Science.gov

Sample records for gap photoluminescence properties

  1. Photoluminescence properties of porous silicon

    NASA Astrophysics Data System (ADS)

    Heben, M. J.; Xiao, Y.; McCullough, J. M.; Tsuo, Y. S.; Pankove, J. I.; Deb, S. K.

    1992-12-01

    A porous silicon (PS) layer can be produced on a crystalline silicon substrate by electrochemical or chemical etching in hydrofluoric acid (HF) solutions. There are many properties that make PS thin films interesting for photovoltaic applications, such as a possible direct band gap that can be adjusted between 1.5 and 1.9 eV, textured surfaces for light trapping, the potential for low cost and large-area fabrication, and the possibility of tandem cell structures with Si. We report the fabrication of large area PS (up to 3` diameter) with quite uniform photoluminescence (PL) properties, and studies of the effects of post-hydrogenation treatments on the intensity and stability of the PL from PS. We have observed that a remote-plasma processing treatment can increase the PL emission intensity from PS prepared under certain conditions by 100 times or more. The emission band is narrower and centered more toward the blue for the remote-plasma processed sample, and the PL emission intensity does not degrade in an air ambient over a period of at least several weeks. This result indicates that PS has the potential to become a stable and useful optoelectronic material.

  2. Degenerate electrical conductive and excitonic photoluminescence properties of epitaxial films of wide gap p-type layered oxychalcogenides, LnCuOCh (Ln=La, Pr and Nd; Ch=S or Se)

    NASA Astrophysics Data System (ADS)

    Hiramatsu, H.; Ueda, K.; Takafuji, K.; Ohta, H.; Hirano, M.; Kamiya, T.; Hosono, H.

    Electrical and photoluminescence properties were investigated for epitaxial films of layered oxychalcogenides, LnCuOCh (Ln=La, Pr, and Nd, Ch=S or Se). Epitaxial films of Mg 10 at.% doped LaCuOS1-xSex are the first demonstration of degenerate conduction with high hole concentration >1020 cm-3 in wide gap p-type semiconductors. Ion substitution varied the excitonic emission energy from 3.21 eV to 2.89 eV while lanthanide and chalcogenide ion substitutions displayed the opposite tendency against cell volume. These unique properties are discussed with respect to the electronic structure originating from the layered crystal structure.

  3. High Photoluminescence Quantum Yield in Band Gap Tunable Bromide Containing Mixed Halide Perovskites.

    PubMed

    Sutter-Fella, Carolin M; Li, Yanbo; Amani, Matin; Ager, Joel W; Toma, Francesca M; Yablonovitch, Eli; Sharp, Ian D; Javey, Ali

    2016-01-13

    Hybrid organic-inorganic halide perovskite based semiconductor materials are attractive for use in a wide range of optoelectronic devices because they combine the advantages of suitable optoelectronic attributes and simultaneously low-cost solution processability. Here, we present a two-step low-pressure vapor-assisted solution process to grow high quality homogeneous CH3NH3PbI3-xBrx perovskite films over the full band gap range of 1.6-2.3 eV. Photoluminescence light-in versus light-out characterization techniques are used to provide new insights into the optoelectronic properties of Br-containing hybrid organic-inorganic perovskites as a function of optical carrier injection by employing pump-powers over a 6 orders of magnitude dynamic range. The internal luminescence quantum yield of wide band gap perovskites reaches impressive values up to 30%. This high quantum yield translates into substantial quasi-Fermi level splitting and high "luminescence or optically implied" open-circuit voltage. Most importantly, both attributes, high internal quantum yield and high optically implied open-circuit voltage, are demonstrated over the entire band gap range (1.6 eV ≤ Eg ≤ 2.3 eV). These results establish the versatility of Br-containing perovskite semiconductors for a variety of applications and especially for the use as high-quality top cell in tandem photovoltaic devices in combination with industry dominant Si bottom cells. PMID:26691065

  4. Synthesis, photoluminescence and magnetic properties of barium vanadate nanoflowers

    SciTech Connect

    Xu, Jing; Hu, Chenguo; Xi, Yi; Peng, Chen; Wan, Buyong; He, Xiaoshan

    2011-06-15

    Graphical abstract: The flower-shaped barium vanadate was obtained for the first time. The photoluminescence and magnetic properties of the barium vanadate nanoflowers were investigated at room temperature. Research highlights: {yields} In the paper, the flower-shaped barium vanadate were obtained for the first time. The CHM method used here is new and simple for preparation of barium vanadate. {yields} The photoluminescence and magnetic properties of the barium vanadate nanoflowers were investigated at room temperature. The strong bluish-green emission was observed. {yields} The ferromagnetic behavior of the barium vanadate nanoflowers was found with saturation magnetization of about 83.50 x 10{sup -3} emu/g, coercivity of 18.89 Oe and remnant magnetization of 4.63 x 10{sup -3} emu/g. {yields} The mechanisms of PL and magnetic property of barium vanadate nanoflowers have been discussed. -- Abstract: The flower-shaped barium vanadate has been obtained by the composite hydroxide mediated (CHM) method from V{sub 2}O{sub 5} and BaCl{sub 2} at 200 {sup o}C for 13 h. XRD and XPS spectrum of the as-synthesized sample indicate it is hexagonal Ba{sub 3}V{sub 2}O{sub 8} with small amount of Ba{sub 3}VO{sub 4.8} coexistence. Scan electron microscope and transmission electron microscope display that the flower-shaped crystals are composed of nanosheets with thickness of {approx}20 nm. The UV-visible spectrum shows that the barium vanadate sample has two optical gaps (3.85 eV and 3.12 eV). Photoluminescence spectrum of the barium vanadate flowers exhibits a visible light emission centered at 492 and 525 nm which might be attributed to VO{sub 4} tetrahedron with T{sub d} symmetry in Ba{sub 3}V{sub 2}O{sub 8}. The ferromagnetic behavior of the barium vanadate nanoflowers has been found with saturation magnetization of about 83.50 x 10{sup -3} emu/g, coercivity of 18.89 Oe and remnant magnetization of 4.63 x 10{sup -3} emu/g, which is mainly due to the presence of a non

  5. Terahertz photoluminescence from S.I.-GaAs by below gap excitation via EL2 level

    SciTech Connect

    Oyama, Yutaka Dezaki, Hikari; Shimizu, Yusaku; Maeda, Kensaku

    2015-01-12

    Terahertz emission by radiative transitions in semi-conductors via shallow impurity states is investigated. We report on the observation of terahertz photoluminescence from S.I.-GaAs by below gap excitation via EL2 level which is located at the center of band gap. In order to investigate the terahertz wave emission mechanisms, the emission spectra and temperature dependence of the emission intensity are evaluated. It is shown that intense terahertz emission from S.I.-GaAs over 120 K is observed due to the thermal recovery of photo-quenched EL2 meta-stable state, and that the emission peak frequency looks to be attributed to the shallow level energy in GaAs.

  6. Efficient Excitonic Photoluminescence in Direct and Indirect Band Gap Monolayer MoS2.

    PubMed

    Steinhoff, A; Kim, J-H; Jahnke, F; Rösner, M; Kim, D-S; Lee, C; Han, G H; Jeong, M S; Wehling, T O; Gies, C

    2015-10-14

    We discuss the photoluminescence (PL) of semiconducting transition metal dichalcogenides on the basis of experiments and a microscopic theory. The latter connects ab initio calculations of the single-particle states and Coulomb matrix elements with a many-body description of optical emission spectra. For monolayer MoS2, we study the PL efficiency at the excitonic A and B transitions in terms of carrier populations in the band structure and provide a quantitative comparison to an (In)GaAs quantum well-structure. Suppression and enhancement of PL under biaxial strain is quantified in terms of changes in the local extrema of the conduction and valence bands. The large exciton binding energy in MoS2 enables two distinctly different excitation methods: above-band gap excitation and quasi-resonant excitation of excitonic resonances below the single-particle band gap. The latter case creates a nonequilibrium distribution of carriers predominantly in the K-valleys, which leads to strong emission from the A-exciton transition and a visible B-peak even if the band gap is indirect. For above-band gap excitation, we predict a strongly reduced emission intensity at comparable carrier densities and the absence of B-exciton emission. The results agree well with PL measurements performed on monolayer MoS2 at excitation wavelengths of 405 nm (above) and 532 nm (below the band gap). PMID:26322814

  7. Photoluminescence characterization of Nd-doped GaP grown by metalorganic chemical vapor deposition

    NASA Astrophysics Data System (ADS)

    Takahei, Kenichiro; Nakagome, Hiroshi

    1992-10-01

    Nd-doped GaP is grown by metalorganic chemical vapor deposition and characterized by photoluminescence measurements. The liquid-helium-temperature luminescence spectra due to Nd intra-4f-shell transitions depend on the growth conditions of the crystals. Some crystals show only a small number of luminescence lines, while some other crystals show many luminescence lines, indicating the presence of many kinds of Nd light emitting centers. Intensities of some luminescence lines begin to decrease at about 50 K and they are below the detection limit at 100 K. However, thermal quenching of some other luminescence lines begins at higher temperatures and their luminescence can be observed up to room temperature. A study on photoexcitation with above- and below-band gap energy photons reveals that some Nd centers can be excited even by below-band gap energy photons, indicating the role of mid-gap levels, in the excitation mechanism, related to the Nd centers. A further comparative study of luminescence characteristics on GaP and GaAs doped with Nd shows that the experimental evidence is consistent with the excitation mechanism proposed for intra-4f-shell luminescence of Yb in InP, where the rare earth 4f shells are excited by way of electron-hole recombination at rare-earth-related trap levels with successive energy transfer.

  8. Photoluminescence properties of S2 molecule trapped in Melanophlogite

    NASA Astrophysics Data System (ADS)

    Messina, Fabrizio; Todaro, Michela; Buscarino, Gianpiero; Vaccaro, Lavinia; Cannas, Marco; Gelardi, Franco M.

    2016-03-01

    We studied the photoluminescence properties of a sample of SiO2-clathrate Melanophlogite, a crystalline microporous material which is found in nature as a rare mineral. Upon β irradiation, the material displays an intense light emission under near-UV illumination. We studied in detail this optical activity by steady-state and time-resolved photoluminescence measurements as a function of temperature. The spectroscopic properties we find can be ascribed to a population of quasi-free molecules trapped within each of the two different types of cage available in the structure of this clathrate, although the spectroscopic properties of the guest molecules are affected by their interactions with the host matrix. Based on the available data, we attribute the observed photoluminescence to trapped S2 molecules, emitting from their excited 3Σ u - or 3Π u electronic states, depending on the cage they are trapped in and on temperature. Our results have an impact on the fundamental understanding of host-guest interactions characteristic of microporous systems such as clathrates. Indeed, the data highlight that even a relatively weak coupling between quasi-free S2 molecules and the two types of cages provided by the Melanophlogite host has a surprisingly complex influence on the optical properties of the guest.

  9. Near-Infrared Photoluminescence Properties of Endohedral Mono- and Dithulium Metallofullerenes.

    PubMed

    Wang, Zhiyong; Izumi, Noriko; Nakanishi, Yusuke; Koyama, Takeshi; Sugai, Toshiki; Tange, Masayoshi; Okazaki, Toshiya; Shinohara, Hisanori

    2016-04-26

    The optical properties of endohedral metallofullerene molecules can be tuned by changing the fullerene size as well as the number of metal atoms inside the fullerene cages. In this work we have synthesized and isolated a series of mono- and dithulium metallofullerenes, including Tm@C82 (isomers I, II, III, IV), Tm@C88 (I-IV), Tm2@C82 (I-III), and (Tm2C2)@C82 (I-III). Near-infrared photoluminescence is observed from the thulium metallofullerenes. By changing the number of Tm ion in the fullerene cage, we have found that one can vary and tune the photoluminescence from 1200 to 1300-2000 nm observed for Tm(2+) (4f(13)) in Tm@C88 and Tm(3+) (4f(12)) in (Tm2C2)@C82, respectively. The photoluminescence intensity depends sensitively on the fullerene cages. (Tm2C2)@C82 (III) exhibits the highest photoluminescence intensity among the three structural isomers because of its large HOMO-LUMO energy gap.

  10. Near-Infrared Photoluminescence Properties of Endohedral Mono- and Dithulium Metallofullerenes.

    PubMed

    Wang, Zhiyong; Izumi, Noriko; Nakanishi, Yusuke; Koyama, Takeshi; Sugai, Toshiki; Tange, Masayoshi; Okazaki, Toshiya; Shinohara, Hisanori

    2016-04-26

    The optical properties of endohedral metallofullerene molecules can be tuned by changing the fullerene size as well as the number of metal atoms inside the fullerene cages. In this work we have synthesized and isolated a series of mono- and dithulium metallofullerenes, including Tm@C82 (isomers I, II, III, IV), Tm@C88 (I-IV), Tm2@C82 (I-III), and (Tm2C2)@C82 (I-III). Near-infrared photoluminescence is observed from the thulium metallofullerenes. By changing the number of Tm ion in the fullerene cage, we have found that one can vary and tune the photoluminescence from 1200 to 1300-2000 nm observed for Tm(2+) (4f(13)) in Tm@C88 and Tm(3+) (4f(12)) in (Tm2C2)@C82, respectively. The photoluminescence intensity depends sensitively on the fullerene cages. (Tm2C2)@C82 (III) exhibits the highest photoluminescence intensity among the three structural isomers because of its large HOMO-LUMO energy gap. PMID:27057619

  11. Enhanced Photoluminescence Properties of Carbon Dots by Doping with Europium.

    PubMed

    Chen, Yuan; Xu, Jiafu; Liu, Bitao; Li, Jiyun; Fang, Xiaomei; Xiong, Liqiong; Peng, Lingling; Han, Tao; Tu, Mingjing

    2016-04-01

    Europium (Eu) doped carbon dots (CDs) were synthesized via a rapid and simple microwave medi- ated method using polyethylene glycol (PEG) as a precursor, and characterized in detail. The results were that these as-prepared CDs showed a uniform and small particle size, and exhibit good pho- tostability and high photoluminescence quantum yields. Additionally, it also found that the doped Eu would change the fluorescence properties, which indicates potential applications in the field of biolabeling. PMID:27451699

  12. Indenopyrans – synthesis and photoluminescence properties

    PubMed Central

    Diac, Andreea Petronela; Ţepeş, Ana-Maria; Soran, Albert; Grosu, Ion; Terec, Anamaria; Roncali, Jean

    2016-01-01

    Summary New indeno[1,2-c]pyran-3-ones bearing different substituents at the pyran moiety were synthesized and their photophysical properties were investigated. In solution all compounds were found to be blue emitters and the trans isomers exhibited significantly higher fluorescence quantum yields (relative to 9,10-diphenylanthracene) as compared to the corresponding cis isomers. The solid-state fluorescence spectra revealed an important red shift of λmax due to intermolecular interactions in the lattice, along with an emission-band broadening, as compared to the solution fluorescence spectra. PMID:27340473

  13. Synthesis, characterization and photoluminescence property of La-doped ZnO nanoparticles

    NASA Astrophysics Data System (ADS)

    Lang, Jihui; Fang, Yue; Zhang, Qi; Wang, Jiaying; Li, Tianshun; Li, Xiuyan; Han, Qiang; Wang, Dandan; Wei, Maobin; Yang, Jinghai

    2016-10-01

    La-doped ZnO nanoparticles were synthesized via a facile and surfactant-free chemical precipitation route, and the effects of lanthanum doping concentration on the structures, morphologies and photoluminescence properties were investigated by XRD, TEM, EDX, PL and UV-Vis absorption spectra. The results showed that the La3+ ions were successfully incorporated into the ZnO host, and the products were well-crystalline. The average size and band gap of La-doped ZnO nanoparticles were varied with the lanthanum doping concentration. The average size of doped nanoparticles was much smaller as compared to that of undoped ZnO. The increasing of lanthanum doping concentration increased the defects in ZnO and resulted in a red shift of UV emission, indicating the narrow band gap in doped nanoparticles. This was probably attributed to the impurity energy levels in band gap introduced by substitutional La3+ ions.

  14. Structural, morphological, optical and photoluminescent properties of spray-deposited ZnSe thin film

    NASA Astrophysics Data System (ADS)

    Lohar, G. M.; Shinde, S. K.; Fulari, V. J.

    2014-11-01

    ZnSe thin films are successfully deposited by spray pyrolysis deposition technique. Deposited thin films are characterized by X-ray diffraction study, and it reveals that spray-deposited ZnSe thin films are polycrystalline with hexagonal crystal structure. Surface morphology is carried out by scanning electron microscopy. It shows cotton-like morphology, and optical properties, such as absorbance, transmittance, reflectance, band gap, refractive index, extinction coefficient are studied. Photoluminescence shows strong emission at 497 nm. Also, spray-deposited ZnSe thin films are hydrophilic in nature, which is shown by contact angle meter.

  15. Leucas aspera mediated multifunctional CeO2 nanoparticles: Structural, photoluminescent, photocatalytic and antibacterial properties.

    PubMed

    Malleshappa, J; Nagabhushana, H; Sharma, S C; Vidya, Y S; Anantharaju, K S; Prashantha, S C; Daruka Prasad, B; Raja Naika, H; Lingaraju, K; Surendra, B S

    2015-01-01

    Spherical shaped cerium dioxide (CeO2) nanoparticles (NPs) were synthesized via bio mediated route using Leucas aspera (LA) leaf extract. The NPs were characterized by PXRD, SEM, UV-Visible techniques. Photoluminescence (PL), photocatalysis and antibacterial properties of NPs were studied. PXRD patterns and Rietveld analysis confirm cubic fluorite structure with space group Fm-3m. SEM results evident that morphology of the NPs was greatly influenced by the concentration of LA leaf extract in the reaction mixture. The band gap energy of the NPs was found to be in the range of 2.98-3.4 eV. The photocatalytic activity of NPs was evaluated by decolorization of Rhodamine-B (RhB) under UVA and Sun light irradiation. CeO2 NPs show intense blue emission with CIE coordinates (0.14, 0.22) and average color coordinated temperature value ∼148,953 K. Therefore the present NPs quite useful for cool LEDs. The superior photocatalytic activity was observed for CeO2 NPs with 20 ml LA under both UVA and Sunlight irradiation. The enhanced photocatalytic activity and photoluminescent properties were attributed to defect induced band gap engineered CeO2 NPs. Further, CeO2 with 20 ml LA exhibit significant antibacterial activity against Escherichia coli (EC) and Staphylococcus aureus (SA). These findings show great promise of CeO2 NPs as multifunctional material for various applications.

  16. Photoluminescence properties of cerium oxide nanoparticles as a function of lanthanum content

    SciTech Connect

    Deus, R.C.; Cortés, J.A.; Ramirez, M.A.; Ponce, M.A.; Andres, J.; Rocha, L.S.R.; and others

    2015-10-15

    Highlights: • CeO{sub 2} nanoparticles were obtained by microwave-hydrothermal method. • Rietveld refinement reveals a cubic structure. • KOH mineralizer agent exhibit weak agglomeration at low temperature and shorter time. - Abstract: The structural and photoluminescent properties at room temperature of CeO{sub 2} and La-doped CeO{sub 2} particles were undertaken. The obtained particles were synthesized by a microwave-assisted hydrothermal method (MAH) under different lanthanum contents. X-ray diffraction (XRD), Fourier transform infrared (FT-IR), Fourier transform Raman (FT-Raman), Ultra-violet spectroscopy (UV–vis) and photoluminescence (PL) measurements were carried out. XRD revealed that the powders are free of secondary phases and crystallize in the cubic structure. Raman data show that increasing La doping content increase oxygen vacancies due to lattice expansion. The UV/vis absorption spectroscopy suggested the presence of intermediate energy levels in the band gap of structurally ordered powders. Lanthanum addition creates oxygen vacancies and shifts the photoluminescence in the low energy range leading to intense PL emission.

  17. Electrospun fluorescein/polymer composite nanofibers and their photoluminescent properties

    NASA Astrophysics Data System (ADS)

    Zhang, Zhi-Hua; Long, Yun-Ze; Yin, Hong-Xin; Sun, Bin; Zheng, Jie; Zhang, Hong-Di; Ji, Xin-Ming; Gu, Chang-Zhi

    2012-09-01

    Fluorescein/polyvinyl pyrrolidone (PVP) composite nanofibers with different fluorescein loadings (with a weight concentration of 0-5.0%) are fabricated via electrospinning. Morphologies, structures and photoluminescent (PL) properties of these straight, helical or wavelike fibers are characterized by scanning electron microscopy (SEM), fluorescence microscopy and a spectrophotometer. It is found that the maximum emission of the as-spun fluorescein/PVP fibers occurs at 510 nm. The PL intensity of the composite fiber increases with fluorescein concentration, then fluorescence quenching appears when the concentration reaches 1.67%. The mechanism of fluorescence quenching of fluorescein is discussed. In addition, the composite fibers exhibit a much stronger PL intensity than fluorescein/PVP bulk film owing to larger specific surface area, which makes them promising materials for biomedical applications such as probes and sensors.

  18. Photoluminescence properties of Mg-doped InN nanowires

    SciTech Connect

    Zhao, Songrui; Liu, Xuedong; Mi, Zetian

    2013-11-11

    In this work, photoluminescence (PL) properties of nearly defect-free Mg-doped InN nanowires were investigated in detail. The low-doped sample exhibits two PL emission peaks up to 152 K, which can be ascribed to the band-to-band recombination and the Mg-acceptor energy level related recombination, respectively. For the high-doped sample, the Mg-acceptor energy level related transition dominates. Detailed power dependent PL studies further indicate that the Mg-acceptor energy level related PL emission is due to the donor-acceptor pair recombination process, which subsequently evolves into the free-to-acceptor recombination with increasing temperature.

  19. Synthesis and photoluminescent and nonlinear optical properties of manganese doped ZnS nanoparticles

    NASA Astrophysics Data System (ADS)

    Nazerdeylami, Somayeh; Saievar-Iranizad, Esmaiel; Dehghani, Zahra; Molaei, Mehdi

    2011-01-01

    In this work we synthesized ZnS:Mn 2+ nanoparticles by chemical method using PVP (polyvinylpyrrolidone) as a capping agent in aqueous solution. The structure and optical properties of the resultant product were characterized using UV-vis optical spectroscopy, X-ray diffraction (XRD), photoluminescence (PL) and z-scan techniques. UV-vis spectra for all samples showed an excitonic peak at around 292 nm, indicating that concentration of Mn 2+ ions does not alter the band gap of nanoparticles. XRD patterns showed that the ZnS:Mn 2+ nanoparticles have zinc blende structure with the average crystalline sizes of about 2 nm. The room temperature photoluminescence (PL) spectrum of ZnS:Mn 2+ exhibited an orange-red emission at 594 nm due to the 4T 1- 6A 1 transition in Mn 2+. The PL intensity increased with increase in the Mn 2+ ion concentration. The second-order nonlinear optical properties of nanoparticles were studied using a continuous-wave (CW) He-Ne laser by z-scan technique. The nonlinear refractive indices of nanoparticles were in the order of 10 -8 cm 2/W with negative sign and the nonlinear absorption indices of these nanoparticles were obtained to be about 10 -3 cm/W with positive sign.

  20. Impact of oxygen bonding on the atomic structure and photoluminescence properties of Si-rich silicon nitride thin films

    SciTech Connect

    Nguyen, P. D.; Sunding, M. F.; Vestland, L. O.; Finstad, T. G.; Olsen, A.; Kepaptsoglou, D. M.; Ramasse, Q. M.

    2012-10-01

    The atomic structure and optical properties of Si-rich silicon nitride thin films have been for decades the subject of intense research, both theoretically and experimentally. It has been established in particular that modifying the chemical composition of this material (e.g., the Si excess concentration) can lead to dramatic differences in its physical, optical, and electrical properties. The present paper reports on how the incorporation of oxygen into silicon nitride networks influences their chemical bonding and photoluminescence properties. Here, by using a combination of analytical scanning transmission electron microscopy and x-ray photoelectron spectroscopy it is demonstrated that the structure of Si-rich silicon nitride with low O content can be described by the co-existence of Si nanocrystals in a Si{sub 3}N{sub 4} matrix, with occasional localized nano-regions of a Si{sub 2}ON{sub 2} phase, depending on the amount of excess Si. Furthermore, it is shown that the structure of silicon nitride with high O content can be adequately described by a so-called random bonding model, according to which the material consists in bonded networks of randomly distributed tetrahedral SiO{sub x}N{sub 4-x} (where x = 0, 1, 2, 3, and 4). Photoluminescence measurements indicate that the effect of O is to introduce a gap state in the band gap of Si{sub 3}N{sub 4} matrix. When a large amount of O is introduced, on the other hand, the photoluminescence measurements are in agreement with a shifted conduction band minimum in the dielectric. For both cases (high and low O content), Si dangling bonds were found to give rise to the deep level in the band gap of the nitride matrix, causing the dominant emission band in the photoluminescence of the films.

  1. Temperature dependence of photoluminescence properties in a thermally activated delayed fluorescence emitter

    SciTech Connect

    Niwa, Akitsugu; Kobayashi, Takashi Nagase, Takashi; Naito, Hiroyoshi; Goushi, Kenichi; Adachi, Chihaya

    2014-05-26

    Using steady-state and time-resolved photoluminescence (PL) spectroscopy, we have investigated the temperature dependence of PL properties of 1,2,3,5-tetrakis(carbazol-9-yl)-4,6-dicyano-benzene (4CzIPN), which have a small energy gap between its singlet and triplet excited states and thus exhibits efficient thermally activated delayed fluorescence [H. Uoyama et al., Nature 492, 235 (2012)]. Below around 100 K, PL quantum efficiency of 4CzIPN thin films is largely suppressed and strong photoexcitation intensity dependence appears. These features can be explained by using rate equations for the densities of singlet and triplet excited states considering a triplet-triplet annihilation process.

  2. Effect of TEA on photoluminescence properties of PbS nanocrystalline thin films

    NASA Astrophysics Data System (ADS)

    Tohidi, Tavakkol; Jamshidi-Ghaleh, Kazem

    2015-03-01

    In this work, the PbS nanocrystalline thin films were prepared by chemical bath deposition method on the glass and unpolished Si(100) substrates. Triethanolamine was used as additive in the aqueous solution, which resulted in the enhancement of the luminescence of nanocrystalline PbS thin films. The introduction of triethanolamine reduced the grain size and increased the optical band gap of the PbS nanoparticles. The crystalline size of PbS films deposited at two different bath temperatures of 25 °C (PbS-25) and 40 °C (PbS-40) and at different deposition times was estimated to be around 5-50 nm by XRD analyses. The films at 60 °C (PbS-60) were prepared and studied. The structural, morphological and optical properties of the obtained films were investigated. The energy-dispersive X-ray of the typical PbS film was presented, which confirmed the formation of PbS. The mechanism of growth of the PbS crystallites at different bath temperatures was described. The confinement was reflected in absorption and photoluminescence spectra. The variation of the photoluminescence intensity of PbS nanocrystals with triethanolamine molarity, deposition time and bath temperature was investigated. The PbS thin films were found to exhibit PL in both the ultraviolet and visible regions via quantum size effects, surface states and excitation wavelength variation. The luminescence of Si(100) substrate and PbS nanocrystalline films deposited on Si(100) were compared, and the results revealed that the PbS nanocrystals altered and notably enhanced the emission features of the Si(100) substrate. The multi-peak fitting using Gaussian function was employed for the photoluminescence spectrum of PbS on Si(100) substrate.

  3. Photoluminescence Properties Research on Graphene Quantum Dots/Silver Composites.

    PubMed

    Wang, Jun; Li, Yan; Zhang, Bo-Ping; Xie, Dan-Dan; Ge, Juan; Liu, Hui

    2016-04-01

    Graphene quantum dots (GQDs) possess unique properties of graphene and exhibit a series of new phenomena of 0 dimension (D) carbon materials. Thus, GQDs have attracted much attention from researchers and have shown great promise for many applications. Recently, many works focus on GQDs-metal ions and metal nanoparticles (NPs). Although, many researches point out that metal ions and metal NPs have significant effect on photoluminescence (PL) feature of GQDs, mainly focus on PL intensity. Here, for the first time, we reported that metal NPs also affected PL peak position which was dependent on the mix mechanism of metal and GQDs. When GQDs-silver (Ag) composite mixed by physical method and excited at a wavelength of 320 nm, PL peak position of composites first showed blue-shifted then red-shifted with increasing of Ag content. However, if GQDs-Ag composite prepared by chemical method, PL peak position of the composites blue-shifted. Furthermore, the shift of PL peak position of GQDs-Ag prepared both for physical and chemical method displayed excitation-dependent feature. When the excitation wavelength approached to Ag SPR peaks, no obvious PL shift was observed. The mechanism for different PL shifts and the phenomenon of excitation-dependent PL shift as well as the formation mechanism of GQDs-Ag composite by chemical method are discussed in detail in this paper. PMID:27451653

  4. Photoluminescence properties and exciton dynamics in monolayer WSe{sub 2}

    SciTech Connect

    Yan, Tengfei; Qiao, Xiaofen; Liu, Xiaona; Tan, Pingheng; Zhang, Xinhui

    2014-09-08

    In this work, comprehensive temperature and excitation power dependent photoluminescence and time-resolved photoluminescence studies are carried out on monolayer WSe{sub 2} to reveal its properties of exciton emissions and related excitonic dynamics. Competitions between the localized and delocalized exciton emissions, as well as the exciton and trion emissions are observed, respectively. These competitions are suggested to be responsible for the abnormal temperature and excitation intensity dependent photoluminescence properties. The radiative lifetimes of both excitons and trions exhibit linear dependence on temperature within the temperature regime below 260 K, providing further evidence for two-dimensional nature of monolayer material.

  5. Photoluminescence properties of Jahn-Teller transition-metal ions

    NASA Astrophysics Data System (ADS)

    Sanz-Ortiz, Marta N.; Rodríguez, Fernando

    2009-09-01

    This work investigates the influence of electron-phonon coupling associated with E ⊗e and T ⊗e Jahn-Teller (JT) effect in different transition-metal (TM) ions on de-excitation phenomena through nonradiative multiphonon relaxation, i.e., photoluminescence (PL) quenching. We developed a configurational curve model which is able to predict from the absorption spectrum whether a given JT-TM ion is PL or quenched. The prediction is made on the basis of an adapted Dexter-Klick-Russell parameter for JT systems, defined in terms of spectroscopic parameters through ΛJT=αΔeabs/Eabs, where Δeabs refers to the splitting of the parent octahedral Eg states by the JT distortion in E ⊗e (α =3/4) or T ⊗e (α =1/4), and Eabs is the energy of the first absorption band involving electronic transition between Eg and T2g. We show that PL in any JT-TM ion occurs whenever ΛJT<0.1 or is quenched if ΛJT>0.2. This result is noteworthy since it allows us to establish structural requirements for the JT-TM ion and the host crystal to be PL. Although PL properties of materials containing TM ions depend on a variety of structural factors such as the electronic configuration, the site symmetry, and the crystal field produced by neighboring atoms, the present model achieves this goal through a simple spectroscopic parameter: ΛJT. In this work we correlated the PL properties of different sixfold-coordinated JT systems such as Ti3+, Cu2+, Mn3+, Cr2+, Fe2+, Co3+, and Ni3+ in halides and oxides with ΛJT obtained from their respective absorption spectra. From this analysis we conclude that depending on the nature of the JT coupling and its strength, PL is either strongly favored or quenched in T ⊗e while it is mostly quenched in E ⊗e systems due to the larger JT distortion.

  6. Properties of Zn-doped GaN. I - Photoluminescence

    NASA Technical Reports Server (NTRS)

    Pankove, J. I.; Berkeyheiser, J. E.; Miller, E. A.

    1974-01-01

    It is shown that zinc in gallium nitride forms an efficient radiative center emitting blue light at 2.86 plus or minus 0.02 eV and acts as a deep acceptor that can render the crystal insulating. A systematic variation of growth conditions indicates that an optimization of the photoluminescence efficiency is possible. Under nonoptimal conditions lower photon energy emission is obtained.

  7. Phosphorus and boron codoping of silicon nanocrystals by ion implantation: Photoluminescence properties

    NASA Astrophysics Data System (ADS)

    Nakamura, Toshihiro; Adachi, Sadao; Fujii, Minoru; Miura, Kenta; Yamamoto, Shunya

    2012-01-01

    The photoluminescence (PL) properties of P or B single-doped Si nanocrystals (Si-nc's) and P and B co-doped Si-nc's are studied. In the single-doped Si-nc samples, PL quenching occurs as a result of the Auger nonradiative recombination process between the photoexcited excitons and free carriers supplied by doped impurities. In the (P, B) co-doped sample, on the other hand, the donor-acceptor (D-A)-pair recombination emission is clearly observed on the long-wavelength side of the intrinsic Si-nc emission peak at ˜900 nm. The D-A-pair recombination energy is found to be smaller than the band-gap energy of bulk Si and is strongly dependent on the number of P and B impurities doped in a Si-nc. PL spectra are measured at 50 and 300 K and found to indicate that strong thermal quenching occurs in a (P, B) co-doped sample at 300 K. This quenching effect is probably because of carrier migration among the donor and acceptor states. The PL decay rate is determined as a function of the emitted-light wavelength for the pure and (P, B) co-doped Si-nc samples.

  8. Synthesis of ZnO flowers and their photoluminescence properties

    SciTech Connect

    Wu Changle; Qiao Xueliang Luo Langli; Li Haijun

    2008-07-01

    Flower-like ZnO nano/microstructures have been synthesized by thermal treatment of Zn(NH{sub 3}){sub 4}{sup 2+} precursor in aqueous solvent, using ammonia as the structure directing agent. A number of techniques, including X-ray diffraction (XRD), field emission scan electron microscopy (FESEM), transmission electron microscopy (TEM), thermal analysis, and photoluminescence (PL) were used to characterize the obtained ZnO structures. The photoluminescence (PL) measurements indicated that the as-synthesized ZnO structures showed UV ({approx}375 nm), blue ({approx}465 nm), and yellow ({approx}585 nm) emission bands when they were excited by a He-Gd laser using 320 nm as the excitation source. Furthermore, it has been interestingly found that the intensity of light emission at {approx}585 nm remarkably decreased when the obtained ZnO nanocrystals were annealed at 600 deg. C for 3 h in air. The reason might be the possible oxygen vacancies and interstitials in the sample decreased at high temperature.

  9. Plasmonically-enhanced mid-infrared photoluminescence in a metal/narrow-gap semiconductor structure

    NASA Astrophysics Data System (ADS)

    Lu, Pengqi; Cai, Chunfeng; Zhang, Bingpo; Liu, Bozhi; Wu, Huizhen; Bi, Gang; Si, Jianxiao

    2016-05-01

    We report the enhancement of the mid-infrared (MIR) luminescence intensity in a nanoscale metal/semiconductor structure by the coupling of surface plasmon polaritons (SPPs) with excitons in a narrow-gap semiconductor. The SPPs are efficiently excited by the total internal reflection photons at a metal/semiconductor interface. The intense electric field induced by SPPs, in turn, greatly changes the radiative recombination rates of the excitons generated by the pumping laser and thus the MIR luminescence intensity. The finding avails the understanding of fundamental science of SPs in narrow-gap semiconductors and the development of novel MIR devices.

  10. Photoluminescence properties of cadmium-selenide quantum dots embedded in a liquid-crystal polymer matrix

    SciTech Connect

    Tselikov, G. I. Timoshenko, V. Yu.; Plenge, J.; Ruehl, E.; Shatalova, A. M.; Shandryuk, G. A.; Merekalov, A. S.; Tal'roze, R. V.

    2013-05-15

    The photoluminescence properties of cadmium-selenide (CdSe) quantum dots with an average size of {approx}3 nm, embedded in a liquid-crystal polymer matrix are studied. It was found that an increase in the quantum-dot concentration results in modification of the intrinsic (exciton) photoluminescence spectrum in the range 500-600 nm and a nonmonotonic change in its intensity. Time-resolved measurements show the biexponential decay of the photoluminescence intensity with various ratios of fast and slow components depending on the quantum-dot concentration. In this case, the characteristic lifetimes of exciton photoluminescence are 5-10 and 35-50 ns for the fast and slow components, respectively, which is much shorter than the times for colloidal CdSe quantum dots of the same size. The observed features of the photoluminescence spectra and kinetics are explained by the effects of light reabsorption, energy transfer from quantum dots to the liquid-crystal polymer matrix, and the effect of the electronic states at the CdSe/(liquid crystal) interface.

  11. Role of plastic deformation mechanisms in the formation of nanostructured silicon and its photoluminescent properties

    NASA Astrophysics Data System (ADS)

    Kulinich, O. A.

    2012-06-01

    The role of plastic deformation mechanisms in the process of obtaining nanostructured silicon layers is demonstrated. The process of obtaining nanostructured silicon consists in growing of silicon oxide layers of various thicknesses on the silicon wafer surface, their subsequent removal, and treatment by selective chemical etchants (SE) before the formation of defectless silicon islands possessing the photoluminescent properties typical of nanostructured silicon. Based on analysis of the photoluminescence intensity spectra of nanostructured silicon islands, the conclusion is drawn on different plastic deformation mechanisms at different thicknesses of thermally grown silicon oxide. Possible mechanisms of displacement of the intensity maximum in the photoluminescence (PL) spectrum toward shorter wavelengths with decreasing nanostructured silicon island sizes are discussed.

  12. Photoluminescence Properties of Sn-Related Donor State in AlxGa1-xAs

    NASA Astrophysics Data System (ADS)

    Kang, Junyong; Iida, Seishi; Huang, Qisheng; Fukuda, Tsuguo

    1993-08-01

    We have investigated the near-gap recombinations in Sn-doped AlxGa1-xAs by photoluminescence. By analyzing the variations of spectral lineshapes under various excitation intensities, only one type of recombination was assigned to associate with the Sn-related donor state, which was different from the hydrogenlike shallow donor states and the DX centers. Phonon replicas were observed to accompany the recombination in the samples with high AlAs mole fractions of direct gaps, as well as in those of indirect gaps. The Franck-Condon shift and the phonon energy of the recombination were found to increase with increasing AlAs mole fraction. This behavior was explained in terms of a variation of local lattice distortion around an ionized Sn-related donor and a weighted average of two local vibrational mode frequencies of the Sn-related donor.

  13. Band-gap narrowing in Mn-doped GaAs probed by room-temperature photoluminescence

    NASA Astrophysics Data System (ADS)

    Prucnal, S.; Gao, K.; Skorupa, I.; Rebohle, L.; Vines, L.; Schmidt, H.; Khalid, M.; Wang, Y.; Weschke, E.; Skorupa, W.; Grenzer, J.; Hübner, R.; Helm, M.; Zhou, S.

    2015-12-01

    The electronic band structure of the (Ga,Mn)As system has been one of the most intriguing problems in solid state physics over the past two decades. Determination of the band structure evolution with increasing Mn concentration is a key issue to understand the origin of ferromagnetism. Here, we present room-temperature photoluminescence and ellipsometry measurements of G a100 %-xM nxAs alloy. The upshift of the valence band is proven by the redshift of the room temperature near band-gap emission from the G a100 %-xM nxAs alloy with increasing Mn content. It is shown that even a doping by 0.02% of Mn affects the valence-band edge, and it merges with the impurity band for a Mn concentration as low as 0.6%. Both x-ray diffraction pattern and high-resolution cross-sectional transmission electron microscopy images confirmed full recrystallization of the implanted layer and GaMnAs alloy formation.

  14. Carbon nanoparticle ionic liquid hybrids and their photoluminescence properties.

    PubMed

    Wei, Ying; Liu, Yang; Li, Haitao; He, Xiaodie; Zhang, Qingguo; Kang, Zhenhui; Lee, Shuit-Tong

    2011-06-01

    A fluorescent carbon nanoparticle ionic liquid hybrids (CNPIL) with high conductivity is synthesized by a facile one-step microwave method from ionic liquid 1-butyl-3-methylimidazolium glutamine salt and Glucose. This CNPIL exhibits excellent PL properties: bright and colorful PL covering the entire visible-NIR spectral range, up conversion PL properties, pH dependent and can be controlled by the reaction condition.

  15. Microwave Synthesis, Characterization, and Photoluminescence Properties of Nanocrystalline Zirconia

    PubMed Central

    Singh, A. K.; Nakate, Umesh T.

    2014-01-01

    We report synthesis of ZrO2 nanoparticles (NPs) using microwave assisted chemical method at 80°C temperature. Synthesized ZrO2 NPs were calcinated at 400°C under air atmosphere and characterized using FTIR, XRD, SEM, TEM, BET, and EDS for their formation, structure, morphology, size, and elemental composition. XRD results revealed the formation of mixed phase monoclinic and tetragonal ZrO2 phases having crystallite size of the order 8.8 nm from most intense XRD peak as obtained using Scherrer formula. Electron microscope analysis shows that the NPs were less than 10 nm and highly uniform in size having spherical morphology. BET surface area of ZrO2 NPs was found to be 65.85 m2/g with corresponding particle size of 16 nm. The band gap of synthesized NPs was found to be 2.49 eV and PL spectra of ZrO2 synthesized NPs showed strong peak at 414 nm, which corresponds to near band edge emission (UV emission) and a relatively weak peak at 475 and 562 nm. PMID:24578628

  16. Photoluminescence and electro-optic properties of small (25-35 nm diameter) quantum boxes

    NASA Astrophysics Data System (ADS)

    Davis, L.; Ko, K. K.; Li, W.-Q.; Sun, H. C.; Lam, Y.; Brock, T.; Pang, S. W.; Bhattacharya, P. K.; Rooks, M. J.

    1993-05-01

    The luminescence and electro-optic properties of buried 25-35 nm quantum boxes have been measured. The quantum boxes were defined by a combination of molecular beam epitaxial growth and regrowth, electron beam lithography, and dry etching. The photoluminescence from 35 nm boxes shows a blue shift of about 15 meV compared to the bulk luminescence and an enhancement, taking into account the fill factor. An enhanced effective linear electrooptic coefficient is observed for the quantum boxes.

  17. XAFS Study on Ag2S Semiconductor Clusters Designed in Nanopores and Their Photoluminescence Properties

    SciTech Connect

    Yuan, Shuai; Tomonari, Masanori; Matsuo, Daisuke; Mori, Kohsuke; Ohmichi, Tetsutaro; Katayama, Iwao; Yamashita, Hiromi

    2007-02-02

    Ag2S clusters were prepared in microporous ZSM-5 and mesoporous AlMCM-41. The state of Ag was analyzed by EXAFS. The pore size of the host has great effects on the photoluminescence property of Ag2S. Compared with Ag2S/ZSM-5, the emission of Ag2S/AlMCM-41 shifts to the longer wavelength region.

  18. Photoluminescent properties of SPAN-80 coated intrinsic and extrinsic ZnO nanostructures

    NASA Astrophysics Data System (ADS)

    Kavita; Kumar, Dinesh; Singh, Karamjit; Kumar, Sunil; Bhatti, H. S.

    2016-05-01

    Semiconductor nanostructures catch the attention due to morphology tunable properties. SPAN-80-Capped intrinsic and extrinsic ZnO nanostructures have been synthesized by the simple wet-chemical synthesis route. Structural behavior (morphology and crystallography) and photoluminescence performance of synthesized nanomaterials have been explored as a function of variable SPAN-80 concentration (0.05-0.125%). Crystallographic studies reveal that the prepared products possess wurtzite structure. Electron microscopy infers that the quantum dots are bunched together to form multifaceted morphology for 0.05% SPAN-80 concentration, whereas rectangular shape has been observed for extreme capping concentration. Photoluminescence properties have affected drastically with the introduction of SPAN-80 during the precipitation reaction. Photoluminescent properties of the synthesized nanostructures are strongly dependent on SPAN-80 concentration. Augmentation of capping concentration from 0.05% to 0.075% diminishes the luminescence quantum yield due to increased surface passivation whereas further addition of capping agent beyond the optimum capping concentration (0.075%) enhances the PL intensity due to increased energy transfer from capping shell to the nanostructure core.

  19. Nanoparticle shape anisotropy and photoluminescence properties: Europium containing ZnO as a Model Case

    NASA Astrophysics Data System (ADS)

    Gerigk, Melanie; Ehrenreich, Philipp; Wagner, Markus R.; Wimmer, Ilona; Reparaz, Juan Sebastian; Sotomayor Torres, Clivia M.; Schmidt-Mende, Lukas; Polarz, Sebastian

    2015-10-01

    against doping than others. Focus was then set on the incorporation of Eu3+ inside the ZnO particles, and it was shown that nanocrystal shape and aspect ratios could be adjusted while maintaining a fixed dopant level. Special PL properties could be observed implying energy transfer from ZnO excited near its band-gap (3.3 eV) to the Eu3+ states mediated by defect luminescence of the nanoparticles. Indications for an influence of shape on photoluminescence (PL) properties were found. Finally, rod-like Eu@ZnO colloids were used as tracers to investigate their uptake into biological samples like HeLa cells. The PL was sufficient for identifying green and red emission under visible light excitation. Electronic supplementary information (ESI) available: ESI-1: Pure ZnO nanorods prepared via the emulsion-based method. ESI-2: Additional analytical data for different M@ZnO particles grown for χM = 0.03% and χM = 0.7%. ESI-3: Proposed effect of cations on the growth of ZnO nanorods. ESI-4: Additional data for differently shaped particles. ESI-5: Additional analytical data for the different Eu@ZnO particles grown for different Eu3+ concentration. ESI-6: Eu@ZnO nanorods with different length. ESI-7: HRTEM analysis of Eu@ZnO. ESI-8: XPS and EPR spectroscopy performed on Eu@ZnO nanorods. ESI-9: Micro-Raman comparison between ZnO and Eu@ZnO nanorods. ESI-10: Additional PL data for Eu@ZnO. See DOI: 10.1039/c5nr02550h

  20. Preparation and photoluminescence properties of Sm3+-doped ZrO2 nanotube arrays

    NASA Astrophysics Data System (ADS)

    Fu, Ning; Wang, Xixin; Ma, Yuanhui; Wang, Mingli; Li, Jiaxin; Zhao, Jianling

    2016-04-01

    Zr-Sm (3 at.% Sm) alloy was prepared through a powder metallurgical method. Sm3+-doped ZrO2 nanotube arrays have been achieved directly by anodizing the Zr-Sm alloy. The effects of electrolyte and annealing temperature on the morphologies and structures of the nanotube arrays were studied. The photoluminescence properties of Sm3+-doped ZrO2 nanotube arrays prepared in aqueous solution and formamide  +  glycerol solution were studied in detail as well. Results show that tetragonal ZrO2 promoted the photoluminescence efficiency of this system. Under excitation at 407 nm, the sample prepared in aqueous solution annealed at 600 °C displayed the strongest emission peak at 571 nm, corresponding to the 4G5/2  →  6H5/2 samarium transition.

  1. Photoluminescence and radiation response properties of Ce3+-doped CsCaCl3 crystalline scintillator

    NASA Astrophysics Data System (ADS)

    Fujimoto, Yutaka; Saeki, Keiichiro; Tanaka, Hironori; Yahaba, Takuma; Yanagida, Takayuki; Koshimizu, Masanori; Asai, Keisuke

    2016-09-01

    In this paper, we report on the photoluminescence and scintillation properties of a newly developed CsCaCl3:Ce (0.5 mol%) crystalline scintillator grown by the vertical Bridgman method. The fluorescence quantum efficiency for the Ce3+ characteristic emission bands centered at around 350–400 nm was 76% under excitation at 330 nm light. The photoluminescence decay time of the Ce3+ was approximately 32 ns. When x-ray excited the crystal, intense emission bands were observed at 350–400 nm, and could be attributed to the Ce3+ emission. The scintillation light yield of the developed crystal was ∼7600 ph MeV‑1 compared to a NaI:Tl commercial scintillator, and the principal scintillation decay time was approximately 340 ns plus two fast components of around 1.6 ns and 45 ns.

  2. Photoluminescence and radiation response properties of Ce3+-doped CsCaCl3 crystalline scintillator

    NASA Astrophysics Data System (ADS)

    Fujimoto, Yutaka; Saeki, Keiichiro; Tanaka, Hironori; Yahaba, Takuma; Yanagida, Takayuki; Koshimizu, Masanori; Asai, Keisuke

    2016-09-01

    In this paper, we report on the photoluminescence and scintillation properties of a newly developed CsCaCl3:Ce (0.5 mol%) crystalline scintillator grown by the vertical Bridgman method. The fluorescence quantum efficiency for the Ce3+ characteristic emission bands centered at around 350-400 nm was 76% under excitation at 330 nm light. The photoluminescence decay time of the Ce3+ was approximately 32 ns. When x-ray excited the crystal, intense emission bands were observed at 350-400 nm, and could be attributed to the Ce3+ emission. The scintillation light yield of the developed crystal was ˜7600 ph MeV-1 compared to a NaI:Tl commercial scintillator, and the principal scintillation decay time was approximately 340 ns plus two fast components of around 1.6 ns and 45 ns.

  3. Investigation on the structural and photoluminescent properties of chromium-doped ceramics cordierite

    NASA Astrophysics Data System (ADS)

    da Silva, M. A. F. M.; Pedro, S. S.; López, A.; Sosman, L. P.

    2016-10-01

    This work presents the investigation about the structural and optical properties of a doped-chromium system containing cordierite (Mg2Al4Si5O18) as main phase. The sample composition and the structural data were obtained from X-ray diffraction (XRD) measurements and the results were analyzed by Rietveld method. Photoluminescence (PL) spectra under several excitation wavelengths and photoluminescence excitation (PLE) measurements were performed. The obtained results from PL and PLE experiments are evidences that Cr3+ occupies octahedral sites in this ceramic system. By correlating the optical results, the crystal field parameter (Dq) and Racah interelectronic repulsion parameters (B and C) were calculated and discussed according to the Tanabe-Sugano (TS) theory for d3 transition metals in octahedral sites.

  4. Temperature-dependent photoluminescence properties of quaternary ZnAgInS quantum dots.

    PubMed

    Zhou, Ping; Zhang, Xiaosong; Liu, Xiaojuan; Xu, Jianping; Li, Lan

    2016-08-22

    A series of ZnAgInS (ZAIS) quantum dots were synthesized and their optical properties were tuned by adjusting the reaction times from 5 to 30 min. The emission spectra were observed ranging from 619 to 667 nm. The temperature-dependent photoluminescence properties of ZAIS QDs were investigated from 10 K to 300 K that show a blue shift of spectra line with increasing intensity as well as broadening of spectral line owing to the coupling of the carrier to acoustic phonon. We have also discussed and investigated the internal luminescence mechanism of ZAIS QDs. PMID:27557228

  5. Synthesis, Characterization and its Photoluminescence Properties of Group I-III-VI2 CuInS2 nanocrystals

    NASA Astrophysics Data System (ADS)

    Oda, Masaru; Miyaoka, Tomotari; Yamada, Shuhei; Tani, Toshiro

    We report the synthesis, characterization, and photoluminescence (PL) properties of colloidal I-III-VI2 CuInS2 and CuInS2/ZnS nanocrystals (NCs). Absorption shoulder and PL bands of the NCs are located at higher energy than those of band gap energy of bulk crystals due to a quantum-confinement effect. The PL band has a relatively large Stokes-shift, broad linewidth, and long decay-time, which suggests that the PL originates from a recombination of confined-excitions associated with donor(s) and/or acceptor(s). We found that quantum yield of the PL depends strongly on the photon-energy of excitation light and that it is up to 40-50% in resonant excitation at the energy positions corresponding to the absorption shoulder. Detailed properties and possible dynamics will be described. We also present preliminary results of PL properties focused on single NCs. There exist highluminescent NCs exhibiting so-called PL blinking as similar with II-VI NCs, while the others are dark NCs. 73.21.La, 78.47.jd, 78.67.Bf, 78.67.Hc

  6. Effects of rapid thermal annealing conditions on GaInNAs band gap blueshift and photoluminescence intensity

    SciTech Connect

    Liverini, V.; Rutz, A.; Keller, U.; Schoen, S.

    2006-06-01

    We have studied the effects of various conditions of rapid thermal annealing (RTA) on 10 nm GaInNAs/GaAs single quantum wells (SQWs) with fixed indium concentration and increasing nitrogen content to obtain photoluminescence (PL) in the telecom wavelength regime of 1.3 and 1.5 {mu}m. Specifically, we analyzed the results of annealing for a fixed short time but at different temperatures and for longer times at a fixed temperature. In all experiments, InGaAs SQWs with the same In concentration were used as references. For both RTA conditions, the well-known blueshift of the band gap energy and the PL intensity improvement show trends that reveal that these are unrelated effects. At high RTA temperatures the PL efficiency reaches a maximum and then drops independently of N content. On the contrary, the blueshift experiences a rapid increase up to 700 deg. C (strong blueshift regime) and it saturates above this temperature (weak blueshift regime). Both these blueshift regimes are related to the nitrogen content in the SQWs but in different ways. In the strong blueshift regime, we could obtain activation energy for the blueshift process in the range of 1.25 eV, which increases with N content. Analysis with high-resolution x-ray diffraction (HRXRD) shows that the blueshift experienced in this regime is not due to a stoichiometric change in the QW. In the weak blueshift regime, the blueshift, which is only partly due to In outdiffusion, saturates more slowly the higher the N content. Annealing at the same temperature (600 deg. C) for a longer time shows that the blueshift saturates earlier than the PL intensity and that samples with higher nitrogen experience a larger blueshift. Only a small In outdiffusion for annealing at high temperatures (>650 deg. C) and long duration was observed. However, this modest stoichiometric change does not explain the large blueshift experienced by the GaInNAs SQWs. We conclude that the mechanism responsible for the drastic blueshift after

  7. Transmission properties of frequency selective structures with air gaps

    NASA Astrophysics Data System (ADS)

    Meng, Zhi-Jun; Wang, Li-Feng; Lü, Ming-Yun; Wu, Zhe

    2010-12-01

    The transmission properties of compound frequency selective structures with dielectric slab and air gaps were investigated by computation and experimentation. Mechanism analyses were also carried out. Results show that the air gaps have a distinct influence on the transmission properties. Resonant frequency of the structure would increase rapidly when the air gap appears. After the gap gets larger to a specific value, generally 1/5 wavelength corresponding to the resonant frequency, the transmission properties would change periodically with the gap thickness. The change of transmission properties in one period has a close relationship with the dielectric thickness. These results provide a new method for designing a bandpass radome of large incidence angle and low loss with the concept of stealth shield radome.

  8. Hydrothermal synthesis, crystal structures and photoluminescence properties of mixed europium-yttrium organic frameworks

    NASA Astrophysics Data System (ADS)

    Han, Yinfeng; Fu, Lianshe; Mafra, Luís; Shi, Fa-Nian

    2012-02-01

    Three mixed europium-yttrium organic frameworks: Eu2-xYx(Mel)(H2O)6 (Mel=mellitic acid or benzene-1,2,3,4,5,6-hexacarboxylic acid, x=0.38 1, 0.74 2, and 0.86 3) have been synthesized and characterized. All the compounds contain a 3-D net with (4, 8)-flu topology. The study indicates that the photoluminescence properties are effectively affected by the different ratios of europium and yttrium ions, the quantum efficiency is increased and the Eu3+ lifetime becomes longer in these MOFs than those of the Eu analog.

  9. Modification of Photoluminescence Properties of ZnO Island Films by Localized Surface Plasmons

    NASA Astrophysics Data System (ADS)

    Zhang, Yang; Li, Xue-Hong; Peng, Cheng-Xiao

    2012-10-01

    The modification of localised surface plasmons of photoluminescence properties of ZnO is studied. It is found that the ultraviolet emission is drastically enhanced, and the visible emission related to the defects is almost completely suppressed, after an Au layer of nanoparticles is deposited on the surface of ZnO island films. This pronounced change in PL spectra is attributed to the efficient electron transfer via the coupling of localised surface plasmons at the interface between the Au nanoparticle layer and ZnO films.

  10. Synthesis and Photoluminescent Properties of Eu²⁺-Doped BaSiF₆ Nanoparticles.

    PubMed

    Zhao, Xin; Hua, Ruinian; Zhang, Wei; Zhao, Jun; Tang, Dongxin; Sun, Zhengang

    2016-01-01

    By adjusting the molar ratio of oleic acid (OA), oleylamine (OM), and 1-octadecene (OD) ligands in reaction solution, Eu²⁺-doped BaSiF₆ nanoparticles were synthesized using a thermal decomposition synthesis route. Eu²⁺ ions have been successfully doped into BaSiF₆ host lattice and strong 4f-4f line emission of the Eu²⁺ in BaSiF₆ matrix is observed. Meanwhile, the photoluminescent (PL) properties of BaSiF₆:Eu²⁺ nanoparticles doping Eu²⁺ ions at different concentrations were also studied. PMID:27398531

  11. Insights into photoluminescence property and photocatalytic activity of cubic and rhombohedral ZnIn 2S 4

    NASA Astrophysics Data System (ADS)

    Shen, Shaohua; Guo, Penghui; Zhao, Liang; Du, Yuanchang; Guo, Liejin

    2011-08-01

    Cubic and rhombohedral ZnIn 2S 4 were synthesized by thermal sulfidation of Zn-In mixed oxide precursor in H 2S atmosphere at different temperatures. Cubic ZnIn 2S 4 was obtained when Zn-In mixed oxide precursor was sulfurized at 400 °C. With sulfidation temperature increasing from 400 to 800 °C, the crystal phase of ZnIn 2S 4 gradually turned from cubic to rhombohedral, which was demonstrated by different analysis techniques such as XRD, Raman, SEM, etc. UV-vis absorption spectra indicated that cubic ZnIn 2S 4 displayed better light absorption property than rhombohedral ZnIn 2S 4, with band gaps calculated to be 2.0 and 2.5 eV, respectively. However, under visible light irradiation, rhombohedral ZnIn 2S 4 photocatalyzed H 2 evolution from aqueous sodium sulfite/sulfide solution efficiently, whereas cubic ZnIn 2S 4 was not active for this reaction. The photoluminescence property revealed the different dynamics of photogenerated carriers, which made a predominant contribution to the increasing photocatalytic performances of ZnIn 2S 4 with crystal phase turning from cubic to rhombohedral.

  12. Three new Ag(I) coordination architectures based on mixed ligands: Syntheses, structures and photoluminescent properties

    SciTech Connect

    Li, Yamin; Xiao, Changyu; Li, Shu; Chen, Qi; Li, Beibei; Liao, Qian; Niu, Jingyang

    2013-04-15

    Three new silver (I) coordination complexes, [Ag{sub 2}(1,2-bdc)(phdat)]{sub n} (1), [Ag{sub 2}(NO{sub 2}-bdc)(phdat)]{sub n} (2), [Ag{sub 4}(nta){sub 3}(phdat)NO{sub 3}]{sub n} (3) (1,2-bdc=phthalic acid dianion, NO{sub 2}-bdc=5-nitro-1,3-benzenedicarboxylic acid dianion, nta=nicotinic acid anion, phdat=2,4-diamine-6-phenyl-1,3,5-triazine) have been hydrothermally synthesized by the reactions of silver nitrate and phdat with the homologous ligands 1,2-H{sub 2}bdc, NO{sub 2}-H{sub 2}bdc, and Hnta, respectively, and characterized by single-crystal X-ray diffractions, IR spectra, elemental analyses thermogravimetric analyses (TGA). The compound 1 exhibits a chiral 3D network with cbs/CrB self-dual topological net, which contains two kinds of single helical chains. For compound 2, the 3D network is comprised of two kinds of similar 2D sheets with the topological symbol of sql-type packed in AABBAA mode by Ag–N/O weakly contacts. And compound 3 has 2D double layer architecture, consisting of the 2D plane with hcb-type topological symbol connected by Ag–O weakly coordinations. The photoluminescent properties associated with the crystal structures of three compounds have also been measured. - Graphical abstract: Three new silver(I) coordination complexes 1–3 have been synthesized and characterized by single-crystal X-ray diffractions, IR spectra, elemental analyses, thermogravimetric analyses (TGA) and photoluminescent spectra. Highlights: ► The compound 1 exhibits a novel chiral 3D network with two kinds of single helical chains. ► 3D or 2D new Ag coordination complexes. ► The photoluminescent properties have been measured.

  13. Optical properties and band gap of single- and few-layer MoTe2 crystals.

    PubMed

    Ruppert, Claudia; Aslan, Ozgur Burak; Heinz, Tony F

    2014-11-12

    Single- and few-layer crystals of exfoliated MoTe2 have been characterized spectroscopically by photoluminescence, Raman scattering, and optical absorption measurements. We find that MoTe2 in the monolayer limit displays strong photoluminescence. On the basis of complementary optical absorption results, we conclude that monolayer MoTe2 is a direct-gap semiconductor with an optical band gap of 1.10 eV. This new monolayer material extends the spectral range of atomically thin direct-gap materials from the visible to the near-infrared.

  14. Optical properties and band gap of single- and few-layer MoTe2 crystals.

    PubMed

    Ruppert, Claudia; Aslan, Ozgur Burak; Heinz, Tony F

    2014-11-12

    Single- and few-layer crystals of exfoliated MoTe2 have been characterized spectroscopically by photoluminescence, Raman scattering, and optical absorption measurements. We find that MoTe2 in the monolayer limit displays strong photoluminescence. On the basis of complementary optical absorption results, we conclude that monolayer MoTe2 is a direct-gap semiconductor with an optical band gap of 1.10 eV. This new monolayer material extends the spectral range of atomically thin direct-gap materials from the visible to the near-infrared. PMID:25302768

  15. Green synthesis of magnesium ion incorporated nanocrystalline hydroxyapatite and their mechanical, dielectric and photoluminescence properties

    SciTech Connect

    Arul, K. Thanigai; Kolanthai, Elayaraja; Manikandan, E.; Bhalerao, G.M.; Chandra, V. Sarath; Ramya, J. Ramana; Mudali, U. Kamachi; Nair, K.G.M.; Kalkura, S.Narayana

    2015-07-15

    Highlights: • Rapid technique to synthesize nanorods of magnesium ion incorporated hydroxyapatite. • Enhanced electrical and mechanical properties. • Improved photoluminescence and wettability on magnesium incorporation. • Increased in vitro bioactivity. - Abstract: Nanocrystalline hydroxyapatite (HAp-Ca{sub 10}(PO{sub 4}){sub 6}(OH){sub 2,} 35 nm) and magnesium (Mg{sup 2+}) ion incorporated HAp were synthesized by microwave technique. XRD (X-ray diffraction), FTIR (Fourier transform infrared spectroscopy), FE-HRTEM (Field emission high resolution transmission electron microscopy), DLS (dynamic light scattering), EDXRF (energy dispersive X-ray fluorescence spectrometry), microhardness, permittivity and alternating current (ac) conductivity, besides the PL (photoluminescence), wettability and in vitro bioactivity of the samples were analysed. EDXRF revealed the Mg{sup 2+} ion incorporation in HAp. The Mg{sup 2+} ion incorporation did not alter the phase but drastically reduced the crystallite size and particle size respectively by 48% and 32%. There was enhanced microhardness (24%) at low level (<13%) and decreased zeta potential of Mg{sup 2+} ion incorporation. The permittivity, ac conductivity, PL, wettability and in vitro bioactivity were enhanced on Mg{sup 2+} ion incorporation. These properties enable them to be a promising candidate for wound healing, bone replacement applications and also as a biosensor.

  16. Photoluminescence and thermoluminescence properties of Y3(Al,Ga)5O12:Tb3+ phosphor

    NASA Astrophysics Data System (ADS)

    Yousif, A.; Som, S.; Swart, H. C.

    2016-01-01

    A comparative study of the structural, photoluminescence (PL) and thermoluminescence (TL) properties of Y3(Al,Ga)5O12:Tb3+ phosphor powder was performed. The scanning electron microscope images showed that the phosphor particles were agglomerated and irregular in shape. The bigger particles consisted of smaller spherically shaped agglomerated particles ranging in size between 0.5 and 1 μm. The UV-VUV synchrotron radiation was used to study the luminescence properties of the phosphor. The TL study was performed after the sample was irradiated by γ-rays obtained from a 60Co target in the dose range of 10-50 Gy. The effect of heating rate on the TL glow curves and trapping parameters was also calculated. The correlation between PL and TL was explored.

  17. Size and dopant-concentration dependence of photoluminescence properties of ion-implanted phosphorus- and boron-codoped Si nanocrystals

    NASA Astrophysics Data System (ADS)

    Nakamura, Toshihiro; Adachi, Sadao; Fujii, Minoru; Sugimoto, Hiroshi; Miura, Kenta; Yamamoto, Shunya

    2015-04-01

    We investigate the nanocrystallite-size and dopant-concentration dependence of the photoluminescence (PL) properties of heavily phosphorus- (P) and boron- (B) codoped Si nanocrystals (Si NCs), prepared using a combination of sputtering and ion implantation techniques. We find that the heavily doped Si NC exhibits three exotic luminescence bands, A, B, and C. The peak energy of band A redshifts with increasing dopant concentration. This band is due to the band-to-band transition at the reduced Si-NC band gap caused by the formation of impurity bands together with band-tailing effects. The PL redshift becomes large when the nanocrystallite size decreases, suggesting the occurrence of the quantum-confinement-induced carrier doping effect. The peak energies of bands B and C are independent of both the concentration and size, indicating that these bands are due to transitions between defect- and/or impurity-related localized states. Band A shows stronger thermal quenching than the PL band in pure (undoped) Si NCs, the magnitude of which depends on the dopant concentration. The stronger thermal quenching in band A is probably due to the thermally induced migration of electrons in the impurity band.

  18. Bandedge optical properties of MBE grown GaAsBi films measured by photoluminescence and photothermal deflection spectroscopy

    NASA Astrophysics Data System (ADS)

    Beaudoin, M.; Lewis, R. B.; Andrews, J. J.; Bahrami-Yekta, V.; Masnadi-Shirazi, M.; O'Leary, S. K.; Tiedje, T.

    2015-09-01

    The bandedge optical properties of GaAsBi films, as thick as 470 nm, with Bi content varying from 0.7% Bi to 2.8% Bi grown by molecular beam epitaxy on GaAs substrates are measured by photoluminescence (PL) and photothermal deflection spectroscopy (PDS). The PDS spectra were fit with a modified Fernelius model which takes into account multiple reflections within the GaAsBi layer and GaAs substrate. Three undoped samples and two samples that are degenerately doped with silicon are studied. The undoped samples show a clear Urbach absorption edge with a composition dependent bandgap that decreases by 56 meV/% Bi and a composition independent Urbach slope parameter of 25 meV due to absorption by Bi cluster states near the valence band. The doped samples show a long absorption tail possibly due to absorption by gap states and free carriers in addition to a Burstein-Moss bandgap shift. PL of the undoped samples shows a lower energy emission peak due to defects not observed in the usually available thin samples (50 nm or less) grown under similar conditions.

  19. CdSe Ring- and Tribulus-Shaped Nanocrystals: Controlled Synthesis, Growth Mechanism, and Photoluminescence Properties

    PubMed Central

    2009-01-01

    With air-stable and generic reagents, CdSe nanocrystals with tunable morphologies were prepared by controlling the temperature in the solution reaction route. Thereinto, the lower reaction temperature facilitates the anisotropic growth of crystals to obtain high-yield CdSe ring- and tribulus-shaped nanocrystals with many branches on their surfaces. The photoluminescence properties are sensitive to the nature of particle and its surface. The products synthesized at room temperature, whose surfaces have many branches, show higher blue shift and narrower emission linewidths (FWHM) of photoluminescence than that of samples prepared at higher temperature, whose surfaces have no branches. Microstructural studies revealed that the products formed through self-assembly of primary crystallites. Nanorings formed through the nonlinear attachment of primary crystallites, and the branches on the surfaces grew by linear attachment at room temperature. And the structure of tribulus-shaped nanoparticle was realized via two steps of aggregation, i.e., random and linear oriented aggregation. Along with the elevation of temperature, the branches on nanocrystal surfaces shortened gradually because of the weakened linear attachment. PMID:20596352

  20. Synthesis, characterization, growth mechanism, photoluminescence and field emission properties of novel dandelion-like gallium nitride

    NASA Astrophysics Data System (ADS)

    Nabi, Ghulam; Cao, Chuanbao; Khan, Waheed S.; Hussain, Sajad; Usman, Zahid; Safdar, Muhammad; Shah, Sajjad Hussain; Khattak, Noor Abass Din

    2011-09-01

    Dandelion-like gallium nitride (GaN) microstructures were successfully synthesized via Ni catalyst assisted chemical vapor deposition method at 1200 °C under NH3 atmosphere by pre-treating precursors with aqueous ammonia. The as-synthesized product was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive X-ray spectroscopy (EDX). X-ray diffraction analysis revealed that as-synthesized dandelion-like GaN was pure and has hexagonal wurtzite structure. SEM results showed that the size of the dandelion-like GaN structure was in the range of 30-60 μm. Dandelion-like GaN microstructures exhibited reasonable field emission properties with the turn-on field of 9.65 V μm-1 (0.01 mA cm-2) and threshold field of 11.35 V μm-1 (1 mA cm-2) which is sufficient for applications of electron emission devices, field emission displays and vacuum micro electronic devices. Optical properties were studied at room temperature by using fluorescence spectrophotometer. Photoluminescence (PL) measurements of dandelion-like GaN showed a strong near-band-edge emission at 370.2 nm (3.35 eV) with blue band emission at 450.4 nm (2.75 eV) and 465.2 nm (2.66 eV) but with out yellow band emission. The room-temperature photoluminescence properties showed that it has also potential application in light-emitting devices. The tentative growth mechanism for the growth of dandelion-like GaN was also described.

  1. Geometrical, response, and gap properties of Lindbladians

    NASA Astrophysics Data System (ADS)

    Albert, Victor V.; Bradlyn, Barry; Fraas, Martin; Jiang, Liang

    We study Lindbladians admitting multi-dimensional steady-state subspaces (SSS) which can be used to store, protect, and process quantum information. We derive an analytical formula for the left eigenmatrices of such Lindbladians corresponding to purely imaginary eigenvalues. This formula resolves how Lindbladian evolution affects perturbative response and geometrical features of the SSS and allows us to generalize recent work to all types of SSS. We show that Hamiltonian and certain jump operator perturbations induce, to first order, exclusively unitary evolution on the SSS. Similarly, the holonomy (generalization of geometric phase) induced on the SSS after adiabatic traversal of a closed path in parameter space is unitary. We derive a new Riemannian metric tensor in parameter space induced by one type of SSS, generalizing the Fubini-Study metric to Lindbladians possessing one or more mixed steady states. We derive a Kubo formula governing linear response of the SSS to Hamiltonian perturbations. Finally, we show that the energy scale governing leakage out of the SSS is different from the conventional Lindbladian dissipative gap.

  2. Synthesis and photoluminescence properties of Ca3B2O6:Tb3+ nanophosphors

    NASA Astrophysics Data System (ADS)

    Manhas, Mohit; Kumar, Vinay; Ntwaeaborwa, O. M.; Swart, H. C.

    2014-04-01

    The green light emitting Tb3+ doped Ca3B2O6 nanophosphors have been synthesized by combustion method at 600°C, and their luminescent properties have been studied. The formation of phosphors has been confirmed by X-ray diffraction (XRD). The photoluminescence (PL) spectra show four emission peaks at 491 nm, 544 nm, 587 and 621 nm. It exhibited a strong green emission located at 544 nm. The effect of different dopant concentrations on emission intensity has also been studied. The maximum photo emission intensity of the Ca3B2O6:Tb3+ was obtained at a dopant concentration of 1.5 mol% of Tb3+.

  3. In situ etching WO{sub 3} nanoplates: Hydrothermal synthesis, photoluminescence and gas sensor properties

    SciTech Connect

    Su, Xintai; Li, Yani; Jian, Jikang; Wang, Jide

    2010-12-15

    A novel hydrothermal process using p-nitrobenzoic acid as structure-directing agent has been employed to synthesize plate-shaped WO{sub 3} nanostructures containing holes. The p-nitrobenzoic acid plays a critical role in the synthesis of such novel WO{sub 3} nanoplates. The morphology, structure and optical property of the WO{sub 3} nanoplates have been characterized by transmission electron microcopy (TEM), scanning electron microcopy (SEM), X-ray diffraction (XRD) and photoluminescence (PL). The lateral size of the nanoplates is 500-1000 nm, and the thickness is about 80 nm. The formation mechanism of WO{sub 3} nanoplates is discussed briefly. The gas sensitivity of WO{sub 3} nanoplates was studied to ethanol and acetone at different operation temperatures and concentrations. Furthermore, the WO{sub 3} nanoplate-based gas sensor exhibits high sensitivity for ethanol and acetone as well as quick response and recovery time at low temperature.

  4. Probing the photoluminescence properties of gold nanoclusters by fluorescence lifetime correlation spectroscopy

    SciTech Connect

    Yuan, C. T. Lin, T. N.; Shen, J. L.; Lin, C. A.; Chang, W. H.; Cheng, H. W.; Tang, J.

    2013-12-21

    Gold nanoclusters (Au NCs) have attracted much attention for promising applications in biological imaging owing to their tiny sizes and biocompatibility. So far, most efforts have been focused on the strategies for fabricating high-quality Au NCs and then characterized by conventional ensemble measurement. Here, a fusion single-molecule technique combining fluorescence correlation spectroscopy and time-correlated single-photon counting can be successfully applied to probe the photoluminescence (PL) properties for sparse Au NCs. In this case, the triplet-state dynamics and diffusion process can be observed simultaneously and the relevant time constants can be derived. This work provides a complementary insight into the PL mechanism at the molecular levels for Au NCs in solution.

  5. Large-scale synthesis well-dispersed ZnS microspheres and their photoluminescence, photocatalysis properties

    SciTech Connect

    Wang Xinjun Wan Fuquan; Han Kun; Chai Chunxia; Jiang Kai

    2008-12-15

    Large-scale and well-dispersed ZnS microspheres were prepared by a simple hydrothermal method using ZnSO{sub 4}{center_dot}7H{sub 2}O and SC(NH{sub 2}){sub 2} as main original reactant and poly(vinyl pyrrolidone) (PVP)(Mr {approx} 10,000) as the surfactant. The products were characterized by X-Ray diffraction, scanning electron microscopy and transmission electron microscopy. The growth process involves a special oriented aggregation of PVP stabilized ZnS nanoparticles into microspheres of 1.5 {approx} 2.0 {mu}m in sizes. The photocatalytic activity of as-prepared ZnS microsphere was evaluated by using methylene blue (MB) as a model organic compound. The optical properties of the products were also examined by means of photoluminescence (PL) spectroscopy.

  6. Structural characterization, electrochemical, photoluminescence and thermal properties of potassium ion-mediated coordination polymer.

    PubMed

    Ceyhan, Gökhan; Köse, Muhammet; Tümer, Mehmet; Dal, Hakan

    2015-05-01

    A polymeric potassium complex of p-nitrophenol was synthesized and characterized by analytical and spectroscopic techniques. Molecular structure of the complex was determined by single crystal X-ray diffraction study. X-ray structural data show that crystals contain polymeric K(+) complex of p-nitrophenol. Asymmetric unit consists of one p-nitrophenolate, one K(+) ion and one water molecule. All bond lengths and angles in the phenyl rings have normal Csp2-Csp2 values and are in the expected ranges. The p-nitrophenolate is close to planar with small distortions by some atoms. Each potassium ion in the polymeric structure is identical and eight-coordinate, bonded to four nitro, two phenolate oxygen atoms from five p-nitrophenolate ligands and two oxygen atoms from two water molecules. Electronic, electrochemical, photoluminescence and thermal properties of the complex were also investigated.

  7. Improved photoluminescence property of CTAB assisted polyaniline-AlZnO nanocomposite

    SciTech Connect

    Mitra, Mousumi; Banerjee, Dipali; Kargupta, Kajari; Ganguly, Saibal

    2015-06-24

    Polyaniline-Al doped ZnO ((PANI-AlZnO:: 70:30) nanocomposite was prepared via in situ chemical oxidative polymerization, while the hexagonal powder of AlZnO was synthesized via sol-gel technique, using Hexadecyltrimethylammonium bromide (CTAB) as a capping agent. The prepared nanocomposite was characterized by High resolution transmission electron microscopy (HRTEM), EDAX, X-ray diffraction (XRD) and Fourier transforms infrared (FTIR) spectra. The optical property of the nanomaterials is examined by photoluminescence (PL) spectra analysis. The XRD pattern confirms the formation of Al doped ZnO as well as PANI. The HRTEM images of the composite showed the formation of hexagonal AlZnO embedded in polyaniline matrix. EDAX spectrum shows the compositional analysis of the nanocomposite. FTIR spectra confirm the formation of nanocomposite of PANI and hexagonal AlZnO. The PL intensity of the nanocomposite is improved as compared to pure AlZnO.

  8. Photon absorption and emission properties of 7 Å SiC nanoclusters: Electronic gap, surface state, and quantum size effect

    NASA Astrophysics Data System (ADS)

    Guo, Xiaoxiao; Chen, Xifang; Fan, Baolu; Zhang, Yumeng; Fan, Jiyang

    2016-07-01

    People know little experimentally about the physical properties of the SiC nanoclusters with sizes of a couple of angstroms. Herein, we study the electronic structure and light absorption/emission properties of the SiC nanoclusters with an average diameter of 7 Å that are fabricated by diminishing the sizes of the SiC microcrystals under high pressure and high temperature. The results reveal that the SiC nanoclusters have an indirect energy gap of 5.1 eV. Unlike the case of larger SiC nanocrystals, the luminescence of the SiC nanoclusters is dominated by two types of oxygen-related surface defects, and the maximum of their photoluminescence/photoluminescence excitation spectrum lies at 4.1/3.3 and 3.8/3.0 eV, respectively. The energy gap of the SiC nanoparticles with reference to bulk value is found to be inversely proportional to the diameter to the power 0.97, which shows slower increase of energy gap with decreasing size than what is predicted by using the first-principles calculations.

  9. Hydrothermal synthesis, crystal structures and photoluminescence properties of mixed europium-yttrium organic frameworks

    SciTech Connect

    Han Yinfeng; Fu Lianshe; Mafra, Luis; Shi, Fa-Nian

    2012-02-15

    Three mixed europium-yttrium organic frameworks: Eu{sub 2-x}Y{sub x}(Mel)(H{sub 2}O){sub 6} (Mel=mellitic acid or benzene-1,2,3,4,5,6-hexacarboxylic acid, x=0.38 1, 0.74 2, and 0.86 3) have been synthesized and characterized. All the compounds contain a 3-D net with (4, 8)-flu topology. The study indicates that the photoluminescence properties are effectively affected by the different ratios of europium and yttrium ions, the quantum efficiency is increased and the Eu{sup 3+} lifetime becomes longer in these MOFs than those of the Eu analog. - Graphical abstract: Three mixed europium and yttrium organic frameworks: Eu{sub 2-x}Y{sub x}(Mel)(H{sub 2}O){sub 6} (Mel=mellitic acid) have been synthesized and characterized. All the compounds contain a 3-D net with (4, 8)-flu topology. The study indicates that the photoluminescence properties are effectively affected by the different ratios of europium and yttrium ions, the quantum efficiency is increased and the Eu{sup 3+} lifetime becomes longer in these MOFs than those of the Eu analog. Highlights: Black-Right-Pointing-Pointer Three (4, 8)-flu topological mixed Eu and Y MOFs were synthesized under mild conditions. Black-Right-Pointing-Pointer Metal ratios were refined by the single crystal data consistent with the EDS analysis. Black-Right-Pointing-Pointer Mixed Eu and Y MOFs show longer lifetime and higher quantum efficiency than the Eu analog. Black-Right-Pointing-Pointer Adding inert lanthanide into luminescent MOFs enlarges the field of luminescent MOFs.

  10. Electronic structure of narrow gap semiconductors: Understanding gap formation and thermoelectric properties

    NASA Astrophysics Data System (ADS)

    Larson, Paul Melvin

    Electronic band structure calculations are invaluable theoretical tools to understand structural, transport, and optical properties of materials. We have used this tool in the search for new high performance thermoelectric materials, which are usually narrow-gap semiconductors. We have studied the electronic structures of these systems both to understand which properties of the band structure are most important for thermoelectric properties and the nature of the gap formation. Narrow-gap semiconductors lie between metals and wide-gap semiconductors, so understanding the nature of the gap formation is very important. The small band gaps in the systems we have studied generally arise from hybridization between different bands. We have used the local density approximation (LDA) and the generalized gradient approximation (GGA) within density functional theory (DFT). These have been implemented using the full-potential linearized augmented planewave (FLAPW) method within the WIEN97 package. This state-of-the-art method is among the most accurate methods for calculating the electronic structure of solids. We have studied four classes of compounds. These include the half-Heusler compounds, the ternary Zintl-phase compounds, the simple chalcogenides, and the complex chalcogenides. The ternary half-Heusler compounds, considered having a stuffed NaCl structure, show promising thermoelectric properties. The band gap formation is understood by starting with the semi-metallic binary NaCl compounds from which they are formed. Adding the transition (or noble) metal atom causes a strong p-d hybridization near the Fermi energy which opens up the band gap. This hybridization also leads to highly anisotropic effective masses at the conduction band minimum which are found in the best thermoelectric materials. Similar band gap formation is found in the ternary Zintl-phase compounds which are considered a stuffed Th3P4 structure. The band gaps in these ternary compounds are larger than

  11. Tuning photoluminescence and surface properties of carbon nanodots for chemical sensing

    NASA Astrophysics Data System (ADS)

    Zhang, Zhaomin; Pan, Yi; Fang, Yaning; Zhang, Lulu; Chen, Junying; Yi, Changqing

    2015-12-01

    Obtaining tunable photoluminescence (PL) with improved emission properties is crucial for successfully implementing fluorescent carbon nanodots (fCDs) in all practical applications such as multicolour imaging and multiplexed detection by a single excitation wavelength. In this study, we report a facile hydrothermal approach to adjust the PL peaks of fCDs from blue, green to orange by controlling the surface passivation reaction during the synthesis. This is achieved by tuning the passivating reagents in a step-by-step manner. The as-prepared fCDs with narrow size distribution show improved PL properties with different emission wavelengths. Detailed characterization of fCDs using elemental analysis, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy suggested that the surface chemical composition results in this tunable PL emission. Surface passivation significantly alters the surface status, resulting in fCDs with either stronger surface oxidation or N element doping that ultimately determine their PL properties. Further experiments suggested that the as-prepared orange luminescent fCDs (O-fCDs) were sensitive and specific nanosensing platforms towards Fe3+ determination in a complex biological environment, emphasizing their potential practical applications in clinical and biological fields.Obtaining tunable photoluminescence (PL) with improved emission properties is crucial for successfully implementing fluorescent carbon nanodots (fCDs) in all practical applications such as multicolour imaging and multiplexed detection by a single excitation wavelength. In this study, we report a facile hydrothermal approach to adjust the PL peaks of fCDs from blue, green to orange by controlling the surface passivation reaction during the synthesis. This is achieved by tuning the passivating reagents in a step-by-step manner. The as-prepared fCDs with narrow size distribution show improved PL properties with different emission wavelengths. Detailed

  12. Insights into photoluminescence property and photocatalytic activity of cubic and rhombohedral ZnIn{sub 2}S{sub 4}

    SciTech Connect

    Shen Shaohua; Guo Penghui; Zhao Liang; Du Yuanchang; Guo Liejin

    2011-08-15

    Cubic and rhombohedral ZnIn{sub 2}S{sub 4} were synthesized by thermal sulfidation of Zn-In mixed oxide precursor in H{sub 2}S atmosphere at different temperatures. Cubic ZnIn{sub 2}S{sub 4} was obtained when Zn-In mixed oxide precursor was sulfurized at 400 deg. C. With sulfidation temperature increasing from 400 to 800 deg. C, the crystal phase of ZnIn{sub 2}S{sub 4} gradually turned from cubic to rhombohedral, which was demonstrated by different analysis techniques such as XRD, Raman, SEM, etc. UV-vis absorption spectra indicated that cubic ZnIn{sub 2}S{sub 4} displayed better light absorption property than rhombohedral ZnIn{sub 2}S{sub 4}, with band gaps calculated to be 2.0 and 2.5 eV, respectively. However, under visible light irradiation, rhombohedral ZnIn{sub 2}S{sub 4} photocatalyzed H{sub 2} evolution from aqueous sodium sulfite/sulfide solution efficiently, whereas cubic ZnIn{sub 2}S{sub 4} was not active for this reaction. The photoluminescence property revealed the different dynamics of photogenerated carriers, which made a predominant contribution to the increasing photocatalytic performances of ZnIn{sub 2}S{sub 4} with crystal phase turning from cubic to rhombohedral. - Graphical Abstract: Rhombohedral ZnIn{sub 2}S{sub 4} showed a superior photocatalytic activity for H{sub 2} evolution than cubic ZnIn{sub 2}S{sub 4}, which was proved to be related with their different dynamics of photogenerated carriers. Highlights: > Cubic and rhombohedral ZnIn{sub 2}S{sub 4} were synthesized by thermal sulfidation. > Rhombohedral ZnIn{sub 2}S{sub 4} could photocatalyze H{sub 2} evolution efficiently. > The dynamics of photogenerated carriers affected the photocatalytic activity.

