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Sample records for electroluminescence efficiency degradation

  1. Electroluminescence efficiencies of erbium in silicon-based hosts

    SciTech Connect

    Cueff, Sébastien E-mail: christophe.labbe@ensicaen.fr; Manel Ramírez, Joan; Berencén, Yonder; Garrido, Blas; Kurvits, Jonathan A.; Zia, Rashid; Rizk, Richard; Labbé, Christophe E-mail: christophe.labbe@ensicaen.fr

    2013-11-04

    We report on room-temperature 1.5 μm electroluminescence from trivalent erbium (Er{sup 3+}) ions embedded in three different CMOS-compatible silicon-based hosts: SiO{sub 2}, Si{sub 3}N{sub 4}, and SiN{sub x}. We show that although the insertion of either nitrogen or excess silicon helps enhance electrical conduction and reduce the onset voltage for electroluminescence, it drastically decreases the external quantum efficiency of Er{sup 3+} ions from 2% in SiO{sub 2} to 0.001% and 0.0004% in SiN{sub x} and Si{sub 3}N{sub 4}, respectively. Furthermore, we present strong evidence that hot carrier injection is significantly more efficient than defect-assisted conduction for the electrical excitation of Er{sup 3+} ions. These results suggest strategies to optimize the engineering of on-chip electrically excited silicon-based nanophotonic light sources.

  2. Efficient electroluminescence from new lanthanide (Eu3+, Sm3+) complexes.

    PubMed

    Yu, Jiangbo; Zhou, Liang; Zhang, Hongjie; Zheng, Youxuan; Li, Huanrong; Deng, Ruiping; Peng, Zeping; Li, Zhefeng

    2005-03-07

    The syntheses, structures, and electroluminescent properties are described for two new lanthanide complexes Ln(HFNH)3phen [HFNH = 4,4,5,5,6,6,6-heptafluoro-1-(2-naphthyl)hexane-1,3-dione; phen = 1,10-phenanthroline; Ln = Eu3+ (1), Sm3+ (2)]. Both complexes exhibit bright photoluminescence at room temperature (RT) due to the characteristic emission of Eu3+ and Sm3+ ion. Several devices using the two complexes as emitters were fabricated. The performances of these devices are among the best reported for devices using europium complex and samarium complex as emitters. The device based on 1 with the structure ITO/TPD (50 nm)/1:CBP (10%, 40 nm)/BCP (20 nm)/AlQ (30 nm)/LiF (1 nm)/Al (200 nm) exhibits the maximum brightness of 957 cd/m2, current efficiency of 4.14 cd/A, and power efficiency of 2.28 lm/W with a pure red Eu3+ ion emission. Especially, at the high brightness of 200 cd/m2, the device of 1 still has a high current efficiency of 2.15 cd/A. The device of 2 with a three-layer structure of ITO/TPD (50 nm)/2 (50 nm)/BCP (20 nm)/LiF (1 nm)/Al (200 nm) gives the maximum brightness of 42 cd/m2, current efficiency of 0.18 cd/A. By the comparison of the electroluminescent properties of devices based on Eu(TTA3phen (TTA = 2-thenoyltrifluoroacteonate) and 1, we conclude that the polyfluoration on the alkyl group of the ligand and the introduction of the long conjugate naphthyl group into the ligand improve the efficiency of 1-doped devices, especially at high current densities.

  3. Analysis of degradation mechanisms in AlInN/GaN HEMTs by electroluminescence technique

    NASA Astrophysics Data System (ADS)

    Berthet, F.; Petitdidier, S.; Guhel, Y.; Trolet, J. L.; Mary, P.; Vivier, A.; Gaquière, C.; Boudart, B.

    2017-01-01

    In this paper, the impact of a severe on-state stress on the IDS (VDS, VGS) characteristics of AlInN/GaN devices is analyzed by electroluminescence technique performed at room temperature. In fact, the devices operate in bias conditions that allow measuring the bell- shaped gate current. To our knowledge, it is the first time that a bell-shaped gate current centered at a positive VGS and measured at room temperature has been shown for an AlInN/GaN transistor. We have also highlighted that electroluminescence spectra are related to the superposition of intraband radiative electron transitions, Fabry-Perot oscillations, and emission bands induced by recombination of electrons due to electron traps. In these conditions, it is not so easy to extract energies levels of electron traps existing in unstressed and stressed AlInN/GaN HEMTs from electroluminescence spectra. Thus, we have also shown that the electrical degradations induced by on-state stress are mainly related to the trapping of hot electron by deep pre-existing electron traps in the devices. Moreover, we have highlighted the existence of two electron traps activated at 1.6 and 1.8 eV in the devices.

  4. Organic electroluminescent devices and method for improving energy efficiency and optical stability thereof

    DOEpatents

    Heller, Christian Maria

    2004-04-27

    An organic electroluminescent device ("OELD") has a controllable brightness, an improved energy efficiency, and stable optical output at low brightness. The OELD is activated with a series of voltage pulses, each of which has a maximum voltage value that corresponds to the maximum power efficiency when the OELD is activated. The frequency of the pulses, or the duty cycle, or both are chosen to provide the desired average brightness.

  5. Degradation and rejuvenation studies of AC electroluminescent ZnS:Cu,Cl phosphors

    NASA Astrophysics Data System (ADS)

    Stanley, Jacob; Jiang, Yu; Bridges, Frank; Carter, Sue A.; Ruhlen, Laurel

    2010-02-01

    We report detailed degradation and rejuvenation studies of AC electroluminescence (EL) of the phosphor ZnS:Cu,Cl, aiming to better understand the physical mechanisms that control EL emission. We find that the AC EL emission spectra vary considerably with the AC driving frequency but all spectra can be fit to a sum of four Gaussians. During degradation, although there is a large overall decrease in amplitude, the shape of the emission spectra measured at a given AC frequency does not change. Annealing the samples after they are significantly degraded can rejuvenate the phosphors with a maximum rejuvenation occurring (for fixed annealing times) near 180 °C. Further, these test cells can be degraded and rejuvenated multiple times. However studies at slightly higher annealing temperatures (240 °C) show significant thermal degradation and, perhaps more importantly, a change in the spectral shape; this likely indicates that two distinct mechanisms are then operative. In extended x-ray absorption fine structure (EXAFS) experiments we find that the CuS nanoprecipitates in the ZnS host (~75% of the Cu is in the CuS precipitates) do not change significantly after the 240 °C anneal; these experiments also provide a more detailed comparison of the local structure about Cu in pure CuS, and in ZnS:Cu,Cl. In addition, the EXAFS experiments also place an upper limit on the fraction of possible interstitial Cu sites, proposed as a blue emission center, at less than 10%. The combined experiments place strong constraints on the mechanisms for degradation and rejuvenation and suggest that EL degradation is most likely caused by either Cu or Cl diffusion under high E-fields, while thermal diffusion at slightly elevated temperatures without E-fields present, re-randomizes the (isolated) dopant distributions. Higher T anneals appear to damage the sharp tips on the precipitates.

  6. Observation of degradation processes of Al electrodes in organic electroluminescence devices by electroluminescence microscopy, atomic force microscopy, scanning electron microscopy, and Auger electron spectroscopy

    NASA Astrophysics Data System (ADS)

    Do, L. M.; Han, E. M.; Niidome, Y.; Fujihira, M.; Kanno, T.; Yoshida, S.; Maeda, A.; Ikushima, A. J.

    1994-11-01

    Degradation of top electrodes is one of the most important factors to determine the lifetimes of organic electroluminescence (EL) devices. An organic EL device (indium thin oxide (ITO/N,N'-diphenyl-N,N'-bis(3-methylphenyl)-(1,1'-biphenyl)-4,4'-diamine (TPD)/tris(8-hydroxy-quinoline)aluminum (Al q(sub 3))/Al) was prepared and a morphological change of the Al top electrode was observed during and/or after applying voltage by atomic force microscopy and scanning electron microscopy (SEM). The change in the electrode surface, i.e., the increase in surface roughness was observed during the current flow. The degradation process started from faint dark core parts and propagated into disks with different rates depending on the magnitude of applied voltage. Degraded sites of the Al electrode, which were analyzed as aluminum oxide by Auger electron spectroscopy, protruded into the air on the organic layers. In SEM images of a life-end electrode, discontinuities due to crevasse formation in the organic layers sandwiched by the ITO base and the metal top electrodes were observed in many places. These results confirm that one of the most crucial factors of the degradation process was deformation of metal and organic layers due to heat, gas evolution, and oxidation caused by applied voltage.

  7. Efficient Blue Electroluminescence Using Quantum-Confined Two-Dimensional Perovskites.

    PubMed

    Kumar, Sudhir; Jagielski, Jakub; Yakunin, Sergii; Rice, Peter; Chiu, Yu-Cheng; Wang, Mingchao; Nedelcu, Georgian; Kim, Yeongin; Lin, Shangchao; Santos, Elton J G; Kovalenko, Maksym V; Shih, Chih-Jen

    2016-10-03

    Solution-processed hybrid organic-inorganic lead halide perovskites are emerging as one of the most promising candidates for low-cost light-emitting diodes (LEDs). However, due to a small exciton binding energy, it is not yet possible to achieve an efficient electroluminescence within the blue wavelength region at room temperature, as is necessary for full-spectrum light sources. Here, we demonstrate efficient blue LEDs based on the colloidal, quantum-confined 2D perovskites, with precisely controlled stacking down to one-unit-cell thickness (n = 1). A variety of low-k organic host compounds are used to disperse the 2D perovskites, effectively creating a matrix of the dielectric quantum wells, which significantly boosts the exciton binding energy by the dielectric confinement effect. Through the Förster resonance energy transfer, the excitons down-convert and recombine radiatively in the 2D perovskites. We report room-temperature pure green (n = 7-10), sky blue (n = 5), pure blue (n = 3), and deep blue (n = 1) electroluminescence, with record-high external quantum efficiencies in the green-to-blue wavelength region.

  8. Thorough subcells diagnosis in a multi-junction solar cell via absolute electroluminescence-efficiency measurements.

    PubMed

    Chen, Shaoqiang; Zhu, Lin; Yoshita, Masahiro; Mochizuki, Toshimitsu; Kim, Changsu; Akiyama, Hidefumi; Imaizumi, Mitsuru; Kanemitsu, Yoshihiko

    2015-01-16

    World-wide studies on multi-junction (tandem) solar cells have led to record-breaking improvements in conversion efficiencies year after year. To obtain detailed and proper feedback for solar-cell design and fabrication, it is necessary to establish standard methods for diagnosing subcells in fabricated tandem devices. Here, we propose a potential standard method to quantify the detailed subcell properties of multi-junction solar cells based on absolute measurements of electroluminescence (EL) external quantum efficiency in addition to the conventional solar-cell external-quantum-efficiency measurements. We demonstrate that the absolute-EL-quantum-efficiency measurements provide I-V relations of individual subcells without the need for referencing measured I-V data, which is in stark contrast to previous works. Moreover, our measurements quantify the absolute rates of junction loss, non-radiative loss, radiative loss, and luminescence coupling in the subcells, which constitute the "balance sheets" of tandem solar cells.

  9. Mechanisms of efficiency enhancement in the doped electroluminescent devices based on a europium complex

    NASA Astrophysics Data System (ADS)

    Zhou, Liang; Zhang, Hongjie; Shi, Weidong; Deng, Ruiping; Li, Zhefeng; Yu, Jiangbo; Guo, Zhiyong

    2008-12-01

    In this study, we investigated the dependence of electroluminescence (EL) efficiency on carrier distribution in the light-emitting layer (EML) of the device based on Eu(TTA)3phen (TTA=thenoyltrifluoroacetone, phen=1,10-phenanthroline) doped 4,4'-N,N'-dicarbazole-biphenyl (CBP) system. We found that EL efficiency increases monotonously with increasing hole injection even when holes are the majority carriers. This phenomenon was attributed to the accumulation of holes in EML, which improves the balance of holes and electrons on Eu(TTA)3phen molecules, thus enhancing the EL efficiency. To further improve the balance of holes and electrons on Eu(TTA)3phen molecules, the injection of electron was gently decreased by modulating the thickness of Al and LiF layers. Interestingly, EL efficiency increases gradually to a maximum and then decreases rapidly with decreasing electron injection. As a result, the device with 80 nm Al and 1.2 nm LiF obtained the maximal current efficiency of 9.53 cd/A, power efficiency of 5.35 lm/W, and external quantum efficiency of 5.15%. Our experimental results demonstrated that the balance of holes and electrons on dye molecules is the precondition for the doped device to obtain high EL efficiency, when carrier trapping is the dominant EL mechanism.

  10. Thorough subcells diagnosis in a multi-junction solar cell via absolute electroluminescence-efficiency measurements

    PubMed Central

    Chen, Shaoqiang; Zhu, Lin; Yoshita, Masahiro; Mochizuki, Toshimitsu; Kim, Changsu; Akiyama, Hidefumi; Imaizumi, Mitsuru; Kanemitsu, Yoshihiko

    2015-01-01

    World-wide studies on multi-junction (tandem) solar cells have led to record-breaking improvements in conversion efficiencies year after year. To obtain detailed and proper feedback for solar-cell design and fabrication, it is necessary to establish standard methods for diagnosing subcells in fabricated tandem devices. Here, we propose a potential standard method to quantify the detailed subcell properties of multi-junction solar cells based on absolute measurements of electroluminescence (EL) external quantum efficiency in addition to the conventional solar-cell external-quantum-efficiency measurements. We demonstrate that the absolute-EL-quantum-efficiency measurements provide I–V relations of individual subcells without the need for referencing measured I–V data, which is in stark contrast to previous works. Moreover, our measurements quantify the absolute rates of junction loss, non-radiative loss, radiative loss, and luminescence coupling in the subcells, which constitute the “balance sheets” of tandem solar cells. PMID:25592484

  11. Fluorene-fluorenone copolymer: Stable and efficient yellow-emitting material for electroluminescent devices

    NASA Astrophysics Data System (ADS)

    Panozzo, S.; Vial, J.-C.; Kervella, Y.; Stéphan, O.

    2002-10-01

    We have synthesized and characterized a new fluorene copolymer exhibiting bright yellow luminescence. In order to ensure a complete π-stacking of the active layer, a 9-fluorenone monomeric unit (FOne) has been used as comonomer in conjunction with the more classical 9,9-di-n-nonylfluorene unit. As expected with fluorene-based materials, when excited at 370 nm, the corresponding dilute copolymer solution photoluminescence spectra exhibit a main peak centered at 450 nm in the blue part of the visible spectrum. However, in the solid state, immediate structural reorganization of the layer occurs, leading to a red-shifted emission (bright yellow emission) centered at 550 nm. The origin of the emitted light has been attributed to excimers and/or aggregates based on short FOne segments and involves mainly exciton transfer between nonaggregated fluorene segments and aggregated ones. It is noteworthy that organic light-emitting devices based on these new materials exhibit no spectral evolution upon device operation. However, although stacking leads generally to a detrimental quenching of the luminescence in the solid state, as for regular poly(alkyl-fluorene), the luminescence efficiency of the fluorene-fluorenone copolymer remains suitable for device preparation. High material stability is attributed to an efficient and fast structural reorganization of the active layer, triggered by the small proportion of fluorenone. High electroluminescence efficiency, when compared to aggregated regular poly(alkyl-fluorene), results from an improved electron injection, a better carrier transport, and the conjunction of an efficient energy transfer from fluorene segments to excimers and/or aggregates with the implication of spin triplet, which is often lacking when using regular semiconducting polymers.

  12. Highly efficient electroluminescence from a heterostructure device combined with emissive layered-perovskite and an electron-transporting organic compound

    NASA Astrophysics Data System (ADS)

    Hattori, Toshiaki; Taira, Takahiro; Era, Masanao; Tsutsui, Tetsuo; Saito, Shugu

    1996-05-01

    Two Pbl-based layer perovskite compounds, which possess cyclohexenylethylamine or phenylbutylamine as an organic ammonium layer, were newly found to exhibit efficient exciton emission due to their self-organized quantum well structure where a lead halide semiconducting layer and an organic ammonium dielectric layer are alternately piled up. We prepared heterostructure electroluminescent devices using the combination of the emissive layered perovskite and an electron-transporting oxadiazole. When the heterostructure devices were driven at 110 K, greenish emission, which corresponded well to the exciton emission, was observed. In the device using the perovskite with an organic layer of cyclohexenythylamine, a high luminance exceeding 4000 cd m -2 and high external EL quantum efficiency of 2.8% were attained at a current density of 50 mA cm -2 at an applied voltage of 24 V.

  13. Rare Earth Complex as Electron Trapper and Energy Transfer Ladder for Efficient Red Iridium Complex Based Electroluminescent Devices.

    PubMed

    Zhou, Liang; Li, Leijiao; Jiang, Yunlong; Cui, Rongzhen; Li, Yanan; Zhao, Xuesen; Zhang, Hongjie

    2015-07-29

    In this work, we experimentally demonstrated the new functions of trivalent rare earth complex in improving the electroluminescent (EL) performances of iridium complex by codoping trace Eu(TTA)3phen (TTA = thenoyltrifluoroacetone, phen = 1,10-phenanthroline) into a light-emitting layer based on PQ2Ir(dpm) (iridium(III)bis(2-phenylquinoly-N,C(2'))dipivaloylmethane). Compared with a reference device, the codoped devices displayed higher efficiencies, slower efficiency roll-off, higher brightness, and even better color purity. Experimental results demonstrated that Eu(TTA)3phen molecules function as electron trappers due to its low-lying energy levels, which are helpful in balancing holes and electrons and in broadening recombination zone. In addition, the matched triplet energy of Eu(TTA)3phen is instrumental in facilitating energy transfer from host to emitter. Finally, highly efficient red EL devices with the highest current efficiency, power efficiency and brightness up to 58.98 cd A(-1) (external quantum efficiency (EQE) of 21%), 61.73 lm W(-1) and 100870 cd m(-2), respectively, were obtained by appropriately decreasing the doping concentration of iridium complex. At certain brightness of 1000 cd m(-2), EL current efficiency up to 51.94 cd A(-1) (EQE = 18.5%) was retained. Our investigation extends the application of rare earth complexes in EL devices and provides a chance to improve the device performances.

  14. Organic electroluminescent structures for new generation of display systems

    NASA Astrophysics Data System (ADS)

    Ermakov, Oleg N.; Kaplunov, Michail G.; Efimov, Oleg N.; Stakharny, Sergey A.

    2007-05-01

    Brief history, modern state and development trends of organic electroluminescent structures technology (so-called OLED technology) are reviewed including research activities in this field in Russia. It's noted that OLED technology is one of the most promising newly emerging display technologies. Due to advantages of these devices (low power consumption, potential flexibility, wide color range) it is particularly well suited for small area display applications (micro displays) such as cell phones, virtual imaging systems, portable electronics. Experimental results for homemade blue light emitting OLED structures and hermetically sealed numeric displays are presented including photoluminescence (PL) and electroluminescence (EL ) current-voltage and brightness characteristics. It is noted that visible electroluminescence is observed at ultra low current level of nearly 1 μA, luminous efficiency exceeding 1 lm/W thus being nearly the same as for super bright inorganic inGaN/IGaN LEDs. Special attention is paid for destabilizing factors (temperature and degradation phenomena) influence on device characteristics.

  15. Improved color purity and electroluminescent efficiency obtained by modulating thicknesses and evaporation rates of hole block and electron transport layers

    NASA Astrophysics Data System (ADS)

    Zhou, Liang; Deng, Ruiping; Feng, Jing; Li, Xiaona; Li, Xiyan; Zhang, Hongjie

    2011-01-01

    In this work, a series of electroluminescent (EL) devices based on trivalent europium (Eu3+) complex Eu(TTA)3phen (TTA = thenoyltrifluoroacetone, phen = 1,10-phenanthroline) were fabricated by selecting 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) and tris(8-hydroxyquinoline) aluminum (Alq3) as hole block and electron transport materials, respectively. Interestingly, we found the transport of electrons decreases gradually with increasing thicknesses and evaporation rates of BCP and Alq3 layers. Analyzing carrier distribution and EL spectra, we conclude that appropriately modulating the thicknesses and evaporation rates is an efficient way to decrease the accumulation of electrons in HBL, thus suppressing the EL of hole block material. On the other hand, decreasing the transport of electrons can also facilitate the balance of holes and electrons on Eu(TTA)3phen molecules, thus further enhancing the EL efficiency. As a result, pure Eu3+ emission with the efficiency as high as 8.49 cd/A was realized by controlling the thicknesses and evaporation rates of BCP and Alq3 layers to be 30 nm and 0.10 nm/s, 40 nm and 0.10 nm/s, respectively.

  16. High-efficiency blue electroluminescence based on coumarin derivative 3-(4-(anthracen-10-yl)phenyl)-benzo[5,6]coumarin.

    PubMed

    Zhang, Hui; Chai, Haifang; Yu, Tianzhi; Zhao, Yuling; Fan, Duowang

    2012-11-01

    The electroluminescent (EL) properties of a new coumarin derivative, 3-(4-(anthracen-10-yl)phenyl)-benzo[5,6]coumarin (APBC), were investigated. The results show that the EL devices comprised of vacuum vapor-deposited films using the derivative as dopant exhibited blue emission that is identical to the photoluminescence of the thin film. The electroluminescence device of ITO/2-TNATA (5 nm)/NPB (40 nm)/CBP : APBC (1.0 wt%, 30 nm)/PBD (30 nm)/LiF (1 nm)/Al (100 nm) gives a maximum luminous efficiency of 2.3 cd/A at the current density of 20 mA/cm(2), and maximum luminance of 5169 cd/m(2) at 16 V. The external quantum efficiency of the device is 1.85 %.

  17. Improved efficiency for green and red emitting electroluminescent devices using the same cohost composed of 9,10-di(2-naphthyl) anthracene and tris-(8-hydroxyquinolinato) aluminum

    NASA Astrophysics Data System (ADS)

    Zhu, Jianzhuo; Li, Wenlian; Chu, Bei; Yang, Dongfang; Zhang, Guang; Liu, Huihui; Chen, Yiren; Su, Zisheng; Wang, Junbo; Wu, Shuanghong

    2009-12-01

    We demonstrate highly efficient green and red fluorescence dyes-doped electroluminescent devices using cohost strategy. The cohost system is composed of tris-(8-hydroxyquinolinato) aluminum (Alq) and 9,10-di(2-naphthyl) anthracene (ADN). The maximum current efficiencies are increased by 54% and 104% for green and red devices by optimizing the ratio between ADN and Alq in the cohost compared to the conventional Alq single-host devices, respectively. We attribute the improvement of efficiencies to balanced hole and electron injection into the emitting layer, the enlarged width of recombination region and the multiple emission processes.

  18. Efficient Deep-Blue Electroluminescence Based on Phenanthroimidazole-Dibenzothiophene Derivatives with Different Oxidation States of the Sulfur Atom.

    PubMed

    Tang, Xiangyang; Shan, Tong; Bai, Qing; Ma, Hongwei; He, Xin; Lu, Ping

    2017-03-02

    Developing efficient deep-blue materials is a long-term research focus in the field of organic light-emitting diodes (OLEDs). In this paper, we report two deep-blue molecules, PITO and PISF, which share similar chemical structures but exhibit different photophysical and device properties. These two molecules consist of phenanthroimidazole and dibenzothiophene analogs. The distinction of their chemical structures lies in the different oxidation states of the S atom. For PITO, the S atom is oxidized and the resulting structure dibenzothiophene S,S-dioxide becomes electron deficient. Therefore, PITO displays remarkable solvatochromism, implying a charge-transfer (CT) excited state formed between the donor (D) phenanthroimidazole and acceptor (A) dibenzothiophene S,S-dioxide. For PISF, it is constituted of phenanthroimidazole and dibenzothiophene in which the S atom is not oxidized. PISF displays locally excited (LE) emission with little solvatochromism. Compared with PISF, the D-A molecule PITO with an electron-deficient group shows a much lower LUMO energy level, which is in favor of electron injection in device. In addition, PITO exhibits more balanced carrier transport. However, PISF is capable of emitting in the shorter wavelength region, which is beneficial to obtain better color purity. The doped electroluminescence (EL) device of the D-A molecule PITO manifests deep-blue emission with CIE coordinates of (0.15, 0.08) and maximum external quantum efficiency (EQE) of 4.67 %. The doped EL device of the LE molecule PISF, however, reveals an even bluer emission with CIE coordinates of (0.15, 0.06) and a maximum EQE of 4.08 %.

  19. Highly efficient electroluminescence from a solution-processable thermally activated delayed fluorescence emitter

    SciTech Connect

    Wada, Yoshimasa; Kubo, Shosei; Suzuki, Katsuaki; Kaji, Hironori; Shizu, Katsuyuki; Tanaka, Hiroyuki; Adachi, Chihaya

    2015-11-02

    We developed a thermally activated delayed fluorescence (TADF) emitter, 2,4,6-tris(4-(9,9-dimethylacridan-10-yl)phenyl)-1,3,5-triazine (3ACR-TRZ), suitable for use in solution-processed organic light-emitting diodes (OLEDs). When doped into 4,4′-bis(carbazol-9-yl)biphenyl (CBP) host at 16 wt. %, 3ACR-TRZ showed a high photoluminescence quantum yield of 98%. Transient photoluminescence decay measurements of the 16 wt. % 3ACR-TRZ:CBP film confirmed that 3ACR-TRZ exhibits efficient TADF with a triplet-to-light conversion efficiency of 96%. This high conversion efficiency makes 3ACR-TRZ attractive as an emitting dopant in OLEDs. Using 3ACR-TRZ as an emitter, we fabricated a solution-processed OLED exhibiting a maximum external quantum efficiency of 18.6%.

  20. Performance evaluation of multi-junction solar cells by spatially resolved electroluminescence microscopy.

    PubMed

    Kong, Lijing; Wu, Zhiming; Chen, Shanshan; Cao, Yiyan; Zhang, Yong; Li, Heng; Kang, Junyong

    2015-01-01

    An electroluminescence microscopy combined with a spectroscopy was developed to visually analyze multi-junction solar cells. Triple-junction solar cells with different conversion efficiencies were characterized by using this system. The results showed that the mechanical damages and material defects in solar cells can be clearly distinguished, indicating a high-resolution imaging. The external quantum efficiency (EQE) measurements demonstrated that different types of defects or damages impacted cell performance in various degrees and the electric leakage mostly degraded the EQE. Meanwhile, we analyzed the relationship between electroluminescence intensity and short-circuit current density J SC. The results indicated that the gray value of the electroluminescence image corresponding to the intensity was almost proportional to J SC. This technology provides a potential way to evaluate the current matching status of multi-junction solar cells.

  1. Self-Host Blue Dendrimer Comprised of Thermally Activated Delayed Fluorescence Core and Bipolar Dendrons for Efficient Solution-Processable Nondoped Electroluminescence.

    PubMed

    Ban, Xinxin; Jiang, Wei; Sun, Kaiyong; Lin, Baoping; Sun, Yueming

    2017-03-01

    A self-host thermally activated delayed fluorescence (TADF) dendrimer POCz-DPS for solution-processed nondoped blue organic light-emitting diodes (OLEDs) was designed and synthesized, in which the bipolar phosphine oxide carbazole moiety was introduced by alkyl chain to ensure balanced charge transfer. The investigation of physical properties showed that the bipolar dendrons not only improve the morphological stability but also restrain the concentration quenching effect of the TADF emissive core. The spin-coated OLEDs featuring POCz-DPS as the host-free blue emitter achieved the highest external quantum efficiency (7.3%) and color purity compared with those of doped or nondoped devices based on the parent molecule DMOC-DPS, which indicates that incorporating the merits of encapsulation and bipolar dendron is an effective way to improve the electroluminescent performance of the TADF emitter used for a solution-processed nondoped device.

  2. Electroluminescence of Giant Stretchability.

    PubMed

    Yang, Can Hui; Chen, Baohong; Zhou, Jinxiong; Chen, Yong Mei; Suo, Zhigang

    2016-06-01

    A new type of electroluminescent device achieves giant stretchability by integrating electronic and ionic components. The device uses phosphor powders as electroluminescent materials, and hydrogels as stretchable and transparent ionic conductors. Subject to cyclic voltage, the phosphor powders luminesce, but the ionic conductors do not electrolyze. The device produces constant luminance when stretched up to an area strain of 1500%.

  3. Enhancing the electroluminescence efficiency of Si NC/SiO2 superlattice-based light-emitting diodes through hydrogen ion beam treatment

    NASA Astrophysics Data System (ADS)

    Fu, Sheng-Wen; Chen, Hui-Ju; Wu, Hsuan-Ta; Chen, Shao-Ping; Shih, Chuan-Feng

    2016-03-01

    This paper presents a novel method for enhancing the electroluminescence (EL) efficiency of ten-period silicon-rich oxide (SRO)/SiO2 superlattice-based light-emitting diodes (LEDs). A hydrogen ion beam (HIB) was used to irradiate each SRO layer of the superlattices to increase the interfacial roughness on the nanoscale and the density of the Si nanocrystals (Si NCs). Fowler-Nordheim (F-N) tunneling was the major mechanism for injecting the carriers into the Si NCs. The barrier height of the F-N tunneling was lowered by forming a nano-roughened interface and the nonradiative Pb centers were passivated through the HIB treatment. Additionally, the reflectance of the LEDs was lowered because of the nano-roughened interface. These factors considerably increased the slope efficiency of EL and the maximum output power of the LEDs. The lighting efficiency increased by an order of magnitude, and the turn-on voltage decreased considerably. This study established an efficient approach for obtaining bright Si NC/SiO2 superlattice-based LEDs.

  4. Enhancing the electroluminescence efficiency of Si NC/SiO2 superlattice-based light-emitting diodes through hydrogen ion beam treatment.

    PubMed

    Fu, Sheng-Wen; Chen, Hui-Ju; Wu, Hsuan-Ta; Chen, Shao-Ping; Shih, Chuan-Feng

    2016-04-07

    This paper presents a novel method for enhancing the electroluminescence (EL) efficiency of ten-period silicon-rich oxide (SRO)/SiO2 superlattice-based light-emitting diodes (LEDs). A hydrogen ion beam (HIB) was used to irradiate each SRO layer of the superlattices to increase the interfacial roughness on the nanoscale and the density of the Si nanocrystals (Si NCs). Fowler-Nordheim (F-N) tunneling was the major mechanism for injecting the carriers into the Si NCs. The barrier height of the F-N tunneling was lowered by forming a nano-roughened interface and the nonradiative Pb centers were passivated through the HIB treatment. Additionally, the reflectance of the LEDs was lowered because of the nano-roughened interface. These factors considerably increased the slope efficiency of EL and the maximum output power of the LEDs. The lighting efficiency increased by an order of magnitude, and the turn-on voltage decreased considerably. This study established an efficient approach for obtaining bright Si NC/SiO2 superlattice-based LEDs.

  5. Synthesis and characterization of copper-doped zinc sulfide nanomaterials for the application of energy efficient electroluminescent lighting

    NASA Astrophysics Data System (ADS)

    Corrado, Carley

    Doped nanocrystals (NCs) compose an important subset of nanomaterials in which a small percentage of dopant ion is introduced into host semiconductor nanocrystals with the affect of altering their optical properties. Their tunable, intense, and stable emission make them ideal candidates for a number of opto-electronic applications, including use as phosphors for solid-state lighting applications. ZnS doped with Cu (ZnS:Cu) is a commonly used bulk phosphor material and a promising candidate for use as a nanophospor material, though the energy states involved in the electronic transitions leading to luminescence are not well understood. To shed light on this topic, ZnS:Cu nanocrystals were synthesized and their optical properties were correlated with their structure using UV-Vis and photoluminescence (PL) spectroscopy, TEM, EXAFS, XRD, and ICP. The dependence of the optical and structural properties on dopant concentration, shell growth, co-doping, and solvent were explored. Through EXAFS study about the local structure of the Cu-dopant, it was found that Cu was located at or near the surface of the nanocrystals. A ZnS shell was grown around the ZnS:Cu nanocrystals resulting in increased dopant-related PL emission due to encapsulation of the dopant into the core of the nanocrystals. ZnS:Cu nanocrystals were also synthesized in an organic solvent to enable fabrication of high quality films for electroluminescent lighting applications. Addition of Br was added as a co-activator with the effect of greatly enhanced Cu-dopant PL emission. Characterization of the local structure of the Br-dopant using EXAFS confirmed substitutional incorporation of the Br into the core of the ZnS nanocrystals. Methods were developed to enhance dopant-related PL emission.

  6. Highly Efficient, Color-Reproducible Full-Color Electroluminescent Devices Based on Red/Green/Blue Quantum Dot-Mixed Multilayer.

    PubMed

    Lee, Ki-Heon; Han, Chang-Yeol; Kang, Hee-Don; Ko, Heejoo; Lee, Changho; Lee, Jonghyuk; Myoung, NoSoung; Yim, Sang-Youp; Yang, Heesun

    2015-11-24

    Over the past few years the performance of colloidal quantum dot-light-emitting diode (QLED) has been progressively improved. However, most of QLED work has been fulfilled in the form of monochromatic device, while full-color-enabling white QLED still remains nearly unexplored. Using red, green, and blue quantum dots (QDs), herein, we fabricate bichromatic and trichromatic QLEDs through sequential solution-processed deposition of poly(9-vinlycarbazole) (PVK) hole transport layer, two or three types of QDs-mixed multilayer, and ZnO nanoparticle electron transport layer. The relative electroluminescent (EL) spectral ratios of constituent QDs in the above multicolored devices are found to inevitably vary with applied bias, leading to the common observation of an increasing contribution of a higher-band gap QD EL over low-band gap one at a higher voltage. The white EL from a trichromatic device is resolved into its primary colors through combining with color filters, producing an exceptional color gamut of 126% relative to National Television Systems Committee (NTSC) color space that a state-of-the-art full-color organic LED counterpart cannot attain. Our trichromatic white QLED also displays the record-high EL performance such as the peak values of 23,352 cd/m(2) in luminance, 21.8 cd/A in current efficiency, and 10.9% in external quantum efficiency.

  7. 2-(2-Hydroxyphenyl)benzimidazole-based four-coordinate boron-containing materials with highly efficient deep-blue photoluminescence and electroluminescence.

    PubMed

    Zhang, Zhenyu; Zhang, Houyu; Jiao, Chuanjun; Ye, Kaiqi; Zhang, Hongyu; Zhang, Jingying; Wang, Yue

    2015-03-16

    Two novel four-coordinate boron-containing emitters 1 and 2 with deep-blue emissions were synthesized by refluxing a 2-(2-hydroxyphenyl)benzimidazole ligand with triphenylborane or bromodibenzoborole. The boron chelation produced a new π-conjugated skeleton, which rendered the synthesized boron materials with intense fluorescence, good thermal stability, and high carrier mobility. Both compounds displayed deep-blue emissions in solutions with very high fluorescence quantum yields (over 0.70). More importantly, the samples showed identical fluorescence in the solution and solid states, and the efficiency was maintained at a high level (approximately 0.50) because of the bulky substituents between the boron atom and the benzimidazole unit, which can effectively separate the flat luminescent units. In addition, neat thin films composed of 1 or 2 exhibited high electron and hole mobility in the same order of magnitude 10(-4), as determined by time-of-flight. The fabricated electroluminescent devices that employed 1 or 2 as emitting materials showed high-performance deep-blue emissions with Commission Internationale de L'Eclairage (CIE) coordinates of (X = 0.15, Y = 0.09) and (X = 0.16, Y = 0.08), respectively. Thus, the synthesized boron-containing materials are ideal candidates for fabricating high-performance deep-blue organic light-emitting diodes.

  8. Electroluminescence-based quality characterization of quantum wells for solar cell applications

    NASA Astrophysics Data System (ADS)

    Toprasertpong, Kasidit; Inoue, Tomoyuki; Delamarre, Amaury; Watanabe, Kentaroh; Guillemoles, Jean-François; Sugiyama, Masakazu; Nakano, Yoshiaki

    2017-04-01

    Material quality is a critical factor which determines the performance, particularly the open-circuit voltage, of multiple quantum well (MQW) solar cells. In this study, we report an electroluminescence-based characterization technique for evaluating luminescence efficiency and Shockley-Read-Hall recombination lifetime in MQW structures as a measure of the material quality. As a demonstration, various structures of InGaAs/GaAsP MQWs inserted in GaAs solar cells are investigated. The complete compensation of strain and the insertion of GaAs interlayers between heterointerfaces result in significant improvement of electroluminescence homogeneity, external luminescence efficiency, and lifetime, agreeing well with the tendency of the open-circuit voltage. We show that this characterization technique can detect even subtle degradations, which are not easily detectable by other typical techniques, such as in-situ reflection, X-ray diffraction, and spectral and transient photoluminescence, but still have a significant impact on the performance of solar cells.

  9. Intense deep blue exciplex electroluminescence from NPB/TPBi:PPh3O-based OLEDs and their intrinsic degradation mechanisms (Conference Presentation)

    NASA Astrophysics Data System (ADS)

    Shinar, Joseph; Hippola, Chamika; Danilovic, Dusan; Bhattacharjee, Ujjal; Petrich, Jacob W.; Shinar, Ruth

    2016-09-01

    We describe intense and efficient deep blue (430 - 440 nm) exciplex emission from NPB/TPBi:PPh3O OLEDs where the luminous efficiency approaches 4 Cd/A and the maximal brightness exceeds 22,000 Cd/m2. Time resolved PL measurements confirm the exciplex emission from NPB:TPBi, as studied earlier by Monkman and coworkers [Adv. Mater. 25, 1455 (2013)]. However, the inclusion of PPh3O improves the OLED performance significantly. The effect of PPh3O on the EL and PL will be discussed. The NPB/TPBi:PPh3O-based OLEDs were also studied by optically and electrically detected magnetic resonance (ODMR and EDMR, respectively). In particular, the amplitude of the negative (EL- and current-quenching) spin 1/2 resonance, previously attributed to enhanced formation of strongly EL-quenching positive bipolarons, increases as the OLEDs degrade in a dry nitrogen atmosphere. This degradation mechanism is discussed in relation to degradation induced by hot polarons that are energized by exciton annihilation.

  10. Electrodeposited, Transverse Nanowire Electroluminescent Junctions.

    PubMed

    Qiao, Shaopeng; Xu, Qiang; Dutta, Rajen K; Le Thai, Mya; Li, Xiaowei; Penner, Reginald M

    2016-09-27

    The preparation by electrodeposition of transverse nanowire electroluminescent junctions (tn-ELJs) is described, and the electroluminescence (EL) properties of these devices are characterized. The lithographically patterned nanowire electrodeposition process is first used to prepare long (millimeters), linear, nanocrystalline CdSe nanowires on glass. The thickness of these nanowires along the emission axis is 60 nm, and the width, wCdSe, along the electrical axis is adjustable from 100 to 450 nm. Ten pairs of nickel-gold electrical contacts are then positioned along the axis of this nanowire using lithographically directed electrodeposition. The resulting linear array of nickel-CdSe-gold junctions produces EL with an external quantum efficiency, EQE, and threshold voltage, Vth, that depend sensitively on wCdSe. EQE increases with increasing electric field and also with increasing wCdSe, and Vth also increases with wCdSe and, therefore, the electrical resistance of the tn-ELJs. Vth down to 1.8(±0.2) V (for wCdSe ≈ 100 nm) and EQE of 5.5(±0.5) × 10(-5) (for wCdSe ≈ 450 nm) are obtained. tn-ELJs produce a broad EL emission envelope, spanning the wavelength range from 600 to 960 nm.

  11. Electroluminescence Imaging Of Space Solar Cells

    NASA Astrophysics Data System (ADS)

    Zimmermann, C. G.

    2011-10-01

    Space solar power is one of the few applications where large area III-V devices are used. Therefore there is great potential for a spatially resolved technique in the inspection, failure investigation and characterization of these devices. Mechanical defects can be identified by electroluminescence imaging unambiguously. The impact of a cell crack on the current distribution in the cell is modeled and the electroluminescence signature of a cell crack is derived. Another qualitative application is failure investigation of cells that suffer degradation, for example in environmental testing. Series resistance problems can be visualized and the location of an environmental attack can be pinpointed on a μm length scale. Finally under the appropriate simplifications, even a quantitative cell characterization can be attempted. Maps of the open circuit voltage and the current at the operating voltage identify shunts quantitatively.

  12. Hybrid electroluminescent devices

    DOEpatents

    Shiang, Joseph John; Duggal, Anil Raj; Michael, Joseph Darryl

    2010-08-03

    A hybrid electroluminescent (EL) device comprises at least one inorganic diode element and at least one organic EL element that are electrically connected in series. The absolute value of the breakdown voltage of the inorganic diode element is greater than the absolute value of the maximum reverse bias voltage across the series. The inorganic diode element can be a power diode, a Schottky barrier diode, or a light-emitting diode.

  13. Mechanically flexible organic electroluminescent device with directional light emission

    DOEpatents

    Duggal, Anil Raj; Shiang, Joseph John; Schaepkens, Marc

    2005-05-10

    A mechanically flexible and environmentally stable organic electroluminescent ("EL") device with directional light emission comprises an organic EL member disposed on a flexible substrate, a surface of which is coated with a multilayer barrier coating which includes at least one sublayer of a substantially transparent organic polymer and at least one sublayer of a substantially transparent inorganic material. The device includes a reflective metal layer disposed on the organic EL member opposite to the substrate. The reflective metal layer provides an increased external quantum efficiency of the device. The reflective metal layer and the multilayer barrier coating form a seal around the organic EL member to reduce the degradation of the device due to environmental elements.

  14. Degradative encryption: An efficient way to protect SPIHT compressed images

    NASA Astrophysics Data System (ADS)

    Xiang, Tao; Qu, Jinyu; Yu, Chenyun; Fu, Xinwen

    2012-11-01

    Degradative encryption, a new selective image encryption paradigm, is proposed to encrypt only a small part of image data to make the detail blurred but keep the skeleton discernible. The efficiency is further optimized by combining compression and encryption. A format-compliant degradative encryption algorithm based on set partitioning in hierarchical trees (SPIHT) is then proposed, and the scheme is designed to work in progressive mode for gaining a tradeoff between efficiency and security. Extensive experiments are conducted to evaluate the strength and efficiency of the scheme, and it is found that less than 10% data need to be encrypted for a secure degradation. In security analysis, the scheme is verified to be immune to cryptographic attacks as well as those adversaries utilizing image processing techniques. The scheme can find its wide applications in online try-and-buy service on mobile devices, searchable multimedia encryption in cloud computing, etc.

  15. [Progress of organometallic complexes and their application to organic electroluminescent materials].

    PubMed

    Zhou, Rui; An, Zhong-Wei; Chai, Sheng-Yong

    2004-08-01

    Organic electroluminescent (EL) material is one of most prospective display materials in flat panel display. Organometallic complexes, which have five or six member ring structures, with high stability, high melting point and high fluorescence quantum efficiency, are widely applied in organic EL devices. The recent progress in organometallic complexes is summarized in terms of the electroluminescence of ligands and metal atoms.

  16. Zinc oxide tetrapods as efficient photocatalysts for organic pollutant degradation

    NASA Astrophysics Data System (ADS)

    Liu, Fangzhou; Leung, Yu Hang; Djurisić, Aleksandra B.; Liao, Changzhong; Shih, Kaimin

    2014-03-01

    Bisphenol A (BPA) and other organic pollutants from industrial wastewater have drawn increasing concern in the past decades regarding their environmental and biological risks, and hence developing strategies of effective degradation of BPA and other organic pollutants is imperative. Metal oxide nanostructures, in particular titanium oxide (TiO2) and zinc oxide (ZnO), have been demonstrated to exhibit efficient photodegradation of various common organic dyes. ZnO tetrapods are of special interest due to their low density of native defects which consequently lead to lower recombination losses and higher photocatalytic efficiency. Tetrapods can be obtained by relatively simple and low-cost vapor phase deposition in large quantity; the micron-scale size would also be advantageous for catalyst recovery. In this study, the photodegradation of BPA with ZnO tetrapods and TiO2 nanostructures under UV illumination were compared. The concentration of BPA dissolved in DI water was analyzed by high-performance liquid chromatography (HPLC) at specified time intervals. It was observed that the photocatalytic efficiency of ZnO tetrapods eventually surpassed Degussa P25 in free-standing form, and more than 80% of BPA was degraded after 60 min. Photodegradation of other organic dye pollutants by tetrapods and P25 were also examined. The superior photocatalytic efficiency of ZnO tetrapods for degradation of BPA and other organic dye pollutants and its correlation with the material properties were discussed.

  17. Efficient Plant Biomass Degradation by Thermophilic Fungus Myceliophthora heterothallica

    PubMed Central

    van den Brink, Joost; van Muiswinkel, Gonny C. J.; Theelen, Bart; Hinz, Sandra W. A.

    2013-01-01

    Rapid and efficient enzymatic degradation of plant biomass into fermentable sugars is a major challenge for the sustainable production of biochemicals and biofuels. Enzymes that are more thermostable (up to 70°C) use shorter reaction times for the complete saccharification of plant polysaccharides compared to hydrolytic enzymes of mesophilic fungi such as Trichoderma and Aspergillus species. The genus Myceliophthora contains four thermophilic fungi producing industrially relevant thermostable enzymes. Within this genus, isolates belonging to M. heterothallica were recently separated from the well-described species M. thermophila. We evaluate here the potential of M. heterothallica isolates to produce efficient enzyme mixtures for biomass degradation. Compared to the other thermophilic Myceliophthora species, isolates belonging to M. heterothallica and M. thermophila grew faster on pretreated spruce, wheat straw, and giant reed. According to their protein profiles and in vitro assays after growth on wheat straw, (hemi-)cellulolytic activities differed strongly between M. thermophila and M. heterothallica isolates. Compared to M. thermophila, M. heterothallica isolates were better in releasing sugars from mildly pretreated wheat straw (with 5% HCl) with a high content of xylan. The high levels of residual xylobiose revealed that enzyme mixtures of Myceliophthora species lack sufficient β-xylosidase activity. Sexual crossing of two M. heterothallica showed that progenies had a large genetic and physiological diversity. In the future, this will allow further improvement of the plant biomass-degrading enzyme mixtures of M. heterothallica. PMID:23241981

  18. Interfused semiconductor nanocrystals: brilliant blue photoluminescence and electroluminescence.

    PubMed

    Jun, Shinae; Jang, Eunjoo

    2005-09-28

    We describe a method for producing blue light-emitting interfused CdSe//ZnS (QE up to 60%) nanocrystals and report the good performance of an electroluminescent device which uses them (external quantum efficiency approximately 1.5 cd A(-1)).

  19. Heck coupling of haloaromatics with octavinylsilsesquioxane: solution processable nanocomposites for application in electroluminescent devices.

    PubMed

    Sellinger, Alan; Tamaki, Ryo; Laine, Richard M; Ueno, Kazunori; Tanabe, Hiroshi; Williams, Evan; Jabbour, Ghassan E

    2005-08-07

    A new solution processable nanocomposite material has been prepared via the Heck coupling of octavinylsilsesquioxane with a selected bromoaromatic hole transport compound. Resultant electroluminescent devices show an 18% improvement in external quantum efficiencies over their small molecule analogues.

  20. Photoluminescence and electroluminescence from Ge/strained GeSn/Ge quantum wells

    NASA Astrophysics Data System (ADS)

    Lin, Chung-Yi; Huang, Chih-Hsiung; Huang, Shih-Hsien; Chang, Chih-Chiang; Liu, C. W.; Huang, Yi-Chiau; Chung, Hua; Chang, Chorng-Ping

    2016-08-01

    Ge/strained GeSn/Ge quantum wells are grown on a 300 mm Si substrate by chemical vapor deposition. The direct bandgap emission from strained GeSn is observed in the photoluminescence spectra and is enhanced by Al2O3/SiO2 passivation due to the field effect. The electroluminescence of the direct bandgap emission of strained GeSn is also observed from the Ni/Al2O3/GeSn metal-insulator-semiconductor tunneling diodes. Electroluminescence is a good indicator of GeSn material quality, since defects in GeSn layers degrade the electroluminescence intensity significantly. At the accumulation bias, the holes in the Ni gate electrode tunnel to the strained n-type GeSn layer through the ultrathin Al2O3 and recombine radiatively with electrons. The emission wavelength of photoluminescence and electroluminescence can be tuned by the Sn content.

  1. A novel lignin degradation bacterial consortium for efficient pulping.

    PubMed

    Wang, Yanxia; Liu, Quan; Yan, Lei; Gao, Yamei; Wang, Yanjie; Wang, Weidong

    2013-07-01

    A lignin degradation bacterial consortium named LDC was screened from the sludge of a reeds pond by a restricted subculture. It could break down 60.9% lignin in reeds at 30°C under conditions of static culture within 15 days. In order to analyze the diversity of LDC, plate isolation, 16S rDNA clone library and ARDRA (Amplified Ribosomal DNA Restriction Analysis) were performed. Six bacterial strains were isolated from LDC and eighteen DNA phylotypes were identified from 230 bacterial analyzed clones. They were classified into Clostridiales(9.1%), Geovibrio thiophilus (5.1%), Desulfomicrobium (10.9%), Pseudomonas sp. (25.2%), Azoarcus sp. (5.1%), Thauera (5.1%), Paenibacillus sp. (5.1%), Cohnella sp. (2.2%), Acinetobacter sp. (3.1%), Microbacterium (7.8%), and uncultured bacterium (21.3%). In addition, physical characteristics of paper hand-sheets between biological pretreatment and chemical pretreatment were compared. The results showed that LDC had the capability of lignin degradation and was efficient for pulping, which would provide a new choice for biopulping.

  2. Efficient degradation of tannic acid by black Aspergillus species.

    PubMed

    Van Diepeningen, Anne D; Debets, Alfons J M; Varga, Janos; van der Gaag, Marijn; Swart, Klaas; Hoekstra, Rolf F

    2004-08-01

    A set of aspergillus strains from culture collections and wild-type black aspergilli isolated on non-selective media were used to validate the use of media with 20% tannic acid for exclusive and complete selection of the black aspergilli. The 20% tannic acid medium proved useful for both quantitative and qualitative selection of all different black aspergilli, including all recognized species: A. carbonarius, A. japonicus, A. aculeatus, A foetidus, A. heteromorphus, A. niger, A. tubingensis and A. brasiliensis haplotypes. Even higher concentrations of tannic acid can be utilized by the black aspergilli suggesting a very efficient tannic acid-degrading system. Colour mutants show that the characteristic ability to grow on high tannic acid concentrations is not causally linked to the other typical feature of these aspergilli, i.e. the formation of brown-black pigments. Sequence analysis of the A. niger genome using the A. oryzae tannase gene yielded eleven tannase-like genes, far more than in related species. Therefore, a unique ecological niche in the degradation of tannic acid and connected nitrogen release seems to be reserved for these black-spored cosmopolitans.

  3. Interplay of point defects, extended defects, and carrier localization in the efficiency droop of InGaN quantum wells light-emitting diodes investigated using spatially resolved electroluminescence and photoluminescence

    SciTech Connect

    Lin, Yue; Zhang, Yong Su, Liqin; Liu, Zhiqiang; Wei, Tongbo; Zhang, Jihong; Chen, Zhong

    2014-01-14

    We perform both spatially resolved electroluminescence (SREL) as a function of injection current and spatially resolved photoluminescence (SRPL) as a function of excitation power on InGaN quantum well blue light-emitting diodes to investigate the underlying physics for the phenomenon of the external quantum efficiency (EQE) droop. SREL allows us to study two most commonly observed but distinctly different droop behaviors on a single device, minimizing the ambiguity trying to compare independently fabricated devices. Two representative devices are studied: one with macroscopic scale material non-uniformity, the other being macroscopically uniform, but both with microscopic scale fluctuations. We suggest that the EQE–current curve reflects the interplay of three effects: nonradiative recombination through point defects, carrier localization due to either In composition or well width fluctuation, and nonradiative recombination of the extended defects, which is common to various optoelectronic devices. By comparing SREL and SRPL, two very different excitation/detection modes, we show that individual singular sites exhibiting either particularly strong or weak emission in SRPL do not usually play any significant and direct role in the EQE droop. We introduce a two-level model that can capture the basic physical processes that dictate the EQE–current dependence and describe the whole operating range of the device from 0.01 to 100 A/cm{sup 2}.

  4. Analysing the effect of crystal size and structure in highly efficient CH3NH3PbI3 perovskite solar cells by spatially resolved photo- and electroluminescence imaging.

    PubMed

    Mastroianni, S; Heinz, F D; Im, J-H; Veurman, W; Padilla, M; Schubert, M C; Würfel, U; Grätzel, M; Park, N-G; Hinsch, A

    2015-12-14

    CH3NH3PbI3 perovskite solar cells with a mesoporous TiO2 layer and spiro-MeOTAD as a hole transport layer (HTL) with three different CH3NH3I concentrations (0.032 M, 0.044 M and 0.063 M) were investigated. Strong variations in crystal size and morphology resulting in diversified cell efficiencies (9.2%, 16.9% and 12.3%, respectively) were observed. The physical origin of this behaviour was analysed by detailed characterization combining current-voltage curves with photo- and electroluminescence (PL and EL) imaging as well as light beam induced current measurements (LBIC). It was found that the most efficient cell shows the highest luminescence and the least efficient cell is most strongly limited by non-radiative recombination. Crystal size, morphology and distribution in the capping layer and in the porous scaffold strongly affect the non-radiative recombination. Moreover, the very non-uniform crystal structure with multiple facets, as evidenced by SEM images of the 0.032 M device, suggests the creation of a large number of grain boundaries and crystal dislocations. These defects give rise to increased trap-assisted non-radiative recombination as is confirmed by high-resolution μ-PL images. The different imaging techniques used in this study prove to be well-suited to spatially investigate and thus correlate the crystal morphology of the perovskite layer with the electrical and radiative properties of the solar cells and thus with their performance.

  5. A multilayer organic electroluminescent device using an organic dye salt

    NASA Astrophysics Data System (ADS)

    Feng, Xueyuan; Gu, Yongdi; Zhang, Jiayu; Cui, Yiping

    2005-01-01

    Organic electroluminescent devices have received considerable attention due to their application in flat-panel displays. To achieve full-color displays, it is necessary to obtain organic layers emitting red, green, and blue light, but it is still a challenge to obtain efficient and stable organic layer emitting red light so far. Recently, we found that an organic salt, trans-4-[p-[N-ethyl-N-(hydroxyethyl)amino]styryl]-N-methylphridinium tetraphenylborate (ASPT), exhibits efficient red-light emission. In this paper, we report a multilayer electrolumicescent device incorporating a hole-transport layer, an ASPT layer, and an electron-transport layer. The dependence of the carrier transport and the luminescence on the device structure is investigated in detail. Compared to the monolayer device, the balance between hole and electron injections is significantly improved for the multilayer device, and thus the electroluminescent efficiency and intensity are enhanced.

  6. Addressing proteolytic efficiency in enzymatic degradation therapy for celiac disease

    PubMed Central

    Rey, Martial; Yang, Menglin; Lee, Linda; Zhang, Ye; Sheff, Joey G.; Sensen, Christoph W.; Mrazek, Hynek; Halada, Petr; Man, Petr; McCarville, Justin L; Verdu, Elena F.; Schriemer, David C.

    2016-01-01

    Celiac disease is triggered by partially digested gluten proteins. Enzyme therapies that complete protein digestion in vivo could support a gluten-free diet, but the barrier to completeness is high. Current options require enzyme amounts on the same order as the protein meal itself. In this study, we evaluated proteolytic components of the carnivorous pitcher plant (Nepenthes spp.) for use in this context. Remarkably low doses enhance gliadin solubilization rates, and degrade gliadin slurries within the pH and temporal constraints of human gastric digestion. Potencies in excess of 1200:1 (substrate-to-enzyme) are achieved. Digestion generates small peptides through nepenthesin and neprosin, the latter a novel enzyme defining a previously-unknown class of prolyl endoprotease. The digests also exhibit reduced TG2 conversion rates in the immunogenic regions of gliadin, providing a twin mechanism for evading T-cell recognition. When sensitized and dosed with enzyme-treated gliadin, NOD/DQ8 mice did not show intestinal inflammation, when compared to mice challenged with only pepsin-treated gliadin. The low enzyme load needed for effective digestion suggests that gluten detoxification can be achieved in a meal setting, using metered dosing based on meal size. We demonstrate this by showing efficient antigen processing at total substrate-to-enzyme ratios exceeding 12,000:1. PMID:27481162

  7. FIrpic: archetypal blue phosphorescent emitter for electroluminescence.

    PubMed

    Baranoff, Etienne; Curchod, Basile F E

    2015-05-14

    FIrpic is the most investigated bis-cyclometallated iridium complex in particular in the context of organic light emitting diodes (OLEDs) because of its attractive sky-blue emission, high emission efficiency, and suitable energy levels. In this Perspective we review the synthesis, structural characterisations, and key properties of this emitter. We also survey the theoretical studies and summarise a series of selected monochromatic electroluminescent devices using FIrpic as the emitting dopant. Finally we highlight important shortcomings of FIrpic as an emitter for OLEDs. Despite the large body of work dedicated to this material, it is manifest that the understanding of photophysical and electrochemical processes are only broadly understood mainly because of the different environment in which these properties are measured, i.e., isolated molecules in solvent vs. device.

  8. Theoretical and material studies on thin-film electroluminescent devices

    NASA Technical Reports Server (NTRS)

    Summers, C. J.; Brennan, K. F.

    1986-01-01

    A highly efficient DC electroluminescent display is presented. A variably spaced superlattice structure is used to produce high energy injection of electrons into a ZnSe:Mn active layer in which impact excitation of the Mn centers can occur. The device is predicted to operate at an applied external bias on order of magnitude less than the best DC electroluminescent device to date. The device is predicted to have comparable brightness, since it operates in the saturation regime. The improved efficiency stems from avoiding significant energy loss to phonons. The electrons sequentially tunnel through a multilayer ZnSe/CaSrF2 stack under bias and emerge into the active layer at an energy equal to the conduction band bending. The injection energy is chosen to coincide with the impact excitation energy of the Mn centers. Different device designs are presented and their performance is predicted.

  9. Study on degrading graphene oxide in wastewater under different conditions for developing an efficient and economical degradation method.

    PubMed

    Li, Ting; Zhang, Chao-Zhi; Gu, Chengyue

    2017-02-13

    With popular application of graphene and graphene oxide (GO), they have been discharged into water. Graphene and GO harm organisms. However, an efficient and economical method for removing graphene and GO in wastewater has seldom been reported. Graphene can be oxidized by hydrogen peroxide to give GO; therefore, degradation of graphene oxide is an important step in the procedure of removal of graphene from water. In this paper, GO degradation via photo-Fenton reaction under different conditions was carried out. Experimental results suggested that GO in wastewater can be efficiently and economically degraded into carbon dioxide and H2O when pH value is 3, concentration of H2O2 and FeCl3 are 35 mM and 5 ppm, respectively. Degradation mechanism of GO was suggested based on UV-vis absorption spectra, scanning electron microscopy, X-ray diffraction and liquid chromatography-mass spectra data of degradation intermediates. This paper suggests an efficient and economical degradation way of GO in wastewater.

  10. Organic solution-processible electroluminescent molecular glasses for non-doped standard red OLEDs with electrically stable chromaticity

    SciTech Connect

    Bi, Xiaoman; Zuo, Weiwei; Liu, Yingliang Zhang, Zhenru; Zeng, Cen; Xu, Shengang; Cao, Shaokui

    2015-10-15

    Highlights: • The D–A–D electroluminescent molecular glasses are synthesized. • Non-doped red electroluminescent film is fabricated by spin-coating. • Red OLED shows stable wavelength, luminous efficiency and chromaticity. • CIE1931 coordinate is in accord with standard red light in PAL system. - Abstract: Organic light-emitting molecular glasses (OEMGs) are synthesized through the introduction of nonplanar donor and branched aliphatic chain into electroluminescent emitters. The target OEMGs are characterized by {sup 1}H NMR, {sup 13}C NMR, IR, UV–vis and fluorescent spectra as well as elemental analysis, TG and DSC. The results indicated that the optical, electrochemical and electroluminescent properties of OEMGs are adjusted successfully by the replacement of electron-donating group. The non-doped OLED device with a standard red electroluminescent emission is achieved by spin-coating the THF solution of OEMG with a triphenylamine moiety. This non-doped red OLED device takes on an electrically stable electroluminescent performance, including the stable maximum electroluminescent wavelength of 640 nm, the stable luminous efficiency of 2.4 cd/A and the stable CIE1931 coordinate of (x, y) = (0.64, 0.35), which is basically in accord with the CIE1931 coordinate (x, y) = (0.64, 0.33) of standard red light in PAL system.

  11. Current transport and electroluminescence mechanisms in thin SiO2 films containing Si nanocluster-sensitized erbium ions

    NASA Astrophysics Data System (ADS)

    Jambois, O.; Berencen, Y.; Hijazi, K.; Wojdak, M.; Kenyon, A. J.; Gourbilleau, F.; Rizk, R.; Garrido, B.

    2009-09-01

    We have studied the current transport and electroluminescence properties of metal oxide semiconductor (MOS) devices in which the oxide layer, which is codoped with silicon nanoclusters and erbium ions, is made by magnetron sputtering. Electrical measurements have allowed us to identify a Poole-Frenkel conduction mechanism. We observe an important contribution of the Si nanoclusters to the conduction in silicon oxide films, and no evidence of Fowler-Nordheim tunneling. The results suggest that the electroluminescence of the erbium ions in these layers is generated by energy transfer from the Si nanoparticles. Finally, we report an electroluminescence power efficiency above 10-3%.

  12. Electroluminescence Efficiency Enhancement using Metal Nanoparticles

    DTIC Science & Technology

    2008-06-22

    the vicinity of isolated metal nanoparticles and their arrays. Using the example of an InGaN /GaN quantum-well active region positioned in close...emitters placed in the vicinity of isolated metal nanoparticles and their arrays. Using the example of an InGaN /GaN quantum-well active region...electron-hole pair states are localized on the scale of the coherent length on the order of a few nanometers at room temperature, the spontaneous

  13. Silicon nanowire hot electron electroluminescence

    NASA Astrophysics Data System (ADS)

    du Plessis, Monuko; Joubert, Trudi-Heleen

    2016-02-01

    This paper investigates the avalanche electroluminescence characteristics of pn junctions formed in silicon nanowires fabricated in a silicon-on-insula*tor (SOI) technology. Since carriers are confined to the nanowires, it is possible to study the effect of electric field strength on device performance while the current density and carrier concentrations are kept constant. This is achieved by varying the nanowire length while keeping the bias current constant, eventually driving the pn junction into the reach-through bias condition. It is observed that photon emission for photon energies higher than 1.2 eV increases when the nanowire length is reduced, while photon emission with energies less than 1.2 eV decreases. The higher electric field in the nanowire at shorter nanowire lengths enhances the high-energy photon emission and attenuates the low energy photon emission.

  14. Distribution of electrical energy consumption for the efficient degradation control of THMs mixture in sonophotolytic process.

    PubMed

    Park, Beomguk; Cho, Eunju; Son, Younggyu; Khim, Jeehyeong

    2014-11-01

    Sonophotolytic degradation of THMs mixture with different electrical energy ratio was carried out for efficient design of process. The total consumed electrical energy was fixed around 50W, and five different energy conditions were applied. The maximum degradation rate showed in conditions of US:UV=1:3 and US:UV=0:4. This is because the photolytic degradation of bromate compounds is dominant degradation mechanism for THMs removal. However, the fastest degradation of total organic carbon was observed in a condition of US:UV=1:3. Because hydrogen peroxide generated by sonication was effectively dissociated to hydroxyl radicals by ultraviolet, the concentration of hydroxyl radical was maintained high. This mechanism provided additional degradation of organics. This result was supported by comparison between the concentration of hydrogen peroxide sole and combined process. Consequently, the optimal energy ratio was US:UV=1:3 for degradation of THMs in sonophotolytic process.

  15. Electroluminescent behaviors in multilayer thin-film electroluminescent devices using 9,10-bisstyrylanthracene derivatives

    NASA Astrophysics Data System (ADS)

    Aminaka, Ei-Ichiro; Tsutsui, Tetsuo; Saito, Shogo

    1994-02-01

    Using nine 9,10-bisstyrylanthracene derivatives (BSA's) with different substituents as emission layer materials, multilayer electroluminescent (EL) devices were fabricated. Among nine BSA's, three BSA's were found to exhibit high EL performance. Four types of devices, a single-layer device with a BSA emission layer, two types of two-layer devices in which BSA emission layers were combined with a triphenylamine dimer as a hole transport layer or an oxadiazole derivative as an electron transport layer, and a three-layer device, were fabricated using the three BSA's. The relationships between the device structures and EL performances of these devices were studied. Ionization potential values in vacuum-deposited films of BSA's were measured. It was found that the introduction of an electron withdrawing group increased electron injection/transport capability, and that of electron donating groups increased hole injection/transport capability. The relative EL efficiencies of various devices were discussed in terms of the electronic nature of BSA's.

  16. Field-effect electroluminescence in silicon nanocrystals.

    PubMed

    Walters, Robert J; Bourianoff, George I; Atwater, Harry A

    2005-02-01

    There is currently worldwide interest in developing silicon-based active optical components in order to leverage the infrastructure of silicon microelectronics technology for the fabrication of optoelectronic devices. Light emission in bulk silicon-based devices is constrained in wavelength to infrared emission, and in efficiency by the indirect bandgap of silicon. One promising strategy for overcoming these challenges is to make use of quantum-confined excitonic emission in silicon nanocrystals. A critical challenge for silicon nanocrystal devices based on nanocrystals embedded in silicon dioxide has been the development of a method for efficient electrical carrier injection. We report here a scheme for electrically pumping dense silicon nanocrystal arrays by a field-effect electroluminescence mechanism. In this excitation process, electrons and holes are both injected from the same semiconductor channel across a tunnelling barrier in a sequential programming process, in contrast to simultaneous carrier injection in conventional pn-junction light-emitting-diode structures. Light emission is strongly correlated with the injection of a second carrier into a nanocrystal that has been previously programmed with a charge of the opposite sign.

  17. Complete Genome Sequence of Pseudomonas aeruginosa FA-HZ1, an Efficient Dibenzofuran-Degrading Bacterium

    PubMed Central

    Ali, Fawad; Hu, Haiyang; Xu, Ping

    2017-01-01

    ABSTRACT Pseudomonas sp. FA-HZ1, an efficient dibenzofuran-degrading bacterium, was isolated from landfill leachate. Here, we present the complete genome sequence of strain FA-HZ1, which contains only one circular chromosome. The complete genome sequence will be essential for revealing the molecular mechanisms of dibenzofuran degradation. PMID:28209830

  18. Complete Genome Sequence of Sphingomonas sp. Strain NIC1, an Efficient Nicotine-Degrading Bacterium

    PubMed Central

    Zhu, Xiongyu; Wang, Weiwei; Xu, Ping

    2016-01-01

    Sphingomonas sp. strain NIC1, an efficient nicotine-degrading bacterium, was isolated from tobacco leaves. Here, we present the complete genome sequence of strain NIC1, which contains one circular chromosome and two circular plasmids. The genomic information will provide insights into its molecular mechanism for nicotine degradation. PMID:27417841

  19. RANDOM ACCESS CONTROL OF ELECTROLUMINESCENT ELEMENTS.

    DTIC Science & Technology

    Cadmium selenide (CdSe) switches were devised to control the luminous emittance of electroluminescent cells in a solid-state display. The technique...purpose of this contract was to establish the feasibility of utilizing the hysteretic effect in cadmium selenide to provide switching and storage to an...array of electroluminescent cells by investigating the cadmium selenide material, by studying panel structure, and by investigating the addressing of

  20. Efficient degradation of sulfamethoxazole by the Fe(II)/HSO5(-) process enhanced by hydroxylamine: Efficiency and mechanism.

    PubMed

    Liu, Guifang; Li, Xuchun; Han, Bangjun; Chen, Liwei; Zhu, Linan; Campos, Luiza C

    2017-01-15

    Fenton or Fenton-like processes have been regarded as feasible methods to degrade a wide variety of contaminants by generating reactive species, but the efficiency is still challenged by the slow transformation from Fe(III) to Fe(II) and pH. This study employed hydroxylamine (HA) to improve the oxidation efficiency of Fe(II)/HSO5(-) (Fe(II)/PMS) process, by selecting sulfamethoxazole (SMX) as the target compound. The degradation efficiency and mechanism of SMX by the HA/Fe(II)/PMS process were elucidated for the first time. Compared with Fe(II)/PMS process, the HA/Fe(II)/PMS process showed about 4 times higher degradation efficiency of SMX at pH 3.0. The analysis of steady-state concentration of Fe species indicated that HA enhanced the transformation of Fe(III) to Fe(II), sustaining the rapid Fenton-like reactions. Both sulfate radicals and hydroxyl radicals accounted for the degradation of SMX, with the latter regarded as the dominant reactive species. Degradation intermediates of SMX were further analyzed, and three main transformation pathways were thus proposed. The HA/Fe(II)/PMS process was also effective in the removal of SMX and total organic carbon from real pharmaceutical wastewater. This work would broaden the scope of application of Fenton and Fenton-like processes enhanced by HA in contaminants treatment.

  1. Quantum efficiencies of the photo-Fenton degradation of atrazine in water.

    PubMed

    Benzaquén, T B; Isla, M A; Alfano, O M

    2012-01-01

    An experimental work in a well-stirred batch recycling reactor for the photo-Fenton degradation of atrazine in water is presented. A study of the quantum efficiency is performed to assess the effectiveness of the photo-Fenton process on the atrazine degradation and total organic carbon (TOC) mineralization. Apparent and absolute quantum efficiencies of degradation and mineralization of an atrazine-based commercial herbicide are determined under different experimental conditions. Higher apparent efficiencies were found for both atrazine degradation and TOC mineralization when the ferric ion and hydrogen peroxide concentrations are increased. Because of the well known stability of the triazine ring, atrazine was not completely mineralized by the photo-Fenton process. However, a TOC reduction of 40% was achieved, being 62.5% of the maximum value that can be reached.

  2. Electric-field-induced strong enhancement of electroluminescence in multilayer molybdenum disulfide

    PubMed Central

    Li, Dehui; Cheng, Rui; Zhou, Hailong; Wang, Chen; Yin, Anxiang; Chen, Yu; Weiss, Nathan O.; Huang, Yu; Duan, Xiangfeng

    2015-01-01

    The layered transition metal dichalcogenides have attracted considerable interest for their unique electronic and optical properties. While the monolayer MoS2 exhibits a direct bandgap, the multilayer MoS2 is an indirect bandgap semiconductor and generally optically inactive. Here we report electric-field-induced strong electroluminescence in multilayer MoS2. We show that GaN–Al2O3–MoS2 and GaN–Al2O3–MoS2–Al2O3-graphene vertical heterojunctions can be created with excellent rectification behaviour. Electroluminescence studies demonstrate prominent direct bandgap excitonic emission in multilayer MoS2 over the entire vertical junction area. Importantly, the electroluminescence efficiency observed in multilayer MoS2 is comparable to or higher than that in monolayers. This strong electroluminescence can be attributed to electric-field-induced carrier redistribution from the lowest energy points (indirect bandgap) to higher energy points (direct bandgap) in k-space. The electric-field-induced electroluminescence is general for other layered materials including WSe2 and can open up a new pathway towards transition metal dichalcogenide-based optoelectronic devices. PMID:26130491

  3. Catalytic liquid marbles: Ag nanowire-based miniature reactors for highly efficient degradation of methylene blue.

    PubMed

    Miao, Yue-E; Lee, Hiang Kwee; Chew, Wee Shern; Phang, In Yee; Liu, Tianxi; Ling, Xing Yi

    2014-06-04

    Ag nanowire-based catalytic liquid marbles are fabricated as miniature reactors, which demonstrate highly efficient, support-free and rate-controllable heterogeneous degradation of methylene blue, with catalytic efficiency close to 100%. Our miniature catalytic liquid marbles are essential for reactions involving highly toxic/hazardous or costly reactants, where small volume preliminary reactions are preferred.

  4. Device Optimization and Transient Electroluminescence Studies of Organic light Emitting Devices

    SciTech Connect

    Lijuan Zou

    2003-08-05

    Organic light emitting devices (OLEDs) are among the most promising for flat panel display technologies. They are light, bright, flexible, and cost effective. And while they are emerging in commercial product, their low power efficiency and long-term degradation are still challenging. The aim of this work was to investigate their device physics and improve their performance. Violet and blue OLEDs were studied. The devices were prepared by thermal vapor deposition in high vacuum. The combinatorial method was employed in device preparation. Both continuous wave and transient electroluminescence (EL) were studied. A new efficient and intense UV-violet light emitting device was developed. At a current density of 10 mA/cm{sup 2}, the optimal radiance R could reach 0.38 mW/cm{sup 2}, and the quantum efficiency was 1.25%. using the delayed EL technique, electron mobilities in DPVBi and CBP were determined to be {approx} 10{sup -5} cm{sup 2}/Vs and {approx} 10{sup -4} cm{sup 2}/Vs, respectively. Overshoot effects in the transient El of blue light emitting devices were also observed and studied. This effect was attributed to the charge accumulation at the organic/organic and organic/cathode interfaces.

  5. Efficient degradation and expression prioritization with small RNAs

    NASA Astrophysics Data System (ADS)

    Mitarai, Namiko; Andersson, Anna M. C.; Krishna, Sandeep; Semsey, Szabolcs; Sneppen, Kim

    2007-09-01

    We build a simple model for feedback systems involving small RNA (sRNA) molecules based on the iron metabolism system in the bacterium E. coli, and compare it with the corresponding system in H. pylori which uses purely transcriptional regulation. This reveals several unique features of sRNA-based regulation that could be exploited by cells. Firstly, we show that sRNA regulation can maintain a smaller turnover of target mRNAs than transcriptional regulation, without sacrificing the speed of response to external shocks. Secondly, we propose that a single sRNA can prioritize the usage of different target mRNAs. This suggests that sRNA regulation would be more common in more complex systems which need to co-regulate many mRNAs efficiently.

  6. Improvement of electroluminescence performance by integration of ZnO nanowires and single-crystalline films on ZnO/GaN heterojunction

    SciTech Connect

    Shi, Zhifeng; Zhang, Yuantao Cui, Xijun; Wu, Bin; Zhuang, Shiwei; Yang, Fan; Zhang, Baolin; Du, Guotong; Yang, Xiaotian

    2014-03-31

    Heterojunction light-emitting diodes based on n-ZnO nanowires/ZnO single-crystalline films/p-GaN structure have been demonstrated for an improved electroluminescence performance. A highly efficient ultraviolet emission was observed under forward bias. Compared with conventional n-ZnO/p-GaN structure, high internal quantum efficiency and light extraction efficiency were simultaneously considered in the proposed diode. In addition, the diode can work continuously for ∼10 h with only a slight degradation in harsh environments, indicating its good reliability and application prospect in the future. This route opens possibilities for the development of advanced nanoscale devices in which the advantages of ZnO single-crystalline films and nanostructures can be integrated together.

  7. Phenol-degrading anode biofilm with high coulombic efficiency in graphite electrodes microbial fuel cell.

    PubMed

    Zhang, Dongdong; Li, Zhiling; Zhang, Chunfang; Zhou, Xue; Xiao, Zhixing; Awata, Takanori; Katayama, Arata

    2017-03-01

    A microbial fuel cell (MFC), with graphite electrodes as both the anode and cathode, was operated with a soil-free anaerobic consortium for phenol degradation. This phenol-degrading MFC showed high efficiency with a current density of 120 mA/m(2) and a coulombic efficiency of 22.7%, despite the lack of a platinum catalyst cathode and inoculation of sediment/soil. Removal of planktonic bacteria by renewing the anaerobic medium did not decrease the performance, suggesting that the phenol-degrading MFC was not maintained by the planktonic bacteria but by the microorganisms in the anode biofilm. Cyclic voltammetry analysis of the anode biofilm showed distinct oxidation and reduction peaks. Analysis of the microbial community structure of the anode biofilm and the planktonic bacteria based on 16S rRNA gene sequences suggested that Geobacter sp. was the phenol degrader in the anode biofilm and was responsible for current generation.

  8. Shifts in Microbial Community and Its Correlation with Degradative Efficiency in a Wastewater Treatment Plant.

    PubMed

    Kapley, Atya; Liu, Ruyin; Jadeja, Niti B; Zhang, Yu; Yang, Min; Purohit, Hemant J

    2015-08-01

    A wastewater treatment plant controls the level of pollution reaching the environment. Yet, despite being the most common aerobic route for treatment of wastewater, the activated sludge process is not utilized to its full potential. This is mainly due to the lack of knowledge base correlating the microbial community in the activated sludge to its degradative performance. In this study, the activated biomass at the treatment site was monitored for five consecutive months. Even though operational parameters were kept constant, the microbial community was observed to change after 3 months. This shift was seen to correlate with 25 % loss of degradative efficiency. Target oxygenases were monitored at two time points, and results indicated that the dominating pathway operating in the common effluent treatment plant (CETP) is the degradation of chlorinated aromatics. This study demonstrates the change in degradative efficiency in a CETP with the change in microbial community and analyzes the parameters influencing the microbial community of activated sludge.

  9. Isolation and identification of Bacillus megaterium YB3 from an effluent contaminated site efficiently degrades pyrene.

    PubMed

    Meena, Sumer Singh; Sharma, Radhey Shyam; Gupta, Priti; Karmakar, Swagata; Aggarwal, Kamal Krishan

    2016-04-01

    Industrial effluents contaminated sites may serve as repositories of ecologically adapted efficient pyrene degrading bacteria. In the present study, six bacterial isolates from industrial effluents were purified using serial enrichment technique and their pyrene degrading potential on pyrene supplemented mineral salt medium was assessed. 16S rRNA sequence analysis showed that they belong to four bacterial genera, namely Acinetobacter, Bacillus, Microbacterium, and Ochrobactrum. Among these isolates, Bacillus megaterium YB3 showed considerably good growth and was further evaluated for its pyrene-degrading efficiency. B. megaterium YB3 could degrade 72.44% of 500 mg L(-1) pyrene within 7 days. GC-MS analysis of ethyl acetate extracted fractions detected two relatively less toxic metabolic intermediates of the pyrene degradation pathway. B. megaterium YB3 also tested positive for catechol 1, 2-dioxygenase and aromatic-ring-hydroxylating dioxygenase indole-indigo conversion assays. Considering the ability and efficiency of B. megaterium YB3 to degrade high pyrene content, the strain can be used as a tool to develop bioremediation technologies for the effective biodegradation of pyrene and possibly other PAHs in the environment.

  10. Evaluation of fuel cell system efficiency and degradation at development and during commercialization

    NASA Astrophysics Data System (ADS)

    Gemmen, R. S.; Johnson, C. D.

    Two primary parameters stand out for characterizing fuel cell system performance. The first and most important parameter is system efficiency. This parameter is relatively easy to define, and protocols for its assessment are already available. Another important parameter yet to be fully considered is system degradation. Degradation is important because customers desire to know how long their purchased fuel cell unit will last. The measure of degradation describes this performance factor by quantifying, for example, how the efficiency of the unit degrades over time. While both efficiency and degradation concepts are readily understood, the coupling between these two parameters must also be understood so that proper testing and evaluation of fuel cell systems is achieved. Tests not properly performed, and results not properly understood, may result in improper use of the evaluation data, producing improper R&D planning decisions and financial investments. This paper presents an analysis of system degradation, recommends an approach to its measurement, and shows how these two parameters are related and how one can be "traded-off" for the other.

