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Sample records for 1s core-shell excitons

  1. Final-state symmetry of Na 1s core-shell excitons in NaCl and NaF

    SciTech Connect

    Nagle, K.P.; Seidler, G.T.; Shirley, E.L.; Fister, T.T.; Bradley, J.A.; Brown, F.C.

    2009-08-13

    We report measurements of the Na 1s contribution to the nonresonant inelastic x-ray scattering (NRIXS) from NaCl and NaF. Prior x-ray absorption studies have observed two pre-edge excitons in both materials. The momentum-transfer dependence (q dependence) of the measured NRIXS cross section and of real-space full multiple scattering and Bethe-Salpeter calculations determine that the higher-energy core excitons are s type for each material. The lower-energy core excitons contribute at most weakly to the NRIXS signal and we propose that these may be surface core excitons, as have been observed in several other alkali halides. The analysis of the orbital angular momentum of these features leads to a discussion of the limited sensitivity of NRIXS measurements to d-type final states when investigating 1s initial states. In this case the s- and p-type final density of states can be characterized by measurements at a small number of momentum transfers. This is in contrast to the case of more complex initial states for which measurements at a large number of momentum transfers are needed to separate the rich admixture of accessible and contributing final-state symmetries.

  2. Exciton Formation and Quenching in a Au/CdS Core/Shell Nanostructure.

    PubMed

    Ziemannn, Dirk; May, Volkhard

    2015-10-15

    An atomistic description is presented of the excited state dynamics in spherical Au/CdS core/shell nanocrystals up to a diameter of 15 nm. Au-core excited states are considered in a multipole plasmon scheme, whereas a tight-binding description combined with a configuration interaction approach is used to compute single electron-hole pair excitations in the CdS-shell. The electron-hole pair energy-shift and screening due to an Au-core polarization is found of minor importance. For the studied system, the energy transfer coupling can be identified as the essential core-shell interaction. Characterizing the CdS-shell excitons by atomic centered transition charges and the Au-core by its multipole plasmon moments, an energy transfer coupling can be introduced that gives a complete microscopic description beyond any dipole-dipole approximation and with values around 10 meV. Together with a considerable plasmon-exciton energy mismatch, these coupling values explain the measured 300 ps lifetime of shell excitons due to energy transfer to the Au-core. PMID:26722776

  3. Influence of Exciton Localization on the Emission and Ultraviolet Photoresponse of ZnO/ZnS Core-Shell Nanowires.

    PubMed

    Fang, Xuan; Wei, Zhipeng; Chen, Rui; Tang, Jilong; Zhao, Haifeng; Zhang, Ligong; Zhao, Dongxu; Fang, Dan; Li, Jinhua; Fang, Fang; Chu, Xueying; Wang, Xiaohua

    2015-05-20

    The structural and optical properties of ZnO and ZnO/ZnS core-shell nanowires grown by a wet chemical method are investigated. The near-bandgap ultraviolet (UV) emission of the ZnO nanowires was enhanced by four times after coating with ZnS. The enhanced emission was attributed to surface passivation of the ZnO nanowires and localized states introduced during ZnS growth. The emission of the ZnO and ZnO/ZnS core-shell nanowires was attributed to neutral donor-bound excitons and localized excitons, respectively. Localized states prevented excitons from diffusing to nonradiative recombination centers, so therefore contributed to the enhanced emission. Emission from the localized exciton was not sensitive to temperature, so emission from the ZnO/ZnS core-shell nanowires was more stable at higher temperature. UV photodetectors based on the ZnO and ZnO/ZnS core-shell nanowires were fabricated. Under UV excitation, the device based on the ZnO/ZnS core-shell nanowires exhibited a photocurrent approximately 40 times higher than that of the device based on the ZnO nanowires. The differing photoresponse of the detectors was consistent with the existence of surface passivation and localized states. This study provides a means for modifying the optical properties of ZnO materials, and demonstrates the potential of ZnO/ZnS core-shell nanowires in UV excitonic emission and detection. PMID:25918945

  4. Excitonic Diffusion in InGaN/GaN Core-Shell Nanowires.

    PubMed

    Shahmohammadi, M; Ganière, J-D; Zhang, H; Ciechonski, R; Vescovi, G; Kryliouk, O; Tchernycheva, M; Jacopin, G

    2016-01-13

    We report on the direct observation of the diffusion of carriers in graded InGaN/GaN quantum wells in a nanowire. By probing the local dynamics at the nanoscale, along the wire for different temperatures between 4 and 250 K, we conclude that this diffusion process is thermally activated. In addition, the analysis of the cathodoluminescence lifetime for different temperatures shows that the carrier motion is isotropic and does not follow the indium gradient. Our observations are interpreted in terms of a hopping process between localized states. We find that the random alloy fluctuations prevent any directional drift of excitons along the In gradient and therefore any carrier accumulation. Our results therefore confirm the potential of core-shell nanowires for lighting devices. Indeed, the short lifetime of m-plane quantum wells together with their large active area and the homogeneous distribution of carrier along the quantum well will decrease influence of any high carrier density effect on the efficiency of these light-emitting diodes. PMID:26674850

  5. Exciton and carrier dynamics in ZnTe-Zn1 -xMgxTe core-shell nanowires

    NASA Astrophysics Data System (ADS)

    Szymura, M.; Kłopotowski, Ł.; Mitioglu, A. A.; Wojnar, P.; Karczewski, G.; Wojtowicz, T.; Maude, D. K.; Plochocka, P.; Kossut, J.

    2016-04-01

    We employ time-resolved photoluminescence combined with scanning electron microscopy and modeling to evaluate the lifetimes of excitons and free carriers in core-shell ZnTe -Zn1 -xMgxTe nanowires. We find that electron tunneling through the shell to the surface controls the decay dynamics. The photoluminescence of single nanowires reveals contributions from an electron-hole plasma. The analysis of its temporal behavior allows one to extract the carrier and exciton lifetimes and monitor the cooling dynamics. In particular, we demonstrate that most of the electrons tunnel out before they cool down or bind into excitons. A semiclassical model allows us to extract the contributions of tunneling and recombination to the photoluminescence decay. We find that the recombination time shortens with increasing temperature as a result of an activation of a phonon-assisted nonradiative process.

  6. Ultraviolet Electroluminescence from ZnS@ZnO Core-Shell Nanowires/p-GaN Introduced by Exciton Localization.

    PubMed

    Fang, Xuan; Wei, Zhipeng; Yang, Yahui; Chen, Rui; Li, Yongfeng; Tang, Jilong; Fang, Dan; Jia, Huimin; Wang, Dengkui; Fan, Jie; Ma, Xiaohui; Yao, Bin; Wang, Xiaohua

    2016-01-27

    We investigate the electroluminescence (EL) from light emitting diodes (LEDs) of ZnO nanowires/p-GaN structure and ZnS@ZnO core-shell nanowires/p-GaN structure. With the increase of forward bias, the emission peak of ZnO nanowires/p-GaN structure heterojunction shows a blue-shift, while the ZnS@ZnO core-shell nanowires/p-GaN structure demonstrates a changing EL emission; the ultraviolet (UV) emission at 378 nm can be observed. This discrepancy is related to the localized states introduced by ZnS particles, which results in a different carrier recombination process near the interfaces of the heterojunction. The localized states capture the carriers in ZnO nanowires and convert them to localized excitons under high forward bias. A strong UV emission due to localized excitons can be observed. Our results indicated that utilizing localized excitons should be a new route toward ZnO-based ultraviolet LEDs with high efficiency. PMID:26710654

  7. Experimental evidence of exciton-plasmon coupling in densely packed dye doped core-shell nanoparticles obtained via microfluidic technique

    NASA Astrophysics Data System (ADS)

    De Luca, A.; Iazzolino, A.; Salmon, J.-B.; Leng, J.; Ravaine, S.; Grigorenko, A. N.; Strangi, G.

    2014-09-01

    The interplay between plasmons and excitons in bulk metamaterials are investigated by performing spectroscopic studies, including variable angle pump-probe ellipsometry. Gain functionalized gold nanoparticles have been densely packed through a microfluidic chip, representing a scalable process towards bulk metamaterials based on self-assembly approach. Chromophores placed at the hearth of plasmonic subunits ensure exciton-plasmon coupling to convey excitation energy to the quasi-static electric field of the plasmon states. The overall complex polarizability of the system, probed by variable angle spectroscopic ellipsometry, shows a significant modification under optical excitation, as demonstrated by the behavior of the ellipsometric angles Ψ and Δ as a function of suitable excitation fields. The plasmon resonances observed in densely packed gain functionalized core-shell gold nanoparticles represent a promising step to enable a wide range of electromagnetic properties and fascinating applications of plasmonic bulk systems for advanced optical materials.

  8. Exciton-trion transitions in single CdSe-CdS core-shell nanocrystals.

    PubMed

    Gómez, Daniel E; van Embden, Joel; Mulvaney, Paul; Fernée, Mark J; Rubinsztein-Dunlop, Halina

    2009-08-25

    We report on the observation of an intermediate state in the blinking of single CdSe/CdS core-shell nanocrystals. This state has a low quantum yield and connects the "on" and "off" states commonly observed in the photoluminescence blinking of individual nanocrystals. We find that the transitions between these two emitting states follow nearly single-exponential statistics. The transitions from the "on" state to this intermediate state result from changes in the surface passivation of the nanocrystal. The data are consistent with photoinduced, adsorption/desorption events that take place at the surface of the nanocrystals. The trion state leads to a reduction in photoluminescence in nanocrystals. PMID:19655720

  9. Exciton-Plasmon Coupling in Metal-Nanoparticle-Decorated ZnO/MgO Core-Shell Nanowires

    NASA Astrophysics Data System (ADS)

    Mayo, Daniel; Marvinney, Claire; Bililign, Ephraim; McBride, James; Mu, Richard; Haglund, Richard

    2014-03-01

    Zinc oxide has emerged as one of the most promising optoelectronic materials due to its direct bandgap of 3.37 eV and large exciton binding energy of 60 meV. Room temperature photoluminescence (PL) spectra for ZnO exhibit a sharply defined exciton recombination peak centered at 3.3 eV and a broad visible defect peak centered around 2.3. A wide range of optoelectronic devices, including LEDs, lasers and sensors, have been developed by tuning ZnO emission through different growth, annealing, and doping conditions. However, one of the most effective methods for PL enhancement is through coupling of localized surface plasmons of metal nanoparticles to the ZnO luminescent centers. ZnO nanowires are decorated variously with Ag, Al, and Au nanoparticles, with an insulating MgO interlayer used to differentiate plasmon-mediated emission due to hot-electron transfer from that due to local field effects. In addition, at specific MgO thicknesses, Fabry-Perot resonators within the core-shell nanowires result in dramatic enhancement of the band-edge PL while the visible emission remains unaffected. A large variation in the band-edge emission occurs for the various nanoparticle species, with Al exhibiting the strongest plasmonic coupling and therefore the highest PL enhancement.

  10. Excitonic fine structure splitting in ZnTe/ZnX (X = S and Se) core/shell nanocrystals: Atomistic tight-binding theory

    NASA Astrophysics Data System (ADS)

    Sukkabot, Worasak

    2016-03-01

    Implementing the atomistic tight-binding theory in the conjunction with a configuration interaction method of coulomb and exchange description, the excitonic fine structure splitting (FSS) in core/shell semiconductor nanocrystals is usually caused by the intrinsic electron-hole exchange interaction. I demonstrate the control of the excitonic fine structure splitting by suitably engineering the type of the band alignments and the thickness of the growth shell. ZnTe/ZnS and ZnTe/ZnSe core/shell nanocrystals exhibiting the type-I and type-II band profile are used to be the simulated candidates with various growth shell thicknesses. The detailed calculations, consisting of single-particle spectra, optical band gaps, ground-state wave function overlaps, ground-state oscillation strengths, ground-state coulomb energies, ground-state exchange energies and excitonic splitting energies, are all sensitive with the type and dimension of the coated shells. The simulations highlight that ZnTe/ZnSe type-II core/shell nanocrystals with the thick growth shell can offer an intensely reduced excitonic splitting as defined by an associated reduction of electron-hole exchange interaction. This insight is important for the theoretical understanding and practical control by the type of the band alignments and sizes in the growth shell for the quantum state of the emitted light from a biexciton cascade recombination process which will be implemented to the entangled photon source in the novel application of quantum information processing.

  11. Photo-induced exciton generation in polyvinylpyrrolidone encapsulated Ag2S core-shells: Electrochemical deposition, regular shape and high order of particle size distribution

    NASA Astrophysics Data System (ADS)

    Mukherjee, Nillohit; Jana, Sumanta; Gopal Khan, Gobinda; Mondal, Anup

    2012-12-01

    Visible light induced frequency switching behavior, exhibited by the electrochemically deposited thin films of polyvinylpyrrolidone (PVP) encapsulated Ag2S nanosphere (core-shell) is shown here. A low frequency (˜40 Hz) pulse was found to be generated upon illumination with 1 Sun due to excitonic transition, which also showed good switching behavior with the "on" and "off" state of the light. Capping of the semiconductor surface by a polymer like PVP reduces the surface states and thus lowers the built in barrier height and the width of depletion region. So, the number of photo generated but non recombining electron-hole pairs (excitons) increases, which put their signature in some unique physical properties like increase in photoluminescence (PL) intensity, light induced frequency switching behavior due to free exciton generation, etc. Here, the depositions were carried out on indium tin oxide coated glass substrates from an aqueous solution of AgNO3, thioacetamide, and PVP. The films were structurally characterized using high resolution X-ray diffraction, field emission scanning electron microscopy, and high resolution transmission electron microscopic techniques. The deposited particles were regular in shape with significantly high order of size distribution. Furrier transform infrared spectroscopy confirmed the presence of PVP as the encapsulating agent. Optical characterization, viz., UV - vis - NIR and NIR-PL revealed noteworthy amount of NIR emission from the deposited material.

  12. Comparative study of the exciton states in CdSe/ZnS core-shell quantum dots under applied electric fields with and without permanent electric dipole moment

    NASA Astrophysics Data System (ADS)

    Cristea, M.

    2016-04-01

    Due to its non-centrosymmetric wurtzite crystal structure, the CdSe dot presents a permanent electric dipole moment. In this paper we study the effect of an electric applied field on the emission wavelength of a CdSe/ZnS core-shell quantum dot with a permanent electric dipole. The electron and hole single-particle energy and wave function in the presence of an electric dipole are obtained in the effective-mass and parabolic-band approximation for various electric field strengths. The Schrödinger equation was solved by use of the finite element method. The exciton binding energy is calculated in the first-order perturbation theory and the optical emission wavelengths are found and compared to the experimental values. We find that the photoluminescence emission can be tuned by varying the electric dipole size, the electric field strength and by an appropriate orientation between the permanent dipole moment and applied electric field.

  13. Exciton delocalization and hot hole extraction in CdSe QDs and CdSe/ZnS type 1 core shell QDs sensitized with newly synthesized thiols

    NASA Astrophysics Data System (ADS)

    Singhal, Pallavi; Ghorpade, Prashant V.; Shankarling, Ganapati S.; Singhal, Nancy; Jha, Sanjay K.; Tripathi, Raj M.; Ghosh, Hirendra N.

    2016-01-01

    The present work describes ultrafast thermalized and hot hole transfer processes from photo-excited CdSe quantum dots (QDs) and CdSe/ZnS core-shell QDs (CSQDs) to newly synthesized thiols. Three thiols namely 2-mercapto-N-phenylacetamide (AAT), 3-mercapto-N-phenylpropanamide (APT) and 3-mercapto-N-(4-methoxyphenyl) propanamide (ADPT) were synthesized and their interaction with both CdSe QDs and CdSe/ZnS CSQDs was monitored. Steady state absorption study suggests the exciton delocalization from CdSe QDs in the presence of the thiols. However similar features were not observed in the presence of a ZnS shell over a CdSe core, instead a broadening in the excitonic peak was observed with both APT and ADPT but not with AAT. This exciton delocalization and broadening in the excitonic peak was also confirmed by ultrafast transient absorption studies. Steady state and time resolved emission studies show hole transfer from photo-excited QDs and CSQDs to the thiols. A signature of hot hole extraction was observed in transient absorption studies which was confirmed by fluorescence upconversion studies. Both hot and thermalized hole transfer rates from CdSe QDs and CdSe/ZnS CSQDs to the thiols were determined using the fluorescence up-conversion technique. Experiments with different ZnS shell thicknesses have been carried out which suggest that hole transfer is possible till 2.5 monolayer of the ZnS shell. To the best of our knowledge we are reporting for the first time the extraction of hot holes from CdSe/ZnS type I CSQDs by a molecular adsorbate.The present work describes ultrafast thermalized and hot hole transfer processes from photo-excited CdSe quantum dots (QDs) and CdSe/ZnS core-shell QDs (CSQDs) to newly synthesized thiols. Three thiols namely 2-mercapto-N-phenylacetamide (AAT), 3-mercapto-N-phenylpropanamide (APT) and 3-mercapto-N-(4-methoxyphenyl) propanamide (ADPT) were synthesized and their interaction with both CdSe QDs and CdSe/ZnS CSQDs was monitored. Steady

  14. Exciton delocalization and hot hole extraction in CdSe QDs and CdSe/ZnS type 1 core shell QDs sensitized with newly synthesized thiols.

    PubMed

    Singhal, Pallavi; Ghorpade, Prashant V; Shankarling, Ganapati S; Singhal, Nancy; Jha, Sanjay K; Tripathi, Raj M; Ghosh, Hirendra N

    2016-01-28

    The present work describes ultrafast thermalized and hot hole transfer processes from photo-excited CdSe quantum dots (QDs) and CdSe/ZnS core-shell QDs (CSQDs) to newly synthesized thiols. Three thiols namely 2-mercapto-N-phenylacetamide (AAT), 3-mercapto-N-phenylpropanamide (APT) and 3-mercapto-N-(4-methoxyphenyl) propanamide (ADPT) were synthesized and their interaction with both CdSe QDs and CdSe/ZnS CSQDs was monitored. Steady state absorption study suggests the exciton delocalization from CdSe QDs in the presence of the thiols. However similar features were not observed in the presence of a ZnS shell over a CdSe core, instead a broadening in the excitonic peak was observed with both APT and ADPT but not with AAT. This exciton delocalization and broadening in the excitonic peak was also confirmed by ultrafast transient absorption studies. Steady state and time resolved emission studies show hole transfer from photo-excited QDs and CSQDs to the thiols. A signature of hot hole extraction was observed in transient absorption studies which was confirmed by fluorescence upconversion studies. Both hot and thermalized hole transfer rates from CdSe QDs and CdSe/ZnS CSQDs to the thiols were determined using the fluorescence up-conversion technique. Experiments with different ZnS shell thicknesses have been carried out which suggest that hole transfer is possible till 2.5 monolayer of the ZnS shell. To the best of our knowledge we are reporting for the first time the extraction of hot holes from CdSe/ZnS type I CSQDs by a molecular adsorbate. PMID:26698125

  15. Optical properties and exciton dynamics of alloyed core/shell/shell Cd(1-x)Zn(x)Se/ZnSe/ZnS quantum dots.

    PubMed

    Fitzmorris, Bob C; Pu, Ying-Chih; Cooper, Jason K; Lin, Yi-Fang; Hsu, Yung-Jung; Li, Yat; Zhang, Jin Z

    2013-04-24

    In this study we introduce a new method for the one-pot synthesis of core/shell/shell alloyed Cd1-xZnxSe/ZnSe/ZnS QDs and examine the effect of the shell coating on the optical properties and exciton dynamics of the alloy core. The photoluminescence (PL) quantum yield is greatly enhanced after shell growth, from 9.6% to 63%. The exciton dynamics were studied by time correlated single photon counting (TCSPC) and fit using integrated singular value decomposition global fitting (i-SVD-GF), which showed the biexponential observed lifetimes on the nanosecond time scale remain the same after shell growth. Using ultrafast transient absorption (TA) spectroscopy and SVD-GF, we have determined that surface passivation by ZnSe and ZnSe/ZnS shells reduces nonradiative recombination primarily on the picosecond time scale. These findings are helpful in directing the development of the next generation of QDs for biological labeling and other applications. PMID:23469824

  16. Cadmium Telluride, Cadmium Telluride/Cadmium Sulfide Core/Shell, and Cadmium Telluride/Cadmium Sulfide/Zinc Sulfide Core/Shell/Shell Quantum Dots Study

    NASA Astrophysics Data System (ADS)

    Yan, Yueran

    aqueous phase can quench CdTe/CdS QDs. Additionally, the stability of the different ligands capped CdTe/CdS QDs was tested by dialysis measurement, the hydrodynamic diameters of CdTe and CdTe/CdS core/shell QDs were measured by dynamic light scattering, and dissolving issue was found when CdTe and CdTe/CdS core/shell QDs were diluted in CHCl3. We have characterized the CdTe core and the CdTe/CdS core/shell QDs by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), small angle X-ray scattering (SAXS), and ICP-OES measurements. We have found that the CdTe core was of a zincblende structure, and the shell was a wurtzite structure. And the CdTe/CdS QDs were core/shell QDs instead of alloying QDs. We have also analyzed the photophysical properties of CdTe and CdTe/CdS core/shell QDs. Time-resolved photoluminescence (PL) measurements showed the emission decay lifetimes in the tens of nanoseconds. Additionally, ultrafast charge carrier relaxation dynamics of the CdTe core and CdTe/CdS core/shell QDs were studied by the femtosecond transient absorption (TA) spectroscopy. The transient absorption spectra of CdTe and CdTe/CdS core/shell QDs showed multiple bleaches, which have been assigned to the 1S3/2(h)-1S(e), 2S3/2(h)-1S(e), and 1P3/2(h)-1P(e) transitions. The spectral shifts of these bleaches after shell deposition have been analyzed in the context of a quasi-type-II carrier distribution in the core/shell samples, and interestingly the red shift was only contributed from the conduction band energy levels shifting to lower energy. In addition, the ultrafast evolution of these bleach features has been examined to extract electron cooling rates in these samples. A fast decay component in the 1S3/2(h)-1S(e) transition of the small CdTe QDs was discovered due to the hole being trapped by the defects on the surface of QD. Further, we have studied the PL quenching process of the air exposed CdTe QDs via the PL decay and transient absorption measurements. Oxygen

  17. Raman scattering from Zn/ZnO core-shell nanoparticles

    NASA Astrophysics Data System (ADS)

    Bajaj, Geetika; Soni, R. K.

    2008-09-01

    We have synthesized Zn/ZnO core-shell nanoparticles by pulsed laser ablation in liquid (PLAL) media using nanosecond pulsed Nd:YAG laser. The formation of crystalline core-shell nanoparticles of varying core and shell thickness with varying SDS concentration is confirmed by HRTEM images. The optical absorption shows distinct features corresponding to ZnO exciton and Zn surface plasmon. Raman spectrum from Zn/ZnO core-shell nanoparticles shows E2(high) phonon modes of the bulk which are insensitive to the size and modes unique to the core-shell structures. Moreover, the surface optical mode is dominant feature of the nonresonant spectrum. We have also examined the wavelength dependence of the phonon modes in Zn/ZnO core-shell structure.

  18. Core-shell nanostructured catalysts.

    PubMed

    Zhang, Qiao; Lee, Ilkeun; Joo, Ji Bong; Zaera, Francisco; Yin, Yadong

    2013-08-20

    Novel nanotechnologies have allowed great improvements in the syn-thesis of catalysts with well-controlled size, shape, and surface properties. Transition metal nanostructures with specific sizes and shapes, for instance, have shown great promise as catalysts with high selectivities and relative ease of recycling. Researchers have already demonstrated new selective catalysis with solution-dispersed or supported-metal nanocatalysts, in some cases applied to new types of reactions. Several challenges remain, however, particularly in improving the structural stability of the catalytic active phase. Core-shell nanostructures are nanoparticles encapsulated and protected by an outer shell that isolates the nanoparticles and prevents their migration and coalescence during the catalytic reactions. The synthesis and characterization of effective core-shell catalysts has been at the center of our research efforts and is the focus of this Account. Efficient core-shell catalysts require porous shells that allow free access of chemical species from the outside to the surface of nanocatalysts. For this purpose, we have developed a surface-protected etching process to prepare mesoporous silica and titania shells with controllable porosity. In certain cases, we can tune catalytic reaction rates by adjusting the porosity of the outer shell. We also designed and successfully applied a silica-protected calcination method to prepare crystalline shells with high surface area, using anatase titania as a model system. We achieved a high degree of control over the crystallinity and porosity of the anatase shells, allowing for the systematic optimization of their photocatalytic activity. Core-shell nanostructures also provide a great opportunity for controlling the interaction among the different components in ways that might boost structural stability or catalytic activity. For example, we fabricated a SiO₂/Au/N-doped TiO₂ core-shell photocatalyst with a sandwich structure that showed

  19. Geometry and B(1s) core excitons of ortho-carborane

    SciTech Connect

    Green, T.A. )

    1991-07-01

    The optimized C{sub 2v} geometry of ortho-carborane, 1,2-C{sub 2}B{sub 10}H{sub 12}, is determined from Hartree-Fock calculations. For this geometry, a carbon atom is substituted for a boron atom at one of the 4 inequivalent boron sites and the ground-state unrestricted Hartree-Fock eigenvalues and molecular orbitals are found. One thus obtains the valence structure of the B(1s) core-excited molecule according to the Z+1 approximation. The eigenvalue of the highest occupied molecular orbital is then subtracted from the experimental B(1s) ionization energy of the same site in ortho-carborane. This determines the excitation energy of the most tightly bound exciton for that site. Three of the sites yield nearly identical excitation energies of 191.9 eV; the fourth site yields an excitation energy of 190.9 eV.

  20. Geometry and B(1s) core excitons of ortho-carborane

    SciTech Connect

    Green, T.A.

    1990-01-01

    The optimized C{sub 2v} geometry of ortho-carborane, 1,2-C{sub 2}B{sub 10}H{sub 12}, is determined from Hartree-Fock calculations. For this geometry, a carbon atom is substituted for a boron atom at one of the 4 inequivalent boron sites and the ground-state unrestricted Hartree-Fock eigenvalues and molecular orbitals are found. One thus obtains the valence structure of the B(1s) core-excited molecule according to the Z + 1 approximation. The eigenvalue of the highest occupied molecular orbital is then subtracted from the experimental B(1s) ionization energy of the same site in ortho-carborane. This determines the excitation energy of the most tightly bound exciton for that site. Three of the sites yield nearly identical excitation energies of 191.9 eV; the fourth site yields an excitation energy of 190.9 eV. 8 refs., 1 fig., 2 tabs.

  1. Engineered Magnetic Core-Shell Structures.

    PubMed

    Alavi Nikje, Mir Mohammad; Vakili, Maryam

    2015-01-01

    In recent years, engineered magnetic core-shell structures are playing an important role in the wide range of various applications. These magnetic core-shell structures have attracted considerable attention because of their unique properties and various applications. Also, the synthesis of engineered magnetic core-shell structures has attracted practical interest because of potential applications in areas such as ferrofluids, medical imaging, drug targeting and delivery, cancer therapy, separations, and catalysis. So far a large number of engineered magnetic core-shell structures have been successfully synthesized. This review article focuses on the recent progress in synthesis and characterization of engineered magnetic core-shell structures. Also, this review gives a brief description of the various application of these structures. It is hoped that this review will play some small part in helping future developments in important field. PMID:26377655

  2. Photon upconversion in core-shell nanoparticles.

    PubMed

    Chen, Xian; Peng, Denfeng; Ju, Qiang; Wang, Feng

    2015-03-21

    Photon upconversion generally results from a series of successive electronic transitions within complex energy levels of lanthanide ions that are embedded in the lattice of a crystalline solid. In conventional lanthanide-doped upconversion nanoparticles, the dopant ions homogeneously distributed in the host lattice are readily accessible to surface quenchers and lose their excitation energy, giving rise to weak and susceptible emissions. Therefore, present studies on upconversion are mainly focused on core-shell nanoparticles comprising spatially confined dopant ions. By doping upconverting lanthanide ions in the interior of a core-shell nanoparticle, the upconversion emission can be substantially enhanced, and the optical integrity of the nanoparticles can be largely preserved. Optically active shells are also frequently employed to impart multiple functionalities to upconversion nanoparticles. Intriguingly, the core-shell design introduces the possibility of constructing novel upconversion nanoparticles by exploiting the energy exchange interactions across the core-shell interface. In this tutorial review, we highlight recent advances in the development of upconversion core-shell nanoparticles, with particular emphasis on the emerging strategies for regulating the interplay of dopant interactions through core-shell nanostructural engineering that leads to unprecedented upconversion properties. The improved control over photon energy conversion will open up new opportunities for biological and energy applications. PMID:25058157

  3. Core-Shell Structured Magnetic Ternary Nanocubes

    SciTech Connect

    Wang, Lingyan; Wang, Xin; Luo, Jin; Wanjala, Bridgid N.; Wang, Chong M.; Chernova, Natalya; Engelhard, Mark H.; Liu, Yao; Bae, In-Tae; Zhong, Chuan-Jian

    2010-12-01

    While transition metal-doped ferrite nanoparticles constitute an important class of soft magnetic nanomaterials with spinel structures, the ability to control the shape and composition would enable a wide range of applications in homogeneous or heterogeneous reactions such as catalysis and magnetic separation of biomolecules. This report describes novel findings of an investigation of core-shell structured MnZn ferrite nanocubes synthesized in organic solvents by manipulating the reaction temperature and capping agent composition in the absence of the conventionally-used reducing agents. The core-shell structure of the highly-monodispersed nanocubes (~20 nm) are shown to consist of an Fe3O4 core and an (Mn0.5Zn0.5)(Fe0.9, Mn1.1)O4 shell. In comparison with Fe3O4 and other binary ferrite nanoparticles, the core-shell structured nanocubes were shown to display magnetic properties regulated by a combination of the core-shell composition, leading to a higher coercivity (~350 Oe) and field-cool/zero-field-cool characteristics drastically different from many regular MnZn ferrite nanoparticles. The findings are discussed in terms of the unique core-shell composition, the understanding of which has important implication to the exploration of this class of soft magnetic nanomaterials in many potential applications such as magnetic resonance imaging, fuel cells, and batteries.

  4. Spectroscopy of colloidal semiconductor core/shell nanoplatelets with high quantum yield.

    PubMed

    Tessier, M D; Mahler, B; Nadal, B; Heuclin, H; Pedetti, S; Dubertret, B

    2013-07-10

    Free standing two-dimensional materials appear as a novel class of structures. Recently, the first colloidal two-dimensional heterostructures have been synthesized. These core/shell nanoplatelets are the first step toward colloidal quantum wells. Here, we study in detail the spectroscopic properties of this novel generation of colloidal nanoparticles. We show that core/shell CdSe/CdZnS nanoplatelets with 80% quantum yield can be obtained. The emission time trace of single core/shell nanoplatelets exhibits reduced blinking compared to core nanoplatelets with a two level emission time trace. At cryogenic temperatures, these nanoplatelets have a quantum yield close to 100% and a stable emission time trace. A solution of core/shell nanoplatelets has emission spectra with a full width half-maximum close to 20 nm, a value much lower than corresponding spherical or rod-shaped heterostructures. Using single particle spectroscopy, we show that the broadening of the emission spectra upon the shell deposition is not due to dispersity between particles but is related to an intrinsic increased exciton-phonon coupling in the shell. We also demonstrate that optical spectroscopy is a relevant tool to investigate the presence of traps induced by shell deposition. The spectroscopic properties of the core/shell nanoplatelets presented here strongly suggest that this new generation of objects will be an interesting alternative to spherical or rod-shaped nanocrystals. PMID:23731211

  5. The influence of interfaces and intra-band transitions on the band gap of CdS/HgS and GaN/X (X=InN, In0.33Ga0.67N) core/shell/shell quantum dot quantum well - A theoretical study

    NASA Astrophysics Data System (ADS)

    Ganesan, P.; Senthilkumar, L.

    2015-11-01

    A theoretical model is presented to calculate the 1s-1s transition energy of an exciton in spherically layered semiconductor quantum-dot quantum-well (QDQW), based on the LCAO variational method using effective mass approximation. The confinement energies of electron and hole and the Coulombic interaction energy between them are calculated for CdS/HgS/CdS, GaN/X/GaN (X=InN, In0.33Ga0.67N) (QDQW) with core/shell/shell structures. The results of the proposed model effectively accommodates the polarization effects at the interfaces of different semiconductor materials in a core/shell/shell structure and elucidates the significant influence of interfaces on the band gap with consistency among previous theoretical and experimental results. The wave function of exciton studied shows significant differences with other theory. The change in the band gap of QDQW is attributed to the exciton excitations by thermal occupation of the lowest dark exciton states at different temperatures. In addition, based on Quantum Confined Stark Effect (QCSE) the effect of high electric field on the charge carriers and the corresponding changes in the band gap has been investigated. The applied electric field provides strong overlap between the electron and hole wave functions as well as increases the binding energy of the exciton, which eventually decreases the band gap.

  6. Tuning biexciton binding and antibinding in core/shell quantum dots

    NASA Astrophysics Data System (ADS)

    McDonald, Peter G.; Tyrrell, Edward J.; Shumway, John; Smith, Jason M.; Galbraith, Ian

    2012-09-01

    We use a path integral quantum Monte Carlo method to simulate excitons and biexcitons in core/shell nanocrystals with Type-I, Type-II, and quasi-Type-II band alignments. Quantum Monte Carlo techniques allow for all quantum correlations to be included when determining the thermal ground state, thus producing accurate predictions of biexciton binding. These subtle quantum correlations are found to cause the biexciton to be binding with Type-I carrier localization and strongly antibinding with Type-II carrier localization, in agreement with experiment for both core/shell nanocrystals and dot in rod nanocrystal structures. Simple treatments based on perturbative approaches are shown to miss this important transition in the biexciton binding. Understanding these correlations offers prospects to engineer strong biexciton antibinding, which is crucial to the design of nanocrystals for single-exciton lasing applications.

  7. Core/shell colloidal semiconductor nanoplatelets.

    PubMed

    Mahler, Benoit; Nadal, Brice; Bouet, Cecile; Patriarche, Gilles; Dubertret, Benoit

    2012-11-14

    We have recently synthesized atomically flat semiconductor colloidal nanoplatelets with quasi 2D geometry. Here, we show that core/shell nanoplatelets can be obtained with a 2D geometry that is conserved. The epitaxial growth of the shell semiconductor is performed at room temperature. We report the detailed synthesis of CdSe/CdS and CdSe/CdZnS structures with different shell thicknesses. The shell growth is characterized both spectroscopically and structurally. In particular, the core/shell structure appears very clearly on high-resolution, high-angle annular dark-field transmission electron microscope images, thanks to the difference of atomic density between the core and the shell. When the nanoplatelets stand on their edge, we can precisely count the number of atomic planes forming the core and the shell. This provides a direct measurement, with atomic precision, of the core nanoplatelets thickness. The constraints exerted by the shell growth on the core is analyzed using global phase analysis. The core/shell nanoplatelets we obtained have narrow emission spectra with full-width at half-maximum close to 20 nm, and quantum yield that can reach 60%. PMID:23057684

  8. Hydrogel Nanofilaments via Core-Shell Electrospinning.

    PubMed

    Nakielski, Paweł; Pawłowska, Sylwia; Pierini, Filippo; Liwińska, Wioletta; Hejduk, Patryk; Zembrzycki, Krzysztof; Zabost, Ewelina; Kowalewski, Tomasz A

    2015-01-01

    Recent biomedical hydrogels applications require the development of nanostructures with controlled diameter and adjustable mechanical properties. Here we present a technique for the production of flexible nanofilaments to be used as drug carriers or in microfluidics, with deformability and elasticity resembling those of long DNA chains. The fabrication method is based on the core-shell electrospinning technique with core solution polymerisation post electrospinning. Produced from the nanofibers highly deformable hydrogel nanofilaments are characterised by their Brownian motion and bending dynamics. The evaluated mechanical properties are compared with AFM nanoindentation tests. PMID:26091487

  9. Magnetic-Plasmonic Core-Shell Nanoparticles

    PubMed Central

    Levin, Carly S.; Hofmann, Cristina; Ali, Tamer A.; Kelly, Anna T.; Morosan, Emilia; Nordlander, Peter; Whitmire, Kenton H.; Halas, Naomi J.

    2013-01-01

    Nanoparticles composed of magnetic cores with continuous Au shell layers simultaneously possess both magnetic and plasmonic properties. Faceted and tetracubic nanocrystals consisting of wüstite with magnetite-rich corners and edges retain magnetic properties when coated with an Au shell layer, with the composite nanostructures showing ferrimagnetic behavior. The plasmonic properties are profoundly influenced by the high dielectric constant of the mixed-iron-oxide nanocrystalline core. A comprehensive theoretical analysis that examines the geometric plasmon tunability over a range of core permittivities enables us to identify the dielectric properties of the mixed-oxide magnetic core directly from the plasmonic behavior of the core-shell nanoparticle. PMID:19441794

  10. Core-shell diodes for particle detectors

    NASA Astrophysics Data System (ADS)

    Jia, Guobin; Plentz, Jonathan; Höger, Ingmar; Dellith, Jan; Dellith, Andrea; Falk, Fritz

    2016-02-01

    High performance particle detectors are needed for fundamental research in high energy physics in the exploration of the Higgs boson, dark matter, anti-matter, gravitational waves and proof of the standard model, which will extend the understanding of our Universe. Future particle detectors should have ultrahigh radiation hardness, low power consumption, high spatial resolution and fast signal response. Unfortunately, some of these properties are counter-influencing for the conventional silicon drift detectors (SDDs), so that they cannot be optimized simultaneously. In this paper, the main issues of conventional SDDs have been analyzed, and a novel core-shell detector design based on micro- and nano-structures etched into Si-wafers is proposed. It is expected to simultaneously reach ultrahigh radiation hardness, low power consumption, fast signal response and high spatial resolution down to the sub-micrometer range, which will probably meet the requirements for the most powerful particle accelerators in the near future. A prototype core-shell detector was fabricated using modern silicon nanotechnology and the functionality was tested using electron-beam-induced current measurements. Such a high performance detector will open many new applications in extreme radiation environments such as high energy physics, astrophysics, high resolution (bio-) imaging and crystallography, which will push these fields beyond their current boundaries.