  13. Temperature dependence of the fundamental band gap parameters in cadmium-rich ZnxCd1-xSe using photoluminescence spectroscopy

    NASA Astrophysics Data System (ADS)

    Gupta, Lalita; Rath, S.; Abbi, S. C.; Jain, F. C.

    2003-10-01

    Thin films of ternary ZnxCd1-xSe were deposited on GaAs (100) substrate using metalorganic- chemical-vapour-deposition (MOCVD) technique. Temperature dependence of the nearband- edge emission from these Cd-rich ZnxCd1-x Se (for x _ 0_025, 0.045) films has been studied using photoluminescence spectroscopy. Relevant parameters that describe temperature variation of the energy and broadening of the fundamental band gap have been evaluated using various models including the two-oscillator model, the Bose-Einstein model and the Varshni model. While all these models suffice to explain spectra at higher temperatures, the two-oscillator model not only explains low temperature spectra adequately but also provides additional information concerning phonon dispersion in these materials.

  14. Photoluminescence properties of Sn-related donor state in Al(x)Ga(1-x)As

    NASA Astrophysics Data System (ADS)

    Kang, Junyog; Iida, Seishi; Huang, Qisheng; Fukuda, Tsuguo

    1993-08-01

    We have investigated the near-gap recombinations in Sn-doped Al(x)Ga(1-x)As by photoluminescence. By analyzing the variations of spectral lineshapes under various excitation intensities, only one type of recombination was assigned to associated with the Sn-related donor state, which was different from the hydrogenlike shallow donor states and the DX centers. Phonon replicas were observed to accompany the recombination in the samples with high AlAs mole fractions of direct gaps, as well as in those of indirect gaps. The Franck-Condon shift and the phonon energy of the recombination were found to increase with increasing AlAs mole fraction. This behavior was explained in terms of a variation of local lattice distortion around an ionized Sn-related donor and a weighted average of two local vibrational mode frequencies of the Sn-related donor.

  15. Monodentate Schiff base ligands: their structural characterization, photoluminescence, anticancer, electrochemical and sensor properties.

    PubMed

    Köse, Muhammet; Ceyhan, Gökhan; Tümer, Mehmet; Demirtaş, Ibrahim; Gönül, İlyas; McKee, Vickie

    2015-02-25

    Two Schiff base compounds, N,N'-bis(2-methoxy phenylidene)-1,5-diamino naphthalene (L(1)) and N,N'-bis(3,4,5-trimethoxy phenylidene)-1,5-diamino naphthalene (L(2)) were synthesized and characterized by the analytical and spectroscopic methods. The electrochemical and photoluminescence properties of the Schiff bases were investigated in the different conditions. The compounds L(1) and L(2) show the reversible redox processes at some potentials. The sensor properties of the Schiff bases were examined and color changes were observed upon addition of the metal cations, such as Hg(II), Cu(II), Co(II) and Al(III). The Schiff base compounds show the bathochromic shift from 545 to 585 nm. The single crystals of the compounds (L(1)) and (L(2)) were obtained from the methanol solution and characterized structurally by the X-ray crystallography technique. The molecule L(2) is centrosymmetric whereas the L(1) has no crystallographically imposed molecular symmetry. However, the molecular structures for these compounds are quite similar, differing principally in the conformation about methoxy groups and the dihedral angle between the two aromatic rings and diamine naphthalene.

  16. The photoluminescence properties of tri-colour silicoaluminate phosphors prepared from oil shale ash

    NASA Astrophysics Data System (ADS)

    Zhang, Hui; Song, Yanhua; Sheng, Ye; Zheng, Keyan; Ding, Shizhou; Yuan, Bo; Xu, Xuechun; Zou, Haifeng

    2015-09-01

    In this paper, high value-added tri-colour phosphors Ba0.96Mg1.88Si2O7:0.02Eu2+, 0.02Dy3+, 0.12Mn2+; CaSr0.995SiO4:0.005Eu2+ and Ba0.91MgAl10O17:0.09Eu2+ were prepared using the white carbon black (hereinafter referred to as WCB) and alumina extracted from oil shale ash as raw materials. The structure and luminescence properties of the samples were characterized by X-ray diffraction (XRD) and photoluminescent spectra. The results show that the red and green phosphors synthesized by WCB exhibited much weaker emission than the phosphors synthesized by pure chemical reagent silica, which is mainly due to the high content of iron in the WCB. After purifying the WCB under laboratory conditions, the luminescence properties were improved and close to that of pure chemical reagent. By comparing with the emission of the samples synthesized with chemical reagents, the results show that the products extracted from oil shale ash can be applied to synthesize luminescent materials which have potential applications in white-light ultraviolet (UV)-LED field.

  17. Effect of graphene on photoluminescence properties of graphene/GeSi quantum dot hybrid structures

    SciTech Connect

    Chen, Y. L.; Ma, Y. J.; Wang, W. Q.; Ding, K.; Wu, Q.; Fan, Y. L.; Yang, X. J.; Zhong, Z. Y.; Jiang, Z. M.; Chen, D. D.; Xu, F.

    2014-07-14

    Graphene has been discovered to have two effects on the photoluminescence (PL) properties of graphene/GeSi quantum dot (QD) hybrid structures, which were formed by covering monolayer graphene sheet on the multilayer ordered GeSi QDs sample surfaces. At the excitation of 488 nm laser line, the hybrid structure had a reduced PL intensity, while at the excitation of 325 nm, it had an enhanced PL intensity. The attenuation in PL intensity can be attributed to the transferring of electrons from the conducting band of GeSi QDs to the graphene sheet. The electron transfer mechanism was confirmed by the time resolved PL measurements. For the PL enhancement, a mechanism called surface-plasmon-polariton (SPP) enhanced absorption mechanism is proposed, in which the excitation of SPP in the graphene is suggested. Due to the resonant excitation of SPP by incident light, the absorption of incident light is much enhanced at the surface region, thus leading to more exciton generation and a PL enhancement in the region. The results may be helpful to provide us a way to improve optical properties of low dimensional surface structures.

  18. Monodentate Schiff base ligands: Their structural characterization, photoluminescence, anticancer, electrochemical and sensor properties

    NASA Astrophysics Data System (ADS)

    Köse, Muhammet; Ceyhan, Gökhan; Tümer, Mehmet; Demirtaş, İbrahim; Gönül, İlyas; McKee, Vickie

    2015-02-01

    Two Schiff base compounds, N,N‧-bis(2-methoxy phenylidene)-1,5-diamino naphthalene (L1) and N,N‧-bis(3,4,5-trimethoxy phenylidene)-1,5-diamino naphthalene (L2) were synthesized and characterized by the analytical and spectroscopic methods. The electrochemical and photoluminescence properties of the Schiff bases were investigated in the different conditions. The compounds L1 and L2 show the reversible redox processes at some potentials. The sensor properties of the Schiff bases were examined and color changes were observed upon addition of the metal cations, such as Hg(II), Cu(II), Co(II) and Al(III). The Schiff base compounds show the bathochromic shift from 545 to 585 nm. The single crystals of the compounds (L1) and (L2) were obtained from the methanol solution and characterized structurally by the X-ray crystallography technique. The molecule L2 is centrosymmetric whereas the L1 has no crystallographically imposed molecular symmetry. However, the molecular structures for these compounds are quite similar, differing principally in the conformation about methoxy groups and the dihedral angle between the two aromatic rings and diamine naphthalene.

  19. Enhanced UV absorbance and photoluminescence properties of ultrasound assisted synthesized gold doped ZnO nanorods

    NASA Astrophysics Data System (ADS)

    Sahu, Dojalisa; Panda, N. R.; Acharya, B. S.; Panda, A. K.

    2014-06-01

    Au doped ZnO (ZnO:Au) nanostructures were synthesized by ultrasound assisted wet chemical method. The concentration of dopant was varied and both structural and optical properties of ZnO:Au were investigated. The crystal structure and morphology of the samples were examined by X-ray diffraction (XRD) and transmission electron microscopy (TEM). These results showed the formation of nanorods of ZnO:Au having wurtzite structure and c-axis orientation. Gradual increase in crystallite size and bond length was also observed with the increase in gold concentration in ZnO intending the expansion of lattice after gold doping. The optical absorption measurements showed high ultraviolet (UV) absorbance property of ZnO:Au with sharp and intense absorption band in this region as compared to pristine ZnO. Photoluminescence (PL) measurements showed excitonic emission band of ZnO around 390 nm for both undoped and Au doped ZnO nanoparticles. Further, a strong emission around 467 nm was observed in the PL spectra of ZnO/ZnO:Au which was attributed to the transitions related to excess of oxygen vacancies. Interestingly, a new band was observed at 582 nm for doped ZnO samples which grew in intensity with doping concentration. This band was ascribed to the gold nanoparticle adsorbed on the surface of ZnO.

  20. Bismuth-, Tin-, and Lead-Containing Metal-Organic Materials: Synthesis, Structure, Photoluminescence, Second Harmonic Generation, and Ferroelectric Properties

    NASA Astrophysics Data System (ADS)

    Wibowo, Arief Cahyo

    Metal-Organic Materials (MOMs) contain metal moieties and organic ligands that combine to form discrete (e.g. metal-organic polyhedra, spheres or nanoballs, metal-organic polygons) or polymeric structures with one-, two-, or three-dimensional periodicities that can exhibit a variety of properties resulting from the presence of the metal moieties and/or ligand connectors in the structure. To date, MOMs with a range of functional attributes have been prepared, including record-breaking porosity, catalytic properties, molecular magnetism, chemical separations and sensing ability, luminescence and NLO properties, multiferroic, ferroelectric, and switchable molecular dielectric properties. We are interested in synthesizing non-centrosymmetric MOM single crystals possessing one of the ten polar space groups required for non-linear optical properties (such as second harmonic generation) and ferroelectric applications. This thesis is divided into two main parts: materials with optical properties, such as photoluminescence and materials for targeted applications such as second harmonic generation and ferroelectric properties. This thesis starts with an introduction describing material having centrosymmetric, non-polar space groups, single crystals structures and their photoluminescence properties. These crystals exhibit very interesting and rare structures as well as interesting photoluminescence properties. Chapters 2-5 of this thesis focus on photoluminescent properties of new MOMs, and detail the exploratory research involving the comparatively rare bismuth, lead, and tin coordination polymers. Specifically, the formation of single white-light emitting phosphors based on the combination of bismuth or lead with pyridine-2,5-dicarboxylate is discussed (Chapter 2). The observation of a new Bi2O2 layer and a new Bi4O 3 chain in bismuth terephthalate-based coordination polymers is presented in Chapter 3, while the formation of diverse structures of tin-based coordination

  1. Semiconducting tin and lead iodide perovskites with organic cations: phase transitions, high mobilities, and near-infrared photoluminescent properties.

    PubMed

    Stoumpos, Constantinos C; Malliakas, Christos D; Kanatzidis, Mercouri G

    2013-08-01

    A broad organic-inorganic series of hybrid metal iodide perovskites with the general formulation AMI3, where A is the methylammonium (CH3NH3(+)) or formamidinium (HC(NH2)2(+)) cation and M is Sn (1 and 2) or Pb (3 and 4) are reported. The compounds have been prepared through a variety of synthetic approaches, and the nature of the resulting materials is discussed in terms of their thermal stability and optical and electronic properties. We find that the chemical and physical properties of these materials strongly depend on the preparation method. Single crystal X-ray diffraction analysis of 1-4 classifies the compounds in the perovskite structural family. Structural phase transitions were observed and investigated by temperature-dependent single crystal X-ray diffraction in the 100-400 K range. The charge transport properties of the materials are discussed in conjunction with diffuse reflectance studies in the mid-IR region that display characteristic absorption features. Temperature-dependent studies show a strong dependence of the resistivity as a function of the crystal structure. Optical absorption measurements indicate that 1-4 behave as direct-gap semiconductors with energy band gaps distributed in the range of 1.25-1.75 eV. The compounds exhibit an intense near-IR photoluminescence (PL) emission in the 700-1000 nm range (1.1-1.7 eV) at room temperature. We show that solid solutions between the Sn and Pb compounds are readily accessible throughout the composition range. The optical properties such as energy band gap, emission intensity, and wavelength can be readily controlled as we show for the isostructural series of solid solutions CH3NH3Sn(1-x)Pb(x)I3 (5). The charge transport type in these materials was characterized by Seebeck coefficient and Hall-effect measurements. The compounds behave as p- or n-type semiconductors depending on the preparation method. The samples with the lowest carrier concentration are prepared from solution and are n-type; p

  2. Cation distribution and photoluminescence properties of Mn-doped ZnGa2O4 nanoparticles

    NASA Astrophysics Data System (ADS)

    Liu, Jian; Duan, Xiulan; Zhang, Yang; Jiang, Huaidong

    2015-06-01

    Mn-doped ZnGa2O4 nanoparticles with the composition of MnxZn1-xGa2O4 (0≤x≤1) were prepared by the citrate sol-gel method. The cation distribution in the nanoparticles was studied by using X-ray photoelectron spectroscopy (XPS) and electron paramagnetic resonance (EPR). The results show that the nanoparticles with the size of 20-48 nm were obtained when the precursor was annealed at 600 °C or above, and the size increases with increasing annealing temperature. The cations (Ga3+, Zn2+ and Mn2+) occupy the tetrahedral (Td) sites as well as the octahedral (Oh) sites of spinel structure in the nanoparticles. Ga3+ ions are located in a large proportion at the octahedral sites and in a small proportion at the tetrahedral sites. The inversion parameter (two times the fraction of Ga3+ in the tetrahedral sites) increases with decreasing annealing temperature and Mn-enrichment. The luminescent properties were studied by using fluorescence spectrophotometer. The photoluminescence (PL) spectra exhibit green and red emissions with excitation wavelength of 304 nm, which is attributed to 4T1(4G)→6A1(6S) transition of Mn2+ ions in the tetrahedral and octahedral sites of MnxZn1-xGa2O4 nanoparticles, respectively.

  3. Photoluminescence and photocatalytic properties of rhombohedral CuGaO2 nanoplates.

    PubMed

    Shi, Linlin; Wang, Fei; Wang, Yunpeng; Wang, Dengkui; Zhao, Bin; Zhang, Ligong; Zhao, Dongxu; Shen, Dezhen

    2016-01-01

    Rhombohedral phase CuGaO2 nanoplates with a diameter of about 10 μm were synthesized via low temperature hydrothermal method. Room temperature and low temperature photoluminescence of the obtained CuGaO2 nanoplates were characterized. CuGaO2 nanoplates exhibited blue emission at room temperature and free exciton emission were appeared at low temperature. The blue emission is originated from defects such as Cu vacancies, which is the possible origin of p-type conductivity. The appearance of free exciton emission can demonstrate the direct bandgap transition behavior of CuGaO2 nanoplates. The as-prepared p-type CuGaO2 nanoplates were further decorated by n-type ZnO nanoparticles via calcination method to fabricate p-n junction nanocomposites. The nanocomposites exhibited enhanced photocatalytic activity which can be ascribed to the effective separation of photogenerated carriers by the internal electrostatic field in the p-n junction region, and the enhanced light absorption properties resulted from sub-bandgap absorption effect of p-n junction. This work has offered a new insight into the design of p-n junction devices using p-type CuGaO2 nanoplates. PMID:26887923

  4. Photoluminescence and photocatalytic properties of rhombohedral CuGaO2 nanoplates

    NASA Astrophysics Data System (ADS)

    Shi, Linlin; Wang, Fei; Wang, Yunpeng; Wang, Dengkui; Zhao, Bin; Zhang, Ligong; Zhao, Dongxu; Shen, Dezhen

    2016-02-01

    Rhombohedral phase CuGaO2 nanoplates with a diameter of about 10 μm were synthesized via low temperature hydrothermal method. Room temperature and low temperature photoluminescence of the obtained CuGaO2 nanoplates were characterized. CuGaO2 nanoplates exhibited blue emission at room temperature and free exciton emission were appeared at low temperature. The blue emission is originated from defects such as Cu vacancies, which is the possible origin of p-type conductivity. The appearance of free exciton emission can demonstrate the direct bandgap transition behavior of CuGaO2 nanoplates. The as-prepared p-type CuGaO2 nanoplates were further decorated by n-type ZnO nanoparticles via calcination method to fabricate p-n junction nanocomposites. The nanocomposites exhibited enhanced photocatalytic activity which can be ascribed to the effective separation of photogenerated carriers by the internal electrostatic field in the p-n junction region, and the enhanced light absorption properties resulted from sub-bandgap absorption effect of p-n junction. This work has offered a new insight into the design of p-n junction devices using p-type CuGaO2 nanoplates.

  5. Morphology evolution and photoluminescence properties of ZnO films electrochemically deposited on conductive glass substrates

    NASA Astrophysics Data System (ADS)

    Cao, Bingqiang; Cai, Weiping; Zeng, Haibo; Duan, Guotao

    2006-04-01

    The current-dependent morphology evolution and photoluminescence properties of zinc oxide (ZnO) films prepared by electrochemical deposition (ECD) method were studied in this paper. It has been shown that the morphologies of ZnO films vary from porous to dense structure, from pillar crystal array to two-dimensional nanosheet covered film, with increase of deposition currents. Correspondingly, orientation of the film evolves from randomly to highly c-axis oriented structure. Current dependence of morphology is attributed to the ECD current-controlled preferential growth velocity along the c axis. All the ZnO films prepared over a wide current range show strong ultraviolet (UV) emission at room temperature, which also shows deposition current dependence in intensity, together with relatively weak defect-related green emission under UV excitations. Further experiments have revealed that a nonradiative relax process and a radiative electron-hole combination process are involved in this defect-related green emission and the excitonic origin of UV emission was also proved.

  6. Structural and photoluminescence properties of terbium-doped zinc oxide nanoparticles

    NASA Astrophysics Data System (ADS)

    Ningthoujam Surajkumar, Singh; Shougaijam Dorendrajit, Singh; Sanoujam Dhiren, Meetei

    2014-05-01

    We present in this paper a study of the structural and photoluminescence (PL) properties of terbium (Tb) doped zinc oxide (ZnO) nanoparticles synthesized by a simple low temperature chemical precipitation method, using zinc acetate and terbium nitrate in an isopropanol medium with diethanolamine (DEA) as the capping agent at 60 °C. The as-prepared samples were heat treated and the PL of the annealed samples were studied. The prepared nanoparticles were characterized with X-ray diffraction (XRD). The XRD patterns show the pattern of typical ZnO nanoparticles and correspond with the standard XRD pattern given by JCPDS card No. 36-1451, showing the hexagonal phase structure. The PL intensity was enhanced due to Tb3+ doping, and it decreased at higher concentrations of Tb3+ doping after reaching a certain optimum concentration. The PL spectra of Tb3+ doped samples exhibited blue, bluish green, and green emissions at 460 nm (5D3 - 7F3), 484 nm (5D4 - 7F6), and 530 nm (5D4 - 7F5), respectively, which were more intense than the emissions for the undoped ZnO sample. Based on the results, an energy level schematic diagram was proposed to explain the possible electron transition processes.

  7. Citrate-Complexation Synthesis and Photoluminescence Properties of Y6MoO12:Eu Nanocrystalline.

    PubMed

    Li, Huaiyong; Pu, Xipeng; Yao, Shujuan; Wang, Xiaoqing; Noh, Hyeon Mi; Jeong, Jung Hyun

    2016-04-01

    Y6MoO12 doped with Eu3+ was synthesized using a citrate-complexation route, and was calcined at 800 °C and 1400 °C, respectively. The structure, morphology and photoluminescence (PL) properties of the samples, and their dependence on the crystallite size were investigated. XRD patterns indicate that the Y6MoO12:Eu3+ powder was obtained at both calcination temperatures, and had a cubic structure. The results also suggest that Y6MoO12:Eu3+ calcined at 800 °C was in the nanocrystalline phase, which was confirmed by the SEM microimage. The crystalline size was about 140 nm. Both phosphors could be excited via three channels: f-f excitation of Eu3+ by blue light, MoO groups excitation by near-UV light, and charge transfer state excitation of Eu3+ by UV light. Both samples yielded red light emissions dominated by the 5D0-7F2 transition at 613 nm. The excitation efficient of the three channels depended on the calcination temperature. The energy transfer from the MoO groups to the Eu3+ ions was more effective in the nanocrystalline phase. The temporal decay feature of the phosphor was also characterized. PMID:27451680

  8. Optical properties of GaSb measured using photoluminescence and photoreflectance spectroscopy

    NASA Astrophysics Data System (ADS)

    Jo, Hyun-Jun; So, Mo Geun; Kim, Jong Su; Lee, Sang Jun

    2016-09-01

    The optical properties of a GaSb layer were investigated using temperature-dependent photoluminescence (PL) and photoreflectance (PR) measurements. The defect-related transitions were observed at 0.714 and 0.728 eV in the PL measurements at 10 K. The band-to-band transition was observed at 0.712 eV in the PL measurement at 300 K. With decreasing temperature, the behavior of the defect-related transition changed slowly compared to the band-to-band transition. The PR spectrum at 300 K showed four signals of E 0 (0.72 eV), E 0 + Δ0 (1.52 eV), E 1 (2.07 eV) and E 1 + Δ1 (2.53 eV). The behavior of the E 1 transition was similar to that of the E 0 transition because the two transitions are band-to-band transitions. The behaviors of the eh transitions from the PL spectra were similar to the results for the E 0 of the PR spectra. The two PR signals of the E 1 transitions using below and above pumping were in good agreement across all temperatures. We confirmed that the below pumping technique was useful in the PR measurement.

  9. Photoluminescence and photocatalytic properties of rhombohedral CuGaO2 nanoplates

    PubMed Central

    Shi, Linlin; Wang, Fei; Wang, Yunpeng; Wang, Dengkui; Zhao, Bin; Zhang, Ligong; Zhao, Dongxu; Shen, Dezhen

    2016-01-01

    Rhombohedral phase CuGaO2 nanoplates with a diameter of about 10 μm were synthesized via low temperature hydrothermal method. Room temperature and low temperature photoluminescence of the obtained CuGaO2 nanoplates were characterized. CuGaO2 nanoplates exhibited blue emission at room temperature and free exciton emission were appeared at low temperature. The blue emission is originated from defects such as Cu vacancies, which is the possible origin of p-type conductivity. The appearance of free exciton emission can demonstrate the direct bandgap transition behavior of CuGaO2 nanoplates. The as-prepared p-type CuGaO2 nanoplates were further decorated by n-type ZnO nanoparticles via calcination method to fabricate p-n junction nanocomposites. The nanocomposites exhibited enhanced photocatalytic activity which can be ascribed to the effective separation of photogenerated carriers by the internal electrostatic field in the p-n junction region, and the enhanced light absorption properties resulted from sub-bandgap absorption effect of p-n junction. This work has offered a new insight into the design of p-n junction devices using p-type CuGaO2 nanoplates. PMID:26887923

  10. Solution-combustion synthesis and photoluminescence properties of YBO3:Tb3+ phosphor powders

    NASA Astrophysics Data System (ADS)

    Onani, Martin O.; Okil, Joseph O.; Dejene, Francis B.

    2014-04-01

    YBO3:Tb3+ nanocrystalline phosphors were successfully deposited by a solution-combustion method, using rare-earth nitrates, urea and boric acid as starting materials. The crystal structure, morphology, chemical composition and photoluminescence properties of the films were investigated by X-ray diffraction (XRD) and atomic force microscopy (AFM). The results of SEM and XRD revealed that the powders were composed of spherical YBO3:Tb3+ nanocrystals with average grain size of between 50 and 100 nm. The electron diffraction spectroscopy (EDS) confirmed the presence of the Y, B, O, and C. The XRD measurements revealed YBO3:Tb3+ (JCPDS:83-1205) structure when annealed at 1000 °C for 2 h. The YBO3:Tb3+ powders exhibited emissions at 490, 545 and 585 nm, which were assigned to the 5D4-7F6, 5D4-7F5 and 5D4-7F4 transitions of Tb3+, respectively. Among them, the green emission at 545 nm (5D4-7F5) was dominant.

  11. Microsphere morphology tuning and photo-luminescence properties of monoclinic Y2WO6

    NASA Astrophysics Data System (ADS)

    Gao, Hong; Bai, Yulong; Zhang, Junying; Tang, Zilong

    2015-04-01

    Effects of the solution pH value and reaction time on the precursor morphology and photoluminescence properties are investigated for hydrothermally prepared monoclinic Y2WO6 phosphors. In the near-neutral environment, sodium dodecyl benzene sulfonate (SDBS) surfactant forms small microspheres micelles as template to synthesize microspherical precursor. H+ ions concentration affects the arrangement of negative ionic surfactant SDBS. As a result, jujube-liked and popcorn-like loose microspheres formed at low pH value. When the pH value is 5.2 and the hydrothermal reaction time reaches 24 h, respectively, the strongest luminescent intensity can be obtained. Under this condition, the precursor presented regular microsphere with diameter of 4.0 μm. After high-temperature heat treatment, the obtained phosphor particles still exhibit microsphere-like shape. Therefore, we provide an effective method to tune the morphology of Y2WO6 phosphors and study the relationship between morphology and luminescent performance.

  12. Enhancing photoluminescence properties of SiC/SiO2 coaxial nanocables by making oxygen vacancies.

    PubMed

    Liu, Wenna; Chen, Junhong; Yang, Tao; Chou, Kuo-Chih; Hou, Xinmei

    2016-09-14

    Coaxial nanocables (CNs) with an SiC core and a SiO2 shell were fabricated at a large scale by a simple and low cost method. The thickness of the SiO2 shell could be controlled by etching in 1 M NaOH aqueous solution for different amounts of time. XRD, SEM, TEM, HRTEM, PL and UV-Vis spectra were adopted to investigate the morphology and optical properties of the obtained SiC/SiO2CNs. Blue photoluminescence was observed at room temperature from the coaxial structure. The intensity of the single emission band at 468 nm (2.65 eV) exhibited a strong dependence on the thickness of the SiO2 layer and was significantly enhanced when the outer SiO2 shell had a thickness of 2.8 nm. The enhancement effect was attributed to oxygen vacancies (OV) and this was verified by deliberately enriching the surface OV through hydrogen treatment. PMID:27503431

  13. Effects of natural oxidation on the photoluminescence properties of Si nanocrystals prepared by pulsed laser ablation

    NASA Astrophysics Data System (ADS)

    Xu, Yanmei; Han, Yinghui

    2014-07-01

    In this work, Si nanocrystals (Si-NCs) have been prepared by pulsed laser ablation technique in dichloromethane, and the microstructure and photoluminescence (PL) properties of the Si-NCs before and after natural oxidation were investigated. Transmission electron microscopy and Raman results show that the average diameter of the Si-NCs is 2.42 nm in the dichloromethane solution. Blue-violet PL with a lifetime of 4.6 ns is observed at room temperature, and the PL peak shifts toward longer wavelength with the red shift of excitation wavelength. The PL excitation spectrum indicates that the bandgap of the Si-NCs in solution is 2.64 eV, which confirms that the blue-violet PL originates from interband transition of Si-NCs caused by quantum confinement effect. The PL peak red shifts to 607 nm after natural oxidation, and the peak lifetime of which is slow down to 13.1 μs. The fixed PL peak excited by different wavelengths and the slow PL decay time indicate that interface defects become the main PL mechanism after natural oxidation. The results will add new information for understanding the PL mechanism of Si-NCs in different environments.

  14. Photoluminescence of heterostructures with GaP{sub 1−x}N{sub x} and GaP{sub 1−x−y}N{sub x}As{sub y} layers grown on GaP and Si substrates by molecular-beam epitaxy

    SciTech Connect

    Lazarenko, A. A. Nikitina, E. V.; Sobolev, M. S.; Pirogov, E. V.; Denisov, D. V.; Egorov, A. Yu.

    2015-04-15

    The structural and optical properties of heterostructures containing GaP{sub 1−x}N{sub x} ternary and GaP{sub 1−x−y}N{sub x}As{sub y} quaternary alloy layers are discussed. The heterostructures are grown by molecular-beam epitaxy on GaP and Si substrates. The structures are studied by the high-resolution X-ray diffraction technique and photoluminescence measurements in a wide temperature range from 10 to 300 K. In the low-temperature photoluminescence spectra of the alloys with a low nitrogen fraction (x < 0.007), two clearly resolved narrow lines attributed to the localized states of nitrogen pairs and the phonon replicas of these lines are observed.

  15. Optical and electronic properties of some semiconductors from energy gaps

    NASA Astrophysics Data System (ADS)

    Tripathy, Sunil K.; Pattanaik, Anup

    2016-03-01

    II-VI and III-V tetrahedral semiconductors have significant potential for novel optoelectronic applications. In the present work, some of the optical and electronic properties of these groups of semiconductors have been studied using a recently proposed empirical relationship for refractive index from energy gap. The calculated values of these properties are also compared with those calculated from some well known relationships. From an analysis of the calculated electronic polarisability of these tetrahedral binary semiconductors from different formulations, we have proposed an empirical relation for its calculation. The predicted values of electronic polarisability of these semiconductors agree fairly well with the known values over a wide range of energy gap. The proposed empirical relation has also been used to calculate the electronic polarisability of some ternary compounds.

  16. Optical Properties and Band Gap of Single- and Few-Layer MoTe2 Crystals

    NASA Astrophysics Data System (ADS)

    Aslan, Ozgur Burak; Ruppert, Claudia; Heinz, Tony

    2015-03-01

    Single- and few-layer crystals of exfoliated MoTe2 have been characterized spectroscopically by photoluminescence, Raman scattering, and optical absorption measurements. We find that MoTe2 in the monolayer limit displays strong photoluminescence. On the basis of complementary optical absorption results, we conclude that monolayer MoTe2 is a direct-gap semiconductor with an optical band gap of 1.10 eV. This new monolayer material extends the spectral range of atomically thin direct-gap materials from the visible to the near-infrared. Supported by the NSF through Grant DMR-1124894 for sample preparation and characterization by the O?ce of Naval Research for analysis. C.R. acknowledges support from the Alexander von Humboldt Foundation.

  17. Size and temperature dependence of the photoluminescence properties of NIR emitting ternary alloyed mercury cadmium telluride quantum dots

    NASA Astrophysics Data System (ADS)

    Jagtap, Amardeep M.; Chatterjee, Abhijit; Banerjee, Arup; Babu Pendyala, Naresh; Koteswara Rao, K. S. R.

    2016-04-01

    Exciton-phonon coupling and nonradiative relaxation processes have been investigated in near-infrared (NIR) emitting ternary alloyed mercury cadmium telluride (CdHgTe) quantum dots. Organically capped CdHgTe nanocrystals of sizes varying from 2.5-4.2 nm have been synthesized where emission is in the NIR region of 650-855 nm. Temperature-dependent (15-300 K) photoluminescence (PL) and the decay dynamics of PL at 300 K have been studied to understand the photophysical properties. The PL decay kinetics shows the transition from triexponential to biexponential on increasing the size of the quantom dots (QDs), informing the change in the distribution of the emitting states. The energy gap is found to be following the Varshni relation with a temperature coefficient of 2.1-2.8  ×  10-4 eV K-1. The strength of the electron-phonon coupling, which is reflected in the Huang and Rhys factor S, is found in the range of 1.17-1.68 for QDs with a size of 2.5-4.2 nm. The integrated PL intensity is nearly constant until 50 K, and slowly decreases up to 140 K, beyond which it decreases at a faster rate. The mechanism for PL quenching with temperature is attributed to the presence of nonradiative relaxation channels, where the excited carriers are thermally stimulated to the surface defect/trap states. At temperatures of different region (<140 K and 140-300 K), traps of low (13-25 meV) and high (65-140 meV) activation energies seem to be controlling the quenching of the PL emission. The broadening of emission linewidth is found to due to exciton-acoustic phonon scattering and exciton-longitudinal optical (LO) phonon coupling. The exciton-acoustic phonon scattering coefficient is found to be enhanced up to 55 μeV K-1 due to a stronger confinement effect. These findings give insight into understanding the photophysical properties of CdHgTe QDs and pave the way for their possible applications in the fields of NIR photodetectors and other optoelectronic devices.

  18. Quantum size effect in the photoluminescence properties of p-type semiconducting transparent CuAlO2 nanoparticles

    NASA Astrophysics Data System (ADS)

    Narayan Banerjee, Arghya; Woo Joo, Sang; Min, Bong-Ki

    2012-12-01

    Photoluminescence properties of CuAlO2 nanoparticles, deposited by a cost-effective direct current sputtering technique, have been studied. The nanoparticles show room-temperature photoluminescence peaks of near-band-edge emission due to recombination of free excitons. A blue-shift in the emission peaks as a decreasing function of the nanoparticle sizes is observed, which is attributed to the quantum confinement effect within the CuAlO2 nanoparticles. Theoretical calculations of bandgap enhancement values are found to be matching fairly well with that of the experimentally obtained values, confirming the existence of the quantum size effect within the nanomaterial. Approximate calculations show that the confinement effect falls within moderate-to-weak confinement regime. X-ray diffraction and electron microscopic measurements confirm the proper phase formation and nanocrystalline structure of the as-deposited nanoparticles. The room-temperature and size-dependent photoluminescence properties of this nanomaterial will be very useful for light emitting diode and similar optoelectronic applications.

  19. Studies on Ferromagnetic and Photoluminescence Properties of ITO and Cu-Doped ITO Nanoparticles Synthesized by Solid State Reaction

    NASA Astrophysics Data System (ADS)

    Babu, S. Harinath; Kaleemulla, S.; Rao, N. Madhusudhana; Krishnamoorthi, C.

    2016-11-01

    Cubic structured indium-tin-oxide (ITO) and copper-doped ITO nanoparticles were synthesized by solid state reaction. The structure, morphology, chemical, magnetic, and photoluminescence properties of the synthesized nanoparticles were studied by x-ray diffraction, field emission scanning electron microscopy, x-ray photoelectron spectroscopy, vibrating sample magnetometry, and photoluminescence spectrophotometry, respectively. Magnetic studies confirmed that the ITO nanoparticles were ferromagnetic at room temperature (300 K) and at 100 K, and it was believed that the observed ferromagnetism may be due to oxygen vacancies and defects present in the system. No hysteresis loop was observed in copper-doped ITO nanoparticles at room temperature and 100 K. The ITO and Cu-doped ITO nanoparticles exhibited two broad emission peaks in the visible region of the electromagnetic spectrum.

  20. Studies on Ferromagnetic and Photoluminescence Properties of ITO and Cu-Doped ITO Nanoparticles Synthesized by Solid State Reaction

    NASA Astrophysics Data System (ADS)

    Babu, S. Harinath; Kaleemulla, S.; Rao, N. Madhusudhana; Krishnamoorthi, C.

    2016-07-01

    Cubic structured indium-tin-oxide (ITO) and copper-doped ITO nanoparticles were synthesized by solid state reaction. The structure, morphology, chemical, magnetic, and photoluminescence properties of the synthesized nanoparticles were studied by x-ray diffraction, field emission scanning electron microscopy, x-ray photoelectron spectroscopy, vibrating sample magnetometry, and photoluminescence spectrophotometry, respectively. Magnetic studies confirmed that the ITO nanoparticles were ferromagnetic at room temperature (300 K) and at 100 K, and it was believed that the observed ferromagnetism may be due to oxygen vacancies and defects present in the system. No hysteresis loop was observed in copper-doped ITO nanoparticles at room temperature and 100 K. The ITO and Cu-doped ITO nanoparticles exhibited two broad emission peaks in the visible region of the electromagnetic spectrum.

  1. Synthesis and Photoluminescence Properties of Li2SrSiO4 Activated with Dy3+ and Sm3+

    NASA Astrophysics Data System (ADS)

    Erdoğmuş, E.

    2015-01-01

    Li2SrSiO4:M (M: Dy3+ and Sm3+) phosphors were synthesized by the conventional solid state reaction. The synthesized materials were characterized by powder XRD. The emission and excitation spectra of these phosphors were measured at room temperature with a spectrofluorometer. The first phosphor, Li2SrSiO4:Dy3+, emits at 479, 573, and 666 nm upon 351 nm excitation. The second phosphor, Li2SrSiO4:Sm3+, emits at 561-571, 594, 647-655, and 703-713 nm upon 399 nm excitation. Also, the dependence of the photoluminescence properties of both phosphors on boric acid concentration was investigated. The results showed that boric acid was effective in improving the photoluminescence intensity of both phosphors.

  2. Investigation on photoluminescence properties and defect chemistry of GdAlO3:Dy3+ Ba2+ phosphors

    NASA Astrophysics Data System (ADS)

    Selvalakshmi, Thangaraj; Sellaiyan, Selvakumar; Uedono, Akira; Semba, Takaaki; Bose, Arumugam Chandra

    2016-08-01

    GdAlO3:Dy3+ Ba2+ phosphors are synthesized by citrate-based sol-gel method. Photoluminescence and positron annihilation studies are used to investigate the emission and defect chemistry of the phosphors respectively. The strong yellow (Dy3+) emission properties of phosphors are discussed for various concentrations of Dy3+ ions. Upon the addition of Ba2+ ion, an enhancement in emission intensity is observed due to the lattice distortions around Dy3+ ion. The positron studies indicate the presence of defects at crystallite boundaries, vacancy clusters and large voids in the materials. The influence of Ba2+ ion on the photoluminescence and lattice distortion around Dy3+ is also explored.

  3. Theoretical and Experimental Insight on Ag2CrO4 Microcrystals: Synthesis, Characterization, and Photoluminescence Properties.

    PubMed

    Silva, Gabriela S; Gracia, Lourdes; Fabbro, Maria T; Serejo Dos Santos, Luis P; Beltrán-Mir, Hector; Cordoncillo, Eloisa; Longo, Elson; Andrés, Juan

    2016-09-01

    Ag2CrO4 microcrystals were synthesized by means of the coprecipitation method without the use of a surfactant under three different conditions. On the basis of the theoretical and experimental results, we describe the relationship among the structural order/disorder effects, morphology, and photoluminescence of the Ag2CrO4 microcrystals. The experimental results were correlated with the theoretical findings for a deeper understanding of the relationship between the electronic structure, morphology, and photoluminescence properties. First-principles computational studies were used to calculate the geometries of bulk Ag2CrO4 and its low-index (001), (011), (110), (010), (111), and (100) facets based on a slab model. A good agreement between the experimental and the theoretical morphologies was found by varying the ratio of the superficial energy values. PMID:27513622

  4. Synthesis, crystal structure and photoluminescent properties of four lanthanide 5-nitroisophthalate coordination polymers

    SciTech Connect

    Huang Yan; Yan Bing; Shao Min

    2009-04-15

    Four new lanthanide coordination polymers, [Y(Hnip)(nip)(H{sub 2}O)].H{sub 2}O (1), [Ln(Hnip)(nip)(H{sub 2}O){sub 2}].2H{sub 2}O [Ln=Eu(2), Tb(3)] and [Y(nip){sub 2}].(H{sub 2}4,4'-bpy){sub 0.5} (4) [5-nip=5-nitroisophthalate, 4,4'-bpy=4,4'-bipyridine], have been hydrothermally synthesized and structurally characterized. Compound 1 features novel lanthanide-carboxylate groups chains composed of three samehanded helical strands intersecting each other through hinged lanthanide atoms, and these chains are cross-linked by phenylene moieties of carboxylate ligands into a 2D layer structure. Compounds 2 and 3 are isomorphous, and contain 1D catenanelike Ln-O-C-O-Ln chains, which are interconnected by phenylene moieties into 2D layer structures. Compound 4, however, displays a 3D architecture sustained by strong hydrogen bonding interactions between the protonated 4,4'-bpy and the carboxyl oxygen atom from [Y{sub 2}(nip){sub 4}]{sup 2-} with 2D layer structure, and 4,4'-bpy as the guest molecules exist in bilayer channel. The studies for the thermal stabilities of the four compounds show that compound 4 is more stable than other compounds. Compound 2 emits characteristic red luminescence of Eu{sup 3+} ions at room temperature, and its luminescent lifetime and quantum efficiency has been determined. - Graphical abstract: Four lanthanide 5-nitroisophthalate coordination polymers have been hydrothermally prepared and resent different structures and thermal stabilities and photoluminescence properties.

  5. Photoluminescence and structural properties of CdSe quantum dot-gelatin composite films

    NASA Astrophysics Data System (ADS)

    Borkovska, L.; Korsunska, N.; Stara, T.; Gudymenko, O.; Kladko, V.; Stroyuk, O.; Raevskaya, A.; Kryshtab, T.

    2014-11-01

    Optical and structural properties of composite films of CdSe quantum dots (QDs) embedded in gelatin matrix have been investigated by photoluminescence (PL), optical absorption and X-ray diffraction (XRD) methods. The optical absorption of the composite in the visible spectral range is found to be determined mainly by light absorption in the QDs. The decrease of the film transparency and the shift of the absorption edge to lower energies observed upon thermal annealing of the films at 140-160 °C are ascribed to the formation of chromophore groups in gelatin matrix. XRD patterns of the composite revealed helix to coil transition in gelatin matrix under thermal annealing of the composite at 100-160 °C. It is found that PL spectra of the composite are dominated by exciton and defect-related emission of the QDs and also contain weak emission of gelatin matrix. It is found that thermal annealing of the composite at 100-160 °C changes PL intensity and produces the shift of the PL bands to lower energies. As the annealed composite was kept in air for several months, the shift of exciton-related PL band position restored partially and the PL intensity increased. It is proposed that the increase of the PL intensity upon the thermal annealing of composite at 140 °C can be used for enhancement of the QD-related PL. Changes that occurred in the PL spectra of composite are ascribed to structural and chemical transformations in gelatin matrix and at the QD/gelatin interface.

  6. Microwave-assisted hydrothermal synthesis of Ag2(W1 -xMox)O4 heterostructures: Nucleation of Ag, morphology, and photoluminescence properties

    NASA Astrophysics Data System (ADS)

    Silva, M. D. P.; Gonçalves, R. F.; Nogueira, I. C.; Longo, V. M.; Mondoni, L.; Moron, M. G.; Santana, Y. V.; Longo, E.

    2016-01-01

    Ag2W1 -xMoxO4 (x = 0.0 and 0.50) powders were synthesized by the co-precipitation (drop-by-drop) method and processed using a microwave-assisted hydrothermal method. We report the real-time in situ formation and growth of Ag filaments on the Ag2W1 -xMoxO4 crystals using an accelerated electron beam under high vacuum. Various techniques were used to evaluate the influence of the network-former substitution on the structural and optical properties, including photoluminescence (PL) emission, of these materials. X-ray diffraction results confirmed the phases obtained by the synthesis methods. Raman spectroscopy revealed significant changes in local order-disorder as a function of the network-former substitution. Field-emission scanning electron microscopy was used to determine the shape as well as dimensions of the Ag2W1 -xMoxO4 heterostructures. The PL spectra showed that the PL-emission intensities of Ag2W1 -xMoxO4 were greater than those of pure Ag2WO4, probably because of the increase of intermediary energy levels within the band gap of the Ag2W1 -xMoxO4 heterostructures, as evidenced by the decrease in the band-gap values measured by ultraviolet-visible spectroscopy.

  7. Controlled fabrication and tunable photoluminescence properties of Mn{sup 2+} doped graphene–ZnO composite

    SciTech Connect

    Luan, Xinglong; Zhang, Yihe Tong, Wangshu; Shang, Jiwu; An, Qi; Huang, Hongwei

    2014-11-15

    Highlights: • Graphene–ZnO composites were synthesized by a mixed solvothermal method. • ZnO quantum dots are distributed uniformly on the graphene sheets. • A possible hypothesis is raised for the influence of graphene oxide on the nucleation of ZnO. • Mn{sup 2+} doped graphene–ZnO composites were fabricated and the emission spectra can be tuned by doping. - Abstract: Graphene–ZnO composites (G–ZnO) with controlled morphology and photoluminescence property were synthesized by a mixed solvothermal method. Mixed solvent were composed by dimethyl sulfoxide and ethylene glycol. Fourier transform infrared spectroscopy, transmission electron microscopy and photoluminescence spectra were used to characterize G–ZnO. Graphene as a substrate can help the distribution and the dispersity of ZnO, and a possible model of the interaction between graphene oxide and ZnO particles is proposed. At the same time, graphene also reduce the size of ZnO particles to about 5 nm. Furthermore, Mn{sup 2+} ions dopes G–ZnO successfully by the mixed solvothermal synthesis and the doping of Mn{sup 2+} makes G–ZnO shift red from 465 nm to 548 nm and 554 nm in the emission spectrum. The changes of the emission spectrum by the adding of Mn{sup 2+} make G–ZnO have tunable photoluminescence spectrum which is desirable for practical applications.

  8. Influence of acetylcholinesterase immobilization on the photoluminescence properties of mesoporous silicon surface

    NASA Astrophysics Data System (ADS)

    Saleem, Muhammad; Rafiq, Muhammad; Seo, Sung-Yum; Lee, Ki Hwan

    2014-07-01

    Acetylcholinesterase immobilized p-type porous silicon surface was prepared by covalent attachment. The immobilization procedure was based on support surface chemical oxidation, silanization, surface activation with cyanuric chloride and finally covalent attachment of free enzyme on the cyanuric chloride activated porous silicon surface. Different pore diameter of porous silicon samples were prepared by electrochemical etching in HF based electrolyte solution and appropriate sample was selected suitable for enzyme immobilization with maximum trapping ability. The surface modification was studied through field emission scanning electron microscope, EDS, FT-IR analysis, and photoluminescence measurement by utilizing the fluctuation in the photoluminescence of virgin and enzyme immobilized porous silicon surface. Porous silicon showed strong photoluminescence with maximum emission at 643 nm and immobilization of acetylcholinesterase on porous silicon surface cause considerable increment on the photoluminescence of porous silicon material while acetylcholinesterase free counterpart did not exhibit any fluorescence in the range of 635-670 nm. The activities of the free and immobilized enzymes were evaluated by spectrophotometric method by using neostigmine methylsulfate as standard enzyme inhibitor. The immobilized enzyme exhibited considerable response toward neostigmine methylsulfate in a dose dependent manner comparable with that of its free counterpart alongside enhanced stability, easy separation from the reaction media and significant saving of enzyme. It was believed that immobilized enzyme can be exploited in organic and biomolecule synthesis possessing technical and economical prestige over free enzyme and prominence of easy separation from the reaction mixture.

  9. MgO:Dy{sup 3+} nanophosphor: Self ignition route, characterization and its photoluminescence properties

    SciTech Connect

    Devaraja, P.B.; Avadhani, D.N.; Nagabhushana, H.; Prashantha, S.C.; Sharma, S.C.; Nagabhushana, B.M.; Nagaswarupa, H.P.; Daruka Prasad, B.

    2014-11-15

    For the first time series of MgO phosphors doped with different concentrations of Dy{sup 3+} (1–9 mol%) were prepared by solution combustion method using glycine as a fuel. The final products were well characterized by powder X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy and transmission electron microscopy. The powder X-ray diffraction patterns of the as-formed product show single cubic phase. The crystallite size estimated using Scherrer's method was found to be in the range 5–15 nm and the same was confirmed by transmission electron microscopy result. Photoluminescence properties of Dy{sup 3+} (1–9 mol%) doped MgO for near ultra violet excitation (325 nm) was studied in order to investigate the possibility of its use in white light emitting diode applications. The emission spectra consists of intra 4f transitions of Dy{sup 3+}, namely {sup 4}F{sub 9/2} → {sup 6}H{sub 15/2} (483 nm), and {sup 4}F{sub 9/2} → {sup 6}H{sub 13/2} (573 nm). Further, the emission at 573 nm shows strong yellow emission and can be applied to the yellow emission of phosphor for the application for near ultraviolet excitation. The intensity of yellow emission was attributed to intrinsic defects, especially oxygen-vacancies, which could assist the energy transfer from the MgO host to the Dy{sup 3+} ions. The Commission International De I-Eclairage chromaticity co-ordinates were calculated from emission spectra, the values (x,y) were very close to the National Television System Committee standard value of white emission. Therefore, the present phosphor was highly useful for display applications. - Graphical Abstract: PL emission spectra and CIE diagram of MgO:Dy{sup 3+} nanophosphor. - Highlights: • MgO:Dy{sup 3+} prepared by simple and low cost LCS method at low temperature (400 °C). • Characteristic emission peaks of Dy{sup 3+} ion at ∼ 483 and 573 nm are recorded. • CIE co-ordinate values located in the white region.

  10. Synthesis, structures, and photoluminescence properties of novel lanthanide tetracyanoplatinates lacking Pt-Pt interactions

    SciTech Connect

    Stojanovic, Milorad; Robinson, Nicholas J.; Chen Xi; Smith, Philip A.; Sykora, Richard E.

    2010-04-15

    The synthesis of a series of lanthanide tetracyanoplatinates all incorporating 2,2':6',2''-terpyridine (terpy) have been carried out by reaction of Ln{sup 3+} nitrate salts with terpy and potassium tetracyanoplatinate. The incorporation of different Ln{sup 3+} cations results in the isolation of [Ln(DMF){sub 2}(C{sub 15}H{sub 11}N{sub 3})(H{sub 2}O){sub 2}(NO{sub 3})]Pt(CN){sub 4} (Ln=La-Nd, Sm-Yb) under otherwise identical reaction conditions. These compounds have been isolated as single crystals and X-ray diffraction has been used to investigate their structural features. All of the reported compounds are isostructural. Crystallographic data for the representative Eu{sup 3+} compound (EuPt) are (MoKalpha, lambda=0.71073 A): monoclinic, space group P2{sub 1}/c, a=10.1234(4) A, b=18.7060(7) A, c=17.1642(5) A, beta=97.249(3){sup o}, V=3224.4(2), Z=4, R(F)=2.78% for 426 parameters with 7724 reflections with I>2sigma(I). The structure consists of a zero-dimensional, ionic salt containing complex [Eu(DMF){sub 2}(C{sub 15}H{sub 11}N{sub 3})(H{sub 2}O){sub 2}(NO{sub 3})]{sup 2+} cations and Pt(CN){sub 4}{sup 2-} anions. The complex cations contain the Eu{sup 3+} ions in a tri-capped trigonal prismatic coordination environment with one terdentate 2,2':6',2''-terpyridine molecule, one bidentate nitrate anion, two O-bound dimethylformamide molecules, and two coordinated water molecules. Photoluminescence data illustrate that EuPt displays intramolecular energy transfer from the coordinated terpy molecule to the Eu{sup 3+} cation. The uncoordinated tetracyanoplatinate anion also exhibits visible emission. - Graphical abstract: The synthesis of an isostructural series of lanthanide tetracyanoplatinates incorporating 2,2':6',2''-terpyridine are presented. Solid-state absorption and luminescence properties are discussed for the Eu{sup 3+} and La{sup 3+} compounds.

  11. Half-oxidized phosphorene: band gap and elastic properties modulation.

    PubMed

    Drissi, L B; Sadki, S; Sadki, K

    2016-04-13

    Based on a first principles approach, we study structural, electronic and elastic properties, as well as stabilities of all possible half-oxidized phosphorene conformers. Stability analysis reveals that oxygen chemisorption is an exothermic process in the six configurations despite the formation of interstitial oxygen bridges in three of them. Electronic structure calculations show that oxidation induces a band gap modulation ranging between 0.54 and 1.57 eV in the generalized gradient approximation corrected to 1.19 and 2.88 eV using GW. The mechanical response of the conformers is sensitively dependent on direction and indicates that the new derivatives are incompressible materials and one configuration has an auxetic behavior. The present results provide a basis for tailoring the electronic and elastic properties of phosphorene via half oxidation. PMID:26964522

  12. Half-oxidized phosphorene: band gap and elastic properties modulation

    NASA Astrophysics Data System (ADS)

    Drissi, L. B.; Sadki, S.; Sadki, K.

    2016-04-01

    Based on a first principles approach, we study structural, electronic and elastic properties, as well as stabilities of all possible half-oxidized phosphorene conformers. Stability analysis reveals that oxygen chemisorption is an exothermic process in the six configurations despite the formation of interstitial oxygen bridges in three of them. Electronic structure calculations show that oxidation induces a band gap modulation ranging between 0.54 and 1.57 eV in the generalized gradient approximation corrected to 1.19 and 2.88 eV using GW. The mechanical response of the conformers is sensitively dependent on direction and indicates that the new derivatives are incompressible materials and one configuration has an auxetic behavior. The present results provide a basis for tailoring the electronic and elastic properties of phosphorene via half oxidation.

  13. Hanford Waste Physical and Rheological Properties: Data and Gaps - 12078

    SciTech Connect

    Kurath, D.E.; Wells, B.E.; Huckaby, J.L.; Mahoney, L.A.; Daniel, R.C.; Burns, C.A.; Tingey, J.M.; Cooley, S.K.

    2012-07-01

    The retrieval, transport, treatment and disposal operations associated with Hanford Tank Wastes involve the handling of a wide range of slurries. Knowledge of the physical and rheological properties of the waste is a key component to the success of the design and implementation of the waste processing facilities. Previous efforts to compile and analyze the physical and rheological properties were updated with new results including information on solids composition and density, particle size distributions, slurry rheology, and particle settling behavior. The primary source of additional data is from a recent series of tests sponsored by the Hanford Waste Treatment and Immobilization Plant (WTP). These tests involved an extensive suite of characterization and bench-scale process testing of 8 waste groups representing approximately 75% of the high-level waste mass expected to be processed through the WTP. Additional information on the morphology of the waste solids was also included. Based on the updated results, a gap analysis to identify gaps in characterization data, analytical methods and data interpretation was completed. (authors)

  14. Hanford Waste Physical and Rheological Properties: Data and Gaps

    SciTech Connect

    Kurath, Dean E.; Wells, Beric E.; Huckaby, James L.; Mahoney, Lenna A.; Daniel, Richard C.; Burns, Carolyn A.; Tingey, Joel M.; Cooley, Scott K.

    2012-03-01

    The retrieval, transport, treatment and disposal operations associated with Hanford Tank Wastes involve the handling of a wide range of slurries. Knowledge of the physical and rheological properties of the waste is a key component to the success of the design and implementation of the waste processing facilities. Previous efforts to compile and analyze the physical and rheological properties were updated with new results including information on solids composition and density, particle size distributions, slurry rheology, and particle settling behavior. The primary source of additional data is from a recent series of tests sponsored by the Hanford Waste Treatment and Immobilization Plant. These tests involved an extensive suite of characterization and bench-scale process testing of 8 waste groups representing approximately 75% of the high-level waste mass expected to be processed through the WTP. Additional information on the morphology of the waste solids was also included. Based on the updated results, a gap analysis to identify gaps in characterization data, analytical methods and data interpretation was completed.

  15. Structural and photoluminescence properties of Ce, Dy, Er-doped ZnO nanoparticles

    SciTech Connect

    Jayachandraiah, C.; Kumar, K. Siva; Krishnaiah, G.

    2015-06-24

    Undoped ZnO and rare earth elements (Ce, Dy and Er with 2 at. %) doped nanoparticles were synthesized by wet chemical co-precipitation method at 90°C with Polyvinylpyrrolidone (PVP) as capping agent. The structural, morphological, compositional and photoluminescence studies were performed with X-ray diffraction (XRD), Transmission electron microscopy (TEM), Energy dispersive spectroscopy (EDS), FTIR spectroscopy and Photoluminescence (PL) respectively. XRD results revealed hexagonal wurtzite structure with average particle size around 18 nm - 14 nm and are compatible with TEM results. EDS confirm the incorporation of Ce, Dy and Er elements into the host ZnO matrix and is validated by FTIR analysis. PL studies showed a broad intensive emission peak at 558 nm in all the samples. The intensity for Er- doped ZnO found maximum with additional Er shoulder peaks at 516nm and 538 nm. No Ce, Dy emission centers were found in spectra.

  16. Structural and photoluminescence properties of Cd and Cu co-doped zinc oxide nanoparticles

    NASA Astrophysics Data System (ADS)

    Samuel, T.; Sujatha, K.; Rao, K. Ramachandra; Rao, M. C.

    2016-05-01

    Cd and Cu co-doped ZnO nanoparticles were synthesized by Polyol method and subsequently have been characterized by their structure, optical and photoluminescence studies. XRD and PSA results revealed the formation of Cd and Cu co-doped ZnO nanoparticles with an average crystallite size of 50 nm and average particle size of 246 nm. From Zeta Potential measurements the Zeta Potential was found to be - 29.2 eV indicating the stability of prepared nanoparticles. From Uv-Vis studies, it is found that the absorption of undoped ZnO is less compared with Cd and Cu co-doped ZnO and the absorbance increases with increase in dopant concentration. Photoluminescence studies revealed that the samples are with high structural and optical quality.

  17. Coherence properties of the photoluminescence from CdS-ZnO nanocomposite thin films.

    PubMed

    Vasa, Parinda; Singh, B P; Ayyub, Pushan

    2005-01-12

    The application of semiconductor quantum dots in important new areas such as random lasing and quantum-information processing requires knowledge of the coherence of the optical emission from such systems. We report the first direct experimental estimation of the coherence in the light emitted by a nanoparticle ensemble. The photoluminescence from a two-phase nanocomposite CdS-ZnO thin film (with a characteristic grain size of 2-3 nm for both the chemical phases) possesses an appreciable degree of spatial and temporal coherence at room temperature. The degree of spatial coherence was estimated from the classical Young's double slit experiment. We also discuss a simple technique for estimating the degree of spectral coherence of the photoluminescence from thin films.

  18. Preparation and Photoluminescence Properties of Ti-Doped Lu2O3 Powder

    NASA Astrophysics Data System (ADS)

    Zeng, G.; Dong, Q.; Bao, W.

    2016-07-01

    A series of Lu2O3:Ti powders was prepared via a co-precipitation route. With the help of X-ray diffraction analysis (XRD), the phase transition temperature of 773 K is confirmed for the powders. It is difficult to reduce the Ti4+ ions in the powders to Ti3+ ions in H2 atmosphere even if the calcination temperature reaches 773 K, which is verified by measurements of X-ray photoelectron spectroscopy and electron paramagnetic resonance spectroscopy. The Lu2O3:Ti powders calcined in H2 demonstrate an ability to emit white light under UV light excitation. The spectral analysis of photoluminescence and photoluminescence excitation reveals that the luminescence emission originates from the clusters (Ti4+-F- V Lu ' ' ' , etc.). The results show t hat Ti4+ ion and F center are noteworthy luminescent centers in developing luminescent materials.

  19. The influence of pressure on the photoluminescence properties of a terbium-adipate framework

    SciTech Connect

    Spencer, Elinor C.; Zhao, Jing; Ross, Nancy L.; Andrews, Michael B.; Surbella, Robert G.; Cahill, Christopher L.

    2013-06-15

    The influence of pressure (over the 0–4.7 GPa range) on the photoluminescence emissions and crystal structure of the known 3D terbium-adipate metal-organic framework material Tb-GWMOF6 has been evaluated by high-pressure single-crystal X-ray diffraction and spectroscopic techniques. The results from this study show that this complex lanthanide framework structure undergoes three phase transitions within the 0–4 GPa pressure range that involve alterations in the number of symmetry independent Tb{sup 3+} ion sites within the crystal lattice. These pressure induced modifications to the structure of Tb-GWMOF6 lead to pronounced changes in the profiles of the {sup 5}D{sub 4}→{sup 7}F{sub 5} emission spectra of this complex. - Graphical abstract: The influence of pressure on the structure and photoluminescence emissions of a 3D terbium-adipate framework. - Highlights: • High-pressure luminescence spectra for a Tb framework were collected. • High-pressure single-crystal XRD experiments were conducted with the Tb Framework. • The framework undergoes two pressure-induced phase transitions. • The three phases of the material show different photoluminescence behaviour.

  20. Photoluminescence from chemically exfoliated MoS2.

    PubMed

    Eda, Goki; Yamaguchi, Hisato; Voiry, Damien; Fujita, Takeshi; Chen, Mingwei; Chhowalla, Manish

    2011-12-14

    A two-dimensional crystal of molybdenum disulfide (MoS2) monolayer is a photoluminescent direct gap semiconductor in striking contrast to its bulk counterpart. Exfoliation of bulk MoS2 via Li intercalation is an attractive route to large-scale synthesis of monolayer crystals. However, this method results in loss of pristine semiconducting properties of MoS2 due to structural changes that occur during Li intercalation. Here, we report structural and electronic properties of chemically exfoliated MoS2. The metastable metallic phase that emerges from Li intercalation was found to dominate the properties of as-exfoliated material, but mild annealing leads to gradual restoration of the semiconducting phase. Above an annealing temperature of 300 °C, chemically exfoliated MoS2 exhibit prominent band gap photoluminescence, similar to mechanically exfoliated monolayers, indicating that their semiconducting properties are largely restored.

  1. Enhanced photoluminescence properties of methylene blue dye encapsulated in nanosized hydroxyapatite/silica particles with core-shell structure

    NASA Astrophysics Data System (ADS)

    Ge, Xiaolu; Li, Chengfeng; Fan, Chengyu; Feng, Xiaoxing; Cao, Bingqiang

    2013-11-01

    Organic dye of methylene blue (MB) was encapsulated in core-shell structured hydroxyapatite/silica particles (HAp/silica-MB) through a modified Stöber method with the addition of polyvinylpyrrolidone molecules. It was found that MB molecules were released from HAp/silica-MB at a slower rate than those from silica-MB in deionized water. In phosphate buffered saline (pH: 7.2-7.4) and acidic solutions (pH: 1.5-1.6), the penetration of ions in the interface influenced the interaction between HAp and MB molecules, which resulted in the rapid release of MB molecules from HAp/silica-MB. From the UV-Vis absorbance spectra, one could see that MB molecules in HAp/silica-MB were weakly aggregated in comparison with those in silica-MB. For HAp/silica-MB, enhanced luminescence properties were observed in the photoluminescence spectra and dual luminescence with two emission peaks were caused by the presence of monomers and dimers. Contrarily, no photoluminescence emission was detected for samples of free MB and silica-MB under the same excitation condition because of the self-quenching effect. It was the adsorption of MB molecules on HAp that had resulted in the enlargement of intramolecular distance and the reduction of self-quenching effect. These hybrid particles with enhanced luminescent properties might find wide applications in the field of bioanalysis, bioseparation, and biomedical imaging.

  2. Raman and photoluminescence properties of type II GaSb/GaAs quantum dots on (001) Ge substrate

    NASA Astrophysics Data System (ADS)

    Zon; Poempool, Thanavorn; Kiravittaya, Suwit; Nuntawong, Noppadon; Sopitpan, Suwat; Thainoi, Supachok; Kanjanachuchai, Songphol; Ratanathammaphan, Somchai; Panyakeow, Somsak

    2016-07-01

    We investigate structural Raman and photoluminescence properties of type II GaSb/GaAs quantum dots (QDs) grown on (001) Ge substrate by molecular beam epitaxy. Array of self-assembled GaSb QDs having an areal density of ˜1.66 × 1010 dots/cm2 is obtained by a growth at relatively low substrate temperature (450 °C) on a GaAs surface segmented into anti-phase domains (APDs). Most of QDs form in one APD area. However, a few QDs can be observed at the APD boundaries. Raman spectroscopy is used to probe the strain in GaAs layer. Slight redshift of both LO and TO GaAs peaks are observed when GaSb QDs are buried into GaAs matrix. Optical properties of capped QDs are characterized by photoluminescence measurement at low temperatures (20 K and 30 K). Emission peaks of GaSb/GaAs QDs are found in the range of 1.0-1.3 eV at both temperatures. Slight redshift is observed when the laser excitation power is increased at 20 K while blueshift of QD peak is observed at 30 K. We attribute this abnormal behavior to the contribution of overlapped GaSb wetting layer peak in the PL emission as well as the feature of type II band structure. [Figure not available: see fulltext.

  3. Energy transfer based photoluminescence properties of (Sm3+ + Eu3+):PEO + PVP polymer films for Red luminescent display device applications

    NASA Astrophysics Data System (ADS)

    Naveen Kumar, K.; Vijayalakshmi, L.; Ratnakaram, Y. C.

    2015-07-01

    Eu3+:PEO + PVP, Sm3+:PEO + PVP and co-doped Sm3+ + Eu3+:PEO + PVP polymer films have successfully been synthesized by solution casting method. For these polymer films, their XRD, FTIR and RAMAN spectral profiles were studied systematically. Both absorption and photoluminescence spectra have been assessed by evaluating their optical properties. The Sm3+:PEO + PVP and Eu3+:PEO + PVP polymer film has displayed a reddish-orange and red emissions at 596 nm and 619 nm respectively under an UV lamp. A reddish-orange emission was found for Sm3+:PEO + PVP polymer film at 596 nm (4G5/2 → 6H7/2) and its lifetime has also been evaluated suitably. Red emission at 619 nm (4G5/2 → 6H7/2) of Eu3+ has been identified for Eu3+:PEO + PVP polymer film and its lifetime are also evaluated. The photoluminescence efficiency of Eu3+ ion has been enhanced due to the addition of Sm3+ by means of an energy transfer process. The energy transfer mechanism, from Sm3+ to Eu3+ has been clearly established. At 0.1 wt% concentration of Sm3+ ions (sensitizer), the photoluminescence efficiency of the Eu3+ ion (activator) has been significantly enhanced in co-doped sample through energy transfer from Sm3+ to Eu3+ in the polymer matrix. The energy transfer process has been analyzed using lifetime decay dynamics. From the obtained results, these polymer materials could be proposed as potential Red luminescent optical materials.

  4. Synthesis, structure and photoluminescence properties of Sm3+-doped BiOBr phosphor

    NASA Astrophysics Data System (ADS)

    Halappa, Pramod; Shivakumara, C.; Saraf, Rohit; Nagabhushana, H.

    2016-05-01

    Well-crystallized tetragonal layered BiOBr and Bi0.95Sm0.05OBr phosphors were prepared by the solid state method. These compounds were characterized using powder X-Ray diffraction and photoluminescence technique. In PL spectra, the electric dipole transitions dominate than other transitions which indicate that the Sm3+ ions occupy a site with an inversion center of BiOBr. CIE chromaticity diagram confirmed that these phosphors can be useful in the fabrication of red component in white light emitting diodes (WLEDs) for display device applications.

  5. Synthesis and photoluminescent properties of SnO-containing germanate and germanosilicate glasses

    NASA Astrophysics Data System (ADS)

    Chernov, A. I.; Denker, B. I.; Ermakov, R. P.; Galagan, B. I.; Iskhakova, L. D.; Sverchkov, S. E.; Velmiskin, V. V.; Dianov, E. M.

    2016-09-01

    Divalent tin-containing germanate glasses have demonstrated wide photoluminescence similar to that of tin silicate glasses discovered recently. In comparison with silicate glasses, the germanate glasses are characterized by longer emission lifetimes (145 ÷ 440 µs), emission peaking at 1.59 ÷ 1.64 µm and the absence of SnO disproportionation into SnO2 and Sn during glass synthesis. The potential fabrication of optical fiber via the SnC2O4 + GeO2 powder in silica tube method was demonstrated.

  6. Effects of thickness layer on the photoluminescence properties of InAlAs/GaAlAs quantum dots

    NASA Astrophysics Data System (ADS)

    Daly, A. Ben; Bernardot, F.; Barisien, T.; Galopin, E.; Lemaître, A.; Maaref, M. A.; Testelin, C.

    2016-09-01

    We investigated the effect of InAlAs layer thickness on exciton-spin relaxation and optical properties of In0.62Al0.38As/Al0.67Ga0.33As QDs. The luminescence properties and carrier dynamics of QDs were studied by the temperature-dependent photoluminescence (PL) and pump-probe measurements. As the total amount of deposited In0.62Al0.38As alloy increased, the central position of the low-energy PL signal decreases, while its full width at half maximum (FWHM) increases. A monotonous redshift of the PL peak was observed with increasing temperature due to the electron-phonon scattering. From the pump-probe measurement, the spin relaxation time decreases with the monolayers at higher temperatures, in agreement with the phonon energy determinate by PL measurements.

  7. Optical properties study of In.08Ga.92As/GaAs using spectral reflectance, photoreflectance and near-infrared Photoluminescence

    NASA Astrophysics Data System (ADS)

    Tounsi, N.; Habchi, M. M.; Chine, Z.; Rebey, A.; El Jani, B.

    2013-07-01

    Optical properties of In.08Ga.92As/GaAs structure grown by metalorganic vapor phase epitaxy have been investigated. Spectral reflectance (SR) and photoreflectance (PR) as well as near-infrared Photoluminescence (PL) were performed in this study. In fact, SR signals in the range 200-1700 nm provided specific parameters of materials such as optical constant spectra, sensitivity to wavelength and critical point energies. In addition, band gap energy was determined by both PR and optical absorption measurements at room temperature. Spin-orbit splitting, internal electric field and electro-optical energy were also calculated. Results provided by previous techniques present a good correlation and complementarities and agree well with the literature. On the other hand, the origins of 12 K PL peaks at 1.42, 1.38 and 1.29 eV, have been identified by performing excitation power (Pex) study. Finally, the peak at 1.38 eV has two regimes of variation with Pex separated by a critical power around 50 mW.

  8. Photoluminescence and electrical properties of polyvinyl alcohol films doped with CdS nanoparticles

    NASA Astrophysics Data System (ADS)

    Ali, Z. I.; Hosni, H. M.; Saleh, H. H.; Ghazy, O. A.

    2016-05-01

    In situ preparation of polyvinyl alcohol (PVA) films doped with cadmium sulfide (CdS) nanoparticles was conducted by gamma radiation. The films were characterized in terms of photoluminescence and electrical conductivity. The photoluminescence results indicated the existence of two emission peaks around 470 and 530 nm, which are due to electron-hole recombination of CdS nanoparticles and surface trapped emission due to the PVA capping, respectively. DC electrical conductivity ( σ DC) measurement in the temperature range from 303 up to 373 K reveals an increase in its value with increasing both Cd2+ ion molar concentration and irradiation dose. AC electrical conductivity ( σ AC) measurement over the same temperature range at an applied field frequency of 10, 100, 500 and 1000 kHz shows an increase behavior with increasing temperature, frequency, Cd2+ ion molar concentration and irradiation dose. Dielectric constant ( ɛ 1) exhibits an increase with temperature, whereas it shows reduced values with increasing frequency, Cd2+ ion molar concentration and irradiation dose. Also, the dielectric loss tangent (tan δ) follows an increasing trend with increasing temperature, Cd2+ ion molar concentration and irradiation dose while it has an opposite trend with increasing frequency. The CdS/PVA nanocomposite films behavior could be explained on the basis of formation of charge-transfer complexes (CTCs) by the CdS nanoparticles doped into the PVA matrix and the role of radiation in enhancing the charge carrier mobility of such CTCs.

  9. Shape controlled synthesis of CaMoO{sub 4} thin films and their photoluminescence property

    SciTech Connect

    Marques, Ana Paula de Azevedo Longo, Valeria M.; Melo, Dulce M.A. de; Pizani, Paulo S.; Leite, Edson R.; Varela, Jose Arana; Longo, Elson

    2008-05-15

    CaMoO{sub 4} (CMO) disordered and ordered thin films were prepared by the complex polymerization method (CPM). The films were annealed at different temperatures and time in a conventional resistive furnace (RF) and in a microwave (MW) oven. The microstructure and surface morphology of the structure were monitored by atomic force microscopy (AFM) and high-resolution scanning electron microscopy (HRSEM). Order and disorder were characterized by X-ray diffraction (XRD) and optical reflectance. A strong photoluminescence (PL) emission was observed in the disordered thin films and was attributed to complex cluster vacancies. The experimental results were compared with density functional and Hartree-Fock calculations. - Graphical abstract: CaMoO{sub 4} thin films were prepared by the complex polymerization method (CPM). The films were annealed at different temperatures and time in a conventional resistive furnace and in a microwave oven. A strong photoluminescence emission was observed in the disordered thin films and was attributed to complex cluster vacancies. The experimental results were confirmed by high level first principle calculations.

  10. Six new coordination polymers constructed by 3-carboxyl-5-oxycarboxymethylpyridinio-1-carboxylate: Crystal structures, topologies, photoluminescent and magnetic properties

    SciTech Connect

    Yuan, Hong-Yan; Han, Min-Min; Jiang, Xian-Rong; Jiang, Zhan-Guo; Feng, Yun-Long

    2013-06-01

    Six new two-dimensional (2D) coordination polymers, [ML(H₂O)₃]ₙ (M=Zn (1), Cd (2), Mn (3), Co (4)), [CdL(H₂O)]ₙ} (5), [CdL(4,4´-bipy)]ₙ·nH₂O (6), (H₂L=3-carboxyl-5-oxycarboxymethylpyridinio-1-carboxylate, 4,4´-bipy=4,4´-bipyridine), have been hydrothermally synthesized and characterized by single crystal X-ray diffraction analyses, IR spectra, and thermogravimetric analyses. 1, 2, 3, 4 are isostructural and feature a binodal (4,6)-connected topology with left- and right-handed helical chains with a pitch of 9.9560 Å. 5 can be topologically presented as an uninodal 6-connected network if the hydrogen bonds are also considered. 6 is a binodal (3,5)-connected 2D layer network. The photoluminescent properties of 1, 2, 5, 6 and magnetic properties of 3, 4 have been studied and discussed. - Graphical abstract: The structural differences show that the ligand, the metal center, and the reaction conditions have great influence on the structure of the final assembly. Highlights: • A new asymmetric flexible tricarboxylate ligand of 3-carboxyl-5-oxycarboxymethylpyridinio-1-carboxylate was synthesized. • Six new two-dimensional (2D) coordination polymers have been hydrothermally obtained. • 1, 2, 3, 4 are isostructural and feature a binodal (4,6)-connected topology with left- and right-handed helical chains. • The photoluminescent properties of 1, 2, 5, 6 and magnetic properties of 3, 4 have been studied.

  11. Enhancement in ferroelectric, pyroelectric and photoluminescence properties in dye doped TGS crystals

    SciTech Connect

    Sinha, Nidhi; Goel, Neeti; Singh, B.K.; Gupta, M.K.; Kumar, Binay

    2012-06-15

    Pure and dye doped (0.1 and 0.2 mol%) Triglycine Sulfate (TGS) single crystals were grown by slow evaporation technique. A pyramidal coloring pattern, along with XRD and FT-IR studies confirmed the dye doping. Decrease in dielectric constant and increase in Curie temperature (T{sub c}) were observed with increasing doping concentration. Low absorption cut off (231 nm) and high optical transparency (>90%) resulting in large band gap was observed in UV-VIS studies. In addition, strong hyper-luminescent emission bands at 350 and 375 nm were observed in which the relative intensity were found to be reversed as a result of doping. In P-E hysteresis loop studies, a higher curie temperature and an improved and more uniform figure of merit over a large region of the ferroelectric phase were observed. The improved dielectric, optical and ferroelectric/pyroelectric properties make the dye doped TGS crystals better candidate for various opto- and piezo-electronics applications. - Graphical abstract: Dye doping in TGS crystal resulted in hourglass morphology, increased hyper-luminescence intensity, improved T{sub c} and figure of merit. Highlights: Black-Right-Pointing-Pointer Amaranth dye doping in TGS crystals resulted in hourglass morphology. Black-Right-Pointing-Pointer Doping resulted in enhancement of Curie temperature from 49 to 53 Degree-Sign C. Black-Right-Pointing-Pointer Low cut off (230 nm) and wider transmittance window observed. Black-Right-Pointing-Pointer Strong hyper-luminescent emission bands at 350 and 375 nm were observed. Black-Right-Pointing-Pointer High and uniform figure of merit in ferroelectric phase was obtained.

  12. The effect of two additional Eu3+ lumophors in two novel trinuclear europium complexes on their photoluminescent properties.

    PubMed

    Yang, Chaolong; Xu, Jing; Ma, Jianying; Zhu, Dongyu; Zhang, Yunfei; Liang, Liyan; Lu, Mangeng

    2013-02-01

    Two novel trinuclear europium complexes based on trisphen(1,3,5-tris{4-((1,10-phenanthroline-[5,6-d]imidazol-2yl)phenoxy)methyl}-2,4,6-trimethyl-benzene) as a second ligand were designed, synthesized, and characterized by FT-IR, (1)H NMR, UV-visible, photoluminescence (PL) spectroscopy, elemental analysis (EA) and ESI-MS. The geometries of these two trinuclear europium complexes were predicted using the Sparkle/PM3 model and suggested a chemical environment of very low symmetry around the lanthanide ions (C(1)), which is in agreement with the luminescent spectra. CV analysis demonstrated that the trinuclear complexes possessed excellent electro-injection abilities. The effects of two additional Eu(3+) lumophors in these trinuclear europium complexes on their photoluminescent properties were investigated in detail. The results indicated that these trinuclear europium complexes exhibited highly luminescent quantum efficiencies and experimental intensity parameters in the solid state. Especially, due to the contribution of the two additional Eu(3+) lumophors in the trinuclear europium complexes, the quantum efficiency of the trinuclear complex Eu(3)(TTA)(9)trisphen was higher (ca. 34%) than the mononuclear europium complex Eu(TTA)(3)imidazophen.

  13. Effect of hydrogen dilution on photoluminescent properties of nanocrystalline SiC films deposited by helicon wave plasma CVD

    NASA Astrophysics Data System (ADS)

    Yu, Wei; Du, Jie; Zhang, Li; Cui, Shuang Kui; Han, Li; Fu, Guang Sheng

    2007-11-01

    Nanocrystalline silicon carbide (nc-SiC) thin films were deposited by helicon wave plasma enhanced chemical vapor deposition (HW-PECVD) technique at different hydrogen dilution ratio (RH). The PL peak energy and intensity were systemically analyzed using photoluminescent (PL) and photoluminescent excitation (PLE) methods. As a whole, the PL intensity shows an increasing trend and the PL peak energy presents continuous blue shifts with increasing hydrogen dilution ratio. In addition, it is found that the spectra band of samples deposited at low RH are composed of two components, the high energy band comes from quantum confinement effect and the low energy band is related to radiation of surface defect. The low energy band has a decreasing trend with increasing hydrogen dilution ratio and even disappears finally at high RH. We explain dependence of PL properties in terms of the variation of film microstructure induced by hydrogen dilution during film deposition. The increasing of PL intensity and the decreasing of the low energy band can both be accounted by the microstructure improvement. The decrease of PL peak energy is related to the size decrease of SiC nanocrystals.

  14. Electrospinning preparation and photoluminescence properties of poly (methyl methacrylate)/Eu{sup 3+} ions composite nanofibers and nanoribbons

    SciTech Connect

    Li, Maoying; Zhang, Zhenyi; Cao, Tieping; Sun, Yangyang; Liang, Pingping; Shao, Changlu; Liu, Yichun

    2012-02-15

    Graphical abstract: Nanofibers and nanoribbons of poly (methyl methacrylate)/Eu{sup 3+} ions composites were successfully prepared by using a simple electrospinning technique. And the photoluminescence properties of the above PMMA/Eu{sup 3+} ions composites were studied. Highlights: Black-Right-Pointing-Pointer Nanofibers and nanoribbons of PMMA/Eu{sup 3+} ions composites are fabricated by electrospinning. Black-Right-Pointing-Pointer Photoluminescence properties of as-electrospun PMMA/Eu{sup 3+} ions composites are studied. Black-Right-Pointing-Pointer The ratios of electric- and magnetic-dipole transitions are enhanced by increasing electrospinning voltage. -- Abstract: Nanofibers and nanoribbons of poly (methyl methacrylate) (PMMA)/Eu{sup 3+} ions composites with different concentration of Eu{sup 3+} ions were successfully prepared by using a simple electrospinning technique. From the results of scanning electron microscopy and energy-dispersive X-ray spectroscopy, we found that the morphology of the as-electrospun PMMA/Eu{sup 3+} ions composites could be changed from fiber to ribbon structure by adjusting the concentration of Eu{sup 3+} ions in the electrospun precursor solution. The coordination between the Eu{sup 3+} ions and PMMA molecules were investigated by Fourier transform infrared spectroscopy and differential thermal analysis. The photoluminescence (PL) properties of the as-electrospun PMMA/Eu{sup 3+} ions composites were studied in comparison to those of the Eu(NO{sub 3}){sub 3} powder. It was showed that the {sup 5}D{sub 0}-{sup 7}F{sub J} (J = 0, 1, 2, 3, 4) emission appeared in the PL spectra of the as-electrospun PMMA/Eu{sup 3+} ions composites, whereas the {sup 5}D{sub 0}-{sup 7}F{sub 0} emission was completely absent in the PL spectra of Eu(NO{sub 3}){sub 3} powder due to the different local environments surrounding Eu{sup 3+} ions. It was interesting to note that the intensity ratios of the electric-dipole and magnetic-dipole transitions for

  15. NaGd(MoO4)2 nanocrystals with diverse morphologies: controlled synthesis, growth mechanism, photoluminescence and thermometric properties

    NASA Astrophysics Data System (ADS)

    Li, Anming; Xu, Dekang; Lin, Hao; Yang, Shenghong; Shao, Yuanzhi; Zhang, Yueli

    2016-08-01

    Pure tetragonal phase, uniform and well-crystallized sodium gadolinium molybdate (NaGd(MoO4)2) nanocrystals with diverse morphologies, e.g. nanocylinders, nanocubes and square nanoplates have been selectively synthesized via oleic acid-mediated hydrothermal method. The phase, structure, morphology and composition of the as-synthesized products are studied. Contents of both sodium molybdate and oleic acid of the precursor solutions are found to affect the morphologies of the products significantly, and oleic acid plays a key role in the morphology-controlled synthesis of NaGd(MoO4)2 nanocrystals with diverse morphologies. Growth mechanism of NaGd(MoO4)2 nanocrystals is proposed based on time-dependent morphology evolution and X-ray diffraction analysis. Morphology-dependent down-shifting photoluminescence properties of NaGd(MoO4)2: Eu3+ nanocrystals, and upconversion photoluminescence properties of NaGd(MoO4)2: Yb3+/Er3+ and Yb3+/Tm3+ nanoplates are investigated in detail. Charge transfer band in the down-shifting excitation spectra shows a slight blue-shift, and the luminescence intensities and lifetimes of Eu3+ are decreased gradually with the morphology of the nanocrystals varying from nanocubes to thin square nanoplates. Upconversion energy transfer mechanisms of NaGd(MoO4)2: Yb3+/Er3+, Yb3+/Tm3+ nanoplates are proposed based on the energy level scheme and power dependence of upconversion emissions. Thermometric properties of NaGd(MoO4)2: Yb3+/Er3+ nanoplates are investigated, and the maximum sensitivity is determined to be 0.01333 K‑1 at 285 K.

