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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. 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

  9. 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

  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. 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.

  15. 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.

  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. 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

  5. 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.

  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. 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

  8. "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.

  9. 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

  10. 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

  11. 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.

  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. 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

  20. 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.

  1. 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.

  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. 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

  4. 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

  5. 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.

  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. 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.

  8. 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.

  9. 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

  10. 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

  11. 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.

  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. 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.

  16. 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.

  17. 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

  18. 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

  19. 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

  20. 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.

  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. 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

  15. 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.

  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. 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

  1. 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.

  2. 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

  3. 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.

  4. 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.

  5. 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.

  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. 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

  8. 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.

  9. 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.

  10. 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.

  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. 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

  16. 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.

  17. 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.

  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. 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

  2. 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

  3. 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

  4. 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.

  5. 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

  6. 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

  7. 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.

  8. 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

  9. 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

  10. 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.

  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. 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

  14. 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

  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. 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

  17. 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.

  18. 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

  19. 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.

  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. 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

  8. 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

  9. 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

  10. 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.

  11. 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.

  12. [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

  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. 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

  15. 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

  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. 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.

  2. 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.

  3. 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.

  4. 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.

  5. 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.

  6. 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

  7. 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

  8. 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.

  9. 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

  10. 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.

  11. 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

  12. 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.

  13. 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.

  14. 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

  15. 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

  16. 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

  17. 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.

  18. 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

  19. 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

  20. 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

  1. 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

  2. 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

  3. 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

  4. 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

  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. 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.

  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. 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

  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. 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

  13. 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

  14. 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

  15. 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.

  16. 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.

  17. 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

  18. 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.

  19. 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

  20. 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.

  1. 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

  2. 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.

  3. 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

  4. 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.

  5. 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

  6. 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

  7. 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.

  8. 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).

  9. 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

  10. 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

  11. 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)

  12. 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.

  13. 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

  14. 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

  15. 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

  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. 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.

  18. 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

  19. 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

  20. 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

  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. 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

  3. 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

  4. 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

  5. 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.

  6. 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

  7. 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.

  8. 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.

  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. 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

  13. 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

  14. 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

  15. 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

  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. 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.

  18. 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.

  19. 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.

  20. Green synthesis and surface properties of Fe3O4@SA core-shell nanocomposites

    NASA Astrophysics Data System (ADS)

    Cao, Huimin; Li, Juchuan; Shen, Yuhua; Li, Shikuo; Huang, Fangzhi; Xie, Anjian

    2014-05-01

    In this paper, a one-step, economic and green approach was explored to prepare Fe3O4 nanoparticles by using L-cysteine as reducer and disperser without any inert gas protection. The Fe3O4 nanoparticles were then modified with stearic acid (SA) to form Fe3O4@SA core-shell nanocomposites. The experiment results indicate that the core-shell nanocomposites prepared could form monolayer on the water surface or films by means of Langmuir-Blodgett (LB) technology due to their hydrophobic and lipophilic properties. Also the composites exhibit paramagnetism, which make product dispersed stably in the oil medium to form magnetic fluid. Moreover, they are developed as sorbents to remove oil from water surface.

  1. Effect of guided resonance modes on emission from GaN core-shell nanorod arrays

    NASA Astrophysics Data System (ADS)

    Anderson, P. Duke; Lin, Chenxi; Povinelli, Michelle L.

    2014-12-01

    We model the process of incoherent emission from quantum wells in GaN core-shell nanorod arrays using finite-difference time-domain simulations. We find that high-intensity features in the emitted field correspond to guided resonance modes near the -point of the photonic band structure. We identify one -point mode whose electric field intensity profile is ideal for core-shell nanorod array geometries. Using this mode, we are able to simultaneously enhance the radiative recombination rate and extraction efficiency relative to an in-filled slab. We determine the conditions on radiative and nonradiative recombination rates for which the nanorod array has a higher internal and external quantum efficiency than a reference slab. We present one nanorod array geometry where the external quantum efficiency is enhanced up to a factor of 25.

  2. Lowering of ground state induced by core-shell structure in strontium titanate

    NASA Astrophysics Data System (ADS)

    Kiat, J. M.; Hehlen, B.; Anoufa, M.; Bogicevic, C.; Curfs, C.; Boyer, B.; Al-Sabbagh, M.; Porcher, F.; Al-Zein, A.

    2016-04-01

    A new ground state of textbook compound strontium titanate (SrTi O3) is obtained by inducing a specific core-shell structure of the particles. Using a combination of high energy synchrotron and neutron diffraction, we demonstrate a lowering of the ferroelastic ground state towards a new antiferrodistortive phase, accompanied with strong shifts of the critical temperature. This new phase is discussed within the Landau theory and compared with the situation in thin films and during pressure experiments. The crucial competition between particle shape anisotropy, surface tension, and shear strain is analyzed. Inducing a specific core-shell structure is therefore an easy way to tailor structural properties and to stabilize new phases that cannot exist in bulk material, just like film deposition on a substrate.

  3. Alternating current dielectrophoresis of core-shell nanoparticles: Experiments and comparison with theory

    NASA Astrophysics Data System (ADS)

    Yang, Chungja

    Nanoparticles are fascinating where physical and optical properties are related to size. Highly controllable synthesis methods and nanoparticle assembly are essential for highly innovative technological applications. Well-defined shaped and sized nanoparticles enable comparisons between experiments, theory and subsequent new models to explain experimentally observed phenomena. Among nanoparticles, nonhomogeneous core-shell nanoparticles (CSnp) have new properties that arise when varying the relative dimensions of the core and the shell. This CSnp structure enables various optical resonances, and engineered energy barriers, in addition to the high charge to surface ratio. Assembly of homogeneous nanoparticles into functional structures has become ubiquitous in biosensors (i.e. optical labeling), nanocoatings, and electrical circuits. Limited nonhomogenous nanoparticle assembly has only been explored. Many conventional nanoparticle assembly methods exist, but this work explores dielectrophoresis (DEP) as a new method. DEP is particle polarization via non-uniform electric fields while suspended in conductive fluids. Most prior DEP efforts involve microscale particles. Prior work on core-shell nanoparticle assemblies and separately, nanoparticle characterizations with dielectrophoresis and electrorotation, did not systematically explore particle size, dielectric properties (permittivity and electrical conductivity), shell thickness, particle concentration, medium conductivity, and frequency. This work is the first, to the best of our knowledge, to systematically examine these dielectrophoretic properties for core-shell nanoparticles. Further, we conduct a parametric fitting to traditional core-shell models. These biocompatible core-shell nanoparticles were studied to fill a knowledge gap in the DEP field. Experimental results (chapter 5) first examine medium conductivity, size and shell material dependencies of dielectrophoretic behaviors of spherical CSnp into 2D and

  4. Core-shell-type magnetic mesoporous silica nanocomposites for bioimaging and therapeutic agent delivery.

    PubMed

    Wang, Yao; Gu, Hongchen

    2015-01-21

    Advances in nanotechnology and nanomedicine offer great opportunities for the development of nanoscaled theranostic platforms. Among various multifunctional nanocarriers, magnetic mesoporous silica nanocomposites (M-MSNs) attract prominent research interest for their outstanding properties and potential biomedical applications. This Research News article highlights recent progress in the design of core-shell-type M-MSNs for both diagnostic and therapeutic applications. First, an overview of synthetic strategies for three representative core-shell-type M-MSNs with different morphologies and structures is presented. Then, the diagnostic functions of M-MSNs is illustrated for magnetic resonance imaging (MRI) applications. Next, magnetic targeted delivery and stimuli-responsive release of drugs, and effective package of DNA/siRNA inside mesopores using M-MSNs as therapeutic agent carriers are discussed. The article concludes with some important challenges that need to be overcome for further practical applications of M-MSNs in nanomedicine. PMID:25238634

  5. Synthesis of Plasmonic Cu2-x Se@ZnS Core@Shell Nanoparticles.

    PubMed

    Wolf, Andreas; Härtling, Thomas; Hinrichs, Dominik; Dorfs, Dirk

    2016-03-01

    We report the synthesis of plasmonic Cu2-x Se@ZnS core@shell nanoparticles (NPs). We used a shell growth approach, starting from Cu2-x Se NPs that have been shown before to exhibit a localized surface plasmon resonance (LSPR). By careful synthesis planning we avoided cation exchange reactions and received core@shell nanoparticles that, after oxidation under air, exhibit a strong LSPR in the NIR. Interestingly, the crystalline, closed ZnS shell that we grew with variable thickness still allowed a slow oxidation of the core under ambient conditions, while the core was effectively protected from reduction, even in the presence of reducing agents such as borane tert-butyamine complex and diisobutylaluminum hydride, giving rise to a stable particle LSPR, also under strongly reducing conditions. PMID:26604183