  11. Band structure of core-shell semiconductor nanowires

    NASA Astrophysics Data System (ADS)

    Pistol, Mats-Erik; Pryor, Craig

    2009-03-01

    We present band structures of strained core-shell nanowires composed of zincblende III-V (binary) semiconductors. We consider all combinations of AlN, GaN, InN, and all combinations of AlP, GaP, AlAs, GaAs, InP, InAs, AlSb, GaSb, and InSb. We compute the γ- and X-conduction band minima as well as the valence band maximum, all as functions of the core and shell radii. The calculations were performed using continuum elasticity theory for the strain, eight-band strain-dependent k.p theory for the γ-point energies, and single band approximation for the X-point conduction minima. We identify structures with type-I, type-II and type-III band alignment, as well as systems in which one material becomes metallic due to a negative band-gap. We identify structures that may support exciton crystals with and without photoexcitation. We have also computed the effective masses, from which the confinement energy may be estimated. All the results [Pistol and Pryor, Phys. Rev. B 78, 115319] are available in graphical and tabular form at www.semiconductor.physics.uiowa.edu

  12. Silica-metal core-shell nanostructures.

    PubMed

    Jankiewicz, B J; Jamiola, D; Choma, J; Jaroniec, M

    2012-01-15

    Silica-metal nanostructures consisting of silica cores and metal nanoshells attract a lot of attention because of their unique properties and potential applications ranging from catalysis and biosensing to optical devices and medicine. The important feature of these nanostructures is the possibility of controlling their properties by the variation of their geometry, shell morphology and shell material. This review is devoted to silica-noble metal core-shell nanostructures; specifically, it outlines the main methods used for the preparation and surface modification of silica particles and presents the major strategies for the formation of metal nanoshells on the modified silica particles. A special emphasis is given to the Stöber method, which is relatively simple, effective and well verified for the synthesis of large and highly uniform silica particles (with diameters from 100 nm to a few microns). Next, the surface chemistry of these particles is discussed with a special focus on the attachment of specific organic groups such as aminopropyl or mercaptopropyl groups, which interact strongly with metal species. Finally, the synthesis, characterization and application of various silica-metal core-shell nanostructures are reviewed, especially in relation to the siliceous cores with gold or silver nanoshells. Nowadays, gold is most often used metal for the formation of nanoshells due to its beneficial properties for many applications. However, other metals such as silver, platinum, palladium, nickel and copper were also used for fabrication of core-shell nanostructures. Silica-metal nanostructures can be prepared using various methods, for instance, (i) growth of metal nanoshells on the siliceous cores with deposited metal nanoparticles, (ii) reduction of metal species accompanied by precipitation of metal nanoparticles on the modified silica cores, and (iii) formation of metal nanoshells under ultrasonic conditions. A special emphasis is given to the seed

  13. No-Core Shell Model and Reactions

    SciTech Connect

    Navratil, Petr; Ormand, W. Erich; Caurier, Etienne; Bertulani, Carlos

    2005-10-14

    There has been a significant progress in ab initio approaches to the structure of light nuclei. Starting from realistic two- and three-nucleon interactions the ab initio no-core shell model (NCSM) can predict low-lying levels in p-shell nuclei. It is a challenging task to extend ab initio methods to describe nuclear reactions. In this contribution, we present a brief overview of the NCSM with examples of recent applications as well as the first steps taken toward nuclear reaction applications. In particular, we discuss cross section calculations of p+6Li and 6He+p scattering as well as a calculation of the astrophysically important 7Be(p,{gamma})8B S-factor.

  14. No-Core Shell Model and Reactions

    SciTech Connect

    Navratil, P; Ormand, W E; Caurier, E; Bertulani, C

    2005-04-29

    There has been a significant progress in ab initio approaches to the structure of light nuclei. Starting from realistic two- and three-nucleon interactions the ab initio no-core shell model (NCSM) can predict low-lying levels in p-shell nuclei. It is a challenging task to extend ab initio methods to describe nuclear reactions. In this contribution, we present a brief overview of the NCSM with examples of recent applications as well as the first steps taken toward nuclear reaction applications. In particular, we discuss cross section calculations of p+{sup 6}Li and {sup 6}He+p scattering as well as a calculation of the astrophysically important {sup 7}Be(p, {gamma}){sup 8}B S-factor.

  15. Multifunctional composite core-shell nanoparticles

    NASA Astrophysics Data System (ADS)

    Wei, Suying; Wang, Qiang; Zhu, Jiahua; Sun, Luyi; Lin, Hongfei; Guo, Zhanhu

    2011-11-01

    In this review paper, the state-of-the-art knowledge of the core-shell multifunctional nanoparticles (MNPs), especially with unique physiochemical properties, is presented. The synthesis methods were summarized from the aspects of both the advantages and the demerits. The core includes the inexpensive and easily oxidized metals and the noble shells include the relatively noble metals, carbon, silica, other oxides, and polymers. The properties including magnetic, optical, anti-corrosion and the surface chemistry of the NPs are thoroughly reviewed. The current status of the applications is reviewed with the detailed examples including the catalysis, giant magnetoresistance (GMR) sensing, electromagnetic interface shielding or microwave absorption, biomedical drug delivery, and the environmental remediation.

  16. Localized surface plasmon mediated energy transfer in the vicinity of core-shell nanoparticle

    NASA Astrophysics Data System (ADS)

    Shishodia, Manmohan Singh; Juneja, Soniya

    2016-05-01

    Multipole spectral expansion based theory of energy transfer interactions between a donor and an acceptor molecule in the vicinity of a core-shell (nanoshell or core@shell) based plasmonic nanostructure is developed. In view of the diverse applications and rich plasmonic features such as tuning capability of surface plasmon (SP) frequencies, greater sensitivity to the change of dielectric environment, controllable redirection of electromagnetic radiation, closed form expressions for Energy Transfer Rate Enhancement Factor (ETREF) near core-shell particle are reported. The dependence of ETREF on different parameters is established through fitting equations, perceived to be of key importance for developing appropriate designs. The theoretical approach developed in the present work is capable of treating higher order multipoles, which, in turn, are also shown to play a crucial role in the present context. Moreover, closed form expressions derived in the present work can directly be used as formula, e.g., for designing SP based biosensors and estimating energy exchange between proteins and excitonic interactions in quantum dots.

  17. Sign-reversed and magnitude-enhanced nonlinear absorption of Au-CdS core-shell hetero-nanorods

    NASA Astrophysics Data System (ADS)

    Nan, Fan; Liang, Shan; Liu, Xiao-Li; Peng, Xiao-Niu; Li, Min; Yang, Zhong-Jian; Zhou, Li; Hao, Zhong-Hua; Wang, Qu-Quan

    2013-04-01

    We synthesis uniform Au-CdS core-shell hetero-nanorods and demonstrate the effective plasmon-exciton interaction induced optical nonlinear enhancement in metal-semiconductor hetero-nanostructures. After growing CdS semiconductor shell onto the Au nanorods, the longitudinal plasmon resonance exhibits considerable red-shift with enlarged absorption intensity. Nonlinear absorption responses transform from saturable absorption to reverse saturable absorption, and effective nonlinear absorption coefficient β is increased from -7.7 to +22.2 cm/GW. The observed behaviors indicate strong plasmon-exciton interaction and great local field enhancement.

  18. Core@shell bimetallic nanoparticle synthesis via anion coordination

    NASA Astrophysics Data System (ADS)

    Serpell, Christopher J.; Cookson, James; Ozkaya, Dogan; Beer, Paul D.

    2011-06-01

    Core@shell structured bimetallic nanoparticles are currently of immense interest due to their unique electronic, optical and catalytic properties. However, their synthesis is non-trivial. We report a new supramolecular route for the synthesis of core@shell nanoparticles, based on an anion coordination protocol—the first to function by binding the shell metal to the surface of the pre-formed primary metal core before reduction. The resultant gold/palladium and platinum/palladium core@shell nanoparticles have been characterized by aberration-corrected scanning transmission electron microscopy (as well as other techniques), giving striking atomic-resolution images of the core@shell architecture, and the unique catalytic properties of the structured nanoparticles have been demonstrated in a remarkable improvement of the selective production of industrially valuable chloroaniline from chloronitrobenzene.

  19. Graded core/shell semiconductor nanorods and nanorod barcodes

    DOEpatents

    Alivisatos, A. Paul; Scher, Erik C.; Manna, Liberato

    2010-12-14

    Graded core/shell semiconductor nanorods and shaped nanorods are disclosed comprising Group II-VI, Group III-V and Group IV semiconductors and methods of making the same. Also disclosed are nanorod barcodes using core/shell nanorods where the core is a semiconductor or metal material, and with or without a shell. Methods of labeling analytes using the nanorod barcodes are also disclosed.

  20. Graded core/shell semiconductor nanorods and nanorod barcodes

    DOEpatents

    Alivisatos, A. Paul; Scher, Erik C.; Manna, Liberato

    2013-03-26

    Graded core/shell semiconductor nanorods and shapped nanorods are disclosed comprising Group II-VI, Group III-V and Group IV semiconductors and methods of making the same. Also disclosed are nanorod barcodes using core/shell nanorods where the core is a semiconductor or metal material, and with or without a shell. Methods of labeling analytes using the nanorod barcodes are also disclosed.

  1. Ab Initio No-Core Shell Model

    SciTech Connect

    Barrett, B R; Navratil, P; Vary, J P

    2011-04-11

    and NNN interactions, characterized by the order of the expansion retained (e.g. 'next-to-next-to leading order' is NNLO), provide a high-quality fit to the NN data and the A = 3 ground-state (g.s.) properties. The derivations of NN, NNN, etc. interactions within meson-exchange and {chi}EFT are well-established but are not subjects of this review. Our focus is solution of the non-relativistic quantum many-body Hamiltonian that includes these interactions using our no core shell model (NCSM) formalism. In the next section we will briefly outline the NCSM formalism and then present applications, results and extensions in later sections.

  2. Simulated evolution process of core-shell microstructures

    NASA Astrophysics Data System (ADS)

    Qin, Tao; Wang, Haipeng; Wei, Bingbo

    2007-08-01

    The evolution process of core-shell microstructures formed in monotectic alloys under the space environment condition was investigated by the numerical simulation method. In order to account for the effect of surface segregation on phase separation, Model H was modified by introducing a surface free energy term into the total free energy of alloy droplet. Three Fe-Cu alloys were taken as simulated examples, which usually exhibit metastable phase separation in undercooled and microgravity states. It was revealed by the dynamic simulation process that the formation of core-shell microstructures depends mainly on surface segregation and Marangoni convection. The phase separation of Fe65Cu35 alloy starts from a dispersed structure and gradually evolves into a triple-layer core-shell micro-structure. Similarly, Fe50Cu50 alloy experiences a structural evolution process of “bicontinuous phase → quadruple-layer core-shell → triple-layer core-shell”, while the microstructures of Fe35Cu65 alloy transfer from the dispersed structure into the final double-layer core-shell morphology. The Cu-rich phase always forms the outer layer because of surface segregation, whereas the internal microstructural evolution is controlled mainly by the Marangoni convection resulting from the temperature gradient.

  3. Dynamics of Intraband and Interband Auger Processes in Colloidal Core-Shell Quantum Dots.

    PubMed

    Rabouw, Freddy T; Vaxenburg, Roman; Bakulin, Artem A; van Dijk-Moes, Relinde J A; Bakker, Huib J; Rodina, Anna; Lifshitz, Efrat; L Efros, Alexander; Koenderink, A Femius; Vanmaekelbergh, Daniël

    2015-10-27

    Conventional colloidal quantum dots (QDs) suffer from rapid energy losses by nonradiative (Auger) processes, leading to sub-ns lifetimes in all excited states but the lowest-energy single exciton. Suppression of interband Auger decay, such as biexciton Auger recombination, has been achieved with the design of heterostructured core-shell QDs. Auger-like processes are also believed to be responsible for rapid intraband hot-electron cooling in QDs. However, the simultaneous effect of shell growth on interband Auger recombination and intraband hot-electron cooling has not been addressed. Here we investigate how the growth of a CdS shell affects these two relaxation processes in CdSe/CdS core-shell QDs. Using a combination of ultrafast pump-push-probe spectroscopy on the QD ensemble and analysis of the photon statistics from single QDs, we find that Auger losses in the biexciton state are suppressed with increasing shell thickness, while hot-electron cooling remains unaffected. Calculations conducted within an eight-band k·p model confirm the experimental dependence of the biexciton Auger decay on the shell thickness, and provide insights into the factors determining the cooling rate of hot carriers. PMID:26389562

  4. Electrochemical synthesis of core-shell magnetic nanowires

    NASA Astrophysics Data System (ADS)

    Ovejero, Jesús G.; Bran, Cristina; Vilanova, Enrique; Kosel, Jürgen; Morales, María P.; Vazquez, Manuel

    2015-09-01

    (Fe, Ni, CoFe) @ Au core-shell magnetic nanowires have been synthesized by optimized two-step potentiostatic electrodeposition inside self-assembled nanopores of anodic aluminium templates. The optimal electrochemical parameters (e.g., potential) have been firstly determined for the growth of continuous Au nanotubes at the inner wall of pores. Then, a magnetic core was synthesized inside the Au shells under suitable electrochemical conditions for a wide spectrum of single elements and alloy compositions (e.g., Fe, Ni and CoFe alloy). Novel opportunities offered by such nanowires are discussed particularly, the magnetic behavior of (Fe, Ni, CoFe) @ Au core-shell nanowires was tested and compared with that of bare nanowires. These core-shell nanowires can be released from the template thereby opening novel opportunities for biofunctionalization of individual nanowires.

  5. Core-shell and segmented polymer-metal composite nanostructures.

    PubMed

    Lahav, Michal; Weiss, Emily A; Xu, Qiaobing; Whitesides, George M

    2006-09-01

    Composite nanostructures (approximately 200 nm wide and several micrometers long) of metal and polyaniline (PANI) in two new variations of core-shell (PANI-Au) and segmented (Au-PANI and Ni-Au-PANI) architectures were fabricated electrochemically within anodized aluminum oxide (AAO) membranes. Control over the structure of these composites (including the length of the gold shells in the core-shell structures) was accomplished by adjusting the time and rate of electrodeposition and the pH of the solution from which the materials were grown. Exposure of the core-shell structures to oxygen plasma removed the PANI and yielded aligned gold nanotubes. In the segmented structures, a self-assembled monolayer (SAM) of thioaniline nucleated the growth of PANI on top of metal nanorods and acted as an adhesion layer between the metal and PANI components. PMID:16968046

  6. Core-Shell Composite Nanoparticles: Synthesis, Characterization, and Applications

    NASA Astrophysics Data System (ADS)

    Sanyal, Sriya

    Nanoparticles are ubiquitous in various fields due to their unique properties not seen in similar bulk materials. Among them, core-shell composite nanoparticles are an important class of materials which are attractive for their applications in catalysis, sensing, electromagnetic shielding, drug delivery, and environmental remediation. This dissertation focuses on the study of core-shell type of nanoparticles where a polymer serves as the core and inorganic nanoparticles are the shell. This is an interesting class of supramolecular building blocks and can "exhibit unusual, possibly unique, properties which cannot be obtained simply by co-mixing polymer and inorganic particles". The one-step Pickering emulsion polymerization method was successfully developed and applied to synthesize polystyrene-silica core-shell composite particles. Possible mechanisms of the Pickering emulsion polymerization were also explored. The silica nanoparticles were thermodynamically favorable to self-assemble at liquid-liquid interfaces at the initial stage of polymerization and remained at the interface to finally form the shells of the composite particles. More importantly, Pickering emulsion polymerization was employed to synthesize polystyrene/poly(N-isopropylacrylamide) (PNIPAAm)-silica core-shell nanoparticles with N-isopropylacrylamide incorporated into the core as a co-monomer. The composite nanoparticles were temperature sensitive and could be up-taken by human prostate cancer cells and demonstrated effectiveness in drug delivery and cancer therapy. Similarly, by incorporating poly-2-(N,N)-dimethylamino)ethyl methacrylate (PDMA) into the core, pH sensitive core-shell composite nanoparticles were synthesized and applied as effective carriers to release a rheological modifier upon a pH change. Finally, the research focuses on facile approaches to engineer the transition of the temperature-sensitive particles and develop composite core-shell nanoparticles with a metallic shell.

  7. "Giant" red and green core/shell quantum dots with high color purity and photostability

    NASA Astrophysics Data System (ADS)

    Huang, Bo; Xu, Ruilin; Zhuo, Ningze; Zhang, Lei; Wang, Haibo; Cui, Yiping; Zhang, Jiayu

    2016-03-01

    "Giant" red CdSe/CdS and green CdSeS/ZnS core/shell quantum dots (QDs), whose color purity were ∼100% and 91%, respectively, were synthesized, and the color gamut could be more than 120% relative to the NTSC color space for the display utilizing these two kinds of QDs. Time-resolved photoluminescence (PL) measurement showed that the PL dynamics was evolved from tri-exponential decay to bi-exponential type with the increase of the shell thickness, and the PL decay characteristics of these giant QDs did not evidently change under long-term UV irradiation, indicating that the thick shell could isolate the effect of the surface's defects on the exciton's recombination within these QDs. Their high photostability could have an advantage in the application on display and white-light LEDs.

  8. Light-Harvesting Nanoparticle Core-Shell Clusters with Controllable Optical Output.

    PubMed

    Sun, Dazhi; Tian, Ye; Zhang, Yugang; Xu, Zhihua; Sfeir, Matthew Y; Cotlet, Mircea; Gang, Oleg

    2015-06-23

    We used DNA self-assembly methods to fabricate a series of core-shell gold nanoparticle-DNA-colloidal quantum dot (AuNP-DNA-Qdot) nanoclusters with satellite-like architecture to modulate optical (photoluminescence) response. By varying the intercomponent distance through the DNA linker length designs, we demonstrate precise tuning of the plasmon-exciton interaction and the optical behavior of the nanoclusters from regimes characterized by photoluminescence quenching to photoluminescence enhancement. The combination of detailed X-ray scattering probing with photoluminescence intensity and lifetime studies revealed the relation between the cluster structure and its optical output. Compared to conventional light-harvesting systems like conjugated polymers and multichromophoric dendrimers, the proposed nanoclusters bring enhanced flexibility in controlling the optical behavior toward a desired application, and they can be regarded as controllable optical switches via the optically pumped color. PMID:25933097

  9. Lithium Intercalation in Core-Shell Materials-Theoretical Analysis

    SciTech Connect

    Suthar, B; Subramanian, VR

    2014-03-04

    Core-shell composite structures are potential candidates for Li-ion battery electrodes as they can take advantage of materials with higher energy density and materials with higher cyclability. This paper derives an analytical solution for isotropic 1-dimensional diffusion with galvanostatic boundary condition in composite slab, cylinder and sphere using separation of variables method. A general interfacial condition has been used to represent the dynamics at the interface of the composite material rendering the solution useful for wide variety of battery materials. Using the derived analytical solution for diffusion, intercalation induced stresses were estimated for spherical core-shell materials. (C) 2014 The Electrochemical Society. All rights reserved.

  10. Fully Crystalline Faceted Fe-Au Core-Shell Nanoparticles.

    PubMed

    Langlois, C; Benzo, P; Arenal, R; Benoit, M; Nicolai, J; Combe, N; Ponchet, A; Casanove, M J

    2015-08-12

    Fe-Au core-shell nanoparticles displaying an original polyhedral morphology have been successfully synthesized through a physical route. Analyses using transmission electron microscopy show that the Au shell forms truncated pyramids epitaxially grown on the (100) facets of the iron cubic core. The evolution of the elastic energy and strain field in the nanoparticles as a function of their geometry and composition is calculated using the finite-element method. The stability of the remarkable centered core-shell morphology experimentally observed is attributed to the weak elastic energy resulting from the low misfit at the Fe/Au (100) interface compared to the surface energy contribution. PMID:26146846

  11. Optimized optical "tractor beam" for core-shell nanoparticles.

    PubMed

    Wang, Neng; Lu, Wanli; Ng, Jack; Lin, Zhifang

    2014-04-15

    It is known that core-shell subwavelength nanoparticles consisting of a dielectric shell and a metallic core can simultaneously support electric and magnetic dipolar resonances, which enhance forward scattering and suppress backward scattering. This creates favorable conditions for optical tractor beam applications. Using the generalized Lorenz-Mie theory and Maxwell stress tensor formulation, we demonstrate how optical pulling forces can be induced and optimized by first-order Bessel beams with appropriate polarization. The transverse stability of the core-shell nanoparticle under ambient damping is also verified by linear stability analysis and dynamical simulation. PMID:24979003

  12. One-step synthesis of gold polyaniline core shell particles

    NASA Astrophysics Data System (ADS)

    Wang, Zhijuan; Yuan, Junhua; Han, Dongxue; Niu, Li; Ivaska, Ari

    2007-03-01

    A one-step method has been developed for synthesizing gold-polyaniline (Au@PANI) core-shell particles by using chlorauric acid (HAuCl4) to oxidize aniline in the presence of acetic acid and Tween 40 at room temperature. SEM images indicated that the resulting core-shell particles were composed of submicrometre-scale Au particles and PANI shells with an average thickness of 25 nm. Furthermore, a possible mechanism concerning the growth of Au@PANI particles was also proposed based on the results of control experiments.

  13. Primary charge carrier dynamics of water-solubilized CdZnS/ZnS core/shell and CdZnS/ZnS·Pd nanoparticle adducts

    NASA Astrophysics Data System (ADS)

    Busby, Erik; Thibert, Arthur; Page, Leah E.; Jawaid, Ali M.; Snee, Preston T.; Larsen, Delmar S.

    2013-06-01

    The primary photodynamics of 5-nm CdZnS core, CdZnS/ZnS core/shell, and CdZnS/ZnS·Pd nanoparticle adducts are characterized with broadband ultrafast transient absorption spectroscopy. Photogenerated excitons in the CdZnS and CdZnS/ZnS nanoparticles exhibit long-lived (>20 ns) lifetimes and further functionalizing of the type-I CdZnS/ZnS core/shells with Pd nanoparticles resulted in rapid exciton quenching (<250 ps) due to the transfer of electrons from the CdZnS core into the Pd nanocrystals via tunneling through the insulating ZnS shell. The shell-induced surface trap passivation and near-unity charge carrier injection efficiency into a platinum-group metal nanoparticle shows potential for enhanced colloidal photocatalytic applications, while enhancing photostability.

  14. To Battle Surface Traps on CdSe/CdS Core/Shell Nanocrystals: Shell Isolation versus Surface Treatment.

    PubMed

    Pu, Chaodan; Peng, Xiaogang

    2016-07-01

    Electronic traps at the inorganic-organic interface of colloidal quantum dots (QDs) are detrimental to their luminescent properties. Several types of interface traps were identified for single-crystalline CdSe/CdS core/shell QDs, which were all found to be extrinsic to either the core/shell structure or their optical performance. The electron traps-presumably excess or unpassivated Cd surface sites-are shallow ones and could be readily isolated from the electron wave function of the excitons with more than ∼2 monolayers of CdS shell. There were two identifiable deep hole traps within the bandgap of the QDs, i.e., the surface adsorbed H2S and unpassivated surface S sites. The surface adsorbed H2S could be removed by either degassing processes or photochemical decomposition of H2S without damaging the QDs. The unpassivated surface S sites could be removed by surface treatment with cadmium carboxylates. Understanding of the surface traps enabled establishment of new phosphine-free synthetic schemes for either single-precursor or successive-ion-layer-adsorption-and-reaction approach, which yielded CdSe/CdS core/shell QDs with near-unity photoluminescence quantum yield and monoexponential photoluminescence decay dynamics with 2-10 monolayers of CdS shell. PMID:27312799

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

    NASA Astrophysics Data System (ADS)

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

    2016-06-01

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

  16. Biocompatible magnetic core-shell nanocomposites for engineered magnetic tissues

    NASA Astrophysics Data System (ADS)

    Rodriguez-Arco, Laura; Rodriguez, Ismael A.; Carriel, Victor; Bonhome-Espinosa, Ana B.; Campos, Fernando; Kuzhir, Pavel; Duran, Juan D. G.; Lopez-Lopez, Modesto T.

    2016-04-01

    The inclusion of magnetic nanoparticles into biopolymer matrixes enables the preparation of magnetic field-responsive engineered tissues. Here we describe a synthetic route to prepare biocompatible core-shell nanostructures consisting of a polymeric core and a magnetic shell, which are used for this purpose. We show that using a core-shell architecture is doubly advantageous. First, gravitational settling for core-shell nanocomposites is slower because of the reduction of the composite average density connected to the light polymer core. Second, the magnetic response of core-shell nanocomposites can be tuned by changing the thickness of the magnetic layer. The incorporation of the composites into biopolymer hydrogels containing cells results in magnetic field-responsive engineered tissues whose mechanical properties can be controlled by external magnetic forces. Indeed, we obtain a significant increase of the viscoelastic moduli of the engineered tissues when exposed to an external magnetic field. Because the composites are functionalized with polyethylene glycol, the prepared bio-artificial tissue-like constructs also display excellent ex vivo cell viability and proliferation. When implanted in vivo, the engineered tissues show good biocompatibility and outstanding interaction with the host tissue. Actually, they only cause a localized transitory inflammatory reaction at the implantation site, without any effect on other organs. Altogether, our results suggest that the inclusion of magnetic core-shell nanocomposites into biomaterials would enable tissue engineering of artificial substitutes whose mechanical properties could be tuned to match those of the potential target tissue. In a wider perspective, the good biocompatibility and magnetic behavior of the composites could be beneficial for many other applications.The inclusion of magnetic nanoparticles into biopolymer matrixes enables the preparation of magnetic field-responsive engineered tissues. Here we

  17. Biocompatible magnetic core-shell nanocomposites for engineered magnetic tissues.

    PubMed

    Rodriguez-Arco, Laura; Rodriguez, Ismael A; Carriel, Victor; Bonhome-Espinosa, Ana B; Campos, Fernando; Kuzhir, Pavel; Duran, Juan D G; Lopez-Lopez, Modesto T

    2016-04-14

    The inclusion of magnetic nanoparticles into biopolymer matrixes enables the preparation of magnetic field-responsive engineered tissues. Here we describe a synthetic route to prepare biocompatible core-shell nanostructures consisting of a polymeric core and a magnetic shell, which are used for this purpose. We show that using a core-shell architecture is doubly advantageous. First, gravitational settling for core-shell nanocomposites is slower because of the reduction of the composite average density connected to the light polymer core. Second, the magnetic response of core-shell nanocomposites can be tuned by changing the thickness of the magnetic layer. The incorporation of the composites into biopolymer hydrogels containing cells results in magnetic field-responsive engineered tissues whose mechanical properties can be controlled by external magnetic forces. Indeed, we obtain a significant increase of the viscoelastic moduli of the engineered tissues when exposed to an external magnetic field. Because the composites are functionalized with polyethylene glycol, the prepared bio-artificial tissue-like constructs also display excellent ex vivo cell viability and proliferation. When implanted in vivo, the engineered tissues show good biocompatibility and outstanding interaction with the host tissue. Actually, they only cause a localized transitory inflammatory reaction at the implantation site, without any effect on other organs. Altogether, our results suggest that the inclusion of magnetic core-shell nanocomposites into biomaterials would enable tissue engineering of artificial substitutes whose mechanical properties could be tuned to match those of the potential target tissue. In a wider perspective, the good biocompatibility and magnetic behavior of the composites could be beneficial for many other applications. PMID:27029891

  18. Controlled alloying of the core-shell interface in CdSe/CdS quantum dots for suppression of Auger recombination.

    PubMed

    Bae, Wan Ki; Padilha, Lazaro A; Park, Young-Shin; McDaniel, Hunter; Robel, Istvan; Pietryga, Jeffrey M; Klimov, Victor I

    2013-04-23

    The influence of a CdSexS1-x interfacial alloyed layer on the photophysical properties of core/shell CdSe/CdS nanocrystal quantum dots (QDs) is investigated by comparing reference QDs with a sharp core/shell interface to alloyed structures with an intermediate CdSexS1-x layer at the core/shell interface. To fully realize the structural contrast, we have developed two novel synthetic approaches: a method for fast CdS-shell growth, which results in an abrupt core/shell boundary (no intentional or unintentional alloying), and a method for depositing a CdSexS1-x alloy layer of controlled composition onto the CdSe core prior to the growth of the CdS shell. Both types of QDs possess similar size-dependent single-exciton properties (photoluminescence energy, quantum yield, and decay lifetime). However the alloyed QDs show a significantly longer biexciton lifetime and up to a 3-fold increase in the biexciton emission efficiency compared to the reference samples. These results provide direct evidence that the structure of the QD interface has a significant effect on the rate of nonradiative Auger recombination, which dominates biexciton decay. We also observe that the energy gradient at the core-shell interface introduced by the alloyed layer accelerates hole trapping from the shell to the core states, which results in suppression of shell emission. This comparative study offers practical guidelines for controlling multicarrier Auger recombination without a significant effect on either spectral or dynamical properties of single excitons. The proposed strategy should be applicable to QDs of a variety of compositions (including, e.g., infrared-emitting QDs) and can benefit numerous applications from light emitting diodes and lasers to photodetectors and photovoltaics. PMID:23521208

  19. Process to make core-shell structured nanoparticles

    DOEpatents

    Luhrs, Claudia; Phillips, Jonathan; Richard, Monique N

    2014-01-07

    Disclosed is a process for making a composite material that contains core-shell structured nanoparticles. The process includes providing a precursor in the form of a powder a liquid and/or a vapor of a liquid that contains a core material and a shell material, and suspending the precursor in an aerosol gas to produce an aerosol containing the precursor. In addition, the process includes providing a plasma that has a hot zone and passing the aerosol through the hot zone of the plasma. As the aerosol passes through the hot zone of the plasma, at least part of the core material and at least part of the shell material in the aerosol is vaporized. Vapor that contains the core material and the shell material that has been vaporized is removed from the hot zone of the plasma and allowed to condense into core-shell structured nanoparticles.

  20. Synthesis of core-shell composites using an inverse surfmer.

    PubMed

    Armando Zaragoza-Contreras, E; Stockton-Leal, Margarita; Hernández-Escobar, Claudia A; Hoshina, Yusuke; Guzmán-Lozano, Josué F; Kobayashi, Takaomi

    2012-07-01

    Anilinium dodecylsulfate was prepared from aniline and sodium dodecylsulfate. The critical micellar concentration of the salt was determined using electrical conductimetry, which revealed that the change of countercation, sodium by anilinium, reduced the critical micellar concentration with respect to the conventional counterpart, sodium dodecylsulfate. The anilinium dodecylsulfate was used as the surfmer in the synthesis of polystyrene/polyaniline core-shell composites, first performing as the surfactant to stabilize the emulsion polymerization of styrene, and later as the monomer to synthesize polyaniline via oxidative polymerization. Here, the surfmer function was directed toward the external phase instead of to the internal phase, as with conventional surfmers with carbon-carbon double bonds. Consequently, the term inverse surfmer is proposed. Analyses of its composite microstructure using electron microscopy and thermogravimetric analysis confirmed the core-shell arrangement. PMID:22520709

  1. Nanocomposite plasmonic fluorescence emitters with core/shell configurations.

    SciTech Connect

    Brener, Igal; Luk, Ting Shan; Miao, Xiaoyu

    2010-06-01

    This paper is focused on the optical properties of nanocomposite plasmonic emitters with core/shell configurations, where a fluorescence emitter is located inside a metal nanoshell. Systematic theoretical investigations are presented for the influence of material type, core radius, shell thickness, and excitation wavelength on the internal optical intensity, radiative quantum yield, and fluorescence enhancement of the nanocomposite emitter. It is our conclusion that: (i) an optimal ratio between the core radius and shell thickness is required to maximize the absorption rate of fluorescence emitters, and (ii) a large core radius is desired to minimize the non-radiative damping and avoid significant quantum yield degradation of light emitters. Several experimental approaches to synthesize these nanocomposite emitters are also discussed. Furthermore, our theoretical results are successfully used to explain several reported experimental observations and should prove useful for designing ultra-bright core/shell nanocomposite emitters.

  2. Rare Earth core/shell nanobarcodes for multiplexed trace biodetection.

    PubMed

    Chen, Lei; Li, Xiaomin; Shen, Dengke; Zhou, Lei; Zhu, Dan; Fan, Chunhai; Zhang, Fan

    2015-06-01

    Multiplexed detection technology has been attractive for its simultaneous assay of several analytes, which play significant roles in applications such as screening for combinatorial chemistry, genetic analysis, and clinical diagnostics. This work reports a novel and potentially powerful encoding system based upon dispersible suspension arrays of multilayer rare earth core/shell nanoparticles that are capable of multiplexed, high-sensitivity reporting for biomolecule detection by the Z-contrast imaging. These nanobarcode arrays are encoded by nanostructure design based on different atomic numbers. With the well-resolved high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) decoding technique, many thousands of unique nanobarcodes can be identified by multilayer core/shell nanostructure. Their applications to multiplexed biodetection of DNA demonstrated the highly sensitive (picomole) features of this novel nanobarcode system. PMID:25951110

  3. Radial modulation doping in core-shell nanowires

    NASA Astrophysics Data System (ADS)

    Dillen, David C.; Kim, Kyounghwan; Liu, En-Shao; Tutuc, Emanuel

    2014-02-01

    Semiconductor nanowires are potential candidates for applications in quantum information processing, Josephson junctions and field-effect transistors and provide a unique test bed for low-dimensional physical phenomena. The ability to fabricate nanowire heterostructures with atomically flat, defect-free interfaces enables energy band engineering in both axial and radial directions. The design of radial, or core-shell, nanowire heterostructures relies on energy band offsets that confine charge carriers into the core region, potentially reducing scattering from charged impurities on the nanowire surface. Key to the design of such nanoscale heterostructures is a fundamental understanding of the heterointerface properties, particularly energy band offsets and strain. The charge-transfer and confinement mechanism can be used to achieve modulation doping in core-shell structures. By selectively doping the shell, which has a larger bandgap, charge carriers are donated and confined in the core, generating a quasi-one-dimensional electron system with higher mobility. Here, we demonstrate radial modulation doping in coherently strained Ge-SixGe1-x core-shell nanowires and a technique to directly measure their valence band offset. Radial modulation doping is achieved by incorporating a B-doped layer during epitaxial shell growth. In contrast to previous work showing site-selective doping in Ge-Si core-shell nanowires, we find both an enhancement in peak hole mobility compared with undoped nanowires and observe a decoupling of electron transport in the core and shell regions. This decoupling stems from the higher carrier mobility in the core than in the shell and allows a direct measurement of the valence band offset for nanowires of various shell compositions.

  4. Synthesis of fullerene@gold core-shell nanostructures.

    PubMed

    Ren, Yupeng; Paira, Priyankar; Nayak, Tapas Ranjan; Ang, Wee Han; Pastorin, Giorgia

    2011-07-21

    A "direct encapsulation" method was developed for the synthesis of highly stable water-soluble fullerene@gold core-shell nanostructures, with gold nanoshells showing either closed or porous morphology. This gold nano-shell coating formed a "nano-oven", capable of decomposing encapsulated fullerene molecules rapidly when irradiated by laser. We envisaged this being a useful tool for chemical reactions as well as a novel scaffold for nano-material synthesis. PMID:21655582

  5. Isolation and Characterization of Monodisperse Core-Shell Nanoparticle Fractions.

    PubMed

    Sánchez-Ferrer, Antoni; Carney, Randy P; Stellacci, Francesco; Mezzenga, Raffaele; Isa, Lucio

    2015-10-20

    Monodispersity is a key property to control the self-assembly of colloidal particles, and is typically reached after fine-tuning of the synthesis conditions. Monodisperse particle fractions can also be separated from polydisperse suspensions via ultracentrifugation. This paper demonstrates the capability of isolating and characterizing suspensions of core-shell iron oxide-polymer nanoparticles with extremely low polydispersity (p < 0.01) and, thus, of complementing nanoparticle synthetic approaches in the pursuit of highly monodisperse materials. PMID:26406563

  6. Graded core/shell semiconductor nanorods and nanorod barcodes

    DOEpatents

    Alivisatos, A. Paul; Scher, Erik C.; Manna, Liberato

    2009-05-19

    Disclosed herein is a graded core/shell semiconductor nanorod having at least a first segment of a core of a Group II-VI, Group III-V or a Group IV semiconductor, a graded shell overlying the core, wherein the graded shell comprises at least two monolayers, wherein the at least two monolayers each independently comprise a Group II-VI, Group III-V or a Group IV semiconductor.