  11. A highly efficient degradation mechanism of methyl orange using Fe-based metallic glass powders.

    PubMed

    Xie, Shenghui; Huang, Ping; Kruzic, Jamie J; Zeng, Xierong; Qian, Haixia

    2016-02-23

    A new Fe-based metallic glass with composition Fe76B12Si9Y3 (at. %) is found to have extraordinary degradation efficiency towards methyl orange (MO, C14H14N3SO3) in strong acidic and near neutral environments compared to crystalline zero-valent iron (ZVI) powders and other Fe-based metallic glasses. The influence of temperature (294-328 K) on the degradation reaction rate was measured using ball-milled metallic glass powders revealing a low thermal activation energy barrier of 22.6 kJ/mol. The excellent properties are mainly attributed to the heterogeneous structure consisting of local Fe-rich and Fe-poor atomic clusters, rather than the large specific surface and strong residual stress in the powders. The metallic glass powders can sustain almost unchanged degradation efficiency after 13 cycles at room temperature, while a drop in degradation efficiency with further cycles is attributed to visible surface oxidation. Triple quadrupole mass spectrometry analysis conducted during the reaction was used to elucidate the underlying degradation mechanism. The present findings may provide a new, highly efficient and low cost commercial method for azo dye wastewater treatment.

  12. A highly efficient degradation mechanism of methyl orange using Fe-based metallic glass powders

    NASA Astrophysics Data System (ADS)

    Xie, Shenghui; Huang, Ping; Kruzic, Jamie J.; Zeng, Xierong; Qian, Haixia

    2016-02-01

    A new Fe-based metallic glass with composition Fe76B12Si9Y3 (at. %) is found to have extraordinary degradation efficiency towards methyl orange (MO, C14H14N3SO3) in strong acidic and near neutral environments compared to crystalline zero-valent iron (ZVI) powders and other Fe-based metallic glasses. The influence of temperature (294–328 K) on the degradation reaction rate was measured using ball-milled metallic glass powders revealing a low thermal activation energy barrier of 22.6 kJ/mol. The excellent properties are mainly attributed to the heterogeneous structure consisting of local Fe-rich and Fe-poor atomic clusters, rather than the large specific surface and strong residual stress in the powders. The metallic glass powders can sustain almost unchanged degradation efficiency after 13 cycles at room temperature, while a drop in degradation efficiency with further cycles is attributed to visible surface oxidation. Triple quadrupole mass spectrometry analysis conducted during the reaction was used to elucidate the underlying degradation mechanism. The present findings may provide a new, highly efficient and low cost commercial method for azo dye wastewater treatment.

  13. A highly efficient degradation mechanism of methyl orange using Fe-based metallic glass powders

    PubMed Central

    Xie, Shenghui; Huang, Ping; Kruzic, Jamie J.; Zeng, Xierong; Qian, Haixia

    2016-01-01

    A new Fe-based metallic glass with composition Fe76B12Si9Y3 (at. %) is found to have extraordinary degradation efficiency towards methyl orange (MO, C14H14N3SO3) in strong acidic and near neutral environments compared to crystalline zero-valent iron (ZVI) powders and other Fe-based metallic glasses. The influence of temperature (294–328 K) on the degradation reaction rate was measured using ball-milled metallic glass powders revealing a low thermal activation energy barrier of 22.6 kJ/mol. The excellent properties are mainly attributed to the heterogeneous structure consisting of local Fe-rich and Fe-poor atomic clusters, rather than the large specific surface and strong residual stress in the powders. The metallic glass powders can sustain almost unchanged degradation efficiency after 13 cycles at room temperature, while a drop in degradation efficiency with further cycles is attributed to visible surface oxidation. Triple quadrupole mass spectrometry analysis conducted during the reaction was used to elucidate the underlying degradation mechanism. The present findings may provide a new, highly efficient and low cost commercial method for azo dye wastewater treatment. PMID:26902824

  14. Phonon-assisted transient electroluminescence in Si

    SciTech Connect

    Cheng, Tzu-Huan; Chu-Su, Yu; Liu, Chien-Sheng; Lin, Chii-Wann

    2014-06-30

    The phonon-replica infrared emission is observed at room temperature from indirect band gap Si light-emitting diode under forward bias. With increasing injection current density, the broadened electroluminescence spectrum and band gap reduction are observed due to joule heating. The spectral-resolved temporal response of electroluminescence reveals the competitiveness between single (TO) and dual (TO + TA) phonon-assisted indirect band gap transitions. As compared to infrared emission with TO phonon-replica, the retarder of radiative recombination at long wavelength region (∼1.2 μm) indicates lower transition probability of dual phonon-replica before thermal equivalent.

  15. Strongly enhanced field-dependent single-molecule electroluminescence

    NASA Astrophysics Data System (ADS)

    Lee, Tae-Hee; Gonzalez, Jose I.; Dickson, Robert M.

    2002-08-01

    Individual, strongly electroluminescent Agn molecules (n = 28 atoms) have been electrically written within otherwise nonemissive silver oxide films. Exhibiting characteristic single-molecule behavior, these individual room-temperature molecules exhibit extreme electroluminescence enhancements (>104 vs. bulk and dc excitation on a per molecule basis) when excited with specific ac frequencies. Occurring through field extraction of electrons with subsequent reinjection and radiative recombination, single-molecule electroluminescence is enhanced by a general mechanism that avoids slow bulk material response. Thus, while we detail strong electroluminescence from single, highly fluorescent Agn molecules, this mechanism also yields strong ac-excited electroluminescence from similarly prepared, but otherwise nonemissive, individual Cu nanoclusters.

  16. Electroluminescent, polycrystalline cadmium selenide nanowire arrays.

    PubMed

    Ayvazian, Talin; van der Veer, Wytze E; Xing, Wendong; Yan, Wenbo; Penner, Reginald M

    2013-10-22

    Electroluminescence (EL) from nanocrystalline CdSe (nc-CdSe) nanowire arrays is reported. The n-type, nc-CdSe nanowires, 400-450 nm in width and 60 nm in thickness, were synthesized using lithographically patterned nanowire electrodeposition, and metal-semiconductor-metal (M-S-M) devices were prepared by the evaporation of two gold contacts spaced by either 0.6 or 5 μm. These M-S-M devices showed symmetrical current voltage curves characterized by currents that increased exponentially with applied voltage bias. As the applied biased was increased, an increasing number of nanowires within the array "turned on", culminating in EL emission from 30 to 50% of these nanowires at applied voltages of 25-30 V. The spectrum of the emitted light was broad and centered at 770 nm, close to the 1.74 eV (712 nm) band gap of CdSe. EL light emission occurred with an external quantum efficiency of 4 × 10(-6) for devices with a 0.60 μm gap between the gold contacts and 0.5 × 10(-6) for a 5 μm gap-values similar to those reported for M-S-M devices constructed from single-crystalline CdSe nanowires. Kelvin probe force microscopy of 5 μm nc-CdSe nanowire arrays showed pronounced electric fields at the gold electrical contacts, coinciding with the location of strongest EL light emission in these devices. This electric field is implicated in the Poole-Frenkel minority carrier emission and recombination mechanism proposed to account for EL light emission in most of the devices that were investigated.

  17. Preparation of ZnO Photocatalyst for the Efficient and Rapid Photocatalytic Degradation of Azo Dyes

    NASA Astrophysics Data System (ADS)

    Chen, Xiaoqing; Wu, Zhansheng; Liu, Dandan; Gao, Zhenzhen

    2017-02-01

    Zinc oxide (ZnO) photocatalysts were synthesized by sol-gel method using zinc acetate as precursor for degradation of azo dyes under UV irradiation. The resultant samples were characterized by different techniques, such as XRD, SEM, and EDX. The influence of preparation conditions such as calcination temperature and composite ratio on the degradation of methyl orange (MO) was investigated. ZnO prepared with a composite ratio of 4:1 and calcination temperature of 400 °C exhibited 99.70% removal rate for MO. The effect of operation parameters on the degradation was also studied. Results showed that the removal rate of azo dyes increased with the increased dosage of catalyst and decreased initial concentration of azo dyes and the acidic condition is favorable for degradation. Furthermore, the kinetics and scavengers of the reactive species during the degradation were also investigated. It was found that the degradation of azo dyes fitted the first-order kinetics and superoxide ions were the main species. The proposed photocatalyst can efficiently and rapidly degrade azo dyes; thus, this economical and environment-friendly photocatalyst can be applied to the treatment of wastewater contaminated with synthetic dyes.

  18. Preparation of ZnO Photocatalyst for the Efficient and Rapid Photocatalytic Degradation of Azo Dyes.

    PubMed

    Chen, Xiaoqing; Wu, Zhansheng; Liu, Dandan; Gao, Zhenzhen

    2017-12-01

    Zinc oxide (ZnO) photocatalysts were synthesized by sol-gel method using zinc acetate as precursor for degradation of azo dyes under UV irradiation. The resultant samples were characterized by different techniques, such as XRD, SEM, and EDX. The influence of preparation conditions such as calcination temperature and composite ratio on the degradation of methyl orange (MO) was investigated. ZnO prepared with a composite ratio of 4:1 and calcination temperature of 400 °C exhibited 99.70% removal rate for MO. The effect of operation parameters on the degradation was also studied. Results showed that the removal rate of azo dyes increased with the increased dosage of catalyst and decreased initial concentration of azo dyes and the acidic condition is favorable for degradation. Furthermore, the kinetics and scavengers of the reactive species during the degradation were also investigated. It was found that the degradation of azo dyes fitted the first-order kinetics and superoxide ions were the main species. The proposed photocatalyst can efficiently and rapidly degrade azo dyes; thus, this economical and environment-friendly photocatalyst can be applied to the treatment of wastewater contaminated with synthetic dyes.

  19. Efficient catalytic effect of CuO nanostructures on the degradation of organic dyes

    NASA Astrophysics Data System (ADS)

    Zaman, S.; Zainelabdin, A.; Amin, G.; Nur, O.; Willander, M.

    2012-11-01

    An efficient catalytic effect of petals and flowers like CuO nanostructures (NSs) on the degradation of two organic dyes, methylene blue (MB) and rhodamine B (RB) were investigated. The highest degradation of 95% in CuO petals and 72% in flowers for MB is observed in 24 h. For RB, the degradation was 85% and 80% in petals and flowers, respectively for 5 h. It was observed that CuO petals appeared to be more active than flowers for degradation of both dyes associated to high specific surface area. The petals and flower like CuO NSs were synthesized using the chemical bath method at 90 °C. The grown CuO NSs were characterized using scanning electron microscopy (SEM), high resolution transmission electron microscopy (HRTEM), and X-ray diffraction (XRD).

  20. Structure–efficiency relationships of cyclodextrin scavengers in the hydrolytic degradation of organophosphorus compounds

    PubMed Central

    Letort, Sophie; Bosco, Michaël; Cornelio, Benedetta; Brégier, Frédérique; Daulon, Sébastien; Gouhier, Géraldine

    2017-01-01

    New derivatives of cyclodextrins were prepared in order to determine the relative importance of the structural key elements involved in the degradation of organophosphorus nerve agents. To avoid a competitive inclusion between the organophosphorus substrate and the iodosobenzoate group, responsible for its degradation, the latter group had to be covalently bound to the cyclodextrin scaffold. Although the presence of the α nucleophile iodosobenzoate was a determinant in the hydrolysis process, an imidazole group was added to get a synergistic effect towards the degradation of the agents. The degradation efficiency was found to be dependent on the relative position of the heterocycle towards the reactive group as well as on the nature of the organophosphorus derivative. PMID:28382180

  1. Catalytic strategy for efficient degradation of nitroaromatic pesticides by using gold nanoflower.

    PubMed

    Mao, Kang; Chen, Yinran; Wu, Zitong; Zhou, Xiaodong; Shen, Aiguo; Hu, Jiming

    2014-11-05

    In this contribution, we report a new type of Au nanoflower-based nitroaromatic pesticide degradation platform that is fast, efficient, and simple. We found a straightforward, economically viable, and "green" approach for the synthesis and stabilization of relatively monodisperse Au nanoflowers by using nontoxic chemical of hydroxylamine (NH2OH) without stabilizer and the adjustment of the pH environment. This experiment shows that these Au nanoflowers function as effective catalyst for the reduction of pendimethalin in the presence of NaBH4 (otherwise unfeasible if NaBH4 is the only agent employed), which was reflected by the UV/vis spectra of the catalytic reaction kinetics. Importantly, the novel degradation platform could be put in use in two different practical soil samples with satisfactory results under laboratory conditions. To demonstrate the feasibility and universality of our design, two other nitroaromatic pesticides, trifluralin, and p-nitrophenol, were selected and were successfully degraded using this degradation platform.

  2. Legibility of electroluminescent instrument panels investigated

    NASA Technical Reports Server (NTRS)

    Mc Lean, M. V.; Miller, G. E.

    1966-01-01

    Legibility studies of several EL /electroluminescent/ displays correlate reading time and accuracy with number size, stroke/width ratio, indicia size, pointer width, contrast, ambient illumination, and color background and and contrast. Human factor criteria established on non-EL displays may not apply to EL displays.

  3. Organic electroluminescent devices having improved light extraction

    DOEpatents

    Shiang, Joseph John

    2007-07-17

    Organic electroluminescent devices having improved light extraction include a light-scattering medium disposed adjacent thereto. The light-scattering medium has a light scattering anisotropy parameter g in the range from greater than zero to about 0.99, and a scatterance parameter S less than about 0.22 or greater than about 3.

  4. Electroluminescent Displays Made With Alternative Dopants

    NASA Technical Reports Server (NTRS)

    Robertson, James B.

    1993-01-01

    Metals and metal fluorides deposited in ZnS to form color phosphors. Single-layer, thin-film electroluminescent display device contains ZnS host layer doped to form green, red, and blue phosphors. Luminescence in chosen colors at chosen intersections between rows and columns produced by application of voltages to appropriate row-and-column pairs of conductors.

  5. Development of gallium aluminum phosphide electroluminescent diodes

    NASA Technical Reports Server (NTRS)

    Chicotka, R. J.; Lorenz, M. R.; Nethercot, A. H.; Pettit, G. D.

    1972-01-01

    Work done on the development of gallium aluminum phosphide alloys for electroluminescent light sources is described. The preparation of this wide band gap semiconductor alloy, its physical properties (particularly the band structure, the electrical characteristics, and the light emitting properties) and work done on the fabrication of diode structures from these alloys are broadly covered.

  6. Degradation of atrazine by UV/chlorine: Efficiency, influencing factors, and products.

    PubMed

    Kong, Xiujuan; Jiang, Jin; Ma, Jun; Yang, Yi; Liu, Weili; Liu, Yulei

    2016-03-01

    In this work, the degradation of atrazine by the combination of UV and chlorine (UV/chlorine) due to the formation of radicals during chlorine photolysis was systematically investigated in terms of efficiency, factors that influence the degradation kinetics, as well as oxidation products. It was found that the degradation efficiency of atrazine was enhanced by UV/chlorine compared to UV or chlorine alone. The degradation efficiency of atrazine was favorable at a lower pH, but was inhibited in the presence of natural organic matters. Meanwhile, the initial chlorine dosage, alkalinity, and chloride barely influenced the degradation efficiency under neutral pH conditions. The degradation of atrazine by UV/chlorine was inhibited in real waters (i.e., surface water and ground water) compared to in deionized water but was still more effective than UV alone. The oxidation products of atrazine resulting from de-alkylation, dechlorination-hydroxylation, alkylic-hydroxylation, alkylic-oxidation, alkylic-hydroxylation-dehydration, deamination-hydroxylation, and dechlorination-hydrogenation in UV/chlorine process were detected, which were slightly different from those formed in UV/H2O2 (commonly used UV-based advanced oxidation process). Particularly, the yields of three primary transformation products (desethyl-atrazine (DEA), desisopropyl-atrazine (DIA), and desethyl-desisopropyl-atrazine (DEIA)) were comparatively quantified in these two processes. The different trend of them formed in UV/chlorine system (DEA:DIA≈4) compared to that formed in UV/H2O2 system (DEA:DIA≈1) could be ascribed to the different reaction reactivities and mechanisms between HO• and Cl• with atrazine.

  7. Contactless Electroluminescence Imaging for Cell and Module Characterization

    SciTech Connect

    Johnston, Steve

    2015-06-14

    Module performance can be characterized by imaging using baseline and periodic images to track defects and degradation. Both thermal images, which can be acquired during sunny operating conditions, and photoluminescence images, which could be acquired at night, can be collected without electrical connection. Electroluminescence (EL) images, which are useful to detect many types of defects such as cracks, interconnect and solder faults, and resistances, have typically required electrical connection to drive current in the cells and modules. Here, a contactless EL imaging technique is proposed, which provides an EL image without the need for electrical connection to drive current through the module. Such EL imaging has the capability to be collected at night without disruption to daytime power generation.

  8. Evaluation of the absolute photoluminescence quantum yields of molecularly doped organic composite films and the electroluminescence efficiencies of molecular light-emitting devices containing oligoheterocycles as efficient emission centers

    NASA Astrophysics Data System (ADS)

    Kushto, Gary P.; Hill, Ian G.; Mitschke, Ullrich; Baeuerle, Peter; Kafafi, Zakya H.

    2001-02-01

    The absolute photoluminescence quantum yields ((Phi) PL) of three end-capped oligothiophene derivatives dispersed in N,N'-((alpha) -naphthyl)-N,N'-diphenyl-1,1'-biphenyl ((alpha) -NPD) have been evaluated and the most efficient of the emitters was used as a dopant in molecular organic LEDs. Composite films of 2,5-bis [5-(4,5,6,7- tetrahydrobenzo[b]thien-2-yl) thien-2-yl]-furan (EC5FUR); 2,5-bis [5-(4,5,6,7- tetrahydrobenzo[b]thien-2-yl) thien-2-yl]-oxazole (EC5OXZ) and 2,5-bis [5-(4,5,6,7- tetrahydrobenzo[b]thien-2-yl)thien-2-yl]-1,3,4- oxadiazole (EC5OXD) doped into (alpha) -NPD were found to have (Phi) PL values of 78, 62 and 28%, respectively. MOLED devices were fabricated using an EC5FUR/(alpha) -NPD composite as the emitting layer and the external quantum efficiencies ((eta) EL) of these devices were evaluated. The results of the device characterization show that the inclusion of EC5FUR in the NPD hole transport layer increases the device (eta) EL to 1.45% at a current density of 10 mA/cm2. In addition, the concentration dependence of the (eta) EL on the EC5FUR dopant in certain device structures when considered in conjunction with the current results of ultraviolet photoemission spectroscopic experiments suggests that this dopant species may be acting as both a hole and electron trap in the (alpha) -NPD host.

  9. Efficiency of uronic acid uptake in marine alginate-degrading fungi

    NASA Astrophysics Data System (ADS)

    Schaumann, K.; Weide, G.

    1995-03-01

    Despite the fact that many marine fungi, including phycomycetes, yeasts, ascomycetes and hyphomycetes, have been recorded from living and/or dead phaeophytes, only a few of these have been shown to be capable of degrading alginic acid or alginates. The degradation is achieved by the action of an exoenzyme complex, comprising alginate lyase, as well as alginate hydrolase activities. The latter was detected only recently by the authors. In this study, the growth of two marine sodiumalginate-degrading deuteromycetes, Asteromyces cruciatus and Dendryphiella salina, was investigated, and the assimilation efficiency of sodiumalginate and its uronic acid degradation products, respectively, was estimated from the economic coefficient (E). E is calculated from the mycelial dry weight, divided by the weight of substrate consumed for this production. The economic coefficient for A. cruciatus was 48.6%, and that of D. salina 38.9%. This indicates that the former species uses the alginate degradation products more efficiently than the latter. The observed E-values for the marine deuteromycetes agree with those from other fungi, e.g. terrestrial species. In general, it is concluded that the marine fungi appear to play a more important role in kelp-based ecosystems than was realized previously.

  10. Efficient degradation of organic pollutants in aqueous solution with bicarbonate-activated hydrogen peroxide.

    PubMed

    Xu, Aihua; Li, Xiaoxia; Xiong, Hui; Yin, Guochuan

    2011-02-01

    Bicarbonate anion is an efficient activator for hydrogen peroxide to generate many active oxygen species including peroxymonocarbonate (HCO(4)(-)), superoxide ion (O(2)(-)) and singlet oxygen ((1)O(2)). This study aims to understand the oxidative degradation of organic pollutants including methyl blue, methyl orange, rhodamine B, and 4-chlorophenol, with H(2)O(2) activated by sodium bicarbonate at room temperature. The obtained results indicate that such a method is apparently efficient in versatile pollutant degradation. Compared with using H(2)O(2) alone under similar pH conditions, the degradation rates of the pollutants were greatly enhanced through adding NaHCO(3). Through LC-MS, FT-IR and the TOC analysis, the degradation of methylene blue was revealed to proceed by the transformation of dimethylamino group in methylene blue to methylamino, aldehyde and nitro group, and the opening of phenyl ring into small molecular compounds and CO(2). The studies using the (1)O(2) scavenger sodium azide and the O(2)(-) indicator nitro blue tetrazolium suggest that the active O(2)(-) intermediate, generated from HCO(4)(-) decomposition, rather than (1)O(2) was involved in the pollutant degradation.

  11. Degradable Molybdenum Oxide Nanosheets with Rapid Clearance and Efficient Tumor Homing Capabilities as a Therapeutic Nanoplatform.

    PubMed

    Song, Guosheng; Hao, Jiali; Liang, Chao; Liu, Teng; Gao, Min; Cheng, Liang; Hu, Junqing; Liu, Zhuang

    2016-02-05

    Molybdenum oxide (MoOx) nanosheets with high near-infrared (NIR) absorbance and pH-dependent oxidative degradation properties were synthesized, functionalized with polyethylene glycol (PEG), and then used as a degradable photothermal agent and drug carrier. The nanosheets, which are relatively stable under acidic pH, could be degraded at physiological pH. Therefore, MoOx-PEG distributed in organs upon intravenous injection would be rapidly degraded and excreted without apparent in vivo toxicity. MoOx-PEG shows efficient accumulation in tumors, the acidic pH of which then leads to longer tumor retention of those nanosheets. Along with the capability of acting as a photothermal agent for effective tumor ablation, MoOx-PEG can load therapeutic molecules with high efficiencies. This concept of inorganic theranostic nanoagent should be relatively stable in tumors to allow imaging and treatment, while being readily degradable in normal organs to enable rapid excretion and avoid long-term retention/toxicity.

  12. Development of a novel high-entropy alloy with eminent efficiency of degrading azo dye solutions

    NASA Astrophysics Data System (ADS)

    Lv, Z. Y.; Liu, X. J.; Jia, B.; Wang, H.; Wu, Y.; Lu, Z. P.

    2016-09-01

    In addition to its scientific importance, the degradation of azo dyes is of practical significance from the perspective of environmental protection. Although encouraging progress has been made on developing degradation approaches and materials, it is still challenging to fully resolve this long-standing problem. Herein, we report that high entropy alloys, which have been emerging as a new class of metallic materials in the last decade, have excellent performance in degradation of azo dyes. In particular, the newly developed AlCoCrTiZn high-entropy alloy synthesized by mechanical alloying exhibits a prominent efficiency in degradation of the azo dye (Direct Blue 6: DB6), as high as that of the best metallic glass reported so far. The newly developed AlCoCrTiZn HEA powder has low activation energy barrier, i.e., 30 kJ/mol, for the degrading reaction and thus make the occurrence of reaction easier as compared with other materials such as the glassy Fe-based powders. The excellent capability of our high-entropy alloys in degrading azo dye is attributed to their unique atomic structure with severe lattice distortion, chemical composition effect, residual stress and high specific surface area. Our findings have important implications in developing novel high-entropy alloys for functional applications as catalyst materials.

  13. Development of a novel high-entropy alloy with eminent efficiency of degrading azo dye solutions.

    PubMed

    Lv, Z Y; Liu, X J; Jia, B; Wang, H; Wu, Y; Lu, Z P

    2016-09-28

    In addition to its scientific importance, the degradation of azo dyes is of practical significance from the perspective of environmental protection. Although encouraging progress has been made on developing degradation approaches and materials, it is still challenging to fully resolve this long-standing problem. Herein, we report that high entropy alloys, which have been emerging as a new class of metallic materials in the last decade, have excellent performance in degradation of azo dyes. In particular, the newly developed AlCoCrTiZn high-entropy alloy synthesized by mechanical alloying exhibits a prominent efficiency in degradation of the azo dye (Direct Blue 6: DB6), as high as that of the best metallic glass reported so far. The newly developed AlCoCrTiZn HEA powder has low activation energy barrier, i.e., 30 kJ/mol, for the degrading reaction and thus make the occurrence of reaction easier as compared with other materials such as the glassy Fe-based powders. The excellent capability of our high-entropy alloys in degrading azo dye is attributed to their unique atomic structure with severe lattice distortion, chemical composition effect, residual stress and high specific surface area. Our findings have important implications in developing novel high-entropy alloys for functional applications as catalyst materials.

  14. Development of a novel high-entropy alloy with eminent efficiency of degrading azo dye solutions

    PubMed Central

    Lv, Z. Y.; Liu, X. J.; Jia, B.; Wang, H.; Wu, Y.; Lu, Z. P.

    2016-01-01

    In addition to its scientific importance, the degradation of azo dyes is of practical significance from the perspective of environmental protection. Although encouraging progress has been made on developing degradation approaches and materials, it is still challenging to fully resolve this long-standing problem. Herein, we report that high entropy alloys, which have been emerging as a new class of metallic materials in the last decade, have excellent performance in degradation of azo dyes. In particular, the newly developed AlCoCrTiZn high-entropy alloy synthesized by mechanical alloying exhibits a prominent efficiency in degradation of the azo dye (Direct Blue 6: DB6), as high as that of the best metallic glass reported so far. The newly developed AlCoCrTiZn HEA powder has low activation energy barrier, i.e., 30 kJ/mol, for the degrading reaction and thus make the occurrence of reaction easier as compared with other materials such as the glassy Fe-based powders. The excellent capability of our high-entropy alloys in degrading azo dye is attributed to their unique atomic structure with severe lattice distortion, chemical composition effect, residual stress and high specific surface area. Our findings have important implications in developing novel high-entropy alloys for functional applications as catalyst materials. PMID:27677462

  15. Theoretical and material studies of thin-film electroluminescent devices

    NASA Technical Reports Server (NTRS)

    Summers, C. J.

    1989-01-01

    Thin-film electroluminescent (TFEL) devices are studied for a possible means of achieving a high resolution, light weight, compact video display panel for computer terminals or television screens. The performance of TFEL devices depends upon the probability of an electron impact exciting a luminescent center which in turn depends upon the density of centers present in the semiconductor layer, the possibility of an electron achieving the impact excitation threshold energy, and the collision cross section itself. Efficiency of such a device is presently very poor. It can best be improved by increasing the number of hot electrons capable of impact exciting a center. Hot electron distributions and a method for increasing the efficiency and brightness of TFEL devices (with the additional advantage of low voltage direct current operation) are investigated.

  16. Composite nanofibers for highly efficient photocatalytic degradation of organic dyes from contaminated water.

    PubMed

    Mohamed, Alaa; El-Sayed, Ramy; Osman, T A; Toprak, M S; Muhammed, M; Uheida, A

    2016-02-01

    In this study highly efficient photocatalyst based on composite nanofibers containing polyacrylonitrile (PAN), carbon nanotubes (CNT), and surface functionalized TiO2 nanoparticles was developed. The composite nanofibers were fabricated using electrospinning technique followed by chemical crosslinking. The surface modification and morphology changes of the fabricated composite nanofibers were examined through SEM, TEM, and FTIR analysis. The photocatalytic performance of the composite nanofibers for the degradation of model molecules, methylene blue and indigo carmine, under UV irradiation in aqueous solutions was investigated. The results demonstrated that high photodegradation efficiency was obtained in a short time and at low power intensity compared to other reported studies. The effective factors on the degradation of the dyes, such as the amount of catalyst, solution pH and irradiation time were investigated. The experimental kinetic data were fitted using pseudo-first order model. The effect of the composite nanofibers as individual components on the degradation efficiency of MB and IC was evaluated in order to understand the overall photodegradation mechanism. The results obtained showed that all the components possess significant effect on the photodegradation activity of the composite nanofibers. The stability studies demonstrated that the photodegradation efficiency can remain constant at the level of 99% after five consecutive cycles.

  17. Efficient adsorption and photocatalytic degradation of Congo red onto hydrothermally synthesized NiS nanoparticles

    NASA Astrophysics Data System (ADS)

    Guo, Hongxu; Ke, Yingchang; Wang, Dongfeng; Lin, Kaili; Shen, Ruxiang; Chen, Jianhua; Weng, Wen

    2013-03-01

    NiS nanoparticles (NiS NPs) have been hydrothermally prepared and characterized by the methods of X-ray diffraction, scanning electronic microscope, X-ray photoelectron spectroscopy, UV-Vis diffuse reflectance spectra, photoluminescence, and thermogravimetric analysis. NiS NPs exhibit fast adsorption in the removal of Congo red (CR) in aqueous solution, in which the pseudo-second-order model was the best to describe the adsorption kinetics, and the intraparticle diffusion was not only the rate-limiting step. The NiS NPs also exhibit efficient photocatalytic activity in the degradation of CR under visible-light irradiation, in which the 30 mg/L CR was almost completely degraded after illumination during 210 min. The •OH radicals in the process of photocatalytic degradation were observed by fluorescence technique.

  18. Efficient and selective degradation of polyethylenes into liquid fuels and waxes under mild conditions.

    PubMed

    Jia, Xiangqing; Qin, Chuan; Friedberger, Tobias; Guan, Zhibin; Huang, Zheng

    2016-06-01

    Polyethylene (PE) is the largest-volume synthetic polymer, and its chemical inertness makes its degradation by low-energy processes a challenging problem. We report a tandem catalytic cross alkane metathesis method for highly efficient degradation of polyethylenes under mild conditions. With the use of widely available, low-value, short alkanes (for example, petroleum ethers) as cross metathesis partners, different types of polyethylenes with various molecular weights undergo complete conversion into useful liquid fuels and waxes. This method shows excellent selectivity for linear alkane formation, and the degradation product distribution (liquid fuels versus waxes) can be controlled by the catalyst structure and reaction time. In addition, the catalysts are compatible with various polyolefin additives; therefore, common plastic wastes, such as postconsumer polyethylene bottles, bags, and films could be converted into valuable chemical feedstocks without any pretreatment.

  19. Efficient and selective degradation of polyethylenes into liquid fuels and waxes under mild conditions

    PubMed Central

    Jia, Xiangqing; Qin, Chuan; Friedberger, Tobias; Guan, Zhibin; Huang, Zheng

    2016-01-01

    Polyethylene (PE) is the largest-volume synthetic polymer, and its chemical inertness makes its degradation by low-energy processes a challenging problem. We report a tandem catalytic cross alkane metathesis method for highly efficient degradation of polyethylenes under mild conditions. With the use of widely available, low-value, short alkanes (for example, petroleum ethers) as cross metathesis partners, different types of polyethylenes with various molecular weights undergo complete conversion into useful liquid fuels and waxes. This method shows excellent selectivity for linear alkane formation, and the degradation product distribution (liquid fuels versus waxes) can be controlled by the catalyst structure and reaction time. In addition, the catalysts are compatible with various polyolefin additives; therefore, common plastic wastes, such as postconsumer polyethylene bottles, bags, and films could be converted into valuable chemical feedstocks without any pretreatment. PMID:27386559

  20. Efficient heterogeneous and environmentally friendly degradation of nerve agents on a tungsten-based POM.

    PubMed

    Mizrahi, Dana M; Saphier, Sigal; Columbus, Ishay

    2010-07-15

    Common (chemical warfare agent) CWA decontaminants exhibit harsh and corrosive characteristics, and are harmful to the environment. In the course of our quest for active sorbents as efficient decontaminants, Keggin-type polyoxometalate (POM) (NH(4))(3)PW(12)O(40) was tested for oxidative degradation of CWAs. Although oxidation did not take place, sarin (GB) and VX were smoothly decontaminated to non-toxic products within 1 and 10 days, respectively. Degradation was carried out directly on the powder, eliminating the need for solvents. Mustard gas (HD), whose degradation is highly dependent on oxidation, was not decontaminated by this POM. Solid state MAS NMR ((31)P and (13)C) was utilized both for POM characterization and for decontamination studies monitoring.

  1. Relationship between phenol degradation efficiency and microbial community structure in an anaerobic SBR.

    PubMed

    Rosenkranz, F; Cabrol, L; Carballa, M; Donoso-Bravo, A; Cruz, L; Ruiz-Filippi, G; Chamy, R; Lema, J M

    2013-11-01

    Phenol is a common wastewater contaminant from various industrial processes, including petrochemical refineries and chemical compounds production. Due to its toxicity to microbial activity, it can affect the efficiency of biological wastewater treatment processes. In this study, the efficiency of an Anaerobic Sequencing Batch Reactor (ASBR) fed with increasing phenol concentrations (from 120 to 1200 mg L(-1)) was assessed and the relationship between phenol degradation capacity and the microbial community structure was evaluated. Up to a feeding concentration of 800 mg L(-1), the initial degradation rate steadily increased with phenol concentration (up to 180 mg L(-1) d(-1)) and the elimination capacity remained relatively constant around 27 mg phenol removed∙gVSS(-1) d(-1). Operation at higher concentrations (1200 mg L(-1)) resulted in a still efficient but slower process: the elimination capacity and the initial degradation rate decreased to, respectively, 11 mg phenol removed∙gVSS(-1) d(-1) and 154 mg L(-1) d(-1). As revealed by Denaturing Gradient Gel Electrophoresis (DGGE) analysis, the increase of phenol concentration induced level-dependent structural modifications of the community composition which suggest an adaptation process. The increase of phenol concentration from 120 to 800 mg L(-1) had little effect on the community structure, while it involved drastic structural changes when increasing from 800 to 1200 mg L(-1), including a strong community structure shift, suggesting the specialization of the community through the emergence and selection of most adapted phylotypes. The thresholds of structural and functional disturbances were similar, suggesting the correlation of degradation performance and community structure. The Canonical Correspondence Analysis (CCA) confirmed that the ASBR functional performance was essentially driven by specific community traits. Under the highest feeding concentration, the most abundant ribotype probably involved in

  2. The oligomeric architecture of the archaeal exosome is important for processive and efficient RNA degradation

    PubMed Central

    Audin, Maxime J. C.; Wurm, Jan Philip; Cvetkovic, Milos A.; Sprangers, Remco

    2016-01-01

    The exosome plays an important role in RNA degradation and processing. In archaea, three Rrp41:Rrp42 heterodimers assemble into a barrel like structure that contains a narrow RNA entrance pore and a lumen that contains three active sites. Here, we demonstrate that this quaternary structure of the exosome is important for efficient RNA degradation. We find that the entrance pore of the barrel is required for nM substrate affinity. This strong interaction is crucial for processive substrate degradation and prevents premature release of the RNA from the enzyme. Using methyl TROSY NMR techniques, we establish that the 3′ end of the substrate remains highly flexible inside the lumen. As a result, the RNA jumps between the three active sites that all equally participate in substrate degradation. The RNA jumping rate is, however, much faster than the cleavage rate, indicating that not all active site:substrate encounters result in catalysis. Enzymatic turnover therefore benefits from the confinement of the active sites and substrate in the lumen, which ensures that the RNA is at all times bound to one of the active sites. The evolution of the exosome into a hexameric complex and the optimization of its catalytic efficiency were thus likely co-occurring events. PMID:26837575

  3. Electroplating sludge derived zinc-ferrite catalyst for the efficient photo-Fenton degradation of dye.

    PubMed

    Cao, Zhenbang; Zhang, Jia; Zhou, Jizhi; Ruan, Xiuxiu; Chen, Dan; Liu, Jianyong; Liu, Qiang; Qian, Guangren

    2017-05-15

    A zinc-dominant ferrite catalyst for efficient degradation of organic dye was prepared by the calcination of electroplating sludge (ES). Characterizations indicated that zinc ferrite (ZnFe2O4) coexisted with Fe2O3 structure was the predominant phase in the calcined electroplating sludge (CES). CES displayed a high decolorization ratio (88.3%) of methylene blue (MB) in the presence of H2O2 combined with UV irradiation. The high efficiency could be ascribed to the photocatalytic process induced by ZnFe2O4 and the photo-Fenton dye degradation by ferrous content, and a small amount of Al and Mg in the sludge might also contribute to the catalysis. Moreover, the degradation capability of dye by CES was supported by the synthetic ZnFe2O4 with different Zn to Fe molar ratio (n(Zn): n(Fe)), as 84.81%-86.83% of dye was removed with n(Zn): n(Fe) ranged from 1:0.5 to 1:3. All synthetic ferrite samples in the simulation achieved adjacent equilibrium decolorization ratio, the flexible proportioning of divalent metal ions (M(2+)) to trivalent metal ions (M(3+)) applied in the synthesis indicated that the catalyst has a high availability. Therefore, an efficacious catalyst for the degradation of dye can potentially be derived from heavy metal-containing ES, it's a novel approach for the reutilization of ES.

  4. Efficient degradation of trichloroethylene in water using persulfate activated by reduced graphene oxide-iron nanocomposite.

    PubMed

    Ahmad, Ayyaz; Gu, Xiaogang; Li, Li; Lv, Shuguang; Xu, Yisheng; Guo, Xuhong

    2015-11-01

    Graphene oxide (GO) and nano-sized zero-valent iron-reduced graphene oxide (nZVI-rGO) composite were prepared. The GO and nZVI-rGO composite were characterized by transmission electron microscopy (TEM), Fourier transform infrared (FTIR), energy-dispersive spectroscopy (EDS), and Raman spectroscopy. The size of nZVI was about 6 nm as observed by TEM. The system of nZVI-rGO and persulfate (PS) was used for the degradation of trichloroethylene (TCE) in water, and showed 26.5% more efficiency as compared to nZVI/PS system. The different parameters were studied to determine the efficiency of nZVI-rGO to activate the PS system for the TCE degradation. By increasing the PS amount, TCE removal was also improved while no obvious effect was observed by varying the catalyst loading. Degradation was decreased as the TCE initial concentration was increased from 20 to 100 mg/L. Moreover, when initial solution pH was increased, efficiency deteriorated to 80%. Bicarbonate showed more negative effect on TCE removal among the solution matrix. To better understand the effects of radical species in the system, the scavenger tests were performed. The •SO4(-) and •O2(-) were predominant species responsible for TCE removal. The nZVI-rGO-activated PS process shows potential applications in remediation of highly toxic organic contaminants such as TCE present in the groundwater. Graphical abstract Persulfate activated by reduced graphene oxide and nano-sized zero-valent iron composite can be used for efficient degradation of trichloroethylene (TCE) in water.

  5. [Electroluminescence character of novel unsymmetry substituted phthalocyanines].

    PubMed

    Xia, Dao-cheng; Li, Wan-cheng; Han, Shuang; Cheng, Chuan-hui; Li, Quan-quan; Wang, Jin; Zhang, Wei; Li, Zhu

    2010-09-01

    The authors for the first time fabricated OLEDs employing novel phthalocynines: 2(3)-(p-tert-butylphenoxy) copper phthalocyanine(1), 2(3),16(17)-di(p-tert-butyl-phenoxy) copper phthalocyanine(2) and 2(3), 9(10), 16(17)-tri (p-tert-butylphenoxy) copper phthalocyanine(3) as light emitting layer, and their electroluminescence character was studied. The final structures of three-layer OLEDs based on copper 2(3)-(p-tert-butylphenoxy) copper phthalocyanine (1) and 2(3), 9(10), 16(17)-tri (p-tert-butylphenoxy) copper phthalocyanine(3) were ITO/NPB(40 nm)/Pc(30 nm)/AlQ(43.5 nm)/LiF (0.5 nm)/Al(120 nm). The structure of three-layer OLED based on 2(3), 9(10), 16(17)-tri (p-tert-butylphenoxy) copper phthalocyanine (3) was ITO/NPB(30 nm)/Pc(30 nm) /BCP(20 nm)/A1Q(30 nm)/LiF (0. 5 nm)/Al(120 nm). Room-temperature electroluminescence was observed at about 869 nmand 1 062 nm for 2(3)-(p-tert-butylphenoxy) copper phthalocyanine(1); room-temperature electroluminescence of 2(3),16(17) -di(p-tert-butyl-phenoxy) copper phthalocyanine(2) was found at about 1050 nm and 1110 nm; and room-temperature electroluminescence of 2(3), 9(10), 16( 17)-tri (p-tert-butylphenoxy) copper phthalocyanine(3) was studied at about 1095 and 1204 nm. The emission wavelengths and the half bandwidths were quite different for the phthalocyanine, which may be due to the differences in the number of substituted and the molecular aggregations in vacuum sublimed films. The difference in Stokes shift relaxation was also induced by the molecular aggregations.

  6. Highly efficient gluten degradation with a newly identified prolyl endoprotease: implications for celiac disease.

    PubMed

    Stepniak, Dariusz; Spaenij-Dekking, Liesbeth; Mitea, Cristina; Moester, Martine; de Ru, Arnoud; Baak-Pablo, Renee; van Veelen, Peter; Edens, Luppo; Koning, Frits

    2006-10-01

    Celiac disease is a T cell-driven intolerance to wheat gluten. The gluten-derived T cell epitopes are proline-rich and thereby highly resistant to proteolytic degradation within the gastrointestinal tract. Oral supplementation with prolyl oligopeptidases has therefore been proposed as a potential therapeutic approach. The enzymes studied, however, have limitations as they are irreversibly inactivated by pepsin and acidic pH, both present in the stomach. As a consequence, these enzymes will fail to degrade gluten before it reaches the small intestine, the site where gluten induces inflammatory T cell responses that lead to celiac disease. We have now determined the usefulness of a newly identified prolyl endoprotease from Aspergillus niger for this purpose. Gluten and its peptic/tryptic digest were treated with prolyl endoprotease, and the destruction of the T cell epitopes was tested using mass spectrometry, T cell proliferation assays, ELISA, reverse-phase HPLC, SDS-PAGE, and Western blotting. We observed that the A. niger prolyl endoprotease works optimally at 4-5 pH, remains stable at 2 pH, and is completely resistant to digestion with pepsin. Moreover, the A. niger-derived enzyme efficiently degraded all tested T cell stimulatory peptides as well as intact gluten molecules. On average, the endoprotease from A. niger degraded gluten peptides 60 times faster than a prolyl oligopeptidase. Together these results indicate that the enzyme from A. niger efficiently degrades gluten proteins. Future studies are required to determine if the prolyl endoprotease can be used as an oral supplement to reduce gluten intake in patients.

  7. An efficient and environment-friendly method of removing graphene oxide in wastewater and its degradation mechanisms.

    PubMed

    Zhang, Chao-Zhi; Li, Ting; Yuan, Yang; Xu, Jianqiang

    2016-06-01

    Graphene and graphene oxide (GO) have already existed in air, water and soil due to their popular application in functional materials. However, degradation of graphene and GO in wastewater has not been reported. Degradation of GO plays a key role in the elimination of graphene and GO in wastewater due to graphene being easily oxidized to GO. In this paper, GO was completely degraded to give CO2 by Photo-Fenton. The degradation intermediates were determined by UV-vis absorption spectra, elemental analysis (EA), fourier transform infrared (FT-IR) and liquid chromatography-mass spectrometry (LC-MS). Experimental results showed that graphene oxide was completely degraded to give CO2 after 28 days. Based on UV, FT-IR, LC-MS spectra and EA data of these degradation intermediates, the degradation mechanisms of GO were supposed. This paper suggests an efficient and environment-friendly method to degrade GO and graphene.

  8. Electroluminescence from ZnO-nanofilm/Si-micropillar heterostructure arrays.

    PubMed

    Chan, Yu Fei; Su, Wei; Zhang, Chang Xing; Wu, Zheng Long; Tang, Ying; Sun, Xiao Qi; Xu, Hai Jun

    2012-10-22

    ZnO-nanofilm/Si-micropillar p-n nanoheterostructure arrays were prepared by growing n-type ZnO onto a p-type nanoporous Si pillar array. Its current-voltage characteristics of nanoheterostructure showed good rectifying behavior with onset voltage of ~1.5 V, forward current density of ~28.7 mA/cm(2) at 2.5 V, leakage current density of ~0.15 mA/cm(2) and rectifying ratio of ~121 at ± 2.5 V. The electron transport across nanohetreostructure obeys the trap-charge-limit current model. Moreover, strong white light electroluminescence from ZnO-nanofilm/Si-micropillar light-emitting diode (LED) has been achieved, which could open up possibilities to build new ZnO/Si-based highly efficient solid-state lighting devices.

  9. Natural Magnetite: an efficient catalyst for the degradation of organic contaminant

    PubMed Central

    HE, Hongping; ZHONG, Yuanhong; LIANG, Xiaoliang; TAN, Wei; ZHU, Jianxi; Yan WANG, Christina

    2015-01-01

    Iron (hydr)oxides are ubiquitous earth materials that have high adsorption capacities for toxic elements and degradation ability towards organic contaminants. Many studies have investigated the reactivity of synthetic magnetite, while little is known about natural magnetite. Here, we first report the reactivity of natural magnetites with a variety of elemental impurities for catalyzing the decomposition of H2O2 to produce hydroxyl free radicals (•OH) and the consequent degradation of p-nitrophenol (p-NP). We observed that these natural magnetites show higher catalytic performance than that of the synthetic pure magnetite. The catalytic ability of natural magnetite with high phase purity depends on the surface site density while that for the magnetites with exsolutions relies on the mineralogical nature of the exsolved phases. The pleonaste exsolution can promote the generation of •OH and the consequent degradation of p-NP; the ilmenite exsolution has little effect on the decomposition of H2O2, but can increase the adsorption of p-NP on magnetite. Our results imply that natural magnetite is an efficient catalyst for the degradation of organic contaminants in nature. PMID:25958854

  10. Natural Magnetite: an efficient catalyst for the degradation of organic contaminant

    NASA Astrophysics Data System (ADS)

    He, Hongping; Zhong, Yuanhong; Liang, Xiaoliang; Tan, Wei; Zhu, Jianxi; Yan Wang, Christina

    2015-05-01

    Iron (hydr)oxides are ubiquitous earth materials that have high adsorption capacities for toxic elements and degradation ability towards organic contaminants. Many studies have investigated the reactivity of synthetic magnetite, while little is known about natural magnetite. Here, we first report the reactivity of natural magnetites with a variety of elemental impurities for catalyzing the decomposition of H2O2 to produce hydroxyl free radicals (•OH) and the consequent degradation of p-nitrophenol (p-NP). We observed that these natural magnetites show higher catalytic performance than that of the synthetic pure magnetite. The catalytic ability of natural magnetite with high phase purity depends on the surface site density while that for the magnetites with exsolutions relies on the mineralogical nature of the exsolved phases. The pleonaste exsolution can promote the generation of •OH and the consequent degradation of p-NP; the ilmenite exsolution has little effect on the decomposition of H2O2, but can increase the adsorption of p-NP on magnetite. Our results imply that natural magnetite is an efficient catalyst for the degradation of organic contaminants in nature.

  11. Assessment of solar driven TiO2-assisted photocatalysis efficiency on amoxicillin degradation.

    PubMed

    Pereira, João H O S; Reis, Ana C; Nunes, Olga C; Borges, Maria T; Vilar, Vítor J P; Boaventura, Rui A R

    2014-01-01

    The objective of this work was to evaluate the efficiency of a solar TiO2-assisted photocatalytic process on amoxicillin (AMX) degradation, an antibiotic widely used in human and veterinary medicine. Firstly, solar photolysis of AMX was compared with solar photocatalysis in a compound parabolic collectors pilot scale photoreactor to assess the amount of accumulated UV energy in the system (Q UV) necessary to remove 20 mg L(-1) AMX from aqueous solution and mineralize the intermediary by-products. Another experiment was also carried out to accurately follow the antibacterial activity against Escherichia coli DSM 1103 and Staphylococcus aureus DSM 1104 and mineralization of AMX by tracing the contents of dissolved organic carbon (DOC), low molecular weight carboxylate anions, and inorganic anions. Finally, the influence of individual inorganic ions on AMX photocatalytic degradation efficiency and the involvement of some reactive oxygen species were also assessed. Photolysis was shown to be completely ineffective, while only 3.1 kJUV L(-1) was sufficient to fully degrade 20 mg L(-1) AMX and remove 61% of initial DOC content in the presence of the photocatalyst and sunlight. In the experiment with an initial AMX concentration of 40 mg L(-1), antibacterial activity of the solution was considerably reduced after elimination of AMX to levels below the respective detection limit. After 11.7 kJUV L(-1), DOC decreased by 71%; 30% of the AMX nitrogen was converted into ammonium and all sulfur compounds were converted into sulfate. A large percentage of the remaining DOC was in the form of low molecular weight carboxylic acids. Presence of phosphate ions promoted the removal of AMX from solution, while no sizeable effects on the kinetics were found for other inorganic ions. Although the AMX degradation was mainly attributed to hydroxyl radicals, singlet oxygen also plays an important role in AMX self-photosensitization under UV/visible solar light.

  12. Transcending the slow bimolecular recombination in lead-halide perovskites for electroluminescence

    PubMed Central

    Xing, Guichuan; Wu, Bo; Wu, Xiangyang; Li, Mingjie; Du, Bin; Wei, Qi; Guo, Jia; Yeow, Edwin K. L.; Sum, Tze Chien; Huang, Wei

    2017-01-01

    The slow bimolecular recombination that drives three-dimensional lead-halide perovskites' outstanding photovoltaic performance is conversely a fundamental limitation for electroluminescence. Under electroluminescence working conditions with typical charge densities lower than 1015 cm−3, defect-states trapping in three-dimensional perovskites competes effectively with the bimolecular radiative recombination. Herein, we overcome this limitation using van-der-Waals-coupled Ruddlesden-Popper perovskite multi-quantum-wells. Injected charge carriers are rapidly localized from adjacent thin few layer (n≤4) multi-quantum-wells to the thick (n≥5) multi-quantum-wells with extremely high efficiency (over 85%) through quantum coupling. Light emission originates from excitonic recombination in the thick multi-quantum-wells at much higher decay rate and efficiency than bimolecular recombination in three-dimensional perovskites. These multi-quantum-wells retain the simple solution processability and high charge carrier mobility of two-dimensional lead-halide perovskites. Importantly, these Ruddlesden-Popper perovskites offer new functionalities unavailable in single phase constituents, permitting the transcendence of the slow bimolecular recombination bottleneck in lead-halide perovskites for efficient electroluminescence. PMID:28239146

  13. Transcending the slow bimolecular recombination in lead-halide perovskites for electroluminescence.

    PubMed

    Xing, Guichuan; Wu, Bo; Wu, Xiangyang; Li, Mingjie; Du, Bin; Wei, Qi; Guo, Jia; Yeow, Edwin K L; Sum, Tze Chien; Huang, Wei

    2017-02-27

    The slow bimolecular recombination that drives three-dimensional lead-halide perovskites' outstanding photovoltaic performance is conversely a fundamental limitation for electroluminescence. Under electroluminescence working conditions with typical charge densities lower than 10(15) cm(-3), defect-states trapping in three-dimensional perovskites competes effectively with the bimolecular radiative recombination. Herein, we overcome this limitation using van-der-Waals-coupled Ruddlesden-Popper perovskite multi-quantum-wells. Injected charge carriers are rapidly localized from adjacent thin few layer (n≤4) multi-quantum-wells to the thick (n≥5) multi-quantum-wells with extremely high efficiency (over 85%) through quantum coupling. Light emission originates from excitonic recombination in the thick multi-quantum-wells at much higher decay rate and efficiency than bimolecular recombination in three-dimensional perovskites. These multi-quantum-wells retain the simple solution processability and high charge carrier mobility of two-dimensional lead-halide perovskites. Importantly, these Ruddlesden-Popper perovskites offer new functionalities unavailable in single phase constituents, permitting the transcendence of the slow bimolecular recombination bottleneck in lead-halide perovskites for efficient electroluminescence.

  14. Transcending the slow bimolecular recombination in lead-halide perovskites for electroluminescence

    NASA Astrophysics Data System (ADS)

    Xing, Guichuan; Wu, Bo; Wu, Xiangyang; Li, Mingjie; Du, Bin; Wei, Qi; Guo, Jia; Yeow, Edwin K. L.; Sum, Tze Chien; Huang, Wei

    2017-02-01

    The slow bimolecular recombination that drives three-dimensional lead-halide perovskites' outstanding photovoltaic performance is conversely a fundamental limitation for electroluminescence. Under electroluminescence working conditions with typical charge densities lower than 1015 cm-3, defect-states trapping in three-dimensional perovskites competes effectively with the bimolecular radiative recombination. Herein, we overcome this limitation using van-der-Waals-coupled Ruddlesden-Popper perovskite multi-quantum-wells. Injected charge carriers are rapidly localized from adjacent thin few layer (n<=4) multi-quantum-wells to the thick (n>=5) multi-quantum-wells with extremely high efficiency (over 85%) through quantum coupling. Light emission originates from excitonic recombination in the thick multi-quantum-wells at much higher decay rate and efficiency than bimolecular recombination in three-dimensional perovskites. These multi-quantum-wells retain the simple solution processability and high charge carrier mobility of two-dimensional lead-halide perovskites. Importantly, these Ruddlesden-Popper perovskites offer new functionalities unavailable in single phase constituents, permitting the transcendence of the slow bimolecular recombination bottleneck in lead-halide perovskites for efficient electroluminescence.

  15. Green synthesis of copper nanoparticles for the efficient removal (degradation) of dye from aqueous phase.

    PubMed

    Sinha, Tanur; Ahmaruzzaman, M

    2015-12-01

    The present work reports the utilization of a common household waste material (fish scales of Labeo rohita) for the synthesis of copper nanoparticles. The method so developed was found to be green, environment-friendly, and economic. The fish scale extracts were acting as a stabilizing and reducing agents. This method avoids the use of external reducing and stabilizing agents, templates, and solvents. The compositional abundance of gelatin may be envisaged for the effective reductive as well as stabilizing potency. The mechanisms for the formation of nanoparticles have also been presented. The synthesized copper nanoparticles formed were predominantly spherical in nature with an average size of nanoparticles in the range of 25-37 nm. The copper nanoparticles showed characteristic Bragg's reflection planes of fcc which was supported by both selected area electron diffraction and X-ray diffraction pattern and showed surface plasmon resonance at 580 nm. Moreover, the energy dispersive spectroscopy pattern also revealed the presence of only elemental copper in the copper nanoparticles. The prepared nanoparticles were used for the remediation of a carcinogenic and noxious textile dye, Methylene blue, from aqueous solution. Approximately, 96 % degradation of Methylene blue dye was observed within 135 min using copper nanoparticles. The probable mechanism for the degradation of the dye has been presented, and the degraded intermediates have been identified using the liquid chromatography-mass spectroscopy technique. The high efficiency of nanoparticles as photocatalysts has opened a promising application for the removal of hazardous dye from industrial effluents contributing indirectly to environmental cleanup process.

  16. Charge collection efficiency degradation induced by MeV ions in semiconductor devices: Model and experiment

    DOE PAGES

    Vittone, Ettore; Pastuovic, Zeljko; Breese, Mark B. H.; ...

    2016-02-08

    This study investigates both theoretically and experimentally the charge collection efficiency (CCE) degradation in silicon diodes induced by energetic ions. Ion Beam Induced Charge (IBIC) measurements carried out on n- and p-type silicon diodes which were previously irradiated with MeV He ions show evidence that the CCE degradation does not only depend on the mass, energy and fluence of the damaging ion, but also depends on the ion probe species and on the polarization state of the device. A general one-dimensional model is derived, which accounts for the ion-induced defect distribution, the ionization profile of the probing ion and themore » charge induction mechanism. Using the ionizing and non-ionizing energy loss profiles resulting from simulations based on the binary collision approximation and on the electrostatic/transport parameters of the diode under study as input, the model is able to accurately reproduce the experimental CCE degradation curves without introducing any phenomenological additional term or formula. Although limited to low level of damage, the model is quite general, including the displacement damage approach as a special case and can be applied to any semiconductor device. It provides a method to measure the capture coefficients of the radiation induced recombination centres. They can be considered indexes, which can contribute to assessing the relative radiation hardness of semiconductor materials.« less

  17. Charge collection efficiency degradation induced by MeV ions in semiconductor devices: Model and experiment

    SciTech Connect

    Vittone, Ettore; Pastuovic, Zeljko; Breese, Mark B. H.; Lopez, Javier Garicia; Jaksic, Milko; Raisanen, Jyrki; Siegele, Rainer; Simon, Aliz; Vizkelethy, Gyorgy

    2016-02-08

    This study investigates both theoretically and experimentally the charge collection efficiency (CCE) degradation in silicon diodes induced by energetic ions. Ion Beam Induced Charge (IBIC) measurements carried out on n- and p-type silicon diodes which were previously irradiated with MeV He ions show evidence that the CCE degradation does not only depend on the mass, energy and fluence of the damaging ion, but also depends on the ion probe species and on the polarization state of the device. A general one-dimensional model is derived, which accounts for the ion-induced defect distribution, the ionization profile of the probing ion and the charge induction mechanism. Using the ionizing and non-ionizing energy loss profiles resulting from simulations based on the binary collision approximation and on the electrostatic/transport parameters of the diode under study as input, the model is able to accurately reproduce the experimental CCE degradation curves without introducing any phenomenological additional term or formula. Although limited to low level of damage, the model is quite general, including the displacement damage approach as a special case and can be applied to any semiconductor device. It provides a method to measure the capture coefficients of the radiation induced recombination centres. They can be considered indexes, which can contribute to assessing the relative radiation hardness of semiconductor materials.

  18. ZnO and cobalt phthalocyanine hybridized graphene: efficient photocatalysts for degradation of rhodamine B

    PubMed Central

    Neelgund, Gururaj M.; Oki, Aderemi; Luo, Zhiping

    2014-01-01

    A novel method has been developed to synthesize graphene-ZnO composite as a highly efficient catalyst by reduction of graphite oxide and in-situ deposition of ZnO nanoparticles by chemical reduction reaction. The graphene-ZnO catalyst is capable of complete degradation of rhodamine B under exposure to natural sunlight. Further, the catalytic efficiency of graphene-ZnO catalyst was enhanced by sensitizing with cobalt phthalocyanine. The formation of graphene-ZnO pcatalyst and its further sensitization with cobalt phthalocyanine was characterized using UV-vis, ATR-IR and Raman spectroscopy, powder XRD and thermogravimetric analysis. The morphology of both graphene-ZnO and graphene-ZnO-CoPC catalysts was analyzed using scanning and transmission electron microscopes. PMID:24972296

  19. Comparison of N-nitrosodiethylamine degradation in water by UV irradiation and UV/O3: efficiency, product and mechanism.

    PubMed

    Xu, Bingbing; Chen, Zhonglin; Qi, Fei; Ma, Jun; Wu, Fengchang

    2010-07-15

    N-nitrosodiethylamine (NDEA) is a member of nitrosamines, which is strong carcinogenic. In order to explore an effective treatment method for NDEA removal from water, sole UV irradiation and UV/O(3) were carried out in this study. The removal efficiency, degradation products and pathways were compared between those two processes. Results showed that NDEA removal efficiency achieved 99% within 15 min by both UV and UV/O(3). Degradation reaction well followed pseudo-first-order kinetics. Water pH had different effect on NDEA degradation in those two processes. Acidic and neutral conditions were good for NDEA degradation by sole UV irradiation. However, NDEA underwent rapid degradation under various pH conditions in the UV/O(3) process. Though the ozone introduction in the UV/O(3) process had little effect on NDEA degradation efficiency, it had significant effect on its degradation products and pathways. Methylamine, dimethylamine, ethylamine and diethylamine were observed as aliphatic amine products of NDEA degradation in both two processes. They were assumed to arise due to N-N bond fission under UV irradiation, or due to the reaction of NDEA and hydroxyl radicals in the UV/O(3) process.

  20. High temperature charging efficiency and degradation behavior of high capacity Ni-MH batteries

    NASA Astrophysics Data System (ADS)

    Choi, Jeon; Kim, Joong

    2001-02-01

    Recently the Ni/MH secondary battery has been studied extensively to achieve higher energy density, longer cycle life and faster charging-discharging rate for electric vehicles and portable computers, and etc. In this work, the charging efficiency of the Ni-MH battery which uses Ni electrode with addition of various compounds and the degradation behavior of the 90Ah battery were studied. The battery using the Ni electrode with Ca(OH)2 addition showed the charging efficiency and the utilization ratio significantly better than electrodes without added compounds. After 418 cycles, the residual capacities at the Ni electrode showed nearly the same values in the upper, middle and lower regions. In the case of the MH electrode, the residual capacity in the upper region appeared lower than that in other regions. As a result of ICP analysis, the amount of dissolved elements in the three regions appeared almost the same. The faster degradation in the upper region of the MH electrode was caused by the TiO2 oxide film formed at the electrode surface because of overcharging. The thickness of the oxide film increases with cycling, so it will form a layer that is not able to allow hydrogen to penetrate into the MH electrode.

  1. Efficient peroxydisulfate activation process not relying on sulfate radical generation for water pollutant degradation.

    PubMed

    Zhang, Tao; Chen, Yin; Wang, Yuru; Le Roux, Julien; Yang, Yang; Croué, Jean-Philippe

    2014-05-20

    Peroxydisulfate (PDS) is an appealing oxidant for contaminated groundwater and toxic industrial wastewaters. Activation of PDS is necessary for application because of its low reactivity. Present activation processes always generate sulfate radicals as actual oxidants which unselectively oxidize organics and halide anions reducing oxidation capacity of PDS and producing toxic halogenated products. Here we report that copper oxide (CuO) can efficiently activate PDS under mild conditions without producing sulfate radicals. The PDS/CuO coupled process is most efficient at neutral pH for decomposing a model compound, 2,4-dichlorophenol (2,4-DCP). In a continuous-flow reaction with an empty-bed contact time of 0.55 min, over 90% of 2,4-DCP (initially 20 μM) and 90% of adsorbable organic chlorine (AOCl) can be removed at the PDS/2,4-DCP molar ratio of 1 and 4, respectively. Based on kinetic study and surface characterization, PDS is proposed to be first activated by CuO through outer-sphere interaction, the rate-limiting step, followed by a rapid reaction with 2,4-DCP present in the solution. In the presence of ubiquitous chloride ions in groundwater/industrial wastewater, the PDS/CuO oxidation shows significant advantages over sulfate radical oxidation by achieving much higher 2,4-DCP degradation capacity and avoiding the formation of highly chlorinated degradation products. This work provides a new way of PDS activation for contaminant removal.

  2. Highly Efficient Photocatalysts and Continuous-Flow Photocatalytic Reactors for Degradation of Organic Pollutants in Wastewater.

    PubMed

    Chang, Sujie; Yang, Xiaoqiu; Sang, Yuanhua; Liu, Hong

    2016-09-06

    One of the most important applications for photocatalysis is engineered water treatment that photodegrades organic pollutants in wastewater at low cost. To overcome the low efficiency of batch degradation methods, continuous-flow photocatalytic reactors have been proposed and have become the most promising method for mass water treatment. However, most commercial semiconductor photocatalysts are granular nanoparticles with low activity and a narrow active light wavelength band; this creates difficulties for direct use in continuous-flow photocatalytic reactors. Therefore, a high-performance photodegradation photocatalyst with proper morphology or structure is key for continuous photocatalytic degradation. Moreover, a well-designed photocatalytic device is another important component for continuous-flow photocatalysis and determines the efficiency of photocatalysis in practical water treatment. This review describes the basic design principles and synthesis of photocatalysts with excellent performance and special morphologies suitable for a filtering photocatalysis process. Certain promising continuous photodegradation reactors are also categorized and summarized. Additionally, selected scientific and technical problems that must be urgently solved are suggested.

  3. Method for producing high energy electroluminescent devices

    DOEpatents

    Meyerson, Bernard S.; Scott, Bruce A.; Wolford, Jr., Donald J.

    1992-09-29

    A method is described for fabricating electroluminescent devices exhibiting visible electroluminescence at room temperature, where the devices include at least one doped layer of amorphous hydrogenated silicon (a-Si:H). The a-Si:H layer is deposited on a substrate by homogeneous chemical vapor deposition (H-CVD) in which the substrate is held at a temperature lower than about 200.degree. C. and the a-Si:H layer is doped in-situ during deposition, the amount of hydrogen incorporated in the deposited layer being 12-50 atomic percent. The bandgap of the a-Si:H layer is between 1.6 and 2.6 eV, and in preferrable embodiments is between 2.0 and 2.6 eV. The conductivity of the a-Si:H layer is chosen in accordance with device requirements, and can be 10.sup.16 -10.sup.19 carriers/cm.sup.2. The bandgap of the a-Si:H layer depends at least in part on the temperature of the substrate on which the layer is deposited, and can be "tuned" by changing the substrate temperature.

  4. Highly efficient degradation of dye pollutants by Ce-doped MoO₃ catalyst at room temperature.

    PubMed

    Jin, Yujian; Li, Na; Liu, Haiqiu; Hua, Xia; Zhang, Qiuying; Chen, Mindong; Teng, Fei

    2014-09-14

    In order to efficiently degrade organic pollutants via an easily operated method, Ce-doped MoO3 (Ce(x)/MoO3) samples are synthesized by a simple impregnation method. The samples are characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), nitrogen sorption isotherms and UV-vis diffused reflectance spectra (UV-DRS), total organic carbon (TOC), infrared spectroscopy (IR) and mass spectrometry (MS) analyses. Furthermore, we have mainly investigated the degradation of different dye pollutants by the Ce(x)/MoO3 samples, including cationic methylene blue (MB), anionic methyl orange (MO), neutral phenol, and a MB-MO mixture dye. For the single-component MB and MO dyes, the highest degradation efficiencies are achieved by Ce(5)/MoO3 and Ce(10)/MoO3 samples. For the MB-MO mixture dyes, the highest degradation efficiency for MB is achieved by a Ce(10)/MoO3 sample. It is surprising that the degradation efficiency of MB in the MB-MO mixture dye solution is higher than that in the single-component MB dye solution, which has been mainly ascribed to the promoting effect of MO. Moreover, a plausible degradation mechanism of the dyes has been proposed and discussed. It should be noted that the degradation reaction is carried out at room temperature and normal atmospheric pressure, and without light irradiation. As a result, this degradation reaction is obviously different from the conventional thermally activated heterogeneous catalysis (or photocatalysis), in which thermal energy (or light irradiation) is indispensable; also different from a sorption technology, in which the pollutants cannot be degraded, but only transformed from one phase to another one. Thus, the reported degradation reaction is a quite promising environmental cleaning technology, which could be widely practically applied.

  5. Unique Kinetic Properties of Phenol-Degrading Variovorax Strains Responsible for Efficient Trichloroethylene Degradation in a Chemostat Enrichment Culture

    PubMed Central

    Futamata, Hiroyuki; Nagano, Yayoi; Watanabe, Kazuya; Hiraishi, Akira

    2005-01-01

    A chemostat enrichment of soil bacteria growing on phenol as the sole carbon source has been shown to exhibit quite high trichloroethylene (TCE)-degrading activities (H. Futamata, S. Harayama, and K. Watanabe, Appl. Environ. Microbiol. 67:4671-4677, 2001). To identify the bacterial populations responsible for the high TCE-degrading activity, a multidisciplinary survey of the chemostat enrichment was conducted by employing molecular-ecological and culture-dependent approaches. Three chemostat enrichment cultures were newly developed under different phenol-loading conditions (0.25, 0.75, and 1.25 g liter−1 day−1) in this study, and the TCE-degrading activities of the enrichments were measured. Among them, the enrichment at 0.75 g liter−1 day−1 (enrichment 0.75) expressed the highest activity. Denaturing gradient gel electrophoresis of PCR-amplified 16S rRNA gene fragments detected a Variovorax ribotype as the strongest band in enrichment 0.75; however, it was not a major ribotype in the other samples. Bacteria were isolated from enrichment 0.75 by direct plating, and their 16S rRNA genes and genes encoding the largest subunit of phenol hydroxylase (LmPHs) were analyzed. Among the bacteria isolated, several strains were affiliated with the genus Variovorax and were shown to have high-affinity-type LmPHs. The LmPH of the Variovorax strains was also detected as the major genotype in enrichment 0.75. Kinetic analyses of phenol and TCE degradation revealed, however, that these strains exhibited quite low affinity for phenol compared to other phenol-degrading bacteria, while they showed quite high specific TCE-degrading activities and relatively high affinity for TCE. Owing to these unique kinetic traits, the Variovorax strains can obviate competitive inhibition of TCE degradation by the primary substrate of the catabolic enzyme (i.e., phenol), contributing to the high TCE-degrading activity of the chemostat enrichments. On the basis of physiological information

  6. Ag-ligand modified tungstovandates and their efficient catalysis degradation properties for methylene blue

    NASA Astrophysics Data System (ADS)

    Zheng, Ran; Zhang, Huixia; Liu, Yunping; Wang, Xiaoxiao; Han, Zhangang

    2017-02-01

    Two polytungstovandates [Ag(mbpy)2][Ag2(mbpy)3][VW5O19]·H2O (1) and [Ag(mbpy)]2[Ag(mbpy)2]4[VW12O40] (2) (mbpy =4,4‧-dimethyl-2,2‧-bipyridyl), had been hydrothermally synthesized and characterized by IR, TG, and single-crystal X-ray diffraction techniques. Single-crystal structural analysis revealed that the polyanionic clusters in two compounds are different: Lindqvist-type in 1 and α-Keggin-type in 2, respectively, while the cationic moieties in them are Ag-mbpy units. The experiments showed that this kind of hybrid crystal materials possesses more efficiently catalytic performance for the degradation of organic dye methylene blue (MB) in water solution under the UV irradiation. The significant degradation rate of MB can reach 89.9%, 94.9% by crystals 1 and 2 (40 mg) in the course of about 5 min.

  7. Direct Blue Dye Degradation Using Titanium Nanostructures Under Energy-Efficient UV-LED Irradiation

    NASA Astrophysics Data System (ADS)

    Jo, Wan-Kuen; Tayade, Rajesh J.

    2016-01-01

    The present study describes the effect of titanium dioxide (TiO2) morphology on the photocatalytic activity under irradiation of ultraviolet light-emitting diode (UV-LED). Different TiO2 nanostructures were synthesized using hydrothermal (nanotubes and nanospheres) and solvothermal (nanoflowers) methods. The morphology, phase composition, bandgap, and chemical properties of the synthesized different TiO2 nanostructures were characterized using x-ray diffraction, scanning electron microscopy, transmission electron microscopy, ultraviolet visible diffuse reflectance spectroscopy (UV-Vis DRS), and Brunauer-Emmett-Teller (BET) analysis. The surface area of the nanotubes was larger than that of the nanospheres and nanoflowers by four- and three-fold, respectively. The photocatalytic activity of the photocatalysts was evaluated by degradation of direct blue-15 dye under UV-LED irradiation in a slurry-type reactor. The photocatalytic activity of the TiO2 nanoflowers was higher than that of TiO2 nanotubes or nanospheres, suggesting that nanoflowers can serve as efficient photocatalysts for dye degradation.

  8. Structuring β-Ga2O3 photonic crystal photocatalyst for efficient degradation of organic pollutants.

    PubMed

    Li, Xiaofang; Zhen, Xiuzheng; Meng, Sugang; Xian, Jiangjun; Shao, Yu; Fu, Xianzhi; Li, Danzhen

    2013-09-03

    Coupling photocatalysts with photonic crystals structure is based on the unique property of photonic crystals in confining, controlling, and manipulating the incident photons. This combination enhances the light absorption in photocatalysts and thus greatly improves their photocatalytic performance. In this study, Ga2O3 photonic crystals with well-arranged skeleton structures were prepared via a dip-coating infiltration method. The positions of the electronic band absorption for Ga2O3 photonic crystals could be made to locate on the red edge, on the blue edge, and away from the edge of their photonic band gaps by changing the pore sizes of the samples, respectively. Particularly, the electronic band absorption of the Ga2O3 photonic crystal with a pore size of 135 nm was enhanced more than other samples by making it locate on the red edge of its photonic band gap, which was confirmed by the higher instantaneous photocurrent and photocatalytic activity for the degradation of various organic pollutants under ultraviolet light irradiation. Furthermore, the degradation mechanism over Ga2O3 photonic crystals was discussed. The design of Ga2O3 photonic crystals presents a prospective application of photonic crystals in photocatalysis to address light harvesting and quantum efficiency problems through manipulating photons or constructing photonic crystal structure as groundwork.

  9. Electroluminescent devices using a layered organic-inorganic perovskite structure as emitter

    NASA Astrophysics Data System (ADS)

    Coelle, Michael; Bruetting, Wolfgang; Schwoerer, Markus; Yahiro, Masayuki; Tsutsui, Tetsuo

    2001-02-01

    Self-organizing layered perovskite compounds like (formula available in paper) naturally form a dielectric quantum-well structure in which semiconducting PbI4 layers and organic (C6H5C2H4NH3) layers are alternately piled up. Due to their low- dimensional semiconductor nature they exhibit a strong absorption and sharp photoluminescence from the exciton band. In electroluminescent devices pure green emission peaking at 520 nm with a very narrow half-width of about 10 nm has been reported. As the organic-inorganic layered structure has promising properties for EL-devices, we investigated two- and three layer structures using this perovskite as emitter material in combination with additional hole and electron injection layers. To get more insight into electrical properties and electroluminescence- mechanisms of this material, temperature dependent current- voltage-luminance characteristics have been measured, showing an increasing onset-voltage for current flow from 2.6 V at room temperature to about 8.8 V at 80 K. Electroluminescence is detected at temperatures below 150 K with onset voltages of about 13 V. At liquid nitrogen temperature efficiencies of (formula available in paper) are obtained.

  10. Highest Efficiency Two-Photon Degradable Copolymer for Remote Controlled Release

    PubMed Central

    Olejniczak, Jason; Sankaranarayanan, Jagadis; Viger, Mathieu L.; Almutairi, Adah

    2013-01-01

    To address the scarcity of polymers that degrade upon absorption of near infrared (NIR) light, we introduce a new polymer containing moieties in its backbone capable of highly efficient NIR-triggered photocleavage. The polymer rapidly undergoes backbone scission in response to both UV-Vis and near infrared light via two-photon absorption, as revealed by gel permeation chromatography. Cleavage of photosensitive groups from the backbone is confirmed by 1H NMR. These polymers were successfully formulated into particles encapsulating a dye that was released upon irradiation with UV-Vis and NIR light, as indicated by changes in fluorescence characteristic of increased solvent interaction with cargo. Thus, this new polymer is readily photocleaved by UV-Vis and NIR light, giving it a variety of potential applications in photopatterning and on-demand release. PMID:24044102

  11. White light-emitting organic electroluminescent devices

    DOEpatents

    Shiang, Joseph John; Duggal, Anil Raj; Parthasarathy, Gautam

    2006-06-20

    A light-emitting device comprises a light-emitting member, which comprises two electrodes, at least two organic electroluminescent ("EL") materials disposed between the electrodes, a charge blocking material disposed between the electrodes, and at least one photoluminescent ("PL") material. The light-emitting member emits electromagnetic ("EM") radiation having a first spectrum in response to a voltage applied across the two electrodes. The PL material absorbs a portion of the EM radiation emitted by the light-emitting member and emits EM radiation having second spectrum different than the first spectrum. Each of the organic EL materials emits EM radiation having a wavelength range selected from the group consisting of blue and red wavelength ranges.

  12. Dielectric relaxation in AC powder electroluminescent devices

    NASA Astrophysics Data System (ADS)

    Zhang, Shuai; Su, Haibin; Tan, Chuan Seng; Wong, Terence Kin Shun; Teo, Ronnie Jin Wah

    2017-01-01

    The dielectric properties of AC powder electroluminescent devices were measured and analyzed using complex impedance spectroscopy to determine the relaxation processes occurring within the devices. The relaxation processes identified were ascribed to the electrode polarization caused by ion accumulation at the electrode/resin interfaces, the Maxwell-Wagner-Sillars effects at the (ZnS or BaTiO3) particle/resin interfaces, and the dipolar reorientation of polymer chains in the resin matrix. Each relaxation process was represented by its corresponding equivalent circuit component. Space charge polarization at the electrodes were represented by a Warburg element, a resistor, and a constant phase element. The resin matrix, ZnS/resin and BaTiO3/resin interfaces could each be modeled by a resistor and a capacitor in parallel. The simulated equivalent circuits for three different printed structures showed good fitting with their experimental impedance results.

  13. Efficient treatment of perfluorohexanoic acid by nanofiltration followed by electrochemical degradation of the NF concentrate.

    PubMed

    Soriano, Álvaro; Gorri, Daniel; Urtiaga, Ane

    2017-04-01

    The present study was aimed at the development of a strategy for removing and degrading perfluorohexanoic acid (PFHxA) from industrial process waters at concentrations in the range 60-200 mg L(-1). The treatment train consisted of nanofiltration (NF) separation followed by electrochemical degradation of the NF concentrate. Using a laboratory-scale system and working in the total recirculation mode, the DowFilm NF270 membrane provided PFHxA rejections that varied in the range 96.6-99.4% as the operating pressure was increased from 2.5 to 20 bar. The NF operation in concentration mode enabled a volume reduction factor of 5 and increased the PFHxA concentration in the retentate to 870 mg L(-1). Results showed that the increase in PFHxA concentration and the presence of calcium sulfate salts did not induce irreversible membrane fouling. The NF retentate was treated in a commercial undivided electrochemical cell provided with two parallel flow-by compartments separated by bipolar boron doped diamond (BDD) electrode, BDD counter anode, and counter cathode. Current densities ranging from 20 to 100 A m(-2) were examined. The electrochemical degradation rate of PFHxA reached 98% and was accompanied by its efficient mineralization, as the reduction of total organic carbon was higher than 95%. Energy consumption, which was 15.2 kWh m(-3) of treated NF concentrate, was minimized by selecting operation at 50 A m(-2). While most of the previous research on the treatment of perfluoroalkyl substances (PFASs) focused on the removal of perfluorooctanoic acid (PFOA) and perfluorooctane sulfonate (PFOS), these compounds have been phased out by chemical manufacturers. Our findings are relevant for the treatment of PFHxA, which appears to be one of the present alternatives to long-chain PFASs thanks to its lower bioaccumulative potential than PFOA and PFOS. However, PFHxA also behaves as a persistent pollutant. Moreover, our results highlight the potential of combining

  14. Solid state carbon nanotube device for controllable trion electroluminescence emission

    NASA Astrophysics Data System (ADS)

    Liang, Shuang; Ma, Ze; Wei, Nan; Liu, Huaping; Wang, Sheng; Peng, Lian-Mao

    2016-03-01

    Semiconducting carbon nanotubes (CNTs) have a direct chirality-dependent bandgap and reduced dimensionality-related quantum confinement effects, which are closely related to the performance of optoelectronic devices. Here, taking advantage of the large energy separations between neutral singlet excitons and charged excitons, i.e. trions in CNTs, we have achieved for the first time all trion electroluminescence (EL) emission from chirality-sorted (8,3) and (8,4) CNT-based solid state devices. We showed that strong trion emission can be obtained as a result of localized impact excitation and electrically injected holes, with an estimated efficiency of ~5 × 10-4 photons per injected hole. The importance of contact-controlled carrier injection (including symmetric and asymmetric contact configurations) and EL spectral stability for gradually increasing bias were also investigated. The realization of electrically induced pure trion emission opens up a new opportunity for CNT film-based optoelectronic devices, providing a new degree of freedom in controlling the devices to extend potential applications in spin or magnetic optoelectronics fields.Semiconducting carbon nanotubes (CNTs) have a direct chirality-dependent bandgap and reduced dimensionality-related quantum confinement effects, which are closely related to the performance of optoelectronic devices. Here, taking advantage of the large energy separations between neutral singlet excitons and charged excitons, i.e. trions in CNTs, we have achieved for the first time all trion electroluminescence (EL) emission from chirality-sorted (8,3) and (8,4) CNT-based solid state devices. We showed that strong trion emission can be obtained as a result of localized impact excitation and electrically injected holes, with an estimated efficiency of ~5 × 10-4 photons per injected hole. The importance of contact-controlled carrier injection (including symmetric and asymmetric contact configurations) and EL spectral stability for

  15. Achieving Pure Deep-Blue Electroluminescence with CIE y≤0.06 via a Rational Design Approach for Highly Efficient Non-Doped Solution-Processed Organic Light-Emitting Diodes.