  6. Core/shell structural transformation and brittle-to-ductile transition in nanowires

    NASA Astrophysics Data System (ADS)

    Yuan, Zaoshi; Nomura, Ken-ichi; Nakano, Aiichiro

    2012-04-01

    Nanowires (NWs) exhibit thermo-mechanical properties that are distinct from their bulk properties, and their understanding is critical for the reliability, manufacturability, and optimization of a wide range of devices consisting of NWs. Here, molecular-dynamics simulation reveals a rich size-temperature "phase diagram" for the mechanical response of a zinc-oxide NW under tension. For smaller diameters and higher temperatures, transitions are found from brittle cleavage to structural transformation-mediated brittle cleavage to ductile failure. Atomistic mechanisms of the unique nano-thermo-mechanical behavior are elucidated as a consequence of surface-structural relaxation, which in particular predicts spontaneous formation of a core/shell structure under tension. The nano-thermo-mechanical phase diagram resolves controversies between previous experiments and theory, and the predicted "intrinsic" core/shell structure may find device applications.

  7. Structural investigations of core-shell nanowires using grazing incidence X-ray diffraction.

    PubMed

    Keplinger, Mario; Mårtensson, Thomas; Stangl, Julian; Wintersberger, Eugen; Mandl, Bernhard; Kriegner, Dominik; Holý, Václav; Bauer, Günther; Deppert, Knut; Samuelson, Lars

    2009-05-01

    The fabrication of core-shell structures is crucial for many nanowire device concepts. For the proper tailoring of their electronic properties, control of structural parameters such as shape, size, diameter of core and shell, their chemical composition, and information on their strain fields is mandatory. Using synchrotron X-ray diffraction studies and finite element simulations, we determined the chemical composition, dimensions, and strain distribution for series of InAs/InAsP core-shell wires grown on Si(111) with systematically varied growth parameters. In particular we detect initiation of plastic relaxation of these structures with increasing shell thickness and/or increasing phosphorus content. We establish a phase diagram, defining the region of parameters leading to pseudomorphic nanowire growth. This is important to avoid extended defects which are detrimental for their electronic properties. PMID:19320494

  8. Surface mode hybridization in the optical response of core-shell particles

    NASA Astrophysics Data System (ADS)

    Thiessen, E.; Heinisch, R. L.; Bronold, F. X.; Fehske, H.

    2016-03-01

    We present an exact rewriting of the Mie coefficients describing the scattering of light by a spherical core-shell particle which enables their interpretation in terms of a hybridization of the two surface modes arising, respectively, at the core-shell and the shell-medium interface. For this particular case, we thus obtain from the Mie theory—analytically for all multipole orders and hence for arbitrarily sized particles—the hybridization scenario, which so far has been employed primarily for small particles in the electrostatic approximation. To demonstrate the strength of the rewriting approach, we also extract the hybridization scenario for a stratified sphere directly from the expansion coefficients for the electromagnetic fields.

  9. Core-Shell Columns in High-Performance Liquid Chromatography: Food Analysis Applications

    PubMed Central

    Preti, Raffaella

    2016-01-01

    The increased separation efficiency provided by the new technology of column packed with core-shell particles in high-performance liquid chromatography (HPLC) has resulted in their widespread diffusion in several analytical fields: from pharmaceutical, biological, environmental, and toxicological. The present paper presents their most recent applications in food analysis. Their use has proved to be particularly advantageous for the determination of compounds at trace levels or when a large amount of samples must be analyzed fast using reliable and solvent-saving apparatus. The literature hereby described shows how the outstanding performances provided by core-shell particles column on a traditional HPLC instruments are comparable to those obtained with a costly UHPLC instrumentation, making this novel column a promising key tool in food analysis. PMID:27143972

  10. Progress in High-Capacity Core-Shell Cathode Materials for Rechargeable Lithium Batteries.

    PubMed

    Myung, Seung-Taek; Noh, Hyung-Joo; Yoon, Sung-June; Lee, Eung-Ju; Sun, Yang-Kook

    2014-02-20

    High-energy-density rechargeable batteries are needed to fulfill various demands such as self-monitoring analysis and reporting technology (SMART) devices, energy storage systems, and (hybrid) electric vehicles. As a result, high-energy electrode materials enabling a long cycle life and reliable safety need to be developed. To ensure these requirements, new material chemistries can be derived from combinations of at least two compounds in a secondary particle with varying chemical composition and primary particle morphologies having a core-shell structure and spherical cathode-active materials, specifically a nanoparticle core and shell, nanoparticle core and nanorod shell, and nanorod core and shell. To this end, several layer core-shell cathode materials were developed to ensure high capacity, reliability, and safety. PMID:26270835

  11. 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

  12. 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.

  13. 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.

  14. 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

  15. 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

  16. 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.

  17. 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

  18. 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

  19. 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.

  20. Epoxy-acrylic core-shell particles by seeded emulsion polymerization.

    PubMed

    Chen, Liang; Hong, Liang; Lin, Jui-Ching; Meyers, Greg; Harris, Joseph; Radler, Michael

    2016-07-01

    We developed a novel method for synthesizing epoxy-acrylic hybrid latexes. We first prepared an aqueous dispersion of high molecular weight solid epoxy prepolymers using a mechanical dispersion process at elevated temperatures, and we subsequently used the epoxy dispersion as a seed in the emulsion polymerization of acrylic monomers comprising methyl methacrylate (MMA) and methacrylic acid (MAA). Advanced analytical techniques, such as scanning transmission X-ray microscopy (STXM) and peak force tapping atomic force microscopy (PFT-AFM), have elucidated a unique core-shell morphology of the epoxy-acrylic hybrid particles. Moreover, the formation of the core-shell morphology in the seeded emulsion polymerization process is primarily attributed to kinetic trapping of the acrylic phase at the exterior of the epoxy particles. By this new method, we are able to design the epoxy and acrylic polymers in two separate steps, and we can potentially synthesize epoxy-acrylic hybrid latexes with a broad range of compositions. PMID:27078740

  1. Transforming powder mechanical properties by core/shell structure: compressible sand.

    PubMed

    Shi, Limin; Sun, Changquan Calvin

    2010-11-01

    Some active pharmaceutical ingredients possess poor mechanical properties and are not suitable for tableting. Using fine sand (silicon dioxide), we show that a core/shell structure, where a core particle (sand) is coated with a thin layer of polyvinylpyrrolidone (PVP), can profoundly improve powder compaction properties. Sand coated with 5% PVP could be compressed into intact tablets. Under a given compaction pressure, tablet tensile strength increases dramatically with the amount of coating. This is in sharp contrast to poor compaction properties of physical mixtures, where intact tablets cannot be made when PVP content is 20% or less. The profoundly improved tabletability of core/shell particles is attributed to the formation of a continuous three-dimensional bonding network in the tablet. PMID:20845444

  2. Thermo-responsive and aqueous dispersible ZnO/PNIPAM core/shell nanoparticles

    NASA Astrophysics Data System (ADS)

    Alem, Halima; Schejn, Aleksandra; Roques-Carmes, Thibault; Ghanbaja, Jaafar; Schneider, Raphaël

    2015-08-01

    In this work, we developed a new process to covalently graft a thermoresponsive polymer on the surface of fluorescent nanocrystals in order to synthesize materials that combine both responsive and fluorescent properties. For the first time, poly(N-isopropylacrylamide) (PNIPAM) was grown by activator regenerated by electron transfer-atom transfer radical polymerization (ARGET-ATRP) from ZnO quantum dots (QDs) by surface-initiated polymerization. This process allowed the formation of fluorescent and responsive ZnO/PNIPAM core/shell QDs while only requiring the use of a ppm amount of copper for the synthesis. The influence of the nature of the silanized layer and the polymerization time on the properties of the final nanomaterials were investigated. Results clearly evidence that both the PNIPAM layer thickness and the temperature affected the luminescence properties of the core/shell nanoparticles, but also that the PNIPAM layer, when it is thick enough, could stabilize the QDs’ optical properties.