  16. NaGd(MoO4)2 nanocrystals with diverse morphologies: controlled synthesis, growth mechanism, photoluminescence and thermometric properties

    PubMed Central

    Li, Anming; Xu, Dekang; Lin, Hao; Yang, Shenghong; Shao, Yuanzhi; Zhang, Yueli

    2016-01-01

    Pure tetragonal phase, uniform and well-crystallized sodium gadolinium molybdate (NaGd(MoO4)2) nanocrystals with diverse morphologies, e.g. nanocylinders, nanocubes and square nanoplates have been selectively synthesized via oleic acid-mediated hydrothermal method. The phase, structure, morphology and composition of the as-synthesized products are studied. Contents of both sodium molybdate and oleic acid of the precursor solutions are found to affect the morphologies of the products significantly, and oleic acid plays a key role in the morphology-controlled synthesis of NaGd(MoO4)2 nanocrystals with diverse morphologies. Growth mechanism of NaGd(MoO4)2 nanocrystals is proposed based on time-dependent morphology evolution and X-ray diffraction analysis. Morphology-dependent down-shifting photoluminescence properties of NaGd(MoO4)2: Eu3+ nanocrystals, and upconversion photoluminescence properties of NaGd(MoO4)2: Yb3+/Er3+ and Yb3+/Tm3+ nanoplates are investigated in detail. Charge transfer band in the down-shifting excitation spectra shows a slight blue-shift, and the luminescence intensities and lifetimes of Eu3+ are decreased gradually with the morphology of the nanocrystals varying from nanocubes to thin square nanoplates. Upconversion energy transfer mechanisms of NaGd(MoO4)2: Yb3+/Er3+, Yb3+/Tm3+ nanoplates are proposed based on the energy level scheme and power dependence of upconversion emissions. Thermometric properties of NaGd(MoO4)2: Yb3+/Er3+ nanoplates are investigated, and the maximum sensitivity is determined to be 0.01333 K−1 at 285 K. PMID:27506629

  17. The synthesis of size-controlled 3C-SiC nanoflakes and their photoluminescent properties

    NASA Astrophysics Data System (ADS)

    Fan, Xiujun; Ye, Ruquan; Peng, Zhiwei; Wang, Juanjuan; Fan, Ailing; Guo, Xia

    2016-06-01

    Size-controlled and high-purity 3C-SiC nanoflakes (NFs) are synthesized on the tips of vertically aligned carbon nanotube (VA-CNT) carpets with a hot-filament chemical vapor deposition (HF-CVD) method. The average diameter and height of SiC NFs can be tuned by changing the thickness of per-deposited Si and growth conditions. The growth process of the SiC NFs is suggested to be dominated by a vapor-solid (VS) mechanism. The prepared SiC NFs exhibit quantum-confinement effects, emitting strong violet-blue photoluminescence (PL) under ultraviolet excitation. The PL peak position changes from 410 to 416 nm as the excitation line increases from 290 to 400 nm. This result opens the possibility for the application of the luminescent solid-state freestanding 3C-SiC NFs in photonics as well as photonics/electronics integration.

  18. Fabrication of Bi-doped In2O3-ITO nanocomposites and their photoluminescence properties

    NASA Astrophysics Data System (ADS)

    Gil Na, Han; Jung, Taek-Kyun; Lee, Ji-Woon; Hyun, Soong-Keun; Kwon, Yong Jung; Mirzaei, Ali; Kim, Tae-Bum; Shin, Young-Chul; Choi, Ho-Joon; Kim, Hyoun Woo; Jin, Changhyun

    2016-09-01

    For the first time, Bi-doped In2O3-indium tin oxide (ITO) nanocomposites were prepared on Si substrates with the assistance of a Au catalyst through the simple gas-phase transport of a mixture of Bi, In, and Sn powders. The square-shaped Bi-doped In2O3-ITO nanostructures were straight, a few hundreds of nanometres in width, and below a few tens of micrometres in length. Electron microscopy, x-ray diffraction, and energy-dispersive x-ray spectroscopy analyses indicated that the Bi-doped In2O3-ITO nanorods were single crystals with a basis of cubic In2O3 structures. The photoluminescence spectra revealed that the Bi-doped In2O3-ITO nanorods had a strong orange emission band centred at approximately 626 nm without any shoulder bands. The enhancement of orange emission might be due to the oxygen deficiencies of structural defects in the nanorods.

  19. Optoelectronic properties analysis of Ti-substituted GaP.

    PubMed

    Tablero, C

    2005-11-01

    A study using first principles of the electronic and optical properties of materials derived from a GaP host semiconductor where one Ti atom is substituted for one of the eight P atoms is presented. This material has a metallic intermediate band sandwiched between the valence and conduction bands of the host semiconductor for 0 < or = U < or = 8 eV where U is the Hubbard parameter. The potential of these materials is that when they are used as an absorber of photons in solar cells, the efficiency is increased significantly with respect to that of the host semiconductor. The results show that the main contribution to the intermediate band is the Ti atom and that this material can absorb photons of lower energy than that of the host semiconductor. The efficiency is increased with respect to that of the host semiconductor mainly because of the absorption from the intermediate to conduction band. As U increases, the contribution of the Ti-d orbitals to the intermediate band varies, increasing the d(z2) character at the bottom of the intermediate band. PMID:16292917

  20. Enhancement of photoluminescence properties in ZnO/AlN bilayer heterostructures grown by atomic layer deposition

    SciTech Connect

    Zhu, Shang-Bin; Lu, Hong-Liang Zhang, Yuan; Sun, Qing-Qing; Zhou, Peng; Ding, Shi-Jin; Zhang, David Wei; Zhang, Qiu-Xiang

    2015-01-15

    The AlN/ZnO bilayer heterostructures were deposited on Si (100) substrate by thermal atomic layer deposition. X-ray diffraction results show that the crystallinity of polycrystalline ZnO layer is enhanced by amorphous AlN capping layer. Compared with ZnO thin film, ZnO/AlN bilayer with 10.7 nm AlN capping layer exhibits three times enhanced near band edge (NBE) emission from the photoluminescence measurements. In addition, the near band edge emission from the ZnO can be further increased by ∼10 times through rapid thermal annealing at 600 °C. The underlying mechanisms for the enhancement of the NBE emission after coating AlN capping layer and thermal treatment are discussed. These results suggest that coating of a thin AlN layer and sequential thermal treatments can effectively tailor the luminescence properties of ZnO film.

  1. Photoluminescence properties of new Zn(II) complexes with 8-hydroxyquinoline ligands: Dependence on volume and electronic effect of substituents

    NASA Astrophysics Data System (ADS)

    Huo, Yanping; Lu, Jiguo; Hu, Sheng; Zhang, Liming; Zhao, Fenghua; Huang, Huarong; Huang, Baohua; Zhang, Li

    2015-03-01

    A series of 2-arylethenyl-8-hydroxyquinoline ligands (A1-A4) with a trimethoxyphenyl, naphthyl, 2-fluoro-4-bromophenyl and anthracenyl group and their corresponding Zn(II) complexes (B1-B4) were synthesized and characterized by means of 1H NMR, ESI-MS, FT-IR and elemental analysis. A1 and A4 were characterized by single-crystal X-ray crystallography. The aggregation behavior of zinc salt and ligands in solution was investigated by several techniques, containing 1H NMR, UV-vis and photoluminescence (PL). The electronic nature and volume of arylethenyl substituents affect the absorption wavelength, the emission color, fluorescence lifetime, fluorescence quantum yield and thermostability of Zn(II) complexes. The experiments corroborated that the properties of Zinc(II) complexes can be tuned by introducing different functional substituents.

  2. Study of photoluminescence properties of CaAl2O4: Eu2+ prepared by combustion synthesis method

    NASA Astrophysics Data System (ADS)

    Hingwe, V. S.; Bajaj, N. S.; Omanwar, S. K.

    2016-05-01

    Eu2+ doped alkaline earth metals such as strontium aluminate, calcium aluminate and barium aluminate prepared by using modified combustion synthesis method at 600°c with Urea as fuel. Crystal structure is determined by using XRD and the sample confirmation by using the FTIR. The effect of the host material on the photoluminescence (PL) and phosphorescence properties were studied by using the Hitachi F-7000 spectrofluorimeter equipped with a 450W Xenon lamp, in the range 200-650 nm. The emission spectra of Eu2+ range from 450 to 500nm in the Blue to aqua region and the transition 4f7-4f6 5d1. The observed emission in CaAl2O4 is 440nm.

  3. Photoluminescent properties of Y2O3:Eu3+ phosphors prepared via urea precipitation in non-aqueous solution

    SciTech Connect

    Sun, Yu; Qi, Jason L.; Lee, M.; Lee, Burtrand I.; Samuels, William D.; Exarhos, Gregory J.

    2004-08-01

    Europium-doped yttrium oxide phosphors were prepared by firing precursors obtained by urea solvothermal method. The nature of solvents plays an important role in determining the structure and chemical composition of the precursor compounds. Amorphous hydroxides/carbonates mixture, amorphous carbonates and crystalline carbonates were obtained by urea solvothermal reactions from ethylenediamine, ethanol and aqueous media, respectively. The morphology and particle size distribution of the phosphor particles were studied by SEM and dynamic laser scattering method. The photoluminescence of the phosphor prepared by urea solvothermal method is improved as compared with that of the phosphor obtained by conventional urea homogeneous precipitation method. Urea solvothermal method provides a possible way to tailor the properties of a variety of carbonates and oxides by exploiting the nature of different solvents.

  4. Composition dependence of photoluminescence properties of In x Al1‑x N/AlGaN quantum wells

    NASA Astrophysics Data System (ADS)

    Zubialevich, V. Z.; Alam, S. N.; Li, H. N.; Parbrook, P. J.

    2016-09-01

    A series of InAlN/AlGaN five quantum well (QW) heterostructures was prepared by metal-organic vapour phase epitaxy to investigate their photoluminescence (PL) properties as a function of indium content in QWs at aluminium content in barriers fixed at 59%. In addition to the expected redshift of the emission spectrum, a strong rise of PL efficiency was observed with increasing indium content from 12.5 to 18%. Use of a higher indium content leads to a further redshift but also to a sudden and sharp degradation of PL efficiency. Reasons for the observed behaviour are discussed in detail, which raise the possibility of a transition to a type II band lineup in the InAlN–AlGaN system.

  5. Synthesis and photoluminescence properties of europium doped Mg-Al layered double hydroxides intercalated with MoO anions

    NASA Astrophysics Data System (ADS)

    Wang, Jun; Pan, Qingrui; Liu, Qi; He, Yang; Mann, Tom; Li, Rumin; Zhang, Milin; Liu, Lianhe

    2012-05-01

    Novel fluorescent Eu-containing layered double hydroxides (Eu-LDHs) were prepared by direct ion-exchange of EuMgAl-NO3 LDHs precursors with MoO anions. The samples were characterized by elemental analyses, powder X-ray diffraction (XRD), Fourier transform infrared (FT-IR), Raman spectra, photoluminescence spectroscopy. The results indicated that Eu3+ ions were likely incorporated into the hydrotalcite lattice and MoO anions were successfully intercalated into interlayer region of the LDHs with the Mo/Al molar ratio close to 0.40. The luminescence properties were largely enhanced compared with the EuMgAl-NO3 LDHs precursors, which were attributed to the energy transfer between Eu3+ and MoO.

  6. Synthesis and photoluminescence properties of core-shell structured YVO4:Eu3+@SiO2 nanocomposites

    NASA Astrophysics Data System (ADS)

    Liu, Lina; Xiao, Hongyu; An, Xiuyun; Zhang, Yongsheng; Qin, Ruifei; Liu, Lishuang; Zhang, Dongmei; Sun, Ruirui; Chen, Linfeng

    2015-01-01

    Well-dispersed YVO4:Eu3+ nanoparticles (NPs) of about 8 nm were synthesized by a precipitation reaction and they were coated with SiO2 by a reverse microemulsion method. The thickness of SiO2 shells was altered by changing the molar ratio of tetraethoxysilane (TEOS)/YVO4:Eu3+. The influence of SiO2 coating on the photoluminescence properties of the YVO4:Eu3+ NPs was studied in detail. With the increase of the SiO2 shell thickness, the intensity ratio of 5D0-7F2/5D0-7F1 becomes lower. It was interesting to observe that the quantum yield of naked YVO4:Eu3+ is higher than that of YVO4:Eu3+@SiO2 nanocomposites, and the result is opposite to a previous reference.

  7. Synthesis and photoluminescence properties of Pb2+ doped inorganic borate phosphor NaSr4(BO3)3

    NASA Astrophysics Data System (ADS)

    Chauhan, A. O.; Koparkar, K. A.; Bajaj, N. S.; Omanwar, S. K.

    2016-05-01

    A series of Inorganic borate phosphors NaSr4(BO3)3 doped with Pb2+ was successfully synthesized by modified solid state diffusion method. The crystal structure and the phase purity of sample were characterized by powder X-ray diffraction (XRD). The photoluminescence properties of synthesized materials were investigated using spectrofluorometer at room temperature. The phosphor show strong broad band emission spectra in UVA region maximum at 370 nm under the excitation of 289 nm. The dependence of the emission intensity on the Pb2+ concentration for the NaSr4(BO3)3 were studied in details. The concentration quenching of Pb2+ doped NaSr4(BO3)3 was observed at 0.02 mol. The Stokes shifts of NaSr4(BO3)3: Pb2+ phosphor was calculated to be 7574 cm-1.

  8. The photoluminescence and structural properties of (Ce, Yb) co-doped silicon oxides after high temperature annealing

    SciTech Connect

    Heng, C. L. Li, J. T.; Su, W. Y.; Yin, P. G.; Finstad, T. G.

    2015-01-28

    We studied the photoluminescence (PL) and structural properties of Ce and Yb co-doped silicon oxide films after high temperature annealing. The PL spectra of Ce{sup 3+} and Yb{sup 3+} ions were sensitive to the structural variation of the films, and the Yb PL intensities were significantly enhanced especially upon 1200 °C annealing. X-ray diffraction, transmission electron microscopy, and X-ray photoelectron spectroscopy, indicated that rare earth silicates and the CeO{sub 2} phase had formed in the oxides. The proportions of the phases varied with the “nominal Si-richness” of the films. Energy transfer from the excited Ce{sup 3+} to Yb{sup 3+} can be inferred from both PL excitation and decay spectra.

  9. Synthesis and photoluminescence properties of a novel reddish orange-emitting Sm3+-doped strontium borosilicate phosphor

    NASA Astrophysics Data System (ADS)

    Sun, Jianfeng; Ding, Debao; Sun, Jiayue

    2016-08-01

    Sr3-2xSmxNaxB2SiO8 phosphors were synthesized by the solid-state reactions. X-ray diffraction, diffuse reflection, photoluminescence excitation and emission, as well as fluorescence decay measurements were utilized to investigate the structural and spectral properties of the samples. The results indicated that Sr3-2xSmxNaxB2SiO8 phosphors could be efficiently excited by the near-ultraviolet light to realize a novel reddish orange luminescence corresponding to the characteristic transitions 4G5/2→6HJ (J = 5/2, 7/2, 9/2, 11/2) of Sm3+ ions, with a maximum intensity at 600 nm. Based on the theoretical calculation, the dipole-dipole interaction was dominantly involved concentration quenching of Sm3+ in the phosphors, and the critical transfer distance (Rc) was determined to be 13.59 Å. Furthermore, Judd-Ofelt analysis was applied to evaluate three phenomenological Judd-Ofelt intensity parameters (Ωλ, λ = 2, 4, 6), and in turn radiative properties such as radiative transition probabilities (AR), radiative lifetimes (τR) and fluorescence branching ratios (βR) for the excited 4G5/2 luminescent level of Sm3+ ions were determined. Upon 402 nm excitation, the composition-optimized Sr2.90Sm0.05Na0.05B2SiO8 exhibited the preferable photoluminescence intensity and CIE coordinates of (0.534, 0.448). These results suggest that the Sm3+-doped Sr3B2SiO8 phosphors are competitive as the reddish orange-emitting phosphor-converted materials for application in near-ultraviolet-pumped LEDs.

  10. A co-precipitation preparation, crystal structure and photoluminescent properties of Er5%:Gd2O3 nanorods

    NASA Astrophysics Data System (ADS)

    Boopathi, G.; Raj, S. Gokul; Kumar, G. Ramesh; Mohan, R.

    2015-06-01

    An inexpensive preparation method is being reported for obtaining erbium doped gadolinium oxide (Er5%:Gd2O3) nanoscale rods. The elongated nanoscale systems, as-formed through a co-precipitation process, are characterized by using X-ray powder diffraction (XRD) patterns, scanning electron microscopy (SEM) with energy dispersive X-ray (EDX) mapping, Ultra Violet-visible (UV-vis.) absorption spectroscopy and photoluminescence (PL) spectroscopy. In addition, the Williamson-Hall (W-H) plot is also performed to distinguish the effect of crystalline size-induced broadening and strain-induced broadening at full-width at half-maximum (FWHM) of the XRD profile. The XRD patterns of as-formed and calcined products show that the phase confirmation. As revealed from the SEM micrographs, the morphology of the products show that the rod-like nanoparticles. The EDX micrographs show that the presence of elements in our samples. The band gap values in calcined samples are found to be in the range of 3.569 eV. Upon 230 nm excitation on calcined samples, three broad emission peaks are observed from PL studies. The possible mechanism for the formation of Er5%:Gd2O3 nanorods is briefly discussed.

  11. A joint experimental and theoretical study on the electronic structure and photoluminescence properties of Al2(WO4)3 powders

    NASA Astrophysics Data System (ADS)

    Batista, F. M. C.; La Porta, F. A.; Gracia, L.; Cerdeiras, E.; Mestres, L.; Siu Li, M.; Batista, N. C.; Andrés, J.; Longo, E.; Cavalcante, L. S.

    2015-02-01

    In this paper, aluminum tungstate Al2(WO4)3 powders were synthesized using the co-precipitation method at room temperature and then submitted to heat treatment processes at different temperatures (100, 200, 400, 800, and 1000 °C) for 2 h. The structure and morphology of the powders were characterized by means of X-ray diffraction (XRD), Rietveld refinement data, and field emission scanning electron microscopy (FE-SEM) images. Their optical properties were examined with ultraviolet-visible (UV-vis) diffuse reflectance spectroscopy and photoluminescence (PL) measurements. XRD patterns and Rietveld refinement data showed that Al2(WO4)3 powders heat treated at 1000 °C for 2 h have a orthorhombic structure with a space group (Pnca) without the presence of deleterious phases. FE-SEM images revealed that these powders are formed by the aggregation of several nanoparticles leading to the growth of microparticles with irregular morphologies and an agglomerated nature. UV-vis spectra indicated that optical band gap energy increased from 3.16 to 3.48 eV) as the processing temperature rose, which was in turn associated with a reduction in intermediary energy levels. First-principle calculations were performed in order to understand the behavior of the PL properties using density functional theory at the B3LYP calculation level on periodic model systems and indicate the presence of stable electronic excited states (singlet). The analyses of the band structures and density of states at both ground and first excited electronic states provide insight into the main features, based on structural and electronic order-disorder effects in octahedral [AlO6] clusters and tetrahedral [WO4] clusters, as constituent building units of this material.

  12. In-dopants effect on the photoluminescence properties of YVO4 nanophosphors.

    PubMed

    Peng, Zifei; Du, Yanyun; Wang, Yuan; Peng, Donghong

    2010-03-01

    The powders of Yttrium vanadate (YVO4) with In-dopants were synthesized by solid-state reactions, and X-ray diffraction (XRD), transmission electron microscopy (TEM), ultraviolet-visible (UV-vis) absorption spectra, photoluminescence (PL) spectra, and the luminescence intensity change were used to characterize the samples. The results of XRD indicated that the YVO4:In3+ samples remained in pure cubic phase. TEM illustrated that the powders mainly consisted of grains with an average size of 100 nm. Under the excitation of 320 nm, the YVO4:In3+ single-crystalline samples exhibited emission ranging from 350 to 700 nm. The emission intensity of YVO4:In3+ increased with increasing indium concentration in the lower indium concentration region until the saturated PL intensity was reached, and the strongest white fluorescence was observed when the In3+ doping concentration was 2% at 900 degrees C. The luminescent intensity of YVO4:In3+ (2%) was 9.6 times as strong as that of non-doped YVO4. The nanophosphors emit white luminescence owing to broad charge transfer in crystal lattice is due to the addition of In3+ to capture the UV radiation. PMID:20355624

  13. Ion Insertion on the Crystal Structure, Photoluminescence, and Dielectric Properties of o-Mullite Nanoparticles

    NASA Astrophysics Data System (ADS)

    Sanad, M. M. S.; Rashad, M. M.; Abdel-Aal, E. A.; El-Shahat, M. F.; Powers, K.

    2014-09-01

    Nanocrystalline Gd3+-doped Gd x Al6- x Si2O13 mullite powders with x from 0.005 to 0.025 have been synthesized via a facile coprecipitation technique. X-ray diffraction results revealed that o-mullite was detected as the major phase for x = 0.0 to 0.01, whereas corundum α-Al2O3 was predominant for x = 0.025. It was found that the volume of the mullite unit cell increased with Gd3+ ion incorporation. Differential scanning calorimetry thermograms evinced that the exothermic peak temperature of mullite shifted to lower values with Gd3+ ion insertion. Transmission electron microscopy observations of pure mullite nanoparticles displayed orthorhombic-like shapes. Meanwhile, at 0.5% Gd3+ ion content, the mullite particles exhibited platelet-like shapes, which distorted into spheroidal-like crystals at high Gd3+ ion contents (1% and 2.5%). The photoluminescence spectra indicated that the intensity of the emission spectra improved considerably with Gd3+ ion doping. On the other hand, dielectric measurements of sintered samples showed that the maximum dielectric loss values were 1.7 and 1.4 at 1.5 MHz and 1.5 GHz, respectively, with 2.5% Gd3+ ion content.

  14. MgO:Eu3+ red nanophosphor: low temperature synthesis and photoluminescence properties.

    PubMed

    Devaraja, P B; Avadhani, D N; Prashantha, S C; Nagabhushana, H; Sharma, S C; Nagabhushana, B M; Nagaswarupa, H P; Premkumar, H B

    2014-01-01

    Nanoparticles of Eu(3+) doped (0-9 mol%) MgO were prepared using low temperature (400°C) solution combustion technique with metal nitrate as precursor and glycine as fuel. The powder X-ray diffraction (PXRD) patterns of the as-formed products show single cubic phase and no further calcination was required. The crystallite size was obtained using Scherer's formula and was found to be 5-6 nm. The effect of Eu(3+) ions on luminescence characteristics of MgO was studied and the results were discussed in detail. These phosphors exhibit bright red emission upon 395 nm excitation. The characteristic photoluminescence (PL) emission peaks at ∼580, 596, 616, 653, 696 and 706 nm ((5)D0→(7)Fj=0, 1, 2, 3, 4) were recorded due to Eu(3+) ions. The electronic transition corresponding to (5)D0→(7)F2 of Eu(3+) ions (616 nm) was stronger than the magnetic dipole transition corresponding to (5)D0→(7)F1 of Eu(3+) ions (596 nm). The international commission on illumination (CIE) chromaticity co-ordinates were calculated from emission spectra, the values (x, y) were very close to national television system committee (NTSC) standard value of red emission. Therefore the present phosphor was highly useful for display applications.

  15. Effects of Forest Gaps on Soil Properties in Castanopsis kawakamii Nature Forest

    PubMed Central

    He, Zhongsheng; Liu, Jinfu; Su, Songjin; Zheng, Shiqun; Xu, Daowei; Wu, Zeyan; Hong, Wei; Wang, James Li-Ming

    2015-01-01

    The aim of this study is to analyze the effects of forest gaps on the variations of soil properties in Castanopsis kawakamii natural forest. Soil physical and chemical properties in various sizes and development stages were studied in C. kawakamii natural forest gaps. The results showed that forest gaps in various sizes and development stages could improve soil pore space structure and water characteristics, which may effectively promote the water absorbing capacity for plant root growth and play an important role in forest regeneration. Soil pore space structure and water characteristics in small gaps showed more obvious improvements, followed by the medium and large gaps. Soil pore space structure and water characteristics in the later development stage of forest gaps demonstrated more obvious improvements, followed by the early and medium development stages. The contents of hydrolysable N and available K in various sizes and development stages of forest gaps were higher than those of non-gaps, whereas the contents of total N, total P, available P, organic matter, and organic carbon were lower. The contents of total N, hydrolysable N, available K, organic matter, and organic carbon in medium gaps were higher than those of large and small gaps. The disturbance of forest gaps could improve the soils’ physical and chemical properties and increase the population species’ richness, which would provide an ecological basis for the species coexistence in C. kawakamii natural forest. PMID:26496710

  16. Effects of Forest Gaps on Soil Properties in Castanopsis kawakamii Nature Forest.

    PubMed

    He, Zhongsheng; Liu, Jinfu; Su, Songjin; Zheng, Shiqun; Xu, Daowei; Wu, Zeyan; Hong, Wei; Wang, James Li-Ming

    2015-01-01

    The aim of this study is to analyze the effects of forest gaps on the variations of soil properties in Castanopsis kawakamii natural forest. Soil physical and chemical properties in various sizes and development stages were studied in C. kawakamii natural forest gaps. The results showed that forest gaps in various sizes and development stages could improve soil pore space structure and water characteristics, which may effectively promote the water absorbing capacity for plant root growth and play an important role in forest regeneration. Soil pore space structure and water characteristics in small gaps showed more obvious improvements, followed by the medium and large gaps. Soil pore space structure and water characteristics in the later development stage of forest gaps demonstrated more obvious improvements, followed by the early and medium development stages. The contents of hydrolysable N and available K in various sizes and development stages of forest gaps were higher than those of non-gaps, whereas the contents of total N, total P, available P, organic matter, and organic carbon were lower. The contents of total N, hydrolysable N, available K, organic matter, and organic carbon in medium gaps were higher than those of large and small gaps. The disturbance of forest gaps could improve the soils' physical and chemical properties and increase the population species' richness, which would provide an ecological basis for the species coexistence in C. kawakamii natural forest.

  17. Electronic properties of Janus silicene: new direct band gap semiconductors

    NASA Astrophysics Data System (ADS)

    Sun, Minglei; Ren, Qingqiang; Wang, Sake; Yu, Jin; Tang, Wencheng

    2016-11-01

    Using first-principles calculations, we propose a new class of materials, Janus silicene, which is silicene asymmetrically functionalized with hydrogen and halogen atoms. Formation energies and phonon dispersion indicated that all the Janus silicene systems exhibit good kinetic stability. As compared to silicane, all Janus silicene systems are direct band gap semiconductors. The band gap of Janus silicene can take any value between 1.91 and 2.66 eV by carefully tuning the chemical composition of the adatoms. In addition, biaxial elastic strain can further reduce the band gap to 1.11 eV (under a biaxial tensile strain up to 10%). According to moderate direct band gap, these materials demonstrate potential applications in optoelectronics, exhibiting a very wide spectral range, and they are expected to be highly stable under ambient conditions.

  18. A green chemical approach to the synthesis of photoluminescent ZnO hollow spheres with enhanced photocatalytic properties

    SciTech Connect

    Patrinoiu, Greta; Tudose, Madalina; Calderon-Moreno, Jose Maria; Birjega, Ruxandra; Budrugeac, Petru; Ene, Ramona; Carp, Oana

    2012-02-15

    ZnO hollow spheres have been synthesized by a simple and environmentally friendly template assisted route. Starch-derived carbonaceous spheres were used as template, impregnated with Zn(CH{sub 3}COO){sub 2}{center_dot}2H{sub 2}O to obtain zinc-containing precursor spheres and thermally treatment at 600 Degree-Sign C, yielding hollow ZnO spherical shells. The precursor spheres and hollow shells were characterized by X-ray diffraction, FTIR spectroscopy, scanning electron microscopy, thermal analysis and room-temperature photoluminescence measurements. The hollow spherical shells with diameters of {approx}150 nm and wall thickness of {approx}20 nm, are polycrystalline, with a mean crystallite size of 22 nm, exhibiting interesting emission features, with a wide multi-peak band covering blue and green regions of the visible spectrum. The photocatalytic activities (under UV and visible light irradiations) of the ZnO spherical shells evaluated for the phenol degradation reaction in aqueous solutions are outstanding, a total phenol conversion being registered in the case of UV irradiation experiments. - Graphical abstract: The photocatalytic reaction initiated by the photoexcitation of the semiconductor (ZnO), leads to the formation of electron-hole, while part of the electron-hole pairs recombine, some holes combine with water to form {center_dot}OH radicals and some electrons convert oxygen to super oxide radical ({center_dot}O{sub 2}{sup -}). Highlights: Black-Right-Pointing-Pointer Green synthesis of ZnO hollow spheres. Black-Right-Pointing-Pointer Starch-derived carbonaceous spheres as spherical hard template. Black-Right-Pointing-Pointer ZnO hollow spheres with notable visible photoluminescence properties. Black-Right-Pointing-Pointer ZnO hollow spheres with photocatalytical activity in degradation/mineralization of phenol.

  19. Biological fabrication of nanostructured silicon-germanium photonic crystals possessing unique photoluminescent and electroluminescent properties

    NASA Astrophysics Data System (ADS)

    Rorrer, Gregory L.; Jeffryes, Clayton; Chang, Chih-hung; Lee, Doo-Hyoung; Gutu, Timothy; Jiao, Jun; Solanki, Raj

    2007-09-01

    Diatoms are single-celled algae which possess silica shells called "frustules" that contain periodic submicron scale features. A diatom cell culture process was used to fabricate a two-dimensional photonic crystal slab of Ge-doped biosilica that possessed 120 nm holes, 330 nm lattice constant, and dielectric constant of 8.5. This material was integrated into an electroluminescent (EL) device by spin coating of the frustules onto indium tin oxide, followed by atomic layer deposition of 400 nm hafnium silicate. No photonic band gap was predicted. However, the EL spectrum possessed resonant UV line emissions that were consistent with photonic band calculations. An EL band gap between 500-640 nm was also observed between blue and red EL line emissions. These EL characteristics have not been observed previously, and are unique to the diatom photonic crystal. This study represents a first step towards the realization of optoelectronic devices which utilize nanoscale components fabricated through cell culture.

  20. Photoluminescence properties and crystallization of silicon quantum dots in hydrogenated amorphous Si-rich silicon carbide films

    SciTech Connect

    Wen, Guozhi; Zeng, Xiangbin Wen, Xixin; Liao, Wugang

    2014-04-28

    Silicon quantum dots (QDs) embedded in hydrogenated amorphous Si-rich silicon carbide (α-SiC:H) thin films were realized by plasma-enhanced chemical vapor deposition process and post-annealing. Fluorescence spectroscopy was used to characterize the room-temperature photoluminescence properties. X-ray photoelectron spectroscopy was used to analyze the element compositions and bonding configurations. Ultraviolet visible spectroscopy, Raman scattering, and high-resolution transmission electron microscopy were used to display the microstructural properties. Photoluminescence measurements reveal that there are six emission sub-bands, which behave in different ways. The peak wavelengths of sub-bands P1, P2, P3, and P6 are pinned at about 425.0, 437.3, 465.0, and 591.0 nm, respectively. Other two sub-bands, P4 is red-shifted from 494.6 to 512.4 nm and P5 from 570.2 to 587.8 nm with temperature increasing from 600 to 900 °C. But then are both blue-shifted, P4 to 500.2 nm and P5 to 573.8 nm from 900 to 1200 °C. The X-ray photoelectron spectroscopy analysis shows that the samples are in Si-rich nature, Si-O and Si-N bonds consumed some silicon atoms. The structure characterization displays that a separation between silicon phase and SiC phase happened; amorphous and crystalline silicon QDs synthesized with increasing the annealing temperature. P1, P2, P3, and P6 sub-bands are explained in terms of defect-related emission, while P4 and P5 sub-bands are explained in terms of quantum confinement effect. A correlation between the peak wavelength shift, as well as the integral intensity of the spectrum and crystallization of silicon QDs is supposed. These results help clarify the probable luminescence mechanisms and provide the possibility to optimize the optical properties of silicon QDs in Si-rich α-SiC: H materials.

  1. Direct band gap wurtzite gallium phosphide nanowires.

    PubMed

    Assali, S; Zardo, I; Plissard, S; Kriegner, D; Verheijen, M A; Bauer, G; Meijerink, A; Belabbes, A; Bechstedt, F; Haverkort, J E M; Bakkers, E P A M

    2013-04-10

    The main challenge for light-emitting diodes is to increase the efficiency in the green part of the spectrum. Gallium phosphide (GaP) with the normal cubic crystal structure has an indirect band gap, which severely limits the green emission efficiency. Band structure calculations have predicted a direct band gap for wurtzite GaP. Here, we report the fabrication of GaP nanowires with pure hexagonal crystal structure and demonstrate the direct nature of the band gap. We observe strong photoluminescence at a wavelength of 594 nm with short lifetime, typical for a direct band gap. Furthermore, by incorporation of aluminum or arsenic in the GaP nanowires, the emitted wavelength is tuned across an important range of the visible light spectrum (555-690 nm). This approach of crystal structure engineering enables new pathways to tailor materials properties enhancing the functionality.

  2. Direct Band Gap Wurtzite Gallium Phosphide Nanowires

    PubMed Central

    2013-01-01

    The main challenge for light-emitting diodes is to increase the efficiency in the green part of the spectrum. Gallium phosphide (GaP) with the normal cubic crystal structure has an indirect band gap, which severely limits the green emission efficiency. Band structure calculations have predicted a direct band gap for wurtzite GaP. Here, we report the fabrication of GaP nanowires with pure hexagonal crystal structure and demonstrate the direct nature of the band gap. We observe strong photoluminescence at a wavelength of 594 nm with short lifetime, typical for a direct band gap. Furthermore, by incorporation of aluminum or arsenic in the GaP nanowires, the emitted wavelength is tuned across an important range of the visible light spectrum (555–690 nm). This approach of crystal structure engineering enables new pathways to tailor materials properties enhancing the functionality. PMID:23464761

  3. Thermal properties and two-dimensional photonic band gaps

    NASA Astrophysics Data System (ADS)

    Elsayed, Hussein A.; El-Naggar, Sahar A.; Aly, Arafa H.

    2014-03-01

    The effect of temperature on a two-dimensional square lattice photonic crystal composed of Si rods arranged in an air background was investigated theoretically using the plane-wave expansion method. Both the thermal expansion effect and thermo-optical effect are considered simultaneously. We have discussed the role of temperature in creating the complete photonic band gap as a function of temperature. Two different shapes of rods, i.e. square and circular, are considered in the presence of the two polarization states, i.e. TE and TM waves. The numerical results show that the photonic band gap can be significantly enlarged compared to the photonic band gap at room temperature. The effect of temperature on the complete photonic band width in the cylindrical rods case is more significant. Cylindrical and square Si rods may work as a temperature sensor or filter, among many other potential applications.

  4. A novel yellow-emitting SrAlSi4N7:Ce3+ phosphor for solid state lighting: Synthesis, electronic structure and photoluminescence properties

    NASA Astrophysics Data System (ADS)

    Ruan, Jian; Xie, Rong-Jun; Funahashi, Shiro; Tanaka, Yoshinori; Takeda, Takashi; Suehiro, Takayuki; Hirosaki, Naoto; Li, Yuan-Qiang

    2013-12-01

    Ce3+-doped and Ce3+/Li+-codoped SrAlSi4N7 phosphors were synthesized by gas pressure sintering of powder mixtures of Sr3N2, AlN, α-Si3N4, CeN and Li3N. The phase purity, electronic crystal structure, photoluminescence properties of SrAlSi4N7:Ce3+(Ce3+/Li+) were investigated in this work. The band structure calculated by the DMol3 code shows that SrAlSi4N7 has a direct band gap of 3.87 eV. The single crystal analysis of Ce3+-doped SrAlSi4N7 indicates a disordered Si/Al distribution and nitrogen vacnacy defects. SrAlSi4N7 was identified as a major phase of the fired powders, and Sr5Al5Si21N35O2 and AlN as minor phases. Both Ce3+ and Ce3+/Li+ doped SrAlSi4N7 phosphors can be efficiently excited by near-UV or blue light and show a broadband yellow emission peaking around 565 nm. A highest external quantum efficiency of 38.3% under the 450 nm excitation was observed for the Ce3+/Li+-doped SrAlSi4N7 (5 mol%). A white light LED lamp with color temperature of 6300 K and color rendering index of Ra=78 was achieved by combining Sr0.97Al1.03Si3.997N\\94\\maccounttest14=t0005_18193 7:Ce3+0.03 with a commercial blue InGaN chip. It indicates that SrAlSi4N7:Ce3+ is a promising yellow emitting down-conversion phosphor for white LEDs.

  5. Large-Scale Synthesis and Systematic Photoluminescence Properties of Monolayer MoS2 on Fused Silica.

    PubMed

    Wan, Yi; Zhang, Hui; Zhang, Kun; Wang, Yilun; Sheng, Bowen; Wang, Xinqiang; Dai, Lun

    2016-07-20

    Monolayer MoS2, with fascinating mechanical, electrical, and optical properties, has generated enormous scientific curiosity and industrial interest. Controllable and scalable synthesis of monolayer MoS2 on various desired substrates has significant meaning in both basic scientific research and device application. Recent years have witnessed many advances in the direct synthesis of single-crystalline MoS2 flakes or their polycrystalline aggregates on numerous diverse substrates, such as SiO2-Si, mica, sapphire, h-BN, and SrTiO3, etc. In this work, we used the dual-temperature-zone atmospheric-pressure chemical vapor deposition method to directly synthesize large-scale monolayer MoS2 on fused silica, the most ordinary transparent insulating material in daily life. We systematically investigated the photoluminescence (PL) properties of monolayer MoS2 on fused silica and SiO2-Si substrates, which have different thermal conductivity coefficients and thermal expansion coefficients. We found that there exists a stronger strain on monolayer MoS2 grown on fused silica, and the strain becomes more obvious as temperature decreases. Moreover, the monolayer MoS2 grown on fused silica exhibits the unique trait of a fractal shape with tortuous edges and has stronger adsorbability. The monolayer MoS2 grown on fused silica may find application in sensing, energy storage, and transparent optoelectronics, etc. PMID:27338112

  6. Large-Scale Synthesis and Systematic Photoluminescence Properties of Monolayer MoS2 on Fused Silica.

    PubMed

    Wan, Yi; Zhang, Hui; Zhang, Kun; Wang, Yilun; Sheng, Bowen; Wang, Xinqiang; Dai, Lun

    2016-07-20

    Monolayer MoS2, with fascinating mechanical, electrical, and optical properties, has generated enormous scientific curiosity and industrial interest. Controllable and scalable synthesis of monolayer MoS2 on various desired substrates has significant meaning in both basic scientific research and device application. Recent years have witnessed many advances in the direct synthesis of single-crystalline MoS2 flakes or their polycrystalline aggregates on numerous diverse substrates, such as SiO2-Si, mica, sapphire, h-BN, and SrTiO3, etc. In this work, we used the dual-temperature-zone atmospheric-pressure chemical vapor deposition method to directly synthesize large-scale monolayer MoS2 on fused silica, the most ordinary transparent insulating material in daily life. We systematically investigated the photoluminescence (PL) properties of monolayer MoS2 on fused silica and SiO2-Si substrates, which have different thermal conductivity coefficients and thermal expansion coefficients. We found that there exists a stronger strain on monolayer MoS2 grown on fused silica, and the strain becomes more obvious as temperature decreases. Moreover, the monolayer MoS2 grown on fused silica exhibits the unique trait of a fractal shape with tortuous edges and has stronger adsorbability. The monolayer MoS2 grown on fused silica may find application in sensing, energy storage, and transparent optoelectronics, etc.

  7. New metal based drug as a therapeutic agent: Spectral, electrochemical, DNA-binding, surface morphology and photoluminescence properties

    NASA Astrophysics Data System (ADS)

    Muslu, Harun; Gölcü, Ayşegül

    2015-07-01

    Cu(II) complexes of non-steroidal anti-inflammatory drug (NSAID) Meloxicam (H2MLX) was synthesized and characterized via spectroscopic and analytical techniques. The thermal behavior of the complex was also analyzed. The photoluminescence properties of the compounds were analyzed under different conditions. The electrochemical properties of both ligand and complex have been analyzed by Cyclic Voltammetry (CV) using glassy carbon electrode. The biological activities of the compounds were evaluated through examining their capacity to bind to fish sperm double strand DNA (FSdsDNA) with absorption spectroscopy and differential pulse voltammetry (DPV). Absorption studies of the interaction of the H2MLX and its Cu(II) complex with FSdsDNA have indicated that these compounds could bind to FSdsDNA, and the binding constants were calculated. The morphology of the FSdsDNA, H2MLX, and Cu(II) complex were analyzed thanks to using scanning electron microscopy (SEM). In the DPV technique, pencil graphite electrode was used as a working electrode. The decrease in the intensity of the guanine oxidation signals was used as an indicator for the interaction mechanism.

  8. Composition-dependent photoluminescence properties of CuInS2/ZnS core/shell quantum dots

    NASA Astrophysics Data System (ADS)

    Hua, Jie; Du, Yuwei; Wei, Qi; Yuan, Xi; Wang, Jin; Zhao, Jialong; Li, Haibo

    2016-06-01

    CuInS2/ZnS (CIS/ZnS) core/shell quantum dots (QDs) with various Cu/In ratios were synthesized using the hot-injection method, and their photoluminescence (PL) properties were investigated by measuring steady-state and time-resolved PL spectroscopy. The emission peak of the CIS/ZnS QDs were tuned from 680 to 580 nm by decreasing the Cu/In precursor ratio from 1/1 to 1/9. As the Cu/In ratio decreases, the PL lifetimes and PL quantum yields (QYs) of CIS/ZnS core/shell QDs increased firstly and then decreased. Two dominant radiative recombination processes were postulated to analyze composition-dependent PL properties, including the recombination from a quantized conduction band to deep defects state and donor-acceptor pair (DAP) recombination. The decrease of PL efficiency resulted from high density defects and traps, which formed at the interface between CIS core and ZnS shell due to the large off-stoichiometry composition. The PL intensity and peak energy for CIS/ZnS core/shell QDs as a function of temperature were also provided. The thermal quenching further confirmed that the PL emission of CIS/ZnS QDs did not come from the recombination of excitons but from the recombination of many kinds of intrinsic defects inside the QDs as emission centers.

  9. Effects of the Template Composition and Coating on the Photoluminescence Properties of ZnS:Mn Nanoparticles

    PubMed Central

    2010-01-01

    Mn-doped ZnS nanocrystals based on low dopant concentrations (0–2%) and coated with a shell of Zn(OH)2 have been prepared via soft template and precipitation reaction. The results indicate that the ZnS:Mn nanocrystal is cubic zinc blende structure and its diameter is 3.02 nm as demonstrated by XRD. Measured by TEM, the morphology of nanocrystals is a spherical shape, and their particle size (3–5 nm) is similar to that of XRD results. Photoluminescence spectra under ultraviolet region shows that the volume ratio of alcohol to water in the template has a great effect on the luminescence properties of ZnS:Mn particles. Compared with unpassivated ZnS:Mn nanocrystals, ZnS:Mn/Zn(OH)2 core/shell nanocrystal exhibits much improved luminescence and higher absolute quantum efficiency. Meanwhile, we simply explore the formation mechanism of ZnS:Mn nanocrystals in alcohol and water system and analyze the reason why alcohol and water cluster structures can affect the luminescent properties of nanoparticle. PMID:20671786

  10. Systhesis, phase transformation and photoluminescence properties of Eu:La(1-x)Gd(x)VO4 nanofibers by electrospinning method.

    PubMed

    Huang, Zuocai; Huang, Siya; Ou, Gang; Pan, Wei

    2012-08-21

    One dimensional Eu:La(1-x)Gd(x)VO(4) nanofibers were successfully prepared via an electrospinning method. Thermogravimetry and differential scanning calorimeter (TG-DSC), X-ray diffraction, Raman spectroscopy, scanning electron microscopy and photoluminescence were used to characterize the samples. The nanofibers crystallized well below 600 °C and with the increase of Gd contents, the nanofibers crystallized in a zircon-type structure. The Raman spectra shifted to higher frequency with the increase of Gd content for zircon Eu:La(1-x)Gd(x)VO(4). The peaks of photoluminescence spectra shift towards longer wavelength when Gd replaces La and when x = 0.4, the photoluminescence intensity reaches its maximum value. The band structure and density of states of m-LaVO(4), t-LaVO(4), t-LaGdVO(4) and t-GdVO(4) were calculated by local-spin density approximation (LSDA) band theory with Hubbard term of U. The band gap of t-LaGdVO(4) is just the average of t-LaVO(4) and t-GdVO(4). In t-LaGdVO(4), La 5p states are highly localized.

  11. Band gap anomaly and topological properties in lead chalcogenides

    NASA Astrophysics Data System (ADS)

    Simin, Nie; Xiao, Yan Xu; Gang, Xu; Zhong, Fang

    2016-03-01

    Band gap anomaly is a well-known issue in lead chalcogenides PbX (X = S, Se, Te, Po). Combining ab initio calculations and tight-binding (TB) method, we have studied the band evolution in PbX, and found that the band gap anomaly in PbTe is mainly related to the high on-site energy of Te 5s orbital and the large s-p hopping originated from the irregular extended distribution of Te 5s electrons. Furthermore, our calculations show that PbPo is an indirect band gap (6.5 meV) semiconductor with band inversion at L point, which clearly indicates that PbPo is a topological crystalline insulator (TCI). The calculated mirror Chern number and surface states double confirm this conclusion. Project supported by the National Natural Science Foundation of China (Grant No. 11204359), the National Basic Research Program of China (Grant No. 2013CB921700), and the Strategic Priority Research Program (B) of the Chinese Academy of Sciences (Grant No. XDB07020100).

  12. γ irradiation induced effects on bismuth active centres and related photoluminescence properties of Bi/Er co-doped optical fibres.

    PubMed

    Sporea, D; Mihai, L; Neguţ, D; Luo, Yanhua; Yan, Binbin; Ding, Mingjie; Wei, Shuen; Peng, Gang-Ding

    2016-01-01

    We investigate the effects of γ irradiation on bismuth active centres (BACs) and related photoluminescence properties of bismuth/erbium co-doped silica fibre (BEDF), [Si] ~28, [Ge] ~1.60, [Al] ~0.10, [Er] ~ <0.10 and [Bi] ~0.10 atom%, fabricated by in-situ solution doping and Modified Chemical Vapor Deposition (MCVD). The samples were irradiated at 1 kGy, 5 kGy, 15 kGy, 30 kGy and 50 kGy doses, and dose rate of 5.5 kGy/h, at room temperature. The optical properties of BEDF samples are tested before and after γ irradiation. We found that high dose γ irradiation could significantly influence the formation and composition of BACs and their photoluminescence performance, as important changes in absorption and emission properties associated with the 830 nm pump produces the direct evidence of γ irradiation effects on BAC-Si. We notice that the saturable to unsaturable absorption ratio at pump wavelength could be increased with high dose γ irradiation, indicating that emission and pump efficiency could be increased by γ irradiation. Our experimental results also reveal good radiation survivability of the BEDF under low and moderate γ irradiation. Our investigation suggests the existence of irradiation related processing available for tailoring the photoluminescence properties and performance of bismuth doped/co-doped fibres. PMID:27440386

  13. γ irradiation induced effects on bismuth active centres and related photoluminescence properties of Bi/Er co-doped optical fibres

    PubMed Central

    Sporea, D.; Mihai, L.; Neguţ, D.; Luo, Yanhua; Yan, Binbin; Ding, Mingjie; Wei, Shuen; Peng, Gang-Ding

    2016-01-01

    We investigate the effects of γ irradiation on bismuth active centres (BACs) and related photoluminescence properties of bismuth/erbium co-doped silica fibre (BEDF), [Si] ~28, [Ge] ~1.60, [Al] ~0.10, [Er] ~ <0.10 and [Bi] ~0.10 atom%, fabricated by in-situ solution doping and Modified Chemical Vapor Deposition (MCVD). The samples were irradiated at 1 kGy, 5 kGy, 15 kGy, 30 kGy and 50 kGy doses, and dose rate of 5.5 kGy/h, at room temperature. The optical properties of BEDF samples are tested before and after γ irradiation. We found that high dose γ irradiation could significantly influence the formation and composition of BACs and their photoluminescence performance, as important changes in absorption and emission properties associated with the 830 nm pump produces the direct evidence of γ irradiation effects on BAC-Si. We notice that the saturable to unsaturable absorption ratio at pump wavelength could be increased with high dose γ irradiation, indicating that emission and pump efficiency could be increased by γ irradiation. Our experimental results also reveal good radiation survivability of the BEDF under low and moderate γ irradiation. Our investigation suggests the existence of irradiation related processing available for tailoring the photoluminescence properties and performance of bismuth doped/co-doped fibres. PMID:27440386

  14. γ irradiation induced effects on bismuth active centres and related photoluminescence properties of Bi/Er co-doped optical fibres

    NASA Astrophysics Data System (ADS)

    Sporea, D.; Mihai, L.; Neguţ, D.; Luo, Yanhua; Yan, Binbin; Ding, Mingjie; Wei, Shuen; Peng, Gang-Ding

    2016-07-01

    We investigate the effects of γ irradiation on bismuth active centres (BACs) and related photoluminescence properties of bismuth/erbium co-doped silica fibre (BEDF), [Si] ~28, [Ge] ~1.60, [Al] ~0.10, [Er] ~ <0.10 and [Bi] ~0.10 atom%, fabricated by in-situ solution doping and Modified Chemical Vapor Deposition (MCVD). The samples were irradiated at 1 kGy, 5 kGy, 15 kGy, 30 kGy and 50 kGy doses, and dose rate of 5.5 kGy/h, at room temperature. The optical properties of BEDF samples are tested before and after γ irradiation. We found that high dose γ irradiation could significantly influence the formation and composition of BACs and their photoluminescence performance, as important changes in absorption and emission properties associated with the 830 nm pump produces the direct evidence of γ irradiation effects on BAC-Si. We notice that the saturable to unsaturable absorption ratio at pump wavelength could be increased with high dose γ irradiation, indicating that emission and pump efficiency could be increased by γ irradiation. Our experimental results also reveal good radiation survivability of the BEDF under low and moderate γ irradiation. Our investigation suggests the existence of irradiation related processing available for tailoring the photoluminescence properties and performance of bismuth doped/co-doped fibres.

  15. Effect of manganese concentration on photoluminescence properties of Zn2SiO4:Mn nanophosphor material

    NASA Astrophysics Data System (ADS)

    Omri, K.; El Mir, L.

    2014-06-01

    Nanophosphor β-Zn2SiO4:Mn with bright yellow light emission were synthesized by a sol-gel process. These samples were prepared by a simple solid-phase reaction under natural atmosphere at 1500 °C after the incorporation of ZnO:Mn nanoparticles, in silica monolith. X-ray diffraction (XRD) and transmission electron microscopy (TEM) were used to characterize the phase purity, particle size and morphology. In addition photoluminescence (PL) was used for optical study. The PL spectrum for the β-Zn2SiO4:Mn nanophosphors showed a dominant peak at 574 nm, which originated from the 4T1 → 6A1 transitions of Mn2+ ions. The level of manganese doping did not greatly affect the crystallinity, but did affect the luminescence of nanophosphors. Upon 255 nm excitation, the luminescence decay time of the yellow emission of β-Zn2SiO4 with a Mn doping concentration of 2 at.% around 574 nm is 13 ms. The characteristics of crystallinity, morphology and luminescence property of the obtained nanophosphors were investigated.

  16. Au and Ag/Au double-shells hollow nanoparticles with improved near infrared surface plasmon and photoluminescence properties.

    PubMed

    Ghosh Chaudhuri, Rajib; Paria, Santanu

    2016-01-01

    Metallic hollow nanoparticles have been continuously drawing researcher's attention because of their excellent improved performance compare to the spherical particles in catalysis, photonics, information storage, surface-enhanced Raman scattering, and sensors applications. In this article we demonstrate a novel route for the synthesis of single and double-shells Au and Ag/Au bimetallic hollow nanoparticles using elemental sulfur as a sacrificial core. We also investigate the optical properties of these new hollow particles and compare with that of pure spherical nanoparticles. The surface plasmon resonance spectra of solid Au, hollow single shell Au, and double shells Ag/Au nanoparticles show that there is gradual shifting of Au peak position towards the higher wavelengths for these three nanoparticles respectively. A similar observation was also found for photoluminescence spectra. In case of double-shells Ag/Au hollow nanoparticles the emission spectrum shifts towards the NIR region with significant higher intensity, which is beneficial for in vivo biomedical applications of these particles.

  17. Rare earth doped SnO2 nanoscaled powders and coatings: enhanced photoluminescence in water and waveguiding properties.

    PubMed

    Gonçalves, R R; Messaddeq, Y; Aegerter, M A; Ribeiro, S J L

    2011-03-01

    Luminescent Eu3+ and Er3+ doped SnO2 powders have been prepared by Sn4+ hydrolysis followed by a controlled growth reaction using a particle's surface modifier in order to avoid particles aggregation. The powders so obtained doped with up to 2 mol% rare earth ions are fully redispersable in water at pH > 8 and present the cassiterite structure. Particles size range from 3 to 10 nm as determined by Photon Correlation Spectroscopy. Rare earth ions were found to be essentially incorporated into the cassiterite structure, substituting for Sn4+, for doping concentration smaller than 0.05 mol%. For higher concentration they are also located at the particles surface. The presence of Eu3+ ions at the surface of the particles hinder their growth and has therefore allowed the preparation of new materials consisting of water redispersable powders coated with Eu(3+)-beta diketonate complexes. Enhanced UV excited photoluminescence was observed in water. SnO2 single layers with thickness up to 200 nm and multilayer coatings were spin coated on borosilicate glass substrates from the colloidal suspensions. Waveguiding properties were evaluated by the prism coupling technique. For a 0.3 microm planar waveguide single propagating mode was observed with attenuation coefficient of 3.5 dB/cm at 632.8 nm. PMID:21449404

  18. Photoluminescence properties of Ho{sup 3+} ion in lithium-fluoroborate glass containing different modifier oxides

    SciTech Connect

    Balakrishna, A. Rajesh, D. Ratnakaram, Y. C.

    2014-04-24

    Trivalent holmium (0.5 mol%) doped lithium fluoro-borate glasses with the chemical compositions 49.5Li{sub 2}B{sub 4}O{sub 7−}20BaF{sub 2−}10NaF−20MO (where M=Mg, Ca, Cd and Pb), 49.5Li{sub 2}B{sub 4}O{sub 7−}20BaF{sub 2−}10NaF−10MgO−10CaO and 49.5Li{sub 2}B{sub 4}O{sub 7−}20BaF{sub 2−}10NaF−10CdO−10PbO were synthesized and investigated their photoluminescence properties. The variation in chemical composition by varying modifier oxides causes changes in the structural spectroscopic behavior of Ho{sup 3+} ions. These changes are examined by UV-VIS- NIR and luminescence spectroscopic techniques. The visible luminescence spectra were obtained by exciting samples at 409 nm radiation.

  19. Positional isomerism-driven two 3D pillar-layered metal-organic frameworks: Syntheses, topological structures and photoluminescence properties

    NASA Astrophysics Data System (ADS)

    Sun, Yayong; Zhao, Siwei; Ma, Haoran; Han, Yi; Liu, Kang; Wang, Lei

    2016-06-01

    Two novel three-dimensional (3D) pillar-layered metal-organic frameworks (MOFs), namely [Zn2(μ2-OH)(boaba)(1,4-bmimb)]n (1) and {[Zn5K2(μ2-H2O)2(boaba)4(1,2-bmimb)2(H2O)2]·H2O}n (2), were prepared by hydrothermal reactions (H3boaba=3,5-bis-oxyacetate-benzoic acid; 1,4-bmimb=1,4-bis((2-methyl-1H-imidazol-1-yl)methyl)benzene; 1,2-bmimb =1,2-bis((2-methyl-1H-imidazol-1-yl)methyl)benzene). Notably, 1 exhibits a (3,5)-connected binodal (63)(69·8)-gra net with binuclear [Zn2(μ2-OH)(COO)]2+ clusters, while 2 shows a novel (4,4,5,9)-connected 4-nodal net constructed from the unique Zn(II)-K(I) heterometal rod-like substructures. The results indicate that the disposition of the 2-methylimidazolyl groups of bis(imidazole) ligands have a significant effect on structural diversity. Moreover, the photoluminescence properties of 1 and 2 have been investigated.

  20. Photoluminescence properties of a new orange-red-emitting Sm(3+)-La3SbO7 phosphor.

    PubMed

    Li, Zeng-Mei; Deng, Li-Gang; Zhao, Shan-Cang; Zhang, Shu-Qiu; Guo, Chang-Ying; Liang, Jing-Yun; Yue, Hui; Wan, Chun-Yan

    2016-03-01

    The antimonate compound La3SbO7 has high chemical stability, lattice stiffness and thermal stability. Orange-red-emitting antimonate-based phosphors La3SbO7:xSm(3+) (x = 0.02, 0.05, 0.08, 0.10, 0.15, 0.20 and 0.25) were synthesized. The phase structure and photoluminescence properties of these phosphors were investigated. The emission spectrum obtained on excitation at 407 nm contained exclusively the characteristic emissions of Sm(3+) at 568, 608, 654 and 716 nm, which correspond to the transitions from (4)G5/2 to (6)H5/2, (6)H7/2, (6)H9/2 and (6)H11/2 of Sm(3+), respectively. The strongest emission was located at 608 nm due to the (4)G5/2→(6)H7/2 transition of Sm(3+), generating bright orange-red light. The critical quenching concentration of Sm(3+) in La3SbO7:Sm(3+) phosphor was determined as 10% and the energy transfer between Sm(3+) was found to be through an exchange interaction. The International Commission on Illumination chromaticity coordinates of the La3SbO7:0.10Sm(3+) phosphors are located in the orange-red region. The La3SbO7:Sm(3+) phosphors may be potentially used as red phosphors for white light-emitting diodes.

  1. Influence of anneal atmosphere on ZnO-nanorod photoluminescent and morphological properties with self-powered photodetector performance

    NASA Astrophysics Data System (ADS)

    Hatch, S. M.; Briscoe, J.; Sapelkin, A.; Gillin, W. P.; Gilchrist, J. B.; Ryan, M. P.; Heutz, S.; Dunn, S.

    2013-05-01

    ZnO nanorods synthesised using an aqueous pH 11 solution are shown to exhibit surface-sensitive morphology post-annealing in oxygen, air, and nitrogen as shown by scanning electron microscopy and transmission electron microscopy analysis. Raman analysis confirms the nanorods were nitrogen-doped and that nitrogen incorporation takes place during the synthesis procedure in the form of N-Hx. A strong green photoluminescence is observed post-annealing for all samples, the intensity of which is dependent on the atmosphere of anneal. This luminescence is linked to zinc vacancies as recent reports have indicated that these defects are energetically favoured with the annealing conditions used herein. ZnO-nanorod/CuSCN diodes are fabricated to examine the effect of material properties on photodetector device performance. The devices exhibit a photocurrent at zero bias, creating a self-powered photodetector. A photocurrent response of 30 μA (at 6 mW cm-2 irradiance) is measured, with a rise time of ˜25 ns, and sensitivity to both UV and visible light (475-525 nm).

  2. Platinum nanoclusters in silica: Photoluminescent properties and their application for enhancing the emission of silicon nanocrystals in an integrated configuration

    NASA Astrophysics Data System (ADS)

    Bornacelli, J.; Silva-Pereyra, H. G.; Rodríguez-Fernández, L.; Avalos-Borja, M.; Oliver, A.

    2016-09-01

    We studied photoluminescence of ion implanted platinum nanoclusters embedded in silica. Pt ions were implanted at 2 MeV and the Pt nanoclusters were then nucleated by thermal treatment under either argon, air, or a reducing atmosphere of hydrogen and nitrogen. The nanoclusters showed broad photoluminescence spectra (400 to 600 nm) with a maximum intensity at 530 nm. The photoluminescence intensity of the Pt nanoclusters was sensitive to the ion fluence used during the ion implantation, and luminescence quenching was observed in samples fabricated at high Pt-ion fluence. A hybrid system composed of silicon nanocrystals and platinum nanoclusters embedded in a silica matrix was also made. The photoluminescence of the hybrid system spanned the entire visible spectrum, and emission from the silicon nanocrystals was enhanced.

  3. Further improvements in program to calculate electronic properties of narrow band gap materials

    NASA Technical Reports Server (NTRS)

    Patterson, James D.

    1991-01-01

    Research into the properties of narrow band gap materials during the period 15 Jun. to 15 Dec. 1991 is discussed. Abstracts and bibliographies from papers presented during this period are reported. Graphs are provided.

  4. Crystal Growth and Photoluminescence Properties of Truncated Cubic BaMgAl10O17:Eu2+ Phosphors for Three-Dimensional Plasma Display Panels.

    PubMed

    Liu, Bitao; Chen, Yuan; Peng, Lingling; Han, Tao; Yu, Hong; Tian, Liangliang; Tu, Mingjing

    2016-04-01

    Monodispersed, truncated cube BaMgAl10O17:Eu2+ phosphors were synthesized by the sol-gel process. Scanning electron microscope (SEM), photoluminescence spectrum, powder X-ray diffraction and decay curves were used to evaluate the truncated cubic BaMgAl10O17:Eu2+ phosphors. The crystal growth process and photoluminescence properties were discussed in detail. The results showed that this truncated cubic morphology can be achieved via a simple sinter process. These truncated cubic BaMgAl10O17:Eu2+ phosphors showed acceptable emission intensity and better thermal properties. This result indicates truncated cubic BaMgAl10O17:Eu2+ phosphors would meet the requirements of plasma display panels (PDPs). PMID:27451727

  5. A new Kagomé lattice coordination polymer based on bismuth and pyridine-2,5-dicarboxylate: structure and photoluminescent properties.

    PubMed

    Wibowo, Arief C; Smith, Mark D; zur Loye, Hans-Conrad

    2011-07-14

    A new Kagomé lattice topology assembled from ML(4) metal-organic polyhedra prepared using bismuth nitrate and pyridine-2,5-dicarboxylate has been obtained via a solvo-thermal reaction. Bi(pydc)(2)·(H(3)O(+))(H(2)O)(0.83) is, to the best of our knowledge, the first example of a bismuth-based coordination polymer to form with a Kagomé topology. Its structure and photoluminescence properties are reported.

  6. Structural and electronic properties of GaAs and GaP semiconductors

    SciTech Connect

    Rani, Anita; Kumar, Ranjan

    2015-05-15

    The Structural and Electronic properties of Zinc Blende phase of GaAs and GaP compounds are studied using self consistent SIESTA-code, pseudopotentials and Density Functional Theory (DFT) in Local Density Approximation (LDA). The Lattice Constant, Equillibrium Volume, Cohesive Energy per pair, Compressibility and Band Gap are calculated. The band gaps calcultated with DFT using LDA is smaller than the experimental values. The P-V data fitted to third order Birch Murnaghan equation of state provide the Bulk Modulus and its pressure derivatives. Our Structural and Electronic properties estimations are in agreement with available experimental and theoretical data.

  7. Synthesis, structure and photoluminescence properties of amine-templated open-framework bismuth sulfates

    SciTech Connect

    Marri, Subba R.; Behera, J.N.

    2014-02-15

    Two organically-templated bismuth sulfates of the compositions, [C{sub 6}N{sub 2}H{sub 14}] [Bi(SO{sub 4}){sub 2}(NO{sub 3})], (1) and [C{sub 4}N{sub 2}H{sub 12}]{sub 4}[Bi{sub 4}(SO{sub 4}){sub 10}(H{sub 2}O){sub 4}], (2), with open architecture have been synthesized and their structures determined by single crystal X-ray diffraction. 1 has a corrugated layered structure with 8-membered aperture wherein the SO{sub 4} tetrahedra and the BiO{sub 8} polyhedra join together to form (4, 4) net sheets of the metal centers while 2 has a three-dimensional structure possessing 8- and 12-membered channels. Both the compounds show good fluorescence properties exhibiting blue luminescence. Time-resolved fluorescence behavior of 1 and 2 shows mean fluorescence life time of 0.9 and 1.0 ns, respectively. - Graphical abstract: Two open-framework bismuth sulfates with the layered and three-dimensional structures have been synthesized and characterized. Both the compounds show good fluorescence properties exhibiting blue luminescence. Display Omitted - Highlights: • Two organically-templated bismuth sulfates with open architecture have been synthesized and characterized. • One has a corrugated layered structure while the other one has a three-dimensional structure possessing channels. • They are novel in that open-framework three-dimensional main group metal sulfates are first to be reported. • They show good fluorescence properties exhibiting blue luminescence.

  8. Cobalt(II) complexes with bis(N-imidazolyl/benzimidazolyl) pyridazine: Structures, photoluminescent and photocatalytic properties

    NASA Astrophysics Data System (ADS)

    Li, Jin-Ping; Fan, Jian-Zhong; Wang, Duo-Zhi

    2016-07-01

    Six new CoII complexes [Co(L1)4(OH)2] (1), {[Co(L1)(H2O)4]·2ClO4}∞ (2), {[Co(L1)(H2O)4]·SiF6}∞ (3), {[Co(L1)3]·2ClO4}∞ (4), [Co(L2)Cl2]∞ (5) and {[Co(L2)2]·SiF6}∞ (6) [L1=3,6-bis(N-imidazolyl) pyridazine, L2=3,6-bis (N-benzimidazolyl) pyridazine] have been synthesized and characterized by elemental analysis, IR spectra and single crystal X-ray diffraction. Complex 1 has a mononuclear structure, while complexes 2 and 3 have 1-D chain structures. Considering the CoII centers were linked by the L1 ligands, the 3-D framework of complex 4 can be rationalized to be a {4^12.6^3} 6-c topological net with the stoichiometry uninodal net. 5 reveals a coordination 1-D zigzag chain structure consisting of a neutral chain [Co(L2)Cl2]n with the CoII centers. Complex 6 has a rhombohedral grid with a (4, 4) topology. The TGA property, fluorescent property and photocatalytic activity of complexes 1-6 have been investigated and discussed.

  9. Fabrication of ZnO photonic amorphous diamond nanostructure from parrot feathers for modulated photoluminescence properties

    NASA Astrophysics Data System (ADS)

    Zhang, Zhengli; Yu, Ke; Liao, Na; Yin, Haihong; Lou, Lei; Yu, Qian; Liao, Yuanyuan; Zhu, Ziqiang

    2011-12-01

    A ZnO photonic amorphous diamond nanostructure was successfully synthesised using a feather barb of the Rosy-Faced Lovebird as supporting template via a facile sol-gel process. Different from ordered structures, an isotropic PBG around 500 nm was evidenced from reflectance spectra and an optical metallurgical microscopy image, which overlaps with the visible emission peak of ZnO. As a result, the inhibition of visible emission inside the PBG and the enhancement of UV emission at the PBG edges have both been observed, which is independent from the incident angle. Moreover, the rapid thermal annealing can also help improve the crystallinity of ZnO and raise the UV/visible emission ratio without affecting the structure. These results can be very useful for the study of the modification of the optical emission properties of ZnO and other semiconductor materials as well as research on ZnO random lasing.

  10. Fabrication and photoluminescence properties of Cr:YAG and Yb,Cr:YAG transparent ceramic

    NASA Astrophysics Data System (ADS)

    Chen, Xingtao; Lu, Tiecheng; Wei, Nian; Lu, Zhongwen; Chen, Lijia; Zhang, Qinghua; Cheng, Gang; Qi, Jianqi

    2015-11-01

    Cr:YAG and Yb/Cr:YAG transparent ceramics containing Ca as charge counter element were fabricated by vacuum sintering technique using the co-precipitation synthesis of raw powders. Their spectral and luminescence properties as well as the influence of Cr3+ concentration on the optical properties of Yb,Cr:YAG ceramic were investigated. Results show the transmittance of 10 at.% Yb, 0.25 at.% Cr:YAG and 0.25 at.% Cr:YAG reaches 83% at 1200 nm and 81% at 1400 nm, respectively. And the Yb,Cr:YAG ceramics exhibit a pore free structure with an average grain size of about 5 μm. After annealing, most of Cr3+ ions transform into Cr4+. In the case of excitation wavelength of 440 nm, a sharp emission peak of 694 nm appeared in the Yb,Cr:YAG ceramic before annealing and the band enhanced with the increase of the Cr3+ concentration, which is attributed to the 4T2g-4A2g fluorescence transition. The emission spectrums and fluorescence decays manifest that both the luminescent intensity and the lifetimes of Yb,Cr:YAG are lower than Yb:YAG ceramic and the lifetimes of Yb,Cr:YAG and Yb:YAG are 0.93 and 2.38 ms, respectively. This results demonstrate the existence of the ground state absorption of Cr4+ in the Yb,Cr:YAG ceramic. Experimental evidence proved that Yb,Cr:YAG transparent ceramics could be a potential material for passive self-Q-switched solid-state laser.

  11. Fabrication and optical properties of non-polar III-nitride air-gap distributed Bragg reflector microcavities

    SciTech Connect

    Tao, Renchun Kako, Satoshi; Arita, Munetaka; Arakawa, Yasuhiko

    2013-11-11

    Using the thermal decomposition technique, non-polar III-nitride air-gap distributed Bragg reflector (DBR) microcavities (MCs) with a single quantum well have been fabricated. Atomic force microscopy reveals a locally smooth DBR surface, and room-temperature micro-photoluminescence measurements show cavity modes. There are two modes per cavity due to optical birefringence in the non-polar MCs, and a systematic cavity mode shift with cavity thickness was also observed. Although the structures consist of only 3 periods (top) and 4 periods (bottom), a quality factor of 1600 (very close to the theoretical value of 2100) reveals the high quality of the air-gap DBR MCs.

  12. Photoluminescence properties of AlN-doped BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} phosphors

    SciTech Connect

    Wang, Yong; Tang, Jianfeng; Ouyang, Xicheng; Liu, Buqiong; Lin, Rong Han

    2013-06-01

    Highlights: ► Ideal hexagonal shape particle size in 5 μm and 2.5–3 μm in thickness are obtained. ► The growth mechanism is studied by a computer simulation. ► The influence of introduced AlN on the sites of Eu{sup 2+} and photoluminescence properties was investigated. - Abstract: The AlN-doped BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} phosphors were synthesized by conventional solid-state reaction. Powder X-ray diffraction (XRD), scanning electron microscope (SEM) and photoluminescence spectrum (PL) were used for characterization. The growth mechanism was carried out by computer simulation with CASTEP application, and revealed that an ideal hexagonal shape, particle size in 5 μm and 2.5–3 μm in thickness, could be obtained by AlN doping. Additionally, due to the low electronegativity of N{sup 3−}, the AlN-doped sample showed 35% increase in PL intensity and improvement of thermal stability. These fine particle size and better photoluminescence properties are expected to be applicable to industrial production of BaMgAl{sub 10}O{sub 17}:Eu{sup 2+} phosphors.

  13. Organic acids and protein compounds causing the photoluminescence properties of natural rubber membranes and the quenching phenomena from Au nanoparticle incorporation.

    PubMed

    Cabrera, Flávio C; Agostini, Deuber L S; Dos Santos, Renivaldo J; Guimarães, Francisco E G; Guerrero, Ariel R; Aroca, Ricardo F; Job, Aldo E

    2014-12-01

    Natural rubber membranes were fabricated using latex from Hevea brasiliensis trees (clone RRIM 600) by casting, and controlling the time and temperature of thermal treatment. Three temperatures were used: 65, 80 and 120 °C and the corresponding annealing times of 6, 8, 10 and 12 h. The centrifugation of the latex produces the constituent phases: solid rubber (F1), serum or protein components (F2) and bottom fraction (F3). The photoluminescence properties could be correlated with organic acid components of latex. Natural rubber membranes were used as the active substrate (reducing agent) for the incorporation of colloidal Au nanoparticles synthesized by in situ reduction at different times. The intensity of photoluminescence bands assigned to the natural rubber decreases with the increase in amount of nanoparticles present on the membrane surface. It can be assumed that Au nanoparticles may be formed by reduction of the Au cation reacting with functional groups that are directly related to photoluminescence properties. However, the quenching of fluorescence may be attributed to the formation of a large amount of metal nanostructures on the natural rubber surface.

  14. Effect of doping of calcium fluoride nanoparticles on the photoluminescence properties of europium complexes with benzoic acid derivatives as secondary ligands and 2-aminopyridine as primary ligand

    NASA Astrophysics Data System (ADS)

    Sharma, Garima; Narula, Anudeep Kumar

    2015-08-01

    The present article reports the synthesis of three Eu(III) complexes [Eu(BA)3(2-ap)] (1), [Eu(HBA)3(2-ap)] (2) and [Eu(ABA)3(2-ap)] (3) (BA = benzoic acid, HBA = 2-hydroxy benzoic acid, ABA = 2-amino benzoic acid and 2-ap = 2-aminopyridine) carried out in ethanol solution. The complexes were further doped with CaF2 nanoparticles and a change in the photoluminescence properties was observed. The compositions and structural investigation of the complexes were determined by elemental analysis and Fourier transform infrared spectroscopy (FTIR) which suggest the coordination of ligands with the central Eu(III) ion. The optical properties of the complexes were studied by Ultraviolet Visible absorption spectroscopy (UV-Vis) and photoluminescence studies (PL). The relative PL intensity was enhanced in the Eu(III) complexes doped with CaF2 nanoparticles as compared to the pure Eu(III) complexes, however the increase in intensity varied in the order of ligands ABA > HBA > BA. The photoluminescence lifetime decay curves also revealed the longer lifetime (τ) and higher quantum efficiency (η) for europium complexes with ABA ligands suggesting the efficient energy transfer and better sensitizing ability of the ligand to europium ion. The morphology of the synthesized compounds were studied by Scanning Electron Microscopy (SEM) revealing spherical morphology with agglomeration of the nanoparticles.

  15. Microstructure, ferromagnetic and photoluminescence properties of ITO and Cr doped ITO nanoparticles using solid state reaction

    NASA Astrophysics Data System (ADS)

    Babu, S. Harinath; Kaleemulla, S.; Rao, N. Madhusudhana; Rao, G. Venugopal; Krishnamoorthi, C.

    2016-11-01

    Indium-tin-oxide (ITO) (In0.95Sn0.05)2O3 and Cr doped indium-tin-oxide (In0.90Sn0.05Cr0.05)2O3 nanoparticles were prepared using simple low cost solid state reaction method and characterized by different techniques to study their structural, optical and magnetic properties. Microstructures, surface morphology, crystallite size of the nanoparticles were studied using X-ray diffractometer (XRD), field emission scanning electron microscope (FE-SEM). From these methods it was found that the particles were about 45 nm. Chemical composition and valence states of the nanoparticles were studied using energy dispersive analysis of X-rays (EDAX) and X-ray photoelectron spectroscopy (XPS). From these techniques it was observed that the elements of indium, tin, chromium and oxygen were present in the system in appropriate ratios and they were in +3, +4, +3 and -2 oxidation states. Raman studies confirmed that the nanoparticle were free from unintentional impurities. Two broad emission peaks were observed at 330 nm and 460 nm when excited wavelength of 300 nm. Magnetic studies were carried out at 300 K and 100 K using vibrating sample magnetometer (VSM) and found that the ITO nanoparticles were ferromagnetic at 100 K and 300 K. Where-as the room temperature ferromagnetism completely disappeared in Cr doped ITO nanoparticles at 100 K and 300 K.

  16. Comparison of photoluminescence properties of HSA-protected and BSA-protected Au25 nanoclusters

    NASA Astrophysics Data System (ADS)

    Tsukamoto, Masato; Kawasaki, Hideya; Saitoh, Tadashi; Inada, Mitsuru; Kansai Univ. Collaboration

    Gold nanoclusters (NCs) have attracted great interest for a wide range of applications. In particular, red light-emitting Au25 NCs have been prepared with various biological ligands. It has been shown that Au25 NCs have Au13-core/6Au2(SR)3-semiring structure. The red luminescence thought to be originated from both core (670 nm) and semiring (625 nm). It is important to reveal a structure of Au25 NCs to facilitate the progress of applications. However, the precise structure of Au25 NCs has not been clarified. There is a possibility of obtaining structural information about Au25 NCs to compare optical properties of the NCs that protected by slightly different molecules. Bovine and human serum albumin (BSA, HSA) are suitable one for this purpose. It has been suggested that rich tyrosine and cysteine residues in these molecules are important to produce the thiolate-protected Au NCs. If Au25 NCs have core/shell structure, only the luminescence of the semiring will be affected by the difference of the albumin molecules. We carefully compared PL characteristics of BSA- and HSA- protected Au25 NCs. As a result, there was no difference in the PL at 670 nm (core), while differences were observed in the PL at 625 nm (semiring). The results support that Au25 NCs have core/semiring structure.

  17. [Temperature-Dependent Photoluminescence Property Studies of SiN(x) Films with nc-Si].

    PubMed

    Liu, Jian-ping; Zheng, Yan; Liu, Hai-xu; Yu, Wei; Ding, Wen-ge; Lai, Wei-dong

    2016-03-01

    Silicon nitride (SiN(x)) films containing nanocrystalline silicon (nc-Si) were deposited on crystalline silicon substrate by facing-target sputtering technique. Thermal annealing process was performed at 450 degrees C for 50 min in a conventional furnace under FG(10% H2, 90% N2) ambient. The photoluminescece (PL) properties of the SiN(x) films with nc-Si were investigated by steady/transient PL spectra measurements by Fluorescence spectrometer with different temperatures. The PL processes could be attributed to the quantum confinement effect of nc-Si and the defects in the film. The PL peak position exhibits a small blue shift with the increasing of the excitation energy, which indicates that the PL portion of the nc-Si increased with smaller size. In addition, the PL lifetime increases and the PL intensity exhibits exponential increase as a result of the decreased temperature which supressed the nonradiative recombination process and then improved the radiative recombination. The PL lifetime of the film significantly reduces with the decreasing of the detection wavelength, which indicates that the PL process related to the the quantum confinement effect strongly depends on temperature. PMID:27400499

  18. Synthesis, crystal structure and photoluminescence property of Eu/Tb MOFs with mixed polycarboxylate ligands

    NASA Astrophysics Data System (ADS)

    Yang, Lu; Zhang, Sheng; Qu, Xiaoni; Yang, Qi; Liu, Xiangyu; Wei, Qing; Xie, Gang; Chen, Sanping

    2015-11-01

    Lanthanide MOFs, [Eu(TCA)(NDC)·H2O]n (1) and [Tb(TCA)(NDC)·H2O]n (2), have been prepared with the mixed aromatic carboxylate ligands, namely, 4,4‧,4″-tricarboxytriphenylamine (H3TCA) and 1,4-naphthalenedicarboxylate (H2NDC). Single-crystal X-ray diffraction analysis reveals that isomorphic 1 and 2 present pillar-layered 3D framework that Eu/Tb(III) bond with carboxylate in various coordination fashions. Optical investigation indicates that the as-prepared compounds feature characteristic luminescence emission bands of Eu/Tb ions in the visible regions at room temperature. Moreover, compound 2 shows a relatively longer luminescence lifetime (τ=0.342 ms) and significantly enhanced quantum yield (Φoverall=11%) comparing with those of 1 (τ=0.335 ms, Φoverall=0.06%). Two Ln-MOFs (Ln=EuIII, TbIII) with mixed polycarboxylate ligands present different luminescent properties.

  19. Thermal annealing effects on photoluminescence properties of carbon-doped silicon-rich oxide thin films implanted with erbium

    NASA Astrophysics Data System (ADS)

    Nikas, Vasileios; Gallis, Spyros; Huang, Mengbing; Kaloyeros, Alain E.

    2011-05-01

    Results are presented from the photoluminescence properties of C-doped Si-rich thin film oxides implanted with Er, as investigated for various postdeposition implantation and subsequent annealing and passivation conditions. In particular, it was found that the near-infrared Er luminescence intensity can be increased by up to a factor of ˜4 after a postdeposition anneal at temperatures of 300-1100 °C. The postdeposition annealing also resulted in an enhancement of the green-red (500-600 nm) PL band associated with the film matrix. Post-Er implantation passivation in an oxygen atmosphere resulted in a gradual reduction in intensity for both the Er and matrix PLs, and led eventually to a complete quenching of both PLs at the highest passivation temperature (900 °C). In contrast, hydrogen passivation increased the matrix PL intensity by a factor up to ˜2, but was found to have negligible effects on Er PL intensity over a wide range of passivation temperatures. Analysis of Er and matrix-related PL characteristics suggests that the matrix luminescence centers are most likely the sensitizers responsible for energy transfer to Er in C-doped silicon oxides. In this context, a discussion is presented of potential types of matrix-related luminescence centers present in such materials, along with the possible mechanisms leading to differences in Er excitation and deexcitation between the C-doped Si-rich oxide films analyzed herein and commonly reported Si-rich oxide materials containing Si nanocrystals.