    PubMed

    Reddy, Saripally Sudhaker; Sree, Vijaya Gopalan; Cho, Woosum; Jin, Sung-Ho

    2016-11-22

    Deep-blue fluorescent emitters with Commission Internationale de l'Eclairage (CIE) y≤0.06 are urgently needed for high-density storage, full-color displays and solid-state lighting. However, developing such emitters with high color purity and efficiency in solution-processable non-doped organic light-emitting diodes (OLEDs) remains an important challenge. Here, we present the synthesis of two new deep-blue fluorescent emitters (AFpTPI and AFmTPI) based on 10-(9,9-diethyl-9H-fluoren-2-yl)-9,9-dimethyl-9,10-dihydroacridine as a core and 1,3- and/or 1,4-phenylene-linked triphenylimidazole (TPI) analogues for non-doped solution-processable OLEDs. Their thermal, photophysical, electrochemical, and device characteristics are explored, and also strongly supported by density functional theory (DFT) study. AFpTPI and AFmTPI exhibit excellent thermal stability (≈450 °C) with high glass transition temperatures (Tg ; 141-152 °C) and deep-blue emission with high quantum yields. Specifically, the solution-processed non-doped device with AFpTPI as an emitter exhibits a maximum external quantum efficiency (EQE) of 4.56 % with CIE coordinates of (0.15, 0.06), which exactly matches the European Broadcasting Union (EBU) blue standard. In addition, AFmTPI also displays good efficiency and better color purity (EQE: 3.37 %; CIE (0.15, 0.05)). To the best of our knowledge, the present work is the first report on non-doped solution-processable OLEDs with efficiency close to 5 % and CIE y≤0.06.

  16. Pd nanoparticles supported on MIL-101/reduced graphene oxide photocatalyst: an efficient and recyclable photocatalyst for triphenylmethane dye degradation.

    PubMed

    Wu, Yan; Luo, Hanjin; Zhang, Li

    2015-11-01

    To improve the photocatalytic efficiency of chromium-based metal-organic framework (MIL-101) photocatalyst, Pd nanoparticles and reduced graphene oxide were used to modify the MIL-101 via a facile method. The resulting novel photocatalyst was characterized by UV-vis diffuse reflectance spectra (DRS), powder X-ray diffraction (XRD), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). It was indicated that the photocatalyst afforded high photocatalytic efficiency for degradation of two triphenylmethane dyes, brilliant green and acid fuchsin, under exposure to visible light irradiation. Cyclic experiments demonstrated that the photocatalyst showed good reusability and stability for the dye degradation.

  17. Introducing saccharic acid as an efficient iron chelate to enhance photo-Fenton degradation of organic contaminants.

    PubMed

    Subramanian, Gokulakrishnan; Madras, Giridhar

    2016-11-01

    The identification of iron chelates that can enhance photo-Fenton degradation is of great interest in the field of advanced oxidation process. Saccharic acid (SA) is a polyhydroxy carboxylic acid and completely non-toxic. Importantly, it can effectively bind Fe(III) as well as induce photoreduction of Fe(III). Despite having these interesting properties, the effect of SA on photo-Fenton degradation has not been studied. Herein, we demonstrate the first assessment of SA as an iron chelate in photo-Fenton process using methylene blue (MB) as a model organic contaminant. Our results demonstrate that SA has the ability to (i) enhance the photo-Fenton degradation of MB by about 11 times at pH 4.5 (ii) intensify photochemical reduction of Fe(III) to Fe(II) by about 17 times and (iii) accelerate the rate of consumption of H2O2 in photo-Fenton process by about 5 times (iv) increase the TOC reduction by about 2 times and (v) improve the photo-Fenton degradation of MB in the presence of a variety of common inorganic ions and organic matter. The influential properties of SA on photo-Fenton degradation is attributed to the efficient photochemical reduction of Fe(III) via LMCT (ligand to metal charge transfer reaction) to Fe(II), which then activated H2O2 to generate OH and accelerated photo-Fenton degradation efficiency. Moreover, the effect of operational parameters such as oxidant: contaminant (H2O2: MB) ratio, catalyst: contaminant (Fe(III)SA: MB) ratio, Fe(III): SA stoichiometry and pH on the degradation of MB by photo-Fenton in the presence of SA is demonstrated. Importantly, SA assisted photo-Fenton caused effective degradation of MB and 4-Chlorophenol under natural sunlight irradiation in natural water matrix. The findings strongly support SA as a deserving iron chelate to enhance photo-Fenton degradation.

  18. Degradation mechanism of laser diodes for 880-nm band

    NASA Astrophysics Data System (ADS)

    DÄ browska, E.; Nakielska, M.; Kozłowska, A.; Teodorczyk, M.; KrzyŻak, K.; Sobczak, G.; Kalbarczyk, J.; MalÄ g, A.

    2013-01-01

    The laser diodes (LD) have numerous applications and promise to become key elements for next generation laser technologies. LD are usually operated under conditions of heavy thermal load. As a result, the devices are affected by aging processes leading to changes of the operation parameters, degradation and, eventually, complete failure. Degradation of high power semiconductor lasers remains a serious problem for practical application of these devices. We investigated the effect of mounting induced strain and defects on the performance of high power laser. In this paper measurements of the temperature distribution and the electroluminescence along the cavity of InGaAs quantum well lasers before and after accelerated aging processes are presented. The electro-optical parameters of the high output power laser diodes, such as emission wavelength, output power, threshold current, slope efficiency, and operating lifetime are presented too.

  19. A P450 gene associated with robust resistance to DDT in ciliated protozoan, Tetrahymena thermophila by efficient degradation.

    PubMed

    Feng, Lifang; Fu, Chengjie; Yuan, Dongxia; Miao, Wei

    2014-04-01

    Analysis of metabolic mechanisms of dichlorodiphenyltrichloroethane (DDT) accumulation and degradation in microorganisms, which could be used to reduce its hazard to higher organisms at the higher in the food chain, have not been investigated. Robust resistance to DDT (grows well in 256 mg/L DDT) and a surprising ability to degrade DDT (more than 70% DDT within 4h) were found in the ciliated protozoan Tetrahymena thermophila. A P450 gene (CYP5013C2) was found to respond specifically to DDT treatment. In the presence of 256 mg/L DDT, cells with overexpressing CYP5013C2 (p450-OE) grew faster and degraded DDT more efficiently than wild-type (WT) cells, while cells with CYP5013C2 partially knocked down (p450-KD) grew slower and exhibited reduced ability to degrade DDT compared to WT cells. Both dichlorodiphenyldichloroethylene (DDE) and dichlorodiphenyldichloroethane (DDD) were detected in cells after exposure to DDT, and the concentration of DDD in the p450-OE strain gradually decreased from 0.5 to 4h. Thus, we argue that this P450 gene (CYP5013C2), by efficiently degrading DDT to DDD, is associated with robust resistance to DDT in Tetrahymena, and that a strain overexpressing this gene has the potential to serve as bioreactor that degrades environmental DDT.

  20. Impact of electrochemical treatment of soil washing solution on PAH degradation efficiency and soil respirometry.

    PubMed

    Mousset, Emmanuel; Huguenot, David; van Hullebusch, Eric D; Oturan, Nihal; Guibaud, Gilles; Esposito, Giovanni; Oturan, Mehmet A

    2016-04-01

    The remediation of a genuinely PAH-contaminated soil was performed, for the first time, through a new and complete investigation, including PAH extraction followed by advanced oxidation treatment of the washing solution and its recirculation, and an analysis of the impact of the PAH extraction on soil respirometry. The study has been performed on the remediation of genuine PAH-contaminated soil, in the following three steps: (i) PAH extraction with soil washing (SW) techniques, (ii) PAH degradation with an electro-Fenton (EF) process, and (iii) recirculation of the partially oxidized effluent for another SW cycle. The following criteria were monitored during the successive washing cycles: PAH extraction efficiency, PAH oxidation rates and yields, extracting agent recovery, soil microbial activity, and pH of soil. Two representative extracting agents were compared: hydroxypropyl-beta-cyclodextrin (HPCD) and a non-ionic surfactant, Tween(®) 80. Six PAH with different numbers of rings were monitored: acenaphthene (ACE), phenanthrene (PHE), fluoranthene (FLA), pyrene (PYR), benzo(a)pyrene (BaP), and benzo(g,h,i)perylene (BghiP). Tween(®) 80 showed much better PAH extraction efficiency (after several SW cycles) than HPCD, regardless of the number of washing cycles. Based on successive SW experiments, a new mathematical relation taking into account the soil/water partition coefficient (Kd*) was established, and could predict the amount of each PAH extracted by the surfactant with a good correlation with experimental results (R(2) > 0.975). More HPCD was recovered (89%) than Tween(®) 80 (79%), while the monitored pollutants were completely degraded (>99%) after 4 h and 8 h, respectively. Even after being washed with partially oxidized solutions, the Tween(®) 80 solutions extracted significantly more PAH than HPCD and promoted better soil microbial activity, with higher oxygen consumption rates. Moreover, neither the oxidation by-products nor the acidic media (p

  1. Improved WO3 photocatalytic efficiency using ZrO2 and Ru for the degradation of carbofuran and ampicillin.

    PubMed

    Gar Alalm, Mohamed; Ookawara, Shinichi; Fukushi, Daisuke; Sato, Akira; Tawfik, Ahmed

    2016-01-25

    The photocatalytic degradation of carbofuran (pesticide) and ampicillin (pharmaceutical) using synthesized WO3/ZrO2 nanoparticles under simulated solar light was investigated. Transmission electron microscopy (TEM), X-ray diffraction (XRD), and Raman spectra analyses were used to characterize the prepared catalysts. The optimum ratio of WO3 to ZrO2 was determined to be 1:1 for the degradation of both contaminants. The degradation of carbofuran and ampicillin by WO3/ZrO2 after 240 min of irradiation was 100% and 96%, respectively. Ruthenium (Ru) was employed as an additive to WO3/ZrO2 to enhance the photocatalytic degradation rate. Ru/WO3/ZrO2 exhibited faster degradation rates than WO3/ZrO2. Furthermore, 100% and 97% degradation of carbofuran and ampicillin, respectively, was achieved using Ru/WO3/ZrO2 after 180 min of irradiation. The durability of the catalyst was investigated by reusing the same suspended catalyst, which achieved 92% of its initial efficiency. The photocatalytic degradation of ampicillin and carbofuran followed pseudo-first order kinetics according to the Langmuir-Hinshelwood model.

  2. Visible electroluminescence in spark-processed silicon

    NASA Astrophysics Data System (ADS)

    Shepherd, Nigel Dexter

    Spark-processing is a novel technique that transforms silicon into a material with unique optical and magnetic properties. In this work, the electroluminescence (EL) from spark-processed silicon (sp-Si) has been studied and characterized. The devices studied have a MOS (metal-oxide-semiconductor) type structure. The EL spectrum is broad, and has a threshold wavelength that extends beyond 350 nm, and peaks at around 650 and 730 nm. The threshold voltage for the EL process is typically in the 5--8 V range. Irrespective of whether the base silicon is n or p-type, EL is observed only under the condition of electron injection into the spark-processed layer. The processing conditions that result in the highest EL intensity have been established. Specifically, the processing parameters that results in the highest device currents and EL intensity are 7--8 kV, 10 mA, 12--13 kHz, around 750 mbar and 10 seconds of spark voltage, current, frequency, pressure and time respectively. It has been also been found that processing in air results in higher EL intensities, compared to processing in ultra-high purity nitrogen or oxygen. These conditions are believed to result in the optimal composition and thickness of the near surface SiOx layers, thought to be the optically active region in sp-Si EL devices. These processing conditions are also believed to result in a surface morphology that facilitates the best coverage by the semitransparent metal film, through which the electroluminescence is emitted. When a tungsten wire is used as the anode for spark-processing, the pattern of emission is a circular band of light. This band consists of small light-emitting spots, separated by non-emitting regions. It is shown that by modifying the anode arrangement, significant improvements to the pattern of emission and EL intensity can be achieved. These improvements are proposed to be due to enhanced coverage by the semitransparent metal film. Based on the results of the EL characterization

  3. The efficiency of turn-over processes in degraded peat as investigated under continuous flow conditions

    NASA Astrophysics Data System (ADS)

    Kleimeier, Christian; Karsten, Ulf; Janssen, Manon; Lennartz, Bernd

    2013-04-01

    Nitrate removal from run-off from agricultural land is in general required to reach a "good chemical status" of surface and groundwater bodies according to the European Water Framework Directive. Removing nitrates via heterotrophic denitrification is highly effective but requires stable anoxic environmental conditions as well as available organic carbon as an electron donator. Constructed wetlands, established on peat soils, through which the nitrate-loaded water is routed, may provide denitrification favorable conditions. A long-term flow experiment (mesocosm) was conducted employing a laboratory container set-up filled with decomposed peat aiming at quantifying the nitrate removal efficiency at various nitrate influx rates. The redox potential was measured at different depths to determine the spatial distribution of denitrificating zones. This new methodological approach allows the observation of biological nitrate turn over without interrupting the adjusted flow rate. We investigated the hydraulic properties and derived transport parameters for the mesocosm by analyzing experimental data from tracer tests. The obtained bromide breakthrough curves (BTC) were subjected to model analysis using the CXTFIT routine of the STANMOD software package. It could be demonstrated that the degraded peat has a dual porosity structure with roughly 40% of the pore water not participating in convective flow and transport processes. Further, the first flushing of mineralized nitrate upon rewetting and onset of flux may compromise any positive clean-up and nitrate removal effects occurring during long-term operation of peat wetlands. The development of the spatial sequence of bacterial cultures is characterized by the redox potential. It is dominated by the available substrates that serve as electron acceptors in bacterial respiration and occurs in a thermodynamically determined top-down order. The zonal development of the nitrate-consuming bacteria was observed and used to describe

  4. Efficient enzymatic degradation process for hydrolysis activity of the Carrageenan from red algae in marine biomass.

    PubMed

    Kang, Dae Hee; Hyeon, Jeong Eun; You, Seung Kyou; Kim, Seung Wook; Han, Sung Ok

    2014-12-20

    Carrageenan is a generic name for a family of polysaccharides obtained from certain species of red algae. New methods to produce useful cost-efficiently materials from red algae are needed to convert enzymatic processes into fermentable sugars. In this study, we constructed chimeric genes cCgkA and cCglA containing the catalytic domain of κ-carrageenase CgkA and λ-carrageenase CglA from Pseudoalteromonas carrageenovora fused with a dockerin domain. Recombinant strains expressing the chimeric carrageenase resulted in a halo formation on the carrageenan plate by alcian blue staining. The recombinant cCgkA and cCglA were assembled with scaffoldin miniCbpA via cohesin and dockerin interaction. Carbohydrate binding module (CBM) in scaffoldin was used as a tag for cellulose affinity purification using cellulose as a support. The hydrolysis process was monitored by the amount of reducing sugar released from carrageenan. Interestingly, these results indicated that miniCbpA, cCgkA and cCglA assembled into a complex and that the dockerin-fused enzymes on the scaffoldin had synergistic activity in the degradation of carrageenan. The observed enhancement of activity by carrageenolytic complex was 3.1-fold-higher compared with the corresponding enzymes alone. Thus, the assemblies of advancement of active enzyme complexes will facilitate the commercial production of useful products from red algae biomass which represents inexpensive and sustainable feed-stocks.

  5. Bioremediation as an efficient method to degrade creosote and improve groundwater quality

    SciTech Connect

    Newbern, V.A.

    1994-09-01

    A hydrogeologic monitoring evaluation was conducted to determine the efficiency of bioremediation on a site at which creosote is used for pressure treating and wood preservation. Initially, pentachlorophenol (PCP) and diesel fuel were incorporated with the creosote. The waste water generated from the process was disposed of in three unlined surface impoundments until 1982. Thirteen monitoring wells were installed between August 1981 and the first half of 1982 where both PCP and creosote releases were found and attributed to the impoundments. A groundwater quality assessment program was initiated in April 1986 and a subsequent pilot groundwater remediation program begun in February 1987. A Corrective Action Plan (CAP) has been in operation since August 1987 and was designed to remediate groundwater from the uppermost water-bearing sand (Bentley sand), which was affected by the impoundment areas. With the CAP, a system of 21 recovery wells set in 4 lines were implemented to withdraw the groundwater. The groundwater was then treated in above-ground bioreactors where microorganisms were introduced to degrade the creosote compounds. Treated groundwater was then discharged to the public waste-water facility or injected to recharge the Bentley sands by the use of either of the two recharge trenches. Both nutrients and oxygen were added to the water prior to injection to increase the in-situ bioremediation of the creosote and PCP contaminants via two air sparging lines. The results demonstrate the reduction of creosote constituents from the groundwater with the use of bioremediation.

  6. High-Capacity and Photoregenerable Composite Material for Efficient Adsorption and Degradation of Phenanthrene in Water.

    PubMed

    Liu, Wen; Cai, Zhengqing; Zhao, Xiao; Wang, Ting; Li, Fan; Zhao, Dongye

    2016-10-18

    We report a novel composite material, referred to as activated charcoal supported titanate nanotubes (TNTs@AC), for highly efficient adsorption and photodegradation of a representative polycyclic aromatic hydrocarbon (PAH), phenanthrene. TNTs@AC was prepared through a one-step hydrothermal method, and is composed of an activated charcoal core and a shell of carbon-coated titanate nanotubes. TNTs@AC offered a maximum Langmuir adsorption capacity of 12.1 mg/g for phenanthrene (a model PAH), which is ∼11 times higher than the parent activated charcoal. Phenanthrene was rapidly concentrated onto TNTs@AC, and subsequently completely photodegraded under UV light within 2 h. The photoregenerated TNTs@AC can then be reused for another adsorption-photodegradation cycle without significant capacity or activity loss. TNTs@AC performed well over a wide range of pH, ionic strength, and dissolved organic matter. Mechanistically, the enhanced adsorption capacity is attributed to the formation of carbon-coated ink-bottle pores of the titanate nanotubes, which are conducive to capillary condensation; in addition, the modified microcarbon facilitates transfer of excited electrons, thereby inhibiting recombination of the electron-hole pairs, resulting in high photocatalytic activity. The combined high adsorption capacity, photocatalytic activity, and regenerability/reusability merit TNTs@AC a very attractive material for concentrating and degrading a host of micropollutants in the environment.

  7. Viral RNA Degradation and Diffusion Act as a Bottleneck for the Influenza A Virus Infection Efficiency

    PubMed Central

    Jolmes, Fabian; Welke, Robert-William; Klipp, Edda; Herrmann, Andreas; Flöttmann, Max

    2016-01-01

    After endocytic uptake, influenza viruses transit early endosomal compartments and eventually reach late endosomes. There, the viral glycoprotein hemagglutinin (HA) triggers fusion between endosomal and viral membrane, a critical step that leads to release of the viral segmented genome destined to reach the cell nucleus. Endosomal maturation is a complex process involving acidification of the endosomal lumen as well as endosome motility along microtubules. While the pH drop is clearly critical for the conformational change and membrane fusion activity of HA, the effect of intracellular transport dynamics on the progress of infection remains largely unclear. In this study, we developed a comprehensive mathematical model accounting for the first steps of influenza virus infection. We calibrated our model with experimental data and challenged its predictions using recombinant viruses with altered pH sensitivity of HA. We identified the time point of virus-endosome fusion and thereby the diffusion distance of the released viral genome to the nucleus as a critical bottleneck for efficient virus infection. Further, we concluded and supported experimentally that the viral RNA is subjected to cytosolic degradation strongly limiting the probability of a successful genome import into the nucleus. PMID:27780209

  8. Transparent organic photodiodes stacked with electroluminescence devices

    NASA Astrophysics Data System (ADS)

    Komatsu, Takahiro; Sakanoue, Kei; Fujita, Katsuhiko; Tsutsui, Tetsuo

    2005-10-01

    Stacked devices that consisted of transparent organic photodiodes (TOPDs) and organic electroluminescence devices (OELs) were demonstrated. TOPDs were prepared by poly-(2-methoxy-5- (2'-ethylhexyloxy)-1,4-phenylene vinylene (MEH-PPV) and [6,6]-phenyl C61-butyric acid methyl ester (PCBM) blend films as an active layer and transparent Au cathode (10 nm thick). These TOPDs showed about 45 % transmittance on average in visible light region (380-780 nm) and good correlation between incident light intensity and output photocurrent. Based on these results, the stacked devices were prepared by introducing OELs on TOPDs through a SiO insulating layer. The structure of OELs was ITO/Carbon/TPD/Alq3/LiF/Al. These stacked devices work as light emitting devices and also photo diodes. Since TOPDs have transparency, OELs can illuminate a paper put on the glass substrate through TOPDs and TOPDs can receive reflective light from the paper. Although the TOPDs also absorb light from OELs directly, the output signals from TOPDs changed according to the black and white pattern of the paper. These results show that the devices act as an image sensor having light emitting layer and light receiving layer in a same area.

  9. Multi-colour electroluminescence of dendronic antennae containing pyrenes as light harvesters.

    PubMed

    Giovanella, Umberto; Mróz, Wojciech; Foggi, Paolo; Fabbrizzi, Pierangelo; Cicchi, Stefano; Botta, Chiara

    2010-02-22

    Dendronic antennae systems containing pyrene units as energy donors and a styrylpyridinium derivative as energy acceptor show efficient energy transfer from the green-emitting pyrene excimer to the red-emitting acceptor. For the third dendron generation the effective screening of the pyrene units on the acceptor provides thin films showing bright red emission. Single-layer light-emitting diodes prepared by properly balancing the dendrons and donor units concentration in polyvinylcarbazole show electroluminescence from the blue, green and red components of the monomeric donor, the donor excimer and the acceptor when excitons are generated in the polymer and subsequently transferred to the molecules by resonant energy transfer.

  10. Electroluminescence Studies on Longwavelength Indium Arsenide Quantum Dot Microcavities Grown on Gallium Arsenide

    DTIC Science & Technology

    2011-12-01

    ELECTROLUMINESCENCE STUDIES ON LONG WAVELENGTH INDIUM ARSENIDE QUANTUM DOT MICROCAVITIES GROWN ON GALLIUM ARSENIDE THESIS John C...11-46 ELECTROLUMINESCENCE STUDIES ON LONGWAVELENGTH INDIUM ARSENIDE QUANTUM DOT MICROCAVITIES GROWN ON GALLIUM ARSENIDE THESIS...58 1 ELECTROLUMINESCENCE STUDIES ON LONGWAVELENGTH INDIUM ARSENIDE QUANTUM DOT MICROCAVITIES GROWN ON GALLIUM ARSENIDE I

  11. Analysis of power supply circuits for electroluminescent panels

    NASA Astrophysics Data System (ADS)

    Drumea, Andrei; Dobre, Robert Alexandru

    2016-12-01

    The electroluminescent panel is a light emitting device that requires for normal operations alternative voltages with peak to peak amplitudes in 100V… 300V range and frequencies in 100Hz … 2 kHz range. Its advantages, when compared with standard light sources like incandescent lamps, gas-discharge lamps or light emitting diodes (LEDs), are lower power consumption, flexible substrate and uniform light without observable luminous points. One disadvantage of electroluminescent panels is the complex power supply required to drive them, but the continuous improvement in passive and active integrated devices for switched mode power supplies will eventually solve this issue. The present paper studies different topologies for these power supplies and the effect of the electric parameters like the amplitude, frequency, waveform of the supplying voltage on the light emission and on power consumption for electroluminescent panels with different size and colors.

  12. Key parameters and practices controlling pesticide degradation efficiency of biobed substrates.

    PubMed

    Karanasios, Evangelos; Karpouzas, Dimitrios G; Tsiropoulos, Nikolaos G

    2012-01-01

    We studied the contribution of each of the components of a compost-based biomixture (BX), commonly used in Europe, on pesticide degradation. The impact of other key parameters including pesticide dose, temperature and repeated applications on the degradation of eight pesticides, applied as a mixture, in a BX and a peat-based biomixture (OBX) was compared and contrasted to their degradation in soil. Incubation studies showed that straw was essential in maintaining a high pesticide degradation capacity of the biomixture, whereas compost, when mixed with soil, retarded pesticide degradation. The highest rates of degradation were shown in the biomixture composed of soil/compost/straw suggesting that all three components are essential for maximum biobed performance. Increasing doses prolonged the persistence of most pesticides with biomixtures showing a higher tolerance to high pesticide dose levels compared to soil. Increasing the incubation temperature from 15 °C to 25 °C resulted in lower t(1/2) values, with biomixtures performing better than soil at the lower temperature. Repeated applications led to a decrease in the degradation rates of most pesticides in all the substrates, with the exception of iprodione and metalaxyl. Overall, our results stress the ability of biomixtures to perform better than soil under unfavorable conditions and extreme pesticide dose levels.

  13. Progress and Prospects in Stretchable Electroluminescent Devices

    NASA Astrophysics Data System (ADS)

    Wang, Jiangxin; Lee, Pooi See

    2017-03-01

    Stretchable electroluminescent (EL) devices are a new form of mechanically deformable electronics that are gaining increasing interests and believed to be one of the essential technologies for next generation lighting and display applications. Apart from the simple bending capability in flexible EL devices, the stretchable EL devices are required to withstand larger mechanical deformations and accommodate stretching strain beyond 10%. The excellent mechanical conformability in these devices enables their applications in rigorous mechanical conditions such as flexing, twisting, stretching, and folding.The stretchable EL devices can be conformably wrapped onto arbitrary curvilinear surface and respond seamlessly to the external or internal forces, leading to unprecedented applications that cannot be addressed with conventional technologies. For example, they are in demand for wide applications in biomedical-related devices or sensors and soft interactive display systems, including activating devices for photosensitive drug, imaging apparatus for internal tissues, electronic skins, interactive input and output devices, robotics, and volumetric displays. With increasingly stringent demand on the mechanical requirements, the fabrication of stretchable EL device is encountering many challenges that are difficult to resolve. In this review, recent progresses in the stretchable EL devices are covered with a focus on the approaches that are adopted to tackle materials and process challenges in stretchable EL devices and delineate the strategies in stretchable electronics. We first introduce the emission mechanisms that have been successfully demonstrated on stretchable EL devices. Limitations and advantages of the different mechanisms for stretchable EL devices are also discussed. Representative reports are reviewed based on different structural and material strategies. Unprecedented applications that have been enabled by the stretchable EL devices are reviewed. Finally, we

  14. Hump-shaped internal collection efficiency of degraded a-Si:H {ital p-i-n} solar cells

    SciTech Connect

    Smole, F.; Topic, M.; Furlan, J.; Kusian, W.

    1997-07-01

    Measured internal collection efficiency (ICE) characteristics of annealed and degraded a-Si:H p-i-n solar cells were used for an analysis of their internal behavior. Using the numerical simulator ASPIN, simulations were performed in order to fit and explain pronounced hump-shaped voltage-dependent ICE characteristics of degraded structures under weak short-wavelength illumination. Agreement with measured ICE characteristics for a degraded cell was obtained only if in addition to the introduction of light-induced dangling bond defect states, their capture cross sections were also increased, in particular the capture cross section for the charged defect states were increased. This caused a change in the occupancy of defect states at the p-i interface and front part of the i layer under forward biases. Consequently, the electric field in the front part of the cell was sustained under higher forward biases, resulting in recovery of the ICE. {copyright} {ital 1997 American Institute of Physics.}

  15. ZnO/Ag nanocomposite: an efficient catalyst for degradation studies of textile effluents under visible light.

    PubMed

    Saravanan, R; Karthikeyan, N; Gupta, V K; Thirumal, E; Thangadurai, P; Narayanan, V; Stephen, A

    2013-05-01

    Degradation of model organic dye and industry effluent was studied using different weight percentages of Ag into ZnO as a catalyst. In this study, the catalysts were prepared by thermal decomposition method, which was employed for the first time in the preparation of ZnO/Ag nanocomposite catalysts. The physical and chemical properties of the prepared samples were studied using various techniques. The specific surface area, which plays an important role in the photocatalytic degradation, was studied using BET analysis and 10 wt.% Ag into ZnO showed the best degrading efficiency. The optical absorption (UV-vis) and emission (PL) properties of the samples were studied and results suggest better photocatalytic properties for 10 wt.% Ag sample compared to other samples.

  16. The effects of the antibiotics ampicillin, florfenicol, sulfamethazine, and tylosin on biogas production and their degradation efficiency during anaerobic digestion.

    PubMed

    Mitchell, Shannon M; Ullman, Jeffrey L; Teel, Amy L; Watts, Richard J; Frear, Craig

    2013-12-01

    The impacts of four common animal husbandry antibiotics (ampicillin, florfenicol, sulfamethazine, and tylosin) on anaerobic digestion (AD) treatment efficiency and the potential for antibiotic degradation during digestion were evaluated. Sulfamethazine and ampicillin exhibited no impact on total biogas production up to 280 and 350 mg/L, respectively, although ampicillin inhibited biogas production rates during early stages of AD. Tylosin reduced biogas production by 10-38% between 130 and 913 mg/L. Florfenicol reduced biogas by ≈ 5%, 40% and 75% at 6.4, 36 and 210 mg/L, respectively. These antibiotic concentrations are higher than commonly seen for mixed feedlot manure, so impacts on full scale AD should be minimal. Antibiotic degradation products were found, confirming AD effectively degraded ampicillin, florfenicol, and tylosin, although some products were persistent throughout the process. Contamination of AD solid and liquid effluents with sulfamethazine and antibiotic transformation products from florfenicol and tylosin could present an environmental concern.

  17. Mercury oxide as an efficient photocatalyst for degradation of rhodamine B dye under visible-light irradiation

    NASA Astrophysics Data System (ADS)

    Li, Datang; Li, Jiayin; Tang, Jianting

    2016-11-01

    In this work, a new visible-light-responsive photocatalyst, mercury oxide (HgO) was successfully developed. Its activity is significantly higher than that of the highly efficient photocatalyst, Ag3PO4 in degradation of rhodamine B (RhB) dye under irradiation of visible light. The HgO photocatalyst can be reused for at least three cycles without obvious loss of its activity in the degradation experiments. It was found that the RhB degradation rate is significantly influenced by the dye solution pH. The ultrahigh photocatalytic activity of HgO is attributed to its strong oxidization-ablility of the photogenerated holes, and high separation-possibility of the photogenerated carriers.

  18. Dual-degradable disulfide-containing PEI-Pluronic/DNA polyplexes: transfection efficiency and balancing protection and DNA release.

    PubMed

    Zhang, Lifen; Chen, Zhenzhen; Li, Yanfeng

    2013-01-01

    Polymeric gene-delivery vectors to achieve lack of toxicity and a balance between protection and DNA release remains a formidable challenge. Incorporating intracellular environment-responsive degradable bonds is an appreciable step toward developing safer transfection agents. In this study, novel, dual-degradable polycation copolymers (Pluronic-diacrylate [PA]-polyethyleneimine [PEI]-SS) were synthesized through the addition of low molecular weight (800 Da) PEI cross-linked with SS (PEI-SS) to PA. Three PA-PEI-SS copolymers (PA-PEI-SS1, 2, and 3) with different PEI-SS to Pluronic molar ratios were investigated and found to strongly condense plasmid DNA into positively charged nanoparticles with an average particle size of approximately 200 nm and to possess higher stability against DNase I digestion and sodium heparin. Disulfide and ester bonds of the copolymers were susceptible to intracellular redox conditions. In vitro experiments demonstrated that the PA-PEI-SS copolymers had significantly lower cytotoxicity and higher transfection efficiency in both BGC-823 and 293T cell lines than the controls of degradable PEI-SS and nondegradable 25 kDa PEI. Transfection activity was influenced by the PEI-SS content in the polymers and PA-PEI-SS1 showed the highest efficiency of the three copolymers. These studies suggest that these dual-degradable copolymers could be used as potential biocompatible gene delivery carriers.

  19. Isolation and characterization of Sphingomonas sp. Y2 capable of high-efficiency degradation of nonylphenol polyethoxylates in wastewater.

    PubMed

    Bai, Naling; Wang, Sheng; Abuduaini, Rexiding; Zhu, Xufen; Zhao, Yuhua

    2016-06-01

    Nonylphenol polyethoxylates (NPEOs), although banned for decades, are still widely used in manufactories and thus affect human lives. In this study, a highly efficient NPEO-degrading bacterium, Sphingomonas sp. Y2, was isolated from sewage sludge by enrichment culture. Strain Y2 ensured the complete removal of NPEO in 48 h and degraded 99.2 % NPEO (1,000 mg L(-1)) within 30 h at a specific growth rate of 0.73 h(-1) in minimum salt medium. To date, this degradation efficiency is the highest reported for NPEO metabolism by a pure bacterium under this condition. Furthermore, the application of this bacterium to wastewater treatment demonstrated that it metabolized 98.5 % NPEO (1,000 mg L(-1)) within 5 days with a specific growth rate of 2.03 day(-1). The degradation intermediates, identified as nonylphenol, short-chain NPEOs and short-chain nonylphenol polyethoxycarboxylates by high-performance liquid chromatography and gas chromatography-mass spectrometry, indicated the sequential exo-cleavage of the EO chain. Additionally, the enzymes involved in the biodegradation were inducible rather than constitutive. Considering that strain Y2 exhibits prominent biodegradation advantages in industrial wastewater treatment, it might serve as a promising potential candidate for in situ bioremediation of contamination by NPEOs and other structurally similar compounds.

  20. Efficient degradation of crystal violet in magnetic CuFe2O4 aqueous solution coupled with microwave radiation.

    PubMed

    Chen, Hongzhe; Yang, Shaogui; Chang, Jiao; Yu, Kai; Li, Dongfang; Sun, Cheng; Li, Aimin

    2012-09-01

    Nanoscale copper ferrite was prepared by co-precipitation method, while citrate acid assisted method was used as reference. Microwave-induced degradation of crystal violet was performed with synthesized copper ferrite, and the behavior of copper ferrite in this process was studied by X-ray photoelectron spectroscopy, SEM/EDS and vector network analyzer. Microwave radiation could greatly enhance the activity of copper ferrite in organic oxidation. The variant of copper and iron on the surface and in the inner core of copper ferrite was studied here. Copper ferrite presents relatively low dielectric loss. Meanwhile, microwave radiation makes a faster degradation than conventional heating process, indicating an indispensable non-thermal effect of microwave with copper ferrite in the process. Microwave induced holes could be responsible for the efficient degradation. The effect of annealing on crystallization and degradation process was considered here, and the intermediates and products were studied by GC-MS and LC-MS to provide a comprehensively evaluation of degradation.

  1. [Selection of a composite microbial system MC1 with efficient and stability cellulose degradation bacteria and its function].

    PubMed

    Cui, Zongjun; Li, Meidan; Piao, Zhe; Huang, Zhiyong; Ishii, Masaharu; Igarashi, Yasuo

    2002-05-01

    Four groups of microbial mix culture with considerable capability of cellulose degradation were selected from four compost heaps, by combining the four groups, a composite microbial system MC1 with highly efficient cellulose degradation was obtained. It was found that 0.48 g of filter paper, 0.49 g of absorbent cotton, 0.19 g of wheat straw, or 0.08 g of wood residue can be degraded by 100 mL of MC1 at 50 degrees C with in 72 hours under static culture. The CM1 saccharification activity was much higher at 24th hours when degrading filter paper that was 122.3 U.mL-1. This capability of degradation maintained more than 20 days when the substrates were continually added. MC1 could be inoculated in a wide pH rang, from 4 to 10; however, the final pH would be changed to neutrality after incubation. The pH would be stability with filter paper between 6.0 and 6.5, and between 8.0 and 8.5 without the filter paper.

  2. Large magneto-conductance and magneto-electroluminescence in exciplex-based organic light-emitting diodes at room temperature

    NASA Astrophysics Data System (ADS)

    Ling, Yongzhou; Lei, Yanlian; Zhang, Qiaoming; Chen, Lixiang; Song, Qunliang; Xiong, Zuhong

    2015-11-01

    In this work, we report on large magneto-conductance (MC) over 60% and magneto-electroluminescence (MEL) as high as 112% at room temperature in an exciplex-based organic light-emitting diode (OLED) with efficient reverse intersystem crossing (ISC). The large MC and MEL are individually confirmed by the current density-voltage characteristics and the electroluminescence spectra under various magnetic fields. We proposed that this type of magnetic field effect (MFE) is governed by the field-modulated reverse ISC between the singlet and triplet exciplex. The temperature-dependent MFEs reveal that the small activation energy of reverse ISC accounts for the large MFEs in the present exciplex-based OLEDs.

  3. Electroluminescence from indirect band gap semiconductor ReS2

    NASA Astrophysics Data System (ADS)

    Gutiérrez-Lezama, Ignacio; Aditya Reddy, Bojja; Ubrig, Nicolas; Morpurgo, Alberto F.

    2016-12-01

    It has been recently claimed that bulk crystals of transition metal dichalcogenide (TMD) ReS2 are direct band gap semiconductors, which would make this material an ideal candidate, among all TMDs, for the realization of efficient opto-electronic devices. The situation is however unclear, because even more recently an indirect transition in the PL spectra of this material has been detected, whose energy is smaller than the supposed direct gap. To address this issue we exploit the properties of ionic liquid gated field-effect transistors (FETs) to investigate the gap structure of bulk ReS2. Using these devices, whose high quality is demonstrated by a record high electron FET mobility of 1100 cm2 V-1 s-1 at 4 K, we can induce hole transport at the surface of the material and determine quantitatively the smallest band gap present in the material, irrespective of its direct or indirect nature. The value of the band gap is found to be 1.41 eV, smaller than the 1.5 eV direct optical transition but in good agreement with the energy of the indirect optical transition, providing an independent confirmation that bulk ReS2 is an indirect band gap semiconductor. Nevertheless, contrary to the case of more commonly studied semiconducting TMDs (e.g., MoS2, WS2, etc) in their bulk form, we also find that ReS2 FETs fabricated on bulk crystals do exhibit electroluminescence when driven in the ambipolar injection regime, likely because the difference between direct and indirect gap is only 100 meV. We conclude that ReS2 does deserve more in-depth investigations in relation to possible opto-electronic applications.

  4. Photoluminescence and electroluminescence of a tripodal compound containing 7-diethylamino-coumarin moiety

    NASA Astrophysics Data System (ADS)

    Yu, Tianzhi; Zhang, Peng; Zhao, Yuling; Zhang, Hui; Meng, Jing; Fan, Duowang; Dong, Wenkui

    2008-12-01

    A novel tripodal compound, tris[2-(7-diethylamino-coumarin-3-carboxamide)ethyl]amine (Tren-C), was synthesized and characterized by elemental analysis, infrared and 1H-NMR spectra. The photoluminescent (PL) and electroluminescent properties of Tren-C were investigated. Tren-C exhibits different colour emissions in solid states and solutions. The electroluminescence devices comprising vacuum vapour-deposited films using the compound as a dopant were fabricated, showing blue emissions that are identical to its PL spectrum in chloroform solutions. With the device structure of indium tin oxide (ITO)/4, 4', 4''-tris-N-naphthyl-N-phenylamino-triphenylamine (2-TNATA) (5 nm)/N, N'-bis-(naphthyl)-N, N'-diphenyl-1, 1'-biphenyl-4, 4'-diamine (NPB) (40 nm)/4, 4'-bis(9-carbazolyl) biphenyl (CBP) : Tren-C (0.5 wt%, 30 nm)/2-(4-biphenylyl)-5-(4-tert-butylphenyl)-1, 3, 4-oxadiazole (Bu-PBD) (30 nm)/LiF (1 nm)/Al (100 nm), a maximum external quantum efficiency of 2.85%, a maximum luminous efficiency of 3.85 cd A-1 and a maximum luminance of 1450 cd m-2 are realized.

  5. Red electroluminescence of ruthenium sensitizer functionalized by sulfonate anchoring groups.

    PubMed

    Shahroosvand, Hashem; Abbasi, Parisa; Mohajerani, Ezeddin; Janghouri, Mohammad

    2014-06-28

    We have synthesized five novel Ru(ii) phenanthroline complexes with an additional aryl sulfonate ligating substituent at the 5-position [Ru(L)(bpy)2](BF4)2 (1), [Ru(L)(bpy)(SCN)2] (2), [Ru(L)3](BF4)2 (3), [Ru(L)2(bpy)](BF4)2 (4) and [Ru(L)(BPhen)(SCN)2] (5) (where L = 6-one-[1,10]phenanthroline-5-ylamino)-3-hydroxynaphthalene 1-sulfonic, bpy = 2,2'-bipyridine, BPhen = 4,7-diphenyl-1,10-phenanthroline), as both photosensitizers for oxide semiconductor solar cells (DSSCs) and light emitting diodes (LEDs). The absorption and emission maxima of these complexes red shifted upon extending the conjugation of the phenanthroline ligand. Ru phenanthroline complexes exhibit broad metal to ligand charge transfer-centered electroluminescence (EL) with a maximum near 580 nm. Our results indicated that a particular structure (2) can be considered as both DSSC and OLED devices. The efficiency of the LED performance can be tuned by using a range of ligands. Device (2) has a luminance of 550 cd m(-2) and maximum efficiency of 0.9 cd A(-1) at 18 V, which are the highest values among the five devices. The turn-on voltage of this device is approximately 5 V. The role of auxiliary ligands in the photophysical properties of Ru complexes was investigated by DFT calculation. We have also studied photovoltaic properties of dye-sensitized nanocrystalline semiconductor solar cells based on Ru phenanthroline complexes and an iodine redox electrolyte. A solar energy to electricity conversion efficiency (η) of 0.67% was obtained for Ru complex (2) under standard AM 1.5 irradiation with a short-circuit photocurrent density (Jsc) of 2.46 mA cm(-2), an open-circuit photovoltage (Voc) of 0.6 V, and a fill factor (ff) of 40%, which are all among the highest values for ruthenium sulfonated anchoring groups reported so far. Monochromatic incident photon to current conversion efficiency was 23% at 475 nm. Photovoltaic studies clearly indicated dyes with two SCN substituents yielded a higher Jsc for the

  6. Heterogeneous Fenton degradation of bisphenol A catalyzed by efficient adsorptive Fe3O4/GO nanocomposites.

    PubMed

    Hua, Zulin; Ma, Wenqiang; Bai, Xue; Feng, Ranran; Yu, Lu; Zhang, Xiaoyuan; Dai, Zhangyan

    2014-06-01

    A new method for the degradation of bisphenol A (BPA) in aqueous solution was developed. The oxidative degradation characteristics of BPA in a heterogeneous Fenton reaction catalyzed by Fe3O4/graphite oxide (GO) were studied. Transmission electron microscopic images showed that the Fe3O4 nanoparticles were evenly distributed and were ∼6 nm in diameter. Experimental results suggested that BPA conversion was affected by several factors, such as the loading amount of Fe3O4/GO, pH, and initial H2O2 concentration. In the system with 1.0 g L(-1) of Fe3O4/GO and 20 mmol L(-1) of H2O2, almost 90% of BPA (20 mg L(-1)) was degraded within 6 h at pH 6.0. Based on the degradation products identified by GC-MS, the degradation pathways of BPA were proposed. In addition, the reused catalyst Fe3O4/GO still retained its catalytic activity after three cycles, indicating that Fe3O4/GO had good stability and reusability. These results demonstrated that the heterogeneous Fenton reaction catalyzed by Fe3O4/GO is a promising advanced oxidation technology for the treatment of wastewater containing BPA.

  7. Marine bacterium strain screening and pyrethroid insecticide-degrading efficiency analysis

    NASA Astrophysics Data System (ADS)

    Sun, Aili; Liu, Jinghua; Shi, Xizhi; Li, Dexiang; Chen, Jiong; Tang, Daojun

    2014-09-01

    A pyrethroid insecticide-degrading bacterium, strain HS-24, was isolated from an offshore seawater environment. The strain, which can degrade cypermethrin (CYP) and deltamethrin (DEL), was identified as Methylophaga sp. The optimal culture and degradation conditions for CYP and DEL by strain HS-24 is pH 7 at 28°C. Under optimum culture conditions, strain HS-24 exhibited a broad degradation concentration range of 100, 200, 400, 600, and 800 mg/L for CYP and DEL. The metabolic intermediates were analyzed by NMR, which provided strong evidence that CYP and DEL removal occurred mainly because of a biological process. The toxicity of the degradation products of strain HS-24 was studied simultaneously by measuring the light output of the luminescence bacterium. This demonstrated that the biodegradation ability of strain HS-24 significantly decreased the toxicity of CYP- and DEL-contaminated aquaculture seawater. Finally, the findings of this paper indicate that strain HS-24 is thus revealed as a biological agent for the remediation of marine aquatic environments.

  8. Complete genome sequence of Streptomyces reticuli, an efficient degrader of crystalline cellulose.

    PubMed

    Wibberg, Daniel; Al-Dilaimi, Arwa; Busche, Tobias; Wedderhoff, Ina; Schrempf, Hildgund; Kalinowski, Jörn; Ortiz de Orué Lucana, Darío

    2016-03-20

    We report the complete, GC-rich genome sequence of the melanin producer Streptomyces reticuli Tü 45 (S. reticuli) that targets and degrades highly crystalline cellulose by the concerted action of a range of biochemically characterized proteins. It consists of a linear 8.3 Mb chromosome, a linear 0.8 Mb megaplasmid, a linear 94 kb plasmid and a circular 76 kb plasmid. Noteworthy, the megaplasmid is the second largest known Streptomyces plasmid. Preliminary analysis reveals, among others, 43 predicted gene clusters for the synthesis of secondary metabolites and 456 predicted genes for binding and degradation of cellulose, other polysaccharides and carbohydrate-containing compounds.

  9. Xylose induces the phyllosphere yeast Pseudozyma antarctica to produce a cutinase-like enzyme which efficiently degrades biodegradable plastics.

    PubMed

    Watanabe, Takashi; Shinozaki, Yukiko; Yoshida, Shigenobu; Koitabashi, Motoo; Sameshima-Yamashita, Yuka; Fujii, Takeshi; Fukuoka, Tokuma; Kitamoto, Hiroko Kuze

    2014-03-01

    There is a need to speed up the degradation of used agricultural mulch films that are made of biodegradable plastics (BPs) in the field. Treating them with BP-degrading enzymes could be a solution to this problem. A cutinase-like enzyme of yeast Pseudozyma antarctica (PaE) has wide specificity of BPs degradation, but needs to be produced efficiently. Here we report that the production of PaE by P. antarctica can be increased by using xylose as carbon source. BP-degradation activity was analyzed using a polybutylene succinate-co-adipate (PBSA) emulsion as the substrate. Strain P. antarctica GB-4(1)W was found to be the best PaE producer among the tested strains. Using a 5-L jar fermentor with xylose fed-batch cultivation, high PaE productivity could be maintained and about 21 U/ml of PaE was obtained in 120 h. This amount was 100 times higher than the amount that we obtained previously (0.21 U/ml by flask cultivation using glycerol as carbon source). Under repeated xylose fed-batch cultivation with 24 h intervals, the maximum PaE production rate (0.34 U/ml/h) was maintained and the highest PaE productivity (28,000 U/2 L/d) was repeatedly obtained for 7 intervals. The activity of filtered jar-culture (crude PaE) was stable over 12 weeks at 4°C. Commercially available BP mulch films (20 μm thickness, cut into 1-cm-squares) were completely degraded by submerging them in crude PaE (2 U/ml) at 30°C in 24 h. These results indicated that concentrated PaE can rapidly degrade the strength of BP mulch films in the field so that they do not interfere with plowing.

  10. Efficient degradation of atrazine by magnetic porous copper ferrite catalyzed peroxymonosulfate oxidation via the formation of hydroxyl and sulfate radicals.

    PubMed

    Guan, Ying-Hong; Ma, Jun; Ren, Yue-Ming; Liu, Yu-Lei; Xiao, Jia-Yue; Lin, Ling-qiang; Zhang, Chen

    2013-09-15

    Magnetic porous copper ferrite (CuFe2O4) showed a notable catalytic activity to peroxymonosulfate (PMS). More than 98% of atrazine was degraded within 15 min at 1 mM PMS and 0.1 g/L CuFe2O4. In contrast, CuFe2O4 exhibited no obvious catalytic activity to peroxodisulfate or H2O2. Several factors affecting the catalytic performance of PMS/CuFe2O4 were investigated. Results showed that the catalytic degradation efficiency of atrazine increased with PMS and CuFe2O4 doses, but decreased with the increase of natural organic matters concentration. The catalytic oxidation also showed a dependence on initial pH. The presence of bicarbonate stimulated atrazine degradation by PMS/CuFe2O4 at low concentrations but inhibited the degradation at high concentrations. Furthermore, the reactive species for atrazine degradation in PMS/CuFe2O4 system were identified as hydroxyl radical (HO) and sulfate radical (SO4(·-)) through competition reactions of atrazine and nitrobenzene, instead of commonly used alcohol scavenging, which was not a reliable method in metal oxide catalyzed oxidation. Surface hydroxyl groups of CuFe2O4 were a critical part in radical generation and the copper on CuFe2O4 surface was an active site to catalyze PMS. The catalytic degradation of atrazine by PMS/CuFe2O4 was also effective under the background of actual waters.

  11. Singlet oxygen as a reactive intermediate in the photodegradation of an electroluminescent polymer

    SciTech Connect

    Scurlock, R.D.; Wang, B.; Ogilby, P.R.; Sheats, J.R.; Clough, R.L.

    1995-10-18

    Singlet molecular oxygen (a{sup 1}{Delta}{sub g}) is shown to be a reactive intermediate in the photoinduced oxidative decomposition of the electroluminescent material poly(2,5-bis(5,6-dihydrocholestanoxy)-1,4-phenylenevinylene) [BCHA-PPV] in both liquid solutions and solid films. Upon irradiation of this polymer in CS{sub 2}, singlet oxygen is produced by energy transfer from the BCHA-PPV triplet state to ground state oxygen with a quantum yield of nearly 0.025. Singlet oxygen reacts with BCHA-PPV, resulting in extensive chain scission of the macromolecule. The reaction with singlet oxygen is unique to the polymer; the monomeric analog of this system, stilbene, does not appreciably react with singlet oxygen. Polymer degradation is proposed to proceed via addition of singlet oxygen in a{sub {pi}} 2+{sub {pi}}2 cycloaddition reaction to the double bond that connects phenylene groups in the macromolecule. 60 refs., 6 figs.

  12. Identification and Characterization of a High Efficiency Aniline Resistance and Degrading Bacterium MC-01.

    PubMed

    Yang, Liu; Ying, Chen; Fang, Ni; Zhong, Yao; Zhao-Xiang, Zhong; Yun, Sun

    2017-01-03

    Biodegradation is one of the important methods for the treatment of industrial wastewater containing aniline. In this paper, a degrading bacterium named MC-01, which could survive in high concentration aniline wastewater, was screened from industrial wastewater containing aniline and sludge. MC-01 was preliminarily identified as Ochrobactrum sp. based on the amplified 16S rDNA gene sequence and Biolog system identification. MC-01 was highly resistant to aniline. After 24-h culture under aniline concentration of 6500 mg/L, the amount of bacterium survived still remained 0.05 × 10(6) CFU/mL. Experiments showed that there was no coupling expression between the growth of MC-01 and aniline degradation. The optimum growth conditions in LB culture were pH 6.0, 30 °C of temperature, and 4% of incubation amount, respectively. And the optimum conditions of aniline degradation of MC-01 were pH 7.0, 45 °C of temperature, and 3.0% of salt concentration, respectively. The degradation rate of MC-01 (48 h) in different aniline concentrations (200~1600 mg/L) was stable under the optimum conditions, which could reach more than 75%.

  13. Layered double hydroxides as efficient photocatalysts for visible-light degradation of Rhodamine B.

    PubMed

    Xia, Sheng-Jie; Liu, Feng-Xian; Ni, Zhe-Ming; Xue, Ji-Long; Qian, Ping-Ping

    2013-09-01

    A series of Zn/M-NO3-LDHs (M=Al, Fe, Ti, and Fe/Ti) have been synthesized by two different methods, and their activities for visible-light photocatalytic degradation on Rhodamine B (RB) were tested. Solids were analyzed by XRD, FT-IR, and ICP characterization, confirming the formation of pure LDH phase with good crystal structure. It was observed that the band gap of these nitrate LDH materials was following this order: Zn/Fe-NO3-LDHs (2.55 eV)>Zn/Fe/Ti-NO3-LDHs (2.88 eV)>Zn/Ti-NO3-LDHs (3.0 3eV)>Zn/Al-NO3-LDHs (3.23 eV); however, the degradation performance of RB by four materials followed the order: Zn/Ti-NO3-LDHs (98%)>Zn/Al-NO3-LDHs (96%)>Zn/Fe/Ti-NO3-LDHs (88%)>Zn/Fe-NO3-LDHs (72%). In addition, a possible mechanism for photocatalytic degradation on RB has also been presumed. Moreover, after three regeneration cycles, the percentage of RB degradation rate was still close to 90%.

  14. Strategies to alleviate poverty and grassland degradation in Inner Mongolia: intensification vs production efficiency of livestock systems.

    PubMed

    Briske, David D; Zhao, Mengli; Han, Guodong; Xiu, Changbai; Kemp, David R; Willms, Walter; Havstad, Kris; Kang, Le; Wang, Zhongwu; Wu, Jianguo; Han, Xingguo; Bai, Yongfei

    2015-04-01

    Semi-nomadic pastoralism was replaced by sedentary pastoralism in Inner Mongolia during the 1960's in response to changes in land use policy and increasing human population. Large increases in numbers of livestock and pastoralist households (11- and 9-fold, respectively) during the past 60 yrs have variously degraded the majority of grasslands in Inner Mongolia (78 M ha) and jeopardize the livelihoods of 24 M human inhabitants. A prevailing strategy for alleviating poverty and grassland degradation emphasizes intensification of livestock production systems to maintain both pastoral livelihoods and large livestock numbers. We consider this strategy unsustainable because maximization of livestock revenue incurs high supplemental feed costs, marginalizes net household income, and promotes larger flock sizes to create a positive feedback loop driving grassland degradation. We offer an alternative strategy that increases both livestock production efficiency and net pastoral income by marketing high quality animal products to an increasing affluent Chinese economy while simultaneously reducing livestock impacts on grasslands. We further caution that this strategy be designed and assessed within a social-ecological framework capable of coordinating market expansion for livestock products, sustainable livestock carrying capacities, modified pastoral perceptions of success, and incentives for ecosystem services to interrupt the positive feedback loop that exists between subsistence pastoralism and grassland degradation in Inner Mongolia.

  15. Bandgap-tailored NiO nanospheres: an efficient photocatalyst for the degradation of crystal violet dye solution

    NASA Astrophysics Data System (ADS)

    Vahini, Raja; Kumar, Puvaneswaran Senthil; Karuthapandian, Swaminathan

    2016-08-01

    Bandgap-tailored NiO nanospheres were successfully synthesized by facile precipitation method for the first time and characterized by XRD, EDX, SEM, TEM, FTIR, UV and PL. Interestingly, the modification of the band gap was observed using UV-Vis (DRS) spectroscopy, and the observed band gap is 3.31 eV. The morphology of the materials was analysed by SEM and TEM which show the sphere like structures of NiO with the particle size of ~20 nm. The efficiency of the materials was examined by the degradation of crystal violet dye under UV light illumination. The complete degradation was achieved within 60 min, and the mechanism of the degradation were also been proposed. In addition, the degradation of rhodamine B (RhB) and methylene blue dye solution was also carried out to extend the practical applications of NiO nanospheres. The involvement of reactive oxidative species (ROS) was found out by trapping experiment, and the ROS is superoxide radical anion.

  16. Green Phosphorescence and Electroluminescence of Sulfur Pentafluoride-Functionalized Cationic Iridium(III) Complexes.

    PubMed

    Shavaleev, Nail M; Xie, Guohua; Varghese, Shinto; Cordes, David B; Slawin, Alexandra M Z; Momblona, Cristina; Ortí, Enrique; Bolink, Henk J; Samuel, Ifor D W; Zysman-Colman, Eli

    2015-06-15

    We report on four cationic iridium(III) complexes [Ir(C^N)2(dtBubpy)](PF6) that have sulfur pentafluoride-modified 1-phenylpyrazole and 2-phenylpyridine cyclometalating (C^N) ligands (dtBubpy = 4,4'-di-tert-butyl-2,2'-bipyridyl). Three of the complexes were characterized by single-crystal X-ray structure analysis. In cyclic voltammetry, the complexes undergo reversible oxidation of iridium(III) and irreversible reduction of the SF5 group. They emit bright green phosphorescence in acetonitrile solution and in thin films at room temperature, with emission maxima in the range of 482-519 nm and photoluminescence quantum yields of up to 79%. The electron-withdrawing sulfur pentafluoride group on the cyclometalating ligands increases the oxidation potential and the redox gap and blue-shifts the phosphorescence of the iridium complexes more so than the commonly employed fluoro and trifluoromethyl groups. The irreversible reduction of the SF5 group may be a problem in organic electronics; for example, the complexes do not exhibit electroluminescence in light-emitting electrochemical cells (LEECs). Nevertheless, the complexes exhibit green to yellow-green electroluminescence in doped multilayer organic light-emitting diodes (OLEDs) with emission maxima ranging from 501 nm to 520 nm and with an external quantum efficiency (EQE) of up to 1.7% in solution-processed devices.

  17. Abnormal strong burn-in degradation of highly efficient polymer solar cells caused by spinodal donor-acceptor demixing

    NASA Astrophysics Data System (ADS)

    Li, Ning; Perea, José Darío; Kassar, Thaer; Richter, Moses; Heumueller, Thomas; Matt, Gebhard J.; Hou, Yi; Güldal, Nusret S.; Chen, Haiwei; Chen, Shi; Langner, Stefan; Berlinghof, Marvin; Unruh, Tobias; Brabec, Christoph J.

    2017-02-01

    The performance of organic solar cells is determined by the delicate, meticulously optimized bulk-heterojunction microstructure, which consists of finely mixed and relatively separated donor/acceptor regions. Here we demonstrate an abnormal strong burn-in degradation in highly efficient polymer solar cells caused by spinodal demixing of the donor and acceptor phases, which dramatically reduces charge generation and can be attributed to the inherently low miscibility of both materials. Even though the microstructure can be kinetically tuned for achieving high-performance, the inherently low miscibility of donor and acceptor leads to spontaneous phase separation in the solid state, even at room temperature and in the dark. A theoretical calculation of the molecular parameters and construction of the spinodal phase diagrams highlight molecular incompatibilities between the donor and acceptor as a dominant mechanism for burn-in degradation, which is to date the major short-time loss reducing the performance and stability of organic solar cells.

  18. Abnormal strong burn-in degradation of highly efficient polymer solar cells caused by spinodal donor-acceptor demixing

    PubMed Central

    Li, Ning; Perea, José Darío; Kassar, Thaer; Richter, Moses; Heumueller, Thomas; Matt, Gebhard J.; Hou, Yi; Güldal, Nusret S.; Chen, Haiwei; Chen, Shi; Langner, Stefan; Berlinghof, Marvin; Unruh, Tobias; Brabec, Christoph J.

    2017-01-01

    The performance of organic solar cells is determined by the delicate, meticulously optimized bulk-heterojunction microstructure, which consists of finely mixed and relatively separated donor/acceptor regions. Here we demonstrate an abnormal strong burn-in degradation in highly efficient polymer solar cells caused by spinodal demixing of the donor and acceptor phases, which dramatically reduces charge generation and can be attributed to the inherently low miscibility of both materials. Even though the microstructure can be kinetically tuned for achieving high-performance, the inherently low miscibility of donor and acceptor leads to spontaneous phase separation in the solid state, even at room temperature and in the dark. A theoretical calculation of the molecular parameters and construction of the spinodal phase diagrams highlight molecular incompatibilities between the donor and acceptor as a dominant mechanism for burn-in degradation, which is to date the major short-time loss reducing the performance and stability of organic solar cells. PMID:28224984

  19. Efficient photocatalytic degradation of gaseous formaldehyde by the TiO{sub 2}/tourmaline composites

    SciTech Connect

    Zhang, Gaoke Qin, Xi

    2013-10-15

    Graphical abstract: - Highlights: • The TiO{sub 2}/tourmaline composites were prepared by a sol–gel method. • The composites exhibited excellent photocatalytic activity and good stability. • The physicochemical property of tourmaline may be favor for the degradation of HCHO. • The mixed-phase of anatase and rutile TiO{sub 2} may be favor for the degradation of HCHO. - Abstract: The TiO{sub 2} supported tourmaline composites were prepared by a sol–gel method and used as a photocatalyst for the degradation of formaldehyde (HCHO). The composites were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), N{sub 2} adsorption–desorption, Fourier transform infrared (FT-IR) spectroscopy and UV–vis diffuse reflectance spectroscopy (UV–vis DRS). The results indicate that the mixed-phase of anatase and rutile exists in the TiO{sub 2}/tourmaline composites. The specific surface area of the TiO{sub 2}/tourmaline composites is much higher than that of the pure TiO{sub 2}. The TiO{sub 2}/tourmaline composites exhibited excellent photocatalytic activity for the degradation of HCHO, which was 6 times higher than that of the pure TiO{sub 2}. Moreover, the excellent photocatalytic activity of the composites was fully maintained after five photocatalytic cycles, which may be attributed to the physicochemical property of tourmaline and the mixed-phase of anatase and rutile in the TiO{sub 2}/tourmaline composites.

  20. Bacteria encapsulated in layered double hydroxides: towards an efficient bionanohybrid for pollutant degradation.

    PubMed

    Halma, Matilte; Mousty, Christine; Forano, Claude; Sancelme, Martine; Besse-Hoggan, Pascale; Prevot, Vanessa

    2015-02-01

    A soft chemical process was successfully used to immobilize Pseudomonas sp. strain ADP (ADP), a well-known atrazine (herbicide) degrading bacterium, within a Mg2Al-layered double hydroxide host matrix. This approach is based on a simple, quick and ecofriendly direct coprecipitation of metal salts in the presence of a colloidal suspension of bacteria in water. It must be stressed that by this process the mass ratio between inorganic and biological components was easily tuned ranging from 2 to 40. This ratio strongly influenced the biological activity of the bacteria towards atrazine degradation. The better results were obtained for ratios of 10 or lower, leading to an enhanced atrazine degradation rate and percentage compared to free cells. Moreover the biohybrid material maintained this biodegradative activity after four cycles of reutilization and 3 weeks storage at 4°C. The ADP@MgAl-LDH bionanohybrid materials were completely characterized by X-ray diffraction (XRD), FTIR spectroscopy, thermogravimetric analysis and scanning and transmission electronic microscopy (SEM and TEM) evidencing the successful immobilization of ADP within the inorganic matrix. This synthetic approach could be readily extended to other microbial whole-cell immobilization of interest for new developments in biotechnological systems.

  1. Efficient photo-catalytic degradation of malachite green using nickel tungstate material as photo-catalyst.

    PubMed

    Helaïli, N; Boudjamaa, A; Kebir, M; Bachari, K

    2017-01-10

    The present study focused on the evaluation of photo-catalytic and photo-electrochemical properties of the photo-catalyst based on nickel tungstate material prepared by a nitrate method through the degradation of malachite green (MG) dye's. The effect of catalyst loading and dye concentration was examined. Physico-chemical, optical, electrical, electrochemical, and photo-electrochemical properties of the prepared material were analyzed by X-ray diffraction (XRD), fourier transform-infrared spectroscopy (FTIR), BET analysis, optical reflectance diffuse (DR), scanning electron microscopy (SEM/EDX), electrical conductivity, cyclic voltammetry (CV), current intensity, mott-shottky, and nyquist. XRD revealed the formation of monoclinic structure with a small particle size. BET surface area of the sample was around 10 m(2)/g. The results show that the degradation of MG was more than 80%, achieved after 3 h of irradiation at pH 4.6 and with a catalyst loading of 75 mg. Also, it was found that the dye photo-degradation obeyed the pseudo-first order kinetic via Langmuir Hinshelwood model.

  2. Molecular characterization of Lactobacillus plantarum DMDL 9010, a strain with efficient nitrite degradation capacity.

    PubMed

    Fei, Yong-tao; Liu, Dong-mei; Luo, Tong-hui; Chen, Gu; Wu, Hui; Li, Li; Yu, Yi-gang

    2014-01-01

    Nitrites commonly found in food, especially in fermented vegetables, are potential carcinogens. Therefore, limiting nitrites in food is critically important for food safety. A Lactobacillus strain (Lactobacillus sp. DMDL 9010) was previously isolated from fermented vegetables by our group, and is not yet fully characterized. A number of phenotypical and genotypical approaches were employed to characterize Lactobacillus sp. DMDL 9010. Its nitrite degradation capacity was compared with four other Lactobacillus strains, including Lactobacillus casei subsp. rhamnosus 719, Lactobacillus delbrueckii subsp. bulgaricu 1.83, Streptococcus thermophilus 1.204, and lactobacillus plantarum 8140, on MRS medium. Compared to these four Lactobacillus strains, Lactobacillus sp. DMDL 9010 had a significantly higher nitrite degradation capacity (P<0.001). Based on 16S rDNA sequencing and sequence comparison, Lactobacillus sp. DMDL 9010 was identified as either Lactobacillus plantarum or Lactobacillus pentosus. To further identify this strain, the flanking regions (922 bp and 806 bp upstream and downstream, respectively) of the L-lactate dehydrogenase 1 (L-ldh1) gene were amplified and sequenced. Lactobacillus sp. DMDL 9010 had 98.92 and 76.98% sequence identity in the upstream region with L. plantarum WCFS1 and L. pentosus IG1, respectively, suggesting that Lactobacillu sp. DMDL 9010 is an L. plantarum strain. It was therefore named L. plantarum DMDL 9010. Our study provides a platform for genetic engineering of L. plantarum DMDL 9010, in order to further improve its nitrite degradation capacity.

  3. Cerium doped red mud catalytic ozonation for bezafibrate degradation in wastewater: Efficiency, intermediates, and toxicity.

    PubMed

    Xu, Bingbing; Qi, Fei; Sun, Dezhi; Chen, Zhonglin; Robert, Didier

    2016-03-01

    In this study, the performance of bezafibrate (BZF) degradation and detoxification in the aqueous phase using cerium-modified red mud (RM) catalysts prepared using different cerium sources and synthesis methods were evaluated. Experimental results showed that the surface cerium modification was responsible for the development of the catalytic activity of RM and this was influenced by the cerium source and the synthesis method. Catalyst prepared from cerium (IV) by precipitation was found to show the best catalytic activity in BZF degradation and detoxification. Reactive oxygen species including peroxides, hydroxyl radicals, and super oxide ions were identified in all reactions and we proposed the corresponding catalytic reaction mechanism for each catalyst that prepared from different cerium source and method. This was supported by the intermediates profiles that were generated upon BZF degradation. The surface and the structural properties of cerium-modified RM were characterized in detail by several analytical methods. Two interesting findings were made: (1) the surface texture (specific surface area and mesoporous volume) influenced the catalytic reaction pathway; and (2) Ce(III) species and oxygen vacancies were generated on the surface of the catalyst after cerium modification. This plays an important role in the development of the catalytic activity.

  4. Strong yellow electroluminescence from manganese-silicon-implanted silicon-dioxide layers

    NASA Astrophysics Data System (ADS)

    Novikov, Sergey; Ovchinnikov, Victor F.; Haerkoenen, Jaakko; Sinkkonen, Juha A.

    2001-05-01

    Room temperature (RT) electroluminescence (EL) was obtained for the first time from Mn enriched Si/SiO2 structure. Si+ or Ar+ stimulated knock-on implantation through 20 nm Mn film with the subsequent annealing was used for EL device fabrication. Devices exhibit bright emission band at the 2.06 eV. The position does neither depend on implanted ion dose nor annealing procedure. EL is visible by naked eye even at current density as low as 1.5x10-6 Acm-2. Continuous wave external quantum efficiency 1.1x10-3 and power efficiency 1.5x10-5 have been achieved.

  5. Ag loaded WO3 nanoplates for efficient photocatalytic degradation of sulfanilamide and their bactericidal effect under visible light irradiation.

    PubMed

    Zhu, Wenyu; Liu, Jincheng; Yu, Shuyan; Zhou, Yan; Yan, Xiaoli

    2016-11-15

    Sulfonamides (SAs) are extensively used antibiotics and their residues in the water bodies propose potential threat to the public. In this study, degradation efficiency of sulfanilamide (SAM), which is the precursor of SAs, using WO3 nanoplates and their Ag heterogeneous as photocatalysts was investigated. WO3 nanoplates with uniform size were synthesized by a facile one step hydrothermal method. Different amount of Ag nanoparticles (Ag NPs) were loaded onto WO3 nanoplates using a photo-reduction method to generate WO3/Ag composites. The physio-chemical properties of synthesized nanomaterials were systematically characterized. Photodegradation of SAM by WO3 and WO3/Ag composites was conducted under visible light irradiation. The results show that WO3/Ag composites performed much better than pure WO3 where the highest removal rate was 96.2% in 5h. Ag as excellent antibacterial agent also endows certain antibacterial efficiency to WO3, and 100% removal efficiency against Escherichia Coli and Bacillus subtilis could be achieved in 2h under visible light irradiation for all three WO3/Ag composites synthesized. The improved performance in terms of SAM degradation and antibacterial activity of WO3/Ag can be attributed to the improved electron-hole pair separation rate where Ag NPs act as effective electron trapper during the photocatalytic process.

  6. Degradation efficiency and mechanism of azo dye RR2 by a novel ozone aerated internal micro-electrolysis filter.

    PubMed

    Zhang, Xian-Bing; Dong, Wen-Yi; Sun, Fei-Yun; Yang, Wei; Dong, Jiao

    2014-07-15

    A newly designed ozone aerated internal micro-electrolysis filter (OIEF) was developed to investigate its degradation efficiencies and correlated reaction mechanisms of RR2 dye. Complete decolorization and 82% TOC removal efficiency were stably achieved in OIEF process. Based on the comprehensive experimental results, an empirical equation was proposed to illustrate the effects of initial dye concentration and ozone dosage rate on color removal. The results indicated that OIEF process could be operated at wide pH range without significant treatment efficiencies change, while the optimum pH for RR2 dye degradation was 9.0. There were 15, 8 and 6 kinds of identified intermediates during ozonation, IE and OIEF treatment processes, respectively. Less identified intermediates and their lower concentrations in OIEF may attribute to its rather excellent mineralization performance. It was found that ozonation, Fe(2+)/Fe(3+) catalyzed ozonation, the redox reactions of electro-reduction and electro-oxidation are the most important mechanisms in OIEF process. The catalytic effect of Fe(2+)/Fe(3+) would induce mutual conversion between dissolved Fe(2+) and Fe(3+), and then decrease the dissolution rate of ZVI. The excellent treatment performance proved that the OIEF process is one promising technology applied for reactive azo dyes and other refractory wastewater treatment.

  7. Efficient visible light-induced degradation of rhodamine B by W(NxS1−x)2 nanoflowers

    PubMed Central

    Liu, Peitao; Zhang, Jingyan; Gao, Daqiang; Ye, Weichun

    2017-01-01

    Here, W(NxS1−x)2 nanoflowers were fabricated by simple sintering process. Photocatalytic activity results indicated our fabricated N-doped WS2 nanoflowers shown outstanding photoactivity of degradating of rhodamine B with visible light. Which is attributed to the high separation efficiency of photoinduced electron–hole pairs, the broadening of the valence band (VB), and the narrowing of energy band gap. Meanwhile, our work provided a novel method to induce surface sulfur vacancies in crystals by introduing impurities atoms for enhancing their photodegradation. PMID:28106096

  8. Ascorbate-Promoted Surface Iron Cycle for Efficient Heterogeneous Fenton Alachlor Degradation with Hematite Nanocrystals.

    PubMed

    Huang, Xiaopeng; Hou, Xiaojing; Jia, Falong; Song, Fahui; Zhao, Jincai; Zhang, Lizhi

    2017-03-15

    This study reports the H2O2 activation with different hematite nanocrystals and ascorbate ions for the herbicide alachlor degradation at pH 5. We found that hematite nanoplates (HNPs) exposed with {001} facets exhibited better catalytic performance than hematite nanocubes (HNCs) exposed with {012} facets, which was attributed to the formation of inner-sphere iron-ascorbate complexes on the hematite facets. The 3-fold undercoordination Fe cations of {001} facet favors the formation of inner-sphere iron-ascorbate complexes, while the 5-fold undercoordination Fe cations of {012} facet has stereo-hindrance effect, disfavoring the complex formation. The surface area normalized alachlor degradation rate constant (23.3 × 10(-4) min(-1) L m(-2)) of HNPs-ascorbate Fenton system was about 2.6 times that (9.1 × 10(-4) min(-1) L m(-2)) of HNCs-ascorbate counterpart. Meanwhile, the 89.0% of dechlorination and 30.0% of denitrification in the HNPs-ascorbate Fenton system were also significantly higher than those (60.9% and 13.1%) of the HNCs-ascorbate one. More importantly, the reductive dissolution of hematite by ascorbate was strongly coupled with the subsequent H2O2 decomposition by surface bound ferrous ions through surface iron cycle on the hematite facets in the hematite-ascorbate Fenton systems. This coupling could significantly inhibit the conversion of surface bound ferrous ions to dissolved ones, and thus account for the stability of hematite nanocrystals. This work sheds light on the internal relationship between iron geochemical cycling and contaminants degradation, and also inspires us to utilize surface iron cycle of widely existent hematite for environmental remediation.

  9. Efficient photocatalytic degradation of rhodamine 6G with a quantum dot-metal organic framework nanocomposite.

    PubMed

    Kaur, Rajnish; Vellingiri, Kowsalya; Kim, Ki-Hyun; Paul, A K; Deep, Akash

    2016-07-01

    The hybrid structures of metal organic frameworks (MOFs) and nanoparticles may offer the realization of effective photocatalytic materials due to combined benefits of the porous and molecular sieving properties of MOF matrix and the functional characteristics of encapsulated nanoparticles. In this study, cadmium telluride (CdTe) quantum dots (QD) are conjugated with a europium-MOF for the synthesis of a novel nanocomposite material with photocatalytic properties. Successful synthesis of a QD/Eu-MOF nanocomposite was characterized with various spectroscopic and microscopic techniques. This QD/Eu-MOF is found to be an effective catalyst to complete the degradation of Rhodamine 6G dye within 50 min.

  10. Efficient photocatalytic degradation of phenol in aqueous solution by SnO2:Sb nanoparticles

    NASA Astrophysics Data System (ADS)

    Al-Hamdi, Abdullah M.; Sillanpää, Mika; Bora, Tanujjal; Dutta, Joydeep

    2016-05-01

    Photodegradation of phenol in the presence of tin dioxide (SnO2) nanoparticles under UV light irradiation is known to be an effective photocatalytic process. However, phenol degradation under solar light is less effective due to the large band gap of SnO2. In this study antimony (Sb) doped tin dioxide (SnO2) nanoparticles were prepared at a low temperature (80 °C) by a sol-gel method and studied for its photocatalytic activity with phenol as a test contaminant. The catalytic degradation of phenol in aqueous media was studied using high performance liquid chromatography and total organic carbon measurements. The change in the concentration of phenol affects the pH of the solution due to the by-products formed during the photo-oxidation of phenol. The photoactivity of SnO2:Sb was found to be a maximum for 0.6 wt.% Sb doped SnO2 nanoparticles with 10 mg L-1 phenol in water. Within 2 h of photodegradation, more than 95% of phenol could be removed under solar light irradiation.

  11. Effect of nitrate ions on the efficiency of sonophotochemical phenol degradation.

    PubMed

    Zaviska, François; Drogui, Patrick; El Hachemi, Errachid M; Naffrechoux, Emmanuel

    2014-01-01

    A sonophotochemical oxidation process has been used for the treatment of an aqueous solution of phenol. The aim of this work is to evaluate the effect of nitrate ions on hydroxyl radical production and on phenol oxidation. It has been demonstrated that ultrasound can produce NOx (nitrate and nitrite), with a production rate of 2.2 μM min(-1). The photolysis of nitrate can significantly improve the hydroxyl radical production. The apparent rate constant for hydroxyl radical production increased from 0.0015 min(-1) to 0.0073 min(-1) while increasing initial nitrate concentration from 0 to 0.5mM. The concentration of hydroxyl radical was directly proportional to the initial nitrate concentration. Using US/UV process, the apparent reaction rate constant of phenol degradation in the presence of nitrate reached 0.020 min(-1), which was relatively lower than the value obtained (0.027 min(-1)) in the absence of nitrate. It appeared that, nitrate ions can inhibit the sonochemical degradation of organic compounds such as phenol.

  12. An efficient fermentation method for the degradation of cyanogenic glycosides in flaxseed.

    PubMed

    Wu, C-F; Xu, X-M; Huang, S-H; Deng, M-C; Feng, A-J; Peng, J; Yuan, J-P; Wang, J-H

    2012-01-01

    Recently, flaxseed has become increasingly popular in the health food market because it contains a considerable amount of specific beneficial nutrients such as lignans and omega-3 fatty acids. However, the presence of cyanogenic glycosides (CGs) in flaxseed severely limits the exploitation of its health benefits and nutritive value. We, therefore, developed an effective fermentation method, optimised by response surface methodology (RSM), for degrading CGs with an enzymatic preparation that includes 12.5% β-glucosidase and 8.9% cyanide hydratase. These optimised conditions resulted in a maximum CG degradation level of 99.3%, reducing the concentration of cyanide in the flaxseed power from 1.156 to 0.015 mg g(-1) after 48 h of fermentation. The avoidance of steam heat to evaporate hydrocyanic acid (HCN) results in lower energy consumption and no environmental pollution. In addition, the detoxified flaxseed retained the beneficial nutrients, lignans and fatty acids at the same level as untreated flaxseed, and this method could provide a new means of removing CGs from other edible plants, such as cassava, almond and sorghum by simultaneously expressing cyanide hydratase and β-glucosidase.