  7. Core-shell upconversion nanoparticle - semiconductor heterostructures for photodynamic therapy.

    PubMed

    Dou, Qing Qing; Rengaramchandran, Adith; Selvan, Subramanian Tamil; Paulmurugan, Ramasamy; Zhang, Yong

    2015-01-01

    Core-shell nanoparticles (CSNPs) with diverse chemical compositions have been attracting greater attention in recent years. However, it has been a challenge to develop CSNPs with different crystal structures due to the lattice mismatch of the nanocrystals. Here we report a rational design of core-shell heterostructure consisting of NaYF4:Yb,Tm upconversion nanoparticle (UCN) as the core and ZnO semiconductor as the shell for potential application in photodynamic therapy (PDT). The core-shell architecture (confirmed by TEM and STEM) enables for improving the loading efficiency of photosensitizer (ZnO) as the semiconductor is directly coated on the UCN core. Importantly, UCN acts as a transducer to sensitize ZnO and trigger the generation of cytotoxic reactive oxygen species (ROS) to induce cancer cell death. We also present a firefly luciferase (FLuc) reporter gene based molecular biosensor (ARE-FLuc) to measure the antioxidant signaling response activated in cells during the release of ROS in response to the exposure of CSNPs under 980 nm NIR light. The breast cancer cells (MDA-MB-231 and 4T1) exposed to CSNPs showed significant release of ROS as measured by aminophenyl fluorescein (APF) and ARE-FLuc luciferase assays, and ~45% cancer cell death as measured by MTT assay, when illuminated with 980 nm NIR light. PMID:25652742

  8. Core - shell upconversion nanoparticle - semiconductor heterostructures for photodynamic therapy

    NASA Astrophysics Data System (ADS)

    Dou, Qing Qing; Rengaramchandran, Adith; Selvan, Subramanian Tamil; Paulmurugan, Ramasamy; Zhang, Yong

    2015-02-01

    Core-shell nanoparticles (CSNPs) with diverse chemical compositions have been attracting greater attention in recent years. However, it has been a challenge to develop CSNPs with different crystal structures due to the lattice mismatch of the nanocrystals. Here we report a rational design of core-shell heterostructure consisting of NaYF4:Yb,Tm upconversion nanoparticle (UCN) as the core and ZnO semiconductor as the shell for potential application in photodynamic therapy (PDT). The core-shell architecture (confirmed by TEM and STEM) enables for improving the loading efficiency of photosensitizer (ZnO) as the semiconductor is directly coated on the UCN core. Importantly, UCN acts as a transducer to sensitize ZnO and trigger the generation of cytotoxic reactive oxygen species (ROS) to induce cancer cell death. We also present a firefly luciferase (FLuc) reporter gene based molecular biosensor (ARE-FLuc) to measure the antioxidant signaling response activated in cells during the release of ROS in response to the exposure of CSNPs under 980 nm NIR light. The breast cancer cells (MDA-MB-231 and 4T1) exposed to CSNPs showed significant release of ROS as measured by aminophenyl fluorescein (APF) and ARE-FLuc luciferase assays, and ~45% cancer cell death as measured by MTT assay, when illuminated with 980 nm NIR light.

  9. Au-Cu2O core-shell nanowire photovoltaics

    NASA Astrophysics Data System (ADS)

    Oener, S. Z.; Mann, S. A.; Sciacca, B.; Sfiligoj, C.; Hoang, J.; Garnett, E. C.

    2015-01-01

    Semiconductor nanowires are among the most promising candidates for next generation photovoltaics. This is due to their outstanding optical and electrical properties which provide large optical cross sections while simultaneously decoupling the photon absorption and charge carrier extraction length scales. These effects relax the requirements for both the minority carrier diffusion length and the amount of semiconductor needed. Metal-semiconductor core-shell nanowires have previously been predicted to show even better optical absorption than solid semiconductor nanowires and offer the additional advantage of a local metal core contact. Here, we fabricate and analyze such a geometry using a single Au-Cu2O core-shell nanowire photovoltaic cell as a model system. Spatially resolved photocurrent maps reveal that although the minority carrier diffusion length in the Cu2O shell is less than 1 μm, the radial contact geometry with the incorporated metal electrode still allows for photogenerated carrier collection along an entire nanowire. Current-voltage measurements yield an open-circuit voltage of 600 mV under laser illumination and a dark diode turn-on voltage of 1 V. This study suggests the metal-semiconductor core-shell nanowire concept could be extended to low-cost, large-scale photovoltaic devices, utilizing for example, metal nanowire electrode grids coated with epitaxially grown semiconductor shells.

  10. Porous Core-Shell Nanostructures for Catalytic Applications

    NASA Astrophysics Data System (ADS)

    Ewers, Trevor David

    Porous core-shell nanostructures have recently received much attention for their enhanced thermal stability. They show great potential in the field of catalysis, as reactant gases can diffuse in and out of the porous shell while the core particle is protected from sintering, a process in which particles coalesce to form larger particles. Sintering is a large problem in industry and is the primary cause of irreversible deactivation. Despite the obvious advantages of high thermal stability, porous core-shell nanoparticles can be developed to have additional interactive properties from the combination of the core and shell together, rather than just the core particle alone. This dissertation focuses on developing new porous core-shell systems in which both the core and shell take part in catalysis. Two types of systems are explored; (1) yolk-shell nanostructures with reducible oxide shells formed using the Kirkendall effect and (2) ceramic-based porous oxide shells formed using sol-gel chemistry. Of the Kirkendall-based systems, Au FexOy and Cu CoO were synthesized and studied for catalytic applications. Additionally, ZnO was explored as a potential shelling material. Sol-gel work focused on optimizing synthetic methods to allow for coating of small gold particles, which remains a challenge today. Mixed metal oxides were explored as a shelling material to make dual catalysts in which the product of a reaction on the core particle becomes a reactant within the shell.

  11. Thermal conductivity modeling of core-shell and tubular nanowires.

    PubMed

    Yang, Ronggui; Chen, Gang; Dresselhaus, Mildred S

    2005-06-01

    The heteroepitaxial growth of crystalline core-shell nanostructures of a variety of materials has become possible in recent years, allowing the realization of various novel nanoscale electronic and optoelectronic devices. The increased surface or interface area will decrease the thermal conductivity of such nanostructures and impose challenges for the thermal management of such devices. In the meantime, the decreased thermal conductivity might benefit the thermoelectric conversion efficiency. In this paper, we present modeling results on the lattice thermal conductivity of core-shell and tubular nanowires along the wire axis direction using the phonon Boltzmann equation. We report the dependence of the thermal conductivity on the surface conditions and the core-shell geometry for silicon core-germanium shell and tubular silicon nanowires at room temperature. The results show that the effective thermal conductivity changes not only with the composition of the constituents but also with the radius of the nanowires and nanopores due to the nature of the ballistic phonon transport. The results in this work have implications for the design and operation of a variety of nanoelectronic devices, optoelectronic devices, and thermoelectric materials and devices. PMID:15943452

  12. Core-shell Au@Pd nanoparticles with enhanced catalytic activity for oxygen reduction reaction via core-shell Au@Ag/Pd constructions

    PubMed Central

    Chen, Dong; Li, Chengyin; Liu, Hui; Ye, Feng; Yang, Jun

    2015-01-01

    Core-shell nanoparticles often exhibit improved catalytic properties due to the lattice strain created in these core-shell particles. Herein, we demonstrate the synthesis of core-shell Au@Pd nanoparticles from their core-shell Au@Ag/Pd parents. This strategy begins with the preparation of core-shell Au@Ag nanoparticles in an organic solvent. Then, the pure Ag shells are converted into the shells made of Ag/Pd alloy by galvanic replacement reaction between the Ag shells and Pd2+ precursors. Subsequently, the Ag component is removed from the alloy shell using saturated NaCl solution to form core-shell Au@Pd nanoparticles with an Au core and a Pd shell. In comparison with the core-shell Au@Pd nanoparticles upon directly depositing Pd shell on the Au seeds and commercial Pd/C catalysts, the core-shell Au@Pd nanoparticles via their core-shell Au@Ag/Pd templates display superior activity and durability in catalyzing oxygen reduction reaction, mainly due to the larger lattice tensile effect in Pd shell induced by the Au core and Ag removal. PMID:26144550

  13. Design of Super-Paramagnetic Core-Shell Nanoparticles for Enhanced Performance of Inverted Polymer Solar Cells.

    PubMed

    Jaramillo, Johny; Boudouris, Bryan W; Barrero, César A; Jaramillo, Franklin

    2015-11-18

    Controlling the nature and transfer of excited states in organic photovoltaic (OPV) devices is of critical concern due to the fact that exciton transport and separation can dictate the final performance of the system. One effective method to accomplish improved charge separation in organic electronic materials is to control the spin state of the photogenerated charge-carrying species. To this end, nanoparticles with unique iron oxide (Fe3O4) cores and zinc oxide (ZnO) shells were synthesized in a controlled manner. Then, the structural and magnetic properties of these core-shell nanoparticles (Fe3O4@ZnO) were tuned to ensure superior performance when they were incorporated into the active layers of OPV devices. Specifically, small loadings of the core-shell nanoparticles were blended with the previously well-characterized OPV active layer of poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM). Upon addition of the core-shell nanoparticles, the performance of the OPV devices was increased up to 25% relative to P3HT-PCBM active layer devices that contained no nanoparticles; this increase was a direct result of an increase in the short-circuit current densities of the devices. Furthermore, it was demonstrated that the increase in photocurrent was not due to enhanced absorption of the active layer due to the presence of the Fe3O4@ZnO core-shell nanoparticles. In fact, this increase in device performance occurred because of the presence of the superparamagnetic Fe3O4 in the core of the nanoparticles as incorporation of ZnO only nanoparticles did not alter the device performance. Importantly, however, the ZnO shell of the nanoparticles mitigated the negative optical effect of Fe3O4, which have been observed previously. This allowed the core-shell nanoparticles to outperform bare Fe3O4 nanoparticles when the single-layer nanoparticles were incorporated into the active layer of OPV devices. As such, the new materials described here present a

  14. The growth and enhanced catalytic performance of Au@Pd core-shell nanodendrites

    NASA Astrophysics Data System (ADS)

    Wang, Haihua; Sun, Zhenhua; Yang, Yi; Su, Dangsheng

    2012-12-01

    Au@Pd core-shell nanodendrites were synthesized by reducing H2PdCl4 with ascorbic acid onto the surface of Au polyhedra at room temperature. The Au@Pd core-shell nanodendrites consisting of a Au core and nanoporous Pd shell, exhibited plasmonic properties and higher catalytic activity in comparison with Au@Pd core-shell nanocubes.Au@Pd core-shell nanodendrites were synthesized by reducing H2PdCl4 with ascorbic acid onto the surface of Au polyhedra at room temperature. The Au@Pd core-shell nanodendrites consisting of a Au core and nanoporous Pd shell, exhibited plasmonic properties and higher catalytic activity in comparison with Au@Pd core-shell nanocubes. Electronic supplementary information (ESI) available: Experimental details, characterization and catalytic performance measurement of Au nanopolyhedra and Au@Pd core-shell nanostructures, TEM image of Au nanopolyhedra and Au@Pd core-shell nanodendrites after four cycles of the Suzuki coupling reaction, TEM and high-resolution images of a single Au@Pd core-shell nanodendrite, and XRD pattern of Au@Pd core-shell nanodendrites, UV-vis spectrum of Au@Pd nanodendrites in the range 200-400 nm, references. See DOI: 10.1039/c2nr32849f

  15. Core-Shell Chitosan Microcapsules for Programmed Sequential Drug Release.

    PubMed

    Yang, Xiu-Lan; Ju, Xiao-Jie; Mu, Xiao-Ting; Wang, Wei; Xie, Rui; Liu, Zhuang; Chu, Liang-Yin

    2016-04-27

    A novel type of core-shell chitosan microcapsule with programmed sequential drug release is developed by the microfluidic technique for acute gastrosis therapy. The microcapsule is composed of a cross-linked chitosan hydrogel shell and an oily core containing both free drug molecules and drug-loaded poly(lactic-co-glycolic acid) (PLGA) nanoparticles. Before exposure to acid stimulus, the resultant microcapsules can keep their structural integrity without leakage of the encapsulated substances. Upon acid-triggering, the microcapsules first achieve burst release due to the acid-induced decomposition of the chitosan shell. The encapsulated free drug molecules and drug-loaded PLGA nanoparticles are rapidly released within 60 s. Next, the drugs loaded in the PLGA nanoparticles are slowly released for several days to achieve sustained release based on the synergistic effect of drug diffusion and PLGA degradation. Such core-shell chitosan microcapsules with programmed sequential drug release are promising for rational drug delivery and controlled-release for the treatment of acute gastritis. In addition, the microcapsule systems with programmed sequential release provide more versatility for controlled release in biomedical applications. PMID:27052812

  16. Enhanced spin-orbit coupling in core/shell nanowires.

    PubMed

    Furthmeier, Stephan; Dirnberger, Florian; Gmitra, Martin; Bayer, Andreas; Forsch, Moritz; Hubmann, Joachim; Schüller, Christian; Reiger, Elisabeth; Fabian, Jaroslav; Korn, Tobias; Bougeard, Dominique

    2016-01-01

    The spin-orbit coupling (SOC) in semiconductors is strongly influenced by structural asymmetries, as prominently observed in bulk crystal structures that lack inversion symmetry. Here we study an additional effect on the SOC: the asymmetry induced by the large interface area between a nanowire core and its surrounding shell. Our experiments on purely wurtzite GaAs/AlGaAs core/shell nanowires demonstrate optical spin injection into a single free-standing nanowire and determine the effective electron g-factor of the hexagonal GaAs wurtzite phase. The spin relaxation is highly anisotropic in time-resolved micro-photoluminescence measurements on single nanowires, showing a significant increase of spin relaxation in external magnetic fields. This behaviour is counterintuitive compared with bulk wurtzite crystals. We present a model for the observed electron spin dynamics highlighting the dominant role of the interface-induced SOC in these core/shell nanowires. This enhanced SOC may represent an interesting tuning parameter for the implementation of spin-orbitronic concepts in semiconductor-based structures. PMID:27491871

  17. TOPICAL REVIEW: Ab initio symplectic no-core shell model

    NASA Astrophysics Data System (ADS)

    Dytrych, T.; Sviratcheva, K. D.; Draayer, J. P.; Bahri, C.; Vary, J. P.

    2008-12-01

    The no-core shell model (NCSM) is a prominent ab initio method that yields a good description of the low-lying states in few-nucleon systems as well as in more complex p-shell nuclei. Nevertheless, its applicability is limited by the rapid growth of the many-body basis with larger model spaces and increasing number of nucleons. The symplectic no-core shell model (Sp-NCSM) aspires to extend the scope of the NCSM beyond the p-shell region by augmenting the conventional spherical harmonic oscillator basis with the physically relevant symplectic \\SpR{3} symmetry-adapted configurations of the symplectic shell model that describe naturally the monopole-quadrupole vibrational and rotational modes, and also partially incorporate α-cluster correlations. In this review, the models underpinning the Sp-NCSM approach, namely, the NCSM, the Elliott SU(3) model and the symplectic shell model, are discussed. Following this, a prescription for constructing translationally invariant symplectic configurations in the spherical harmonic oscillator basis is given. This prescription is utilized to unveil the extent to which symplectic configurations enter into low-lying states in 12C and 16O nuclei calculated within the framework of the NCSM with the JISP16 realistic nucleon-nucleon interaction. The outcomes of this proof-of-principle study are presented in detail.

  18. Enhanced spin-orbit coupling in core/shell nanowires

    NASA Astrophysics Data System (ADS)

    Furthmeier, Stephan; Dirnberger, Florian; Gmitra, Martin; Bayer, Andreas; Forsch, Moritz; Hubmann, Joachim; Schüller, Christian; Reiger, Elisabeth; Fabian, Jaroslav; Korn, Tobias; Bougeard, Dominique

    2016-08-01

    The spin-orbit coupling (SOC) in semiconductors is strongly influenced by structural asymmetries, as prominently observed in bulk crystal structures that lack inversion symmetry. Here we study an additional effect on the SOC: the asymmetry induced by the large interface area between a nanowire core and its surrounding shell. Our experiments on purely wurtzite GaAs/AlGaAs core/shell nanowires demonstrate optical spin injection into a single free-standing nanowire and determine the effective electron g-factor of the hexagonal GaAs wurtzite phase. The spin relaxation is highly anisotropic in time-resolved micro-photoluminescence measurements on single nanowires, showing a significant increase of spin relaxation in external magnetic fields. This behaviour is counterintuitive compared with bulk wurtzite crystals. We present a model for the observed electron spin dynamics highlighting the dominant role of the interface-induced SOC in these core/shell nanowires. This enhanced SOC may represent an interesting tuning parameter for the implementation of spin-orbitronic concepts in semiconductor-based structures.

  19. Biocompatible core-shell magnetic nanoparticles for cancer treatment

    SciTech Connect

    Sharma, Amit M.; Qiang, You; Meyer, Daniel R.; Souza, Ryan; Mcconnaughoy, Alan; Muldoon, Leslie; Baer, Donald R.

    2008-04-01

    Non-toxic magnetic nanoparticles (MNPs) have expanded the treatment delivery options in the medical world. With a size range from 2 to 200 nm MNPs can be compiled with most of the small cells and tissues in living body. Monodispersive iron-iron oxide core shell nanoparticles were prepared in our novel cluster deposition system. This unique method of preparing the core shell MNPs gives nanoparticles very high magnetic moment. We tested the nontoxicity and uptake of MNPs coated with/without dextrin by incubating them with rat LX-1 small cell lung cancer cells (SCLC). Since core iron enhances the heating effect [7] the rate of oxidation of iron nanoparticles was tested in deionized water at certain time interval. Both coated and noncoated MNPs were successfully uptaken by the cells, indicating that the nanoparticles were not toxic. The stability of MNPs was verified by X-ray diffraction (XRD) scan after 0, 24, 48, 96, 204 hours. Due to the high magnetic moment offered by MNPs produced in our lab, we predict that even in low applied external alternating field desired temperature can be reached in cancer cells in comparison to the commercially available nanoparticles. Moreover, our MNPs do not require additional anti-coagulating agents and provide a cost effective means of treatment with significantly lower dosage in the body in comparison to commercially available nanoparticles.

  20. Enhanced spin–orbit coupling in core/shell nanowires

    PubMed Central

    Furthmeier, Stephan; Dirnberger, Florian; Gmitra, Martin; Bayer, Andreas; Forsch, Moritz; Hubmann, Joachim; Schüller, Christian; Reiger, Elisabeth; Fabian, Jaroslav; Korn, Tobias; Bougeard, Dominique

    2016-01-01

    The spin–orbit coupling (SOC) in semiconductors is strongly influenced by structural asymmetries, as prominently observed in bulk crystal structures that lack inversion symmetry. Here we study an additional effect on the SOC: the asymmetry induced by the large interface area between a nanowire core and its surrounding shell. Our experiments on purely wurtzite GaAs/AlGaAs core/shell nanowires demonstrate optical spin injection into a single free-standing nanowire and determine the effective electron g-factor of the hexagonal GaAs wurtzite phase. The spin relaxation is highly anisotropic in time-resolved micro-photoluminescence measurements on single nanowires, showing a significant increase of spin relaxation in external magnetic fields. This behaviour is counterintuitive compared with bulk wurtzite crystals. We present a model for the observed electron spin dynamics highlighting the dominant role of the interface-induced SOC in these core/shell nanowires. This enhanced SOC may represent an interesting tuning parameter for the implementation of spin–orbitronic concepts in semiconductor-based structures. PMID:27491871

  1. Acoustic phonons and strain in core/shell nanowires

    NASA Astrophysics Data System (ADS)

    Kloeffel, Christoph; Trif, Mircea; Loss, Daniel

    2014-09-01

    We study theoretically the low-energy phonons and the static strain in cylindrical core/shell nanowires (NWs). Assuming pseudomorphic growth, isotropic media, and a force-free wire surface, we derive algebraic expressions for the dispersion relations, the displacement fields, and the stress and strain components from linear elasticity theory. Our results apply to NWs with arbitrary radii and arbitrary elastic constants for both core and shell. The expressions for the static strain are consistent with experiments, simulations, and previous analytical investigations; those for phonons are consistent with known results for homogeneous NWs. Among other things, we show that the dispersion relations of the torsional, longitudinal, and flexural modes change differently with the relative shell thickness, and we identify new terms in the corresponding strain tensors that are absent for uncapped NWs. We illustrate our results via the example of Ge/Si core/shell NWs and demonstrate that shell-induced strain has large effects on the hole spectrum of these systems.

  2. Organized thiol functional groups in mesoporous core shell colloids

    SciTech Connect

    Marchena, Martin H.; Granada, Mara; Bordoni, Andrea V.; Joselevich, Maria; Troiani, Horacio; Williams, Federico J.; Wolosiuk, Alejandro

    2012-03-15

    The co-condensation in situ of tetraethoxysilane (TEOS) and mercaptopropyltrimethoxysilane (MPTMS) using cetyltrimethylammonium bromide (CTAB) as a template results in the synthesis of multilayered mesoporous structured SiO{sub 2} colloids with 'onion-like' chemical environments. Thiol groups were anchored to an inner selected SiO{sub 2} porous layer in a bilayered core shell particle producing different chemical regions inside the colloidal layered structure. X-Ray Photoelectron Spectroscopy (XPS) shows a preferential anchoring of the -SH groups in the double layer shell system, while porosimetry and simple chemical modifications confirm that pores are accessible. We can envision the synthesis of interesting colloidal objects with defined chemical environments with highly controlled properties. - Graphical abstract: Mesoporous core shell SiO{sub 2} colloids with organized thiol groups. Highlights: Black-Right-Pointing-Pointer Double shell mesoporous silica colloids templated with CTAB. Black-Right-Pointing-Pointer Sequential deposition of mesoporous SiO{sub 2} layers with different chemistries. Black-Right-Pointing-Pointer XPS shows the selective functionalization of mesoporous layers with thiol groups.

  3. Thermoelectric properties of porous multi-walled carbon nanotube/polyaniline core/shell nanocomposites.

    PubMed

    Zhang, Kun; Davis, Marauo; Qiu, Jingjing; Hope-Weeks, Louisa; Wang, Shiren

    2012-09-28

    Porous polyaniline (PANI)-coated multi-walled carbon nanotube (MWNT) core/shell nanohybrids were fabricated through in situ polymerization and subsequently assembled into macroscopic composites. N(2) adsorption/desorption analysis indicated that the volume of nanopores increased significantly, which could make a significant contribution to phonon scattering. Thermal annealing was also carried out to improve the Seebeck coefficient of the as-produced nanocomposites. The optimal sample showed electrical conductivity of 14.1 S cm(-1), a Seebeck coefficient of 79.8 μV K(-1) and thermal conductivity of 0.27 W mK(-1), resulting in a highest figure of merit (ZT) of 0.01 at a very low loading of MWNTs (<1 wt%). These results will provide a potential direction to enhance thermoelectric performance of organic materials and also facilitate the application of organic materials in thermal energy harvesting or cooling. PMID:22947620

  4. Thermoelectric properties of porous multi-walled carbon nanotube/polyaniline core/shell nanocomposites

    NASA Astrophysics Data System (ADS)

    Zhang, Kun; Davis, Marauo; Qiu, Jingjing; Hope-Weeks, Louisa; Wang, Shiren

    2012-09-01

    Porous polyaniline (PANI)-coated multi-walled carbon nanotube (MWNT) core/shell nanohybrids were fabricated through in situ polymerization and subsequently assembled into macroscopic composites. N2 adsorption/desorption analysis indicated that the volume of nanopores increased significantly, which could make a significant contribution to phonon scattering. Thermal annealing was also carried out to improve the Seebeck coefficient of the as-produced nanocomposites. The optimal sample showed electrical conductivity of 14.1 S cm-1, a Seebeck coefficient of 79.8 μV K-1 and thermal conductivity of 0.27 W mK-1, resulting in a highest figure of merit (ZT) of 0.01 at a very low loading of MWNTs (<1 wt%). These results will provide a potential direction to enhance thermoelectric performance of organic materials and also facilitate the application of organic materials in thermal energy harvesting or cooling.

  5. Enhancement of Thermoelectric Performance by Reducing Phonon Thermal Conductance in Multiple Core-shell Nanowires

    PubMed Central

    Zhou, Wu-Xing; Chen, Ke-Qiu

    2014-01-01

    The thermoelectric properties of multiple core-shell nanowires are investigated by using nonequilibrium Green's function method and molecular dynamics simulations. The results show that the thermoelectric performance of multiple core-shell NWs can be improved observably with the increase of shell number compared with the single component NWs due to the significant reduction of phonon thermal conductance. The ZT value of multiple core-shell NWs can reach three times greater than that of the single component GaSb NWs at room temperature. Moreover, the ZT values of both the core-shell NWs and single component NWs are increased with the increasing temperature, but the ZT value of core-shell NWs increases more slowly than that of single component NWs. These results show that the single component NWs is suitable as thermoelectric material at much high temperature, but the multiple core-shell NWs is more suitable as thermoelectric material at room temperature. PMID:25413874

  6. Suppression of non-radiative surface recombination by N incorporation in GaAs/GaNAs core/shell nanowires

    PubMed Central

    Chen, Shula L.; Chen, Weimin M.; Ishikawa, Fumitaro; Buyanova, Irina A.

    2015-01-01

    III-V semiconductor nanowires (NWs) such as GaAs NWs form an interesting artificial materials system promising for applications in advanced optoelectronic and photonic devices, thanks to the advantages offered by the 1D architecture and the possibility to combine it with the main-stream silicon technology. Alloying of GaAs with nitrogen can further enhance performance and extend device functionality via band-structure and lattice engineering. However, due to a large surface-to-volume ratio, III-V NWs suffer from severe non-radiative carrier recombination at/near NWs surfaces that significantly degrades optical quality. Here we show that increasing nitrogen composition in novel GaAs/GaNAs core/shell NWs can strongly suppress the detrimental surface recombination. This conclusion is based on our experimental finding that lifetimes of photo-generated free excitons and free carriers increase with increasing N composition, as revealed from our time-resolved photoluminescence (PL) studies. This is accompanied by a sizable enhancement in the PL intensity of the GaAs/GaNAs core/shell NWs at room temperature. The observed N-induced suppression of the surface recombination is concluded to be a result of an N-induced modification of the surface states that are responsible for the nonradiative recombination. Our results, therefore, demonstrate the great potential of incorporating GaNAs in III-V NWs to achieve efficient nano-scale light emitters. PMID:26100755

  7. Simultaneous in-situ synthesis and characterization of Co@Cu core-shell nanoparticle arrays

    DOE PAGESBeta

    McKeown, Joseph T.; Wu, Yueying; Fowlkes, Jason D.; Rack, Philip D.; Campbell, Geoffrey H.

    2014-12-23

    Core-shell nanostructures have attracted much attention due to their unique and tunable properties relative to bulk structures of the same materials, making core-shell nanoparticles candidates for a variety of applications with multiple functionalities.[1,2] Intriguing magnetic behavior can be tailored by variation of size, interface, crystal orientation, and composition, and core-shell nanostructures with noble-metal shells yield novel optical responses[3] and enhanced electrocatalytic activity.[4

  8. Core-size-dependent catalytic properties of bimetallic Au/Ag core-shell nanoparticles.

    PubMed

    Haldar, Krishna Kanta; Kundu, Simanta; Patra, Amitava

    2014-12-24

    Bimetallic core-shell nanoparticles have recently emerged as a new class of functional materials because of their potential applications in catalysis, surface enhanced Raman scattering (SERS) substrate and photonics etc. Here, we have synthesized Au/Ag bimetallic core-shell nanoparticles with varying the core diameter. The red-shifting of the both plasmonic peaks of Ag and Au confirms the core-shell structure of the nanoparticles. Transmission electron microscopy (TEM) analysis, line scan EDS measurement and UV-vis study confirm the formation of core-shell nanoparticles. We have examined the catalytic activity of these core-shell nanostructures in the reaction between 4-nitrophenol (4-NP) and NaBH4 to form 4-aminophenol (4-AP) and the efficiency of the catalytic reaction is found to be increased with increasing the core size of Au/Ag core-shell nanocrystals. The catalytic efficiency varies from 41.8 to 96.5% with varying core size from 10 to 100 nm of Au/Ag core-shell nanoparticles, and the Au100/Ag bimetallic core-shell nanoparticle is found to be 12-fold more active than that of the pure Au nanoparticles with 100 nm diameter. Thus, the catalytic properties of the metal nanoparticles are significantly enhanced because of the Au/Ag core-shell structure, and the rate is dependent on the size of the core of the nanoparticles. PMID:25456348

  9. Stability of core-shell nanowires in selected model solutions

    NASA Astrophysics Data System (ADS)

    Kalska-Szostko, B.; Wykowska, U.; Basa, A.; Zambrzycka, E.

    2015-03-01

    This paper presents the studies of stability of magnetic core-shell nanowires prepared by electrochemical deposition from an acidic solution containing iron in the core and modified surface layer. The obtained nanowires were tested according to their durability in distilled water, 0.01 M citric acid, 0.9% NaCl, and commercial white wine (12% alcohol). The proposed solutions were chosen in such a way as to mimic food related environment due to a possible application of nanowires as additives to, for example, packages. After 1, 2 and 3 weeks wetting in the solutions, nanoparticles were tested by Infrared Spectroscopy, Atomic Absorption Spectroscopy, Transmission Electron Microscopy and X-ray diffraction methods.

  10. Magnetization processes in core/shell exchange-spring structures

    NASA Astrophysics Data System (ADS)

    Jiang, J. S.

    2015-05-01

    The magnetization reversal processes in cylindrical and spherical soft core/hard shell exchange-spring structures are investigated via the analytical nucleation theory and are verified with numerical micromagnetic simulations. At small core sizes, the nucleation of magnetic reversal proceeds via the modified bulging mode, where the transverse component of the magnetization is only semi-coherent in direction and the nucleation field contains a contribution from self-demagnetization. For large core sizes, the modified curling mode, where the magnetization configuration is vortex-like, is favored at nucleation. The preference for the modified curling mode is beneficial in that the flux-closure allows cylindrical and spherical core/shell exchange-spring elements to be densely packed into bulk permanent magnets without affecting the nucleation field, thereby offering the potential for high energy product.

  11. Vertical Ge/Si Core/Shell Nanowire Junctionless Transistor.

    PubMed

    Chen, Lin; Cai, Fuxi; Otuonye, Ugo; Lu, Wei D

    2016-01-13

    Vertical junctionless transistors with a gate-all-around (GAA) structure based on Ge/Si core/shell nanowires epitaxially grown and integrated on a ⟨111⟩ Si substrate were fabricated and analyzed. Because of efficient gate coupling in the nanowire-GAA transistor structure and the high density one-dimensional hole gas formed in the Ge nanowire core, excellent P-type transistor behaviors with Ion of 750 μA/μm were obtained at a moderate gate length of 544 nm with minimal short-channel effects. The experimental data can be quantitatively modeled by a GAA junctionless transistor model with few fitting parameters, suggesting the nanowire transistors can be fabricated reliably without introducing additional factors that can degrade device performance. Devices with different gate lengths were readily obtained by tuning the thickness of an etching mask film. Analysis of the histogram of different devices yielded a single dominate peak in device parameter distribution, indicating excellent uniformity and high confidence of single nanowire operation. Using two vertical nanowire junctionless transistors, a PMOS-logic inverter with near rail-to-rail output voltage was demonstrated, and device matching in the logic can be conveniently obtained by controlling the number of nanowires employed in different devices rather than modifying device geometry. These studies show that junctionless transistors based on vertical Ge/Si core/shell nanowires can be fabricated in a controlled fashion with excellent performance and may be used in future hybrid, high-performance circuits where bottom-up grown nanowire devices with different functionalities can be directly integrated with an existing Si platform. PMID:26674542

  12. Dual emission in asymmetric ``giant'' PbS/CdS/CdS core/shell/shell quantum dots

    NASA Astrophysics Data System (ADS)

    Zhao, Haiguang; Sirigu, Gianluca; Parisini, Andrea; Camellini, Andrea; Nicotra, Giuseppe; Rosei, Federico; Morandi, Vittorio; Zavelani-Rossi, Margherita; Vomiero, Alberto

    2016-02-01

    Semiconducting nanocrystals optically active in the infrared region of the electromagnetic spectrum enable exciting avenues in fundamental research and novel applications compatible with the infrared transparency windows of biosystems such as chemical and biological optical sensing, including nanoscale thermometry. In this context, quantum dots (QDs) with double color emission may represent ultra-accurate and self-calibrating nanosystems. We present the synthesis of giant core/shell/shell asymmetric QDs having a PbS/CdS zinc blende (Zb)/CdS wurtzite (Wz) structure with double color emission close to the near-infrared (NIR) region. We show that the double emission depends on the excitation condition and analyze the electron-hole distribution responsible for the independent and simultaneous radiative exciton recombination in the PbS core and in the CdS Wz shell, respectively. These results highlight the importance of the driving force leading to preferential crystal growth in asymmetric QDs, and provide a pathway for the rational control of the synthesis of double color emitting giant QDs, leading to the effective exploitation of visible/NIR transparency windows.Semiconducting nanocrystals optically active in the infrared region of the electromagnetic spectrum enable exciting avenues in fundamental research and novel applications compatible with the infrared transparency windows of biosystems such as chemical and biological optical sensing, including nanoscale thermometry. In this context, quantum dots (QDs) with double color emission may represent ultra-accurate and self-calibrating nanosystems. We present the synthesis of giant core/shell/shell asymmetric QDs having a PbS/CdS zinc blende (Zb)/CdS wurtzite (Wz) structure with double color emission close to the near-infrared (NIR) region. We show that the double emission depends on the excitation condition and analyze the electron-hole distribution responsible for the independent and simultaneous radiative exciton

  13. Hydrothermal synthesis of high-quality type-II CdTe/CdSe core/shell quantum dots with dark red emission.

    PubMed

    Liu, Ning; Yang, Ping

    2014-08-01

    A hydrothermal method was used to synthesize type-II CdTe/CdSe core/shell quantum dots (QDs) using the thilglycolic acid (TGA) capped CdTe QDs as cores, which show a number of advantages. Because of the spatial separation of carriers the low excited states of CdTe/CdSe QDs, they exhibit many novel properties that are fundamentally different from the type-I QDs. On the other hand, our experiment results show that the wave function of the hole of the exciton in the CdTe core extends well into the CdSe shell. The results also reveal that a thick shell can confine the electrons inside the particles and thereby improve the PL efficiency and prolong the lifetime of the core/shell QDs. We use the UV-vis absorption and fluorescence spectrum measurements on growing particles in detail. We found that the fluorescence of the CdTe/CdSe QDs was strongly dependent on the thick of the shell and size of the core as well as the unique type-II heterostructure, which make the type-II core/shell QDs more suitable in photovoltaic or photoconduction applications. PMID:25936008

  14. The diamagnetic susceptibility of a donor in a semiconductor core shell quantum dot

    SciTech Connect

    Sudharshan, M. S.; Subhash, P.; Shaik, Nagoor Babu; Kalpana, P.; Jayakumar, K.; Reuben, A. Merwyn Jasper D.

    2015-06-24

    The effect of Aluminium concentration, shell thickness and size of the core shell Quantum Dot on the Diamagnetic Susceptibility of a donor in the Core Shell Quantum Dot is calculated in the effective mass approximation using the variational method. The results are presented and discussed.

  15. Iron(ii)-triazole core-shell nanocomposites: toward multistep spin crossover materials.

    PubMed

    Wang, Yu-Xia; Qiu, Dan; Xi, Sai-Fei; Ding, Zheng-Dong; Li, Zaijun; Li, Yunxing; Ren, Xuehong; Gu, Zhi-Guo

    2016-06-28

    The first SCO@SCO core-shell nanomaterials have been synthesized by the step-by-step microemulsion method. The observed gyroscopic core-shell nanocomposites exhibit three-step spin crossover behaviour with thermal hysteresis at around room temperature. This offers an efficient and novel strategy for the development of multistable SCO materials. PMID:27263855

  16. A novel approach to the construction of core shell gold polyaniline nanoparticles

    NASA Astrophysics Data System (ADS)

    Dong, Yang; Ma, Ying; Zhai, Tianyou; Zeng, Yi; Fu, Hongbing; Yao, Jiannian

    2007-11-01

    Uniform core-shell gold-polyaniline (Au-PANI) nanoparticles were successfully fabricated by in situ polymerization of aniline using poly(N-isopropylacrylamide)-co-poly(acrylic acid) (PNIPAM-co-PAA)/AuNP hybrid microgel particles as a template. TEM images gave direct evidence of the core-shell nanostructure of Au-PANI particles, which were composed of gold nanoparticles as the core and polyaniline as the shell. The shell thickness of as-prepared core-shell Au-PANI nanoparticles can be easily tuned by controlling the reaction time. A possible mechanism for the formation of core-shell Au-PANI nanostructures was proposed. This novel synthetic method may be extended to the synthesis of other core-shell nanostructures with diverse functionality and high colloidal stability.