  3. The composition-dependent mechanical properties of Ge/Si core shell nanowires

    NASA Astrophysics Data System (ADS)

    Liu, X. W.; Hu, J.; Pan, B. C.

    2008-09-01

    The Stillinger-Weber potential is used to study the composition-dependent Young's modulus for Ge-core/Si-shell and Si-core/Ge-shell nanowires. Here, the composition is defined as a ratio of the number of atoms of the core to the number of atoms of a core-shell nanowire. For each concerned Ge-core/Si-shell nanowire with a specified diameter, we find that its Young's modulus increases to a maximal value and then decreases as the composition increases. Whereas Young's modulus of the Si-core/Ge-shell nanowires increase nonlinearly in a wide compositional range. Our calculations reveal that these observed trends of Young's modulus of core-shell nanowires are essentially attributed to the different components of the cores and the shells, as well as the different strains in the interfaces between the cores and the shells.

  4. Controlled self-assembly of multiferroic core-shell nanoparticles exhibiting strong magneto-electric effects

    SciTech Connect

    Sreenivasulu, Gollapudi; Hamilton, Sean L.; Lehto, Piper R.; Srinivasan, Gopalan; Popov, Maksym; Chavez, Ferman A.

    2014-02-03

    Ferromagnetic-ferroelectric composites show strain mediated coupling between the magnetic and electric sub-systems due to magnetostriction and piezoelectric effects associated with the ferroic phases. We have synthesized core-shell multiferroic nano-composites by functionalizing 10–100 nm barium titanate and nickel ferrite nanoparticles with complementary coupling groups and allowing them to self-assemble in the presence of a catalyst. The core-shell structure was confirmed by electron microscopy and magnetic force microscopy. Evidence for strong strain mediated magneto-electric coupling was obtained by static magnetic field induced variations in the permittivity over 16–18 GHz and polarization and by electric field induced by low-frequency ac magnetic fields.

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

    NASA Astrophysics Data System (ADS)

    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

    2016-06-01

    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.

  6. Picomolar detection of mercuric ions by means of gold-silver core-shell nanorods

    NASA Astrophysics Data System (ADS)

    Chen, Shouhui; Liu, Dingbin; Wang, Zhihua; Sun, Xiaolian; Cui, Daxiang; Chen, Xiaoyuan

    2013-07-01

    We report an ultrasensitive and selective probe for detection of mercuric ions using gold-silver core-shell nanorods as the substrate of surface-enhanced Raman scattering. The detection limit of this probe for mercuric ions can be as low as 1 pM. The efficiency of this probe in complex samples was evaluated by allowing detection of spiked mercuric ions in river water and fish samples.We report an ultrasensitive and selective probe for detection of mercuric ions using gold-silver core-shell nanorods as the substrate of surface-enhanced Raman scattering. The detection limit of this probe for mercuric ions can be as low as 1 pM. The efficiency of this probe in complex samples was evaluated by allowing detection of spiked mercuric ions in river water and fish samples. Electronic supplementary information (ESI) available: See DOI: 10.1039/c3nr01603j

  7. General Method for the Synthesis of Ultrastable Core/Shell Quantum Dots by Aluminum Doping.

    PubMed

    Li, Zhichun; Yao, Wei; Kong, Long; Zhao, Yixin; Li, Liang

    2015-10-01

    Semiconductor quantum dots (QDs) have attracted extensive attention in various applications because of their unique optical and electronic properties. However, long-term photostability remains a challenge for their practical application. Here, we present a simple method to enhance the photostability of QDs against oxidation by doping aluminum into the shell of core/shell QDs. We demonstrate that Al in the coating shell can be oxidized to Al2O3, which can serve as a self-passivation layer on the surface of the core/shell QDs and effectively stop further photodegradation during long-term light irradiation. The prepared CdSe/CdS:Al QDs survived 24 h without significant degradation when they were subjected to intense illumination under LED light (450 nm, 0.35 W/cm(2)), whereas conventional CdSe/CdS QDs were bleached within 3 h. PMID:26389704

  8. 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.

  9. Fabrication of Te@Au core-shell hybrids for efficient ethanol oxidation

    NASA Astrophysics Data System (ADS)

    Jin, Huile; Wang, Demeng; Zhao, Yuewu; Zhou, Huan; Wang, Shun; Wang, Jichang

    2012-10-01

    Using Au nanoparticles to catalyze the oxidation of alcohols has garnered increasing attention due to its potential application in direct alcohol fuel cells. In this research Te@Au core-shell hybrids were fabricated for the catalytic oxidation of ethanol, where the preparation procedure involved the initial production of Te crystals with different microstructures and the subsequent utilization of the Te crystal as a template and reducing agent for the production of Te@Au hybrids. The as-prepared core-shell hybrids were characterized by scanning electron microscopy, transmission electron microscopy, energy-dispersive X-ray spectroscopy, and X-ray diffraction techniques. Electrochemical measurements illustrate that the hybrids have great electrocatalytic activity and stability toward ethanol oxidation in alkaline media. The enhanced electrocatalytic property may be attributed to the cooperative effects between the metal and semiconductor and the presence of a large number of active sites on the hybrids surface.

  10. 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.

  11. On axisymmetric/diamond-like mode transitions in axially compressed core-shell cylinders

    NASA Astrophysics Data System (ADS)

    Xu, Fan; Potier-Ferry, Michel

    2016-09-01

    Recent interests in curvature- and stress-induced pattern formation and pattern selection motivate the present study. Surface morphological wrinkling of a cylindrical shell supported by a soft core subjected to axial compression is investigated based on a nonlinear 3D finite element model. The post-buckling behavior of core-shell cylinders beyond the first bifurcation often leads to complicated responses with surface mode transitions. The proposed finite element framework allows predicting and tracing these bifurcation portraits from a quantitative standpoint. The occurrence and evolution of 3D instability modes including sinusoidally deformed axisymmetric patterns and non-axisymmetric diamond-like modes will be highlighted according to critical dimensionless parameters. Besides, the phase diagram obtained from dimensional analyses and numerical results could be used to guide the design of core-shell cylindrical systems to achieve the desired instability patterns.

  12. Organic phase synthesis of noble metal-zinc chalcogenide core-shell nanostructures.

    PubMed

    Kumar, Prashant; Diab, Mahmud; Flomin, Kobi; Rukenstein, Pazit; Mokari, Taleb

    2016-10-15

    Multi-component nanostructures have been attracting tremendous attention due to their ability to form novel materials with unique chemical, optical and physical properties. Development of hybrid nanostructures that are composed of metal-semiconductor components using a simple approach is of interest. Herein, we report a robust and general organic phase synthesis of metal (Au or Ag)-Zinc chalcogenide (ZnS or ZnSe) core-shell nanostructures. This synthetic protocol also enabled the growth of more compositionally complex nanostructures of Au-ZnSxSe1-x alloys and Au-ZnS-ZnSe core-shell-shell. The optical and structural properties of these hybrid nanostructures are also presented. PMID:27428852

  13. Controlled Release from Core-Shell Nanoporous Silica Particles for Corrosion Inhibition of Aluminum Alloys

    DOE PAGESBeta

    Jiang, Xingmao; Jiang, Ying-Bing; Liu, Nanguo; Xu, Huifang; Rathod, Shailendra; Shah, Pratik; Brinker, C. Jeffrey

    2011-01-01

    Ceriumore » m (Ce) corrosion inhibitors were encapsulated into hexagonally ordered nanoporous silica particles via single-step aerosol-assisted self-assembly. The core/shell structured particles are effective for corrosion inhibition of aluminum alloy AA2024-T3. Numerical simulation proved that the core-shell nanostructure delays the release process. The effective diffusion coefficient elucidated from release data for monodisperse particles in water was 1.0 × 10 − 14  m 2 s for Ce 3+ compared to 2.5 × 10 − 13  m 2 s for NaCl. The pore size, pore surface chemistry, and the inhibitor solubility are crucial factors for the application. Microporous hydrophobic particles encapsulating a less soluble corrosion inhibitor are desirable for long-term corrosion inhibition.« less

  14. Ab Initio Study of 40Ca with an Importance Truncated No-Core Shell Model

    SciTech Connect

    Roth, R; Navratil, P

    2007-05-22

    We propose an importance truncation scheme for the no-core shell model, which enables converged calculations for nuclei well beyond the p-shell. It is based on an a priori measure for the importance of individual basis states constructed by means of many-body perturbation theory. Only the physically relevant states of the no-core model space are considered, which leads to a dramatic reduction of the basis dimension. We analyze the validity and efficiency of this truncation scheme using different realistic nucleon-nucleon interactions and compare to conventional no-core shell model calculations for {sup 4}He and {sup 16}O. Then, we present the first converged calculations for the ground state of {sup 40}Ca within no-core model spaces including up to 16{h_bar}{Omega}-excitations using realistic low-momentum interactions. The scheme is universal and can be easily applied to other quantum many-body problems.