  13. Efficient activation of peroxymonosulfate by magnetic Mn-MGO for degradation of bisphenol A.

    PubMed

    Du, Jiangkun; Bao, Jianguo; Liu, Ying; Ling, Haibo; Zheng, Han; Kim, Sang Hoon; Dionysiou, Dionysios D

    2016-12-15

    A heterogeneous manganese/magnetite/graphene oxide (Mn-MGO) hybrid catalyst was fabricated through the reduction of KMnO4 by ethylene glycol in the presence of magnetite/GO (MGO) particles. The Mn-MGO catalyst exhibited high efficacy and long-term stability in activating peroxymonosulfate (PMS) to generate sulfate radicals for the removal of bisphenol A (BPA) from water. The results of the batch experiments indicated that an increase in the catalyst dose and solution pH could enhance BPA degradation in the coupled Mn-MGO/PMS system. Regardless of the initial pH, the solution pH significantly dropped after the reaction, which was caused by catalytic PMS activation. The production of sulfate radicals and hydroxyl radicals was validated through radical quenching and electron paramagnetic resonances (EPR) tests. BPA degradation pathways were proposed on the basis of LC-MS and GC-MS analyses. Finally, a possible mechanism of catalytic PMS activation was proposed that involved electron transfer from MnO or Mn2O3 to PMS with the generation of sulfate radicals, protons and MnO2, as well as the simultaneous reduction of MnO2 by PMS.

  14. Multilayer white light-emitting organic electroluminescent device.

    PubMed

    Kido, J; Kimura, M; Nagai, K

    1995-03-03

    Organic electroluminescent devices are light-emitting diodes in which the active materials consist entirely of organic materials. Here, the fabrication of a white light-emitting organic electroluminescent device made from vacuum-deposited organic thin films is reported. In this device, three emitter layers with different carrier transport properties, each emitting blue, green, or red light, are used to generate white light. Bright white light, over 2000 candelas per square meter, nearly as bright as a fluorescent lamp, was successfully obtained at low drive voltages such as 15 to 16 volts. The applications of such a device include paper-thin light sources, which are particularly useful for places that require lightweight illumination devices, such as in aircraft and space shuttles. Other uses are a backlight for liquid crystal display as well as full color displays, achieved by combining the emitters with micropatterned color filters.

  15. Quantifying Solar Cell Cracks in Photovoltaic Modules by Electroluminescence Imaging

    SciTech Connect

    Spataru, Sergiu; Hacke, Peter; Sera, Dezso; Glick, Stephen; Kerekes, Tamas; Teodorescu, Remus

    2015-06-14

    This article proposes a method for quantifying the percentage of partially and totally disconnected solar cell cracks by analyzing electroluminescence images of the photovoltaic module taken under high- and low-current forward bias. The method is based on the analysis of the module's electroluminescence intensity distribution, applied at module and cell level. These concepts are demonstrated on a crystalline silicon photovoltaic module that was subjected to several rounds of mechanical loading and humidity-freeze cycling, causing increasing levels of solar cell cracks. The proposed method can be used as a diagnostic tool to rate cell damage or quality of modules after transportation. Moreover, the method can be automated and used in quality control for module manufacturers, installers, or as a diagnostic tool by plant operators and diagnostic service providers.

  16. White electroluminescence of n-ZnO:Al/p-diamond heterostructure devices

    NASA Astrophysics Data System (ADS)

    Yang, Can; Wang, Xiao-Ping; Wang, Li-Jun; Pan, Xiu-Fang; Li, Song-Kun; Jing, Long-Wei

    2013-08-01

    An n-ZnO:Al/p-boron-doped diamond heterostructure electroluminescent device is produced, and a rectifying behavior can be observed. The electroluminescence spectrum at room temperature exhibits two visible bands centred at 450 nm-485 nm (blue emission) and 570 nm-640 nm (yellow emission). Light emission with a luminance of 15 cd/m2 is observed from the electroluminescent device at a forward applied voltage of 85 V, which is distinguished from white light by the naked eye.

  17. Efficient degradation of Acid Orange 7 in aqueous solution by iron ore tailing Fenton-like process.

    PubMed

    Zheng, Jianming; Gao, Zhanqi; He, Huan; Yang, Shaogui; Sun, Cheng

    2016-05-01

    An effective method based on iron ore tailing Fenton-like process was studied for removing an azo dye, Acid Orange 7 (AO7) in aqueous solution. Five tailings were characterized by X-ray fluorescence spectroscope (XFS), Brunner-Emmet-Teller (BET) measurement, and Scanning Electron Microscope (SEM). The result of XFS showed that Fe, Si and Ca were the most abundant elements and some toxic heavy metals were also present in the studied tailings. The result of BET analysis indicated that the studied tailings had very low surface areas (0.64-5.68 m(2) g(-1)). The degradation efficiencies of AO7 were positively correlated with the content of iron oxide and cupric oxide, and not related with the BET surface area of the tailings. The co-existing metal elements, particularly Cu, might accelerate the heterogeneous Fenton-like reaction. The effects of other parameters on heterogeneous Fenton-like degradation of AO7 by a converter slag iron tailing (tailing E) which contains highest iron oxide were also investigated. The tailing could be reused 10 times without significant decrease of the catalytic capacity. Very low amount of iron species and almost undetectable toxic elements were leached in the catalytic degradation of AO7 by the tailing E. The reaction products were identified by gas chromatography-mass spectrometry and a possible pathway of AO7 degradation was proposed. This study not only provides an effective method for removing azo dyes in polluted water by employing waste tailings as Fenton-like catalysts, but also uses waste tailings as the secondary resource.

  18. Theoretical and material studies on thin-film electroluminescent devices

    NASA Technical Reports Server (NTRS)

    Summers, C. J.; Brennan, K. F.

    1986-01-01

    Electroluminescent materials and device technology were assessed. The evaluation strongly suggests the need for a comprehensive theoretical and experimental study of both materials and device structures, particularly in the following areas: carrier generation and multiplication; radiative and nonradiative processes of luminescent centers; device modeling; new device concepts; and single crystal materials growth and characterization. Modeling of transport properties of hot electrons in ZnSe and the generation of device concepts were initiated.

  19. Optical sensors and multisensor arrays containing thin film electroluminescent devices

    DOEpatents

    Aylott, Jonathan W.; Chen-Esterlit, Zoe; Friedl, Jon H.; Kopelman, Raoul; Savvateev, Vadim N.; Shinar, Joseph

    2001-12-18

    Optical sensor, probe and array devices for detecting chemical biological, and physical analytes. The devices include an analyte-sensitive layer optically coupled to a thin film electroluminescent layer which activates the analyte-sensitive layer to provide an optical response. The optical response varies depending upon the presence of an analyte and is detected by a photodetector and analyzed to determine the properties of the analyte.

  20. Efficient visible-light photocatalytic degradation of sulfadiazine sodium with hierarchical Bi₇O₉I₃under solar irradiation.

    PubMed

    Xu, MengMeng; Zhao, YaLei; Yan, QiShe

    2015-01-01

    Bi₇O₉I₃, a kind of visible-light-responsive photocatalyst, with hierarchical micro/nano-architecture was successfully synthesized by oil-bath heating method, with ethylene glycol as solvent, and applied to degrade sulfonamide antibiotics. The as-prepared product was characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), UV-visible diffuse reflection spectra and scanning electron microscopy (SEM). XRD and XPS tests confirmed that the product was indeed Bi₇O₉I₃. The result of SEM observation shows that the as-synthesized Bi₇O₉I₃ consists of a large number of micro-sheets with parallel rectangle structure. The optical test exhibited strong photoabsorption in visible light irradiation, with 617 nm of absorption edges. Moreover, the difference in the photocatalytic efficiency of as-prepared Bi₇O₉I₃ at different seasons of a whole year was investigated in this study. The chemical oxygen demand removal efficiency and concentration of NO(3)(-) and SO(4)(2-) of solution after reaction were also researched to confirm whether degradation of the pollutant was complete; the results indicated a high mineralization capacity of Bi₇O₉I₃. The as-synthesized Bi₇O₉I₃exhibits an excellent oxidizing capacity of sulfadiazine sodium and favorable stability during the photocatalytic reaction.

  1. Graphene-SnO2 composites for highly efficient photocatalytic degradation of methylene blue under sunlight.

    PubMed

    Seema, Humaira; Christian Kemp, K; Chandra, Vimlesh; Kim, Kwang S

    2012-09-07

    Graphene sheets decorated with SnO(2) nanoparticles (RGO-SnO(2)) were prepared via a redox reaction between graphene oxide (GO) and SnCl(2). Graphene oxide (GO) was reduced to graphene (RGO) and Sn(2+) was oxidized to SnO(2) during the redox reaction, leading to a homogeneous distribution of SnO(2) nanoparticles on RGO sheets. The scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images show uniform distribution of the nanoparticles on the RGO surface and high-resolution transmission electron microscopy (HRTEM) shows an average particle size of 3-5 nm. The RGO-SnO(2) composite showed an enhanced photocatalytic degradation activity for the organic dye methylene blue under sunlight compared to bare SnO(2) nanoparticles. This result leads us to believe that the RGO-SnO(2) composite could be used in catalytic photodegradation of other organic dyes.

  2. Preparation of immobilized coating Fenton-like catalyst for high efficient degradation of phenol.

    PubMed

    Wang, Jiankang; Yao, Zhongping; Wang, Yajing; Xia, Qixing; Chu, Huiya; Jiang, Zhaohua

    2017-03-06

    In this study, solid acid amorphous Fe3O4/SiO2 ceramic coating decorated with sulfur on Q235 carbon steel as Fenton-like catalyst for phenol degradation was successfully prepared by plasma electrolytic oxidation (PEO) in silicate electrolyte containing Na2S2O8 as sulfur source. The surface morphology and phase composition were characterized by SEM, EDS, XRD and XPS analyses. NH3-TPD was used to evaluate surface acidity of PEO coating. The results indicated that sulfur decorated amorphous Fe3O4/SiO2 ceramic coatings with porous structure and higher acid strength had the similar pore size and the surface became more and more uneven with the increase of Na2S2O8 in the silicate electrolyte. The Fenton-like catalytic activity of sulfur decorated PEO coatings was also evaluated. In contrast to negligible catalytic activity of sulfur undecorated PEO coating, catalytic activity of sulfur decorated PEO coating was excellent and PEO coating prepared with 3.0 g Na2S2O8 had the highest catalytic activity which could degrade 99% of phenol within 8 min under circumneutral pH. The outstanding performance of sulfur decorated PEO coating was attributed to strong acidic microenvironment and more Fe(2+) on the surface. The strong acid sites played a key factor in determining catalytic activity of catalyst. In conclusion, rapid phenol removal under circumneutral pH and easier separation endowed it potential application in wastewater treatment. In addition, this strategy of preparing immobilized solid acid coating could provide guidance for designing Fenton-like catalyst with excellent catalytic activity and easier separation.

  3. Efficient degradation of rhodamine B using modified graphite felt gas diffusion electrode by electro-Fenton process.

    PubMed

    Tian, Jiangnan; Olajuyin, Ayobami Matthew; Mu, Tingzhen; Yang, Maohua; Xing, Jianmin

    2016-06-01

    The electro-Fenton (EF) process treatment of 0.1-M (rhodamine B) RhB solution was studied with different graphite cathode materials, and graphite felt (GF) was selected as a promising material in further investigation. Then, the degradation performances of gas diffusion electrode (GDE) and graphite felt (GF) were compared, and GDE was confirmed to be more efficient in RhB removal. The operational parameters such as Fe(2+) dosage and current density were optimized, and comparison among different modified methods-polytetrafluoroethylene-carbon black (PTFE-CB), polytetrafluoroethylene-carbon nanotube (PTFE-CNT), electrodeposition-CB, and electrodeposition-CNT-showed 98.49 % RhB removal by PTFE-CB-modified cathode in 0.05 M Na2SO4 at a current density of 50 A/m(2) and an air flow rate of 1 L/min after 20 min. Meanwhile, after cathode modified by PTFE-CB, the mineralization efficiency and mineralization current efficiency performed absolutely better than the pristine one. Cyclic voltammograms, SEM images, contact angles, and BET surface area were carried out to demonstrate stronger current responses and higher hydrophilicity of GF after modified. The value of biochemical oxygen demand/chemical oxygen demand (BOD5/COD) increased from 0.049 to 0.331 after 90-min treatment, suggesting the solution was biodegradable, and the modified cathode was confirmed to be stable after ten circle runs. Finally, a proposed degradation pathway of RhB was put forward.

  4. Pretreatment combining ultrasound and sodium percarbonate under mild conditions for efficient degradation of corn stover.

    PubMed

    Nakashima, Kazunori; Ebi, Yuuki; Kubo, Masaki; Shibasaki-Kitakawa, Naomi; Yonemoto, Toshikuni

    2016-03-01

    Ultrasound (US) can be used to disrupt microcrystalline cellulose to give nanofibers via ultrasonic cavitation. Sodium percarbonate (SP), consisting of sodium carbonate and hydrogen peroxide, generates highly reactive radicals, which cause oxidative delignification. Here, we describe a novel pretreatment technique using a combination of US and SP (US-SP) for the efficient saccharification of cellulose and hemicellulose in lignocellulosic corn stover. Although US-SP pretreatment was conducted under mild condition (i.e., at room temperature and atmospheric pressure), the pretreatment greatly increased lignin removal and cellulose digestibility. We also determined the optimum US-SP treatment conditions, such as ultrasonic power output, pretreatment time, pretreatment temperature, and SP concentration for an efficient cellulose saccharification. Moreover, xylose could be effectively recovered from US-SP pretreated biomass without the formation of microbial inhibitor furfural.

  5. Immobilization of degradative bacteria in polyurethane-based foams: embedding efficiency and effect on bacterial activity

    SciTech Connect

    Wilde, E.W.; Radway, J.C.; Hazen, T.C.; Hermann, P.

    1996-09-03

    The immobilization of TCE-degrading bacterium Burkholderia cepacia was evaluated using hydrophilic polyurethane foam. The influence of several foam formulation parameters upon cell retention was examined. Surfactant type was a major determinant of retention, with a lecithin- based compound retaining more cells than pluronic or silicone based surfactants. Excessive amounts of surfactant led to increased washout of bacteria. Increasing the biomass concentration from 4.8% to 10.5% caused fewer cells to be washed out. Embedding at reduced temperature did not significantly affect retention, while the use of a silane binding agent gave inconsistent results. The optimal formulation retained all but 0.2% of total embedded cells during passage of 2 liters of water through columns containing 2 g of foam. All foam formulations tested reduced the culturability of embedded cells by several orders of magnitude. However, O{sub 2} and CO{sub 2} evolution rates of embedded cells were never less than 50% of unembedded cells. Nutrient amendments stimulated an increase in cell volume and ribosomal activity as indicated by hybridization studies using fluorescently labeled ribosomal probes. these results indicated that, although immobilized cells were nonculturable, they were metabolically active and thus could be used for biodegradation of toxic compounds.

  6. Highly efficient photocatalytic degradation of organic dyes by Cu doped ZnO nanostructures.

    PubMed

    Kuriakose, Sini; Satpati, Biswarup; Mohapatra, Satyabrata

    2015-10-14

    Copper doped ZnO nanostructures have been synthesized by a facile wet chemical method. Structural properties of as-synthesized nanomaterials have been studied by X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) with energy dispersive X-ray spectroscopy, while UV-visible absorption spectroscopy and Raman spectroscopy have been used to study their optical properties. Sunlight driven photocatalytic degradation of methylene blue (MB) and methyl orange (MO) dyes in water was used to evaluate the photocatalytic activities of Cu doped ZnO nanostructures using UV-visible absorption spectroscopy. The results showed that there is an optimum Cu doping level which leads to the highly enhanced photocatalytic activity of Cu doped ZnO nanostructures, as compared to pure ZnO nanostructures. A mechanism for the enhanced photocatalytic activity of Cu-ZnO nanostructures is tentatively proposed. The enhanced photocatalytic activity of Cu-ZnO nanostructures is attributed to the combined effects of improved separation of photogenerated charge carriers due to optimal Cu doping in ZnO nanostructures and the formation of ZnO-CuO nanoheterojunctions.

  7. Sprayed nanostructured TiO2 films for efficient photocatalytic degradation of textile azo dye.

    PubMed

    Stambolova, Irina; Shipochka, Capital Em Cyrillicaria; Blaskov, Vladimir; Loukanov, Alexandrе; Vassilev, Sasho

    2012-12-05

    Spray pyrolysis procedure for preparation of nanostructured TiO(2) films with higher photocatalytic effectiveness and longer exploitation life is presented in this study. Thin films of active nanocrystalline TiO(2) were obtained from titanium isopropoxide, stabilized with acetyl acetone and characterized by X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM) and X-ray diffraction (XRD). The activity of sprayed nanostructured TiO(2) is tested for photocatalytic degradation of Reactive Black 5 dye with concentrations up to 80 ppm. Interesting result of the work is the reduction of toxicity after photocatalytic treatment of RB5 with TiO(2), which was confirmed by the lower percentage of mortality of Artemia salina. It was proved that the film thickness, conditions of post deposition treatment and the type of the substrate affected significantly the photocatalytic reaction. Taking into account that the parameters are interdependent, it is necessary to optimize the preparation conditions in order to synthesize photocatalytic active films.

  8. Highly efficient visible light mediated azo dye degradation through barium titanate decorated reduced graphene oxide sheets

    NASA Astrophysics Data System (ADS)

    Rastogi, Monisha; Kushwaha, H. S.; Vaish, Rahul

    2016-03-01

    This study investigates BaTiO3 decorated reduced graphene oxide sheets as a potential visible light active catalyst for dye degradation (Rhodamine B). The composites were prepared through conventional hydrothermal synthesis technique using hydrazine as a reducing agent. A number of techniques have been employed to affirm the morphology, composition and photocatalytic properties of the composites; these include UV-visible spectrophotoscopy that assisted in quantifying the concentration difference of Rhodamine B. The phase homogeneity of the composites was examined through x-ray powder diffraction (XRD) and high resolution transmission electron microscopy (HRTEM) was employed to confirm the orientation of the BaTiO3 particles over the reduced graphene oxide sheets. Photoluminescence (PL) emission spectra assisted in determining the surface structure and excited state of the catalyst. Fourier transformed-infrared (FTIR) spectra investigated the vibrations and adsorption peak of the composites, thereby ascertaining the formation of reduced graphene oxide. In addition, diffuse reflectance spectroscopy (DRS) demonstrated an enhanced absorption in the visible region. The experimental investigations revealed that graphene oxide acted as charge collector and simultaneously facilitated surface adsorption and photo-sensitization. It could be deduced that BaTiO3-reduced graphene oxide composites are of significant interest the field of water purification through solar photocatalysis. [Figure not available: see fulltext.

  9. RAPID COMMUNICATION: Self-quenching of excited europium ions in Eu(DBM)3bath-based organic electroluminescent devices

    NASA Astrophysics Data System (ADS)

    Liang, C. J.; Wong, T. C.; Hung, L. S.; Lee, S. T.; Hong, Z. R.; Li, W. L.

    2001-06-01

    Luminance-current characteristics of organic electroluminescent devices based on the europium complex of europium(dibenzoylmethanato)3 (bathophenanthroline) (Eu(DBM)3bath) have been investigated. Transient measurements were carried out to study the decay process of excited Eu3+ ions. A comparison of experimental data and theoretical calculation shows that biexcitonic quenching among the excited Eu3+ ions is an important channel in their decay process, and this quenching process is a primary cause for our observation of a rapid decrease in quantum efficiency with increasing current density. Extending the recombination zone is found to be beneficial to reducing this defective effect. The mechanism of the quenching process is also discussed.

  10. Extremely low amplified spontaneous emission threshold and blue electroluminescence from a spin-coated octafluorene neat film

    NASA Astrophysics Data System (ADS)

    Kim, D.-H.; Sandanayaka, A. S. D.; Zhao, L.; Pitrat, D.; Mulatier, J. C.; Matsushima, T.; Andraud, C.; Ribierre, J. C.; Adachi, C.

    2017-01-01

    We report on the photophysical, amplified spontaneous emission (ASE), and electroluminescence properties of a blue-emitting octafluorene derivative in spin-coated films. The neat film shows an extremely low ASE threshold of 90 nJ/cm2, which is related to its high photoluminescence quantum yield of 87% and its large radiative decay rate of 1.7 × 109 s-1. Low-threshold organic distributed feedback semiconductor lasers and fluorescent organic light-emitting diodes with a maximum external quantum efficiency as high as 4.4% are then demonstrated, providing evidence that this octafluorene derivative is a promising candidate for organic laser applications.

  11. Highly efficient photocatalytic degradation of methylene blue by PoPD/TiO2 nanocomposite

    PubMed Central

    Dong, Wenping; Cui, Guanwei; Ren, Zongming

    2017-01-01

    The poly-o-phenylenediamine (PoPD)/TiO2 nanocomposite was successfully synthesized via ‘in situ’ oxidative polymerization method. The modified photocatalysts were characterized by BET, scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier-transform infrarad spectra (FT-IR), thermogravimrtic analysis (TGA), X-ray photoelectron spectroscopy (XPS), Ultraviolet-visible diffuse reflectance spectrum (UV-Vis DRS) and Photocurrent Test. The results showed that the PoPD exists on the surface of TiO2, the presence of PoPD does not impact on the lattice structure and grain size of TiO2, and the presence of PoPD enhances the visible response and photoelectric property. The photocatalytic degradation of methylene blue (MB) was chosen as a model reaction to evaluate the photocatalytic activities of TiO2 and PoPD/TiO2. The optimal preparation condition was the molar ratio of oPD to TiO2 = 3:1, HCl concentration = 1.2 mol/L, the molar ratio of APS to oPD = 1:1. The apparent first-order rate constant kapp of PoPD/TiO2 nanocomposite was 0.0098 min-1, which is 6 times higher than TiO2 (0.0016 min-1). Meanwhile, the PoPD/TiO2 nanocomposites showed excellent photocatalytic stability, and the photocatalytic stability was depended on the stability of structure. At last, the photocatalytic mechanism of POPD/TiO2 nanocomposites was also proposed based on the synergetic effect between TiO2 and PoPD. PMID:28329007

  12. Highly efficient photocatalytic degradation of methylene blue by PoPD/TiO2 nanocomposite.

    PubMed

    Yang, Chuanxi; Zhang, Ming; Dong, Wenping; Cui, Guanwei; Ren, Zongming; Wang, Weiliang

    2017-01-01

    The poly-o-phenylenediamine (PoPD)/TiO2 nanocomposite was successfully synthesized via 'in situ' oxidative polymerization method. The modified photocatalysts were characterized by BET, scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier-transform infrarad spectra (FT-IR), thermogravimrtic analysis (TGA), X-ray photoelectron spectroscopy (XPS), Ultraviolet-visible diffuse reflectance spectrum (UV-Vis DRS) and Photocurrent Test. The results showed that the PoPD exists on the surface of TiO2, the presence of PoPD does not impact on the lattice structure and grain size of TiO2, and the presence of PoPD enhances the visible response and photoelectric property. The photocatalytic degradation of methylene blue (MB) was chosen as a model reaction to evaluate the photocatalytic activities of TiO2 and PoPD/TiO2. The optimal preparation condition was the molar ratio of oPD to TiO2 = 3:1, HCl concentration = 1.2 mol/L, the molar ratio of APS to oPD = 1:1. The apparent first-order rate constant kapp of PoPD/TiO2 nanocomposite was 0.0098 min-1, which is 6 times higher than TiO2 (0.0016 min-1). Meanwhile, the PoPD/TiO2 nanocomposites showed excellent photocatalytic stability, and the photocatalytic stability was depended on the stability of structure. At last, the photocatalytic mechanism of POPD/TiO2 nanocomposites was also proposed based on the synergetic effect between TiO2 and PoPD.

  13. Self-Organized TiO₂-MnO₂ Nanotube Arrays for Efficient Photocatalytic Degradation of Toluene.

    PubMed

    Nevárez-Martínez, María C; Kobylański, Marek P; Mazierski, Paweł; Wółkiewicz, Jolanta; Trykowski, Grzegorz; Malankowska, Anna; Kozak, Magda; Espinoza-Montero, Patricio J; Zaleska-Medynska, Adriana

    2017-03-31

    Vertically oriented, self-organized TiO₂-MnO₂ nanotube arrays were successfully obtained by one-step anodic oxidation of Ti-Mn alloys in an ethylene glycol-based electrolyte. The as-prepared samples were characterized by scanning electron microscopy (SEM), energy-dispersive X-ray spectroscopy (EDX), UV-Vis absorption, photoluminescence spectroscopy, X-ray diffraction (XRD), and micro-Raman spectroscopy. The effect of the applied potential (30-50 V), manganese content in the alloy (5-15 wt. %) and water content in the electrolyte (2-10 vol. %) on the morphology and photocatalytic properties was investigated for the first time. The photoactivity was assessed in the toluene removal reaction under visible light, using low-powered LEDs as an irradiation source (λmax = 465 nm). Morphology analysis showed that samples consisted of auto-aligned nanotubes over the surface of the alloy, their dimensions were: diameter = 76-118 nm, length = 1.0-3.4 μm and wall thickness = 8-11 nm. It was found that the increase in the applied potential led to increase the dimensions while the increase in the content of manganese in the alloy brought to shorter nanotubes. Notably, all samples were photoactive under the influence of visible light and the highest degradation achieved after 60 min of irradiation was 43%. The excitation mechanism of TiO₂-MnO₂ NTs under visible light was presented, pointing out the importance of MnO₂ species for the generation of e(-) and h⁺.

  14. Efficiency degradation due to tracking errors for point focusing solar collectors

    NASA Technical Reports Server (NTRS)

    Hughes, R. O.

    1978-01-01

    An important parameter in the design of point focusing solar collectors is the intercept factor which is a measure of efficiency and of energy available for use in the receiver. Using statistical methods, an expression of the expected value of the intercept factor is derived for various configurations and control law implementations. The analysis assumes that a radially symmetric flux distribution (not necessarily Gaussian) is generated at the focal plane due to the sun's finite image and various reflector errors. The time-varying tracking errors are assumed to be uniformly distributed within the threshold limits and allows the expected value calculation.

  15. BiOCl/TiO2 heterojunction network with high energy facet exposed for highly efficient photocatalytic degradation of benzene

    NASA Astrophysics Data System (ADS)

    Wang, Xiaoxia; Ni, Qian; Zeng, Dawen; Liao, Guanglan; Wen, Yanwei; Shan, Bin; Xie, Changsheng

    2017-02-01

    Benzene is known for its difficulty of degradation as well as enormous harmful intermediates released during degradation, which arouses urgent demand for highly efficient photocatalysts as solution. In this paper, we fabricated a 3D hierarchical structure of 2D single crystalline BiOCl nanosheets with high energy (001) facets exposed using 1D single-crystalline TiO2 nanorod array as supporting framework and charge transfer tunnel. Compared to releasing various intermediates by the TiO2 nanorod array during photocatalysis, the BiOCl/TiO2 heterojunction network exhibited phenomenal photocatalytic activity for fully degradation of 150 ppm gaseous benzene within 80 min, yielding stoichiometric 900 ppm CO2 with excellent repeat stability. The outstanding photocatalytic performance is ascribed to the charge separation across the BiOCl/TiO2 interface, which is evidenced by density functional theory (DFT) based calculation as well as photoluminescence and photocurrent experiments. Furthermore, the internal electric fields of BiOCl and TiO2 nanorod high-speed transferring tunnel also make contributes to the charge separation. Then the reserved holes at (001) facets of BiOCl, which is believed to be the major actives for gaseous photocatalysis, can migrate to the surface oxygen vacancies for decomposing benzene with oxygen molecules. In addition, the scavenging effect due to oxygen vacancies on (001) facet of BiOCl is also responsible for the excellent and sustainable photocatalytic activity. This work reveals an approach for novel photocatalysts by building band-aligned 3D heterojunction network with high energy facet exposed as active sites.

  16. Efficient visible-light photocatalytic degradation system assisted by conventional Pd catalysis

    PubMed Central

    Yu, Yanlong; He, Tao; Guo, Lingju; Yang, Yajun; Guo, Limei; Tang, Yue; Cao, Yaan

    2015-01-01

    Different approaches like doping and sensitization have been used to develop photocatalysts that can lead to high reactivity under visible-light illumination, which would allow efficient utilization of solar irradiation and even interior lighting. We demonstrated a conceptually different approach by changing reaction route via introducing the idea of conventional Pd catalysis used in cross-coupling reactions into photocatalysis. The –O–Pd–Cl surface species modified on Ni-doped TiO2 can play a role the same as that in chemical catalysis, resulting in remarkably enhanced photocatalytic activity under visible-light irradiation. For instance, Pd/Ni-TiO2 has much higher activity than N-TiO2 (about 3 ~ 9 times for all of the 4-XP systems) upon irradiation with wavelength of 420 nm. The catalytically active Pd(0) is achieved by reduction of photogenerated electrons from Ni-TiO2. Given high efficient, stable Pd catalysts or other suitable chemical catalysts, this concept may enable realization of the practical applications of photocatalysis. PMID:25825365

  17. Efficient degradation of phenol using iron-montmorillonite as a Fenton catalyst: Importance of visible light irradiation and intermediates.

    PubMed

    Wei, Xipeng; Wu, Honghai; He, Guangping; Guan, Yufeng

    2017-01-05

    Iron-montmorillonite (Fe-Mt) with delaminated structures was synthesized via the introduction of iron oxides into Na-montmorillonite. Fe-Mt showed significant increases in the available iron content, surface area and pore volume, along with a slight increase in the basal spacing from d001=1.26 (Na-Mt) to 1.53nm (Fe-Mt). The Fenton process was efficient for phenol removal using Fe-Mt as a catalyst under visible light irradiation, and the process had two-stage pseudo-first order kinetics. The overall reaction had a higher degradation rate even when it was only irradiated with visible light for the first 40min period. Further investigation confirmed that the irradiation increased the presence of certain intermediates. Among them, 1,4-benzoquinone, hydroquinone, and catechol all enhanced the Fenton reaction rates. Either catechol or hydroquinone was added to the Fenton system with Fe-Mt/H2O2 with or without visible light irradiation, and they both accelerated phenol degradation because catechol and hydroquinone are capable of reductively and effectively transforming Fe(III) into Fe(II). The concentrations of dissolved total Fe increased with the increase in the oxalic acid concentration, which can strongly chelate Fe(III). Hence, iron was released from Fe-Mt, and reductive transformation played an important role in promoting the Fenton reaction process for phenol removal.

  18. Efficient adsorption and photocatalytic degradation of Rhodamine B under visible light irradiation over BiOBr/montmorillonite composites.

    PubMed

    Xu, Chengqun; Wu, Honghai; Gu, Feng Long

    2014-06-30

    BiOBr/Na-montmorillonite composites (BiOBr-Mt) were prepared under laboratory ambient conditions by using the surfactant cetyltrimethylammonium bromide (CTAB) as the Br source and template, and the as-synthesized samples were characterized by XRD, FT-IR, FESEM, TEM equipped with EDS, BET and UV-vis DRS techniques. Interestingly, the particle size of BiOBr can be controlled by CTAB modified Na-montmorillonite. The photocatalytic activity of the as-prepared was further evaluated by decomposition of Rhodamine B (RhB) under visible light irradiation; the obtained results revealed that the BiOBr-Mt sample had strong photoabsorption in the visible light region. It has higher photocatalytic activity than pure BiOBr alone. There exists an efficient adsorption for RhB onto BiOBr-Mt contrast to that onto the pure BiOBr. The adsorption processes can be well described by pseudo-second-order kinetic model; meanwhile, the adsorption behaviors can be described by both Freundlich and Langmuir equations but the former was better. Additionally, the relevant adsorption and degradation mechanisms were explored and the possible mechanisms were presented. The photocatalytic activity has high effect both in acidic and basic conditions on the degradation reaction but in acidic condition is more favorable. After three recycles, BiOBr-Mt did not exhibit any significant loss of photocatalytic activity, confirming the photocatalyst was essentially stable.

  19. Humic acid degradation by the synthesized flower-like Ag/ZnO nanostructure as an efficient photocatalyst.

    PubMed

    Ghaneian, Mohammad Taghi; Morovati, Pouran; Ehrampoush, Mohammad Hassan; Tabatabaee, Masoumeh

    2014-01-01

    Nano-sized flower-like Ag/ZnO was synthesized by a simple method using zinc acetate and silver acetate under hydrothermal condition. Powder X-ray diffraction (PXRD) and transmission electron microscopy (TEM) were used to characterize the structure and morphology of the synthesized powder. Nano flower-like Ag/ZnO was used as a photocatalyst for degradation of humic acid in aqueous solution. The disappearance of HA was analyzed by measuring the absorbance of sample at special wavelength (254 nm). The effects of various parameters such as amount of photocatalyst, pH, initial humic acid concentration and irradiation time on degradation rate were systematically investigated. Photodegradation efficiency was small when the photolysis was carried out in the absence of Ag/ZnO and it was also negligible in the absence of light. Approximately 70% of humic acid (50 mg/L) has been eliminated after 40 minutes in the presences of catalyst (catalyst dose o.6 g/L and pH =7) and UVA irradiation. While, 100% of humic acid has been eliminated with solar irradiation.

  20. ZrO2/MoS2 heterojunction photocatalysts for efficient photocatalytic degradation of methyl orange

    NASA Astrophysics Data System (ADS)

    Prabhakar Vattikuti, Surya Veerendra; Byon, Chan; Reddy, Chandragiri Venkata

    2016-10-01

    We report a simple solution-chemistry approach for the synthesis of ZrO2/MoS2 hybrid photocatalysts, which contain MoS2 as a cocatalyst. The material is usually obtained by a wet chemical method using ZrO(NO3)2 or (NH4)6Mo7O24·4H2O and C8H6S as precursors. The structural features of obtained materials were characterized by X-ray diffraction (XRD), highresolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), thermal analysis (TG-DTA), N2 adsorption-desorption, and photoluminescence (PL). The influence on the photocatalytic activity of the MoS2 cocatalyst concentration with ZrO2 nanoparticles was studied. The MZr-2 hybrid sample had the highest photocatalytic activity for the degradation of methyl orange (MO), which was 8.45 times higher than that of pristine ZrO2 ascribed to high specific surface area and absorbance efficiency. Recycling experiments revealed that the reusability of the MZr-2 hybrid was due to the low photocorrosive effect and good catalytic stability. PL spectra confirmed the electronic interaction between ZrO2 and MoS2. The photoinduced electrons could be easily transferred from CB of ZrO2 to the MoS2 cocatalyst, which facilitate effective charge separation and enhanced the photocatalytic degradation in the UV region. A photocatalytic mechanism is proposed. It is believed that the ZrO2/MoS2 hybrid structure has promise as a photocatalyst with low cost and high efficiency for photoreactions.

  1. Reduced sampling efficiency causes degraded Vernier hyperacuity with normal aging: Vernier acuity in position noise.

    PubMed

    Li, Roger W; Brown, Brian; Edwards, Marion H; Ngo, Charlie V; Chat, Sandy W; Levi, Dennis M

    2012-01-01

    Vernier acuity, a form of visual hyperacuity, is amongst the most precise forms of spatial vision. Under optimal conditions Vernier thresholds are much finer than the inter-photoreceptor distance. Achievement of such high precision is based substantially on cortical computations, most likely in the primary visual cortex. Using stimuli with added positional noise, we show that Vernier processing is reduced with advancing age across a wide range of noise levels. Using an ideal observer model, we are able to characterize the mechanisms underlying age-related loss, and show that the reduction in Vernier acuity can be mainly attributed to the reduction in efficiency of sampling, with no significant change in the level of internal position noise, or spatial distortion, in the visual system.

  2. Correlation between excitation of Alfven modes and degradation of ICRF heating efficiency in TFTR

    SciTech Connect

    Bernabei, S.; Chang, Z.; Darrow, D.

    1997-05-01

    Alfven modes are excited by energetic ions in TFTR during intense minority ICRF heating. There is a clear threshold in rf power above which the modes are destabilized. The net effect of these modes is the increase of the fast ion losses, with an associated saturation of the ion tail energy and of the efficiency of the heating. Typically, several modes are excited with progressive n-numbers, with frequencies in the neighborhood of 200 kHz. Results suggest that Energetic Particle Modes (EPM), mostly unseen by the Mirnov coils, are generated near the center and are responsible for the ion losses. Stronger global TAE modes, which are destabilized by the stream of displaced fast ions, appear responsible only for minor losses.

  3. Degradation efficiencies of azo dye Acid Orange 7 by the interaction of heat, UV and anions with common oxidants: persulfate, peroxymonosulfate and hydrogen peroxide.

    PubMed

    Yang, Shiying; Wang, Ping; Yang, Xin; Shan, Liang; Zhang, Wenyi; Shao, Xueting; Niu, Rui

    2010-07-15

    In this paper, the degradation of azo dye Acid Orange 7 (AO7) by three common peroxides (persulfate (PS), peroxymonosulfate (PMS) or hydrogen peroxide (H(2)O(2))) under various activation conditions, i.e., heat (25-80 degrees C), UV light (254 nm), or anions (SO(4)(2-), NO(3)(-), CO(3)(2-), HCO(3)(-), HPO(4)(2-), and Cl(-)), was investigated. The order of AO7 degradation efficiencies by heat activation is PS>PMS>H(2)O(2). PS oxidation activated by heat (>50 degrees C) is an effective degradation technology, while PMS and H(2)O(2) are hardly activated. When assisted by UV, peroxides could all be activated and degrade AO7 quickly. The order is PS>H(2)O(2)>PMS. We activated peroxides, for the first time, by using some anions and compared the subsequently degradation efficiencies of AO7. It was found that PMS could be activated by some anions, but PS and H(2)O(2) cannot. The activation efficiencies of PMS by SO(4)(2-) and NO(3)(-) are negligible, whereas remarkable by HCO(3)(-), HPO(4)(2-), Cl(-) and CO(3)(2-). For HCO(3)(-), HPO(4)(2-) and Cl(-), the activation efficiencies become higher with the increase of anion concentration. For CO(3)(2-), however, the activation efficiency is higher at lower concentration.

  4. Luminescent Photoelectrochemical Cells. 6. Spatial Aspects of the Photoluminescence and Electroluminescence of Cadmium Selenide Electrodes.

    DTIC Science & Technology

    1981-10-06

    NO. 8 Luminescent Photoelectrochemical Cells. 6. Spatial Aspects of the Photoluminescence and Electroluminescence of Cadmium Selenide Electrodes by...Photoelectrochemistry; photoluminescence; electroluminescence; cadmium selenide electrodes 20. ABSTRACT (Continue. on reverse aide flnocosee7 and...REPORT A PERIOD COVERED Luminescent Photoelectrochemical Cells. 6.1 1 Spatial Aspects of the Photoluminescence and Elect roluminescence of Cadmium

  5. Electroluminescence and cathodoluminescence from polyethylene and polypropylene films: Spectra reconstruction from elementary components and underlying mechanisms

    SciTech Connect

    Qiao, B.; Teyssedre, G.; Laurent, C.

    2016-01-14

    The mechanisms of electroluminescence from large band gap polymers used as insulation in electric components are still under debate. It becomes important to unravel the underlying physics of the emission because of increasing thermo-electric stress and a possible relationship between electroluminescence and field withstand. We report herein on the cathodoluminescence spectra of polyethylene and polypropylene films as a way to uncover the nature of its contributions to electroluminescence emission. It is shown that spectra from the two materials are structured around four elementary components, each of them being associated with a specific process contributing to the overall emission with different weights depending on excitation conditions and on materials. The cathodoluminescence and electroluminescence spectra of each material are reconstructed from the four spectral components and their relative contribution are discussed. It is shown that electroluminescence from polyethylene and polypropylene has the same origin pointing towards generic mechanisms in both.

  6. [Photoluminescent and electroluminescent properties of a new rare earth terbium complex].

    PubMed

    Wang, Li; Zhang, Xi-qing; Lin, Peng; Xiong, De-pin; Huang, Shi-hua; Yu, Tian-zhi

    2004-06-01

    Pure green and narrowbandwidth emission from an organic electroluminescent device was presented by using arare earth terbium (III) complex as the emissive layer. The structure of the device was ITO/PVK/Tb/PBD/LiF/Al. It was proved that this new kind of rare earth complex has excellent photoluminescent and electroluminescent properties. The electroluminescent spectrum of the device was very similar to that of the terbium (III) complex film. The electroluminescent mechanism of the device was proposed by measuring and analyzing the spectra and electroluminescent property of the device. It is proposed that the excited carriers of PVK and PBD were captured by Tb3+ and light was emitted when the electrons and holes recombined at Tb3+.

  7. Efficient degradation of rice straw in the reactors packed by carbon fiber textiles.

    PubMed

    Sasaki, Kengo; Morita, Masahiko; Hirano, Shin-Ichi; Sasaki, Daisuke; Ohmura, Naoya; Igarashi, Yasuo

    2010-07-01

    We have reported for the first time that agricultural and cellulosic waste, i.e., rice straw was directly applied to methanogenic bioreactors containing carbon fiber textiles (CFT) as supporting material. Addition of CFT to the methanogenic bioreactors enhanced the conversion of dichromate chemical oxygen demand of the substrate to methane (41%) to a greater extent than bioreactors without CFT (9%). In addition, removal of rice straw as a suspended solid was increased from 31% (in bioreactors without CFT) to 57% (in those with CFT). Methanogenic 16S rRNA gene analysis showed that the abundance of acetoclastic methanogen, genus Methanosarcina, was about 11 times higher in bioreactors with CFT (suspended fraction plus retained fraction to CFT) than in bioreactors without CFT (suspended fraction), resulting in lower concentration of acetate in bioreactors with CFT (0.4 mM) than in those without CFT (29.7 mM). On the other hand, the abundance of hydrogenotrophic methanogen, genus Methanobacterium, in bioreactors with CFT was similar to those without CFT. Bacterial communities in bioreactors with CFT were different from those in bioreactors without CFT. Our results indicated that specific microbial community and cooperative relationships between microorganisms in reactors containing CFT facilitated efficient decomposition of rice straw and its conversion to methane.

  8. Kinetic analysis and energy efficiency of phenol degradation in a plasma-photocatalysis system.

    PubMed

    Wang, Hui-juan; Chen, Xiao-yang

    2011-02-28

    Combination of two kinds of advanced oxidation processes (AOPs) is an effective approach to control wastewater pollution. In this research, a pulsed discharge plasma system with multi-point-to-plate electrode and an immobilized TiO(2) photocatalysis system is coupled to oxidize target pollutant in aqueous solution. Kinetic analysis (pseudo-first order kinetic constant, k) and energy efficiency (energy yield value at 50% phenol conversion, G(50)) of phenol oxidation in different reaction systems (plasma alone and plasma-photocatalysis) are reviewed to account for the synergistic mechanism of plasma and photocatalysis. The experimental results show that higher k and G(50) of phenol oxidation can be obtained in the plasma-photocatalysis system under the conditions of different gas bubbling varieties, initial solution pH and radical scavenger addition. Moreover, the investigation tested hydroxyl radical (OH) is the most important species for phenol removal in the synergistic system of plasma-photocatalysis as well as in the plasma alone system.

  9. Electroluminescence from completely horizontally oriented dye molecules

    NASA Astrophysics Data System (ADS)

    Komino, Takeshi; Sagara, Yuta; Tanaka, Hiroyuki; Oki, Yuji; Nakamura, Nozomi; Fujimoto, Hiroshi; Adachi, Chihaya

    2016-06-01

    A complete horizontal molecular orientation of a linear-shaped thermally activated delayed fluorescent guest emitter 2,6-bis(4-(10Hphenoxazin-10-yl)phenyl)benzo[1,2-d:5,4-d'] bis(oxazole) (cis-BOX2) was obtained in a glassy host matrix by vapor deposition. The orientational order of cis-BOX2 depended on the combination of deposition temperature and the type of host matrix. Complete horizontal orientation was obtained when a thin film with cis-BOX2 doped in a 4,4'-bis(N-carbazolyl)-1,1'-biphenyl (CBP) host matrix was fabricated at 200 K. The ultimate orientation of guest molecules originates from not only the kinetic relaxation but also the kinetic stability of the deposited guest molecules on the film surface during film growth. Utilizing the ultimate orientation, a highly efficient organic light-emitting diode with the external quantum efficiency of 33.4 ± 2.0% was realized. The thermal stability of the horizontal orientation of cis-BOX2 was governed by the glass transition temperature (Tg) of the CBP host matrix; the horizontal orientation was stable unless the film was annealed above Tg.

  10. Blue-red electroluminescence from hybrid Eu:phosphors/ZnO-nanowires/p-GaN LED

    NASA Astrophysics Data System (ADS)

    Viana, B.; Pauporte, T.; Lupan, O.; Devis, L.; Gacoin, T.

    2014-03-01

    Nanowire (NW) based light emitting diodes (LEDs) have drawn great research interest due to many advantages compared to thin film based devices. Marked improved performances are expected from nanostructured active layers for light emission. Semiconducting oxide nanowires can act as direct waveguides and favor emitted light extraction without use of lens and reflectors in LEDs. Moreover, the use of ZnO wires avoids the presence of grain boundaries and then the emission efficiency is boosted by the absence of non-radiative recombinations at the joint defects. In this context, europium (Eu):Chelate/ZnO:Mg-nanowires/p-GaN light-emitting-diode (LED) structures have been fabricated showing near-UV/violet electroluminescence and red emission from trivalent europium. Fabricated LED structures exhibit UV-blue light at about 380 nm coming from the n-(ZnO:Mg)/p-GaN and a sharp red emission at ˜611 nm related to the intra-4f transition of Eu ions. It is found that in the case of the ZnO:Mg, the emission wavelength is slightly shifted to smaller wavelength to be well adapted to the trivalent europium excitation band. Radiative energy transfer is achieved through strong overlap between the emission wavelength from n-(ZnO:Mg)/p- GaN heterojunction and chelate ligand intensive absorption band. Indeed the Eu:chelate/(ZnO:Mg)-nanowires/p-GaN structure appears well adapted to UV/blue and red dual emission. Our results shows that the design of LEDs based on the chelate ligands are important issue to enhance the performance of electroluminescence devices based on ZnO nanowire arrays/p-GaN heterojunction and rare-earth metal complexes.

  11. Dispenser printed electroluminescent lamps on textiles for smart fabric applications

    NASA Astrophysics Data System (ADS)

    de Vos, Marc; Torah, Russel; Tudor, John

    2016-04-01

    Flexible electroluminescent (EL) lamps are fabricated onto woven textiles using a novel dispenser printing process. Dispenser printing utilizes pressurized air to deposit ink onto a substrate through a syringe and nozzle. This work demonstrates the first use of this technology to fabricate EL lamps. The luminance of the dispenser printed EL lamps is compared to screen-printed EL lamps, both printed on textile, and also commercial EL lamps on polyurethane film. The dispenser printed lamps are shown to have a 1.5 times higher luminance than the best performing commercially available lamp, and have a comparable performance to the screen-printed lamps.

  12. Mechanosynthesis of a phenylenedivinylidenebisquinoline. Optical, morphological and electroluminescence properties

    NASA Astrophysics Data System (ADS)

    Gutiérrez, A. R.; Vázquez, R. A.; Moggio, I.; Arias, E.; Coreño, O.; Maldonado, J. L.; Ramos-Ortíz, G.; Rodríguez, O.; Jiménez-Barrera, R. M.

    2015-04-01

    A phenylenedivinylidenebisquinoline oligomer was obtained by reacting quinaldine with 2,5-bis(octyloxy)terephtalaldehyde via the Knoevenagel reaction by mechanosynthesis. The product was characterized by 1H Homo-J-Resolved NMR, 13C NMR, FT-IR, Fluorescence, UV-Vis spectroscopy and by FAB+ mass spectrometry. X-ray diffraction studies indicate that the molecule is semicrystalline, while laser scanning confocal microscopy shows that the emission comes from the crystals. As a consequence, the morphology and accordingly the PL values in spun films can be changed by varying the spinning conditions. Intrinsic electroluminescent properties are reported using the ITO/M1AMec/Al single layer configuration.

  13. Degradable and biocompatible nanoparticles decorated with cyclic RGD peptide for efficient drug delivery to hepatoma cells in vitro.

    PubMed

    Loyer, Pascal; Bedhouche, Wahib; Huang, Zhi Wei; Cammas-Marion, Sandrine

    2013-10-01

    Amphiphilic derivatives of poly(benzyl malate) were synthesized and characterized with the aim of being used as degradable and biocompatible building blocks for the design of functional nanoparticles (NPs). An anti-cancer model drug, doxorubicin, has been successfully encapsulated into the prepared NPs and its release profile has been evaluated in water and in culture medium. NPs bearing biotin molecules were prepared either for site-specific drug delivery via the targeting of biotin receptors overexpressed on the surface of several cancer cells, or for grafting biotinylated cyclic RGD peptide onto their surface using the strong and highly specific interactions between biotin and the streptavidin protein. We have shown that this binding did not affect dramatically the physico-chemical properties of the corresponding NPs. Cyclic RGD grafted fluorescent NPs were more efficiently uptaken by the HepaRG hepatoma cells than biotinylated fluorescent NPs. Furthermore, the targeting of HepaRG hepatoma cells with NPs bearing cyclic RGD was very efficient and much weaker for HeLa and HT29 cell lines confirming that cyclic RGD is a suitable targeting agent for liver cells. Our results also provide a new mean for rapid screening of short hepatotropic peptides in order to design NPs showing specific liver targeting properties.

  14. Rapid, Efficient and Versatile Strategies for Functionally Sophisticated Polymers and Nanoparticles: Degradable Polyphosphoesters and Anisotropic Distribution of Chemical Functionalities

    NASA Astrophysics Data System (ADS)

    Zhang, Shiyi

    The overall emphasis of this dissertation research included two kinds of asymmetrically-functionalized nanoparticles with anisotropic distributions of chemical functionalities, three degradable polymers synthesized by organocatalyzed ring-opening polymerizations, and two polyphosphoester-based nanoparticle systems for various biomedical applications. Inspired by the many hierarchical assembly processes that afford complex materials in Nature, the construction of asymmetrically-functionalized nanoparticles with efficient surface chemistries and the directional organization of those building blocks into complex structures have attracted much attention. The first method generated a Janus-faced polymer nanoparticle that presented two orthogonally click-reactive surface chemistries, thiol and azido. This robust method involved reactive functional group transfer by templating against gold nanoparticle substrates. The second method produced nanoparticles with sandwich-like distribution of crown ether functionalities through a stepwise self-assembly process that utilized crown ether-ammonium supramolecular interactions to mediate inter-particle association and the local intra-particle phase separation of unlike hydrophobic polymers. With the goal to improve the efficiency of the production of degradable polymers with tunable chemical and physical properties, a new type of reactive polyphosphoester was synthesized bearing alkynyl groups by an organocatalyzed ring-opening polymerization, the chemical availability of the alkyne groups was investigated by employing "click" type azide-alkyne Huisgen cycloaddition and thiol-yne radical-mediated reactions. Based on this alkyne-functionalized polyphosphoester polymer and its two available "click" type reactions, two degradable nanoparticle systems were developed. To develop the first system, the well defined poly(ethylene oxide)-block-polyphosphester diblock copolymer was transformed into a multifunctional Paclitaxel drug

  15. Efficient degradation of lignocellulosic plant biomass without pretreatment by the 9 thermophilic anaerobe, Anaerocellum thermophilum DSM 6725

    SciTech Connect

    Yang, Sung-Jae; Kataeva, Irina; Hamilton-Brehm, Scott; Engle, Nancy L; Tschaplinski, Timothy J; Doeppke, Crissa; Davis, Dr. Mark F.; Westpheling, Janet; Adams, Michael W. W.

    2009-01-01

    Very few cultivated microorganisms can degrade lignocellulosic biomass without chemical pretreatment. We show here that 'Anaerocellum thermophilum' DSM 6725, an anaerobic bacterium that grows optimally at 75 C, efficiently utilizes various types of untreated plant biomass, as well as crystalline cellulose and xylan. These include hardwoods such as poplar, low-lignin grasses such as napier and Bermuda grasses, and high-lignin grasses such as switchgrass. The organism did not utilize only the soluble fraction of the untreated biomass, since insoluble plant biomass (as well as cellulose and xylan) obtained after washing at 75 C for 18 h also served as a growth substrate. The predominant end products from all growth substrates were hydrogen, acetate, and lactate. Glucose and cellobiose (on crystalline cellulose) and xylose and xylobiose (on xylan) also accumulated in the growth media during growth on the defined substrates but not during growth on the plant biomass. A. thermophilum DSM 6725 grew well on first- and second-spent biomass derived from poplar and switchgrass, where spent biomass is defined as the insoluble growth substrate recovered after the organism has reached late stationary phase. No evidence was found for the direct attachment of A. thermophilum DSM 6725 to the plant biomass. This organism differs from the closely related strain A. thermophilum Z-1320 in its ability to grow on xylose and pectin. Caldicellulosiruptor saccharolyticus DSM 8903 (optimum growth temperature, 70 C), a close relative of A. thermophilum DSM 6725, grew well on switchgrass but not on poplar, indicating a significant difference in the biomass-degrading abilities of these two otherwise very similar organisms.

  16. Carbon Conversion Efficiency and Limits of Productive Bacterial Degradation of Methyl tert-Butyl Ether and Related Compounds▿

    PubMed Central

    Müller, Roland H.; Rohwerder, Thore; Harms, Hauke

    2007-01-01

    The utilization of the fuel oxygenate methyl tert-butyl ether (MTBE) and related compounds by microorganisms was investigated in a mainly theoretical study based on the YATP concept. Experiments were conducted to derive realistic maintenance coefficients and Ks values needed to calculate substrate fluxes available for biomass production. Aerobic substrate conversion and biomass synthesis were calculated for different putative pathways. The results suggest that MTBE is an effective heterotrophic substrate that can sustain growth yields of up to 0.87 g g−1, which contradicts previous calculation results (N. Fortin et al., Environ. Microbiol. 3:407-416, 2001). Sufficient energy equivalents were generated in several of the potential assimilatory routes to incorporate carbon into biomass without the necessity to dissimilate additional substrate, efficient energy transduction provided. However, when a growth-related kinetic model was included, the limits of productive degradation became obvious. Depending on the maintenance coefficient ms and its associated biomass decay term b, growth-associated carbon conversion became strongly dependent on substrate fluxes. Due to slow degradation kinetics, the calculations predicted relatively high threshold concentrations, Smin, below which growth would not further be supported. Smin strongly depended on the maximum growth rate μmax, and b and was directly correlated with the half maximum rate-associated substrate concentration Ks, meaning that any effect impacting this parameter would also change Smin. The primary metabolic step, catalyzing the cleavage of the ether bond in MTBE, is likely to control the substrate flux in various strains. In addition, deficits in oxygen as an external factor and in reduction equivalents as a cellular variable in this reaction should further increase Ks and Smin for MTBE. PMID:17220260

  17. Near-infrared roll-off-free electroluminescence from highly stable diketopyrrolopyrrole light emitting diodes

    NASA Astrophysics Data System (ADS)

    Sassi, Mauro; Buccheri, Nunzio; Rooney, Myles; Botta, Chiara; Bruni, Francesco; Giovanella, Umberto; Brovelli, Sergio; Beverina, Luca

    2016-09-01

    Organic light emitting diodes (OLEDs) operating in the near-infrared spectral region are gaining growing relevance for emerging photonic technologies, such as lab-on-chip platforms for medical diagnostics, flexible self-medicated pads for photodynamic therapy, night vision and plastic-based telecommunications. The achievement of efficient near-infrared electroluminescence from solution-processed OLEDs is, however, an open challenge due to the low photoluminescence efficiency of most narrow-energy-gap organic emitters. Diketopyrrolopyrrole-boron complexes are promising candidates to overcome this limitation as they feature extremely high photoluminescence quantum yield in the near-infrared region and high chemical stability. Here, by incorporating suitably functionalized diketopyrrolopyrrole derivatives emitting at ~760 nm in an active matrix of poly(9,9-dioctylfluorene-alt-benzothiadiazole) and without using complex light out-coupling or encapsulation strategies, we obtain all-solution-processed NIR-OLEDs with external quantum efficiency as high as 0.5%. Importantly, our test-bed devices show no efficiency roll-off even for high current densities and high operational stability, retaining over 50% of the initial radiant emittance for over 50 hours of continuous operation at 10 mA/cm2, which emphasizes the great applicative potential of the proposed strategy.

  18. Synthesis and electroluminescent properties of anthracene derivatives containing electron-withdrawing oxide moieties

    SciTech Connect

    Yoon, Jhin-yeong; Na, Eun Jae; Park, Soo Na; Lee, Seok Jae; Kim, Young Kwan; Yoon, Seung Soo

    2014-10-15

    Highlights: • Blue fluorescent material is important for application in full-color displays. • We have synthesized emitters based on anthracene connected with oxide moieties. • 1C shows a highly efficient blue EL emission due to electron-injection property. - Abstract: A series of new blue-emitting materials: (4-(10-(naphthalen-2-yl)anthracen-9-yl)phenyl)(phenyl)methanone (1); 9-(naphthalen-2-yl)-10-(4-((diphenyl)phosphine oxide)phenyl)anthracene (2); 9-(naphthalen-2-yl)-10-(4-(phenylsulfonyl)phenyl)anthracene (3) were designed and synthesized via Suzuki cross-coupling reaction. Multilayer OLEDs were fabricated in the following sequence: ITO (180 nm)/NPB (50 nm)/blue materials 1–3 (30 nm)/TPBi (15 nm)/Liq (2 nm)/Al (100 nm). All devices showed the efficient blue EL emissions. In particular, the device using 1 as an emitter exhibited efficient blue electroluminescent properties with a maximum luminous, power, external quantum efficiency and CIE coordinates of 0.36 cd/A, 0.90 lm/W, 0.55% at 20 mA/cm{sup 2} and (x = 0.16, y = 0.20) at 10.0 V, respectively.

  19. Near-infrared roll-off-free electroluminescence from highly stable diketopyrrolopyrrole light emitting diodes

    PubMed Central

    Sassi, Mauro; Buccheri, Nunzio; Rooney, Myles; Botta, Chiara; Bruni, Francesco; Giovanella, Umberto; Brovelli, Sergio; Beverina, Luca

    2016-01-01

    Organic light emitting diodes (OLEDs) operating in the near-infrared spectral region are gaining growing relevance for emerging photonic technologies, such as lab-on-chip platforms for medical diagnostics, flexible self-medicated pads for photodynamic therapy, night vision and plastic-based telecommunications. The achievement of efficient near-infrared electroluminescence from solution-processed OLEDs is, however, an open challenge due to the low photoluminescence efficiency of most narrow-energy-gap organic emitters. Diketopyrrolopyrrole-boron complexes are promising candidates to overcome this limitation as they feature extremely high photoluminescence quantum yield in the near-infrared region and high chemical stability. Here, by incorporating suitably functionalized diketopyrrolopyrrole derivatives emitting at ~760 nm in an active matrix of poly(9,9-dioctylfluorene-alt-benzothiadiazole) and without using complex light out-coupling or encapsulation strategies, we obtain all-solution-processed NIR-OLEDs with external quantum efficiency as high as 0.5%. Importantly, our test-bed devices show no efficiency roll-off even for high current densities and high operational stability, retaining over 50% of the initial radiant emittance for over 50 hours of continuous operation at 10 mA/cm2, which emphasizes the great applicative potential of the proposed strategy. PMID:27677240

  20. Low degradable protein supply to increase nitrogen efficiency in lactating dairy cows and reduce environmental impacts at barn level.

    PubMed

    Edouard, N; Hassouna, M; Robin, P; Faverdin, P

    2016-02-01

    Generally, <30% of dairy cattle's nitrogen intake is retained in milk. Large amounts of nitrogen are excreted in manure, especially in urine, with damaging impacts on the environment. This study explores the effect of lowering dietary degradable nitrogen supplies--while maintaining metabolisable protein--on dairy cows' performance, nitrogen use efficiency and gas emissions (NH3, N2O, CH4) at barn level with tied animals. Two dietary N concentrations (CP: 12% DM for LowN; 18% DM for HighN) were offered to two groups of three lactating dairy cows in a split-plot design over four periods of 2 weeks. Diets were formulated to provide similar metabolisable protein supply, with degradable N either in deficit or in excess (PDIN of 84 and 114 g/kg DM for LowN and HighN, respectively). Cows ingested 0.8 kg DM/day less on the LowN diet, which was also 2.5% less digestible. Milk yield and composition were not significantly affected. N exported in milk was 5% lower (LowN: 129 g N/day; HighN: 136 g N/day; P<0.001) but milk protein yield was not significantly affected (LowN: 801 g/day; HighN: 823 g/day; P=0.10). Cows logically ingested less nitrogen on the LowN diet (LowN: 415 g N/day; HighN: 626 g N/day; P<0.001) resulting in a higher N use efficiency (N milk/N intake; LowN: 0.31; HighN: 0.22; P<0.001). N excreted in urine was almost four times lower on the LowN diet (LowN: 65 g N/day; HighN: 243 g N/day; P<0.001) while urinary urea N concentration was eightfold lower (LowN: 4.6 g/l; HighN: 22.9 g/l; P<0.001). Ammonia emission (expressed in g/h in order to remove periods of the day with potential interferences with volatile molecules from feed) was also lower on the LowN diet (LowN: 1.03 g/h per cow; HighN: 1.25 g/h per cow; P<0.05). Greenhouse gas emissions (N2O and CH4) at barn level were not significantly affected by the amount of dietary N. Offering low amounts of degradable protein with suitable metabolisable protein amounts to cattle improved nitrogen use efficiency and

  1. Synthesis, photophysical and electroluminescent properties of novel iridium (III) complexes based on 5-methyl-2-phenylbenzo[d]oxazole derivatives

    NASA Astrophysics Data System (ADS)

    Li, Xiao; Chi, Hai-Jun; Dong, Yan; Xiao, Guo-Yong; Lei, Peng; Zhang, Dong-Yu; Cui, Zheng

    2013-12-01

    A new series of phosphorescent iridium (III) complexes based on 5-methyl-2-phenylbenzo[d]oxazole derivatives as main ligands, i.e. bis(5-methyl-2- phenylbenzo[d]oxazole-N,C2‧)iridium(acetylacetonate) [(mpbo)2Ir(acac)], bis(2-(4-fluorophenyl)-5-methylbenzo[d]oxazole-N,C2‧)iridium(acetylacetonate) [(fmbo)2Ir(acac)] and bis(5-methyl-2-p-tolylbenzo[d]oxazole-N,C2‧) iridium(acetylacetonate) [(mtbo)2Ir(acac)], were synthesized for organic light-emitting diodes (OLEDs), and their photophysical, electroluminescent properties were investigated. All complexes have high thermal stability and emit intense phosphorescence from green to yellow at room temperature with high quantum efficiencies and relatively short lifetimes. The OLED based on (fmbo)2Ir(acac) as dopant emitter showed very high luminance of 26,004 cd m-2 and luminance efficiency of 18.5 cd A-1. The evidences indicated that this series of iridium (III) complexes were potential candidates for applications in organic electroluminescent devices.

  2. Electroluminescence mechanisms in organic light emitting devices employing a europium chelate doped in a wide energy gap bipolar conducting host

    NASA Astrophysics Data System (ADS)

    Adachi, Chihaya; Baldo, Marc A.; Forrest, Stephen R.

    2000-06-01

    The mechanism for energy transfer leading to electroluminescence (EL) of a lanthanide complex, Eu(TTA)3phen (TTA=thenoyltrifluoroacetone,phen=1,10-phenanthroline), doped into 4,4'-N,N'-dicarbazole-biphenyl (CBP) host is investigated. With the device structure of anode/hole transport layer/Eu(TTA)3phen(1%):CPB/electron transport layer/cathode, we achieve a maximum external EL quantum efficiency (η) of 1.4% at a current density of 0.4 mA/cm2. Saturated red Eu3+ emission based on 5Dx-7Fx transitions is centered at a wavelength of 612 nm with a full width at half maximum of 3 nm. From analysis of the electroluminescent and photoluminescent spectra, and the current density-voltage characteristics, we conclude that direct trapping of holes and electrons and subsequent formation of the excitons occurs on the dopant, leading to high quantum efficiencies at low current densities. With increasing current between 1 and 100 mA/cm2, however, a significant decrease of η along with an increase in CBP host emission is observed. We demonstrate that the decrease in η at high current densities can be explained by triplet-triplet annihilation.

  3. High-sensitivity strain visualization using electroluminescence technologies

    NASA Astrophysics Data System (ADS)

    Xu, Jian; Jo, Hongki

    2016-04-01

    Visualizing mechanical strain/stress changes is an emerging area in structural health monitoring. Several ways are available for strain change visualization through the color/brightness change of the materials subjected to the mechanical stresses, for example, using mechanoluminescence (ML) materials and mechanoresponsive polymers (MRP). However, these approaches were not effectively applicable for civil engineering system yet, due to insufficient sensitivity to low-level strain of typical civil structures and limitation in measuring both static and dynamic strain. In this study, design and validation for high-sensitivity strain visualization using electroluminescence technologies are presented. A high-sensitivity Wheatstone bridge, of which bridge balance is precisely controllable circuits, is used with a gain-adjustable amplifier. The monochrome electroluminescence (EL) technology is employed to convert both static and dynamic strain change into brightness/color change of the EL materials, through either brightness change mode (BCM) or color alternation mode (CAM). A prototype has been made and calibrated in lab, the linearity between strain and brightness change has been investigated.

  4. DDT degradation efficiency and ecotoxicological effects of two types of nano-sized zero-valent iron (nZVI) in water and soil.

    PubMed

    El-Temsah, Yehia S; Sevcu, Alena; Bobcikova, Katerina; Cernik, Miroslav; Joner, Erik J

    2016-02-01

    Nano-scale zero-valent iron (nZVI) has been conceived for cost-efficient degradation of chlorinated pollutants in soil as an alternative to e.g permeable reactive barriers or excavation. Little is however known about its efficiency in degradation of the ubiquitous environmental pollutant DDT and its secondary effects on organisms. Here, two types of nZVI (type B made using precipitation with borohydride, and type T produced by gas phase reduction of iron oxides under H2) were compared for efficiency in degradation of DDT in water and in a historically (>45 years) contaminated soil (24 mg kg(-1) DDT). Further, the ecotoxicity of soil and water was tested on plants (barley and flax), earthworms (Eisenia fetida), ostracods (Heterocypris incongruens), and bacteria (Escherichia coli). Both types of nZVI effectively degraded DDT in water, but showed lower degradation of aged DDT in soil. Both types of nZVI had negative impact on the tested organisms, with nZVI-T giving least adverse effects. Negative effects were mostly due to oxidation of nZVI, resulting in O2 consumption and excess Fe(II) in water and soil.

  5. Mn/Ti-doped carbon xerogel for efficient catalysis of microcystin-LR degradation in the water surface discharge plasma reactor.

    PubMed

    Xin, Qing; Zhang, Yi; Li, Zhongjian; Lei, Lecheng; Yang, Bin

    2015-11-01

    The novel catalysts of Mn/Ti-doped carbon xerogel (CX) were synthesized for efficient degradation of microcystin-LR (MC-LR) in the water surface discharge plasma reactor. The degradation efficiency of 79.7% was obtained in 6 min with 0.5 wt% Ti impregnation of CX, and it would be increased with higher amount of Ti. In particular, Mn-doped CX resulted in larger mesoporous particle diameter and higher porosity in the matrix, and thereby, the highest efficiency of 88.6% was achieved for CX-Ti-Mn. The possible degradation pathway of MC-LR was elucidated on the basis of the LC-MS analysis. It demonstrated that Adda chain was cleaved from the MC-LR cyclic peptide by OH radical attack after plasma discharge in the presence of catalysts, and the generated nontoxic products can be further easily degraded in the biological treatment. Therefore, Mn/Ti-doped carbon xerogel is promising as the catalyst for the improvement of MC-LR degradation in the water surface discharge plasma reactor.

  6. Optical properties of heavily doped GaAs nanowires and electroluminescent nanowire structures.

    PubMed

    Lysov, A; Offer, M; Gutsche, C; Regolin, I; Topaloglu, S; Geller, M; Prost, W; Tegude, F-J

    2011-02-25

    We present GaAs electroluminescent nanowire structures fabricated by metal organic vapor phase epitaxy. Electroluminescent structures were realized in both axial pn-junctions in single GaAs nanowires and free-standing nanowire arrays with a pn-junction formed between nanowires and substrate, respectively. The electroluminescence emission peak from single nanowire pn-junctions at 10 K was registered at an energy of around 1.32 eV and shifted to 1.4 eV with an increasing current. The line is attributed to the recombination in the compensated region present in the nanowire due to the memory effect of the vapor-liquid-solid growth mechanism. Arrayed nanowire electroluminescent structures with a pn-junction formed between nanowires and substrate demonstrated at 5 K a strong electroluminescence peak at 1.488 eV and two shoulder peaks at 1.455 and 1.519 eV. The main emission line was attributed to the recombination in the p-doped GaAs. The other two lines correspond to the tunneling-assisted photon emission and band-edge recombination in the abrupt junction, respectively. Electroluminescence spectra are compared with the micro-photoluminescence spectra taken along the single p-, n- and single nanowire pn-junctions to find the origin of the electroluminescence peaks, the distribution of doping species and the sharpness of the junctions.

  7. Kinetics and energy efficiency for the degradation of 1,4-dioxane by electro-peroxone process.

    PubMed

    Wang, Huijiao; Bakheet, Belal; Yuan, Shi; Li, Xiang; Yu, Gang; Murayama, Seiichi; Wang, Yujue

    2015-08-30

    Degradation of 1,4-dioxane by ozonation, electrolysis, and their combined electro-peroxone (E-peroxone) process was investigated. The E-peroxone process used a carbon-polytetrafluorethylene cathode to electrocatalytically convert O2 in the sparged ozone generator effluent (O2 and O3 gas mixture) to H2O2. The electro-generated H2O2 then react with sparged O3 to yield aqueous OH, which can in turn oxidize pollutants rapidly in the bulk solution. Using p-chlorobenzoic acid as OH probe, the pseudo-steady concentration of OH was determined to be ∼0.744×10(-9)mM in the E-peroxone process, which is approximately 10 and 186 times of that in ozonation and electrolysis using a Pt anode. Thanks to its higher OH concentration, the E-peroxone process eliminated 96.6% total organic carbon (TOC) from a 1,4-dioxane solution after 2h treatment with a specific energy consumption (SEC) of 0.376kWhg(-1) TOCremoved. In comparison, ozonation and electrolysis using a boron-doped diamond anode removed only ∼6.1% and 26.9% TOC with SEC of 2.43 and 0.558kWhg(-1) TOCremoved, respectively. The results indicate that the E-peroxone process can significantly improve the kinetics and energy efficiency for 1,4-dioxane mineralization as compared to the two individual processes. The E-peroxone process may thus offer a highly effective and energy-efficient alternative to treat 1,4-dioxane wastewater.

  8. Electroluminescence of hot electrons in AlGaN/GaN high-electron-mobility transistors under radio frequency operation

    SciTech Connect

    Brazzini, Tommaso Sun, Huarui; Uren, Michael J.; Kuball, Martin; Casbon, Michael A.; Lees, Jonathan; Tasker, Paul J.; Jung, Helmut; Blanck, Hervé

    2015-05-25

    Hot electrons in AlGaN/GaN high electron mobility transistors are studied during radio frequency (RF) and DC operation by means of electroluminescence (EL) microscopy and spectroscopy. The measured EL intensity is decreased under RF operation compared to DC at the same average current, indicating a lower hot electron density. This is explained by averaging the DC EL intensity over the measured load line used in RF measurements, giving reasonable agreement. In addition, the hot electron temperature is lower by up to 15% under RF compared to DC, again at least partially explainable by the weighted averaging along the specific load line. However, peak electron temperature under RF occurs at high V{sub DS} and low I{sub DS} where EL is insignificant suggesting that any wear-out differences between RF and DC stress of the devices will depend on the balance between hot-carrier and field driven degradation mechanisms.

  9. Efficient immobilization of mushroom tyrosinase utilizing whole cells from Agaricus bisporus and its application for degradation of bisphenol A.

    PubMed

    Kampmann, Markus; Boll, Stefan; Kossuch, Jan; Bielecki, Julia; Uhl, Stefan; Kleiner, Beatrice; Wichmann, Rolf

    2014-06-15

    A simple and efficient procedure for preparation and immobilization of tyrosinase enzyme was developed utilizing whole cells from the edible mushroom Agaricus bisporus, without the need for enzyme purification. Tyrosinase activity in the cell preparation remained constant during storage at 21 °C for at least six months. The cells were entrapped in chitosan and alginate matrix capsules and characterized with respect to their resulting tyrosinase activity. A modification of the alginate with colloidal silica enhanced the activity due to retention of both cells and tyrosinase from fractured cells, which otherwise leached from matrix capsules. The observed activity was similar to the activity that was obtained with immobilized isolated tyrosinase in the same material. Mushroom cells in water were susceptible to rapid inactivation, whereas the immobilized cells maintained 73% of their initial activity after 30 days of storage in water. Application in repeated batch experiments resulted in almost 100% conversion of endocrine disrupting bisphenol A (BPA) for 11 days, under stirring conditions, and 50-60% conversion after 20 days, without stirring under continuous usage. The results represent the longest yet reported application of immobilized tyrosinase for degradation of BPA in environmental water samples.

  10. Highly efficient electrochemical degradation of perfluorooctanoic acid (PFOA) by F-doped Ti/SnO2 electrode.

    PubMed

    Yang, Bo; Jiang, Chaojin; Yu, Gang; Zhuo, Qiongfang; Deng, Shubo; Wu, Jinhua; Zhang, Hong

    2015-12-15

    The novel F-doped Ti/SnO2 electrode prepared by SnF4 as the single-source precursor was used for electrochemical degradation of aqueous perfluorooctanoic acid (PFOA). Higher oxidation reactivity and significantly longer service life were achieved for Ti/SnO2-F electrode than Ti/SnO2-X (X=Cl, Br, I, or Sb) electrode, which could decomposed over 99% of PFOA (50 mL of 100 mg L(-1)) within 30-min electrolysis. The property of Ti/SnO2-F electrode and its electrooxidation mechanism were investigated by XRD, SEM-EDX, EIS, LSV, and interfacial resistance measurements. We propose that the similar ionic radii of F and O as well as strong electronegativity of F caused its electrochemical stability with high oxygen evolution potential (OEP) and smooth surface to generate weakly adsorbed OH. The preparation conditions of electrode were also optimized including F doping amount, calcination temperature, and dip coating times, which revealed the formation process of electrode. Additionally, the major mineralization product, F(-), and low concentration of shorter chain perfluorocarboxylic acids (PFCAs) were detected in solution. So the reaction pathway of PFOA electrooxidation was proposed by intermediate analysis. These results demonstrate that Ti/SnO2-F electrode is promising for highly efficient treatment of PFOA in wastewater.

  11. Facile synthesis of Au-ZnO plasmonic nanohybrids for highly efficient photocatalytic degradation of methylene blue

    NASA Astrophysics Data System (ADS)

    Kuriakose, Sini; Sahu, Kavita; Khan, Saif A.; Tripathi, A.; Avasthi, D. K.; Mohapatra, Satyabrata

    2017-02-01

    Au-ZnO plasmonic nanohybrids were synthesized by a facile two step process. In the first step, nanostructured ZnO thin films were prepared by carbothermal evaporation followed by thermal annealing in oxygen atmosphere. Deposition of ultrathin Au films onto the nanostructured ZnO thin films by sputtering combined with thermal annealing resulted in the formation of Au-ZnO plasmonic nanohybrid thin films. The structural, optical, plasmonic and photocatalytic properties of the Au-ZnO nanohybrid thin films were studied. XRD studies on the Au-ZnO hybrid thin films revealed the presence of Au and ZnO nanostructures. UV-visible absorption studies showed two peaks corresponding to the excitonic absorption of ZnO nanostructures in the UV region and the surface plasmon resonance (SPR) absorption of Au nanoparticles in the visible region. The Au-ZnO nanohybrid thin films annealed at 400 °C showed enhanced photocatalytic activity as compared to nanostructrured ZnO thin films towards sun light driven photocatalytic degradation of methylene blue (MB) dye in water. The observed enhanced photocatalytic activity of Au-ZnO plasmonic nanohybrids is attributed to the efficient suppression of the recombination of photogenerated charge carriers in ZnO due to the strong electron scavenging action of Au nanoparticles combined with the improved sun light utilization capability of Au-ZnO nanohybrids coming from the plasmonic response of Au nanoparticles decorating ZnO nanostructures.

  12. Positive role of incorporating P-25 TiO2 to mesoporous-assembled TiO2 thin films for improving photocatalytic dye degradation efficiency.

    PubMed

    Sreethawong, Thammanoon; Ngamsinlapasathian, Supachai; Yoshikawa, Susumu

    2014-09-15

    In this work, a simple and effective strategy to improve the photocatalytic dye degradation efficiency of the mesoporous-assembled TiO2 nanoparticle thin films by incorporating small contents of commercial P-25 TiO2 during the thin film preparation was developed. The mesoporous-assembled TiO2 nanoparticles were synthesized by a sol-gel method with the aid of a mesopore-directing surfactant, followed by homogeneously mixing with P-25 TiO2 prior to the thin film coating on glass substrate. The mesoporous-assembled TiO2 film with 5 wt.% P-25 TiO2 incorporation and calcined at 400°C provided an improved photocatalytic Acid Black (AB) dye degradation efficiency. The increase in number of coated layers to the optimum four layers of the aforementioned film was found to further improve the degradation efficiency. The recyclability test of this 5 wt.% P-25 TiO2-incorporated mesoporous-assembled TiO2 film with four coated layers revealed that it can be reused for multiple cycles without a requirement of post-treatment while the degradation efficiency was retained.

  13. Electroluminescence et radiation thermique dans les nanotubes de carbone

    NASA Astrophysics Data System (ADS)

    Adam, Elyse

    We present here a spectroscopic study of the light emission properties of different nanotube devices with the aim to clarify the different mechanisms leading to the light emission. The first study consists of taking measurements from a thick (˜ 450 nm) macroscopic suspended carbon nanotube film connected between two electrodes. A significant increase of the temperature is expected when voltage is applied since thermal dissipation by the substrate is suppressed for this configuration. In imaging mode, we observed that infrared light is emitted from the entire area of the film instead of being localized. This observation demonstrates that the light emission arise from thermal emission. Spectra measured on this device all present a smooth response, characteristic of that of a blackbody. As expected for a pure thermal source, the results fit well the Planck formula. Because the Planck formula is temperature dependant, it became possible to extract a lower limit of the temperature of the film as a function of voltage. The temperature increases more or less from 350K to 600K when the voltage increases from 0.1V to 1.6V. The second study is made using a sub-monolayer network of carbon nanotubes interconnected together to form a semiconducting layer. The large number of tube-tube junctions in the networks limits the current and prevents the temperature to rise significantly at higher bias. The intimate contact between the network and the substrate also prevent the temperature of the film to increase significantly due to a good thermalizaton. Hence, electroluminescence from excitonic recombination is expected to be dominant over heat radiation for this type of devices. First, spatial resolution measurements on long channel network devices shows that the light-emitting zone is always located near the minority charge injector contact. This result demonstrates that light emission arises from electroluminescence in network from a bipolar current. Thermal emission can therefore

  14. Permeation impact on metallization degradation

    NASA Astrophysics Data System (ADS)

    Peike, C.; Hoffmann, S.; Hülsmann, P.; Weiß, K.-A.; Koehl, M.; Bentz, P.