  20. Structural phase transitions and photoluminescence properties of oxonitridosilicate phosphors under high hydrostatic pressure

    PubMed Central

    Lazarowska, Agata; Mahlik, Sebastian; Grinberg, Marek; Li, Guogang; Liu, Ru-Shi

    2016-01-01

    Spectroscopic properties of a series of (Sr0.98-xBaxEu0.02)Si2O2N2 (0 ≤ x ≤ 0.98) compounds has been studied under high hydrostatic pressure applied in a diamond anvil cell up to 200 kbar. At ambient pressure the crystal structures of (Sr0.98-xBaxEu0.02)Si2O2N2 (0 ≤ x ≤ 0.98) are related to the ratio of strontium to barium and three different phases exists: orthorhombic Pbcn(0.78 ≤ x ≤ 0.98), triclinic P1 (0 < x ≤ 0.65) and triclinic P1 (0.65 < x < 0.78). It was found that Eu2+ luminescence reveals abrupt changes under pressure (decay time, energy and shape) which indicate the variation of the local symmetry and crystal field strength in Eu2+ sites. These changes are attributed to the reversible pressure-induced structural phase transitions of triclinic (Sr0.98-xBaxEu0.02)Si2O2N2 into orthorhombic structure. Pressure in which phase transition occurs decreases linearly with increasing of Ba composition in (Sr0.98-xBaxEu0.02)Si2O2N2 series. Additionally, very different pressure shifts of the Eu2+ luminescence in different phases of (Sr0.98-xBaxEu0.02)Si2O2N2:Eu from −40 cm−1/kbar to 0 cm−1/kbar have been observed. This effect is explained by different interaction of the Eu2+ 5d electron with the second coordination sphere around the impurity cations. PMID:27734847

  1. Structural phase transitions and photoluminescence properties of oxonitridosilicate phosphors under high hydrostatic pressure

    NASA Astrophysics Data System (ADS)

    Lazarowska, Agata; Mahlik, Sebastian; Grinberg, Marek; Li, Guogang; Liu, Ru-Shi

    2016-10-01

    Spectroscopic properties of a series of (Sr0.98-xBaxEu0.02)Si2O2N2 (0 ≤ x ≤ 0.98) compounds has been studied under high hydrostatic pressure applied in a diamond anvil cell up to 200 kbar. At ambient pressure the crystal structures of (Sr0.98-xBaxEu0.02)Si2O2N2 (0 ≤ x ≤ 0.98) are related to the ratio of strontium to barium and three different phases exists: orthorhombic Pbcn(0.78 ≤ x ≤ 0.98), triclinic P1 (0 < x ≤ 0.65) and triclinic P1 (0.65 < x < 0.78). It was found that Eu2+ luminescence reveals abrupt changes under pressure (decay time, energy and shape) which indicate the variation of the local symmetry and crystal field strength in Eu2+ sites. These changes are attributed to the reversible pressure-induced structural phase transitions of triclinic (Sr0.98-xBaxEu0.02)Si2O2N2 into orthorhombic structure. Pressure in which phase transition occurs decreases linearly with increasing of Ba composition in (Sr0.98-xBaxEu0.02)Si2O2N2 series. Additionally, very different pressure shifts of the Eu2+ luminescence in different phases of (Sr0.98-xBaxEu0.02)Si2O2N2:Eu from ‑40 cm‑1/kbar to 0 cm‑1/kbar have been observed. This effect is explained by different interaction of the Eu2+ 5d electron with the second coordination sphere around the impurity cations.

  2. Synthesis, structural characterization and photoluminescence properties of a novel La(III) complex

    NASA Astrophysics Data System (ADS)

    Köse, Muhammet; Ceyhan, Gökhan; Atcı, Emine; McKee, Vickie; Tümer, Mehmet

    2015-05-01

    In this study, a novel La(III) complex [La(H2L)2(NO3)3(MeOH)] of a Schiff base ligand was synthesized and characterized by spectroscopic and analytical methods. Single crystals of the complex suitable for X-ray diffraction study were obtained by slow diffusion of diethyl ether into a MeOH solution of the complex which was found to crystallise as [La(H2L)2(NO3)3(MeOH)]ṡ2MeOHṡH2O. The structure was solved in monoclinic crystal system, P21/n space group with unit cell parameters a = 10.5641(11), b = 12.6661(16), c = 16.0022(17) Å, α = 67.364(2), β = 83.794(2)°, γ = 70.541(2)°, V = 1862.9(4) Å3 and Z = 2 with R final value of 0.526. In the complex, the La(III) ion is ten-coordinated by O atoms, five of which come from three nitrate ions, four from the two Schiff base ligands and one from MeOH oxygen atom. The Schiff base ligands in the structure are in a zwitter ion form with the phenolic H transferred to the imine N atom. Thermal properties of the La(III) complex were examined by thermogravimetric analysis and the complex was found to be thermally stable up to 310 °C. The Schiff base ligand and its La(II) complex were screened for their in vitro antimicrobial activity against Bacillus megaterium, Staphylococcus aureus, Bacillus subtilis, Micrococcus luteus (Gram positive bacteria), Klebsiella pneumonia, Escherichia coli, Enterobacter aerogenes, Pseudomonas aeruginosa (Gram negative bacteria), Candida albicans,Yarrowia lipolytica (fungus) and Saccharomyces cerevisiae (yeast). The complex shows more antimicrobial activity than the free ligand.

  3. Remarkable changes in the photoluminescent properties of Y2Ce2O7:Eu(3+) red phosphors through modification of the cerium oxidation states and oxygen vacancy ordering.

    PubMed

    Raj, Athira K V; Prabhakar Rao, P; Sreena, T S; Sameera, S; James, Vineetha; Renju, U A

    2014-11-21

    A new series of red phosphors based on Eu(3+)-doped yttrium cerate [Y1.9Ce2O7:0.1Eu(3+), Y2Ce1.9O7:0.1Eu(3+) and Y2Ce2-xO7:xEu(3+) (x = 0.05, 0.10, 0.15, 0.20, 0.25 and 0.50)] was prepared via a conventional solid-state method. The influence of the substitution of Eu(3+) at the aliovalent site on the photoluminescent properties was determined by powder X-ray diffraction, FT Raman spectroscopy, X-ray photoelectron spectroscopy, transmission electron microscopy, scanning electron microscopy with energy-dispersive spectroscopy, UV-visible absorption spectroscopy, photoluminescence spectroscopy and lifetime measurements. The substitution of Eu(3+) at the Ce(4+) site induces a structural transition from a defect fluorite to a C-type structure, which increases the oxygen vacancy ordering and the distortion of the Eu(3+) environment, and decreases the formation of Ce(3+) states. In contrast, phosphors with isovalent substitution at the Y(3+) site exhibit the biphasic nature of defect fluorite and a C-type structure, thereby increasing the number of Ce(3+) oxidation states. These modifications resulted in remarkable changes in the photoluminescent properties of Y2Ce1.9O7:0.1Eu(3+) red phosphors, with emission intensities 3.8 times greater than those of the Ce0.9O2:0.1Eu(3+) and Y1.9Ce2O7:0.1Eu(3+). The photoluminescent properties of Y2Ce2-xO7:xEu(3+) were studied at different Eu(3+) concentrations under excitation with blue light. These phosphors emit intense red light due to the (5)D0-(7)F2 transition under excitation at 466 nm and no concentration quenching is observed with up to 50 mol% Eu(3+). They show increased lifetimes in the range 0.62-0.72 ms at Eu(3+) concentrations. The cation ordering linked to the oxygen vacancy ordering led to the uniform distribution of Eu(3+) ions in the lattice, thus allowing higher doping concentrations without quenching and consequently increasing the lifetime of the (5)D0 states. Our results demonstrate that significant improvements in

  4. Photoluminescence and thermoluminescence properties of Sr{sub 3}Al{sub 2}O{sub 6}:Tb{sup 3+}

    SciTech Connect

    Page, Pallavi; Ghildiyal, Rahul; Murthy, K.V.R.

    2008-02-05

    Photoluminescence and thermoluminescence characteristics of the SrO-Al{sub 2}O{sub 3} system doped with terbium have been studied and reported here. The phosphor was synthesized by a reflux sol-gel technique. With a view to study the dosimetric properties, the effect of beta irradiation has been studied in detail; further, concentration quenching effects observed in the emission of various terbium doped phosphors have led to optimization of dopant content. A case is made to project the phosphor as an efficient green light emitting material with good dosimetric properties.

  5. Vacuum consumable arc remelting electrode gap control strategies based on drop short properties

    NASA Astrophysics Data System (ADS)

    Zanner, F. J.

    1981-12-01

    An investigation was conducted to determine the influence of electrode gap on the properties of drop shorts during vacuum consumable arc remelting. The goal of this work was to yield an electrode gap control strategy based on easily measured electrical parameters. For a particular alloy, at one current level and low pressure (<4 X 10-3 Torr), this goal was achieved, in that drop short period was found to be highly correlated with electrode gap. However, this model was found to be constrained by statistics which require counting 100 drop shorts in order to obtain a valid measurement. Other control strategies involving anode spikes, drop short resistance, and energy/resistance ratios were also evaluated and these properties showed poor correlation with electrode gap.

  6. Vibration band-gap properties of three-dimensional Kagome lattices using the spectral element method

    NASA Astrophysics Data System (ADS)

    Wu, Zhi-Jing; Li, Feng-Ming; Zhang, Chuanzeng

    2015-04-01

    The spectral element method (SEM) is extended to investigate the vibration band-gap properties of three-dimensional (3D) Kagome lattices. The dynamic stiffness matrix of the 3D element which contains bending, tensional and torsional components is derived. The spectral equations of motion of the whole 3D Kagome lattice are then established. Comparing with frequency-domain solutions calculated by the finite element method (FEM), the accuracy and the feasibility of the SEM solutions are verified. It can be shown that the SEM is suitable for analyzing the vibration band-gap properties. Due to the band-gap characteristics, the periodic 3D Kagome lattice has the performance of vibration isolation. The influences of the structural and material parameters on the vibration band-gaps are discussed and a new type of 3D Kagome lattice is designed to obtain the improved vibration isolation capability.

  7. Photoluminescence and thermoluminescence properties of Tb{sup 3+} doped K{sub 3}Gd(PO{sub 4}){sub 2} nanophosphor

    SciTech Connect

    Gupta, Palvi; Bedyal, A.K.; Kumar, Vinay; Khajuria, Y.; Lochab, S.P.; Pitale, S.S.; Ntwaeaborwa, O.M.; Swart, H.C.

    2014-12-15

    Energy level diagram of Tb{sup 3+} ion in the K{sub 3}Gd(PO{sub 4}){sub 2} host lattice. - Highlights: • First time, a detailed TL and PL study on undoped and Tb{sup 3+} doped K{sub 3}Gd(PO{sub 4}){sub 2} nanophosphor. • Combustion method was employed to synthesize the Tb{sup 3+} doped K{sub 3}Gd(PO{sub 4}){sub 2} nanophosphor. • Mechanism of excitation and emission in undoped and Tb{sup 3+} doped K{sub 3}Gd(PO{sub 4}){sub 2} nanophosphor was given. - Abstract: Tb{sup 3+} doped nanoparticulate K{sub 3}Gd(PO{sub 4}){sub 2} phosphor was prepared by combustion method using urea as a fuel. The structure, optical and luminescent properties of the phosphor were studied by X-ray diffraction (XRD), scanning electron microscopy (SEM), diffuse reflectance spectroscopy (DRS), photoluminescence spectroscopy (PL), and thermoluminescence (TL) spectroscopy. In undoped K{sub 3}Gd(PO{sub 4}){sub 2}, the excitation and emission peaks at 273 nm and 323 nm belongs to the {sup 8}S{sub 7/2} → {sup 6}I{sub J(J=7/2)} and {sup 6}P{sub J(J=7/2)} → {sup 8} S{sub 7/2} transitions of Gd{sup 3+} while green emission was observed in the Tb{sup 3+} doped K{sub 3}Gd(PO{sub 4}){sub 2}. TL study was carried out after exposing the samples to γ-radiations (0.1–5 kGy) in the K{sub 3}Gd(PO{sub 4}){sub 2}:Tb{sup 3+} (1.5 mol%). The calculated kinetic parameters were compared with different methods. The band gap of the phosphor was estimated as 5.80 eV. The green shade of the Tb{sup 3+} ion with the CIE coordinates (x, y) as (0.29, 0.54) was in good agreement with the well known green phosphors.

  8. BaCdSnS4 and Ba3CdSn2S8: syntheses, structures, and non-linear optical and photoluminescence properties.

    PubMed

    Zhen, Ni; Wu, Kui; Wang, Ying; Li, Qiang; Gao, Wenhui; Hou, Dianwei; Yang, Zhihua; Jiang, Huaidong; Dong, Yongjun; Pan, Shilie

    2016-06-28

    Two non-centrosymmetric metal chalcogenides, BaCdSnS4 and Ba3CdSn2S8, were synthesized using a high temperature solid-state reaction in an evacuated silica tube. Although the two compounds have the same building units in their structures, namely CdS4, SnS4 and BaS8 units, both of them have different structures. BaCdSnS4 crystallizes in the orthorhombic space group Fdd2 and its structure can be characterized by the two-dimensional ∞[Cd-Sn-S] layers composed of corner- and edge-sharing CdS4 and SnS4 tetrahedra with Ba atoms located between the two adjacent ∞[Cd-Sn-S] layers. Ba3CdSn2S8 crystallizes in the space group I4[combining macron]3d of the orthorhombic system and the CdS4 and SnS4 groups are connected with each other via corner-sharing to form a three-dimensional framework, which is different from the 2D ∞[Cd-Sn-S] layer structure in BaCdSnS4. The UV-vis-NIR diffuse-reflectance spectra show that the experimental band gaps are about 2.30 eV for BaCdSnS4 and 2.75 eV for Ba3CdSn2S8, respectively. IR and Raman measurement results indicate that their transparent ranges are up to 25 μm. Second-order NLO measurements show that BaCdSnS4 exhibits strong powder second-harmonic generation (SHG) intensities at 2.09 μm laser pumping that are ∼5 and 0.7 times that of AgGaS2 in the particle size 38-55 and 150-200 μm, respectively, whereas Ba3CdSn2S8 only exhibits SHG intensities of about 0.8 and 0.1 times that of AgGaS2 at the same particle sizes. The origin of the NLO response in BaCdSnS4 may originate from the macroscopic arrangement of the SnS4 and CdS4 tetrahedra. Furthermore, the photoluminescence properties of the two compounds have also been investigated and show obvious blue and green light emission. PMID:27272926

  9. Heating Profile Effect on Morphology, Crystallinity, and Photoluminescent Properties of Y2O3:Eu3+ Phosphor Nanofibers Prepared Using an Electrospinning Method

    NASA Astrophysics Data System (ADS)

    Munir, Muhammad Miftahul; Yun, Ki Myoung; Iskandar, Ferry; Yabuki, Akihiro; Okuyama, Kikuo

    2007-10-01

    Europium-doped yttrium oxide (Y2O3:Eu3+) nanofibers were successfully prepared via an electrospinning method followed by annealing at temperatures up to 1200 °C. Mixed solutions of yttrium nitrate, europium nitrate and poly(vinyl pyrrolidone) (PVP) were used as precursors. Poly(vinyl pyrrolidone) polymer was used as a template for obtaining fiber morphology and was then removed during the annealing process to yield Y2O3:Eu3+ fibers. The fibers were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier-transform infrared (FTIR), and photoluminescence (PL) spectrometry. The effect of the heating profile on the morphology, crystallinity, and photoluminescent properties of the nanofibers was systematically investigated. The diameter of the prepared fibers decreased with increasing temperature and a high heating rate caused the polymer to melt quickly and cross-links to form between the fibers. In addition, crystallite size and photoluminescent intensity of Y2O3:Eu3+ phosphor fibers increased with increasing temperature.

  10. Effects of site substitutions and concentration on the structural, optical and visible photoluminescence properties of Er doped BaTiO3 thin films prepared by RF magnetron sputtering

    NASA Astrophysics Data System (ADS)

    Maneeshya, L. V.; Thomas, P. V.; Joy, K.

    2015-08-01

    The structural, optical and visible photoluminescence of the Erbium (Er) doped BaTiO3 (BT:Er) thin films were studied in terms of Er3+ substitutions for Ba and Ti sites with different Er3+ doping concentrations (0, 1, 3 and 5 wt%). X-ray diffraction pattern of BT:Er films with different Er3+ concentration showed tetragonal phase with preferred orientation along (1 0 1) plane. The lattice constant of BT:Er film of 1 wt% Er3+ shrank and then expanded for higher concentration. This indicates that Er3+ ions are completely incorporated into the host lattice by substituting for Ba2+ sites for 1 wt% Er3+ and then Ti4+ sites for higher Er3+ concentration in the BaTiO3 host. The crystallite size decreased for 1 wt% and then increased for higher Er (3 and 5 wt%) concentrations. The Scanning electron microscopy images revealed well patterned arrangement of larger spherical grains with neck formation. X-ray photoelectron spectroscopy analysis confirmed the presence of barium, titanium, erbium and oxygen in BT:Er films. An average transmittance >80% in visible region were observed for all the films. Optical band gap energy of BT:Er films were found to vary with increase in Er3+ concentration. The high refractive index >2 of these films can be used in optical application and anti-reflection coatings. Photoluminescence spectra of the films exhibited an increase in the emission intensity up to 3 wt% of Er3+ and then a decrease, due to self quenching. The improved optical properties of BT:Er films makes suitable for optical applications.

  11. Isotropic properties of the photonic band gap in quasicrystals with low-index contrast

    NASA Astrophysics Data System (ADS)

    Priya Rose, T.; di Gennaro, E.; Abbate, G.; Andreone, A.

    2011-09-01

    We report on the formation and development of the photonic band gap in two-dimensional 8-, 10-, and 12-fold symmetry quasicrystalline lattices of low-index contrast. Finite-size structures made of dielectric cylindrical rods were studied and measured in the microwave region, and their properties were compared with a conventional hexagonal crystal. Band-gap characteristics were investigated by changing the direction of propagation of the incident beam inside the crystal. Various angles of incidence from 0∘ to 30∘ were used to investigate the isotropic nature of the band gap. The arbitrarily high rotational symmetry of aperiodically ordered structures could be practically exploited to manufacture isotropic band-gap materials, which are perfectly suitable for hosting waveguides or cavities.

  12. Ab-initio study of structural, electronic, and transport properties of zigzag GaP nanotubes.

    PubMed

    Srivastava, Anurag; Jain, Sumit Kumar; Khare, Purnima Swarup

    2014-03-01

    Stability and electronic properties of zigzag (3 ≤ n ≤ 16) gallium phosphide nanotubes (GaP NTs) have been analyzed by employing a systematic ab-intio approach based on density functional theory using generalized gradient approximation with revised Perdew Burke Ernzerhoff type parameterization. Diameter dependence of bond length, buckling, binding energy, and band gap has been investigated and the analysis shows that the bond length and buckling decreases with increasing diameter of the tube, highest binding energy of (16, 0) confirms this as the most stable amongst all the NTs taken into consideration. The present GaP NTs shows direct band gap and it increases with diameter of the tubes. Using a two probe model for (4, 0) NT the I-V relationship shows an exponential increase in current on applying bias voltage beyond 1.73 volt.

  13. Photoluminescence and electrical properties of Eu-doped (Na0.5Bi0.5)TiO3 ferroelectric single crystals

    NASA Astrophysics Data System (ADS)

    Zhang, Haiwu; Zhao, Xiangyong; Deng, Hao; Chen, Chao; Lin, Di; Li, Xiaobing; Yan, Jun; Luo, Haosu

    2014-02-01

    Eu3+-doped Na0.5Bi0.5TiO3 (Eu:NBT) single crystals were grown by a top-seeded solution growth method. Photoluminescence emission and excitation spectra of Eu:NBT were investigated. The two transitions in 7F0 → 5D0 excitation spectra reveal that Eu3+ ions were incorporated into two adjacent crystallographic sites in NBT, i.e., Bi3+ and Na+ sites. The former has a symmetrical surrounding, while the later has a disordered environment, which was confirmed by decay curve measurements. The dielectric dispersion behavior was depressed and the piezoelectric and ferroelectric properties were improved after Eu doping.

  14. Theoretical study of optical properties of anti phase domains in GaP

    SciTech Connect

    Tea, E.; Vidal, J.; Laribi, S.; Guillemoles, J.-F.; Pedesseau, L.; Cornet, C.; Jancu, J.-M.; Even, J.; Durand, O.

    2014-02-14

    III-V/Si heterostructures are currently investigated for silicon photonics and solar energy conversion. In particular, dilute nitride alloy GaAsPN grown on a GaP/Si platform exhibits lattice match with Si and an optimal band gap configuration for tandem solar cell devices. However, monolithic “coherent” growth of the GaP thin layer on Si suffers from the nucleation of extended structural defects, which can hamper device operation as well as the GaP/Si interface level and through their propagation inside the overall heterostructure. However, the effect of such structural defects on optical and transport properties is actually not well understood in details. In this letter, we investigate the anti phase domains defect (also called inversion domains) by means of ab initio calculations giving insights into the alteration of optical and transport properties of GaP due to the defective GaP/Si interface.

  15. [Preparation and Photoluminescent Properties of Ce³⁺-Activated LaPO₄ Nanocrystals and Core/Shell Structure].

    PubMed

    Li, Zhen-ya; Huang, Shi-ming; Gu, Mu; Liu, Xiao-lin

    2015-11-01

    Hydrophobic, monodisperse LaPO₄: Ce³⁺ nanoparticles, LaPO₄:Ce³⁺/LaPO₄ and LaPO₄:Ce³⁺/LaPO₄: Ce³⁺/ LaPO₄ core/shell structure nanocrystals were synthesized via a high-temperature organic solution approach. The as-synthesized samples were characterized by X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR) and photoluminescence spectroscopy (PL). The results show that: all the samples are a monoclinic phase, Because of the size small nanoparticles, the diffraction peaks of the sample occurs width phenomenon. The LaPO₄:Ce³⁺ nano- crystals exhibits the characteristic emission of Ce³⁺ ions, the photoluminescence intensity increases first and then decreases with the increasing doping concentration of Ce³⁺ ions, and the best doping amount is 6 at %, with the increasing doping amount, the photoluminescence intensity decreases which may caused by the concentration quenching. Compared to LaPO₄:Ce³⁺ nanoparti- cles, the photoluminescence intensity of LaPO₄:Ce³⁺/LaPO₄ and LaPO₄: Ce³⁺/LaPO₄: Ce³⁺/LaPO₄ core/shell structure nanocrystals improves about 41% and 95% respectively, this may be a synergy of larger particle size of nanocrystals and surface passivation effect. FTIR spectra data shows that the absorption peak at 1545 and 1461 cm⁻¹ corresponded to the asymmetric and symmetric stretching vibration of --COO⁻, the separation, Δ, between the two peaks is 84 cm⁻¹, The mechanism of the sample surface modification by the organics might be that the oxygen atoms of the carboxyl are coordinated with the lanthunum ions by a bidentate mode.

  16. Microstructure and photoluminescent properties of Sr{sub 2}SiO{sub 4}:Eu{sup 3+} phosphors with various NH{sub 4}Cl flux concentrations

    SciTech Connect

    Chen, Huang-Yu; Chang, Shoou-Jinn

    2012-06-15

    Graphical abstract: This paper describes effects of NH{sub 4}Cl concentration on microstructural and luminescent characteristics of Sr{sub 2}SiO{sub 4}:Eu{sup 3+} phosphors using microwave assisted sintering at 1200 °C for 1 h. The results showed the improved photoluminescence properties of microwave sintered Sr{sub 2}SiO{sub 4}:Eu{sup 3+} phosphors by adding NH{sub 4}Cl flux. Highlights: ► NH{sub 4}Cl flux improved the luminescence properties of microwave sintered phosphors. ► The particle sizes were enlarged from 1 μm to 10 μm as the NH{sub 4}Cl flux was added. ► The maximum photoluminescence intensity was appeared as adding 1 wt% NH{sub 4}Cl flux. ► The decay times of Sr{sub 2}SiO{sub 4}:Eu{sup 3+} phosphors with NH{sub 4}Cl flux were around 2.47–2.52 ms. -- Abstract: In this paper, effect of NH{sub 4}Cl flux concentrations (0, 1, 2, 3 and 4 wt%) on the crystal structure, morphology and photoluminescent properties of Sr{sub 2}SiO{sub 4}:Eu{sup 3+} phosphors synthesized by a microwave sintering at 1200 °C for 1 h was investigated and discussed. X-ray powder diffraction analysis showed the crystal structure was not affected and the pure Sr{sub 2}SiO{sub 4} phase was formed without second phase or phases of starting materials when adding with the NH{sub 4}Cl flux. The SEM images indicated that increase of the NH{sub 4}Cl flux enlarged the particle size of the phosphor particles. The photo-luminescence results showed the addition of 1 wt% NH{sub 4}Cl flux much improved the emission intensity at λ{sub em} of 617 nm as the excitation spectrum at λ{sub ex} of 395 nm. The decay times of Sr{sub 2}SiO{sub 4}:Eu{sup 3+} phosphors with different NH{sub 4}Cl flux concentrations were obtained around 2.47–2.52 ms.

  17. Syntheses, structures and photoluminescent properties of three d{sup 10} coordination architectures based on in-situ 1,3,5-triazine derivatives

    SciTech Connect

    Xiao, Changyu; Li, Yamin; Lun, Huijie; Cui, Caiyan; Xu, Yanqing

    2013-12-15

    In the presence of aromatic carboxylic acids, three new d{sup 10} transition metal coordination polymers, [Ag(PAHT)]{sub n}(1), [Ag{sub 2}(HCA)]{sub n}(2) and [Cu{sub 6}(CA){sub 2}(H{sub 2}O)]{sub n}(3) (HPAHT=2-phenyl-4-amino-6-hydroxy-1,3,5-triazine, H{sub 3}CA=cyanuric acid) have been synthesized based on in-situ 1,3,5-triazine derivatives resulting from 2,4-diamino-6-phenyl-1,3,5-triazine, 2-chloro-4,6-diamino-1,3,5-triazine and melamine under hydrothermal conditions. Complexes 1–3 have been characterized by single-crystal X-ray diffraction, IR spectra, elemental analysis and thermogravimetric analysis (TGA). The compound 1 exhibits a uninodal three-connected 3D network with a rare lig LiGe type topology, which contains right-handed and left-handed [Ag(PAHT)]{sub n} helical chains. For compound 2, the 3D network is comprised of 2D sheet by strongly Ag–O and weakly Ag(I)…Ag(I) interactions. In compound 3, it is infrequently observed that dodecanuclear copper(I) units as secondary building units (SBUs) construct 3D network by the ligands CA{sup 3−} with a rare uninodal 10-connected bct topology (3{sup 12}.4{sup 28}.5{sup 5}). The photoluminescent properties of three compounds have also been measured. - Graphical abstract: Three d{sup 10} transition metal coordination polymers 1–3 have been hydrothermally synthesized and characterized by single-crystal X-ray diffraction, IR spectra, elemental analysis, photoluminescent spectra and thermogravimetric analysis (TGA). - Highlights: • The compound 1 exhibits a new 3D network with two kinds of single helical chains. • New 3D d{sup 10} transition metal coordination polymers. • The photoluminescent properties have been measured.

  18. Anisotropic Effective Mass, Optical Property, and Enhanced Band Gap in BN/Phosphorene/BN Heterostructures.

    PubMed

    Hu, Tao; Hong, Jisang

    2015-10-28

    Phosphorene is receiving great research interests because of its peculiar physical properties. Nonetheless, the phosphorus has a trouble of degradation due to oxidation. Hereby, we propose that the electrical and optical anisotropic properties can be preserved by encapsulating into hexagonal boron nitride (h-BN). We found that the h-BN contributed to enhancing the band gap of the phosphorene layer. Comparing the band gap of the pristine phosphorene layer, the band gap of the phosphorene/BN(1ML) system was enhanced by 0.15 eV. It was further enhanced by 0.31 eV in the BN(1ML)/phosphorene/BN(1ML) trilayer structure. However, the band gap was not further enhanced when we increased the thickness of the h-BN layers even up to 4 MLs. Interestingly, the anisotropic effective mass and optical property were still preserved in BN/phosphorene/BN heterostructures. Overall, we predict that the capping of phosphorene by the h-BN layers can be an excellent solution to protect the intrinsic properties of the phosphorene.

  19. Electronic properties of unstrained unrelaxed narrow gap InAs x Sb1-x alloys

    NASA Astrophysics Data System (ADS)

    Suchalkin, S.; Ludwig, J.; Belenky, G.; Laikhtman, B.; Kipshidze, G.; Lin, Y.; Shterengas, L.; Smirnov, D.; Luryi, S.; Sarney, W. L.; Svensson, S. P.

    2016-03-01

    The electronic properties of unstrained unrelaxed InAs x Sb1-x alloys have been determined in a wide range of alloy compositions using IR magnetospectroscopy, magnetotransport and IR photoluminescence. All studied alloys have n-type background doping with electron concentration decreasing with the Sb content. The composition dependence of the background doping concentration follows an empirical exponential law in a wide range of compositions. Both bandgap and electron effective mass dependence on alloy composition exhibit negative bowing reaching lowest values at x  =  0.63: E g  =  0.10 eV, m*  =  0.0082 m 0 at 4.2 K. The bowing coefficient of 0.038 m 0 obtained for the electron effective mass is in good agreement with that obtained from the Kane model.

  20. Annealing effects on the structure, photoluminescence, and magnetic properties of GaN/Mn{sub 3}O{sub 4} core-shell nanowires

    SciTech Connect

    Kim, Hyo Sung; Na, Han Gil; Yang, Ju Chan; Jung, Jong Hoon; Koo, Yong Sung; Hur, Nam Jung; Kim, Hyoun Woo

    2010-10-15

    Nanowires consisting of GaN/Mn{sub 3}O{sub 4} were prepared using a two-step approach that involved dipping the as-synthesized GaN nanowires into an aqueous manganese acetate solution. To examine the effects of annealing, GaN/Mn{sub 3}O{sub 4} core-shell nanowires were heated thermally to 700 {sup o}C in N{sub 2} ambient. Transmission electron microscopy showed that the continuous Mn{sub 3}O{sub 4} shell layer had agglomerated to expose a bare GaN core surface after thermal annealing. The magnetic measurements showed that the ferromagnetic behavior of the GaN nanowires had been suppressed by coating with the Mn{sub 3}O{sub 4} shell, without significant change by the subsequent thermal annealing. The GaN/Mn{sub 3}O{sub 4} core-shell nanowires exhibited blue, green, and red photoluminescence (PL) emission. The red emission was enhanced by thermal annealing. This paper discusses the associated mechanism for the variations in PL and magnetic properties of GaN/Mn{sub 3}O{sub 4} core-shell nanowires. - Abstract: Novel GaN/Mn{sub 3}O{sub 4} core-shell nanowires were synthesized and the effects of thermal annealing on the structure, photoluminescence, and magnetic properties were investigated.

  1. Single layer of silicon quantum dots in silicon oxide matrix: Investigation of forming gas hydrogenation on photoluminescence properties and study of the composition of silicon rich oxide layers

    NASA Astrophysics Data System (ADS)

    Aliberti, P.; Shrestha, S. K.; Li, Ruoyu; Green, M. A.; Conibeer, G. J.

    2011-07-01

    Structures consisting of a single layer of silicon quantum dots in a SiO 2 matrix show interesting optoelectronic properties and potential use as energy selective filters, which are a crucial component for the realization of the hot carrier solar cell. In this work single layer silicon quantum dots in SiO 2 have been realized using a magnetron sputtering technique. Quantum dots are formed by annealing of a silicon rich oxide layer deposited between a thermally grown SiO 2 layer and a sputtered SiO 2 layer. The effects of a forming gas post-hydrogenation process on the photoluminescence of the single layer of quantum dots have been investigated in order to understand the photoluminescence mechanism. It was found that for sputtered silicon quantum dots in SiO 2 matrix the photoemission mechanisms are primarily due to quantum confinement and does not strongly rely on matrix defects. In addition, physical and optical properties of several thick silicon rich oxide layers, with different chemical compositions, have been investigated in order to optimize the stoichiometry of silicon rich oxide in the single layers.

  2. Giant blue shifted photoluminescence peak from the edges of CVD grown monolayer MoS2

    NASA Astrophysics Data System (ADS)

    Yore, Alexander; Crumrine, Wendy; Smithe, Kirby; Pop, Eric; Wang, Bin; Newaz, Akm

    To probe the electronic and optical properties of direct band-gap monolayer transition metal dichalcogenides, such as band structure and excitons, micro-photoluminescence spectroscopy has become an attractive and standard tool. Here, we present our experimental work on spatial scanning of photoluminescence of monolayer MoS2 grown by chemical vapor deposition (CVD) using an ultrasmall blue laser (wavelength 405 nm) beam spot with beam diameter as small as ~ 200 nm. We have observed a giant blue shift, as large as ~ 40 nm or ~ 100 meV, of the A-excitonic peak in the photoluminescence spectra from the edges when compared to luminescence from the inside. This giant blue shift may result from the following: (i) compressive strain at the edges; (ii) the enhanced dielectric screening caused by the increased electron density at the metallic Mo-edges; and (iii) chemical impurities.

  3. Control of Photoluminescence of Carbon Nanodots via Surface Functionalization using Para-substituted Anilines

    PubMed Central

    Kwon, Woosung; Do, Sungan; Kim, Ji-Hee; Seok Jeong, Mun; Rhee, Shi-Woo

    2015-01-01

    Carbon nanodots (C-dots) are a kind of fluorescent carbon nanomaterials, composed of polyaromatic carbon domains surrounded by amorphous carbon frames, and have attracted a great deal of attention because of their interesting properties. There are still, however, challenges ahead such as blue-biased photoluminescence, spectral broadness, undefined energy gaps and etc. In this report, we chemically modify the surface of C-dots with a series of para-substituted anilines to control their photoluminescence. Our surface functionalization endows our C-dots with new energy levels, exhibiting long-wavelength (up to 650 nm) photoluminescence of very narrow spectral widths. The roles of para-substituted anilines and their substituents in developing such energy levels are thoroughly studied by using transient absorption spectroscopy. We finally demonstrate light-emitting devices exploiting our C-dots as a phosphor, converting UV light to a variety of colors with internal quantum yields of ca. 20%. PMID:26218869

  4. Elucidating Quantum Confinement in Graphene Oxide Dots Based On Excitation-Wavelength-Independent Photoluminescence.

    PubMed

    Yeh, Te-Fu; Huang, Wei-Lun; Chung, Chung-Jen; Chiang, I-Ting; Chen, Liang-Che; Chang, Hsin-Yu; Su, Wu-Chou; Cheng, Ching; Chen, Shean-Jen; Teng, Hsisheng

    2016-06-01

    Investigating quantum confinement in graphene under ambient conditions remains a challenge. In this study, we present graphene oxide quantum dots (GOQDs) that show excitation-wavelength-independent photoluminescence. The luminescence color varies from orange-red to blue as the GOQD size is reduced from 8 to 1 nm. The photoluminescence of each GOQD specimen is associated with electron transitions from the antibonding π (π*) to oxygen nonbonding (n-state) orbitals. The observed quantum confinement is ascribed to a size change in the sp(2) domains, which leads to a change in the π*-π gap; the n-state levels remain unaffected by the size change. The electronic properties and mechanisms involved in quantum-confined photoluminescence can serve as the foundation for the application of oxygenated graphene in electronics, photonics, and biology. PMID:27192445

  5. Photoluminescent Properties of Y2O3:Eu3+ Phosphors Prepared via Urea Precipitation in Non-Aqueous Solution

    SciTech Connect

    Sun, Yu; Qi, Lai; Lee, M; Lee, Burtrand I.; Samuels, William D.; Exarhos, Gregory J.

    2004-08-02

    Europium-doped yttrium oxide phosphors were obtained by firing precursors prepared by urea precipitation in ethanol and ethylenediamine. The precipitation in non-aqueous solution was carried out in an autoclave at 150 C to allow the decomposition of urea. The photoluminescent intensities of the phosphors prepared in ethanol and ethylenediamine increased by about 30% compared to that of the phosphor prepared by the conventional urea homogeneous precipitation in aqueous solution. Amorphous carbonates and amorphous hydroxides/carbonates mixtures were identified as precursors from ethanol and ethylenediamine, respectively. The morphology and particle size were studied by SEM and dynamic laser scattering method.

  6. Effects of morphology on the structural and photoluminescence properties of co-precipitation derived GdVO4:Dy3+

    NASA Astrophysics Data System (ADS)

    Kumari, Puja; Manam, J.

    2016-10-01

    Herein, Dy3+ doped GdVO4 samples with various morphologies were prepared by the co-precipitation method at low temperature, and the effects of different morphologies on the structural and optical behaviors have been reported. The obtained samples were stabilized to the stable tetragonal structure. The IR and FESEM study were carried out to see the vibrational bonds position and surface morphology. At present PL, PLE, diffuse reflectance and decay curves have been discussed in detail. The morphology dependent photoluminescence studies were resulted to a suitable sample for the lighting and display applications.

  7. Indium nitride: A narrow gap semiconductor

    SciTech Connect

    Wu, J.; Walukiewicz, W.; Yu, K.M.; Ager III, J.W.; Haller, E.E.; Lu, H.; Schaff, W.J.

    2002-08-14

    The optical properties of wurtzite InN grown on sapphire substrates by molecular-beam epitaxy have been characterized by optical absorption, photoluminescence, and photomodulated reflectance techniques. All these three characterization techniques show an energy gap for InN between 0.7 and 0.8 eV, much lower than the commonly accepted value of 1.9 eV. The photoluminescence peak energy is found to be sensitive to the free electron concentration of the sample. The peak energy exhibits a very weak hydrostatic pressure dependence and a small, anomalous blueshift with increasing temperature. The bandgap energies of In-rich InGaN alloys were found to be consistent with the narrow gap of InN. The bandgap bowing parameter was determined to be 1.43 eV in InGaN.

  8. Photoluminescence properties of rare-earth-doped (Er³⁺,Yb³⁺) Y₂O₃ nanophosphors by a combustion synthesis method.

    PubMed

    Kaur, Manmeet; Bisen, D P; Brahme, N; Singh, Prabhjot; Sahu, I P

    2016-05-01

    In this work, we report the synthesis of Y2O3:Er(3+), Y2O3:Yb(3+) and Y2O3:Er(3+),Yb(3+) nanophosphors by the combustion synthesis method using urea as fuel. The doping agents were incorporated in the form of erbium nitrate and ytterbium nitrate. X-Ray diffraction (XRD) patterns revealed that the synthesized particles have a body-centered cubic structure with space group Ia-3. The photoluminescence (PL) properties were investigated after UV and infrared irradiation at room temperature. A strong characteristic emission of Er(3+) and Yb(3+) ions was identified, and the influence of doping concentration on the PL properties was systematically studied. Energy transfer from Yb(3+) to Er(3+) ions was observed in Y2O3 nanophosphors. The obtained result may be useful in potential applications such as bioimaging.

  9. Photoluminescence, enhanced ferroelectric, and dielectric properties of Pr{sup 3+}-doped SrBi{sub 2}Nb{sub 2}O{sub 9} multifunctional ceramics

    SciTech Connect

    Zou, Hua; Yu, Yao; Li, Jun; Cao, Qiufeng; Wang, Xusheng; Hou, Junwei

    2015-09-15

    Pr{sup 3+}-doped SrBi{sub 2}Nb{sub 2}O{sub 9} (SBN) multifunctional ceramics were synthesized by the conventional solid state method. The photoluminescence (PL) excitation and emission spectra, enhanced ferroelectric and dielectric properties were investigated. The X-ray diffraction (XRD) and FESEM analyses indicated that the samples were simple phase and uniform flake-structure. Under the 250–350 nm ultraviolet (UV) excitations, the red emission was obtained and the optimal emission intensity was investigated when Pr doping level was 0.005 mol. With the increasing of the Pr{sup 3+} ion contents, the ferroelectric properties were enhanced obviously. As a new multifunctional material, the Pr{sup 3+}-doped SBN ceramics could be used for a wide range of application, such as integrated electro-optical devices.

  10. Simultaneous observation of up/down conversion photoluminescence and colossal permittivity properties in (Er+Nb) co-doped TiO2 materials

    NASA Astrophysics Data System (ADS)

    Tse, Mei-Yan; Tsang, Ming-Kiu; Wong, Yuen-Ting; Chan, Yi-Lok; Hao, Jianhua

    2016-07-01

    We have investigated the optical and dielectric properties of rutile TiO2 doped with Nb and Er, i.e., (Er0.5Nb0.5)xTi1-xO2. The up/downconversion photoluminescence was observed in the visible and near-infrared region from the materials under 980 nm laser diode excitation. The upconversion emissions are attributed to the energy transfer between Er ions in the excited states. Moreover, the dielectric measurements indicate that the fabricated materials simultaneously present colossal permittivity properties with relatively low dielectric loss. Our work demonstrates the coexistence of both interesting luminescence and attractive dielectric characteristics in (Er+Nb) co-doped TiO2, showing the potential for multifunctional applications.

  11. Reflectivity properties of graphene with a nonzero mass-gap parameter

    NASA Astrophysics Data System (ADS)

    Klimchitskaya, G. L.; Mostepanenko, V. M.

    2016-05-01

    The reflectivity properties of graphene with a nonzero mass-gap parameter are investigated in the framework of a Dirac model using the polarization tensor in (2 +1 ) -dimensional space-time. For this purpose, a more simple explicit representation for the polarization tensor along the real frequency axis is found. The approximate analytic expressions for the polarization tensor and for the reflectivities of graphene are obtained in different frequency regions at any temperature. We show that the nonzero mass-gap parameter has a profound effect on the reflectivity of graphene. Specifically, at zero temperature the reflectivity of gapped graphene goes to zero with vanishing frequency. At nonzero temperature the same reflectivities are equal to unity at zero frequency. We also find the resonance behavior of the reflectivities of gapped graphene at both zero and nonzero temperature at the border frequency determined by the width of the gap. At nonzero temperature the reflectivities of graphene drop to zero in the vicinity of some frequency smaller than the border frequency. Our analytic results are accompanied with numerical computations performed over a wide frequency region. The developed formalism can be used in devising nanoscale optical detectors and optoelectronic switches and in other optical applications of graphene.

  12. Synthesis, characterization and photoluminescence properties of Bi3+ co-doped CaSiO3:Eu3+ nanophosphor

    NASA Astrophysics Data System (ADS)

    Madesh Kumar, M.; Hari Krishna, R.; Nagabhushana, B. M.; Shivakumara, C.

    2015-03-01

    Ceramic luminescent powders with the composition Ca0.96-xEu0.04BixSiO3 (x = 0.01-0.05) were prepared by solution combustion method. The nanopowders are characterized by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR) and photoluminescence (PL) techniques. PXRD patterns of calcined (950 °C for 3 h) Ca0.96-xEu0.04BixSiO3 powders exhibit monoclinic phase with mean crystallite sizes ranging from 28 to 48 nm. SEM micrographs show the products are foamy, agglomerated and fluffy in nature due to the large amount of gases liberated during combustion reaction. TEM micrograph shows the crystalline characteristics of the nanoparticles. Upon 280 nm excitation, the photoluminescence of the Ca0.96-xEu0.04BixSiO3 particles show red emission at 611 nm corresponding to 5D0→7F2 transition. It is observed that PL intensity increases with Bi3+ concentration. Our work demonstrates very interesting energy transfer from Bi3+ to Eu3+ in CaSiO3 host.

  13. The influece of forest gaps on some properties of humus in a managed beech forest, northern Iran

    NASA Astrophysics Data System (ADS)

    Vajari, K. A.

    2015-10-01

    The present research focuses on the effect of eight-year-old artificially created gaps on some properties of humus in managed beech-dominated stand in Hyrcanian forest of northern Iran. In this study, six-teen gaps were sampled in site and were classified into four classes (small, medium, large, and very large) with four replications for each. Humus sampling was carried out at the centre and at the cardinal points within each gap as well as in the adjacent closed stand, separately, as composite samples. The variables of organic carbon, P, K, pH, and total N were measured for each sample. It was found that the gap size had significant effect only on total N (%) and organic carbon (%) in beech stand. The amount of potassium clearly differed among three positions in beech forest. The adjacent stand had higher significantly potassium than center and edge of gaps. Different amount of potassium was detected in gap center and gap edge. Comparison of humus properties between gaps and its adjacent stand pointed to the higher amount of potassium in adjacent stand than that in gaps but there was no difference between them regarding other humus properties. According to the results, it can be concluded that there is relatively similar condition among gaps and closed adjacent stands in terms of humus properties eight years after logging in the beech stand.

  14. The importance of temperature dependent energy gap in the understanding of high temperature thermoelectric properties

    NASA Astrophysics Data System (ADS)

    Singh, Saurabh; Pandey, Sudhir K.

    2016-10-01

    In this work, we show the importance of temperature dependent energy band gap, E g (T), in understanding the high temperature thermoelectric (TE) properties of material by considering LaCoO3 (LCO) and ZnV2O4 (ZVO) compounds as a case study. For the fix value of band gap, E g , deviation in the values of α has been observed above 360 K and 400 K for LCO and ZVO compounds, respectively. These deviation can be overcomed by consideration of temperature dependent band gap. The change in used value of E g with respect to temperature is ∼4 times larger than that of In As. This large temperature dependence variation in E g can be attributed to decrement in the effective on-site Coulomb interaction due to lattice expansion. At 600 K, the value of ZT for n and p-doped, LCO is ∼0.35 which suggest that it can be used as a potential material for TE device. This work clearly suggest that one should consider the temperature dependent band gap in predicting the high temperature TE properties of insulating materials.

  15. Warm white light emitting ThO{sub 2}:Sm{sup 3+} nanorods: Cationic surfactant assisted reverse micellar synthesis and Photoluminescence properties

    SciTech Connect

    Gupta, Santosh K.; Gupta, Ruma; Natarajan, V.; Godbole, S.V.

    2014-01-01

    Graphical abstract: - Highlights: • ThO{sub 2}:Sm{sup 3+} nanoparticles have been synthesized using cationic surfactant assisted reverse micellar route. • HRTEM shows the formation of thoria nanorods. • Photoluminescence investigation shows host as well as samarium ion emission. • Time resolved fluorescence spectroscopy shows the presence of two types of samarium ion in thoria host. - Abstract: Sm{sup 3+} activated thorium oxide nanorods were synthesized by cationic surfactant assisted reverse micellar route. Phase purity, morphological and luminescent properties were investigated by X-ray diffraction, high resolution transmission electron microscopy and photoluminescence spectroscopy. Upon UV light excitation (245 nm), ThO{sub 2}:Sm{sup 3+} exhibited host emission at 447 nm, along with characteristic emission lines of Sm{sup 3+} at 569, 609, 662 and 716 nm. Lifetime spectroscopy shows the presence of two types of Sm{sup 3+} (τ = 1.1 ms and 4.9 ms) with different asymmetric ratios.

  16. Coordination mechanism, characterization, and photoluminescence properties of spinel ZnAl2O4 nanoparticles prepared by a modified polyacrylamide gel route

    NASA Astrophysics Data System (ADS)

    Sun, Guangzhuang; Sun, Guangai; Zhong, Mian; Wang, Shifa; Zu, Xiaotao; Xiang, Xia

    2016-03-01

    Single-phase ZnAl2O4 nanoparticles with the spinel structure were successfully synthesized using a modified polyacrylamide gel method according to the atomic ratio of Zn to Al = 1: 1.8. The as-prepared samples were characterized by means of X-ray powder diffraction (XRD), thermogravimetric analysis (TG), differential scanning calorimetry analysis (DSC), field-emission scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR), and photoluminescence (PL) spectra. XRD patterns show that the pure phase of ZnAl2O4 is obtained after heating the xerogel at 900°C for 5 h in air. The SEM images reveal that the ZnAl2O4 nanoparticles have a narrow particle size distribution and the average particle size is around 45 nm. Photoluminescence (PL) spectra demonstrate the single phase ZnAl2O4 nanoparticles have an emission peak located at 469 nm when excited by 350 nm light. The phase structure, coordination mechanism, and luminescence properties have been discussed on the basis of the experimental results.

  17. Controlled synthesis, characterization and photoluminescence property of olive-like tetragonal α-Nd{sub 2}(MoO{sub 4}){sub 3}

    SciTech Connect

    Zhang, Youjin; Zheng, Ao; Yang, Xiaozhi; He, Hongmei; Fan, Yun

    2012-09-15

    Highlights: ► The olive-like tetragonal α-Nd{sub 2}(MoO{sub 4}){sub 3} was gained with EDTA assisted hydrothermal method. ► The product was characterized by XRD, XPS, FTIR, FESEM, and PL. ► The possible formation mechanism for olive-like α-Nd{sub 2}(MoO{sub 4}){sub 3} was proposed. ► The PL in visible region of the olive-like α-Nd{sub 2}(MoO{sub 4}){sub 3} was studied. -- Abstract: The olive-like tetragonal α-Nd{sub 2}(MoO{sub 4}){sub 3} was obtained by a convenient and facile complex agent assisted hydrothermal method. The product was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR) spectroscopy, field-emission scanning electron microscopy (FESEM) and photoluminescence (PL). The possible formation mechanism of the olive-like α-Nd{sub 2}(MoO{sub 4}){sub 3} was proposed. The photoluminescence property in visible region of the olive-like tetragonal α-Nd{sub 2}(MoO{sub 4}){sub 3} was studied.

  18. Microbundles of zinc oxide nanorods: Assembly in ionic liquid [EMIM]{sup +}[BF{sub 4}]{sup -}, photoluminescence and photocatalytic properties

    SciTech Connect

    Wang Li; Xu Shenzhi; Li Huijun; Chang Lixian; Zhisu; Zeng Minghua; Wang Lina; Huang Yineng

    2011-03-15

    A simple, efficient and low-temperature approach for the assembly of hierarchical Zinc oxide (ZnO) microstructures in ionic liquid [EMIM]{sup +}[BF{sub 4}]{sup -} is reported. The as-obtained ZnO superstructures are composed of microbundles of nanorods from the center points, with the diameter and length in the range of 100-150 nm and 2-4 {mu}m, which have been characterized by X-ray diffraction, scanning and transmission electron microscopy, and photoluminescence spectroscopy. The ZnO microstructures exhibit significant defect-related green-yellow emission and high photodegradation of dye Methyl Orange (5x10{sup -5} mol/L) under UV excitation within 80 min. -- Graphical abstract: Easy formation of microbundles of ZnO nanorods were accomplished in low temperature with [EMIM]{sup +}[BF{sub 4}]{sup -} (1-ethyl-3-methylimidazolium tetrafluoroborate) ionic liquid, which exhibit significant green-yellow photoluminescence property and high photodegradation of Methyl Orange dye. Display Omitted Research highlights: {yields} Ionic liquid assisted solid-state route was introduced into synthesis of ZnO nanorods. {yields} The distinctive microbundles ZnO nanorod assembles was evidenced by SEM and TEM. {yields} ZnO nano-material exhibited high efficiency in photodegradation of Methyl Orange.

  19. Synthesis, structure and photoluminescence of (PLAGH){sub 2}[ZnCl{sub 4}] and comparative analysis of photoluminescence properties with tris(2,2′-bipyridine)ruthenium(II)

    SciTech Connect

    Radanović, Mirjana M.; Jelić, Miodrag G.; Romčević, Nebojša Ž.; Boukos, Nikos; Vojinović-Ješić, Ljiljana S.; Leovac, Vukadin M.; Hadžić, Branka B.; Bajac, Branimir M.; Nađ, Laslo F.; Chandrinou, Chrysoula; Baloš, Sebastian S.

    2015-10-15

    Highlights: • New zinc(II) complex with pyridoxalaminoguanidine was synthesized. • The enhancement of the photoluminescence due to the compound formation was achieved. • Very high photoluminescence of Zn(II) compound was noticed. • Comparative analysis of photoluminescence with tris(2,2′-bipyridine) ruthenium(II) was provided. - Abstract: The first compound of zinc(II) containing pyridoxalaminoguanidine has been synthesized and characterized by elemental analysis, infrared spectra, conductometric measurements and X-ray crystallography. Single crystals of the compound were obtained in the reaction of methanolic solution of zinc(II) chloride and pyridoxalaminoguanidine hydrochloride. In this compound the coordination of chelate ligand is absent and tetrachlorido complex of zinc(II) with pyridoxalaminuguanidinium cation as contraion is obtained. Photoluminescence spectra were measured. Lorentzian multipeak technique was used to determine peak wavelengths and their intensities. Photoluminescence spectroscopy upon 325, 488 and 514 nm laser excitation light was used to obtain results. This novel compound of zinc(II) was compared to the well-known organic light emitting diode material—ruthenium(II) complex with bypiridine i.e., tris(2,2′-bipyridine)ruthenium(II), under the same circumstances and the identical experimental setup. A scheme of energy levels and transitions is proposed to explain the obtained experimental results.

  20. Engineering of the band gap and optical properties of thin films of yttrium hydride

    SciTech Connect

    You, Chang Chuan; Mongstad, Trygve; Maehlen, Jan Petter; Karazhanov, Smagul

    2014-07-21

    Thin films of oxygen-containing yttrium hydride show photochromic effect at room temperature. In this work, we have studied structural and optical properties of the films deposited at different deposition pressures, discovering the possibility of engineering the optical band gap by variation of the oxygen content. In sum, the transparency of the films and the wavelength range of photons triggering the photochromic effect can be controlled by variation of the deposition pressure.

  1. Synthesis of the tube-brush-shaped SiC nanowire array on carbon fiber and its photoluminescence properties.

    PubMed

    Chen, Jianjun; Wu, Renbing; Pan, Yi

    2010-10-01

    Tube-brush-shaped nanostructure of SiC nanowires was synthesized on polyacrylonitrile-based carbon fibers. The morphology and microstructure of the nanowires were characterized by X-ray powder diffraction, field emission scanning electron microscopy and high-resolution transmission electron microscopy. A quasi-periodically twin structure with (111) plane as the boundary along the SiC nanowires was observed. The vapor-solid growth mechanism of the SiC nanowire brush is also discussed. Moreover, some separated blue-shifted photoluminescence peaks around 469 nm were measured. The separated blue-shifted emission peaks are attributed to the quantum confinement of nanoscaled twin segments along each nanowire rather than the apparent diameters of the nanowires. The SiC nanowire brushes hopefully can find potential applications in nanotechnology. PMID:21137760

  2. Sn-filled Si nanotubes fabricated by the facile DC arc discharge method and their photoluminescence property

    NASA Astrophysics Data System (ADS)

    Feng, J. J.; Yan, P. X.; Yang, Q.; Chen, J. T.; Yan, D.

    2008-10-01

    High-yield preparation of polycrystalline Si nanotubes (SiNTs) filled with single-crystal Sn was achieved by the DC arc discharge method. The Sn/Si nanocables were identified by X-ray diffraction (XRD), field-emission scanning electron microscope (FE-SEM), transmission electron microscope (TEM) and photoluminescence (PL). The results show that the Sn/Si coaxial nanocables have homogeneous diameters of about 20-30 nm and lengths ranging from several ten to several hundred nanometers. Most of them are composed of an oval-shaped tip and a tapered hollow body. The possible growth mechanism is vapor-liquid-solid (VLS) model. The PL spectrum shows two characteristic emissions at 491 nm (blue emission) and 572 nm (yellow emission). The origin of luminescence was also discussed.

  3. Photoluminescence properties of thermographic phosphors YAG:Dy and YAG:Dy, Er doped with boron and nitrogen

    NASA Astrophysics Data System (ADS)

    Chepyga, Liudmyla M.; Jovicic, Gordana; Vetter, Andreas; Osvet, Andres; Brabec, Christoph J.; Batentschuk, Miroslaw

    2016-08-01

    This paper investigates Dy3+-doped and Dy3+, Er3+-co-doped yttrium aluminum garnets (YAG) with the admixture of boron nitride with the aim of using them as efficient thermographic phosphors at high temperatures. The phosphors were synthesized using a conventional high-temperature solid-state method. The influence of two fluxes, B2O3 and LiF/NH4F, and the effect of activator and coactivator concentrations were investigated. Additionally, the effect of B3+ and N3- substituting for Al3+ and O2- ions, respectively, in the YAG:Dy3+ co-doped with Er3+ was studied for the first time. The changes in the host lattice led to a much stronger photoluminescence compared with the samples without B3+ and N3- substitution. The admixture of BN also improves the thermal sensitivity of the YAG:Dy and YAG:Dy, Er thermographic phosphors.

  4. Investigation to the deep center related properties of low temperature grown InPBi with Hall and photoluminescence

    SciTech Connect

    Wang, Peng; Pan, Wenwu; Wu, Xiaoyan; Wang, Kai; Yue, Li; Gong, Qian; Wang, Shumin

    2015-12-15

    InP{sub 1-x}Bi{sub x} epilayers with bismuth (Bi) concentration x= 1.0% were grown on InP by gas source molecular beam epitaxy (GS-MBE) at low temperature (LT). Bi incorporation decreased the intrinsic free electron concentration of low temperature grown InP indicated by hall analysis. It is concluded that deep level center was introduced by Bi. Influence of Si doping on the InP{sub 1-x}Bi{sub x} films Photoluminescence (PL) was investigated. N-type doping in the InP{sub 1-x}Bi{sub x} epilayers was found to be effective at PL enhancement. Blue shift of InPBi PL emission wavelength was observed as the Si doping concentration increasing. Two independent peaks were fitted and their temperature dependence behavior was observed to be distinct obviously. Two individual radiative recombination processes were expected to be involved.

  5. Hydrothermal processes for Tm 3+ -doped GdV O 4 nanocrystalline morphologies and their photoluminescence properties

    NASA Astrophysics Data System (ADS)

    Calderón-Villajos, R.; Zaldo, C.; Cascales, C.

    Controlled reaction conditions in simple, template-free hydrothermal processes yield pure tetragonal zircon-type I 41 / amd TmGdV O4 nanocrystals with well-defined specific morphologies and sizes. Nitrate reagents under mild conditions (180 ∘C, pH=7, autogenous pressure) produce from square, hexagon and lozenge nanocrystals with sides starting in 20 nm, to porous spindles, nanotubes, nanorods and nanobelts depending of the reaction times. They exhibit photoluminescence in ˜1.95 μm similar to bulk single crystals. For the lowest Tm3+ concentration (0.2 % mol) in GdV O4 measured 3H4 and 3F4 fluorescence lifetimes τ are very near to their radiative values, τrad.

  6. Photoluminescence properties of the rare-earth ions in the TiO{sub 2} host nanofibers prepared via electrospinning

    SciTech Connect

    Wang Haiying; Wang Yu; Yang Yang; Li Xiang; Wang Ce

    2009-02-04

    Luminescent rare-earth (RE) ions doped TiO{sub 2} nanofibers have been prepared by electrospinning of a mixture solution of rare-earth acetylacetone (RE(C{sub 5}H{sub 7}O{sub 2}){sub 3})/titanium tetraisopropoxide (Ti (OiPr){sub 4})/poly(vinyl pyrrolidone) (PVP) (RE = Eu, Er, Ce, Pr), followed by calcination at high temperature. Scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD) analyses demonstrated the morphology and the structure of the rare-earth doped TiO{sub 2} nanofibers. Exciting the nanofibers results in an energy transfer from surface states of TiO{sub 2} to that of the rare-earth ions and the photoluminescence is observed from the crystal field states of the rare-earth ions.

  7. Photoluminescent green carbon nanodots from food-waste-derived sources: large-scale synthesis, properties, and biomedical applications.

    PubMed

    Park, So Young; Lee, Hyun Uk; Park, Eun Sik; Lee, Soon Chang; Lee, Jae-Won; Jeong, Soon Woo; Kim, Chi Hyun; Lee, Young-Chul; Huh, Yun Suk; Lee, Jouhahn

    2014-03-12

    We have developed a simple approach for the large-scale synthesis of water-soluble green carbon nanodots (G-dots) from many kinds of large food waste-derived sources. About 120 g of G-dots per 100 kg of food waste can be synthesized using our simple and environmentally friendly synthesis approach. The G-dots exhibit a high degree of solubility in water because of the abundant oxygen-containing functional groups around their surface. The narrow band of photoluminescence emission (400-470 nm) confirms that the size of the G-dots (∼4 nm) is small because of a similar quantum effects and emission traps on the surfaces. The G-dots have excellent photostability; their photoluminescence intensity decreases slowly (∼8%) under continuous excitation with a Xe lamp for 10 days. We carried out cell viability assay to assess the effect of cytotoxicity by introducing G-dots in cells such as Chinese hamster ovary cells (CHO-K1), mouse muscle cells (C2C12), and African green monkey kidney cells (COS-7), up to a concentration of 2 mg mL(-1) for 24 h. Due to their high photostability and low cytotoxicity, these G-dots are excellent probes for in vitro bioimaging. Moreover, the byproducts (not including G-dots) of G-dot synthesis from large food-waste derived sources promoted the growth and development of seedlings germinated on 3DW-supplemented gauze. Because of the combined advantages of green synthesis, high aqueous stability, high photostability, and low cytotoxicity, the G-dots show considerable promise in various areas, including biomedical imaging, solution state optoelectronics, and plant seed germination and/or growth.

  8. Bright photoluminescent hybrid mesostructured silica nanoparticles.

    PubMed

    Miletto, Ivana; Bottinelli, Emanuela; Caputo, Giuseppe; Coluccia, Salvatore; Gianotti, Enrica

    2012-07-28

    Bright photoluminescent mesostructured silica nanoparticles were synthesized by the incorporation of fluorescent cyanine dyes into the channels of MCM-41 mesoporous silica. Cyanine molecules were introduced into MCM-41 nanoparticles by physical adsorption and covalent grafting. Several photoluminescent nanoparticles with different organic loadings have been synthesized and characterized by X-ray powder diffraction, high resolution transmission electron microscopy and nitrogen physisorption porosimetry. A detailed photoluminescence study with the analysis of fluorescence lifetimes was carried out to elucidate the cyanine molecules distribution within the pores of MCM-41 nanoparticles and the influence of the encapsulation on the photoemission properties of the guests. The results show that highly stable photoluminescent hybrid materials with interesting potential applications as photoluminescent probes for diagnostics and imaging can be prepared by both methods. PMID:22706523

  9. Synthesis and photoluminescence properties of Ca{sub 3}B{sub 2}O{sub 6}:Tb{sup 3+} nanophosphors

    SciTech Connect

    Manhas, Mohit; Kumar, Vinay; Ntwaeaborwa, O. M.; Swart, H. C.

    2014-04-24

    The green light emitting Tb{sup 3+} doped Ca{sub 3}B{sub 2}O{sub 6} nanophosphors have been synthesized by combustion method at 600°C, and their luminescent properties have been studied. The formation of phosphors has been confirmed by X-ray diffraction (XRD). The photoluminescence (PL) spectra show four emission peaks at 491 nm, 544 nm, 587 and 621 nm. It exhibited a strong green emission located at 544 nm. The effect of different dopant concentrations on emission intensity has also been studied. The maximum photo emission intensity of the Ca{sub 3}B{sub 2}O{sub 6}:Tb{sup 3+} was obtained at a dopant concentration of 1.5 mol% of Tb{sup 3+}.

  10. Photoluminescence properties of NaPbB{sub 5}O{sub 9}:Dy{sup 3+} new material for white light applications

    SciTech Connect

    Rajesh, D. Ratnakaram, Y. C.

    2014-04-24

    Keeping in view of the recent increased interest towards phosphor materials and its applications, an attempt has been made in the present paper to analyze the new NaPbB{sub 5}O{sub 9}:Dy{sub 3+} phosphor with different Dy{sub 3+} concentrations. Special attention is paid to investigate their crystal structure, morphology and luminescence properties. X-ray diffraction (XRD) results confirm the formation of NaPbB{sub 5}O{sub 9}:Dy{sub 3+} phosphor powder. The scanning electron microscope (SEM) images show that the grains are in micrometer range. Photoluminescence spectra are recorded with different excitation wavelengths for the investigated phosphor and analyzed the variation of intensity of emission bands with Dy{sub 3+} ion concentration. Color co-ordinates are calculated and are used to characterize the color of the phosphor.

  11. Structural variations and photoluminescent properties of a series of metal-organic frameworks constructed from 5-(4-carboxybenzoylamino)-isophthalic acid

    SciTech Connect

    Zhao, Wen; Zhang, Li-Juan; Zhao, Xiao-Li

    2013-06-01

    Five new metal-organic frameworks (MOFs) with 5-(4-carboxybenzoylamino)-isophthalic acid (H₃L), namely, [Cd₉L₆(DMA)₆]·4DMA (1), [Cd₃L₂(H₂O)₉]·4H₂O (2), [LaL(H₂O)₄]·2H₂O (3), [CeL(H₂O)₄]·H₂O (4) and [Tb(HL)(H₂L)(H₂O)₃]·5H₂O (5) (DMA=N,N-dimethylacetamide), have been synthesized. Complex 1 shows a three-dimensional architecture generated from linkage of Cd–O chains via L³⁻ ligands. Minor variations in synthetic conditions of 1 afforded 2, which features an interesting 2D→3D catenation architecture containing helical chains. Complexes 3 and 4 are isostructural and each feature a two-dimensional architecture constructed from the linkage of L³⁻ with Ln³⁺. Complex 5 displays a chain-like structure, of which the most interesting feature is the existence of free carboxylic acid (–COOH) group which may confer unique functionality. Moreover, the investigations of the thermal stability, powder X-ray diffractions and solid-state photoluminescent properties for these crystalline materials have been carried out. - Graphical Abstract: Solvothermal reactions of tricarboxylate ligand H₃L with Cd²⁺/Ln³⁺ has yielded a series of new MOFs containing interesting structural motifs. Highlights: • A tricarboxylate ligand whose coordinating functionalities are not symmetry equivalent is employed to construct MOFs. • Complex 2 features an interesting 2D→3D catenation architecture containing helical chains. • Complex 3 feature chain-like structure containing free – COOH group, which may confer unique functionality. • Photoluminescent properties and thermal behaviors for 1–5 have been reported.

  12. A co-precipitation preparation, crystal structure and photoluminescent properties of Er5%:Gd{sub 2}O{sub 3} nanorods

    SciTech Connect

    Boopathi, G. Mohan, R.; Raj, S. Gokul; Kumar, G. Ramesh

    2015-06-24

    An inexpensive preparation method is being reported for obtaining erbium doped gadolinium oxide (Er5%:Gd{sub 2}O{sub 3}) nanoscale rods. The elongated nanoscale systems, as-formed through a co-precipitation process, are characterized by using X-ray powder diffraction (XRD) patterns, scanning electron microscopy (SEM) with energy dispersive X-ray (EDX) mapping, Ultra Violet-visible (UV-vis.) absorption spectroscopy and photoluminescence (PL) spectroscopy. In addition, the Williamson–Hall (W–H) plot is also performed to distinguish the effect of crystalline size-induced broadening and strain-induced broadening at full-width at half-maximum (FWHM) of the XRD profile. The XRD patterns of as-formed and calcined products show that the phase confirmation. As revealed from the SEM micrographs, the morphology of the products show that the rod-like nanoparticles. The EDX micrographs show that the presence of elements in our samples. The band gap values in calcined samples are found to be in the range of 3.569 eV. Upon 230 nm excitation on calcined samples, three broad emission peaks are observed from PL studies. The possible mechanism for the formation of Er5%:Gd{sub 2}O{sub 3} nanorods is briefly discussed.

  13. Optical Properties of Neutral and Charged Low Band Gap Alternating Copolyfluorenes: TD-DFT Investigation

    NASA Astrophysics Data System (ADS)

    Ding, Yong; Zhao, Jun-feng; Wang, Xiang-si; Liu, Sha-sha; Ma, Feng-cai

    2009-08-01

    Electronic structure and optical properties of neutral and charged low band gap alternating copolyfluorenes (Green 1, which is based on alternating repeating units consisting of alkyl-substituted fluorene and a thiophene-[1,2,5]thiadiazolo-[3,4]quinoxaline-thiophene (T-TDQ-T) unit were investigated theoretically with time-dependent density functional theory (TD-DFT) method, and their excited state properties were further analyzed with 2D site and 3D cube representations. For neutral Green 1, the band gap, binding energy, exciton binding energy, and nuclear relaxation energy were obtained. The transition dipole moments of neutral and charged Green 1 are compared using 3D transition density, which reveals the orientation and strength of transition dipole moments. The charge redistribution of neutral and charged Green 1 upon excitation are displayed and compared with 3D charge difference density. The electron-hole coherences of neutral and charged Green 1 upon excitation are investigated with 2D site representation (transition density matrix). The excited state properties of neutral Green 1 calculated with TD-DFT method are compared with that calculated with ZINDO method, which reveals the importance of electron-electron interaction (in TD-DFT) in the excited state properties.

  14. Extraordinary room-temperature photoluminescence in triangular WS2 monolayers.

    PubMed

    Gutiérrez, Humberto R; Perea-López, Nestor; Elías, Ana Laura; Berkdemir, Ayse; Wang, Bei; Lv, Ruitao; López-Urías, Florentino; Crespi, Vincent H; Terrones, Humberto; Terrones, Mauricio

    2013-08-14

    Individual monolayers of metal dichalcogenides are atomically thin two-dimensional crystals with attractive physical properties different from those of their bulk counterparts. Here we describe the direct synthesis of WS2 monolayers with triangular morphologies and strong room-temperature photoluminescence (PL). The Raman response as well as the luminescence as a function of the number of S-W-S layers is also reported. The PL weakens with increasing number of layers due to a transition from direct band gap in a monolayer to indirect gap in multilayers. The edges of WS2 monolayers exhibit PL signals with extraordinary intensity, around 25 times stronger than that at the platelet's center. The structure and chemical composition of the platelet edges appear to be critical for PL enhancement.

  15. EPR and photoluminescence properties of green light emitting LaAl11O18:Mn2+ phosphors

    NASA Astrophysics Data System (ADS)

    Singh, Vijay; Chakradhar, R. P. S.; Rao, J. L.; Jho, Young-Dahl

    2012-06-01

    The LaAl11O18:Mn2+ powder phosphor has been prepared using a self-propagating synthesis. Formation and homogeneity of the LaAl11O18:Mn2+ phosphor has been verified by X-ray diffraction and energy dispersive X-ray analysis respectively. The EPR spectra of Mn2+ ions exhibit resonance signals with effective g values at g≈4.8 and g≈1.978. The signal at g≈1.978 exhibits six-line hyperfine structure and is due to Mn2+ ions in an environment close to tetrahedral symmetry, whereas the resonance at g≈4.8 is attributed to the rhombic surroundings of the Mn2+ ions. It is observed that the number of spins participating in resonance for g≈1.978 increases with decreasing temperature obeying the Boltzmann law. Upon 451 nm excitation, the photoluminescence spectrum exhibits a green emission peak at 514 nm due to 4T1 (G)→6A1 (S) transition of Mn2+ ions. The crystal field parameter Dq and Racah inter-electronic repulsion parameters B and C have been evaluated from the excitation spectrum.

  16. Self-assembled ZnO nanoparticles on ZnO microsheet: ultrafast synthesis and tunable photoluminescence properties

    NASA Astrophysics Data System (ADS)

    Brahma, Sanjaya; Khatei, Jayakrishna; Sunkara, S.; Lo, K.-Y.; Shivashankar, S. A.

    2015-06-01

    We report on the tunable photoluminescence characteristics of porous ZnO microsheets fabricated within 1-5 min of microwave irradiation in the presence of a capping agent such as citric acid, and mixture of citric acid with polyvinylpyrrolidone (PVP). The UV emission intensity reduces to 60% and visible emission increases tenfold when the molar concentration of citric acid is doubled. Further diminution of the intensity of UV emission (25%) is observed when PVP is mixed with citric acid. The addition of nitrogen donor ligands to the parent precursor leads to a red shift in the visible luminescence. The deep level emission covers the entire visible spectrum and gives an impression of white light emission from these ZnO samples. The detailed luminescence mechanism of our ZnO samples is described with the help of a band diagram constructed by using the theoretical models that describe the formation energy of the defect energy levels within the energy band structure. Oxygen vacancies play the key role in the variation of the green luminescence in the ZnO microsheets. Our research findings provide an insight that it is possible to retain the microstructure and simultaneously introduce defects into ZnO. The growth of the ZnO microsheets may be due to the self assembly of the fine sheets formed during the initial stage of nucleation.

  17. Structure and photoluminescent properties of a ZnS/Si nanoheterostructure based on a silicon nanoporous pillar array

    NASA Astrophysics Data System (ADS)

    Xu, Hai Jun; Li, Xin Jian

    2009-07-01

    A silicon nanoporous pillar array (Si-NPA) is a silicon hierarchical structure with regularly patterned surface morphology. Through a heterogeneous reaction process, the nanocrystallites of zinc sulfide (nc-ZnS) were grown onto the Si-NPA and a uniquely patterned core/shell nanoheterostructure array (ZnS/Si-NPA) was obtained. The pillars of the ZnS/Si-NPA were constructed by an outermost shell of a nc-ZnS membrane, an innermost core of a nanoporous silicon pillar and an interface with nc-ZnS embedded into an amorphous SiO2 matrix. The photoluminescence (PL) spectrum of the ZnS/Si-NPA showed that in addition to the two blue PL bands peaked at ~412 and ~491 nm observed in the Si-NPA, a green PL band at ~537 nm was observed in the ZnS/Si-NPA when it was excited by 300 nm ultraviolet light. Based on these experimental results, the two blue PL bands of the ZnS/Si-NPA came from a Si-NPA substrate, while the green PL band was attributed to the emission from the surface states of sulfur vacancies of nc-ZnS. The broad PL from blue to red in the visible region realized in the ZnS/Si-NPA might be applied in solid-state lighting devices with white light emission.

  18. Electrical, dielectric, photoluminescence and magnetic properties of ZnO nanoparticles co-doped with Co and Cu

    NASA Astrophysics Data System (ADS)

    Ashokkumar, M.; Muthukumaran, S.

    2015-01-01

    X-ray diffraction spectra of Zn0.96-xCu0.04CoxO (0≤x≤0.04) nanoparticles synthesized by co-precipitation method confirmed the hexagonal wurtzite structure without any secondary phase formation. The dielectric dispersion was high at lower frequencies and almost frequency independent at higher frequencies. The observed higher dielectric constant, dielectric loss and ac conductivity in Co=2% doped Zn0.96Cu0.04O samples was explained in terms of average crystalline size and number of nano-dipoles. Photoluminescence spectra of undoped and Co-doped Zn0.96Cu0.04O samples showed four distinct bands, (i) ultra violet emission bands around 382-391 nm, (ii) violet emission band centered at 417 nm, (iii) blue emission bands centered at 478 nm and (iv) green emission bands centered at 523 nm. The observed minimum of Igreen/Iblue revealed that Co=1% doped Zn0.96Cu0.04O sample had minimum defects sites and vacancies and it saturated after Co=3% doping. Undoped Zn0.96Cu0.04O sample had higher magnetization and it was suppressed by Co-doping due to the enhanced antiferromagnetic interaction between neighbouring Cu-Cu ion.

  19. Raman and photoluminescence properties of highly Cu doped ZnO nanowires fabricated by vapor-liquid-solid process.

    PubMed

    Zhu, Huichao; Iqbal, Javed; Xu, Hongjun; Yu, Dapeng

    2008-09-28

    Highly Cu doped ZnO nanowires have been fabricated by vapor-liquid-solid (VLS) process. The average concentration of Cu in the ZnO nanowires is estimated to be 6 at. %. The ultrafine synthesized nanowires have diameters nearly 80 nm, while their average length lies in the range of 40 to 90 mum. Raman spectroscopy shows that the Cu doped ZnO nanowires have a typical wurtzite structure. High resolution transmission electron microscopy (HRTEM) investigations of individual nanowires demonstrate that the nanowires have single crystalline structure in which the growth direction is oriented along the c axis. Room temperature photoluminescence spectrum of as prepared nanowires shows two emissions in UV and visible regions that can be ascribed to the near band edge (NBE) transition and defects respectively, while the spectrum of the annealed nanowires exhibits a red shift in UV and a suppression in visible bands. Furthermore, the low temperature (10 K) PL spectrum illustrates a novel dominant blue emission relating to the different valence states of Cu atoms in ZnO, which is explained on the basis of Dingle model.

  20. Photoluminescence Properties and Energy Transfer in a Novel Yellow Emitting Phosphor GdTaO4: Dy3+.

    PubMed

    Zhang, Hijuan; Tan, Xinyu; Wang, Yuhua

    2016-04-01

    The phosphor Dy3+ doped M type gadolinium orthotantalate GdTaO4 was prepared successfully by traditional solid state reaction and the photoluminescence of GdTaO4: xDy3+ (0.01 ≤ x ≤ 0.10) has been investigated under ultraviolet and vacuum ultraviolet excitation. In the excitation spectra of GdTaO4: Dy3+, the overlap appears between the host lattice excitation, the excitation lines of Gd3+ and the f-f transitions of Dy3+, which indicates that the energy transfer could occur from the host to the Dy3+ ions. In the emission spectra of the samples, the intense emissions of Dy3+ have been expectably revealed both upon excitation at 365 nm and 147 nm. And the chromaticity coordinates of GdTaO4: xDy3+ have been correspondingly calculated. The results indicate that GdTaO4: Dy3+ would be a novel yellow emitting phosphor applied in light emitting diodes (LEDs), plasma display panels (PDPs) and mercury-free fluorescent tubes. PMID:27451754

  1. Time-resolved photoluminescence properties of ion-beam-synthesized β-FeSi2 and Si-implanted Si

    NASA Astrophysics Data System (ADS)

    Terai, Yoshikazu; Maeda, Yoshihito

    2015-07-01

    Temporal decay characteristics of 1.54 µm photoluminescence (PL) were investigated in β-FeSi2 and Si-implanted Si samples grown by ion-beam-synthesis (IBS). In the samples, the band-edge PL of β-FeSi2 (A-band) and the dislocation-related PL (D1-band) of Si were both observed at ˜0.8 eV. Regarding the dependence of the PL decay curves on excitation power density (P), PL decay curves without extrinsic effects were obtained at a low P of P ≤ 4.3 mW/cm2. The PL decay times obtained at a low P showed clear differences between the A-band and the D1-line. The result showed that the band-edge PL of β-FeSi2 was distinguished from the dislocation-related PL of Si by the PL decay times. The intrinsic PL decay times of β-FeSi2 were determined to be τ1 = 70-100 ns and τ2 = 550-670 ns at 5 K.

  2. A green chemical approach to the synthesis of photoluminescent ZnO hollow spheres with enhanced photocatalytic properties

    NASA Astrophysics Data System (ADS)

    Patrinoiu, Greta; Tudose, Madalina; Calderón-Moreno, Jose Maria; Birjega, Ruxandra; Budrugeac, Petru; Ene, Ramona; Carp, Oana

    2012-02-01

    ZnO hollow spheres have been synthesized by a simple and environmentally friendly template assisted route. Starch-derived carbonaceous spheres were used as template, impregnated with Zn(CH3COO)2·2H2O to obtain zinc-containing precursor spheres and thermally treatment at 600 °C, yielding hollow ZnO spherical shells. The precursor spheres and hollow shells were characterized by X-ray diffraction, FTIR spectroscopy, scanning electron microscopy, thermal analysis and room-temperature photoluminescence measurements. The hollow spherical shells with diameters of ∼150 nm and wall thickness of ∼20 nm, are polycrystalline, with a mean crystallite size of 22 nm, exhibiting interesting emission features, with a wide multi-peak band covering blue and green regions of the visible spectrum. The photocatalytic activities (under UV and visible light irradiations) of the ZnO spherical shells evaluated for the phenol degradation reaction in aqueous solutions are outstanding, a total phenol conversion being registered in the case of UV irradiation experiments.

  3. Absorption and photoluminescence properties of Er-doped and Er/Yb codoped soda-silicate laser glasses

    SciTech Connect

    Li, S.F.; Zhang, Q.Y.; Lee, Y.P.

    2004-11-01

    Er-doped and Er/Yb codoped soda-silicate laser glasses with various concentrations of Er and Yb were fabricated. The absorption and the photoluminescence (PL) spectra were measured and analyzed. For the Er- doped soda-slilicate glasses, the optimum Er concentration for the PL intensity at 1536 nm turns out to be 0.5 at. %, and the full width at half maximum (FWHM) of PL spectrum increases from 18 to 26 nm, with the increase of the concentration from 0.1 to 0.8 at. %. The PL intensity of Er/Yb codoped soda-silicate glasses with an Er concentration of 0.5 at. % is enhanced approximately by four times, and the optimum Yb concentration for the PL intensity at 1536 nm is analyzed to be 3.0 at. %. The PL spectrum becomes broader with increasing the Yb concentration, up to a FWHM of 80 nm at 6.0 at. %. Yb. The relation between the absorption and PL spectra, together with the mechanism of PL broadening, has also been addressed.

  4. Shape tailored green synthesis of CeO2:Ho3+ nanopowders, its structural, photoluminescence and gamma radiation sensing properties

    NASA Astrophysics Data System (ADS)

    Malleshappa, J.; Nagabhushana, H.; Kavyashree, D.; Prashantha, S. C.; Sharma, S. C.; Premkumar, H. B.; Shivakumara, C.

    2015-06-01

    CeO2:Ho3+ (1-9 mol%) nanopowders have been prepared by efficient and environmental friendly green combustion method using Aloe vera gel as fuel for the first time. The final products are well characterized by powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), fourier transform infrared (FTIR). Bell, urchin, core shell and flower like morphologies are observed with different concentrations of the A. vera gel. It is apparent that by adjusting the concentration of the gel, considerable changes in the formation of CeO2:Ho3+ nano structures can be achieved. Photoluminescence (PL) studies show green (543, 548 nm) and red (645, 732 nm) emissions upon excited at 400 nm wavelength. The emission peaks at ∼526, 548, 655 and 732 nm are associated with the transitions of 5F3 → 5I8, 5S2 → 5I8, 5F5 → 5I8 and 5S2 → 5I7, respectively. Three TL glow peaks are observed at 118, 267 and 204 °C for all the γ irradiated samples which specify the surface and deeper traps. Linear TL response in the range 0.1-2 kGy shows that phosphor is fairly useful as γ radiation dosimeter. Kinetic parameters associated with the glow peaks are estimated using Chen's half width method. The CIE coordinate values show that phosphor is quite useful for the possible applications in WLEDs as orange red phosphor.