  17. Design, synthesis and applications of core-shell, hollow core, and nanorattle multifunctional nanostructures.

    PubMed

    El-Toni, Ahmed Mohamed; Habila, Mohamed A; Labis, Joselito Puzon; ALOthman, Zeid A; Alhoshan, Mansour; Elzatahry, Ahmed A; Zhang, Fan

    2016-02-01

    With the evolution of nanoscience and nanotechnology, studies have been focused on manipulating nanoparticle properties through the control of their size, composition, and morphology. As nanomaterial research has progressed, the foremost focus has gradually shifted from synthesis, morphology control, and characterization of properties to the investigation of function and the utility of integrating these materials and chemical sciences with the physical, biological, and medical fields, which therefore necessitates the development of novel materials that are capable of performing multiple tasks and functions. The construction of multifunctional nanomaterials that integrate two or more functions into a single geometry has been achieved through the surface-coating technique, which created a new class of substances designated as core-shell nanoparticles. Core-shell materials have growing and expanding applications due to the multifunctionality that is achieved through the formation of multiple shells as well as the manipulation of core/shell materials. Moreover, core removal from core-shell-based structures offers excellent opportunities to construct multifunctional hollow core architectures that possess huge storage capacities, low densities, and tunable optical properties. Furthermore, the fabrication of nanomaterials that have the combined properties of a core-shell structure with that of a hollow one has resulted in the creation of a new and important class of substances, known as the rattle core-shell nanoparticles, or nanorattles. The design strategies of these new multifunctional nanostructures (core-shell, hollow core, and nanorattle) are discussed in the first part of this review. In the second part, different synthesis and fabrication approaches for multifunctional core-shell, hollow core-shell and rattle core-shell architectures are highlighted. Finally, in the last part of the article, the versatile and diverse applications of these nanoarchitectures in

  18. Design, synthesis and applications of core-shell, hollow core, and nanorattle multifunctional nanostructures

    NASA Astrophysics Data System (ADS)

    El-Toni, Ahmed Mohamed; Habila, Mohamed A.; Labis, Joselito Puzon; Alothman, Zeid A.; Alhoshan, Mansour; Elzatahry, Ahmed A.; Zhang, Fan

    2016-01-01

    With the evolution of nanoscience and nanotechnology, studies have been focused on manipulating nanoparticle properties through the control of their size, composition, and morphology. As nanomaterial research has progressed, the foremost focus has gradually shifted from synthesis, morphology control, and characterization of properties to the investigation of function and the utility of integrating these materials and chemical sciences with the physical, biological, and medical fields, which therefore necessitates the development of novel materials that are capable of performing multiple tasks and functions. The construction of multifunctional nanomaterials that integrate two or more functions into a single geometry has been achieved through the surface-coating technique, which created a new class of substances designated as core-shell nanoparticles. Core-shell materials have growing and expanding applications due to the multifunctionality that is achieved through the formation of multiple shells as well as the manipulation of core/shell materials. Moreover, core removal from core-shell-based structures offers excellent opportunities to construct multifunctional hollow core architectures that possess huge storage capacities, low densities, and tunable optical properties. Furthermore, the fabrication of nanomaterials that have the combined properties of a core-shell structure with that of a hollow one has resulted in the creation of a new and important class of substances, known as the rattle core-shell nanoparticles, or nanorattles. The design strategies of these new multifunctional nanostructures (core-shell, hollow core, and nanorattle) are discussed in the first part of this review. In the second part, different synthesis and fabrication approaches for multifunctional core-shell, hollow core-shell and rattle core-shell architectures are highlighted. Finally, in the last part of the article, the versatile and diverse applications of these nanoarchitectures in

  19. Core-shell interaction and its impact on the optical absorption of pure and doped core-shell CdSe/ZnSe nanoclusters

    NASA Astrophysics Data System (ADS)

    Wang, Xinqin; Cui, Yingqi; Yu, Shengping; Zeng, Qun; Yang, Mingli

    2016-04-01

    The structural, electronic, and optical properties of core-shell nanoclusters, (CdSe)x@(CdSe)y and their Zn-substituted complexes of x = 2-4 and y = 16-28, were studied with density functional theory calculations. The substitution was applied in the cores, the shells, and/or the whole clusters. All these clusters are characterized by their core-shell structures in which the core-shell interaction was found different from those in core or in shell, as reflected by their bondlengths, volumes, and binding energies. Moreover, the core and shell combine together to compose a new cluster with electronic and optical properties different from those of separated individuals, as reflected by their HOMO-LUMO gaps and optical absorptions. With the substitution of Cd by Zn, the structural, electronic, and optical properties of clusters change regularly. The binding energy increases with Zn content, attributed to the strong Zn-Se bonding. For the same core/shell, the structure with a CdSe shell/core has a narrower gap than that with a ZnSe shell/core. The optical absorption spectra also change accordingly with Zn substitution. The peaks blueshift with increasing Zn concentration, accompanying with shape variations in case large number of Cd atoms are substituted. Our calculations reveal the core-shell interaction and its influence on the electronic and optical properties of the core-shell clusters, suggesting a composition-structure-property relationship for the design of core-shell CdSe and ZnSe nanoclusters.

  20. Cloaking core-shell nanoparticles from conducting electrons in solids.

    PubMed

    Liao, Bolin; Zebarjadi, Mona; Esfarjani, Keivan; Chen, Gang

    2012-09-21

    In this Letter, we aim at making nanoparticles embedded in a host semiconductor with a size comparable to electronic wavelengths "invisible" to the electron transport. Inspired by the recent progress made in optics and working within the framework of the expansion of partial waves, we demonstrate that the opposite effects imposed by potential barriers and wells of a core-shell nanoparticle on the phase shifts associated with the scattered electron wave could make the scattering cross section of the first two partial waves vanish simultaneously. We show that this is sufficient to cloak the nanoparticle from being detected by electrons with specific energy in the sense that a total scattering cross section smaller than 0.01% of the physical cross section can be obtained and a 4 orders of magnitude difference in the total scattering cross section can be presented within an energy range of only 40 meV, indicating possible applications of the "electron cloaks" as novel electronic switches and sensors, and in efficient energy harvesting and conversion technologies. PMID:23005976

  1. Recent Developments in No-Core Shell-Model Calculations

    SciTech Connect

    Navratil, P; Quaglioni, S; Stetcu, I; Barrett, B R

    2009-03-20

    We present an overview of recent results and developments of the no-core shell model (NCSM), an ab initio approach to the nuclear many-body problem for light nuclei. In this aproach, we start from realistic two-nucleon or two- plus three-nucleon interactions. Many-body calculations are performed using a finite harmonic-oscillator (HO) basis. To facilitate convergence for realistic inter-nucleon interactions that generate strong short-range correlations, we derive effective interactions by unitary transformations that are tailored to the HO basis truncation. For soft realistic interactions this might not be necessary. If that is the case, the NCSM calculations are variational. In either case, the ab initio NCSM preserves translational invariance of the nuclear many-body problem. In this review, we, in particular, highlight results obtained with the chiral two- plus three-nucleon interactions. We discuss efforts to extend the applicability of the NCSM to heavier nuclei and larger model spaces using importance-truncation schemes and/or use of effective interactions with a core. We outline an extension of the ab initio NCSM to the description of nuclear reactions by the resonating group method technique. A future direction of the approach, the ab initio NCSM with continuum, which will provide a complete description of nuclei as open systems with coupling of bound and continuum states is given in the concluding part of the review.

  2. Nonlocal dielectric effects in core-shell nanowires.

    SciTech Connect

    McMahon, J. M.; Gray, S. K.; Schatz, G. C.

    2010-01-01

    We study the optical spectra and near fields of core-shell nanowires (nanoshells), using a recently developed finite-difference method that allows for a spatially nonlocal dielectric response. We first analyze the parameters of the nonlocal model by making comparisons with related experimental data and previous theoretical work. We then investigate how nonlocal effects are dependent on nanoshell features, such as shell thickness, overall size, and the ratio of core radius to shell radius. We demonstrate that the shell thickness along the longitudinal direction of the incident light is the primary controlling factor of nonlocal effects, which appear as anomalous absorption resonances and blueshifts in the localized surface plasmon resonance (LSPR) positions, relative to local theory. In addition, we show that the amount of blueshift depends on the order of the LSPR. The optical responses of nanoshells immersed in various refractive index (RI) environments are also studied. We show that the nonlocal anomalous absorption features are relatively insensitive to RI changes, but the blueshift of the dipolar LSPR varies nonlinearly.

  3. Homogeneous Protein Analysis by Magnetic Core-Shell Nanorod Probes.

    PubMed

    Schrittwieser, Stefan; Pelaz, Beatriz; Parak, Wolfgang J; Lentijo-Mozo, Sergio; Soulantica, Katerina; Dieckhoff, Jan; Ludwig, Frank; Altantzis, Thomas; Bals, Sara; Schotter, Joerg

    2016-04-13

    Studying protein interactions is of vital importance both to fundamental biology research and to medical applications. Here, we report on the experimental proof of a universally applicable label-free homogeneous platform for rapid protein analysis. It is based on optically detecting changes in the rotational dynamics of magnetically agitated core-shell nanorods upon their specific interaction with proteins. By adjusting the excitation frequency, we are able to optimize the measurement signal for each analyte protein size. In addition, due to the locking of the optical signal to the magnetic excitation frequency, background signals are suppressed, thus allowing exclusive studies of processes at the nanoprobe surface only. We study target proteins (soluble domain of the human epidermal growth factor receptor 2 - sHER2) specifically binding to antibodies (trastuzumab) immobilized on the surface of our nanoprobes and demonstrate direct deduction of their respective sizes. Additionally, we examine the dependence of our measurement signal on the concentration of the analyte protein, and deduce a minimally detectable sHER2 concentration of 440 pM. For our homogeneous measurement platform, good dispersion stability of the applied nanoprobes under physiological conditions is of vital importance. To that end, we support our measurement data by theoretical modeling of the total particle-particle interaction energies. The successful implementation of our platform offers scope for applications in biomarker-based diagnostics as well as for answering basic biology questions. PMID:27023370

  4. Supramolecular core-shell nanoparticles for photoconductive device applications.

    PubMed

    Cheng, Chih-Chia; Chen, Jem-Kun; Shieh, Yeong-Tarng; Lee, Duu-Jong

    2016-08-12

    We report a breakthrough discovery involving supramolecular-based strategies to construct novel core-shell heterojunction nanoparticles with hydrophilic adenine-functionalized polythiophene (PAT) as the core and hydrophobic phenyl-C61-butyric acid methyl ester (PCBM) as the shell, which enables the conception of new functional supramolecular assemblies for constructing functional nanomaterials for applications in optoelectronic devices. The generated nanoparticles exhibit uniform spherical shape, well-controlled tuning of particle size with narrow size distributions, and excellent electrochemical stability in solution and the solid state owing to highly efficient energy transfer from PAT to PCBM. When the PAT/PCBM nanoparticles were fabricated into a photoconducting layer in an electronic device, the resulting device showed excellent electric conduction characteristics, including an electrically-tunable voltage-controlled switch, and high short-circuit current and open-circuit voltage. These observations demonstrate how the self-assembly of PAT/PCBM into specific nanostructures may help to promote efficient charge generation and transport processes, suggesting potential for a wide variety of applications as a promising candidate material for bulk heterojunction polymer devices. PMID:27353003

  5. Mesoscale modeling of functional properties in core-shell nanoparticles

    NASA Astrophysics Data System (ADS)

    Mangeri, John; Heinonen, Olle; Karpeev, Dmitry; Nakhmanson, Serge

    2015-03-01

    Core-shell nanoparticle systems of Zn-ZnO and ZnO-TiO2 are studied computationally using the highly scalable MOOSE finite-element framework, developed at Idaho National Lab. The elastic anisotropic mismatch of the core and shell create an imprinting effect within the shell that produces a wide variation of strains. Due to this diversity of strains, the sharp band gap edges of the bulk semiconductor are observed to be ``thinned-out'' much like amorphous silicon. We show that a variety of factors, such as particle size, core-to-shell volume ratio, applied hydrostatic pressure, shell microstructure, as well as the effect of surface elasticity, can influence the distribution of optical band-gap values within the particle, which may prove useful within the field of photovoltaics. Part of the work by O.H. was supported by Award 70NANB14H012 from U.S. Department of Commerce, National Institute of Standards and Technology as part of the Center for Hierarchical Material Design.

  6. Radial pressure measurement in core/shell nanocrystals

    NASA Astrophysics Data System (ADS)

    Ithurria, Sandrine; Guyot-Sionnest, Philippe; Mahler, Benoît; Dubertret, Benoît

    2009-02-01

    Quantum dots are nanometre-sized semiconductor particles exhibiting unique size-dependent electronic properties. In order to passivate the nanocrystals surface and to protect them from oxidation, we grow a shell composed of a second semiconductor with a larger bandgap on the core (for example a core / shell CdS / ZnS). However, the lattice mismatch between the two materials (typically 7% between ZnS and CdS) induces mechanical stress which can lead to dislocations. To better understand these mechanisms, it is important to be able to measure the pressure induced on the semiconductor core. We used a nanocrystal doped with manganese ions Mn2+, which provide a phosphorescence signal depending on the local pressure. A few dopant atoms per nanoparticle were placed at controlled radial positions in a ZnS shell formed layer by layer. The experimental pressure measurements are in very good agreement with a simple spherically symmetric elastic continuum model[1]. Using manganese as a pressure gauge could be used to better understand some structural phenomena observed in these nanocrystals, such as crystalline phases transition, or shell cracking.

  7. Cloaking Core-Shell Nanoparticles from Conducting Electrons in Solids

    NASA Astrophysics Data System (ADS)

    Liao, Bolin; Zebarjadi, Mona; Esfarjani, Keivan; Chen, Gang

    2012-09-01

    In this Letter, we aim at making nanoparticles embedded in a host semiconductor with a size comparable to electronic wavelengths “invisible” to the electron transport. Inspired by the recent progress made in optics and working within the framework of the expansion of partial waves, we demonstrate that the opposite effects imposed by potential barriers and wells of a core-shell nanoparticle on the phase shifts associated with the scattered electron wave could make the scattering cross section of the first two partial waves vanish simultaneously. We show that this is sufficient to cloak the nanoparticle from being detected by electrons with specific energy in the sense that a total scattering cross section smaller than 0.01% of the physical cross section can be obtained and a 4 orders of magnitude difference in the total scattering cross section can be presented within an energy range of only 40 meV, indicating possible applications of the “electron cloaks” as novel electronic switches and sensors, and in efficient energy harvesting and conversion technologies.

  8. Interface states and bio-conjugation of CdSe/ZnS core-shell quantum dots

    NASA Astrophysics Data System (ADS)

    Torchynska, T. V.

    2009-03-01

    The paper presents the results of photoluminescence (PL) and Raman scattering studies of non-conjugated and bio-conjugated CdSe/ZnS core-shell quantum dots (QDs). The commercial CdSe/ZnS QDs used are characterized by color emission with maxima at 605-610 nm (2.03-2.05 eV). PL spectra of non-conjugated QDs are the superposition of PL bands related to exciton emission in the CdSe core (2.03-2.05 eV) and to hot electron-hole emission via defect states at the CdSe/ZnS interface (2.37 and 2.68 eV). QD conjugation was performed with biomolecules—the antihuman interleukin 10 antibody (antihuman IL10). The PL spectra of bio-conjugated QDs have been changed dramatically: only one PL band related to exciton emission in the CdSe core was detected in bio-conjugated QDs. To explain this effect a model has been proposed which assumes that the QD bio-conjugation process is accompanied by the recharging of acceptor-like interface states at the CdSe/ZnS interface. A comparative analysis of normalized PL spectra of non-conjugated CdSe/ZnS QDs with different intensities of interface state PL has confirmed the proposed electron-hole recombination model in QDs.

  9. Origin of radiative recombination and manifestations of localization effects in GaAs/GaNAs core/shell nanowires

    SciTech Connect

    Chen, S. L.; Filippov, S.; Chen, W. M.; Buyanova, I. A.; Ishikawa, Fumitaro

    2014-12-22

    Radiative carrier recombination processes in GaAs/GaNAs core/shell nanowires grown by molecular beam epitaxy on a Si substrate are systematically investigated by employing micro-photoluminescence (μ-PL) and μ-PL excitation (μ-PLE) measurements complemented by time-resolved PL spectroscopy. At low temperatures, alloy disorder is found to cause localization of photo-excited carriers leading to predominance of optical transitions from localized excitons (LE). Some of the local fluctuations in N composition are suggested to lead to strongly localized three-dimensional confining potential equivalent to that for quantum dots, based on the observation of sharp and discrete PL lines within the LE contour. The localization effects are found to have minor influence on PL spectra at room temperature due to thermal activation of the localized excitons to extended states. Under these conditions, photo-excited carrier lifetime is found to be governed by non-radiative recombination via surface states which is somewhat suppressed upon N incorporation.

  10. Radial composition variations in the shells of GaAs/AlGaAs core-shell nanowires

    NASA Astrophysics Data System (ADS)

    Nilsen, J. S.; Reinertsen, J. F.; Mosberg, A.; Fauske, V. T.; Munshi, A. M.; Dheeraj, D. L.; Fimland, B. O.; Weman, H.; van Helvoort, A. T. J.

    2015-10-01

    GaAs nanowires (NWs) are seen as promising building blocks for future optoelectronic devices. To ensure reproducible properties, a high NW uniformity is required. Here, a substantial number of both position-controlled and randomly grown self-catalyzed GaAs/AlGaAs core-shell NWs are compared. Single NWs are characterized by correlated microphotoluminescence (µ-PL) spectroscopy and transmission electron microscopy (TEM). TEM is done in the <110>- and <112>-projections, and on the <111>-cross-section of the NWs. The position-control grown NWs showed a higher degree of uniformity in morphology. All NWs on both samples had a predominantly stacking fault free zinc blende structure, with a main optical response around the GaAs free exciton energy. However, NW-to-NW structural variations in the tip region and radial compositional variations in the shell are present in both samples. These structural features could be the origin of variations in the optical response just below and above the free exciton energy. This correlated study demonstrates that the observed distinct, sharp PL peaks in the 1.6 - 1.8 eV energy range present in several NWs, are possibly related to radial compositional variations in the AlGaAs shell rather than the structural defects in the tip region.

  11. Crystal Phase Quantum Dots in the Ultrathin Core of GaAs-AlGaAs Core-Shell Nanowires.

    PubMed

    Loitsch, Bernhard; Winnerl, Julia; Grimaldi, Gianluca; Wierzbowski, Jakob; Rudolph, Daniel; Morkötter, Stefanie; Döblinger, Markus; Abstreiter, Gerhard; Koblmüller, Gregor; Finley, Jonathan J

    2015-11-11

    Semiconductor quantum dots embedded in nanowires (NW-QDs) can be used as efficient sources of nonclassical light with ultrahigh brightness and indistinguishability, needed for photonic quantum information technologies. Although most NW-QDs studied so far focus on heterostructure-type QDs that provide an effective electronic confinement potential using chemically distinct regions with dissimilar electronic structure, homostructure NWs can localize excitons at crystal phase defects in leading to NW-QDs. Here, we optically investigate QD emitters embedded in GaAs-AlGaAs core-shell NWs, where the excitons are confined in an ultrathin-diameter NW core and localized along the axis of the NW core at wurtzite (WZ)/zincblende (ZB) crystal phase defects. Photoluminescence (PL)-excitation measurements performed on the QD-emission reveal sharp resonances arising from excited electronic states of the axial confinement potential. The QD-like nature of the emissive centers are suggested by the observation of a narrow PL line width, as low as ~300 μeV, and confirmed by the observation of clear photon antibunching in autocorrelation measurements. Most interestingly, time-resolved PL measurements reveal a very short radiative lifetime <1 ns, indicative of a transition from a type-II to type-I band alignment of the WZ/ZB crystal interface in GaAs due to the strong quantum confinement in the ultrathin NW core. PMID:26455732

  12. Multicomponent (Ce, Cu, Ni) oxides with cage and core-shell structures: tunable fabrication and enhanced CO oxidation activity

    NASA Astrophysics Data System (ADS)

    Liu, Wei; Tang, Ke; Lin, Ming; June, Lay Ting Ong; Bai, Shi-Qiang; Young, David James; Li, Xu; Yang, Yan-Zhao; Hor, T. S. Andy

    2016-05-01

    Solvothermal synthesis of Cu2O cubes from Cu(OAc)2 in ethanol provided templates for tunable formation of novel multicomponent composites: hollow CeO2-Cu2O (1), core-shell NiO@Cu2O (2) and hollow CeO2-NiO-Cu2O (3). Composites 1-3 catalyze the oxidation of CO at a lower temperature than the parent Cu2O cubes.Solvothermal synthesis of Cu2O cubes from Cu(OAc)2 in ethanol provided templates for tunable formation of novel multicomponent composites: hollow CeO2-Cu2O (1), core-shell NiO@Cu2O (2) and hollow CeO2-NiO-Cu2O (3). Composites 1-3 catalyze the oxidation of CO at a lower temperature than the parent Cu2O cubes. Electronic supplementary information (ESI) available: Experimental section: materials and characterization; synthesis of materials; catalytic test. Tables S1-S3 and Fig. S1-S8. See DOI: 10.1039/c6nr02383e

  13. In vitro hyperthermia with improved colloidal stability and enhanced SAR of magnetic core/shell nanostructures.

    PubMed

    Patil, R M; Thorat, N D; Shete, P B; Otari, S V; Tiwale, B M; Pawar, S H

    2016-02-01

    Magnetic core/shell nanostructures of Fe3O4 nanoparticles coated with oleic acid and betaine-HCl were studied for their possible use in magnetic fluid hyperthermia (MFH). Their colloidal stability and heat induction ability were studied in different media viz. phosphate buffer solution (PBS), saline solution and glucose solution with different physiological conditions and in human serum. The results showed enhanced colloidal stability in these media owing to their high zeta potential values. Heat induction studies showed that specific absorption rates (SAR) of core/shells were 82-94W/g at different pH of PBS and concentrations of NaCl and glucose. Interestingly, core/shells showed 78.45±3.90W/g SAR in human serum. The cytotoxicity of core/shells done on L929 and HeLa cell lines using 3-(4,5-dimethylthiazol-2-yl)2,5-diphenyl tetrazolium bromide and trypan blue dye exclusion assays showed >89% and >80% cell viability for 24 and 48h respectively. Core/shell structures were also found to be very efficient for in vitro MFH on cancer cell line. About 95% cell death was occurred in 90min after hyperthermia treatment. The mechanism of cell death was found to be elevated ROS generation in cells after exposure to core/shells in external magnetic field. This study showed that these core/shells have a great potential to be used in in vivo MFH. PMID:26652424

  14. Development of magnetic luminescent core/shell nanocomplex particles with fluorescence using Rhodamine 6G

    SciTech Connect

    Lee, Hee Uk; Song, Yoon Seok; Park, Chulhwan; Kim, Seung Wook

    2012-12-15

    Graphical abstract: Display Omitted Highlights: ► A simple method was developed to synthesize Co-B/SiO{sub 2}/dye/SiO{sub 2} composite particles. ► The magnetic particle shows that highly luminescent and core/shell particles are formed. ► Such core/shell particles can be easily suspended in water. ► The magnetic particles could detect fluorescence for the application of biosensor. -- Abstract: A simple and reproducible method was developed to synthesize a novel class of Co-B/SiO{sub 2}/dye/SiO{sub 2} composite core/shell particles. Using a single cobalt core, Rhodamine 6G of organic dye molecules was entrapped in a silica shell, resulting in core/shell particles of ∼200 nm diameter. Analyses using a variety of techniques such as transmission electron microscopy, X-ray photoelectron spectroscopy, vibration sample magnetometry, confocal laser scanning microscopy, and fluorescence intensity demonstrated that dye molecules were trapped inside the core/shell particles. A photoluminescence investigation showed that highly luminescent and photostable core/shell particles were formed. Such core/shell particles can be easily suspended in water. The synthesized magnetic particles could be used to detect fluorescence on glass substrate arrays for bioassay and biosensor applications.

  15. Formation of core-shell structure in high entropy alloy coating by laser cladding

    NASA Astrophysics Data System (ADS)

    Zhang, Hui; Wu, Wanfei; He, Yizhu; Li, Mingxi; Guo, Sheng

    2016-02-01

    The formation of core-shell structure is an interesting phenomenon occurring during the solidification process, due to the liquid phase separation. The formation of core-shell structure in high-entropy alloys, a new class of advanced metallic materials, has not been reported previously, and thus constitutes an intriguing scientific question. Here, we firstly report the formation of core-shell structure in one laser cladded high-entropy alloy, where we show the nanosized-Y2O3 powder addition, serves as the catalyst for the liquid phase separation.

  16. Influences of external vs. core-shell mixing on aerosol optical properties at various relative humidities.

    PubMed

    Ramachandran, S; Srivastava, Rohit

    2013-05-01

    Aerosol optical properties of external and core-shell mixtures of aerosol species present in the atmosphere are calculated in this study for different relative humidities. Core-shell Mie calculations are performed using the values of radii, refractive indices and densities of aerosol species that act as core and shell, and the core-shell radius ratio. The single scattering albedo (SSA) is higher when the absorbing species (black carbon, BC) is the core, while for a sulfate core SSA does not vary significantly as the BC in the shell dominates the absorption. Absorption gets enhanced in core-shell mixing of absorbing and scattering aerosols when compared to their external mixture. Thus, SSA is significantly lower for a core-shell mixture than their external mixture. SSA is more sensitive to core-shell ratio than mode radius when BC is the core. The extinction coefficient, SSA and asymmetry parameter are higher for external mixing when compared to BC (core)-water soluble aerosol (shell), and water soluble aerosol (core)-BC (shell) mixtures in the relative humidity range of 0 to 90%. Spectral SSA exhibits the behaviour of the species which acts as a shell in core-shell mixing. The asymmetry parameter for an external mixture of water soluble aerosol and BC is higher than BC (core)-water soluble aerosol (shell) mixing and increases as function of relative humidity. The asymmetry parameter for the water soluble aerosol (core)-BC (shell) is independent of relative humidity as BC is hydrophobic. The asymmetry parameter of the core-shell mixture decreases when BC aerosols are involved in mixing, as the asymmetry parameter of BC is lower. Aerosol optical depth (AOD) of core-shell mixtures increases at a higher rate when the relative humidity exceeds 70% in continental clean and urban aerosol models, whereas AOD remains the same when the relative humidity exceeds 50% in maritime aerosol models. The SSA for continental aerosols varies for core-shell mixing of water soluble

  17. PVP induce self-seeding process for growth of Au@Ag core@shell nanocomposites

    NASA Astrophysics Data System (ADS)

    Eisa, Wael H.; Al-Ashkar, Emad; El-Mossalamy, S. M.; Ali, Safaa S. M.

    2016-05-01

    A novel self-seeding route is developed for fabrication of metallic nanocomposites of gold (core) and silver (shell) (Au@Ag core@shell). Herein, polyvinylpyrrolidone (PVP) is used as both reducing and stabilizing agent. The surface plasmon resonance (SPR) of Au@Ag core@shell can be tuned by controlling the thickness of the Ag shell. The different growth stages of the Au@Ag core@shell have been traced by in situ UV-vis absorption spectra. Transmission electron microscopy (TEM), X-ray diffraction (XRD) and Fourier transform infrared spectroscopy are used for the characterization of the prepared samples.

  18. Advanced piezoresistance of extended metal-insulator core-shell nanoparticle assemblies.

    PubMed

    Athanassiou, E K; Krumeich, F; Grass, R N; Stark, W J

    2008-10-17

    Assembled metal-insulator nanoparticles with a core-shell geometry provide access to materials containing a large number (>10(6)) of tunneling barriers. We demonstrate the production of ceramic coated metal nanoparticles exhibiting an exceptional pressure-sensitive conductivity. We further show that graphene bi- and trilayers on 20 nm copper nanoparticles are insulating in such a core-shell geometry and show a similar pressure-dependent conductivity. This demonstrates that core-shell metal-insulator assemblies offer a route to alternative sensing materials. PMID:18999701

  19. Ab initio no-core shell model with continuum

    NASA Astrophysics Data System (ADS)

    Navratil, Petr

    2008-04-01

    The ab initio no-core shell model (NCSM) is a many-body approach to nuclear structure of light nuclei. The NCSM adopts an effective interaction theory to transform fundamental inter-nucleon interactions into effective interactions for a specified nucleus in a selected harmonic oscillator basis space [1]. The method is capable of predicting nuclear structure from inter-nucleon forces derived from quantum chromodynamics by means of chiral effective field theory [2]. NCSM extensions to the microscopic description of nuclear reactions are now under development. In my talk, I will first discuss our recent calculations of the ^4He total photo-absorption cross section using two- and three-nucleon interactions from chiral effective field theory [3]. I will then outline our effort to augment the NCSM by the resonating group method (RGM) technique to develop a new method capable of describing simultaneously both bound states and nuclear reactions on light nuclei [4]. This approach, which preserves translational symmetry and the Pauli principle, will allow us to calculate cross sections of reactions important for astrophysics and describe weakly-bound systems from first principles. I will present our first phase shift results for neutron scattering off ^3H, ^4He and ^7Li and proton scattering off ^3He, ^4He and ^7Be using realistic nucleon-nucleon potentials. 3mm [1] P. Navr'atil, J. P. Vary and B. R. Barrett, Phys. Rev. C 62, 054311 (2000). [2] P. Navr'atil and V. G. Gueorguiev and J. P. Vary, W. E. Ormand and A. Nogga, Phys. Rev. Lett. 99, 042501 (2007). [3] S. Quaglioni and P. Navr'atil, Phys. Lett. B 652, 370 (2007). [4] S. Quaglioni and P. Navr'atil, arXiv:0712.0855.

  20. Design of efficient dye-sensitized solar cells with patterned ZnO-ZnS core-shell nanowire array photoanodes

    NASA Astrophysics Data System (ADS)

    Chen, Xiang; Bai, Zhiming; Yan, Xiaoqin; Yuan, Haoge; Zhang, Guangjie; Lin, Pei; Zhang, Zheng; Liu, Yichong; Zhang, Yue

    2014-04-01

    The fabrication of photoanodes with a high light-harvesting ability, direct electron pathway and low exciton recombination is a key challenge in dye-sensitized solar cells (DSSCs) today. In this paper, large-scale patterned ZnO-ZnS core-shell nanowire arrays (NWAs) are designed and fabricated as such photoanodes for the fist time. By using the NWA photoanodes with a hexagonal symmetry and FTO-Pt cathodes with an Al reflecting layer, the resulting DSSCs demonstrate a maxiumum efficiency of 2.09%, which is an improvement of 140% compared to the reference cells with line symmetry and no reflecting layer. This improvement is attributed to the enhanced light-harvesting ability of the patterned NWAs, as well as to the remarkable double absorption caused by the Al reflecting layer. Additionally, the ZnO core provides a direct electron pathway and the ZnS shell simultaneously reduces exciton recombination. This study shows an effective method to improve the performance of DSSCs which could be extended to other nanodevices and nanosystems.The fabrication of photoanodes with a high light-harvesting ability, direct electron pathway and low exciton recombination is a key challenge in dye-sensitized solar cells (DSSCs) today. In this paper, large-scale patterned ZnO-ZnS core-shell nanowire arrays (NWAs) are designed and fabricated as such photoanodes for the fist time. By using the NWA photoanodes with a hexagonal symmetry and FTO-Pt cathodes with an Al reflecting layer, the resulting DSSCs demonstrate a maxiumum efficiency of 2.09%, which is an improvement of 140% compared to the reference cells with line symmetry and no reflecting layer. This improvement is attributed to the enhanced light-harvesting ability of the patterned NWAs, as well as to the remarkable double absorption caused by the Al reflecting layer. Additionally, the ZnO core provides a direct electron pathway and the ZnS shell simultaneously reduces exciton recombination. This study shows an effective method to

  1. Controllable fabrication of PS/Ag core-shell-shaped nanostructures

    PubMed Central

    2012-01-01

    In this paper, based on the previous steps, a facile in situ reduction method was developed to controllably prepare polystyrene/Ag (PS/Ag) core-shell-shaped nanostructures. The crucial procedure includes surface treatment of polystyrene core particles by cationic polyelectrolyte polyethyleneimine, in situ formation of Ag nanoparticles, and immobilization of the Ag nanoparticles onto the surface of the polystyrene colloids via functional group NH from the polyethyleneimine. The experimental parameters, such as the reaction temperature, the reaction time, and the silver precursors were optimized for improvement of dispersion and Ag coat coverage of the core-shell-shaped nanostructures. Ultimately, the optimum parameters were obtained through a series of experiments, and well-dispersed, uniformly coated PS/Ag core-shell-shaped nanostructures were successfully fabricated. The formation mechanism of the PS/Ag core-shell-shaped nanostructures was also explained. PMID:23092195

  2. Size-Dependent Specific Surface Area of Nanoporous Film Assembled by Core-Shell Iron Nanoclusters

    DOE PAGESBeta

    Antony, Jiji; Nutting, Joseph; Baer, Donald R.; Meyer, Daniel; Sharma, Amit; Qiang, You

    2006-01-01

    Nmore » anoporous films of core-shell iron nanoclusters have improved possibilities for remediation, chemical reactivity rate, and environmentally favorable reaction pathways. Conventional methods often have difficulties to yield stable monodispersed core-shell nanoparticles. We produced core-shell nanoclusters by a cluster source that utilizes combination of Fe target sputtering along with gas aggregations in an inert atmosphere at 7 ∘ C . Sizes of core-shell iron-iron oxide nanoclusters are observed with transmission electron microscopy (TEM). The specific surface areas of the porous films obtained from Brunauer-Emmett-Teller (BET) process are size-dependent and compared with the calculated data.« less

  3. Synthesis and characterization of Zn 3P 2/ZnS core/shell nanowires

    NASA Astrophysics Data System (ADS)

    Sun, T.; Wu, P. C.; Guo, Z. D.; Dai, Y.; Meng, H.; Fang, X. L.; Shi, Z. J.; Dai, L.; Qin, G. G.

    2011-05-01

    Fully-surrounded Zn3P2/ZnS core/shell nanowires (NWs) were synthesized for the first time via a two-step method: a catalyst free chemical vapor deposition followed by a low-pressure vulcanization process. Field emission scanning electron microscopy, high-resolution transmission electron microscopy, and high-angle angular dark field scanning transmission electron microscopy were used to characterize the morphologies, crystal structure, and element composition of the core/shell NWs. The band structure analysis demonstrates that the Zn3P2/ZnS core-shell NW type-II heterostructures have bright potential in photovoltaic nanodevice applications. The core/shell NW growth method used here can be extended to other material system.

  4. Design of polyelectrolyte core-shells with DNA to control TMPyP binding.

    PubMed

    Serra, Vanda Vaz; Teixeira, Raquel; Andrade, Suzana M; Costa, Sílvia M B

    2016-10-01

    The interaction of DNA with 5,10,15,20-tetrakis(4-N-methylpyridiniumyl)porphyrin (TMPyP) in polyelectrolyte core-shells obtained via layer by layer adsorption of poly(sodium 4-styrenesulfonate), PSS, and poly(allylamine hydrochloride), PAH, polyelectrolytes was followed by steady state, time resolved fluorescence and by Fluorescence Lifetime Imaging Microscopy (FLIM). Our results show that DNA adsorption onto polyelectrolyte core-shell changes the TMPyP interaction within PSS/PAH core-shells structure and increase significantly the TMPyP uptake. Specific DNA/TMPyP interactions are also altered by DNA adsorption favouring porphyrin intercalation onto GC pair rich regions. Circular dichroism (CD) spectra reveal that DNA undergoes important conformational changes upon adsorption onto the core-shell surface, which are reverted upon TMPyP encapsulation. PMID:27285535

  5. Engineered magnetic core shell nanoprobes: Synthesis and applications to cancer imaging and therapeutics

    PubMed Central

    Mandal, Samir; Chaudhuri, Keya

    2016-01-01

    Magnetic core shell nanoparticles are composed of a highly magnetic core material surrounded by a thin shell of desired drug, polymer or metal oxide. These magnetic core shell nanoparticles have a wide range of applications in biomedical research, more specifically in tissue imaging, drug delivery and therapeutics. The present review discusses the up-to-date knowledge on the various procedures for synthesis of magnetic core shell nanoparticles along with their applications in cancer imaging, drug delivery and hyperthermia or cancer therapeutics. Literature in this area shows that magnetic core shell nanoparticle-based imaging, drug targeting and therapy through hyperthermia can potentially be a powerful tool for the advanced diagnosis and treatment of various cancers. PMID:26981204

  6. Study of photodynamic activity of Au@SiO2 core-shell nanoparticles in vitro.

    PubMed

    Meena, K S; Dhanalekshmi, K I; Jayamoorthy, K

    2016-06-01

    Metal-semiconductor core-shell type Au@SiO2 nanoparticles were prepared by Stober's method. They were characterized by absorption, XRD, HR-TEM and EDAX techniques. The resulting modified core-shell nanoparticles shows that the formation of singlet oxygen, which was confirmed by ESR technique. The photohemolysis studies were carried out under two different experimental conditions. It is observed that the photohemolysis increases with concentration as well as light dose. Cell viability of the core-shell nanoparticles against HeLa cell lines were studied by MTT assay method. The outcomes of the present study indicate that, the Au@SiO2 core-shell nanoparticles are extremely stable with a very high photodynamic efficiency under visible light illumination. PMID:27040225

  7. Water-soluble core/shell nanoparticles for proton therapy through particle-induced radiation

    NASA Astrophysics Data System (ADS)

    Park, Jeong Chan; Jung, Myung-Hwan; Kim, Maeng Jun; Kim, Kye-Ryung

    2015-02-01

    Metallic nanoparticles have been used in biomedical applications such as magnetic resonance imaging (MRI), therapy, and drug delivery systems. Metallic nanoparticles as therapeutic tools have been demonstrated using radio-frequency magnetic fields or near-infrared light. Recently, therapeutic applications of metallic nanomaterials combined with proton beams have been reported. Particle-induced radiation from metallic nanoparticles, which can enhance the therapeutic effects of proton therapy, was released when the nanoparticles were bombarded by a high-energy proton beam. Core/shell nanoparticles, especially Au-coated magnetic nanoparticles, have drawn attention in biological applications due to their attractive characteristics. However, studies on the phase transfer of organic-ligand-based core/shell nanoparticles into water are limited. Herein, we demonstrated that hydrophobic core/shell structured nanomaterials could be successfully dispersed in water through chloroform/surfactant mixtures. The effects of the core/shell nanomaterials and the proton irradiation on Escherichia coli (E. coli) were also explored.