    2012-10-01

    The degradation of the inorganic components in a PV module is, besides polymer degradation, one of the most important aspects of PV module aging. Especially the corrosion of the cell metallization may lead to significant decreases in PV module performance. But in which way the metallization corrosion is affected by the permeation of atmospheric gases is not understood, yet. In order to investigate this permeation impact, laminates with a systematic variation of back-sheet and encapsulation materials as well as different laminate set-ups were made. Two different kinds of encapsulation (EVA and PVB) and four different back-sheet materials (TAPT, PA and two different TPT foils) were used. Standard cells with a two and three bus bar set-up were used. The laminates were subjected to damp-heat aging tests with a relative humidity of 80% at 80°C and 90°C, respectively. The degradation was investigated by means of electroluminescence imaging, Raman spectroscopy and microscopy. Special attention was paid to the spatial distribution of corrosion effects on the cell. Furthermore, the occurrence of a typical damp-heat induced damage, apparent as a shaded area in the electroluminescence images, should be investigated. A corrosion of the grid and the ribbons could be observed. EDX measurements revealed the grid corrosion to go along with the formation of needles of lead compounds from the silver paste.

  15. Guest concentration, bias current, and temperature-dependent sign inversion of magneto-electroluminescence in thermally activated delayed fluorescence devices

    NASA Astrophysics Data System (ADS)

    Deng, Junquan; Jia, Weiyao; Chen, Yingbing; Liu, Dongyu; Hu, Yeqian; Xiong, Zuhong

    2017-03-01

    Non-emissive triplet excited states in devices that undergo thermally activated delayed fluorescence (TADF) can be up-converted to singlet excited states via reverse intersystem crossing (RISC), which leads to an enhanced electroluminescence efficiency. Exciton-based fluorescence devices always exhibit a positive magneto-electroluminescence (MEL) because intersystem crossing (ISC) can be suppressed effectively by an external magnetic field. Conversely, TADF devices should exhibit a negative MEL because RISC is suppressed by the external magnetic field. Intriguingly, we observed a positive MEL in TADF devices. Moreover, the sign of the MEL was either positive or negative, and depended on experimental conditions, including doping concentration, current density and temperature. The MEL observed from our TADF devices demonstrated that ISC in the host material and RISC in the guest material coexisted. These competing processes were affected by the experimental conditions, which led to the sign change of the MEL. This work gives important insight into the energy transfer processes and the evolution of excited states in TADF devices.

  16. Guest concentration, bias current, and temperature-dependent sign inversion of magneto-electroluminescence in thermally activated delayed fluorescence devices

    PubMed Central

    Deng, Junquan; Jia, Weiyao; Chen, Yingbing; Liu, Dongyu; Hu, Yeqian; Xiong, Zuhong

    2017-01-01

    Non-emissive triplet excited states in devices that undergo thermally activated delayed fluorescence (TADF) can be up-converted to singlet excited states via reverse intersystem crossing (RISC), which leads to an enhanced electroluminescence efficiency. Exciton-based fluorescence devices always exhibit a positive magneto-electroluminescence (MEL) because intersystem crossing (ISC) can be suppressed effectively by an external magnetic field. Conversely, TADF devices should exhibit a negative MEL because RISC is suppressed by the external magnetic field. Intriguingly, we observed a positive MEL in TADF devices. Moreover, the sign of the MEL was either positive or negative, and depended on experimental conditions, including doping concentration, current density and temperature. The MEL observed from our TADF devices demonstrated that ISC in the host material and RISC in the guest material coexisted. These competing processes were affected by the experimental conditions, which led to the sign change of the MEL. This work gives important insight into the energy transfer processes and the evolution of excited states in TADF devices. PMID:28295056

  17. A rhenium complex with diamine ligand containing oxadiazole group and fluorine atom: Synthesis, characterization, photoluminescence and electroluminescence performances

    NASA Astrophysics Data System (ADS)

    Yang, Wensheng; Yang, Wan; Liu, Weisheng; Qin, Wenwu

    2013-03-01

    In this paper, a diamine ligand of 2-(4-fluorophenyl)-5-(pyridin-2-yl)-1,3,4-oxadiazole (FPYOZ), which owned both enlarged conjugation chain with electron-pulling group and fluorine atom, was synthesized. Its corresponding Re(I) complex was also synthesized and studied in detail, including single crystal analysis, electronic structure, photophysical performance, thermal stability and electrochemical property. Single crystal analysis suggested that there was a coordination ability difference between the N atom from pyridine ring and the one from oxadiazole moiety. Theoretical calculation on the complex suggested that the onset electronic transition owned a mixed character of metal-to-ligand-charge-transfer and ligand-to-ligand-charge-transfer. Upon photoexcitation of 375 nm, this complex showed a yellow emission peaking at 537 nm with excited state lifetime of 8.35 μs. Cyclic voltammetry result suggested that this complex owned HOMO and LUMO energy levels of -5.37 eV and -3.04 eV. The decomposition temperature of this complex was as high as 300 °C, as revealed by thermogravimetric analysis data. The optimal electroluminescence device using this complex as the emitting dopant showed an electroluminescence peaking at 562 nm, with a maximum luminance of 6250 cd/m2 and a maximum current efficiency of 7.3 cd/A.

  18. CONDENSED MATTER: ELECTRONIC STRUCTURE, ELECTRICAL, MAGNETIC, AND OPTICAL PROPERTIES: A New Conducting Polymer Electrode for Organic Electroluminescence Devices

    NASA Astrophysics Data System (ADS)

    Qu, Shu; Peng, Jing-Cu

    2008-08-01

    Conducting polymer polydimethylsiloxane (PDMS) is studied for the high performance electrode of organic electroluminescence devices. A method to prepare the electrode consisting of a SiC thin film and PDMS is investigated. By using ultra thin SiC films with different thicknesses, the organic electroluminescence devices are obtained in an ultra vacuum system with the model device PDMS/SiC/PPV/Alq3, where PPV is poly para-phenylene vinylene and Alq3 is tris(8-hydroxyquinoline) aluminium. The capacitance-voltage (C - V), capacitance-frequency (C - F), current-voltage (I - V), radiation intensity-voltage (R - V) and luminance efficiency-voltage (E - V) measurements are systematically studied to investigate the conductivity, Fermi alignment and devices properties in organic semiconductors. Scanning Kelvin probe measurement shows that the work function ofPDMS/SiC anode with a 2.5-nm SiC over layer can be increased by as much as 0.28 eV, compared to the conventional ITO anode. The result is attributed to the charge transfer effect and ohmic contacts at the interface.

  19. Construction of a Rapid Feather-Degrading Bacterium by Overexpression of a Highly Efficient Alkaline Keratinase in Its Parent Strain Bacillus amyloliquefaciens K11.

    PubMed

    Yang, Lian; Wang, Hui; Lv, Yi; Bai, Yingguo; Luo, Huiying; Shi, Pengjun; Huang, Huoqing; Yao, Bin

    2016-01-13

    Keratinase is essential to degrade the main feather component, keratin, and is of importance for wide industrial applications. In this study, Bacillus amyloliquefaciens strain K11 was found to have significant feather-degrading capacity (completely degraded whole feathers within 24 h). The keratinase encoding gene, kerK, was expressed in Bacillus subtilis SCK6. The purified recombinant KerK showed optimal activity at 50 °C and pH 11.0 and degraded whole feathers within 0.5 h in the presence of DTT. The recombinant plasmids harboring kerK were extracted from B. subtilis SCK6 and transformed into B. amyloliquefaciens K11. As a result, the recombinant B. amyloliquefaciens K11 exhibited enhanced feather-degrading capacity with shortened reaction time within 12 h and increased keratinolytic activity (1500 U/mL) by 6-fold. This efficient and rapid feather-degrading character makes the recombinant strain of B. amyloliquefaciens K11 have potential for applications in feather meal preparation and waste feather disposal.

  20. Single-photon electroluminescence for on-chip quantum networks

    NASA Astrophysics Data System (ADS)

    Bentham, C.; Hallett, D.; Prtljaga, N.; Royall, B.; Vaitiekus, D.; Coles, R. J.; Clarke, E.; Fox, A. M.; Skolnick, M. S.; Itskevich, I. E.; Wilson, L. R.

    2016-10-01

    An electrically driven single-photon source has been monolithically integrated with nano-photonic circuitry. Electroluminescent emission from a single InAs/GaAs quantum dot (QD) is channelled through a suspended nanobeam waveguide. The emission line has a linewidth of below 6 μeV, demonstrating the ability to have a high coherence, electrically driven, waveguide coupled QD source. The single-photon nature of the emission is verified by g ( 2 ) ( τ ) correlation measurements. Moreover, in a cross-correlation experiment, with emission collected from the two ends of the waveguide, the emission and propagation of single photons from the same QD is confirmed. This work provides the basis for the development of electrically driven on-chip single-photon sources, which can be readily coupled to waveguide filters, directional couplers, phase shifters, and other elements of quantum photonic networks.

  1. Highly stretchable electroluminescent skin for optical signaling and tactile sensing.

    PubMed

    Larson, C; Peele, B; Li, S; Robinson, S; Totaro, M; Beccai, L; Mazzolai, B; Shepherd, R

    2016-03-04

    Cephalopods such as octopuses have a combination of a stretchable skin and color-tuning organs to control both posture and color for visual communication and disguise. We present an electroluminescent material that is capable of large uniaxial stretching and surface area changes while actively emitting light. Layers of transparent hydrogel electrodes sandwich a ZnS phosphor-doped dielectric elastomer layer, creating thin rubber sheets that change illuminance and capacitance under deformation. Arrays of individually controllable pixels in thin rubber sheets were fabricated using replica molding and were subjected to stretching, folding, and rolling to demonstrate their use as stretchable displays. These sheets were then integrated into the skin of a soft robot, providing it with dynamic coloration and sensory feedback from external and internal stimuli.

  2. Improving the diversity of manufacturing electroluminescent flat panel displays

    SciTech Connect

    Moss, T.S.; Samuels, J.A.; Smith, D.C.

    1995-09-01

    Crystalline calcium thiogallate with a cerium dopant has been deposited by metal-organic chemical vapor deposition (MOCVD) at temperatures below 600{degrees}C on a low cost glass substrate. An EL luminance of 1.05 fL was observed 40 volts above threshold at 60 Hz. This is more than an order of magnitude improvement over earlier crystalline-as-deposited thiogallate materials. These results pave the way for the use of MOCVD as a potential method for processing full color thin-film electroluminescent (TFEL) flat panel displays. The formation of the CaGa{sub 2}S{sub 4}:Ce phosphor requires precise control over a number of deposition parameters including flow rates, substrate temperature, and reactor pressure. The influence of these parameters will be discussed in terms of structure, uniformity, and TFEL device performance.

  3. Flat-panel, full-color, electroluminescent display

    NASA Astrophysics Data System (ADS)

    Robertson, James B.

    1987-08-01

    This invention relates to a flat-panel, electroluminescent display capable of achieving full color and is particularly useful in achieving a bright display with high resolution. The invention uses red, green and blue phosphors in two layers separated by layers of insulating material and layers of electrodes that are used to excite the phosphors. In operation, the display is addressed by supplying sufficient voltage between selected electrodes. This places an electric field across the phosphor at each picture element located between the overlap of the selected electrodes causing the phosphor to emit light at this location. These and other matrix-addressed displays can be addressed line-at-a-time (row or column) fashion in rapid enough sequence to display information at standard TV frame rates.

  4. Electroluminescence from single-wall carbon nanotube network transistors.

    PubMed

    Adam, E; Aguirre, C M; Marty, L; St-Antoine, B C; Meunier, F; Desjardins, P; Ménard, D; Martel, R

    2008-08-01

    The electroluminescence (EL) properties from single-wall carbon nanotube network field-effect transistors (NNFETs) and small bundle carbon nanotube field effect transistors (CNFETs) are studied using spectroscopy and imaging in the near-infrared (NIR). At room temperature, NNFETs produce broad (approximately 180 meV) and structured NIR spectra, while they are narrower (approximately 80 meV) for CNFETs. EL emission from NNFETs is located in the vicinity of the minority carrier injecting contact (drain) and the spectrum of the emission is red shifted with respect to the corresponding absorption spectrum. A phenomenological model based on a Fermi-Dirac distribution of carriers in the nanotube network reproduces the spectral features observed. This work supports bipolar (electron-hole) current recombination as the main mechanism of emission and highlights the drastic influence of carrier distribution on the optoelectronic properties of carbon nanotube films.

  5. Optical properties of inorganic electroluminescent devices with nanostripe electrodes

    NASA Astrophysics Data System (ADS)

    Nonaka, Toshihiro; Yamamoto, Shin-ichi

    2016-03-01

    In this paper, we report on the luminescence (emission) characteristics of a laminated dispersion-type inorganic electroluminescent (EL) device with a nanostripe electrode made of thin Al film, instead of a conventional indium-tin oxide (ITO) transparent electrode, on the emission side of the device. The transmittance of the Al nanostripe electrode, with 60-nm line-and-space widths, was 45%. We compared an inorganic EL device positioned between two thin films of Al and the inorganic EL device with the Al nanostripe electrode using electric field simulations and actual experiments. We were able to apply the same electric field intensity to the phosphor layer in the conventional structure and to the new structure. Therefore, with an Al nanostripe electrode on one side of the EL device, it is possible to fabricate an ITO-free display.

  6. Structural, morphological and electroluminescence studies of Zno:Co nanophosphor

    NASA Astrophysics Data System (ADS)

    Singh, Anju; Vishwakarma, H. L.

    2016-09-01

    The nanoparticles of zinc oxide (ZnO) doped with various concentrations of cobalt (Co) were synthesized by chemical precipitation method in the presence of capping agent polyvinylpyrrolidone (PVP). The effect of doping concentration on structural and morphological properties has been studied by X-ray diffraction (XRD) and scanning electron microscope (SEM). Cell volume, bond length, texture coefficient, lattice constants and dislocation density are also studied. Here, we also compared the interplaner spacing and relative peak intensities from their standard values with different angles. Crystallite sizes have been calculated by Debye-Scherrer's formula whose values are decreasing with increase in cobalt content up to 3 %. It has been seen that the growth orientation of the prepared ZnO nanorods was (101). The XRD analysis also ensures that ZnO has a hexagonal (wurtzite) crystal structure. The electroluminescence (EL) cells were prepared by placing pure and cobalt-doped ZnO nanoparticles between ITO-coated conducting glass plate and aluminium foil. Alternating voltage of various frequencies was applied, and EL brightness at different voltages was measured and corresponding current was also recorded. The voltage dependence of electroluminescence (EL) brightness of the ZnO:Co shows exponential increase. The linear voltage-current characteristic indicates ohmic nature. The EL brightness at a particular voltage is found to increase by increasing Co doping, but for higher percentage of Co the EL brightness is reduced. It is also seen that Co does not influence the threshold voltage. The brightness is also affected by increasing the frequency of AC signal.

  7. Industrial innovations for tomorrow: Advances in industrial energy-efficiency technologies. Degradable plastic made from potato peels

    SciTech Connect

    Not Available

    1992-07-01

    Stimulated by public demand and state and federal legislation, industry has begun to develop bio- and photo- degradable plastics. so far, however, none of these degradable plastics meets all of the criteria for success - adequate physical and mechanical properties for the desired use, cost-effectiveness, and 100% degradability. Polylactic acid (PLA) plastic is one degradable plastic that shows promise. It has the desired properties and is 100% degradable. However, PLA plastic made by conventional techniques is not cost effective. Made from lactic acid, which is typically made form petroleum using a very costly synthesis process. Lactic acid can also be made from carbohydrates (starches), found in food processing wastes such as potato wastes, cheese whey, and sorghum. Conversion of starch to simple sugars, and fermentation of these sugars can produce lactic acid.

  8. Selection and screening of microbial consortia for efficient and ecofriendly degradation of plastic garbage collected from urban and rural areas of Bangalore, India.

    PubMed

    Skariyachan, Sinosh; Megha, M; Kini, Meghna Niranjan; Mukund, Kamath Manali; Rizvi, Alya; Vasist, Kiran

    2015-01-01

    Industrialization and urbanization have led to massive accumulation of plastic garbage all over India. The persistence of plastic in soil and aquatic environment has become ecological threat to the metropolitan city such as Bangalore, India. Present study investigates an ecofriendly, efficient and cost-effective approach for plastic waste management by the screening of novel microbial consortia which are capable of degrading plastic polymers. Plastic-contaminated soil and water samples were collected from six hot spots of urban and rural areas of Bangalore. The plastic-degrading bacteria were enriched, and degradation ability was determined by zone of clearance method. The percentage of polymer degradation was initially monitored by weight loss method, and the main isolates were characterized by standard microbiology protocols. These isolates were used to form microbial consortia, and the degradation efficiency of the consortia was compared with individual isolate and known strains obtained from the Microbial Type Culture Collection (MTCC) and Gene Bank, India. One of the main enzymes responsible for polymer degradation was identified, and the biodegradation mechanism was hypothesized by bioinformatics studies. From this study, it is evident that the bacteria utilized the plastic polymer as a sole source of carbon and showed 20-50% weight reduction over a period of 120 days. The two main bacteria responsible for the degradation were microbiologically characterized to be Pseudomonas spp. These bacteria could grow optimally at 37 °C in pH 9.0 and showed 35-40% of plastic weight reduction over 120 days. These isolates were showed better degradation ability than known strains from MTCC. The current study further revealed that the microbial consortia formulated by combining Psuedomonas spp. showed 40 plastic weight reduction over a period of 90 days. Further, extracellular lipase, one of the main enzymes responsible for polymer degradation, was identified. The

  9. Self-Assembly of Rod-Coil Block Copolymers and Their Application in Electroluminescent Devices

    SciTech Connect

    Tao, Yuefei; Ma, Biwu; Segalman, Rachel A.

    2008-11-18

    The formation of alternating electron transporting and hole transporting 15 nm lamellae within the active layer of an organic light-emitting diode (OLED) is demonstrated to improve device performance. A new multifunctional bipolar rod-coil block copolymer containing a poly(alkoxy phenylenevinylene) (PPV) rod-shaped block as the hole transporting and emitting material and a poly(vinyloxadiazole) coil-shaped electron transporting block is synthesized. This new block copolymer is the active material of a self-assembling multicomponent electroluminescent device that can be deposited in a single step. In the thin film, grazing incidence X-ray scattering and transmission electron microscopy demonstrate that the layers form grains which are oriented bimodally: parallel and perpendicular from the anode. In this mixed orientation, the device demonstrates better performance than those with either pure PPV or a blend of the two analogous homopolymers as the active materials, i.e., higher external quantum efficiency (EQE) and brightness. This improved device performance is mainly attributed to the bipolar functionality and microphase separation of the block copolymer, which provide highly efficient hole and electron recombination at the nanodomain interfaces.

  10. Self-Assembly of Rod-Coil Block Copolymers And Their Application in Electroluminescent Devices

    SciTech Connect

    Tao, Y.; Ma, B.; Segalman, R.A.

    2009-05-26

    The formation of alternating electron transporting and hole transporting 15 nm lamellae within the active layer of an organic light-emitting diode (OLED) is demonstrated to improve device performance. A new multifunctional bipolar rod-coil block copolymer containing a poly(alkoxy phenylenevinylene) (PPV) rod-shaped block as the hole transporting and emitting material and a poly(vinyloxadiazole) coil-shaped electron transporting block is synthesized. This new block copolymer is the active material of a self-assembling multicomponent electroluminescent device that can be deposited in a single step. In the thin film, grazing incidence X-ray scattering and transmission electron microscopy demonstrate that the layers form grains which are oriented bimodally: parallel and perpendicular from the anode. In this mixed orientation, the device demonstrates better performance than those with either pure PPV or a blend of the two analogous homopolymers as the active materials, i.e., higher external quantum efficiency (EQE) and brightness. This improved device performance is mainly attributed to the bipolar functionality and microphase separation of the block copolymer, which provide highly efficient hole and electron recombination at the nanodomain interfaces.

  11. Strong visible electroluminescence from silicon nanocrystals embedded in a silicon carbide film

    SciTech Connect

    Huh, Chul Kim, Tae-Youb; Ahn, Chang-Geun; Kim, Bong Kyu

    2015-05-25

    We report the strong visible light emission from silicon (Si) nanocrystals (NCs) embedded in a Si carbide (SiC) film. Compared to Si NC light-emitting diode (LED) by employing the Si nitride (SiN{sub x}) film as a surrounding matrix, the turn-on voltage of the Si NC LED with the SiC film was significantly decreased by 4 V. This was attributed to a smaller barrier height for injecting the electrons into the Si NCs due to a smaller band gap of SiC film than a SiN{sub x} film. The electroluminescence spectra increases with increasing forward voltage, indicating that the electrons are efficiently injected into the Si NCs in the SiC film. The light output power shows a linear increase with increasing forward voltage. The light emission originated from the Si NCs in a SiC film was quite uniform. The power efficiency of the Si NC LED with the SiC film was 1.56 times larger than that of the Si NC LED with the SiN{sub x} film. The Si NCs in a SiC film show unique advantages and are a promising candidate for application in optical devices.

  12. Fabrication of efficient visible light activated Cu-P25-graphene ternary composite for photocatalytic degradation of methyl blue

    NASA Astrophysics Data System (ADS)

    Jin, Zheng; Duan, Wubiao; Liu, Bo; Chen, Xidong; Yang, Feihua; Guo, Jianping

    2015-11-01

    Cu-P25-graphene nanocomposite was fabricated through hydrothermal method at relatively low temperature. The technique used is P25-graphene (PG) binary composite was firstly prepared by P25 and graphite oxide (GO), and then Cu2+ ions were impregnated into PG composite. The prepared samples were characterized by X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), transmission electron microscopy (TEM), UV-vis diffuse reflectance spectroscopy (DRS) and photoluminescence (PL) spectrum respectively. As the results showed, the Cu-P25-graphene (CPG) nanocomposites possessed the extended light absorption in visible light and better charge separation capability as compared to the pure P25 and PG system. Moreover, CPG-4 (4 mM Cu(NO3)2) showed the highest degradation rate of methyl blue (MB) under the visible light, which the removal efficiency can reach 98% after 100 min. The corresponding hydrogen evolution rate of CPG-4 was 7.9 times than pure P25. It was concluded that the synergistic effects of Cu2+ ions and graphene narrowed the band gap of TiO2 and promoted charge separation, which played significant roles for the enhancement of photoactivity of CPG composite catalysts. In addition, it was observed that the photodegradation of MB followed the first order reaction kinetics. The effects of pH values of MB solution for photocatalysts had also been investigated. The result confirmed that the optimum values of pH were found to be 7. Finally, the stability test of photocatalysts was carried out and the photocatalytic mechanism was explained concretely.

  13. Simultaneous enhancement of photo- and electroluminescence in white organic light-emitting devices by localized surface plasmons of silver nanoclusters

    NASA Astrophysics Data System (ADS)

    Yu, Jingting; Zhu, Wenqing; Shi, Guanjie; Zhai, Guangsheng; Qian, Bingjie; Li, Jun

    2017-02-01

    White organic light-emitting devices (WOLEDs) with enhanced current efficiency and negligible color shifting equipped with an internal color conversion layer (CCL) were fabricated. They were attained by embedding a single layer of silver nanoclusters (SNCs) between the CCL and light-emitting layer (EML). The simultaneous enhancement of the photoluminescence (PL) of the CCL and electroluminescence (EL) of the EML were realized by controlling the thickness and size of the SNCs to match the localized surface plasmon resonance spectrum with the PL spectrum of the CCL and the EL spectrum of the EML. The WOLED with optimal SNCs demonstrated a 25.81% enhancement in current efficiency at 60 mA cm‑2 and good color stability over the entire range of current density.

  14. Bright Multicolor Bandgap Fluorescent Carbon Quantum Dots for Electroluminescent Light-Emitting Diodes.

    PubMed

    Yuan, Fanglong; Wang, Zhibin; Li, Xiaohong; Li, Yunchao; Tan, Zhan'ao; Fan, Louzhen; Yang, Shihe

    2017-01-01

    Multicolor bandgap fluorescent carbon quantum dots (MCBF-CQDs) from blue to red with quantum yield up to 75% are synthesized using a solvothermal method. For the first time, monochrome electroluminescent light-emitting diodes (LEDs) with MCBF-CQDs directly as an active emission layer are fabricated. The maximum luminance of blue LEDs reaches 136 cd m(-2) , which is the best performance for CQD-based monochrome electroluminescent LEDs.

  15. Degradation by acetic acid for crystalline Si photovoltaic modules

    NASA Astrophysics Data System (ADS)

    Masuda, Atsushi; Uchiyama, Naomi; Hara, Yukiko

    2015-04-01

    The degradation of crystalline Si photovoltaic modules during damp-heat test was studied using some test modules with and without polymer film insertion by observing electrical and electroluminescence properties and by chemical analyses. Acetic acid generated by the hydrolysis decomposition of ethylene vinyl acetate used as an encapsulant is the main origin of degradation. The change in electroluminescence images is explained on the basis of the corrosion of electrodes by acetic acid. On the other hand, little change was observed at the pn junction even after damp-heat test for a long time. Therefore, carrier generation occurs even after degradation; however, such generated carriers cannot be collected owing to corrosion of electrodes. The guiding principle that module structure and module materials without saving acetic acid into the modules was obtained.

  16. DHA inhibits protein degradation more efficiently than EPA by regulating the PPARγ/NFκB pathway in C2C12 myotubes.

    PubMed

    Wang, Yue; Lin, Qiao-wei; Zheng, Pei-pei; Zhang, Jian-song; Huang, Fei-ruo

    2013-01-01

    This study was conducted to evaluate the mechanism by which n-3 PUFA regulated the protein degradation in C2C12 myotubes. Compared with the BSA control, EPA at concentrations from 400 to 600 µM decreased total protein degradation (P < 0.01). However, the total protein degradation was decreased when the concentrations of DHA ranged from 300 µM to 700 µM (P < 0.01). DHA (400 µM, 24 h) more efficiently decreased the I κ B α phosphorylation and increased in the I κ B α protein level than 400 µM EPA (P < 0.01). Compared with BSA, 400 µM EPA and DHA resulted in a 47% or 68% induction of the NF κ B DNA binding activity, respectively (P < 0.01). Meanwhile, 400 µM EPA and DHA resulted in a 1.3-fold and 2.0-fold induction of the PPAR γ expression, respectively (P < 0.01). In C2C12 myotubes for PPAR γ knockdown, neither 400 µM EPA nor DHA affected the levels of p-I κ B α , total I κ B α or NF κ B DNA binding activity compared with BSA (P > 0.05). Interestingly, EPA and DHA both still decreased the total protein degradation, although PPAR γ knockdown attenuated the suppressive effects of EPA and DHA on the total protein degradation (P < 0.01). These results revealed that DHA inhibits protein degradation more efficiently than EPA by regulating the PPAR γ /NF- κ B pathway in C2C12 myotubes.

  17. Efficient on-site degradation of high concentration of spent deicing fluids: A laboratory study. Final report

    SciTech Connect

    Strong, J.M.; Waltz, M.

    1997-10-01

    The on-site treatment of antifreeze compounds and aircraft deicing fluids (ethylene glycol and propylene glycol) will reduce disposal costs, decrease environmental impact, minimize the potential for additional spills/contamination and meet the goals of pollution prevention by reducing the amount of hazardous materials generated. The authors have identified bacteria that can degrade 1-10% glycol waste at room temperatures of ca. 23C. A second subculture was isolated that could degrade glycol waste at ca. 4C.

  18. Fabrication of Sc2O3-magneli phase titanium composite electrode and its application in efficient electrocatalytic degradation of methyl orange

    NASA Astrophysics Data System (ADS)

    Bai, Hongmei; He, Ping; Chen, Jingchao; Liu, Kaili; Lei, Hong; Dong, Faqin; Zhang, Xingquan; Li, Hong

    2017-04-01

    Sc2O3-magneli phase titanium (Sc2O3-MPT) composite electrode was successfully fabricated via a simple pressing-sintering method and used for electrocatalytic degradation of methyl orange (MO). It was shown that Sc2O3 was successfully composited with MPT. Compared with MPT electrode, Sc2O3-MPT composite electrode had less spherical particles and more pores. Linear scanning voltammetry indicated that Sc2O3-MPT composite electrode presented higher oxygen evolution overpotential than MPT electrode, suggesting that Sc2O3-MPT electrode was much more suitable for the degradation of MO. The electrocatalytic degradation of MO was evaluated under different parameters including current density, temperature, initial pH and electrolysis time. Under the optimal parameters (current density 10 mA cm-2, temperature 25 °C, initial pH 3 and electrolysis time 120 min), the degradation efficiency of MO on Sc2O3-MPT composite electrode reached up to 90.16%. All these results demonstrated that Sc2O3-MPT composite electrode was effective for electrocatalytic degradation of MO and had a great potential application in the treatment of dyes wastewater.

  19. TiO₂ supported over SBA-15: an efficient photocatalyst for the pesticide degradation using solar light.

    PubMed

    Phanikrishna Sharma, M V; Durga Kumari, V; Subrahmanyam, M

    2008-11-01

    Photocatalytic degradation and mineralization of pesticides are studied over TiO(2) supported mesoporous SBA-15 composite system using solar light. TiO(2) is immobilized over SBA-15 by solid sate dispersion method. The catalysts are characterized by XRD, surface area, UV-Vis diffused reflectance spectra, SEM and TEM. The detailed photocatalytic degradation studies are carried out over TiO(2), SBA-15 and different TiO(2) wt% supported SBA-15. The activity evaluation parameters such as catalyst amount, pH, and pollutant initial concentration are studied taking isoproturon as a model compound and established conditions for pesticide degradation. The optimum degradation is achieved over 10 wt% TiO(2)/SBA-15 within 30 min and the reaction is following pseudo-first order kinetics. The isoproturon mineralization is monitored with TOC reduction and it takes around 9h for disappearance. The commercial pesticide solutions containing imidacloprid and phosphamidon are also successfully degraded over these composites with the established conditions. The data indicates that 10 wt% TiO(2)/SBA-15 composite is an effective and highly active system for the pesticide degradations.

  20. Electroluminescent layers based on ZnS:Cu deposited into matrices of porous anodic Al2O3

    NASA Astrophysics Data System (ADS)

    Valeev, R. G.; Petukhov, D. I.; Chukavin, A. I.; Bel'tyukov, A. N.

    2016-02-01

    It is suggested to use a new nanocomposite material—nanostructures of copper-doped zinc sulfide in a matrix of porous aluminum oxide—as a light-emitting layer of electroluminescent sources of light. The material was deposited by thermal evaporation in a vacuum. The microstructure of the layers, impurity distribution in the electroluminescent-phosphor layer, and electroluminescence spectra at various copper concentrations in ZnS:Cu were studied.

  1. High-efficiency sono-solar-induced degradation of organic dye by the piezophototronic/photocatalytic coupling effect of FeS/ZnO nanoarrays

    NASA Astrophysics Data System (ADS)

    Guo, Xiao; Fu, Yongming; Hong, Deyi; Yu, Binwei; He, Haoxuan; Wang, Qiang; Xing, Lili; Xue, Xinyu

    2016-09-01

    Highly-efficient sono-solar-induced degradation of organic dye by the piezophototronic/photocatalytic coupling effect of FeS/ZnO nanoarrays was achieved. A steel screen was used as the substrate for supporting FeS/ZnO nanoarrays, and the nanoarrays were vertically and uniformly grown on the substrate via a wet-chemical route. Under ultrasonic and solar irradiation, FeS/ZnO nanoarrays have high sono-photocatalytic activity for degrading methylene blue in water. The photogenerated carriers can be separated by a piezoelectric field and a built-in electric field, resulting in a low recombination rate and high photocatalytic efficiency. The piezophototronic and photocatalytic effects were coupled together. The experimental/theoretical data indicate that this novel wastewater treatment can co-use mechanical and solar energy in nature, and so is a promising technology for environment improvement.

  2. Luminescent photoelectrochemical cells. 6. Spatial aspects of the photoluminescence and electroluminescence of cadmium selenide electrodes

    SciTech Connect

    Streckert, H.H.; Tong, J.; Ellis, A.B.

    1982-01-27

    Samples of single-crystal, n-type CdSe emit when excited with ultraband gap excitation. The emission band (lambda/sub max/ approx. = 720 nm) is near the band gap of CdSe (approx. 1.7 eV); its energy, decay time, and temperature dependence are consistent with its description as edge emission. Photoluminescence (PL) spectra can be dependent on excitation wavelength and show evidence of self-absorption effects: PL spectra obtained with 457.9-nm excitation are broadened in the high-energy portion of the band relative to spectra obtained with more deeply penetrating 632.9-nm excitation. Measured PL efficiencies, theta/sub r/, are approx.10/sup -4/ in air at 295 K. When CdSe is used as the photoanode of photoelectrochemical cells employing aqueous polychalcogenide electrolytes, emission is quenched by the passage of photocurrent resulting from ultraband gap excitation. Electroluminescence (EL) can be observed from CdSe when the semiconductor is used as a dark cathode in aqueous, alkaline peroxydisulfate electrolyte. The EL spectrum is similar to the PL spectrum, suggesting the involvement of a common emissive excited state. Differences in the breadths of the spectra, however, indicate that, on average, EL is produced nearer to the semiconductor-electrolyte interface than PL under comparable experimental conditions. Measured EL efficiencies, theta/sub EL/, approaching 10/sup -3/ at -1.50 V vs SCE are comparable to PL efficiencies measured at this potential in hydroxide solution and provide evidence that the emissive excited state can be efficiently populated in an EL experiment; these lower-limit estimates of theta/sub EL/ and theta/sub r/ decline in passing to potentials near the onset of EL, approx.-0.9 V vs SCE. Spatial features of these comparisons are discussed.

  3. Surface Lattice Resonances for Enhanced and Directional Electroluminescence at High Current Densities.

    PubMed

    Zakharko, Yuriy; Held, Martin; Graf, Arko; Rödlmeier, Tobias; Eckstein, Ralph; Hernandez-Sosa, Gerardo; Hähnlein, Bernd; Pezoldt, Jörg; Zaumseil, Jana

    2016-12-21

    Hybrid photonic-plasmonic modes in periodic arrays of metallic nanostructures offer a promising trade-off between high-quality cavities and subdiffraction mode confinement. However, their application in electrically driven light-emitting devices is hindered by their sensitivity to the surrounding environment and to charge injecting metallic electrodes in particular. Here, we demonstrate that the planar structure of light-emitting field-effect transistor (LEFET) ensures undisturbed operation of the characteristic modes. We incorporate a square array of gold nanodisks into the charge transporting and emissive layer of a polymer LEFET in order to tailor directionality and emission efficiency via the Purcell effect and variation of the fractional local density of states in particular. Angle- and polarization-resolved spectra confirm that the enhanced electroluminescence correlates with the dispersion curves of the surface lattice resonances supported by these structures. These LEFETs reach current densities on the order of 10 kA/cm(2), which may pave the way toward practical optoelectronic devices with tailored emission patterns and potentially electrically pumped plasmonic lasers.

  4. First full-color thin film electroluminescent (TFEL) display product: the FC-2

    NASA Astrophysics Data System (ADS)

    Laakso, C.; Barrow, W. A.; Coovert, R.; Dickey, Eric; Flegal, T.; Fullman, M.; King, Christopher N.; Tuenge, Richard T.; Sun, Sey-Shing; Schaus, Christian F.

    1995-04-01

    Planar has developed the first manufacturable, full color, high contrast, 320.256 line thin film electroluminescent (TFEL) display; the FC-2. Three primary tasks in developing the FC-2 were (1) blue phosphor improvement, (2) unique panel structure development for enhanced optical properties, and (3) application of high density interconnects. We review progress in the development of the cerium doped, alkaline earth thiogallate compounds for blue emission. ZnS:Mn is filtered for red emission and ZnS:Tb is used for green. The panel structure reported optimizes key performance parameters by enhancing the fill factor, frequency of operation, and power efficiency. It uses a `dual substrate' approach, placing the blue phosphor on one substrate and the red/green on the other. We describe panel fabrication processes and assembly techniques utilized. We also describe the electronic driver and addressing schemes used to maximize the brightness. The high interconnect density in this 5' diagonal display demands an improved driver interconnect scheme. Planar has developed a chip on glass (COG) process with the driver chips bonded directly to the glass substrate and wire bonded to the rows, columns, and control electronics. This approach is compared to conventional tape carrier package (TCP) and flex interconnects. Mechanical, optical and electrical panel performance specifications are reported together with some exiting areas of future development.

  5. Near-infrared electroluminescence at room temperature from neodymium-doped gallium nitride thin films

    SciTech Connect

    Kim, Joo Han; Holloway, Paul H.

    2004-09-06

    Strong near-infrared (NIR) electroluminescence (EL) at room temperature from neodymium (Nd)-doped gallium nitride (GaN) thin films is reported. The Nd-doped GaN films were grown by radio-frequency planar magnetron cosputtering of separate GaN and metallic Nd targets in a pure nitrogen ambient. X-ray diffraction data did not identify the presence of any secondary phases and revealed that the Nd-doped GaN films had a highly textured wurtzite crystal structure with the c-axis normal to the surface of the film. The EL devices were fabricated with a thin-film multilayered structure of Al/Nd-doped GaN/Al{sub 2}O{sub 3}-TiO{sub 2}/indium-tin oxide and tested at room temperate. Three distinct NIR EL emission peaks were observed from the devices at 905, 1082, and 1364 nm, arising from the radiative relaxation of the {sup 4}F{sub 3sol2} excited-state energy level to the {sup 4}I{sub 9sol2}, {sup 4}I{sub 11sol2}, and {sup 4}I{sub 13sol2} levels of the Nd{sup 3+} ion, respectively. The threshold voltage for all the three emission peaks was {approx}150 V. The external power efficiency of the fabricated EL devices was {approx}1x10{sup -5} measured at 40 V above the threshold voltage.

  6. Improved electroluminescence with reversed bilayers of thiophene/phenylene co-oligomer derivatives

    NASA Astrophysics Data System (ADS)

    Dokiya, Shohei; Sasaki, Fumio; Hotta, Shu; Yanagi, Hisao

    2016-03-01

    Organic electroluminescence (EL) devices were fabricated with bilayered thiophene/phenylene co-oligomer (TPCO) derivatives: p-type 5,5‧-bis(4-biphenylyl)-2,2‧-bithiophene (BP2T) and n-type 5,5‧-bis(4‧-cyanobiphenyl-4-yl)-2,2‧-bithiophene (BP2T-CN). Two types of EL device, Al:Li/BP2T-CN/BP2T/ITO (device A) and Au/BP2T/BP2T-CN/ITO (device B), were investigated using vapor-deposited films of BP2T and BP2T-CN by changing the order of deposition onto the indium-tin-oxide (ITO)/glass substrate. The EL performance was significantly improved for device B in which the two molecules had a lying orientation suitable for efficient carrier injection and transport as well as surface emission. In device A, on the other hand, the standing BP2T orientation resulted in much lower current density and EL intensity.

  7. Surface Lattice Resonances for Enhanced and Directional Electroluminescence at High Current Densities

    PubMed Central

    2016-01-01

    Hybrid photonic-plasmonic modes in periodic arrays of metallic nanostructures offer a promising trade-off between high-quality cavities and subdiffraction mode confinement. However, their application in electrically driven light-emitting devices is hindered by their sensitivity to the surrounding environment and to charge injecting metallic electrodes in particular. Here, we demonstrate that the planar structure of light-emitting field-effect transistor (LEFET) ensures undisturbed operation of the characteristic modes. We incorporate a square array of gold nanodisks into the charge transporting and emissive layer of a polymer LEFET in order to tailor directionality and emission efficiency via the Purcell effect and variation of the fractional local density of states in particular. Angle- and polarization-resolved spectra confirm that the enhanced electroluminescence correlates with the dispersion curves of the surface lattice resonances supported by these structures. These LEFETs reach current densities on the order of 10 kA/cm2, which may pave the way toward practical optoelectronic devices with tailored emission patterns and potentially electrically pumped plasmonic lasers. PMID:28042593

  8. Incorporation of electroluminescence and electrochemiluminescence in one organic light-emitting device

    NASA Astrophysics Data System (ADS)

    Zhen, Changgua; Chuai, Yutao; Lao, Chunfeng; Huang, Lan; Zou, Dechun; Lee, Do Nam; Kim, Byeong Hyo

    2005-08-01

    The incorporation of electroluminescence and electrochemiluminescence in one light-emitting device with the configuration of indium tin oxide (ITO)/[Ru(bpy)2(dimbpy)](PF6)2/Alq3(30nm)/NPB(45nm)/Ag(60nm) is investigated. When the ITO and Ag electrodes are negatively and positively biased respectively, the color of the emission changes from green to light yellow-white within 100 s. So there is only one recombination zone in the bulk of the Alq3 at the initial stage of the operation, followed by the formation of another recombination zone in the bulk of the [Ru(bpy)2(dimbpy)](PF6)2. This directly indicates the existence of unipolar injection (electron injection) process in the ruthenium complex layer. The external quantum efficiency of the device is 1.4% compared with 0.45% of the ITO /[Ru(bpy)2(dimbpy)](PF6)2/Ag device, improved by twofold. Furthermore, this hybrid device provides a feasible way to control the emission of a wide spectrum of colors including red, green, yellow, and white.

  9. Comparative studies of operational parameters of degradation of azo dyes in visible light by highly efficient WOx/TiO2 photocatalyst.

    PubMed

    Sajjad, Ahmed Khan Leghari; Shamaila, Sajjad; Tian, Baozhu; Chen, Feng; Zhang, Jinlong

    2010-05-15

    The multidimensional aspects of the photocatalytic activity were investigated in a systematic way by employing the dyes Acid Orange 7 (AO7) and Methyl Orange (MO) as substrates in terms of their degradation or conversion rates. 4.0% WO(x)/TiO(2) nanocomposite demonstrated the best reactivity under visible light, allowing more efficient usage of solar light. The reduced form of W decreased the band gap and inhibited electron hole recombination efficiently. This composite was characterized by X-ray diffraction spectroscopy (XRD), UV-vis diffuse reflectance spectroscopy (DRS), transmission electron microscopy (TEM) and energy dispersive X-ray spectroscopy (EDX). A series of experiments were conducted to investigate the operational parameters under visible light irradiation such as optimization of nanocomposites wt%, change of pH, reuse of catalyst and initial dye concentration. The kinetics of the dyes degradation was found to follow the Langmuir-Hinshelwood model. Decomposition or mineralization was investigated with the changes of absorption spectra, pH, degradation efficiency and TOC removal in visible irradiation systems. FT-IR spectroscopy of these adsorbed dyes on WO(x)/TiO(2) powder provided an insight to the mode of its adsorption on WO(x)/TiO(2). It was found that the dye adsorbed on WO(x)/TiO(2) underwent a series of oxidation steps which lead to decolorization and formation of a number of intermediates mainly aromatic and aliphatic acids. These intermediates were quantified by GC/GC-MS.

  10. Investigation Into Efficiency of a Novel Glycol Chitosan-Bestatin Conjugate to Protect Thymopoietin Oligopeptides From Enzymatic Degradation.

    PubMed

    Zhang, Yong; Feng, Jiao; Cui, Lili; Zhang, Yuebin; Li, Wenzhao; Li, Chunlei; Shi, Nianqiu; Chen, Yan; Kong, Wei

    2016-02-01

    In this study, a novel glycol chitosan (GCS)-bestatin conjugate was synthesized and evaluated to demonstrate its efficacy in protecting thymopoietin oligopeptides from aminopeptidase-mediated degradation. Moreover, the mechanism and relative susceptibility of three thymopoietin oligopeptides, thymocartin (TP4), thymopentin (TP5), and thymotrinan (TP3), to enzymatic degradation were investigated and compared at the molecular level. Initial investigations indicated that formation of the GCS-bestatin conjugate, with a substitution degree of 7.0% (moles of bestatin per mole of glycol glucosamine unit), could significantly protect all 3 peptides from aminopeptidase-mediated degradation in a concentration-dependent manner. The space hindrance and loss of one pair of hydrogen bonds, resulting from the covalent conjugation of chitosan with bestatin, did not affect the specific interaction between bestatin and aminopeptidase. Moreover, TP4 displayed a higher degradation clearance compared with those of TP5 and TP3 under the same experimental conditions. The varying levels of susceptibility of these 3 peptides to aminopeptidase (TP4 > TP5 > TP3) were closely related to differences in their binding energies to enzyme, which mainly involved Van der Waals forces and electrostatic interactions, as supported by the results of molecular dynamics simulations. These results suggest that GCS-bestatin conjugate might be useful in the delivery of thymopoietin oligopeptides by mucosal routes, and that TP3 and TP5 are better alternatives to TP4 for delivery because of their robust resistance against enzymatic degradation.

  11. Impact of hydrodynamics on pollutant degradation and energy efficiency of VUV/UV and H2O2/UV oxidation processes.

    PubMed

    Bagheri, Mehdi; Mohseni, Madjid

    2015-12-01

    The Vacuum-UV/UV process, an incipient catalyst/chemical-free advanced oxidation process (AOP), is potentially a cost-effective solution for the removal of harmful micropollutants from water. Utilizing a novel mechanistic numerical model, this work aimed to establish a thorough understanding of the degradation mechanisms in the VUV/UV process operating under continuous flow conditions, when compared with the widely applied H2O2/UV AOP. Of particular interest was the examination of the impact of flow characteristics (hydrodynamics) on the degradation efficacy of a target micropollutant during the VUV/UV and H2O2/UV AOPs. While hydroxyl radical (OH) oxidation was the dominant degradation pathway in both processes, the degradation efficacy of the VUV/UV process showed much stronger correlation with the extent of mixing in the photoreactor. Under a uniform flow regime, the degradation efficiency of the target pollutant achieved by the H2O2/UV process with 2- and 5 ppm H2O2 was greater than that provided by the VUV/UV process. Nonetheless, introduction of mixing and circulation zones to the VUV/UV reactor resulted in superior performance compared with the H2O2/UV AOP. Based on the electrical energy-per-order (EEO) analysis, incorporation of circulation zones resulted in a reduction of up to 50% in the overall energy cost of the VUV/UV AOP, while the corresponding reduction for the 5-ppm H2O2/UV system was less than 5%. Furthermore, the extent of OH scavenging of natural organic matter (NOM) on energy efficiency of the VUV/UV and H2O2/UV AOPs under continuous flow conditions was assessed using the EEO analysis.

  12. [Screening of a Highly Efficient Quinoline-degrading Strain and Its Enhanced Biotreatment on Coking Waste Water].

    PubMed

    Li, Jing; Li, Wen-ying

    2015-04-01

    A bacterial strain, which could utilize quinoline as the sole carbon, nitrogen and energy source, was isolated from the activated sludge in a coking wastewater treatment plant. According to the 16S rRNA gene sequence analysis, the strain was identified as Acidovorax sp. Taken into consideration of both the growth and the quinoline degradation of the strain, the optimized degradation conditions were acquired as following: 10% inoculum, pH value of 8.0-10.0, 35 degrees C and 150 r x min(-1). The process of its growth was simulated by Haldane kinetic model under different initial quinoline concentrations, the fitted curve had a good correlation with test measured values. Furthermore, coking wastewater was bioaugmented by the mixed strains of DQS-01 and D2 with enhanced process in a moving bed biofilm reactor, and the COD degradation rate was 87.4% within 72 h.

  13. Intense green-yellow electroluminescence from Tb+-implanted silicon-rich silicon nitride/oxide light emitting devices

    NASA Astrophysics Data System (ADS)

    Berencén, Y.; Wutzler, R.; Rebohle, L.; Hiller, D.; Ramírez, J. M.; Rodríguez, J. A.; Skorupa, W.; Garrido, B.

    2013-09-01

    High optical power density of 0.5 mW/cm2, external quantum efficiency of 0.1%, and population inversion of 7% are reported from Tb+-implanted silicon-rich silicon nitride/oxide light emitting devices. Electrical and electroluminescence mechanisms in these devices were investigated. The excitation cross section for the 543 nm Tb3+ emission was estimated under electrical pumping, resulting in a value of 8.2 × 10-14 cm2, which is one order of magnitude larger than one reported for Tb3+:SiO2 light emitting devices. These results demonstrate the potentiality of Tb+-implanted silicon nitride material for the development of integrated light sources compatible with Si technology.

  14. Direct band gap electroluminescence from bulk germanium at room temperature using an asymmetric fin type metal/germanium/metal structure

    SciTech Connect

    Wang, Dong Maekura, Takayuki; Kamezawa, Sho; Yamamoto, Keisuke; Nakashima, Hiroshi

    2015-02-16

    We demonstrated direct band gap (DBG) electroluminescence (EL) at room temperature from n-type bulk germanium (Ge) using a fin type asymmetric lateral metal/Ge/metal structure with TiN/Ge and HfGe/Ge contacts, which was fabricated using a low temperature (<400 °C) process. Small electron and hole barrier heights were obtained for TiN/Ge and HfGe/Ge contacts, respectively. DBG EL spectrum peaked at 1.55 μm was clearly observed even at a small current density of 2.2 μA/μm. Superlinear increase in EL intensity was also observed with increasing current density, due to superlinear increase in population of elections in direct conduction band. The efficiency of hole injection was also clarified.

  15. Remarkable improvement in electroluminescence benefited from appropriate electron injection and transporting in ultraviolet organic light-emitting diode

    NASA Astrophysics Data System (ADS)

    You, Fengjiao; Mo, Bingjie; Liu, Liming; Wang, Honghang; Bin Wei; Xu, Jiwen; Zhang, Xiaowen

    2016-08-01

    Suitable thickness of LiF and 4,7-diphenyl-1, 10-phenanthroline with slightly weakened electron injection and transporting is proposed to match the intractable hole injection capacity in ultraviolet organic light-emitting diode (UV OLED). By using this strategy, the device performance is remarkably improved. With 4,4‧-bis(carbazol-9-yl)biphenyl (CBP) and 3-(4-biphenyl)-4-phenyl-5-tert-butylphenyl-1,2,4-triazole (TAZ) as emitters, the UV OLED shows maximum radiance of 5.8 mW/cm2 and external quantum efficiency of 2.1% with emission peak of ~380 nm predominantly from TAZ and noticeable shoulder emission of ~410 nm from CBP. The retarded electron injection and transporting contribute to optimizing hole-electron recombination zone and balance within the emitting layers, which accounts for the improved electroluminescent intensity. The detailed mechanism is further clarified with impedance spectroscopy.

  16. In-situ mapping of electroluminescent enhancement of light-emitting diodes grown on patterned sapphire substrates

    NASA Astrophysics Data System (ADS)

    Su, Jung-Chieh; Lee, Chung-Hao; Huang, Yi-Hsuan; Yang, Henglong

    2017-02-01

    The mechanism for enhancing extraction efficiency of light emitting diodes (LEDs) grown on patterned sapphire substrates (PSSs) was observed by the in-situ lateral electroluminescence (EL) mapping using optical microscopy equipped with a laser energy profiler. The observed spatial intensity distribution of epilayers, varying from epilayer to epilayer on the lateral surface of the PSS LED chip, revealed that the perimeter scattering on the convex facets of PSSs converges the propagation of emitted light with random directionality into a spot near the top surface of the buffer layer. Moreover, this in-situ sidewall mapping implied that the enhancement of light extraction of the PSS LED is due to reducing the total internal reflection effect, resulting from the spot located closer to the LED/air interface. Simulated results and EL images of convex patterns on the PSS surface were consistent with sidewall surface-based observations.

  17. Determining the degradation efficiency and mechanisms of ethyl violet using HPLC-PDA-ESI-MS and GC-MS

    PubMed Central

    2012-01-01

    Background The discharge of wastewater that contains high concentrations of reactive dyes is a well-known problem associated with dyestuff activities. In recent years, semiconductor photocatalysis has become more and more attractive and important since it has a great potential to contribute to such environmental problems. One of the most important aspects of environmental photocatalysis is in the selection of semiconductor materials like ZnO and TiO2, which are close to being two of the ideal photocatalysts in several respects. For example, they are relatively inexpensive, and they provide photo-generated holes with high oxidizing power due to their wide band gap energy. In this work, nanostructural ZnO film on the Zn foil of the Alkaline-Manganese Dioxide-Zinc Cell was fabricated to degrade EV dye. The major innovation of this paper is to obtain the degradation mechanism of ethyl violet dyes resulting from the HPLC-PDA-ESI-MS analyses. Results The fabrication of ZnO nanostructures on zinc foils with a simple solution-based corrosion strategy and the synthesis, characterization, application, and implication of Zn would be reported in this study. Other objectives of this research are to identify the reaction intermediates and to understand the detailed degradation mechanism of EV dye, as model compound of triphenylmethane dye, with active Zn metal, by HPLC-ESI-MS and GC-MS. Conclusions ZnO nanostructure/Zn-foils had an excellent potential for future applications on the photocatalytic degradation of the organic dye in the environmental remediation. The intermediates of the degradation process were separated and characterized by the HPLC-PDA-ESI-MS and GC-MS, and twenty-six intermediates were characterized in this study. Based on the variation of the amount of intermediates, possible degradation pathways for the decolorization of dyes are also proposed and discussed. PMID:22748361

  18. Matrix-assisted resonant infrared pulsed laser ablation of electroluminescent dendrimers

    NASA Astrophysics Data System (ADS)

    Torres-Pagan, Ricardo Daniel

    The deposition techniques for polymer thin films in organic light emitting diodes are limited to wet methods since molecular pyrolysis prevents the use of dry vacuum thermal evaporation methods. Wet methods have critical limitations such as poor thickness control, drying patterns and re-dissolution of previous layers. In this work, a novel approach, Matrix-Assisted Resonant Infrared Pulsed Laser Ablation (RIM-PLA) has been studied as an alternative deposition method for electroluminescent polymer films. RIM-PLA was successfully used for the deposition of two model dendrimers: fluorescent and phosphorescent Ir-cored. A free-electron laser was tuned to resonance frequencies for the vibrational modes of two solid matrix solvents: chloroform (C-H stretch; C-H bending) and toluene (C-H stretch; C=C stretch). The temperature-dependent absorption coefficients for each resonance mode were measured. Targets made from flash-frozen, low-concentration solutions of the dendrimers were irradiated at each frequency while varying fluence and exposure times. The molecular structure integrity of the targets was characterized. The deposited films were characterized to assess structure fidelity, roughness and topography, and luminance. All RIM-PLA deposited films were compared with spin-coated films. The ablation characteristics for each mode were found to be dependent on the solvent and not the dendrimer. Calculations from a temperature-rise model show that FEL pulsed-irradiation results in heating rates on the order of 108--109 K/s, resulting in metastable condensed targets. Thermodynamic and kinetic relations were used to calculate the relevance of three ablation mechanisms: normal vaporization, normal boiling and phase explosion. The latter mechanism has a critical threshold (> 0.8 Tc) for each solvent, and proceeds through spinodal decay followed by rapid homogeneous nucleation of vapor bubbles within the focal volume. For both chloroform modes, the primary ablation mechanism was

  19. The preparation of ZnS:Mn electroluminescent layers by MOCVD using new manganese sources

    NASA Astrophysics Data System (ADS)

    Migita, M.; Kanehisa, O.; Shiiki, M.; Yamamoto, H.

    1988-12-01

    In the preparation of ZnS:Mn polycrystalline films by MOCVD, CPM [(C 5H 5) 2Mn: di-π-cyclopentadienyl manganese] and BCPM [(CH 3C 5H 4) 2Mn: bismethylcyclopentadienyl manganese] are employed as new doping sources, and are compared with previously reported TCM [(CH 3C 5H 4)Mn(CO) 3: tricarbonyl methylcyclopentadienyl manganese]. In contrast to TCM, which is only partially decomposed even at 400 ˜ 500°C, CPM and BCPM are completely decomposed around the optimum growth temperature of ZnS, i.e. 280-350°C. When thermally decomposed, TCM produces a by-product containing Mn and carbonyl, which does not contribute to the luminescence, but CPM and BCPM do not. By these advantages, the double-insulator type electroluminescent (EL) devices prepared with CPM or BCPM show higher luminance than those prepared with TCM. A 500 nm thick ZnS:Mn layer by CPM gives the maximum efficiency ( ηmax) of 4.8 lm/W and a saturated luminance ( Lsat) of 4300 cd/m 2 at 1 kHz sine wave excitation. By BCPM, Lsat of 3150 cd/m 2 was obtained. Meanwhile, the devices prepared with TCM in this investigation show Lsat to be less than 1000 cd/m 2 and a low efficiency of less than 1 lm/W. By the combination with red filters, ZnS:Mn by MOCVD with CPM or BCPM can also provide efficient red EL. When a glass filter (the cut-off wavelength is 590 nm) is used, the EL device prepared with CPM gives Lsat=1420 cd/m 2 and ηmax=1.6 lm/W (the color coordinates, x=0.626 and y=0.373) at 1 kHz sine wave excitation.

  20. Red, green, blue and white organic electroluminescent devices

    NASA Astrophysics Data System (ADS)

    Tsou, Chuan-Cheng; Lu, Huei-Tzong; Yokoyama, Meiso

    2005-06-01

    Full-color capability is an essential feature in organic electroluminescent (OEL) devices for flat panel display. This work presents novel designs for red, green, blue and white OEL devices. Indium tin oxide (ITO) was used as a glass substrate and N, N'-bis-(1-naphthyl)- N, N'-diphenyl-1,1-biphenyl-4-4'-diamine (NPB) as a hole transport layer (HTL). Bathocuproine (BCP) was used as a hole-blocking layer (HBL), DCM2, as a red fluorescent dye, was doped into the BCP layer. Tris-(8-hydroxy-quinoline) aluminum (Alq 3) was used in the electron transport layer (ETL), and aluminum (Al) was used as a cathode in OEL devices with the configuration ITO/NPB (30 nm)/BCP:DCM2 ( x%, 30 nm)/Alq 3 (40 nm)/Al. A green OEL device is obtained by employing this structure without a BCP:DCM2 ( x %) layer; a blue OEL device is obtained by using a BCP layer without the DCM2 dopant. The red OEL device is obtained by doping 10% DCM2 in the BCP layer. The white OEL device is produced by doping 1% DCM2 in the BCP layer. The CIE x and y coordinates of the white OEL device are 0.32 and 0.32, respectively.

  1. Synthesis, photophysics, electrochemistry, thermal stability and electroluminescent performances of a new europium complex with bis(β-diketone) ligand containing carbazole group.

    PubMed

    Liu, Jian; Liang, Quan-Bin; Wu, Hong-Bin

    2016-09-07

    We synthesized a new europium complex [Eu(ecbpd)3 (Phen)] with bis(β-diketone) ligand containing a carbazole group, in which ecbpd and Phen are dehydro-3,3'-(9-ethyl-9H-carbazole-3,6-diyl)bis(1-phenylpropane-1,3-dione) and 1,10-phenanthroline, respectively. Its UV/vis and photoluminescent spectra, quantum yield, luminescence lifetime, electrochemistry, thermal stability and electroluminescent performances were studied. This europium complex showed low efficiency luminescence, which is probably due to the mismatching energy levels of its ligand and Eu(3)(+) , as well as the double Eu(3)(+) core resonance.

  2. White light from an electroluminescent diode made from poly(3(4-octylphenyl)-2,2min -bithiophene) and an oxadiazole derivative

    NASA Astrophysics Data System (ADS)

    Berggren, M.; Gustafsson, G.; Inganas, O.; Andersson, M. R.; Hjertberg, T.; Wennerstrom, O.

    1994-12-01

    We report on an electroluminescent diode emitting red, green, and blue light simultaneously. The device is based on a thin polymer layer, poly(3-(4-octylphenyl)-2,2 min-bithiophene) and a thick molecular layer, 2-(4-biphenylyl)-5-(4-tertbutyl-phenyl)1,3,5-oxadiazole. The quantum efficiency for light conversion is 0.3% and the turn-on voltage for light emission is 7 V. In this arcitcle we present electric and spectroscopic characterizations. A mechanism for the light emission, based on electron and hole recombination between the two organic layers, is proposed.

  3. Degradation of microcystin-LR by highly efficient AgBr/Ag3PO4/TiO2 heterojunction photocatalyst under simulated solar light irradiation

    NASA Astrophysics Data System (ADS)

    Wang, Xin; Utsumi, Motoo; Yang, Yingnan; Li, Dawei; Zhao, Yingxin; Zhang, Zhenya; Feng, Chuanping; Sugiura, Norio; Cheng, Jay Jiayang

    2015-01-01

    A novel photocatalyst AgBr/Ag3PO4/TiO2 was developed by a simple facile in situ deposition method and used for degradation of mirocystin-LR. TiO2 (P25) as a cost effective chemical was used to improve the stability of AgBr/Ag3PO4 under simulated solar light irradiation. The photocatalytic activity tests for this heterojunction were conducted under simulated solar light irradiation using methyl orange as targeted pollutant. The results indicated that the optimal Ag to Ti molar ratio for the photocatalytic activity of the resulting heterojunction AgBr/Ag3PO4/TiO2 was 1.5 (named as 1.5 BrPTi), which possessed higher photocatalytic capacity than AgBr/Ag3PO4. The 1.5 BrPTi heterojunction was also more stable than AgBr/Ag3PO4 in photocatalysis. This highly efficient and relatively stable photocatalyst was further tested for degradation of the hepatotoxin microcystin-LR (MC-LR). The results suggested that MC-LR was much more easily degraded by 1.5 BrPTi than by AgBr/Ag3PO4. The quenching effects of different scavengers proved that reactive h+ and •OH played important roles for MC-LR degradation.

  4. Efficient degradation of chlorimuron-ethyl by a bacterial consortium and shifts in the aboriginal microorganism community during the bioremediation of contaminated-soil.

    PubMed

    Li, Chunyan; Lv, Tongyang; Liu, Wanjun; Zang, Hailian; Cheng, Yi; Li, Dapeng

    2017-05-01

    Excessive application of chlorimuron-ethyl has led to soil contamination and limited crop rotation; therefore, tactics to decrease and eliminate residual chlorimuron-ethyl in the environment have attracted increasing attention. In this study, two chlorimuron-ethyl-degrading bacterial strains (Rhodococcus sp. D310-1; Enterobacter sp. D310-5) were used to ferment and prepare a chlorimuron-ethyl-degrading bacterial consortium. To improve the degradation efficiency of the bacterial consortium, the cultivation conditions were optimized using response surface methodology (RSM). The maximum biodegradation rate (87.42%) was obtained under optimal conditions (carbon concentration, 9.21gL(-1); temperature, 26.15°C; pH, 6.95). The rate of chlorimuron-ethyl degradation by the bacterial consortium in the chlorimuron-ethyl-contaminated soil was monitored and reached 80.02% at the end of a 60-d incubation period. Illumina MiSeq sequencing results showed that microbial diversity was high, and 33 phyla were identified in the analyzed samples. Proteobacteria, Acidobacteria, Acidobacteria, Firmicutes and Bacteroidetes were present in relatively high abundances in the samples. The bacterial consortium made a positive impact on the remediation of chlorimuron-ethyl-contaminated soil and somewhat altered the composition of the bacterial community in the chlorimuron-ethyl-contaminated soil. These findings provide highly valuable information on the production of bacterial consortium for the remediation of chlorimuron-ethyl and other sulfonylurea-herbicide-contaminated soil.

  5. A novel method developed for estimating mineralization efficiencies and its application in PC and PEC degradations of large molecule biological compounds with unknown chemical formula.

    PubMed

    Li, Guiying; Liu, Xiaolu; An, Taicheng; Wong, Po Keung; Zhao, Huijun

    2016-05-15

    A new method to estimate the photocatalytic (PC) and photoelectrocatalytic (PEC) mineralization efficiencies of large molecule biological compounds with unknown chemical formula in water was firstly developed and experimentally validated. The method employed chemical oxidation under the standard dichromate chemical oxygen demand (COD) conditions to obtain QCOD values of model compounds with unknown chemical formula. The measured QCOD values were used as the reference to replace QCOD values of model compounds for calculation of the mineralization efficiencies (in %) by assuming the obtained QCOD values are the measure of the theoretical charge required for the complete mineralization of organic pollutants. Total organic carbon (TOC) was also employed as a reference to confirm the mineralization capacity of dichromate chemical oxidation. The developed method was applied to determine the degradation extent of model compounds, such as bovine serum albumin (BSA), lecithin and bacterial DNA, by PC and PEC. Incomplete PC mineralization of all large molecule biological compounds was observed, especially for BSA. But the introduction of electrochemical technique into a PC oxidation process could profoundly improve the mineralization efficiencies of model compounds. PEC mineralization efficiencies of bacterial DNA was the highest, while that of lecithin was the lowest. Overall, PEC degradation method was found to be much effective than PC method for all large molecule biological compounds investigated, with PEC/PC mineralization ratios followed an order of BSA > lecithin > DNA.

  6. Degradation of 2,6-di-tert-butylphenol by an isolated high-efficiency bacterium strain.

    PubMed

    Zhang, Ya-lei; Fang, Zhen-wei; Xu, De-qiang; Xiao, Yi-ping; Zhao, Jian-fu; Qiang, Zhi-min

    2005-01-01

    An aerobic bacterium strain, F-3-4, capable of effectively degrading 2, 6-ditert-butylphenol (2, 6-DTBP), was isolated and screened out from an acrylic fiber wastewater and the biofilm in the wastewater treatment facilities. This strain was identified as Alcaligenes sp. through morphological, physiological and biochemical examinations. After cultivation, the strain was enhanced by 26.3% in its degradation capacity for 2,6-DTBP. Results indicated that the strain was able to utilize 2,6-DTBP, lysine, lactamine, citrate, n-utenedioic acid and malic acid as the sole carbon and energy source, alkalinize acetamide, asparagine, L-histidine, acetate, citrate and propionate, but failed to utilize glucose, D-fructose, D-seminose, D-xylose, serine and phenylalanine as the sole carbon and energy source. The optimal growth conditions were determined to be: temperature 37 degrees C, pH 7.0, inoculum size 0.1% and shaker rotary speed 250 r/min. Under the optimal conditions, the degradation kinetics of 2,6-DTBP with an initial concentration of 100 mg/L was studied. Results indicated that 62.4% of 2,6-DTBP was removed after 11 d. The degradation kinetics could be expressed by Eckenfelder equation with a half life of 9.38 d. In addition, the initial concentration of 2,6-DTBP played an important role on the degradation ability of the strain. The maximum initial concentration of 2,6-DTBP was determined to be 200 mg/L. Above this level, the strain was overloaded and exhibited significant inhibition.

  7. Improvement of ethanol productivity and energy efficiency by degradation of inhibitors using recombinant Zymomonas mobilis (pHW20a-fdh).

    PubMed

    Dong, Hong-Wei; Fan, Li-Qiang; Luo, Zichen; Zhong, Jian-Jiang; Ryu, Dewey D Y; Bao, Jie

    2013-09-01

    Toxic compounds, such as formic acid, furfural, and hydroxymethylfurfural (HMF) generated during pretreatment of corn stover (CS) at high temperature and low pH, inhibit growth of Zymomonas mobilis and lower the conversion efficiency of CS to biofuel and other products. The inhibition of toxic compounds is considered as one of the major technical barriers in the lignocellulose bioconversion. In order to detoxify and/or degrade these toxic compounds by the model ethanologenic strain Z. mobilis itself in situ the fermentation medium, we constructed a recombinant Z. mobilis ZM4 (pHW20a-fdh) strain that is capable of degrading toxic inhibitor, formate. This is accomplished by cloning heterologous formate dehydrogenase gene (fdh) from Saccharomyces cerevisiae and by coupling this reaction of NADH regeneration reaction system with furfural and HMF degradation in the recombinant Z. mobilis strain. The NADH regeneration reaction also improved both the energy efficiency and cell physiological activity of the recombinant organism, which were definitely confirmed by the improved cell growth, ethanol yield, and ethanol productivity during fermentation with CS hydrolysate.

  8. Hybrid electroluminescent device based on MEH-PPV and ZnO

    NASA Astrophysics Data System (ADS)

    Hewidy, Dina.; Gadallah, A.-S.; Fattah, G. Abdel

    2017-02-01

    Hybird organic/inorganic electroluminescent device based on the structure of glass/ITO/PEDOT:PSS/MEH-PPV/ZnO/ZnO submicrorods/Al has been manufactured. Spin coating has been used to deposit both PEDOT:PSS and MEH-PPV. Two-step process has been used to synthesis ZnO submicrorods, namely, spin coating and chemical bath deposition. Changing the dimensions of the ZnO submicrorods in this layer structure has been investigated to improve the performance of the organic/inorganic electroluminescence device. Such layer structure provides electroluminescence with narrow emission bands due to a high gain with this structure. X-ray diffraction patterns and scanning electron microscope images show that ZnO submicrorods have hexagon structure. Current-voltage curve for the structure has been reported. Electroluminescence curves (electroluminescence intensity versus wavelength) at different bias voltages have been presented and these results show narrowing in full width at half maximum in the spectra at high current density compared to photoluminescence excitation. The narrowing in the spectrum has been explained.

  9. Fourier transform infrared spectroscopy approach for measurements of photoluminescence and electroluminescence in mid-infrared.

    PubMed

    Zhang, Y G; Gu, Y; Wang, K; Fang, X; Li, A Z; Liu, K H

    2012-05-01

    An improved Fourier transform infrared spectroscopy approach adapting to photoluminescence and electroluminescence measurements in mid-infrared has been developed, in which diode-pumped solid-state excitation lasers were adopted for photoluminescence excitation. In this approach, three different Fourier transform infrared modes of rapid scan, double modulation, and step scan were software switchable without changing the hardware or connections. The advantages and limitations of each mode were analyzed in detail. Using this approach a group of III-V and II-VI samples from near-infrared extending to mid-infrared with photoluminescence intensities in a wider range have been characterized at room temperature to demonstrate the validity and overall performances of the system. The weaker electroluminescence of quantum cascade lasers in mid-infrared band was also surveyed at different resolutions. Results show that for samples with relatively strong photoluminescence or electroluminescence out off the background, rapid scan mode is the most preferable. For weaker photoluminescence or electroluminescence overlapped with background, double modulation is the most effective mode. To get a better signal noise ratio when weaker photoluminescence or electroluminescence signal has been observed in double modulation mode, switching to step scan mode should be an advisable option despite the long data acquiring time and limited resolution.

  10. Electroluminescence Observation of Microcrack Growth Behavior of Crystalline Silicon Solar Modules Fabricated by Hot-Air Soldering Technology

    NASA Astrophysics Data System (ADS)

    Lin, Keh-Moh; Lee, Yang-Hsien; Wang, Li-Kuo; Chen, Li-Wei; Yang, Sian-Yi; Chen, Yi-Chia; Liu, De-Chih; Huang, Ming-Yuan; Wu, Zhen-Cheng; Chen, Chien-Pin

    In this study, the quality degradation of Si-based photovoltaic (PV) modules during the aging process was observed by using electroluminescent (EL) technology and was verified by the IV curve measurements in order to find out the occurring timing of damages on solar cells. Furthermore, the influences of solder materials and soldering temperatures on the performance of the PV modules were also studied. Experiment results show that, high soldering temperatures which induce high thermal stress can easily lead to the power loss of the PV modules. Besides, the mechanical properties of the solar cells itself can also affect the degradation rate of the PV modules. On PV modules soldered with SnPb (SP) solder, more than 80% of cell damages occurred during the soldering and encapsulation processes. When SnAgPb (SAP) solder was used, a small part of the cell damages didn't emerge until the initial stage of the thermal cycling test (TC.) This phenomenon is attributed to the reduction of residual stress between the ribbon and the silver paste because of the good wettability of SAP solder.

  11. Electroluminescent devices formed using semiconductor nanocrystals as an electron transport media and method of making such electroluminescent devices

    DOEpatents

    Alivisatos, A. Paul; Colvin, Vickie

    1996-01-01

    An electroluminescent device is described, as well as a method of making same, wherein the device is characterized by a semiconductor nanocrystal electron transport layer capable of emitting visible light in response to a voltage applied to the device. The wavelength of the light emitted by the device may be changed by changing either the size or the type of semiconductor nanocrystals used in forming the electron transport layer. In a preferred embodiment the device is further characterized by the capability of emitting visible light of varying wavelengths in response to changes in the voltage applied to the device. The device comprises a hole processing structure capable of injecting and transporting holes, and usually comprising a hole injecting layer and a hole transporting layer; an electron transport layer in contact with the hole processing structure and comprising one or more layers of semiconductor nanocrystals; and an electron injecting layer in contact with the electron transport layer for injecting electrons into the electron transport layer. The capability of emitting visible light of various wavelengths is principally based on the variations in voltage applied thereto, but the type of semiconductor nanocrystals used and the size of the semiconductor nanocrystals in the layers of semiconductor nanometer crystals may also play a role in color change, in combination with the change in voltage.

  12. Bifunctional star-burst amorphous molecular materials for OLEDs: achieving highly efficient solid-state luminescence and carrier transport induced by spontaneous molecular orientation.

    PubMed

    Kim, Jun Yun; Yasuda, Takuma; Yang, Yu Seok; Adachi, Chihaya

    2013-05-21

    Bifunctional star-burst amorphous molecular materials displaying both efficient solid-state luminescence and high hole-transport properties are developed in this study. A high external electroluminescence quantum efficiency up to 5.9% is attained in OLEDs employing the developed amorphous materials. It is revealed that the spontaneous horizontal orientation of these light-emitting molecules in their molecular-condensed states leads to a remarkable enhancement of the electroluminescence efficiencies and carrier-transport properties.

  13. Methods and apparatus of spatially resolved electroluminescence of operating organic light-emitting diodes using conductive atomic force microscopy

    NASA Technical Reports Server (NTRS)

    Hersam, Mark C. (Inventor); Pingree, Liam S. C. (Inventor)

    2008-01-01

    A conductive atomic force microscopy (cAFM) technique which can concurrently monitor topography, charge transport, and electroluminescence with nanometer spatial resolution. This cAFM approach is particularly well suited for probing the electroluminescent response characteristics of operating organic light-emitting diodes (OLEDs) over short length scales.

  14. Efficient APC/C substrate degradation in cells undergoing mitotic exit depends on K11 ubiquitin linkages

    PubMed Central

    Min, Mingwei; Mevissen, Tycho E. T.; De Luca, Maria; Komander, David; Lindon, Catherine

    2015-01-01

    The ubiquitin proteasome system (UPS) directs programmed destruction of key cellular regulators via posttranslational modification of its targets with polyubiquitin chains. These commonly contain Lys-48 (K48)–directed ubiquitin linkages, but chains containing atypical Lys-11 (K11) linkages also target substrates to the proteasome—for example, to regulate cell cycle progression. The ubiquitin ligase called the anaphase-promoting complex/cyclosome (APC/C) controls mitotic exit. In higher eukaryotes, the APC/C works with the E2 enzyme UBE2S to assemble K11 linkages in cells released from mitotic arrest, and these are proposed to constitute an improved proteolytic signal during exit from mitosis. We tested this idea by correlating quantitative measures of in vivo K11-specific ubiquitination of individual substrates, including Aurora kinases, with their degradation kinetics tracked at the single-cell level. All anaphase substrates tested by this methodology are stabilized by depletion of K11 linkages via UBE2S knockdown, even if the same substrates are significantly modified with K48-linked polyubiquitin. Specific examination of substrates depending on the APC/C coactivator Cdh1 for their degradation revealed Cdh1-dependent enrichment of K11 chains on these substrates, whereas other ubiquitin linkages on the same substrates added during mitotic exit were Cdh1-independent. Therefore we show that K11 linkages provide the APC/C with a means to regulate the rate of substrate degradation in a coactivator-specified manner. PMID:26446837

  15. The interplay of Hrd3 and the molecular chaperone system ensures efficient degradation of malfolded secretory proteins

    PubMed Central

    Mehnert, Martin; Sommermeyer, Franziska; Berger, Maren; Kumar Lakshmipathy, Sathish; Gauss, Robert; Aebi, Markus; Jarosch, Ernst; Sommer, Thomas

    2015-01-01

    Misfolded proteins of the secretory pathway are extracted from the endoplasmic reticulum (ER), polyubiquitylated by a protein complex termed the Hmg-CoA reductase degradation ligase (HRD-ligase), and degraded by cytosolic 26S proteasomes. This process is termed ER-associated protein degradation (ERAD). We previously showed that the membrane protein Der1, which is a subunit of the HRD-ligase, is involved in the export of aberrant polypeptides from the ER. Unexpectedly, we also uncovered a close spatial proximity of Der1 and the substrate receptor Hrd3 in the ER lumen. We report here on a mutant Hrd3KR that is selectively defective for ERAD of soluble proteins. Hrd3KR displays subtle structural changes that affect its positioning toward Der1. Furthermore, increased quantities of the ER-resident Hsp70-type chaperone Kar2 and the Hsp40-type cochaperone Scj1 bind to Hrd3KR. Of note, deletion of SCJ1 impairs ERAD of model substrates and causes the accumulation of client proteins at Hrd3. Our data imply a function of Scj1 in the removal of malfolded proteins from the receptor Hrd3, which facilitates their delivery to downstream-acting components like Der1. PMID:25428985

  16. Tunneling electron induced molecular electroluminescence from individual porphyrin J-aggregates

    SciTech Connect

    Meng, Qiushi; Zhang, Chao; Zhang, Yang E-mail: zcdong@ustc.edu.cn; Zhang, Yao; Liao, Yuan; Dong, Zhenchao E-mail: zcdong@ustc.edu.cn

    2015-07-27

    We investigate molecular electroluminescence from individual tubular porphyrin J-aggregates on Au(111) by tunneling electron excitations in an ultrahigh-vacuum scanning tunneling microscope (STM). High-resolution STM images suggest a spiral tubular structure for the porphyrin J-aggregate with highly ordered “brickwork”-like arrangements. Such aggregated nanotube is found to behave like a self-decoupled molecular architecture and shows red-shifted electroluminescence characteristics of J-aggregates originated from the delocalized excitons. The positions of the emission peaks are found to shift slightly depending on the excitation sites, which, together with the changes in the observed spectral profiles with vibronic progressions, suggest a limited exciton coherence number within several molecules. The J-aggregate electroluminescence is also found unipolar, occurring only at negative sample voltages, which is presumably related to the junction asymmetry in the context of molecular excitations via the carrier injection mechanism.