  5. Synthesis and photoluminescence properties of cerium-doped terbium-yttrium aluminum garnet phosphor for white light-emitting diodes applications

    NASA Astrophysics Data System (ADS)

    Wang, Jun; Han, Tao; Lang, Tianchun; Tu, Mingjing; Peng, Lingling

    2015-11-01

    Cerium-doped terbium-yttrium aluminum garnet phosphors were synthesized using the solid-state reaction method. The crystalline phase, morphology, and photoluminescence properties were characterized by x-ray diffraction (XRD), scanning electron microscope (SEM), and fluorescence spectrophotometer, respectively. The XRD results indicate that with an increase of the amount of x (Tb3+), all of the samples have a pure garnet crystal structure without secondary phases. The SEM images reveal that the samples are composed of sphere-like crystallites, which exhibit different degrees of agglomeration. The luminescent properties of Ce ions in )Al5O12∶Ce0.1 have been studied, and it was found that the emission band shifted toward a longer wavelength. The redshift is attributed to the lowering of the 5d energy level centroid of Ce, which can be explained by the nephelauxetic effect and compression effect. These phosphors were coated on blue light-emitting diode (LED) chips to fabricate white light-emitting diodes (WLEDs), and their color-rendering indices, color temperatures, and luminous efficiencies were measured. As a consequence of the addition of Tb, the blue LED pumped )Al5O12∶Ce0.1 phosphors WLEDs showed good optical properties.

  6. Impact of hydrostatic pressure on the crystal structure and photoluminescence properties of Mn4+-doped BaTiF6 red phosphor.

    PubMed

    Wang, Yonggang; Wen, Ting; Tang, Lingyun; Yang, Liuxiang; Yang, Wenge; Zhao, Yusheng

    2015-04-28

    High-efficiency red phosphors with non-rare-earth activators are emerging as an alternative for next generation solid-state warm white LEDs. Their optical properties depend strongly on the local site symmetry and the crystal field strength. Herein we present the pressure tuning of structural and photoluminescence (PL) properties of Mn(4+)-doped BaTiF6 up to 40 GPa. In situ high pressure synchrotron X-ray diffraction, Raman and PL spectroscopy studies show that the crystal symmetry changes from trigonal at ambient pressure to monoclinic from 0.5 GPa and triclinic above 14 GPa, attributed to the distortion of (Ti/Mn)F6 octahedra. The red emission peaks shift monotonically to longer wavelengths due to the reinforced crystal field strength within MnF6 octahedra as pressure increases. A detailed comparison of emission shift rate, PL intensity and FWHM between Mn(4+)-doped BaTiF6 and ruby (Cr(3+)-doped Al2O3) was performed using neon pressure transmission medium. This demonstration provides not only an efficient way to artificially tune the emission properties of practically useful phosphors by means of hydrostatic pressure, but also alternative candidates as potential pressure gauges for high pressure techniques. PMID:25811812

  7. Impact of hydrostatic pressure on the crystal structure and photoluminescence properties of Mn4+-doped BaTiF6 red phosphor.

    PubMed

    Wang, Yonggang; Wen, Ting; Tang, Lingyun; Yang, Liuxiang; Yang, Wenge; Zhao, Yusheng

    2015-04-28

    High-efficiency red phosphors with non-rare-earth activators are emerging as an alternative for next generation solid-state warm white LEDs. Their optical properties depend strongly on the local site symmetry and the crystal field strength. Herein we present the pressure tuning of structural and photoluminescence (PL) properties of Mn(4+)-doped BaTiF6 up to 40 GPa. In situ high pressure synchrotron X-ray diffraction, Raman and PL spectroscopy studies show that the crystal symmetry changes from trigonal at ambient pressure to monoclinic from 0.5 GPa and triclinic above 14 GPa, attributed to the distortion of (Ti/Mn)F6 octahedra. The red emission peaks shift monotonically to longer wavelengths due to the reinforced crystal field strength within MnF6 octahedra as pressure increases. A detailed comparison of emission shift rate, PL intensity and FWHM between Mn(4+)-doped BaTiF6 and ruby (Cr(3+)-doped Al2O3) was performed using neon pressure transmission medium. This demonstration provides not only an efficient way to artificially tune the emission properties of practically useful phosphors by means of hydrostatic pressure, but also alternative candidates as potential pressure gauges for high pressure techniques.

  8. Structural and Electronic Properties of a Wide-Gap Quaternary Solid Solution: \\(Zn, Mg\\) \\(S, Se\\)

    NASA Astrophysics Data System (ADS)

    Saitta, A. M.; de Gironcoli, S.; Baroni, S.

    1998-06-01

    The structural properties of the (Zn, Mg) (S, Se) solid solutions are determined by a combination of the computational alchemy and the cluster expansion methods with Monte Carlo simulations. We determine the phase diagram of the alloy and show that the homogeneous phase is characterized by a large amount of short-range order occurring among first-nearest neighbors. Electronic-structure calculations performed using the special quasirandom structure approach indicate that the energy gap of the alloy is rather sensitive to this short-range order.

  9. The properties of photoconductivity of the Ila-type diamond related to the band gap structure

    NASA Astrophysics Data System (ADS)

    Altukhov, A. A.; Feshchenko, V. S.; Shepelev, V. A.; Popov, A. V.

    2016-08-01

    We investigate the properties of the photosensitivity spectra of the UV photodetectors based on natural diamond. The effect of the structural defects associated with nitrogen impurities to the photosensitivity is analyzed. We confirm that the polychrome light bias application enhances the photosensitivity of these detectors in the spectral range 240-340 nm due to the quasi-two-photon absorption which originates due to the complicated structure of the band gap impurity states of a natural diamond. The possibility to influence the photosensitivity spectra in the λ<220 nm spectral range of these detectors by the polychrome light bias application is revealed.

  10. Characteristic properties of Raman scattering and photoluminescence on ZnO crystals doped through phosphorous-ion implantation

    NASA Astrophysics Data System (ADS)

    Jeong, T. S.; Yu, J. H.; Mo, H. S.; Kim, T. S.; Lim, K. Y.; Youn, C. J.; Hong, K. J.

    2014-02-01

    P-doped ZnO was fabricated by means of the ion-implantation method. At the Raman measurement, the blue shift of the E2high mode and A1(LO) phonon of the inactive mode were observed after the P-ion implantation. It suggested to be caused by the compressive stress. Thus, Hall effect measurement indicates that the acceptor levels exists in P-doped ZnO while still maintaining n-type ZnO. From the X-ray photoelectron spectroscopy, the chemical bond formation of the P2p3/2 spectrum consisted of 2(P2O5) molecules. Therefore, the implanted P ions were substituted to the Zn site in ZnO. From the photoluminescence (PL) spectra, P-related PL peaks were observed in the energy ranges of 3.1 and 3.5 eV, and its origin was analyzed at PZn-2VZn complexes, acting as a shallow acceptor. With increasing temperatures, the neutral-acceptor bound-exciton emission, (A0, X), shows a tendency to quench the intensity and extend the emission linewidth. From the relations of the intensity and the linewidth as a function of temperature, the broadening of linewidth was believed to the result that the vibration mode of E2high participates in the broadening process of (A0, X) and the change of luminescent intensity was attributed to the partial dissociation of (A0, X). Consequently, these facts indicate that the acceptor levels existed in P-doped ZnO layer by the ion implantation.

  11. A 3D porous zinc MOF constructed from a flexible tripodal ligand: Synthesis, structure, and photoluminescence property

    SciTech Connect

    Wen Lili; Wang Dong'e; Wang Chenggang; Wang Feng; Li Dongfeng Deng Kejian

    2009-03-15

    A new metal-organic framework, [Zn{sub 5}(trencba){sub 2}(OH){sub 2}Cl{sub 2}.4H{sub 2}O] (1) [H{sub 3}trencba=N,N,N',N',N'',N''-tris[(4-carboxylate-2-yl)methyl]-tris (2-aminoethyl)amine], constructed from a flexible tripodal ligand based on C{sub 3} symmetric tris(2-aminoethyl)amine, has been synthesized hydrothermally and characterized by elemental analysis, IR, TG, XRD and single-crystal X-ray diffraction analysis. Compound 1 contains an unprecedented linear penta-nuclear zinc cluster fragment. Each ligand links four penta-nuclear fragments, and every fragment links eight ligands to generate a three-dimensional non-interpenetrated porous framework. The uncoordinated water molecules were observed trapped in the void pores. Compound 1 represents the first example of (6,8)-connected 3D bi-nodal framework based on a single kind of organic ligand. The photoluminescence measurements showed that complex 1 exhibits relatively stronger blue emissions at room temperature than that of the ligand. - Graphical abstract: The MOF [Zn{sub 5}(trencba){sub 2}(OH){sub 2}Cl{sub 2}.4H{sub 2}O] (H{sub 3}trencba=N,N,N',N',N',N'-tris[(4-carboxylate-2-yl)methyl]-tris (2-aminoethyl)amine) reveals a (6,8)-connected bi-nodal three-dimensional porous framework with unprecedented penta-nuclear fragment, which appears to be a good candidate of hybrid inorganic-organic photoactive materials.

  12. Characteristic properties of Raman scattering and photoluminescence on ZnO crystals doped through phosphorous-ion implantation

    SciTech Connect

    Jeong, T. S.; Yu, J. H.; Mo, H. S.; Kim, T. S.; Lim, K. Y.; Youn, C. J.; Hong, K. J.

    2014-02-07

    P-doped ZnO was fabricated by means of the ion-implantation method. At the Raman measurement, the blue shift of the E{sub 2}{sup high} mode and A{sub 1}(LO) phonon of the inactive mode were observed after the P-ion implantation. It suggested to be caused by the compressive stress. Thus, Hall effect measurement indicates that the acceptor levels exists in P-doped ZnO while still maintaining n-type ZnO. From the X-ray photoelectron spectroscopy, the chemical bond formation of the P2p{sub 3/2} spectrum consisted of 2(P{sub 2}O{sub 5}) molecules. Therefore, the implanted P ions were substituted to the Zn site in ZnO. From the photoluminescence (PL) spectra, P-related PL peaks were observed in the energy ranges of 3.1 and 3.5 eV, and its origin was analyzed at P{sub Zn}-2V{sub Zn} complexes, acting as a shallow acceptor. With increasing temperatures, the neutral-acceptor bound-exciton emission, (A{sup 0}, X), shows a tendency to quench the intensity and extend the emission linewidth. From the relations of the intensity and the linewidth as a function of temperature, the broadening of linewidth was believed to the result that the vibration mode of E{sub 2}{sup high} participates in the broadening process of (A{sup 0}, X) and the change of luminescent intensity was attributed to the partial dissociation of (A{sup 0}, X). Consequently, these facts indicate that the acceptor levels existed in P-doped ZnO layer by the ion implantation.

  13. Energy Dependence and Scaling Property of Localization Length near a Gapped Flat Band

    NASA Astrophysics Data System (ADS)

    Ge, Li; Tureci, Hakan

    Using a tight-binding model for a one-dimensional Lieb lattice, we show that the localization length near a gapped flat band behaves differently from the typical Urbach tail in a band gap: instead of reducing monotonically as the energy E moves away from the flat band energy Ef, the presence of the flat band causes a nonmonotonic energy dependence of the localization length. This energy dependence follows a scaling property when the energy is within the spread (W) of uniformly distributed diagonal disorder, i.e. the localization length is only a function of (E-Ef)/W. Several other lattices are compared to distinguish the effect of the flat band on the localization length, where we eliminate, shift, or duplicate the flat band, without changing the dispersion relations of other bands. Using the top right element of the Green's matrix, we derive an analytical relation between the density of states and the localization length, which shines light on these properties of the latter, including a summation rule for its inverse. This work is partially supported by NSF under Grant No. DMR-1506987.

  14. Enhanced photoluminescence and Raman properties of Al-Doped ZnO nanostructures prepared using thermal chemical vapor deposition of methanol assisted with heated brass.

    PubMed

    Thandavan, Tamil Many K; Gani, Siti Meriam Abdul; San Wong, Chiow; Md Nor, Roslan

    2015-01-01

    Vapor phase transport (VPT) assisted by mixture of methanol and acetone via thermal evaporation of brass (CuZn) was used to prepare un-doped and Al-doped zinc oxide (ZnO) nanostructures (NSs). The structure and morphology were characterized by field emission scanning electron microscopy (FESEM) and x-ray diffraction (XRD). Photoluminescence (PL) properties of un-doped and Al-doped ZnO showed significant changes in the optical properties providing evidence for several types of defects such as zinc interstitials (Zni), oxygen interstitials (Oi), zinc vacancy (Vzn), singly charged zinc vacancy (VZn-), oxygen vacancy (Vo), singly charged oxygen vacancy (Vo+) and oxygen anti-site defects (OZn) in the grown NSs. The Al-doped ZnO NSs have exhibited shifted PL peaks at near band edge (NBE) and red luminescence compared to the un-doped ZnO. The Raman scattering results provided evidence of Al doping into the ZnO NSs due to peak shift from 145 cm-1 to an anomalous peak at 138 cm-1. Presence of enhanced Raman signal at around 274 and 743 cm-1 further confirmed Al in ZnO NSs. The enhanced D and G band in all Al-doped ZnO NSs shows possible functionalization and doping process in ZnO NSs.

  15. Synthesis and photoluminescent properties of cuboid-like Y2(C2O4)3:Tb3+ green-emitting phosphors

    NASA Astrophysics Data System (ADS)

    Ye, Menglin; Zhou, Liqun; Hong, Fei; Li, Ling; Xia, Qinghua; Yang, Kunzhou; Xiong, Xing

    2015-09-01

    In this paper, the Tb3+-doped Y2(C2O4)3 phosphors were prepared using the hydrothermal method in the presence of surfactants. XRD, SEM and fluorescence spectroscopy were used to study the structure and luminescence properties of the material. The effects of surfactants and pH values on the morphologies and photoluminescent properties of Y2(C2O4)3:Tb3+ phosphors were investigated, respectively. When surfactant CA (Citric Acid) and pH 1.5 were employed, homogeneous cuboid-like structure phosphor was obtained, and it was composed of a small number of homogeneous particles with sizes of 2-4 μm and showed higher luminescent intensity than phosphors prepared with surfactants EDTA, Glycine and PEG. Under the 370 nm radiation excitation, Y2-x(C2O4)3:xTb3+ phosphors exhibit green emission (546 nm) corresponding to the 5D4 → 7F5 transition of Tb3+. The emission intensity of this phosphor can be influenced by Tb3+ doping concentration and the maximum intensity of luminescence is observed at the Tb3+ concentration around x = 1.4. The corresponding concentration quenching mechanism is verified as quadrupole-quadrupole interaction. The CIE chromaticity coordinates values of Y0.6 (C2O4)3:1.4Tb3+ almost locate in the green region.

  16. Enhanced Photoluminescence and Raman Properties of Al-Doped ZnO Nanostructures Prepared Using Thermal Chemical Vapor Deposition of Methanol Assisted with Heated Brass

    PubMed Central

    Thandavan, Tamil Many K.; Gani, Siti Meriam Abdul; San Wong, Chiow; Md. Nor, Roslan

    2015-01-01

    Vapor phase transport (VPT) assisted by mixture of methanol and acetone via thermal evaporation of brass (CuZn) was used to prepare un-doped and Al-doped zinc oxide (ZnO) nanostructures (NSs). The structure and morphology were characterized by field emission scanning electron microscopy (FESEM) and x-ray diffraction (XRD). Photoluminescence (PL) properties of un-doped and Al-doped ZnO showed significant changes in the optical properties providing evidence for several types of defects such as zinc interstitials (Zni), oxygen interstitials (Oi), zinc vacancy (Vzn), singly charged zinc vacancy (VZn-), oxygen vacancy (Vo), singly charged oxygen vacancy (Vo+) and oxygen anti-site defects (OZn) in the grown NSs. The Al-doped ZnO NSs have exhibited shifted PL peaks at near band edge (NBE) and red luminescence compared to the un-doped ZnO. The Raman scattering results provided evidence of Al doping into the ZnO NSs due to peak shift from 145 cm-1 to an anomalous peak at 138 cm-1. Presence of enhanced Raman signal at around 274 and 743 cm-1 further confirmed Al in ZnO NSs. The enhanced D and G band in all Al-doped ZnO NSs shows possible functionalization and doping process in ZnO NSs. PMID:25756598

  17. Enhanced photoluminescence and Raman properties of Al-Doped ZnO nanostructures prepared using thermal chemical vapor deposition of methanol assisted with heated brass.

    PubMed

    Thandavan, Tamil Many K; Gani, Siti Meriam Abdul; San Wong, Chiow; Md Nor, Roslan

    2015-01-01

    Vapor phase transport (VPT) assisted by mixture of methanol and acetone via thermal evaporation of brass (CuZn) was used to prepare un-doped and Al-doped zinc oxide (ZnO) nanostructures (NSs). The structure and morphology were characterized by field emission scanning electron microscopy (FESEM) and x-ray diffraction (XRD). Photoluminescence (PL) properties of un-doped and Al-doped ZnO showed significant changes in the optical properties providing evidence for several types of defects such as zinc interstitials (Zni), oxygen interstitials (Oi), zinc vacancy (Vzn), singly charged zinc vacancy (VZn-), oxygen vacancy (Vo), singly charged oxygen vacancy (Vo+) and oxygen anti-site defects (OZn) in the grown NSs. The Al-doped ZnO NSs have exhibited shifted PL peaks at near band edge (NBE) and red luminescence compared to the un-doped ZnO. The Raman scattering results provided evidence of Al doping into the ZnO NSs due to peak shift from 145 cm-1 to an anomalous peak at 138 cm-1. Presence of enhanced Raman signal at around 274 and 743 cm-1 further confirmed Al in ZnO NSs. The enhanced D and G band in all Al-doped ZnO NSs shows possible functionalization and doping process in ZnO NSs. PMID:25756598

  18. Facile fabrication and photoluminescence properties of rare-earth-doped Gd₂O₃ hollow spheres via a sacrificial template method.

    PubMed

    Gao, Yu; Zhao, Qian; Fang, Qinghong; Xu, Zhenhe

    2013-08-21

    Rare-earth-doped gadolinium oxide (Gd₂O₃) hollow spheres were successfully fabricated on a large scale by using PS spheres as sacrificed templates and urea as a precipitating agent, which involved the deposition of an inorganic coating Gd(OH)CO3 on the surface of PS spheres and subsequent calcination in the air. Various approaches including X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Fourier transform infrared (FT-IR), thermogravimetric and differential thermal analysis (TG-DTA), as well as photoluminescence spectroscopies were used to characterize the samples. The results indicate that the sample is composed of uniform hollow Gd₂O₃ spheres with a mean particle size of about 2.3 μm and these hollow spheres have the mesoporous shell that are composed of a large amount of nanoparticles. The possible mechanism of evolution from PS spheres to the amorphous precursor and to the final hollow Gd₂O₃ spheres have been proposed. The as-obtained samples show strong light emission with different colors corresponding to different Ln³⁺ ions under ultraviolet-visible light and electron-beam excitation. Under 980 nm NIR irradiation, Gd₂O₃:Ln³⁺ (Ln³⁺ = Yb³⁺/Er³⁺, Yb³⁺/Tm³⁺ and Yb³⁺/Ho³⁺) exhibit characteristic up-conversion (UC) emissions of red (Er³⁺, ²H11/2, ⁴S3/2, ⁴F9/2 → ⁴I15/2), blue (Tm³⁺, ¹G₄ → ³H₆) and green (Ho³⁺, ⁵F₄, ⁵S₂ → ⁵I₈), respectively. These merits of multicolor emissions in the visible region endow these kinds of materials with potential applications in the field of light display systems, lasers, optoelectronic devices, and MRI contrast agents.

  19. New in situ generated acylhydrazidate-coordinated complexes and acylhydrazide molecules: Synthesis, structural characterization and photoluminescence property

    NASA Astrophysics Data System (ADS)

    Wang, Yan-Ning; Huo, Qi-Sheng; Zhang, Ping; Yu, Jie-Hui; Xu, Ji-Qing

    2016-10-01

    By utilizing the hydrothermal in situ acylation of organic acids with N2H4, three acylhydrazidate-coordinated compounds [Mn(L1)2(H2O)2] (L1 = 2,3-quinolinedicarboxylhydrazidate; HL1 = 2,3-dihydropyridazino[4,5-b] quinoline-1,4-dione) 1, [Mn2(ox)(L2)2(H2O)6]·2H2O (L2 = benzimidazolate-5,6-dicarboxylhydrazide; HL2 = 6,7-dihydro-1H-imidazo[4,5-g]phthalazine-5,8-dione; ox = oxalate) 2, and [Cd(HL3)(bpy)] (L3 = 4,5-di(3‧-carboxylphenyl)phthalhydrazidate; H3L3 = 6,7-dihydro-1H-imidazo[4,5-g]phthalazine-5,8-dione; bpy = 2,2‧-bipyridine) 3, as well as two acylhydrazide molecules L4 (L4 = oxepino[2,3,4-de:7,6,5-d‧e‧]diphthalazine-4,10(5H,9H)-dione) 4 and L5 (L5 = 4,5-dibromophthalhydrazide; L5 = 6,7-dibromo-2,3-dihydrophthalazine-1,4-dione) 5 were obtained. X-ray single-crystal diffraction analysis reveals that (i) 1 only possesses a mononuclear structure, but it self-assembles into a 2-D supramolecular network via the Nhydrazinesbnd H ⋯ Nhydrazine and Owsbnd H ⋯ Ohydroxylimino interactions; (ii) 2 exhibits a dinuclear structure. Ox acts as the linker, while L2 just serves as a terminal ligand; (iii) In 3, L3 acts as a 3-connected node to propagate the 7-coordinated Cd2 + centers into a 1-D double-chain structure; (iv) 4 is a special acylhydrazide molecule. Two sbnd OH groups for the intermediates 3,3‧-biphthalhydrazide further lose one water molecule to form 4; (v) 5 is a common monoacylhydrazide molecule. Via the Nhydrazinesbnd H ⋯ Ohydrazine, Ohydroxyliminosbnd H ⋯ Oacylamino and the π ⋯ π interactions, it self-assembles into a 2-D supramolecular network. The photoluminescence analysis reveals that 4 emits light with the maxima at 510 nm.

  20. Structural, photoluminescent and photocatalytic properties of TiO2:Eu3+ coatings formed by plasma electrolytic oxidation

    NASA Astrophysics Data System (ADS)

    Stojadinović, Stevan; Radić, Nenad; Grbić, Boško; Maletić, Slavica; Stefanov, Plamen; Pačevski, Aleksandar; Vasilić, Rastko

    2016-05-01

    In this paper, we used plasma electrolytic oxidation (PEO) of titanium in water solution containing 10 g/L Na3PO4·12H2O + 2 g/L Eu2O3 powder for preparation of TiO2:Eu3+ coatings. The surfaces of obtained coatings exhibit a typical PEO porous structure. The energy dispersive X-ray spectroscopy analysis showed that the coatings are mainly composed of Ti, O, P, and Eu; it is observed that Eu content in the coatings increases with PEO time. The X-ray diffraction analysis indicated that the coatings are crystallized and composed of anatase and rutile TiO2 phases, with anatase being the dominant one. X-ray photoelectron spectroscopy revealed that Ti 2p spin-orbit components of TiO2:Eu3+ coatings are shifted towards higher binding energy, with respect to pure TiO2 coatings, suggesting that Eu3+ ions are incorporated into TiO2 lattice. Diffuse reflectance spectroscopy showed that TiO2:Eu3+ coatings exhibit evident red shift with respect to the pure TiO2 coatings. Photoluminescence (PL) emission spectra of TiO2:Eu3+ coatings are characterized by sharp emission bands in orange-red region ascribed to f-f transitions of Eu3+ ions from excited level 5D0 to lower levels 7FJ (J = 0, 1, 2, 3, and 4). The excitation PL spectra of TiO2:Eu3+ coatings can be divided into two regions: the broad band region from 250 nm to 350 nm associated with charge transfer state of Eu3+ and the series of sharp peaks in the range from 350 nm to 550 nm corresponding to direct excitation of the Eu3+ ions. It is observed that the intensity of peaks in excitation and emission PL spectra increases with the concentration of Eu3+, but the peak positions remain practically unchanged. The ratio of PL emission for electric and magnetic dipole transitions indicates highly asymmetric environment around Eu3+ ions. The photocatalytic activity (PA) of TiO2:Eu3+ coatings is evaluated by measuring the photodegradation of methyl orange under simulated sunlight conditions. It is shown that PEO time, i.e., the amount

  1. Preparation, photoluminescent properties and luminescent dynamics of BaAlF{sub 5}:Eu{sup 2+} nanophosphors

    SciTech Connect

    Zhang, Wei; Hua, Ruinian; Liu, Tianqing; Zhao, Jun; Na, Liyan; Chen, Baojiu

    2014-12-15

    Graphical abstract: Rice-shaped BaAlF{sub 5}:Eu{sup 2+} nanophosphors were synthesized via one-pot hydrothermal process. The as-prepared BaAlF{sub 5}:Eu{sup 2+} are composed of many particles with an average diameter of 40 nm. When excited at 260 nm, the sharp line emission located at 361 nm of Eu{sup 2+} was observed. The optimum doping concentration of Eu{sup 2+} was confirmed to be 5 mol%. The strong ultraviolet emission of Eu{sup 2+} ions in BaAlF{sub 5}:Eu{sup 2+} nanoparticles suggests that these nanoparticles may have potential applications for sensing, solid-state lasers and spectrometer calibration. - Highlights: • BaAlF{sub 5}:Eu{sup 2+} nanophosphors were synthesized via a mild hydrothermal process. • The Van and Huang models were used to research the mechanism of concentration quenching. • The optimum doping concentration of Eu2+ was confirmed to be 5 mol%. - Abstract: Eu{sup 2+}-doped BaAlF{sub 5} nanophosphors were synthesized via a facile one-pot hydrothermal method. The final products were characterized by X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), and photoluminescence (PL) spectroscopy. XRD results showed that the prepared samples are single-phase. The FE-SEM and TEM images indicated that the prepared BaAlF{sub 5}:Eu{sup 2+} nanophosphors are composed of many rice-shaped particles with an average diameter of 40 nm. When excited at 260 nm, BaAlF{sub 5}:Eu{sup 2+} nanophosphors exhibit the sharp line emissions of Eu{sup 2+} at room temperature. The optimum doping concentration of Eu{sup 2+} was confirmed to be 5 mol%. The Van and Huang models were used to study the mechanism of concentration quenching and the electric dipole–dipole interaction between Eu{sup 2+} can be deduced to be a dominant for quenching fluorescence in BaAlF{sub 5}:Eu{sup 2+} nanophosphors. The strong ultraviolet emission of Eu{sup 2+} in BaAlF{sub 5}:Eu{sup 2+} nanophosphors suggests that

  2. Green engineered ZnO nanopowders by Banyan Tree and E. tirucalli plant latex: auto ignition route, photoluminescent and photocatalytic properties

    NASA Astrophysics Data System (ADS)

    Anilkumar, M. R.; Nagaswarupa, H. P.; Anantharaju, K. S.; Gurushantha, K.; Pratapkumar, C.; Prashantha, S. C.; Shashi Shekhar, T. R.; Nagabhushana, H.; Sharma, S. C.; Vidya, Y. S.; Prasad, Daruka

    2015-03-01

    A simple and eco-friendly solution combustion route was used to prepare ZnO nanoparticles (ZNPs) using Banyan Tree (BT) and Euphorbia tirucalli (ET) plant latexes as fuels. The final products were characterized by powder x-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FTIR), UV-visible, scanning electron microcopy (SEM) and transmission electron microscopy (TEM). The PXRD result reveals the formation of hexagonal phase with Wurtzite structure. The crystallite size obtained from TEM was found to be ˜20-25 nm. SEM results reveal rose-like morphology with BT latex and hexagonal shaped with ET latex. The energy band gap of ZNPs obtained by BT and ET latex were found to be 3.20 and 3.38 eV, respectively. Photoluminescence (PL) emission peaks at ˜421, 458, 505, 522, 628 and 695 nm were observed in both the samples when excited at 383 nm. These emission peaks were mainly attributed to deep level oxygen (blue-green) defect and exciton (UV) defects, respectively. The international commission on illumination (CIE) chromaticity co-ordinates, as well as co-ordinated color temperature (CCT), were estimated from the emission spectra; the values (x, y) were very close to national television system committee (NTSC) standard values of pure white emission. Photocatalytic activity (PCA) of ZNPs prepared was studied in detail. The ZNPs prepared using BT latex showed highest PCA under sunlight. The results demonstrate that the synthesized product could be quite useful for display applications as well as photocatalyst. Further, the material prepared by this route was found to be non-toxic, environmentally friendly and could be a potential alternative to economical routes.

  3. A Mathematical Solution to the Theoretical Band Gap Underestimation: Predictive Calculations of Properties of Semiconductors

    NASA Astrophysics Data System (ADS)

    Bagayoko, Diola

    2008-03-01

    Most density functional theory (DFT) calculations find band gaps that are 30-50 percent smaller than the experimental ones, as illustrated in this presentation that recalls some popular explanations of this band gap problem, i.e., self-interaction effects and derivative discontinuities of the exchange correlation energy. A survey of the increasingly numerous approaches aimed at resolving the theoretical underestimation follows these explanations. These approaches include the Green function and screened Coulomb approximation (GWA), time dependent density functional theory (TDDFT), the exact exchange and screened exchange methods, and the use of local density approximation (LDA) potentials plus additional potentials located at atomic sites. Using the Rayleigh theorem, we describe a basis set and variational effect inherently associated with calculations that employ a linear combination of atomic orbitals (LCAO) in a variational approach of the Rayleigh-Ritz type. This description concomitantly shows a source of large underestimation errors in calculated band gaps, i.e., an often dramatic lowering of some unoccupied energies on account of the Rayleigh theorem as opposed to the Hamiltonian. We present the Bagayoko, Zhao, and Williams (BZW) method [Phys. Rev. B 60, 1563 (1999); PRB 74, 245214 (2006); and PRB 76, 037101 (2007)] that follows from the description of the aforementioned effect and that leads (a) to DFT and LDA calculated band gaps of semiconductors in agreement with experiment and (b) theoretical predictions of band gaps that are confirmed by experiment. Unlike most calculations, BZW computations solve, self-consistently, a system of two coupled equations. DFT-BZW calculated effective masses and optical properties (dielectric functions) also agree with measurements. We illustrate ten years of success of the BZW method with its results for GaN, C, Si, 3C-SIC, 4H-SiC, ZnO, AlAs, Ge, ZnSe, w-InN, InAs, and AlN. We conclude with a request to revisit beliefs

  4. Auxiliary aromatic-acid effect on the structures of a series of Zn{sup II} coordination polymers: Syntheses, crystal structures, and photoluminescence properties

    SciTech Connect

    Xu Yanhong; Lan Yaqian; Shao Kuizhan; Su Zhongmin; Liao Yi

    2010-04-15

    Five novel Zn{sup II}-(pyridyl)imidazole derivative coordination polymers, [Zn(L){sub 2}] (1), [Zn{sub 2}(mu{sub 3}-OH)L(m-BDC)] (2), [Zn{sub 2}(mu{sub 3}-OH)L(p-BDC)].H{sub 2}O (3), [Zn{sub 2}L(BTC)(H{sub 2}O)].2.5H{sub 2}O (4) and [Zn{sub 3.5}(mu{sub 3}-OH)L{sub 2}(BTEC)(H{sub 2}O)].H{sub 2}O (5) (L=4-((2-(pyridine-2-yl)-1H-imidazol-1-yl)methyl)benzoic acid, p-H{sub 2}BDC=1,4-benzenedicarboxylic acid, m-H{sub 2}BDC=1,3-benzenedicarboxylic acid, H{sub 3}BTC=1,3,5-benzenetricarboxylic acid, H{sub 4}BTEC=1,2,4,5-benzenetetracarboxylic acid), were successfully synthesized under hydrothermal conditions through varying auxiliary aromatic-acid ligands and structurally characterized by X-ray crystallography. Compound 1 exhibits a 1D chain linked via double L bridges. Compound 2 features a well-known pcu topology with bent dicarboxylate ligand (m-H{sub 2}BDC) as an auxiliary ligand, while 3 displays a bcu network with linear dicarboxylate ligand (p-H{sub 2}BDC) as an auxiliary ligand. The structure of compound 4 is a novel 3D (3,5)-connected network with (4.6{sup 2})(4.6{sup 4}.8{sup 2}.10.12{sup 2}) topology. It is interesting that compound 5 shows an intricate (3,4,8)-connected framework with (4.6{sup 2})(4{sup 2}.6{sup 3}.8)(4{sup 2}.6{sup 4})(4{sup 2}.6{sup 18}.7.8{sup 6}.10) topology. In addition, their infrared spectra (IR), X-ray powder diffraction (XPRD) and photoluminescent properties were also investigated in detail. - Graphical abstract: Five novel Zn{sup II}-organic architectures have been hydrothermally synthesized through varying auxiliary aromatic-acid ligands and characterized by X-ray diffraction, the photoluminescence properties of compounds 1-5 were studied.

  5. Investigation on multiferroic, optical and photoluminescence properties of CoFe2O4/(Pb1-xSrx)TiO3 nanostructured composite thin films

    NASA Astrophysics Data System (ADS)

    Bala, Kanchan; Sharma, Pankaj; Negi, N. S.

    2016-11-01

    Multiferroic nanostructured composite thin films consisting of CoFe2O4 (CFO) and Pb1-xSrxTiO3 (PST; x = 0.1, 0.2, 0.3, 0.4 and 0.5) layers have been deposited on Pt/TiO2/SiO2/Si and quartz substrates by using metallo-organic decomposition process and spin coating. The effect of Sr content on the multiferroic and optical properties have been investigated. The phase purity such as spinel structure of CFO and perovskite structure of PST has been verified by X-ray diffraction. Cross-sectional scanning electron microscopy images revealed clear interface between CFO and PST layers without any noticeable diffusion. The multiferroic properties of CFO/PST composite films have been confirmed by magnetic and ferroelectric hysteresis loops with low leakage current density. The residual strain sensitivity of multiferroic and optical properties has been observed in the composite films. The decrease in saturation magnetization and saturation polarization with increase in Sr content has been observed which could be attributed to the decrease in residual strain of CFO/PST composite films. The magnetic phase transition temperature of the CFO/PST composite films is also reduced. The optical refractive index decreases with increase of amount of Sr content. The photoluminescence spectra of the CFO/PST composite films possess a blue shift which can be attributed to the Pb and oxygen vacancies as localized sensitizing centers. We show that the multiferroic and optical properties of the CFO/PST composite films are highly sensitive to the heterostructure strains which can be controlled by Sr content.

  6. Gap Analysis of Material Properties Data for Ferritic/Martensitic HT-9 Steel

    SciTech Connect

    Brown, Neil R.; Serrano De Caro, Magdalena; Rodriguez, Edward A.

    2012-08-28

    The US Department of Energy (DOE), Office of Nuclear Energy (NE), is supporting the development of an ASME Code Case for adoption of 12Cr-1Mo-VW ferritic/martensitic (F/M) steel, commonly known as HT-9, primarily for use in elevated temperature design of liquid-metal fast reactors (LMFR) and components. In 2011, Los Alamos National Laboratory (LANL) nuclear engineering staff began assisting in the development of a small modular reactor (SMR) design concept, previously known as the Hyperion Module, now called the Gen4 Module. LANL staff immediately proposed HT-9 for the reactor vessel and components, as well as fuel clad and ducting, due to its superior thermal qualities. Although the ASME material Code Case, for adoption of HT-9 as an approved elevated temperature material for LMFR service, is the ultimate goal of this project, there are several key deliverables that must first be successfully accomplished. The most important key deliverable is the research, accumulation, and documentation of specific material parameters; physical, mechanical, and environmental, which becomes the basis for an ASME Code Case. Time-independent tensile and ductility data and time-dependent creep and creep-rupture behavior are some of the material properties required for a successful ASME Code case. Although this report provides a cursory review of the available data, a much more comprehensive study of open-source data would be necessary. This report serves three purposes: (a) provides a list of already existing material data information that could ultimately be made available to the ASME Code, (b) determines the HT-9 material properties data missing from available sources that would be required and (c) estimates the necessary material testing required to close the gap. Ultimately, the gap analysis demonstrates that certain material properties testing will be required to fulfill the necessary information package for an ASME Code Case.

  7. The influence of the number of pulses on the morphological and photoluminescence properties of SrAl 2O 4:Eu 2+,Dy 3+ thin films prepared by pulsed laser deposition

    NASA Astrophysics Data System (ADS)

    Nsimama, P. D.; Ntwaeaborwa, O. M.; Coetsee, E.; Swart, H. C.

    2009-12-01

    The current work reports on the influence of the number of laser pulses on the morphological and photoluminescence properties of SrAl 2O 4:Eu 2+,Dy 3+ thin films prepared by the pulsed laser deposition (PLD) technique. Atomic force microscopy (AFM) was used to study the surface topography and morphology of the films. The AFM data showed that the film deposited using a higher number of laser pulses was packed with a uniform layer of coarse grains. In addition, the surface of this film was shown to be relatively rougher than the films deposited at a lower number of pulses. Photoluminescence (PL) data were collected using the Cary Eclipse fluorescence spectrophotometer equipped with a monochromatic xenon lamp. An intense green photoluminescence was observed at 517 nm from the films prepared using a higher number of laser pulses. Consistent with the PL data, the decay time of the film deposited using a higher number of pulses was characteristically longer than those of the other films. The effects of laser pulses on morphology, topography and photoluminescence intensity of the SrAl 2O 4:Eu 2+,Dy 3+ thin films are discussed.

  8. Hydrothermal synthesis of Y{sub 2}O{sub 3} coated Y{sub 2}O{sub 3}:Eu{sup 3+} nanotubes for enhanced photoluminescence properties

    SciTech Connect

    Gao, Linhui; Wang, Guangfa; Zhu, Hongliang; Zhou, Weijie; Ou, Guofu

    2015-10-15

    Highlights: • Eu{sup 3+} doped Y{sub 2}O{sub 3} nanotubes. • Hydrothermal synthesis of Y{sub 2}O{sub 3} coated Y{sub 2}O{sub 3}:Eu{sup 3+} nanostructures assissted with a further heat treatment. • Tunable coating ratios of Y{sub 2}O{sub 3} coated Y{sub 2}O{sub 3}:Eu{sup 3+} nanophosphor. • Enhanced photoluminescence intensity of Y{sub 2}O{sub 3}:Eu{sup 3+} more than 60% by Y{sub 2}O{sub 3} surface coating. - Abstract: Novel Y{sub 2}O{sub 3} coated Y{sub 2}O{sub 3}:Eu{sup 3+} nanotubes with different coating ratios were synthesized successfully by a facile two-step process, including hydrothermal synthesis of Y(OH){sub 3} coated Y(OH){sub 3}:Eu{sup 3+} as precursors and then calcination of them at 1000 °C for 2 h. X-ray diffraction patterns and field emission scanning electron microscope images indicated these Y{sub 2}O{sub 3} coated Y{sub 2}O{sub 3}:Eu{sup 3+} phosphors possess tubular nanostructures. The photoluminescence properties of Y{sub 2}O{sub 3} coated Y{sub 2}O{sub 3}:Eu{sup 3+} were systematically investigated by photoluminescence spectra, and photoluminescence enhancement was observed after proper coating. In other words, the coating ratio played a crucial role in photoluminescence efficiency. When it was 1/9, the photoluminescence intensity of {sup 5}D{sub 0} → {sup 7}F{sub 2} emission (about 613 nm) was 60% higher than that of Y{sub 2}O{sub 3}: Eu{sup 3+} phosphors under 255 nm excitation. Therefore, surface coating may be an alternative route for enhanced photoluminescence properties of the Y{sub 2}O{sub 3}:Eu{sup 3+} red-emitting phosphor.

  9. Photoluminescence and cathodoluminescence properties of Eu{sup 3+} ions activated AMoO{sub 4} (A = Mg, Ca, Sr, Ba) phosphors

    SciTech Connect

    Du, Peng; Yu, Jae Su

    2015-10-15

    Highlights: • Under 393 nm excitation, strong red emission located at 615 nm was observed in all the samples. • The Eu{sup 3+}-activated CaMoO{sub 4} phosphor exhibited the strongest PL properties. • The CIE chromaticity coordinate of Eu{sup 3+}-activated CaMoO{sub 4} phosphor was (0.647,0.352). • The color purity of Eu{sup 3+}-activated CaMoO{sub 4} phosphor was 92.8%. • Strong CL properties were observed in the Eu{sup 3+}-activated CaMoO{sub 4} phosphor. - Abstract: Eu{sup 3+}-activated AMoO{sub 4} (A = Mg, Ca, Sr, Ba) phosphors were synthesized by a solid-state reaction method. Photoluminescence and cathodoluminescence (CL) spectra as well as X-ray diffraction patterns were measured to characterize the fabricated samples. Under 393 nm excitation, strong red emissions located at ∼615 nm corresponding to the {sup 5}D{sub 0} → {sup 7}F{sub 2} transition of Eu{sup 3+} ions were observed in all the samples. Compared with other Eu{sup 3+} ions activated AMoO{sub 4} (A = Mg, Sr, Ba) phosphors, Eu{sup 3+}-activated CaMoO{sub 4} phosphor exhibited the strongest red emission intensity with better Commission Internationale de L’Eclairage chromaticity coordinate and higher color purity. Furthermore, the CL results indicated that the Eu{sup 3+}-activated CaMoO{sub 4} phosphor had excellent luminescence properties.

  10. Pentamodal property and acoustic band gaps of pentamode metamaterials with different cross-section shapes

    NASA Astrophysics Data System (ADS)

    Huang, Yan; Lu, Xuegang; Liang, Gongying; Xu, Zhuo

    2016-03-01

    Pentamodal property and acoustic band gaps of pentamode metamaterials with different cross-section shapes, including regular triangle, square, pentagon, hexagon and circle, have been comparatively studied by finite-element method. Results show that for the varying diameters of circumcircles in thick and thin ends of unit (D and d), the ratio of bulk modulus to shear modulus (B / G) and bandgaps of these five structures perform similar changing tendency. With the increasing d, B / G decreases and the single-mode bandgap moves toward high-frequency direction with the decreasing normalized bandwidth (Δω /ωg). With the increasing D, B / G keeps around the respective average value, and the single-mode bandgap firstly moves to high-frequency then to low-frequency direction with the firstly increasing and then decreasing Δω /ωg. Complete bandgap appears as D reaching to critical value for each given d, then moves to high-frequency direction. For same parameters the triangle case has highest B / G and acoustic band gaps with lower frequency and broader bandwidth.

  11. Accurate prediction of band gaps and optical properties of HfO2

    NASA Astrophysics Data System (ADS)

    Ondračka, Pavel; Holec, David; Nečas, David; Zajíčková, Lenka

    2016-10-01

    We report on optical properties of various polymorphs of hafnia predicted within the framework of density functional theory. The full potential linearised augmented plane wave method was employed together with the Tran-Blaha modified Becke-Johnson potential (TB-mBJ) for exchange and local density approximation for correlation. Unit cells of monoclinic, cubic and tetragonal crystalline, and a simulated annealing-based model of amorphous hafnia were fully relaxed with respect to internal positions and lattice parameters. Electronic structures and band gaps for monoclinic, cubic, tetragonal and amorphous hafnia were calculated using three different TB-mBJ parametrisations and the results were critically compared with the available experimental and theoretical reports. Conceptual differences between a straightforward comparison of experimental measurements to a calculated band gap on the one hand and to a whole electronic structure (density of electronic states) on the other hand, were pointed out, suggesting the latter should be used whenever possible. Finally, dielectric functions were calculated at two levels, using the random phase approximation without local field effects and with a more accurate Bethe-Salpether equation (BSE) to account for excitonic effects. We conclude that a satisfactory agreement with experimental data for HfO2 was obtained only in the latter case.

  12. Composition dependence of photoluminescence properties of poly(9,9-di-n-hexylfluorenyl-2,7-diyl) with perovskite-structured SrTiO3 nanocomposites

    NASA Astrophysics Data System (ADS)

    Din, U. K. N.; Salleh, M. M.; Aziz, T. H. T.; Umar, A. A.

    2016-05-01

    Nanocomposite thin films of poly(9,9-di-n-hexylfluorenyl-2,7-diyl) (PHF) with 10-50 wt% perovskite-structured SrTiO3 nanoparticles (designated as PHF:SrTiO3) were prepared by spin coating. The photoluminescence (PL) properties of the nanocomposites thin films were studied. The incorporation of SrTiO3 nanoparticles into the nanocomposite thin films enhanced the original PL intensities of the host PHF thin films. The intensities of the PL peak for the nanocomposite thin films were dependent on the amount of SrTiO3 nanoparticles in the films and the homogeneity of the nanoparticle distribution. The distribution of the SrTiO3 nanoparticles contributed to the overlapping molecular orbital sites in PHF:SrTiO3, which promoted the excited electrons from the conduction band of SrTiO3 transferred to the excited energy level of the PHF host material. In this case, the perovskite-structured SrTiO3 nanoparticles act as sensitizers.

  13. Photoluminescence and phosphorescence properties of SrZn(PO):Eux2+,Mny2+ phosphor for UV-based white-LEDs

    NASA Astrophysics Data System (ADS)

    Jeong, Junho; Jayasimhadri, M.; Sueb Lee, Ho; Jang, Kiwan; Soo Yi, Soung; Hyun Jeong, Jung; Kim, Changdae

    2009-07-01

    SrZn(PO)2:Eux2+,Mny2+ (SZP: Eux2+, Mny2+) phosphors ( x=0, 0.01 and y=0, 0.01) were prepared by using a stoichiometric solid-state reaction method and their photoluminescence and phosphorescence decay properties were investigated. The emission spectrum of SrZn 2(PO 4) 2: Eu0.012+, Mn0.012+ measured under 400 nm excitation was composed of the violettish blue and the emerald green emissioins centered at 421 and 547 nm, respectively. The excitation wavelength of the emission peak at 547 nm was about 421 nm in the excitation spectrum of SZP: Mn0.012+. Since, this value is equal to the transition energy of Eu 2+, the energy transfer from Eu 2+ to Mn 2+ in SZP: Eu0.012+, Mn0.012+ phosphor has been demonstrated. The CIE chromaticity coordinates of SZP: Eu0.012+, Mn0.012+ phosphor were (0.330, 0.328) under the excitation wavelength 375 nm at room temperature. The phosphorescence from SZP: Eu0.012+, Mn0.012+ could be seen by naked eyes for few seconds and it has persisted for about 4.4 h while monitoring by using a PMT spectrometer. Therefore, SZP: Eux2+, Mny2+phosphor may be a potential candidate for the UV-based white light-emitting diodes (LEDs).

  14. Syntheses, structures and photoluminescent properties of three d10 coordination architectures based on in-situ 1,3,5-triazine derivatives

    NASA Astrophysics Data System (ADS)

    Xiao, Changyu; Li, Yamin; Lun, Huijie; Cui, Caiyan; Xu, Yanqing

    2013-12-01

    In the presence of aromatic carboxylic acids, three new d10 transition metal coordination polymers, [Ag(PAHT)]n(1), [Ag2(HCA)]n(2) and [Cu6(CA)2(H2O)]n(3) (HPAHT=2-phenyl-4-amino-6-hydroxy-1,3,5-triazine, H3CA=cyanuric acid) have been synthesized based on in-situ 1,3,5-triazine derivatives resulting from 2,4-diamino-6-phenyl-1,3,5-triazine, 2-chloro-4,6-diamino-1,3,5-triazine and melamine under hydrothermal conditions. Complexes 1-3 have been characterized by single-crystal X-ray diffraction, IR spectra, elemental analysis and thermogravimetric analysis (TGA). The compound 1 exhibits a uninodal three-connected 3D network with a rare lig LiGe type topology, which contains right-handed and left-handed [Ag(PAHT)]n helical chains. For compound 2, the 3D network is comprised of 2D sheet by strongly Ag-O and weakly Ag(I)…Ag(I) interactions. In compound 3, it is infrequently observed that dodecanuclear copper(I) units as secondary building units (SBUs) construct 3D network by the ligands CA3- with a rare uninodal 10-connected bct topology (312.428.55). The photoluminescent properties of three compounds have also been measured.

  15. Microwave sol-gel derived NaCaGd(MoO4)3:Er3+/Yb3+ phosphors and their upconversion photoluminescence properties

    NASA Astrophysics Data System (ADS)

    Lim, Chang Sung

    2016-05-01

    Ternary molybdate NaCaGd1-x(MoO4)3:Er3+/Yb3+ phosphors with the proper doping concentrations of Er3+ and Yb3+ (x = Er3+ + Yb3+, Er3+ = 0, 0.05, 0.1, 0.2 and Yb3+ = 0, 0.2, 0.45) were successfully synthesized by microwave sol-gel method for the first time. Well-crystallized particles formed after heat-treatment at 900 °C for 16 h showed a fine and homogeneous morphology with particle sizes of 3-5 μm. The optical properties were examined comparatively using photoluminescence emission and Raman spectroscopy. Under excitation at 980 nm, the doped particles exhibited a strong 525-nm emission band, a weak 550-nm emission band in the green region, which correspond to the 2H11/2 → 4I15/2 and 4S3/2 → 4I15/2 transitions, and a very weak 655-nm emission band in the red region, which corresponds to the 4F9/2 → 4I15/2 transition. The optimal Yb3+:Er3+ ratio was obtained to be 9:1, as indicated by the composition-dependent quenching effect of Er3+ ions. The pump power dependence of upconversion emission intensity and Commission Internationale de L'Eclairage chromaticity coordinates of the phosphors were evaluated in detail.

  16. The effect of citric acid on morphology and photoluminescence properties of white light emitting ZnO-SiO2 nanocomposites

    NASA Astrophysics Data System (ADS)

    Sivakami, R.; Thiyagarajan, P.

    2016-07-01

    The white light emitting ZnO-SiO2 nanocomposites were synthesized by sol-gel combustion method using zinc nitrate, citric acid and tetraethoxysilane. To analyze the effect of fuel content on the photoluminescence properties of ZnO-SiO2 nanocomposites, the citric acid content was varied as 1, 5, and 10 moles with respect to one mole of zinc. The SEM images of the nanocomposites revealed the spherical, flower and platelet like morphology with variation in citric acid content and annealing temperatures. The ZnO-SiO2 nanocomposites prepared with various Zn:CA ratio excited at UV (280 nm), near UV (365 nm), violet (405 nm) and blue (465 nm) wavelength showed blue and greenish-yellow emission. Among all ratios, the ZnO-SiO2 nanocomposites with Zn:CA - 1:1 ratio showed the intense broad band emission compared to Zn:CA - 1:5 and 1:10 values. This particular composition of sample excited under violet (405 nm) LED source shows white light, as confirmed by the CIE chromaticity coordinates (x = 0.342, y = 0.318).

  17. Investigations on photoluminescence and cathodoluminescence properties of Ca3La6(SiO4)6:Tb3 +, Mn2 +

    NASA Astrophysics Data System (ADS)

    Zhang, Jia; Zhou, Beibei; Wang, Xichen

    2016-08-01

    Tb3 +/Mn2 + activated Ca3La6(SiO4)6 (CLS) phosphors were prepared by solid-state reaction method, and their photoluminescence and cathodoluminescence (CL) properties were investigated. The CLS:Tb3 + sample shows a yellowish green emission under 377 nm excitation, and the excitation spectrum reveals the excitation peaks between 340 and 390 nm can match with the near-ultraviolet LED chip. Excellent thermal stability has been obtained in the CLS:Tb3 + phosphor by studying the temperature dependence of the Tb3 + emission intensity. By introducing Mn2 + into CLS:Tb3 +, tunable emissions are generated due to the efficient energy transfer from Tb3 + to Mn2 +. The CL spectrum of CLS:Tb3 + displays that the characteristic 5D4-7FJ (J = 6 - 3) transitions of Tb3 + are found under electron beam excitation. The above investigation results imply that the CLS:Tb3 +, Mn2 + phosphors could have potential applications on LEDs and FEDs.

  18. Redox properties of a single (7,5)single-walled carbon nanotube determined by an in situ photoluminescence spectroelectrochemical method.

    PubMed

    Hong, Liu; Mouri, Shinichiro; Miyauchi, Yuhei; Matsuda, Kazunari; Nakashima, Naotoshi

    2014-11-01

    The determination of electronic states of single-walled carbon nanotubes (SWNTs) has been a central issue in science and nanotechnology of carbon nanotubes. We here describe the oxidation and reduction potentials of a single SWNT determined by in situ photoluminescence (PL) spectroelectrochemical measurements. By PL imaging and single SWNT PL spectroscopy, the stepwise quenching behavior of the PL from a single (7,5)SWNT was detected as the outer-applied potentials increased. Based on the analysis of the obtained potential-dependent PL plots using the Nernst equation, the oxidation and reduction potentials of the (7,5) tube are successfully determined as 0.41 V and -0.38 V vs. Ag/AgCl, respectively, which shift from those of the bulk (7,5)SWNTs. We further observed a PL blueshift and narrowing of the line width as the external-applied potential to the single SWNT increases. The present results are important for understanding the electronic properties of a single (n,m)SWNT and its applications.

  19. Lanthanide-thiophene-2,5-dicarboxylate frameworks: ionothermal synthesis, helical structures, photoluminescent properties, and single-crystal-to-single-crystal guest exchange.

    PubMed

    Zhan, Cai-Hong; Wang, Fei; Kang, Yao; Zhang, Jian

    2012-01-01

    Eight three-dimensional lanthanide-thiophene-2,5-dicarboxylate frameworks, [Ln(TDC)(2)]·(choline) (1-6; Ln = Gd, Nd, Eu, Er, Tb, Dy; TDC = thiophene-2,5-dicarboxylate), [Yb(TDC)(2)(e-urea)]·(choline)·H(2)O (7; e-urea = ethyleneurea), [Nd(2)(TDC)(3)(e-urea)(4)]·3(e-urea) (8) have been successfully prepared in deep eutectic solvents (choline chloride/e-urea), respectively. Compounds 1-7 are anionic frameworks with 8-connected bcu topology, while compound 8 features a neutral 6-connected rob-type framework with guest e-urea molecules. In these structures, lanthanide ions show dicapped trigonal prism, pentagonal bipyramid, and tricapped trigonal prism coordination configurations, respectively, and the TDC ligands exhibit different coordination modes. Versatile helical substructures are presented in these compounds. The photoluminescent properties of compounds 3 (Eu) and 8 (Nd) were studied. Moreover, compound 8 can perform single-crystal-to-single-crystal guest exchange. The ethanol-exchange mechanism of 8 can be ascribed to the kinetically controlled flexibility (KCF). PMID:22136232

  20. Symmetry properties of n-doped (Cd,Mn)Te quantum well photoluminescence spectra: An exemplary evidence for anisotropy-induced valence-band mixing

    NASA Astrophysics Data System (ADS)

    Koudinov, A. V.; Kehl, C.; Astakhov, G.; Geurts, J.; Wojtowicz, T.; Karczewski, G.

    2016-05-01

    The symmetry properties of photoluminescence spectra of an n-doped (001)-Cd0.99Mn0.01Te quantum well provide a simple and intuitive demonstration of the valence-band mixing induced by spontaneous in-plane anisotropy of the sample. The spectra were taken with linear-polarization resolution in an in-plane external magnetic field. They consisted of several features which are characteristic for a two-dimensional electron gas. Because the quantum well layer contained "magnetic" ions of Mn, the spectra showed pronounced polarization-dependent modifications induced by the magnetic field. With the field applied, a 90° rotation of the sample about the surface normal axis resulted in a clearly different spectrum, meaning that the nominally equivalent [110 ] and [1 1 ¯ 0 ] in-plane directions in the sample are not equivalent in fact. But, remarkably, the additional 90° rotations of both the polarizer and the analyzer restored the initial spectrum. This combined invariance regarding simultaneous 90° rotation of the sample and reversal of the polarization configuration was known earlier for spin-flip Raman spectra only. Our present observations are interpreted in terms of an intermixing of valence subbands leading to a pseudoisotropic g-factor of the ground-state holes.

  1. Topological evolution and photoluminescent properties of a series of divalent zinc-based metal-organic frameworks tuned via ancillary ligating spacers

    NASA Astrophysics Data System (ADS)

    Lian, Xiao-Min; Zhao, Wen; Zhao, Xiao-Li

    2013-04-01

    The combination of divalent zinc ions, 4-(4-carboxybenzamido)benzoic acid and exo-bidendate bipyridine ligands gave rise to a series of new MOFs: [ZnL(bipy)]·DMF·H2O (1), [ZnL(bpe)]·1.5H2O (2), [ZnL(bpa)]·4H2O (3) and [ZnL(bpp)]·1.75H2O (4) (MOF=metal-organic framework, bipy=4,4'-bipyridine, bpe=trans-1,2-bis(4-pyridyl)ethylene, bpa=1,2-bis(4-pyridinyl)ethane, bpp=1,3-bis(4-pyridinyl)propane, H2L=4,4'-(carbonylimino)dibenzoic acid). Fine tune over the topology of the MOFs was achieved via systematically varying the geometric length of the second ligating bipyridine ligands. Single-crystal X-ray analysis reveals that complex 1 has a triply interpenetrated three-dimensional (3D) framework with elongated primitive cubic topology, whereas isostructural complexes 2 and 3 each possesses a 6-fold interpenetrated diamondiod 3D framework. Further expansion of the length of the bipyridine ligand to bpp leads to the formation of 4, which features an interesting entangled architecture of 2D→3D parallel polycatenation. In addition, the thermogravimetric analyses and solid-state photoluminescent properties of the selected complexes are investigated.

  2. Synthesis and photoluminescence properties of a red-emitting phosphor, K2SiF6:Mn4+, for use in three-band white LED applications

    NASA Astrophysics Data System (ADS)

    Yeo, Byul-Ee; Cho, Young-Sik; Huh, Young-Duk

    2016-01-01

    K2SiF6:Mn4+ phosphors were prepared by redox precipitation at room temperature from mixed aqueous solutions of SiO2, HF, KMnO4, and H2O2. The optimal conditions required to obtain the brightest red emission spectra of the K2SiF6:Mn4+ phosphors were examined. The K2SiF6:Mn4+ phosphors emitted deep red light with three strong peaks at 615, 630, and 650 nm under 465 nm excitation, the emission wavelength of a commercial blue LED. K2SiF6:Mn4+ and SrGa2S4:Eu2+ phosphors were used to produce the red and green emission bands under excitation from a commercial blue LED, respectively. The photoluminescence properties of the three-band white LEDs fabricated by coating K2SiF6:Mn4+ and SrGa2S4:Eu2+ phosphors onto the commercial blue LED chip were investigated.

  3. Role of crystallite size on the photoluminescence properties of SrIn{sub 2}O{sub 4}:Eu{sup 3+} phosphor synthesized by different methods

    SciTech Connect

    Lakshminarasimhan, N. Varadaraju, U.V.

    2008-09-15

    Photoluminescence (PL) of Eu{sup 3+} was studied in SrIn{sub 2}O{sub 4} host lattice. A complete solid solubility of Eu{sup 3+} has been found in the series SrIn{sub 2-x}Eu{sub x}O{sub 4} [x=0-2.0]. The phase formation at a relatively low temperature and in a very short duration was achieved by combustion synthesis (CS). Concentration quenching of luminescence has been observed in SrIn{sub 2-x}Eu{sub x}O{sub 4} [x=0.1-2.0] and the critical concentration for maximum emission was found to be with x=0.3. In order to find the role of crystallite size on the PL properties of SrIn{sub 2}O{sub 4}:Eu{sup 3+}, the results obtained with phosphors synthesized by solid state reaction (SSR) and CS methods were compared. - Graphical abstract: Comparison of PL excitation and emission of Eu{sup 3+} in SrIn{sub 2}O{sub 4} synthesized by solid state reaction (SSR) and combustion synthesis (CS) methods revealing a decrease in intensity for CS method.

  4. One-pot synthesis and photoluminescence properties of core/porous-shell olive-like BaWO4 microstructure by a template-assisted hydrothermal method

    NASA Astrophysics Data System (ADS)

    Zhang, Suyue; Wang, Yunlong; Wang, Cuiping; Zhang, Hui; Shen, Yuhua; Xie, Anjian

    2016-02-01

    Core/porous-shell olive-like crystalline BaWO4 is synthesized by a combined simple hydrothermal method and soft template approach. The prepared product shows an olive-like shape with diameter of ˜2 μm, length of ˜4 μm, and the thickness of the shell of about 65 nm, which are orderly assembled by many nanoparticles. A possible formation mechanism of olive-like BaWO4 microstructure involving interfacial recognization of ions, nucleation, aggregation, in situ growth and Ostwald ripening process is proposed. Polyacrylic acid sodium (PAAS) as a template plays an important role in inducing the nucleation and growth of olive-like BaWO4 microcrystalline. Other shapes of BaWO4 microcrystalline are also fabricated by varying the concentration of PAAS and Ba2+. The olive-like product with a core-shell structure which exists a large number of pores on crystal surface shows excellent photoluminescence property, which have potentially applied prospects in fields such as light display systems etc.

  5. Photoluminescence properties and energy levels of RE (RE = Pr, Sm, Er, Tm) in layered-CaZnOS oxysulfide

    SciTech Connect

    Zhang, Zhi-Jun; Feng, Ang; Chen, Xiang-Yang; Zhao, Jing-Tai

    2013-12-07

    RE{sup 3+} (RE = Pr, Sm, Er, Tm)-activated CaZnOS samples were prepared by a solid-state reaction method at high temperature, and their photoluminescence properties were investigated. Doping with RE{sup 3+} (RE = Pr, Sm, Er, Tm) into layered-CaZnOS resulted in typical RE{sup 3+} (RE = Pr, Sm, Er, Tm) f-f line absorptions and emissions, as well as the charge transfer band of Sm{sup 3+} at about 3.3 eV. The energy level scheme containing the position of the 4f and 5d levels of all divalent and trivalent lanthanide ions with respect to the valence and conduction bands of CaZnOS has been constructed based on the new data presented in this work, together with the data from literature on Ce{sup 3+} and Eu{sup 2+} doping in CaZnOS. The detailed energy level scheme provides a platform for interpreting the optical spectra and could be used to comment on the valence stability of the lanthanide ions in CaZnOS.

  6. Investigations on photoluminescence and cathodoluminescence properties of Ca3La6(SiO4)6:Tb(3+), Mn(2.).

    PubMed

    Zhang, Jia; Zhou, Beibei; Wang, Xichen

    2016-08-01

    Tb(3+)/Mn(2+) activated Ca3La6(SiO4)6 (CLS) phosphors were prepared by solid-state reaction method, and their photoluminescence and cathodoluminescence (CL) properties were investigated. The CLS:Tb(3+) sample shows a yellowish green emission under 377nm excitation, and the excitation spectrum reveals the excitation peaks between 340 and 390nm can match with the near-ultraviolet LED chip. Excellent thermal stability has been obtained in the CLS:Tb(3+) phosphor by studying the temperature dependence of the Tb(3+) emission intensity. By introducing Mn(2+) into CLS:Tb(3+), tunable emissions are generated due to the efficient energy transfer from Tb(3+) to Mn(2+). The CL spectrum of CLS:Tb(3+) displays that the characteristic (5)D4-(7)FJ (J=6-3) transitions of Tb(3+) are found under electron beam excitation. The above investigation results imply that the CLS:Tb(3+), Mn(2+) phosphors could have potential applications on LEDs and FEDs.

  7. Synthesis and Photoluminescence Properties of Sr2Be2B2O7 Doped with Dy3+, Sm3+, Tb3+, and Pb2+

    NASA Astrophysics Data System (ADS)

    Pekgözlü, İ.; Karabulut, H.; Mergen, A.; Basak, A. S.

    2016-07-01

    Pure and Dy3+-, Sm3+-, Tb3+-, and Pb2+-doped Sr2Be2B2O7 materials were prepared by a solution combustion synthesis method. The phase analysis of all synthesized materials was carried out using powder XRD. The photoluminescent properties of Dy3+-, Sm3+-, Tb3+-, and Pb2+-doped Sr2Be2B2O7 materials were investigated using a spectrofl uorometer at room temperature. The fi rst luminescent material, Sr2Be2B2O7:Dy3+, emits 478-493, 573, and 661 nm upon excitation with 344 nm; Sr2Be2B2O7:Sm3+ emits 563-574, 599-613, 647-666, and 705-713 nm upon excitation with 395 nm; Sr2Be2B2O7:Tb3+ emits 489, 545, 584-591, and 622 nm upon excitation with 248 nm; Sr2Be2B2O7:Pb2+ emits 371 nm upon excitation with 281 nm. Also, the dependence of the emission intensity on the activator ion (Dy3+, Sm3+, Tb3+, and Pb2+) concentration for the Sr2Be2B2O7 was studied. It was observed that the concentration quenching of Dy3+, Sm3+, Tb3+, and Pb2+ in Sr2Be2B2O7 is 0.05, 0.02, 0.07, and 0.02 mol.%, respectively.

  8. Effect of cell gap on electro-optical properties of polymer dispersed liquid crystal lens for smart electronic glasses

    NASA Astrophysics Data System (ADS)

    Kim, Jaeyong; Han, Jeong In

    2014-07-01

    Polymer dispersed liquid crystal (PDLC) lenses with a cell gap of 11 μm and 30 μm were made from a uniformly dispersed mixture of 40% prepolymer (NOA 65, Norland optical adhesive 65) and 60% E7 liquid crystal. PDLC's mixture between two ITO coated glasses was polymerized by UV (ultraviolet) curing in the polymerization induced phase separation (PIPS) process. Decline of cell gap is a physical approach to improve the electrooptical properties, while cooling or doping of SiO2 nanoparticles is the microstructural approach to enhance the properties, because the electric field applied to the liquid crystal molecules in LC droplets is inversely proportional to the cell gap. A smaller cell gap significantly and effectively increases the electric field applied to PDLCD devices. The driving voltages and slope for the sample with a cell gap of 11 μm and 30 μm were drastically improved. The driving voltage and the slope of the linear region of PDLC lens with narrow cell gap of 11 μm were drastically enhanced compared to those of the samples with 30 μm cell gap and the cooled and doped samples. These improvements were due to the increase of the applied electric field. However, the response time and contrast ratio were deteriorated. It seems that this deterioration was caused by the sticking or fixing of liquid crystal molecules in LC (liquid crystal) droplets by the intensive electric field applied to the PDLC device.

  9. Crystal structure, electronic structure, and photoluminescent properties of SrMoO{sub 4}:Tb{sup 3+} phosphors

    SciTech Connect

    Park, Sung Wook; Moon, Byung Kee; Jeong, Jung Hyun; Bae, Jong Seong; Kim, Jung Hwan

    2015-10-15

    Highlights: • SrMoO{sub 4}:Tb{sup 3+} phosphor samples were synthesized at different temperatures. • The crystal and electronic structures, and luminescence properties were studied. • The excitation peak shifts to red with increasing the sintering temperature. • The luminescence mechanism of SrMoO{sub 4}:Tb{sup 3+} was suggested. - Abstract: The experimental and theoretical studies of the optical properties of SrMoO{sub 4}:Tb{sup 3+} phosphors were carried out. The structural, optical, and electronical properties of the phosphors were systematically studied. The phosphor samples were crystallized at different temperatures via a sol–gel method. Excitation spectra of SrMoO{sub 4}:Tb{sup 3+} powder samples exhibited gradual red shift and luminescent intensity changed with increasing the sintering temperature. Such spectral changes depend strongly on the crystallographic properties such as lattice parameters and crystallinity. The shift of the excitation spectra is mainly ascribed to the covalent bond interaction between Mo−O bonds. An energy band model was demonstrated to describe the luminescence mechanism in the material.

  10. Low Band Gap Thiophene-Perylene Diimide Systems with Tunable Charge Transport Properties

    SciTech Connect

    Balaji, Ganapathy; Kale, Tejaswini S.; Keerthi, Ashok; Della Pelle, Andrea M.; Thayumanavan, S.; Vallyaveettil, Surech

    2010-11-30

    Perylenediimide-pentathiophene systems with varied architecture of thiophene units were synthesized. The photophysical, electrochemical, and charge transport behavior of the synthesized compounds were studied. Both molecules showed a low band gap of ~1.4 eV. Surprisingly, the molecule with pentathiophene attached via β-position to the PDI unit upon annealing showed a predominant hole mobility of 1 × 10-4 cm2 V-1 s-1 whereas the compound with branched pentathiophene attached via β-position showed an electron mobility of 9.8 × 10-7 cm2 V-1 s-1. This suggests that charge transport properties can be tuned by simply varying the architecture of pentathiophene units.

  11. The role of deep centers in formation of dosimetric properties of wide-gap materials

    NASA Astrophysics Data System (ADS)

    Nikiforov, S. V.; Kortov, V. S.

    2014-11-01

    The direct and indirect methods of experimental detection of deep traps in wide-gap insulators are described. The experimentally observed effects of influence of deep traps with different nature on luminescent and dosimetric properties of materials are analyzed. It is established that the most wide-spread and well-studied effects are the sensitization and superlinearity of dose response. They are interpreted in terms of the kinetic model of competitive electron traps. Taking into account the temperature dependence of capture probability by deep traps in this model allows one to explain some new effects associated with luminescence thermal quenching. The luminescence model of Al2O3:C single crystal is described. In this model the temperature dependence of competitive interaction between the main and deep traps is caused by thermal ionization of excited states of F-centers.

  12. Giant photoluminescence enhancement in tungsten-diselenide–gold plasmonic hybrid structures

    PubMed Central

    Wang, Zhuo; Dong, Zhaogang; Gu, Yinghong; Chang, Yung-Huang; Zhang, Lei; Li, Lain-Jong; Zhao, Weijie; Eda, Goki; Zhang, Wenjing; Grinblat, Gustavo; Maier, Stefan A.; Yang, Joel K. W.; Qiu, Cheng-Wei; Wee, Andrew T. S.

    2016-01-01

    Impressive properties arise from the atomically thin nature of transition metal dichalcogenide two-dimensional materials. However, being atomically thin limits their optical absorption or emission. Hence, enhancing their photoluminescence by plasmonic nanostructures is critical for integrating these materials in optoelectronic and photonic devices. Typical photoluminescence enhancement from transition metal dichalcogenides is 100-fold, with recent enhancement of 1,000-fold achieved by simultaneously enhancing absorption, emission and directionality of the system. By suspending WSe2 flakes onto sub-20-nm-wide trenches in gold substrate, we report a giant photoluminescence enhancement of ∼20,000-fold. It is attributed to an enhanced absorption of the pump laser due to the lateral gap plasmons confined in the trenches and the enhanced Purcell factor by the plasmonic nanostructure. This work demonstrates the feasibility of giant photoluminescence enhancement in WSe2 with judiciously designed plasmonic nanostructures and paves a way towards the implementation of plasmon-enhanced transition metal dichalcogenide photodetectors, sensors and emitters. PMID:27150276

  13. Giant photoluminescence enhancement in tungsten-diselenide-gold plasmonic hybrid structures

    NASA Astrophysics Data System (ADS)

    Wang, Zhuo; Dong, Zhaogang; Gu, Yinghong; Chang, Yung-Huang; Zhang, Lei; Li, Lain-Jong; Zhao, Weijie; Eda, Goki; Zhang, Wenjing; Grinblat, Gustavo; Maier, Stefan A.; Yang, Joel K. W.; Qiu, Cheng-Wei; Wee, Andrew T. S.

    2016-05-01

    Impressive properties arise from the atomically thin nature of transition metal dichalcogenide two-dimensional materials. However, being atomically thin limits their optical absorption or emission. Hence, enhancing their photoluminescence by plasmonic nanostructures is critical for integrating these materials in optoelectronic and photonic devices. Typical photoluminescence enhancement from transition metal dichalcogenides is 100-fold, with recent enhancement of 1,000-fold achieved by simultaneously enhancing absorption, emission and directionality of the system. By suspending WSe2 flakes onto sub-20-nm-wide trenches in gold substrate, we report a giant photoluminescence enhancement of ~20,000-fold. It is attributed to an enhanced absorption of the pump laser due to the lateral gap plasmons confined in the trenches and the enhanced Purcell factor by the plasmonic nanostructure. This work demonstrates the feasibility of giant photoluminescence enhancement in WSe2 with judiciously designed plasmonic nanostructures and paves a way towards the implementation of plasmon-enhanced transition metal dichalcogenide photodetectors, sensors and emitters.

  14. Study of structural and photoluminescent properties of Ca8Eu2(PO4)6O2.

    PubMed

    Silva, C C; Filho, F P; Sombra, A S B; Rosa, I L V; Leite, E R; Longo, E; Varela, J A

    2008-03-01

    In this work it is presented for the first time the nanostructured hydroxyapatites doped with 0.5, 1.0 and 2.0 wt% of Eu(3+) prepared at room temperature by the mechanical alloying technique. X-ray diffraction powder (XRD), infrared (IR) and Raman scattering spectroscopy, scanning electron microscopy (SEM), microhardness measurements as well as luminescent data of Eu(3+) were used to investigate the structural and optical properties of these nanomaterials. The electrical and dielectrical analyses were used with the intention of having a better comprehension about the electromagnetic fields in pure and doped hydroxyapatites.

  15. Structural, electronic and photoluminescence properties of Eu3+-doped CaYAlO4 obtained by using citric acid complexes as precursors

    NASA Astrophysics Data System (ADS)

    Perrella, R. V.; Júnior, C. S. Nascimento; Góes, M. S.; Pecoraro, E.; Schiavon, M. A.; Paiva-Santos, C. O.; Lima, H.; Couto dos Santos, M. A.; Ribeiro, S. J. L.; Ferrari, J. L.

    2016-07-01

    The search for new materials that meet the current technological demands for photonic applications, make the Rare Earth ions embedded in inorganic oxides as excellent candidates for several technological devices. This work presents the synthesis of Eu3+-doped CaYAlO4 using citric acid as ligand to form a complex precursor. The methodology used has big draw due to its easy handling and low cost of the materials. The thermal analysis of viscous solutions was evaluated and the obtained compounds show the formation of a polycrystalline tetragonal phase. Rietveld refinement was used to understand the structural and the cell parameters of the crystalline phase as a function of temperature of heat-treatment. Crystallite size and microstrain were determined and were shown to have a direct relationship with the temperature of the heat-treatment. The band-gap of the CaYAlO4 doped with 1 and 10 mol% of Eu3+ showed values close to 4.30 eV, resulting in their transparency in the visible region between 330 and 750 nm. Besides the intense photoluminescence from Eu3+, a study was conducted to evaluate the possible position of the Eu3+ in the CaYAlO4 as host lattice. Lifetime of the emission decay from Eu3+ excited state 5D0 show that CaYAlO4 is a good host to rare earth ions, once it can avoid clustering of these ions in concentration as high as 10 mol%. The predictions of the sublevels of the 7F1 crystal field level are discussed through the method of equivalent nearest neighbours (MENN). The intensity parameters (Ωλ, λ = 2 and 4) are reproduced with physically reasonable values of average polarizabilities. The set of charge factors used in both calculations are in good agreement with the charge of the europium ion described by the Batista-Longo improved model (BLIM). The quantum efficiencies of the materials were calculated based on Judd-Ofelt theory. Based on the results obtained in this work, the materials have potential use in photonic devices such as lasers and solid

  16. Transition metal coordination polymers based on tetrabromoterephthalic and bis(imidazole) ligands: Syntheses, structures, topological analysis and photoluminescence properties

    NASA Astrophysics Data System (ADS)

    Zhang, Xiaowei; Xing, Peiqi; Geng, Xiujuan; Sun, Daofeng; Xiao, Zhenyu; Wang, Lei

    2015-09-01

    Eight new coordination polymers (CPs), namely, [Zn(1,2-mbix)(tbtpa)]n (1), [Co(1,2-mbix)(tbtpa)]n (2), [CdCl(1,2-mbix)(tbtpa)0.5]n (3), {[Cd(1,2-bix)(tbtpa)]·H2O}n (4), {[Cd0.5(1,2-bix)(tbtpa)0.5]·H2O}n (5), {[Co0.5(1,2-bix)(tbtpa)0.5]·2H2O}n (6), {[Co(1,2-bix)(tbtpa)]·H2O}n (7) and {[Co(1,2-bix)(tbtpa)]·Diox·2H2O}n (8), were synthesized under solvothermal conditions based on mix-ligand strategy (H2tbtpa=tetrabromoterephthalic acid and 1,2-mbix=1,2-bis((2-methyl-1H-imidazol-1-yl)methyl)benzene, 1,2-bix=1,2-bis(imidazol-1-ylmethyl)benzene). All of the CPs have been structurally characterized by single-crystal X-ray diffraction analyses and further characterized by elemental analyses, IR spectroscopy, powder X-ray diffraction (PXRD), and thermogravimetric analyses (TGA). X-ray diffraction analyses show that 1 and 2 are isotypics which have 2D highly undulated networks with (4,4)-sql topology with the existence of C-H ⋯Br interactions; for 3, it has a 2D planar network with (4,4)-sql topology with the occurrence of C-H ⋯Cl interactions other than C-H ⋯Br interactions; 4 shows a 3D 2-fold interpenetrated nets with rare 65·8-mok topology which has a self-catention property. As the same case as 1 and 2, 5 and 6 are also isostructural with planar layers with 44-sql topology which further assembled into 3D supramolecular structure through the interdigitated stacking fashion and the C-Br ⋯Cph interactions. As for 7, it has a 2D slightly undulated networks with (4,4)-sql topology which has one dimension channel. While 8 has a 2-fold interpenetrated networks with (3,4)-connect jeb topology with point symbol {63}{65·8}. And their structures can be tuned by conformations of bis(imidazol) ligands and solvent mixture. Besides, the TGA properties for all compounds and the luminescent properties for 1, 3, 4, 5 are discussed in detail.

  17. Photoluminescence imaging of electronic-impurity-induced exciton quenching in single-walled carbon nanotubes.

    PubMed

    Crochet, Jared J; Duque, Juan G; Werner, James H; Doorn, Stephen K

    2012-02-01

    The electronic properties of single-walled carbon nanotubes can be altered by surface adsorption of electronic impurities or dopants. However, fully understanding the influence of these impurities is difficult because of the inherent complexity of the solution-based colloidal chemistry of nanotubes, and because of a lack of techniques for directly imaging dynamic processes involving these impurities. Here, we show that photoluminescence microscopy can be used to image exciton quenching in semiconducting single-walled carbon nanotubes during the early stages of chemical doping with two different species. The addition of AuCl(3) leads to localized exciton-quenching sites, which are attributed to a mid-gap electronic impurity level, and the adsorbed species are also found sometimes to be mobile on the surface of the nanotubes. The addition of H(2)O(2) leads to delocalized exciton-quenching hole states, which are responsible for long-range photoluminescence blinking, and are also mobile.

  18. Propagation properties and dispersion characteristics of the tapered gap plasmonic waveguides

    NASA Astrophysics Data System (ADS)

    Sheikhi, Kamran; Granpayeh, Nosrat; Ahmadi, Vahid

    2016-08-01

    In this study, we numerically analyse the propagation properties and dispersion characteristics of the tapered gap plasmonic waveguides (TGPWs). Using the finite element method, the waveguide parameters such as modal field distribution and complex propagation constant are calculated for different geometrical parameters over a wide spectral range. Moreover, using a kind of active medium with appropriate gain, the required gains for lossless propagation are obtained. Results show that the propagation properties and dispersion characteristics of the waveguide along with the value of required gain for achieving lossless propagation can be well controlled by adjusting the geometrical parameters of the waveguide. The simulation results indicate that the calculated gain values are obtainable using the existing semiconductor technology such as InGaAsP-InGaAlAs multi-quantum well and InAs/GaAs quantum dot active medium at the wavelength of 1550 nm. The strong mode confinement of the TGPWs can be used for achieving strong nonlinear effects. Furthermore, due to optical energy confinement in nanoscale, optical nanofocusing devices based on TGPWs are attainable. TGPWs can be utilized in the field of nanotechnology to fulfil the photonic devices integration.

  19. Electronic properties of graphene nano-flakes: Energy gap, permanent dipole, termination effect, and Raman spectroscopy

    SciTech Connect

    Singh, Sandeep Kumar Peeters, F. M.; Neek-Amal, M.

    2014-02-21

    The electronic properties of graphene nano-flakes (GNFs) with different edge passivation are investigated by using density functional theory. Passivation with F and H atoms is considered: C{sub N{sub c}} X{sub N{sub x}} (X = F or H). We studied GNFs with 10 < N{sub c} < 56 and limit ourselves to the lowest energy configurations. We found that: (i) the energy difference Δ between the highest occupied molecular orbital and the lowest unoccupied molecular orbital decreases with N{sub c}, (ii) topological defects (pentagon and heptagon) break the symmetry of the GNFs and enhance the electric polarization, (iii) the mutual interaction of bilayer GNFs can be understood by dipole-dipole interaction which were found sensitive to the relative orientation of the GNFs, (iv) the permanent dipoles depend on the edge terminated atom, while the energy gap is independent of it, and (v) the presence of heptagon and pentagon defects in the GNFs results in the largest difference between the energy of the spin-up and spin-down electrons which is larger for the H-passivated GNFs as compared to F-passivated GNFs. Our study shows clearly the effect of geometry, size, termination, and bilayer on the electronic properties of small GNFs. This study reveals important features of graphene nano-flakes which can be detected using Raman spectroscopy.

  20. Effect of ZnO on the physical properties and optical band gap of soda lime silicate glass.

    PubMed

    Zaid, Mohd Hafiz Mohd; Matori, Khamirul Amin; Aziz, Sidek Hj Abdul; Zakaria, Azmi; Ghazali, Mohd Sabri Mohd

    2012-01-01

    This manuscript reports on the physical properties and optical band gap of five samples of soda lime silicate (SLS) glass combined with zinc oxide (ZnO) that were prepared by a melting and quenching process. To understand the role of ZnO in this glass structure, the density, molar volume and optical band gaps were investigated. The density and absorption spectra in the Ultra-Violet-Visible (UV-Visible) region were recorded at room temperature. The results show that the densities of the glass samples increased as the ZnO weight percentage increased. The molar volume of the glasses shows the same trend as the density: the molar volume increased as the ZnO content increased. The optical band gaps were calculated from the absorption edge, and it was found that the optical band gap decreased from 3.20 to 2.32 eV as the ZnO concentration increased.