  8. One-pot aerosol synthesis of ordered hierarchical mesoporous core-shell silica nanoparticles.

    PubMed

    Areva, S; Boissière, C; Grosso, D; Asakawa, T; Sanchez, C; Lindén, M

    2004-07-21

    A mixed surfactant approach has been successfully employed in an aerosol-based synthesis of spherical silica particles exhibiting a new core-shell structure where the shell and the core exhibit different ordered mesoporosity and pore sizes. PMID:15263952

  9. Tunable mechanical and thermal properties of ZnS/CdS core/shell nanowires

    NASA Astrophysics Data System (ADS)

    Mandal, Taraknath; Dasgupta, Chandan; Maiti, Prabal K.

    2015-03-01

    Using all-atom molecular dynamics (MD) simulations, we have studied the mechanical properties of ZnS/CdS core/shell nanowires. Our results show that the coating of a few-atomic-layer CdS shell on the ZnS nanowire leads to a significant change in the stiffness of the core/shell nanowires compared to the stiffness of pure ZnS nanowires. The binding energy between the core and shell region decreases due to the lattice mismatch at the core-shell interface. This reduction in binding energy plays an important role in determining the stiffness of a core/shell nanowire. We have also investigated the effects of the shell on the thermal conductivity and melting behavior of the nanowires.

  10. Coordination polymer core/shell structures: Preparation and up/down-conversion luminescence.

    PubMed

    Li, Bingmei; Xu, Hualan; Xiao, Chen; Shuai, Min; Chen, Weimin; Zhong, Shengliang

    2016-10-01

    Coordination polymer (CP) core-shell nanoparticles with Gd-based CP (GdCP) as core and Eu-based CP (EuCP) as shell have been successfully prepared. Allantoin was employed as the organic building block without the assistance of any template. The composition, size and structure of the core-shell nanospheres were well characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy dispersive X-ray (EDX), powder X-ray diffraction (PXRD), Fourier transform infrared spectroscopy (FT-IR), thermo-gravimetric analysis (TG). Results show that the resultant cores are uniform nanospheres with diameter of approximately 45nm, while the diameters of the core-shell nanospheres are increased to approximately 60nm. The core-shell products show enhanced luminescence efficiency than the core under 980nm laser excitation and decreased down-conversion luminescence when excited at 394nm. PMID:27344485

  11. Introduction of biotin or folic acid into polypyrrole magnetite core-shell nanoparticles

    SciTech Connect

    Nan, Alexandrina; Turcu, Rodica; Liebscher, Jürgen

    2013-11-13

    In order to contribute to the trend in contemporary research to develop magnetic core shell nanoparticles with better properties (reduced toxicity, high colloidal and chemical stability, wide scope of application) in straightforward and reproducible methods new core shell magnetic nanoparticles were developed based on polypyrrole shells functionalized with biotin and folic acid. Magnetite nanoparticles stabilized by sebacic acid were used as magnetic cores. The morphology of magnetite was determined by transmission electron microscopy TEM, while the chemical structure investigated by FT-IR.

  12. Synthesis and cytotoxicity study of magnesium ferrite-gold core-shell nanoparticles.

    PubMed

    Nonkumwong, Jeeranan; Pakawanit, Phakkhananan; Wipatanawin, Angkana; Jantaratana, Pongsakorn; Ananta, Supon; Srisombat, Laongnuan

    2016-04-01

    In this work, the core-magnesium ferrite (MgFe2O4) nanoparticles were prepared by hydrothermal technique. Completed gold (Au) shell coating on the surfaces of MgFe2O4 nanoparticles was obtained by varying core/shell ratios via a reduction method. Phase identification, morphological evolution, optical properties, magnetic properties and cytotoxicity to mammalian cells of these MgFe2O4 core coated with Au nanoparticles were examined by using a combination of X-ray diffraction, scanning electron microscopy, transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy, UV-visible spectroscopy (UV-vis), vibrating sample magnetometry and resazurin microplate assay techniques. In general, TEM images revealed different sizes of the core-shell nanoparticles generated from various core/shell ratios and confirmed the completed Au shell coating on MgFe2O4 core nanoparticles via suitable core/shell ratio with particle size less than 100nm. The core-shell nanoparticle size and the quality of coating influence the optical properties of the products. The UV-vis spectra of complete coated MgFe2O4-Au core-shell nanoparticles exhibit the absorption bands in the near-Infrared (NIR) region indicating high potential for therapeutic applications. Based on the magnetic property measurement, it was found that the obtained MgFe2O4-Au core-shell nanoparticles still exhibit superparamagnetism with lower saturation magnetization value, compared with MgFe2O4 core. Both of MgFe2O4 and MgFe2O4-Au core-shell also showed in vitro non-cytotoxicity to mouse areola fibroblast (L-929) cell line. PMID:26838832

  13. Core-shell palladium nanoparticle@metal-organic frameworks as multifunctional catalysts for cascade reactions.

    PubMed

    Zhao, Meiting; Deng, Ke; He, Liangcan; Liu, Yong; Li, Guodong; Zhao, Huijun; Tang, Zhiyong

    2014-02-01

    Uniform core-shell Pd@IRMOF-3 nanostructures, where single Pd nanoparticle core is surrounded by amino-functionalized IRMOF-3 shell, are prepared by a facile mixed solvothermal method. When used as multifunctional catalysts, the Pd@IRMOF-3 nanocomposites exhibit high activity, enhanced selectivity, and excellent stability in the cascade reaction. Both experimental evidence and theoretical calculations reveal that the high catalytic performance of Pd@IRMOF-3 nanocomposites originates from their unique core-shell structures. PMID:24437922

  14. Synthesis and optical properties of three-dimensional porous core-shell nanoarchitectures.

    PubMed

    Qian, Li-Hua; Ding, Yi; Fujita, Takeshi; Chen, Ming-Wei

    2008-05-01

    Three-dimensional porous core-shell nanostructures consisting of gold skeletons and silver shells were fabricated by controllable electroless plating. Optical properties of the 3D nanocomposite with a heterogeneous interface exhibit a significant shell-thickness dependence. The porous core-shell structure with an optimized shell thickness of approximately 3-5 nm exhibits a considerable improvement in surface-enhanced Raman scattering. This study has important implications in the functionalization of nanoporous metals by surface modification. PMID:18355096

  15. From Superatomic Au25(SR)18- to Superatomic M@Au24(SR)18q Core-shell Clusters.

    SciTech Connect

    Jiang, Deen; Dai, Sheng

    2009-01-01

    Au{sub 25}(SR){sub 18}{sup -} belongs to a new type of superatom that features an icosahedral Au{sub 13} core-shell structure and a protective layer of six RS(Au-SR){sub 2} motifs. This superatom has a magic number of 8 free electrons that fully fill the 1s and 1p levels of the electron-shell model. By applying this superatom concept to the core-substitution chemistry of Au{sub 25}(SR){sub 18}{sup -}, we first scanned the periodic table for the potential core atom M by applying a simple rule derived from the 8-electron count and then optimized the selected candidates by density functional theory calculations to create many series of M{at}Au{sub 24}(SR){sub 18}{sup q} core-shell nanoclusters. We found that 16 elements from groups 1, 2, and 10-14 of the periodic table can maintain both electronic and geometric structures of the original Au{sub 25}(SR){sub 18}{sup -} magic cluster, indicating that the electron-counting rule based on the superatom concept is powerful in predicting viable M{at}Au{sub 24}(SR){sub 18}{sup q} clusters. Our work opens up a promising area for experimental exploration.

  16. Magnetite and magnetite/silver core/shell nanoparticles with diluted magnet-like behavior

    SciTech Connect

    Garza-Navarro, Marco; Gonzalez, Virgilio; Ortiz, Ubaldo; De la Rosa, Elder

    2010-01-15

    In the present work is reported the use of the biopolymer chitosan as template for the preparation of magnetite and magnetite/silver core/shell nanoparticles systems, following a two step procedure of magnetite nanoparticles in situ precipitation and subsequent silver ions reduction. The crystalline and morphological characteristics of both magnetite and magnetite/silver core/shell nanoparticles systems were analyzed by high resolution transmission electron microscopy (HRTEM) and nanobeam diffraction patterns (NBD). The results of these studies corroborate the core/shell morphology and the crystalline structure of the magnetite core and the silver shell. Moreover, magnetization temperature dependent, M(T), measurements show an unusual diluted magnetic behavior attributed to the dilution of the magnetic ordering in the magnetite and magnetite/silver core/shell nanoparticles systems. - Graphical abstract: Biopolymer chitosan was used as stabilization media to synthesize both magnetite and magnetite/silver core/shell nanoparticles. Results of HRTEM and NBD patterns confirm core/shell morphology of the obtained nanoparticles. It was found that the composites show diluted magnet-like behavior.

  17. Folate-targeting magnetic core-shell nanocarriers for selective drug release and imaging.

    PubMed

    Wang, Hanjie; Wang, Sheng; Liao, Zhenyu; Zhao, Peiqi; Su, Wenya; Niu, Ruifang; Chang, Jin

    2012-07-01

    One of the most urgent medical requirements for cancer diagnosis and treatment is how to construct a multifunctional vesicle for simultaneous diagnostic imaging and therapeutic applications. In our study, superparamagnetic iron oxide nanocrystals (SPIONs) and doxorubicin hydrochloride (DOX) are co-encapsulated into PLGA/polymeric liposome core-shell nanocarriers for achieving simultaneous magnetic resonance imaging and targeting drug delivery. The core-shell nanocarrier was self-assembled from a hydrophobic PLGA core and a hydrophilic folate coated PEGlated lipid shell. The experiment showed that folate-targeting magnetic core-shell nanocarriers show clear core-shell structure, excellent magnetism and controlled drug release behavior. Importantly, the core-shell nanoparticles achieve the possibility of co-delivering drugs and SPIONs to the same cells for enhancing magnetic resonance imaging (MRI) effect and improving drug delivery efficiency simultaneously. Our data suggests that the folate-targeting magnetic core-shell nanocarriers (FMNs) could provide effective cancer-targeting and MRI as well as drug delivery. The FMNs may become a useful nanomedical carrier system for cancer diagnosis and treatment. PMID:22525087

  18. Environmentally responsive core/shell particles via electrohydrodynamic co-jetting of fully miscible polymer solutions.

    PubMed

    Kazemi, Abbass; Lahann, Joerg

    2008-10-01

    Herein it is demonstrated that electrohydrodynamic co-jetting is not limited to Janus-type particles, but can also be used for the preparation of core/shell particles. Using side-by-side flow of miscible polymer solutions, electrohydrodynamic co-jetting offers an elegant and scalable route towards preparation of core/shell particles with otherwise difficult-to-prepare particle architectures, including particles with hydrophilic shell and core. Throughout this study, electrohydrodynamic co-jetting of aqueous solutions consisting of a mixture of PAAm-co-AA and PAA is used, and a range of different types of particles with distinct compartments are observed. Transition from Janus particles to core/shell particles appears to be caused by changes in the relative conductivity of the two jetting solutions. After crosslinking, the core/shell particles are stable in aqueous solution and exhibit reproducible swelling behavior while maintaining the original core/shell geometry. In addition, the pH-responsiveness of the particles is demonstrated by repeatedly switching the environmental pH between 1.3 and 12. Moreover, the core/shell particles show surprising uptake selectivity. For instance, a 450% increase in uptake of 6-carboxyfluorescein over rhodamine B base is found. PMID:18819137

  19. Cu-Ag core-shell nanoparticles with enhanced oxidation stability for printed electronics

    NASA Astrophysics Data System (ADS)

    Lee, Changsoo; Kim, Na Rae; Koo, Jahyun; Jong Lee, Yung; Lee, Hyuck Mo

    2015-11-01

    In this work, we synthesized uniform Cu-Ag core-shell nanoparticles using a facile two-step process that consists of thermal decomposition and galvanic displacement methods. The core-shell structure of these nanoparticles was confirmed through characterization using transmission electron microscopy, energy-dispersive spectroscopy, and x-ray diffraction. Furthermore, we investigated the oxidation stability of the Cu-Ag core-shell nanoparticles in detail. Both qualitative and quantitative x-ray photoelectron spectroscopy analyses confirm that the Cu-Ag core-shell nanoparticles have considerably higher oxidation stability than Cu nanoparticles. Finally, we formulated a conductive ink using the synthesized nanoparticles and coated it onto glass substrates. Following the sintering process, we compared the resistivity of the Cu-Ag core-shell nanoparticles with that of the Cu nanoparticles. The results of this study clearly show that the Cu-Ag core-shell nanoparticles can potentially be used as an alternative to Ag nanoparticles because of their superior oxidation stability and electrical properties.

  20. Magnetic core-shell nanoparticles for drug delivery by nebulization

    PubMed Central

    2013-01-01

    Background Aerosolized therapeutics hold great potential for effective treatment of various diseases including lung cancer. In this context, there is an urgent need to develop novel nanocarriers suitable for drug delivery by nebulization. To address this need, we synthesized and characterized a biocompatible drug delivery vehicle following surface coating of Fe3O4 magnetic nanoparticles (MNPs) with a polymer poly(lactic-co-glycolic acid) (PLGA). The polymeric shell of these engineered nanoparticles was loaded with a potential anti-cancer drug quercetin and their suitability for targeting lung cancer cells via nebulization was evaluated. Results Average particle size of the developed MNPs and PLGA-MNPs as measured by electron microscopy was 9.6 and 53.2 nm, whereas their hydrodynamic swelling as determined using dynamic light scattering was 54.3 nm and 293.4 nm respectively. Utilizing a series of standardized biological tests incorporating a cell-based automated image acquisition and analysis procedure in combination with real-time impedance sensing, we confirmed that the developed MNP-based nanocarrier system was biocompatible, as no cytotoxicity was observed when up to 100 μg/ml PLGA-MNP was applied to the cultured human lung epithelial cells. Moreover, the PLGA-MNP preparation was well-tolerated in vivo in mice when applied intranasally as measured by glutathione and IL-6 secretion assays after 1, 4, or 7 days post-treatment. To imitate aerosol formation for drug delivery to the lungs, we applied quercitin loaded PLGA-MNPs to the human lung carcinoma cell line A549 following a single round of nebulization. The drug-loaded PLGA-MNPs significantly reduced the number of viable A549 cells, which was comparable when applied either by nebulization or by direct pipetting. Conclusion We have developed a magnetic core-shell nanoparticle-based nanocarrier system and evaluated the feasibility of its drug delivery capability via aerosol administration. This study has

  1. Engineering of lead chalcogenide nanostructures for carrier multiplication: Core/shell, 1D, and 2D

    NASA Astrophysics Data System (ADS)

    Lin, Qianglu

    Near infrared emitting semiconductors have been used widely in industry especially in solar-cell fabrications. The efficiency of single junction solar-cell can reach the Shockley-Queisser limit by using optimum band gap material such as silicon and cadmium telluride. The theoretical efficiency can be further enhanced through carrier multiplication, in which a high energy photon is absorbed and more than one electron-hole pair can be generated, reaching more than 100% quantum efficiency in the high energy region of sunlight. The realization of more than unity external quantum efficiency in lead selenide quantum dots solar cell has motivated vast investigation on lowering the carrier multiplication threshold and further improving the efficiency. This dissertation focuses on synthesis of lead chalcogenide nanostructures for their optical spectroscopy studies. PbSe/CdSe core/shell quantum dots were synthesized by cation exchange to obtain thick shells (up to 14 monolayers) for studies of visible and near infrared dual band emissions and carrier multiplication efficiency. By examining the reaction mechanism, a thermodynamic and a kinetic model are introduced to explain the vacancy driven cation exchange. As indicated by the effective mass model, PbSe/CdSe core/shell quantum dots has quasi-type-II band alignment, possessing electron delocalized through the entire quantum dot and hole localized in the core, which breaks down the symmetry of energy levels in the conduction and valence band, leading to hot-hole-assisted efficient multi-exciton generation and a lower carrier multiplication threshold to the theoretical value. For further investigation of carrier multiplication study, PbTe, possessing the highest efficiency among lead chalcogenides due to slow intraband cooling, is synthesized in one-dimensional and two-dimensional nanostructures. By using dodecanethiol as the surfactant, PbTe NRs can be prepared with high uniformity in width and resulted in fine quantum

  2. Investigating photoinduced charge transfer in double- and single-emission PbS@CdS core@shell quantum dots

    NASA Astrophysics Data System (ADS)

    Zhao, Haiguang; Liang, Hongyan; Gonfa, Belete Atomsa; Chaker, Mohamed; Ozaki, Tsuneyuki; Tijssen, Peter; Vidal, François; Ma, Dongling

    2013-12-01

    structure model was proposed to explain the origin of double emissions from monodisperse QDs. Their charge transfer behavior was investigated by monitoring photoluminescence (PL) intensity variation with the introduction of electron or hole scavengers. It was found that the PL quenching of the PbS core is more efficient than that of the CdS shell, suggesting more efficient charge transfer from the core to scavengers, although the opposite was expected. Further measurements of the PL lifetime followed by wave function calculations disclosed that the time scale is the critical factor explaining the more efficient charge transfer from the core than from the shell. The charge transfer behavior was also examined on a series of single-emission core@shell QDs with either different core sizes or different shell thicknesses and dominant factors were identified. Towards photovoltaic applications, these PbS@CdS QDs were attached onto multi-walled carbon nanotubes (MWCNTs) and their charge transfer behavior was compared with that in the PbS-QD/MWCNT system. Results demonstrate that although the CdS shell serves as an electron transfer barrier, the electrons excited in the PbS cores can still be transferred into the MWCNTs efficiently when the shell thickness is ~0.7 nm. Considering their higher stability, these core@shell QDs are very promising for the development of highly efficient QD-based photovoltaic devices. Electronic supplementary information (ESI) available: The PL and absorption spectra of PbS@CdS QDs in solution and in films with and without the combination of MWCNTs, Gaussian curve fit to the PL spectra of representative QD film samples, PL lifetime and charge transfer rate from QDs to electron or hole scavengers, radial distribution functions for 1s electron levels of the PbS@CdS core@shell QD with a different core size and constant shell thickness. See DOI: 10.1039/c3nr03691j

  3. Enhanced antibacterial activity of bimetallic gold-silver core-shell nanoparticles at low silver concentration

    NASA Astrophysics Data System (ADS)

    Banerjee, Madhuchanda; Sharma, Shilpa; Chattopadhyay, Arun; Ghosh, Siddhartha Sankar

    2011-12-01

    Herein we report the development of bimetallic Au@Ag core-shell nanoparticles (NPs) where gold nanoparticles (Au NPs) served as the seeds for continuous deposition of silver atoms on its surface. The core-shell structure and morphology were examined by UV-Vis spectroscopy, transmission electron microscopy (TEM), energy dispersive X-ray (EDX) analysis and X-ray diffraction (XRD). The core-shell NPs showed antibacterial activity against both Gram negative (Escherichia coli and Pseudomonas aeruginosa) and Gram positive (Enterococcus faecalis and Pediococcus acidilactici) bacteria at low concentration of silver present in the shell, with more efficacy against Gram negative bacteria. TEM and flow cytometric studies showed that the core-shell NPs attached to the bacterial surface and caused membrane damage leading to cell death. The enhanced antibacterial properties of Au@Ag core-shell NPs was possibly due to the more active silver atoms in the shell surrounding gold core due to high surface free energy of the surface Ag atoms owing to shell thinness in the bimetallic NP structure.Herein we report the development of bimetallic Au@Ag core-shell nanoparticles (NPs) where gold nanoparticles (Au NPs) served as the seeds for continuous deposition of silver atoms on its surface. The core-shell structure and morphology were examined by UV-Vis spectroscopy, transmission electron microscopy (TEM), energy dispersive X-ray (EDX) analysis and X-ray diffraction (XRD). The core-shell NPs showed antibacterial activity against both Gram negative (Escherichia coli and Pseudomonas aeruginosa) and Gram positive (Enterococcus faecalis and Pediococcus acidilactici) bacteria at low concentration of silver present in the shell, with more efficacy against Gram negative bacteria. TEM and flow cytometric studies showed that the core-shell NPs attached to the bacterial surface and caused membrane damage leading to cell death. The enhanced antibacterial properties of Au@Ag core-shell NPs was

  4. Magnetic and optical properties of multifunctional core-shell radioluminescence nanoparticles.

    PubMed

    Chen, Hongyu; Colvin, Daniel C; Qi, Bin; Moore, Thomas; He, Jian; Mefford, O Thompson; Alexis, Frank; Gore, John C; Anker, Jeffrey N

    2012-07-01

    When X-rays irradiate radioluminescence nanoparticles, they generate visible and near infrared light that can penetrate through centimeters of tissue. X-ray luminescence tomography (XLT) maps the location of these radioluminescent contrast agents at high resolution by scanning a narrow X-ray beam through the tissue sample and collecting the luminescence at every position. Adding magnetic functionality to these radioluminescent particles would enable them to be guided, oriented, and heated using external magnetic fields, while their location and spectrum could be imaged with XLT and complementary magnetic resonance imaging. In this work, multifunctional monodispersed magnetic radioluminescent nanoparticles were developed as potential drug delivery carriers and radioluminescence imaging agents. The particles consisted of a spindle-shaped magnetic γ-Fe2O3 core and a radioluminescent europium-doped gadolinium oxide shell. Particles with solid iron oxide cores displayed saturation magnetizations consistent with their ~13% core volume, however, the iron oxide quenched their luminescence. In order to increase the luminescence, we partially etched the iron oxide core in oxalic acid while preserving the radioluminescent shell. The core size was controlled by the etching time which in turn affected the particles' luminescence and magnetic properties. Particles with intermediate core sizes displayed both strong magnetophoresis and luminescence properties. They also served as MRI contrast agents with relaxivities of up to 58 mM(-1)s(-1) (r2) and 120 mM(-1)s(-1) (r2*). These particles offer promising multimodal MRI/fluorescence/X-ray luminescence contrast agents. Our core-shell synthesis technique offers a flexible method to control particle size, shape, and composition for a wide range of biological applications of magnetic/luminescent nanoparticles. PMID:24520183

  5. Synthesis of monodisperse TiO2-paraffin core-shell nanoparticles for improved dielectric properties.

    PubMed

    Balasubramanian, Balamurugan; Kraemer, Kristin L; Reding, Nicholas A; Skomski, Ralph; Ducharme, Stephen; Sellmyer, David J

    2010-04-27

    Core-shell structures of oxide nanoparticles having a high dielectric constant, and organic shells with large breakdown field are attractive candidates for large electrical energy storage applications. A high growth temperature, however, is required to obtain the dielectric oxide nanoparticles, which affects the process of core-shell formation and also leads to poor control of size, shape, and size-distribution. In this communication, we report a new synthetic process to grow core-shell nanoparticles by means of an experimental method that can be easily adapted to synthesize core-shell structures from a variety of inorganic-organic or inorganic-inorganic materials. Monodisperse and spherical TiO2 nanoparticles were produced at room temperature as a collimated cluster beam in the gas phase using a cluster-deposition source and subsequently coated with uniform paraffin nanoshells using in situ thermal evaporation, prior to deposition on substrates for further characterization and device processing. The paraffin nanoshells prevent the TiO2 nanoparticles from contacting each other and also act as a matrix in which the volume fraction of TiO2 nanoparticles was varied by controlling the thickness of the nanoshells. Parallel-plate capacitors were fabricated using dielectric core-shell nanoparticles having different shell thicknesses. With respect to the bulk paraffin, the effective dielectric constant of TiO2-paraffin core-shell nanoparticles is greatly enhanced with a decrease in the shell thickness. The capacitors show a minimum dielectric dispersion and low dielectric losses in the frequency range of 100 Hz-1 MHz, which are highly desirable for exploiting these core-shell nanoparticles for potential applications. PMID:20359188

  6. Electrochemiluminescence immunosensor for highly sensitive detection of 8-hydroxy-2'-deoxyguanosine based on carbon quantum dot coated Au/SiO2 core-shell nanoparticles.

    PubMed

    Zhang, Ting-Ting; Zhao, Hui-Min; Fan, Xin-Fei; Chen, Shuo; Quan, Xie

    2015-01-01

    An electrochemiluminescence (ECL) immunosensor using Pt electrode modified with carbon quantum dot (CQDs) coated Au/SiO2 core-shell nanoparticles was proposed for sensitive detection of 8-hydroxy-2'-deoxyguanosine (8-OHdG) in this work. Rabbit anti-8-OHdG antibody was covalently bound to CQDs on the surface of Au/SiO2 core-shell nanoparticles. Through signal amplification of Au/SiO2 core-shell nanoparticles, 8-fold enhancement of the ECL signals was achieved. Under optimal conditions, a good linear range from 0.2 to 200 ng mL(-1) with a low detection limit of 0.085 ng mL(-1) (S/N=3) for 8-OHdG detection was obtained. Interfering substances tests showed that the corresponding ECL intensity (ΔECL) of 8-OHdG is 8-18 times higher than that of guanine, uric acid (UA) and ascorbic acid, demonstrating its good selectivity for 8-OHdG detection. The ECL immunosensor exhibits long-term stability with a relative standard deviation (RSD) of 8.5% even after 16 cycles of continuous potential scans. The result of analytical detection of 8-OHdG in real samples was satisfactory. The proposed ECL immunosensor shows good performance with high sensitivity, specificity, repeatability, stability and provided a powerful tool for 8-OHdG monitoring in clinical samples. PMID:25281118

  7. Hydrogel Encapsulation of Cells in Core-Shell Microcapsules for Cell Delivery.

    PubMed

    Nguyen, Duy Khiem; Son, Young Min; Lee, Nae-Eung

    2015-07-15

    A newly designed 3D core-shell microcapsule structure composed of a cell-containing liquid core and an alginate hydrogel shell is fabricated using a coaxial dual-nozzle electrospinning system. Spherical alginate microcapsules are successfully generated with a core-shell structure and less than 300 μm in average diameter using this system. The thickness of the core and shell can be easily controlled by manipulating the core and shell flow rates. Cells encapsulated in core-shell microcapsules demonstrate better cell encapsulation and immune protection than those encapsulated in microbeads. The observation of a high percentage of live cells (≈80%) after encapsulation demonstrates that the voltage applied for generation of microcapsules does not significantly affect the viability of encapsulated cells. The viability of encapsulated cells does not change even after 3 d in culture, which suggests that the core-shell structure with culture medium in the core can maintain high cell survival by providing nutrients and oxygen to all cells. This newly designed core-shell structure can be extended to use in multifunctional platforms not only for delivery of cells but also for factor delivery, imaging, or diagnosis by loading other components in the core or shell. PMID:25963828

  8. Platinum Monolayer on IrFe Core-Shell Nanoparticle Electrocatalysts for the Oxygen Reduction Reaction

    SciTech Connect

    K Sasaki; K Kuttiyiel; D Su; R Adzic

    2011-12-31

    We synthesized high activity and stability platinum monolayer on IrFe core-shell nanoparticle electrocatalysts. Carbon-supported IrFe core-shell nanoparticles were synthesized by chemical reduction and subsequent thermal annealing. The formation of Ir shells on IrFe solid-solution alloy cores has been verified by scanning transmission electron microscopy coupled with energy-loss spectroscopy (EELS) and in situ X-ray absorption spectroscopy. The Pt monolayers were deposited on IrFe core-shell nanoparticles by galvanic replacement of underpotentially deposited Cu adatoms on the Ir shell surfaces. The specific and Pt mass activities for the ORR on the Pt monolayer on IrFe core-shell nanoparticle electrocatalyst are 0.46 mA/cm{sup 2} and 1.1 A/mg{sub Pt}, which are much higher than those on a commercial Pt/C electrocatalyst. High durability of Pt{sub ML}/IrFe/C has also been demonstrated by potential cycling tests. These high activity and durability observed can be ascribed to the structural and electronic interaction between the Pt monolayer and the IrFe core-shell nanoparticles.

  9. Hypersonic vibrations of Ag@SiO2 (cubic core)-shell nanospheres.

    PubMed

    Sun, Jing Ya; Wang, Zhi Kui; Lim, Hock Siah; Ng, Ser Choon; Kuok, Meng Hau; Tran, Toan Trong; Lu, Xianmao

    2010-12-28

    The intriguing optical and catalytic properties of metal-silica core-shell nanoparticles, inherited from their plasmonic metallic cores together with the rich surface chemistry and increased stability offered by their silica shells, have enabled a wide variety of applications. In this work, we investigate the confined vibrational modes of a series of monodisperse Ag@SiO(2) (cubic core)-shell nanospheres synthesized using a modified Stöber sol-gel method. The particle-size dependence of their mode frequencies has been mapped by Brillouin light scattering, a powerful tool for probing hypersonic vibrations. Unlike the larger particles, the observed spheroidal-like mode frequencies of the smaller ones do not scale with inverse diameter. Interestingly, the onset of the deviation from this linearity occurs at a smaller particle size for higher-energy modes than for lower-energy ones. Finite element simulations show that the mode displacement profiles of the Ag@SiO(2) core-shells closely resemble those of a homogeneous SiO(2) sphere. Simulations have also been performed to ascertain the effects that the core shape and the relative hardness of the core and shell materials have on the vibrations of the core-shell as a whole. As the vibrational modes of a particle have a bearing on its thermal and mechanical properties, the findings would be of value in designing core-shell nanostructures with customized thermal and mechanical characteristics. PMID:21087022

  10. Dual Drug Release Electrospun Core-Shell Nanofibers with Tunable Dose in the Second Phase

    PubMed Central

    Qian, Wei; Yu, Deng-Guang; Li, Ying; Liao, Yao-Zu; Wang, Xia; Wang, Lu

    2014-01-01

    This study reports a new type of drug-loaded core-shell nanofibers capable of providing dual controlled release with tunable dose in the second phase. The core-shell nanofibers were fabricated through a modified coaxial electrospinning using a Teflon-coated concentric spinneret. Poly(vinyl pyrrolidone) and ethyl cellulose were used as the shell and core polymer matrices respectively, and the content of active ingredient acetaminophen (APAP) in the core was programmed. The Teflon-coated concentric spinneret may facilitate the efficacious and stable preparation of core-shell nanofibers through the modified coaxial electrospinning, where the core fluids were electrospinnable and the shell fluid had no electrospinnability. The resultant nanofibers had linear morphologies and clear core-shell structures, as observed by the scanning and transmission electron microscopic images. APAP was amorphously distributed in the shell and core polymer matrices due to the favorite second-order interactions, as indicated by the X-ray diffraction and FTIR spectroscopic tests. The results from the in vitro dissolution tests demonstrated that the core-shell nanofibers were able to furnish the desired dual drug controlled-release profiles with a tunable drug release amount in the second phase. The modified coaxial electrospinning is a useful tool to generate nanostructures with a tailored components and compositions in their different parts, and thus to realize the desired functional performances. PMID:24406731

  11. [Scattering properties of core-shell structure of mist wrapped dust particles].

    PubMed

    Feng, Shi-qi; Song, Wei; Wang, Yan; Miao, Xin-hui; Xu, Li-jun; Liu, Yu; Li, Cheng; Li Wen-long; Wang, Yi-ran; Cai, Hong-xing

    2014-12-01

    The authors have investigated the optical properties of core-shell structure of mist wrapped dust particles based on the method of discrete dipole approximation (DDA). The influence on the thickness of the elliptical core-shell structure were calculated which the ratio of long axis and short axis is 2:1, and the change of scattering angle for scattering characteristics. The results shows that the thickness of outer layer increase from 1.2 to 4.8 μm with the scattering and extinction coefficient of double core-shell layers particles decrease from 3.4 and 3.43 to 2.543 and 2.545, when the size of inner core isn't change. And scattering relative strength also increased obviously. The thickness of inner core increase from 0.6 to 2.4 μm with the of scattering and extinction coefficient change from 2.59 and 2.88 to 2.6 and 2.76 when thickness of outer remain constant. Effect of the thickness of visible outer layer on the scattering characteristics of double core-shell layers particles is greater, because of the interaction between scattering light and outer materials. The scattering relative intensity decrease with wavelength increased, while increased with the scale of core-shell structure increase. The results make a promotion on the study of the transportation characteristics of laser and scattering characteristics when the atmospheric aerosol and water mist interact together. PMID:25881412

  12. Core-shell morphology and characterization of carbon nanotube nanowires click coupled with polypyrrole

    NASA Astrophysics Data System (ADS)

    Rana, Sravendra; Cho, Jae Whan

    2011-07-01

    Core-shell nanowires having multiwalled carbon nanotubes (MWNT) as a core and polypyrrole (PPy) as a shell were synthesized using Cu(I)-catalyzed azide-alkyne cycloaddition click chemistry. According to transmission electron microscopy measurements, the uniform PPy layers of 10-20 nm in thickness were formed well on the MWNT's surface. In particular 'grafting from' click coupling was more effective in obtaining uniform and stable core-shell nanowires as well as in the reaction yield, compared to 'grafting to' click coupling. This is due to chemical bond formation between PPy and MWNT in equal intervals along the longitudinal direction of the MWNT, achieved by 'grafting from' click coupling. As a result, the core-shell nanowires were very stable even in the sonication of nanowires and showed an enhanced electrical conductivity of 80 S cm - 1, due to the synergetic interaction between MWNTs and PPy, which is higher than the conductivity of pure MWNTs and pure PPy. In addition, the core-shell nanowires could show better NO2 gas sensing properties compared to pure MWNTs and pure PPy as well as MWNT/PPy composites prepared by in situ polymerization. The synthesized core-shell nanowires would play an important role in preparing electrical and sensing devices.

  13. Suppression of auger recombination in ""giant"" core/shell nanocrystals

    SciTech Connect

    Garcia Santamaria, Florencio; Vela, Javier; Schaller, Richard D; Hollingsworth, Jennifer A; Klimov, Victor I; Chen, Yongfen

    2009-01-01

    Many potential applications of semiconductor nanocrystals are hindered by nonradiative Auger recombination wherein the electron-hole (exciton) recombination energy is transferred to a third charge carrier. This process severely limits the lifetime and bandwidth of optical gain, leads to large nonradiative losses in light emitting diodes and photovoltaic cells, and is believed to be responsible for intermittency ('blinking') of emission from single nanocrystals. The development of nanostructures in which Auger recombination is suppressed has been a longstanding goal in colloidal nanocrystal research. Here, we demonstrate that such suppression is possible using so-called 'giant' nanocrystals that consist of a small CdSe core and a thick CdS shell. These nanostructures exhibit a very long biexciton lifetime ({approx}10 ns) that is likely dominated by radiative decay instead of non-radiative Auger recombination. As a result of suppressed Auger recombination, even high-order multiexcitons exhibit high emission efficiencies, which allows us to demonstrate optical amplification with an extraordinarily large bandwidth (>500 me V) and record low excitation thresholds.

  14. Dual emission in asymmetric "giant" PbS/CdS/CdS core/shell/shell quantum dots.

    PubMed

    Zhao, Haiguang; Sirigu, Gianluca; Parisini, Andrea; Camellini, Andrea; Nicotra, Giuseppe; Rosei, Federico; Morandi, Vittorio; Zavelani-Rossi, Margherita; Vomiero, Alberto

    2016-02-21

    Semiconducting nanocrystals optically active in the infrared region of the electromagnetic spectrum enable exciting avenues in fundamental research and novel applications compatible with the infrared transparency windows of biosystems such as chemical and biological optical sensing, including nanoscale thermometry. In this context, quantum dots (QDs) with double color emission may represent ultra-accurate and self-calibrating nanosystems. We present the synthesis of giant core/shell/shell asymmetric QDs having a PbS/CdS zinc blende (Zb)/CdS wurtzite (Wz) structure with double color emission close to the near-infrared (NIR) region. We show that the double emission depends on the excitation condition and analyze the electron-hole distribution responsible for the independent and simultaneous radiative exciton recombination in the PbS core and in the CdS Wz shell, respectively. These results highlight the importance of the driving force leading to preferential crystal growth in asymmetric QDs, and provide a pathway for the rational control of the synthesis of double color emitting giant QDs, leading to the effective exploitation of visible/NIR transparency windows. PMID:26837955

  15. Synthesis, Characterization, and Functionalization of Hybrid Au/CdS and Au/ZnS Core/Shell Nanoparticles.

    PubMed

    Tobias, Andrew; Qing, Song; Jones, Marcus

    2016-01-01

    Plasmonic nanoparticles are an attractive material for light harvesting applications due to their easily modified surface, high surface area and large extinction coefficients which can be tuned across the visible spectrum. Research into the plasmonic enhancement of optical transitions has become popular, due to the possibility of altering and in some cases improving photo-absorption or emission properties of nearby chromophores such as molecular dyes or quantum dots. The electric field of the plasmon can couple with the excitation dipole of a chromophore, perturbing the electronic states involved in the transition and leading to increased absorption and emission rates. These enhancements can also be negated at close distances by energy transfer mechanism, making the spatial arrangement of the two species critical. Ultimately, enhancement of light harvesting efficiency in plasmonic solar cells could lead to thinner and, therefore, lower cost devices. The development of hybrid core/shell particles could offer a solution to this issue. The addition of a dielectric spacer between a gold nanoparticles and a chromophore is the proposed method to control the exciton plasmon coupling strength and thereby balance losses with the plasmonic gains. A detailed procedure for the coating of gold nanoparticles with CdS and ZnS semiconductor shells is presented. The nanoparticles show high uniformity with size control in both the core gold particles and shell species allowing for a more accurate investigation into the plasmonic enhancement of external chromophores. PMID:26967555

  16. Quantum dot cosensitized solar cell based on PMOT@CdSe@ZnO core shell nanostructures with dual emission

    NASA Astrophysics Data System (ADS)

    Sehgal, Preeti; Narula, Anudeep Kumar

    2016-01-01

    Quantum dot sensitized solar cell based on poly(3-methoxythiophene) (PMOT)@CdSe@ZnO core shell nanostructure were synthesized where PMOT serves as hole transport material, CdSe acts as a photosensitizer which enhances visible range absorption and also helps in injection of electrons from PMOT to ZnO where ZnO provides channel for efficient electron transport. The properties of the device were assessed with and without CdSe quantum dots and effect of annealing was also observed on the device. After the addition of CdSe QDs, the visible light absorption of PMOT@ZnO was enhanced due to increase in surface area. PMOT@CdSe@ZnO exhibited dual emission, where CdSe and ZnO exhibited visible and UV emission respectively. The interface formed between PMOT and CdSe improves the charge separation. The better photovoltaic measurement of PMOT@CdSe@ZnO over CdSe@ZnO indicates that PMOT efficiently dissociate excitons at interface and suppress the interfacial charge recombination. A power conversion efficiency of 0.989% was attained for the device PMOT@CdSe@ZnO with Voc=0.56 V and Jsc=2.5 mA/cm2. Upon annealing, the efficiency of the device was enhanced to 1.1609% with Voc=0.58, Jsc=3.2 mA/cm2.