  17. Large Size Color-tunable Electroluminescence from Cationic Iridium Complexes-based Light-emitting Electrochemical Cells

    PubMed Central

    Zeng, Qunying; Li, Fushan; Guo, Tailiang; Shan, Guogang; Su, Zhongmin

    2016-01-01

    Solution-processable light-emitting electrochemical cells (LECs) with simple device architecture have become an attractive candidate for application in next generation lighting and flat-panel displays. Herein, single layer LECs employing two cationic Ir(III) complexes showing highly efficient blue-green and yellow electroluminescence with peak current efficiency of 31.6 cd A−1 and 40.6 cd A−1, respectively, have been reported. By using both complexes in the device, color-tunable LECs with a single spectral peak in the wavelength range from 499 to 570 nm were obtained by varying their rations. In addition, the fabrication of efficient LECs was demonstrated based on low cost doctor-blade coating technique, which was compatible with the roll to roll fabrication process for the large size production. In this work, for the first time, 4 inch LEC devices by doctor-blade coating were fabricated, which exhibit the efficiencies of 23.4 cd A−1 and 25.4 cd A−1 for the blue-green and yellow emission, respectively. The exciting results indicated that highly efficient LECs with controllable color could be realized and find practical application in large size lighting and displays. PMID:27278527

  18. Large Size Color-tunable Electroluminescence from Cationic Iridium Complexes-based Light-emitting Electrochemical Cells

    NASA Astrophysics Data System (ADS)

    Zeng, Qunying; Li, Fushan; Guo, Tailiang; Shan, Guogang; Su, Zhongmin

    2016-06-01

    Solution-processable light-emitting electrochemical cells (LECs) with simple device architecture have become an attractive candidate for application in next generation lighting and flat-panel displays. Herein, single layer LECs employing two cationic Ir(III) complexes showing highly efficient blue-green and yellow electroluminescence with peak current efficiency of 31.6 cd A‑1 and 40.6 cd A‑1, respectively, have been reported. By using both complexes in the device, color-tunable LECs with a single spectral peak in the wavelength range from 499 to 570 nm were obtained by varying their rations. In addition, the fabrication of efficient LECs was demonstrated based on low cost doctor-blade coating technique, which was compatible with the roll to roll fabrication process for the large size production. In this work, for the first time, 4 inch LEC devices by doctor-blade coating were fabricated, which exhibit the efficiencies of 23.4 cd A‑1 and 25.4 cd A‑1 for the blue-green and yellow emission, respectively. The exciting results indicated that highly efficient LECs with controllable color could be realized and find practical application in large size lighting and displays.

  19. Electroluminescence of carbon ‘quantum' dots - From materials to devices

    NASA Astrophysics Data System (ADS)

    Veca, L. Monica; Diac, Andreea; Mihalache, Iuliana; Wang, Ping; LeCroy, Gregory E.; Pavelescu, Emil Mihai; Gavrila, Raluca; Vasile, Eugeniu; Terec, Anamaria; Sun, Ya-Ping

    2014-10-01

    Carbon ‘quantum' dots or carbon dots have emerged as a new class of luminescent nanomaterials. While photoluminescence properties of carbon dots had targeted optical imaging and related usage, their unique excited state redox processes responsible for the luminescence emissions may find potentially significant optoelectronic applications. In this regard, we investigated the electroluminescence properties of the carbon dots integrated into multilayer light emitting diode devices. The devices emitted white light with a slight blue color, visible to naked eyes, thus validating the expectation that carbon dots may potentially serve as a new platform for electroluminescent nanomaterials.

  20. An IBM-Compatible 640 X 200 Electroluminescent (EL) Display Monitor

    NASA Astrophysics Data System (ADS)

    Gullick, Paul; Schmachtenberg, Richard; Laakso, Carl

    1986-05-01

    An electroluminescent flat-panel display has been developed and recently introduced that fills any of the needs of the portable computer market. The display is very thin, yet rugged enough for the rigors of portability. It is highly integrated, and very reliable. It has the crisp and clear display image that is typical of high quality electroluminescent displays. The unit has a pixel matrix organization and pixel dimensions that are not only asthetically and ergonomically pleasing, but also make the display compatible with the most widely used software packages run on today's personal computers (Figure 1).

  1. A novel method of synthesis of small band gap SnS nanorods and its efficient photocatalytic dye degradation.

    PubMed

    Das, Dipika; Dutta, Raj Kumar

    2015-11-01

    A facile one pot method has been developed for synthesis of stable (ξ=-37.5 mV), orthorhombic structured SnS nanorods capped with mercaptoacetic acid by precipitation method. The SnS nanorods were measured to be about 45 nm long with a diameter of 20 nm, as studied by transmission electron microscopy (TEM). The band gap of the MAA capped SnS nanorods was 1.81 eV, measured by diffused reflectance spectroscopy and was larger than the bulk SnS. The relative positions of highest valence band and lowest conduction band were determined from theoretical band structure calculation as 1.58 eV and -0.23 eV, respectively. The UV-Visible-NIR fluorescence emission spectrum of the SnS nanorods revealed intense emission peak at 1000 nm (1.239 eV) and weaker peaks at 935 nm, 1080 nm, 1160 nm which is likely to be due to Sn(2+) vacancies. The as-synthesized SnS nanorods exhibited more than 95% sunlight induced photocatalytic degradation of trypan blue in 4 h, following first order kinetics with high rate of degradation (k) (0.0124 min(-1)). The observed dye degradation is attributable to generation of reactive oxygen species (ROS), confirmed from terephthalic acid assay. The ROS generation has been explained on the basis of interaction between photoexcited electrons from conduction band with molecular oxygen adhered to the surface of nanorods owing to favourable redox potentials of O2/O2(-) (-0.20 eV) in normal hydrogen electrode (NHE) scale.

  2. Synthesis and characterization of zinc doped nano TiO2 for efficient photocatalytic degradation of Eriochrome Black T

    NASA Astrophysics Data System (ADS)

    Singla, Pooja; Sharma, Manoj; Singh, Kulvir; Pandey, O. P.

    2013-06-01

    Sol-gel method was used to synthesize undoped and zinc doped TiO2 with varied dopant concentrations using titanium tetraisopropoxide and zinc acetate as precursors. The synthesized catalyst samples were characterized by various techniques such as X-ray powder diffraction (XRD), UV-vis diffuse reflectance (DRS). The photocatalytic activity was determined by means of degradation of azo dye Eriochrome Black T. The results revealed that Zn doped TiO2 nanoparticles exhibited better results as compared to undoped TiO2 nanoparticles. Zn doped TiO2 (0.7mol %) nanoparticles exhibited the highest photocatalytic activity.

  3. Self-assembly graphitic carbon nitride quantum dots anchored on TiO2 nanotube arrays: An efficient heterojunction for pollutants degradation under solar light.

    PubMed

    Su, Jingyang; Zhu, Lin; Geng, Ping; Chen, Guohua

    2016-10-05

    In this study, an efficient heterojunction was constructed by anchoring graphitic carbon nitride quantum dots onto TiO2 nanotube arrays through hydrothermal reaction strategy. The prepared graphitic carbon nitride quantum dots, which were prepared by solid-thermal reaction and sequential dialysis process, act as a sensitizer to enhance light absorption. Furthermore, it was demonstrated that the charge transfer and separation in the formed heterojunction were significantly improved compared with pristine TiO2. The prepared heterojunction was used as a photoanode, exhibiting much improved photoelectrochemical capability and excellent photo-stability under solar light illumination. The photoelectrocatalytic activities of prepared heterojunction were demonstrated by degradation of RhB and phenol in aqueous solution. The kinetic constants of RhB and phenol degradation using prepared photoelectrode are 2.4 times and 4.9 times higher than those of pristine TiO2, respectively. Moreover, hydroxyl radicals are demonstrated to be dominant active radicals during the pollutants degradation.

  4. Self-degrading niosomes for encapsulation of hydrophilic and hydrophobic drugs: An efficient carrier for cancer multi-drug delivery.

    PubMed

    Sharma, Varsha; Anandhakumar, Sundaramurthy; Sasidharan, Manickam

    2015-11-01

    In this study, we have examined the encapsulation and release of hydrophilic and hydrophobic drugs in self-degrading niosomes as a unique method for anticancer therapy. Niosomes were prepared by amphiphilic self-assembly of Tween 80 and cholesterol through film hydration method. Encapsulation studies with two active molecules curcumin and doxorubicin hydrochloride (Dox) showed that curcumin is supposed to accumulate in the shell whereas Dox accumulates in the inner aqueous core of the niosome. Confocal studies indicated that nile red adsorbs preferentially to the head group of the Tween 80 and forms two separate layers in the shell. It was also seen that the niosomes undergo self-degradation in PBS through a sequential process, forming interconnected pores followed by complete collapse after 1week. The release profile shows two phases: i) initial Dox release in the first two days, followed by ii) curcumin release over 7days. Enhanced (synergistic) cytotoxicity was observed for dual-drug loaded niosomes against HeLa cell lines. Thus these niosomes are shown to offer a promising delivery system for hydrophobic and hydrophilic drugs collectively.

  5. Preparation and characterization of Cu{sub 2}O-TiO{sub 2}: Efficient photocatalytic degradation of methylene blue

    SciTech Connect

    Xu Yuehua Liang Dahui; Liu Manle; Liu Dingzhong

    2008-12-01

    A series of copper-deposited titania were prepared by photoreduction method under irradiation with a 125-W high-pressure mercury lamp. From XPS and AES results, the deposited-copper formed Ti-O-Cu bond on the surface of TiO{sub 2}, and the Cu species on the surface of copper-deposited TiO{sub 2} can be identified as Cu(I). The photocatalytic degradation activity of methylene blue for the Cu{sub 2}O-TiO{sub 2} series increased with increasing Cu{sub 2}O-deposited content, and then decreased. The highest photocatalytic degradation activity of methylene blue was obtained for 0.16% Cu{sub 2}O-TiO{sub 2}. When copper-deposited content reached to 0.32%, the photocatalytic activity was lower than that of pure TiO{sub 2}. It is shown that Cu{sub 2}O on the surface of TiO{sub 2} can trap electrons from the TiO{sub 2} conduction band, and the electrons trapped on the Cu{sub 2}O-TiO{sub 2} site are subsequently transferred to the surrounding adsorbed O{sub 2}, thereby avoiding electron-hole recombination, and enhancing the photocatalytic activity. Excess copper loading may screen the photocatalyst from the UV source, so the photocatalytic activity diminishes with increasing Cu{sub 2}O.

  6. Highly ordered Ti-SBA-15: Efficient H{sub 2} adsorbent and photocatalyst for eco-toxic dye degradation

    SciTech Connect

    Das, Swapan K.; Bhunia, Manas K.; Bhaumik, Asim

    2010-06-15

    Highly ordered 2D-hexagonal mesoporous titanium silicate Ti-SBA-15 materials (space group p6mm) have been synthesized hydrothermally in acidic medium employing amphiphilic tri-block copolymer, Pluronic F127 as structure directing agent. Samples are characterized by powder X-ray diffraction, transmission electron microscopy, scanning electron microscopy, FT IR spectroscopy, UV-visible diffuse reflectance measurements, N{sub 2} adsorption/desorption and TG-DTA analysis. XRD and TEM results suggested the presence of highly ordered mesophase with hexagonal pore arrangements. BET surface area for Ti-SBA-15 (924 m{sup 2} g{sup -1}) is considerably higher than the pure silica SBA-15 (611 m{sup 2} g{sup -1}) prepared following the same synthetic route. UV-visible and FT-IR studies suggested the incorporation of mostly tetrahedral titanium (IV) species, along with some six-coordinated sites in the silicate network. This material shows very good H{sub 2} adsorption capacity at higher pressure and excellent catalytic activity in the photocatalytic degradation of ecologically abundant dye methylene blue. - Graphical abstract: Highly ordered 2D-hexagonal mesoporous Ti-SBA-15 materials are synthesized hydrothermally, which show high H{sub 2} adsorption capacity and excellent activity in the photocatalytic degradation of ecologically abundant dye methylene blue.

  7. Ce-Fe-reduced graphene oxide nanocomposite as an efficient catalyst for sulfamethazine degradation in aqueous solution.

    PubMed

    Wan, Zhong; Wang, Jianlong

    2016-09-01

    A heterogeneous Fenton catalyst Ce(0)-Fe(0)-reduced graphene oxide (Ce-Fe-RGO) was synthesized with chemical reduction methods and used for degradation of sulfamethazine. The introduction of Ce and graphene increased the dispersibility of iron particles which was confirmed by SEM and TEM. The results of VSM analysis showed good magnetism of Ce-Fe-RGO. The catalyst performance was compared with other kinds of catalysts (Fe(0) and Ce(0)-Fe(0)) for degradation of sulfamethazine. The results showed that Ce(0)-Fe-RGO had good catalytic performance and adsorption. X-ray diffraction showed the change of iron oxide on catalyst surface after use. The total sulfur (TS), total nitrogen (TN), total organic carbon (TOC), and intermediates, such as small organic molecular and anion ions, were analyzed by IC under different pH conditions. Finally, the possible catalytic mechanism was tentatively proposed based on inhibitor experimental results and XPS characterization. The main active species was hydroxyl radical on catalyst surface and the transition between Ce(3+) and Ce(4+) which enhanced the reduction from Fe(3+) to Fe(2+) and formation of ·OH and ·O2 (-).

  8. Laccase-syringaldehyde-mediated degradation of trace organic contaminants in an enzymatic membrane reactor: Removal efficiency and effluent toxicity.

    PubMed

    Nguyen, Luong N; van de Merwe, Jason P; Hai, Faisal I; Leusch, Frederic D L; Kang, Jinguo; Price, William E; Roddick, Felicity; Magram, Saleh F; Nghiem, Long D

    2016-01-01

    Redox-mediators such as syringaldehyde (SA) can improve laccase-catalyzed degradation of trace organic contaminants (TrOCs) but may increase effluent toxicity. The degradation performance of 14 phenolic and 17 non-phenolic TrOCs by a continuous flow enzymatic membrane reactor (EMR) at different TrOC and SA loadings was assessed. A specific emphasis was placed on the investigation of the toxicity of the enzyme (laccase), SA, TrOCs and the treated effluent. Batch tests demonstrated significant individual and interactive toxicity of the laccase and SA preparations. Reduced removal of resistant TrOCs by the EMR was observed for dosages over 50μg/L. SA addition at a concentration of 10μM significantly improved TrOC removal, but no removal improvement was observed at the elevated SA concentrations of 50 and 100μM. The treated effluent showed significant toxicity at SA concentrations beyond 10μM, providing further evidence that higher dosage of SA must be avoided.

  9. Newly isolated Penicillium oxalicum A592-4B secretes enzymes that degrade milled rice straw with high efficiency.

    PubMed

    Aoyama, Akihisa; Kurane, Ryuichiro; Matsuura, Akira; Nagai, Kazuo

    2015-01-01

    An enzyme producing micro-organism, which can directly saccharify rice straw that has only been crushed without undergoing the current acid or alkaline pretreatment, was found. From the homology with the ITS, 28S rDNA sequence, the strain named A592-4B was identified as Penicillium oxalicum. Activities of the A592-4B enzymes and commercial enzyme preparations were compared by Novozymes Cellic CTec2 and Genencore GC220. In the present experimental condition, activity of A592-4B enzymes was 2.6 times higher than that of CTec2 for degrading milled rice straw. Furthermore, even when a quarter amount of A592-4B enzyme was applied to the rice straw, the conversion rate was still higher than that by CTec2. By utilizing A592-4B enzymes, improved lignocellulose degradation yields can be achieved without pre-treatment of the substrates; thus, contributing to cost reduction as well as reducing environmental burden.

  10. Phosphorescent Iridium(III) Complexes Bearing Fluorinated Aromatic Sulfonyl Group with Nearly Unity Phosphorescent Quantum Yields and Outstanding Electroluminescent Properties.

    PubMed

    Zhao, Jiang; Yu, Yue; Yang, Xiaolong; Yan, Xiaogang; Zhang, Huiming; Xu, Xianbin; Zhou, Guijiang; Wu, Zhaoxin; Ren, Yixia; Wong, Wai-Yeung

    2015-11-11

    A series of heteroleptic functional Ir(III) complexes bearing different fluorinated aromatic sulfonyl groups has been synthesized. Their photophysical features, electrochemical behaviors, and electroluminescent (EL) properties have been characterized in detail. These complexes emit intense yellow phosphorescence with exceptionally high quantum yields (ΦP > 0.9) at room temperature, and the emission maxima of these complexes can be finely tuned depending upon the number of the fluorine substituents on the pendant phenyl ring of the sulfonyl group. Furthermore, the electrochemical properties and electron injection/transporting (EI/ET) abilities of these Ir(III) phosphors can also be effectively tuned by the fluorinated aromatic sulfonyl group to furnish some desired characters for enhancing the EL performance. Hence, the maximum luminance efficiency (ηL) of 81.2 cd A(-1), corresponding to power efficiency (ηP) of 64.5 lm W(-1) and external quantum efficiency (ηext) of 19.3%, has been achieved, indicating the great potential of these novel phosphors in the field of organic light-emitting diodes (OLEDs). Furthermore, a clear picture has been drawn for the relationship between their optoelectronic properties and chemical structures. These results should provide important information for developing highly efficient phosphors.

  11. INTERNATIONAL CONFERENCE ON SEMICONDUCTOR INJECTION LASERS SELCO-87: Determination of the quantum efficiency of InGaAsP/InP double heterostructures from spontaneous emission measurements

    NASA Astrophysics Data System (ADS)

    Rheinländer, B.; Anton, A.; Heilmann, R.; Oelgart, G.; Gottschalch, V.

    1988-11-01

    A method was developed for determination of the suitability of epitaxial InGaAsP/InP double heterostructures in fabrication of ridge-waveguide lasers. The method is based on determination of the quantum efficiency of electroluminescence.

  12. Crude oil degradation efficiency of a recombinant Acinetobacter baumannii strain and its survival in crude oil-contaminated soil microcosm.

    PubMed

    Mishra, Sanjeet; Sarma, Priyangshu M; Lal, Banwari

    2004-06-15

    A hydrocarbon degrading Acinetobacter baumannii S30 strain, isolated from crude oil-contaminated soil, was inserted with the lux gene from the luciferase gene cassette luxCDABE. Soil microcosms were designed to study the degradation efficacy for total petroleum hydrocarbon (TPH) of crude oil by lux-tagged A. baumannii S30 pJES. Bioaugmentation of a TPH-contaminated microcosm with A baumannii S30 pJES showed that TPH levels were reduced from 89.3 to 53.9 g/kg soil in 90 days. Biodegradation of TPH by A baumannii S30 pJES was also monitored in shake flask conditions, which showed a reduction of initial TPH levels by over 50% at the end of 120 h. A lux-PCR-based approach along with the standard dilution plating with selective antibiotics was successfully utilized to monitor the survivability of the lux-tagged strain A. baumannii S30 pJES in soil microcosms and stability of the lux insert in the host strain A. baumannii S30. The selective plating technique indicated the population of A. baumannii S30 pJES to be 6.5+/-0.13 x 10(8) CFU/g at day zero (just after bioaugmentation) and 2.09+/-0.08 x 10(8) CFU/g of soil after 90 days of incubation. lux-PCR confirmed the stability of the insert in all the randomly selected colonies of A. baumannii strains from the antibiotic plates. The lux insert was stable after 50 generations in Luria Bertini broth and storage at -70 degrees C as glycerol stocks for over a year. These results revealed that the lux insert was stable and lux-tagged A. baumannii S30 strain could survive in a TPH-contaminated soil microcosm and could degrade TPH in the soil microcosm conditions. It can be used as an effective marker to monitor the survival of augmented strains at a bioremediation site.

  13. Terminal PEGylated DNA–Gold Nanoparticle Conjugates Offering High Resistance to Nuclease Degradation and Efficient Intracellular Delivery of DNA Binding Agents

    PubMed Central

    2015-01-01

    Over the past 10 years, polyvalent DNA–gold nanoparticle (DNA–GNP) conjugate has been demonstrated as an efficient, universal nanocarrier for drug and gene delivery with high uptake by over 50 different types of primary and cancer cell lines. A barrier limiting its in vivo effectiveness is limited resistance to nuclease degradation and nonspecific interaction with blood serum contents. Herein we show that terminal PEGylation of the complementary DNA strand hybridized to a polyvalent DNA–GNP conjugate can eliminate nonspecific adsorption of serum proteins and greatly increases its resistance against DNase I-based degradation. The PEGylated DNA–GNP conjugate still retains a high cell uptake property, making it an attractive intracellular delivery nanocarrier for DNA binding reagents. We show that it can be used for successful intracellular delivery of doxorubicin, a widely used clinical cancer chemotherapeutic drug. Moreover, it can be used for efficient delivery of some cell-membrane-impermeable reagents such as propidium iodide (a DNA intercalating fluorescent dye currently limited to the use of staining dead cells only) and a diruthenium complex (a DNA groove binder), for successful staining of live cells. PMID:26237203

  14. Novel AgI-decorated β-Bi₂O₃ nanosheet heterostructured Z-scheme photocatalysts for efficient degradation of organic pollutants with enhanced performance.

    PubMed

    Zhang, Zhengyuan; Jiang, Deli; Xing, Chaosheng; Chen, Linlin; Chen, Min; He, Minqiang

    2015-07-07

    The low photocatalytic activity of single semiconductor photocatalysts mainly originates from their fast recombination of photogenerated electron-hole pairs. Constructing nanosheet-based composite photocatalysts is an effective way to enhance the charge separation efficiency of photogenerated electron-hole pairs. In this work, AgI-decorated β-Bi2O3 nanosheet heterostructured photocatalysts were prepared by a facile method. The as-obtained AgI/β-Bi2O3 heterostructures exhibited enhanced visible-light-driven photocatalytic activity towards the degradation of methyl orange (MO) and tetracycline hydrochloride (TC) in aqueous solution. The optimum photocatalytic activity of 20%-AgI/β-Bi2O3 for the degradation of MO was about 4.1 and 6.2 times higher than that of AgI and β-Bi2O3. The photocatalytic activity enhancement of AgI/β-Bi2O3 heterostructures could be ascribed to the formation of a Z-scheme system, which results in the efficient space separation of photo-induced charge carriers.

  15. Iron oxychloride (FeOCl): an efficient Fenton-like catalyst for producing hydroxyl radicals in degradation of organic contaminants.

    PubMed

    Yang, Xue-jing; Xu, Xi-meng; Xu, Jing; Han, Yi-fan

    2013-10-30

    An iron oxychloride (FeOCl) catalyst was developed for oxidative degradation of persistent organic compounds in aqueous solutions. Exceptionally high activity for the production of hydroxyl radical (OH·) by H2O2 decomposition was achieved, being 2-4 orders of magnitudes greater than that over other Fe-based heterogeneous catalysts. The relationship of catalyst structure and performance has been established by using multitechniques, such as XRD, HRTEM, and EPR. The unique structural configuration of iron atoms and the reducible electronic properties of FeOCl are responsible for the excellent activity. This study paves the way toward the rational design of relevant catalysts for applications, such as wastewater treatment, soil remediation, and other emerging environmental problems.

  16. The effect of polysaccharide-degrading wine yeast transformants on the efficiency of wine processing and wine flavour.

    PubMed

    Louw, C; La Grange, D; Pretorius, I S; van Rensburg, P

    2006-10-01

    Commercial polysaccharase preparations are applied to winemaking to improve wine processing and quality. Expression of polysaccharase-encoding genes in Saccharomyces cerevisiae allows for the recombinant strains to degrade polysaccharides that traditional commercial yeast strains cannot. In this study, we constructed recombinant wine yeast strains that were able to degrade the problem-causing grape polysaccharides, glucan and xylan, by separately integrating the Trichoderma reesei XYN2 xylanase gene construct and the Butyrivibrio fibrisolvens END1 glucanase gene cassette into the genome of the commercial wine yeast strain S. cerevisiae VIN13. These genes were also combined in S. cerevisiae VIN13 under the control of different promoters. The strains that were constructed were compared under winemaking conditions with each other and with a recombinant wine yeast strain expressing the endo-beta-1,4-glucanase gene cassette (END1) from B. fibrisolvens and the endo-beta-1,4-xylanase gene cassette (XYN4) from Aspergillus niger, a recombinant strain expressing the pectate lyase gene cassette (PEL5) from Erwinia chrysanthemi and the polygalacturonase-encoding gene cassette (PEH1) from Erwinia carotovora. Wine was made with the recombinant strains using different grape cultivars. Fermentations with the recombinant VIN13 strains resulted in significant increases in free-flow wine when Ruby Cabernet must was fermented. After 6 months of bottle ageing significant differences in colour intensity and colour stability could be detected in Pinot Noir and Ruby Cabernet wines fermented with different recombinant strains. After this period the volatile composition of Muscat d'Alexandria, Ruby Cabernet and Pinot Noir wines fermented with different recombinant strains also showed significant differences. The Pinot Noir wines were also sensorial evaluated and the tasting panel preferred the wines fermented with the recombinant strains.

  17. Design of binary SnO2-CuO nanocomposite for efficient photocatalytic degradation of malachite green dye

    NASA Astrophysics Data System (ADS)

    Kumar, Aniket; Rout, Lipeeka; Achary, L. Satish Kumar; Mohanty, Anurag; Marpally, Jyoshna; Chand, Pradyumna Kumar; Dash, Priyabrat

    2016-04-01

    Semiconductor mediated photocatalysis has got enormous consideration as it has shown immense potential in addressing the overall energy and environmental issues. To overcome the earlier drawbacks concerning quick charge recombination and limited visible-light absorption of semiconductor photocatalysts, numerous methods have been produced in the past couple of decades and the most broadly utilized one is to develop the photocatalytic heterojunctions. In our work, a series of SnO2-CuO nanocomposites of different compositions were synthesized by a combustion method and have been investigated in detail by various characterization techniques, such as wide angle X-ray diffraction (XRD), UV-vis spectroscopy, transmission electron microscopy (TEM), and field emission scanning electron microscopy (FE-SEM). The results revealed that the crystal structure and optical properties of the nanocomposites were almost same for all the compositions. FE-SEM images showed that the shape of SnO2-CuO was spherical in nature and the 1: 1 Sn/Cu sample had a well-proportioned morphology. The malachite green dye was used for the photocatalytic studies in a photoreactor and monitored with a UV-visible spectrometer for different composition ratio of metal (Sn: Cu) such as 1:1, 1:2, 2:1, 1:0.5 and 0.5:1. The 1:1 ratio nanocomposite showed excellent photocatalytic degradation of 96 % compared to pure SnO2 and CuO. The mechanism of degradation and charge separation ability of the nanocomposite are also explored using photocurrent measurement study.

  18. Ag{sub 3}PO{sub 4}/ZnO: An efficient visible-light-sensitized composite with its application in photocatalytic degradation of Rhodamine B

    SciTech Connect

    Liu, Wei; Wang, Mingliang; Xu, Chunxiang; Chen, Shifu; Fu, Xianliang

    2013-01-15

    Graphical abstract: The free OH radicals generated in the VB of ZnO play the primary role in the visible-light photocatalytic degradation of RhB in Ag{sub 3}PO{sub 4}/ZnO system. The accumulated electrons in the CB of Ag{sub 3}PO{sub 4} can be transferred to O{sub 2} adsorbed on the surface of the composite semiconductors and H{sub 2}O{sub 2} yields. H{sub 2}O{sub 2} reacts with electrons in succession to produce active ·OH to some extent. Display Omitted Highlights: ► Efficient visible-light-sensitized Ag{sub 3}PO{sub 4}/ZnO composites were successfully prepared. ► Effect of Ag{sub 3}PO{sub 4} content on the catalytic activity of Ag{sub 3}PO{sub 4}/ZnO is studied in detail. ► Rate constant of RhB degradation over Ag{sub 3}PO{sub 4}(3.0 wt.%)/ZnO is 3 times that of Ag{sub 3}PO{sub 4}. ► The active species in RhB degradation are examined by adding a series of scavengers. ► Visible light degradation mechanism of RhB over Ag{sub 3}PO{sub 4}/ZnO is systematically studied. -- Abstract: The efficient visible-light-sensitized Ag{sub 3}PO{sub 4}/ZnO composites with various weight percents of Ag{sub 3}PO{sub 4} were prepared by a facile ball milling method. The photocatalysts were characterized by XRD, DRS, SEM, EDS, XPS, and BET specific area. The ·OH radicals produced during the photocatalytic reaction was detected by the TA–PL technique. The photocatalytic property of Ag{sub 3}PO{sub 4}/ZnO was evaluated by photocatalytic degradation of Rhodamine B under visible light irradiation. Significantly, the results revealed that the photocatalytic activity of the composites was much higher than that of pure Ag{sub 3}PO{sub 4} and ZnO. The rate constant of RhB degradation over Ag{sub 3}PO{sub 4}(3.0 wt.%)/ZnO is 3 times that of single-phase Ag{sub 3}PO{sub 4}. The optimal percentage of Ag{sub 3}PO{sub 4} in the composite is 3.0 wt.%. It is proposed that the ·OH radicals produced in the valence band of ZnO play the leading role in the photocatalytic degradation of

  19. Photo- and electroluminescence of mixed-ligand Eu(III) complexes

    NASA Astrophysics Data System (ADS)

    Eremina, N. S.; Meshkova, S. B.; Degtyarenko, K. M.; Kopylova, T. N.; Topilova, Z. M.; Gadirov, R. M.; Samsonova, L. G.

    2012-05-01

    Spectral and luminescent properties of mixed-ligand Eu(III) complexes were studied in solutions and in polyvinylcarbazole (PVC) thin films. Trends in their variations were found depending on the complex structure and excitation mode. The electroluminescence was observed in ITO/PEDOT/Eu complex:PVC/CaMg/Al devices. Their current-voltage and voltage-brightness characteristics were investigated.

  20. Temperature Dependence of D.C. and Pulsed Electroluminescence in Anthracene Crystals,

    DTIC Science & Technology

    appears. The spectral distribution of the electroluminescence is independent of the second electrode material, though differences in the time dependence ...shown in the different current and temperature dependence of the intensity of the major vibrational progression of the emission. Included argon

  1. An observation of direct-gap electroluminescence in GaAs structures with Ge quantum wells

    SciTech Connect

    Aleshkin, V. Ya.; Dikareva, N. V.; Dubinov, A. A.; Zvonkov, B. N.; Kudryavtsev, K. E.; Nekorkin, S. M.

    2015-02-15

    A light-emitting diode structure based on GaAs with eight narrow Ge quantum wells is grown by laser sputtering. An electroluminescence line polarized predominately in the plane parallel to the constituent layers of the structure is revealed. The line corresponds to the direct optical transitions in momentum space in the Ge quantum wells.

  2. The energy transfer mechanism of a photoexcited and electroluminescent organic hybrid thin film of blue, green, and red laser dyes

    NASA Astrophysics Data System (ADS)

    Li, Weiling; Zhang, Jing; Zheng, Yanqiong; Chen, Guo; Cai, Miao; Wei, Bin

    2015-04-01

    Though optically pumped lasing has been realized for years, electrically pumped lasing has not yet been achieved in organic semiconductor devices. In order to make a better understanding of the laser mechanisms of the organic materials, we prepared organic thin films consisting of three efficient laser dyes of a blue emitter, 4″,4″'-N,N-diphenylamine-4,4'-diphenyl-1,1'-binaphthyl (BN), a green emitter, 1,4-bis[2-[4-[N,N-di(p-tolyl)amino] phenyl]vinyl]benzene (DSB), and a red emitter, 4-(dicyanomethylene)-2-t-butyl-6(1,1,7,7-tetramethyljulolidy-l-9-enyl)-4H-pyran (DCJTB) with different doping concentrations for the first time to investigate the cascade energy transfer process. The energy transfer schemes in the co-doped thin films in photoluminescence and electroluminescence have been investigated. The results indicated that the DSB molecules acted as a bridge to deliver energy more effectively from the host (BN) to the guest (DCJTB). Meanwhile, the maximum current efficiency ( C E) and power efficiency ( P E) of the organic light-emitting devices (OLEDs) with the emitting layer of lower doping concentration were 13.5 cd/A and 14.1 lm/W, respectively.

  3. Rational design of hyperbranched 3D heteroarrays of SrS/CdS: synthesis, characterization and evaluation of photocatalytic properties for efficient hydrogen generation and organic dye degradation

    NASA Astrophysics Data System (ADS)

    Khan, Ziyauddin; Chetia, Tridip Ranjan; Qureshi, Mohammad

    2012-05-01

    Hyperbranched 3D SrS/CdS nanostructures were synthesized using a one pot hydrothermal method. Transmission Electron Microscopy (TEM) and Field Emission-Scanning Electron Microscopy (FE-SEM) analysis showed the formation of flower-like structure and the crystalline phase was confirmed by powder X-ray diffraction. The prepared 3D SrS/CdS exhibited improved photocatalytic activity for water splitting leading to H2 generation (AQY 10%) and nearly complete degradation of methyl orange (MO) dye. The dye degradation followed first order kinetics and the apparent reaction rate constant (kapp) was 0.136 min-1. The present 3D SrS/CdS structure promise to be efficient photocatalysts due to (i) the facile intersystem charge transfer resulting from their band alignment (ii) enhanced specific surface area and (iii) crystallinity.Hyperbranched 3D SrS/CdS nanostructures were synthesized using a one pot hydrothermal method. Transmission Electron Microscopy (TEM) and Field Emission-Scanning Electron Microscopy (FE-SEM) analysis showed the formation of flower-like structure and the crystalline phase was confirmed by powder X-ray diffraction. The prepared 3D SrS/CdS exhibited improved photocatalytic activity for water splitting leading to H2 generation (AQY 10%) and nearly complete degradation of methyl orange (MO) dye. The dye degradation followed first order kinetics and the apparent reaction rate constant (kapp) was 0.136 min-1. The present 3D SrS/CdS structure promise to be efficient photocatalysts due to (i) the facile intersystem charge transfer resulting from their band alignment (ii) enhanced specific surface area and (iii) crystallinity. Electronic supplementary information (ESI) available: Schematic experimental setup for photocatalytic hydrogen generation, TEM of CdS NWs and SrS NPs, FESEM images of 3D SrS/CdS, Low resolution TEM images for 3D SrS/CdS, EDX and SAED, SEM of SrS/CdS at different ratios, progress of hydrogen production at different time interval, different UV

  4. Self-assembly of ultrathin Cu2MoS4 nanobelts for highly efficient visible light-driven degradation of methyl orange

    NASA Astrophysics Data System (ADS)

    Zhang, Ke; Chen, Wenxing; Lin, Yunxiang; Chen, Haiping; Haleem, Yasir A.; Wu, Chuanqiang; Ye, Fei; Wang, Tianxing; Song, Li

    2015-10-01

    We demonstrate ultrathin self-assembled Cu2MoS4 nanobelts synthesized by using Cu2O as the starting sacrificial template via a hydrothermal method. The nanobelts exhibit strong light absorption over a broad wavelength spectrum, suggesting their potential application as photocatalysts. The photocatalytic activity of nanobelts is evaluated by the degradation of Methyl Orange (MO) dye under visible light irradiation. Notably, the nanobelts can completely degrade 100 mL of 15 mg mL-1 MO in 20 minutes with excellent recycling and structural stability, suggesting their excellent photocatalytic performance. In comparison with a sheet-like sample, the high efficiency of the self-assembled Cu2MoS4 nanobelts is attributed to a high surface area and a unique band gap, agreeing with the nitrogen adsorption analysis and photoluminescence spectra. This study offers a self-assembled synthetic route to create new multifunctional nanoarchitectures composed of atomic layers, and thus may open a window for greatly extending potential applications in water pollution treatment, photocatalytic water-splitting, solar cells and other related fields.We demonstrate ultrathin self-assembled Cu2MoS4 nanobelts synthesized by using Cu2O as the starting sacrificial template via a hydrothermal method. The nanobelts exhibit strong light absorption over a broad wavelength spectrum, suggesting their potential application as photocatalysts. The photocatalytic activity of nanobelts is evaluated by the degradation of Methyl Orange (MO) dye under visible light irradiation. Notably, the nanobelts can completely degrade 100 mL of 15 mg mL-1 MO in 20 minutes with excellent recycling and structural stability, suggesting their excellent photocatalytic performance. In comparison with a sheet-like sample, the high efficiency of the self-assembled Cu2MoS4 nanobelts is attributed to a high surface area and a unique band gap, agreeing with the nitrogen adsorption analysis and photoluminescence spectra. This study

  5. Copper-promoted circumneutral activation of H2O2 by magnetic CuFe2O4 spinel nanoparticles: Mechanism, stoichiometric efficiency, and pathway of degrading sulfanilamide.

    PubMed

    Feng, Yong; Liao, Changzhong; Shih, Kaimin

    2016-07-01

    To evaluate the heterogeneous degradation of sulfanilamide by external energy-free Fenton-like reactions, magnetic CuFe2O4 spinel nanoparticles (NPs) were synthesized and used as catalysts for activation of hydrogen peroxide (H2O2). The physicochemical properties of the CuFe2O4 NPs were characterized with several techniques, including X-ray diffraction, X-ray photoelectron spectroscopy, transmission electron microscopy, and magnetometry. In the catalytic experiments, CuFe2O4 NPs/H2O2 oxidation showed the best degradation performance in the circumneutral conditions that resulted from the presence of Cu(II) on the surface of the CuFe2O4 NPs. The surface area-normalized pseudo-first-order rate constants were calculated as 2.60 × 10(-2) L m(-1) min(-1), 2.58 × 10(-3) L m(-1) min(-1), 1.92 × 10(-3) L m(-1) min(-1), and 7.30 × 10(-4) L m(-1) min(-1) for CuO, CuFe2O4 NPs, Fe3O4, and α-Fe2O3 catalysts, respectively. Thus, solid state Cu(II) was more reactive and efficient than Fe(III) in the circumneutral activation of H2O2; this finding was further supported by the results regarding the stoichiometric efficiency of H2O2. The effects of experimental parameters such as the oxidant dosage and catalyst loading were investigated. The mechanism for H2O2 activation on the spinel surface was explored and could be explained by the solid redox cycles of Fe(II)/Fe(III) and Cu(II)/Cu(I). Based on the products detected, a degradation pathway via the CS bond cleavage is proposed for the degradation of sulfanilamide. The findings of this study suggest that copper can be used as a doping metal to improve the reactivity and expand the effective pH range of iron oxides.

  6. Fe-based MOFs for efficient adsorption and degradation of acid orange 7 in aqueous solution via persulfate activation

    NASA Astrophysics Data System (ADS)

    Li, Xianghui; Guo, Weilin; Liu, Zhonghua; Wang, Ruiqin; Liu, Hua

    2016-04-01

    Fe-based metal-organic frameworks (MOFs) including MIL-101(Fe), MIL-100(Fe), MIL-53(Fe), and MIL-88B(Fe) prepared via a facile solvothermal process were introduced as both adsorbents and catalysts to generate powerful radicals from persulfate for acid orange 7 (AO7) removal in aqueous solution. Various catalysts were described and characterized by X-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy and X-ray photoelectron spectra. Because of the high specific surface area of the materials, we studied the adsorption isotherms of the four MILs by the fitting of Langmuir adsorption isotherm. Meanwhile, the catalytic activities in persulfate oxidation system were investigated. The results showed that the sequence of the materials ability in the combination of adsorption and degradation was MIL-101(Fe) > MIL-100(Fe) > MIL-53(Fe) > MIL-88B(Fe), which had a close connection with the activity of metal ion in active site of the catalysts and their different cages in size. Moreover, the reactive species in MILs/persulfate system were identified as sulfate radicals and hydroxyl radicals. The reaction mechanism for persulfate activation over MILs was also studied.

  7. How endogenous plant cell-wall degradation mechanisms can help achieve higher efficiency in saccharification of biomass.

    PubMed

    Tavares, Eveline Q P; De Souza, Amanda P; Buckeridge, Marcos S

    2015-07-01

    Cell-wall recalcitrance to hydrolysis still represents one of the major bottlenecks for second-generation bioethanol production. This occurs despite the development of pre-treatments, the prospect of new enzymes, and the production of transgenic plants with less-recalcitrant cell walls. Recalcitrance, which is the intrinsic resistance to breakdown imposed by polymer assembly, is the result of inherent limitations in its three domains. These consist of: (i) porosity, associated with a pectin matrix impairing trafficking through the wall; (ii) the glycomic code, which refers to the fine-structural emergent complexity of cell-wall polymers that are unique to cells, tissues, and species; and (iii) cellulose crystallinity, which refers to the organization in micro- and/or macrofibrils. One way to circumvent recalcitrance could be by following cell-wall hydrolysis strategies underlying plant endogenous mechanisms that are optimized to precisely modify cell walls in planta. Thus, the cell-wall degradation that occurs during fruit ripening, abscission, storage cell-wall mobilization, and aerenchyma formation are reviewed in order to highlight how plants deal with recalcitrance and which are the routes to couple prospective enzymes and cocktail designs with cell-wall features. The manipulation of key enzyme levels in planta can help achieving biologically pre-treated walls (i.e. less recalcitrant) before plants are harvested for bioethanol production. This may be helpful in decreasing the costs associated with producing bioethanol from biomass.

  8. Nano-Titania Photocatalyst Loaded on W-MCM-41 Support and Its Highly Efficient Degradation of Methylene Blue

    NASA Astrophysics Data System (ADS)

    Shankar, H.; Saravanan, R.; Narayanan, V.; Stephen, A.

    2011-07-01

    Most of the azo dyes produced in textile, printing, paper manufacturing, pulp processing and pharmaceutical industries contain different organic contaminants. These dyes can enter the body through ingestion and the high content in living systems can prove to be carcinogenic. Therefore photocatalytic degradation of such toxic organic compounds in water, in the presence of semiconductor powders has received much attention over the last two decades. Nanocrystalline titanium dioxide, TiO2, is a well studied and commonly used material for photocatalytic applications. However, the control of particle size, monodispersity, large catalytic surface for sufficient adsorption of organic pollutants, recovery and recycle of TiO2 nanoparticles are challenging tasks. Hence in the present study, titania was introduced into the nanopores (2-10 nm size) of MCM-41 to produce stable nanoparticles of uniform size and shape. Further, in order to lengthen the life time of the excited electrons/holes during photoreaction, tungsten atoms were incorporated in to the MCM-41 silica matrix in addition to titania loading.

  9. Bifunctional-nanotemplate assisted synthesis of nanoporous SrTiO₃ photocatalysts toward efficient degradation of organic pollutant.

    PubMed

    Ouyang, Shuxin; Li, Peng; Xu, Hua; Tong, Hua; Liu, Lequan; Ye, Jinhua

    2014-12-24

    Nanoporous SrTiO3 photocatalysts were fabricated via a novel technique, the nanotemplate assisted sol-gel hydrothermal reaction. In the alkaline-environment hydrothermal reaction, the SiO2 nanotemplate not only served as pore generator but also worked on adjusting the local reaction environment around the SrTiO3 nanocrystals. This contributed to a continuous modulation between the surface area and the crystallinity of the photocatalyst. The photocatalytic activities of the nanoporous SrTiO3 samples were evaluated by the degradation of gaseous isopropyl alcohol (IPA). Due to an optimal equilibrium between surface area and crystallinity, a SrTiO3 sample synthesized via adding 40% template (STO-SiO2-40%) showed the highest activity, which achieves 40 and 8 times of enhancement of CO2 evolution in comparison with the sample prepared without template and a commercial nano-SrTiO3, respectively. The photodegradation mechanism of IPA over this sample was also investigated in detail. This synthetic technique is also available to prepare the other nanoporous titanates, such as doped SrTiO3 samples and alkali-metal titanates.

  10. Characterization and modeling of radiation damages via internal radiative efficiency in multi-junction solar cells

    NASA Astrophysics Data System (ADS)

    Zhu, Lin; Yoshita, Masahiro; Nakamura, Tetsuya; Imaizumi, Mitsuru; Kim, Changsu; Mochizuki, Toshimitsu; Chen, Shaoqiang; Kanemitsu, Yoshihiko; Akiyama, Hidefumi

    2016-03-01

    In order to understand the radiation effects in space-used multi-junction solar cells, we characterized degradations of internal radiative efficiency (ηint i ) in respective subcells in InGaP/GaAs double-junction solar cells after 1-MeV electron irradiations with different electrons fluences (Φ) via absolute electroluminescence (EL) measurements, because ηint i purely represents material-quality change due to radiation damage, independently from cell structures. We analyzed the degradation of ηint i under different Φ and found that the data of ηint i versus Φ in moderate and high Φ regions are very similar and almost independent of subcell materials, while the difference in beginning-of-life qualities of InGaP and GaAs materials causes dominant difference in sub-cell sensitivity to the low radiation damages. Finally, a simple model was proposed to explain the mechanism in degradation of ηint i, and also well explained the degradation behavior in open-circuit voltage for these multi-junction solar cells.

  11. Comparison of halide impacts on the efficiency of contaminant degradation by sulfate and hydroxyl radical-based advanced oxidation processes (AOPs).

    PubMed

    Yang, Yi; Pignatello, Joseph J; Ma, Jun; Mitch, William A

    2014-02-18

    The effect of halides on organic contaminant destruction efficiency was compared for UV/H2O2 and UV/S2O8(2-) AOP treatments of saline waters; benzoic acid, 3-cyclohexene-1-carboxylic acid, and cyclohexanecarboxylic acid were used as models for aromatic, alkene, and alkane constituents of naphthenic acids in oil-field waters. In model freshwater, contaminant degradation was higher by UV/S2O8(2-) because of the higher quantum efficiency for S2O8(2-) than H2O2 photolysis. The conversion of (•)OH and SO4(•-) radicals to less reactive halogen radicals in the presence of seawater halides reduced the degradation efficiency of benzoic acid and cyclohexanecarboxylic acid. The UV/S2O8(2-) AOP was more affected by Cl(-) than the UV/H2O2 AOP because oxidation of Cl(-) is more favorable by SO4(•-) than (•)OH at pH 7. Degradation of 3-cyclohexene-1-carboxylic acid, was not affected by halides, likely because of the high reactivity of halogen radicals with alkenes. Despite its relatively low concentration in saline waters compared to Cl(-), Br(-) was particularly important. Br(-) promoted halogen radical formation for both AOPs resulting in ClBr(•-), Br2(•-), and CO3(•-) concentrations orders of magnitude higher than (•)OH and SO4(•-) concentrations and reducing differences in halide impacts between the two AOPs. Kinetic modeling of the UV/H2O2 AOP indicated a synergism between Br(-) and Cl(-), with Br(-) scavenging of (•)OH leading to BrOH(•-), and further reactions of Cl(-) with this and other brominated radicals promoting halogen radical concentrations. In contaminant mixtures, the conversion of (•)OH and SO4(•-) radicals to more selective CO3(•-) and halogen radicals favored attack on highly reactive reaction centers represented by the alkene group of 3-cyclohexene-1-carboxylic acid and the aromatic group of the model compound, 2,4-dihydroxybenzoic acid, at the expense of less reactive reaction centers such as aromatic rings and alkane groups

  12. Efficient photocatalytic degradation of organic pollutants by magnetically recoverable nitrogen-doped TiO2 nanocomposite photocatalysts under visible light irradiation.

    PubMed

    Hamzezadeh-Nakhjavani, Sahar; Tavakoli, Omid; Akhlaghi, Seyed Parham; Salehi, Zeinab; Esmailnejad-Ahranjani, Parvaneh; Arpanaei, Ayyoob

    2015-12-01

    Preparation of novel nanocomposite particles (NCPs) with high visible-light-driven photocatalytic activity and possessing recovery potential after advanced oxidation process (AOP) is much desired. In this study, pure anatase phase titania (TiO2) nanoparticles (NPs) as well as three types of NCPs including nitrogen-doped titania (TiO2-N), titania-coated magnetic silica (Fe3O4 cluster@SiO2@TiO2 (FST)), and a novel magnetically recoverable TiO2 nanocomposite photocatalyst containing nitrogen element (Fe3O4 cluster@SiO2@TiO2-N (FST-N)) were successfully synthesized via a sol-gel process. The photocatalysts were characterized by X-ray diffraction (XRD), Fourier transform infrared (FT-IR) spectroscopy, field emission scanning electron microscopy (FE-SEM) with an energy-dispersive X-ray (EDX) spectroscopy analysis, X-ray photoelectron spectroscopy (XPS), UV-vis diffuse reflectance spectroscopy (DRS), and vibrating sample magnetometer (VSM). The photocatalytic activity of as-prepared samples was further investigated and compared with each other by degradation of phenol, as a model for the organic pollutants, in deionized (DI) water under visible light irradiation. The TiO2-N (55 ± 1.5%) and FST-N (46 ± 1.5%) samples exhibited efficient photocatalytic activity in terms of phenol degradation under visible light irradiation, while undoped samples were almost inactive under same operating conditions. Moreover, the effects of key operational parameters, the optimum sample calcination temperature, and reusability of FST-N NCPs were evaluated. Under optimum conditions (calcination temperature of 400 °C and near-neutral reaction medium), the obtained results revealed efficient degradation of phenol for FST-N NCPs under visible light irradiation (46 ± 1.5%), high yield magnetic separation and efficient reusability of FST-N NCPs (88.88% of its initial value) over 10 times reuse.

  13. Integrated ternary nanocomposite of TiO2/NiO/reduced graphene oxide as a visible light photocatalyst for efficient degradation of o-chlorophenol.

    PubMed

    Sharma, Ajit; Lee, Byeong-Kyu

    2016-10-01

    This study investigated a novel approach for the synthesis of an integrated ternary nanocomposite which could act as a good photo-catalyst under visible light irradiation for the removal of organic pollutants from aqueous environments. The photo-catalyst included nickel oxide (NiO) as a dopant, and reduced graphene oxide (RGO) as a good carbon basal support for enhancement of the photo-catalytic activity of TiO2. Under irradiation with visible light, the ternary nanocomposite (TiO2/NiO-RGO) system generates e(-)/h(+) pairs, and then reacts with H2O and O2(-) molecules to produce oxy-radicals which can be used for the mineralization of o-chlorophenol from aqueous solution. The characteristic of all photo-catalysts were investigated by UV-Vis analysis, with surface area and pore size measurements by Brunauer-Emmett-Teller (BET), crystallinity by X-ray diffraction (XRD), elemental composition by X-ray photoelectron spectroscopy (XPS), and morphology by scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM/EDX). The functional groups were measured by Fourier transform infrared (FT-IR) spectroscopy before and after o-chlorophenol degradation. TiO2/NiO-RGO was capable of achieving 88.4% photo-degradation of 100 mg/L o-chlorophenol (100 mL) within 8 h with addition of 0.01% H2O2 under visible light irradiation at pH 6.5. The photo-degradation followed a pseudo-first-order reaction. The TiO2/NiO-RGO nanocomposite retained its high removal efficiency, even after four photo-catalytic cycles.

  14. Photo- and electroluminescent properties of bithiophene disubstituted 1,3,4-thiadiazoles and their application as active components in organic light emitting diodes

    NASA Astrophysics Data System (ADS)

    Grykien, Remigiusz; Luszczynska, Beata; Glowacki, Ireneusz; Kurach, Ewa; Rybakiewicz, Renata; Kotwica, Kamil; Zagorska, Malgorzata; Pron, Adam; Tassini, Paolo; Maglione, Maria Grazia; Mauro, Anna De Girolamo Del; Fasolino, Tommaso; Rega, Romina; Pandolfi, Giuseppe; Minarini, Carla; Aprano, Salvatore

    2014-11-01

    Photo- and electroluminescence of five bithiophene disubstituted 1,3,4-thiadiazoles, constituting a new class of solution processable materials for organic opto-electronics, were studied. It was found that the introduction of alkyl solubilizing substituents bathochromically shifted the photo- and electroluminescence bands. The most pronounced effect was observed for the substitution at the Cα position which changed the emitting light color from bluish to green. All five derivatives were tested in host/guest type organic light emitting diodes (OLEDs) with either poly(N-vinylcarbazole) (PVK) or poly(N-vinylcarbazole) + 2-tert-butylphenyl-5-biphenyl-1,3,4-oxadiazole (PVK + PBD) matrices. The latter matrix turned out especially well suited for these guest molecules yielding devices of varying color coordinates. The best luminance (750 cd/m2) was measured for 2,5-bis(5‧-octyl-2,2‧-bithiophene-5-yl)-1,3,4-thiadiazole with the luminous efficiency exceeding 0.4 cd/A.

  15. A highly efficient immobilized ZnO/Zn photoanode for degradation of azo dye Reactive Green 19 in a photocatalytic fuel cell.

    PubMed

    Lee, Sin-Li; Ho, Li-Ngee; Ong, Soon-An; Wong, Yee-Shian; Voon, Chun-Hong; Khalik, Wan Fadhilah; Yusoff, Nik Athirah; Nordin, Noradiba

    2017-01-01

    Photocatalytic fuel cell (PFC) is a potential wastewater treatment technology that can generate electricity from the conversion of chemical energy of organic pollutants. An immobilized ZnO/Zn fabricated by sonication and heat attachment method was applied as the photoanode and Pt/C plate was used as the cathode of the PFC in this study. Factors that affect the decolorization efficiency and electricity generation of the PFC such as different initial dye concentrations and pH were investigated. Results revealed that the degradation of Reactive Green 19 (RG19) was enhanced in a closed circuit PFC compared with that of a opened circuit PFC. Almost 100% decolorization could be achieved in 8 h when 250 mL of 30 mg L(-1) of RG19 was treated in a PFC without any supporting electrolyte. The highest short circuit current of 0.0427 mA cm(-2) and maximum power density of 0.0102 mW cm(-2) was obtained by PFC using 30 mg L(-1) of RG19. The correlation between dye degradation, conductivity and voltage output were also investigated and discussed.

  16. Design of a novel Cu₂O/TiO₂/carbon aerogel electrode and its efficient electrosorption-assisted visible light photocatalytic degradation of 2,4,6-trichlorophenol.

    PubMed

    Wang, Yabo; Zhang, Ya-Nan; Zhao, Guohua; Tian, Hongyi; Shi, Huijie; Zhou, Tianchen

    2012-08-01

    Cu(2)O/TiO(2) heterojunction photocatalyst is built on carbon aerogel (CA) substrate with good adsorption properties by sol impregnation and seed-mediated synthesis approach. The Cu(2)O/TiO(2)/CA electrode has excellent electrosorptive and high efficient photocatalytic properties. Its morphology and surface chemical composition are characterized with SEM, TEM, X-ray diffraction (XRD) and Raman spectra. The UV-vis diffuse reflectance spectra show that the optical absorption edge for Cu(2)O/TiO(2)/CA appears at 636 nm. Under visible-light (λ > 420 nm) irradiation, the photocurrent density increment on Cu(2)O/TiO(2)/CA is 60 times of that on Cu(2)O/TiO(2)/FTO. The electrochemical characteristic is investigated with electrochemical impedance spectrum (EIS). The Cu(2)O/TiO(2)/CA electrode is further applied in the electrosorptive photodegradation of the 2,4,6-trichlorophenol (2,4,6-TCP) wastewater. The result shows that the removal ratio of 2,4,6-TCP in 5.5 h on Cu(2)O/TiO(2)/CA is 96.3% and the TOC removal is 91.3%. The intermediates generated in the degradation process are analyzed by GC-MS and HPLC. The possible mechanism of visible light photocatalytic degradation of 2,4,6-TCP on Cu(2)O/TiO(2)/CA is also studied.

  17. Different types of degradable vectors from low-molecular-weight polycation-functionalized poly(aspartic acid) for efficient gene delivery.

    PubMed

    Dou, X B; Hu, Y; Zhao, N N; Xu, F J

    2014-03-01

    Poly(aspartic acid) (PAsp) has been employed as the potential backbone for the preparation of efficient gene carriers, due to its low cytotoxicity, good biodegradability and excellent biocompatibility. In this work, the degradable linear or star-shaped PBLA was first prepared via ring-opining polymerization of β-benzyl-L-aspartate N-carboxy anhydride (BLA-NCA) initiated by ethylenediamine (ED) or ED-functionalized cyclodextrin cores. Then, PBLA was functionalized via aminolysis reaction with low-molecular-weight poly(2-(dimethylamino)ethyl methacrylate) with one terminal primary amine group (PDMAEMA-NH2), followed by addition of excess ED or ethanolamine (EA) to complete the aminolysis process. The obtained different types of cationic PAsp-based vectors including linear or star PAsp-PDM-NH2 and PAsp-PDM-OH exhibited good condensation capability and degradability, benefiting gene delivery process. In comparison with gold standard polyethylenimine (PEI, ∼ 25 kDa), the cationic PAsp-based vectors, particularly star-shaped ones, exhibited much better transfection performances.

  18. In situ H(+)-mediated formation of singlet oxygen from NaBiO3 for oxidative degradation of bisphenol A without light irradiation: Efficiency, kinetics, and mechanism.

    PubMed

    Ding, Yaobin; Xia, Xiangli; Ruan, Yufeng; Tang, Heqing

    2015-12-01

    Bisphenol A (BPA) is a ubiquitous environmental contaminant with endocrine disruption potential. This study explored the efficiency, kinetics, and mechanism of BPA removal from weakly acidic solutions by using NaBiO3 as a source of singlet oxygen. It was observed that the use of NaBiO3 (1gL(-1)) could eliminate almost all (more than 97%) of the added BPA (0.1mmolL(-1)) in solutions at pH 5.0 in 60min. The degradation of BPA followed pseudo-first-order kinetics over the pH range from 3 to 9, and the pseudo-first-order rate constant (k) was dependent on pH, NaBiO3 concentration and the coexisting compounds. As solution pH was decreased from 9 to 3 or NaBiO3 concentration was increased from 0.5 to 2gL(-1), the k value was increased logarithmically. Humic acid and Fe(3+) showed little effect on the BPA removal, but Mn(2+) exhibited exceptionally enhancing effect on the degradation of BPA. The involved reactive species were identified as singlet oxygen by using radical scavenger probes and ESR measurement, and the generated singlet oxygen was confirmed to be generated from the decomposition of NaBiO3 mediated by H(+) ions.

  19. Ultrasonic-assisted one-pot preparation of ZnO/Ag3VO4 nanocomposites for efficiently degradation of organic pollutants under visible-light irradiation

    NASA Astrophysics Data System (ADS)

    Kiantazh, Fariba; Habibi-Yangjeh, Aziz

    2015-11-01

    We report a facile ultrasonic-assisted one-pot method for preparation of ZnO/Ag3VO4 nanocomposites with different mole fractions of silver vanadate. The preparation method has considerable merits such as short preparation time, large-scale, and one-pot strategy. The resultant samples were fairly characterized by means of XRD, EDX, SEM, TEM, UV-vis DRS, FT-IR, and PL techniques. Visible-light activity of the resultant samples was investigated by degradation of rhodamine B (RhB), methylene blue (MB), and methyl orange (MO). Among the prepared nanocomposites, the ZnO/Ag3VO4 nanocomposite with 0.073 mole fraction of Ag3VO4 exhibited the best activity and excessive amount of Ag3VO4 resulted in decrease of the activity. Photocatalytic activity of this nanocomposite under visible-light irradiation is about 21, 56, and 2.8-fold higher than that of the ZnO sample in degradation of RhB, MB, and MO, respectively. The highly enhanced activity of the nanocomposite was attributed to greater generation of electron-hole pairs, due to photosensitizing role of Ag3VO4 under visible-light irradiation, and efficiently separation of the photogenerated electron-hole pairs, due to formation of n-n heterojunction between the counterparts. Furthermore, it was revealed that the photocatalytic activity largely depends on ultrasonic irradiation time, calcination temperature, and scavengers of the reactive species.

  20. Novel Na2Mo4O13/α-MoO3 hybrid material as highly efficient CWAO catalyst for dye degradation at ambient conditions

    NASA Astrophysics Data System (ADS)

    Zhang, Zhang; Yang, Ruoyan; Gao, Yanshan; Zhao, Yufei; Wang, Junyang; Huang, Liang; Guo, Jiang; Zhou, Tuantuan; Lu, Peng; Guo, Zhanhu; Wang, Qiang

    2014-10-01

    We report a novel hybrid material Na2Mo4O13/α-MoO3 as highly efficient catalytic wet air oxidation (CWAO) catalyst, which showed the highest ever activity at room temperature and atmosphere pressure for the degradation of cationic red GTL. SEM and TEM analyses indicated that this hybrid catalyst has bamboo-shaped nanofiber morphology. In view of practical applications, the influence of some key parameters including operation temperature, catalyst calcination temperature, and the volume of dye wastewater have been optimized. The mechanism for the superior catalytic performance was investigated. XRD, XPS, and ESR suggested the Na2Mo4O13/α-MoO3 hybrid catalyst possesses more O2- ions in the oxygen deficient regions than neat α-MoO3, promoting the formation of active .OH radicals and resulting in a higher activity. Considering the facile preparation and its superior activity, this novel catalyst is promising for practical dye wastewater treatment.

  1. Growth of Fe2O3/SnO2 nanobelt arrays on iron foil for efficient photocatalytic degradation of methylene blue

    NASA Astrophysics Data System (ADS)

    Lei, Rui; Ni, Hongwei; Chen, Rongsheng; Zhang, Bowei; Zhan, Weiting; Li, Yang

    2017-04-01

    Tin(IV) oxide has been intensively employed in optoelectronic devices due to its excellent electrical and optical properties. But the high recombination rates of the photogenerated electron-hole pairs of SnO2 nanomaterials often results in low photocatalytic efficiency. Herein, we proposed a facile route to prepare a novel Fe2O3/SnO2 heterojunction structure. The nanobelt arrays grown on iron foil naturally form a Schottky-type contact and provide a direct pathway for the photogenerated excitons. Hence, the Fe2O3/SnO2 nanobelt arrays exhibit much improved photocatalytic performance with the degradation rate constant on the Fe2O3/SnO2 film of approximately 12 times to that of α-Fe2O3 nanobelt arrays.

  2. A passivated codoping approach to tailor the band edges of TiO2 for efficient photocatalytic degradation of organic pollutants

    NASA Astrophysics Data System (ADS)

    Wang, Dan; Zou, Yanhong; Wen, Shuangchun; Fan, Dianyuan

    2009-07-01

    We propose an effective passivated codoping approach to tailor the band edges of TiO2 by doping the host with group IVA and group VIB impurities to passive donor-acceptor complexes. A way of achieving p-type TiO2 is found, which can outspread the application range of TiO2 semiconductor. It is demonstrated that the carbon (C)/tungsten (W) codoped TiO2 has a substantial increase in the valence band edge, while leaving the conduction band edge almost unchanged, thus improving the efficiency of photocatalytic degradation of organic pollutants. In principle, the suggested approach for overcoming the p-type doping bottleneck can be applied to other wide-band-gap semiconductors.

  3. Coupling of Nanocrystalline Anatase TiO2 to Porous Nanosized LaFeO3 for Efficient Visible-Light Photocatalytic Degradation of Pollutants

    PubMed Central

    Humayun, Muhammad; Li, Zhijun; Sun, Liqun; Zhang, Xuliang; Raziq, Fazal; Zada, Amir; Qu, Yang; Jing, Liqiang

    2016-01-01

    In this work we have successfully fabricated nanocrystalline anatase TiO2/perovskite-type porous nanosized LaFeO3 (T/P-LFO) nanocomposites using a simple wet chemical method. It is clearly demonstrated by means of atmosphere-controlled steady-state surface photovoltage spectroscopy (SPS) responses, photoluminescence spectra, and fluorescence spectra related to the formed OH− radical amount that the photogenerated charge carriers in the resultant T/P-LFO nanocomposites with a proper mole ratio percentage of TiO2 display much higher separation in comparison to the P-LFO alone. This is highly responsible for the improved visible-light activities of T/P-LFO nanocomposites for photocatalytic degradation of gas-phase acetaldehyde and liquid-phase phenol. This work will provide a feasible route to synthesize visible-light responsive nano-photocatalysts for efficient solar energy utilization.

  4. Mn(2+)-mediated homogeneous Fenton-like reaction of Fe(III)-NTA complex for efficient degradation of organic contaminants under neutral conditions.

    PubMed

    Li, Yifan; Sun, Jianhui; Sun, Sheng-Peng

    2016-08-05

    In this work, we report a novel Mn(2+)-mediated Fenton-like process based on Fe(III)-NTA complex that is super-efficient at circumneutral pH range. Kinetics experiments showed that the presence of Mn(2+) significantly enhanced the effectiveness of Fe(III)-NTA complex catalyzed Fenton-like reaction. The degradation rate constant of crotamiton (CRMT), a model compound, by the Fe(III)- NTA_Mn(2+) Fenton-like process was at least 1.6 orders of magnitude larger than that in the absence of Mn(2+). Other metal ions such as Ca(2+), Mg(2+), Co(2+) and Cu(2+) had no impacts or little inhibitory effect on the Fe(III)-NTA complex catalyzed Fenton-like reaction. The generation of hydroxyl radical (HO) and superoxide radical anion (O2(-)) in the Fe(III)-NTA_Mn(2+) Fenton-like process were suggested by radicals scavenging experiments. The degradation efficiency of CRMT was inhibited significantly (approximately 92%) by the addition of HO scavenger 2-propanol, while the addition of O2(-) scavenger chloroform resulted in 68% inhibition. Moreover, the results showed that other chelating agents such as EDTA- and s,s-EDDS-Fe(III) catalyzed Fenton-like reactions were also enhanced significantly by the presence of Mn(2+). The mechanism involves an enhanced generation of O2(-) from the reactions of Mn(2+)-chelates with H2O2, indirectly promoting the generation of HO by accelerating the reduction rate of Fe(III)-chelates to Fe(II)- chelates.

  5. Kinetic Monte Carlo simulation of the efficiency roll-off, emission color, and degradation of organic light-emitting diodes (Presentation Recording)

    NASA Astrophysics Data System (ADS)

    Coehoorn, Reinder; van Eersel, Harm; Bobbert, Peter A.; Janssen, Rene A. J.

    2015-10-01

    The performance of Organic Light Emitting Diodes (OLEDs) is determined by a complex interplay of the charge transport and excitonic processes in the active layer stack. We have developed a three-dimensional kinetic Monte Carlo (kMC) OLED simulation method which includes all these processes in an integral manner. The method employs a physically transparent mechanistic approach, and is based on measurable parameters. All processes can be followed with molecular-scale spatial resolution and with sub-nanosecond time resolution, for any layer structure and any mixture of materials. In the talk, applications to the efficiency roll-off, emission color and lifetime of white and monochrome phosphorescent OLEDs [1,2] are demonstrated, and a comparison with experimental results is given. The simulations show to which extent the triplet-polaron quenching (TPQ) and triplet-triplet-annihilation (TTA) contribute to the roll-off, and how the microscopic parameters describing these processes can be deduced properly from dedicated experiments. Degradation is treated as a result of the (accelerated) conversion of emitter molecules to non-emissive sites upon a triplet-polaron quenching (TPQ) process. The degradation rate, and hence the device lifetime, is shown to depend on the emitter concentration and on the precise type of TPQ process. Results for both single-doped and co-doped OLEDs are presented, revealing that the kMC simulations enable efficient simulation-assisted layer stack development. [1] H. van Eersel et al., Appl. Phys. Lett. 105, 143303 (2014). [2] R. Coehoorn et al., Adv. Funct. Mater. (2015), publ. online (DOI: 10.1002/adfm.201402532)

  6. Hydrogenated TiO2 nanobelts as highly efficient photocatalytic organic dye degradation and hydrogen evolution photocatalyst.

    PubMed

    Tian, Jian; Leng, Yanhua; Cui, Hongzhi; Liu, Hong

    2015-12-15

    TiO2 nanobelts have gained increasing interest because of its outstanding properties and promising applications in a wide range of fields. Here we report the facile synthesis of hydrogenated TiO2 (H-TiO2) nanobelts, which exhibit excellent UV and visible photocatalytic decomposing of methyl orange (MO) and water splitting for hydrogen production. The improved photocatalytic property can be attributed to the Ti(3+) ions and oxygen vacancies in TiO2 nanobelts created by hydrogenation. Ti(3+) ions and oxygen vacancies can enhance visible light absorption, promote charge carrier trapping, and hinder the photogenerated electron-hole recombination. This work offers a simple strategy for the fabrication of a wide solar spectrum of active photocatalysts, which possesses significant potential for more efficient photodegradation, photocatalytic water splitting, and enhanced solar cells using sunlight as light source.

  7. Highly Efficient Gluten Degradation by Lactobacilli and Fungal Proteases during Food Processing: New Perspectives for Celiac Disease▿

    PubMed Central

    Rizzello, Carlo G.; De Angelis, Maria; Di Cagno, Raffaella; Camarca, Alessandra; Silano, Marco; Losito, Ilario; De Vincenzi, Massimo; De Bari, Maria D.; Palmisano, Francesco; Maurano, Francesco; Gianfrani, Carmen; Gobbetti, Marco

    2007-01-01

    Presently, the only effective treatment for celiac disease is a life-long gluten-free diet. In this work, we used a new mixture of selected sourdough lactobacilli and fungal proteases to eliminate the toxicity of wheat flour during long-time fermentation. Immunological (R5 antibody-based sandwich and competitive enzyme-linked immunosorbent assay [ELISA] and R5 antibody-based Western blot), two-dimensional electrophoresis, and mass spectrometry (matrix-assisted laser desorption ionization-time of flight, strong-cation-exchange-liquid chromatography/capillary liquid chromatography-electrospray ionization-quadrupole-time of flight [SCX-LC/CapLC-ESI-Q-TOF], and high-pressure liquid chromatography-electrospray ionization-ion trap mass spectrometry) analyses were used to determine the gluten concentration. Assays based on the proliferation of peripheral blood mononuclear cells (PBMCs) and gamma interferon production by PBMCs and intestinal T-cell lines (iTCLs) from 12 celiac disease patients were used to determine the protein toxicity of the pepsin-trypsin digests from fermented wheat dough (sourdough). As determined by R5-based sandwich and competitive ELISAs, the residual concentration of gluten in sourdough was 12 ppm. Albumins, globulins, and gliadins were completely hydrolyzed, while ca. 20% of glutenins persisted. Low-molecular-weight epitopes were not detectable by SCX-LC/CapLC-ESI-Q-TOF mass spectrometry and R5-based Western blot analyses. The kinetics of the hydrolysis of the 33-mer by lactobacilli were highly efficient. All proteins extracted from sourdough activated PBMCs and induced gamma interferon production at levels comparable to the negative control. None of the iTCLs demonstrated immunoreactivity towards pepsin-trypsin digests. Bread making was standardized to show the suitability of the detoxified wheat flour. Food processing by selected sourdough lactobacilli and fungal proteases may be considered an efficient approach to eliminate gluten toxicity

  8. Construction and Characterization of Vitreoscilla Hemoglobin (VHb) with Enhanced Peroxidase Activity for Efficient Degradation of Textile Dye.

    PubMed

    Zhang, Zidong; Li, Wei; Li, Haichao; Zhang, Jing; Zhang, Yuebin; Cao, Yufeng; Ma, Jianzhang; Li, Zhengqiang

    2015-09-01

    Pollution resulting from the discharge of textile dyes into water systems has become a major global concern. Because peroxidases are known for their ability to decolorize and detoxify textile dyes, the peroxidase activity of Vitreoscilla hemoglobin (VHb) has recently been studied. It is found that VHb and variants of this enzyme show great promise for enzymatic decolorization of dyes and may play a role in achieving their successful removal from industrial wastewater. The level of VHb peroxidase activity correlates with two amino acid residues present within the conserved distal pocket, at positions 53 and 54. In this work, sitedirected mutagenesis of these residues was performed and resulted in improved VHb peroxidase activity. The double mutant, Q53H/P54C, shows the highest dye decolorization and removal efficiency, with 70% removal efficiency within 5 min. UV spectral studies of Q53H/P54C reveals a more compact structure and an altered porphyrin environment (λSoret = 413 nm) relative to that of wild-type VHb (λSoret = 406), and differential scanning calorimetry data indicate that the VHb variant protein structure is more stable. In addition, circular dichroism spectroscopic studies indicate that this variant's increased protein structural stability is due to an increase in helical structure, as deduced from the melting temperature, which is higher than 90°C. Therefore, the VHb variant Q53H/P54C shows promise as an excellent peroxidase, with excellent dye decolorization activity and a more stable structure than wild-type VHb under high-temperature conditions.

  9. Observation of near infrared and enhanced visible emissions from electroluminescent devices with organo samarium(III) complex

    NASA Astrophysics Data System (ADS)

    Chu, B.; Li, W. L.; Hong, Z. R.; Zang, F. X.; Wei, H. Z.; Wang, D. Y.; Li, M. T.; Lee, C. S.; Lee, S. T.

    2006-11-01

    Samarium (dibenzoylmethanato)3 bathophenanthroline (Sm(DBM)3 bath) was employed as an emitting and electron transport layer in organic light emitting diodes (OLEDs), and narrow electroluminescent (EL) emissions of a Sm3+ ion were observed in the visible and near infrared (NIR) region, differing from those of the same devices with Eu3+- or Tb3+-complex EL devices with the same structure. The EL emissions of the Sm3+-devices originate from transitions from 4G5/2 to the lower respective levels of Sm3+ ions. A maximum luminance of 490 cd m-2 at 15 V and an EL efficiency of 0.6% at 0.17 mA cm-2 were obtained in the visible region, and the improved efficiency should be attributed to introducing a transitional layer between the N,N'-diphenyl-N,N'-bis(3-methylphenyl)-1,1'-diphenyl-4,4'-diamine (TPD) film and the Sm(DBM)3 bath film and the avoidance of interfacial exciplex emission in devices. Sharp emissions of Sm3+ ions in the NIR region were also observed under a lower threshold value less than 4.5 V.

  10. Photoluminescent and Electroluminescent Properties of Cd sub 0.95 Mn sub 0.05 Se Electrodes.

    DTIC Science & Technology

    1984-09-28

    electroluminescence, cadmium manganese selenide electrodes, photoelectrochemistry, dead-layer model 10. ABSTRACT (Contlave on Fvors&a side 110080080Y d...to map the electric field in theme solids, grown by a modified Bridgman method. , DD P1’H"I. 1473 CITION Of I NOV 66 IS OSSOLCTE nlssfe 012.L.014501...used to map the electric field in these solids, grown by a modified Bridgman method. 1. INTRODUCTION Photoluminescence (PL) and electroluminescence (EL

  11. Efficient photocatalytic degradation of acid fuchsin in aqueous solution using separate porous tetragonal-CuFe2O4 nanotubes.

    PubMed

    Jing, Panpan; Li, Jianan; Pan, Lining; Wang, Jianbo; Sun, Xiaojun; Liu, Qingfang

    2015-03-02

    To develop a new promising magnetic photocatalyst, homogeneous tetragonal-CuFe2O4 (t-CuFe2O4) nanotubes were successfully synthesized via the electrospinning technique followed by heating treatment. The detailed investigation of chemical phase and microstructure reveals that the obtained samples are inversely spinel CuFe2O4 nanotubes with an average diameter of about 272±2nm, which are assembled by numerous CuFe2O4 single crystal nanoparticles with regular polyhedron structure and possess a very outstanding porous feature. Furthermore, element mapping, UV-vis adsorption spectrum, N2 adsorption-desorption isotherm, and magnetic hysteresis loop indicate that these t-CuFe2O4 nanotubes have uniform component distribution, strong light response in the range of 200 nm-800 nm, considerable specific surface area of 12.8 m(2)/g and porosity of 15.5 nm, and enough magnetization of about 18 emu/g. Therefore, the t-CuFe2O4 nanotubes show an excellent catalytic activity and durability for the photodecomposition of acid fuchsin dye in aqueous solution under a simulated sunlight source. Furthermore, these CuFe2O4 nanotubes could be acted as an eco-friendly and recyclable photocatalyst because they can be efficiently separated from the residual solution. Finally, a mechanism is presented for the significant photocatalytic performance of the porous CuFe2O4 nanotubes.

  12. Self-assembling process of Oxalamide compounds and their nucleation efficiency in bio-degradable Poly(hydroxyalkanoate)s

    NASA Astrophysics Data System (ADS)

    Ma, Piming; Deshmukh, Yogesh S.; Wilsens, Carolus H. R. M.; Ryan Hansen, Michael; Graf, Robert; Rastogi, Sanjay

    2015-08-01

    One of the key requirements in semi-crystalline polyesters, synthetic or bio-based, is the control on crystallization rate and crystallinity. One of the limiting factors in the commercialization of the bio-based polyesters, for example polyhydroxyalkanoates synthesized by bacteria for energy storage purposes, is the slow crystallization rate. In this study, we show that by tailoring the molecular structure of oxalamide compounds, it is possible to dissolve these compounds in molten poly(hydroxybutyrate) (PHB), having a hydroxyvalerate co-monomer content of less than 2 mol%. Upon cooling the polymer melt, the homogeneously dispersed oxalamide compound crystallizes just below the melting temperature of the polymer. The phase-separated compound reduces the nucleation barrier of the polymer, thus enhancing the crystallization rate, nucleation density and crystallinity. The findings reported in this study provide a generic route for the molecular design of oxalamide-based compounds that can be used for enhancing nucleation efficiency of semi-crystalline bio-based polyesters.

  13. Self-assembling process of Oxalamide compounds and their nucleation efficiency in bio-degradable Poly(hydroxyalkanoate)s

    PubMed Central

    Ma, Piming; Deshmukh, Yogesh S.; Wilsens, Carolus H.R.M.; Ryan Hansen, Michael; Graf, Robert; Rastogi, Sanjay

    2015-01-01

    One of the key requirements in semi-crystalline polyesters, synthetic or bio-based, is the control on crystallization rate and crystallinity. One of the limiting factors in the commercialization of the bio-based polyesters, for example polyhydroxyalkanoates synthesized by bacteria for energy storage purposes, is the slow crystallization rate. In this study, we show that by tailoring the molecular structure of oxalamide compounds, it is possible to dissolve these compounds in molten poly(hydroxybutyrate) (PHB), having a hydroxyvalerate co-monomer content of less than 2 mol%. Upon cooling the polymer melt, the homogeneously dispersed oxalamide compound crystallizes just below the melting temperature of the polymer. The phase-separated compound reduces the nucleation barrier of the polymer, thus enhancing the crystallization rate, nucleation density and crystallinity. The findings reported in this study provide a generic route for the molecular design of oxalamide-based compounds that can be used for enhancing nucleation efficiency of semi-crystalline bio-based polyesters. PMID:26290334

  14. Nanostructured AgBr loaded TiO2: An efficient sunlight active photocatalyst for degradation of Reactive Red 120.

    PubMed

    Velmurugan, Rengasamy; Sreedhar, Bojja; Swaminathan, Meenakshisundaram

    2011-07-30

    The AgBr loaded TiO2 catalyst was prepared by a feasible approach with AgBr and tetraisopropyl orthotitanate and characterized by BET surface area measurement, diffuse reflectance spectra (DRS), scanning electron microscope (SEM), energy dispersive spectra (EDS), X-ray diffraction (XRD), transmission electron microscope (TEM) and atomic force microscope (AFM) analysis. The results of characterization reveal that AgBr loaded TiO2 has a nanostructure. Formation of the nanostructure in AgBr loaded TiO2 results in substantial shifting of the absorption edge of TiO2 to red and enhancement of visible light absorption. Electrochemical impedance spectroscopy measurements reveal that AgBr loaded TiO2 has a higher photoconductivity than prepared TiO2 due to higher separation efficiency of electron-hole pairs. Cyclic voltammetric studies reveal enhanced conductivity in AgBr loaded TiO2, which causes an increase in its photocatalytic activity. AgBr loaded TiO2 exhibited a higher photocatalytic activity than TiO2-P25 and prepared TiO2 in the photodegradation of Reactive Red 120 (RR 120).