  1. Branch-shaped NaGdF{sub 4}:Eu{sup 3+} nanocrystals: Selective synthesis, and photoluminescence properties

    SciTech Connect

    Wang Shangbing; Li Qing; Pei Lizhai; Zhang Qianfeng

    2010-08-15

    The branch-shaped NaGdF{sub 4}:Eu{sup 3+} nanocrystals (NCs) were synthesized by using polyvinylpyrrolidone (PVP) as a capping agent in ethylene glycol (EG) solution. The NCs were readily dispersed into water or ethanol to form a relatively stable suspension, which may facilitate their applications in biological fields. Meanwhile, the crystal structures of the NCs were tunable from the mixture of the {alpha}-(cubic) and {beta}-(hexagonal) phases to the pure {beta}-phase by varying the F{sup -}/Ln{sup 3+} molar ratio or the reaction temperature. The pure {beta}-phase NCs were obtained at relatively high F{sup -}/Ln{sup 3+} molar ratio and reaction temperature. In addition, the Eu{sup 3+}-doping concentration-dependent optical properties of the NaGdF{sub 4}:Eu{sup 3+} NCs were investigated in detail. The result shows that the emissions from high energy level transitions (e.g., {sup 5}D{sub 1}, {sup 5}D{sub 2}, and {sup 5}D{sub 3}) are significantly impaired with increasing the Eu{sup 3+}-doping concentration due to the cross-relaxation process, and the emission at 612 nm is predominant since the doped Eu{sup 3+} ions locate in the crystal fields without inversion center.

  2. Three complexes of Cu(I) cluster with flexible and rigid ligands: Synthesis, characterization and photoluminescent properties

    NASA Astrophysics Data System (ADS)

    Sun, Shu; Liu, Li-Juan; Ma, Wang-Yang; Zhou, Wei-Xia; Li, Jun; Zhang, Feng-Xing

    2015-05-01

    Three new Cu(I) cluster complexes, viz. [(Cu4I4)(Cu2I2)(dimb)3]n (1; dimb=1,4-diimidazol-1-ylbutane), [(Cu3I2)(dimb)(dmtz)]n (2; dmtz=3,5-dimethyl-1,2,4-triazole), and [Cu6(mbt)6] (3; mbt=2-mercaptobenzothiazole), have been solvothermally synthesized and structurally characterized. In 1, a Cu4I4 cubane core as a 4-connecting node, connects the neighboring nodes either through single dimb or μ2-[(Cu2I2)(dimb)2] linkers, affording an undulated 2D (4,4) net. Parallel interpenetration occurs between the adjacent nets and thus the overall 2D→3D network is formed. Complex 2 is constructed by 2D (4,4) topological plane grid layers of AB stacking. The core, a distorted triangular bipyramidal Cu3I2 cluster, is acted as a 4-connecting node and connected with dimb and μ3-dmtz to form the layer. Complex 3 contains a (Cu6S6) core in discrete paddle-wheel molecule, which serves as a 4-connecting node to link equivalent ones via π···π interaction, forming 2D (4,4) layers. Solid-state luminescence properties and thermogravimetric analyses of 1, 2 and 3 were investigated.

  3. Photoluminescence and energy transfer properties of Eu2+ and Tb3+ co-doped gamma aluminum oxynitride powders

    NASA Astrophysics Data System (ADS)

    Zhang, Jiantao; Ma, Chaoyang; Wen, Zicheng; Du, Miaomiao; Long, Jiaqi; Ma, Ran; Yuan, Xuanyi; Li, Junting; Cao, Yongge

    2016-08-01

    Gamma-AlON: 0.2Eu2+, Tb3+ phosphors were firstly synthesized via a high temperature solid-state reaction. For the phosphors, luminescence properties as well as energy transfer mechanism were investigated in detail. The energy transfer from Eu2+ to Tb3+ in the γ-AlON host was ascribed to the dipole-dipole mechanism, and the efficiency and critical distance in the energy transfer process were also estimated. γ-AlON: 0.2Eu2+, Tb3+ phosphors showed a broad-band emission centered at about 405 nm and other several emission peaks, which were assigned to the 5d-4f transition of Eu2+ ions and the 5D4-7FJ (J = 6, 5, 4, and 3) characteristic transitions of Tb3+ ions, respectively. The results indicated that γ-AlON: 0.2Eu2+, Tb3+ phosphors have great potential application in white light-emitting diodes due to its broad-band excitation in the ultraviolet range and the high-efficient green light emission.

  4. Synthesis and photoluminescent properties of geometrically hindered cis-tris(diphenylaminofluorene) as precursors to light-emitting devices.

    PubMed

    Kang, Nam-Goo; Kokubo, Ken; Jeon, Seaho; Wang, Min; Lee, Chang-Lyoul; Canteenwala, Taizoon; Tan, Loon-Seng; Chiang, Long Y

    2015-03-13

    A novel highly luminescent tris-fluorenyl ring-interconnected chromophore tris(DPAF-C9) was synthesized using a C3 symmetrical triaminobenzene core as the synthon. This structure bears three light-harvesting 2-diphenylamino-9,9-dialkylfluorenyl (DPAF) ring moieties with each attached by two branched 3',5',5'-trimethylhexyl (C9) arms. A major stereoisomer was chromatographically isolated and characterized to possess a 3D structural configuration of cis-conformer in a cup-form. Molecular calculation at B3LYP/6-31G* level revealed the unexpected stability of this cis-cup-conformer of tris(DPAF-C9) better than that of the stereoisomer in a propeller-form and the trans-conformer. The structural geometry is proposed to be capable of minimizing the aggregation related self-quenching effect in the condensed phase. Fluorescence emission wavelength of tris(DPAF-C9) was found to be in a close range to that of PVK that led to its potential uses as the secondary blue hole-transporting material for enhancing the device property toward the modulation of PLED performance.

  5. Gap-junctional properties of electrically coupled skate horizontal cells in culture.

    PubMed

    Qian, H; Malchow, R P; Ripps, H

    1993-01-01

    Whole-cell voltage-clamp recordings were used to examine the unusual pharmacological properties of the electrical coupling between rod-driven horizontal cells in skate retina as revealed previously by receptive-field measurements (Qian & Ripps, 1992). The junctional resistance was measured in electrically coupled cell pairs that had been enzymatically isolated and maintained in culture; the typical value was about 19.92 M omega (n = 45), more than an order of magnitude lower than the nonjunctional membrane resistance. These data and the intercellular spread of the fluorescent dye Lucifer Yellow provide a good indication that skate horizontal cells are well coupled. The junctional conductance between cells was not modulated by the neurotransmitters dopamine (200 microM) or GABA (1 mM), nor was it affected by the membrane-permeable analogues of cAMP or cGMP, or the adenylate cyclase activator, forskolin. Although resistant to agents that have been reported to alter horizontal-cell coupling in cone-driven horizontal cells, the junctional conductance between paired horizontal cells of skate was greatly reduced by the application of 20 mM acetate, which is known to effectively reduce intracellular pH. Together with the results obtained in situ on the receptive-field properties of skate horizontal cells, these findings indicate that the gap-junctional properties of rod-driven horizontal cells of the skate are fundamentally different from those of cone-driven horizontal cells in other species. This raises the possibility that there is more than one class of electrical synapse on vertebrate horizontal cells. PMID:8485091

  6. Crystal structure, thermally stability and photoluminescence properties of novel Sr{sub 10}(PO{sub 4}){sub 6}O:Eu{sup 2+} phosphors

    SciTech Connect

    Guo, Qingfeng; Liao, Libing Mei, Lefu; Liu, Haikun

    2015-03-15

    A series of novel luminescent phosphors Sr{sub 10}(PO{sub 4}){sub 6}O:Eu{sup 2+} with apatite structure were synthesized via a high temperature solid-state reaction. The phase structure, photoluminescence (PL) properties, the PL thermal stability, as well as the fluorescence decay curves of the samples were investigated to characterize the resulting samples, and the selected Sr{sub 9.97}(PO{sub 4}){sub 6}O:0.03Eu{sup 2+} phosphor exhibits strong thermal quenching resistance, retaining the luminance of 88.73% at 150 °C. The quenching concentration of Eu{sup 2+} in Sr{sub 10}(PO{sub 4}){sub 6}O was about 0.03 attributing to the dipole–quadrupole interaction. The Sr{sub 10}(PO{sub 4}){sub 6}O:Eu{sup 2+} phosphor exhibited a broad-band blue emission at 439 nm upon excitation at 346 nm. The results indicate that Sr{sub 10}(PO{sub 4}){sub 6}O:Eu{sup 2+} phosphors have potential applications as near UV-convertible phosphors for white-light UV LEDs. - Graphical abstract: Sr{sub 10}(PO{sub 4}){sub 6}O:Eu{sup 2+} phosphors have potential applications as near UV-convertible phosphors for white-light UV LEDs. - Highlights: • Sr{sub 9.97}(PO{sub 4}){sub 6}O:0.03Eu{sup 2+} phosphor exhibits strong thermal quenching resistance. • Two different Eu{sup 2+} emission centers exists in Sr{sub 10}(PO{sub 4}){sub 6}O. • The activation energy was also estimated for the Eu{sup 2+} luminescence center.

  7. Synthesis and photoluminescence properties of silver(I) complexes based on N-benzoyl-L-glutamic acid and N-donor ligands with different flexibility

    NASA Astrophysics Data System (ADS)

    Yan, Ming-Jie; Feng, Qi; Song, Hui-Hua

    2016-05-01

    By changing the N-donor ancillary ligand, three novel silver (I) complexes {[Ag(HbzgluO) (4,4‧-bipy)]·H2O}n (1), {[Ag2(HbzgluO)2 (bpe)2]·2H2O}n (2) and {[Ag(HbzgluO)(bpp)]·2H2O}n (3) (H2bzgluO = N-benzoyl-L-glutamic acid, 4,4‧-bipy = 4,4ˊ-bipyridine, bpe = 1,2-di(4-pyridyl)ethane, bpp = 1,3-di(4-pyridyl)propane) were synthesized. Their structures have been determined by single-crystal X-ray diffraction analyses and further characterized by elemental analyses, IR spectra, powder X-ray diffraction (PXRD), and thermogravimetric analyses (TGA). In this study, the N-donor ligands are changed from rigidity (4,4‧-bipy), quasi-flexibility (bpe) to flexibility (bpp), the structures of complexes also change. Complex 1 features a 1D chain structure which is further linked together to construct a 2D supramolecular structure through hydrogen bonds. Complex 2 is a 1D double-chains configuration which eventually forms a 3D supramolecular network via hydrogen bonding interactions. Whereas, complex 3 exhibits a 2D pleated grid structure which is linked by hydrogen bonding interactions into a 3D supramolecular network. The present observations demonstrate that the modulation of coordination polymers with different structures can accomplish by changing the spacer length of N-donor ligands. In addition, the solid-state circular dichroism (CD) spectra indicated that compound 2 exhibited negative cotton effect which originated from the chiral ligands H2bzgluO and the solid-state fluorescence spectra of the three complexes demonstrated the auxiliary ligands have influence on the photoluminescence properties of the complexes.

  8. Photoluminescence properties of novel red-emitting NaSrBO3:Eu3+ phosphor for near-UV light-emitting diodes

    NASA Astrophysics Data System (ADS)

    Yang, Fan; Liang, Yujun; Liu, Mingyu; Li, Xuejing; Zhang, Mengfei; Wang, Nan

    2013-03-01

    A series of NaSrBO3:xEu3+ and NaSr1-2xBO3:xEu3+, xM+ (M=Li, Na, K) phosphors were synthesized by the solid state reaction. The crystal structure, photoluminescence properties and concentration quenching of NaSrBO3:Eu3+ phosphors were systematically investigated. The excitation spectra indicate that the phosphors can be efficiently excited by 394 nm, which is matched well with the emission wavelength of near-UV LED chip. All the samples show the characteristic red emission of Eu3+ ions (5D0→7FJ, J=0, 1, 2, 3 and 4). The maximum intensity of luminescence is observed at the Eu3+ concentration around x=0.11. The concentration quenching of Eu3+ in NaSrBO3:Eu3+ phosphor can be mainly attributed to quadrupole-quadrupole interaction. The relative emission intensities of Eu3+ (5D0→7F2) in NaSrBO3:Eu3+ phosphors with Li+, Na+ or K+ introduced as charge compensator are significantly enhanced, and the phosphors added with K+ ions show the strongest emission. The emission intensities of NaSr1-2xBO3:xEu3+, xM+ (M=Li, Na, K) are about 1.47, 1.64 and 2.08 times than that of commercial red phosphor Y2O2S:Eu3+. These results indicate that NaSr1-2xBO3:xEu3+, xM+ (M=Li, Na, K) phosphors exhibit potential applications in the field of near-UV LED as an efficient red-emitting phosphors.

  9. Rare earth (Eu{sup 3+}, Tb{sup 3+}) mesoporous hybrids with calix[4]arene derivative covalently linking MCM-41: Physical characterization and photoluminescence property

    SciTech Connect

    Li Yajuan; Yan Bing; Wang Li

    2011-09-15

    MCM-41 mesoporous silica has been functionalized with two kinds of macrocylic calixarene derivatives Calix[4] and Calix[4]Br (Calix[4]=P-tert-butylcalix[4]arene, Calix[4]Br=5.11,17.23-tetra-tert-butyl-25.27-bihydroxy- 26.28-bibromopropoxycalix[4]arene) through condensation approach of tetraethoxysilane (TEOS) in the presence of the cetyltrimethylammonium bromide (CTAB) surfactant as a template. Novel organic-inorganic mesoporous luminescent hybrid containing RE{sup 3+} (Eu{sup 3+}, Tb{sup 3+}) complexes covalently attached to the functionalized ordered mesoporous MCM-41, which are designated as RE-Calix[4]-MCM-41 and RE-Calix[4]Br-MCM-41, respectively, are obtained by sol-gel process. It is found that they all have high surface area, uniform in the mesostructure and good crystallinity. Measurement of the photoluminescence properties show the mesoporous material covalently bonded Tb{sup 3+} complexes (Tb-Calix[4]-MCM-41 and Tb-Calix[4]Br-MCM-41) exhibit the stronger characteristic emission of Tb{sup 3+} and longer lifetime than the corresponding Eu-containing materials Eu-Calix[4]-MCM-41 and Eu-Calix[4]Br-MCM-41 due to the triplet state energy of modified organic ligands Calix[4]-Si and Calix[4]Br-Si match with the emissive energy level of Tb{sup 3+} very well. - Graphical abstract: MCM-41 mesoporous silica is functionalized with two kinds of macrocylic calixarene derivatives and luminescent organic-inorganic mesoporous hybrids containing Ln{sup 3+} complexes covalently attached to the functionalized ordered mesoporous MCM-41. Highlights: > Novel linkages of functionalized calixarene derivative. > New rare earth mesoporous hybrids. > Luminescence in visible region.

  10. Microwave sol-gel synthesis and upconversion photoluminescence properties of CaGd2(WO4)4:Er3+/Yb3+ phosphors with incommensurately modulated structure

    NASA Astrophysics Data System (ADS)

    Lim, Chang Sung; Aleksandrovsky, Aleksandr; Molokeev, Maxim; Oreshonkov, Aleksandr; Atuchin, Victor

    2015-08-01

    CaGd2-x(WO4)4:Er3+/Yb3+ phosphors with the doping concentrations of Er3+ and Yb3+ (x=Er3++Yb3+, Er3+=0.05, 0.1, 0.2 and Yb3+=0.2, 0.45) have been successfully synthesized by the microwave sol-gel method. The crystal structure of CaGd2-x(WO4)4:Er3+/Yb3+ tungstates have been refined, and upconversion photoluminescence properties have been investigated. The synthesized particles, being formed after the heat-treatment at 900 °C for 16 h, showed a well crystallized morphology. Under the excitation at 980 nm, CaGd2(WO4)4:Er3+/Yb3+ particles exhibited a strong 525-nm and a weak 550-nm emission bands in the green region and a very weak 655-nm emission band in the red region. The Raman spectrum of undoped CaGd2(WO4)4 revealed about 12 narrow lines. The strongest band observed at 903 cm-1 was assigned to the ν1 symmetric stretching vibration of WO4 tetrahedrons. The spectra of the samples doped with Er and Yb obtained under the 514.5 nm excitation were dominated by Er3+ luminescence preventing the recording of these samples Raman spectra. Concentration quenching of the erbium luminescence at 2H11/2→4I15/2 transition is weak in the range of erbium doping level xEr=0.05-0.2, while, for transition 4S3/2→4I15/2, the signs of concentration quenching become pronounced at xEr=0.2.

  11. Electrically tuned photoluminescence in large pitch cholesteric liquid crystal

    SciTech Connect

    Middha, Manju Kumar, Rishi Raina, K. K.

    2014-04-24

    Cholesteric liquid crystals are known as 1-D photonic band gap materials due to their periodic helical supramolecular structure and larger birefringence. Depending upon the helical twisted pitch length, they give the characteristic contrast due to selective Bragg reflections when viewed through the polarizing optical microscope and hence affect the electro-optic properties. So the optimization of chiral dopant concentration in nematic liquid crystal leads to control the transmission of polarized light through the microscope. Hence transmission based polarizing optical microscope is used for the characterization of helical pitch length in the optical texture. The unwinding of helical pitch was observed with the application of electric field which affects the intensity of photoluminescence.

  12. Synthesis, photoluminescence and biological properties of terbium(III) complexes with hydroxyketone and nitrogen containing heterocyclic ligands.

    PubMed

    Poonam; Kumar, Rajesh; Boora, Priti; Khatkar, Anurag; Khatkar, S P; Taxak, V B

    2016-01-01

    The ternary terbium(III) complexes [Tb(HDAP)3⋅biq], [Tb(HDAP)3⋅dmph] and [Tb(HDAP)3⋅bathophen] were prepared by using methoxy substituted hydroxyketone ligand HDAP (2-hydroxy-4,6-dimethoxyacetophenone) and an ancillary ligand 2,2-biquinoline or 5,6-dimethyl-1,10-phenanthroline or bathophenanthroline respectively. The ligand and synthesized complexes were characterised based on elemental analysis, FT-IR and (1)H NMR. Thermal behaviour of the synthesized complexes illustrates the general decomposition patterns of the complexes by thermogravimetric analysis. Photophysical properties such as excitation spectra, emission spectra and luminescence decay curves of the complexes were investigated in detail. The main green emitting peak at 548nm can be attributed to (5)D4→(7)F5 of Tb(3+) ion. Thus, these complexes might be used to make a bright green light-emitting diode for display purpose. In addition the in vitro antibacterial activities of HDAP and its Tb(III) complexes against Bacillus subtilis, Staphylococcus aureus, Escherichia coli and antifungal activities against Candida albicans and Aspergillus niger are reported. The Tb(3+) complexes were found to be more potent antimicrobial agent as compared to the ligand. Among all these complexes, [Tb(HDAP)3⋅bathophen] exhibited excellent antimicrobial activity which proves its potential usefulness as an antimicrobial agent. Furthermore, in vitro antioxidant activity tests were carried out by using DPPH method which indicates that the complexes have considerable antioxidant activity when compared with the standard ascorbic acid.

  13. Synthesis, photoluminescence and biological properties of terbium(III) complexes with hydroxyketone and nitrogen containing heterocyclic ligands

    NASA Astrophysics Data System (ADS)

    Poonam; Kumar, Rajesh; Boora, Priti; Khatkar, Anurag; Khatkar, S. P.; Taxak, V. B.

    2016-01-01

    The ternary terbium(III) complexes [Tb(HDAP)3ṡbiq], [Tb(HDAP)3ṡdmph] and [Tb(HDAP)3ṡbathophen] were prepared by using methoxy substituted hydroxyketone ligand HDAP (2-hydroxy-4,6-dimethoxyacetophenone) and an ancillary ligand 2,2-biquinoline or 5,6-dimethyl-1,10-phenanthroline or bathophenanthroline respectively. The ligand and synthesized complexes were characterised based on elemental analysis, FT-IR and 1H NMR. Thermal behaviour of the synthesized complexes illustrates the general decomposition patterns of the complexes by thermogravimetric analysis. Photophysical properties such as excitation spectra, emission spectra and luminescence decay curves of the complexes were investigated in detail. The main green emitting peak at 548 nm can be attributed to 5D4 → 7F5 of Tb3+ ion. Thus, these complexes might be used to make a bright green light-emitting diode for display purpose. In addition the in vitro antibacterial activities of HDAP and its Tb(III) complexes against Bacillus subtilis, Staphylococcus aureus, Escherichia coli and antifungal activities against Candida albicans and Aspergillus niger are reported. The Tb3+ complexes were found to be more potent antimicrobial agent as compared to the ligand. Among all these complexes, [Tb(HDAP)3ṡbathophen] exhibited excellent antimicrobial activity which proves its potential usefulness as an antimicrobial agent. Furthermore, in vitro antioxidant activity tests were carried out by using DPPH method which indicates that the complexes have considerable antioxidant activity when compared with the standard ascorbic acid.

  14. Tunable photoluminescence properties of Sr(1-y)CayMoO4:Sm3+ phosphors (0 ≤ y < 1).

    PubMed

    Cao, Renping; Chen, Kangbin; Liu, Pan; Cao, Chunyan; Xu, Yongchun; Ao, Hui; Tang, Pengjie

    2015-11-01

    A series of Sr(1-x-y)CayMoO4:xSm(3+) (0 ≤ x ≤ 7 mol% and 0 ≤ y < 1) phosphors was synthesized by a conventional solid-state reaction method in air, and their structural and spectroscopic properties were investigated. The optimal doping concentration of Sm(3+) in SrMoO4:Sm(3+) phosphor is 5 mol%. Under excitation with 275 nm, in Sr(1-x-y)CayMoO4:xSm(3+) (0 ≤ x ≤ 7 mol% and 0 ≤ y < 1) phosphors, the emission band of the host was found to overlap with the excitation bands peaking at ~ 500 nm of Sm(3+) ion, and the energy transfer from MoO4 (2-) group to Sm(3+) ion can also be observed. The International Commission on Illumination (CIE) chromaticity coordinates of Sr(0.95-y)CayMoO4:0.05Sm(3+) phosphors with excitation 275 nm varied systematically from an orange (0.4961, 0.3761) (y = 0) to a white color (0.33, 0.3442) (y = 0.95) with increasing calcium oxide (CaO) concentration. However, Sr(0.95-y)CayMoO4:0.05Sm(3+) phosphors with excitation at 404 nm only showed red emission and the energy transfer between MoO4(2-) group to Sm(3+) ion was not observed. The complex mechanisms of luminescence and energy transfer are discussed by energy level diagrams of MoO4(2-) group and Sm(3+) ion. PMID:25645573

  15. Enhanced photoluminescence of C 60 incorporated into interlayers of hydrotalcite

    NASA Astrophysics Data System (ADS)

    Ding, Weiping; Gu, Gang; Zhong, Wei; Zang, Wen-Cheng; Du, Youwei

    1996-11-01

    Strong photoluminescence of sodium-reduced C 60 incorporated into interlayers of hydrotalcite is observed. This phenomenon is correlated to the fact that the reduced C 60 is positioned between positively charged layers of the anion clay. The interaction between the layers and reduced C 60 alters the photophysical properties of C 60 and relaxes the electron transition inhibition, thus enhancing photoluminescence.

  16. Three complexes of Cu(I) cluster with flexible and rigid ligands: Synthesis, characterization and photoluminescent properties

    SciTech Connect

    Sun, Shu; Liu, Li-Juan; Ma, Wang-Yang; Zhou, Wei-Xia; Li, Jun; Zhang, Feng-Xing

    2015-05-15

    Three new Cu(I) cluster complexes, viz. [(Cu{sub 4}I{sub 4})(Cu{sub 2}I{sub 2})(dimb){sub 3}]{sub n} (1; dimb=1,4-diimidazol-1-ylbutane), [(Cu{sub 3}I{sub 2})(dimb)(dmtz)]{sub n} (2; dmtz=3,5-dimethyl-1,2,4-triazole), and [Cu{sub 6}(mbt){sub 6}] (3; mbt=2-mercaptobenzothiazole), have been solvothermally synthesized and structurally characterized. In 1, a Cu{sub 4}I{sub 4} cubane core as a 4-connecting node, connects the neighboring nodes either through single dimb or μ{sub 2}-[(Cu{sub 2}I{sub 2})(dimb){sub 2}] linkers, affording an undulated 2D (4,4) net. Parallel interpenetration occurs between the adjacent nets and thus the overall 2D→3D network is formed. Complex 2 is constructed by 2D (4,4) topological plane grid layers of AB stacking. The core, a distorted triangular bipyramidal Cu{sub 3}I{sub 2} cluster, is acted as a 4-connecting node and connected with dimb and μ{sub 3}-dmtz to form the layer. Complex 3 contains a (Cu{sub 6}S{sub 6}) core in discrete paddle-wheel molecule, which serves as a 4-connecting node to link equivalent ones via π···π interaction, forming 2D (4,4) layers. Solid-state luminescence properties and thermogravimetric analyses of 1, 2 and 3 were investigated. - Graphical abstract: Complexes based on Cu(I) clusters possess two-fold 2D→3D parallel interpenetrating (1), triple emissions (2) and near-infrared emission (3). - Highlights: • Complex 1 represents two-fold 2D→3D parallel interpenetrating framework. • Complex 2 shows triple emissions. • Complex 3 displays a quite intense near-infrared (NIR) emission. • These complexes have good thermal stability.

  17. Preparation and Photoluminescence Properties of Eu2+-Doped Oxyapatite-Type SrxLa10-x (SiO4)6O3-x/2

    NASA Astrophysics Data System (ADS)

    Cui, Zhao-Feng; Yuan, Shuang-Long; Yang, Yun-Xia; François, Chevire; Franck, Tessier; Chen, Guo-Rong

    2011-01-01

    Eu2+-doped oxyapatite SrxLa10-x(SiO4)6O3-x/2 phosphors are prepared by solid-state reaction at high temperatures under reducing atmosphere. Their crystal structures and photoluminescence are investigated by x-ray diffraction (XRD) and fluorescence spectroscopy, respectively. The XRD results indicate that the samples are pure oxyapatite phase (P63/m space group). The fluorescence spectra show two peaks corresponding to two sites (4f and 6h sites) for Eu2+ in the host lattice. As the Eu2+ content influences the intensity ratio of the two observed emission peaks, the photoluminescence mechanism is discussed.

  18. Arc voltage distribution properties as a function of melting current, electrode gap, and CO pressure during vacuum arc remelting

    SciTech Connect

    Williamson, R.L.; Zanner, F.J.; Grose, S.M.

    1997-10-01

    An industrial vacuum arc remelting experiment was carried out at Cytemp Specialty Steel Corp. (Titusville, PA) during which a 0.432-m-diameter Alloy 718 electrode was remelted into a 0.508-m-diameter ingot. The purpose of the experiment was to investigate the response of the arc voltage distribution properties (mean, standard deviation, and skewness) and the drip-short frequency to melting current, electrode gap, and CO pressure. The responses were characterized by recording and analyzing changes in the temporally averaged properties. Each independent variable was systematically varied in accordance with a modified Yates order factor space experimental design within the following ranges: melting current, 5,000 to 11,200 A; electrode gap, 0.004 to 0.056 m; and CO pressure, 0.40 to 14.7 Pa. Statistical models were developed describing the correlation between the averaged arc voltage distribution properties and the independent variables. The models demonstrate that all of the voltage distribution properties, as well as the drip-short frequency, are directly related to electrode gap. An arc column model is presented to account for the mean arc voltage properties and the model is used to estimate the arc column pressure. The potential usefulness of the distribution properties as process diagnostics and control responses is evaluated.

  19. Photoluminescence properties of a new orange–red emitting Sm{sup 3+}-doped Y{sub 2}Mo{sub 4}O{sub 15} phosphor

    SciTech Connect

    Deng, Huajuan; Zhao, Ze; Wang, Jing; Hei, Zhoufei; Li, Mengxue; Noh, Hyeon Mi; Jeong, Jung Hyun; Yu, Ruijin

    2015-08-15

    A series of novel Y{sub 2}Mo{sub 4}O{sub 15}:xSm{sup 3+} ( (0.01 ≤ x ≤ 0.20) phosphors for white light-emitting (W-LEDs) were successfully prepared by the solid state reaction technology at 973 K for 12 h. X-ray diffraction and photoluminescence spectra were utilized to characterize the structure and luminescence properties of the as-synthesized phosphors. The emission spectra of the Y{sub 2}Mo{sub 4}O{sub 15}:Sm{sup 3+} phosphors consisted of some sharp emission peaks of Sm{sup 3+} ions centered at 565 nm, 605 nm, 650 nm, and 712 nm. The strongest one is located at 605 nm due to {sup 4}G{sub 5/2}–{sup 6}H{sub 7/2} transition of Sm{sup 3+}, generating bright orange–red light. The optimum dopant concentration of Sm{sup 3+} ions in Y{sub 2}Mo{sub 4}O{sub 15}:xSm{sup 3+} is around 5 mol% and the critical transfer distance of Sm{sup 3+} is calculated as 23.32 Å. The CIE chromaticity coordinates of the Y{sub 2}Mo{sub 4}O{sub 15}:0.05Sm{sup 3+} phosphors were located in the orange reddish region. The Y{sub 2}Mo{sub 4}O{sub 15}:Sm{sup 3+} phosphors may be potentially used as red phosphors for white light-emitting diodes. - Graphical abstract: The excitation spectrum of Y{sub 2}Mo{sub 4}O{sub 15}:Sm{sup 3+} is composed of a broad band and some sharp f–f transitions. Under 407 nm excitation, the phosphor presents some sharp emission peaks of Sm{sup 3+} ions. - Highlights: • An orange–red emitting Y{sub 2}Mo{sub 4}O{sub 15}:Sm{sup 3+} phosphor has been firstly synthesized. • Their structures, luminescent properties have also been investigated. • The optical absorption edge for the molybdate lies around 325 nm. • The CIE chromaticity coordinates were located in the orange reddish region.

  20. Topological evolution and photoluminescent properties of a series of divalent zinc-based metal–organic frameworks tuned via ancillary ligating spacers

    SciTech Connect

    Lian, Xiao-Min; Zhao, Wen; Zhao, Xiao-Li

    2013-04-15

    The combination of divalent zinc ions, 4-(4-carboxybenzamido)benzoic acid and exo-bidendate bipyridine ligands gave rise to a series of new MOFs: [ZnL(bipy)]·DMF·H{sub 2}O (1), [ZnL(bpe)]·1.5H{sub 2}O (2), [ZnL(bpa)]·4H{sub 2}O (3) and [ZnL(bpp)]·1.75H{sub 2}O (4) (MOF=metal-organic framework, bipy=4,4′-bipyridine, bpe=trans-1,2-bis(4-pyridyl)ethylene, bpa=1,2-bis(4-pyridinyl)ethane, bpp=1,3-bis(4-pyridinyl)propane, H{sub 2}L=4,4′-(carbonylimino)dibenzoic acid). Fine tune over the topology of the MOFs was achieved via systematically varying the geometric length of the second ligating bipyridine ligands. Single-crystal X-ray analysis reveals that complex 1 has a triply interpenetrated three-dimensional (3D) framework with elongated primitive cubic topology, whereas isostructural complexes 2 and 3 each possesses a 6-fold interpenetrated diamondiod 3D framework. Further expansion of the length of the bipyridine ligand to bpp leads to the formation of 4, which features an interesting entangled architecture of 2D→3D parallel polycatenation. In addition, the thermogravimetric analyses and solid-state photoluminescent properties of the selected complexes are investigated. - Graphical abstract: The incorporation of exo-bidendate bipyridine spacers into the Zn–H{sub 2}L system has yielded a series of new MOFs exhibiting topological evolution from 3-fold interpenetration to 6-fold interpenetration and 2D→3D parallel polycatenation. Highlights: ► The effect of the pyridyl-based spacers on the formation of MOFs was explored. ► Fine tune over the topology of the MOFs was achieved. ► An interesting structure of 2D→3D parallel polycatenation is reported.

  1. Investigation on the properties of omnidirectional photonic band gaps in two-dimensional plasma photonic crystals

    NASA Astrophysics Data System (ADS)

    Zhang, Hai-Feng; Liu, Shao-Bin; Li, Bing-Xiang

    2016-01-01

    The properties of omnidirectional photonic band gaps (OBGs) in two-dimensional plasma photonic crystals (2D PPCs) are theoretically investigated by the modified plane wave expansion method. In the simulation, we consider the off-plane incident wave vector. The configuration of 2D PPCs is the triangular lattices filled with the nonmagnetized plasma cylinders in the homogeneous and isotropic dielectric background. The calculated results show that the proposed 2D PPCs possess a flatbands region and the OBGs. Compared with the OBGs in the conventional 2D dielectric-air PCs, it can be obtained more easily and enlarged in the 2D PPCs with a similar structure. The effects of configurational parameters of the PPCs on the OBGs also are studied. The simulated results demonstrate that the locations of OBGs can be tuned easily by manipulating those parameters except for changing plasma collision frequency. The achieved OBGs can be enlarged by optimizations. The OBGs of two novel configurations of PPCs with different cross sections are computed for a comparison. Both configurations have the advantages of obtaining the larger OBGs compared with the conventional configuration, since the symmetry of 2D PPCs is broken by different sizes of periodically inserted plasma cylinders or connected by the embedded plasma cylinders with thin veins. The analysis of the results shows that the bandwidths of OBGs can be tuned by changing geometric and physical parameters of such two PPCs structures. The theoretical results may open a new scope for designing the omnidirectional reflectors or mirrors based on the 2D PPCs.

  2. Superfluidity and collective properties of excitonic polaritons in gapped graphene in a microcavity

    NASA Astrophysics Data System (ADS)

    Berman, Oleg L.; Kezerashvili, Roman Ya.; Ziegler, Klaus

    2012-12-01

    We predict the formation and superfluidity of polaritons in an optical microcavity formed by excitons in gapped graphene embedded there and microcavity photons. The Rabi splitting related to the creation of an exciton in a graphene layer in the presence of the band gap is obtained. It is demonstrated that the Rabi splitting decreases when the energy gap increases, while the larger value of the dielectric constant of the microcavity gives a smaller value for the Rabi splitting. The analysis of collective excitations as well as the sound velocity is presented. We show that the superfluid density ns and temperature of the Kosterlitz-Thouless phase transition Tc are decreasing functions of the energy gap.

  3. Optical and photoelectric properties of anodic oxide films on GaAs, GaP, and GaAs/sub 0. 6/P/sub 0. 4/

    SciTech Connect

    Kashkarov, P.K.; Obraztsov, A.N.; Sorokin, I.N.; Sosnovskikh, Yu.N.

    1987-03-01

    The authors investigate the optical absorption spectra and the photoconductivities of anodic oxide film based on GaAs, GaP, and GaAs/sub 0.6/P/sub 0.4/ in the range of light energy quanta 2-6.2 eV. Anodic oxide film (AOF) was studied on the surface of single crystals of GaAs and epitaxial layers of p-type Gap and AsAs/sub 0.6/P/sub 0.4/ of the n-type. The structures of the oxides were monitored by electron diffraction. The photoconductivity of the AOF was investigated. The absorption of the AOF in the visible and near-UV ranges was estimated by comparing the spectra of excitation of photoluminescence at 80 K for specimens coated with an AOF and specimens with the AOF removed by etching in HCl.

  4. Gap Junctions

    PubMed Central

    Nielsen, Morten Schak; Axelsen, Lene Nygaard; Sorgen, Paul L.; Verma, Vandana; Delmar, Mario; Holstein-Rathlou, Niels-Henrik

    2013-01-01

    Gap junctions are essential to the function of multicellular animals, which require a high degree of coordination between cells. In vertebrates, gap junctions comprise connexins and currently 21 connexins are known in humans. The functions of gap junctions are highly diverse and include exchange of metabolites and electrical signals between cells, as well as functions, which are apparently unrelated to intercellular communication. Given the diversity of gap junction physiology, regulation of gap junction activity is complex. The structure of the various connexins is known to some extent; and structural rearrangements and intramolecular interactions are important for regulation of channel function. Intercellular coupling is further regulated by the number and activity of channels present in gap junctional plaques. The number of connexins in cell-cell channels is regulated by controlling transcription, translation, trafficking, and degradation; and all of these processes are under strict control. Once in the membrane, channel activity is determined by the conductive properties of the connexin involved, which can be regulated by voltage and chemical gating, as well as a large number of posttranslational modifications. The aim of the present article is to review our current knowledge on the structure, regulation, function, and pharmacology of gap junctions. This will be supported by examples of how different connexins and their regulation act in concert to achieve appropriate physiological control, and how disturbances of connexin function can lead to disease. © 2012 American Physiological Society. Compr Physiol 2:1981-2035, 2012. PMID:23723031

  5. Structural and photoluminescent properties of nanowires formed by the metal-assisted chemical etching of monocrystalline silicon with different doping level

    SciTech Connect

    Georgobiani, V. A. Gonchar, K. A.; Osminkina, L. A.; Timoshenko, V. Yu.

    2015-08-15

    Silicon-nanowire layers grown by the metal-assisted chemical etching of (100)-oriented p-type monocrystalline silicon substrates with a resistivity of 10 and 0.001 Ω · cm are studied by electron microscopy, Raman scattering, and photoluminescence measurements. It is established that nanowires grown on lightly doped substrates are structurally nonporous and formed as crystalline cores covered by nanocrystals 3–5 nm in dimensions. Nanowires grown on heavily doped substrates are structurally porous and contain both small nanocrystals and coarser crystallites with equilibrium charge carriers that influence interband radiative recombination. It is found that the photoluminescence intensity of nanowires in the spectral range 1.3–2.0 eV depends on the presence of molecular oxygen.

  6. Optical properties of Ge-rich G e1 -xS ix alloys: Compositional dependence of the lowest direct and indirect gaps

    NASA Astrophysics Data System (ADS)

    Xu, Chi; Gallagher, J. D.; Senaratne, C. L.; Menéndez, J.; Kouvetakis, J.

    2016-03-01

    Ge-rich G e1 -xS ix alloys have been investigated using spectroscopic ellipsometry and photoluminescence at room temperature. Special emphasis was placed on the compositional dependence of the lowest-energy interband transitions. For x ≤0.05 , a compositional range of particular interest for modern applications, we find E0=0.799 (1 ) +3.214 (45 ) x +0.080 (44 ) x2 (in eV) for the lowest direct gap. The compositional dependence of the indirect gap is obtained from photoluminescence as Eind=0.659 (4 ) +1.18 (17 ) x (in eV). We find no significant discrepancies between these results and the extrapolations from measurements at higher Si concentrations. Such discrepancies had been suggested by recent work on G e1 -xS ix films on Si. Accurate knowledge of the interband transition energies is an important requirement for the design of devices incorporating Ge-rich G e1 -xS ix alloys and for the understanding of more complex systems, such as ternary G e1 -x -yS ixS ny alloys, in terms of its binary constituents.

  7. Highly Photoluminescent Molybdenum Oxide Quantum Dots: One-Pot Synthesis and Application in 2,4,6-Trinitrotoluene Determination.

    PubMed

    Xiao, Sai Jin; Zhao, Xiao Jing; Hu, Ping Ping; Chu, Zhao Jun; Huang, Cheng Zhi; Zhang, Li

    2016-03-01

    As a well-studied transition-metal semiconductor material, MoOx has a wider band gap than molybdenum disulfide (MoS2), and its property varies dramatically for the existence of several different allotropes and suboxide phases of molybdenum oxides (MoOx, x < 3). In this manuscript, a one-pot method possessing the advantages of one pot, easily prepared, rapid, and environmentally friendly, has been developed for facile synthesis of highly photoluminescent MoOx quantum dots (MoOx QDs), in which commercial molybdenum disulfide (MoS2) powder and hydrogen peroxide (H2O2) are employed as the precursor and oxidant, respectively. The obtained MoOx QDs can be further utilized as an efficient photoluminescent probe, and a new turn-off sensor is developed for 2,4,6-trinitrotoluene (TNT) determination based on the fact that the photoluminescence of MoOx QDs can be quenched by the Meisenheimer complexes formed in the strong alkali solution through the inner filter effect (IFE). Under the optimal conditions, the decreased photoluminescence of MoOx QDs shows a good linear relationship to the concentration of TNT ranging from 0.5 to 240.0 μM, and the limit of detection was 0.12 μM (3σ/k). With the present turn-off sensor, TNT in river water samples can be rapidly and selectively detected without tedious sample pretreatment processes.

  8. A new silicon phase with direct band gap and novel optoelectronic properties

    SciTech Connect

    Guo, Yaguang; Wang, Qian; Kawazoe, Yoshiyuki; Jena, Puru

    2015-09-23

    Due to the compatibility with the well-developed Si-based semiconductor industry, there is considerable interest in developing silicon structures with direct energy band gaps for effective sunlight harvesting. In this paper, using silicon triangles as the building block, we propose a new silicon allotrope with a direct band gap of 0.61 eV, which is dynamically, thermally and mechanically stable. Symmetry group analysis further suggests that dipole transition at the direct band gap is allowed. Additionally, this new allotrope displays large carrier mobility (~104 cm/V · s) at room temperature and a low mass density (1.71 g/cm3), making it a promising material for optoelectronic applications.

  9. A new silicon phase with direct band gap and novel optoelectronic properties

    DOE PAGESBeta

    Guo, Yaguang; Wang, Qian; Kawazoe, Yoshiyuki; Jena, Puru

    2015-09-23

    Due to the compatibility with the well-developed Si-based semiconductor industry, there is considerable interest in developing silicon structures with direct energy band gaps for effective sunlight harvesting. In this paper, using silicon triangles as the building block, we propose a new silicon allotrope with a direct band gap of 0.61 eV, which is dynamically, thermally and mechanically stable. Symmetry group analysis further suggests that dipole transition at the direct band gap is allowed. Additionally, this new allotrope displays large carrier mobility (~104 cm/V · s) at room temperature and a low mass density (1.71 g/cm3), making it a promising materialmore » for optoelectronic applications.« less

  10. A New Silicon Phase with Direct Band Gap and Novel Optoelectronic Properties

    PubMed Central

    Guo, Yaguang; Wang, Qian; Kawazoe, Yoshiyuki; Jena, Puru

    2015-01-01

    Due to the compatibility with the well-developed Si-based semiconductor industry, there is considerable interest in developing silicon structures with direct energy band gaps for effective sunlight harvesting. In this paper, using silicon triangles as the building block, we propose a new silicon allotrope with a direct band gap of 0.61 eV, which is dynamically, thermally and mechanically stable. Symmetry group analysis further suggests that dipole transition at the direct band gap is allowed. In addition, this new allotrope displays large carrier mobility (~104 cm/V · s) at room temperature and a low mass density (1.71 g/cm3), making it a promising material for optoelectronic applications. PMID:26395926

  11. Electronic properties of metal-induced gap states formed at alkali-halide/metal interfaces

    NASA Astrophysics Data System (ADS)

    Kiguchi, Manabu; Yoshikawa, Genki; Ikeda, Susumu; Saiki, Koichiro

    2005-04-01

    The spatial distribution and site distribution of metal-induced gap states (MIGS) are studied by thickness-dependent near-edge x-ray absorption fine structure (NEXAFS) and by comparing the cation and anion-edge NEXAFS. The thickness-dependent NEXAFS shows that the decay length of MIGS depends on an alkali-halide rather than a metal, and it is larger for alkali-halides with smaller band gap energies. By comparing the Cl-edge and K-edge NEXAFS for KCl/Cu (001) , MIGS are found to be states localizing at anion sites.

  12. Photoluminescence of Diamondoid Crystals

    SciTech Connect

    Clay, William; Sasagawa, Takao; Iwasa, Akio; Liu, Zhi; Dahl, Jeremy E.; Carlson, Robert M.K.; Kelly, Michael; Melos, Nicholas; Shen, Zhi-Xun; /Stanford U., Phys. Dept. /Stanford U., Appl. Phys. Dept. /Stanford U., Geballe Lab. /SIMES, Stanford

    2012-04-03

    The photoluminescence of diamondoids in the solid state is examined. All of the diamondoids are found to photoluminesce readily with initial excitation wavelengths ranging from 233 nm to 240 nm (5.3 eV). These excitation energies are more than 1 eV lower than any previously studied saturated hydrocarbon material. The emission is found to be heavily shifted from the absorption, with emission wavelengths of roughly 295 nm (4.2 eV) in all cases. In the dissolved state, however, no uorescence is observed for excitation wavelengths as short as 200 nm. We also discuss predictions and measurements of the quantum yield. Our predictions indicate that the maximum yield may be as high as 25%. Our measurement of one species, diamantane, gives a yield of 11%, the highest ever reported for a saturated hydrocarbon, even though it was likely not at the optimal excitation wavelength.

  13. Properties of MIS structures based on graded-gap HgCdTe grown by molecular beam epitaxy

    SciTech Connect

    Voitsekhovskii, A. V. Nesmelov, S. N.; Dzyadookh, S. M.; Varavin, V. S.; Dvoretskii, S. A.; Mikhailov, N. N.; Sidorov, Yu. G.; Vasiliev, V. V.

    2008-11-15

    The effect of near-surface graded-gap layers on the electrical characteristics of MIS structures fabricated based on heteroepitaxial Hg{sub 1-x} Cd{sub x}Te films grown by molecular beam epitaxy with a two-layer SiO{sub 2}/Si{sub 3}N{sub 4} insulator and anodic oxide film is studied experimentally. It is shown that a larger modulation of capacitance (depth and width of the valley) is observed compared with the structures without the graded-gap layer. The field dependences of photovoltage of MIS structures with the graded-gap layers had a classical form and were characterized by a drop only in the enrichment region. For the structures without the graded-gap layer with x = 0.22, a drop in the voltage dependence of the photocurrent is observed in the region of pronounced inversion. This drop is governed by limitation of the space charge region by processes of tunneling generation via deep levels. The properties of the HgCdTe-insulator interfaces are studied.

  14. Mechanisms behind blue, green, and red photoluminescence emissions in CaWO4 and CaMoO4 powders

    NASA Astrophysics Data System (ADS)

    Campos, A. B.; Simões, A. Z.; Longo, E.; Varela, J. A.; Longo, V. M.; de Figueiredo, A. T.; De Vicente, F. S.; Hernandes, A. C.

    2007-07-01

    A combined experimental and theoretical study was conducted to analyze the photoluminescence (PL) properties of ordered and disordered CaWO4 (CW) and CaMoO4 (CM) powders. Two mechanisms were found to be responsible for photoluminescence emission in CW and CM powders. The first one, in the disordered powders, was caused by oxygen complex vacancies [MO3•VOx], [MO3•VO•] and [MO3•VO••], where M =W or Mo, which leads to additional levels in the band gap. The second mechanism, in ordered powders, was caused by an intrinsic slight distortion of the [WO4] or [MoO4] tetrahedral in the short range.

  15. Effect of Thermal Annealing on the Band GAP and Optical Properties of Chemical Bath Deposited ZnSe Thin Films

    NASA Astrophysics Data System (ADS)

    Ezema, F. I.; Ekwealor, A. B. C.; Osuji, R. U.

    2006-05-01

    Zinc selenide (ZnSe) thin films were deposited on glass substrate using the chemical bath deposition method at room temperature from aqueous solutions of zinc sulphate and sodium selenosulfate in which sodium hydroxide was employed as complexing agents. The `as-deposited' ZnSe thin films are red in color and annealed in oven at 473 K for 1 hour and on a hot plate in open air at 333 K for 5 minutes, affecting the morphological and optical properties. Optical properties such as absorption coefficient a and extinction coefficient k, were determined using the absorbance and transmission measurement from Unico UV-2102 PC spectrophotometer, at normal incidence of light in the wavelength range of 200-1000 nm. The films have transmittance in VIS-NIR regions that range between 26 and 87%. From absorbance and transmittance spectra, the band gap energy determined ranged between 1.60 eV and 1.75 for the `as deposited' samples, and the annealed samples exhibited a band gap shift of 0.15 eV. The high transmittance of the films together with its large band gap made them good materials for selective coatings for solar cells.

  16. Structural, optical and electrical properties of tin oxide thin films for application as a wide band gap semiconductor

    SciTech Connect

    Sethi, Riti; Ahmad, Shabir; Aziz, Anver; Siddiqui, Azher Majid

    2015-08-28

    Tin oxide (SnO) thin films were synthesized using thermal evaporation technique. Ultra pure metallic tin was deposited on glass substrates using thermal evaporator under high vacuum. The thickness of the tin deposited films was kept at 100nm. Subsequently, the as-deposited tin films were annealed under oxygen environment for a period of 3hrs to obtain tin oxide films. To analyse the suitability of the synthesized tin oxide films as a wide band gap semiconductor, various properties were studied. Structural parameters were studied using XRD and SEM-EDX. The optical properties were studied using UV-Vis Spectrophotometry and the electrical parameters were calculated using the Hall-setup. XRD and SEM confirmed the formation of SnO phase. Uniform texture of the film can be seen through the SEM images. Presence of traces of unoxidised Sn has also been confirmed through the XRD spectra. The band gap calculated was around 3.6eV and the optical transparency around 50%. The higher value of band gap and lower value of optical transparency can be attributed to the presence of unoxidised Sn. The values of resistivity and mobility as measured by the Hall setup were 78Ωcm and 2.92cm{sup 2}/Vs respectively. The reasonable optical and electrical parameters make SnO a suitable candidate for optoelectronic and electronic device applications.

  17. Photoluminescence and compositional-structural properties of ion-beam sputter deposited Er-doped TiO{sub 2−x}N{sub x} films: Their potential as a temperature sensor

    SciTech Connect

    Scoca, D. Morales, M.; Merlo, R.; Alvarez, F.; Zanatta, A. R.

    2015-05-28

    Er-doped TiO{sub 2−x}N{sub x} films were grown by Ar{sup +} ion-beam sputtering a Ti + Er target under different N{sub 2} + O{sub 2} high-purity atmospheres. The compositional-structural properties of the samples were investigated after thermal annealing the films up to 1000 °C under a flow of oxygen. Sample characterization included x-ray photoelectron spectroscopy, grazing incidence x-ray diffraction, Raman scattering, and photoluminescence experiments. According to the experimental data, both composition and atomic structure of the samples were very sensitive to the growth conditions and annealing temperature. In the as-deposited form, the N-rich TiO{sub 2−x}N{sub x} films presented TiN crystallites and no photoluminescence. As the thermal treatments proceed, the films were transformed into TiO{sub 2} and Er{sup 3+}-related light emission were observed in the visible and near-infrared ranges at room-temperature. Whereas the development of TiO{sub 2} occurred due to the insertion-diffusion of oxygen in the films, light emission originated because of optical bandgap widening and/or structural-chemical variations in the vicinity of the Er{sup 3+} ions. Finally, the photoluminescence results in the visible range suggested the potential of the present samples in producing an optically based temperature sensor in the ∼150–500 K range.

  18. Structural and optical properties of size controlled Si nanocrystals in Si{sub 3}N{sub 4} matrix: The nature of photoluminescence peak shift

    SciTech Connect

    Zelenina, A. Hiller, D.; Gutsch, S.; Zacharias, M.; Dyakov, S. A.; Trouillet, V.; Bruns, M.; Mirabella, S.; Löper, P.; López-Conesa, L.; López-Vidrier, J.; Peiró, F.; Garrido, B. [MIND-IN2UB, Departament d’Electrònica, Universitat de Barcelona, C Estradé, S. [MIND-IN2UB, Departament d’Electrònica, Universitat de Barcelona, C CCiT, Scientific and Technical Centers, Universitat de Barcelona, C and others

    2013-11-14

    Superlattices of Si{sub 3}N{sub 4} and Si-rich silicon nitride thin layers with varying thickness were prepared by plasma enhanced chemical vapor deposition. After high temperature annealing, Si nanocrystals were formed in the former Si-rich nitride layers. The control of the Si quantum dots size via the SiN{sub x} layer thickness was confirmed by transmission electron microscopy. The size of the nanocrystals was well in agreement with the former thickness of the respective Si-rich silicon nitride layers. In addition X-ray diffraction evidenced that the Si quantum dots are crystalline whereas the Si{sub 3}N{sub 4} matrix remains amorphous even after annealing at 1200 °C. Despite the proven Si nanocrystals formation with controlled sizes, the photoluminescence was 2 orders of magnitude weaker than for Si nanocrystals in SiO{sub 2} matrix. Also, a systematic peak shift was not found. The SiN{sub x}/Si{sub 3}N{sub 4} superlattices showed photoluminescence peak positions in the range of 540–660 nm (2.3–1.9 eV), thus quite similar to the bulk Si{sub 3}N{sub 4} film having peak position at 577 nm (2.15 eV). These rather weak shifts and scattering around the position observed for stoichiometric Si{sub 3}N{sub 4} are not in agreement with quantum confinement theory. Therefore theoretical calculations coupled with the experimental results of different barrier thicknesses were performed. As a result the commonly observed photoluminescence red shift, which was previously often attributed to quantum-confinement effect for silicon nanocrystals, was well described by the interference effect of Si{sub 3}N{sub 4} surrounding matrix luminescence.

  19. Effects of Ligand Geometry on the Photophysical Properties of Photoluminescent Eu(III) and Sm(III) 1-Hydroxypyridin-2-one Complexes in Aqueous Solution.

    PubMed

    Daumann, Lena J; Tatum, David S; Andolina, Christopher M; Pacold, Joseph I; D'Aléo, Anthony; Law, Ga-lai; Xu, Jide; Raymond, Kenneth N

    2016-01-01

    A series of 10 tetradentate 1-hydroxy-pyridin-2-one (1,2-HOPO) ligands and corresponding eight-coordinated photoluminescent Eu(III) and Sm(III) complexes were prepared. Generally, the ligands differ by the linear (nLI) aliphatic linker length, from 2 to 8 methylene units between the bidentate 1,2-HOPO chelator units. The photoluminescent quantum yields (Φtot) were found to vary with the linker length, and the same trend was observed for the Eu(III) and Sm(III) complexes. The 2LI and 5LI bridged complexes are the brightest (Φtotxε). The change in ligand wrapping pattern between 2LI and 5LI complexes observed by X-ray diffraction (XRD) is further supported by density functional theory (DFT) calculations. The bimodal Φtot trends of the Eu(III) and Sm(III) complexes are rationalized by the change in ligand wrapping pattern as the bridge (nLI) is increased in length.

  20. Influence of γ-radiation on photoluminescence properties of YPO4:Eu3+,Ce3+ and YPO4:Dy3+,Ce3+ phosphors

    NASA Astrophysics Data System (ADS)

    Gurugubelli, Sudheer; Dadhich, Anima S.; Saha, Abhijit; Babu Mukkamala, Saratchandra

    2015-10-01

    Hexagonal YPO4 phosphors doped with Eu3+/Dy3+ and co-doped with Ce3+ were synthesized by a hydrothermal route assisted using lauric acid as a capping agent. The prepared phosphors were characterized by transmission electron microscopy, infrared spectroscopy, powder X-ray diffraction and photoluminescence spectra. YPO4: Eu3+ gives two red emission peaks at 587 and 610 nm corresponding to 5D0→7F1 and 5D0→7F2 transitions, respectively. YPO4: Dy3+ exhibits two emission peaks at 485 nm (blue) and 575 nm (yellow) corresponding to 4F9/2→6H15/2 and 4F9/2→6H13/2 transitions, respectively. Ce3+ ions enhanced the emission intensity as a co-dopant in both phosphors. Moreover, the effect of γ-radiation in the dose range 5-300 kGy on the photoluminescence behaviour of YPO4:Eu3+,Ce3+ and YPO4:Dy3+,Ce3+ was also investigated. Quenching of emission intensity, after irradiation at 5 and 300 kGy, was observed in both the phosphors due to loss of excess energy through a non-radiative relaxation process.

  1. A novel yellow-emitting SrAlSi{sub 4}N{sub 7}:Ce{sup 3+} phosphor for solid state lighting: Synthesis, electronic structure and photoluminescence properties

    SciTech Connect

    Ruan, Jian; Xie, Rong-Jun; Funahashi, Shiro; Tanaka, Yoshinori; Takeda, Takashi; Suehiro, Takayuki; Hirosaki, Naoto; Li, Yuan-Qiang

    2013-12-15

    Ce{sup 3+}-doped and Ce{sup 3+}/Li{sup +}-codoped SrAlSi{sub 4}N{sub 7} phosphors were synthesized by gas pressure sintering of powder mixtures of Sr{sub 3}N{sub 2}, AlN, α-Si{sub 3}N{sub 4}, CeN and Li{sub 3}N. The phase purity, electronic crystal structure, photoluminescence properties of SrAlSi{sub 4}N{sub 7}:Ce{sup 3+}(Ce{sup 3+}/Li{sup +}) were investigated in this work. The band structure calculated by the DMol{sup 3} code shows that SrAlSi{sub 4}N{sub 7} has a direct band gap of 3.87 eV. The single crystal analysis of Ce{sup 3+}-doped SrAlSi{sub 4}N{sub 7} indicates a disordered Si/Al distribution and nitrogen vacnacy defects. SrAlSi{sub 4}N{sub 7} was identified as a major phase of the fired powders, and Sr{sub 5}Al{sub 5}Si{sub 21}N{sub 35}O{sub 2} and AlN as minor phases. Both Ce{sup 3+} and Ce{sup 3+}/Li{sup +} doped SrAlSi{sub 4}N{sub 7} phosphors can be efficiently excited by near-UV or blue light and show a broadband yellow emission peaking around 565 nm. A highest external quantum efficiency of 38.3% under the 450 nm excitation was observed for the Ce{sup 3+}/Li{sup +}-doped SrAlSi{sub 4}N{sub 7} (5 mol%). A white light LED lamp with color temperature of 6300 K and color rendering index of Ra=78 was achieved by combining Sr{sub 0.97}Al{sub 1.03}Si{sub 3.997}N/94/maccounttest14=t0005{sub 1}8193 {sub 7}:Ce{sup 3+}{sub 0.03} with a commercial blue InGaN chip. It indicates that SrAlSi{sub 4}N{sub 7}:Ce{sup 3+} is a promising yellow emitting down-conversion phosphor for white LEDs. - Graphical abstract: One-phosphor converted white light-emitting diode (LED) was fabricated by combining a blue LED chip and a yellow-emitting SrAlSi4N7:Ce{sup 3+} phosphor (see inset), which has the color rendering index of 78 and color temperature of 6300 K. - Highlights: • We reported a new yellow nitride phosphor suitable for solid state lighting. • We solved the crystal structure and evidenced a disordered Si/Al distribution. • We fabricated a high color rendering

  2. Photoluminescence of Mn+ doped GaAs

    NASA Astrophysics Data System (ADS)

    Zhou, Huiying; Qu, Shengchun; Liao, Shuzhi; Zhang, Fasheng; Liu, Junpeng; Wang, Zhanguo

    2010-10-01

    Photoluminescence is one of the most useful techniques to obtain information about optoelectronic properties and defect structures of materials. In this work, the room-temperature and low temperature photoluminescence of Mn-doped GaAs were investigated, respectively. Mn-doped GaAs structure materials were prepared by Mn+ ion implantation at room temperature into GaAs. The implanted samples were subsequently annealed at various temperatures under N2 atmosphere to recrystallize the samples and remove implant damage. A strong peak was found for the sample annealed at 950 °C for 5 s. Transitions near 0.989 eV (1254 nm), 1.155 eV (1074 nm) and 1.329 eV (933 nm) were identified and formation of these emissions was analyzed for all prepared samples. This structure material could have myriad applications, including information storage, magnet-optical properties and energy level engineering.

  3. The down-conversion and up-conversion photoluminescence properties of Na{sub 0.5}Bi{sub 0.5}TiO{sub 3}:Yb{sup 3+}/Pr{sup 3+} ceramics

    SciTech Connect

    Huang, Yinpeng; Luo, Laihui Wang, Jia; Zuo, Qianghui; Yao, Yongjie; Li, Weiping

    2015-07-28

    Na{sub 0.5}Bi{sub 0.5−x−y}Yb{sub x}Pr{sub y}TiO{sub 3} (NBT:xYb/yPr) ceramics with different Yb and Pr contents are prepared. Both the down-conversion (DC) and up-conversion (UC) photoluminescence (PL) of the ceramics via 453 and 980 nm excitation, respectively, are investigated. The effect of Yb{sup 3+} and Pr{sup 3+} doping contents on the DC and UC PL is significantly different from each other. Furthermore, the UC PL of the ceramics as a function of temperatures is measured to investigate the UC process in detail. Based on energy level diagram of Pr{sup 3+} and Yb{sup 3+} ions and the DC and UC PL spectra, the DC and UC PL mechanisms of Pr{sup 3+} and Yb{sup 3+} ions are discussed. Especially, the UC PL mechanism is clarified, which is different from the previously reported literature. Also, the temperature sensing properties of the ceramics are studied based on the photoluminescence ratio technique, using the thermal coupling energy levels of Pr{sup 3+}.

  4. Structural Stability and Optical Properties of Nanomaterials with Reconstructed Surfaces

    SciTech Connect

    Puzder, A; Williamson, A; Reboredo, F; Galli, G

    2003-10-24

    The authors present density functional and quantum Monte Carlo calculations of the stability and optical properties of semiconductor nanomaterials with reconstructed surfaces. they predict the relative stability of silicon nanostructures with reconstructed and unreconstructed surfaces, and show that surface step geometries unique to highly curved surfaces dramatically reduce the optical gaps and decrease excitonic lifetimes. These predictions provide an explanation of both the variations in the photoluminescence spectra of colloidally synthesized nanoparticles and observed deep gap levels in porous silicon.

  5. The properties of photonic band gaps for three-dimensional plasma photonic crystals in a diamond structure

    SciTech Connect

    Zhang Haifeng; Liu Shaobin; Kong Xiangkun, Chenchen; Bian Borui

    2013-04-15

    In this paper, the properties of photonic band gaps (PBGs) for two types of three-dimensional plasma photonic crystals (PPCs) composed of isotropic dielectric and unmagnetized plasma with diamond lattices are theoretically investigated for electromagnetic waves based on a modified plane wave expansion method. The equations for type-1 structure are theoretically deduced, which depend on the diamond lattices realization (dielectric spheres immersed in plasma background). The influences of dielectric constant of dielectric, plasma collision frequency, filling factor, and plasma frequency on PBGs are investigated, respectively, and some corresponding physical explanations and the possible methods to realize the three-dimensional PPCs in experiments are also given. From the numerical results, it has been shown that not only the locations but also the gap/midgap ratios of the PBGs for two types of PPCs can be tuned by plasma frequency, filling factor, and the relative dielectric constant, respectively. However, the plasma collision frequency has no effect on the frequency ranges and gap/midgap ratios of the PBGs for two types of PPCs.

  6. The properties of photonic band gaps for three-dimensional plasma photonic crystals in a diamond structure

    NASA Astrophysics Data System (ADS)

    Zhang, Hai-Feng; Liu, Shao-Bin; Kong, Xiang-Kun; Chen-Chen; Bian, Bo-Rui

    2013-04-01

    In this paper, the properties of photonic band gaps (PBGs) for two types of three-dimensional plasma photonic crystals (PPCs) composed of isotropic dielectric and unmagnetized plasma with diamond lattices are theoretically investigated for electromagnetic waves based on a modified plane wave expansion method. The equations for type-1 structure are theoretically deduced, which depend on the diamond lattices realization (dielectric spheres immersed in plasma background). The influences of dielectric constant of dielectric, plasma collision frequency, filling factor, and plasma frequency on PBGs are investigated, respectively, and some corresponding physical explanations and the possible methods to realize the three-dimensional PPCs in experiments are also given. From the numerical results, it has been shown that not only the locations but also the gap/midgap ratios of the PBGs for two types of PPCs can be tuned by plasma frequency, filling factor, and the relative dielectric constant, respectively. However, the plasma collision frequency has no effect on the frequency ranges and gap/midgap ratios of the PBGs for two types of PPCs.

  7. Influence of optical gaps on signal and noise properties of luminescent screen x-ray detectors

    NASA Astrophysics Data System (ADS)

    Koch, Andreas

    2004-05-01

    X-ray detection with luminescent screens requires optical signal transfer as an intermediate step between x-ray detection and conversion to an electronic signal. Luminescent screens may be granular (phosphor screens), structured (e.g. CsI) or transparent (scintillators). The optical signal is imaged with lenses, fibre optics, electron optics or by proximity focussing to an electronic detector. Poor focussing or poor optical contact may degrade the signal and noise transfer characteristics, i.e. modulation transfer function (MTF) and detective quantum efficiency (DQE). The case when x-rays are detected with granular luminescent screens, imaged onto flat panel electronic detectors is considered here. The detector assembly often requires layers of glue or protective thin films creating optical gaps, in which light is spread, hence spatial resolution is degraded. The noise spectrum is not necessarily changed the same way. Its exact shape depends on the dominant noise sources in a given detector configuration under the specific operating conditions: The noise of the primary x-ray quanta, noise aliasing and direct x-ray detection by the electronic detection layer are the main contributions in this investigation. Especially at high spatial frequencies small optical gaps in conjunction with white quantum noise from direct x-ray absorption of the electronic imager degrade DQE: A gap of 40 μm between luminescent screen and detector reduces the DQE by 33% at the Nyquist frequency. This was demonstrated with an a-Si imager of 143-μm pixel size and a Lanex Fine luminescent screen operated at 100 kV.

  8. Visible photoluminescence of the deposited germanium-oxide prepared from clusters in the gas phase

    NASA Astrophysics Data System (ADS)

    Negishi, Yuichi; Nagao, Satoshi; Nakamura, Yoshiaki; Nakajima, Atsushi; Kamei, Shinichi; Kaya, Koji

    2000-11-01

    Optical properties of the deposited germanium-oxide (Ge-O) prepared from the laser ablation of GeO2 were investigated. When the GenOm clusters, having the compositions mainly at n=m, were deposited onto a substrate as a precursor, strong visible photoluminescence peaked at 500 nm was observed under the excitation of 325 nm laser light. X-ray photoelectron spectroscopy for the deposited Ge-O on the substrate consistently shows the substantial component of the oxidation state of Ge2+, which shows the contributions from 1:1 composition of Ge2+-O2-. Correspondingly, the electronic structures of the germanium-oxide cluster were studied by using photoelectron spectroscopy in gas phase. Our developed method of the halogen atom doping enables us to determine the highest occupied molecular orbital-the lowest unoccupied molecular orbital gap of the corresponding neutral GenOn clusters experimentally, and it was found that the gap of the GenOn (n=2-5) clusters reasonably corresponds to the energy of the visible light. These results imply that the GenOn clusters can be ascribed to the origin of the visible photoluminescence.

  9. Gap Opening as a Probe of Circumsolar and Circumplanetary Gas Disk Properties

    NASA Astrophysics Data System (ADS)

    Estrada, P. R.; Mosqueira, I.

    2002-09-01

    We expect that the largest objects forming in the solar nebula and giant-planet subnebulae truncated the gas disks in which they were formed, thus preventing gas outside their orbits from accreting onto the primary (Mosqueira and Estrada 2002a,b). The criterion for gap opening depends on two uncertain parameters; namely, the turbulent viscosity of the gas, and the damping length of the waves launched by the secondary in the neighborhood of resonant locations in the disk. In light of the difficulty of maintaining gas turbulence in disks with a positive radial gradient in specific angular momentum in the absence of a source of ``stirring'' (Ryu and Goodman 1992; Balbus et al. 1996), we adopt an inviscid disk. Regarding the second issue, there has been recent progress in characterizing the damping length of acoustic waves under several disk conditions. In a 2-D isothermal disk, wave steepening is likely to result in wave dissipation in a lengthscale of order ~ rL, where rL is the radial location of a Lindblad resonance and this distance has a weak dependence on the mass of the secondary (Goodman and Rafikov 2001). In an optically thick, vertically thermally stratified, disk the radial lengthscale for ``wave-channeling'' and wave dissipation is ~ rL/m, where m is the azimuthal wavenumber (Lubow and Ogilvie 1998; Bate et al. 2002). In a 3-D vertically isothermal gas disk, a significant fraction of the angular momentum flux may be transported by waves with non-zero vertical group velocity and possible radial damping lengths of the order ~ H, where H is the nebula scale-height (Bate et al. 2002; Mosqueira and Houben, this conference). The above can be used to compute the inertial mass (Ward and Hourigan 1989) and constrain the surface density of the disk at the time of gap opening. Here we do so for Jupiter in the solar disk (M2/M_1 = 9.5 x 10-4), Ganymede in the jovian disk (M2/M_1 = 7.8 x 10-5), Titan in the saturnian disk (M2/M_1 = 2.4 x 10-4), and Titania in the

  10. Photoluminescence of a Plasmonic Molecule.

    PubMed

    Huang, Da; Byers, Chad P; Wang, Lin-Yung; Hoggard, Anneli; Hoener, Ben; Dominguez-Medina, Sergio; Chen, Sishan; Chang, Wei-Shun; Landes, Christy F; Link, Stephan

    2015-07-28

    Photoluminescent Au nanoparticles are appealing for biosensing and bioimaging applications because of their non-photobleaching and non-photoblinking emission. The mechanism of one-photon photoluminescence from plasmonic nanostructures is still heavily debated though. Here, we report on the one-photon photoluminescence of strongly coupled 50 nm Au nanosphere dimers, the simplest plasmonic molecule. We observe emission from coupled plasmonic modes as revealed by single-particle photoluminescence spectra in comparison to correlated dark-field scattering spectroscopy. The photoluminescence quantum yield of the dimers is found to be surprisingly similar to the constituent monomers, suggesting that the increased local electric field of the dimer plays a minor role, in contradiction to several proposed mechanisms. Aided by electromagnetic simulations of scattering and absorption spectra, we conclude that our data are instead consistent with a multistep mechanism that involves the emission due to radiative decay of surface plasmons generated from excited electron-hole pairs following interband absorption. PMID:26165983

  11. Tunable photoluminescence and spectrum split from fluorinated to hydroxylated graphene

    NASA Astrophysics Data System (ADS)

    Gong, Peiwei; Wang, Jinqing; Sun, Weiming; Wu, Di; Wang, Zhaofeng; Fan, Zengjie; Wang, Honggang; Han, Xiuxun; Yang, Shengrong

    2014-02-01

    Tunable control over the functionalization of graphene is significantly important to manipulate its structure and optoelectronic properties. Yet the chemical inertness of this noble carbon material poses a particular challenge for its decoration without forcing reaction conditions. Here, a mild, operationally simple and controllable protocol is developed to synthesize hydroxylated graphene (HOG) from fluorinated graphene (FG). We successfully demonstrate that under designed alkali environment, fluorine atoms on graphene framework are programmably replaced by hydroxyl groups via a straightforward substitution reaction pathway. Element constituent analyses confirm that homogeneous C-O bonds are successfully grafted on graphene. Rather different from graphene oxide, the photoluminescence (PL) emission spectrum of the obtained HOG becomes split when excited with UV radiation. More interestingly, such transformation from FG facilitates highly tunable PL emission ranging from greenish white (0.343, 0.392) to deep blue (0.156, 0.094). Additionally, both experimental data and density function theory calculation indicate that the chemical functionalization induced structural rearrangement is more important than the chemical decoration itself in tuning the PL emission band tail and splitting energy gaps. This work not only presents a new way to effectively fabricate graphene derivatives with tunable PL performance, but also provides an enlightening insight into the PL origin of graphene related materials.Tunable control over the functionalization of graphene is significantly important to manipulate its structure and optoelectronic properties. Yet the chemical inertness of this noble carbon material poses a particular challenge for its decoration without forcing reaction conditions. Here, a mild, operationally simple and controllable protocol is developed to synthesize hydroxylated graphene (HOG) from fluorinated graphene (FG). We successfully demonstrate that under designed

  12. Reflectance properties of two-dimensional sonic band-gap crystals.

    PubMed

    Sanchis, L; Cervera, F; Sánchez-Dehesa, J; Sánchez-Pérez, J V; Rubio, C; Martínez-Sala, R

    2001-06-01

    An analysis of the reflectance of sonic band-gap crystals consisting of square arrays of rigid cylinders in air is presented. The standing wave formed in front of the structures is studied both experimentally and theoretically. Experiments have been performed with a mobile robotized microphone that obtains pressure maps on the plane perpendicular to the axes of the cylinders. Enhancements of the standing wave ratio (SWR) are observed in frequency regions where attenuation bands appear in zero-order transmission experiments. Also, the SWR presents oscillations that can be related to the finite dimension of the structure (Fabry-Perot effect). Both features are well described by calculations based on a double-scattering approach.

  13. Improvement of program to calculate electronic properties of narrow band gap materials

    NASA Technical Reports Server (NTRS)

    Patterson, James D.; Abdelhakiem, Wafaa

    1991-01-01

    The program was improved by reprogramming it so it will run on both a SUN and a VAX. Also it is easily transportable as it is on a disk for use on a SUN. A computer literature search resulted in some improved parameters for Hg(1-x)Cd(x)Te and a table of parameters for Hg(1-x)Zn(x)Te. The effects of neutral defects were added to the program, and it was found, as expected, that they contribute very little to the mobility at temperatures of interest. The effect were added of varying the following parameters: dielectric constants, screening parameters, disorder energies, donor and acceptor concentrations, momentum matrix element, different expressions for energy gap, and transverse effective charge.

  14. Phase diagram, correlation gap, and critical properties of the Coulomb glass

    NASA Astrophysics Data System (ADS)

    Palassini, Matteo; Goethe, Martin

    2009-03-01

    We investigate the lattice Coulomb glass model in three dimensions via extensive Monte Carlo simulations. 1. No evidence for an equilibrium glass phase is found down to very low temperatures, contrary to mean-field predictions, although the correlation length increases rapidly near T=0. 2. The single-particle density of states near the Coulomb gap satisfies the scaling law g(e,T)=T^λf(e/T) with λ 2.2. 3. A charge-ordered phase exists at low disorder. The phase transition from the fluid to the charge ordered phase is consistent with the Random Field Ising universality class, which shows that the interaction is effectively screened at moderate temperature. Results from nonequilibrium simulations will also be briefly discussed. Reference: M.Goethe and M.Palassini, arXiv:0810.1047

  15. Phase diagram, correlation gap, and critical properties of the coulomb glass.

    PubMed

    Goethe, Martin; Palassini, Matteo

    2009-07-24

    We investigate the lattice Coulomb glass model in three dimensions via Monte Carlo simulations. No evidence for an equilibrium glass phase is found down to very low temperatures, although the correlation length increases rapidly near T = 0. A charge-ordered phase exists at low disorder. The transition to this phase is consistent with the random field Ising universality class, which shows that the interaction is effectively screened at moderate temperature. For large disorder, the single-particle density of states near the Coulomb gap satisfies the scaling relation g(epsilon, T) = T;{delta}f(|epsilon|/T) with delta = 2.01 +/- 0.05 in agreement with the prediction of Efros and Shklovskii. For decreasing disorder, a crossover to a larger effective exponent occurs due to the proximity of the charge-ordered phase.

  16. Reflectance properties of two-dimensional sonic band-gap crystals.

    PubMed

    Sanchis, L; Cervera, F; Sánchez-Dehesa, J; Sánchez-Pérez, J V; Rubio, C; Martínez-Sala, R

    2001-06-01

    An analysis of the reflectance of sonic band-gap crystals consisting of square arrays of rigid cylinders in air is presented. The standing wave formed in front of the structures is studied both experimentally and theoretically. Experiments have been performed with a mobile robotized microphone that obtains pressure maps on the plane perpendicular to the axes of the cylinders. Enhancements of the standing wave ratio (SWR) are observed in frequency regions where attenuation bands appear in zero-order transmission experiments. Also, the SWR presents oscillations that can be related to the finite dimension of the structure (Fabry-Perot effect). Both features are well described by calculations based on a double-scattering approach. PMID:11425100

  17. Self-assembly drives quantum dot photoluminescence.

    PubMed

    Plain, J; Sonnefraud, Y; Viste, P; Lérondel, G; Huant, S; Royer, P

    2009-03-01

    Engineering the spectral properties of quantum dots can be achieved by a control of the quantum dots organization on a substrate. Indeed, many applications of quantum dots as LEDs are based on the realization of a 3D architecture of quantum dots. In this contribution, we present a systematic study of the quantum dot organization obtained on different chemically modified substrates. By varying the chemical affinity between the quantum dots and the substrate, the quantum dot organization is strongly modified from the 2D monolayer to the 3D aggregates. Then the photoluminescence of the different obtained samples has been systematically studied and correlated with the quantum dot film organization. We clearly show that the interaction between the substrate and the quantum dot must be stronger than the quantum dot-quantum dot interaction to avoid 3D aggregation and that these organization strongly modified the photoluminescence of the film rather than intrinsic changes of the quantum dot induced by pure surface chemistry.

  18. Structure and photoluminescent properties of green-emitting terbium-doped GdV1-x Px O4 phosphor prepared by solution combustion method.

    PubMed

    Motloung, S J; Shaat, S K K; Tshabalala, K G; Ntwaeaborwa, O M

    2016-08-01

    Terbium-doped gadolinium orthovanadate (GdVO4 :Tb(3+) ), orthophosphate monohydrate (GdPO4 ·H2 O:Tb(3+) ) and orthovanadate-phosphate (GdV,PO4 :Tb(3+) ) powder phosphors were synthesized using a solution combustion method. X-Ray diffraction analysis confirmed the formation of crystalline GdVO4 , GdPO4 ·H2 O and GdV,PO4 . Scanning electron microscopy images showed that the powder was composed of an agglomeration of particles of different shapes, ranging from spherical to oval to wire-like structures. The chemical elements present were confirmed by energy dispersive spectroscopy, and the stretching mode frequencies were determined by Fourier transform infrared spectroscopy. UV-visible spectroscopy spectra showed a strong absorption band with a maximum at 200 nm assigned to the absorption of VO4 (3-) and minor excitation bands assigned to f → f transitions of Tb(3+) . Four characteristic emission peaks were observed at 491, 546, 588 and 623 nm, and are attributed to (5) D4  → (7) Fj (j = 6, 5, 4 and 3). The photoluminescent prominent green emission peak ((5) D4  → (7) F5 ) was centred at 546 nm. The structure and possible mechanism of light emission from GdV1-x Px O4 :% Tb(3+) are discussed. Copyright © 2016 John Wiley & Sons, Ltd.

  19. Diversity of electronic transitions and photoluminescence properties of p-type cuprous oxide films: A temperature-dependent spectral transmittance study

    SciTech Connect

    Yu, W. L. E-mail: zghu@ee.ecnu.edu.cn; Lin, Y. Z.; Zhu, X. W.; Cai, S. S.; Chen, L. L.; Shao, H. H.; Hu, Z. G. E-mail: zghu@ee.ecnu.edu.cn; Han, M. J.

    2015-01-28

    Cuprous oxide films have been deposited on quartz substrates by a sol-gel method under various annealing temperatures. The X-ray diffraction analysis and Raman scattering show that all the films are of pure Cu{sub 2}O phase. From comparison of photoluminescence with 488 and 325 nm laser excitations, the electronic transition energies and intensities present the annealing-temperature dependent behavior. The electronic band structures of the Cu{sub 2}O film annealed at 800 °C, especially for the contribution of exciton series and high energy transitions, have been investigated by temperature dependent transmittance. The extracted refraction index and the high frequency dielectric constant both abruptly decrease until the temperature rises up to 100 K. Six transitions can be clearly identified and the red shift trend of E{sub o3}-E{sub o5} transition energies with increasing the temperature can be found. Moreover, the anomalous behavior takes place at about 200 K from the E{sub o6} transition. The singularities indicate that the change in the crystalline and electronic band structure occurs as the temperature near 100 K and 200 K for the film.

  20. Facile green fabrication of nanostructure ZnO plates, bullets, flower, prismatic tip, closed pine cone: Their antibacterial, antioxidant, photoluminescent and photocatalytic properties

    NASA Astrophysics Data System (ADS)

    Madan, H. R.; Sharma, S. C.; Udayabhanu; Suresh, D.; Vidya, Y. S.; Nagabhushana, H.; Rajanaik, H.; Anantharaju, K. S.; Prashantha, S. C.; Sadananda Maiya, P.

    2016-01-01

    Green synthesis of multifunctional Zinc oxide nanoparticles (NPs) with a variety of morphologies were achieved by low temperature solution combustion route employing neem (Azadirachta indica) extract as fuel. The nanoparticles were characterized by PXRD, FTIR, XPS, Raman and UV-Visible spectroscopic studies. The Morphologies were studied by SEM and TEM analysis. The NPs were subjected for photoluminescence, photocatalytic, antibacterial and antioxidant activity studies. PXRD pattern confirmed the hexagonal wurtzite structure of the product. SEM images indicated the transformation of mushroom like hexagonal disks to bullets, buds, cones, bundles and closed pine cone structured NPs with increase in the concentration of neem extract in reaction mixture. The NPs exhibited prominent green emission due to the presence of intrinsic defect centers. The as-formed bullet shaped ZnO with 4 ml of neem extract was found to decolorize Methylene blue (MB) under Sunlight and UV light irradiation. The antibacterial studies indicated that ZnO NPs of concentration 500, 750 and 1000 μg resulted in significant antibacterial activity on Klebsiella aerogenes and Staphylococcus aureus but not against Escherichia coli and Pseudomonas aeruginosa in agar well diffusion method. Further, ZnO NPs exhibited significant antioxidant activity against scavenging DPPH free radicals. The current investigation demonstrated green engineering method for the synthesis of multifunctional ZnO NPs with interesting morphologies using neem extract.

  1. Effects of post-annealing treatment on the structure and photoluminescence properties of CdS/PS nanocomposites prepared by sol-gel method

    NASA Astrophysics Data System (ADS)

    Zhang, Hong-yan

    2016-03-01

    CdS nanocrystals have been successfully grown on porous silicon (PS) by sol-gel method. The plan-view field emission scanning electron microscopy (FESEM) shows that the pore size of PS is smaller than 5 μm in diameter and the agglomerates of CdS are broadly distributed on the surface of PS substrate. With the increase of annealing time, the CdS nanoparticles grow in both length and diameter along the preferred orientation. The cross-sectional FESEM images of ZnO/PS show that CdS nanocrystals are uniformly penetrated into all PS layers and adhere to them very well. photoluminescence (PL) spectra demonstrate that the intensity of PL peak located at about 425 nm has almost no change after the annealing time increases. The range of emission wavelength of CdS/PS is from 425 nm to 455 nm and the PL intensity is decreasing with the annealing temperature increasing from 100 °C to 200 °C.

  2. Photoluminescent mixed ligand complexes of CuX (X = Cl, Br, I) with PPh3 and a polydentate imino-pyridyl ligand - Syntheses, structural variations and catalytic property

    NASA Astrophysics Data System (ADS)

    Ghorai, Anupam; Mondal, Jahangir; Patra, Goutam K.

    2015-10-01

    Three ternary copper(I) complexes [CuI2Cl2(L1)(PPh3)4] (1), [CuI2Br2(L1) (PPh3)4] (2) and [CuI2(μ-I)2 (μ-L1) (PPh3)2]n (3) have been prepared by reactions of CuX (X = Cl, Br and I) with PPh3 and the polydentate imino-pyridyl ligand L1. These complexes have been characterized by elemental analysis, IR, UV-Vis, NMR and X-ray crystallography. From single crystal structural analysis it has been found that complexes 1 and 2 are homo-dinuclear having non-bridging halide ions whereas complex 3 is a 1-D zig-zag co-ordination polymer containing bridged iodide ions. Complexes 1, 2 and 3 are photoluminescent at room temperature in chloroform whereas ligand L1 is non-emissive. The E½ values of the CuIsbnd CuII couple of 1, 2 and 3 are 0.98 V, 0.92 V and 0.42 V respectively (vs Ag/AgCl in 1 M KCl, scan rate 100 mV s-1). All three complexes function as effective catalysts for the synthesis of 2-substituted benzoxazoles.