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

    SciTech Connect

    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]

  16. LaF3 core/shell nanoparticles for subcutaneous heating and thermal sensing in the second biological-window

    NASA Astrophysics Data System (ADS)

    Ximendes, Erving Clayton; Rocha, Uéslen; Kumar, Kagola Upendra; Jacinto, Carlos; Jaque, Daniel

    2016-06-01

    We report on Ytterbium and Neodymium codoped LaF3 core/shell nanoparticles capable of simultaneous heating and thermal sensing under single beam infrared laser excitation. Efficient light-to-heat conversion is produced at the Neodymium highly doped shell due to non-radiative de-excitations. Thermal sensing is provided by the temperature dependent Nd3+ → Yb3+ energy transfer processes taking place at the core/shell interface. The potential application of these core/shell multifunctional nanoparticles for controlled photothermal subcutaneous treatments is also demonstrated.

  17. Optical trapping of core-shell magnetic microparticles by cylindrical vector beams

    SciTech Connect

    Zhong, Min-Cheng; Gong, Lei; Li, Di; Zhou, Jin-Hua; Wang, Zi-Qiang; Li, Yin-Mei

    2014-11-03

    Optical trapping of core-shell magnetic microparticles is experimentally demonstrated by using cylindrical vector beams. Second, we investigate the optical trapping efficiencies. The results show that radially and azimuthally polarized beams exhibit higher axial trapping efficiencies than the Gaussian beam. Finally, a trapped particle is manipulated to kill a cancer cell. The results make possible utilizing magnetic particles for optical manipulation, which is an important advantage for magnetic particles as labeling agent in targeted medicine and biological analysis.

  18. Tailoring thermal conductivity of silicon/germanium nanowires utilizing core-shell architecture

    NASA Astrophysics Data System (ADS)

    Sarikurt, S.; Ozden, A.; Kandemir, A.; Sevik, C.; Kinaci, A.; Haskins, J. B.; Cagin, T.

    2016-04-01

    Low-dimensional nanostructured materials show large variations in their thermal transport properties. In this work, we investigate the influence of the core-shell architecture on nanowire (1D) thermal conductivity and evaluate its validity as a strategy to achieve a better thermoelectric performance. To obtain the thermal conductivity values, equilibrium molecular dynamics simulations are conducted for core-shell nanowires of silicon and germanium. To explore the parameter space, we have calculated thermal conductivity values of the Si-core/Ge-shell and Ge-core/Si-shell nanowires having different cross-sectional sizes and core contents at several temperatures. Our results indicate that (1) increasing the cross-sectional area of pristine Si and pristine Ge nanowires increases the thermal conductivity, (2) increasing the Ge core size in the Ge-core/Si-shell structure results in a decrease in the thermal conductivity at 300 K, (3) the thermal conductivity of the Si-core/Ge-shell nanowires demonstrates a minima at a specific core size, (4) no significant variation in the thermal conductivity is observed in nanowires for temperatures larger than 300 K, and (5) the predicted thermal conductivity within the frame of applied geometrical constraints is found to be around 10 W/(mK) for the Si and Ge core-shell architecture with a smooth interface. The value is still higher than the amorphous limit (1 W/(mK)). This represents a significant reduction in thermal conductivity with respect to their bulk crystalline and pristine nanowire forms. Furthermore, we observed additional suppression of thermal conductivity through the introduction of interface roughness to Si/Ge core-shell nanowires.

  19. Controllable synthesis of a novel hedgehog-like core/shell structure

    SciTech Connect

    Wang Shumin; Tian Hongwei; Pei Yanhui; Meng Qingnan; Chen Jianli; Wang Huan; Zeng Yi; Zheng Weitao; Liu Yichun

    2012-02-15

    A novel hedgehog-like core/shell structure, consisting of a high density of vertically aligned graphene sheets and a thin graphene shell/a copper core (VGs-GS/CC), has been synthesized via a simple one-step synthesis route using radio-frequency plasma-enhanced chemical vapor deposition (RF-PECVD). Scanning and transmission electron microscopy investigations show that the morphology of this core/shell material could be controlled by deposition time. For a short deposition time, only multilayer graphene shell tightly surrounds the copper particle, while as the deposition time is relative long, graphene sheets extend from the surface of GS/CC. The GS can protect CC particles from oxidation. The growth mechanism for the obtained GS/CC and VGs-GS/CC has been revealed. Compared to VGs, VGs-GS/CC material exhibits a better electron field emission property. This investigation opens a possibility for designing a core/shell structure of different carbon-metal hybrid materials for a wide variety of practical applications. - Graphical abstract: With increasing deposition time, graphene sheets extend from the surface of GS/CC, causing the multilayer graphene encapsulated copper to be converted into vertically aligned graphene sheets-graphene shell/copper core structure. Highlights: Black-Right-Pointing-Pointer A novel hedgehog-like core/shell structure has been synthesized. Black-Right-Pointing-Pointer The structure consists of vertical graphene sheets-graphene shell and copper core. Black-Right-Pointing-Pointer The morphology of VGs-GS/CC can be controlled by choosing a proper deposition time. Black-Right-Pointing-Pointer With increasing deposition time, graphene sheets extend from the surface of GS/CC. Black-Right-Pointing-Pointer VGs-GS/CC exhibits a better electron field emission property as compared with VGs.

  20. Non-volatile transistor memory devices using charge storage cross-linked core-shell nanoparticles.

    PubMed

    Lo, Chen-Tsyr; Watanabe, Yu; Oya, Hiroshi; Nakabayashi, Kazuhiro; Mori, Hideharu; Chen, Wen-Chang

    2016-06-01

    Solution processable cross-linked core-shell poly[poly(ethylene glycol)methylether methacrylate]-block-poly(2,5-dibromo-3-vinylthiophene) (poly(PEGMA)m-b-poly(DB3VT)n) nanoparticles are firstly explored as charge storage materials for transistor-type memory devices owing to their efficient and controllable ability in electric charge transfer and trapping. PMID:27180874

  1. Spatially resolved Raman spectroscopy on indium-catalyzed core-shell germanium nanowires: size effects.

    PubMed

    Xiang, Y; Zardo, I; Cao, L Y; Garma, T; Heiss, M; Morante, J R; Arbiol, J; Brongersma, M L; Fontcuberta I Morral, A

    2010-03-12

    The structure of indium-catalyzed germanium nanowires is investigated by atomic force microscopy, scanning confocal Raman spectroscopy and transmission electron microscopy. The nanowires are formed by a crystalline core and an amorphous shell. We find that the diameter of the crystalline core varies along the nanowire, down to few nanometers. Phonon confinement effects are observed in the regions where the crystalline region is the thinnest. The results are consistent with the thermally insulating behavior of the core-shell nanowires. PMID:20154375

  2. Gap state related blue light emitting boron-carbon core shell structures

    NASA Astrophysics Data System (ADS)

    Singh, Paviter; Kaur, Manpreet; Singh, Bikramjeet; Kaur, Gurpreet; Singh, Kulwinder; Kumar, Manjeet; Bala, Rajni; Thakur, Anup; Kumar, Akshay

    2016-05-01

    Boron- carbon core shell structures have been synthesized by solvo-thermal synthesis route. The synthesized material is highly pure. X-ray diffraction analysis confirms the reduction of reactants in to boron and carbon. Scanning Electron Microscopy (SEM) analysis showed that the shell is uniform with average thickness of 340 nm. Photo luminescence studies showed that the material is blue light emitting with CIE color coordinates: x=0.16085, y=0.07554.