  15. Isolation and evaluation of native cellulose degrading microorganisms for efficient bioconversion of weed biomass and rice straw.

    PubMed

    Mahanta, K; Jha, D K; Rajkhowa, D J; Kumar, Manoj

    2014-07-01

    Cellulose decomposing microorganisms (CDMs) are important for efficient bioconversion of plant biomasses. To this end, we isolated seven fungal isolates (Aspergillus wentii, Fusarium solani, Mucor sp., Penicillum sp., Trichoderma harzaianum, Trichoderma sp.1 and Trichoderma sp.2) and three bacterial isolates (bacterial isolate I, II and III) from partially decomposed farm yard manure, rice straw and vermicompost, and evaluated them for decomposition of rice straw (Oryza sativa), Ipomoea camea and Eichhornia crassipes biomass. CDMs inoculation, in general, reduced the composting period by 14-28 days in rice straw, 14-34 days in Eichhornia and 10-28 days in Ipomoea biomass over control. Of the 10 CDMs tested, Mucor sp. was found to be the most effective as Mucor-inoculated biomass required minimum time, i.e. 84, 68 and 80 days respectively for composting of rice straw, Eichhornia and Ipomoea biomass as against 112, 102 and 108 days required under their respective control. CDMs inoculation also narrowed down the C:N ratio of the composts which ranged from 19.1-22.7, 12.9-14.7 and 10.5-13.1 in rice straw, Eichhornia and Ipomoea biomass respectively as against 24.1, 17.1 and 16.2 in the corresponding control treatments. Aspergillus wentii, Fusarium solani, Mucor sp., and Penicillum sp. were found most effective (statistically at par) in reducing C:N ratio and causing maximum loss of carbon and dry matter in composted materials. These benefits of CDMs inoculation were also accompanied by significant increase in NPK contents in the composted materials.

  16. Micropollutant degradation, bacterial inactivation and regrowth risk in wastewater effluents: Influence of the secondary (pre)treatment on the efficiency of Advanced Oxidation Processes.

    PubMed

    Giannakis, Stefanos; Voumard, Margaux; Grandjean, Dominique; Magnet, Anoys; De Alencastro, Luiz Felippe; Pulgarin, César

    2016-10-01

    In this work, disinfection by 5 Advanced Oxidation Processes was preceded by 3 different secondary treatment systems present in the wastewater treatment plant of Vidy, Lausanne (Switzerland). 5 AOPs after two biological treatment methods (conventional activated sludge and moving bed bioreactor) and a physiochemical process (coagulation-flocculation) were tested in laboratory scale. The dependence among AOPs efficiency and secondary (pre)treatment was estimated by following the bacterial concentration i) before secondary treatment, ii) after the different secondary treatment methods and iii) after the various AOPs. Disinfection and post-treatment bacterial regrowth were the evaluation indicators. The order of efficiency was Moving Bed Bioreactor > Activated Sludge > Coagulation-Flocculation > Primary Treatment. As far as the different AOPs are concerned, the disinfection kinetics were: UVC/H2O2 > UVC and solar photo-Fenton > Fenton or solar light. The contextualization and parallel study of microorganisms with the micropollutants of the effluents revealed that higher exposure times were necessary for complete degradation compared to microorganisms for the UV-based processes and inversed for the Fenton-related ones. Nevertheless, in the Fenton-related systems, the nominal 80% removal of micropollutants deriving from the Swiss legislation, often took place before the elimination of bacterial regrowth risk.

  17. Novel Fe3O4@SiO2@Ag@Ni trepang-like nanocomposites: High-efficiency and magnetic recyclable catalysts for organic dye degradation

    NASA Astrophysics Data System (ADS)

    Li, Chao; Sun, Jun-Jie; Chen, Duo; Han, Guang-Bing; Yu, Shu-Yun; Kang, Shi-Shou; Mei, Liang-Mo

    2016-08-01

    A facile step-by-step approach is developed for synthesizing the high-efficiency and magnetic recyclable Fe3O4@SiO2@Ag@Ni trepang-like nanocomposites. This method involves coating Fe2O3 nanorods with a uniform silica layer, reduction in 10% H2/Ar atmosphere to transform the Fe2O3 into magnetic Fe3O4, and finally depositing Ag@Ni core-shell nanoparticles on the L-lysine modified surface of Fe3O4@SiO2 nanorods. The fabricated nanocomposites are further characterized by x-ray diffraction, transmission electron microscopy, scanning electron microscope, Fourier transform infrared spectroscopy, and inductively coupled plasma mass spectroscopy. The Fe3O4@SiO2@Ag@Ni trepang-like nanocomposites exhibit remarkably higher catalytic efficiency than monometallic Fe3O4@SiO2@Ag nanocomposites toward the degradation of Rhodamine B (RhB) at room temperature, and maintain superior catalytic activity even after six cycles. In addition, these samples could be easily separated from the catalytic system by an external magnet and reused, which shows great potential applications in treating waste water. Project supported by the National Basic Research Program of China (Grant No. 2015CB921502), the National Natural Science Foundation of China (Grant Nos. 11474184 and 11174183), the 111 Project (Grant No. B13029), and the Fundamental Research Funds of Shandong University, China.

  18. Light-induced efficient molecular oxygen activation on a Cu(II)-grafted TiO2/graphene photocatalyst for phenol degradation.

    PubMed

    Zhang, Hui; Guo, Liang-Hong; Wang, Dabin; Zhao, Lixia; Wan, Bin

    2015-01-28

    An efficient photocatalytic process involves two closely related steps: charge separation and the subsequent surface redox reaction. Herein, a ternary hybrid photocatalytic system was designed and fabricated by anchoring Cu(II) clusters onto a TiO2/reduced graphene oxide (RGO) composite. Microscopic and spectroscopic characterization revealed that both TiO2 nanoparticles and Cu(II) clusters were highly dispersed on a graphene sheet with intimate interfacial contact. Compared with pristine TiO2, the TiO2/RGO/Cu(II) composite yielded an almost 3-fold enhancement in the photodegradation rate toward phenol degradation under UV irradiation. Electron spin resonance (ESR) spectra and electrochemical measurements demonstrated that the improved photocatalytic activity of this ternary system benefitted from the synergetic effect between RGO and Cu(II), which facilitates the interfacial charge transfer and simultaneously achieves in situ generation of H2O2 via two-electron reduction of O2. These results highlight the importance to harmonize the charge separation and surface reaction process in achieving high photocatalytic efficiency for practical application.

  19. Mechanism of hot electron electroluminescence in GaN-based transistors

    NASA Astrophysics Data System (ADS)

    Brazzini, Tommaso; Sun, Huarui; Sarti, Francesco; Pomeroy, James W.; Hodges, Chris; Gurioli, Massimo; Vinattieri, Anna; Uren, Michael J.; Kuball, Martin

    2016-11-01

    The nature of hot electron electroluminescence (EL) in AlGaN/GaN high electron mobility transistors is studied and attributed to Bremsstrahlung. The spectral distribution has been corrected, for the first time, for interference effects due to the multilayered device structure, and this was shown to be crucial for the correct interpretation of the data, avoiding artefacts in the spectrum and misinterpretation of the results. An analytical expression for the spectral distribution of emitted light is derived assuming Bremsstrahlung as the only origin and compared to the simplified exponential model for the high energy tail commonly used for electron temperature extraction: the electron temperature obtained results about 20% lower compared to the approximated exponential model. Comparison of EL intensity for devices from different wafers illustrated the dependence of EL intensity on the material quality. The polarization of electroluminescence also confirms Bremsstrahlung as the dominant origin of the light emitted, ruling out other possible main mechanisms.

  20. Analysis of defect-related inhomogeneous electroluminescence in InGaN/GaN QW LEDs

    NASA Astrophysics Data System (ADS)

    Ren, C. X.; Rouet-Leduc, B.; Griffiths, J. T.; Bohacek, E.; Wallace, M. J.; Edwards, P. R.; Hopkins, M. A.; Allsopp, D. W. E.; Kappers, M. J.; Martin, R. W.; Oliver, R. A.

    2016-11-01

    The inhomogeneous electroluminescence (EL) of InGaN/GaN quantum well light emitting diode structures was investigated in this study. Electroluminescence hyperspectral images showed that inhomogeneities in the form of bright spots exhibited spectrally blue-shifted and broadened emission. Scanning electron microscopy combined with cathodoluminescence (SEM-CL) was used to identify hexagonal pits at the centre of approximately 20% of these features. Scanning transmission electron microscopy imaging with energy dispersive X-ray spectroscopy (STEM-EDX) indicated there may be p-doped AlGaN within the active region caused by the presence of the pit. Weak beam dark-field TEM (WBDF-TEM) revealed the presence of bundles of dislocations associated with the pit, suggesting the surface features which cause the inhomogeneous EL may occur at coalescence boundaries, supported by trends in the number of features observed across the wafer.

  1. Interface-Free Area-Scalable Self-Powered Electroluminescent System Driven by Triboelectric Generator

    PubMed Central

    Yan Wei, Xiao; Kuang, Shuang Yang; Yang Li, Hua; Pan, Caofeng; Zhu, Guang; Wang, Zhong Lin

    2015-01-01

    Self-powered system that is interface-free is greatly desired for area-scalable application. Here we report a self-powered electroluminescent system that consists of a triboelectric generator (TEG) and a thin-film electroluminescent (TFEL) lamp. The TEG provides high-voltage alternating electric output, which fits in well with the needs of the TFEL lamp. Induced charges pumped onto the lamp by the TEG generate an electric field that is sufficient to excite luminescence without an electrical interface circuit. Through rational serial connection of multiple TFEL lamps, effective and area-scalable luminescence is realized. It is demonstrated that multiple types of TEGs are applicable to the self-powered system, indicating that the system can make use of diverse mechanical sources and thus has potentially broad applications in illumination, display, entertainment, indication, surveillance and many others. PMID:26338365

  2. Enhancement of Organic Electroluminescent Intensity by Doping Hole-Property Polymers

    NASA Astrophysics Data System (ADS)

    Wang, Guangming; Wu, Haiming; Yuan, Chunwei; Wei, Yu

    1995-09-01

    Organic electroluminescent (EL) diodes with one-layer poly(3-octylthiophene) (P3OT) and P3OT doped with poly(N-vinylcarbazole) (PVK) (P3OT/PVK) as EL emitting layer sandwiched between indium/tin oxide (ITO) and aluminium electrodes have been fabricated by spin coating onto ITO respectively. The P3OT/PVK EL diode starts to emit red-orange light at 5 V in our experiment, the luminance and the current for the P3OT/PVK EL diode at bias voltage was compared with those for the only P3OT EL diode, indicating that the PVK dopant has power over the P3OT electroluminescence.

  3. Interface-Free Area-Scalable Self-Powered Electroluminescent System Driven by Triboelectric Generator.

    PubMed

    Wei, Xiao Yan; Kuang, Shuang Yang; Li, Hua Yang; Pan, Caofeng; Zhu, Guang; Wang, Zhong Lin

    2015-09-04

    Self-powered system that is interface-free is greatly desired for area-scalable application. Here we report a self-powered electroluminescent system that consists of a triboelectric generator (TEG) and a thin-film electroluminescent (TFEL) lamp. The TEG provides high-voltage alternating electric output, which fits in well with the needs of the TFEL lamp. Induced charges pumped onto the lamp by the TEG generate an electric field that is sufficient to excite luminescence without an electrical interface circuit. Through rational serial connection of multiple TFEL lamps, effective and area-scalable luminescence is realized. It is demonstrated that multiple types of TEGs are applicable to the self-powered system, indicating that the system can make use of diverse mechanical sources and thus has potentially broad applications in illumination, display, entertainment, indication, surveillance and many others.

  4. High-efficiency white organic light-emitting diodes using thermally activated delayed fluorescence

    SciTech Connect

    Nishide, Jun-ichi; Hiraga, Yasuhide; Nakanotani, Hajime; Adachi, Chihaya

    2014-06-09

    White organic light-emitting diodes (WOLEDs) have attracted much attention recently, aimed for next-generation lighting sources because of their high potential to realize high electroluminescence efficiency, flexibility, and low-cost manufacture. Here, we demonstrate high-efficiency WOLED using red, green, and blue thermally activated delayed fluorescence materials as emissive dopants to generate white electroluminescence. The WOLED has a maximum external quantum efficiency of over 17% with Commission Internationale de l'Eclairage coordinates of (0.30, 0.38).

  5. Quantum Dots for Wide Color Gamut Displays from Photoluminescence to Electroluminescence

    NASA Astrophysics Data System (ADS)

    Kang, Yongyin; Song, Zhicheng; Jiang, Xiaofang; Yin, Xia; Fang, Long; Gao, Jing; Su, Yehua; Zhao, Fei

    2017-02-01

    Monodisperse quantum dots (QDs) were prepared by low-temperature process. The remarkable narrow emission peak of the QDs helps the liquid crystal displays (LCD) and electroluminescence displays (QD light-emitting diode, QLED) to generate wide color gamut performance. The range of the color gamut for QD light-converting device (QLCD) is controlled by both the QDs and color filters (CFs) in LCD, and for QLED, the optimized color gamut is dominated by QD materials.

  6. Electroluminescence of cubic boron nitride single crystal flakes with color-zoning

    NASA Astrophysics Data System (ADS)

    Liu, Xiuhuan; Wang, Shuang; Chen, Zhanguo; Jia, Gang; Bian, Tianliang; Hou, Lixin; Wang, Qi; Liu, Nian

    2015-04-01

    The current-voltage (I-V) characteristics and phenomena of electroluminescence of cubic boron nitride (cBN) single crystal flakes with color-zoning under extremely non-uniform electric fields (ENUEFs) induced by needle-plate electrodes were observed. When a cBN flake with sizes of 0.3×0.3×0.1 mm3 was tightly fixed between the tungsten needle and brass plate electrodes in the atmosphere, the I-V relationship exhibited nonlinearity, and peculiar phenomena of electroluminescence with bright blue-violet light appeared at the bias voltage in a range of 700-1200 V. The current-controlled differential negative resistance was synchronously observed. The electroluminescent phenomena were somewhat different for cases of the needle electrode respectively contacting to the amber and transparent zones. The electroluminescent radiations of cBN flakes biased at voltages with a range of 600-1550 V were also investigated in vacuum. In a vacuum chamber, the green emitting phosphor spread around the cBN flake might be excited by the vacuum ultraviolet (VUV) emission from the cBN crystal, and the green fluorescence was observed by naked eyes. The VUV radiation spectrum with a peak wavelength of 149 nm was measured. In the atmosphere, the blue-violet light emission may be the gas discharge resulted from the air ionization induced by the VUV emission from the cBN crystal under the ENUEF, and the ENUEF subsequently keeps the air discharging. The VUV emission from the cBN crystal under the ENUEF can be caused by the original interband transition and the subsequent intraband transfer for electrons, and the final electron-hole direct recombination.

  7. Quantum Dots for Wide Color Gamut Displays from Photoluminescence to Electroluminescence.

    PubMed

    Kang, Yongyin; Song, Zhicheng; Jiang, Xiaofang; Yin, Xia; Fang, Long; Gao, Jing; Su, Yehua; Zhao, Fei

    2017-12-01

    Monodisperse quantum dots (QDs) were prepared by low-temperature process. The remarkable narrow emission peak of the QDs helps the liquid crystal displays (LCD) and electroluminescence displays (QD light-emitting diode, QLED) to generate wide color gamut performance. The range of the color gamut for QD light-converting device (QLCD) is controlled by both the QDs and color filters (CFs) in LCD, and for QLED, the optimized color gamut is dominated by QD materials.

  8. Electroluminescence from a diamond device with ion-beam-micromachined buried graphitic electrodes

    NASA Astrophysics Data System (ADS)

    Forneris, J.; Battiato, A.; Gatto Monticone, D.; Picollo, F.; Amato, G.; Boarino, L.; Brida, G.; Degiovanni, I. P.; Enrico, E.; Genovese, M.; Moreva, E.; Traina, P.; Verona, C.; Verona Rinati, G.; Olivero, P.

    2015-04-01

    Focused MeV ion microbeams are suitable tools for the direct writing of conductive graphitic channels buried in an insulating diamond bulk, as demonstrated in previous works with the fabrication of multi-electrode ionizing radiation detectors and cellular biosensors. In this work we investigate the suitability of the fabrication method for the electrical excitation of color centers in diamond. Differently from photoluminescence, electroluminescence requires an electrical current flowing through the diamond sub-gap states for the excitation of the color centers. With this purpose, buried graphitic electrodes with a spacing of 10 μm were fabricated in the bulk of a detector-grade CVD single-crystal diamond sample using a scanning 1.8 MeV He+ micro-beam. The current flowing in the gap region between the electrodes upon the application of a 450 V bias voltage was exploited as the excitation pump for the electroluminescence of different types of color centers localized in the above-mentioned gap. The bright light emission was spatially mapped using a confocal optical microscopy setup. The spectral analysis of electroluminescence revealed the emission from neutrally-charged nitrogen-vacancy centers (NV0, λZPL = 575 nm), as well as from cluster crystal dislocations (A-band, λ = 400-500 nm). Moreover, an electroluminescence signal with appealing spectral features (sharp emission at room temperature, low phonon sidebands) from He-related defects was detected (λZPL = 536.3 nm, λZPL = 560.5 nm); a low and broad peak around λ = 740 nm was also observed and tentatively ascribed to Si-V or GR1 centers. These results pose interesting future perspectives for the fabrication of electrically-stimulated single-photon emitters in diamond for applications in quantum optics and quantum cryptography.

  9. Electroluminescence and Spectral Shift of CdS Nanoparticles on Si Wafer

    DTIC Science & Technology

    2002-01-01

    emitting active layer is simply fabricated by the spin - coating technique. Electroluminescence (EL) can be easily achieved by quantum tunneling of...percolatior, solutions for spin - coating purpose were produced by dissolving the nanoparicles in ethanol with a concentration of 1% (w/v). Fabrication of...diffusing easier. Conclusions The CdS nanoparticles prepared by chemical method are ready for spin - coating and EL device fabrication. The observed a

  10. Electroluminescence spectra of rare-earth-doped ZnS 1-XSe X thin films

    NASA Astrophysics Data System (ADS)

    Miura, Noboru; Ogawa, Kiyoshi; Kobayashi, Shuko; Matsumoto, Hironaga; Nakano, Ryotaro

    1994-04-01

    Electroluminescence has been measured for ZnS 1- XSe X thin films doped with rare-earth ions. As X increases the band-gap energy of the host decreases. The emission levels of trivalent rare-earth ions are not observed when the band-gap energy is narrower than the excitation levels. This is because of the energy transfer between the host and the emission center.

  11. Molding resonant energy transfer by colloidal crystal: Dexter transfer and electroluminescence

    NASA Astrophysics Data System (ADS)

    González-Urbina, Luis; Kolaric, Branko; Libaers, Wim; Clays, Koen

    2010-05-01

    Building photonic crystals by combination of colloidal ordering and metal sputtering we were able to construct a system sensitive to an electrical field. In corresponding crystals we embedded the Dexter pair (Ir(ppy3) and BAlq) and investigated the influence of the band gap on the resonant energy transfer when the system is excited by light and by an electric field respectively. Our investigations extend applications of photonic crystals into the field of electroluminescence and LED technologies.

  12. Efficient photocatalytic degradation of rhodamine-B by Fe doped CuS diluted magnetic semiconductor nanoparticles under the simulated sunlight irradiation

    NASA Astrophysics Data System (ADS)

    Sreelekha, N.; Subramanyam, K.; Amaranatha Reddy, D.; Murali, G.; Rahul Varma, K.; Vijayalakshmi, R. P.

    2016-12-01

    The present work is planned for a simple, inexpensive and efficient approach for the synthesis of Cu1-xFexS (x = 0.00, 0.01, 0.03, 0.05 and 0.07) nanoparticles via simplistic chemical co-precipitation route by using ethylene diamine tetra acetic acid (EDTA) as a capping molecules. As synthesized nanoparticles were used as competent catalysts for degradation of rhodamine-B organic dye pollutant. The properties of prepared samples were analyzed with energy dispersive analysis of X-rays (EDAX), X-ray diffraction (XRD), transmission electron microscopy (TEM), UV-visible optical absorption spectroscopy, Fourier transform infrared (FTIR) spectra, Raman spectra and vibrating sample magnetometer (VSM). EDAX spectra corroborated the existence of Fe in prepared nanoparticles within close proximity to stoichiometric ratio. XRD, FTIR and Raman patterns affirmed that configuration of single phase hexagonal crystal structure as that of (P63/mmc) CuS, without impurity crystals. The average particle size estimated by TEM scrutiny is in the assortment of 5-10 nm. UV-visible optical absorption measurements showed that band gap narrowing with increasing the Fe doping concentration. VSM measurements revealed that 3% Fe doped CuS nanoparticles exhibited strong ferromagnetism at room temperature and changeover of magnetic signs from ferromagnetic to the paramagnetic nature with increasing the Fe doping concentration in CuS host lattice. Among all Fe doped CuS nanoparticles, 3% Fe inclusion CuS sample shows better photocatalytic performance in decomposition of RhB compared with the pristine CuS. Thus as synthesized Cu0·97Fe0·03S nanocatalysts are tremendously realistic compounds for photocatalytic fictionalization in the direction of organic dye degradation under visible light.

  13. Ag/AgBr/g-C{sub 3}N{sub 4}: A highly efficient and stable composite photocatalyst for degradation of organic contaminants under visible light

    SciTech Connect

    Cao, Jing; Zhao, Yijie; Lin, Haili; Xu, Benyan; Chen, Shifu

    2013-10-15

    Graphical abstract: Ag/AgBr/g-C{sub 3}N{sub 4} composite photocatalysts displayed excellent photocatalytic activities on the degradation of methyl orange (MO) under visible light. The improved photocatalytic performance and stability of Ag/AgBr/g-C{sub 3}N{sub 4} originated from the synergetic effects of AgBr/g-C{sub 3}N{sub 4} interface and metallic Ag nanoparticles. ·O{sub 2}−, one of the reactive species, was responsible for the photodegradation of MO compared to H+ and ·OH. - Highlights: • Novel Ag/AgBr/g-C{sub 3}N{sub 4} composite photocatalyst was reported. • Ag/AgBr/g-C{sub 3}N{sub 4} had novel energy band combination between AgBr and g-C{sub 3}N{sub 4}. • Synergetic effects of AgBr/g-C{sub 3}N{sub 4} interface and metallic Ag nanoparticles. • Electron trapping role of metallic Ag dominated the stability of Ag/AgBr/g-C{sub 3}N{sub 4}. - Abstract: Novel Ag/AgBr/g-C{sub 3}N{sub 4} composite photocatalysts were constructed via deposition–precipitation method and extensively characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM) and UV–vis diffuse reflectance spectroscopy (DRS). Under visible light (λ > 420 nm), Ag/AgBr/g-C{sub 3}N{sub 4} composite photocatalysts displayed much higher photocatalytic activities than those of Ag/AgBr and g-C{sub 3}N{sub 4} for degradation of methyl orange (MO). 50% Ag/AgBr/g-C{sub 3}N{sub 4} presented the best photocatalytic performance, which was mainly attributed to the synergistic effects of AgBr/g-C{sub 3}N{sub 4} interface and the in situ metallic Ag nanoparticles for efficiently separating electron–hole pairs. Furthermore, Ag/AgBr/g-C{sub 3}N{sub 4} remained good photocatalytic activity through 5 times of cycle experiments. Additionally, the radical scavengers experiment indicated that ·O{sub 2}{sup −} was the main reactive species for the MO degradation under visible light.

  14. Photo- and electroluminescence properties of lanthanide tungstate-doped porous anodic aluminum oxide

    NASA Astrophysics Data System (ADS)

    Staninski, Krzysztof; Piskuła, Zbigniew; Kaczmarek, Małgorzata

    2017-02-01

    A new cathode material for the potential use in light-emitting devices, based on porous anodic alumina (PAA), aluminum and ITO layers has been synthesized. Porous alumina samples with ordered pore arrays were prepared electrochemically from high purity Al sheet in H2SO4 and H3PO4. To be able to apply the matrix obtained in the electroluminescence cell, the thickness of the barrier layer of aluminum oxide was decreased by slow reduction of the anodization voltage to zero. The luminescence and electroluminescence (EL) properties of the Al2O3 matrix admixtured with Eu3+ and Tb3+ ions as well as europium and terbium tungstates, were determined. The particles of inorganic luminophore were synthesized on the walls of the matrix cylindrical nanopores in the two-step process of immersion in solutions of TbCl3 or EuCl3 and Na2WO4. The effect of the nanopores diameter and the thickness of the porous Al2O3 layer on the intensity and relative yield of electroluminescence was analyzed, the best results were obtained for 80-90 μm PAA layers with 140 nm nanopores.

  15. Optical and electroluminescent properties of a number of new derivatives of divinyl dibenzothiophene sulfone

    NASA Astrophysics Data System (ADS)

    Kukhto, A. V.; Kopylova, T. N.; Gadirov, R. M.; Degtyarenko, K. N.; Nikonova, E. N.; Solodova, T. A.; Kukhto, I. N.

    2016-02-01

    Photoluminescent and electroluminescent properties of four new bipolar linear derivatives of divinyl dibenzothiophene sulfone are studied. It is found that amorphous films of solutions, as well as films of the compounds under study in the poly(N-vinylcarbazole) matrix, have a rather high quantum yield of photoluminescence in the blue and blue-green spectrum regions. Bright blue electroluminescence is obtained in the samples with a structure of ITO/PEDOT:PSS/TPD/OC/LiF/Al using vacuum deposition of the compounds under study and in the single-layer ITO/PEDOT:PSS/PVK:OC/LiF/Al structure when applied from the solution with a threshold voltage of 2.5-3.5 V. The influence of a molecule structure on the spectra and quantum yield of fluorescence as well as on the electroluminescent properties of the compounds is shown. Results of quantum-chemical calculations in the context of the density functional theory of the structure and characteristics of main molecular orbitals are presented.

  16. Time-resolved electroluminescence studies of III-nitride ultraviolet photonic-crystal light-emitting diodes

    NASA Astrophysics Data System (ADS)

    Shakya, J.; Lin, J. Y.; Jiang, H. X.

    2004-09-01

    Transient responses of III-nitride photonic-crystal (PC) ultraviolet (UV) light-emitting diodes (LEDs) were measured by picosecond time-resolved electroluminescence (EL) spectroscopy. Triangular arrays of PCs with different diameters/periodicities were fabricated on 333nmUV LEDs for enhancing light extraction efficiency using electron-beam lithography and inductively coupled-plasma dry etching. With the incorporation of PCs on LEDs, the EL decay time constant τ decreases systematically with the increase of the etched sidewall area indicating the strong effect of the surface recombination. The surface recombination velocities on the p-type epitaxial surface and on the sidewall of etched holes on LEDs were determined to be 1.73×104cm /s and 1.48×105cm/s, respectively. The angular distribution of light emission from LEDs with PCs shows slight narrowing in far-field pattern. Because of the increased transient response along with enhanced light extraction, the incorporation of PCs in UV LEDs provide an effective method to control the modulation speed of UV LEDs, which could be very useful for many applications.

  17. First proof of topological signature in the high pressure xenon gas TPC with electroluminescence amplification for the NEXT experiment

    DOE PAGES

    Ferrario, P.

    2016-01-19

    The NEXT experiment aims to observe the neutrinoless double beta decay of xenon in a high-pressure 136Xe gas TPC using electroluminescence (EL) to amplify the signal from ionization. One of the main advantages of this technology is the possibility to reconstruct the topology of events with energies close to Qββ. This paper presents the first demonstration that the topology provides extra handles to reject background events using data obtained with the NEXT-DEMO prototype. Single electrons resulting from the interactions of 22Na 1275 keV gammas and electron-positron pairs produced by conversions of gammas from the 228Th decay chain were used tomore » represent the background and the signal in a double beta decay. Furthermore, these data were used to develop algorithms for the reconstruction of tracks and the identification of the energy deposited at the end-points, providing an extra background rejection factor of 24.3 ± 1.4 (stat.)%, while maintaining an efficiency of 66.7 ± 1% for signal events.« less

  18. First proof of topological signature in the high pressure xenon gas TPC with electroluminescence amplification for the NEXT experiment

    SciTech Connect

    Ferrario, P.

    2016-01-19

    The NEXT experiment aims to observe the neutrinoless double beta decay of xenon in a high-pressure 136Xe gas TPC using electroluminescence (EL) to amplify the signal from ionization. One of the main advantages of this technology is the possibility to reconstruct the topology of events with energies close to Qββ. This paper presents the first demonstration that the topology provides extra handles to reject background events using data obtained with the NEXT-DEMO prototype. Single electrons resulting from the interactions of 22Na 1275 keV gammas and electron-positron pairs produced by conversions of gammas from the 228Th decay chain were used to represent the background and the signal in a double beta decay. Furthermore, these data were used to develop algorithms for the reconstruction of tracks and the identification of the energy deposited at the end-points, providing an extra background rejection factor of 24.3 ± 1.4 (stat.)%, while maintaining an efficiency of 66.7 ± 1% for signal events.

  19. Shell-dependent electroluminescence from colloidal CdSe quantum dots in multilayer light-emitting diodes

    NASA Astrophysics Data System (ADS)

    Jing, Pengtao; Zheng, Jinju; Zeng, Qinghui; Zhang, Youlin; Liu, Xiaomin; Liu, Xueyan; Kong, Xianggui; Zhao, Jialong

    2009-02-01

    We report electroluminescence (EL) of colloidal CdSe/CdS, CdSe/ZnS, and CdSe/CdS/CdZnS/ZnS core/shell quantum dots (QDs) in multilayer light-emitting diodes (LEDs) fabricated by spin coating a near monolayer of the core/shell QDs on cross-linkable hole transporting layers. It is found that CdSe/CdS QD-LEDs exhibit a faster decrease in EL quantum efficiency (˜2% at a brightness of 100 cd/m2) with increasing current density and lower maximum brightness than those of CdSe/ZnS QD-LEDs. A more significant redshift and spectral broadening of the EL observed in CdSe core/shell QDs with a CdS or CdS/CdZnS/ZnS shell than with a ZnS shell indicate that the electron wave function can penetrate into the shell under electric field. The difference in device performance and EL spectra results from conduction band offsets between the CdSe cores and CdS or ZnS shells, suggesting the existence of the exciton ionization in the QD-LEDs.

  20. Reduction of molecular aggregation and its application to the high-performance blue perylene-doped organic electroluminescent device

    NASA Astrophysics Data System (ADS)

    Mi, B. X.; Gao, Z. Q.; Lee, C. S.; Lee, S. T.; Kwong, H. L.; Wong, N. B.

    1999-12-01

    A nonplanar derivative of perylene, 2,5,8,11-tetra-tertbutylperylene (TBPe), was synthesized via the Friedel-Crafts alkylation reaction. Electroluminescent (EL) devices were made using TBPe or perylene as a dopant in bis(2-methyl-8-quinolinolato)(para-phenylphenolato)aluminum(III) and their EL performance was compared. Similar to the device doped with the parent perylene molecule, the device doped with TBPe also emitted strongly in the blue. As the concentration of TBPe increased from 1% to 5%, the color coordinates in CIE 1931 chromaticity of the TBPe-doped device changed only slightly from (0.168,0.273) to (0.175,0.273), whereas the perylene-doped device exhibited a much larger shift from (0.165,0.196) to (0.178,0.252). The constancy of EL color and efficiency with respect to TBPe dopant concentration is attributable to diminishing molecular aggregation in the nonplanar perylene derivative, TBPe, due to the steric hindrance of the tert-butyl groups.

  1. Improved electroluminescence of quantum dot light-emitting diodes enabled by a partial ligand exchange with benzenethiol

    NASA Astrophysics Data System (ADS)

    Kim, Daekyoung; Fu, Yan; Kim, Jungwoo; Lee, Ki-heon; Kim, Hyoungsub; Yang, Heesun; Chae, Heeyeop

    2016-06-01

    In this study, benzenethiol ligands were applied to the surface of CdSe@ZnS core@shell quantum dots (QDs) and their effect on the performance of quantum dot light-emitting diodes (QD-LEDs) was investigated. Conventional long-chained oleic acid (OA) and trioctylphosphine (TOP) capping ligands were partially replaced by short-chained benzenethiol ligands in order to increase the stability of QDs during purification and also improve the electroluminescence performance of QD-LEDs. The quantum yield of the QD solution was increased from 41% to 84% by the benzenethiol ligand exchange. The mobility of the QD films with benzenethiol ligands approximately doubled to 2.42 × 10-5 cm2 V-1 s-1 from 1.19 × 10-5 cm2 V-1 s-1 compared to the device consisting of OA/TOP-capped QDs, and an approximately 1.8-fold improvement was achieved over QD-LEDs fabricated with bezenethiol ligand-exchanged QDs with respect to the maximum luminance and current efficiency. The turn-on voltage decreased by about -0.6 V through shifting the energy level of the QDs with benzenethiol ligands compared to conventional OA and TOP ligands.

  2. Combined thermotherapy and cryotherapy for efficient virus eradication: relation of virus distribution, subcellular changes, cell survival and viral RNA degradation in shoot tips.

    PubMed

    Wang, Qiaochun; Cuellar, Wilmer J; Rajamäki, Minna-Liisa; Hirata, Yukimasa; Valkonen, Jari P T

    2008-03-01

    Accumulation of viruses in vegetatively propagated plants causes heavy yield losses. Therefore, supply of virus-free planting materials is pivotal to sustainable crop production. In previous studies, Raspberry bushy dwarf virus (RBDV) was difficult to eradicate from raspberry (Rubus idaeus) using the conventional means of meristem tip culture. As shown in the present study, it was probably because this pollen-transmitted virus efficiently invades leaf primordia and all meristematic tissues except the least differentiated cells of the apical dome. Subjecting plants to thermotherapy prior to meristem tip culture heavily reduced viral RNA2, RNA3 and the coat protein in the shoot tips, but no virus-free plants were obtained. Therefore, a novel method including thermotherapy followed by cryotherapy was developed for efficient virus eradication. Heat treatment caused subcellular alterations such as enlargement of vacuoles in the more developed, virus-infected cells, which were largely eliminated following subsequent cryotherapy. Using this protocol, 20-36% of the treated shoot tips survived, 30-40% regenerated and up to 35% of the regenerated plants were virus-free, as tested by ELISA and reverse transcription loop-mediated isothermal amplification. Novel cellular and molecular insights into RBDV-host interactions and the factors influencing virus eradication were obtained, including invasion of shoot tips and meristematic tissues by RBDV, enhanced viral RNA degradation and increased sensitivity to freezing caused by thermotherapy, and subcellular changes and subsequent death of cells caused by cryotherapy. This novel procedure should be helpful with many virus-host combinations in which virus eradication by conventional means has proven difficult.

  3. Novel Na2Mo4O13/α-MoO3 hybrid material as highly efficient CWAO catalyst for dye degradation at ambient conditions

    PubMed Central

    Zhang, Zhang; Yang, Ruoyan; Gao, Yanshan; Zhao, Yufei; Wang, Junyang; Huang, Liang; Guo, Jiang; Zhou, Tuantuan; Lu, Peng; Guo, Zhanhu; Wang, Qiang

    2014-01-01

    We report a novel hybrid material Na2Mo4O13/α-MoO3 as highly efficient catalytic wet air oxidation (CWAO) catalyst, which showed the highest ever activity at room temperature and atmosphere pressure for the degradation of cationic red GTL. SEM and TEM analyses indicated that this hybrid catalyst has bamboo-shaped nanofiber morphology. In view of practical applications, the influence of some key parameters including operation temperature, catalyst calcination temperature, and the volume of dye wastewater have been optimized. The mechanism for the superior catalytic performance was investigated. XRD, XPS, and ESR suggested the Na2Mo4O13/α-MoO3 hybrid catalyst possesses more O2− ions in the oxygen deficient regions than neat α-MoO3, promoting the formation of active ·OH radicals and resulting in a higher activity. Considering the facile preparation and its superior activity, this novel catalyst is promising for practical dye wastewater treatment. PMID:25348943

  4. Direct evidence of molecular aggregation and degradation mechanism of organic light-emitting diodes under joule heating: an STM and photoluminescence study.

    PubMed

    Gong, Jian-Ru; Wan, Li-Jun; Lei, Sheng-Bin; Bai, Chun-Li; Zhang, Xiao-Hong; Lee, Shuit-Tong

    2005-02-10

    The Joule heating effect on electroluminescent efficiency is important in the degradation origin of organic light-emitting diodes (OLED). Scanning tunneling microscopy (STM) and photoluminescence (PL) measurements were performed on the guest molecule BT (1,4-bis(benzothiazole-vinyl) benzene), host molecule TPBI (2, 2',2' '-(1,3,5-phenylene)tris-[1-phenyl-1H-benzimidazole]), and their mixture deposited on an HOPG surface to study the OLED degradation mechanism due to thermal heating. At room temperature, BT and TPBI in the mixed layer show good compatibility and high PL intensity, but at higher temperatures, they show phase separation and aggregation into their own domains and a concomitant decrease in PL intensity. The PL intensity loss suggests ineffective energy transfer from TPBI to BT due to phase separation, which may cause OLED degradation. Scanning tunneling spectroscopy (STS) results show that the band gaps of TPBI and BT remain unchanged with the annealing temperature, suggesting that the heat-induced decay of OLED is related to the interfacial structural change rather than the respective molecular band gap. The results provide direct evidence showing how the molecular structures of the mixed layer vary and affect the PL intensity due to temperature.

  5. Efficient Degradation of TCE in Groundwater Using Pd and Electro-generated H2 and O2: A Shift in Pathway from Hydrodechlorination to Oxidation in the Presence of Ferrous Ions

    PubMed Central

    Yuan, Songhu; Mao, Xuhui; Alshawabkeh, Akram N.

    2012-01-01

    Degradation of trichloroethylene (TCE) in simulated groundwater by Pd and electro-generated H2 and O2 is investigated in the absence and presence of Fe(II). In the absence of Fe(II), hydrodechlorination dominates TCE degradation, with accumulation of H2O2 up to 17 mg/L. Under weak acidity, low concentrations of oxidizing •OH radical are detected due to decomposition of H2O2, slightly contributing to TCE degradation via oxidation. In the presence of Fe(II), the degradation efficiency of TCE at 396 μM improves to 94.9% within 80 min. The product distribution proves that the degradation pathway shifts from 79% hydrodechlorination in the absence of Fe(II) to 84% •OH oxidation in the presence of Fe(II). TCE degradation follows zeroth-order kinetics with rate constants increasing from 2.0 to 4.6 μM/min with increasing initial Fe(II) concentration from 0 to 27.3 mg/L at pH 4. A good correlation between TCE degradation rate constants and •OH generation rate constants confirms that •OH is the predominant reactive species for TCE oxidation. Presence of 10 mM Na2SO4, NaCl, NaNO3, NaHCO3, K2SO4, CaSO4 and MgSO4 does not significantly influence degradation, but sulfite and sulfide greatly enhance and slightly suppresses degradation, respectively. A novel Pd-based electrochemical process is proposed for groundwater remediation. PMID:22315993

  6. Solution-Processable Silicon Phthalocyanines in Electroluminescent and Photovoltaic Devices.

    PubMed

    Zysman-Colman, Eli; Ghosh, Sanjay S; Xie, Guohua; Varghese, Shinto; Chowdhury, Mithun; Sharma, Nidhi; Cordes, David B; Slawin, Alexandra M Z; Samuel, Ifor D W

    2016-04-13

    Phthalocyanines and their main group and metal complexes are important classes of organic semiconductor materials but are usually highly insoluble and so frequently need to be processed by vacuum deposition in devices. We report two highly soluble silicon phthalocyanine (SiPc) diester compounds and demonstrate their potential as organic semiconductor materials. Near-infrared (λ(EL) = 698-709 nm) solution-processed organic light-emitting diodes (OLEDs) were fabricated and exhibited external quantum efficiencies (EQEs) of up to 1.4%. Binary bulk heterojunction solar cells employing P3HT or PTB7 as the donor and the SiPc as the acceptor provided power conversion efficiencies (PCE) of up to 2.7% under simulated solar illumination. Our results show that soluble SiPcs are promising materials for organic electronics.

  7. Solution-Processable Silicon Phthalocyanines in Electroluminescent and Photovoltaic Devices

    PubMed Central

    2016-01-01

    Phthalocyanines and their main group and metal complexes are important classes of organic semiconductor materials but are usually highly insoluble and so frequently need to be processed by vacuum deposition in devices. We report two highly soluble silicon phthalocyanine (SiPc) diester compounds and demonstrate their potential as organic semiconductor materials. Near-infrared (λEL = 698–709 nm) solution-processed organic light-emitting diodes (OLEDs) were fabricated and exhibited external quantum efficiencies (EQEs) of up to 1.4%. Binary bulk heterojunction solar cells employing P3HT or PTB7 as the donor and the SiPc as the acceptor provided power conversion efficiencies (PCE) of up to 2.7% under simulated solar illumination. Our results show that soluble SiPcs are promising materials for organic electronics. PMID:26990151

  8. Electroluminescence of thin-film CdTe solar cells and modules

    NASA Astrophysics Data System (ADS)

    Raguse, John Michael

    Thin-film photovoltaics has the potential to be a major source of world electricity. Mitigation of non-uniformities in thin-film solar cells and modules may help improve photovoltaic conversion efficiencies. In this manuscript, a measurement technique is discussed in detail which has the capability of detecting such non-uniformities in a form useful for analysis. Thin-film solar cells emit radiation while operating at forward electrical bias, analogous to an LED, a phenomena known as electroluminescence (EL). This process relatively is inefficient for polycrystalline CdTe devices, on the order of 10-4%, as most of the energy is converted into heat, but still strong enough for many valuable measurements. A EL system was built at the Colorado State University Photovoltaics Laboratory to measure EL from CdTe cells and modules. EL intensity normalized to exposure time and injection current density has been found to correlate very well with the difference between ideal and measured open-circuit voltage from devices that include a GaAs cell, an AlGaAs LED, and several CdTe cells with variations in manufacturing. Furthermore, these data points were found to be in good agreement when overlaid with calibrated data from two additional sources. The magnitude of the inverse slope of the fit is in agreement with the thermal voltage and the intercept was found to have a value near unity, in agreement with theory. The expanded data set consists of devices made from one of seven different band gaps and spans eight decades of EQELED efficiencies. As expected, cells which exhibit major failure of light-dark J-V superposition did not follow trend of well-behaved cells. EL images of selected defects from CdTe cells and modules are discussed and images are shown to be highly sensitive to defects in devices, since the intensity depends exponentially on the cells' voltages. The EL technique has proven to be a useful high-throughput tool for screening of cells. In addition to EL images

  9. Synthesis and electroluminescent properties of a novel electroluminescence material of bis-2-(4-(diphenylphosphino)phenyl)benzo[d]oxazole (DPB).

    PubMed

    Hoanh, Trinh Dac; Kim, Ik-Hwan; Kim, Dong-Eun; Shin, Hoon-Kyu; Kwon, Young-Soo; Chang, Sang-Mok; Lee, Burm-Jong

    2014-08-01

    A new light-emissive material, bis-2-(4-(diphenylphosphino)phenyl)benzo[d]oxazole (DPB), has been synthesized and characterized by FT-NMR, FT-IR, UV-Vis and elemental analysis. DPB has the band gap of 4.3 eV between HOMO and LUMO levels. The photoluminescence (PL) of DPB was measured at 410 nm from the chloroform solution. The electroluminescent (EL) devices with structures of ITO/NPB/DPB/LiF/Al and ITO/NPB/DPB/Alq3/LiF/Al were constructed and showed maximum emission at 540 nm. The device using DPB as emitting material showed the luminance of 1000 cd/m2 at 11 V. The CIE chromaticity of the device showed near the region of white color emission.

  10. Alpha-1,4-glucan lyase, a new class of starch/glycogen degrading enzyme. I. Efficient purification and characterization from red seaweeds.

    PubMed

    Yu, S; Kenne, L; Pedersén, M

    1993-03-21

    This study presents the first purification and characterization of an alpha-1,4-glucan lyase. The enzyme degraded alpha-1,4-glucan to produce 1,5-anhydrofructose. A simple and efficient purification procedure has been developed and the enzyme has been purified to homogeneity from two red seaweeds Gracilariopsis lemaneiformis and Gracilaria verrucosa. alpha-1,4-Glucan lyase was apparently a single polypeptide as a molecular weight of 111,000 was observed in SDS-gel electrophoresis, and 98,000 by gel filtration chromatography on Sephacryl S-200. Amino acid composition analysis of the enzyme showed high amounts of Asp/Asn, Gly and Glu/Gln. The isoelectric point of the enzyme was 3.9, as revealed by isoelectrofocusing. The concentrations of maltotriose, maltose and amylopectin that yield half of the maximum activity were 798 micrograms ml-1 (1.58 mM), 1,418 micrograms ml-1 (4.14 mM) and 1,600 micrograms ml-1, respectively. alpha-1,4-Glucan lyase exhibited a wide pH optimum range from pH 2.5 to 7.0 for maltose and from pH 3.5 to 7.5 for amylopectin. The optimal temperature for activity of the algal lyase was 50 degrees C when maltose or amylopectin was used as a substrate under the assay conditions. The Arrhenius activation energies were 45.8 and 44.0 kJ mol-1 for maltose and amylopectin as substrate, respectively. Only one form of alpha-1,4-glucan lyase was found in cell-free extracts of the two red seaweeds.

  11. Module Degradation Mechanisms Studied by a Multi-Scale Approach

    SciTech Connect

    Johnston, Steve; Al-Jassim, Mowafak; Hacke, Peter; Harvey, Steven P.; Jiang, Chun-Sheng; Gerber, Andreas; Guthrey, Harvey; Moutinho, Helio; Albin, David; To, Bobby; Tynan, Jerry; Moseley, John; Aguiar, Jeffery; Xiao, Chuanxiao; Waddle, John; Nardone, Marco

    2016-11-21

    A key pathway to meeting the Department of Energy SunShot 2020 goals is to reduce financing costs by improving investor confidence through improved photovoltaic (PV) module reliability. A comprehensive approach to further understand and improve PV reliability includes characterization techniques and modeling from module to atomic scale. Imaging techniques, which include photoluminescence, electroluminescence, and lock-in thermography, are used to locate localized defects responsible for module degradation. Small area samples containing such defects are prepared using coring techniques and are then suitable and available for microscopic study and specific defect modeling and analysis.

  12. Electroluminescence from nonpolar n-ZnO/p-AlGaN heterojunction light-emitting diode on r-sapphire

    NASA Astrophysics Data System (ADS)

    Chen, Jingwen; Zhang, Jun; Dai, Jiangnan; Wu, Feng; Wang, Shuai; Chen, Cheng; Long, Hanling; Liang, Renli; Zhao, Chong; Chen, Changqing; Tang, Zhiwu; Cheng, Hailing; He, Yunbin; Li, Mingkai

    2017-03-01

    Nonpolar a-plane n-ZnO/p-AlGaN heterojunction light-emitting diodes (LEDs) have been prepared on r-sapphire substrate using metal organic chemical vapor deposition and a pulsed laser deposition method. The dominant electroluminescence emission at 390 nm from the interband transition in n-ZnO layer under a forward bias was observed. Interestingly, electroluminescence with emission at 385 nm based on an avalanche mechanism was also achieved under reverse bias. The mechanisms of both the electroluminescence and I–V characteristics are discussed in detail by considering the avalanche effect. It is demonstrated that the crystalline quality of n-ZnO, not the p-AlGaN, is what affects the performance of the nonpolar ZnO based avalanche LED.

  13. Magnetic carbon-supported cobalt derived from a Prussian blue analogue as a heterogeneous catalyst to activate peroxymonosulfate for efficient degradation of caffeine in water.

    PubMed

    Lin, Kun-Yi Andrew; Chen, Bo-Jau

    2017-01-15

    Extensive usage of caffeine (CAF) as a medicine and additives in beverages has led to increasing presence of CAF in wastewater and even drinking water. To remove CAF, peroxymonosulfate (PMS), is adopted to generate sulfate radical to degrade CAF in water. To facilitate PMS activation, a magnetic carbon-supported cobalt (MC/Co) hybrid material is prepared via carbonization of a cobalt-containing Prussian blue analogue framework (Co3[Co(CN)6]2). The resultant MC/Co contains Co and Co3O4 nanoparticles supported on a carbon matrix, making it an attractive magnetic catalyst to activate PMS for degrading CAF. MC/Co-activated PMS was shown to degrade CAF much more effectively than PMS and Co3O4-activated PMS. Parameters affecting CAF degradation by MC/Co-activated PMS were also examined, including MC/Co and PMS concentrations, temperature, pH, and salt. Effects of radical quenchers were also examined to provide insights into the CAF degradation mechanism. MC/Co-activated PMS was much more favorable at higher temperatures than ambient temperature, and under neutral conditions. Nevertheless, the presence of concentrated NaCl noticeably hindered CAF degradation. Through examining effects of radical quenchers, the mechanism of CAF degradation by MC/Co-activated PMS was attributed primarily to sulfate radicals and hydroxyl radicals to a lesser extent. The degradation products of CAF by MC/Co-activated PMS were also identified and a possible degradation pathway is proposed. MC/Co can activate PMS over multiple cycles without loss of catalytic activity. These findings demonstrate that MC/Co, simply prepared from simple carbonization of Co3[Co(CN)6]2 can be a promising heterogeneous catalyst for activating PMS to degrade CAF.

  14. Quantum-chemical investigation of the structure and electronic absorption spectra of electroluminescent zinc complexes

    NASA Astrophysics Data System (ADS)

    Minaev, B. F.; Baryshnikov, G. V.; Korop, A. A.; Minaeva, V. A.; Kaplunov, M. G.

    2013-01-01

    Using the quantum chemical methods of the density functional theory and of the electron density topological analysis, we have studied the structure of two recently synthesized electroluminescent zinc complexes, one with aminoquinoline ligands and the other with a Schiff base (N,O-donor). The energies and intensities of vertical excitations for the molecules under study have been calculated in terms of the PM3 semiempirical approximation taking into account the configurational interaction between singly excited singlet excited states. Good agreement between calculation results and experimental data on the electron density topological characteristics and on the visible and UV absorption spectra has been obtained.

  15. Room-temperature electroluminescence from two-dimensional lead halide perovskites

    NASA Astrophysics Data System (ADS)

    Li, Renzhi; Yi, Chang; Ge, Rui; Zou, Wei; Cheng, Lu; Wang, Nana; Wang, Jianpu; Huang, Wei

    2016-10-01

    Room-temperature electroluminescence (EL) is demonstrated from a light-emitting diode (LED) based on two-dimensional lead halide perovskites, (C6H5NH3)2PbI4. The device has a multilayer structure of ITO/Poly(3,4-ethylenedioxythiophene):Poly(styrenesulfonate)/(C6H5CH2NH3)2PbI4/Bathophenanthroline/Al. The EL emission peaks at 526 nm with a narrow full width at half maximum of 15 nm, which origins from perovskite exciton emission. The LED device exhibits a maximum luminance of ˜9 cd m-2 at a bias of 5 V.

  16. Double side electroluminescence from p-NiO/n-ZnO nanowire heterojunctions

    SciTech Connect

    Wang, J.-Y.; Chen, Y.-T.; Chen, C.-T.; Chen, Y.-L.; Chen, Y.-F.; Lee, C.-Y.; Lin, C.-F.

    2009-09-28

    Double side light emission devices based on p-NiO/n-ZnO nanowire heterojunctions have been fabricated on indium tin oxide substrate by radio frequency magnetron sputtering combined with hydrothermal process. According to the energy band alignment, the detected broad visible and narrow ultraviolet electroluminescence arise from defect and band edge transitions in ZnO nanowires, respectively. The unique property of the double side emission is due to the nature of the large band gap of NiO film. It provides a good opportunity for the emission of a light emitting device with different colors on the top and back sides, simultaneously.

  17. Photomechanical modification of ZnS microcrystal to enhance electroluminescence by ultrashort-pulse laser processing

    NASA Astrophysics Data System (ADS)

    Nabesaka, Kyohei; Ishikawa, Yasuaki; Hosokawa, Yoichiroh; Uraoka, Yukiharu

    2017-02-01

    A ZnS microcrystal was treated with an ultrashort-pulse laser and applied to an inorganic electroluminescence (EL) phosphor. We found that the emission intensity of the EL phosphor was increased by laser-induced photomechanical modification. The pulse duration dependence of the emission enhancement and structural analysis by scanning electron microscopy indicated that the structural modification was induced inside the ZnS microcrystal, although a mechanical grinding would induce the structural modification mainly on the crystal surface. The results suggested a new way of enhancing the emission of inorganic EL devices.

  18. White-blue electroluminescence from a Si quantum dot hybrid light-emitting diode

    SciTech Connect

    Xin, Yunzi; Nishio, Kazuyuki; Saitow, Ken-ichi

    2015-05-18

    A silicon (Si) quantum dot (QD)-based hybrid inorganic/organic light-emitting diode (LED) was fabricated via solution processing. This device exhibited white-blue electroluminescence at a low applied voltage of 6 V, with 78% of the effective emission obtained from the Si QDs. This hybrid LED produced current and optical power densities 280 and 350 times greater than those previously reported for such device. The superior performance of this hybrid device was obtained by both the prepared Si QDs and the optimized layer structure and thereby improving carrier migration through the hybrid LED and carrier recombination in the homogeneous Si QD layer.

  19. Reduced graphene oxide nanosheets decorated with Au-Pd bimetallic alloy nanoparticles towards efficient photocatalytic degradation of phenolic compounds in water

    NASA Astrophysics Data System (ADS)

    Darabdhara, Gitashree; Boruah, Purna K.; Borthakur, Priyakshree; Hussain, Najrul; Das, Manash R.; Ahamad, Tansir; Alshehri, Saad M.; Malgras, Victor; Wu, Kevin C.-W.; Yamauchi, Yusuke

    2016-04-01

    Reduced graphene oxide nanosheets decorated with Au-Pd bimetallic alloy nanoparticles are successfully prepared via a chemical approach consisting of reducing the metal precursors using ascorbic acid as reductant at an elevated temperature. The prepared nanocomposite is employed as a photocatalyst for the degradation of organic contaminants such as phenol, 2-chlorophenol (2-CP), and 2-nitrophenol (2-NP). The complete degradation of phenol is achieved after 300 min under natural sunlight irradiation whereas the degradation of 2-CP and 2-NP is completed after 180 min. The activity of the photocatalyst is evaluated considering several parameters such as the initial phenol concentration, the photocatalyst loading, and the pH of the solution. The degradation kinetics of all the compounds is carefully studied and found to follow a linear Langmuir-Hinshelwood model. Furthermore, the reusability of the photocatalyst is successfully achieved up to five cycles and the catalyst exhibits an excellent stability.Reduced graphene oxide nanosheets decorated with Au-Pd bimetallic alloy nanoparticles are successfully prepared via a chemical approach consisting of reducing the metal precursors using ascorbic acid as reductant at an elevated temperature. The prepared nanocomposite is employed as a photocatalyst for the degradation of organic contaminants such as phenol, 2-chlorophenol (2-CP), and 2-nitrophenol (2-NP). The complete degradation of phenol is achieved after 300 min under natural sunlight irradiation whereas the degradation of 2-CP and 2-NP is completed after 180 min. The activity of the photocatalyst is evaluated considering several parameters such as the initial phenol concentration, the photocatalyst loading, and the pH of the solution. The degradation kinetics of all the compounds is carefully studied and found to follow a linear Langmuir-Hinshelwood model. Furthermore, the reusability of the photocatalyst is successfully achieved up to five cycles and the catalyst

  20. A novel electroluminescent device based on a reduced graphene oxide wrapped phosphor (ZnS:Cu,Al) and hexagonal-boron nitride for high-performance luminescence.

    PubMed

    Gupta, Bipin Kumar; Singh, Satbir; Kedawat, Garima; Kanika; Kumar, Pawan; Gangwar, Amit Kumar; Narayanan, Tharangattu N; Marti, Angel A; Vajtai, Robert; Ajayan, P M

    2017-04-06

    Reduced graphene oxide (rGO) has recently emerged as a very promising family of exotic carbon material with augmented performance in electronic and optoelectronic devices. Herein, we report an efficient and novel inorganic electroluminescent device geometry, where a new phosphor composite, reduced graphene oxide wrapped ZnS:Cu,Al, acts as an active emitting layer and an exfoliated hexagonal boron nitride (h-BN) as a dielectric layer. The roles of rGO in the active layer as a conductive support and local electric field enhancing agent are attributed to its wrinkles being unraveled compared with other carbon exotic nano-forms such as carbon nanotubes, graphite, charcoal and activated carbon, which significantly improves the brightness of the device (∼50 cd m(-2) for 0.50 wt% rGO/ZnS:Cu,Al at 10 kHz and 110 V with an external quantum efficiency of ∼6.3% ± 0.1% and current efficiency of ∼0.81 ± 0.09 cd A(-1)). This new and facile strategy to construct the luminescent devices could be a paradigm shift towards cost effective, highly stable in air (for several days) and energy efficient next generation display devices.

  1. Plasmon-enhanced molecular electroluminescence: Effects of nonlinear excitation and molecular cooperativity

    NASA Astrophysics Data System (ADS)

    Zhang, Yuan; May, Volkhard

    2014-06-01

    Plasmon enhanced electroluminescence of a single as well as a couple of molecules is discussed theoretically. The considered system is formed by a metal nanoparticle (MNP) placed in the proximity of a junction with molecules sandwiched between a left and a right lead. In continuing recent work on a junction with a single molecule [Phys. Rev. B 88, 155426 (2013), 10.1103/PhysRevB.88.155426] the case of strong charge injection and resulting further enhanced electroluminescence is investigated. Photoemission and plasmon excitation saturate if the molecule-lead coupling enters a range of about 50 meV. This saturation appears long before the molecule-lead coupling approaches the limit at which the considered sequential type of charge transfer becomes invalid. Turning to junctions with up to five molecules stronger plasmon excitation is achieved and a noticeable population of the second and third excited dipole plasmon level appears. This goes along with a nonlinear increase of the photoemission intensity and a decrease of the emission linewidth displaying the onset of cooperative molecule-MNP coupling.

  2. [The role of BCP in electroluminescence of multilayer organic light-emitting devices].

    PubMed

    Deng, Zhao-Ru; Yang, Sheng-Yi; Lou, Zhi-Dong; Meng, Ling-Chuan

    2009-03-01

    As a hole-blocking layer, 2,9-dimethyl-4,7-diphenyl-1,10-phenanthroline (BCP) is usually used in blue and white light electroluminescent devices. The ability of blocking holes of BCP layer depends on its thickness, and basically holes can tunnel through thin BCP layer. In order to know the role of BCP layer in electroluminescence (EL) of multilayer organic light-emitting diodes (OLEDs), in the present paper, the authors designed a multilayer OLED ITO/NPB/BCP/Alq3 : DCJTB/Alq3/Al and investigated the influence of thickness of BCP on the EL spectra of multilayer OLEDs at different applied voltages. The experimental data show that thin BCP layer can block holes partially and tune the energy transfer between different emissive layers, and in this way, it is easy to obtain white emission, but its EL spectra will change with the applied voltages. The EL spectra of multilayer device will remain relatively stable when BCP layer is thick enough, and the holes can hardly tunnel through when the thickness of BCP layer is more than 15 nm. Furthermore, the stability of EL spectra of the multilayer OLED at different applied voltages was discussed.

  3. Investigation of thioglycerol stabilized ZnS quantum dots in electroluminescent device performance

    NASA Astrophysics Data System (ADS)

    Ethiraj, Anita Sagadevan; Rhen, Dani; Lee, D. H.; Kang, Dae Joon; Kulkarni, S. K.

    2016-05-01

    The present work is focused on the investigation of thioglycerol (TG) stabilized Zinc Sulfide Quantum dots (ZnS QDs) in the hybrid electroluminescence (EL) device. Optical absorption spectroscopy clearly indicates the formation of narrow size distributed ZnS in the quantum confinement regime. X-ray Diffraction (XRD), Photoluminescence (PL), Energy Dispersive X-ray Spectroscopy (EDS) data supports the same. The hybrid EL device with structure of ITO (indium tin oxide)//PEDOT:PSS ((poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonate)//HTL (α NPD- N,N'-diphenyl-N,N'-bis(1-naphthyl)-(1,1'-phenyl)-4,4'-diamine// PVK:ZnS QDs//ETL(PBD- 2-tert-butylphenyl- 5-biphenyl-1,3,4-oxadiazole)//LiF:Al (Device 1) was fabricated. Reference device without the ZnS QDs were also prepared (Device 2). The results show that the ZnS QDs based device exhibited bright electroluminescence emission of 24 cd/m2 at a driving voltage of 16 Volts under the forward bias conditions as compared to the reference device without the ZnS QDs, which showed 6 cd/m2 at ˜22 Volts.

  4. Determining the Origin of Half-bandgap-voltage Electroluminescence in Bifunctional Rubrene/C60 Devices

    NASA Astrophysics Data System (ADS)

    Chen, Qiusong; Jia, Weiyao; Chen, Lixiang; Yuan, De; Zou, Yue; Xiong, Zuhong

    2016-05-01

    Lowering the driving voltage of organic light-emitting diodes (OLEDs) is an important approach to reduce their energy consumption. We have fabricated a series of bifunctional devices (OLEDs and photovoltaics) using rubrene and fullerene (C60) as the active layer, in which the electroluminescence threshold voltage(~1.1 V) was half the value of the bandgap of rubrene. Magneto-electroluminescence (MEL) response of planner heterojunction diodes exhibited a small increase in response to a low magnetic field strength (<20 mT) however, a very large decay was observed at a high magnetic field strength (>20 mT). When a hole-transport layer with a low mobility was included in these devices, the MEL response reversed in shape, and simultaneously, the EL threshold voltage became larger than the bandgap voltage. When bulk heterojunction device was examined, the amplitude of MEL curves presented an anomalous voltage-dependence. Following an analysis of the MEL responses of these devices, we proposed that the EL of half-bandgap-voltage device originated from bimolecular triplet-triplet annihilation in the rubrene film, rather than from singlet excitons that formed via an interface auger recombination. This work provides critical insight into the mechanisms of OLED emission and will help advance the applications of bifunctional devices.

  5. Wavelength-Tunable Electroluminescent Light Sources from Individual Ga-Doped ZnO Microwires.

    PubMed

    Jiang, Mingming; He, Gaohang; Chen, Hongyu; Zhang, Zhenzhong; Zheng, Lingxia; Shan, Chongxin; Shen, Dezhen; Fang, Xiaosheng

    2017-03-07

    Electrically driven wavelength-tunable light emission from biased individual Ga-doped ZnO microwires (ZnO:Ga MWs) is demonstrated. Single crystalline ZnO:Ga MWs with different Ga-doping concentrations have been synthesized using a one-step chemical vapor deposition method. Strong electrically driven light emission from individual ZnO:Ga MW based devices is realized with tunable colors, and the emission region is localized toward the center of the wires. Increasing Ga-doping concentration in the MWs can lead to the redshift of electroluminescent emissions in the visible range. Interestingly, owing to the lack of rectification characteristics, relevant electrical measurement results show that the alternating current-driven light emission functions excellently on the ZnO:Ga MWs. Consequently, individual ZnO:Ga MWs, which can be analogous to incandescent sources, offer unique possibilities for future electroluminescence light sources. This typical multicolor emitter can be used to rival and complement other conventional semiconductor devices in displays and lighting.

  6. Preparation, characterization and electroluminescence studies of ZnO nanorods for optoelectronic device applications

    NASA Astrophysics Data System (ADS)

    Singh, Anju; Vishwakarma, H. L.

    2015-07-01

    In this work, ZnO nanorods were achieved by a simple chemical precipitation method in the presence of capping agent Poly Vinyl Pyrrolidone (PVP) at room temperature. X-Ray Diffraction (XRD) result indicates that the synthesized undoped ZnO nanorods have wurtzite hexagonal structure without any impurities. It has been seen that the growth orientation of the prepared ZnO nanorods were (101). XRD analysis revealed that the nanorods having the crystallite size 49 nm. The Scanning Electron Microscopy (SEM) image confirmed the size and shape of these nanorods. The diameter of nanorods has been found that 1.52 µm to 1.61 µm and the length of about 4.89 µm. It has also been found that at room temperature Ultra Violet Visible (UV-VIS) absorption band is around 355 nm (blue shifted as compared to bulk). Electroluminescence (EL) studies show that emission of light is possible at very small threshold voltage and increases rapidly with increasing applied voltage. It is seen that smaller ZnO nanoparticles give higher electroluminescence brightness starting at lower threshold voltage. The brightness is also affected by increasing the frequency of AC signal.

  7. Preparation, characterization and electroluminescence studies of ZnO nanorods for optoelectronic device applications

    SciTech Connect

    Singh, Anju; Vishwakarma, H. L.

    2015-07-31

    In this work, ZnO nanorods were achieved by a simple chemical precipitation method in the presence of capping agent Poly Vinyl Pyrrolidone (PVP) at room temperature. X-Ray Diffraction (XRD) result indicates that the synthesized undoped ZnO nanorods have wurtzite hexagonal structure without any impurities. It has been seen that the growth orientation of the prepared ZnO nanorods were (101). XRD analysis revealed that the nanorods having the crystallite size 49 nm. The Scanning Electron Microscopy (SEM) image confirmed the size and shape of these nanorods. The diameter of nanorods has been found that 1.52 µm to 1.61 µm and the length of about 4.89 µm. It has also been found that at room temperature Ultra Violet Visible (UV-VIS) absorption band is around 355 nm (blue shifted as compared to bulk). Electroluminescence (EL) studies show that emission of light is possible at very small threshold voltage and increases rapidly with increasing applied voltage. It is seen that smaller ZnO nanoparticles give higher electroluminescence brightness starting at lower threshold voltage. The brightness is also affected by increasing the frequency of AC signal.

  8. Sky-Blue Organic Light Emitting Diode with 37% External Quantum Efficiency Using Thermally Activated Delayed Fluorescence from Spiroacridine-Triazine Hybrid.

    PubMed

    Lin, Ting-An; Chatterjee, Tanmay; Tsai, Wei-Lung; Lee, Wei-Kai; Wu, Meng-Jung; Jiao, Min; Pan, Kuan-Chung; Yi, Chih-Lung; Chung, Chin-Lung; Wong, Ken-Tsung; Wu, Chung-Chih

    2016-08-01

    Extremely efficient sky-blue organic electroluminescence with external quantum efficiency of ≈37% is achieved in a conventional planar device structure, using a highly efficient thermally activated delayed fluorescence emitter based on the spiroacridine-triazine hybrid and simultaneously possessing nearly unitary (100%) photoluminescence quantum yield, excellent thermal stability, and strongly horizontally oriented emitting dipoles (with a horizontal dipole ratio of 83%).

  9. Highly efficient phosphorescent organic light-emitting devices based on Re(CO)3Cl-bathophenanthroline

    NASA Astrophysics Data System (ADS)

    Li, Jiang; Si, Zhenjun; Liu, Chunbo; Li, Chuannan; Zhao, Feifei; Duan, Yu; Chen, Ping; Liu, Shiyong; Li, Bin

    2007-05-01

    Highly efficient orange organic electroluminescent devices based on Re(CO)3Cl-bathophenanthroline have been fabricated. A device with 9 wt% shows the highest efficiencies of 13.8 cd A-1 (luminance efficiency), 8.69 lm W-1 (power efficiency) and 5.24% (external quantum efficiency). Maximum luminance over 4000 cd m-2 is obtained. By discussing the mechanisms, it is believed that trapping contributes mostly to these relatively much higher efficiencies.

  10. Visible and near infrared emitting thin film electroluminescent gallium nitride doped with rare earths

    NASA Astrophysics Data System (ADS)

    Kim, Joo Han

    Visible and near-infrared (NIR) light-emitting thin-film electroluminescent gallium nitride (GaN) doped with rare earth (RE) elements was studied. The rare-earth-doped GaN thin films were prepared by radio frequency (RF) planar magnetron co-sputtering of separate targets consisting of a GaN compound target and a metallic rare earth target in a pure nitrogen atmosphere. The luminescence of rare-earth-doped GaN was shown to be a strong function of its structure and properties, and growth parameters affected the structure and properties of the GaN host films. A phase transition from the thermodynamically stable wurtzite to the metastable zinc-blende structure at room temperature in GaN host films was observed upon increasing the impact energy of the bombarding species, thereby increasing the compressive stress in the GaN film. The switch from wurtzite to zinc-blende GaN occurred at a compressive internal stress of ˜1 GPa. The internal compressive stress above this threshold value apparently stabilizes the zinc-blende GaN phase at room temperature. Field emission scanning electron microscopy (FESEM) and atomic force microscopy (AFM) showed that the impact by hyperthermal species yielded a highly condensed fibrous GaN microstructure with a smooth surface morphology due to annihilation of porosity by knock-on and bombardment-induced adatom mobility. X-ray diffraction and texture analyses showed that the GaN films deposited at a low pressure had a predominant cubic phase with a preferred crystallographic orientation of the [111] direction perpendicular to the surface of the film. X-ray rocking curve data revealed that cubic GaN films grown with a lower growth rate exhibited a more highly [111]-textured structure. Alternating-current thin-film electroluminescent (ACTFEL) devices were fabricated based on GaN doped with rare earth (RE) elements. Visible electroluminescent light emission peaks at 475 (blue), 530 (green), and 614 nm (red) were demonstrated at room temperature

  11. Correlating electroluminescence characterization and physics-based models of InGaN/GaN LEDs: Pitfalls and open issues

    SciTech Connect

    Calciati, Marco; Vallone, Marco; Zhou, Xiangyu; Ghione, Giovanni; Goano, Michele Bertazzi, Francesco; Meneghini, Matteo; Meneghesso, Gaudenzio; Zanoni, Enrico; Verzellesi, Giovanni; Zhu, Dandan; Humphreys, Colin

    2014-06-15

    Electroluminescence (EL) characterization of InGaN/GaN light-emitting diodes (LEDs), coupled with numerical device models of different sophistication, is routinely adopted not only to establish correlations between device efficiency and structural features, but also to make inferences about the loss mechanisms responsible for LED efficiency droop at high driving currents. The limits of this investigative approach are discussed here in a case study based on a comprehensive set of current- and temperature-dependent EL data from blue LEDs with low and high densities of threading dislocations (TDs). First, the effects limiting the applicability of simpler (closed-form and/or one-dimensional) classes of models are addressed, like lateral current crowding, vertical carrier distribution nonuniformity, and interband transition broadening. Then, the major sources of uncertainty affecting state-of-the-art numerical device simulation are reviewed and discussed, including (i) the approximations in the transport description through the multi-quantum-well active region, (ii) the alternative valence band parametrizations proposed to calculate the spontaneous emission rate, (iii) the difficulties in defining the Auger coefficients due to inadequacies in the microscopic quantum well description and the possible presence of extra, non-Auger high-current-density recombination mechanisms and/or Auger-induced leakage. In the case of the present LED structures, the application of three-dimensional numerical-simulation-based analysis to the EL data leads to an explanation of efficiency droop in terms of TD-related and Auger-like nonradiative losses, with a C coefficient in the 10{sup −30} cm{sup 6}/s range at room temperature, close to the larger theoretical calculations reported so far. However, a study of the combined effects of structural and model uncertainties suggests that the C values thus determined could be overestimated by about an order of magnitude. This preliminary

  12. Efficient degradation of Methylene Blue dye over highly reactive Cu doped strontium titanate (SrTiO3) nanoparticles photocatalyst under visible light.

    PubMed

    Rahman, Qazi Inamur; Ahmad, Musheer; Misra, Sunil Kumar; Lohani, Minaxi

    2012-09-01

    Visible light induced photocatalysts of Cu doped SrTiO3 (Cu/SrTiO3) nanoparticles with the size -60-75 nm were prepared via facile sol-gel method. The morphological, optical, crystalline properties and compositions of synthesized Cu/SrTiO3 nanoparticles were thoroughly characterized by field emission scanning electron microscopy (FE-SEM), powder X-ray diffraction (XRD), ultra violet-visible spectroscopy (UV-Vis) and energy dispersive X-ray (EDX). A significant red shift in the UV-diffused reflectance spectrum was observed and the absorption edge shifted to visible region by the Cu doping. Surprisingly, the band gap of SrTiO3 was changed from 3.2 eV drop to 2.96 eV. The photocatalytic activity of the synthesized Cu/SrTiO3 nanoparticles was demonstrated for the degradation of Methylene Blue dye under visible light irradiation. The formation of new acceptor region in Cu/SrTiO3 was responsible for high photocatalytic activity of Cu/SrTiO3 nanoparticles. The results showed that the Methylene Blue dye was degraded by -66% within time span of 2 h over the Cu/SrTiO3 nanoparticles. This dye degradation reaction followed the Langmuir-Hinshelwood kinetics and also exhibited first order reaction rate. The calculated rate constant for the degradation reaction following first order kinetics was k = 0.0016 min(-1).

  13. Tailored synthesis of CuS nanodisks from a new macrocyclic precursor and their efficient catalytic properties on methylene blue dye degradation

    NASA Astrophysics Data System (ADS)

    Islam, D. A.; Chakraborty, A.; Bhattacharya, B.; Sarkar, U.; Acharya, H.

    2016-05-01

    In this study, CuS nanodisks have been synthesized from a tetraaza (N4) macrocyclic complex precursor by a facile wet chemical method. The crystallinity and morphology of the as-synthesized products were characterized by X-ray diffraction and transmission electron microscopy, which confirm a phase pure crystalline CuS nanostructures with 15 to 20 nm in dimension with 5 nm thickness. A possible formation mechanism and growth process of the CuS nanodisks are discussed using thiourea and tetraaza ligand as the sulfur donor and stabilizing agent, respectively. Cyclic N4 ligand also acts as a binding agent to template-guide the oriented growth of CuS nanodisks. The optimized geometry of ligands and complexes was calculated using B3YLP functional, which indicates that the HOMO in the complex located on metal center and N atoms are weakly bonded to the metal center. The catalytic activity of CuS nanodisks toward MB degradation with light displays the higher MB degradation rate than under dark in the presence of H2O2. The C t/ C 0 plot as a function of time displays the higher MB degradation activity of CuS nanoparticles with H2O2. The recycle stability of CuS nanoparticles was even found to be >80 % after five cycles studied by repeating the MB degradation with same CuS nanoparticles sample.

  14. Efficient visible light photo-fenton-like degradation of organic pollutants using in situ surface-modified BiFeO3 as a catalyst.

    PubMed

    An, Junjian; Zhu, Lihua; Zhang, Yingying; Tang, Heqing

    2013-06-01

    The visible light photo-Fenton-like catalytic performance of BiFeO3 nanoparticles was investigated using Methyl Violet (MV), Rhodamine B (RhB) and phenol as probes. Under optimum conditions, the pseudo first-order rate constant (k) was determined to be 2.21 x 10(-2), 5.56 x 10(-2) and 2.01 x 10(-2) min(-1) for the degradation of MV (30 micromol/L), RhB (10 micromol/L) and phenol (3 mmol/L), respectively, in the BiFeO3-H2O2-visible light (Vis) system. The introduction of visible light irradiation increased the k values of MV, RhB and phenol degradation 3.47, 1.95 and 2.07 times in comparison with those in dark. Generally, the k values in the BiFeO3-H2O2-Vis system were accelerated by increasing BiFeO3 load and H2O2 concentration, but decreased with increasing initial pollutant concentration. To further enhance the degradation of pollutants at high concentrations, BiFeO3 was modified with the addition of surface modifiers. The addition of ethylenediamineteraacetic acid (EDTA, 0.4 mmol/L) increased the k value of MV degradation (60 micromol/L) from 1.01 x 10(-2) min(-1) in the BiFeO3-H2O2-Vis system to 1.30 min(-1) in the EDTA-BiFeO3-H2O2-Vis system by a factor of 128. This suggests that in situ surface modification can enable BiFeO3 nano-particles to be a promising visible light photo-Fenton-like catalyst for the degradation of organic pollutants.

  15. Efficient Photocatalytic Degradation of Norfloxacin in Aqueous Media by Hydrothermally Synthesized Immobilized TiO2/Ti Films with Exposed {001} Facets.

    PubMed

    Sayed, Murtaza; Shah, Luqman Ali; Khan, Javed Ali; Shah, Noor S; Nisar, Jan; Khan, Hasan M; Zhang, Pengyi; Khan, Abdur Rahman

    2016-12-22

    In this study, a novel immobilized TiO2/Ti film with exposed {001} facets was prepared via a facile one-pot hydrothermal route for the degradation of norfloxacin from aqueous media. The effects of various hydrothermal conditions (i.e., solution pH, hydrothermal time (HT) and HF concentration) on the growth of {001} faceted TiO2/Ti film were investigated. The maximum photocatalytic performance of {001} faceted TiO2/Ti film was observed when prepared at pH 2.62, HT of 3 h and at HF concentration of 0.02 M. The as-prepared {001} faceted TiO2/Ti films were fully characterized by field-emission scanning electron microscope (FE-SEM), X-ray diffraction (XRD), high resolution transmission electron microscope (HR-TEM), and X-ray photoelectron spectroscopy (XPS). More importantly, the as-prepared {001} faceted TiO2/Ti film exhibited excellent photocatalytic performance toward degradation of norfloxacin in various water matrices (Milli-Q water, tap water, river water and synthetic wastewater). The individual influence of various anions (SO4(2-), HCO3(-), NO3(-), Cl(-)) and cations (K(+), Ca(2+), Mg(2+), Cu(2+), Na(+), Fe(3+)) usually present in the real water samples on the photocatalytic performance of as-prepared TiO2/Ti film with exposed {001} facet was investigated. The mechanistic studies revealed that (•)OH is mainly involved in the photocatalytic degradation of norfloxacin by {001} faceted TiO2/Ti film. In addition, norfloxacin degradation byproducts were investigated, on the basis of which degradation schemes were proposed.

  16. Magnetic recoverable MnFe₂O₄ and MnFe₂O₄-graphene hybrid as heterogeneous catalysts of peroxymonosulfate activation for efficient degradation of aqueous organic pollutants.