  3. Facile green fabrication of nanostructure ZnO plates, bullets, flower, prismatic tip, closed pine cone: Their antibacterial, antioxidant, photoluminescent and photocatalytic properties.

    PubMed

    Madan, H R; Sharma, S C; Udayabhanu; Suresh, D; Vidya, Y S; Nagabhushana, H; Rajanaik, H; Anantharaju, K S; Prashantha, S C; Sadananda Maiya, P

    2016-01-01

    Green synthesis of multifunctional Zinc oxide nanoparticles (NPs) with a variety of morphologies were achieved by low temperature solution combustion route employing neem (Azadirachta indica) extract as fuel. The nanoparticles were characterized by PXRD, FTIR, XPS, Raman and UV-Visible spectroscopic studies. The Morphologies were studied by SEM and TEM analysis. The NPs were subjected for photoluminescence, photocatalytic, antibacterial and antioxidant activity studies. PXRD pattern confirmed the hexagonal wurtzite structure of the product. SEM images indicated the transformation of mushroom like hexagonal disks to bullets, buds, cones, bundles and closed pine cone structured NPs with increase in the concentration of neem extract in reaction mixture. The NPs exhibited prominent green emission due to the presence of intrinsic defect centers. The as-formed bullet shaped ZnO with 4ml of neem extract was found to decolorize Methylene blue (MB) under Sunlight and UV light irradiation. The antibacterial studies indicated that ZnO NPs of concentration 500, 750 and 1000μg resulted in significant antibacterial activity on Klebsiella aerogenes and Staphylococcus aureus but not against Escherichia coli and Pseudomonas aeruginosa in agar well diffusion method. Further, ZnO NPs exhibited significant antioxidant activity against scavenging DPPH free radicals. The current investigation demonstrated green engineering method for the synthesis of multifunctional ZnO NPs with interesting morphologies using neem extract.

  4. Facile green fabrication of nanostructure ZnO plates, bullets, flower, prismatic tip, closed pine cone: Their antibacterial, antioxidant, photoluminescent and photocatalytic properties.

    PubMed

    Madan, H R; Sharma, S C; Udayabhanu; Suresh, D; Vidya, Y S; Nagabhushana, H; Rajanaik, H; Anantharaju, K S; Prashantha, S C; Sadananda Maiya, P

    2016-01-01

    Green synthesis of multifunctional Zinc oxide nanoparticles (NPs) with a variety of morphologies were achieved by low temperature solution combustion route employing neem (Azadirachta indica) extract as fuel. The nanoparticles were characterized by PXRD, FTIR, XPS, Raman and UV-Visible spectroscopic studies. The Morphologies were studied by SEM and TEM analysis. The NPs were subjected for photoluminescence, photocatalytic, antibacterial and antioxidant activity studies. PXRD pattern confirmed the hexagonal wurtzite structure of the product. SEM images indicated the transformation of mushroom like hexagonal disks to bullets, buds, cones, bundles and closed pine cone structured NPs with increase in the concentration of neem extract in reaction mixture. The NPs exhibited prominent green emission due to the presence of intrinsic defect centers. The as-formed bullet shaped ZnO with 4ml of neem extract was found to decolorize Methylene blue (MB) under Sunlight and UV light irradiation. The antibacterial studies indicated that ZnO NPs of concentration 500, 750 and 1000μg resulted in significant antibacterial activity on Klebsiella aerogenes and Staphylococcus aureus but not against Escherichia coli and Pseudomonas aeruginosa in agar well diffusion method. Further, ZnO NPs exhibited significant antioxidant activity against scavenging DPPH free radicals. The current investigation demonstrated green engineering method for the synthesis of multifunctional ZnO NPs with interesting morphologies using neem extract. PMID:26241826

  5. Electronic Structures, Bonding Configurations, and Band-Gap-Opening Properties of Graphene Binding with Low-Concentration Fluorine

    SciTech Connect

    Duan, Yuhua; Stinespring, Charter D.; Chorpening, Benjamin

    2015-06-18

    To better understand the effects of low-level fluorine in graphene-based sensors, first-principles density functional theory (DFT) with van der Waals dispersion interactions has been employed to investigate the structure and impact of fluorine defects on the electrical properties of single-layer graphene films. The results show that both graphite-2H and graphene have zero band gaps. When fluorine bonds to a carbon atom, the carbon atom is pulled slightly above the graphene plane, creating what is referred to as a CF defect. The lowest-binding energy state is found to correspond to two CF defects on nearest neighbor sites, with one fluorine above the carbon plane and the other below the plane. Overall this has the effect of buckling the graphene. The results further show that the addition of fluorine to graphene leads to the formation of an energy band (BF) near the Fermi level, contributed mainly from the 2p orbitals of fluorine with a small contribution from the porbitals of the carbon. Among the 11 binding configurations studied, our results show that only in two cases does the BF serve as a conduction band and open a band gap of 0.37 eV and 0.24 eV respectively. The binding energy decreases with decreasing fluorine concentration due to the interaction between neighboring fluorine atoms. The obtained results are useful for sensor development and nanoelectronics.

  6. Electronic Structures, Bonding Configurations, and Band-Gap-Opening Properties of Graphene Binding with Low-Concentration Fluorine

    DOE PAGESBeta

    Duan, Yuhua; Stinespring, Charter D.; Chorpening, Benjamin

    2015-06-18

    To better understand the effects of low-level fluorine in graphene-based sensors, first-principles density functional theory (DFT) with van der Waals dispersion interactions has been employed to investigate the structure and impact of fluorine defects on the electrical properties of single-layer graphene films. The results show that both graphite-2H and graphene have zero band gaps. When fluorine bonds to a carbon atom, the carbon atom is pulled slightly above the graphene plane, creating what is referred to as a CF defect. The lowest-binding energy state is found to correspond to two CF defects on nearest neighbor sites, with one fluorine abovemore » the carbon plane and the other below the plane. Overall this has the effect of buckling the graphene. The results further show that the addition of fluorine to graphene leads to the formation of an energy band (BF) near the Fermi level, contributed mainly from the 2p orbitals of fluorine with a small contribution from the porbitals of the carbon. Among the 11 binding configurations studied, our results show that only in two cases does the BF serve as a conduction band and open a band gap of 0.37 eV and 0.24 eV respectively. The binding energy decreases with decreasing fluorine concentration due to the interaction between neighboring fluorine atoms. The obtained results are useful for sensor development and nanoelectronics.« less

  7. The lithium content and other properties of F2-G5 giants in the Hertzsprung Gap

    NASA Technical Reports Server (NTRS)

    Wallerstein, George; Bohm-Vitense, Erika; Vanture, Andrew D.; Gonzalez, Guillermo

    1994-01-01

    As stars of 2-5 solar mass evolve across the Hertzsprung Gap they should first deplete their surface lithium by convective dilution and then, when convection penetrates deeper, begin to bring CN processed material to their surfaces. To investigate this process we have observed 52 giants, 25 of which have known C/N ratios, for their Li abundances. After eliminating four stars that may actually be dwarfs and including the two components of Capella analyzed by Pilachowski and Sowell we have compared our (Li/Fe) ratios with models of Swenson. For stars showing v sin i greater than 50 km/s we find (Li/Fe) to be uneffected by mixing for B - V less than 0.7 as predicted. For stars cooler than B - V = 0.7 both v sin i and (Li/Fe) drop to smaller values. For the sharp lined stars (v sin i less than 50 km/s) we find a drop in Li between B - V = 0.45 and 0.60 which cannot be understood in terms of dilution by convection. Various possible causes of such an early depletion or dilution of surface Li are discussed including diffusion at the base of the convection zone, mass loss possibly enhanced by pulsation, and magnetic activity as in the magnetic A and B type stars. The models of Richer & Michaud (1993) with diffusion point toward a satisfactory solution. A few giants with low v sin i values stand out with much higher than expected (Li/Fe) values despite their cool effective temperatures. We do not understand why those stars have not depleted their lithium as have most giants of similar color. The correlation of (N/C) with (Li/Fe) follows expectations in so far as almost all stars with enhanced (N/C) have depleted their Li as well.

  8. Analysis of photonic band gap in dispersive properties of tunable three-dimensional photonic crystals doped by magnetized plasma

    SciTech Connect

    Zhang HaiFeng; Liu Shaobin; Yang Huan; Kong Xiangkun

    2013-03-15

    In this paper, the magnetooptical effects in dispersive properties for two types of three-dimensional magnetized plasma photonic crystals (MPPCs) containing homogeneous dielectric and magnetized plasma with diamond lattices are theoretically investigated for electromagnetic (EM) wave based on plane wave expansion (PWE) method, as incidence EM wave vector is parallel to the external magnetic field. The equations for two types of MPPCs with diamond lattices (dielectric spheres immersed in magnetized plasma background or vice versa) are theoretically deduced. The influences of dielectric constant, plasma collision frequency, filling factor, the external magnetic field, and plasma frequency on the dispersive properties for both types of structures are studied in detail, respectively, and some corresponding physical explanations are also given. From the numerical results, it has been shown that the photonic band gaps (PBGs) for both types of MPPCs can be manipulated by plasma frequency, filling factor, the external magnetic field, and the relative dielectric constant of dielectric, respectively. Especially, the external magnetic field can enlarge the PBG for type-2 structure (plasma spheres immersed in dielectric background). However, the plasma collision frequency has no effect on the dispersive properties of two types of three-dimensional MPPCs. The locations of flatbands regions for both types of structures cannot be tuned by any parameters except for plasma frequency and the external magnetic field. The analytical results may be informative and of technical use to design the MPPCs devices.

  9. Analysis of photonic band gap in dispersive properties of tunable three-dimensional photonic crystals doped by magnetized plasma

    NASA Astrophysics Data System (ADS)

    Zhang, Hai-Feng; Liu, Shao-Bin; Yang, Huan; Kong, Xiang-Kun

    2013-03-01

    In this paper, the magnetooptical effects in dispersive properties for two types of three-dimensional magnetized plasma photonic crystals (MPPCs) containing homogeneous dielectric and magnetized plasma with diamond lattices are theoretically investigated for electromagnetic (EM) wave based on plane wave expansion (PWE) method, as incidence EM wave vector is parallel to the external magnetic field. The equations for two types of MPPCs with diamond lattices (dielectric spheres immersed in magnetized plasma background or vice versa) are theoretically deduced. The influences of dielectric constant, plasma collision frequency, filling factor, the external magnetic field, and plasma frequency on the dispersive properties for both types of structures are studied in detail, respectively, and some corresponding physical explanations are also given. From the numerical results, it has been shown that the photonic band gaps (PBGs) for both types of MPPCs can be manipulated by plasma frequency, filling factor, the external magnetic field, and the relative dielectric constant of dielectric, respectively. Especially, the external magnetic field can enlarge the PBG for type-2 structure (plasma spheres immersed in dielectric background). However, the plasma collision frequency has no effect on the dispersive properties of two types of three-dimensional MPPCs. The locations of flatbands regions for both types of structures cannot be tuned by any parameters except for plasma frequency and the external magnetic field. The analytical results may be informative and of technical use to design the MPPCs devices.

  10. Photoluminescence by Interstellar Dust

    NASA Astrophysics Data System (ADS)

    Vijh, U. P.

    2005-08-01

    In this dissertation, we report on our study of interstellar dust through the process of photoluminescence (PL). We present the discovery of a new band of dust PL, blue luminescence (BL) with λpeak˜370 nm in the proto-planetary nebula known as the Red Rectangle (RR). We attribute this to fluorescence by small, 3-4-ringed polycyclic aromatic hydrocarbon (PAH) molecules. Further analysis reveals additional independent evidence for the presence of small PAHs in this nebula. Detection of BL using long-slit spectroscopic observations in other ordinary reflection nebulae suggests that the BL carrier is an ubiquitous component of the ISM and is not restricted to the particular environment of the RR. We present the spatial distribution of the BL in these nebulae and find that the BL is spatially correlated with IR emission structures attributed to aromatic emission features (AEFs), attributed to PAHs. The carrier of the dust-associated photoluminescence process causing the extended red emission (ERE), known now for over twenty five years, remains unidentified. We constrain the character of the ERE carrier by determining the wavelengths of the radiation that initiates the ERE -- λ < 118 nm. We note that under interstellar conditions most PAH molecules are ionized to the di-cation stage by photons with E > 10.5 eV and that the electronic energy level structure of PAH di-cations is consistent with fluorescence in the wavelength band of the ERE. In the last few chapters of the dissertation we present first results from ongoing work: i) Using narrow-band imaging, we present the optical detection of the circum-binary disk of the RR in the light of the BL, and show that the morphology of the BL and ERE emissions in the RR nebula are almost mutually exclusive. It is very suggestive to attribute them to different ionization stages of the same family of carriers such as PAH molecules. ii) We also present a pure spectrum of the BL free of scattered light, resolved into seven

  11. Effect of Electronic Acceptor Segments on Photophysical Properties of Low-Band-Gap Ambipolar Polymers

    PubMed Central

    Li, Yuanzuo; Cui, Jingang; Zhao, Jianing; Liu, Jinglin; Song, Peng; Ma, Fengcai

    2013-01-01

    Stimulated by a recent experimental report, charge transfer and photophysical properties of donor-acceptor ambipolar polymer were studied with the quantum chemistry calculation and the developed 3D charge difference density method. The effects of electronic acceptor strength on the structure, energy levels, electron density distribution, ionization potentials, and electron affinities were also obtained to estimate the transporting ability of hole and electron. With the developed 3D charge difference density, one visualizes the charge transfer process, distinguishes the role of molecular units, and finds the relationship between the role of DPP and excitation energy for the three polymers during photo-excitation. PMID:23365549

  12. Spectral and thermodynamic properties of electrons in mobility gap states of covalent glasses

    NASA Astrophysics Data System (ADS)

    Klinger, M. I.; Karpov, V. G.

    1981-07-01

    Spectral and thermodynamic properties of electrons (holes) in covalent semiconducting glasses are considered in which self-trapping of electron (hole) pairs is realized with negative effective correlation energy U -. Unlike the Anderson model, electron (hole) pairing is restricted to a small part of the glass bonds. Ranges of the U - values are found in which either pair effects (suppression of paramagnetism etc.) or single-particle effects predominate; the concentration of the pair states and of the occupied ones can roughly be estimated and can be fairly high. The problem of the coexistence of the Fermi level pinning and effective diamagnetism in glasses is discussed. Some related effects are briefly considered.

  13. Study of photoluminescence and thermoluminescence properties of BaAl2O4 (Eu2+, Dy3+) phosphor synthesized by solution combustion method

    NASA Astrophysics Data System (ADS)

    Pathak, Pushpraj; Kurchania, Rajnish

    2016-10-01

    Eu and Dy co-doped barium aluminate phosphor was successfully synthesized by combustion method using urea as a fuel. Phase formation was confirmed by powder X-ray diffraction (PXRD) analysis. The calculated average crystallite size was found to be ~34.62 nm. Scanning electron microscopy (SEM) images acquired at different (low and high) magnifications reveal that the crystallites have no uniform shape and size. This was due to the non-uniform distribution of temperature and mass flow in the combustion technique. Fourier Transform Infra-red (FTIR) spectrum was recorded to confirm the phase formation and also to identify any impurity if present in the prepared phosphor. Photoluminescence (PL) measurement was carried out to investigate the incorporation of dopant into the host lattice. Thermoluminescence (TL) behaviour of synthesized phosphor was studied after the irradiation with Cobalt-60 gamma rays (Eavg=1.25 MeV) as well as 6 and 16 MV (Mega Voltage) X-ray photons, at various dose levels. The glow curves of irradiated samples exhibit only one peak at 115 °C at each dose level. With the increases of radiation dose an increase in total intensity has been observed. No appreciable shift in peak positions has been observed. Trapping parameters were evaluated to understand the characteristics of prepared phosphor. A simple glow peak with relatively high intensity is one of the important factors, which make this phosphor useful for monitoring the ionizing radiations in nuclear industries, gamma irradiators, high energy accelerators, nuclear reactors etc. where medium and high level of exposure is involved. It could also be applicable for accidental and retrospective dose assessment.

  14. 1D to 3D and Chiral to Noncentrosymmetric Metal-Organic Complexes Controlled by the Amount of DEF Solvent: Photoluminescent and NLO Properties.

    PubMed

    Wen, Yuehong; Sheng, Tianlu; Zhuo, Chao; Zhu, Xiaoquan; Hu, Shengmin; Cao, Wenhai; Li, Haoran; Zhang, Hao; Wu, Xintao

    2016-05-01

    A mixture of 2D and 1D metal-organic complexes, [ZnL(H2O)2·G1·DEF·2H2O]n (1a: G1 = naphthalene-2,7-disulfonate; DEF = N,N-diethylformamide) and [ZnL(H2O)3·G1·DEF·2H2O]n (2), has been prepared from a hydrogenated Schiff base L and Zn(II) in a DEF-contained solvent system under mild conditions. The yields of 1a and 2 are equivalent; however, they can be tuned by varying the amount of DEF solvent. Increasing the use of DEF tends to form pure 1a, while decreasing it generates 2. Without DEF, another novel 3D four-connected CdSO4 (cds) framework [ZnL(H2O)2·G1·2H2O]n (3) composed of alternated right-handed and left-handed helical chains has been constructed. The amount of DEF solvent has a significant impact on the diverse coordination architectures of 1-3, which is rare in the preparation of metal-organic complexes. The photoluminescence of complexes 1-3 along with naphthalene-2,7-disulfonate has been investigated in the solid state. The luminescent emission of G1 was enhanced greatly after being confined into metal-organic networks. In addition, complexes 1-3 display second-harmonic generation efficiencies, which are approximately 0.58, 0.42, 0.32, and 0.52 times as much as that of potassium dihydrogen phosphate.

  15. 1D to 3D and Chiral to Noncentrosymmetric Metal-Organic Complexes Controlled by the Amount of DEF Solvent: Photoluminescent and NLO Properties.

    PubMed

    Wen, Yuehong; Sheng, Tianlu; Zhuo, Chao; Zhu, Xiaoquan; Hu, Shengmin; Cao, Wenhai; Li, Haoran; Zhang, Hao; Wu, Xintao

    2016-05-01

    A mixture of 2D and 1D metal-organic complexes, [ZnL(H2O)2·G1·DEF·2H2O]n (1a: G1 = naphthalene-2,7-disulfonate; DEF = N,N-diethylformamide) and [ZnL(H2O)3·G1·DEF·2H2O]n (2), has been prepared from a hydrogenated Schiff base L and Zn(II) in a DEF-contained solvent system under mild conditions. The yields of 1a and 2 are equivalent; however, they can be tuned by varying the amount of DEF solvent. Increasing the use of DEF tends to form pure 1a, while decreasing it generates 2. Without DEF, another novel 3D four-connected CdSO4 (cds) framework [ZnL(H2O)2·G1·2H2O]n (3) composed of alternated right-handed and left-handed helical chains has been constructed. The amount of DEF solvent has a significant impact on the diverse coordination architectures of 1-3, which is rare in the preparation of metal-organic complexes. The photoluminescence of complexes 1-3 along with naphthalene-2,7-disulfonate has been investigated in the solid state. The luminescent emission of G1 was enhanced greatly after being confined into metal-organic networks. In addition, complexes 1-3 display second-harmonic generation efficiencies, which are approximately 0.58, 0.42, 0.32, and 0.52 times as much as that of potassium dihydrogen phosphate. PMID:27093469

  16. Characterization of PVT Grown ZnSe by Low Temperature Photoluminescence

    NASA Technical Reports Server (NTRS)

    Wang, Ling Jun

    1998-01-01

    ZnSe, a II-VI semiconductor with a large direct band gap of 2.7 eV at room temperature and 2.82 eV at 10 K, is considered a promising material for optoelectric applications in the blue-green region of the spectrum. Photoemitting devices and diode laser action has been demonstrated as a result of decades of research. A key issue in the development of II-VI semiconductors is the control of the concentration of the various impurities. The II-VI semiconductors seem to defy the effort of high level doping due to the well known self compensation of the donors and the acceptors. A good understanding of roles of the impurities and the behavior of the various intrinsic defects such as vacancies, interstitials and their complexes with impurities is necessary in the development and application of these materials. Persistent impurities such as Li and Cu have long played a central role in the photoelectronic properties of many II-VI compounds, particularly ZnSe. The shallow centers which may promote useful electrical conductivity are of particular interest. They contribute the richly structured near gap edge luminescence, containing weak to moderate phonon coupling and therefore very accessible information about the energy states of the different centers. Significance of those residual impurities which may contribute such centers in II-VI semiconductors must be fully appreciated before improved control of their electrical properties may be possible. Low temperature photoluminescence spectroscopy is an important source of information and a useful tool of characterization of II-VI semiconductors such as ZnSe. The low temperature photoluminescence spectrum of a ZnSe single crystal typically consists of a broad band emission peaking at 2.34 eV, known as the Cu-green band, and some very sharp lines near the band gap. These bands and lines are used to identify the impurity ingredients and the defects. The assessment of the quality of the crystal based on the photoluminescence

  17. Bridging the gap between structures and properties: An investigation and evaluation of students' representational competence

    NASA Astrophysics Data System (ADS)

    Underwood, Sonia Miller

    The heart of learning chemistry is the ability to connect a compound's structure to its function; Lewis structures provide an essential link in this process. In many cases, their construction is taught using an algorithmic approach, containing a set of step-by-step rules. We believe that this approach is in direct conflict with the precepts of meaningful learning. From a sequential, mixed methods study, we found that students have much difficulty constructing these structures and that the step-by-step rules do not make use of students' relevant prior knowledge. This causes students to develop "home grown" rules when unsure of how to progress with the construction process. It also became clear that most students are uncertain of the importance of Lewis structures since they perceive them as being useful only for obtaining structural information but not property information. Using responses from student interviews and open ended questions, the Information from Lewis Structures Survey (ILSS) was developed, validated, and found reliable to assess students' representational competence by determining their understanding of the purpose of Lewis structures. Since students had many problems with the relationship of structures and properties, an alternative curriculum was evaluated to determine if it could help students develop a more meaningful understanding of this process. This instruction was part of a larger NSF-funded general chemistry curriculum redesign called Chemistry, Life, the Universe and Everything (CLUE). Using a control and treatment group, the effectiveness of this new curriculum was evaluated for two main aspects: 1. the students' ability to construct Lewis structures using OrganicPad and 2. the students' representational competence using the ILSS. Through four main studies (a pilot study, instructor effect study, main study, and retention study), we found that the CLUE curriculum helps students develop more expert-like strategies for constructing Lewis

  18. Influence of Au nanoparticles on the photoluminescent and electrical properties of Bi{sub 3.6}Eu{sub 0.4}Ti{sub 3}O{sub 12} ferroelectric thin films

    SciTech Connect

    Su, Li; Qin, Ni E-mail: stsbdh@mail.sysu.edu.cn; Xie, Wei; Fu, Jianhui; Bao, Dinghua E-mail: stsbdh@mail.sysu.edu.cn

    2014-07-21

    Au-doped Bi{sub 3.6}Eu{sub 0.4}Ti{sub 3}O{sub 12} (BET) thin films were prepared on fused silica and Pt/Ti/SiO{sub 2}/Si substrates by a chemical solution deposition method. The existence of Au nanoparticles (NPs) has been confirmed by X-ray diffraction, X-ray photoelectron spectroscopy, and transmission electron microscope analysis. Enhanced photoluminescence (PL) of Eu{sup 3+} ions was obtained in a wide range of Au doping level. Role of the Au NPs in the PL enhancement was investigated by means of optical absorption, excitation, and emission spectra, as well as decay lifetime measurements. The results indicated that the intra-4f transition of Eu{sup 3+} ions can be intensively activated by the coupling of the charge transfer band of BET with the {sup 5}D{sub 0} state of Eu{sup 3+} ions. The influence of Au NPs on the PL properties of Eu{sup 3+} ions in the present thin films was attributed to the band bending at Au/BET interface and the localized surface plasma resonance absorption of Au NPs in the visible light region. The dielectric and ferroelectric properties of Au-doped BET thin films were investigated as well.

  19. Thin-Film Photoluminescent Properties and the Atomistic Model of Mg2TiO4 as a Non-rare Earth Matrix Material for Red-Emitting Phosphor

    NASA Astrophysics Data System (ADS)

    Huang, Chieh-Szu; Chang, Ming-Chuan; Huang, Cheng-Liang; Lin, Shih-kang

    2016-08-01

    Thin-film electroluminescent devices are promising solid-state lighting devices. Red light-emitting phosphor is the key component to be integrated with the well-established blue light-emitting diode chips for stimulating natural sunlight. However, environmentally hazardous rare-earth (RE) dopants, e.g. Eu2+ and Ce2+, are commonly used for red-emitting phosphors. Mg2TiO4 inverse spinel has been reported as a promising matrix material for "RE-free" red light luminescent material. In this paper, Mg2TiO4 inverse spinel is investigated using both experimental and theoretical approaches. The Mg2TiO4 thin films were deposited on Si (100) substrates using either spin-coating with the sol-gel process, or radio frequency sputtering, and annealed at various temperatures ranging from 600°C to 900°C. The crystallinity, microstructures, and photoluminescent properties of the Mg2TiO4 thin films were characterized. In addition, the atomistic model of the Mg2TiO4 inverse spinel was constructed, and the electronic band structure of Mg2TiO4 was calculated based on density functional theory. Essential physical and optoelectronic properties of the Mg2TiO4 luminance material as well as its optimal thin-film processing conditions were comprehensively reported.

  20. Microwave sol–gel synthesis and upconversion photoluminescence properties of CaGd{sub 2}(WO{sub 4}){sub 4}:Er{sup 3+}/Yb{sup 3+} phosphors with incommensurately modulated structure

    SciTech Connect

    Lim, Chang Sung; Aleksandrovsky, Aleksandr; Molokeev, Maxim; Oreshonkov, Aleksandr; Atuchin, Victor

    2015-08-15

    CaGd{sub 2−x}(WO{sub 4}){sub 4}:Er{sup 3+}/Yb{sup 3+} phosphors with the doping concentrations of Er{sup 3+} and Yb{sup 3+} (x=Er{sup 3+}+Yb{sup 3+}, Er{sup 3+}=0.05, 0.1, 0.2 and Yb{sup 3+}=0.2, 0.45) have been successfully synthesized by the microwave sol–gel method. The crystal structure of CaGd{sub 2−x}(WO{sub 4}){sub 4}:Er{sup 3+}/Yb{sup 3+} tungstates have been refined, and upconversion photoluminescence properties have been investigated. The synthesized particles, being formed after the heat-treatment at 900 °C for 16 h, showed a well crystallized morphology. Under the excitation at 980 nm, CaGd{sub 2}(WO{sub 4}){sub 4}:Er{sup 3+}/Yb{sup 3+} particles exhibited a strong 525-nm and a weak 550-nm emission bands in the green region and a very weak 655-nm emission band in the red region. The Raman spectrum of undoped CaGd{sub 2}(WO{sub 4}){sub 4} revealed about 12 narrow lines. The strongest band observed at 903 cm{sup −1} was assigned to the ν{sub 1} symmetric stretching vibration of WO{sub 4} tetrahedrons. The spectra of the samples doped with Er and Yb obtained under the 514.5 nm excitation were dominated by Er{sup 3+} luminescence preventing the recording of these samples Raman spectra. Concentration quenching of the erbium luminescence at {sup 2}H{sub 11/2}→{sup 4}I{sub 15/2} transition is weak in the range of erbium doping level x{sub Er}=0.05–0.2, while, for transition {sup 4}S{sub 3/2}→{sup 4}I{sub 15/2}, the signs of concentration quenching become pronounced at x{sub Er}=0.2. - Graphical abstract: CaGd{sub 2−x}(WO{sub 4}){sub 4}:Er{sup 3+}/Yb{sup 3+} phosphors with the doping concentrations of Er{sup 3+} and Yb{sup 3+} (x=Er{sup 3+}+Yb{sup 3+}, Er{sup 3+}=0.05, 0.1, 0.2 and Yb{sup 3+}=0.2, 0.45) have been successfully synthesized by the microwave sol–gel method and the crystal structure refinement, and upconversion photoluminescence properties have been investigated. - Highlights: • CaGd{sub 2−x}(WO{sub 4}){sub 4}:Er{sup 3+}/Yb

  1. Synthesis and photoluminescence properties of Dy{sup 3+} doped white light emitting CdTa{sub 2}O{sub 6} phosphors

    SciTech Connect

    İlhan, Mustafa; Ekmekçi, Mete Kaan

    2015-03-15

    The undoped and CdTa{sub 2}O{sub 6}:Dy{sup 3+} (0.2≤x≤2.0 mol%) phosphors were synthesized at 1100 °C for 12 h by the conventional solid state reaction method. The synthesized CdTa{sub 2}O{sub 6}:Dy{sup 3+} phosphors were characterized by X-ray diffraction (XRD), Scanning electron microscopy (SEM), Energy dispersive spectroscopy (EDS) and Photoluminescence (PL) analyses. The PL spectra showed the presence of excitation peaks between 310 and 440 nm due to the 4f–4f transitions of Dy{sup 3+}. The emission of Dy{sup 3+} ions at 353.0 nm excitation was observed at 487.1 nm (blue) and 577.8 nm (yellow) due to the {sup 4}F{sub 9/2}→{sup 6}H{sub 15/2} transitions and {sup 4}F{sub 9/2}→{sup 6}H{sub 13/2} transitions, respectively. The PL analysis results also showed that the emissions increase with the increasing Dy{sup 3+} ion content. The emissions increased with the doping concentration of up to 1 mol%, and above this level decreased due to concentration quenching effect. The CIE chromaticity color coordinates (x,y) of the CdTa{sub 2}O{sub 6}:Dy{sup 3+} phosphors were found to be in the white light region of the chromaticity diagram. - Graphical abstract: Emission spectra at λ{sub ex}=353.0 nm and CIE chromaticity coordinate diagram of CdTa{sub 2}O{sub 6}:Dy{sup 3+} phosphors. - Highlights: • Pure and CdTa{sub 2}O{sub 6}:Dy{sup 3+} was produced by solid state reaction method. • CdTa{sub 2}O{sub 6}:Dy{sup 3+} phosphor exhibited blue and yellow emissions due to the {sup 4}F{sub 9/2}→{sup 6}H{sub 15/2} and {sup 4}F{sub 9/2}→{sup 6}H{sub 13/2} transitions. • The CCT value for 1.0 mol% CdTa{sub 2}O{sub 6}:Dy{sup 3+} was 5133 K which was located in the cool white daylight region. • Dy{sup 3+} doped CdTa{sub 2}O{sub 6} phosphor has potential in the production of white LEDs.

  2. Room temperature ferromagnetism and photoluminescence in Cu-doped ZnO nanocrystals.

    PubMed

    Kong, Liming; Yu, Bin; Xu, Xiaoyong; Pan, Jing; Su, Yuanchang; Hu, Jingguo

    2014-08-01

    The Zn(1-x)Cu(x)O (x = 0.0-3.5%) nanocrystals have been synthesized by a simple sol-gel method. X-ray diffraction, optical absorption and photoluminescence measurements were employed to validate consistently the incorporation of Cu ions into the ZnO wurtzite lattice without formation of secondary phases for Zn(1-x)Cu(x)O (x < 2.0%). Meanwhile, it was found that the substituted Cu-doping leads to the reduction of the band gap and the appearance of the structured green emission. Magnetization measurement showed that the low Cu-doping (x < 1.0%) develops the ferromagnetism, but the high Cu-doping destroys sharply the ferromagnetism due to the formation of the antiferromagnetic coupling among the neighboring Cu ions. It is indicated that the rational Cu-doping can tune optical and magnetic properties in ZnO.

  3. Photoluminescence study in diaminobenzene functionalized graphene oxide

    SciTech Connect

    Gupta, Abhisek E-mail: cnssks@iacs.res.in; Saha, Shyamal K. E-mail: cnssks@iacs.res.in

    2014-10-15

    Being an excellent electronic material graphene is a very poor candidate for optoelectronic applications. One of the major strategies to develop the optical property in GO is the functionalization of graphene oxide (GO). In the present work GO sheets are functionalized by o-phenylenediamine to achieve diaminobenzene functionalized GO composite (DAB-GO). Formation of DAB-GO composite is further characterized by FTIR, UV, Raman studies. Excellent photoluminescence is observed in DAB-GO composite via passivation of the surface reactive sites by ring-opening amination of epoxides of GO.

  4. Photoluminescence study in diaminobenzene functionalized graphene oxide

    NASA Astrophysics Data System (ADS)

    Gupta, Abhisek; Saha, Shyamal K.

    2014-10-01

    Being an excellent electronic material graphene is a very poor candidate for optoelectronic applications. One of the major strategies to develop the optical property in GO is the functionalization of graphene oxide (GO). In the present work GO sheets are functionalized by o-phenylenediamine to achieve diaminobenzene functionalized GO composite (DAB-GO). Formation of DAB-GO composite is further characterized by FTIR, UV, Raman studies. Excellent photoluminescence is observed in DAB-GO composite via passivation of the surface reactive sites by ring-opening amination of epoxides of GO.

  5. Photoluminescence in anthracene and it's derivatives

    NASA Astrophysics Data System (ADS)

    Vyas, Arpita; Mirgane, Nitin A.; Moharil, S. V.; Muley, Aarti Iyer

    2016-05-01

    The anthracene and it's derivative 9-chloro acridine and Anthracene-9-ylmethylacetate have prepared in Poly vinyl alcohol(PVOH). Their photoluminescence properties have studied. The pure anthracene has an emission at 424 and 443nm. The intense peak is observed at 465nm and shoulder at 407nm. The derivatives of anthracene Anthracene-9-ylmethylacetate shows an emission around 440nm for the excitation at 393nm and 9-chloro acridine shows emission around 360nm for the excitation at 290nm. The major problem of this organic material is the stability. The composites prepared in the medium of PVOH are more stable.

  6. Structure, upconversion photoluminescence, and dielectric properties of Ho{sup 3+}- and Yb{sup 3+}-codoped tetragonal tungsten bronze Sr{sub 4}La{sub 2}Ti{sub 4}Nb{sub 6}O{sub 30}

    SciTech Connect

    Wei, T.; Li, C.P.; Zhou, Q.J.; Li, Z.P.; Li, P.; Wu, J.; Yang, X.F.

    2015-04-15

    Highlights: • TTB-type SLTN: Ho-Ybx with space group P4/mbm was determined. • UC photoluminescence of SLTN: Ho-Ybx ceramics was first reported. • Bright UC green emission was observed at room temperature. • Two-photon energy transfer process was confirmed for the UC processes. • Temperature stability of dielectric permittivity was improved for SLTN: Ho-Ybx. - Abstract: Ho{sup 3+}- and Yb{sup 3+}-codoped Sr{sub 4}La{sub 2}Ti{sub 4}Nb{sub 6}O{sub 30} (Sr{sub 4}La{sub 1.94–x}Ho{sub 0.06}Yb{sub x}Ti{sub 4}Nb{sub 6}O{sub 30}, abbreviated as SLTN: Ho-Ybx) ceramics have been synthesized, and their structural, up-conversion (UC) photoluminescence, and dielectric properties have been carefully investigated. Through Rietveld structural refinement, SLTN: Ho-Ybx samples are determined as single tetragonal tungsten bronze (TTB) phase with space group P4/mbm in which larger Sr{sup 2+} ions fill the A{sub 2}-sites, relative smaller La{sup 3+}, Ho{sup 3+}, and Yb{sup 3+} ions occupy the A{sub 1}-sites, while Ti{sup 4+} and Nb{sup 4+} ions fill the B-sites. Under 980 nm near infrared (NIR) excitation, bright UC green emission, relatively weak red and near-infrared (NIR) emissions, originating from {sup 5}F{sub 4}/{sup 5}S{sub 2} → {sup 5}I{sub 8}, {sup 5}F{sub 5} → {sup 5}I{sub 8}, and {sup 5}F{sub 4}/{sup 5}S{sub 2} → {sup 5}I{sub 7} transitions of Ho{sup 3+} ions, are confirmed for SLTN: Ho-Ybx. Two-photon energy transfer process is proved through pumping laser power dependence of emission intensity measurement. Furthermore, the influence of Ho{sup 3+}- and Yb{sup 3+}- ions on the dielectric properties of SLTN: Ho-Ybx is also investigated and the temperature stability of dielectric permittivity is improved.

  7. Over 11% Efficiency in Tandem Polymer Solar Cells Featured by a Low-Band-Gap Polymer with Fine-Tuned Properties.

    PubMed

    Zheng, Zhong; Zhang, Shaoqing; Zhang, Jianqi; Qin, Yunpeng; Li, Wanning; Yu, Runnan; Wei, Zhixiang; Hou, Jianhui

    2016-07-01

    Highly efficient polymer solar cells with tandem structure are fabricated by using two excellent photovoltaic polymers and a highly transparent intermediate recombination layer. Power conversion efficiencies over 11% can be realized featured by a low-band-gap polymer with fine-tuned properties.

  8. Over 11% Efficiency in Tandem Polymer Solar Cells Featured by a Low-Band-Gap Polymer with Fine-Tuned Properties.

    PubMed

    Zheng, Zhong; Zhang, Shaoqing; Zhang, Jianqi; Qin, Yunpeng; Li, Wanning; Yu, Runnan; Wei, Zhixiang; Hou, Jianhui

    2016-07-01

    Highly efficient polymer solar cells with tandem structure are fabricated by using two excellent photovoltaic polymers and a highly transparent intermediate recombination layer. Power conversion efficiencies over 11% can be realized featured by a low-band-gap polymer with fine-tuned properties. PMID:27136384

  9. Synthesis and photoluminescence properties of Ca{sub 19}Mg{sub 2}(PO{sub 4}){sub 14}:Sm{sup 3+} red phosphor for white light emitting diodes

    SciTech Connect

    Zhu, Ge; Ci, Zhipeng; Shi, Yurong; Wang, Yuhua

    2014-07-01

    Highlights: • A novel red phosphor Ca{sub 19}Mg{sub 2}(PO{sub 4}){sub 14}:Sm{sup 3+} was synthesized and investigated firstly. • The structure and characteristic luminescence properties are discussed. • The excellent thermal stability was found and investigated. • It has good color saturation, the CIE is close to that of commercial Y{sub 2}O{sub 3}:Eu{sup 3+}. - Abstract: A series of Sm{sup 3+} doped Ca{sub 19}Mg{sub 2}(PO{sub 4}){sub 14} red phosphors were successfully synthesized. X-ray diffraction analysis indicates that all the samples are single phased. The luminescence property is investigated in detail by measuring their photoluminescence excitation and emission spectra. Ca{sub 19}Mg{sub 2}(PO{sub 4}){sub 14}:Sm{sup 3+} phosphors show strong absorption in 400–410 nm region, which is suitable for application in LEDs. When excited at 403 nm, Ca{sub 19}Mg{sub 2}(PO{sub 4}){sub 14}:Sm{sup 3+} phosphor can emit red emission with CIE chromaticity coordinates (0.615, 0.384). The optimal doping concentration of Sm{sup 3+} doped Ca{sub 19}Mg{sub 2}(PO{sub 4}){sub 14} is measured to be 0.02. The thermal quenching property is also measured and compared with the commercial red phosphor Y{sub 2}O{sub 3}:Eu{sup 3+} (Topstar, TXC-RIA). The results indicate Ca{sub 19}Mg{sub 2}(PO{sub 4}){sub 14}:Sm{sup 3+} phosphors have potential to serve as a red phosphor for white LEDs.

  10. Photoluminescence and photocatalytic properties of BiOCl and Bi{sub 24}O{sub 31}Cl{sub 10} nanostructures synthesized by electrolytic corrosion of metal Bi

    SciTech Connect

    Chen, G.; Fang, G.L.; Tang, G.D.

    2013-03-15

    Highlights: ► We report a facile method to synthesize bismuth oxychlorides. ► The BiOCl nanosheets have both ultraviolet-blue emission zone and visible emission zone. ► The Bi{sub 24}O{sub 31}Cl{sub 10} nanostructure is a direct electron transition semiconductor. ► The broad and intensive UV emission were observed in Bi{sub 24}O{sub 31}Cl{sub 10} nanostructure. - Abstract: Nanostructured BiOCl and Bi{sub 24}O{sub 31}Cl{sub 10} have been synthesized by electrolytic corrosion of metal Bi. The photocatalysis and photoluminescence (PL) properties of BiOCl and Bi{sub 24}O{sub 31}Cl{sub 10} nanostructures have been investigated. Nanosheets with a thickness of ∼10 nm and in-plane size of 30–60 nm were obtained in the as-synthesized BiOCl. The emission spectra excited at 360 nm consist of two broad emission bands: ultraviolet-blue and visible. The visible emission is responsible for the photocatalytic activity of BiOCl under visible light irradiation. The nanostructured Bi{sub 24}O{sub 31}Cl{sub 10}, self-assembled by uniform nanosheets with a thickness of 10–20 nm, exhibits a broad and strong blue shift UV emission at room temperature.

  11. Dicarboxylate-controlled three Zn(II) coordination polymers incorporating flexible 1,2-bis(imidazol-1‧-yl)ethane ligand: Syntheses, structures, thermal stabilities and photoluminescent properties

    NASA Astrophysics Data System (ADS)

    Hao, Hong-Jun; Sun, Di; Liu, Fu-Jing; Huang, Rong-Bin; Zheng, Lan-Sun

    2012-03-01

    Three mixed-ligand Zn(II) coordination polymers (CPs) of the formula {[Zn2(bime)2(adip)2]ṡ(H2O)5}n (1), {[Zn(bime)(ipa)]ṡ(H2O)3}n (2), {[Zn(bime)(tpa)]ṡ(H2O)ṡ(CH3OH)}n (3) (bime = 1,2-bis(imidazol-1'-yl)ethane, H2adip = adipic acid, H2ipa = isophthalic acid and H2tpa = terephthalic acid) were synthesized. All CPs have been characterized by element analysis, powder X-ray diffraction (PXRD), IR and X-ray single-crystal diffraction. Complexes 1 and 2 exhibit similar wavy two-dimensional (2D) sheets with 44-sql topology. Compared to 1, complex 2 contains a larger window owing to the different conformation of bime ligand. In both 1 and 2, we observed 1D water chain filling in the 44-sql net. In 3, the bime acts as a bidentate ligand and the tpa adopts a μ2-η1,η1 coordinated mode which links the Zn(II) ions to form a 2D 63-hcb net. The results suggest that the dicarboxylates play crucial roles in the formation of the different structures. In addition, the thermal stabilities and the photoluminescence properties of them were also investigated.

  12. Four M(II)-coordination polymers (M = Zn(II) and Cd(II)) based on a flexible 1,2-bis(pyridin-3-yloxy)ethane ligand: Syntheses, structures and photoluminescent properties

    NASA Astrophysics Data System (ADS)

    Ge, Jing-Yuan; Cheng, Jun-Yan; Wang, Peng; Liu, Qi-Kui; Dong, Yu-Bin

    2014-01-01

    Four coordination polymers, namely {[Zn(L)2](ClO4)2}n (1), [Zn(L)(ipa)]n (2), [Cd(L)(chdc)ṡ2H2O]n (3) and [Cd(L)0.5(pydc)ṡ0.5H2O]n (4) (H2ipa = isophthalic acid, H2chdc = cyclohexane-1,4-dicarboxylic acid, H2pydc = pyridine-2,6-dicarboxylic acid), have been synthesized based on a flexible ligand 1,2-bis(pyridin-3-yloxy)ethane (L) under hydrothermal conditions. Their structures are determined by X-ray single-crystal analyses, IR spectra and X-ray powder diffractions (XRPD). In 1, the infinite 2D square sheets arrange regularly to form 1D channels containing ClO4- anions. 2 exhibits wave-like network, which is further extended into a 3D framework via interlayer C-H⋯X (X = π, O) interactions. With different co-ligands, 3 shows a 2D structure, while 4 exhibits a intriguing 3D supramolecular framework. In 1-4, L adopts different conformations in the solid state. The various conformations of L, with the different co-ligands, play an important role in structural diversity. The thermogravimetric analyses and photoluminescent properties of them were also investigated.

  13. Photoluminescence and phosphorescence properties of MAl 2O 4:Eu 2+, Dy 3+ (M=Ca, Ba, Sr) phosphors prepared at an initiating combustion temperature of 500 °C

    NASA Astrophysics Data System (ADS)

    Mothudi, B. M.; Ntwaeaborwa, O. M.; Botha, J. R.; Swart, H. C.

    2009-12-01

    Eu 2+ and Dy 3+ co-doped calcium aluminate, barium aluminate and strontium aluminate phosphors were synthesized at an initiating combustion temperature of 500 °C using urea as an organic fuel. The crystallinity of the phosphors was investigated by using X-ray diffraction (XRD) and the morphology was determined by a scanning electron microscope (SEM). The low temperature monoclinic structure for both CaAl 2O 4 and SrAl 2O 4 and the hexagonal structure of BaAl 2O 4 were observed. The effect of the host materials on the photoluminescence (PL) and phosphorescence properties were investigated by using a He-Cd Laser and a Cary Eclipse fluorescence spectrophotometer, respectively. The broad band emission spectra observed at 449 nm for CaAl 2O 4:Eu 2+, Dy 3+, 450 nm (with a shoulder-peak at 500 nm) for BaAl 2O 4:Eu 2+, Dy 3+ and 528 nm for SrAl 2O 4:Eu 2+, Dy 3+ are attributed to the 4f 65d 1 to 4f 7 transition in the Eu 2+ ion in the different hosts.

  14. Effects R3+ on the photoluminescent properties of Ca2R8(SiO4)6O2:A (R = Y,La,Gd;A = Eu3+,Tb3+) phosphor films prepared by the sol gel process

    NASA Astrophysics Data System (ADS)

    Han, X. M.; Lin, J.; Zhou, H. L.; Yu, M.; Zhou, Y. H.; Pang, M. L.

    2004-04-01

    Using CaCO3, metal oxides (all dissolved by nitric acid) and tetraethoxysilane Si(OC2H5)4 (TEOS) as the main starting materials, Ca2R8(SiO4)6O2:A (R = Y,La,Gd;A = Eu3+,Tb3+) phosphor films have been dip-coated on quartz glass substrates through the sol-gel process. X-ray diffraction (XRD), atomic force microscope (AFM), scanning electron microscope (SEM) and photoluminescence (PL) spectra as well as lifetimes were used to characterize the resulting films. The results of XRD indicated that the 1000 °C annealed films are isomorphous and crystallize with the silicate oxyapatite structure. AFM and SEM studies revealed that the phosphor films consisted of homogeneous particles ranging from 30 to 90 nm, with an average thickness of 1.30 µm. The Eu3+ and Tb3+ show similar spectral properties independent of R3+ in the films due to their isomorphous crystal structures. However, both the emission intensity and lifetimes of Eu3+ and Tb3+ in Ca2R8(SiO4)6O2 (R = Y, La, Gd) films decrease in the sequence of R = Gd>R = Y>R = La, which have been explained in accordance with the crystal structures.

  15. Nonaqueous sol-gel chemistry applied to atomic layer deposition: tuning of photonic band gap properties of silica opals.

    PubMed

    Marichy, Catherine; Dechézelles, Jean-Francois; Willinger, Marc-Georg; Pinna, Nicola; Ravaine, Serge; Vallée, Renaud

    2010-05-01

    Combining both electromagnetic simulations and experiments, it is shown that the photonic pseudo band gap (PPBG) exhibited by a silica opal can be fully controlled by Atomic Layer Deposition (ALD) of titania into the pores of the silica spheres constituting the opal. Different types of opals were assembled by the Langmuir-Blodgett technique: homogeneous closed packed structures set up of, respectively, 260 and 285 nm silica spheres, as well as opal heterostructures consisting of a monolayer of 430 nm silica spheres embedded within 10 layers of 280 nm silica spheres. For the stepwise infiltration of the opals with titania, titanium isopropoxide and acetic acid were used as metal and oxygen sources, in accordance with a recently published non-aqueous approach to ALD. A shift of the direct PPBG, its disappearance, and the subsequent appearance and shifting of the inverse PPBG are observed as the opal is progressively filled. The close agreement between simulated and experimental results is striking, and promising in terms of predicting the properties of advanced photonic materials. Moreover, this work demonstrates that the ALD process is rather robust and can be applied to the coating of complex nanostructures.

  16. Effect of a bearing gap on hemolytic property in a hydrodynamically levitated centrifugal blood pump with a semi-open impeller.

    PubMed

    Kosaka, Ryo; Nishida, Masahiro; Maruyama, Osamu; Yambe, Tomoyuki; Imachi, Kou; Yamane, Takashi

    2013-01-01

    We have developed a hydrodynamically levitated centrifugal blood pump with a semi-open impeller for long-term circulatory assist. The pump uses hydrodynamic bearings to enhance durability and reliability without additional displacement-sensors or control circuits. However, a narrow bearing gap of the pump has a potential for hemolysis. The purpose of this study is to develop the hydrodynamically levitated centrifugal blood pump with a semi-open impeller, and to evaluate the effect of a bearing gap on hemolytic property. The impeller levitates using a spiral-groove type thrust bearing, and a herringbone-groove type radial bearing. The pump design was improved by adopting a step type thrust bearing and optimizing the pull-up magnetic force. The pump performance was evaluated by a levitation performance test, a hemolysis test and an animal experiment. In these tests, the bearing gap increased from 1 to 63 μm. In addition, the normalized index of hemolysis (NIH) improved from 0.415 to 0.005 g/100 l, corresponding to the expansion of the bearing gap. In the animal experiment for 24 h, the plasma-free hemoglobin remained within normal ranges (<4.0 mg/dl). We confirmed that the hemolytic property of the pump was improved to the acceptable level by expanding the bearing gap greater than 60 μm. PMID:23442235

  17. Effect of a bearing gap on hemolytic property in a hydrodynamically levitated centrifugal blood pump with a semi-open impeller.

    PubMed

    Kosaka, Ryo; Nishida, Masahiro; Maruyama, Osamu; Yambe, Tomoyuki; Imachi, Kou; Yamane, Takashi

    2013-01-01

    We have developed a hydrodynamically levitated centrifugal blood pump with a semi-open impeller for long-term circulatory assist. The pump uses hydrodynamic bearings to enhance durability and reliability without additional displacement-sensors or control circuits. However, a narrow bearing gap of the pump has a potential for hemolysis. The purpose of this study is to develop the hydrodynamically levitated centrifugal blood pump with a semi-open impeller, and to evaluate the effect of a bearing gap on hemolytic property. The impeller levitates using a spiral-groove type thrust bearing, and a herringbone-groove type radial bearing. The pump design was improved by adopting a step type thrust bearing and optimizing the pull-up magnetic force. The pump performance was evaluated by a levitation performance test, a hemolysis test and an animal experiment. In these tests, the bearing gap increased from 1 to 63 μm. In addition, the normalized index of hemolysis (NIH) improved from 0.415 to 0.005 g/100 l, corresponding to the expansion of the bearing gap. In the animal experiment for 24 h, the plasma-free hemoglobin remained within normal ranges (<4.0 mg/dl). We confirmed that the hemolytic property of the pump was improved to the acceptable level by expanding the bearing gap greater than 60 μm.

  18. Ultrafast spectroscopic measurement of the optical and electronic properties of narrow-band-gap semiconductor laser materials

    NASA Astrophysics Data System (ADS)

    Anson, Scott Allen

    1999-12-01

    Semiconductor lasers operating in the mid-infrared region of the spectrum (2-5 μm) are of interest for a variety of potential applications and therefore are currently the focus of intense research and development. One of the main impediments to the development of these lasers is a non-radiative loss process know as Auger recombination. It is this loss mechanism that leads to the relatively low temperature operation of these lasers. In addition to Auger recombination, there is an interest in suppressing laser which can lead to the degradation and catastrophic failure of devices at high output powers. The tendency for filament formation is suppressed in materials with small linewidth enhancement factors. To improve the performance of these semiconductor lasers, band structure engineering techniques have been employed to the design of narrow band-gap III-V semiconductor active regions based on GaInSb/InAs superlattices. These superlattice structures are designed to have favorable material properties that allow for the suppression of Auger recombination and a reduction of the linewidth enhancement factor. In addition to Auger recombination and the linewidth enhancement factor, a number of other optical and electronic properties in these superlattice structures are also of interest, including the differential gain, differential index, Shockley-Read-Hall recombination, and in-plane carrier diffusion. In this dissertation measurements of the optical and electronic properties in these structures conducted using two ultrafast spectroscopic techniques, time-resolved differential transmission and photogenerated transient grating is discussed. These ultrafast spectroscopic measurements are performed using 140 fs pump pulses from a mode-locked Ti:sapphire laser operating at 840 nm and 170 fs probe pulses from a synchronously-pumped optical parametric oscillator which is tunable between 2.65 to 4.4 μm. The measurements show that these superlattices have favorable material

  19. The Tellurophosphate K[subscript 4]P[subscript 8]Te[subscript 4]: Phase-Change Properties, Exfoliation, Photoluminescence in Solution and Nanospheres

    SciTech Connect

    Chung, In; Song, Jung-Hwan; Kim, Myung Gil; Malliakas, Christos D.; Karst, Angela L.; Freeman, Arthur J.; Weliky, David P.; Kanatzidis, Mercouri G.

    2009-12-14

    We describe the inorganic polymer K{sub 4}P{sub 8}Te{sub 4} which is soluble, giving solutions that exhibit white emission upon 355 nm laser irradiation. An indirect band gap semiconductor (E{sub g} {approx} 1.4 eV), K{sub 4}P{sub 8}Te{sub 4} crystallizes in the space group P2{sub 1}/m, with a = 6.946(1) {angstrom}, b = 6.555(1) {angstrom}, c = 9.955(2) {angstrom}, and {beta} = 90.420(3){sup o} at 173(2) K. The compound features infinite chains of [P{sub 8}Te{sub 4}{sup 4-}] with covalent P-Te bonding and exhibits reversible crystal-glass phase-change behavior. When deposited from solution, the material forms highly crystalline K{sub 4}P{sub 8}Te{sub 4} nanospheres. The thermal analysis, FT-IR, UV-vis diffuse reflectance, {sup 31}P magic angle spinning solid-state NMR spectroscopy, and pair distribution function (PDF) analysis for the crystal and glass forms and ab initio electronic structure calculations by the screened-exchange local density function approximation are also reported. Speciation of K{sub 4}P{sub 8}Te{sub 4} in solution studied with {sup 31}P solution-state NMR spectroscopy, electrospray ionization mass spectrometry, and PDF analysis indicate exfoliation of [P{sub 8}Te{sub 4}{sup 4-}] chains followed by rearrangement into molecular species.

  20. Synthesis and photoluminescence properties of rhenium(I) complexes based on 2,2':6',2''-terpyridine derivatives with hole-transporting units.

    PubMed

    Wang, Dong; Xu, Qiu-Lei; Zhang, Song; Li, Hong-Yan; Wang, Cheng-Cheng; Li, Tian-Yi; Jing, Yi-Ming; Huang, Wei; Zheng, You-Xuan; Accorsi, Gianluca

    2013-02-28

    Based on 2,2′:6′,2′′-terpyridine ligands (L1), five terpyridine derivatives, namely 4′-carbazol-9-yl-2,2′:6′,2′′-terpyridine (L2), 4′-diphenylamino-2,2′:6′,2′′-terpyridine (L3), 4′-bis(4-tert-butylphenyl)amino-2,2′:6′,2′′-terpyridine (L4), 4′-[naphthalen-1-yl-(phenyl)amino]-2,2′:6′,2′′-terpyridine (L5), 4′-[naphthalen-2-yl(phenyl)amino]-2,2′:6′,2′′-terpyridine (L6) and their corresponding Re(I) complexes ReL(n)(CO)3Cl (n = 1–6) have been synthesized and characterized by elemental analysis and 1H NMR spectroscopy. The X-ray crystal structure of ReL3(CO)3Cl has also been obtained. The luminescence spectra of ReL2(CO)3Cl–ReL5(CO)3Cl, obtained in CH2Cl2 solution at room temperature, show strong dπ (Re) → π* (diimine) MLCT character (λ(max) 600 nm) and a small red shift relative to ReL1(CO)3Cl. This, confirmed by the study of the triplet energy levels of the L1–L6 ligands at low temperature (77 K rigid matrix), indicates that the introduction of electron-donating moieties on the terpyridine unit decreases the triplet levels of the ligands, leading to a reduction of the energy gap between d and π* orbitals. In the solid state, upon MLCT excitation, all the complexes show an even stronger emission and a blue spectral shift (λ(max) ∼ 550 nm) compared to those obtained in solution.

  1. A study on the magnetic and photoluminescence properties of Eu(n+) and Sm3+ doped Fe3O4 nanoparticles.

    PubMed

    Huan, Weiwei; Cheng, Chao; Yang, Yuxiang; Yuan, Hongming; Li, Yongxia

    2012-06-01

    In this paper, Eu(n+), Sm3+ doped Fe3O4 nanoparticles were prepared via solvothermal method, in which Ferric chloride is used as the iron source, and anhydrous EuCl3, SmCl3 as doping source. Eu, Sm valence in doped Fe3O4 nanoparticles, and effects of Eu, Sm doping amount on their structure, morphology, magnetic properties and PL properties were discussed. The results show, the Eu ions had doped Fe3O4 nanoparticles in the mixed-valence state, when the Eu and Sm doping amount were increased, the doped Fe3O4 nanoparticles changed from hollow nanospheres into spherical particles, and finally changed into uniform cube-shaped particles with 13 nm in diameter. Moreover, the doping sites for doping ions in doped Fe3O4 nanoparticles were discussed from Rietveld analysis of XRD pattern of the doped Fe3O4 nanoparticles. And the changes of the magnetic and PL properties with the doping amount were further discussed. It was found that higher Sm(3+)-doping amount led to stronger magnetic dipole transitions, while the Eu(n+)-doping amount had little effect on the magnetic dipole transitions, thus resulting in different changes in their saturation magnetization with doping amount. PMID:22905509

  2. Solid state reaction synthesis and photoluminescence properties of Dy{sup 3+} doped Ca{sub 3}Sc{sub 2}Si{sub 3}O{sub 12} phosphor

    SciTech Connect

    Long, Qiang; Wang, Chuang; Li, Yanyan; Ding, Jianyan; Wang, Xicheng; Wang, Yuhua

    2015-11-15

    Highlights: • Ca{sub 3−x}Sc{sub 2}Si{sub 3}O{sub 12}:xDy{sup 3+} (0.01 ≤ x ≤ 0.03) was successfully synthesized under a reducing atmosphere. • The thermal stability of the Ca{sub 2.975}Sc{sub 2}Si{sub 3}O{sub 12}:0.025Dy{sup 3+} is superior to commercial phosphors in theory and experiment. • The optimal chromaticity coordinates of Ca{sub 3}Sc{sub 2}Si{sub 3}O{sub 12}:Dy{sup 3+} is (x = 0.3425, y = 0.3343) upon 350 nm excitation. - Abstract: The white emission phosphor Ca{sub 3}Sc{sub 2}Si{sub 3}O{sub 12}:Dy{sup 3+} was synthesized by the solid-state reaction. Phase analysis and characteristic luminescence properties are investigated by X-ray diffraction and photoluminescence spectra measurement. Ca{sub 3}Sc{sub 2}Si{sub 3}O{sub 12}:Dy{sup 3+} phosphor shows strong absorption in 350–410 nm region and exhibits white emission with CIE chromaticity coordinates of (0.3425, 0.3343). Its emission intensity at 250 °C remained 74% of that measured at room temperature. Moreover, the activation energy is also calculated through the Arrhenius equation. The result shows that the thermostability of Ca{sub 3}Sc{sub 2}Si{sub 3}O{sub 12}:Dy{sup 3+} is superior than that of commercial phosphor Ca{sub 3}Sc{sub 2}Si{sub 3}O{sub 12}:Ce{sup 3+}. The outstanding luminescent properties indicate that Ca{sub 3}Sc{sub 2}Si{sub 3}O{sub 12}:Dy{sup 3+} could be a potential white light emission phosphor.

  3. Designing a heterotrinuclear Cu(II)-Ni(II)-Cu(II) complex from a mononuclear Cu(II) Schiff base precursor with dicyanamide as a coligand: synthesis, crystal structure, thermal and photoluminescence properties.

    PubMed

    Hopa, Cigdem; Cokay, Ismail

    2016-08-01

    Schiff bases are considered `versatile ligands' in coordination chemistry. The design of polynuclear complexes has become of interest due to their facile preparations and varied synthetic, structural and magnetic properties. The reaction of the `ligand complex' [CuL] {H2L is 2,2'-[propane-1,3-diylbis(nitrilomethanylylidene)]diphenol} with Ni(OAc)2·4H2O (OAc is acetate) in the presence of dicyanamide (dca) leads to the formation of bis(dicyanamido-1κN(1))bis(dimethyl sulfoxide)-2κO,3κO-bis{μ-2,2'-[propane-1,3-diylbis(nitrilomethanylylidene)]diphenolato}-1:2κ(6)O,O':O,N,N',O';1:3κ(6)O,O':O,N,N',O'-dicopper(II)nickel(II), [Cu2Ni(C17H16N2O2)2(C2N3)2(C2H6OS)2]. The complex shows strong absorption bands in the frequency region 2155-2269 cm(-1), which clearly proves the presence of terminal bonding dca groups. A single-crystal X-ray study revealed that two [CuL] units coordinate to an Ni(II) atom through the phenolate O atoms, with double phenolate bridges between Cu(II) and Ni(II) atoms. Two terminal dca groups complete the distorted octahedral geometry around the central Ni(II) atom. According to differential thermal analysis-thermogravimetric analysis (DTA-TGA), the title complex is stable up to 423 K and thermal decomposition starts with the release of two coordinated dimethyl sulfoxide molecules. Free H2L exhibits photoluminescence properties originating from intraligand (π-π*) transitions and fluorescence quenching is observed on complexation of H2L with Cu(II).

  4. Designing a heterotrinuclear Cu(II)-Ni(II)-Cu(II) complex from a mononuclear Cu(II) Schiff base precursor with dicyanamide as a coligand: synthesis, crystal structure, thermal and photoluminescence properties.

    PubMed

    Hopa, Cigdem; Cokay, Ismail

    2016-08-01

    Schiff bases are considered `versatile ligands' in coordination chemistry. The design of polynuclear complexes has become of interest due to their facile preparations and varied synthetic, structural and magnetic properties. The reaction of the `ligand complex' [CuL] {H2L is 2,2'-[propane-1,3-diylbis(nitrilomethanylylidene)]diphenol} with Ni(OAc)2·4H2O (OAc is acetate) in the presence of dicyanamide (dca) leads to the formation of bis(dicyanamido-1κN(1))bis(dimethyl sulfoxide)-2κO,3κO-bis{μ-2,2'-[propane-1,3-diylbis(nitrilomethanylylidene)]diphenolato}-1:2κ(6)O,O':O,N,N',O';1:3κ(6)O,O':O,N,N',O'-dicopper(II)nickel(II), [Cu2Ni(C17H16N2O2)2(C2N3)2(C2H6OS)2]. The complex shows strong absorption bands in the frequency region 2155-2269 cm(-1), which clearly proves the presence of terminal bonding dca groups. A single-crystal X-ray study revealed that two [CuL] units coordinate to an Ni(II) atom through the phenolate O atoms, with double phenolate bridges between Cu(II) and Ni(II) atoms. Two terminal dca groups complete the distorted octahedral geometry around the central Ni(II) atom. According to differential thermal analysis-thermogravimetric analysis (DTA-TGA), the title complex is stable up to 423 K and thermal decomposition starts with the release of two coordinated dimethyl sulfoxide molecules. Free H2L exhibits photoluminescence properties originating from intraligand (π-π*) transitions and fluorescence quenching is observed on complexation of H2L with Cu(II). PMID:27487333

  5. Structural and photoluminescence properties of Dy3+ co-doped and Eu2+ activated MAl2O4 (M = Ba, Ca, Sr) nanophosphors

    NASA Astrophysics Data System (ADS)

    Dejene, F. B.; Kebede, M. A.; Redi-Abshiro, M.; Kgarebe, B. V.

    2013-09-01

    Long afterglow alkaline earth aluminates MAl2O4:Eu, Dy (M: Ca, Sr, Ba) phosphors are generally synthesized by the solid-state process which is more feasible than other conventional processes in terms of operation and large-scale production. However, the constituents of phosphors synthesized using this process are usually not mixed well, the particles agglomerates and very high temperature requirement to synthesize the final powder make it undesirable. In order to circumvent these problems, MAl2O4:Eu, Dy (Ca, Ba, Sr) phosphors were prepared at low temperatures (500 °C) by the solution-combustion of corresponding metal nitrate-urea solution mixtures, over a time of 5-10 min. In order to elucidate the relationship between the constituent, structure and PL properties product's particle size, morphological and structural properties were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), energy dispersive X-ray spectrometer (EDS), while the characteristic luminescence properties were investigated using emission spectra. The low temperature monoclinic structure for both CaAl2O4 and SrAl2O4 and the hexagonal structure of BaAl2O4 were observed. The emission spectra of these phosphors indicated that all of them are broad band, and the only emission peaks around 448, 490 and 515 nm of CaAl2O4:Eu, Dy, BaAl2O4:Eu, Dy and SrAl2O4:Eu, Dy, respectively, are due to 5d → 4f transition of Eu2+. The decay curves implied that these phosphors contain fast, medium and slow-decay process. The Dy3+ trap levels may be considered to be responsible for the long afterglow phosphorescence at room temperature.

  6. Influence of structural distortions upon photoluminescence properties of Eu{sup 3+} and Tb{sup 3+} activated Na{sub 3}Ln(BO{sub 3}){sub 2} (Ln=Y, Gd) borates

    SciTech Connect

    Asiri Naidu, S.; Boudin, S.; Varadaraju, U.V.; Raveau, B.

    2012-06-15

    The comparative study of the structure and photoluminescence (PL) properties of the Eu{sup 3+} and Tb{sup 3+} activated Na{sub 3}Ln(BO{sub 3}){sub 2}, with Ln=Y, Gd, showed the important role of the host lattice structure upon PL. Higher emission intensities of Eu{sup 3+} and Tb{sup 3+} are observed for Na{sub 3}Gd(BO{sub 3}){sub 2} than for Na{sub 3}Y(BO{sub 3}){sub 2}, through direct Eu{sup 3+} excitation at 395 nm for Eu{sup 3+} doped borates, and through Gd{sup 3+} excitation around 280 nm for Tb{sup 3+} doped borates. This higher performance for Na{sub 3}Gd(BO{sub 3}){sub 2} is due to the less regular environment of Eu{sup 3+} (Tb{sup 3+}) in the Gd sites than in the Y sites and to energy transfer from Gd{sup 3+} to Eu{sup 3+}(Tb{sup 3+}). The smaller critical concentration in Na{sub 3}Ln{sub 1-x}Tb{sub x}(BO{sub 3}){sub 2} observed for Ln=Gd, x=0.5, compared to x=0.6 for Ln=Y, is explained by shorter Ln-Ln distances (4.11 A for Gd-Gd vs. 4.59 A for Y-Y). Both Na{sub 3}Y{sub 0.4}Tb{sub 0.6}(BO{sub 3}){sub 2} and Na{sub 3}Gd{sub 0.5}Tb{sub 0.5}(BO{sub 3}){sub 2} show intense green emission under UV excitation. - Graphical abstract: The PL properties of Eu{sup 3+} and Tb{sup 3+} are studied in Na{sub 3}Ln(BO{sub 3}){sub 2} (Ln=Y, Gd) borates. Eu{sup 3+} and Tb{sup 3+}exhibits higher emission intensity in Na{sub 3}Gd(BO{sub 3}){sub 2} compared to Na{sub 3}Y(BO{sub 3}){sub 2} due to the less regular environment of the Gd{sup 3+} ion. Energy transfer from Gd{sup 3+} to Tb{sup 3+} is observed. Highlights: Black-Right-Pointing-Pointer Crystal structure of Na{sub 3}Gd(BO{sub 3}){sub 2} by X-ray powder diffraction. Black-Right-Pointing-Pointer Photoluminescence properties of Eu{sup 3+} and Tb{sup 3+} doped Na{sub 3}Ln(BO{sub 3}){sub 2} (Ln=Y, Gd). Black-Right-Pointing-Pointer Higher Eu{sup 3+} and Tb{sup 3+} emission for Na{sub 3}Gd(BO{sub 3}){sub 2} due to an irregular environment of Gd{sup 3+}. Black-Right-Pointing-Pointer Higher Eu{sup 3+} and Tb{sup 3+} emission

  7. Preparation and photoluminescence study of mesoporous indium hydroxide nanorods

    SciTech Connect

    Li, Changyu; Lian, Suoyuan; Liu, Yang; Liu, Shouxin; Kang, Zhenhui

    2010-02-15

    Mesoporous indium hydroxide nanorods were successfully synthesized by a mild one-step one-pot method. The obtained samples were characterized by X-ray diffraction, transmission electron microscopy with selected area electron diffraction, N{sub 2} adsorption, ultraviolet-visible absorption and photoluminescence, respectively. Transmission electron microscopy showed that there were some pores in the samples, which were mainly composed of rod-like shapes with length of 300 nm and diameter of 90 nm. N{sub 2} adsorption/desorption measurements confirmed that the prepared powder was mesoporous with average pore diameter of 3.1 nm. The ultraviolet-visible absorption spectroscopy analysis indicated that the band gap energy of the samples was 5.15 eV. Photoluminescence spectrum showed that there were two strong emissions under ultraviolet light irradiation. The growth mechanism of indium hydroxide nanorods and the role of cetyltrimethyl ammonium bromide were also discussed.

  8. Structural phase analysis, band gap tuning and fluorescence properties of Co doped TiO2 nanoparticles

    NASA Astrophysics Data System (ADS)

    Alamgir; Khan, Wasi; Ahmad, Shabbir; Mehedi Hassan, M.; Naqvi, A. H.

    2014-12-01

    This paper reports on structural and optical properties of Co (0, 3, 5 & 7 mol%) doped TiO2 (titania) nanoparticles (NPs) synthesized by employing acid modified sol-gel method. The crystalline phase of the pure and doped NPs was observed with X-ray diffraction (XRD) followed by Raman scattering technique. Field emission scanning electron microscope and transmission electron microscopy give the morphological details. Fourier transform infrared spectra indicate the bonding interactions of Co ions with the titania lattice framework. Optical studies were attained with UV-visible absorption and fluorescence emission spectroscopy. XRD analysis reveals that all prepared samples have pure anatase phase with tetragonal symmetry devoid of any other secondary phase. The average crystallite size of all samples was calculated using Scherrer's formula and was found to vary from 8 to 10 nm with doping concentration of Co. The Raman spectroscopy further confirmed the formation of TiO2 in anatase structure in both pure and Co doped TiO2 NPs. The most intense Raman active Eg peak of TiO2 NPs shifted to higher energy on doping. Both UV-visible and fluorescence spectra show a blue shift in their absorption and band edge emission subsequently on increasing with Co percentage in titania host matrix, wherever there is an indication of quantum confinement effect with widening of band gap on decreasing in NPs size. There is also a possibility of strong Coulomb interaction effect on the optical processes involving the Co ions. However, the intensities of different emission spectra are not the same but decrease profoundly for doping samples due to concentration quenching effect.

  9. Influence of optical band gap and particle size on the catalytic properties of Sm/SnO2-TiO2 nanoparticles

    NASA Astrophysics Data System (ADS)

    Javaid, Shaghraf; Farrukh, Muhammad Akhyar; Muneer, Iqra; Shahid, Maryam; Khaleeq-ur-Rahman, Muhammad; Umar, Akrajas Ali

    2015-06-01

    In this work, samarium (Sm) supported on tin oxide-titanium oxide (SnO2/TiO2) nanoparticles (Sm/SnO2-TiO2) were synthesized by sol-gel, ultrasonic and hydrothermal methods; and the optical and catalytic properties of Sm/SnO2-TiO2 nanoparticles was observed. Effect of synthetic methods on nanoparticles size and percentage composition of anatase and rutile phase in TiO2 was evaluated. The Sm/SnO2-TiO2 nanoparticles were characterized by Transmission Electron Microscopy, Scanning Electron Microscopy, Energy Dispersive X-ray spectroscopy, Powder X-ray Diffraction, Thermogravimetric Analysis and Fourier Transmission Infrared Spectroscopy. However, UV-Vis and solid phase spectroscopy were used to determine the catalytic efficiency and optical band gap, respectively. It was found out that nanoparticles synthesized by sol-gel and hydrothermal method have small optical band gap as compare to nanoparticles synthesized by ultrasonic method and ultimately showed more catalytic activity toward degradation of dye due to red shift in the optical band gap (shifting of wavelength to visible region). A direct relationship between particle size and optical band gap was investigated. It was observed that Sm reduced the optical band gap and increased catalytic efficiency when supported on SnO2/TiO2.

  10. Thin film GaP for solar cell application

    NASA Astrophysics Data System (ADS)

    Morozov, I. A.; Gudovskikh, A. S.; Kudryashov, D. A.; Nikitina, E. V.; Kleider, J.-P.; Myasoedov, A. V.; Levitskiy, V.

    2016-08-01

    A new approach to the silicon based heterostructures technology consisting of the growth of III-V compounds (GaP) on a silicon substrate by low-temperature plasma enhanced atomic layer deposition (PE-ALD) is proposed. The basic idea of the method is to use a time modulation of the growth process, i.e. time separated stages of atoms or precursors transport to the growing surface, migration over the surface, and crystal lattice relaxation for each monolayer. The GaP layers were grown on Si substrates by PE-ALD at 350°C with phosphine (PH3) and trimethylgallium (TMG) as sources of III and V atoms. Scanning and transmission electron microscopy demonstrate that the grown GaP films have homogeneous amorphous structure, smooth surface and a sharp GaP/Si interface. The GaP/Si heterostructures obtained by PE-ALD compare favourably to that conventionally grown by molecular beam epitaxy (MBE). Indeed, spectroscopic ellipsometry measurements indicate similar interband optical absorption while photoluminescence measurements indicate higher charge carrier effective lifetime. The better passivation properties of GaP layers grown by PE-ALD demonstrate a potential of this technology for new silicon based photovoltaic heterostructure

  11. Photoluminescence quenching and charge transfer in artificial heterostacks of monolayer transition metal dichalcogenides and few-layer black phosphorus.

    PubMed

    Yuan, Jiangtan; Najmaei, Sina; Zhang, Zhuhua; Zhang, Jing; Lei, Sidong; M Ajayan, Pulickel; Yakobson, Boris I; Lou, Jun

    2015-01-27

    Transition metal dichalcogenides monolayers and black phosphorus thin crystals are emerging two-dimensional materials that demonstrated extraordinary optoelectronic properties. Exotic properties and physics may arise when atomic layers of different materials are stacked together to form van der Waals solids. Understanding the important interlayer couplings in such heterostructures could provide avenues for control and creation of characteristics in these artificial stacks. Here we systematically investigate the optical and optoelectronic properties of artificial stacks of molybdenum disulfide, tungsten disulfide, and black phosphorus atomic layers. An anomalous photoluminescence quenching was observed in tungsten disulfide-molybdenum disulfide stacks. This was attributed to a direct to indirect band gap transition of tungsten disulfide in such stacks while molybdenum disulfide maintains its monolayer properties by first-principles calculations. On the other hand, due to the strong build-in electric fields in tungsten disulfide-black phosphorus or molybdenum disulfide-black phosphorus stacks, the excitons can be efficiently splitted despite both the component layers having a direct band gap in these stacks. We further examine optoelectronic properties of tungsten disulfide-molybdenum disulfide artificial stacks and demonstrate their great potentials in future optoelectronic applications.

  12. Two new Zn(II) and Cd(II) coordinastion polymers based on amino-tetrazole and phenylcarboxylate: Syntheses, topological structures and photoluminescent properties

    SciTech Connect

    Liu, Dong-Sheng; Sui, Yan; Chen, Weng-Tong; Huang, Jian-Gen; Chen, Jian-Zhong; Huang, Chang-Cang

    2012-12-15

    Two Zn(II) and Cd(II) compounds with the in-situ generated ligand of 5-amino-tetrazolate (atz{sup -}) were prepared from the hydrothermal reactions of the corresponding Cd or Zn(II) salts with phenylcarboxylate, and characterized by elemental analysis, IR spectroscopy, and TGA. The results of X-ray crystallographic analysis reveal that compound [Zn{sub 2}(BZA)(atz){sub 2}(OH)]{sub n} (1) (BZA=benzoic acid) presents a two-dimensional (2D) 'hcb' topological network constructed from the ZnN{sub 2}O{sub 2} tetrahedra. In compound [Cd{sub 6}(atz){sub 6}(PTA){sub 3}]{sub n} (2) (PTA=terephthalic acid), the identical [Cd{sub 3}(atz){sub 3})]{sup 3+}{sub n} clusters are connected by atz ligands to generate a 2D cationic layer, and the neighboring cationic layers are pillared by PTA giving birth to 3D network. After simplifying, the complicated 3D network of 2 can be presented as an unprecedented (4, 4, 10)-connected trinodal topology. The formations of the structures show a good example that using the combination of the in-situ generated ligand and other coligand synthetic strategy can construct interesting topological structures. The thermal stabilities and fluorescent properties of the complexes have also been studied. - Graphical abstract: Two d{sup 10} metal complexes have been synthesized by employing mixed-ligand synthetic approach. Complex 1 presents a 2D 'hcb' topological network. Complex 2 shows an unprecedented (4, 4, 10)-connected trinodal topology. Highlights: Black-Right-Pointing-Pointer Coligand synthetic strategy was applied to obtain new MOFs with useful properties. Black-Right-Pointing-Pointer Two new Zn(II) and Cd(II) complexes were constructed from the mixed-ligand. Black-Right-Pointing-Pointer Topologically, compound 2 presented an unprecedented (4, 4, 10)-connected trinodal topology. Black-Right-Pointing-Pointer The two compounds may be excellent candidates for potential photoactive material.

  13. Spectroscopic and sub optical band gap properties of e-beam irradiated ultra-high molecular weight polyethylene

    NASA Astrophysics Data System (ADS)

    Khan, Hamna; Gahfoor, Bilal; Mehmood, Malik Sajjad; Ahmad, Manzoor; Yasin, Tariq; Ikram, Masroor

    2015-12-01

    Muller matrix spectro-polarimeter has been used to study the absorption behavior of pristine and e-beam irradiated (30, 65,100 kGy) ultra-high molecular weight polyethylene (UHMWPE) over the visible spectral range i.e. 400-800 nm. As a result, significant changes occur in the absorption behavior of irradiated samples due to radiation induced physical and chemical changes. To analyze these (radiation induced) changes in polymer matrix, Urbach edge method is employed for the calculation of optical activation energy. In addition to this, direct and indirect energy band gaps along the number of carbon atoms in C=C unsaturation have been determined by using modified Urbach formula and Tauc's equation, respectively. The results obtained during study reveal that Urbach energy decreases with radiation treatment and has a lower value for 100 kGy sample i.e. Eu=71.63 meV. The values of direct and indirect energy band gaps are also following the decreasing trend with e-beam irradiation. Moreover, indirect energy gaps are found to have lower values as compared to direct energy gaps. The number of carbon atoms in clusters (as estimated from modified Tauc's equation) has been found to vary from ∼6 to 8 for direct energy band gaps and from ∼9 to 11 for indirect energy band gaps.

  14. Exploring the Electronic Band Structure of Organometal Halide Perovskite via Photoluminescence Anisotropy of Individual Nanocrystals.

    PubMed

    Täuber, Daniela; Dobrovolsky, Alexander; Camacho, Rafael; Scheblykin, Ivan G

    2016-08-10

    Understanding electronic processes in organometal halide perovskites, flourishing photovoltaic, and emitting materials requires unraveling the origin of their electronic transitions. Light polarization studies can provide important information regarding transition dipole moment orientations. Investigating individual methylammonium lead triiodide perovskite nanocrystals enabled us to detect the polarization of photoluminescence intensity and photoluminescence excitation, hidden in bulk samples by ensemble averaging. Polarization properties of the crystals were correlated with their photoluminescence spectra and electron microscopy images. We propose that distortion of PbI6 octahedra leads to peculiarities of the electronic band structure close to the band-edge. Namely, the lowest band transition possesses a transition dipole moment along the apical Pb-I-Pb bond resulting in polarized photoluminescence. Excitation of photoluminescence above the bandgap is unpolarized because it involves molecular orbitals delocalized both in the apical and equatorial directions of the perovskite octahedron. Trap-assisted emission at 77 K, rather surprisingly, was polarized similar to the bandgap emission.

  15. Photoluminescence and energy storage traps in CaTiO{sub 3}:Pr{sup 3+}

    SciTech Connect

    Zhang, Xianmin; Cao, Chunyan; Zhang, Chenghua; Xie, Shiyao; Xu, Guangwen; Zhang, Jiahua; Wang, Xiao-jun

    2010-12-15

    Red-emitting CaTiO{sub 3}:Pr{sup 3+} phosphors are fabricated using a solid state method and structurally characterized by X-ray diffraction and field emission scanning electron microscopy. The optical properties are investigated using photoluminescence emission, excitation, photoluminescence decay curves, diffused reflectance and thermoluminescence spectra, and persistent phosphorescence decay curves. The optimal fabrication temperatures for photoluminescence and persistent phosphorescence are found at 1200-1300 {sup o}C for photoluminescence and 1400 {sup o}C for persistent phosphorescence. The energy storage traps for persistent phosphorescence in the system are analyzed based on the dependence of photoluminescence and persistent phosphorescence on sintering temperature. The distribution of energy storage traps is further characterized by thermoluminescence spectra and the parameters of the traps are calculated. Oxygen vacancies as the main trapping centers play the key role for persistent phosphorescence in CaTiO{sub 3}:Pr{sup 3+}.