  3. SYNTHESIS AND APPLICATIONS OF Fe3O4/SiO2 CORE-SHELL MATERIALS.

    PubMed

    Sonmez, Maria; Georgescu, Mihai; Alexandrescu, Laurentia; Gurau, Dana; Ficai, Anton; Ficai, Denisa; Andronescu, Ecaterina

    2015-01-01

    Multifunctional nanoparticles based on magnetite/silica core-shell, consisting of iron oxides coated with silica matrix doped with fluorescent components such as organic dyes (fluorescein isothiocyanate - FITC, Rhodamine 6G) or quantum dots, have drawn remarkable attention in the last years. Due to the bi-functionality of these types of nanoparticles (simultaneously having magnetic and fluorescent properties), they are successfully used in highly efficient human stem cell labeling, magnetic carrier for photodynamic therapy, drug delivery, hyperthermia and other biomedical applications. Another application of core-shell-based nanoparticles, in which the silica is functionalized with aminosilanes, is for immobilization and separation of various biological entities such as proteins, antibodies, enzymes etc. as well as in environmental applications, as adsorbents for heavy metal ions. In vitro tests on human cancerous cells, such as A549 (human lung carcinoma), breast, human cervical cancer, THP-1 (human acute monocytic leukaemia) etc. , were conducted to assess the potential cytotoxic effects that may occur upon contact of nanoparticles with cancerous tissue. Results show that core-shell nanoparticles doped with cytostatics (cisplatin, doxorubicin, etc.), are easily adsorbed by affected tissue and in some cases lead to an inhibition of cell proliferation and induce cell death by apoptosis. The goal of this review is to summarize the advances in the field of core-shell materials, particularly those based on magnetite/silica with applicability in medicine and environmental protection. This paper briefly describes synthesis methods of silica-coated magnetite nanoparticles (Stöber method and microemulsion), the method of encapsulating functional groups based on aminosilanes in silica shell, as well as applications in medicine of these types of simple or modified nanoparticles for cancer therapy, MRI, biomarker immobilization, drug delivery, biocatalysis etc., and in

  4. MAGNETIC CORE SHELL STRUCTURES: from 0D to 1D assembling.

    PubMed

    Ficai, Denisa; Ficai, Anton; Dinu, Elena; Oprea, Ovidiu; Sonmez, Maria; Keler, Memduh Kagan; Sahin, Yesim Muge; Ekren, Nazmi; Inan, Ahmet Talat; Daglilar, Sibel; Gunduz, Oguzhan

    2015-01-01

    Material research and development studies are focused on different techniques of bringing out nanomaterials with desired characteristics and properties. From the point of view of materials development, nowadays scientists are strongly focused on obtaining materials with predefined characteristics and properties. The morphology control seems to be a determinant factor and increasing attention is devoted to this aspect. At this moment it is possible to engineer the material's features by using different methods and materials combination for both medical and industrial applications. In the applications of chemistry and synthesis, biology, mechanics, optics solar cells and microelectronics tailoring the adjustable parameters of stoichiometry, chemical structure, shape and segregation are evaluated and opens new fields. Because of the magnetic features of nanoparticles and durable particle size, less than 100 nm, this study is aiming to describe their uses in practical applications. That's why the whole hydrodynamic magnetic core shell topic will be reviewed on this paper. Additionally, the properties acting in general sight in solid-state physics are utilized for material selection and for defining issue connecting the core, shell structure and their producing properties. Here, in the study of core/shell nanoparticle various physical and chemical synthesis routes and the effect of electrospun method are briefly discussed. Starting from a real void of the scientific literature, the existent data related to the 1D magnetic electrospun materials are reviewed. The perspectives in the medical, environmental or energetic sector is great and bring some real advantages related to the 0D core@shell structures because both mechanical and biological properties are dependent on the morphology of the materials. PMID:26377653

  5. Process Development of Gallium Nitride Phosphide Core-Shell Nanowire Array Solar Cell

    NASA Astrophysics Data System (ADS)

    Chuang, Chen

    Dilute Nitride GaNP is a promising materials for opto-electronic applications due to its band gap tunability. The efficiency of GaNxP1-x /GaNyP1-y core-shell nanowire solar cell (NWSC) is expected to reach as high as 44% by 1% N and 9% N in the core and shell, respectively. By developing such high efficiency NWSCs on silicon substrate, a further reduction of the cost of solar photovoltaic can be further reduced to 61$/MWh, which is competitive to levelized cost of electricity (LCOE) of fossil fuels. Therefore, a suitable NWSC structure and fabrication process need to be developed to achieve this promising NWSC. This thesis is devoted to the study on the development of fabrication process of GaNxP 1-x/GaNyP1-y core-shell Nanowire solar cell. The thesis is divided into two major parts. In the first parts, previously grown GaP/GaNyP1-y core-shell nanowire samples are used to develop the fabrication process of Gallium Nitride Phosphide nanowire solar cell. The design for nanowire arrays, passivation layer, polymeric filler spacer, transparent col- lecting layer and metal contact are discussed and fabricated. The property of these NWSCs are also characterized to point out the future development of Gal- lium Nitride Phosphide NWSC. In the second part, a nano-hole template made by nanosphere lithography is studied for selective area growth of nanowires to improve the structure of core-shell NWSC. The fabrication process of nano-hole templates and the results are presented. To have a consistent features of nano-hole tem- plate, the Taguchi Method is used to optimize the fabrication process of nano-hole templates.

  6. Photochemical processes in doped argon-neon core-shell clusters: the effect of cage size on the dissociation of molecular oxygen.

    PubMed

    Laarmann, T; Wabnitz, H; von Haeften, K; Möller, T

    2008-01-01

    The caging effect of the host environment on photochemical reactions of molecular oxygen is investigated using monochromatic synchrotron radiation and spectrally resolved fluorescence. Oxygen doped clusters are formed by coexpansion of argon and oxygen, by pickup of molecular oxygen or by multiple pickup of argon and oxygen by neon clusters. Sequential pickup provides radially ordered core-shell structures in which a central oxygen molecule is surrounded by argon layers of variable thickness inside large neon clusters. Pure argon and core-shell argon-neon clusters excited with approximately 12 eV monochromatic synchrotron radiation show strong fluorescence in the vacuum ultraviolet (vuv) spectral range. When the clusters are doped with O2, fluorescence in the visible (vis) spectral range is observed and the vuv radiation is found to be quenched. Energy-resolved vis fluorescence spectra show the 2 1Sigma+-->1 1Sigma+(ArO(1S)-->ArO(1D)) transition from argon oxide as well as the vibrational progression A '3Delta u(nu'=0)-->X 3Sigmag*(nu") of O2 indicating that molecular oxygen dissociates and occasionally recombines depending on the experimental conditions. Both the emission from ArO and O2 as well the vuv quenching by oxygen are found to depend on the excitation energy, providing evidence that the energy transfer from the photoexcited cluster to the embedded oxygen proceeds via the O2+ ground state. The O2+ decays via dissociative recombination and either reacts with Ar resulting in electronically excited ArO or it recombines to O2 within the Ar cage. Variation of the Ar layer thickness in O2-Ar-Ne core-shell clusters shows that a stable cage is formed by two solvation layers. PMID:18190199

  7. Nanocellulose Derivative/Silica Hybrid Core-Shell Chiral Stationary Phase: Preparation and Enantioseparation Performance.

    PubMed

    Zhang, Xiaoli; Wang, Litao; Dong, Shuqing; Zhang, Xia; Wu, Qi; Zhao, Liang; Shi, Yanping

    2016-01-01

    Core-shell silica microspheres with a nanocellulose derivative in the hybrid shell were successfully prepared as a chiral stationary phase by a layer-by-layer self-assembly method. The hybrid shell assembled on the silica core was formed using a surfactant as template by the copolymerization reaction of tetraethyl orthosilicate and the nanocellulose derivative bearing triethoxysilyl and 3,5-dimethylphenyl groups. The resulting nanocellulose hybrid core-shell chiral packing materials (CPMs) were characterized and packed into columns, and their enantioseparation performance was evaluated by high performance liquid chromatography. The results showed that CPMs exhibited uniform surface morphology and core-shell structures. Various types of chiral compounds were efficiently separated under normal and reversed phase mode. Moreover, chloroform and tetrahydrofuran as mobile phase additives could obviously improve the resolution during the chiral separation processes. CPMs still have good chiral separation property when eluted with solvent systems with a high content of tetrahydrofuran and chloroform, which proved the high solvent resistance of this new material. PMID:27153055

  8. Modeling heterogeneous polymer-grafted nanoparticle networks having biomimetic core-shell structure

    NASA Astrophysics Data System (ADS)

    Mbanga, Badel L.; Yashin, Victor V.; Holten-Andersen, Niels; Balazs, Anna C.