  17. Doxorubicin/gold-loaded core/shell nanoparticles for combination therapy to treat cancer through the enhanced tumor targeting.

    PubMed

    Kim, Kyungim; Oh, Keun Sang; Park, Dal Yong; Lee, Jae Young; Lee, Beom Suk; Kim, In San; Kim, Kwangmeyung; Kwon, Ick Chan; Sang, Yoon Kim; Yuk, Soon Hong

    2016-04-28

    A combination therapy consisting of radiotherapy and chemotherapy is performed using the core/shell nanoparticles (NPs) containing gold NPs and doxorubicin (DOX). Gold NPs in the core/shell NPs were utilized as a radiosensitizer. To examine the morphology and size distribution of the core/shell NPs, transmittance electron microscopy and dynamic light scattering were used. The in vitro release behavior, cellular uptake and toxicity were also observed to verify the functionality of the core/shell NPs as a nanocarrier. To demonstrate the advantage of the core/shell NPs over traditional gold NPs reported in the combination therapy, we evaluated the accumulation behavior of the core/shell NPs at the tumor site using the biodistribution. Antitumor efficacy was observed with and without radiation to evaluate the role of gold NPs as a radiosensitizer. PMID:26970205

  18. Enhanced UV Emission From Silver/ZnO And Gold/ZnO Core-Shell Nanoparticles: Photoluminescence, Radioluminescence, And Optically Stimulated Luminescence

    NASA Astrophysics Data System (ADS)

    Guidelli, E. J.; Baffa, O.; Clarke, D. R.

    2015-09-01

    The optical properties of core-shell nanoparticles consisting of a ZnO shell grown on Ag and Au nanoparticle cores by a solution method have been investigated. Both the ZnO/Ag and ZnO/Au particles exhibit strongly enhanced near-band-edge UV emission from the ZnO when excited at 325 nm. Furthermore, the UV intensity increases with the metal nanoparticle concentration, with 60-fold and 17-fold enhancements for the ZnO/Ag and ZnO/Au, core-shell nanoparticles respectively. Accompanying the increase in UV emission, there is a corresponding decrease in the broad band defect emission with nanoparticle concentration. Nonetheless, the broad band luminescence increases with laser power. The results are consistent with enhanced exciton emission in the ZnO shells due to coupling with surface plasmon resonance of the metal nanoparticles. Luminescence measurements during and after exposure to X-rays also exhibit enhanced UV luminescence. These observations suggest that metal nanoparticles may be suitable for enhancing optical detection of ionizing radiation.

  19. Enhanced UV Emission From Silver/ZnO And Gold/ZnO Core-Shell Nanoparticles: Photoluminescence, Radioluminescence, And Optically Stimulated Luminescence.

    PubMed

    Guidelli, E J; Baffa, O; Clarke, D R

    2015-01-01

    The optical properties of core-shell nanoparticles consisting of a ZnO shell grown on Ag and Au nanoparticle cores by a solution method have been investigated. Both the ZnO/Ag and ZnO/Au particles exhibit strongly enhanced near-band-edge UV emission from the ZnO when excited at 325 nm. Furthermore, the UV intensity increases with the metal nanoparticle concentration, with 60-fold and 17-fold enhancements for the ZnO/Ag and ZnO/Au, core-shell nanoparticles respectively. Accompanying the increase in UV emission, there is a corresponding decrease in the broad band defect emission with nanoparticle concentration. Nonetheless, the broad band luminescence increases with laser power. The results are consistent with enhanced exciton emission in the ZnO shells due to coupling with surface plasmon resonance of the metal nanoparticles. Luminescence measurements during and after exposure to X-rays also exhibit enhanced UV luminescence. These observations suggest that metal nanoparticles may be suitable for enhancing optical detection of ionizing radiation. PMID:26365945

  20. Core shell particles consisting of cobalt ferrite and silica as model ferrofluids [CoFe 2O 4-SiO 2 core shell particles

    NASA Astrophysics Data System (ADS)

    Wagner, Joachim; Autenrieth, Tina; Hempelmann, Rolf

    2002-11-01

    Nearly monodisperse core shell particles consisting of a magnetic core of cobalt ferrite (CoFe 2O 4) and a shell of silica (SiO 2) are prepared via a modified Stöber synthesis. The core shell structure is confirmed by TEM, the size distribution of the whole particles was determined by means of photon correlation spectroscopy and small angle X-ray scattering. Due to charged surface groups of the silica shells and the magnetic moments of the cores, these particles interact both via a screened Coulomb potential and via a magnetic dipole potential. If stray ions are removed in the presence of a mixed bed ion exchanger, the electrostatic repulsion induces colloidal crystallisation. The lattice constant is influenced by the interaction with a magnetic field gradient, indicated by a blue shift of the Laue spots towards increasing field gradient.

  1. A New Class of Silica Crosslinked Micellar Core-Shell /nanoparticles."

    SciTech Connect

    Huo, Qisheng; Liu, Jun; Wang, Li Q.; Jiang, Yingbing; Lambert, Timothy N.; Fang, Erica

    2006-05-17

    Micellar nanoparticles made of surfactants and polymers have attracted wide attention in the materials and biomedical community for controlled drug delivery, molecular imaging and sensing; however, their long-term stability remains a topic of intense study. Here we report a new class of robust, ultrafine (10nm) silica core-shell nanoparticles formed from silica crosslinked, individual block copolymer micelles. Compared with pure polymer micelles, the new core-shell nanoparticles have significantly improved stability and do not break down during dilution. They also achieve much higher loading capacity for a wide range of chemicals, with the entrapped molecules slowly released over a much longer period of time. A wide range of functional groups can be easily incorporated through co-condensation with the silica matrix. The potential to deliver hydrophobic agents into cancer cells has been demonstrated. Because of their unique properties, these novel core-shell nanoparticles could potentially provide a new nanomedicine platform for imaging, detection and treatment.

  2. Lithography-Free Fabrication of Core-Shell GaAs Nanowire Tunnel Diodes.

    PubMed

    Darbandi, A; Kavanagh, K L; Watkins, S P

    2015-08-12

    GaAs core-shell p-n junction tunnel diodes were demonstrated by combining vapor-liquid-solid growth with gallium oxide deposition by atomic layer deposition for electrical isolation. The characterization of an ensemble of core-shell structures was enabled by the use of a tungsten probe in a scanning electron microscope without the need for lithographic processing. Radial tunneling transport was observed, exhibiting negative differential resistance behavior with peak-to-valley current ratios of up to 3.1. Peak current densities of up to 2.1 kA/cm(2) point the way to applications in core-shell photovoltaics and tunnel field effect transistors. PMID:26189994

  3. A pathway for the growth of core-shell Pt-Pd nanoparticles

    SciTech Connect

    Narula, Chaitanya Kumar; Yang, Xiaofan; Li, Chen; Pennycook, Stephen J; Lupini, Andrew R

    2015-10-12

    In this study, the aging of both Pt-Pd nanoparticles and core-shell Pt-Pd nanoparticles has been reported to result in alloying of Pt with Pd. In comparison to monometallic Pt catalysts, the growth of Pd-Pt bimetallics is slower; however, the mechanism of growth of particles and the mechanism by which Pd improves the hydrothermal durability of bimetallic Pd-Pt particles remains uncertain. In our work on hydrothermal aging of core-shell Pt-Pd nanoparticles, synthesized by solution methods, with varying Pd:Pt ratio of 1:4, 1:1, and 4:1, we compare the growth of core-shell Pt-Pd nanoparticles and find that particles grow by migrating and joining together. The unique feature of the observed growth is that Pd shells from both particles open up and join, allowing the cores to merge. At high temperatures, alloying occurs in good agreement with reports by other workers.

  4. Nitride stabilized PtNi core-shell nanocatalyst for high oxygen reduction activity.

    PubMed

    Kuttiyiel, Kurian A; Sasaki, Kotaro; Choi, Yongman; Su, Dong; Liu, Ping; Adzic, Radoslav R

    2012-12-12

    We describe a route to the development of novel PtNiN core-shell catalysts with low Pt content shell and inexpensive NiN core having high activity and stability for the oxygen reduction reaction (ORR). The PtNiN synthesis involves nitriding Ni nanoparticles and simultaneously encapsulating it by 2-4 monolayer-thick Pt shell. The experimental data and the density functional theory calculations indicate nitride has the bifunctional effect that facilitates formation of the core-shell structures and improves the performance of the Pt shell by inducing both geometric and electronic effects. Synthesis of inexpensive NiN cores opens up possibilities for designing of various transition metal nitride based core-shell nanoparticles for a wide range of applications in energy conversion processes. PMID:23194259

  5. Controlled nanostructuring of multiphase core-shell nanowires by a template-assisted electrodeposition approach

    NASA Astrophysics Data System (ADS)

    Shi, Dawei; Chen, Junyang; Riaz, Saira; Zhou, Wenping; Han, Xiufeng

    2012-08-01

    Multiphase core-shell nanowires have been fabricated by controlling the ion transport processes of the microfluids in the nanochannels of the template. Both forced convection and pulsed potential induced migration can be applied to tune the morphologies of the nanostructures obtained by manipulating the ion transport during electrodeposition. The morphology and content of the core-shell structure were studied by field emission scanning electron microscope (FESEM) analysis, transmission electron microscope (TEM) analysis and energy dispersive spectrometry (EDS), respectively. The magnetic properties were analyzed by vibrating sample magnetometer (VSM) analysis. A magnetically hard core and soft shell constitutes the multiphase composite nanostructure. The unique magnetic hysteresis curve indicates the decoupled magnetic reversal processes of the two components. Our work provides deeper insights into the formation mechanisms of a new core-shell nanostructure, which may have potential applications in novel spintronics devices.

  6. Electrosprayed core-shell polymer-lipid nanoparticles for active component delivery

    NASA Astrophysics Data System (ADS)

    Eltayeb, Megdi; Stride, Eleanor; Edirisinghe, Mohan

    2013-11-01

    A key challenge in the production of multicomponent nanoparticles for healthcare applications is obtaining reproducible monodisperse nanoparticles with the minimum number of preparation steps. This paper focus on the use of electrohydrodynamic (EHD) techniques to produce core-shell polymer-lipid structures with a narrow size distribution in a single step process. These nanoparticles are composed of a hydrophilic core for active component encapsulation and a lipid shell. It was found that core-shell nanoparticles with a tunable size range between 30 and 90 nm and a narrow size distribution could be reproducibly manufactured. The results indicate that the lipid component (stearic acid) stabilizes the nanoparticles against collapse and aggregation and improves entrapment of active components, in this case vanillin, ethylmaltol and maltol. The overall structure of the nanoparticles produced was examined by multiple methods, including transmission electron microscopy and differential scanning calorimetry, to confirm that they were of core-shell form.

  7. Production of Polymer Core-Shell Colloids with High Uniformity via Coaxial Electrospray

    NASA Astrophysics Data System (ADS)

    Hwang, Yoon Kyun; Jeong, Unyong

    2008-03-01

    Although nanofibers fabricated by electrospinning have been attracting wide interest, the production of colloids by electrospraying has not much studied so far. We have developed a simple method for the production of core-shell colloids with high uniformity by means of the coaxial electrospray. Contrary to usual coaxial setup, the inner nozzle was set to touch the inside wall of the outer nozzle for reproducible production. A polymer solution for the core was introduced through the outer nozzle and another solution for the shell was provided through the inner nozzle. The structure of the colloids was dependent on the polymer concentration, relative feed ratio between the polymer solutions. Especially, core-shell structured colloids are our primary interest due to their promising uses in drug-delivery systems, cosmetics, and food industries. This talk will present the production of core-shell colloids consisting of two polymer components.

  8. Platinum-Maghemite Core-Shell Nanoparticles Using a Sequential Synthesis

    SciTech Connect

    Teng, X.; Black, D.; Watkins, N.J.; Gao, Y.; Yang, H.

    2003-01-11

    OAK-B135 Pt{at}Fe2O3 core-shell nanoparticles have been made using a sequential synthetic method. Platinum nanoparticles were synthesized via reduction of platinum acetylacetonate in octyl ether, and layers of iron oxide were subsequently deposited on the surface of Pt nanoparticles through thermal decomposition of iron pentacarbonyl. The core-shell nanoparticles were characterized by powder X-ray diffraction, high-resolution transmission electron microscopy, and X-ray photoemission spectroscopy. Thickness of the shell can be controlled by changing concentrations of the reactants and the reaction conditions. These Pt{at}Fe2O3 core-shell nanoparticles could have potential applications in catalysis and as precursors for making property-tunable magnetic nanoparticles, thin films, and nanocomposites.

  9. Thermoelectric characteristic of the rough InN/GaN core-shell nanowires

    SciTech Connect

    Wu, Chao-Wei; Wu, Yuh-Renn

    2014-09-14

    An analysis to model the thermoelectric (TE) effects of the rough InN/GaN core-shell nanowires (NWs) with wire diameter ranging from 25 nm to 100 nm is proposed. The elastic continuum model is employed to calculate the phonon dispersion relation curves and the related phonon group velocity. Within the framework of Boltzmann transport equations and relaxation time approximation, the electrical conductivity, Seebeck coefficient, electronic thermal conductivity, and the lattice thermal conductivity is obtained. Simulation results indicate that TE properties of the rough InN/GaN core-shell NWs are strongly affected by the surface roughness and the diameter of NWs. The optimized condition of the proposed rough InN/GaN core-shell TE NWs is studied in this paper and the highest ZT obtained in the calculation is 0.8598 at 300 K and 1.713 at 1000 K.

  10. Study of core-shell platinum-based catalyst for methanol and ethylene glycol oxidation

    NASA Astrophysics Data System (ADS)

    Kaplan, D.; Alon, M.; Burstein, L.; Rosenberg, Yu.; Peled, E.

    A Ru core-Pt shell, XC72-supported catalyst was synthesized in a two-step process: first, by deposition of Ru on XC72 by the polyol process and then by deposition of Pt on the XC72-supported Ru, with NaBH 4 as reducing agent. The structure and composition of this core-shell catalyst were determined by EDS, XPS, TEM and XRD. Electrochemical characterization was determined with the use of cyclic voltammetry and chronoamperometry. The methanol and ethylene glycol oxidation activities of the core-shell catalyst were studied at 80 °C and compared to those of a commercial catalyst. It was found to be significantly better (in terms of A g -1 of Pt) in the case of methanol oxidation and worse in the case of ethylene glycol oxidation. Possible reasons for the lower ethylene glycol oxidation activity of the core-shell catalyst are discussed.

  11. Photonic bandgap of inverse opals prepared from core-shell spheres.

    PubMed

    Liu, Bo-Tau; Lin, Ya-Li; Huang, Shao-Xian

    2012-01-01

    In this study, we synthesized monodispersed polystyrene (PS)-silica core-shell spheres with various shell thicknesses for the fabrication of photonic crystals. The shell thickness of the spheres was controlled by various additions of tetraethyl orthosilicate during the shell growth process. The shrinkage ratio of the inverse opal photonic crystals prepared from the core-shell spheres was significantly reduced from 14.7% to within 3%. We suspected that the improvement resulted from the confinement of silica shell to the contraction of PS space during calcination. Due to the shell effect, the inverse opals prepared from the core-shell spheres have higher filling fraction and larger wavelength of stop band maximum. PMID:22894600

  12. Preparation of highly dispersed core/shell-type titania nanocapsules containing a single Ag nanoparticle.

    PubMed

    Sakai, Hideki; Kanda, Takashi; Shibata, Hirobumi; Ohkubo, Takahiro; Abe, Masahiko

    2006-04-19

    Core/shell-type titania nanocapsules containing a single Ag nanoparticle were prepared. Ag nanoparticles were prepared using the reduction of silver nitrate with hydrazine in the presence of cetyltrimethylammonium bromide (CTAB) as protective agent. The sol-gel reaction of titanium tetraisopropoxide (TTIP) was used to prepare core/shell-type titania nanocapsules with CTAB-coated Ag nanoparticles as the core. TEM observations revealed that the size of the core (Ag particle) and the thickness of the shell (titania) of the core/shell particles obtained are about 10 nm and 5-10 nm, respectively. In addition, the nanocapsules were found to be dispersed in the medium as individual particles without aggregation. Moreover, titania coating caused the surface plasmon absorption of Ag nanoparticles to shift toward the longer wavelength side. PMID:16608315

  13. Highly responsive core-shell microactuator arrays for use in viscous and viscoelastic fluids

    PubMed Central

    Fiser, Briana L.; Shields, Adam R.; Falvo, M. R.; Superfine, R.

    2015-01-01

    We present a new fabrication method to produce arrays of highly responsive polymer-metal core-shell magnetic microactuators. The core-shell fabrication method decouples the elastic and magnetic structural components such that the actuator response can be optimized by adjusting the core-shell geometry. Our microstructures are 10 μm long, 550 nm in diameter, and electrochemically fabricated in particle track-etched membranes, comprising a poly(dimethylsiloxane) core with a 100 nm Ni shell surrounding the upper 3–8 μm. The structures can achieve deflections of nearly 90° with moderate magnetic fields and are capable of driving fluid flow in a fluid 550 times more viscous than water. PMID:26405376

  14. Polyethylenimine-immobilized core-shell nanoparticles: synthesis, characterization, and biocompatibility test.

    PubMed

    Ratanajanchai, Montri; Soodvilai, Sunhapas; Pimpha, Nuttaporn; Sunintaboon, Panya

    2014-01-01

    Herein, we prepared PEI-immobilized core-shell particles possessing various types of polymer cores via a visible light-induced surfactant-free emulsion polymerization (SFEP) of three vinyl monomers: styrene (St), methyl methacrylate (MMA), and 2-hydroxyethyl methacrylate (HEMA). An effect of monomers on the polymerization and characteristics of resulting products was investigated. Monomers with high polarity can provide high monomer conversion, high percentage of grafted PEI, stable particles with uniform size distribution but less amino groups per particles. All prepared nanoparticles exhibited a core-shell nanostructure, containing PEI on the shell with hydrodynamic size around 140-230nm. For in-vitro study in Caco-2 cells, we found that the incorporation of PEI into these core-shell nanoparticles can significantly reduce its cytotoxic effect and also be able to internalized within the cells. Accordingly, these biocompatible particles would be useful for various biomedical applications, including gene transfection and intracellular drug delivery. PMID:24268272

  15. Controlled nanostructuring of multiphase core-shell nanowires by a template-assisted electrodeposition approach.

    PubMed

    Shi, Dawei; Chen, Junyang; Riaz, Saira; Zhou, Wenping; Han, Xiufeng

    2012-08-01

    Multiphase core-shell nanowires have been fabricated by controlling the ion transport processes of the microfluids in the nanochannels of the template. Both forced convection and pulsed potential induced migration can be applied to tune the morphologies of the nanostructures obtained by manipulating the ion transport during electrodeposition. The morphology and content of the core-shell structure were studied by field emission scanning electron microscope (FESEM) analysis, transmission electron microscope (TEM) analysis and energy dispersive spectrometry (EDS), respectively. The magnetic properties were analyzed by vibrating sample magnetometer (VSM) analysis. A magnetically hard core and soft shell constitutes the multiphase composite nanostructure. The unique magnetic hysteresis curve indicates the decoupled magnetic reversal processes of the two components. Our work provides deeper insights into the formation mechanisms of a new core-shell nanostructure, which may have potential applications in novel spintronics devices. PMID:22751156

  16. Ethanol sensing of SnO2-WO3 core/shell nanowires

    NASA Astrophysics Data System (ADS)

    Park, Sunghoon; Kim, Soohyun; Sun, Gun-Joo; Choi, Seung-Bok; Lee, Sangmin; Lee, Chongmu

    2015-09-01

    SnO2-WO3 core/shell nanowires were synthesized by the thermal evaporation of Sn powders in an oxidizing ambient followed by the thermal evaporation of WO3 powders. Their C2H5OH gas sensing properties were then examined. The C2H5OH gas sensing properties were improved remarkably by formation of the SnO2-WO3 heterostructures. The SnO2-WO3 core/shell nanowire sensors showed a much stronger and faster response to C2H5OH gas than the pristine SnO2-nanowire sensors. The enhanced sensing performance of the SnO2-WO3 core/shell nanowires towards C2H5OH gas can be accounted for by the potential barrier-controlled carrier-transport mechanism combined with the surface-depletion mechanism. [Figure not available: see fulltext.

  17. Electrosprayed core-shell polymer-lipid nanoparticles for active component delivery.

    PubMed

    Eltayeb, Megdi; Stride, Eleanor; Edirisinghe, Mohan

    2013-11-22

    A key challenge in the production of multicomponent nanoparticles for healthcare applications is obtaining reproducible monodisperse nanoparticles with the minimum number of preparation steps. This paper focus on the use of electrohydrodynamic (EHD) techniques to produce core-shell polymer-lipid structures with a narrow size distribution in a single step process. These nanoparticles are composed of a hydrophilic core for active component encapsulation and a lipid shell. It was found that core-shell nanoparticles with a tunable size range between 30 and 90 nm and a narrow size distribution could be reproducibly manufactured. The results indicate that the lipid component (stearic acid) stabilizes the nanoparticles against collapse and aggregation and improves entrapment of active components, in this case vanillin, ethylmaltol and maltol. The overall structure of the nanoparticles produced was examined by multiple methods, including transmission electron microscopy and differential scanning calorimetry, to confirm that they were of core-shell form. PMID:24164775

  18. Solution-Processed Copper/Reduced-Graphene-Oxide Core/Shell Nanowire Transparent Conductors.

    PubMed

    Dou, Letian; Cui, Fan; Yu, Yi; Khanarian, Garo; Eaton, Samuel W; Yang, Qin; Resasco, Joaquin; Schildknecht, Christian; Schierle-Arndt, Kerstin; Yang, Peidong

    2016-02-23

    Copper nanowire (Cu NW) based transparent conductors are promising candidates to replace ITO (indium-tin-oxide) owing to the high electrical conductivity and low-cost of copper. However, the relatively low performance and poor stability of Cu NWs under ambient conditions limit the practical application of these devices. Here, we report a solution-based approach to wrap graphene oxide (GO) nanosheets on the surface of ultrathin copper nanowires. By mild thermal annealing, GO can be reduced and high quality Cu r-GO core-shell NWs can be obtained. High performance transparent conducting films were fabricated with these ultrathin core-shell nanowires and excellent optical and electric performance was achieved. The core-shell NW structure enables the production of highly stable conducting films (over 200 days stored in air), which have comparable performance to ITO and silver NW thin films (sheet resistance ∼28 Ω/sq, haze ∼2% at transmittance of ∼90%). PMID:26820809

  19. Preparation and Biocompatibility of Gold@ Polypyrrole-Chitosan with Core-Shell Nanostructure.

    PubMed

    Wu, Yun; Wang, Yanyan; Chen, Hui; Ge, Shanshan; Zhang, Jinling; Mao, Chun; Ding, Hongyan; Shen, Jian

    2016-03-01

    A two-step method for preparing Au@polypyrrole-chitosan core-shell nanoparticles (Au @ PPy-CS NPs) was fabricated by in situ polymerization of pyrrole monomer on the surface of Au spheres in chitosan solution. Transmission electron microscopy (TEM) images showed the presence of core-shell structure of nanoparticles. Energy-Dispersive Spectroscopy (EDS) and Fourier transform infrared (FTIR) spectroscopy were adopted to verify the shell is polypyrrole-chitosan. Ultraviolet-visible (UV-vis) and X-ray diffraction (XRD) showed that Au was present in the core-shell nanoparticles. The biocompatibility of Au @ PPy-CS NPs was characterized by in vitro for hemolysis assay and cytotoxicity experiments. Results indicated the Au @ PPy-CS NPs had good blood compatibility and low cytotoxicity. The Au @ PPy-CS NPs we proposed provide a promising platform of blood circulation system for early illness diagnosis and therapy. PMID:27455639

  20. Tuning g factors of core-shell nanoparticles by controlled positioning of magnetic impurities

    NASA Astrophysics Data System (ADS)

    Sanders, G. D.; Musfeldt, J. L.; Stanton, C. J.

    2016-02-01

    We present a theoretical platform for modeling the electronic and magneto-optic properties of magnetically doped core-shell nanoparticles that has, as a central prediction, a mechanism by which the g factors in these nanoparticles can be tuned over a wide range by controlled positioning of magnetic impurities. We illustrate this effect for wide-gap Mn-doped CdS-ZnS core-shell particles and point out several unexpected trends that merit extended experimental investigation. The ability to tune g factors will make core-shell nanostructures viable candidates for spintronic applications, and the comprehensive modeling approach outlined here will be a powerful tool for predicting their properties as well as for optimizing the design of novel spintronic devices.

  1. Cracking the Si Shell Growth in Hexagonal GaP-Si Core-Shell Nanowires.

    PubMed

    Conesa-Boj, S; Hauge, H I T; Verheijen, M A; Assali, S; Li, A; Bakkers, E P A M; Fontcuberta i Morral, A

    2015-05-13

    Semiconductor nanowires have increased the palette of possible heterostructures thanks to their more effective strain relaxation. Among these, core-shell heterostructures are much more sensitive to strain than axial ones. It is now accepted that the formation of misfit dislocations depends both on the lattice mismatch and relative dimensions of the core and the shell. Here, we show for the first time the existence of a new kind of defect in core-shell nanowires: cracks. These defects do not originate from a lattice mismatch (we demonstrate their appearance in an essentially zero-mismatch system) but from the thermal history during the growth of the nanowires. Crack defects lead to the development of secondary defects, such as type-I1 stacking faults and Frank-type dislocations. These results provide crucial information with important implications for the optimized synthesis of nanowire-based core-shell heterostructures. PMID:25922878

  2. Heterogeneous core/shell fluoride nanocrystals with enhanced upconversion photoluminescence for in vivo bioimaging

    NASA Astrophysics Data System (ADS)

    Hao, Shuwei; Yang, Liming; Qiu, Hailong; Fan, Rongwei; Yang, Chunhui; Chen, Guanying

    2015-06-01

    We report on heterogeneous core/shell CaF2:Yb3+/Ho3+@NaGdF4 nanocrystals of 17 nm with efficient upconversion (UC) photoluminescence (PL) for in vivo bioimaging. Monodisperse core/shell nanostructures were synthesized using a seed-mediated growth process involving two quite different approaches of liquid-solid-solution and thermal decomposition. They exhibit green emission with a sharp band around 540 nm when excited at ~980 nm, which is about 39 times brighter than the core CaF2:Yb3+/Ho3+ nanoparticles. PL decays at 540 nm revealed that such an enhancement arises from efficient suppression of surface-related deactivation from the core nanocrystals. In vivo bioimaging employing water-dispersed core/shell nanoparticles displayed high contrast against the background.We report on heterogeneous core/shell CaF2:Yb3+/Ho3+@NaGdF4 nanocrystals of 17 nm with efficient upconversion (UC) photoluminescence (PL) for in vivo bioimaging. Monodisperse core/shell nanostructures were synthesized using a seed-mediated growth process involving two quite different approaches of liquid-solid-solution and thermal decomposition. They exhibit green emission with a sharp band around 540 nm when excited at ~980 nm, which is about 39 times brighter than the core CaF2:Yb3+/Ho3+ nanoparticles. PL decays at 540 nm revealed that such an enhancement arises from efficient suppression of surface-related deactivation from the core nanocrystals. In vivo bioimaging employing water-dispersed core/shell nanoparticles displayed high contrast against the background. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr02287h

  3. Auger and Carrier Trapping Dynamics in Core/Shell Quantum Dots Having Sharp and Alloyed Interfaces.

    PubMed

    Beane, Gary A; Gong, Ke; Kelley, David F

    2016-03-22

    The role of interface sharpness in controlling the excited state dynamics in CdSe/ZnSe core/shell particles is examined here. Particles composed of CdSe/ZnSe with 2.4-4.0 nm diameter cores and approximately 4 monolayer shells are synthesized at relatively low temperature, ensuring a sharp core-shell interface. Subsequent annealing results in cadmium and zinc interdiffusion, softening the interface. TEM imaging and absorption spectra reveal that annealing results in no change in the particle sizes. Annealing results in a 5-10 nm blue shift in the absorption spectrum, which is compared to calculated spectral shifts to characterize the extent of metal interdiffusion. The one- and two-photon dynamics are measured using time-resolved absorption spectroscopy. We find that biexcitons undergo biexponential decays, with fast and slow decay times differing by about an order of magnitude. The relative magnitudes of the fast and slow components depend on the sharpness of the core-shell interface, with larger fast component amplitudes associated with a sharp core-shell interface. The slow component is assigned to Auger recombination of band edge carriers and the fast decay component to Auger recombination of holes that are trapped in defects produced by lattice strain. Annealing of these particles softens the core-shell interface and thereby reduces the amount of lattice strain and diminishes the magnitude of the fast decay component. The time constant of the slow biexciton Auger recombination component changes only slightly upon softening of the core-shell interface. PMID:26895220

  4. Facile preparation of hybrid core-shell nanorods for photothermal and radiation combined therapy.

    PubMed

    Deng, Yaoyao; Li, Erdong; Cheng, Xiaju; Zhu, Jing; Lu, Shuanglong; Ge, Cuicui; Gu, Hongwei; Pan, Yue

    2016-02-11

    The hybrid platinum@iron oxide core-shell nanorods with high biocompatibility were synthesized and applied for combined therapy. These hybrid nanorods exhibit a good photothermal effect on cancer cells upon irradiation with a NIR laser. Furthermore, due to the presence of a high atomic number element (platinum core), the hybrid nanorods show a synergistic effect between photothermal and radiation therapy. Therefore, the as-prepared core-shell nanorods could play an important role in facilitating synergistic therapy between photothermal and radiation therapy to achieve better therapeutic efficacy. PMID:26818657

  5. Anisotropic In distribution in InGaN core-shell nanowires

    SciTech Connect

    Leclere, C.; Renevier, H.; Katcho, N. A.; Tourbot, G.; Daudin, B.; Proietti, M. G.

    2014-07-07

    In this work, we investigate the local atomic structure of defect-free homogeneous and self-organized core-shell structure nanowires by means of X-ray Absorption Fine Structure (XAFS) Spectroscopy at the In L{sub III} and K edges and Multiwavelength Anomalous Diffraction. The results are interpreted by comparison of the experimental data with X-ray absorption calculations carried out with ab initio structural models. Extended-XAFS data analysis at In K-edge shows an anisotropic In distribution in the second nearest neighbors pointing out to a deviation from randomness in In distribution for the core-shell sample.

  6. Highly stable, luminescent core-shell type methylammonium-octylammonium lead bromide layered perovskite nanoparticles.

    PubMed

    Bhaumik, Saikat; Veldhuis, Sjoerd A; Ng, Yan Fong; Li, Mingjie; Muduli, Subas Kumar; Sum, Tze Chien; Damodaran, Bahulayan; Mhaisalkar, Subodh; Mathews, Nripan

    2016-06-01

    A new protocol for the synthesis of a highly stable (over 2 months under ambient conditions) solution-processed core-shell type structure of mixed methylammonium-octylammonium lead bromide perovskite nanoparticles (5-12 nm), having spherical shape, color tunability in the blue to green spectral region (438-521 nm) and a high photoluminescence quantum yield (PLQY) of up to 92% is described. The color tunability, high PLQY and stability are due to the quantum confinement imparted by the crystal engineering associated with core-shell nanoparticle formation during growth. PMID:27165565

  7. Symplectic Symmetry and the Ab Initio No-Core Shell Model

    SciTech Connect

    Draayer, Jerry P.; Dytrych, Tomas; Sviratcheva, Kristina D.; Bahri, Chairul; Vary, James P.; /Iowa State U. /LLNL, Livermore /SLAC

    2007-03-14

    The symplectic symmetry of eigenstates for the 0{sub gs}{sup +} in {sup 16}O and the 0{sub gs}{sup +} and lowest 2{sup +} and 4{sup +} configurations of {sup 12}C that are well-converged within the framework of the no-core shell model with the JISP16 realistic interaction is examined. These states are found to project at the 85-90% level onto very few symplectic representations including the most deformed configuration, which confirms the importance of a symplectic no-core shell model and reaffirms the relevance of the Elliott SU(3) model upon which the symplectic scheme is built.

  8. Real-Time Imaging of the Formation of Au-Ag Core-Shell Nanoparticles.

    PubMed

    Tan, Shu Fen; Chee, See Wee; Lin, Guanhua; Bosman, Michel; Lin, Ming; Mirsaidov, Utkur; Nijhuis, Christian A

    2016-04-27

    We study the overgrowth process of silver-on-gold nanocubes in dilute, aqueous silver nitrate solution in the presence of a reducing agent, ascorbic acid, using in situ liquid-cell electron microscopy. Au-Ag core-shell nanostructures were formed via two mechanistic pathways: (1) nuclei coalescence, where the Ag nanoparticles absorbed onto the Au nanocubes, and (2) monomer attachment, where the Ag atoms epitaxially deposited onto the Au nanocubes. Both pathways lead to the same Au-Ag core-shell nanostructures. Analysis of the Ag deposition rate reveals the growth modes of this process and shows that this reaction is chemically mediated by the reducing agent. PMID:27043921

  9. Synthesis of AgatCrO2 core-shell nanoparticles

    NASA Astrophysics Data System (ADS)

    Sharma, Preetam K.; Sharma, Priyanka; Biswas, S.; Nagawat, A. K.

    2013-06-01

    Half metallic ferromagnetic Chromium Oxide (CrO2) with 100% spin polarization is thought as an excellent candidate for magnetic nano-tag for Giant magnetoresistive biosensor. We have investigated the chemical synthesis and direct mixing approaches for the synthesis of Ag@CrO2 core shell nanoparticles. For chemical synthesis two mild reducing agents namely polyvinyl alcohol (PVA) and ethylene glycol (EG) were used. Our investigations suggest that the direct mixing and subsequent annealing at 300°C for 2 h is the better method to realize Ag@CrO2 core shell nanoparticles.

  10. Improved oxygen reduction activity on the Ih Cu@Pt core-shell nanoparticles

    NASA Astrophysics Data System (ADS)

    Yang, Zongxian; Geng, Zhixia; Zhang, Yanxing; Wang, Jinlong; Ma, Shuhong

    2011-09-01

    The minimum energy path (MEP) for the dissociation of O 2 on the Ih Cu@Pt12 core-shell nanoparticle. Ih Cu@Pt12 is the most stable among the symmetric Cu@Pt12 core-shell isomers. O 2 prefers to be adsorbed on the Ih Cu@Pt12 with the t-b-t configuration. The Ih Cu@Pt12 has enhanced activity for O 2 dissociation and O diffusion. Ih Cu@Pt12 nanoparticle is a good candidate for being the ORR catalyst.

  11. Recent advances in the synthesis of Fe3O4@AU core/shell nanoparticles

    NASA Astrophysics Data System (ADS)

    Salihov, Sergei V.; Ivanenkov, Yan A.; Krechetov, Sergei P.; Veselov, Mark S.; Sviridenkova, Natalia V.; Savchenko, Alexander G.; Klyachko, Natalya L.; Golovin, Yury I.; Chufarova, Nina V.; Beloglazkina, Elena K.; Majouga, Alexander G.

    2015-11-01

    Fe3O4@Au core/shell nanoparticles have unique magnetic and optical properties. These nanoparticles are used for biomedical applications, such as magnetic resonance imaging, photothermal therapy, controlled drug delivery, protein separation, biosensors, DNA detection, and immunosensors. In this review, recent methods for the synthesis of core/shell nanoparticles are discussed. We divided all of the synthetic methods in two groups: methods of synthesis of bi-layer structures and methods of synthesis of multilayer composite structures. The latter methods have a layer of "glue" material between the core and the shell.