  16. A study of photoluminescence properties and performance improvement of Cd-doped ZnO quantum dots prepared by the sol–gel method

    PubMed Central

    2012-01-01

    In the present work, ZnO quantum dots (QDs) have been prepared by the sol–gel method, and the performance of the QDs has been improved. The effect of Cd concentration on the structural and luminescent properties of the QDs, as well as the effect of the mass ratio of trioctylphosphine oxide (TOPO)/octadecylamine (ODA), has been investigated. The ZnO and Cd-doped ZnO QDs have hexagonal wurtzite structures and are 3 to 6 nm in diameter. When the Cd content was increased, the QD particle size was reduced; this effect was confirmed in the corresponding ultraviolet–visible spectra. The fluorescence intensity was simultaneously enhanced significantly. Both the UV and fluorescence spectra were blue-shifted. The luminous intensity was further enhanced when the QDs were modified with TOPO/ODA. Fourier transform infrared and X-ray diffraction techniques proved that the polymer successfully coated the surfaces of the QDs. A TOPO/ODA mass ratio of 1:2 was determined to result in the best optical performance among the different ratios examined. The results showed that the described synthetic method is appropriate for the preparation of doped QDs with high-fluorescence quantum efficiency. PMID:22809232

  17. Color-tunable photoluminescence and energy transfer properties of single-phase Ba10(PO4)6O:Eu2+, Mn2+ phosphors

    NASA Astrophysics Data System (ADS)

    Guo, Qingfeng; Liao, Libing; Mei, Lefu; Liu, Haikun

    2015-12-01

    Single-phase Ba10-x-y(PO4)6O:xEu2+,yMn2+ samples with apatite structure have been synthesized via a solid-state reaction method. The phase structure, luminescence properties, lifetime, PL thermal stability, as well as fluorescence decay curves of the samples were investigated. Effective energy transfer occurs from Eu2+ to Mn2+ in Ba10(PO4)6O and a possible mechanism of the energy-transfer from Eu2+ to Mn2+ is proposed. The critical distances Rc was calculated by concentration quenching and turned out to be about 0.817 nm (xc=0.21). The CIE and thermally stable luminescence behaviors of Ba9.94(PO4)6O:0.06Eu2+ phosphor were also studied in detail. All the results indicate that Ba10-x-y(PO4)6O:xEu2+, yMn2+ phosphors have potential applications as near UV-convertible phosphors for white light-emitting diodes.

  18. Photoluminescence and electrical properties of Eu3+-doped Na0.5Bi4.5Ti4O15-based ferroelectrics under blue light excitation

    NASA Astrophysics Data System (ADS)

    Jiang, Xing-an; Jiang, Xiang-ping; Chen, Chao; Tu, Na; Chen, Yun-jing; Zhang, Ban-chao

    2016-03-01

    Na0.5Bi4.5- x Eu x Ti4O15 (NBT- x Eu3+) ceramics with x = 0, 0.05, 0.10, 0.15, 0.20, 0.25, 0.30 and 0.40 were prepared by conventional ceramics processing. NBT-0.25Eu3+ ceramics show the strongest red and orange emissions corresponding to the 5D0 → 7F2 (617 nm) and 5D0 → 7F1 (596 nm) transitions, respectively. The strongest excitation band around 465 nm matches well with the emission wavelength of commercial InGaN-based blue LED chip, indicating that Eu3+-doped NBT ceramics may be used as potential environmental friendly red-orange phosphor for W-LEDs application. As an inherent ferroelectric and piezoelectric material, the electrical properties of this potentially multifunctional electro-optical material have been also studied. The introduction of Eu3+ distinctly increased the Curie temperature ( T C ) of NBT- x Eu3+ ceramics from 640°C to 711°C as x ranges from 0 to 0.40. For higher temperature applications, the electrical conductivity was also investigated. The conduction of charge carriers in high-temperature range originates from the conducting electrons from the ionization of oxygen vacancies. High T C and low tan δ makes Eu3+-doped NBTceramic also suitable for high temperature piezoelectric sensor applications and electro-optical integration.

  19. Energy transfer based photoluminescence properties of co-doped (Er3+ + Pr3+): PEO + PVP blended polymer composites for photonic applications

    NASA Astrophysics Data System (ADS)

    Naveen Kumar, K.; Kang, Misook; Bhaskar Kumar, G.; Ratnakaram, Y. C.

    2016-04-01

    Er3+, Pr3+ singly doped and co-doped PEO + PVP polymer composites have been synthesized by conventional solution casting method. The structural analysis has been carried out for all these polymer composites from XRD analysis. Raman spectral studies confirm the ion-polymer interactions and polymer complex formation. Thermal properties of pure polymer film has also been clearly elucidated by TG/DTA profiles. Well defined optical absorption bands pertaining to Er3+ and Pr3+ are observed in the absorption spectral profile and these bands are assigned with corresponding electronic transitions. The polymer films containing singly doped Er3+ and Pr3+ ions have displayed green and red emissions at 510 nm (2H11/2 → 4I15/2) and 688 nm (3P0 → 3F3) respectively under UV excitation source. Comparing the emission spectra of singly Er3+ and co-doped Er3+ + Pr3+: PEO + PVP polymer films, a significant red emission pertaining to Pr3+ions is remarkably enhanced in co-doped polymer system. This could be ascribed to possible energy transfer from Er3+ to Pr3+ in co-doped polymer system. The energy transfer mechanism is clearly demonstrated using their emission performances, overlapped spectral profiles and also life time decay dynamics. Thus, it could be suggested that Er3+: PEO + PVP, Pr3+: PEO + PVP and (Er3+ + Pr3+): PEO + PVP blended polymer films are potential materials for several photonic applications.

  20. Preparation and Photoluminescence Properties of SrAl2O4:Eu2+,RE3+ Green Nanophosphors for Display Device Applications

    NASA Astrophysics Data System (ADS)

    Singh, Devender; Tanwar, Vijeta; Samantilleke, Anura P.; Mari, Bernabe; Bhagwan, Shri; Kadyan, Pratap Singh; Singh, Ishwar

    2016-06-01

    An efficient rapid gel combustion process was used to prepare divalent-europium-doped strontium aluminate (SrAl2O4:Eu2+/Eu2+,Dy3+/Eu2+,Dy3+,Nd3+) nanophosphors in the presence of boron flux in air. The prepared nanophosphors emitted green light at 507 nm upon excitation at 360 nm. The emission of green light was observed due to the 4 f 65 d 1 → 4 f 7 transition of Eu2+ ions. The absence of the characteristic sharp emission peak at 612 nm for Eu3+ (5D0 → 7F2) indicates that efficient reduction of Eu3+ to Eu2+ occurred in the presence of the boron flux (H3BO3) as reducing agent. The x-ray diffraction pattern suggested monoclinic crystallinity, while transmission electron microscopy revealed the average size of the prepared materials to be between 20 nm and 50 nm. Coactivators in the lattices such as Dy3+ alone or Dy3+ with Nd3+ produced long persistence and enhancement of the optoelectronic properties of the prepared materials.

  1. Differences in photoluminescence properties and thermal degradation between nanoparticle and bulk particle BaMgAl10O17:Eu2+ phosphors under UV?VUV irradiation.

    PubMed

    Liu, Bitao; Xin, Shuangyu; Li, Fenghua; Zhang, Jiachi; Wang, Yuhua

    2014-05-01

    BaMgAl10O17:Eu2+ (BAM) phosphors used for plasma display panels and three-band fluorescence lamps are exposed to an oxidizing environment at about 500 degrees C, which is currently unavoidable in actual applications. We investigated the mechanism of the luminance degradation of BAM caused by annealing at 500 degrees C based on the difference in luminance degradation of bulk particle and nanoparticle samples under various excitation source irradiations. When the samples were excited by the different light sources, more than 30% degradation of luminance occurred under 147 nm while less than 10% degradation occurred under 254 nm both for nanoparticle and bulk particle samples. In addition, the luminescence degradation of nanophosphors shows a different tendency compared to the bulk phosphors. With a model based on the particle size and excitation light penetration depth, we demonstrate that the degradation is still mainly ascribed to the oxidized of divalent Eu. The differences in luminescence properties between nanophosphors and bulk phosphors are also illustrated by this model. As a result, the potential industrial applications of nanophosphors are evaluated.

  2. Ultra-fast photoluminescence as a diagnostic for laser damage initiation

    SciTech Connect

    Laurence, T A; Bude, J D; Shen, N; Miller, P E; Steele, W A; Guss, G; Adams, J J; Wong, L L; Feit, M D; Suratwala, T I

    2009-10-30

    Using high-sensitivity confocal time-resolved photoluminescence (CTP) techniques, we report an ultra-fast photoluminescence (40ps-5ns) from impurity-free surface flaws on fused silica, including polished, indented or fractured surfaces of fused silica, and from laser-heated evaporation pits. This fast photoluminescence (PL) is not associated with slower point defect PL in silica which has characteristic decay times longer than 5ns. Fast PL is excited by the single photon absorption of sub-band gap light, and is especially bright in fractures. Regions which exhibit fast PL are strongly absorptive well below the band gap, as evidenced by a propensity to damage with 3.5eV ns-scale laser pulses, making CTP a powerful non-destructive diagnostic for laser damage in silica. The use of CTP to provide insights into the nature of damage precursors and to help develop and evaluate new damage mitigation strategies will be presented.

  3. Co-precipitation synthesis of Y2O2SO4:Eu3+ nanophosphor and comparison of photoluminescence properties with Y2O3:Eu3+ and Y2O2S:Eu3+ nanophosphors

    NASA Astrophysics Data System (ADS)

    Lian, Jingbao; Qin, Hua; Liang, Ping; Liu, Feng

    2015-10-01

    Eu3+ ions activated yttrium oxysulfate (Y2O2SO4:Eu3+) nanophosphor has been successfully synthesized by a co-precipitation method from commercially available Y(NO3)3·6H2O, Eu(NO3)3·6H2O, (NH4)2SO4 and NH3·H2O as the starting materials. Detailed characterizations of the synthetic products were obtained by differential thermal analysis, thermogravimetry and derivative thermogravimetry (DTA-TG-DTG), Fourier transform infrared spectroscopy (FT-IR), X-ray diffractometry (XRD), transmission electron microscopy (TEM), and photoluminescence (PL) spectroscopy. The results revealed that the precursor was composed of amorphous yttrium hydroxide sulfate when (NH4)2SO4 was introduced in the reaction system. Moreover, the precursor could be converted into pure Y2O2SO4 phase by calcining at 800 °C for 2 h in air and pure Y2O2S phase could be obtained by calcining Y2O2SO4 at 800 °C for 1 h in hydrogen atmosphere. The as-synthesized Y2O2SO4 phosphor particles are quasi-spherical in shape, slight aggregation and about 20-30 nm in size. PL spectra of the Y2O2SO4:Eu3+ nanophosphor under 270 nm ultraviolet (UV) light excitation show a red emission at 620 nm as the most prominent peak, which attributes to the 5D0→7F2 transition of Eu3+ ions. The quenching concentration of Eu3+ ions was 5 mol%, and its corresponding fluorescence lifetime was 1.49 ms according to the linear fitting result. Furthermore, the Y2O3 nanophosphor was synthesized by similar reaction and comparison of PL properties among three kinds of Eu3+ activated nanophosphors was also systematically discussed.

  4. Photoluminescence and Energy Transfer Properties with Y+SiO4 Substituting Ba+PO4 in Ba3Y(PO4)3:Ce(3+)/Tb(3+), Tb(3+)/Eu(3+) Phosphors for w-LEDs.

    PubMed

    Li, Kai; Liang, Sisi; Shang, Mengmeng; Lian, Hongzhou; Lin, Jun

    2016-08-01

    A series of Ce(3+), Tb(3+), Eu(3+) doped Ba2Y2(PO4)2(SiO4) (BYSPO) phosphors were synthesized via the high-temperature solid-state reaction route. X-ray diffraction, high-resolution transmission electron microscopy, Fourier transform infrared, solid-state NMR, photoluminescence (PL) including temperature-dependent PL, and fluorescent decay measurements were conducted to characterize and analyze as-prepared samples. BYSPO was obtained by the substitution of Y+SiO4 for Ba+PO4 in Ba3Y(PO4)3 (BYPO). The red shift of PL emission from 375 to 401 nm occurs by comparing BYSPO:0.14Ce(3+) with BYPO:0.14Ce(3+) under 323 nm UV excitation. More importantly, the excitation edge can be extended from 350 to 400 nm, which makes it be excited by UV/n-UV chips (330-410 nm). Tunable emission color from blue to green can be observed under 365 nm UV excitation based on the energy transfer from Ce(3+) to Tb(3+) ions after codoping Tb(3+) into BYSPO:0.14Ce(3+). Moreover, energy transfer from Tb(3+) to Eu(3+) ions also can be found in BYSPO:Tb(3+),Eu(3+) phosphors, resulting in the tunable color from green to orange red upon 377 nm UV excitation. Energy transfer properties were demonstrated by overlap of excitation spectra, variations of emission spectra, and decay times. In addition, energy transfer mechanisms from Ce(3+) to Tb(3+) and Tb(3+) to Eu(3+) in BYSPO were also discussed in detail. Quantum yields and CIE chromatic coordinates were also presented. Generally, the results suggest their potential applications in UV/n-UV pumped LEDs. PMID:27415966

  5. Photoluminescence properties of rare earths (Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+} and Tm{sup 3+}) activated NaInW{sub 2}O{sub 8} wolframite host lattice

    SciTech Connect

    Asiri Naidu, S.; Boudin, S.; Varadaraju, U.V.; Raveau, B.

    2012-01-15

    The photoluminescence (PL) studies on NaIn{sub 1-x}RE{sub x}W{sub 2}O{sub 8}, with RE=Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+} and Tm{sup 3+} phases have shown that the relative contribution of the host lattice and of the intra-f-f emission of the activators to the PL varies with the nature of the rare earth cation. In the case of Dy{sup 3+} and Tm{sup 3+} activators, with yellow and blue emission, respectively, the energy transfer from host to the activator plays a major role. In contrast for Eu{sup 3+}, with intense red emission, the host absorption is less pronounced and the intra-f-f transitions of the Eu{sup 3+} ions play a major role, whereas for Tb{sup 3+} intra-f-f transitions are only observed, giving rise to green emission. - Graphical abstract: NaInW{sub 2}O{sub 8} double tungstate doped with Eu{sup 3+}, Dy{sup 3+}, Tb{sup 3+}and Tm{sup 3+} shows characteristic emission of intense red for Eu{sup 3+}, yellow for Dy{sup 3+}, green for Tb{sup 3+} and blue for Tm{sup 3+}. Highlights: Black-Right-Pointing-Pointer Characteristic emissions of rare earths (Eu{sup 3+}, Tb{sup 3+}, Dy{sup 3+} and Tm{sup 3+}) are observed NaInW{sub 2}O{sub 8} wolframite. Black-Right-Pointing-Pointer Energy transfer from host to the activators (Eu{sup 3+} Dy{sup 3+} Tm{sup 3+} is observed. Black-Right-Pointing-Pointer PL properties of rare earth ions depend on minor structural variations in the host lattice.

  6. Photoluminescence and Energy Transfer Properties with Y+SiO4 Substituting Ba+PO4 in Ba3Y(PO4)3:Ce(3+)/Tb(3+), Tb(3+)/Eu(3+) Phosphors for w-LEDs.

    PubMed

    Li, Kai; Liang, Sisi; Shang, Mengmeng; Lian, Hongzhou; Lin, Jun

    2016-08-01

    A series of Ce(3+), Tb(3+), Eu(3+) doped Ba2Y2(PO4)2(SiO4) (BYSPO) phosphors were synthesized via the high-temperature solid-state reaction route. X-ray diffraction, high-resolution transmission electron microscopy, Fourier transform infrared, solid-state NMR, photoluminescence (PL) including temperature-dependent PL, and fluorescent decay measurements were conducted to characterize and analyze as-prepared samples. BYSPO was obtained by the substitution of Y+SiO4 for Ba+PO4 in Ba3Y(PO4)3 (BYPO). The red shift of PL emission from 375 to 401 nm occurs by comparing BYSPO:0.14Ce(3+) with BYPO:0.14Ce(3+) under 323 nm UV excitation. More importantly, the excitation edge can be extended from 350 to 400 nm, which makes it be excited by UV/n-UV chips (330-410 nm). Tunable emission color from blue to green can be observed under 365 nm UV excitation based on the energy transfer from Ce(3+) to Tb(3+) ions after codoping Tb(3+) into BYSPO:0.14Ce(3+). Moreover, energy transfer from Tb(3+) to Eu(3+) ions also can be found in BYSPO:Tb(3+),Eu(3+) phosphors, resulting in the tunable color from green to orange red upon 377 nm UV excitation. Energy transfer properties were demonstrated by overlap of excitation spectra, variations of emission spectra, and decay times. In addition, energy transfer mechanisms from Ce(3+) to Tb(3+) and Tb(3+) to Eu(3+) in BYSPO were also discussed in detail. Quantum yields and CIE chromatic coordinates were also presented. Generally, the results suggest their potential applications in UV/n-UV pumped LEDs.

  7. Origin of photoluminescence from silicon nanowires prepared by metal induced etching (MIE)

    SciTech Connect

    Saxena, Shailendra K. Rai, Hari. M.; Late, Ravikiran; Sagdeo, Pankaj R.; Kumar, Rajesh

    2015-05-15

    In this present study the origin of luminescence from silicon nanowires (SiNws) has been studied. SiNWs are fabricated on Si substrate by metal induced chemical etching (MIE). Here it is found that the band gap of SiNWs is higher than the gap of luminescent states in SiNWs which leads to the effect of Si=O bond. The band gap is estimated from diffuse reflectance analysis. Here we observe that band gap can be tailored depending on size (quantum confinement) but photoluminescence (PL) from all the sample is found to be fixed at 1.91 eV. This study is important for the understanding of origin of photoluminescence.

  8. Diverse Cd(II) compounds based on N-benzoyl-L-glutamic acid and N-donor ligands: Structures and photoluminescent properties

    NASA Astrophysics Data System (ADS)

    Ma, Ning; Guo, Wei-Ying; Song, Hui-Hua; Yu, Hai-Tao

    2016-01-01

    Five new Cd(II) coordination polymers with N-benzoyl-L-glutamic acid (H2bzgluO) and different N-donor ligands, [Cd(bzgluO)(2,2‧-bipy)(H2O)]n (1), [Cd(bzgluO)(2,4‧-bipy)2(H2O)·3H2O]n (2), [Cd(bzgluO)(phen)·H2O]n (3), [Cd(bzgluO)(4,4‧-bipy)(H2O)]n (4), [Cd(bzgluO)(bpp)(H2O)·2H2O]n (5) were synthesized (2,2‧-bipy=2,2‧-bipyridine, 2,4‧-bipy=2,4‧-bipyridine, phen=1,10-phenanthroline, 4,4‧-bipy=4,4‧-bipyridine, bpp=1,3-di(4-pyridyl)propane). Compounds 1-2 exhibit a 1D single-chain structure. Compound 1 generates a 2D supramolecular structure via π-π stacking and hydrogen bonding, 3D architecture of compound 2 is formed by hydrogen bonding. Compound 3 features a 1D double-chain structure, which are linked by π-π interactions into a 2D supramolecular layer. Compounds 4-5 display a 2D network structure. Neighboring layers of 4 are extended into a 3D supramolecular architecture through hydrogen bonding. The structural diversity of these compounds is attributed to the effect of ancillary N-donor ligands and coordination modes of H2bzgluO. Luminescent properties of 1-5 were studied at room temperature. Circular dichroism of compounds 1, 2 and 5 were investigated.

  9. Inter-band optoelectronic properties in quantum dot structure of low band gap III-V semiconductors

    SciTech Connect

    Dey, Anup; Maiti, Biswajit; Chanda, Debasree

    2014-04-14

    A generalized theory is developed to study inter-band optical absorption coefficient (IOAC) and material gain (MG) in quantum dot structures of narrow gap III-V compound semiconductor considering the wave-vector (k{sup →}) dependence of the optical transition matrix element. The band structures of these low band gap semiconducting materials with sufficiently separated split-off valance band are frequently described by the three energy band model of Kane. This has been adopted for analysis of the IOAC and MG taking InAs, InSb, Hg{sub 1−x}Cd{sub x}Te, and In{sub 1−x}Ga{sub x}As{sub y}P{sub 1−y} lattice matched to InP, as example of III–V compound semiconductors, having varied split-off energy band compared to their bulk band gap energy. It has been found that magnitude of the IOAC for quantum dots increases with increasing incident photon energy and the lines of absorption are more closely spaced in the three band model of Kane than those with parabolic energy band approximations reflecting the direct the influence of energy band parameters. The results show a significant deviation to the MG spectrum of narrow-gap materials having band nonparabolicity compared to the parabolic band model approximations. The results reflect the important role of valence band split-off energies in these narrow gap semiconductors.

  10. Structure and photoluminescence properties of Na{sub 2}Y{sub 2}B{sub 2}O{sub 7}:Ce{sup 3+},Tb{sup 3+} phosphors for solid-state lighting application

    SciTech Connect

    Wen, Dawei; Yang, Hui; Yang, Guanhui; Shi, Jianxin Wu, Mingmei Su, Qiang

    2014-05-01

    Novel phosphors of Na{sub 2}Y{sub 2}B{sub 2}O{sub 7}:Ce{sup 3+} and Na{sub 2}Y{sub 2}B{sub 2}O{sub 7}:Ce{sup 3+},Tb{sup 3+} were synthesized by a solid-state process and characterized with X-ray diffraction, photoluminescence (PL), PL excitation (PLE), and fluorescence decay time. The relationship between the observed Ce{sup 3+} emission properties and the crystal structure of Na{sub 2}Y{sub 2}B{sub 2}O{sub 7} is built and the result shows that Ce{sup 3+} ions occupy two non-equivalent Y{sup 3+} sites in the host. The codoping of Tb{sup 3+} in Na{sub 2}Y{sub 2}B{sub 2}O{sub 7}:Ce{sup 3+} can tune the emitting colour from blue to green and increase the luminescence quantum efficiency to 75.2% by the energy transfer of Ce{sup 3+}→Tb{sup 3+}. The energy transfer processes of Ce{sup 3+}–Ce{sup 3+} and Ce{sup 3+}–Tb{sup 3+} are analysed and determined to be electric dipole–dipole and dipole–quadrupole, respectively. The broad PLE spectra of Na{sub 2}Y{sub 2}B{sub 2}O{sub 7}:Ce{sup 3+} and Na{sub 2}Y{sub 2}B{sub 2}O{sub 7}:Ce{sup 3+},Tb{sup 3+} are well matched with the emission from near UV LED chips, which indicates that they are promising blue and green phosphors for phosphor-converted white LEDs. - Graphical abstract: Colour-tunable phosphors Na{sub 2}Y{sub 2}B{sub 2}O{sub 7}:Ce{sup 3+},Tb{sup 3+} with optimal quantum yield of 75.2% are synthesized and the phosphors can be served as n-UV pumped materials for LEDs. - Highlights: • Green phosphor Na{sub 2}Y{sub 2}B{sub 2}O{sub 7}:Ce{sup 3+},Tb{sup 3+} with quantum efficiency of 75.2% for n-UV application is synthesized. • The site occupation of Ce{sup 3+} in Na{sub 2}Y{sub 2}B{sub 2}O{sub 7} is investigated with the crystal structure and photoluminescence spectra. • The energy transfer of Ce{sup 3+}–Ce{sup 3+} and Ce{sup 3+}–Tb{sup 3+}, which is responsible to the tunable emitting colour of the phosphor, is demonstrated and the mechanism is studied.

  11. Photoluminescence of a single complex plasmonic nanoparticle

    PubMed Central

    Zhang, Tianyue; Lu, Guowei; Shen, Hongming; Shi, Kebin; Jiang, Yuanyuan; Xu, Dongsheng; Gong, Qihuang

    2014-01-01

    We report detailed investigations of the photoluminescence (PL) generated from an individual gold nanoflower, a highly branched plasmonic nanoparticle. Compared to nanostructures with simple shapes, such as spheres, nanorods, and bipyramids, nanoflowers exhibit more distinct features, i.e., the PL spectra and far-field emission patterns are strongly dependent on the wavelength and polarization of the excitation light. The experimental results are qualitatively explained using theoretical calculations. In addition, the intrinsic PL signal is highly dominated by localized surface plasmon resonances. The crucial role of plasmonic coupling in complex nanostructures during the plasmon-enhanced PL process is highlighted. The findings contribute to a deeper understanding of the PL properties of metallic nanoparticles. This study will be beneficial for several potential applications, including optical imaging and sensing in the fields of materials science and biology. PMID:24463794

  12. Simulation of J-aggregate microcavity photoluminescence

    NASA Astrophysics Data System (ADS)

    Michetti, Paolo; La Rocca, Giuseppe C.

    2008-05-01

    We have developed a model in order to account for the photoexcitation dynamics of J-aggregate films and strongly coupled J-aggregate microcavities. The J aggregates are described as a disordered Frenkel exciton system in which relaxation occurs due to the presence of a thermal bath of molecular vibrations. The correspondence between the photophysics in J-aggregate films and that in J-aggregate microcavities is obtained by introducing a model polariton wave function mixing cavity photon modes and J-aggregate super-radiant excitons. With the same description of the material properties, we have calculated both absorption and luminescence spectra for the J-aggregate film and the photoluminescence of strongly coupled organic microcavities. The model is able to account for the fast relaxation dynamics in organic microcavities following nonresonant pumping and explains the temperature dependence of the ratio between the upper polariton and the lower polariton luminescence.

  13. A comparative study on the effects of air gap wind and walking motion on the thermal properties of Arabian Thawbs and Chinese Cheongsams.

    PubMed

    Cui, Zhiying; Fan, Jintu; Wu, Yuenshing

    2016-08-01

    This paper reports on an experimental investigation on the effects of air gap, wind and walking motion on the thermal properties of traditional Arabian thawbs and Chinese cheongsams. Total thermal resistance (It) and vapour resistance (Re) were measured using the sweating fabric manikin - 'Walter', and the air gap volumes of the garments were determined by a 3D body scanner. The results showed the relative changes of It and Re of thawbs due to wind and walking motion are greater than those of cheongsams, which provided an explanation of why thawbs are preferred in extremely hot climate. It is further shown that thermal insulation and vapour resistance of thawbs increase with the air gap volume up to about 71,000 cm(3) and then decrease gradually. Thawbs with higher air permeability have significantly lower evaporative resistance particularly under windy conditions demonstrating the advantage of air permeable fabrics in body cooling in hot environments. Practitioner Summary: This paper aims to better understand the thermal insulation and vapour resistance of traditional Arabian thawbs and Chinese cheongsams, and the relationship between the thermal properties and their fit and design. The results of this study provide a scientific basis for designing ethnic clothing used in hot environments.

  14. Photoluminescence of spray pyrolysis deposited ZnO nanorods

    PubMed Central

    2011-01-01

    Photoluminescence of highly structured ZnO layers comprising well-shaped hexagonal rods is presented. The ZnO rods (length 500-1,000 nm, diameter 100-300 nm) were grown in air onto a preheated soda-lime glass (SGL) or ITO/SGL substrate by low-cost chemical spray pyrolysis method using zinc chloride precursor solutions and growth temperatures in the range of 450-550°C. We report the effect of the variation in deposition parameters (substrate type, growth temperature, spray rate, solvent type) on the photoluminescence properties of the spray-deposited ZnO nanorods. A dominant near band edge (NBE) emission is observed at 300 K and at 10 K. High-resolution photoluminescence measurements at 10 K reveal fine structure of the NBE band with the dominant peaks related to the bound exciton transitions. It is found that all studied technological parameters affect the excitonic photoluminescence in ZnO nanorods. PACS: 78.55.Et, 81.15.Rs, 61.46.Km PMID:21711895

  15. Nonlinear photoluminescence spectrum of single gold nanostructures.

    PubMed

    Knittel, Vanessa; Fischer, Marco P; de Roo, Tjaard; Mecking, Stefan; Leitenstorfer, Alfred; Brida, Daniele

    2015-01-27

    We investigate the multiphoton photoluminescence characteristics of gold nanoantennas fabricated from single crystals and polycrystalline films. By exciting these nanostructures with ultrashort pulses tunable in the near-infrared range, we observe distinct features in the broadband photoluminescence spectrum. By comparing antennas of different crystallinity and shape, we demonstrate that the nanoscopic geometry of plasmonic devices determines the shape of the emission spectra. Our findings rule out the contribution of the gold band structure in shaping the photoluminescence.

  16. Photoinduced spectral changes of photoluminescent gold nanoclusters

    NASA Astrophysics Data System (ADS)

    Matulionytė, Marija; Marcinonytė, Raminta; Rotomskis, Ričardas

    2015-05-01

    Ultrasmall photoluminescent gold nanoclusters (Au NCs), composed of several atoms with sizes up to a few nanometers, have recently stimulated extensive interest. Unique molecule-like behaviors, low toxicity, and facile synthesis make photoluminescent Au NCs a very promising alternative to organic fluorophores and semiconductor quantum dots (QDs) in broad ranges of biomedical applications. However, using gold nanoparticles (Au NPs) for bioimaging might cause their degradation under continuous excitation with UV light, which might result in toxicity. We report spectral changes of photoluminescent 2-(N-morpholino) ethanesulfonic acid (MES)-coated (Au-MES) NCs under irradiation with UV/blue light. Photoluminescent water soluble Au-MES NCs with a photoluminescence (PL) band maximum at 476 nm (λex=420 nm) were synthesized. Under irradiation with 402 nm wavelength light the size of photoluminescent Au-MES NCs decreased (λem=430 nm). Irradiating the sample solution with 330 nm wavelength light, nonluminescent Au NPs were disrupted, and photoluminescent Au NCs (λem=476 nm) were formed. Irradiation with 330 nm wavelength light did not directly affect photoluminescent Au-MES NCs, however, increase in PL intensity indicated the formation of photoluminescent Au NCs from the disrupted nonluminescent Au NPs. This study gives a good insight into the photostability of MES-coated Au NPs under continuous excitation with UV/blue light.

  17. Synthesis and photoluminescence behavior of difluoroboron complexes with β-diketone ligands

    NASA Astrophysics Data System (ADS)

    Wang, Dun-Jia; Kang, Yan-Fang; Fan, Ling; Hu, Yan-Jun; Zheng, Jing

    2013-12-01

    Five new difluoroboron complexes with 4-pyridyl-β-diketones were synthesized and their structures were confirmed by elemental analysis, IR, 1H NMR, ESI-MS and UV-vis spectroscopy. Their photoluminescence behavior was studied in DMF solution and solid state. The quantum yields (Φu) of complexes 2a-2e in DMF solution were measured relative to quinine sulfate and their lifetime values (τ) were calculated according to the luminescence decay curves in the solid state. From these data, the difluoroboron complexes exhibited the excellent photoluminescence properties. Especially, the complexes 2d and 2e displayed the stronger photoluminescence intensity, much higher quantum yield and longer lifetime value as compared to complexes 2a, 2b and 2c. The results indicate that the substituents at the 4-position on benzene ring have a significant impacts on the photoluminescence properties of the difluoroboron complexes.

  18. Improved photoluminescence characteristics of order-disorder AlGaInP quantum wells at room and elevated temperatures

    SciTech Connect

    Mukherjee, Kunal; Fitzgerald, Eugene A.; Deotare, Parag B.

    2015-04-06

    A set of nominally undoped CuPt-B type ordered (Al{sub x}Ga{sub 1−x}){sub 0.5}In{sub 0.5}P quantum-wells with disordered (Al{sub 0.7}Ga{sub 0.3}){sub 0.5}In{sub 0.5}P barriers were grown and characterized using transmission electron microscopy and photoluminescence spectroscopy. Such structures are potentially beneficial for light emitting devices due to the possibility of greater carrier confinement, reduced scattering into the indirect valleys, and band-offset adjustment beyond what is possible with strain and composition. Furthermore, the possibility of independently tuning the composition and the order-parameter of the quantum-well allows for the decoupling of the carrier confinement and the aluminum content and aids in the identification of carrier loss mechanisms. In this study, sharp order-disorder interfaces were achieved via the control of growth temperature between 650 °C and 750 °C using growth pauses. Improved high-temperature (400 K) photoluminescence intensity was obtained from quantum-wells with ordered Ga{sub 0.5}In{sub 0.5}P as compared to disordered Ga{sub 0.5}In{sub 0.5}P due to greater confinement. Additionally, in the ordered samples with a higher Al/Ga ratio to counter the band-gap reduction, the photoluminescence intensity at high temperature was as bright as that from conventional disordered heterostructures and had slightly improved wavelength stability. Room-temperature time-resolved luminescence measurements indicated a longer radiative lifetime in the ordered quantum-well with reduced scattering into the barrier. These results show that in samples of good material quality, the property controlling the luminescence intensity is the carrier confinement and not the presence of ordering or the aluminum content.

  19. Influence of electron beam irradiation on structural and optical properties of α-Ag2WO4 nanoparticles.

    PubMed

    A, Sreedevi; K P, Priyanka; K K, Babitha; S, Ganesh; Varghese, T

    2016-09-01

    The influence of 8MeV electron beam irradiation on the structural and optical properties of silver tungstate (α-Ag2WO4) nanoparticles synthesized by chemical precipitation method was investigated. The dose dependent effect of electron irradiation was investigated by various characterization techniques such as, X-ray diffraction, scanning electron microscopy, UV-vis absorption spectroscopy, photoluminescence and Raman spectroscopy. Systematic studies confirm that electron beam irradiation induces non-stoichiometry, defects and particle size variation on α-Ag2WO4, which in turn results changes in optical band gap, photoluminescence spectra and Raman bands.

  20. Nonlinear broadband photoluminescence of graphene induced by femtosecond laser irradiation

    SciTech Connect

    Liu, Wei-Tao; Wu, S.W.; Schuck, P.J.; Salmeron, Miquel; Shen, Y.R.; Wang, F.

    2010-07-01

    Upon femtosecond laser irradiation, a bright, broadband photoluminescence is observed from graphene at frequencies well above the excitation frequency. Analyses show that it arises from radiative recombination of a broad distribution of nonequilibrium electrons and holes, generated by rapid scattering between photoexcited carriers within tens of femtoseconds after the optical excitation. Its highly unusual characteristics come from the unique electronic and structural properties of graphene.

  1. Time Resolved Photoluminescence Studies of ZnO and Zn2SnO4 Nanowires for Solar Cells Applications

    NASA Astrophysics Data System (ADS)

    Yakami, Baichhabi Raj; Mahat, Meg; Chen, Jiajun; Lu, Liyou; Wang, Wenyong; Pikal, Jon M.

    2013-03-01

    Sensitized nanowires (NWs) are a promising option for solar cells. They serve as the support structure for the absorbing centers, provide interfacial charge separation, and transport to the anode. Most work has focused on binary oxides, but ternary oxides have advantages due to flexibility in the properties of the oxide. Here we report on the photoluminescence (PL) and Time Resolved PL (TRPL) of Zinc oxide (ZnO) and Zinc Tin Oxide (ZTO) NWs grown by Chemical Vapor Deposition. The ZnO NWs show strong band gap emission and weak but resolvable defect emission peaks. The PL from the ZTO NWs does not show any band gap emission and absorption measurements confirm that these NWs have a direct forbidden transition. The ZTO NWs do have a board visible emission peak, which is usually attributed defects and oxygen vacancies. TRPL of the band gap emission in ZnO NWs yield a carrier lifetime of 1.4ns. The TRPL of the defect peaks in ZTO NWs are more complicated, showing a multi-exponential decay but with an overall decay rate similar to the ZnO NWs. This indicates that the expected increase in carrier lifetime in the ZTO NWs is not currently realized likely due to defect recombination, and additional optimization of the NW growth process may yield improved performance. DOE

  2. Intrinsic photoluminescence of diatom shells in sensing applications

    NASA Astrophysics Data System (ADS)

    De Tommasi, E.; Rendina, I.; Rea, I.; De Stefano, M.; Lamberti, A.; De Stefano, L.

    2009-05-01

    Diatoms are monocellular micro-algae provided with external valves, the frustules, made of amorphous hydrated silica. Frustules present patterns of regular arrays of holes, the areolae, characterized by sub-micrometric dimensions. Frustules from centric diatoms are characterized by a radial disposition of areolae and exhibit several optical properties, such as photoluminescence, lens-like behavior and, in general, photonic-crystal-like behavior as long as confinement of electromagnetic field is concerned. In particular, intrinsic photoluminescence from frustules is strongly influenced by the surrounding atmosphere: on exposure to gases, the induced luminescence changes both in the optical intensity and peaks positions. To give specificity against a target analyte, a key feature for an optical sensor, a biomolecular probe, which naturally recognizes its ligand, can be covalently linked to the diatom surface. We explored the photoluminescence emission properties of frustules of Coscinodiscus wailesii centric species, characterized by a diameter of about 100-200 μm, on exposure to different vapours and in presence of specific bioprobes interacting with target analytes. Very high sensitivities have been observed due to the characteristic morphology of diatoms shells. Particular attention has been devoted to the emission properties of single frustules.

  3. Detection of immunocomplex formation by enhanced photoluminescence of antibody-functionalized diatom biosilica

    NASA Astrophysics Data System (ADS)

    Gale, Debra K.; Gutu, Timothy; Jiao, Jun; Chang, Chih-Hung; Rorrer, Gregory L.

    2009-05-01

    Diatoms are single-celled photosynthetic algae that make silica shells or "frustules" with intricate features patterned at the nano and microscales. In this study, antibody-functionalized diatom biosilica frustules serve as a biosensor platform for selective and label free antibody-antigen immunocomplex formation by enhanced photoluminescence. Biosilica frustules of 10 micron diameter were isolated from cells of the centric marine diatom Cyclotella sp. They were then mounted on glass and covalently functionalized with the model antibody Rabbit Immunoglobulin G (IgG) to yield a uniform nanostructured surface that selectively binds to its complimentary antigen, Goat anti-Rabbit IgG. Diatom frustules possess an intrinsic capacity to emit blue light when excited with a UV laser light source, a property called photoluminescence. Binding the antibody-functionalized diatom frustule with its complimentary antigen selectively enhanced the intrinsic photoluminescence intensity of the diatom frustule by a factor of three, whereas challenging the antibody-functionalized diatom frustule with a non-complimentary antigen, Goat anti-human IgG did not change the intrinsic photoluminescence intensity. The nucleophilic immunocomplex increases the photoluminescence by donating electrons to non-radiative sites on the photoluminescent diatom biosilica, thereby decreasing non-radiative electron decay and increasing radiative emission. The intensified photoluminescence intensity is correlated to the antigen, goat anti-rabbit IgG concentration, with a binding constant of 2.8 +/- 0.7x10-7 M.

  4. Blue Photoluminescence From Silacyclobutene Compounds

    NASA Astrophysics Data System (ADS)

    Pernisz, Udo

    1999-04-01

    Organosilicon compounds in which the Si atom is bound to an aromatic moiety such as a phenyl group, exhibit strong blue photoluminescence when excited with UV light (for example at a wavelength of 337 nm). This phenomenon was investigated quantitatively at room temperature and at the temperature of liquid nitrogen (78 K) by measuring the emission and excitation spectra of the total luminescence, and of the phosphorescence, for a silacyclobutene compound in which two phenyl groups are joined across the C=C double bond of the ring. The effect of a series of organic substituents on the Si atom was investigated as well as the time dependence of the phosphorescence intensity decay for this class of materials. A tentative model of the energy levels in this compound is proposed. The observation of visible blue emission -- in contrast to photoluminescence in the UV from the aromatic groups -- is explained by the Si-C bond lowering the energy of the molecular orbitals, an effect that is currently under study for a range of Si-containing compounds. Synthesis of the silacyclobutene compounds was performed at the laboratory of Prof. N. Auner, now at J.W. Goethe Universität, Frankfurt, Germany. His contributions, and those of his collaborators, to the work reported here are gratefully acknowledged.

  5. Optical properties of amorphous Ge1- x Se x and Ge1- x- y Se x As y thin films — optical gap bowing and phonon modes

    NASA Astrophysics Data System (ADS)

    Lee, Hosuk; So, Hyeon Seob; Lee, Hosun; Shin, Hae-Young; Yoon, Seokhyun; Ahn, Hyung-Woo; Kim, Su-Dong; Lee, Suyoun; Jeong, Doo-Seok; Cheong, Byung-ki

    2014-06-01

    We investigated the optical properties of Ge1- x Se x and Ge1- x- y Se x As y amorphous films by using spectroscopic ellipsometry and Raman spectroscopy. The dielectric functions and absorption coefficients ( α) of the amorphous films were determined from the measured ellipsometric angles (Ψ,Δ). We obtained the optical gap energies and the Urbach energies from the absorption coefficients and found a strong bowing effect in the optical gap energy of Ge1- x- y Se x As y , where the endpoint binaries were Ge0.50Se0.50 and Ge0.31As0.69. Based on the correlation between the optical gap energies and the Urbach energies, we attributed the large bowing parameter to electronic disorder. Using Raman spectroscopy, we measured the phonon modes and discussed the composition dependence of the phonon peak frequencies and lineshapes in terms of structural units. Based on the composition dependence of the phonons in Ge1- x- y Se x As y , we identified the phonon modes of Ge0.31As0.69. A resonant Raman phenomenon was observed in Ge0.40Se0.60 at a laser excitation of 514 nm (2.41 eV). We verified that this laser energy corresponded to the transition energy of Ge0.40Se0.60 by using the second derivative of the dielectric function of Ge0.40Se0.60.

  6. Strong correlation of the electrical properties, up-conversion photoluminescence, and phase structure in Er3+/Yb3+ co-doped (1 - x)K0.5Na0.5NbO3-xLiNbO3 ceramics

    NASA Astrophysics Data System (ADS)

    Wang, Jia; Luo, Laihui; Huang, Yinpeng; Li, Weiping; Wang, Feifei

    2015-11-01

    Er3+ and Yb3+ co-doped (1 - x)K0.5Na0.5NbO3-xLiNbO3 (KNN-xLN:Er/Yb, x = 0.04-0.09) ceramics were prepared to investigate their phase structures and piezoelectric, ferroelectric, and up-conversion photoluminescence properties. With increasing LN content, x, KNN-xLN:Er/Yb ceramics at room temperature evolve from the orthorhombic phase to the polymorphic phase and finally to the tetragonal phase. All the ferroelectric and piezoelectric properties and the Ir/Ig ratio of integrated intensities of red and green emission bands reach maximum values within the polymorphic phase transition of the KNN-0.06LN:Er/Yb ceramic. In this work, we find a close correlation between the electrical properties, up-conversion photoluminescence, and phase structure of KNN-xLN:Er/Yb ceramics. This correlation is discussed based on the Judd-Ofelt and crystallographic symmetry theories.

  7. Mind the gap: investigating why the physical and orbital properties of 'hot' and 'cold' Classical KBOs mismatch.

    NASA Astrophysics Data System (ADS)

    Peixinho, N.; Miloni, O.

    2011-10-01

    We have generated orbital parameters for 700 Classical Kuiper Belt Objects (CKBOs) and simulated their orbital evolution for 500 Myr. We have noticed that, during their orbital evolution, objects with initial orbital inclinations ˜ 5° - 10° make larger inclination excursions that others. Since the inclination variation of these objects is approximately pendulum-like, they spend more time at the extrema and less time at their (central) initial inclination, hence they are less likely to be seen there. We will discuss this phenomenon and analyze if it could be responsible for the observed inclination density gap at i ˜5° of the unbiased distribution of CKBOs.

  8. A self-consistent optimization of multicomponent solution properties: Ab initio molecular dynamic simulations and the MgO-SiO2 miscibility gap under pressure

    NASA Astrophysics Data System (ADS)

    Harvey, Jean-Philippe; Gheribi, Aïmen E.; Asimow, Paul D.

    2015-07-01

    We propose a new approach to parameterizing the Gibbs energy of a multicomponent solution as a function of temperature, pressure and composition. It uses the quasichemical model in the second nearest neighbor approximation and considers both a polynomial representation (for low pressure) and an exponential decay representation (for moderate-to-high pressure) of the excess molar volume νxs to extend thermodynamic behavior to elevated pressure. This approach differs from previous configuration-independent regular or associated solution-type models of multicomponent silicate liquids at elevated pressure and can account for any structural or short-range order data that may be available. A simultaneous least squares fit of the molar volume and the molar enthalpy of mixing data obtained from First Principles Molecular Dynamics (FPMD) simulations at various pressures enables complete parameterization of the excess thermodynamic properties of the solution. Together with consistently optimized properties of coexisting solids, this enables prediction of pressure-temperature-composition phase diagrams associated with melting. Although the method is extensible to natural multicomponent systems, we apply the procedure as a first test case to the important planetary model system MgO-SiO2 using FPMD data found in the literature. One key result of this optimization, which depends only on the derived excess properties of the liquid phase, is that the consolute temperature of the SiO2-rich miscibility gap is predicted to decrease with increasing pressure. This appears to be in disagreement with available experimental constraints and suggests possible thermodynamic inconsistency between FPMD data and experimental phase equilibrium data in the 0-5 GPa pressure range. We propose a new thermodynamic consistency criterion relating the signs of νxs and other excess properties and discuss the need for precise calculations of derivatives of excess properties. Finally, the potential

  9. Design and properties of intermediate-sized narrow band-gap conjugated molecules relevant to solution-processed organic solar cells.

    PubMed

    Liu, Xiaofeng; Sun, Yanming; Hsu, Ben B Y; Lorbach, Andreas; Qi, Li; Heeger, Alan J; Bazan, Guillermo C

    2014-04-16

    Increases in the molecular length of narrow band gap conjugated chromophores reveal potentially beneficial optical and electronic properties, thermal stabilities, and high power conversion efficiencies when integrated into optoelectronic devices, such as bulk heterojunction organic solar cells. With the objective of providing useful information for understanding the transition from small-sized molecules to polymers, as well as providing a general chemical design platform for extracting relationships between molecular structure and bulk properties, we set out to vary the electron affinity of the molecular backbone. Therefore, a series of donor (D)-acceptor (A) alternating narrow band gap conjugated chromophores were synthesized based on the general molecular frameworks: D(1)-A(1)-D(2)-A(2)-D(2)-A(1)-D(1) and D(1)-A(1)-D(2)-A(2)-D(2)-A(2)-D(2)-A(1)-D(1). When the central electron-accepting moiety (A(2)) was varied or modified, two classes of molecules could be compared. First, we showed that the alteration of one single electron-accepting group, while maintaining the shape of the molecular framework, can effectively impact the optical properties and energy levels of the molecules. DFT ground state structure optimizations show similar "U" shape conformations among these molecules. Second, we examined how the site-specific introduction of fluorine atom(s) modifies the thermal properties in the solid state, while maintaining relatively similar optical and electrochemical features of interest. Structure-property relationship of such molecular systems could be rationally evaluated in the aspects of thermal-responsive molecular organizations in the solid state and dipole moments both in the ground and excited states. The impact of molecular structure on charge carrier mobilities in field effect transistors and the performance of photovoltaic devices were also studied.

  10. Photoluminescent and thermal properties of (Sr{sub 0.995−x−y−z}Ca{sub x}Ba{sub y}Mg{sub z}){sub 2}SiO{sub 4}:0.01Eu{sup 2+} phosphors for warm white light-emitting diodes

    SciTech Connect

    Li, Yao; Ci, Zhipeng; Peng, Yingquan; Wang, Yuhua; Liu, Chunjuan

    2015-01-15

    Highlights: • The photoluminescent property of Sr{sub 2}SiO{sub 4}:Eu{sup 2+} is improved by doping Ca{sup 2+} and Ba{sup 2+}. • The emission spectra red-shift obviously by doping Ca{sup 2+} into Sr{sub 2}SiO{sub 4}:Eu{sup 2+}. • The thermal stability is enhanced by doping Ba{sup 2+} into (Sr,Ca){sub 2}SiO{sub 4}:Eu{sup 2+}. • The improved phosphors can combine blue-LED chips to generate warm white light. - Abstract: A series of phosphors (Sr{sub 0.995−x−y−z}Ca{sub x}Ba{sub y}Mg{sub z}){sub 2}SiO{sub 4}:0.01Eu{sup 2+} (0 ≤ x ≤ 0.45, 0 ≤ y ≤ 0.015, 0 ≤ z ≤ 0.35) were synthesized by solid state reaction. Their phase compositions and photoluminescent properties were investigated in detail. The X-ray diffraction analysis indicates the impurity phase of SrSiO{sub 3} is formed only when z ≥ 0.25. A photoluminescence investigation shows, with x increasing the emission spectra of the phosphors (0 ≤ x ≤ 0.45, 0 ≤ y ≤ 0.015, z = 0) obviously red-shift, the corresponding color tones shift from yellow to orange–yellow and their CCTs reduce from 2875 to 2237 K. All the results are beneficial for the phosphors to combining blue light-emitting diode chips to generate warm white light. Besides, the thermal stability of the phosphor (x = 0.36, y = z = 0) is enhanced by doping Ba{sup 2+}, due to the greater activation energy for the compounds containing barium.

  11. Connexin26 Mutations Causing Palmoplantar Keratoderma and Deafness Interact with Connexin43, Modifying Gap Junction and Hemichannel Properties.

    PubMed

    Shuja, Zunaira; Li, Leping; Gupta, Shashank; Meşe, Gülistan; White, Thomas W

    2016-01-01

    Mutations in GJB2 (connexin [Cx]26) cause either deafness or deafness associated with skin diseases. That different disorders can be caused by distinct mutations within the same gene suggests that unique channel activities are influenced by each class of mutation. We have examined the functional characteristics of two human mutations, Cx26-H73R and Cx26-S183F, causing palmoplantar keratoderma (PPK) and deafness. Both failed to form gap junction channels or hemichannels when expressed alone. Coexpression of the mutants with wild-type Cx43 showed a transdominant inhibition of Cx43 gap junction channels, without reductions in Cx43 protein synthesis. In addition, the presence of mutant Cx26 shifted Cx43 channel gating and kinetics toward a more Cx26-like behavior. Coimmunoprecipitation showed Cx43 being pulled down more efficiently with mutant Cx26 than wild-type, confirming the enhanced formation of heteromeric connexons. Finally, the formation of heteromeric connexons resulted in significantly increased Cx43 hemichannel activity in the presence of Cx26 mutants. These findings suggest a common mechanism whereby Cx26 mutations causing PPK and deafness transdominantly influence multiple functions of wild-type Cx43. They also implicate a role for aberrant hemichannel activity in the pathogenesis of PPK and further highlight an emerging role for Cx43 in genetic skin diseases.

  12. Sol-gel production of Cu/Al co-doped zinc oxide: Effect of Al co-doping concentration on its structure and optoelectronic properties

    NASA Astrophysics Data System (ADS)

    Bu, Ian Yi-Yu

    2014-12-01

    Sol-gel deposition of ZnO:Cu:Al thin films were co-doped different Cu:Al ratio. The optoelectronic and structural properties of the resultant film were evaluated using scanning electron microscopy, X-ray diffraction, energy dispersive spectroscopy, photoluminescence spectroscopy and UV-VIS spectroscopy. It was found that the Al content leads to narrowing of the band gap and that excessive Al doping concentration greater than 5 at% degrade the film's properties.

  13. Raman spectroscopy and time-resolved photoluminescence of BN and BxCyNz nanotubes

    SciTech Connect

    Wu, J.; Han, Wei-Qiang; Walukiewicz, W.; Ager III, J.W.; Shan, W.; Haller,E.E.; Zettl, A.

    2004-01-21

    We report Raman and time-resolved photoluminescence spectroscopic studies of multiwalled BN and B{sub x}C{sub y}N{sub z} nanotubes. The Raman spectroscopy shows that the as-grown B{sub x}C{sub y}N{sub z} charge recombination, respectively. Comparison of the photoluminescence of BN nanotubes to that decay process is characterized by two time constants that are attributed to intra- and inter-BN sheet nanotubes as predicted by theory. nanotubes are radially phase separated into BN shells and carbon shells. The photoluminescence of hexagonal BN is consistent with the existence of a spatially indirect band gap in multi-walled BN.

  14. Effect of low temperature anneals and nonthermal treatments on the properties of gap fill oxides used in SiGe and III-V devices

    NASA Astrophysics Data System (ADS)

    Ryan, E. Todd; Morin, Pierre; Madan, Anita; Mehta, Sanjay

    2016-07-01

    Silicon dioxide is used to electrically isolate CMOS devices such as fin field effect transistors by filling gaps between the devices (also known as shallow trench isolation). The gap fill oxide typically requires a high temperature anneal in excess of 1000 °C to achieve adequate electrical properties and oxide densification to make the oxide compatible with subsequent fabrication steps such as fin reveal etch. However, the transition from Si-based devices to high mobility channel materials such as SiGe and III-V semiconductors imposes more severe thermal limitations on the processes used for device fabrication, including gap fill oxide annealing. This study provides a framework to quantify and model the effect of anneal temperature and time on the densification of a flowable silicon dioxide as measured by wet etch rate. The experimental wet etch rates allowed the determination of the activation energy and anneal time dependence for oxide densification. Dopant and self-diffusion can degrade the channel material above a critical temperature. We present a model of self-diffusion of Ge and Si in SiGe materials. Together these data allowed us to map the thermal process space for acceptable oxide wet etch rate and self-diffusion. The methodology is also applicable to III-V devices, which require even lower thermal budget. The results highlight the need for nonthermal oxide densification methods such as ultraviolet (UV) and plasma treatments. We demonstrate that several plasma treatments, in place of high temperature annealing, improved the properties of flowable oxide. In addition, UV curing prior to thermal annealing enables acceptable densification with dramatically reduced anneal temperature.

  15. Photoluminescence in modulation-doped GaAs/Ga1-xAlxAs heterojunctions

    NASA Astrophysics Data System (ADS)

    Shen, J. X.; Oka, Y.; Hu, C. Y.; Ossau, W.; Landwehr, G.; Friedland, K.-J.; Hey, R.; Ploog, K.; Weimann, G.

    1999-03-01

    We investigated the physical properties of modulation-doped GaAs/Ga1-xAlxAs heterojunctions by photoluminescence. We found two types of transitions and attributed them to the space direct excitons in the GaAs flat band region and the space indirect excitons near the heterojunction notch. We propose the vertical transport of photoexcited carriers prior to the actual exciton formation under the influence of the two-dimensional carrier gas. Therefore, the photoluminescence intensities of the two types of excitons are correlated. The vertical transport model explains successfully the experimental results of the optically detected cyclotron resonance, the photoluminescence intensity oscillation with magnetic field and the long rise time of the photoluminescence intensity for the excitonic transitions.

  16. Bridging the Design-Manufacturing-Materials Data Gap: Material Properties for Optimum Design and Manufacturing Performance in Light Vehicle Steel-Intensive Body Structures

    NASA Astrophysics Data System (ADS)

    Zuidema, Blake K.

    2012-09-01

    As safety and fuel economy regulations become increasingly more challenging around the world, light vehicle manufacturers are facing increasing pressure to reduce the weight of their vehicles cost effectively while maintaining or improving safety performance. Optimum light vehicle steel body structure weight and performance are achieved when the constraints of design, manufacturing, and material properties are considered simultaneously. ArcelorMittal has invested heavily over the past several years to close the gap between material property knowledge and the inter-relation between material performance and design and manufacturing efficiency. Knowledge gained through this process is presented and the importance of achieving this simultaneous 3-way optimization is illustrated by a lightweight steel door design example from ArcelorMittal's S-in motion catalog of lightweight steel solutions.

  17. Effects of the Cu off-stoichiometry on transport properties of wide gap p-type semiconductor, layered oxysulfide LaCuSO

    SciTech Connect

    Goto, Yosuke Tanaki, Mai; Okusa, Yuki; Matoba, Masanori; Kamihara, Yoichi; Shibuya, Taizo; Yasuoka, Kenji

    2014-07-14

    Layered oxysulfide LaCu{sub 1−x}SO (x = 0–0.03) was prepared to elucidate the effect of Cu off-stoichiometry on their electrical and thermal transport properties. Electrical resistivity drastically decreases down from ∼10{sup 5} Ω·cm to ∼10{sup −1} Ω·cm as a result of Cu deficiency (x = 0.01) at 300 K. Thermal conductivity of the samples at 300 K, which is dominated by lattice components, is estimated to be 2.3(3) Wm{sup −1}K{sup −1}. Stoichiometric LaCuSO has an optical band gap of 3.1 eV, while broad optical absorption at photon energies of approximately 2.1 eV was observed for Cu-deficient samples. Density functional theory calculation suggests that these broad absorption structures probably originate from the in-gap states generated by the sulfur vacancies created to compensate the charge imbalance due to Cu off-stoichiometry. These results clearly demonstrate that Cu deficiency plays a crucial role in determining the electrical transport properties of Cu-based p-type transparent semiconductors.

  18. Modulation of mixed-phase titania photoluminescence by oxygen adsorption

    SciTech Connect

    Pallotti, D.; Orabona, E.; Amoruso, S.; Maddalena, P.; Lettieri, S.

    2014-07-21

    We investigate the effect of oxygen (O{sub 2}) adsorption on photoluminescence properties of mixed-phase titania nanoparticle films deposited by femtosecond pulsed laser deposition, aiming to assess preliminary conclusions about the feasibility of opto-chemical sensing based on titania. We evidence that O{sub 2} produces opposite responses in rutile and anatase photoluminescence efficiency, highlighting interesting potentialities for future double-parametric optical sensing based on titania. The results evidence an important role of lattice oxygen atoms, suggesting that the standard Schottky barrier mechanism driving the response toward gas species in most used metal-oxide sensors (e.g., tin dioxide) is not the only active mechanism in titania.

  19. Radioluminescence and photoluminescence of Th:CaF2 crystals

    PubMed Central

    Stellmer, Simon; Schreitl, Matthias; Schumm, Thorsten

    2015-01-01

    We study thorium-doped CaF2 crystals as a possible platform for optical spectroscopy of the 229Th nuclear isomer transition. We anticipate two major sources of background signal that might cover the nuclear spectroscopy signal: VUV-photoluminescence, caused by the probe light, and radioluminescence, caused by the radioactive decay of 229Th and its daughters. We find a rich photoluminescence spectrum at wavelengths above 260 nm, and radioluminescence emission above 220 nm. This is very promising, as fluorescence originating from the isomer transition, predicted at a wavelength shorter than 200 nm, could be filtered spectrally from the crystal luminescence. Furthermore, we investigate the temperature-dependent decay time of the luminescence, as well as thermoluminescence properties. Our findings allow for an immediate optimization of spectroscopy protocols for both the initial search for the nuclear transition using synchrotron radiation, as well as future optical clock operation with narrow-linewidth lasers. PMID:26502749

  20. Photoluminescence Imaging Characterization of Thin-Film InP

    SciTech Connect

    Johnston, Steve; Allende Motz, Alyssa; Moore, James; Zheng, Maxwell; Javey, Ali; Bermel, Peter

    2015-06-14

    Indium phosphide grown using a novel vapor-liquid-solid method is a promising low-cost material for III-V single-junction photovoltaics. In this work, we characterize the properties of these materials using photoluminescence (PL) imaging, time-resolved photoluminescence (TRPL), and microwave-reflection photoconductive decay (u-PCD). PL image data clearly shows the emergence of a self-similar dendritic growth network from nucleation sites, while zoomed-in images show grain structure and grain boundaries. Single photon TRPL data shows initial surface-dominated recombination, while two-photon excitation TRPL shows a lifetime of 10 ns. Bulk carrier lifetime may be as long as 35 ns as measured by u-PCD, which can be less sensitive to surface recombination.

  1. Radioluminescence and photoluminescence of Th:CaF2 crystals.

    PubMed

    Stellmer, Simon; Schreitl, Matthias; Schumm, Thorsten

    2015-01-01

    We study thorium-doped CaF2 crystals as a possible platform for optical spectroscopy of the (229)Th nuclear isomer transition. We anticipate two major sources of background signal that might cover the nuclear spectroscopy signal: VUV-photoluminescence, caused by the probe light, and radioluminescence, caused by the radioactive decay of (229)Th and its daughters. We find a rich photoluminescence spectrum at wavelengths above 260 nm, and radioluminescence emission above 220 nm. This is very promising, as fluorescence originating from the isomer transition, predicted at a wavelength shorter than 200 nm, could be filtered spectrally from the crystal luminescence. Furthermore, we investigate the temperature-dependent decay time of the luminescence, as well as thermoluminescence properties. Our findings allow for an immediate optimization of spectroscopy protocols for both the initial search for the nuclear transition using synchrotron radiation, as well as future optical clock operation with narrow-linewidth lasers. PMID:26502749

  2. Gap Resolution

    2009-06-16

    With the continued improvements of next generation DNA sequencing technologies and their advantages over traditional Sanger sequencing, the Joint Genome Institute (JGI) has modified its sequencing pipeline to take advantage of the benefits of such technologies. Currently, standard 454 Titanium, paired end 454 Titanium, and Illumina GAll data are generated for all microbial projects and then assembled using draft assemblies at a much greater throughput than before. However, it also presents us with new challenges.more » In addition to the increased throughput, we also have to deal with a larger number of gaps in the Newbler genome assemblies. Gaps in these assemblies are usually caused by repeats (Newbler collapses repeat copies into individual contigs, thus creating gaps), strong secondary structures, and artifacts of the PCR process (specific to 454 paired end libraries). Some gaps in draft assemblies can be resolved merely by adding back the collapsed data from repeats. To expedite gap closure and assembly improvement on large numbers of these assemblies, we developed software to address this issue.« less

  3. Montmorillonite-chitosan-silver sulfadiazine nanocomposites for topical treatment of chronic skin lesions: in vitro biocompatibility, antibacterial efficacy and gap closure cell motility properties.

    PubMed

    Sandri, Giuseppina; Bonferoni, Maria Cristina; Ferrari, Franca; Rossi, Silvia; Aguzzi, Carola; Mori, Michela; Grisoli, Pietro; Cerezo, Pilar; Tenci, Marika; Viseras, Cesar; Caramella, Carla

    2014-02-15

    Silver compounds and especially silver sulfadiazine (AgSD) are reported as effective antimicrobial agents against almost all known bacteria, fungi and some viruses. However, AgSD has been shown to be cytotoxic toward fibroblasts and keratinocytes in vitro and consequently to retard wound healing in vivo. The aim of the present work was to evaluate the in vitro biocompatibility (cytotoxicity and proliferation), antimicrobial efficacy and cell motility gap closure (assay of wound closure) of MT/CS nanocomposites loaded with silver sulfadiazine (AgSD). It is envisioned to be administered as a powder or a dressing for cutaneous application in the treatment of skin ulcers. The loading of AgSD in MT/CS nanocomposites aimed at preventing the delay in wound healing, by decreasing the cytotoxicity of AgSD and maintaining its antimicrobial properties. Nanocomposites were prepared by using different amounts of MT (100-2000 mg) and 40 ml of a 1% (w/w) chitosan glutamate aqueous solution. The relative amounts of AgSD and chitosan in the systems were assessed by suitable analytic methods. The nanocomposite prepared using 100mg of MT was characterized for in vitro biocompatibility and proliferation and for wound healing using normal human dermal fibroblasts (NHDF). Antimicrobial properties were evaluated against four reference bacterial strains: Staphylococcus aureus, Streptococcus pyogenes, Escherichia coli, and Pseudomonas aeruginosa. AgSD loaded in the 100 MT/CS nanocomposite showed good in vitro biocompatibility and gap closure properties (fibroblasts) and maintained AgSD antimicrobial properties, especially against P. aeruginosa, that often complicates skin lesions. PMID:24507371

  4. Modeling of band gap properties of GaInNP alloys lattice matched to GaAs

    NASA Astrophysics Data System (ADS)

    Buyanova, I. A.; Izadifard, M.; Chen, W. M.; Hong, Y. G.; Tu, C. W.

    2006-01-01

    Compositional and temperature dependences of the band gap energies of GaInNP alloys, which are lattice matched to GaAs, are determined and modeled by a band anticrossing (BAC) interaction between the localized state of the isolated NP and extended host states. The BAC parameters are deduced as EN=2.1±0.1eV and CMN=1.7±0.2eV. The low value of the coupling parameter CMN implies weaker coupling of the N level with the host matrix, presumably due to short range ordering effects, similar to the case of GaInNAs alloys with a high In content. The obtained information is important for future modeling of the electronic structure of the alloys.

  5. Ancillary ligand-assisted assembly of C{sub 3}-symmetric 4,4′,4″-nitrilotribenzoic acid with divalent Zn{sup 2+} ions: Syntheses, topological structures, and photoluminescence properties

    SciTech Connect

    Cui, Li-Ting; Niu, Yan-Fei; Han, Jie; Zhao, Xiao-Li

    2015-07-15

    4,4′,4″-nitrilotribenzoic acid (H{sub 3}L), a C{sub 3}-symmetric ligand, was found to self-assemble into two polymorphs driven by intermolecular hydrogen-bonding interactions. Reactions of this ligand with Zn{sup 2+} under solvothermal conditions resulted in four new coordination polymers bearing interesting structural motifs: [Zn{sub 2}(L){sub 2}(py){sub 2}]·2(H{sub 2}NMe{sub 2}){sup +}·DMF·2H{sub 2}O (1), [Zn{sub 2}(L)(H{sub 2}L)(bipy)]·1.5H{sub 2}O·Guest (2), [Zn{sub 2}(L){sub 2}(bipy)]·2(H{sub 2}NMe{sub 2}){sup +}·2DMF (3), and [Zn{sub 3}(L){sub 2}(bpa)]·2H{sub 2}O·Guest (4) (H{sub 3}L=4,4′,4′′-nitrilotribenzoic acid, DMF=dimethylformamide, py=pyridine, bipy=4,4′-bipyridine, bpa=1,2-bis(4-pyridyl)diazene). Single-crystal structural analysis revealed that compound 1 exhibits a rare example of twofold interpenetrating anionic 3D (3,3)-net framework containing helical channels, whereas in 2, the 3D pillar-layer structure generated from bipy-pillared Zn{sub 2}(L)(H{sub 2}L) layer is further reinforced by intermolecular hydrogen bonding among pairs of free –COOH units. Compound 3 shows an interesting entangled architecture of 2D→3D parallel polycatenation consisting five-coordinated Zn{sup 2+} ions. Compound 4 displays a 3D pillar-layer framework with trimeric Zn{sub 3}(CO{sub 2}){sub 6} serving as secondary building unit (SBU). The syntheses, structures, thermal stabilities, powder X-ray diffractions and solid-state photoluminescence properties for these crystalline materials have been carried out. In addition, supramolecular assembly of H{sub 3}L under solvothermal conditions will also be addressed. - Graphical abstract: Supramolecular assembly of 4,4′,4′′-nitrilotribenzoic acid and its ligand behavior toward Zn{sup 2+} were investigated, which exhibit two polymorphs of the free acid and four metal coordination polymers bearing interesting structural motifs. - Highlights: • Two polymorphs of H{sub 3}L showing different hydrogen

  6. Crossing the Gap

    ERIC Educational Resources Information Center

    Lockette, Tim

    2009-01-01

    In a nation where education is funded largely by local property taxes, schools in wealthy communities have plenty of funds to spend on programs that get their kids ready for college. Schools in poor communities scrimp and save to get the job done--or hope that funding from the state will help fill in the gap. This article describes how students…

  7. Synthesis, structural characterization and study of blue shift in optical properties of zinc oxide nano particles prepared by chemical route method

    NASA Astrophysics Data System (ADS)

    Taunk, P. B.; Das, R.; Bisen, D. P.; Tamrakar, Raunak Kumar

    2015-12-01

    We report the synthesis and optical properties of ZnO nano particle using TEA (Tri Ethanol Amine) and without TEA by chemical route method. By decreasing the concentration of TEA, reaction rate is decreases and inter planner spacing d is increases, band gap is increased from 4.1 to 4.8 eV. In case of without TEA band gap is obtained 3.4 eV. Morphology, growth and the nature of crystalline of the powder samples were performed by X- ray Diffraction (XRD); UV spectrophotometer, scanning electron microscope (SEM) and Photoluminescence (PL). Luminescence properties are discussed by probing the photoluminescence properties of ZnO nano particles with TEA at different molar concentrations.

  8. Activation of extended red emission photoluminescence in carbon solids by exposure to atomic hydrogen and UV radiation

    NASA Technical Reports Server (NTRS)

    Furton, Douglas G.; Witt, Adolf N.

    1993-01-01

    We report on new laboratory results which relate directly to the observation of strongly enhanced extended red emission (ERE) by interstellar dust in H2 photodissociation zones. The ERE has been attributed to photoluminescence by hydrogenated amorphous carbon (HAC). We are demonstrating that exposure to thermally dissociated atomic hydrogen will restore the photoluminescence efficiency of previously annealed HAC. Also, pure amorphous carbon (AC), not previously photoluminescent, can be induced to photoluminesce by exposure to atomic hydrogen. This conversion of AC into HAC is greatly enhanced by the presence of UV irradiation. The presence of dense, warm atomic hydrogen and a strong UV radiation field are characteristic environmental properties of H2 dissociation zones. Our results lend strong support to the HAC photoluminescence explanation for ERE.

  9. Enhanced band-edge photoluminescence from ZnO-passivated ZnO nanoflowers by atomic layer deposition

    PubMed Central

    2013-01-01

    The ZnO nanoflowers were synthesized by reactive vapor deposition. A secondary nucleation in the stalk/leaves interface was suggested. The photoluminescence revealed that there were many oxygen vacancies in the nanoflowers. To tune the optical properties of ZnO nanoflowers, ZnO thin films with varying thicknesses were coated on the nanoflowers by atomic layer deposition, which can distinctly improve the band-edge photoluminescence properties. PMID:23442577

  10. Photoluminescence of carbon dots from mesoporous silica

    NASA Astrophysics Data System (ADS)

    Nelson, D. K.; Razbirin, B. S.; Starukhin, A. N.; Eurov, D. A.; Kurdyukov, D. A.; Stovpiaga, E. Yu; Golubev, V. G.

    2016-09-01

    Photophysical properties of carbon dots were investigated under various excitation conditions and over a wide temperature region - from room to liquid helium temperatures. The carbon dots (CDs) were synthesized using mesoporous silica particles as a reactor and (3-aminopropyl)triethoxysilane (APTES) as a precursor. The photoluminescence spectra of CDs exhibit a strong dependence on the excitation wavelength and demonstrate a significant inhomogeneous broadening. Lowering sample temperature reveals the doublet structure of the spectra, which is associated with the vibronic structure of radiative transitions. The vibration energy ∼1200 cm-1 is close to the energy of Csbnd O stretching vibration. Long-lived phosphorescence of carbon dots with its decay time ∼0.2 s at T = 80 K was observed. The fluorescence and phosphorescence spectra are shown to be spectrally separated. The long-lived component of the emission was ascribed to optically forbidden triplet-singlet transitions. The value of the singlet-triplet splitting was found to be about 0.3 eV. Photo-induced polarization of the luminescence of carbon dots was revealed. The degree of the linear polarization is dependent on the wavelengths of both excitation and emitted light. The effect indicates a hidden anisotropy of optical dipole transitions in the dots and demonstrates the loss of the dipole orientation during the electron energy relaxation.

  11. Structural properties and band offset determination of p-channel mixed As/Sb type-II staggered gap tunnel field-effect transistor structure

    SciTech Connect

    Zhu, Y.; Jain, N.; Hudait, M. K.; Mohata, D. K.; Datta, S.; Lubyshev, D.; Fastenau, J. M.; Liu, A. K.

    2012-09-10

    The structural properties and band offset determination of p-channel staggered gap In{sub 0.7}Ga{sub 0.3}As/GaAs{sub 0.35}Sb{sub 0.65} heterostructure tunnel field-effect transistor (TFET) grown by molecular beam epitaxy (MBE) were investigated. High resolution x-ray diffraction revealed that the active layers are strained with respect to 'virtual substrate.' Dynamic secondary ion mass spectrometry confirmed an abrupt junction profile at the In{sub 0.7}Ga{sub 0.3}As/GaAs{sub 0.35}Sb{sub 0.65} heterointerface and minimal level of intermixing between As and Sb atoms. The valence band offset of 0.37 {+-} 0.05 eV was extracted from x-ray photoelectron spectroscopy. A staggered band lineup was confirmed at the heterointerface with an effective tunneling barrier height of 0.13 eV. Thus, MBE-grown staggered gap In{sub 0.7}Ga{sub 0.3}As/GaAs{sub 0.35}Sb{sub 0.65} TFET structures are a promising p-channel option to provide critical guidance for the future design of mixed As/Sb type-II based complementary logic and low power devices.

  12. Electronic properties of metal-induced gap states at insulator/metal interfaces: Dependence on the alkali halide and the possibility of excitonic mechanism of superconductivity

    NASA Astrophysics Data System (ADS)

    Arita, Ryotaro; Tanida, Yoshiaki; Kuroki, Kazuhiko; Aoki, Hideo

    2004-03-01

    Motivated from the experimental observation of metal-induced gap states (MIGS) at insulator/metal interfaces by Kiguchi et al. [Phys. Rev. Lett. 90, 196803 (2003)], we have theoretically investigated the electronic properties of MIGS at interfaces between various alkali halides and a metal represented by a jellium with the first-principles density-functional method. We have found that, on top of the usual evanescent state, MIGS generally have appreciable amplitudes on halogen sites with a pz-like character, whose penetration depth (λ) is as large as half the lattice constant of bulk alkali halides. This implies that λ, while little dependent on the carrier density in the jellium, is dominated by the energy gap of the alkali halide, and is scaled by the lattice constant, where λLiF<λLiCl<λLiI. We also propose a possibility of the MIGS working favorably for the exciton-mediated superconductivity, especially in a system where ˜10 Å of metal is sandwiched by alkali halide substrates.

  13. Structural properties and band offset determination of p-channel mixed As/Sb type-II staggered gap tunnel field-effect transistor structure

    NASA Astrophysics Data System (ADS)

    Zhu, Y.; Jain, N.; Mohata, D. K.; Datta, S.; Lubyshev, D.; Fastenau, J. M.; Liu, A. K.; Hudait, M. K.

    2012-09-01

    The structural properties and band offset determination of p-channel staggered gap In0.7Ga0.3As/GaAs0.35Sb0.65 heterostructure tunnel field-effect transistor (TFET) grown by molecular beam epitaxy (MBE) were investigated. High resolution x-ray diffraction revealed that the active layers are strained with respect to "virtual substrate." Dynamic secondary ion mass spectrometry confirmed an abrupt junction profile at the In0.7Ga0.3As/GaAs0.35Sb0.65 heterointerface and minimal level of intermixing between As and Sb atoms. The valence band offset of 0.37 ± 0.05 eV was extracted from x-ray photoelectron spectroscopy. A staggered band lineup was confirmed at the heterointerface with an effective tunneling barrier height of 0.13 eV. Thus, MBE-grown staggered gap In0.7Ga0.3As/GaAs0.35Sb0.65 TFET structures are a promising p-channel option to provide critical guidance for the future design of mixed As/Sb type-II based complementary logic and low power devices.

  14. Time-Resolved Photoluminescence and Photovoltaics

    SciTech Connect

    Metzger, W. K.; Ahrenkiel, R. K.; Dippo, P.; Geisz, J.; Wanlass, M. W.; Kurtz, S.

    2005-01-01

    The time-resolved photoluminescence (TRPL) technique and its ability to characterize recombination in bulk photovoltaic semiconductor materials are reviewed. Results from a variety of materials and a few recent studies are summarized and compared.

  15. Emergence of new red-shifted carbon nanotube photoluminescence based on proximal doped-site design

    NASA Astrophysics Data System (ADS)

    Shiraki, Tomohiro; Shiraishi, Tomonari; Juhász, Gergely; Nakashima, Naotoshi

    2016-06-01

    Single-walled carbon nanotubes (SWNTs) show unique photoluminescence (PL) in the near-infrared (NIR) region. Here we propose a concept based on the proximal modification in local covalent functionalization of SWNTs. Quantum mechanical simulations reveal that the SWNT band gap changes specifically based on the proximal doped-site design. Thus, we synthesize newly-designed bisdiazonium molecules and conduct local fucntionalisation of SWNTs. Consequently, new red-shifted PL (E112*) from the bisdiazonium-modified SWNTs with (6, 5) chirality is recognized around 1250 nm with over ~270 nm Stokes shift from the PL of the pristine SWNTs and the PL wavelengths are shifted depending on the methylene spacer lengths of the modifiers. The present study revealed that SWNT PL modulation is enable by close-proximity-local covalent modification, which is highly important for fundamental understanding of intrinsic SWNT PL properties as well as exciton engineering-based applications including photonic devices and (bio)imaging/sensing.

  16. Emergence of new red-shifted carbon nanotube photoluminescence based on proximal doped-site design

    NASA Astrophysics Data System (ADS)

    Shiraki, Tomohiro; Shiraishi, Tomonari; Juhász, Gergely; Nakashima, Naotoshi

    2016-06-01

    Single-walled carbon nanotubes (SWNTs) show unique photoluminescence (PL) in the near-infrared (NIR) region. Here we propose a concept based on the proximal modification in local covalent functionalization of SWNTs. Quantum mechanical simulations reveal that the SWNT band gap changes specifically based on the proximal doped-site design. Thus, we synthesize newly-designed bisdiazonium molecules and conduct local fucntionalisation of SWNTs. Consequently, new red-shifted PL (E112*) from the bisdiazonium-modified SWNTs with (6, 5) chirality is recognized around 1250 nm with over ~270 nm Stokes shift from the PL of the pristine SWNTs and the PL wavelengths are shifted depending on the methylene spacer lengths of the modifiers. The present study revealed that SWNT PL modulation is enable by close-proximity-local covalent modification, which is highly important for fundamental understanding of intrinsic SWNT PL properties as well as exciton engineering–based applications including photonic devices and (bio)imaging/sensing.

  17. Effect of capping agent concentration on thermoluminescence and photoluminescence of copper-doped zinc sulfide nanoparticles.

    PubMed

    Wanjari, Lata; Bisen, D P; Brahme, Namita; Sahu, Ishwar Prasad; Sharma, Ravi

    2015-08-01

    Copper-doped zinc sulfide (ZnS:Cu) nanoparticles with varying concentrations of capping agent were prepared using a chemical route technique. These particles were characterized by scanning electron microscopy (SEM), transmission electron microscopy and X-ray diffraction (XRD). Optical absorption studies showed that the absorption edge shifted towards the blue region as the concentration of the capping agent increased. Using effective mass approximation, calculation of the nanoparticle size indicated that effective band gap energy increases with decreasing particle size. The thermoluminescence (TL) properties of sodium hexameta phosphate (SHMP)-passivated ZnS:Cu nanoparticles were investigated after UV irradiation at room temperature. The TL glow curve of capped ZnS:Cu showed variations in TL peak position and intensity with the change in capping agent concentration. The photoluminescence (PL) spectra of ZnS:Cu nanoparticles excited at 254 nm exhibited a broad green emission band peaking around 510 nm, which confirmed the characteristic feature of Zn(2+) as well as Cu(2+) ions as the luminescent centres in the lattice. The PL spectra of ZnS:Cu nanoparticles with increasing capping agent concentrations revealed that the emission becomes more intense and shifted towards shorter wavelengths as the sizes of the samples were reduced.

  18. Temperature-dependent photoluminescence spectra of GaN epitaxial layer grown on Si (111) substrate

    NASA Astrophysics Data System (ADS)

    Zhao, Dan-Mei; Zhao, De-Gang; Jiang, De-Sheng; Liu, Zong-Shun; Zhu, Jian-Jun; Chen, Ping; Liu, Wei; Li, Xiang; Shi, Ming

    2015-10-01

    In this paper, the temperature-dependent photoluminescence (PL) properties of GaN grown on Si (111) substrate are studied. The main emission peaks of GaN films grown on Si (111) are investigated and compared with those grown on sapphire substrates. The positions of free and bound exciton luminescence peaks, i.e., FXA and D0X peaks, of GaN films grown on Si (111) substrates undergo red shifts compared with those grown on sapphire. This is attributed to the fact that the GaN films grown on sapphire are under the action of compressive stress, while those grown on Si (111) substrate are subjected to tensile stress. Furthermore, the positions of these peaks may be additionally shifted due to different stress conditions in the real sample growth. The emission peaks due to stacking faults are found in GaN films grown on Si (111) and an S-shaped temperature dependence of PL spectra can be observed, owing to the influence of the quantum well (QW) emission by the localized states near the conduction band gap edge and the temperature-dependent distribution of the photo-generated carriers. Project supported by the National Natural Science Foundation of China (Grant Nos. 61474110, 61377020, 61376089, 61223005, and 61176126) and the National Science Fund for Distinguished Young Scholars of China (Grant No. 60925017).

  19. Emergence of new red-shifted carbon nanotube photoluminescence based on proximal doped-site design

    PubMed Central

    Shiraki, Tomohiro; Shiraishi, Tomonari; Juhász, Gergely; Nakashima, Naotoshi

    2016-01-01

    Single-walled carbon nanotubes (SWNTs) show unique photoluminescence (PL) in the near-infrared (NIR) region. Here we propose a concept based on the proximal modification in local covalent functionalization of SWNTs. Quantum mechanical simulations reveal that the SWNT band gap changes specifically based on the proximal doped-site design. Thus, we synthesize newly-designed bisdiazonium molecules and conduct local fucntionalisation of SWNTs. Consequently, new red-shifted PL (E112*) from the bisdiazonium-modified SWNTs with (6, 5) chirality is recognized around 1250 nm with over ~270 nm Stokes shift from the PL of the pristine SWNTs and the PL wavelengths are shifted depending on the methylene spacer lengths of the modifiers. The present study revealed that SWNT PL modulation is enable by close-proximity-local covalent modification, which is highly important for fundamental understanding of intrinsic SWNT PL properties as well as exciton engineering–based applications including photonic devices and (bio)imaging/sensing. PMID:27345862

  20. The properties of photonic band gap and surface plasmon modes in the three-dimensional magnetized photonic crystals as the mixed polarized modes considered

    NASA Astrophysics Data System (ADS)

    Zhang, Hai-Feng; Liu, Shao-Bin; Jiang, Yu-Chi

    2015-04-01

    In this paper, the properties of photonic band gap (PBG) and surface plasmon modes in the three-dimensional (3D) magnetized plasma photonic crystals (MPPCs) with face-centered-cubic (fcc) lattices are theoretically investigated based on the plane wave expansion (PWE) method, in which the homogeneous magnetized plasma spheres are immersed in the homogeneous dielectric background, as the Voigt effects of magnetized plasma are considered (the incidence electromagnetic wave vector is perpendicular to the external magnetic field at any time). The dispersive properties of all of the EM modes are studied because the PBG is not only for the extraordinary and ordinary modes but also for the mixed polarized modes. The equations for PBGs also are theoretically deduced. The numerical results show that the PBG and a flatbands region can be observed. The effects of the dielectric constant of dielectric background, filling factor, plasma frequency and plasma cyclotron frequency (the external magnetic field) on the dispersive properties of all of the EM modes in such 3D MPPCs are investigated in detail, respectively. Theoretical simulations show that the PBG can be manipulated by the parameters as mentioned above. Compared to the conventional dielectric-air PCs with similar structure, the larger PBG can be obtained in such 3D MPPCs. It is also shown that the upper edge of flatbands region cannot be tuned by the filling factor and dielectric constant of dielectric background, but it can be manipulated by the plasma frequency and plasma cyclotron frequency.