    Inspired by the remarkable mechanical properties of such biological structures as mussel adhesive fibers, we use 3D computational modeling to study the behavior of heterogeneous polymer-grafted nanoparticle (PGN) networks under tensile deformation. The building block of a PGN network is a nanoparticle with grafted polymer chains whose free ends' reactive groups can form both permanent and labile bonds with the end chains on the nearby particles. The tunable behavior of cross-linked PGN networks makes them excellent candidates for designing novel materials with enhanced mechanical properties. Here, we consider the PGN networks having the core-shell structures, in which the type and strength of the inter-particle bonds in the outer shell differ from those in the core. Using the computer simulations, we obtain and compare the ultimate tensile properties (strength, toughness, ductility) and the strain recovery properties for the uniform samples and various core-shell structures. We demonstrate that the core-shell structures could be designed to obtain highly resilient self-healing materials

  9. Au-Cu{sub 2}O core-shell nanowire photovoltaics

    SciTech Connect

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

    2015-01-12

    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-Cu{sub 2}O core-shell nanowire photovoltaic cell as a model system. Spatially resolved photocurrent maps reveal that although the minority carrier diffusion length in the Cu{sub 2}O 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. Microfluidic fabrication of cholesteric liquid crystal core-shell structures toward magnetically transportable microlasers.

    PubMed

    Chen, Lu-Jian; Gong, Ling-Li; Lin, Ya-Li; Jin, Xin-Yi; Li, Han-Ying; Li, Sen-Sen; Che, Kai-Jun; Cai, Zhi-Ping; Yang, Chaoyong James

    2016-04-01

    We report a magnetically transportable microlaser with cholesteric liquid crystal (CLC) core-shell structure, operating in band-edge mode. The dye doped CLC shells as a water-in-oil-in-water (W/O/W) double emulsion were fabricated by microfluidics. Water-dispersible Fe3O4 magnetic nanoparticles were incorporated in the inner aqueous phase by taking advantage of the immiscibility with the middle CLC oil phase. The influence of temperature and shell thickness on laser properties was discussed in detail. The non-invasive manipulation of microlasers was realized under a magnetic field. The dependence of velocity on the viscosity of the carrying fluid and size of the core-shell structure was theoretically analyzed and experimentally investigated using a prototype electromagnetic platform. We also discussed the design principles for this type of DDCLC core-shell structure. Such magnetically transportable microlasers offer promise in in-channel illumination applications requiring active control inside micro-channels. PMID:26923221

  11. Tunable core-shell particles generated from smart water-soluble chitosan seeds.

    PubMed

    Xiao, Congming; You, Rongrui; Dong, Yanrui; Zhang, Zhongxin

    2016-05-20

    A chain-like route was presented to create various core-shell particles with soft, aqueous or inorganic cores respectively. Water-soluble chitosan (WSC) gel particles were obtained through gelating the aqueous WSC solution of 0.02g/mL at its isoelectric point. Then, polyelectrolyte complexes were formed and surrounded on the outer surfaces of WSC gel particles by immersing the particles in 2wt% aqueous sodium alginate. Soft WSC cores in these core-shell particles disappeared after maintaining the particles in 1M HCl for 6h. The cores of obtained particles at this step became aqueous, and could be further transformed into inorganic ones via contacting the particles with copper sulfate and sodium sulfide aqueous solutions successively. The composition of the shell was verified with Fourier transform infrared spectroscopy. The formation of various core-shell particles was confirmed with digital photographic observation, thermogravimetric and fluorescence analyses. The whole process was a chain-like one and was able to stop at any stage to harvest a corresponding target. PMID:26917373

  12. Microstructure and electronic behavior of PtPd@Pt core-shell nanowires

    SciTech Connect

    Han, Wei-Qiang; Su, Dong; Murphy, Michael; Ward, Matthew; Sham, Tsun-Kong; Wu, Lijun; Zhu, Yimei; Hu, Yongfeng; Aoki, Toshihiro

    2010-07-19

    PtPd{at}Pt core-shell ultrathin nanowires were prepared using a one-step phase-transfer approach. The diameters of the nanowires range from 2 to 3 nm, and their lengths are up to hundreds of nanometers. Line scanning electron energy loss spectra showed that PtPd bimetallic nanowires have a core-shell structure, with a PtPd alloy core and a Pt monolayer shell. X-ray absorption near edge structure (XANES) spectra reveal that a strong Pt-Pd interaction exists in this nanowire system in that there is PtPd alloying and/or interfacial interaction. Extended x-ray absorption fine structures (EXAFS) further confirms the PtPd@Pt core-shell structure. The bimetallic nanowires were determined to be face-centered cubic structures. The long-chain organic molecules of n-dodecyl trimethylammonium bromide and octadecylamine, used as surfactants during synthesis, were clearly observed using aberration-corrected TEM operated at 80 KV. The interaction of Pt and surfactants was also revealed by EXAFS.

  13. Nanomagnetism of Core-Shell Magnetic Nanoparticles and Application in Spent Nuclear Fuel Separation

    NASA Astrophysics Data System (ADS)

    Tarsem Singh, Maninder Kaur

    This dissertation presents the study on novel core-shell magnetic nanoparticles (NPs) with unique magnetic properties. Understanding the fundamental physics of antiferromagnetic - ferromagnetic interactions is essential to apply in different applications. Chromium (Cr) doped and undoped core-shell iron/iron-oxide NPs have been synthesized using cluster deposition system and studied with respect to their nanostructures, morphologies, sizes, chemical composition and magnetic properties. The room-temperature magnetic properties of Fe based NPs shows the strong dependence of intra/inter-particle interaction on NP size. The Cr-doped Fe NP shows the origin of sigma-FeCr phase at very low Cr concentration (2 at.%) unlike others reported at high Cr content and interaction reversal from dipolar to exchange interaction. A theoretical model of watermelon is constructed based on the experimental results and core-shell NP system in order to explain the physics of exchange interaction in Cr-doped Fe particles. The magnetic nanoparticle---chelator separation nanotechnology is investigated for spent nuclear fuel recycling and is reported 97% and 80% of extraction for Am(III) and Pu(IV) actinides respectively. If the long-term heat generating actinides such as Am(III) can be efficiently removed from the used fuel raffinates, the volume of material that can be placed in a given amount of repository space can be significantly increased. As it is a simple, versatile, compact, and cost efficient process that minimizes secondary waste and improves storage performance.

  14. Solution-Blown Core-Shell Self-Healing Nano- and Microfibers.

    PubMed

    Lee, Min Wook; Yoon, Sam S; Yarin, Alexander L

    2016-02-24

    Self-healing microfibers with core-shell geometry were studied. A commercial binary epoxy was encased in solution-blown polymer nano-/microfibers in the 0.2-2.6 μm diameter range. The core-shell microfibers were formed by coaxial nozzles, which encapsulated the epoxy resin and its hardener in separate cores. Solution blowing, the fiber-forming process used in this work, was at least 30 times faster than the electrospinning method used previously and has already been scaled up to the industrial level. These core-shell microfibers show self-healing capability, in which epoxy and hardener are released from the cores of damaged fibers, resulting in polymerization. The epoxy used had a higher strength and shorter solidification time than poly(dimethylsiloxane) (PDMS) used previously. Also, the larger fiber diameters in the present study facilitated faster release of the epoxy resin and its hardener from the fiber cores, shortening the solidification time in comparison to the previous studies. Blister tests were conducted, which measured the adhesion energy of microfiber mats to substrates and the cohesion energy between layers of microfiber mats before and after fatigue damage followed by self-healing. PMID:26836581