    PubMed

    Yao, Yunjin; Cai, Yunmu; Lu, Fang; Wei, Fengyu; Wang, Xiaoyao; Wang, Shaobin

    2014-04-15

    Magnetic iron based materials are generally effective for many catalytic reactions and can be magnetically recovered after application, showing advantages than other metal oxides. In the present work, magnetic MnFe2O4 nanoparticle and MnFe2O4-reduced graphene oxide (rGO) hybrid were prepared and used as catalysts to activate peroxymonosulfate (PMS) to oxidatively degrade various organic pollutants in water. From a process of chemical deposition and reduction, MnFe2O4-rGO hybrids were produced with nanosized MnFe2O4 particles (ca. 13.2 nm). It was found that MnFe2O4 or MnFe2O4-rGO presented high activity in activating PMS to produce sulfate radicals for degradation of organic dyes (Methyl violet, Methyl orange, Methylene blue, Orange II and Rhodamine B) and could be separated with a magnet without any loss. The reaction kinetics, effect of different ion species CL(-),HCO3(-),CH3COO(-)and NO3(-) and Cl(-) strength, reaction temperature (25-65°C), catalytic stability, as well as degradation mechanism were comprehensively studied. The lower activation energy on MnFe2O4-rGO (25.7 kJ/mol) justify the higher chemical performance than that of MnFe2O4 (31.7 kJ/mol), suggesting that graphene plays a significant role in the enhanced degradation of dyes. More importantly, the as-prepared MnFe2O4 and MnFe2O4-rGO hybrid exhibited stable performance to remove the organic pollutants in wastewater with easy recycling and good stability by successive degradation experiments.

  17. Size-Controlled TiO2 nanocrystals with exposed {001} and {101} facets strongly linking to graphene oxide via p-Phenylenediamine for efficient photocatalytic degradation of fulvic acids.

    PubMed

    Yan, Wen-Yuan; Zhou, Qi; Chen, Xing; Yang, Yong; Zhang, Yong; Huang, Xing-Jiu; Wu, Yu-Cheng

    2016-08-15

    Photocatalytic degradation is one of the most promising methods for removal of fulvic acids (FA), which is a typical category of natural organic contamination in groundwater. In this paper, TiO2/graphene nanocomposites (N-RGO/TiO2) were prepared via simple chemical functionalization and one-step hydrothermal method for efficient photodegradation of FA under illumination of a xenon lamp as light source. Here, p-phenylenediamine was used as not only the linkage chemical agent between TiO2 nanocrystals and graphene, but also the nitrogen dopant for TiO2 nanocrystals and graphene. During the hydrothermal process, facets of TiO2 nanocrystals were modulated with addition of HF, and sizes of TiO2 nanocrystals were controlled by the contents of graphene oxide functionalized with p-phenylenediamine (RGO-NH2). The obtained N-RGO/TiO2 nanocomposites exhibited a much higher photocatalytic activity and stability for degradation of methyl blue (MB) and FA compared with other TiO2 samples under xenon lamp irradiation. For the third cycle, the 10wt%N-RGO/TiO2 catalyst maintains high photoactivity (87%) for the degradation of FA, which is much better than the TiO2-N/F (61%) in 3h. This approach supplies a new strategy to design and synthesize metal oxide and graphene oxide nanocomposites with highly efficient photocatalytic performance.

  18. Transient electroluminescence dynamics in small molecular organic light-emitting diodes

    SciTech Connect

    Gan, Z; Liu, R; Shinar, R; Shinar, J

    2010-09-14

    Intriguing electroluminescence (EL) spikes, following a voltage pulse applied to small molecular OLEDs, are discussed, elucidating carrier and exciton quenching dynamics and their relation to device structure. At low temperatures, all devices exhibit spikes at {approx} 70-300 ns and {mu}s-long tails. At 295 K only those with a hole injection barrier, carrier-trapping guest-host emitting layer, and no strong hole-blocking layer exhibit the spikes. They narrow and appear earlier under post-pulse reverse bias. The spikes and tails are in agreement with a revised model of recombination of correlated charge pairs (CCPs) and initially unpaired charges. Decreased post-pulse field-induced dissociative quenching of singlet excitons and CCPs, and possibly increased post-pulse current of holes that 'turn back' toward the recombination zone after having drifted beyond it are suspected to cause the spikes amplitude, which exceeds the dc EL.

  19. Observation of 1.5 μm photoluminescence and electroluminescence from a holmium organic complex

    NASA Astrophysics Data System (ADS)

    Zang, F. X.; Li, W. L.; Hong, Z. R.; Wei, H. Z.; Li, M. T.; Sun, X. Y.; Lee, C. S.

    2004-06-01

    Electroluminescence (EL) and photoluminescence in both the visible and near-infrared spectral range were observed from a holmium(dibenzoylmethanato)3(bathophenanthroline) [Ho(DBM)3bath]. Five peaks at 580nm, 660nm, 980nm, 1200nm, and 1500nm, respectively, were attributed to the internal 4f electronical transitions of the Ho3+ ions. Except for the emissions of the Ho3+ ions, a broadband exciplex emission from 480nmto670nm appeared in the EL cases. The emission intensity of the exciplex at organic interface showed a tendency to saturation beyond a certain driving voltage, while the emissions of the Ho3+ ions kept increasing. This evolution of visible EL spectra was discussed in terms of the extension of the charge recombination zone. The 1500nm emission corresponding to the F55→I65 transition suggests that the Ho(DBM)3bath is a potential candidate for optical communications.

  20. Sensitized photo- and electroluminescence from Er complexes mixed with Ir complex

    NASA Astrophysics Data System (ADS)

    Zhang, Dongyu; Li, Wenlian; Chu, Bei; Li, Xiao; Han, Liangliang; Zhu, Jianzhuo; Li, Tianle; Bi, Defeng; Yang, Dongfang; Yan, Fei; Liu, Huihui; Wang, Dan

    2008-03-01

    We investigated the sensitized effect of fac-tris(2-phenylpyridine) iridium [Ir(ppy)3] on tris-(dibenzoylmethanato)-mono-(bathophenanthroline) erbium (Er-DB) for 1.5μm near-infrared emission. Compared with the neat Er-DB film, the blend film composed of Er-DB and Ir(ppy)3 with a 1:1 of the weight ratio shows 20 times and 4 times enhancement on intensity of photoluminescence (PL) and electroluminescence (EL), respectively. The improvement in both PL and EL intensities was conjectured to be the result of the energy transfer from Ir(ppy)3 to Er-DB complex, and the detailed mechanisms of the enhancement were also discussed.

  1. Electron mobility of rare earth complexes measured by transient electroluminescence method

    NASA Astrophysics Data System (ADS)

    Zang, F. X.; Lengyel, O.; Li, Wenlian; Hong, Z. R.; Liu, Ze; Lee, C. S.; Lee, S. T.

    2006-09-01

    Electron mobility of gadolinium/europium (dibenzoylmethanato) 3(bathophenanthroline) (Gd/Eu(DBM) 3 bath) was measured by transient electroluminescence (EL) method. Although electron mobility of the two complexes were expected to be same, the value of mobility (1.2 × 10 -4 cm 2/Vs at electric field of 1 MV/cm) of Eu(DBM) 3 bath complex was bigger than that (8 × 10 -5 cm 2/Vs at electric field of 1 MV/cm) of Gd(DBM) 3 bath complex. It was found to be related to the different luminescent mechanisms of active materials and recombination zones in the devices. According to this, penetration length of hole injected into electron transport layer of Eu(DBM) 3 bath was estimated.

  2. Automatic Detection and Evaluation of Solar Cell Micro-Cracks in Electroluminescence Images Using Matched Filters

    SciTech Connect

    Spataru, Sergiu; Hacke, Peter; Sera, Dezso

    2016-11-21

    A method for detecting micro-cracks in solar cells using two dimensional matched filters was developed, derived from the electroluminescence intensity profile of typical micro-cracks. We describe the image processing steps to obtain a binary map with the location of the micro-cracks. Finally, we show how to automatically estimate the total length of each micro-crack from these maps, and propose a method to identify severe types of micro-cracks, such as parallel, dendritic, and cracks with multiple orientations. With an optimized threshold parameter, the technique detects over 90 % of cracks larger than 3 cm in length. The method shows great potential for quantifying micro-crack damage after manufacturing or module transportation for the determination of a module quality criterion for cell cracking in photovoltaic modules.

  3. Probe beam-free detection of terahertz wave by electroluminescence induced by intense THz pulse

    NASA Astrophysics Data System (ADS)

    Shin, J.; Jin, Z.; Nosaka, Y.; Nakazawa, T.; Kodama, R.

    2016-03-01

    Recently, a table-top fs laser system can generate MW terahertz (THz) pulse with its electric field higher than 100 kV/cm can be generated by several schemes. Such a strong THz field can directly drive electrons inside various materials. Here, we demonstrated a direct THz electric field detection method by measuring the electroluminescence induced by intense THz pulse inside commonly available light emitting diode. An intense THz wave obtained by the two-color laser scheme was focused onto LED along with an external DC bias to induce luminescence which we found proportional to the amplitude of the incident THz field. The scheme can be useful to realize a low-cost, probe-free THz detection and imaging system.

  4. Homogeneous Synthesis and Electroluminescence Device of Highly Luminescent CsPbBr3 Perovskite Nanocrystals.

    PubMed

    Wei, Song; Yang, Yanchun; Kang, Xiaojiao; Wang, Lan; Huang, Lijian; Pan, Daocheng

    2017-03-06

    Highly luminescent CsPbBr3 perovskite nanocrystals (PNCs) are homogeneously synthesized by mixing toluene solutions of PbBr2 and cesium oleate at room temperature in open air. We found that PbBr2 can be easily dissolved in nonpolar toluene in the presence of tetraoctylammonium bromide, which allows us to homogeneously prepare CsPbBr3 perovskite quantum dots and prevents the use of harmful polar organic solvents, such as N,N-dimethylformamide, dimethyl sulfoxide, and N-methyl-2-pyrrolidone. Additionally, this method can be extended to synthesize highly luminescent CH3NH3PbBr3 perovskite quantum dots. An electroluminescence device with a maximal luminance of 110 cd/m(2) has been fabricated by using high-quality CsPbBr3 PNCs as the emitting layer.

  5. Light-emitting device with organic electroluminescent material and photoluminescent materials

    DOEpatents

    McNulty, Thomas Francis; Duggal, Anil Raj; Turner, Larry Gene; Shiang, Joseph John

    2005-06-07

    A light-emitting device comprises a light-emitting member, which comprises two electrodes and an organic electroluminescent material disposed between the electrodes, and at least one organic photoluminescent ("PL") material. The light-emitting member emits light having a first spectrum in response to a voltage applied across the two electrodes. The organic PL material absorbs a portion of the light emitted by the light-emitting member and emits light having second spectrum different than the first spectrum. The light-emitting device can include an inorganic PL material that absorbs another portion of the light emitted from the light-emitting member and emits light having a third spectrum different than both the first and the second spectra.

  6. Photo and electroluminescence from PECVD grown a-Si:H/SiO 2 multilayers

    NASA Astrophysics Data System (ADS)

    Ovchinnikov, V.; Malinin, A.; Sokolov, V.; Kilpelä, O.; Sinkkonen, J.

    2001-06-01

    Multilayers (ML) of a-Si:H/SiO 2 have been grown using plasma enhanced chemical vapor deposition. Room-temperature photoluminescence (PL) and electroluminescence (EL) in the range 1.35-1.8 eV has been observed in as-deposited and annealed samples. A noticeable redshift of the PL peak has been detected by increasing the a-Si:H layer thickness in the range 0.7-2.1 nm, as well as the annealing temperature (700-1200°C). The strong correlation between PL and EL spectra indicates that light emission from a-Si:H/SiO 2 ML can be attributed to the same luminescence centers in Si layers and nanoclusters. The luminescence mechanism can be interpreted in terms of quantum and spatial confinement of carriers.

  7. Two-phase Cryogenic Avalanche Detector with electroluminescence gap operated in argon doped with nitrogen

    NASA Astrophysics Data System (ADS)

    Bondar, A.; Buzulutskov, A.; Dolgov, A.; Nosov, V.; Shekhtman, L.; Shemyakina, E.; Sokolov, A.

    2017-02-01

    A two-phase Cryogenic Avalanche Detector (CRAD) with electroluminescence (EL) gap, operated in argon doped with a minor (49±7 ppm) admixture of nitrogen, has been studied. The EL gap was optically read out using cryogenic PMTs located on the perimeter of the gap. We present the results of the measurements of the N2 content, detector sensitivity to X-ray-induced signals, EL gap yield and electron lifetime in the liquid. The detector sensitivity, at a drift field in liquid Ar of 0.6 kV/cm, was measured to be 9 and 16 photoelectrons recorded at the PMTs per keV of deposited energy at 23 and 88 keV respectively. Such two-phase detectors, with enhanced sensitivity to the S2 (ionization-induced) signal, are relevant in the field of argon detectors for dark matter search and low energy neutrino detection.

  8. Room temperature direct-bandgap electroluminescence from a horizontal Ge ridge waveguide on Si

    NASA Astrophysics Data System (ADS)

    He, Chao; Liu, Zhi; Cheng, Bu-Wen

    2016-12-01

    We report a lateral Ge-on-Si ridge waveguide light emitting diode (LED) grown by ultrahigh vacuum chemical vapor deposition (UHV-CVD). Direct-bandgap electroluminescence (EL) of Ge waveguide under continuous current is observed at room temperature. The heat-enhancing luminescence and thermal radiation-induced superlinear increase of edge output optical power are found. The spontaneous emission and thermal radiation based on the generalized Planck radiation law are calculated and fit very well to the experimental results. The Ge waveguides with different lengths are studied and the shorter one shows stronger EL intensity. Project supported by the National Basic Research Program of China (Grant No. 2013CB632103), the National Natural Science Foundation of China (Grant Nos. 61176013 and 61036003), and the Science Fund from Beijing Science and Technology Commission, China (Grant No. Z151100003315019).

  9. Enhanced electroluminescence from nanoscale silicon p+ -n junctions made with an anodic aluminum oxide pattern.

    PubMed

    Hong, T; Chen, T; Ran, G Z; Wen, J; Li, Y Z; Dai, T; Qin, G G

    2010-01-15

    An enhancement of the electroluminescence (EL) from nanoscale silicon p(+)-n junctions made with an anodic aluminum oxide (AAO) pattern was demonstrated. The nanoporous AAO pattern with a pore density of 1.4 x 10(10) cm(-2) and a pore diameter of 50 +/- 10 nm was fabricated by the two-step anodic oxidation method on a n-type silicon wafer. The nanoscale AAO patterned Si p(+)-n junctions achieved an EL enhancement factor up to about 5 compared to the unpatterned Si p(+)-n junctions. The enhancement may originate from a reduction of nonradiative recombination due to partial passivation of the Si surface by the AAO pattern and improvement of the light extraction due to surface nanotextures.

  10. Room-temperature direct band-gap electroluminescence from germanium (111)-fin light-emitting diodes

    NASA Astrophysics Data System (ADS)

    Tani, Kazuki; Saito, Shin-ichi; Oda, Katsuya; Miura, Makoto; Wakayama, Yuki; Okumura, Tadashi; Mine, Toshiyuki; Ido, Tatemi

    2017-03-01

    Germanium (Ge) (111) fins of 320 nm in height were successfully fabricated using a combination of flattening sidewalls of a silicon (Si) fin structure by anisotropic wet etching with tetramethylammonium hydroxide, formation of thin Ge fins by selective Si oxidation in SiGe layers, and enlargement of Ge fins by Ge homogeneous epitaxial growth. The excellent electrical characteristics of Ge(111) fin light-emitting diodes, such as an ideality factor of 1.1 and low dark current density of 7.1 × 10‑5 A cm‑2 at reverse bias of ‑2 V, indicate their good crystalline quality. A tensile strain of 0.2% in the Ge fins, which originated from the mismatch of the thermal expansion coefficients between Ge and the covering SiO2 layers, was expected from the room-temperature photoluminescence spectra, and room-temperature electroluminescence corresponding to the direct band-gap transition was observed from the Ge fins.

  11. Electroluminescence from individual air-suspended carbon nanotubes within split-gate structures

    NASA Astrophysics Data System (ADS)

    Higashide, N.; Uda, T.; Yoshida, M.; Ishii, A.; Kato, Y. K.

    Electrically induced light emission from chirality-identified single-walled carbon nanotubes are investigated by utilizing split-gate field-effect devices fabricated on silicon-on-insulator substrates. We begin by etching trenches through the top silicon layer into the buried oxide, and the silicon layer is thermally oxidized for use as local gates. We partially remove the oxide and form gate electrodes, then contacts for nanotubes are deposited on both sides of the trench. Catalyst particles are placed on the contacts, and nanotubes are grown over the trench by chemical vapor deposition. We use photoluminescence microscopy to locate the nanotubes and perform excitation spectroscopy to identify their chirality. Gate-induced photoluminescence quenching is used to confirm carrier doping, and electroluminescence intensity is investigated as a function of the split-gate and bias voltages. Work supported by JSPS (KAKENHI 24340066, 26610080), MEXT (Photon Frontier Network Program, Nanotechnology Platform), Canon Foundation, and Asahi Glass Foundation.

  12. Democratizing an electroluminescence imaging apparatus and analytics project for widespread data acquisition in photovoltaic materials

    NASA Astrophysics Data System (ADS)

    Fada, Justin S.; Wheeler, Nicholas R.; Zabiyaka, Davis; Goel, Nikhil; Peshek, Timothy J.; French, Roger H.

    2016-08-01

    We present a description of an electroluminescence (EL) apparatus, easily sourced from commercially available components, with a quantitative image processing platform that demonstrates feasibility for the widespread utility of EL imaging as a characterization tool. We validated our system using a Gage R&R analysis to find a variance contribution by the measurement system of 80.56%, which is typically unacceptable, but through quantitative image processing and development of correction factors a variance contribution by the measurement system of 2.41% was obtained. We further validated the system by quantifying the signal-to-noise ratio (SNR) and found values consistent with other systems published in the literature, at SNR values of 10-100, albeit at exposure times of greater than 1 s compared to 10 ms for other systems. This SNR value range is acceptable for image feature recognition, providing the opportunity for widespread data acquisition and large scale data analytics of photovoltaics.

  13. Democratizing an electroluminescence imaging apparatus and analytics project for widespread data acquisition in photovoltaic materials.

    PubMed

    Fada, Justin S; Wheeler, Nicholas R; Zabiyaka, Davis; Goel, Nikhil; Peshek, Timothy J; French, Roger H

    2016-08-01

    We present a description of an electroluminescence (EL) apparatus, easily sourced from commercially available components, with a quantitative image processing platform that demonstrates feasibility for the widespread utility of EL imaging as a characterization tool. We validated our system using a Gage R&R analysis to find a variance contribution by the measurement system of 80.56%, which is typically unacceptable, but through quantitative image processing and development of correction factors a variance contribution by the measurement system of 2.41% was obtained. We further validated the system by quantifying the signal-to-noise ratio (SNR) and found values consistent with other systems published in the literature, at SNR values of 10-100, albeit at exposure times of greater than 1 s compared to 10 ms for other systems. This SNR value range is acceptable for image feature recognition, providing the opportunity for widespread data acquisition and large scale data analytics of photovoltaics.

  14. Experimental and theoretical study of photo- and electroluminescence of divinyldiphenyl and divinylphenanthrene derivatives

    NASA Astrophysics Data System (ADS)

    Samsonova, L. G.; Valiev, R. R.; Degtyarenko, K. M.; Sunchugashev, D. A.; Kukhta, I. N.; Kukhta, A. V.; Kopylova, T. N.

    2017-02-01

    Electronic absorption and luminescence spectra of four new compounds of divinyldiphenyl and divinylphenanthrene derivatives are investigated experimentally in tetrahydrofuran solutions and thin films obtained by thermal vacuum deposition and by spin coating of these substances embedded into polyvinylcarbazole matrix. Molecular geometry optimizations and electronic spectra have been calculated in the framework of XMC-QDPT2/6-31G (d, p) and TDDFT/B3LYP/6-31G (d, p) levels of theory. We have fabricated and studied OLED devices with the structure ITO/PEDOT:PSS/NPD/L/Ca/Al and ITO/PEDOT:PSS/PVK + L/Ca, where L is the luminophore. It is demonstrated that the photo-and electroluminescence spectra of divinyldiphenyl are not identical and undergo strong changes depending on the method of sample preparation.

  15. Spectral features and voltage effects in high-field electroluminescence of AlN filamentary nanocrystals

    NASA Astrophysics Data System (ADS)

    Weinstein, I. A.; Vokhmintsev, A. S.; Chaikin, D. V.; Afonin, Yu. D.

    2016-11-01

    The high-field electroluminescence (EL) spectra for Al-rich AlN nanowhiskers varying applied voltage were studied. The observed 2.70 eV emission, which can be considered as superposition of two Gaussian bands in 2.75 and 2.53 eV, was analyzed. It was shown that Fowler-Nordheim effect took place in EL mechanism with participation of capturing levels of ON- and VN-centers when AlN nanowhiskers were exposed to an external field of 2.5 ÷ 10 V/μm. Obtained results and made conclusions are in a good agreement with independent electron field emission measurements for different one-dimensional AlN nanostructures.

  16. The pure white light emission from three-layer electroluminescent device

    NASA Astrophysics Data System (ADS)

    Chen, Zhijian; Ogino, Kenji; Miyata, Seizo; Lu, Youmei; Watanabe, Toshiyuki

    2002-04-01

    We have synthesized a red fluorescent dye of 4-dicyanomethylene- 2,6-di-(4-dimethylaminobenzaldehyde)-γ-pyran (DCDM), and fabricated electroluminescent devices of glass/indium-tin oxide/N,N'-diphenyl-N, N'-(3-methyphenyl)-1,1'-biphenyl-4,4'-diamine (TPD), doped with different concentration of DCDM and 2.5wt.% of 9-cyanoanthracene (CNA), 50 nm/2,9-dimethy-4,7-diphenyl-1,10-phenanthroline (BCP), 40 nm/tris-(8-hydroxyquiniline) aluminium (Alq3), 5 nm/Ag : Mg, 500 nm/Ag cap, 100 nm. The Commission International de 1' Eclairage (CIE) colour coordinates traverses along a straight line in the CIE chromaticity diagram with the concentration of DCDM. By adjusting the concentration of the fluorescent dyes, the pure white light emission was obtained at the CIE coordinates of x = 0.34 and y = 0.35.

  17. Effect of annealing treatment on electroluminescence from GaN/Si nanoheterostructure array.

    PubMed

    Han, Chang Bao; He, Chuan; Meng, Xiao Bo; Wan, Ya Rui; Tian, Yong Tao; Zhang, Ying Jiu; Li, Xin Jian

    2012-02-27

    A GaN/Si nanoheterostructure array was prepared by growing GaN nanostructures on silicon nanoporous pillar array (Si-NPA). Based on as-grown and annealed GaN/Si-NPA, two light-emitting diodes (LEDs) were fabricated. It was found that after the annealing treatment, both the turn-on voltage and the leakage current density of the nanoheterostructure varied greatly, together with the electroluminescence (EL) changed from a yellow band to a near infrared band. The EL variation was attributed to the radiative transition being transformed from a defect-related recombination in GaN to an interfacial recombination of GaN/Si-NPA. Ours might have provided an effective approach for fabricating GaN/Si-based LEDs with different emission wavelengths.

  18. Tunable white light from photo- and electroluminescence of ZnO nanoparticles

    NASA Astrophysics Data System (ADS)

    Oliva, Jorge; Perez Mayen, Leonardo; De la Rosa, Elder; Diaz-Torres, Luis A.; Torres Castro, Alejandro; Salas, Pedro

    2014-01-01

    Tunable white light emission was obtained from ZnO nanorods with lengths ranging from 125 to 165 nm and quantum dots with an average size of 5 nm, synthesized with dodecylamine (DCA) as surfactant. It was possible to tailor the emission from cool to warm white light by changing the concentration of DCA in the synthesis process. The CIE coordinates for the white light obtained were (0.33, 0.32) in the case of photoluminescence and (0.31, 0.33) for electroluminescence from ZnO-based LEDs with a turn-on voltage of 4 and 6 V and a maximum current consumption of 2.32 mA at 10 V.

  19. The electroluminescence mechanism of Er³⁺ in different silicon oxide and silicon nitride environments

    SciTech Connect

    Rebohle, L. Wutzler, R.; Braun, M.; Helm, M.; Skorupa, W.; Berencén, Y.; Ramírez, J. M.; Garrido, B.; Hiller, D.

    2014-09-28

    Rare earth doped metal-oxide-semiconductor (MOS) structures are of great interest for Si-based light emission. However, several physical limitations make it difficult to achieve the performance of light emitters based on compound semiconductors. To address this point, in this work the electroluminescence (EL) excitation and quenching mechanism of Er-implanted MOS structures with different designs of the dielectric stack are investigated. The devices usually consist of an injection layer made of SiO₂ and an Er-implanted layer made of SiO₂, Si-rich SiO₂, silicon nitride, or Si-rich silicon nitride. All structures implanted with Er show intense EL around 1540 nm with EL power efficiencies in the order of 2 × 10⁻³ (for SiO₂:Er) or 2 × 10⁻⁴(all other matrices) for lower current densities. The EL is excited by the impact of hot electrons with an excitation cross section in the range of 0.5–1.5 × 10⁻¹⁵cm⁻². Whereas the fraction of potentially excitable Er ions in SiO₂ can reach values up to 50%, five times lower values were observed for other matrices. The decrease of the EL decay time for devices with Si-rich SiO₂ or Si nitride compared to SiO₂ as host matrix implies an increase of the number of defects adding additional non-radiative de-excitation paths for Er³⁺. For all investigated devices, EL quenching cross sections in the 10⁻²⁰ cm² range and charge-to-breakdown values in the range of 1–10 C cm⁻² were measured. For the present design with a SiO₂ acceleration layer, thickness reduction and the use of different host matrices did not improve the EL power efficiency or the operation lifetime, but strongly lowered the operation voltage needed to achieve intense EL.

  20. COUGAR: a liquid nitrogen cooled InGaAs camera for astronomy and electro-luminescence

    NASA Astrophysics Data System (ADS)

    Van Bogget, Urbain; Vervenne, Vincent; Vinella, Rosa Maria; van der Zanden, Koen; Merken, Patrick; Vermeiren, Jan

    2014-06-01

    A SWIR FPA was designed and manufactured with 640*512 pixels, 20 μm pitch and InGaAs detectors for electroluminescence characterization and astronomical applications in the [0.9 - 1.55 μm] range. The FPA is mounted in a liquid nitrogen dewar and is operated by a low noise frontend electronics. One of the biggest problem in designing sensors and cameras for electro-luminescence measurements is the autoillumination of the detectors by the readout circuit. Besides of proper shielding of the detectors, the ROIC shall be optimized for minimal electrical activity during the integration time of the very-weak signals coming from the circuit under test. For this reason a SFD (or Source Follower per Detector) architecture (like in the Hawaii sensor) was selected, resulting in a background limited performance of the detector. The pixel has a (somewhat arbitrary) full well capacity of 400 000 e- and a sensitivity of 2.17 μV/e-. The dark signal is app. 1 e-/pixel/sec and with the appropriate Fowler sampling the dark noise lowers below 5 e-rms. The power consumption of the circuit is limited 2 mW, allowing more than 24 hours of operation on less than 1 l of liquid nitrogen. The FPA is equipped with 4 outputs (optional readout on one single channel) and is capable of achieving 3 frames per second. Due to the non-destructive readout it is possible to determine in a dynamic way the optimal integration time for each observation. The Cougar camera is equipped with ultra-low noise power supply and bias lines; the electronics contain also a 24 bit AD converter to fully exploit the sensitivity of the FPA and the camera.

  1. Photoluminescence and electroluminescence characteristics of CaSiN2:Eu phosphor

    NASA Astrophysics Data System (ADS)

    Lee, Soon S.; Lim, Sungkyoo; Sun, Sey-Shing; Wager, John F.

    1997-11-01

    Photoluminescenc eand electroluminescence of CaSiN2:Eu materials were investigted to develop a new phosphor for thin film electroluminescence (TFEL) device applications. Ca3N2 and Si3N4 powders were mixed to form CaSiN2 hostmaterials and Eu was added as the luminescent center. The mixed powermatrials were cold pressed under the pressure of 1 Kg/cm2 to make pellets, and fired at 1400 degrees Celsius for 2 hours under N2H2 envrionemtn. Th ex-ry diffraction(CRD) patterns of synthesizd materals wer well matched with CaSiN2 of joint committee for powder diffraction standards (JCPDS) csrad. When illuminated by ultravilet rays, th enew phosphors emitted very bright red ligh of peak wav lenegth centered at 620 nm. Th TFEL devices with CaSiN2:Eu phosphor layser swre grown by sputter depositonof CaSiN2:Eu target. Red light emission was observed when the peak amplitude of the applied voltge exceeded 116 V.l The luminance was shown to increase sharply withth increase of the applied voltage. The maximum luminance was 1.62 Cd/m2 at the applied peak voltage of 276 V. The red emission from CaSiN2:Eu TFEL device seems to result from electronic transition of Eu3+ ions.The emission spectra of TFEl devices matchwell withth ephotoluminescence spectra of CaSiN2:Ey powders. The new devices structure and fabrication processes for the iimprovement of emission intenityof CaSiN2:Eu TFEl devices ar under investigation.

  2. The Effect of the Oxygen Plasma Treatment for ITO and ZnO Nanorods on the Electroluminescence of ZnO Nanorod/MEH-PPV Heterostructure Devices

    NASA Astrophysics Data System (ADS)

    Zhao, Su-Ling; Wang, Yong-Sheng; Gao, Song; Yang, Yi-Fan; Xu, Zheng

    2013-03-01

    Series devices of ITO/ZnO/ZnO nanorods/MEH-PPV/Al have been fabricated. ITO and ZnO nanorods of some devices are treated by O2 plasma. The electroluminescence of different devices is detected under different biases. UV electroluminescence of ZnO nanorods at 380nm is observed in all the devices. The intensity of 380nm increases when both ITO and ZnO nanorods are treated. The turn-on voltage of the treated device is lower than that of the non-treated device, and the EL power is enhanced. When the thickness of MEH-PPV is sufficiently thin, only 380 nm electroluminescence, besides a weak defect emission at 760 nm, is detected. The enhancement mechanism of the electroluminescence of the treated devices is discussed.

  3. Synthesis, photophysical, electrochemical and electroluminescent properties of a novel iridium(III) complex based on 2-phenylbenzo[d]oxazole derivative.

    PubMed

    Li, Xiao; Yu, Xiao-Ting; Chi, Hai-Jun; Dong, Yan; Xiao, Guo-Yong; Lei, Peng; Zhang, Dong-Yu; Cui, Zheng

    2013-12-01

    A new phosphorescent iridium (III) complex based on 2-(4-tert-butylphenyl)-5-methylbenzo[d]oxazole as main ligand, i.e. bis(2-(4-tert-butylphenyl)-5-methylbenzo[d]oxazole-N,C(2'))iridium(acetylacetonate) [(tmbo)2Ir(acac)], was synthesized for organic light-emitting diodes (OLEDs), and its photophysical, electrochemical and electroluminescent properties were investigated. The complex displayed strong phosphorescence emission, high decomposition temperature, short phosphorescent lifetime and reversible redox electrochemical behavior. The OLEDs based on (tmbo)2Ir(acac) as dopant emitter exhibited maximum luminance efficiency of 26.1cdA(-1) and high luminance of 16,445 cd m(-2). Interestingly, highly doped device based on (tmbo)2Ir(acac) showed high efficiency with negligible roll-off under a wide range of driving current density, which was mainly attributed to the effect of bulky steric hindrance of multi-methyl groups on this complex and its short phosphorescent lifetime.

  4. Synthesis, photophysical, electrochemical and electroluminescent properties of a novel iridium(III) complex based on 2-phenylbenzo[d]oxazole derivative

    NASA Astrophysics Data System (ADS)

    Li, Xiao; Yu, Xiao-Ting; Chi, Hai-Jun; Dong, Yan; Xiao, Guo-Yong; Lei, Peng; Zhang, Dong-Yu; Cui, Zheng

    2013-12-01

    A new phosphorescent iridium (III) complex based on 2-(4-tert-butylphenyl)-5-methylbenzo[d]oxazole as main ligand, i.e. bis(2-(4-tert-butylphenyl)-5-methylbenzo[d]oxazole-N,C2‧)iridium(acetylacetonate) [(tmbo)2Ir(acac)], was synthesized for organic light-emitting diodes (OLEDs), and its photophysical, electrochemical and electroluminescent properties were investigated. The complex displayed strong phosphorescence emission, high decomposition temperature, short phosphorescent lifetime and reversible redox electrochemical behavior. The OLEDs based on (tmbo)2Ir(acac) as dopant emitter exhibited maximum luminance efficiency of 26.1 cd A-1 and high luminance of 16,445 cd m-2. Interestingly, highly doped device based on (tmbo)2Ir(acac) showed high efficiency with negligible roll-off under a wide range of driving current density, which was mainly attributed to the effect of bulky steric hindrance of multi-methyl groups on this complex and its short phosphorescent lifetime.

  5. Synthesis and electroluminescence characterization of a new aluminum complex, [8-hydroxyquinoline] bis [2, 2'bipyridine] aluminum Al(Bpy)2q

    NASA Astrophysics Data System (ADS)

    Rahul, Kumar; Ritu, Srivastava; Punita, Singh

    2016-01-01

    We have synthesized and characterized a new electroluminescent material, [8-hydroxyquinoline] bis [2,2'bipyridine] aluminum. A solution of this material Al(Bpy)2q in toluene showed absorption maxima at 380 nm, which was attributed to the moderate energy (π-π*) transitions of the aromatic rings. The photoluminescence spectrum of Al(Bpy)2q in the toluene solution showed a peak at 518 nm. This material shows thermal stability up to 300 °C. The structure of the device is ITO/F4-TCNQ (1 nm)/α-NPD (35 nm)/Al(Bpy)2q (35 nm)/ BCP (6 nm)/Alq3 (28 nm)/LiF (1 nm)/Al (150 nm). This device exhibited a luminescence peak at 515 nm (CIE coordinates, x = 0.32, y = 0.49). The maximum luminescence of the device was 214 cd/m2 at 21 V. The maximum current efficiency of OLED was 0.12 cd/A at 13 V and the maximum power efficiency was 0.03 lm/W at 10 V.

  6. Electronic properties of anthracene derivatives for blue light emitting electroluminescent layers in organic light emitting diodes: a density functional theory study.

    PubMed

    Raghunath, P; Reddy, M Ananth; Gouri, C; Bhanuprakash, K; Rao, V Jayathirtha

    2006-01-26

    Molecular level parameters are investigated computationally to understand the factors that are responsible for the higher efficiency in derivatives of 9,10-bis(1-naphthyl)anthracene (alpha-ADN), 9,10-bis(2-naphthyl)anthracene (beta-ADN), their tetramethyl derivatives (alpha,beta-TMADN) and the t-Bu derivative (beta-TBADN) as blue light emitting electroluminescent (EL) layers in organic light emitting diodes (OLEDs). DFT studies at the B3LYP/6-31G(d,p) level have been carried out on the substituted anthracenes. The absorption spectra are simulated using time dependent DFT methods (TD-DFT) whereas the emission spectra are approximated by optimizing the excited state by HF/CI-Singles and then carrying out the vertical CI calculations by the TD-DFT method. The reorganization energy for estimating the hole and electron transport is calculated. The transfer integrals between parallely stacked molecules in the bulk state are estimated by calculating the electronic splitting. The substituted anthracenes are compared with unsubstituted anthracene and yet untested 9,10-dianthrylanthracene (TANTH). A larger and slower buildup of the electrons and holes in the EL layer, due to the higher reorganization energy and smaller electronic coupling between the adjacent molecules could lead to an increase in hole-electron recombination in the layer and thus increase the efficiency.

  7. Zinc finger-inspired nanohydrogels with glutathione/pH triggered degradation based on coordination substitution for highly efficient delivery of anti-cancer drugs.

    PubMed

    Zhang, Zihao; Wan, Jiaxun; Sun, Luyan; Li, Yongjing; Guo, Jia; Wang, Changchun

    2016-03-10

    Biodegradable materials used for drug delivery are of great demand due to their ability to degrade into low molecular weight species and further excrete from the body by metabolism. Herein, we report a new kind of zinc(II) crosslinked poly(methacrylic acid) nanohydrogels (ZCLNs) inspired by zinc finger proteins with dual stimuli-triggered degradation (glutathione and pH) for the first time. Compared with the disulfide bond crosslinked nanohydrogels, this new kind of ZCLNs is beneficial to the degradation of a wide range of cells, including normal cells. Ex vivo fluorescence images showed that the DOX-loaded folate-PEG conjugated zinc(II)-crosslinked polymeric nanohydrogels (FPZCLNs-15) preferentially accumulated in tumor tissue and the accumulation in normal tissues was much less compared with DOX-loaded PZCLNs-15 (non-targeted nanohydrogels) and free DOX, the FPZCLNs-15 (targeting system) delivered DOX to the tumor site with approximately 3.6- and 1.6-fold higher than free DOX and PZCLNs-15, respectively. Meanwhile, the PZCLNs-15 and FPZCLNs-15 reduced the concentration of DOX in the heart by 3.2- and 5.0-fold respectively, as compared to the free DOX. Moreover, a superior tumor growth inhibition and negligible damage to normal organs like the heart and kidney, which is reported to be vulnerable to DOX-associated side effects, are further demonstrated.

  8. A novel iron-containing polyoxometalate heterogeneous photocatalyst for efficient 4-chlorophennol degradation by H2O2 at neutral pH

    NASA Astrophysics Data System (ADS)

    Zhai, Qian; Zhang, Lizhong; Zhao, Xiufeng; Chen, Han; Yin, Dongju; Li, Jianhui

    2016-07-01

    An iron-containing polyoxometalate (FeШLysSiW) was synthesized from ferric chloride (FeIII), lysine (Lys) and silicotungstic acid (SiW), and characterized using ICP-AES, TG, FT-IR, UV-vis DRS, XRD and SEM. The chemical formula of FeШLysSiW was determined as [Fe(H2O)5(C6H14N2O2)]HSiW12O40·8H2O, with Keggin-structured SiW12O404- heteropolyanion and lysine moiety. As a heterogeneous catalyst, the as prepared FeШLysSiW showed good performance in the degradation of 4-chlorophenol by H2O2 in both the dark and irradiated systems. Under the conditions of 4-chlorophenol 100 mg/L, FeШLysSiW 1.0 g/L, H2O2 20 mmol/L and pH 6.5, 4-chlorophenol could be completely degraded in ca. 40 min in the dark and ca. 15 min upon irradiation. Prolonging the reaction time to 3 h, the TOC removal reached to ca. 71.3% in the dark and ca. 98.8% under irradiation. The catalytic activity of FeШLysSiW stems from synergetic effect of ferric iron and SiW12O404- in the catalyst, corresponding to Fenton-like catalysis and photocatalysis, respectively. The enhanced degradation of 4-CP under irradiation is due to the simultaneous oxidation of 4-CP through the Fenton-like and photocatalytic processes. The high catalytic activity of FeШLysSiW is also strongly related to the chemisorption of H2O2 on FeШLysSiW surface by hydrogen bonding, which promotes both the Fenton-like and photocatalytic processes.

  9. Nickel-doped cobalt ferrite nanoparticles: efficient catalysts for the reduction of nitroaromatic compounds and photo-oxidative degradation of toxic dyes.

    PubMed

    Singh, Charanjit; Goyal, Ankita; Singhal, Sonal

    2014-07-21

    This study deals with the exploration of NixCo₁-xFe₂O₄ (x = 0.0, 0.2, 0.4, 0.6, 0.8, 1.0) ferrite nanoparticles as catalysts for reduction of 4-nitrophenol and photo-oxidative degradation of Rhodamine B. The ferrite samples with uniform size distribution were synthesized using the reverse micelle technique. The structural investigation was performed using powder X-ray diffraction, high-resolution transmission electron microscopy, energy dispersive X-ray and scanning tunneling microscopy. The spherical particles with ordered cubic spinel structure were found to have the crystallite size of 4-6 nm. Diffused UV-visible reflectance spectroscopy was employed to investigate the optical properties of the synthesized ferrite nanoparticles. The surface area calculated using BET method was found to be highest for Co₀.₄Ni₀.₆Fe₂O₄ (154.02 m(2) g(-1)). Co₀.₄Ni₀.₆Fe₂O₄ showed the best catalytic activity for reduction of 4-nitrophenol to 4-aminophenol in the presence of NaBH4 as reducing agent, whereas CoFe₂O₄ was found to be catalytically inactive. The reduction reaction followed pseudo-first order kinetics. The effect of varying the concentration of catalyst and NaBH₄ on the reaction rates was also scrutinized. The photo-oxidative degradation of Rhodamine B, enhanced oxidation efficacy was observed with the introduction of Ni(2+) in to the cobalt ferrite lattice due to octahedral site preference of Ni(2+). Almost 99% degradation was achieved in 20 min using NiFe₂O₄ nanoparticles as catalyst.

  10. Impact of trace element addition on degradation efficiency of volatile fatty acids, oleic acid and phenyl acetate and on microbial populations in a biogas digester.

    PubMed

    Karlsson, Anna; Einarsson, Peter; Schnürer, Anna; Sundberg, Carina; Ejlertsson, Jörgen; Svensson, Bo H

    2012-10-01

    The effect of trace element addition on anaerobic digestion of food industry- and household waste was studied using two semi-continuous lab-scale reactors, one (R30+) was supplied with Fe, Co and Ni, while the other (R30) acted as a control. Tracer analysis illustrated that methane production from acetate proceeded through syntrophic acetate oxidation (SAO) in both digesters. The effect of the trace elements was also evaluated in batch assays to determine the capacity of the microorganisms of the two digesters to degrade acetate, phenyl acetate, oleic acid or propionate, butyrate and valerate provided as a cocktail. The trace elements addition improved the performance of the process giving higher methane yields during start-up and early operation and lower levels of mainly acetate and propionate in the R30+ reactor. The batch assay showed that material from R30+ gave effects on methane production from all substrates tested. Phenyl acetate was observed to inhibit methane formation in the R30 but not in the R30+ assay. A real-time PCR analysis targeting methanogens on the order level as well as three SAO bacteria showed an increase in Methanosarcinales in the R30+ reactor over time, even though SAO continuously was the dominating pathway for methane production. Possibly, this increase explains the low VFA-levels and higher degradation rates observed in the R30+ batch incubations. These results show that the added trace elements affected the ability of the microflora to degrade VFAs as well as oleic acid and phenyl acetate in a community, where acetate utilization is dominated by SAO.

  11. Fabrication and efficient photocatalytic degradation of methylene blue over CuO/BiVO{sub 4} composite under visible-light irradiation

    SciTech Connect

    Jiang Haiqing Endo, Hiromitsu; Natori, Hirotaka; Nagai, Masayuki; Kobayashi, Koichi

    2009-03-05

    CuO/BiVO{sub 4} composite photocatalysts were prepared by solution combustion synthesis method and impregnation technique. X-ray diffraction, X-ray photoelectron spectroscopy, field-emission scan electron microscopy and UV-vis diffusion reflectance spectra were used to identify the physical properties and photophysical properties of CuO/BiVO{sub 4} composite photocatalysts. The photocatalysts exhibit the enhanced photocatalytic properties for degradation of methylene blue under visible-light ({lambda} > 420 nm). The mechanism of improved photocatalytic activity is also discussed.

  12. Sub-bandgap Voltage Electroluminescence and Magneto-oscillations in a WSe2 Light-Emitting van der Waals Heterostructure.

    PubMed

    Binder, Johannes; Withers, Freddie; Molas, Maciej R; Faugeras, Clement; Nogajewski, Karol; Watanabe, Kenji; Taniguchi, Takashi; Kozikov, Aleksey; Geim, Andre K; Novoselov, Kostya S; Potemski, Marek

    2017-03-08

    We report on experimental investigations of an electrically driven WSe2 based light-emitting van der Waals heterostructure. We observe a threshold voltage for electroluminescence significantly lower than the corresponding single particle band gap of monolayer WSe2. This observation can be interpreted by considering the Coulomb interaction and a tunneling process involving excitons, well beyond the picture of independent charge carriers. An applied magnetic field reveals pronounced magneto-oscillations in the electroluminescence of the free exciton emission intensity with a 1/B periodicity. This effect is ascribed to a modulation of the tunneling probability resulting from the Landau quantization in the graphene electrodes. A sharp feature in the differential conductance indicates that the Fermi level is pinned and allows for an estimation of the acceptor binding energy.

  13. Exciplex electroluminescence and photoluminescence spectra of the new organic materials based on zinc complexes of sulphanylamino-substituted ligands

    PubMed Central

    2012-01-01

    We have investigated the electroluminescence spectra of the electroluminescent devices based on the new zinc complexes of amino-substituted benzothiazoles and quinolines containing the C-N-M-N chains in their chelate cycles. The spectra exhibit strong exciplex bands in the green to yellow region 540 to 590 nm due to interaction of the excited states of zinc complexes and triaryl molecules of the hole-transporting layer. For some devices, the intrinsic luminescence band of 460 nm in the blue region is also observed along with the exciplex band giving rise to an almost white color of the device emission. The exciplex band can be eliminated if the material of the hole-transporting layer is not a triarylamine derivative. We have also found the exciplex emission in the photoluminescence spectra of the films containing blends of zinc complex and triphenylamine material. PMID:22471942

  14. The effect of absorption and coherent interference in the photoluminescence and electroluminescence spectra of SRO/SRN MIS capacitors.

    PubMed

    Juvert, Joan; González-Fernández, Alfredo Abelardo; Llobera, Andreu; Domínguez, Carlos

    2013-04-22

    In this paper we present a technique that can be used to study the effect of absorption and coherent interference in the luminescence of multilayer structures. We apply the technique to the measured photoluminescence and electroluminescence spectra of MIS capacitors where the insulator is composed of a silicon rich oxide (SRO)/silicon rich nitride (SRN) bilayer structure. We remove the effect of the multilayer stack on the measured photoluminescence spectrum of the samples without the metal contact to find the intrinsic spectrum. Then we apply the effect of the MIS structure on the intrinsic spectrum in order to calculate the electroluminescence spectrum. Good agreement with the experimentally measured EL spectrum is found. We discuss which parameters affect the spectra most significantly.

  15. Electro- and photoluminescence imaging as fast screening technique of the layer uniformity and device degradation in planar perovskite solar cells

    NASA Astrophysics Data System (ADS)

    Soufiani, Arman Mahboubi; Tayebjee, Murad J. Y.; Meyer, Steffen; Ho-Baillie, Anita; Sung Yun, Jae; MacQueen, Rowan W.; Spiccia, Leone; Green, Martin A.; Hameiri, Ziv

    2016-07-01

    In this study, we provide insights into planar structure methylammonium lead triiodide (MAPbI3) perovskite solar cells (PSCs) using electroluminescence and photoluminescence imaging techniques. We demonstrate the strength of these techniques in screening relatively large area PSCs, correlating the solar cell electrical parameters to the images and visualizing the features which contribute to the variation of the parameters extracted from current density-voltage characterizations. It is further used to investigate one of the major concerns about perovskite solar cells, their long term stability and aging. Upon storage under dark in dry glovebox condition for more than two months, the major parameter found to have deteriorated in electrical performance measurements was the fill factor; this was elucidated via electroluminescence image comparisons which revealed that the contacts' quality degrades. Interestingly, by deploying electroluminescence imaging, the significance of having a pin-hole free active layer is demonstrated. Pin-holes can grow over time and can cause degradation of the active layer surrounding them.

  16. Efficiency of Cu2O/BiVO4 particles prepared with a new soft procedure on the degradation of dyes under visible-light irradiation

    NASA Astrophysics Data System (ADS)

    Aguilera-Ruiz, Eduardo; García-Pérez, Ulises M.; de la Garza-Galván, María; Zambrano-Robledo, Patricia; Bermúdez-Reyes, Bárbara; Peral, José

    2015-02-01

    Cu2O/BiVO4 composites with different concentrations of Cu2O were synthesized by a simple impregnation method at 200 °C under N2 atmosphere for 4 h. The as-synthesized samples were characterized by X-ray powder diffraction, scanning electron microscopy, UV-vis diffuse reflection absorption and vis photoluminescence. The morphology of the as-synthesized composites with different weight ratios of Cu2O is composed by quasi-spherical and dendrite-like particles. The photocatalytic performance of the Cu2O/BiVO4 composites was evaluated by degradation of methyl orange solutions under visible-LED irradiation. The results obtained show that the photocatalytic behavior of the p-n heterojunction Cu2O/BiVO4 composites was better than pure Cu2O and BiVO4. The variation of the reaction parameters, such as solution pH and presence of O2, improved the photocatalytic performance of Cu2O/BiVO4 composite. Meanwhile, a possible mechanism for methyl orange photocatalytic degradation over Cu2O/BiVO4 photocatalysts was proposed. The chemical stability and reusability of Cu2O/BiVO4 powders were also investigated.

  17. Microbial degradation of lignin: how a bulky recalcitrant polymer is efficiently recycled in nature and how we can take advantage of this

    PubMed Central

    Ruiz‐Dueñas, Francisco J.; Martínez, Ángel T.

    2009-01-01

    Summary Lignin is the second most abundant constituent of the cell wall of vascular plants, where it protects cellulose towards hydrolytic attack by saprophytic and pathogenic microbes. Its removal represents a key step for carbon recycling in land ecosystems, as well as a central issue for industrial utilization of plant biomass. The lignin polymer is highly recalcitrant towards chemical and biological degradation due to its molecular architecture, where different non‐phenolic phenylpropanoid units form a complex three‐dimensional network linked by a variety of ether and carbon–carbon bonds. Ligninolytic microbes have developed a unique strategy to handle lignin degradation based on unspecific one‐electron oxidation of the benzenic rings in the different lignin substructures by extracellular haemperoxidases acting synergistically with peroxide‐generating oxidases. These peroxidases posses two outstanding characteristics: (i) they have unusually high redox potential due to haem pocket architecture that enables oxidation of non‐phenolic aromatic rings, and (ii) they are able to generate a protein oxidizer by electron transfer to the haem cofactor forming a catalytic tryptophanyl‐free radical at the protein surface, where it can interact with the bulky lignin polymer. The structure–function information currently available is being used to build tailor‐made peroxidases and other oxidoreductases as industrial biocatalysts. PMID:21261911

  18. A Stability-Indicating HPLC-DAD Method for Determination of Ferulic Acid into Microparticles: Development, Validation, Forced Degradation, and Encapsulation Efficiency

    PubMed Central

    Toledo, Maria da Graça; Pupo, Yasmine Mendes; Padilha de Paula, Josiane; Zanin, Sandra Maria Warumby

    2015-01-01

    A simple stability-indicating HPLC-DAD method was validated for the determination of ferulic acid (FA) in polymeric microparticles. Chromatographic conditions consisted of a RP C18 column (250 mm × 4.60 mm, 5 μm, 110 Å) using a mixture of methanol and water pH 3.0 (48 : 52 v/v) as mobile phase at a flow rate of 1.0 mL/min with UV detection at 320 nm. The developed method was validated as per ICH guidelines with respect to specificity, linearity, limit of quantification, limit of detection, accuracy, precision, and robustness provided suitable results regarding all parameters investigated. The calibration curve was linear in the concentration range of 10.0–70.0 μg/mL with a correlation coefficient >0.999. Precision (intraday and interday) was demonstrated by a relative standard deviation lower than 2.0%. Accuracy was assessed by the recovery test of FA from polymeric microparticles (99.02% to 100.73%). Specificity showed no interference from the components of polymeric microparticles or from the degradation products derived from acidic, basic, and photolytic conditions. In conclusion, the method is suitable to be applied to assay FA as bulk drug and into polymeric microparticles and can be used for studying its stability and degradation kinetics. PMID:26075139

  19. The MIT domain of UBPY constitutes a CHMP binding and endosomal localization signal required for efficient epidermal growth factor receptor degradation.

    PubMed

    Row, Paula E; Liu, Han; Hayes, Sebastian; Welchman, Rebecca; Charalabous, Panagoula; Hofmann, Kay; Clague, Michael J; Sanderson, Christopher M; Urbé, Sylvie

    2007-10-19

    We have identified and characterized a Microtubule Interacting and Transport (MIT) domain at the N terminus of the deubiquitinating enzyme UBPY/USP8. In common with other MIT-containing proteins such as AMSH and VPS4, UBPY can interact with CHMP proteins, which are known to regulate endosomal sorting of ubiquitinated receptors. Comparison of binding preferences for the 11 members of the human CHMP family between the UBPY MIT domain and another ubiquitin isopeptidase, AMSH, reveals common interactions with CHMP1A and CHMP1B but a distinct selectivity of AMSH for CHMP3/VPS24, a core subunit of the ESCRT-III complex, and UBPY for CHMP7. We also show that in common with AMSH, UBPY deubiquitinating enzyme activity can be stimulated by STAM but is unresponsive to its cognate CHMPs. The UBPY MIT domain is dispensable for its catalytic activity but is essential for its localization to endosomes. This is functionally significant as an MIT-deleted UBPY mutant is unable to rescue its binding partner STAM from proteasomal degradation or reverse a block to epidermal growth factor receptor degradation imposed by small interfering RNA-mediated depletion of UBPY.

  20. A Stability-Indicating HPLC-DAD Method for Determination of Ferulic Acid into Microparticles: Development, Validation, Forced Degradation, and Encapsulation Efficiency.

    PubMed

    Nadal, Jessica Mendes; Toledo, Maria da Graça; Pupo, Yasmine Mendes; Padilha de Paula, Josiane; Farago, Paulo Vitor; Zanin, Sandra Maria Warumby

    2015-01-01

    A simple stability-indicating HPLC-DAD method was validated for the determination of ferulic acid (FA) in polymeric microparticles. Chromatographic conditions consisted of a RP C18 column (250 mm × 4.60 mm, 5 μm, 110 Å) using a mixture of methanol and water pH 3.0 (48 : 52 v/v) as mobile phase at a flow rate of 1.0 mL/min with UV detection at 320 nm. The developed method was validated as per ICH guidelines with respect to specificity, linearity, limit of quantification, limit of detection, accuracy, precision, and robustness provided suitable results regarding all parameters investigated. The calibration curve was linear in the concentration range of 10.0-70.0 μg/mL with a correlation coefficient >0.999. Precision (intraday and interday) was demonstrated by a relative standard deviation lower than 2.0%. Accuracy was assessed by the recovery test of FA from polymeric microparticles (99.02% to 100.73%). Specificity showed no interference from the components of polymeric microparticles or from the degradation products derived from acidic, basic, and photolytic conditions. In conclusion, the method is suitable to be applied to assay FA as bulk drug and into polymeric microparticles and can be used for studying its stability and degradation kinetics.

  1. Features of the electroluminescence spectra of quantum-confined silicon p{sup +}-n heterojunctions in the infrared spectral region

    SciTech Connect

    Bagraev, N. T.; Klyachkin, L. E.; Kuzmin, R. V. Malyarenko, A. M.; Mashkov, V. A.

    2013-11-15

    The results of studying the characteristics of optical emission in various regions of quantum-confined silicon p{sup +}-n heterojunctions heavily doped with boron are analyzed. The results obtained allow one to conclude that near-infrared electroluminescence arises near the heterointerface between the nanostructured wide-gap silicon p{sup +}-barrier heavily doped with boron and n-type silicon (100), the formation of which included the active involvement of boron dipole centers.

  2. Electroluminescence enhancement of glass/ITO/PEDOT:PSS/MEH-PPV/PEDOT:PSS/Al OLED by thermal annealing

    NASA Astrophysics Data System (ADS)

    Hewidy, Dina; Gadallah, A.-S.; Fattah, G. Abdel

    2017-02-01

    Manufacturing of glass/ITO/PEDOT:PSS/MEH-PPV/PEDOT:PSS/Al organic light emitting diode (OLED) by depositing PEDOT:PSS/MEH-PPV/PEDOT:PSS using spin coating has been reported. The roles of PEDOT:PSS in the structure have been reported. It allows transportation of holes from ITO to the highest occupied molecular orbit (HOMO) of MEH-PPV. In additions, it allows transportation of electrons from Al to lowest unoccupied molecular orbit (LUMO) of MEH:PPV. Further, it confines electrons in the LUMO of MEH:PPV due to the higher barrier of PEDOT:PSS of LUMO. The effect of thermal annealing on the current-voltage curve as well as on the electroluminescence intensity has been reported. The results show that the current increased from 25 mA to 52 mA at 7 V, when the sample was thermally annealed at 150 °C. Such enhancement in electrical injection leads to enhancement of the electroluminescence to a factor of 4.7 at the peak luminescence wavelength (∼592 nm). Reasons for electroluminescence improvement caused by thermal annealing have been proposed.

  3. Pd-catalytic in situ generation of H2O2 from H2 and O2 produced by water electrolysis for the efficient electro-fenton degradation of rhodamine B.

    PubMed

    Yuan, Songhu; Fan, Ye; Zhang, Yucheng; Tong, Man; Liao, Peng

    2011-10-01

    A novel electro-Fenton process was developed for wastewater treatment using a modified divided electrolytic system in which H2O2 was generated in situ from electro-generated H2 and O2 in the presence of Pd/C catalyst. Appropriate pH conditions were obtained by the excessive H+ produced at the anode. The performance of the novel process was assessed by Rhodamine B (RhB) degradation in an aqueous solution. Experimental results showed that the accumulation of H2O2 occurred when the pH decreased and time elapsed. The maximum concentration of H2O2 reached 53.1 mg/L within 120 min at pH 2 and a current of 100 mA. Upon the formation of the Fenton reagent by the addition of Fe2+, RhB degraded completely within 30 min at pH 2 with a pseudo first order rate constant of 0.109 ± 0.009 min(-1). An insignificant decline in H2O2 generation and RhB degradation was found after six repetitions. RhB degradation was achieved by the chemisorption of H2O2 on the Pd/C surface, which subsequently decomposed into •OH upon catalysis by Pd0 and Fe2+. The catalytic decomposition of H2O2 to •OH by Fe2+ was more powerful than that by Pd0, which was responsible for the high efficiency of this novel electro-Fenton process.

  4. Microbial degradation of herbicides.

    PubMed

    Singh, Baljinder; Singh, Kashmir

    2016-01-01

    Herbicides remain the most effective, efficient and economical way to control weeds; and its market continues to grow even with the plethora of generic products. With the development of herbicide-tolerant crops, use of herbicides is increasing around the world that has resulted in severe contamination of the environment. The strategies are now being developed to clean these substances in an economical and eco-friendly manner. In this review, an attempt has been made to pool all the available literature on the biodegradation of key herbicides, clodinafop propargyl, 2,4-dichlorophenoxyacetic acid, atrazine, metolachlor, diuron, glyphosate, imazapyr, pendimethalin and paraquat under the following objectives: (1) to highlight the general characteristic and mode of action, (2) to enlist toxicity in animals, (3) to pool microorganisms capable of degrading herbicides, (4) to discuss the assessment of herbicides degradation by efficient microbes, (5) to highlight biodegradation pathways, (6) to discuss the molecular basis of degradation, (7) to enlist the products of herbicides under degradation process, (8) to highlight the factors effecting biodegradation of herbicides and (9) to discuss the future aspects of herbicides degradation. This review may be useful in developing safer and economic microbiological methods for cleanup of soil and water contaminated with such compounds.

  5. Strong room temperature electroluminescence from lateral p-SiGe/i-Ge/n-SiGe heterojunction diodes on silicon-on-insulator substrate

    NASA Astrophysics Data System (ADS)

    Lin, Guangyang; Yi, Xiaohui; Li, Cheng; Chen, Ningli; Zhang, Lu; Chen, Songyan; Huang, Wei; Wang, Jianyuan; Xiong, Xihuan; Sun, Jiaming

    2016-10-01

    A lateral p-Si0.05Ge0.95/i-Ge/n-Si0.05Ge0.95 heterojunction light emitting diode on a silicon-on-insulator (SOI) substrate was proposed, which is profitable to achieve higher luminous extraction compared to vertical junctions. Due to the high carrier injection ratio of heterostructures and optical reflection at the SiO2/Si interface of the SOI, strong room temperature electroluminescence (EL) at around 1600 nm from the direct bandgap of i-Ge with 0.30% tensile strain was observed. The EL peak intensity of the lateral heterojunction is enhanced by ˜4 folds with a larger peak energy than that of the vertical Ge p-i-n homojunction, suggesting that the light emitting efficiency of the lateral heterojunction is effectively improved. The EL peak intensity of the lateral heterojunction, which increases quadratically with injection current density, becomes stronger for diodes with a wider i-Ge region. The CMOS compatible fabrication process of the lateral heterojunctions paves the way for the integration of the light source with the Ge metal-oxide-semiconductor field-effect-transistor.

  6. Synthesis, crystal structures and photo- and electro-luminescence of copper(I) complexes containing electron-transporting diaryl-1,3,4-oxadiazole.

    PubMed

    Yu, Tianzhi; Liu, Peng; Chai, Haifang; Kang, Jundan; Zhao, Yuling; Zhang, Hui; Fan, Duowang

    2014-05-01

    Two mononuclear Cu(I) complexes based on 2-(2-pyridyl)benzimidazolyl derivative ligand containing electron-transporting 1,3,4-oxadiazole group (L), [Cu(L)(PPh(3))2](BF(4)) and [Cu(L)(DPEphos)](BF(4)), where L = 1-(4-(5-(4-tert-butylphenyl)-1,3,4-oxadiazol-2-yl)benzyl)-2-(pyridin-2-yl)benzimidazole and DPEphos = bis[2-(diphenylphosphino)phenyl]ether, have been successfully synthesized and characterized. The X-ray crystal structure analyses of the ligand L and the complex [Cu(L)(PPh(3))2](BF(4)) were described. The photophysical properties of the complexes were examined by using UV-vis, photoluminescence spectroscopic analysis. The doped light-emitting devices using the Cu(I) complexes as dopants were fabricated. With no electron transporting layers employed in the devices, yellow electroluminescence from Cu(I) complexes were observed. The devices based on the complex [Cu(L)(DPEphos)](BF4) possess better performance as compared with the devices fabricated by the complex [Cu(L)(PPh(3))2](BF(4)). The devices with the structure of ITO/MoO(3) (2 nm)/NPB (40 nm)/CBP:[Cu(L)(DPEphos)](BF(4)) (8 wt%, 30 nm)/BCP (30 nm)/LiF (1 nm)/Al (150 nm) exhibit a maximum efficiency of 3.04 cd/A and a maximum brightness of 4,758 cd/m(2).

  7. Photovoltaic Degradation Risk: Preprint

    SciTech Connect

    Jordan, D. C.; Kurtz, S. R.

    2012-04-01

    The ability to accurately predict power delivery over the course of time is of vital importance to the growth of the photovoltaic (PV) industry. Important cost drivers include the efficiency with which sunlight is converted into power, how this relationship changes over time, and the uncertainty in this prediction. An accurate quantification of power decline over time, also known as degradation rate, is essential to all stakeholders - utility companies, integrators, investors, and researchers alike. In this paper we use a statistical approach based on historical data to quantify degradation rates, discern trends and quantify risks related to measurement uncertainties, number of measurements and methodologies.

  8. Ag-Decorated Localized Surface Plasmon-Enhanced Ultraviolet Electroluminescence from ZnO Quantum Dot-Based/GaN Heterojunction Diodes by Optimizing MgO Interlayer Thickness

    NASA Astrophysics Data System (ADS)

    Chen, Cheng; Chen, Jingwen; Zhang, Jun; Wang, Shuai; Zhang, Wei; Liang, Renli; Dai, Jiangnan; Chen, Changqing

    2016-10-01

    We demonstrate the fabrication and characterization of localized surface plasmon (LSP)-enhanced n-ZnO quantum dot (QD)/MgO/p-GaN heterojunction light-emitting diodes (LEDs) by embedding Ag nanoparticles (Ag-NPs) into the ZnO/MgO interface. The maximum enhancement ration of the Ag-NP-decorated LEDs in electroluminescence (EL) is 4.3-fold by optimizing MgO electron-blocking layer thickness. The EL origination was investigated qualitatively in terms of photoluminescence (PL) results. Through analysis of the energy band structure of device and carrier transport mechanisms, it suggests that the EL enhancement is attributed to the increased rate of spontaneous emission and improved internal quantum efficiency induced by exciton-LSP coupling.

  9. A new series of short axially symmetrically and asymmetrically 1,3,6,8-tetrasubstituted pyrenes with two types of substituents: Syntheses, structures, photophysical properties and electroluminescence

    NASA Astrophysics Data System (ADS)

    Zhang, Ran; Zhang, Tengfei; Xu, Lu; Han, Fangfang; Zhao, Yun; Ni, Zhonghai

    2017-01-01

    A new series of short axially symmetrically (4a and 4b) and asymmetrically (4c and 4d) 1,3,6,8-tetrasubstituted pyrene-based compounds with two phenyl moieties and two diphenylamine units on the pyrene core were designed and synthesized based on stepwise synthetic strategy. These compounds were structurally characterized and their photoelectric properties were investigated by spectroscopy, electrochemical and theoretical studies. The structures of 4a and 4b were determined by single-crystal X-ray diffraction analysis, indicating that the compounds are twisted by the peripheral substituents and the intermolecular π-π interactions have been efficiently interrupted. The four compounds exhibit high absolute fluorescence quantum yields (VF) in dichloromethane (83.31-88.45%) and moderate VFs in film states (20.78-38.68%). In addition, compounds 4a and 4b display relatively higher absolute VFs than those of 4c and 4d in film states. All the compounds exhibit high thermal stability with decomposition temperatures above 358 °C and the values of 4c and 4d are higher than 4a and 4b. Compounds 4a and 4b can form morphologically stable amorphous thin films with Tg values of 146 °C and 149 °C, respectively. However, there are no obvious Tg observed in compounds 4c and 4d. Electroluminescent devices using 4a and 4b as doped emission layer show promising device performance with low turn-on voltage (3.0 V), maximum brightness around 15100 cd/m2 and 16100 cd/m2, maximum luminance efficiency of 12.4 cd/A and 13.6 cd/A and maximum external quantum efficiency of 5.34% and 5.63%, respectively.

  10. Origin of White Electroluminescence in Graphene Quantum Dots Embedded Host/Guest Polymer Light Emitting Diodes

    PubMed Central

    Kyu Kim, Jung; Bae, Sukang; Yi, Yeonjin; Jin Park, Myung; Jin Kim, Sang; Myoung, NoSoung; Lee, Chang-Lyoul; Hee Hong, Byung; Hyeok Park, Jong

    2015-01-01

    Polymer light emitting diodes (PLEDs) using quantum dots (QDs) as emissive materials have received much attention as promising components for next-generation displays. Despite their outstanding properties, toxic and hazardous nature of QDs is a serious impediment to their use in future eco-friendly opto-electronic device applications. Owing to the desires to develop new types of nano-material without health and environmental effects but with strong opto-electrical properties similar to QDs, graphene quantum dots (GQDs) have attracted great interest as promising luminophores. However, the origin of electroluminescence from GQDs incorporated PLEDs is unclear. Herein, we synthesized graphene oxide quantum dots (GOQDs) using a modified hydrothermal deoxidization method and characterized the PLED performance using GOQDs blended poly(N-vinyl carbazole) (PVK) as emissive layer. Simple device structure was used to reveal the origin of EL by excluding the contribution of and contamination from other layers. The energy transfer and interaction between the PVK host and GOQDs guest were investigated using steady-state PL, time-correlated single photon counting (TCSPC) and density functional theory (DFT) calculations. Experiments revealed that white EL emission from the PLED originated from the hybridized GOQD-PVK complex emission with the contributions from the individual GOQDs and PVK emissions. PMID:26067060

  11. Infrared and visible emission from organic electroluminescent devices based on praseodymium complex

    NASA Astrophysics Data System (ADS)

    Hong, Ziruo; Liang, Chunjun; Li, Ruigang; Zang, Faxin; Fan, Di; Li, Wenlian; Hung, L. S.; Lee, S. T.

    2001-09-01

    Praseodymium(dibenzoylmethanato)3(bathophenanthroline) [Pr(DBM)3bath] was employed as an emitting and electron transport layer, and N,N'-diphenyl-N,N'-bis(3-methylphenyl)-1, 1'-biphenyl-4,4'-diamine (TPD) as a hole transport layer in organic electroluminescent (EL) devices. Bilayer device TPD/Pr(DBM)3bath and trilayer devices TPD/TPD:Pr(DBM)3bath/Pr(DBM)3bath with a different ratio of TPD to the Pr-complex were fabricated. Emission bands at 608 nm (1D2→3H6), 890 nm (1D2→3F2), 1015 nm (1D2→3F3), 1065 nm (1D2→3F4) and 1550 nm (1D2→1G4) originating from the internal f-f transitions of a Pr3+ ion were observed from EL devices using both bilayer and trilayer structures. Decreasing the ratio of TPD to the Pr-complex, the emission of the 1D2→3H6 transition was promoted and that from the exciplex suppressed, which was explained in terms of energy transfer from the ligand to the central ion.

  12. Size-dependent electroluminescence from Si quantum dots embedded in amorphous SiC matrix

    NASA Astrophysics Data System (ADS)

    Rui, Yunjun; Li, Shuxin; Xu, Jun; Song, Chao; Jiang, Xiaofan; Li, Wei; Chen, Kunji; Wang, Qimin; Zuo, Yuhua

    2011-09-01

    Si quantum dots (QDs) were formed by thermal annealing the hydrogenated amorphous silicon carbide films (a-SiCx:H) with different C/Si ratio x, which were controlled by using a different gas ratio R of methane to silane during the deposition process. By adjusting x and post annealing temperature, the QD size can be changed from 1.4 to 4.2 nm accordingly, which was verified by the Raman spectra and transmission electron microscopy images. Size-dependent electroluminescence (EL) was observed, and the EL intensity was higher for the sample containing small-sized Si QDs due to the quantum confinement effect (QCE). The EL peak energy as a function of the Si QDs size was in good agreement with a modified effective mass approximation (EMA) model. The calculated finite barrier potential of the Si QDs embedded in SiC matrix is 0.4 and 0.8 eV for conduction and valence band, respectively. Moreover, the current-voltage properties and the linear relationship between the integrated EL intensity and injection current indicate that the carrier transport is dominated by Fowler-Nordheim tunneling and the EL mechanism is originated from the bipolar recombination of electron-hole pairs at Si QDs. Our results demonstrate Si QDs embedded in amorphous SiC matrix has the potential application in Si-based light emitting devices and the third-generation solar cells.

  13. Modeling of electroluminescence in SrS:Ce ACTFEL display devices

    NASA Astrophysics Data System (ADS)

    Dhillon, Tarlochan Singh

    The main objective of this study was to model electroluminescence behavior of ACTFEL display devices. Qualitative comparison of the predicted results with measurable characteristics is given. It is intended to explain certain unusual behavior that other models cannot explain fully. In particular, aspects of leading and trailing edge luminance peaks, oscillations in luminance, luminance peaks due to denting in applied voltage and multiple interfacial states are analyzed. Also, optimum concentration of activators has been analytically modeled for any phosphor to get maximum light output without causing appreciable quenching. Maximum light output for ZnS:Mn yellow devices is at about 2% Mn by weight. The beginning trailing edge peak (BTE) in SrS:Ce devices can be explained based on capture of electrons by ionized activators from the bulk traps due to their proximity. Oscillations in luminance are modeled due to distinct, widely separated and deep interfacial energy states when interface of two materials is rough. It has been observed that leading edge peak and luminance peak due to denting at leading edge are intercoupled and are partially created due to impact excitation and partially due to capture of electrons by ionized activators. Luminance vs. time graph of two interfacial energy states does not match very well with the experimental results. Luminance vs. time graph for multiple energy states matches better with experimental results.

  14. Ultrathin GaN quantum disk nanowire LEDs with sub-250 nm electroluminescence

    NASA Astrophysics Data System (ADS)

    Sarwar, A. T. M. Golam; May, Brelon J.; Chisholm, Matthew F.; Duscher, Gerd J.; Myers, Roberto C.

    2016-04-01

    By quantum confining GaN at monolayer thickness with AlN barriers inside of a nanowire, deep ultraviolet LEDs are demonstrated. Full three-dimensional strain dependent energy band simulations are carried out within multiple quantum disk (MQD) GaN/AlN nanowire superlattice heterostructures. It is found that, even within the same nanowire MQD, the emission energy of the ultrathin GaN QDs varies from disk to disk due to the changing strain distribution and polarization charge induced energy band bending along the axial nanowire direction. MQD heterostructures are grown by plasma-assisted molecular beam epitaxy to form self-assembled catalyst-free nanowires with 1 to 2 monolayer thick GaN insertions within an AlN matrix. Photoluminescence peaks are observed at 295 nm and 283 nm from the 2 ML and 1 ML thick MQD samples, respectively. Polarization-doped nanowire LEDs are grown incorporating 1 ML thick GaN MQD active regions from which we observe deep ultraviolet electroluminescence. The shortest LED wavelength peak observed is 240 nm and attributed to electron hole recombination within 1 ML thick GaN QDs.

  15. Electroluminescence from ZnO/Si heterojunctions fabricated by PLD with bias voltage application

    SciTech Connect

    Seno, Yuuki; Konno, Daisuke; Komiyama, Takao; Chonan, Yasunori; Yamaguchi, Hiroyuki; Aoyama, Takashi

    2014-02-21

    Electroluminescence (EL) for ZnO films has been investigated by fabricating n-ZnO/p-Si heterojunctions and changing the VI/II (O/Zn) ratio of the films. In the photoluminescence (PL) spectra, both the near band edge (NBE) emission and the defect-related emission were observed, while in the EL spectra only defect-related emission was observed. The EL spectra were divided into three components: green (550 nm), yellow (618 nm) and red (700 nm) bands; and their intensities were compared. As the VI/II (O/Zn) ratio was increased, the red band emission intensity decreased and the green band emission intensity increased. This implies that the oxygen and the zinc vacancies are related to the red and the green band emissions, respectively. Electron transitions from the conduction band minimum (Ec) to the deep energy levels of these vacancies are suggested to cause the red and the green luminescences while the energy levels of the Zn interstitials are close to the Ec in the band gap and no NBE emission is observed.

  16. Investigations on electroluminescent tapes and foils in relation to their applications in automotive

    NASA Astrophysics Data System (ADS)

    Plotog, Ioan

    2015-02-01

    The electroluminescent (EL) tapes or foils having barrier films for an additional level of protection against the toughest environments conditions, offer a large area of applications. The EL lights, due to their characteristics, began to be used not only in the entertainment industry, but also for automotive and aerospace applications. In the paper, the investigations regarding EL foils technical performances in relation to their applications as light sources in automotive ambient light were presented. The experiments were designed based on the results of EL foils electrical properties previous investigations done in laboratory conditions, taking into account the range of automotive ambient temperatures for sinusoidal alternative supply voltage. The measurements for different temperatures were done by keeping the EL foils into electronic controlled oven that ensures the dark enclosure offering conditions to use a lux-meter in order to measure and maintain under control light emission intensity. The experiments results define the EL foils characteristics as load in automotive ambient temperatures condition, assuring so the data for optimal design of a dedicated inverter.

  17. Pure circular polarization electroluminescence at room temperature with spin-polarized light-emitting diodes.

    PubMed

    Nishizawa, Nozomi; Nishibayashi, Kazuhiro; Munekata, Hiro

    2017-02-21

    We report the room-temperature electroluminescence (EL) with nearly pure circular polarization (CP) from GaAs-based spin-polarized light-emitting diodes (spin-LEDs). External magnetic fields are not used during device operation. There are two small schemes in the tested spin-LEDs: first, the stripe-laser-like structure that helps intensify the EL light at the cleaved side walls below the spin injector Fe slab, and second, the crystalline AlO x spin-tunnel barrier that ensures electrically stable device operation. The purity of CP is depressively low in the low current density (J) region, whereas it increases steeply and reaches close to the pure CP when J > 100 A/cm(2) There, either right- or left-handed CP component is significantly suppressed depending on the direction of magnetization of the spin injector. Spin-dependent reabsorption, spin-induced birefringence, and optical spin-axis conversion are suggested to account for the observed experimental results.

  18. Electroluminescence from GeSn heterostructure pin diodes at the indirect to direct transition

    SciTech Connect

    Gallagher, J. D.; Menéndez, J.; Senaratne, C. L.; Sims, P.; Kouvetakis, J.; Aoki, T.

    2015-03-02

    The emission properties of GeSn heterostructure pin diodes have been investigated. The devices contain thick (400–600 nm) Ge{sub 1−y}Sn{sub y} i-layers spanning a broad compositional range below and above the crossover Sn concentration y{sub c} where the Ge{sub 1−y}Sn{sub y} alloy becomes a direct-gap material. These results are made possible by an optimized device architecture containing a single defected interface thereby mitigating the deleterious effects of mismatch-induced defects. The observed emission intensities as a function of composition show the contributions from two separate trends: an increase in direct gap emission as the Sn concentration is increased, as expected from the reduction and eventual reversal of the separation between the direct and indirect edges, and a parallel increase in non-radiative recombination when the mismatch strains between the structure components is partially relaxed by the generation of misfit dislocations. An estimation of recombination times based on the observed electroluminescence intensities is found to be strongly correlated with the reverse-bias dark current measured in the same devices.

  19. Blue and green electroluminescence from CdSe nanocrystal quantum-dot-quantum-wells

    SciTech Connect

    Lu, Y. F.; Cao, X. A.

    2014-11-17

    CdS/CdSe/ZnS quantum dot quantum well (QDQW) nanocrystals were synthesized using the successive ion layer adsorption and reaction technique, and their optical properties were tuned by bandgap and strain engineering. 3-monolayer (ML) CdSe QWs emitted blue photoluminescence at 467 nm with a spectral full-width-at-half-maximum of ∼30 nm. With a 3 ML ZnS cladding layer, which also acts as a passivating and strain-compensating layer, the QDQWs acquired a ∼35% quantum yield of the QW emission. Blue and green electroluminescence (EL) was obtained from QDQW light-emitting devices with 3–4.5 ML CdSe QWs. It was found that as the peak blueshifted, the overall EL was increasingly dominated by defect state emission due to poor hole injection into the QDQWs. The weak EL was also attributed to strong field-induced charge separation resulting from the unique QDQW geometry, weakening the oscillator strength of optical transitions.

  20. Ultrathin GaN quantum disk nanowire LEDs with sub-250 nm electroluminescence

    SciTech Connect

    Chisholm, Matthew F.; Golam Sarwar, A. T. M.; Myers, Roberto C.; Mays, Brelon J.; Duscher, Gerd J.

    2016-03-18

    By quantum confining GaN at monolayer thickness with AlN barriers inside of a nanowire, deep ultraviolet LEDs are demonstrated. Full three-dimensional strain dependent energy band simulations are carried out within multiple quantum disk (MQD) GaN/AlN nanowire superlattice heterostructures. It is found that, even within the same nanowire MQD, the emission energy of the ultrathin GaN QDs varies from disk to disk due to the changing strain distribution and polarization charge induced energy band bending along the axial nanowire direction. MQD heterostructures are grown by plasma-assisted molecular beam epitaxy to form self-assembled catalyst-free nanowires with 1 to 2 monolayer thick GaN insertions within an AlN matrix. Photoluminescence peaks are observed at 295 nm and 283 nm from the 2 ML and 1 ML thick MQD samples, respectively. Polarization-doped nanowire LEDs are grown incorporating 1 ML thick GaN MQD active regions from which we observe deep ultraviolet electroluminescence. As a result, the shortest LED wavelength peak observed is 240 nm and attributed to electron hole recombination within 1 ML thick GaN QDs.