  12. Controllable synthesis of Cu-Ni core-shell nanoparticles and nanowires with tunable magnetic properties.

    PubMed

    Guo, Huizhang; Jin, Jiarui; Chen, Yuanzhi; Liu, Xiang; Zeng, Deqian; Wang, Laisen; Peng, Dong-Liang

    2016-05-25

    Cu seeds were used to direct the epitaxial growth of Ni shell to form Cu-Ni core-shell cubes, tetrahexahedrons and nanowires. The controllable epitaxial growth of Ni shells on Cu cores provided selectively exposed surfaces and morphologies as well as tunable magnetic properties. PMID:27147395

  13. Core-shell structured TiO2@polydopamine for highly active visible-light photocatalysis.

    PubMed

    Mao, Wen-Xin; Lin, Xi-Jie; Zhang, Wei; Chi, Zi-Xiang; Lyu, Rong-Wen; Cao, An-Min; Wan, Li-Jun

    2016-06-01

    This communication reports that the TiO2@polydopamine nanocomposite with a core-shell structure could be a highly active photocatalyst working under visible light. A very thin layer of polydopamine at around 1 nm was found to be critical for the degradation of Rhodamine B. PMID:27165843

  14. Synthesis and characterization of core-shell acrylate based latex and study of its reactive blends.

    PubMed

    Liu, Xiang; Fan, Xiao-Dong; Tang, Min-Feng; Nie, Ying

    2008-03-01

    Techniques in resin blending are simple and efficient method for improving the properties of polymers, and have been used widely in polymer modification field. However, polymer latex blends such as the combination of latexes, especially the latexes with water-soluble polymers, were rarely reported. Here, we report a core-shell composite latex synthesized using methyl methacrylate (MMA), butyl acrylate (BA), 2-ethylhexyl acrylate (EHA) and glycidyl methacrylate (GMA) as monomers and ammonium persulfate and sodium bisulfite redox system as the initiator. Two stages seeded semi-continuous emulsion polymerization were employed for constructing a core-shell structure with P(MMA-co-BA) component as the core and P(EHA-co-GMA) component as the shell. Results of Transmission Electron Microscopy (TEM) and Dynamics Light Scattering (DLS) tests confirmed that the particles obtained are indeed possessing a desired core-shell structural character. Stable reactive latex blends were prepared by adding the latex with waterborne melamine-formaldehyde resin (MF) or urea-formaldehyde resin (UF). It was found that the glass transition temperature, the mechanical strength and the hygroscopic property of films cast from the latex blends present marked enhancements under higher thermal treatment temperature. It was revealed that the physical properties of chemically reactive latexes with core-shell structure could be altered via the change of crosslinking density both from the addition of crosslinkers and the thermal treatment. PMID:19325753

  15. Enhanced functionalization of Mn2O3@SiO2 core-shell nanostructures

    NASA Astrophysics Data System (ADS)

    Vaidya, Sonalika; Thaplyal, Pallavi; Ganguli, Ashok Kumar

    2011-12-01

    Core-shell nanostructures of Mn2O3@SiO2, Mn2O3@amino-functionalized silica, Mn2O3@vinyl-functionalized silica, and Mn2O3@allyl-functionalized silica were synthesized using the hydrolysis of the respective organosilane precursor over Mn2O3 nanoparticles dispersed using colloidal solutions of Tergitol and cyclohexane. The synthetic methodology used is an improvement over the commonly used post-grafting or co-condensation method as it ensures a high density of functional groups over the core-shell nanostructures. The high density of functional groups can be useful in immobilization of biomolecules and drugs and thus can be used in targeted drug delivery. The high density of functional groups can be used for extraction of elements present in trace amounts. These functionalized core-shell nanostructures were characterized using TEM, IR, and zeta potential studies. The zeta potential study shows that the hydrolysis of organosilane to form the shell results in more number of functional groups on it as compared to the shell formed using post-grafting method. The amino-functionalized core-shell nanostructures were used for the immobilization of glucose and L -methionine and were characterized by zeta potential studies.

  16. Synthesis and Characterization of Core-Shell Acrylate Based Latex and Study of Its Reactive Blends

    PubMed Central

    Liu, Xiang; Fan, Xiao-Dong; Tang, Min-Feng; Nie, Ying

    2008-01-01

    Techniques in resin blending are simple and efficient method for improving the properties of polymers, and have been used widely in polymer modification field. However, polymer latex blends such as the combination of latexes, especially the latexes with water-soluble polymers, were rarely reported. Here, we report a core-shell composite latex synthesized using methyl methacrylate (MMA), butyl acrylate (BA), 2-ethylhexyl acrylate (EHA) and glycidyl methacrylate (GMA) as monomers and ammonium persulfate and sodium bisulfite redox system as the initiator. Two stages seeded semi-continuous emulsion polymerization were employed for constructing a core-shell structure with P(MMA-co-BA) component as the core and P(EHA-co-GMA) component as the shell. Results of Transmission Electron Microscopy (TEM) and Dynamics Light Scattering (DLS) tests confirmed that the particles obtained are indeed possessing a desired core-shell structural character. Stable reactive latex blends were prepared by adding the latex with waterborne melamine-formaldehyde resin (MF) or urea-formaldehyde resin (UF). It was found that the glass transition temperature, the mechanical strength and the hygroscopic property of films cast from the latex blends present marked enhancements under higher thermal treatment temperature. It was revealed that the physical properties of chemically reactive latexes with core-shell structure could be altered via the change of crosslinking density both from the addition of crosslinkers and the thermal treatment. PMID:19325753

  17. In-situ Liquid Phase Epitaxy: Another Strategy to Synthesize Heterostructured Core-shell Composites

    NASA Astrophysics Data System (ADS)

    Wen, Zhongsheng; Wang, Guanqin

    2016-04-01

    Core-shell Nb2O5/TiO2 composite with hierarchical heterostructure is successfully synthesized In-situ by a facile template-free and acid-free solvothermal method based on the mechanism of liquid phase epitaxy. The chemical circumstance change induced by the alcoholysis of NbCl5 is utilized tactically to trigger core-shell assembling In-situ. The tentative mechanism for the self-assembling of core-shell structure and hierarchical structure is explored. The microstructure and morphology changes during synthesis process are investigated systematically by using X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and transmission electron microscopy. The dramatic alcoholysis of NbCl5 has been demonstrated to be the fundamental factor for the formation of the spherical core, which changes the acid circumstance of the solution and induces the co-precipitation of TiO2. The homogeneous co-existence of Nb2O5/TiO2 in the core and the co-existence of Nb/Ti ions in the reaction solution facilitate the In-situ nucleation and epitaxial growth of the crystalline shell with the same composition as the core. In-situ liquid phase epitaxy can offer a different strategy for the core-shell assembling for oxide materials.

  18. In-situ Liquid Phase Epitaxy: Another Strategy to Synthesize Heterostructured Core-shell Composites

    PubMed Central

    Wen, Zhongsheng; Wang, Guanqin

    2016-01-01

    Core-shell Nb2O5/TiO2 composite with hierarchical heterostructure is successfully synthesized In-situ by a facile template-free and acid-free solvothermal method based on the mechanism of liquid phase epitaxy. The chemical circumstance change induced by the alcoholysis of NbCl5 is utilized tactically to trigger core-shell assembling In-situ. The tentative mechanism for the self-assembling of core-shell structure and hierarchical structure is explored. The microstructure and morphology changes during synthesis process are investigated systematically by using X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and transmission electron microscopy. The dramatic alcoholysis of NbCl5 has been demonstrated to be the fundamental factor for the formation of the spherical core, which changes the acid circumstance of the solution and induces the co-precipitation of TiO2. The homogeneous co-existence of Nb2O5/TiO2 in the core and the co-existence of Nb/Ti ions in the reaction solution facilitate the In-situ nucleation and epitaxial growth of the crystalline shell with the same composition as the core. In-situ liquid phase epitaxy can offer a different strategy for the core-shell assembling for oxide materials. PMID:27121200

  19. In-situ Liquid Phase Epitaxy: Another Strategy to Synthesize Heterostructured Core-shell Composites.

    PubMed

    Wen, Zhongsheng; Wang, Guanqin

    2016-01-01

    Core-shell Nb2O5/TiO2 composite with hierarchical heterostructure is successfully synthesized In-situ by a facile template-free and acid-free solvothermal method based on the mechanism of liquid phase epitaxy. The chemical circumstance change induced by the alcoholysis of NbCl5 is utilized tactically to trigger core-shell assembling In-situ. The tentative mechanism for the self-assembling of core-shell structure and hierarchical structure is explored. The microstructure and morphology changes during synthesis process are investigated systematically by using X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy and transmission electron microscopy. The dramatic alcoholysis of NbCl5 has been demonstrated to be the fundamental factor for the formation of the spherical core, which changes the acid circumstance of the solution and induces the co-precipitation of TiO2. The homogeneous co-existence of Nb2O5/TiO2 in the core and the co-existence of Nb/Ti ions in the reaction solution facilitate the In-situ nucleation and epitaxial growth of the crystalline shell with the same composition as the core. In-situ liquid phase epitaxy can offer a different strategy for the core-shell assembling for oxide materials. PMID:27121200

  20. Liquid immiscibility and core-shell morphology formation in ternary Al–Bi–Sn alloys

    SciTech Connect

    Dai, R.; Zhang, J.F.; Zhang, S.G. Li, J.G.

    2013-07-15

    The effects of composition on liquid immiscibility, macroscopic morphology, microstructure and phase transformation in ternary Al–Bi–Sn alloys were investigated. Three types of morphology, the core-shell type, the stochastic droplet type and uniform dispersion type, of Al–Bi–Sn particles prepared by a jet breakup process were distinguished, and the relationships between which were discussed. The phase transformation behaviors of the Al–Bi–Sn alloys were studied by thermal analysis, in agreement with the microstructural observation and microanalysis. The liquid immiscibility and formation of the core-shell morphology in Al–Bi–Sn alloys are easily achieved when the composition lies in the liquid miscibility gap. The particles exhibit a high melting point Al-rich core with a low melting point Sn–Bi-rich solder shell, showing promise for application as high-density electronic packaging materials. - Highlights: • The liquid demixing, morphology and microstructure in Al–Bi–Sn alloys were studied. • Three types of morphology were classified and discussed. • The conditions for formation of the core-shell morphology were obtained. • The phase transition behaviors agree with the microstructure characterization. • The Al/Sn–Bi core-shell particles show promise for use in electronic packaging.

  1. Photo-physical properties enhancement of bare and core-shell quantum dots

    NASA Astrophysics Data System (ADS)

    Mumin, Md Abdul; Akhter, Kazi Farida; Charpentier, Paul A.

    2014-03-01

    Semiconductor nanocrystals (NCs) (also known as quantum dots, QDs) have attracted immense attention for their size-tunable optical properties that makes them impressive candidates for solar cells, light emitting devices, lasers, as well as biomedical imaging. However monodispersity, high and consistent photoluminescence, photostability, and biocompatibility are still major challenges. This work focuses on optimizing the photophysical properties and biocompatibility of QDs by forming core-shell nanostructures and their encapsulation by a carrier. Highly luminescent CdS and CdS-ZnS core-shell QDs with 5 nm sizes were synthesized using a facile approach based on pyrolysis of the single molecule precursors. After capping the CdS QDs with a thin layer of ZnS to reduce toxicity, the photoluminescence and photostability of the core-shell QDs was significantly enhanced. To make both the bare and core/shell structure QDs more resistant against photochemical reactions, a mesoporous silica layer was grown on the QDs through a reverse microemulsion technique based on hydrophobic interaction. This encapsulation enhanced the quantum yield and photostability compared to the bare QDs by providing much stronger resistance to oxidation and Oswald ripening of QDs. Encapsulation also improved biocompatibility of QDs that was evaluated with human umbilical vein endothelial cell lines (HUVEC).

  2. Copper nanowire-graphene core-shell nanostructure for highly stable transparent conducting electrodes.

    PubMed

    Ahn, Yumi; Jeong, Youngjun; Lee, Donghwa; Lee, Youngu

    2015-03-24

    A copper nanowire-graphene (CuNW-G) core-shell nanostructure was successfully synthesized using a low-temperature plasma-enhanced chemical vapor deposition process at temperatures as low as 400 °C for the first time. The CuNW-G core-shell nanostructure was systematically characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, Raman, and X-ray photoelectron spectroscopy measurements. A transparent conducting electrode (TCE) based on the CuNW-G core-shell nanostructure exhibited excellent optical and electrical properties compared to a conventional indium tin oxide TCE. Moreover, it showed remarkable thermal oxidation and chemical stability because of the tight encapsulation of the CuNW with gas-impermeable graphene shells. The potential suitability of CuNW-G TCE was demonstrated by fabricating bulk heterojunction polymer solar cells. We anticipate that the CuNW-G core-shell nanostructure can be used as an alternative to conventional TCE materials for emerging optoelectronic devices such as flexible solar cells, displays, and touch panels. PMID:25712446

  3. A new class of PANI-Ag core-shell nanorods with sensing dimensions.

    PubMed

    Shukla, Vineet K; Yadav, Poonam; Yadav, Raghvendra S; Mishra, Priya; Pandey, Avinash C

    2012-07-01

    A single-step, cost-effective and eco-safe synthesis of a new class of homogeneous silver-polyaniline (PANI-Ag) core-shell nanorods is carried out via mild photolysis by ultraviolet radiation from sunlight (SUN UV-radiation). X-ray diffraction (XRD) of these core-shell nanorods gives two additional peaks from PANI centered at 2θ = 20.5° and 24. 9°. A validation of the core-shell structural information is given by transmission electron spectroscopy (TEM) whereas the tubular shape morphology is determined by scanning electron microscopy (SEM). UV-Vis. absorption shows a strong blue-shift along with photoluminescence emission. Fourier transform-infrared spectroscopy (FT-IR) and energy dispersive X-ray spectroscopy (EDX) also support the core-shell formation. Thermogravimetric analysis (TGA) shows good thermal stability and allows excellent detection of hydrogen peroxide and hydrazine. The cyclic voltammetry (CV) results show excellent electro-activation, indicating its promising potential in sensing of clinical and environmental analytes. PMID:22669315

  4. Poly(Glycerol sebacate)/gelatin core/shell fibrous structure for regeneration of myocardial infarction.

    PubMed

    Ravichandran, Rajeswari; Venugopal, Jayarama Reddy; Sundarrajan, Subramanian; Mukherjee, Shayanti; Ramakrishna, Seeram

    2011-05-01

    Heart failure remains the leading cause of death in many industrialized nations owing to the inability of the myocardial tissue to regenerate. The main objective of this work was to develop a cardiac patch that is biocompatible and matches the mechanical properties of the heart muscle for myocardial infarction. The present study was to fabricate poly (glycerol sebacate)/gelatin (PGS/gelatin) core/shell fibers and gelatin fibers alone by electrospinning for cardiac tissue engineering. PGS/gelatin core/shell fibers, PGS used as a core polymer to impart the mechanical properties and gelatin as a shell material to achieve favorable cell adhesion and proliferation. These core/shell fibers were characterized by scanning electron microscopy, contact angle, Fourier transform infrared spectroscopy, and tensile testing. The cell-scaffold interactions were analyzed by cell proliferation, confocal analysis for the expression of marker proteins like actinin, troponin-T, and platelet endothelial cell adhesion molecule, and scanning electron microscopy to analyze cell morphology. Dual immunofluorescent staining was performed to further confirm the cardiogenic differentiation of mesenchymal stem cells by employing mesenchymal stem cell-specific marker protein CD 105 and cardiac-specific marker protein actinin. The results observed that PGS/gelatin core/shell fibers have good potential biocompatibility and mechanical properties for fabricating nanofibrous cardiac patch and would be a prognosticating device for the restoration of myocardium. PMID:21247338

  5. Core-shell TiO2@ZnO nanorods for efficient ultraviolet photodetection.

    PubMed

    Panigrahi, Shrabani; Basak, Durga

    2011-05-01

    Core-shell TiO(2)@ZnO nanorods (NRs) have been fabricated by a simple two step method: growth of ZnO NRs' array by an aqueous chemical technique and then coating of the NRs with a solution of titanium isopropoxide [Ti(OC(3)H(7))(4)] followed by a heating step to form the shell. The core-shell nanocomposites are composed of single-crystalline ZnO NRs, coated with a thin TiO(2) shell layer obtained by varying the number of coatings (one, three and five times). The ultraviolet (UV) emission intensity of the nanocomposite is largely quenched due to an efficient electron-hole separation reducing the band-to-band recombinations. The UV photoconductivity of the core-shell structure with three times TiO(2) coating has been largely enhanced due to photoelectron transfer between the core and the shell. The UV photosensitivity of the nanocomposite becomes four times larger while the photocurrent decay during steady UV illumination has been decreased almost by 7 times compared to the as-grown ZnO NRs indicating high efficiency of these core-shell structures as UV sensors. PMID:21483939

  6. Core-shell TiO2@ZnO nanorods for efficient ultraviolet photodetection

    NASA Astrophysics Data System (ADS)

    Panigrahi, Shrabani; Basak, Durga

    2011-05-01

    Core-shell TiO2@ZnO nanorods (NRs) have been fabricated by a simple two step method: growth of ZnO NRs' array by an aqueous chemical technique and then coating of the NRs with a solution of titanium isopropoxide [Ti(OC3H7)4] followed by a heating step to form the shell. The core-shell nanocomposites are composed of single-crystalline ZnO NRs, coated with a thin TiO2 shell layer obtained by varying the number of coatings (one, three and five times). The ultraviolet (UV) emission intensity of the nanocomposite is largely quenched due to an efficient electron-hole separation reducing the band-to-band recombinations. The UV photoconductivity of the core-shell structure with three times TiO2 coating has been largely enhanced due to photoelectron transfer between the core and the shell. The UV photosensitivity of the nanocomposite becomes four times larger while the photocurrent decay during steady UV illumination has been decreased almost by 7 times compared to the as-grown ZnO NRs indicating high efficiency of these core-shell structures as UV sensors.

  7. Comparison of methanol and ethylene glycol oxidation by alloy and Core-Shell platinum based catalysts

    NASA Astrophysics Data System (ADS)

    Kaplan, D.; Burstein, L.; Rosenberg, Yu.; Peled, E.

    2011-10-01

    Two Core-Shell, RuCore-PtShell and IrNiCore-PtRuShell, XC72-supported catalyst were synthesized in a two-step deposition process with NaBH4 as reducing agent. The structure and composition of the Core-Shell catalysts were determined by EDS, XPS and XRD. Electrochemical characterization was performed with the use of cyclic voltammetry. Methanol and ethylene glycol oxidation activities of the Core-Shell catalysts (in terms of surface and mass activities) were studied at 80 °C and compared to those of a commercial Pt-Ru alloy catalyst. The surface activity of the alloy based catalyst, in the case of methanol oxidation, was found to be superior as a result of optimized surface Pt:Ru composition. However, the mass activity of the PtRu/IrNi/XC72 was higher than that of the alloy based catalyst by ∼50%. Regarding ethylene glycol oxidation, while the surface activity of the alloy based catalyst was slightly higher than that of the Pt/Ru/XC72 catalyst, the latter showed ∼66% higher activities in terms of A g-1 of Pt. These results show the potential of Core-Shell catalysts for reducing the cost of catalysts for DMFC and DEGFC.

  8. Novel ZnO/Fe₂O₃ Core-Shell Nanowires for Photoelectrochemical Water Splitting.

    PubMed

    Hsu, Yu-Kuei; Chen, Ying-Chu; Lin, Yan-Gu

    2015-07-01

    A facile and simple fabrication of Fe2O3 as a shell layer on the surface of ZnO nanowires (NW) as a core-shell nanoelectrode is applied for the photoelectrochemical (PEC) splitting of water. An ZnO NW array of core diameter ∼80 nm was grown on a fluorine-doped tin-oxide (FTO) substrate with a hydrothermal method; subsequent deposition and annealing achieved a shell structure of the Fe2O3 layer of thickness a few nm. Fe2O3 in the α phase and ZnO in the wurtzite phase were identified as the structures of the shell and core, respectively, through analysis with X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. The ZnO/Fe2O3 core-shell NW showed an excellent PEC response to the oxidation of water, and also benefited from a negative shift of onset potential because of an n/n heterojunction structure. A detailed energy diagram of the ZnO/Fe2O3 core-shell NW was investigated with a Mott-Schottky analysis. This novel core-shell nanostructure can hence not only exhibit a great potential for the solar generation of hydrogen, but also offer a blueprint for the future design of photocatalysts. PMID:26053274

  9. Platinum-coated non-noble metal-noble metal core-shell electrocatalysts

    DOEpatents

    Adzic, Radoslav; Zhang, Junliang; Mo, Yibo; Vukmirovic, Miomir

    2015-04-14

    Core-shell particles encapsulated by a thin film of a catalytically active metal are described. The particles are preferably nanoparticles comprising a non-noble core with a noble metal shell which preferably do not include Pt. The non-noble metal-noble metal core-shell nanoparticles are encapsulated by a catalytically active metal which is preferably Pt. The core-shell nanoparticles are preferably formed by prolonged elevated-temperature annealing of nanoparticle alloys in an inert environment. This causes the noble metal component to surface segregate and form an atomically thin shell. The Pt overlayer is formed by a process involving the underpotential deposition of a monolayer of a non-noble metal followed by immersion in a solution comprising a Pt salt. A thin Pt layer forms via the galvanic displacement of non-noble surface atoms by more noble Pt atoms in the salt. The overall process is a robust and cost-efficient method for forming Pt-coated non-noble metal-noble metal core-shell nanoparticles.

  10. Controlled Synthesis of Pd/Pt Core Shell Nanoparticles Using Area-selective Atomic Layer Deposition

    PubMed Central

    Cao, Kun; Zhu, Qianqian; Shan, Bin; Chen, Rong

    2015-01-01

    We report an atomic scale controllable synthesis of Pd/Pt core shell nanoparticles (NPs) via area-selective atomic layer deposition (ALD) on a modified surface. The method involves utilizing octadecyltrichlorosilane (ODTS) self-assembled monolayers (SAMs) to modify the surface. Take the usage of pinholes on SAMs as active sites for the initial core nucleation, and subsequent selective deposition of the second metal as the shell layer. Since new nucleation sites can be effectively blocked by surface ODTS SAMs in the second deposition stage, we demonstrate the successful growth of Pd/Pt and Pt/Pd NPs with uniform core shell structures and narrow size distribution. The size, shell thickness and composition of the NPs can be controlled precisely by varying the ALD cycles. Such core shell structures can be realized by using regular ALD recipes without special adjustment. This SAMs assisted area-selective ALD method of core shell structure fabrication greatly expands the applicability of ALD in fabricating novel structures and can be readily applied to the growth of NPs with other compositions. PMID:25683469

  11. Fluorescent core-shell silica nanoparticles: an alternative radiative materials platform

    NASA Astrophysics Data System (ADS)

    Herz, Erik; Burns, Andrew; Lee, Stephanie; Sengupta, Prabuddha; Bonner, Daniel; Ow, Hooisweng; Liddell, Chekesha; Baird, Barbara; Wiesner, Ulrich

    2006-02-01

    We report on monodisperse fluorescent core-shell silica nanoparticles (C dots) with enhanced brightness and photostability as compared to parent free dye in aqueous solution. Dots containing either tetramethylrhodamine or 7-nitrobenz-2-oxa-1,3-diazole dyes with diameters ranging from tens of nanometers to microns are discussed. The benefits of the core-shell architecture are described in terms of enhanced fluorescent yield of the fluorophores in the quasi-solid-state environment within the particle as compared with parent free dye in water. Several applications of these particles in the fields of photonics and the life sciences are discussed. Specifically, fluorescent core-shell silica nanoparticles are investigated as an active medium for photonic building blocks assembled on zinc sulfide-based seed particles. Initial assembly results for these composite raspberry structures are shown. Finally, applications in the life sciences are explored, including targeting of specific antibody receptors using these single-emission nanoparticles. We expand on single-emission core-shell architecture to incorporate environmentally-sensitive fluorophores to create quantitative ratiometric nanoscale sensors capable of interrogating chemical concentrations on the sub-cellular to molecular levels and demonstrate initial results of intracellular pH imaging. The concept of a single particle laboratory (SPL) is introduced as an active investigator of its environment.

  12. Nanostructured core-shell Ni deposition on SiC particles by alkaline electroless coating

    NASA Astrophysics Data System (ADS)

    Uysal, M.; Karslioğlu, R.; Alp, A.; Akbulut, H.

    2011-10-01

    In this study, core-shell nanostructured nickel formation on silicon carbide (SiC) ceramic powders was achieved through the electroless deposition method using alkaline solutions. To produce a nano core-shell Ni deposition on the SiC surfaces, process parameters such as pH values, the type of reducer material, deposition temperature, stirring rate and activation procedure among others were determined. Full coverage of core-shell nickel structures on SiC surfaces was achieved with a grain size of between 100 and 300 nm, which was approximately the same deposition thickness on the SiC surfaces. The surface morphology of the coated SiC particles showed a homogenous distribution of nanostructured nickel grains characterized by scanning electron microscopy and X-ray diffraction techniques. The nanostructures of the crystalline Ni coatings were observed to be attractive for achieving both good bonding and dense structure. The thin core shell-structure of Ni on the SiC surfaces was assessed as a beneficial reinforcement for possible metal matrix composite manufacturing.

  13. In Situ Synthesis of Catalytic Active Au Nanoparticles onto Gibbsite-Polydopamine Core-Shell Nanoplates.

    PubMed

    Cao, Jie; Mei, Shilin; Jia, He; Ott, Andreas; Ballauff, Matthias; Lu, Yan

    2015-09-01

    We report a facile method to synthesize anisotropic platelike gibbsite-polymer core-shell particles. Dopamine is self-polymerized on the surface of gibbsite nanoplates and forms a homogeneous layer on it. Transmission electron microscopy characterization of the resulting latexes demonstrates the formation of well-defined platelike core-shell particles. Reaction time and ultrasonification are found to be important factors to control the thickness of the polymer shell and avoid aggregation. Good control over the platelike morphology and 100% encapsulation efficiency have been achieved via this novel route. The resulting well-defined gibbsite-polydamine (G-PDA) core-shell nanoplates show excellent colloidal stability and can form opal-like columnar crystal with iridescent Bragg reflection after modest centrifugation. In addition, G-PDA core-shell nanoplates can serve both as reductant and stabilizer for the generation of Au nanoparticles (NPs) in situ. Au NPs with tunable size have been formed on the G-PDA particle surface, which show efficient catalytic activity for the reduction of 4-nitrophenol and Rhodamine B (RhB) in the presence of borohydride. Such nanocatalysts can be easily deposited on silicon substrate by spin-coating due to the large contact area of platelike G-PDA particles and the strong adhesive behavior of the PDA layer. The substrate-deposited nanocatalyst can be easily recycled which show excellent reusability for the reduction of RhB. PMID:26266398

  14. Controlled Release of Ciprofloxacin from Core-Shell Nanofibers with Monolithic or Blended Core.

    PubMed

    Zupančič, Špela; Sinha-Ray, Sumit; Sinha-Ray, Suman; Kristl, Julijana; Yarin, Alexander L

    2016-04-01

    Sustained controlled drug release is one of the prominent contributions for more successful treatment outcomes in the case of several diseases. However, the incorporation of hydrophilic drugs into nanofibers, a promising novel delivery system, and achieving a long-term sustained release still pose a challenging task. In this work we demonstrated a robust method of avoiding burst release of drugs and achieving a sustained drug release from 2 to 4 weeks using core-shell nanofibers with poly(methyl methacrylate) (PMMA) shell and monolithic poly(vinyl alcohol) (PVA) core or a novel type of core-shell nanofibers with blended (PVA and PMMA) core loaded with ciprofloxacin hydrochloride (CIP). It is also shown that, for core-shell nanofibers with monolithic core, drug release can be manipulated by varying flow rate of the core PVA solution, whereas for core-shell nanofibers with blended core, drug release can be manipulated by varying the ratios between PMMA and PVA in the core. During coaxial electrospinning, when the solvent from the core evaporates in concert with the solvent from the shell, the interconnected pores spanning the core and the shell are formed. The release process is found to be desorption-limited and agrees with the two-stage desorption model. Ciprofloxacin-loaded nanofiber mats developed in the present work could be potentially used as local drug delivery systems for treatment of several medical conditions, including periodontal disease and skin, bone, and joint infections. PMID:26950163

  15. Core-shell potassium niobate nanowires for enhanced nonlinear optical effects.

    PubMed

    Richter, J; Steinbrück, A; Zilk, M; Sergeyev, A; Pertsch, T; Tünnermann, A; Grange, R

    2014-05-21

    We demonstrate the synthesis as well as the optical characterization of core-shell nanowires. The wires consist of a potassium niobate (KNbO3) core and a gold shell. The nonlinear optical properties of the core are combined with the plasmonic resonance of the shell and offer an enhanced optical signal in the near infrared spectral range. We compare two different functionalization schemes of the core material prior to the shell growth process: silanization and polyelectrolyte. We show that the latter leads to a smoother and complete core-shell nanostructure and an easier-to-use synthesis process. A Mie-theory based theoretical approach is presented to model the enhanced second-harmonic generated (SHG) signal of the core-shell wires, illustrating the influence of the fabrication-induced varying geometrical factors of wire radius and shell thickness. A spectroscopic measurement on a core-shell nanowire shows a strong localized surface plasmon resonance close to 900 nm, which matches with the SHG resonance obtained from nonlinear optical experiments with the same nanowire. According to the simulation, this corresponds to a wire radius of 35 nm and a shell thickness of 7.5 nm. By comparing SHG signals measured from an uncoated nanowire and the coated one, we obtain a 250 times enhancement factor. This is less than the calculated enhancement, which considers a cylindrical nanowire with a perfectly smooth shell. Thus, we explain this discrepancy mainly with the roughness of the synthesized gold shell. PMID:24675780

  16. Hydrothermal synthesis of core-shell TiO2 to enhance the photocatalytic hydrogen evolution

    NASA Astrophysics Data System (ADS)

    Jiang, Jinghui; Zhou, Han; Zhang, Fan; Fan, Tongxiang; Zhang, Di

    2016-04-01

    A hydrothermal approach was designed to synthesize core-shell TiO2 with interior cavity by making sodium dodecyl sulfonate (SDS) as the surfactant and the mixture of water and ethanol as the solvent. The control experiment of solvent reveals ethanol and water are responsible for the formation of sphere and interior cavity, respectively. Besides, SDS can assist the growth of core-shell structure, and the sizes of sphere and interior cavity can be tuned by regulating the reaction time or temperature. UV-vis absorption proves core-shell structure with interior cavity can increase the absorption of incident light to enhance the optical activity of final product. The calculated bandgap and photoluminescence (PL) analyses reveal the coexistence of rutile in final product can optimize the bandgap to 3.03 eV and delay the charge recombination. As a result, an effective photocatalytic hydrogen evolution under full spectrum irradiation can be harvested by the as-synthesized core-shell spheres to reach a quantum yield, approximately 9.57% at 340 nm wavelength.

  17. Role of the interfaces in multiple networked one-dimensional core-shell nanostructured gas sensors.

    PubMed

    Park, Sunghoon; Ko, Hyunsung; Kim, Soohyun; Lee, Chongmu

    2014-06-25

    This study examined the gas sensing mechanism of multiple networked core-shell nanowire sensors. The ethanol gas sensing properties of In2O3/ZnO core-shell nanowires synthesized by the thermal evaporation of indium powder in an oxidizing atmosphere followed by the atomic layer deposition of ZnO were examined as an example. The pristine In2O3 nanowires and In2O3-core/ZnO-shell nanowires exhibited responses of ∼30% and ∼196%, respectively, to 1000 ppm ethanol at 300 °C. The response of the core-shell nanostructures to ethanol also showed a strong dependence on the shell layer width. The strongest response to ethanol was obtained with a shell layer thickness of ∼44 nm corresponding to 2λD, where λD is the Debye length of ZnO. The enhanced sensing properties of the core-shell nanowires toward ethanol can be explained based on the potential barrier-controlled carrier transport model combined with the surface depletion model; the former is predominant over the latter. PMID:24850501

  18. Facile preparation of hybrid core-shell nanorods for photothermal and radiation combined therapy

    NASA Astrophysics Data System (ADS)

    Deng, Yaoyao; Li, Erdong; Cheng, Xiaju; Zhu, Jing; Lu, Shuanglong; Ge, Cuicui; Gu, Hongwei; Pan, Yue

    2016-02-01

    The hybrid platinum@iron oxide core-shell nanorods with high biocompatibility were synthesized and applied for combined therapy. These hybrid nanorods exhibit a good photothermal effect on cancer cells upon irradiation with a NIR laser. Furthermore, due to the presence of a high atomic number element (platinum core), the hybrid nanorods show a synergistic effect between photothermal and radiation therapy. Therefore, the as-prepared core-shell nanorods could play an important role in facilitating synergistic therapy between photothermal and radiation therapy to achieve better therapeutic efficacy.The hybrid platinum@iron oxide core-shell nanorods with high biocompatibility were synthesized and applied for combined therapy. These hybrid nanorods exhibit a good photothermal effect on cancer cells upon irradiation with a NIR laser. Furthermore, due to the presence of a high atomic number element (platinum core), the hybrid nanorods show a synergistic effect between photothermal and radiation therapy. Therefore, the as-prepared core-shell nanorods could play an important role in facilitating synergistic therapy between photothermal and radiation therapy to achieve better therapeutic efficacy. Electronic supplementary information (ESI) available: Details of general experimental procedures. See DOI: 10.1039/c5nr09102k

  19. Photo-physical properties enhancement of bare and core-shell quantum dots

    SciTech Connect

    Mumin, Md Abdul Akhter, Kazi Farida Charpentier, Paul A.

    2014-03-31

    Semiconductor nanocrystals (NCs) (also known as quantum dots, QDs) have attracted immense attention for their size-tunable optical properties that makes them impressive candidates for solar cells, light emitting devices, lasers, as well as biomedical imaging. However monodispersity, high and consistent photoluminescence, photostability, and biocompatibility are still major challenges. This work focuses on optimizing the photophysical properties and biocompatibility of QDs by forming core-shell nanostructures and their encapsulation by a carrier. Highly luminescent CdS and CdS-ZnS core-shell QDs with 5 nm sizes were synthesized using a facile approach based on pyrolysis of the single molecule precursors. After capping the CdS QDs with a thin layer of ZnS to reduce toxicity, the photoluminescence and photostability of the core-shell QDs was significantly enhanced. To make both the bare and core/shell structure QDs more resistant against photochemical reactions, a mesoporous silica layer was grown on the QDs through a reverse microemulsion technique based on hydrophobic interaction. This encapsulation enhanced the quantum yield and photostability compared to the bare QDs by providing much stronger resistance to oxidation and Oswald ripening of QDs. Encapsulation also improved biocompatibility of QDs that was evaluated with human umbilical vein endothelial cell lines (HUVEC)

  20. Piezoelectric constants for ZnO calculated using classical polarizable core-shell potentials

    NASA Astrophysics Data System (ADS)

    Dai, Shuangxing; Dunn, Martin L.; Park, Harold S.

    2010-11-01

    We demonstrate the feasibility of using classical atomistic simulations, i.e. molecular dynamics and molecular statics, to study the piezoelectric properties of ZnO using core-shell interatomic potentials. We accomplish this by reporting the piezoelectric constants for ZnO as calculated using two different classical interatomic core-shell potentials: that originally proposed by Binks and Grimes (1994 Solid State Commun. 89 921-4), and that proposed by Nyberg et al (1996 J. Phys. Chem. 100 9054-63). We demonstrate that the classical core-shell potentials are able to qualitatively reproduce the piezoelectric constants as compared to benchmark ab initio calculations. We further demonstrate that while the presence of the shell is required to capture the electron polarization effects that control the clamped ion part of the piezoelectric constant, the major shortcoming of the classical potentials is a significant underprediction of the clamped ion term as compared to previous ab initio results. However, the present results suggest that overall, these classical core-shell potentials are sufficiently accurate to be utilized for large scale atomistic simulations of the piezoelectric response of ZnO nanostructures.

  1. A facile route to synthesize core/shell structured carbon/magnetic nanoparticles hybrid and their magnetic properties

    SciTech Connect

    Qi, Xiaosi; Xu, Jianle; Zhong, Wei; Du, Youwei

    2015-07-15

    Graphical abstract: Controllable synthesis of core/shell structured carbon/magnetic nanoparticles hybrid and their tunable magnetic properties. - Highlights: • The paper reports a simple route for core/shell structured carbon/magnetic nanoparticles hybrid. • By controlling the temperature, Fe{sub 3}O{sub 4}@CNCs, Fe@HCNTs and Fe@LCNTs were produced selectively. • The magnetic properties of the obtained core/shell structured hybrid could be tuned effectively. - Abstract: By controlling the pyrolysis temperature, core/shell structured Fe{sub 3}O{sub 4}/carbon nanocages, Fe/helical carbon nanotubes and Fe/low helicity of carbon nanotubes could be synthesized selectively over Fe{sub 2}O{sub 3} nanotubes generated by a hydrothermal method. The transmission electron microscopic and scanning electron microscopic investigations revealed that the efficiency of generating core/shell structured hybrid was high, exceeding 90%. Because of the magnetic nanoparticles tightly wrapped in graphitic layers, the obtained core/shell structured hybrids showed high stability and good magnetic properties. And the magnetic properties of the obtained core/shell structured hybrid could be tuned by the decomposition temperature and time. Therefore, a simple, inexpensive and environment-benign route was proposed to produce magnetism-tunable core/shell structured hybrid in large quantities.