  15. Core-Shell CdS-Cu₂S Nanorod Array Solar Cells.

    PubMed

    Wong, Andrew Barnabas; Brittman, Sarah; Yu, Yi; Dasgupta, Neil P; Yang, Peidong

    2015-06-10

    As an earth-abundant p-type semiconductor, copper sulfide (Cu2S) is an attractive material for application in photovoltaic devices. However, it suffers from a minority carrier diffusion length that is less than the length required for complete light absorption. Core-shell nanowires and nanorods have the potential to alleviate this difficulty because they decouple the length scales of light absorption and charge collection. To achieve this geometry using Cu2S, cation exchange was applied to an array of CdS nanorods to produce well-defined CdS-Cu2S core-shell nanorods. Previous work has demonstrated single-nanowire photovoltaic devices from this material system, but in this work, the cation exchange chemistry has been applied to nanorod arrays to produce ensemble-level devices with microscale sizes. The core-shell nanorod array devices show power conversion efficiencies of up to 3.8%. In addition, these devices are stable when measured in air after nearly one month of storage in a desiccator. These results are a first step in the development of large-area nanostructured Cu2S-based photovoltaics that can be processed from solution. PMID:25993088

  16. PMMA/PMMA core-shell particles with ellipsoidal, fluorescent cores: accessing rotational dynamics.

    PubMed

    Klein, Matthias K; Klinkenberg, Nele; Schuetter, Stefan; Saenger, Nicolai; Pfleiderer, Patrick; Zumbusch, Andreas

    2015-03-10

    For several decades, nonaqueous dispersions of PMMA particles have played an important role in colloid research. They have found application as colloidal model systems, which are used to probe glassy dynamics or to explore crystal nucleation. To date, most research has focused on spherical particles, in which only translational motion can be investigated. Recently, however, there has been a surge of interest in analyzing also rotational dynamics. In this contribution, we introduce a new class of core-shell particles, which can be used as rotational probes. The colloids described herein are composed of shape anisotropic, fluorescent cores covered with nonfluorescent PMMA shells. The core-shell particles are built up in four steps. In a first step, we produce fluorescent and photo-cross-linkable PMMA colloids. In the second step, these particles are thermomechanically elongated and fixed in defined ellipsoidal shapes by photo-cross-linking. Subsequently, we cover the cross-linked, fluorescent core with a nonfluorescent PMMA shell. The shape of the resulting core-shell colloids is tunable between the initial anisotropic and perfect spherical shape. For shaping, we apply a simple solvent swelling procedure. As one option, this method yields perfect PMMA spheres with ellipsoidal, fluorescent centers. We also report morphological particle characterization using various fluorescence microscopy techniques. Finally, we demonstrate that the rotational dynamics of individual colloids can be tracked and analyzed. PMID:25654438

  17. Vertically aligned P(VDF-TrFE) core-shell structures on flexible pillar arrays

    PubMed Central

    Choi, Yoon-Young; Yun, Tae Gwang; Qaiser, Nadeem; Paik, Haemin; Roh, Hee Seok; Hong, Jongin; Hong, Seungbum; Han, Seung Min; No, Kwangsoo

    2015-01-01

    PVDF and P(VDF-TrFE) nano- and micro- structures have been widely used due to their potential applications in several fields, including sensors, actuators, vital sign transducers, and energy harvesters. In this study, we developed vertically aligned P(VDF-TrFE) core-shell structures using high modulus polyurethane acrylate (PUA) pillars as the support structure to maintain the structural integrity. In addition, we were able to improve the piezoelectric effect by 1.85 times from 40 ± 2 to 74 ± 2 pm/V when compared to the thin film counterpart, which contributes to the more efficient current generation under a given stress, by making an effective use of the P(VDF-TrFE) thin top layer as well as the side walls. We attribute the enhancement of piezoelectric effects to the contributions from the shell component and the strain confinement effect, which was supported by our modeling results. We envision that these organic-based P(VDF-TrFE) core-shell structures will be used widely as 3D sensors and power generators because they are optimized for current generations by utilizing all surface areas, including the side walls of core-shell structures. PMID:26040539

  18. Gold/Copper Sulphide core/shell nanoparticles for Photothermal Therapy

    NASA Astrophysics Data System (ADS)

    Bala Lakshmanan, Santana; Zou, Xiaoju; Chen, Wei

    2011-10-01

    One of the biggest successes in photothermal therapy (PTT) is the use of gold (Au) nanoparticles. But its disadvantage is that it is too expensive and in addition the NIR absorption in gold nanostructures is from surface plasmon resonance which is dependent on the dielectric constant of the surrounding matrix. Thus the plasmon absorption maxima would shift for in-vivo observations compared to in-vitro. Alternatively, Copper sulphide (CuS) nanoparticles, developed recently, have also been used for PTT. Their advantage over gold nanostructures is that they have NIR absorption around 1100 nm which originates from the d-d transition of Cu2+ ions unlike surface plasmon resonance in gold nanostructures. Therefore, in this paper, we combined the above two nanoparticle systems and developed a new type of agent -Gold/Copper Sulphide (Au/CuS) core/shell nanostructure that has better photothermal conversion efficiency and also overcomes the limitations of the existing nanoparticle systems for PTT. The TEM results confirmed the core/shell structure of Au/CuS nanostructures. From UV-Vis-NIR spectrometer we obtained that these core/shell nanostructures have maximum absorbance at 1100 nm and absorption intensity much higher than only Au and only CuS nanoparticles systems. This, in turn attributed to the relatively high photothermal conversion efficiency of Au/CuS nanostructures.

  19. Directed Fluid Flow Produced by Arrays of Magnetically Actuated Core-Shell Biomimetic Cilia

    NASA Astrophysics Data System (ADS)

    Fiser, B. L.; Shields, A. R.; Evans, B. A.; Superfine, R.

    2010-03-01

    We have developed a novel core-shell microstructure that we use to fabricate arrays of flexible, magnetically actuated biomimetic cilia. Our biomimetic cilia mimic the size and beat shape of biological cilia in order to replicate the transport of fluid driven by cilia in many biological systems including the determination of left-right asymmetry in the vertebrate embryonic nodal plate and mucociliary clearance in the lung. Our core-shell structures consist of a flexible poly(dimethylsiloxane) (PDMS) core surrounded by a shell of nickel approximately forty nanometers thick; by using a core-shell structure, we can tune the mechanical and magnetic properties independently. We present the fabrication process and the long-range transport that occurs above the beating biomimetic cilia tips and will report on progress toward biomimetic cilia induced flow in viscoelastic fluids similar to mucus in the human airway. These flows may have applications in photonics and microfluidics, and our structures may be further useful as sensors or actuators in microelectromechanical systems.

  20. Novel Organically Modified Core-Shell Clay for Epoxy Composites-"SOBM Filler 1".

    PubMed

    Iheaturu, Nnamdi Chibuike; Madufor, Innocent Chimezie

    2014-01-01

    Preparation of a novel organically modified clay from spent oil base drilling mud (SOBM) that could serve as core-shell clay filler for polymers is herein reported. Due to the hydrophilic nature of clay, its compatibility with polymer matrix was made possible through modification of the surface of the core clay sample with 3-aminopropyltriethoxysilane (3-APTES) compound prior to its use. Fourier transform infrared (FT-IR) spectroscopy was used to characterize clay surface modification. Electron dispersive X-ray diffraction (EDX) and scanning electron microscopy (SEM) were used to expose filler chemical composition and morphology, while electrophoresis measurement was used to examine level of filler dispersion. Results show an agglomerated core clay powder after high temperature treatment, while EDX analysis shows that the organically modified clay is composed of chemical inhomogeneities, wherein elemental compositions in weight percent vary from one point to the other in a probe of two points. Micrographs of the 3-APTES coupled SOBM core-shell clay filler clearly show cloudy appearance, while FT-IR indicates 25% and 5% increases in fundamental vibrations band at 1014 cm(-1) and 1435 cm(-1), respectively. Furthermore, 3-APTES coupled core-shell clay was used to prepare epoxy composites and tested for mechanical properties. PMID:27355022