  2. Synthesis and properties MFe2O4 (M = Fe, Co) nanoparticles and core-shell structures

    NASA Astrophysics Data System (ADS)

    Yelenich, O. V.; Solopan, S. O.; Greneche, J. M.; Belous, A. G.

    2015-08-01

    Individual Fe3-xO4 and CoFe2O4 nanoparticles, as well as Fe3-xO4/CoFe2O4 core/shell structures were synthesized by the method of co-precipitation from diethylene glycol solutions. Core/shell structure were synthesized with CoFe2O4-shell thickness of 1.0, 2.5 and 3.5 nm. X-ray diffraction patterns of individual nanoparticles and core/shell are similar and indicate that all synthesized samples have a cubic spinel structure. Compares Mössbauer studies of CoFe2O4, Fe3-xO4 nanoparticles indicate superparamagnetic properties at 300 K. It was shown that individual magnetite nanoparticles are transformed into maghemite through oxidation during the synthesis procedure, wherein the smallest nanoparticles are completely oxidized while a magnetite core does occur in the case of the largest nanoparticles. The Mössbauer spectra of core/shell nanoparticles with increasing CoFe2O4-shell thickness show a gradual decrease in the relative intensity of the quadrupole doublet and significant decrease of the mean isomer shift value at both RT and 77 K indicating a decrease of the superparamagnetic relaxation phenomena. Specific loss power for the prepared ferrofluids was experimentally calculated and it was determined that under influence of ac-magnetic field magnetic fluid based on individual CoFe2O4 and Fe3-xO4 particles are characterized by very low heating temperature, when magnetic fluids based on core/shell nanoparticles demonstrate higher heating effect.

  3. Lithography-free shell-substrate isolation for core-shell GaAs nanowires.

    PubMed

    Haggren, Tuomas; Perros, Alexander Pyymaki; Jiang, Hua; Huhtio, Teppo; Kakko, Joona-Pekko; Dhaka, Veer; Kauppinen, Esko; Lipsanen, Harri

    2016-07-01

    A facile and scalable lithography-free technique(5) for the rapid construction of GaAs core-shell nanowires incorporating shell isolation from the substrate is reported. The process is based on interrupting NW growth and applying a thin spin-on-glass (SOG) layer to the base of the NWs and resuming core-shell NW growth. NW growth occurred in an atmospheric pressure metalorganic vapour phase epitaxy (MOVPE) system with gold nanoparticles used as catalysts for the vapour-liquid-solid growth. It is shown that NW axial core growth and radial shell growth can be resumed after interruption and even exposure to air. The SOG residues and native oxide layer that forms on the NW surface are shown to prevent or perturb resumption of epitaxial NW growth if not removed. Both HF etching and in situ annealing of the air-exposed NWs in the MOVPE were shown to remove the SOG residues and native oxide layer. While both procedures are shown capable of removing the native oxide and enabling resumption of epitaxial NW growth, in situ annealing produced the best results and allowed construction of pristine core-shell NWs. No growth occurred on SOG and it was observed that axial NW growth was more rapid when a SOG layer covered the substrate. The fabricated p-core/n-shell NWs exhibited diode behaviour upon electrical testing. The isolation of the NW shells from the substrate was confirmed by scanning electron microscopy and electrical measurements. The crystal quality of the regrown core-shell NWs was verified with a high resolution transmission electron microscope. The reported technique potentially provides a pathway using MOVPE for scalable and high-throughput production of shell-substrate isolated core-shell NWs on an industrial scale. PMID:27242347

  4. Determining the size distribution of core-shell spheres and other complex particles by laser diffraction.

    PubMed

    Lagasse, R R; Richards, D Wayne

    2003-11-01

    The goal of this work is to determine the size distribution of hollow glass spheres by laser diffraction, an experiment which involves measuring angle-dependent scattering of light from particles dispersed in a liquid. The proprietary software supplied with commercial instruments is not strictly applicable to our two-layer, glass-shell, hollow-core spheres because it requires that the particles have spatially homogeneous properties. We therefore developed Fortran code to compute the scattering from core-shell spherical particles. The results show that the scattering from representative hollow glass particles diverges from homogeneous sphere scattering when the radius decreases from 10 to 3 microm. Additionally, scattering measurements on two core-shell hollow glass powders were analyzed using the exact core-shell optical model and homogeneous sphere approximations. In both cases, the size distribution determined using the exact core-shell model differs from that determined using the homogeneous-sphere approximation when the distribution covers radii smaller than about 10 microm, as expected. The size distribution based on the exact core-shell optical model was determined using a new algorithm. Although the basic equations used in the algorithm have been published previously, they are developed here in a different form, which can be implemented using Fortran and MatLab routines available commercially and in the public domain. This algorithm could be used to determine the size distribution of other kinds of particles, such as cylindrical rods, as long as their angle-dependent scattering could be computed. PMID:14554168

  5. Core-shell nanophosphor architecture: toward efficient energy transport in inorganic/organic hybrid solar cells.

    PubMed

    Li, Qinghua; Yuan, Yongbiao; Chen, Zihan; Jin, Xiao; Wei, Tai-huei; Li, Yue; Qin, Yuancheng; Sun, Weifu

    2014-08-13

    In this work, a core-shell nanostructure of samarium phosphates encapsulated into a Eu(3+)-doped silica shell has been successfully fabricated, which has been confirmed by X-ray diffraction, transmission electron microscopy (TEM), and high-resolution TEM. Moreover, we report the energy transfer process from the Sm(3+) to emitters Eu(3+) that widens the light absorption range of the hybrid solar cells (HSCs) and the strong enhancement of the electron-transport of TiO2/poly(3-hexylthiophene) (P3HT) bulk heterojunction (BHJ) HSCs by introducing the unique core-shell nanoarchitecture. Furthermore, by applying femtosecond transient absorption spectroscopy, we successfully obtain the electron transport lifetimes of BHJ systems with or without incorporating the core-shell nanophosphors (NPs). Concrete evidence has been provided that the doping of core-shell NPs improves the efficiency of electron transfers from donor to acceptor, but the hole transport almost remains unchanged. In particular, the hot electron transfer lifetime was shortened from 30.2 to 16.7 ps, i.e., more than 44% faster than pure TiO2 acceptor. Consequently, a notable power conversion efficiency of 3.30% for SmPO4@Eu(3+):SiO2 blended TiO2/P3HT HSCs is achieved at 5 wt % as compared to 1.98% of pure TiO2/P3HT HSCs. This work indicates that the core-shell NPs can efficiently broaden the absorption region, facilitate electron-transport of BHJ, and enhance photovoltaic performance of inorganic/organic HSCs. PMID:24967836

  6. Proteresis of Cu2O/CuO core-shell nanoparticles: Experimental observations and theoretical considerations

    NASA Astrophysics Data System (ADS)

    Wu, Sheng Yun; Ji, Jhong-Yi; Shih, Po-Hsun; Gandhi, Ashish Chhaganlal; Chan, Ting-Shan

    2014-11-01

    A study of "proteresis (inverted hysteresis)" in core-shell, Cu2O/CuO nanoparticles, is presented. Crystal and characteristic sizes are determined using the x-ray absorption near-edge structure method for the weak ferromagnetic core (Cu2O) and antiferromagnetic shell (CuO) nanoparticles. A core-shell anisotropic energy model is established to describe the observed proteretic behavior in Cu2O/CuO core-shell nanocrystals. The proteresis loop triggered by the applied magnetic field can be tentatively attributed to core-shell exchange coupling induced by the surface of the Cu2O core, hinting at a possible way to tune the strength of the exchange inter-coupling energy that can control the dynamic of proteresis and hysteresis in a core-shell system.

  7. Dynamic evolution process of multilayer core-shell microstructures within containerlessly solidifying Fe(50)Sn(50) immiscible alloy.

    PubMed

    Wang, W L; Wu, Y H; Li, L H; Geng, D L; Wei, B

    2016-03-01

    Multilayer core-shell structures are frequently formed in polymers and alloys when temperature and concentration fields are well symmetrical spatially. Here we report that two- to five-layer core-shell microstructures were the dominant structural morphology of a binary Fe(50)Sn(50) immiscible alloy solidified under the containerless and microgravity states within a drop tube. Three dimensional phase field simulation reveals that both the uniformly dispersive structure and the multilayer core-shells are the various metastable and transitional states of the liquid phase separation process. Only the two-layer core-shell is the most stable microstructure with the lowest chemical potential. Because of the suppression of Stokes motion, solutal Marangoni migration becomes important to drive the evolution of core-shell structures. PMID:27078410

  8. Dynamic evolution process of multilayer core-shell microstructures within containerlessly solidifying F e50S n50 immiscible alloy

    NASA Astrophysics Data System (ADS)

    Wang, W. L.; Wu, Y. H.; Li, L. H.; Geng, D. L.; Wei, B.

    2016-03-01

    Multilayer core-shell structures are frequently formed in polymers and alloys when temperature and concentration fields are well symmetrical spatially. Here we report that two- to five-layer core-shell microstructures were the dominant structural morphology of a binary F e50S n50 immiscible alloy solidified under the containerless and microgravity states within a drop tube. Three dimensional phase field simulation reveals that both the uniformly dispersive structure and the multilayer core-shells are the various metastable and transitional states of the liquid phase separation process. Only the two-layer core-shell is the most stable microstructure with the lowest chemical potential. Because of the suppression of Stokes motion, solutal Marangoni migration becomes important to drive the evolution of core-shell structures.

  9. Excitonic condensation in spatially separated one-dimensional systems

    SciTech Connect

    Abergel, D. S. L.

    2015-05-25

    We show theoretically that excitons can form from spatially separated one-dimensional ground state populations of electrons and holes, and that the resulting excitons can form a quasicondensate. We describe a mean-field Bardeen-Cooper-Schrieffer theory in the low carrier density regime and then focus on the core-shell nanowire giving estimates of the size of the excitonic gap for InAs/GaSb wires and as a function of all the experimentally relevant parameters. We find that optimal conditions for pairing include small overlap of the electron and hole bands, large effective mass of the carriers, and low dielectric constant of the surrounding media. Therefore, one-dimensional systems provide an attractive platform for the experimental detection of excitonic quasicondensation in zero magnetic field.

  10. Core-shell potassium niobate nanowires for enhanced nonlinear optical effects

    NASA Astrophysics Data System (ADS)

    Richter, J.; Steinbrück, A.; Zilk, M.; Sergeyev, A.; Pertsch, T.; Tünnermann, A.; Grange, R.

    2014-04-01

    We demonstrate the synthesis as well as the optical characterization of core-shell nanowires. The wires consist of a potassium niobate (KNbO3) core and a gold shell. The nonlinear optical properties of the core are combined with the plasmonic resonance of the shell and offer an enhanced optical signal in the near infrared spectral range. We compare two different functionalization schemes of the core material prior to the shell growth process: silanization and polyelectrolyte. We show that the latter leads to a smoother and complete core-shell nanostructure and an easier-to-use synthesis process. A Mie-theory based theoretical approach is presented to model the enhanced second-harmonic generated (SHG) signal of the core-shell wires, illustrating the influence of the fabrication-induced varying geometrical factors of wire radius and shell thickness. A spectroscopic measurement on a core-shell nanowire shows a strong localized surface plasmon resonance close to 900 nm, which matches with the SHG resonance obtained from nonlinear optical experiments with the same nanowire. According to the simulation, this corresponds to a wire radius of 35 nm and a shell thickness of 7.5 nm. By comparing SHG signals measured from an uncoated nanowire and the coated one, we obtain a 250 times enhancement factor. This is less than the calculated enhancement, which considers a cylindrical nanowire with a perfectly smooth shell. Thus, we explain this discrepancy mainly with the roughness of the synthesized gold shell.We demonstrate the synthesis as well as the optical characterization of core-shell nanowires. The wires consist of a potassium niobate (KNbO3) core and a gold shell. The nonlinear optical properties of the core are combined with the plasmonic resonance of the shell and offer an enhanced optical signal in the near infrared spectral range. We compare two different functionalization schemes of the core material prior to the shell growth process: silanization and polyelectrolyte

  11. Strong exciton-photon coupling with colloidal quantum dots in a high-Q bilayer microcavity

    SciTech Connect

    Giebink, Noel C; Wiederrecht, Gary P.; Wasielewski, Michael R

    2011-01-01

    We demonstrate evanescently coupled bilayer microcavities with Q -factors exceeding 250 fabricated by a simple spin-coating process. The cavity architecture consists of a slab waveguide lying upon a low refractive index spacer layer supported by a glass substrate. For a lossless guide layer, the cavity Q depends only on the thickness of the low index spacer and in principle can reach arbitrarily high values. We demonstrate the versatility of this approach by constructing cavities with a guide layer incorporating CdSe/ZnS core/shell quantum dots, where we observe strong coupling and hybridization between the 1S(e)-1S{sub 3/2} (h) and 1S(e)-2S{sub 3/2} (h) exciton states mediated by the cavity photon. This technique greatly simplifies the fabrication of high-Q planar microcavities for organic and inorganic quantum dot thin films and opens up new opportunities for the study of nonlinear optical phenomena in these materials.

  12. One-pot synthesis of hematite@graphene core@shell nanostructures for superior lithium storage

    NASA Astrophysics Data System (ADS)

    Chen, Dezhi; Quan, Hongying; Liang, Junfei; Guo, Lin

    2013-09-01

    Novel hematite@graphene composites have been successfully synthesized by a one-pot surfactant governed approach under mild wet-chemical conditions. A series of characterizations including X-ray diffraction (XRD), Raman spectrum, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) indicated that the hematite nanoparticles with relatively uniform size were encapsulated by graphene layers and were able to form core-shell nanostructures. The electrochemical properties of hematite@graphene core-shell nanostructures as anodes for lithium-ion batteries were evaluated by galvanostatic charge-discharge and AC impedance spectroscopy techniques. The as-prepared hematite@graphene core-shell nanostructures exhibited a high reversible specific capacity of 1040 mA h g-1 at a current density of 200 mA g-1 (0.2 C) after 180 cycles and excellent rate capability and long cycle life. Furthermore, a reversible capacity as high as 500 mA h g-1 was still achieved after 200 cycles even at a high rate of 6 C. The electrochemical test results show that the hematite@graphene composites prepared by the one-pot wet chemical method are promising anode materials for lithium-ion batteries.Novel hematite@graphene composites have been successfully synthesized by a one-pot surfactant governed approach under mild wet-chemical conditions. A series of characterizations including X-ray diffraction (XRD), Raman spectrum, scanning electron microscopy (SEM) and transmission electron microscopy (TEM) indicated that the hematite nanoparticles with relatively uniform size were encapsulated by graphene layers and were able to form core-shell nanostructures. The electrochemical properties of hematite@graphene core-shell nanostructures as anodes for lithium-ion batteries were evaluated by galvanostatic charge-discharge and AC impedance spectroscopy techniques. The as-prepared hematite@graphene core-shell nanostructures exhibited a high reversible specific capacity of 1040 mA h g-1 at a

  13. Spherical core-shell magnetic particles constructed by main-chain palladium N-heterocyclic carbenes

    NASA Astrophysics Data System (ADS)

    Zhao, Huaixia; Li, Liuyi; Wang, Jinyun; Wang, Ruihu

    2015-02-01

    The encapsulation of the functional species on magnetic core is a facile approach for the synthesis of core-shell magnetic materials, and surface encapsulating matrices play crucial roles in regulating their properties and applications. In this study, two core-shell palladium N-heterocyclic carbene (NHC) particles (Fe3O4@PNP1 and Fe3O4@PNP2) were prepared by a one-pot reaction of semi-rigid tripodal imidazolium salts and palladium acetate in the presence of magnetite nanoparticles. The magnetite nanoparticles are encapsulated inside the main-chain palladium, which act as cores. The conjugated effects of triphenyltriazine and triphenylbenzene in the imidazolium salts have important influence on their physical properties and catalytic performances. Fe3O4@PNP2 shows better recyclability than Fe3O4@PNP1. Unexpectedly, Pd(ii) is well maintained after six consecutive catalytic runs in Fe3O4@PNP2, and Pd(0) and Pd(ii) coexist in Fe3O4@PNP1 under the same conditions; moreover, the morphologies of these spherical core-shell particles show no significant variation after six consecutive catalytic runs.The encapsulation of the functional species on magnetic core is a facile approach for the synthesis of core-shell magnetic materials, and surface encapsulating matrices play crucial roles in regulating their properties and applications. In this study, two core-shell palladium N-heterocyclic carbene (NHC) particles (Fe3O4@PNP1 and Fe3O4@PNP2) were prepared by a one-pot reaction of semi-rigid tripodal imidazolium salts and palladium acetate in the presence of magnetite nanoparticles. The magnetite nanoparticles are encapsulated inside the main-chain palladium, which act as cores. The conjugated effects of triphenyltriazine and triphenylbenzene in the imidazolium salts have important influence on their physical properties and catalytic performances. Fe3O4@PNP2 shows better recyclability than Fe3O4@PNP1. Unexpectedly, Pd(ii) is well maintained after six consecutive catalytic runs in

  14. Smart micelle@polydopamine core-shell nanoparticles for highly effective chemo-photothermal combination therapy

    NASA Astrophysics Data System (ADS)

    Zhang, Ruirui; Su, Shishuai; Hu, Kelei; Shao, Leihou; Deng, Xiongwei; Sheng, Wang; Wu, Yan

    2015-11-01

    In this investigation, we have designed and synthesized a novel core-shell polymer nanoparticle system for highly effective chemo-photothermal combination therapy. A nanoscale DSPE-PEG micelle encapsulating doxorubicin (Dox-M) was designed as a core, and then modified by a polydopamine (PDA) shell for photothermal therapy and bortezomib (Btz) administration (Dox-M@PDA-Btz). The facile conjugation of Btz to the catechol-containing PDA shell can form a reversible pH-sensitive boronic acid-catechol conjugate to create a stimuli-responsive drug carrier system. As expected, the micelle@PDA core-shell nanoparticles exhibited satisfactory photothermal efficiency, which has potential for thermal ablation of malignant tissues. In addition, on account of the PDA modification, both Dox and Btz release processes were pH-dependent and NIR-dependent. Both in vitro and in vivo studies illustrated that the Dox-M@PDA-Btz nanoparticles coupled with laser irradiation could enhance the cytotoxicity, and thus combinational therapy efficacy was achieved when integrating Dox, Btz, and PDA into a single nanoplatform. Altogether, our current study indicated that the micelle@polydopamine core-shell nanoparticles could be applied for NIR/pH-responsive sustained-release and synergized chemo-photothermal therapy for breast cancer.In this investigation, we have designed and synthesized a novel core-shell polymer nanoparticle system for highly effective chemo-photothermal combination therapy. A nanoscale DSPE-PEG micelle encapsulating doxorubicin (Dox-M) was designed as a core, and then modified by a polydopamine (PDA) shell for photothermal therapy and bortezomib (Btz) administration (Dox-M@PDA-Btz). The facile conjugation of Btz to the catechol-containing PDA shell can form a reversible pH-sensitive boronic acid-catechol conjugate to create a stimuli-responsive drug carrier system. As expected, the micelle@PDA core-shell nanoparticles exhibited satisfactory photothermal efficiency, which has

  15. Magnetic response of hybrid ferromagnetic and antiferromagnetic core-shell nanostructures

    NASA Astrophysics Data System (ADS)

    Khan, U.; Li, W. J.; Adeela, N.; Irfan, M.; Javed, K.; Wan, C. H.; Riaz, S.; Han, X. F.

    2016-03-01

    The synthesis of FeTiO3-Ni(Ni80Fe20) core-shell nanostructures by a two-step method (sol-gel and DC electrodeposition) has been demonstrated. XRD analysis confirms the rhombohedral crystal structure of FeTiO3(FTO) with space group R3&cmb.macr;. Transmission electron microscopy clearly depicts better morphology of nanostructures with shell thicknesses of ~25 nm. Room temperature magnetic measurements showed significant enhancement of magnetic anisotropy for the permalloy (Ni80Fe20)-FTO over Ni-FTO core-shell nanostructures. Low temperature magnetic measurements of permalloy-FeTiO3 core-shell structure indicated a strong exchange bias mechanism with magnetic coercivity below the antiferromagnetic Neel temperature (TN = 59 K). The exchange bias is attributed to the alignment of magnetic moments in the antiferromagnetic material at low temperature. Our scheme opens a path towards optimum automotive systems and wireless communications wherein broader bandwidths and smaller sizes are required.The synthesis of FeTiO3-Ni(Ni80Fe20) core-shell nanostructures by a two-step method (sol-gel and DC electrodeposition) has been demonstrated. XRD analysis confirms the rhombohedral crystal structure of FeTiO3(FTO) with space group R3&cmb.macr;. Transmission electron microscopy clearly depicts better morphology of nanostructures with shell thicknesses of ~25 nm. Room temperature magnetic measurements showed significant enhancement of magnetic anisotropy for the permalloy (Ni80Fe20)-FTO over Ni-FTO core-shell nanostructures. Low temperature magnetic measurements of permalloy-FeTiO3 core-shell structure indicated a strong exchange bias mechanism with magnetic coercivity below the antiferromagnetic Neel temperature (TN = 59 K). The exchange bias is attributed to the alignment of magnetic moments in the antiferromagnetic material at low temperature. Our scheme opens a path towards optimum automotive systems and wireless communications wherein broader bandwidths and smaller sizes are

  16. Investigation of linear optical absorption coefficients in core-shell quantum dot (QD) luminescent solar concentrators (LSCs)

    NASA Astrophysics Data System (ADS)

    Ebrahimipour, Bahareh Alsadat; Askari, Hassan Ranjbar; Ramezani, Ali Behjat

    2016-09-01

    The interlevel absorption coefficient of CdSe/ZnS and ZnS/CdSe core-shell Quantum Dot (QD) in luminescent solar concentrators (LSCs) is reported. By considering the quantum confinement effects, the wave functions and eigenenergies of electrons in the nonperturebative system consists of a core-shell QD have been numerically calculated under the frame work of effective-mass approximation by solving a three-dimensional Schrӧdinger equation. And then the absorption coefficient is obtained under density matrix approximation considering in the polymer sheets of the concentrator including the core-shell QDs. The effect of the hetero-structure geometry upon the energy spectrum and absorption coefficient associated to interlevel transitions was also considered. The results show that the core-shell QDs can absorb the photons with higher energy in solar spectrum as compared to the inverted core-shell. And with a small shell layer diameter, the core-shell QDs produce larger linear absorption coefficients and consequently higher efficiency values, however it is inversed for inverted core-shell QDs. The work described here gives a detailed insight into the promise of QD-based LSCs and the optoelectronic devices applications.

  17. Palladium–platinum core-shell icosahedra with substantially enhanced activity and durability towards oxygen reduction

    SciTech Connect

    Wang, Xue; Choi, Sang-Il; Roling, Luke T.; Luo, Ming; Ma, Cheng; Zhang, Lei; Chi, Miaofang; Liu, Jingyue; Xie, Zhaoxiong; Herron, Jeffrey A.; Mavrikakis, Manos; Xia, Younan

    2015-07-02

    Conformal deposition of platinum as ultrathin shells on facet-controlled palladium nanocrystals offers a great opportunity to enhance the catalytic performance while reducing its loading. Here we report such a system based on palladium icosahedra. Owing to lateral confinement imposed by twin boundaries and thus vertical relaxation only, the platinum overlayers evolve into a corrugated structure under compressive strain. For the core-shell nanocrystals with an average of 2.7 platinum overlayers, their specific and platinum mass activities towards oxygen reduction are enhanced by eight- and sevenfold, respectively, relative to a commercial catalyst. Density functional theory calculations indicate that the enhancement can be attributed to the weakened binding of hydroxyl to the compressed platinum surface supported on palladium. After 10,000 testing cycles, the mass activity of the core-shell nanocrystals is still four times higher than the commercial catalyst. Ultimately, these results demonstrate an effective approach to the development of electrocatalysts with greatly enhanced activity and durability.

  18. Palladium-platinum core-shell icosahedra with substantially enhanced activity and durability towards oxygen reduction

    NASA Astrophysics Data System (ADS)

    Wang, Xue; Choi, Sang-Il; Roling, Luke T.; Luo, Ming; Ma, Cheng; Zhang, Lei; Chi, Miaofang; Liu, Jingyue; Xie, Zhaoxiong; Herron, Jeffrey A.; Mavrikakis, Manos; Xia, Younan

    2015-07-01

    Conformal deposition of platinum as ultrathin shells on facet-controlled palladium nanocrystals offers a great opportunity to enhance the catalytic performance while reducing its loading. Here we report such a system based on palladium icosahedra. Owing to lateral confinement imposed by twin boundaries and thus vertical relaxation only, the platinum overlayers evolve into a corrugated structure under compressive strain. For the core-shell nanocrystals with an average of 2.7 platinum overlayers, their specific and platinum mass activities towards oxygen reduction are enhanced by eight- and sevenfold, respectively, relative to a commercial catalyst. Density functional theory calculations indicate that the enhancement can be attributed to the weakened binding of hydroxyl to the compressed platinum surface supported on palladium. After 10,000 testing cycles, the mass activity of the core-shell nanocrystals is still four times higher than the commercial catalyst. These results demonstrate an effective approach to the development of electrocatalysts with greatly enhanced activity and durability.

  19. The preparation and properties of monodisperse core-shell silica magnetic microspheres.

    PubMed

    Lou, Min-yi; Jia, Qiu-ling; Wang, De-ping; Liu, Bing; Huang, Wen-hai

    2008-01-01

    The monodisperse core-shell silica magnetic microspheres (MMS) were synthesized by sol-gel method gelling in the emulsion. Optical microscope (OM), field emission scanning electron microscope (FESEM), nitrogen adsorption and desorption Brunauer Emmett Teller Procedure (BET) isotherms and Barrett-Joyner-Halenda (BJH) pore size distribution measurements, X-ray diffraction (XRD), energy dispersive spectrometer (EDS) and vibrating sample magnetometer (VSM) were used to characterize the appearance, size distribution, phase, specific surface area, chemical composition and magnetic property of silica MMS. The results showed that silica MMS prepared through sol-gel method with acid-alkali two-step catalyze and gelling in emulsion exhibited the superior core-shell structure and size distribution of the microspheres concentrated in about 20 mum. The main phase of microspheres was amorphous silica and spinel ferroferric oxide. Meanwhile, the microspheres remained the superparamagnetic behavior and could be used as biomaterials. PMID:17597357

  20. The Core-Shell Approach to Formation of Ordered Nanoporous Materials

    SciTech Connect

    Chang, Jeong H.; Wang, Li Q.; Shin, Yongsoon; Jeong, Byeongmoon; Birnbaum, Jerome C.; Exarhos, Gregory J.

    2002-03-04

    This work describes a novel core-shell approach for the preparation of ordered nanoporous ceramic materials that involve a self-assembly process at the molecular level using MPEG-b-PDLLA bloack copolymers. This approach provides for rapid self-assembly and structural reorganization at room temperature. Selected MPEG-b-PDLLA block copolymers were synthesized with systematic variation of the chain lengths of the resident hydrophilic and hydrophobic blocks. This allows the micelle size to be systematically varied. Results from this work are used to understand the formation mechanism of nanoporous structures in which the pore size and wall thickness are closely dependent on the size of hydrophobic cores and hydrophilic shells of the block copolymer templates. The core-shell mechanism for nanoporous structure evolution is based on the size and contrasting micellar packing arrangements that are controlled by the copolymer.

  1. Controlled Growth of Ordered III-Nitride Core-Shell Nanostructure Arrays for Visible Optoelectronic Devices

    NASA Astrophysics Data System (ADS)

    Rishinaramangalam, Ashwin K.; Ul Masabih, Saadat Mishkat; Fairchild, Michael N.; Wright, Jeremy B.; Shima, Darryl M.; Balakrishnan, Ganesh; Brener, Igal; Brueck, S. R. J.; Feezell, Daniel F.

    2015-05-01

    We demonstrate the growth of ordered arrays of nonpolar core-shell nanowalls and semipolar core-shell pyramidal nanostripes on c-plane (0001) sapphire substrates using selective-area epitaxy and metal organic chemical vapor deposition. The nanostructure arrays are controllably patterned into LED mesa regions, demonstrating a technique to impart secondary lithography features into the arrays. We study the dependence of the nanostructure cores on the epitaxial growth conditions and show that the geometry and morphology are strongly influenced by growth temperature, V/III ratio, and pulse interruption time. We also demonstrate the growth of InGaN quantum well shells on the nanostructures and characterize the structures by using micro-photoluminescence and cross-section scanning tunneling electron microscopy.

  2. Intraband Luminescence from HgSe/CdS Core/Shell Quantum Dots.

    PubMed

    Deng, Zhiyou; Guyot-Sionnest, Philippe

    2016-02-23

    HgSe/CdS core/shell CQD are synthesized, and the changes in the optical absorption and luminescence are investigated. While HgSe quantum dots are naturally n-doped after synthesis, both as colloidal solutions and as films, the HgSe/CdS core/shell dots in solution lose the n-doping, as seen from the optical absorption in solution. However, n-doping is regained in films, and the intraband luminescence of the films of HgSe/CdS is greater than that of the cores. The shell also vastly improves the stability of the quantum dots films against sintering at 200 °C. After annealing at that temperature, the HgSe/CdS films retain a narrow intraband emission and sustain a higher laser power leading to brighter emission at 5 μm. PMID:26820380

  3. Template-Directed Synthesis of Porous and Protective Core-Shell Bionanoparticles.

    PubMed

    Li, Shaobo; Dharmarwardana, Madushani; Welch, Raymond P; Ren, Yixin; Thompson, Christina M; Smaldone, Ronald A; Gassensmith, Jeremiah J

    2016-08-26

    Metal-organic frameworks (MOFs) are promising high surface area coordination polymers with tunable pore structures and functionality; however, a lack of good size and morphological control over the as-prepared MOFs has persisted as an issue in their application. Herein, we show how a robust protein template, tobacco mosaic virus (TMV), can be used to regulate the size and shape of as-fabricated MOF materials. We were able to obtain discrete rod-shaped TMV@MOF core-shell hybrids with good uniformity, and their diameters could be tuned by adjusting the synthetic conditions, which can also significantly impact the stability of the core-shell composite. More interestingly, the virus particle underneath the MOF shell can be chemically modified using a standard bioconjugation reaction, showing mass transportation within the MOF shell. PMID:27485579

  4. TiN/VN composites with core/shell structure for supercapacitors

    SciTech Connect

    Dong, Shanmu; Chen, Xiao; Gu, Lin; Zhou, Xinhong; Wang, Haibo; Liu, Zhihong; Han, Pengxian; Yao, Jianhua; Wang, Li; Cui, Guanglei; Chen, Liquan

    2011-06-15

    Research highlights: {yields} Vanadium and titanium nitride nanocomposite with core-shell structure was prepared. {yields} TiN/VN composites with different V:Ti molar ratios were obtained. {yields} TiN/VN composites can provide promising electronic conductivity and favorable capacity storage. -- Abstract: TiN/VN core-shell composites are prepared by a two-step strategy involving coating of commercial TiN nanoparticles with V{sub 2}O{sub 5}.nH{sub 2}O sols followed by ammonia reduction. The highest specific capacitance of 170 F g{sup -1} is obtained when scanned at 2 mV s{sup -1} and a promising rate capacity performance is maintained at higher voltage sweep rates. These results indicate that these composites with good electronic conductivity can deliver a favorable capacity performance.

  5. Freestanding three-dimensional core-shell nanoarrays for lithium-ion battery anodes.

    PubMed

    Tan, Guoqiang; Wu, Feng; Yuan, Yifei; Chen, Renjie; Zhao, Teng; Yao, Ying; Qian, Ji; Liu, Jianrui; Ye, Yusheng; Shahbazian-Yassar, Reza; Lu, Jun; Amine, Khalil

    2016-01-01

    Structural degradation and low conductivity of transition-metal oxides lead to severe capacity fading in lithium-ion batteries. Recent efforts to solve this issue have mainly focused on using nanocomposites or hybrids by integrating nanosized metal oxides with conducting additives. Here we design specific hierarchical structures and demonstrate their use in flexible, large-area anode assemblies. Fabrication of these anodes is achieved via oxidative growth of copper oxide nanowires onto copper substrates followed by radio-frequency sputtering of carbon-nitride films, forming freestanding three-dimensional arrays with core-shell nano-architecture. Cable-like copper oxide/carbon-nitride core-shell nanostructures accommodate the volume change during lithiation-delithiation processes, the three-dimensional arrays provide abundant electroactive zones and electron/ion transport paths, and the monolithic sandwich-type configuration without additional binders or conductive agents improves energy/power densities of the whole electrode. PMID:27256920

  6. Potential of electrospun core-shell structured gelatin-chitosan nanofibers for biomedical applications.

    PubMed

    Jalaja, K; Naskar, Deboki; Kundu, Subhas C; James, Nirmala R

    2016-01-20

    Coaxial electrospinning is an upcoming technology that has emerged from the conventional electrospinning process in order to realize the production of nanofibers of less spinnable materials with potential applications. The present work focuses on the production of chitosan nanofibers in a benign route, using natural polymer as core template, mild solvent system and naturally derived cross-linkers. Nanofibers with chitosan as shell are fabricated by coaxial electrospinning with highly spinnable gelatin as core using aqueous acetic acid as solvent. For maintaining the biocompatibility and structural integrity of the core-shell nanofibers, cross-linking is carried out using naturally derived cross-linking agents, dextran aldehyde and sucrose aldehyde. The biological evaluation of gelatin/chitosan mat is carried out using human osteoblast like cells. The results show that the cross-linked core-shell nanofibers are excellent matrices for cell adhesion and proliferation. PMID:26572452

  7. Evidence for Symplectic Symmetry in Ab Initio No-Core Shell Model Results for Light Nuclei

    SciTech Connect

    Dytrych, Tomas; Sviratcheva, Kristina D.; Bahri, Chairul; Draayer, Jerry P.; Vary, James P.; /Iowa State U. /LLNL, Livermore /SLAC

    2007-04-24

    Clear evidence for symplectic symmetry in low-lying states of {sup 12}C and {sup 16}O is reported. Eigenstates of {sup 12}C and {sup 16}O, determined within the framework of the no-core shell model using the JISP16 NN realistic interaction, typically project at the 85-90% level onto a few of the most deformed symplectic basis states that span only a small fraction of the full model space. The results are nearly independent of whether the bare or renormalized effective interactions are used in the analysis. The outcome confirms Elliott's SU(3) model which underpins the symplectic scheme, and above all, points to the relevance of a symplectic no-core shell model that can reproduce experimental B(E2) values without effective charges as well as deformed spatial modes associated with clustering phenomena in nuclei.

  8. Facile synthesis 3D flexible core-shell graphene/glass fiber via chemical vapor deposition

    NASA Astrophysics Data System (ADS)

    Yang, Cheng; Xu, Yuanyuan; Zhang, Chao; Sun, Zhencui; Chen, Chuansong; Li, Xiuhua; Jiang, Shouzhen; Man, Baoyuan

    2014-08-01

    Direct deposition of graphene layers on the flexible glass fiber surface to form the three-dimensional (3D) core-shell structures is offered using a two-heating reactor chemical vapor deposition system. The two-heating reactor is utilized to offer sufficient, well-proportioned floating C atoms and provide a facile way for low-temperature deposition. Graphene layers, which are controlled by changing the growth time, can be grown on the surface of wire-type glass fiber with the diameter from 30 nm to 120 um. The core-shell graphene/glass fiber deposition mechanism is proposed, suggesting that the 3D graphene films can be deposited on any proper wire-type substrates. These results open a facile way for direct and high-efficiency deposition of the transfer-free graphene layers on the low-temperature dielectric wire-type substrates.

  9. Core-shell nanoparticles as scavengers for hydrophobic molecules in biological systems

    NASA Astrophysics Data System (ADS)

    Wong, Jeffrey

    2005-11-01

    Core-shell nanoparticles containing hydrophobic cores and hydrophilic shells were synthesized based on a tertiary microemulsion system. Due to their hydrophobic interior, this system is proposed to work as a scavenger of non polar species, like pesticides or drugs present in concentrations higher than what the body can tolerate. The ability to control the core and shell sizes using different molecules to fill the core was studied with different techniques. Hydrophobic fluorescent dyes were used as model non polar molecules to study the uptake abilities of the system synthesized. Derivatization of the surface of the core-shell particles with different groups, including biotin and poly(ethylene glycol) was performed to improve the biocompatibility of the system. Binding to streptavidin via the biotin units on the surface was performed to study the biocompatibility of the derivatized nanocapsules in biological relevant systems.

  10. Enhancement of Electrochromic Durability of a Film Made of Silica-Polyaniline Core-Shell Nanoparticles

    NASA Astrophysics Data System (ADS)

    Hwang, Taejin; Lee, Heungyeol; Kim, Hohyeong; Kim, Gyuntak; Mun, Gyeongjin

    Enhancing the operation life time or the electrochemical durability is one of the key issues in electrochromic material studies. It is generally accepted that the inorganic-organic hybrid structure is one of the effective ways to enhance the chemical stability of the material. In this study, an electrochromic film made of silica-polyaniline core-shell composite nanoparticles was tested. The composite particles were prepared through a chemical dispersion polymerization of aniline in an aqueous colloidal solution of silica. The synthesized particles were then dispersed into ethanol and the solution was deposited onto an Indium Tin Oxide (ITO)-coated glass substrate. The electrochromic characterization on the prepared films was performed using the cyclovoltammetry and the optical response to a switching potential. The results showed that the inorganic-organic core-shell hybrid nanoparticle could be a promising choice for the enhancement of electrochromic durability.