  1. Non-resonant Mie scattering: Emergent optical properties of core-shell polymer nanowires

    PubMed Central

    Khudiyev, Tural; Huseyinoglu, Ersin; Bayindir, Mehmet

    2014-01-01

    We provide the in-depth characterization of light-polymer nanowire interactions in the context of an effective Mie scattering regime associated with low refractive index materials. Properties of this regime sharply contrast with these of resonant Mie scattering, and involve the formation of strictly forward-scattered and coupling-free optical fields in the vicinity of core-shell polymer nanowires. Scattering from these optical fields is shown to be non-resonant in nature and independent from incident polarization. In order to demonstrate the potential utility of this scattering regime in one-dimensional (1D) polymeric nanostructures, we fabricate polycarbonate (PC) - polyvinylidene difluoride (PVDF) core-shell nanowires using a novel iterative thermal drawing process that yields uniform and indefinitely long core-shell nanostructures. These nanowires are successfully engineered for novel nanophotonics applications, including size-dependent structural coloration, efficient light capture on thin-film solar cells, optical nano-sensors with ultrahigh sensitivity and a mask-free photolithography method suitable for the straightforward production of 1D nanopatterns. PMID:24714206

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

    DOE PAGESBeta

    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 joiningmore » 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.« less

  3. Computational Atomistic Modeling of Bi-Magnetic Core-Shell Nanoparticles

    NASA Astrophysics Data System (ADS)

    Sahay, Rahul; Peralta, Juan; Caruntu, Gabriel

    Since its discovery, there has been an increasing interest in the modeling of magnetic phenomena found in materials that present exchange bias. In particular, ferro-antiferromagnetic core-shell nanoparticles are an interesting case in which the magnetic properties of the nanostructure can be altered by adjusting their size, shape, and composition. Here we present a computational scheme that efficiently models the magnetic behavior of bi-magnetic core-shell nanostructures. Using a Heisenberg-Dirac-van Vleck Hamiltonian in combination with a continuous spin model, we simulate a wide range of hysteresis diagrams displaying exchange bias. Furthermore, we will demonstrate our efforts towards improving the efficiency of the simulation algorithms, aiming to afford magnetic atomistic simulations of large nanostructures by using a method based on a tessellated unit sphere to account for spin orientations. Our results allow for further semi-quantitative comparisons with existing experimental data and provide a means to discover new phenomena associated with these core-shell nanoparticles and other nanostructures. NSF DMR-1206920.

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

    PubMed

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

    2015-12-14

    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. PMID:26556382

  5. Multi-photon excited luminescence of magnetic FePt core-shell nanoparticles

    PubMed Central

    Seemann, K.M.; Kuhn, B.

    2014-01-01

    We present magnetic FePt nanoparticles with a hydrophilic, inert, and biocompatible silico-tungsten oxide shell. The particles can be functionalized, optically detected, and optically manipulated. To show the functionalization the fluorescent dye NOPS was bound to the FePt core-shell nanoparticles with propyl-triethoxy-silane linkers and fluorescence of the labeled particles were observed in ethanol (EtOH). In aqueous dispersion the NOPS fluorescence is quenched making them invisible using 1-photon excitation. However, we observe bright luminescence of labeled and even unlabeled magnetic core-shell nanoparticles with multi-photon excitation. Luminescence can be detected in the near ultraviolet and the full visible spectral range by near infrared multi-photon excitation. For optical manipulation, we were able to drag clusters of particles, and maybe also single particles, by a focused laser beam that acts as optical tweezers by inducing an electric dipole in the insulated metal nanoparticles. In a first application, we show that the luminescence of the core-shell nanoparticles is bright enough for in vivo multi-photon imaging in the mouse neocortex down to cortical layer 5. PMID:25071977

  6. Coercivity enhancement in Ce-Fe-B based magnets by core-shell grain structuring

    NASA Astrophysics Data System (ADS)

    Ito, M.; Yano, M.; Sakuma, N.; Kishimoto, H.; Manabe, A.; Shoji, T.; Kato, A.; Dempsey, N. M.; Givord, D.; Zimanyi, G. T.

    2016-05-01

    Ce-based R2Fe14B (R= rare-earth) nano-structured permanent magnets consisting of (Ce,Nd)2Fe14B core-shell grains separated by a non-magnetic grain boundary phase, in which the relative amount of Nd to Ce is higher in the shell of the magnetic grain than in its core, were fabricated by Nd-Cu infiltration into (Ce,Nd)2Fe14B hot-deformed magnets. The coercivity values of infiltrated core-shell structured magnets are superior to those of as-hot-deformed magnets with the same overall Nd content. This is attributed to the higher value of magnetocrystalline anisotropy of the shell phase in the core-shell structured infiltrated magnets compared to the homogeneous R2Fe14B grains of the as-hot-deformed magnets, and to magnetic isolation of R2Fe14B grains by the infiltrated grain boundary phase. First order reversal curve (FORC) diagrams suggest that the higher anisotropy shell suppresses initial magnetization reversal at the edges and corners of the R2Fe14B grains.

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

    PubMed

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

    2016-03-21

    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[combining macron]. 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. PMID:26931335

  8. Agx@WO3 core-shell nanostructure for LSP enhanced chemical sensors

    PubMed Central

    Xu, Lijie; Yin, Ming-Li; (Frank) Liu, Shengzhong

    2014-01-01

    Exceptional properties of graphene have triggered intensive research on other 2D materials. Surface plasmon is another subject being actively explored for many applications. Herein we report a new class of core-shell nanostructure in which the shell is made of a 2D material for effective plasmonic propagation. We have designed a much enhanced chemical sensor made of plasmonic Agx@(2D-WO3) that combines above advantages. Specifically, the sensor response increases from 38 for Agx-WO3 mixture to 217 for the Agx@(2D-WO3) core-shell structure; response and recovery time are shortened considerably to 2 and 5 seconds; and optimum sensor working temperature is lowered from 370°C to 340°C. Light irradiation is found to increase the Agx@(2D-WO3) sensor response, particularly at blue wavelength where it resonates with the absorption of Ag nanoparticles. Raman scattering shows significantly enhanced intensity for both the 2D-WO3 shell and surface adsorbates. Both the resonance sensor enhancement and the Raman suggest that the improved sensor performance is due to nanoplasmonic mechanism. It is demonstrated that (1) 2D material can be used as the shell component of a core-shell nanostructure, and (2) surface plasmon can effectively boost sensor performance. PMID:25339285

  9. Enhanced Electrorheological Properties of Elastomers Containing TiO₂/Urea Core-Shell Particles.

    PubMed

    Niu, Chenguang; Dong, Xufeng; Qi, Min

    2015-11-11

    Polar molecule-coated core-shell particles have been used to prepare electrorheological (ER) fluids with high performance. Inspired by those studies, TiO2/urea core-shell structured particles were fabricated and used to prepare novel ER elastomers, whose properties were compared with the ER elastomers with bare TiO2 particles. Particles characterization results illustrate the TiO2/urea particles present little change in size, morphology and crystal structure with respect to the bare amorphous TiO2 particles, while clear core-shell structure is observed. Compared with the bare TiO2 particles filled elastomer, the TiO2/urea particles filled elastomer presents higher dielectric constant, indicating enhanced polarization. The viscoelastic properties of the two elastomers under different strain amplitude, frequency and electric field were tested. The results indicate that the TiO2/urea particles filled elastomer shows higher storage modulus G' and higher relative ER effect within the low field strength region from 0 to 2 kV/mm. Coating polar molecules is an effective method to improve the ER performance for ER elastomers. PMID:26492099

  10. Core-Shell Processing of Natural Pigment: Upper Palaeolithic Red Ochre from Lovas, Hungary.

    PubMed

    Sajó, István E; Kovács, János; Fitzsimmons, Kathryn E; Jáger, Viktor; Lengyel, György; Viola, Bence; Talamo, Sahra; Hublin, Jean-Jacques

    2015-01-01

    Ochre is the common archaeological term for prehistoric pigments. It is applied to a range of uses, from ritual burials to cave art to medications. While a substantial number of Palaeolithic paint mining pits have been identified across Europe, the link between ochre use and provenance, and their antiquity, has never yet been identified. Here we characterise the mineralogical signature of core-shell processed ochre from the Palaeolithic paint mining pits near Lovas in Hungary, using a novel integration of petrographic and mineralogical techniques. We present the first evidence for core-shell processed, natural pigment that was prepared by prehistoric people from hematitic red ochre. This involved combining the darker red outer shell with the less intensely coloured core to efficiently produce an economical, yet still strongly coloured, paint. We demonstrate the antiquity of the site as having operated between 14-13 kcal BP, during the Epigravettian period. This is based on new radiocarbon dating of bone artefacts associated with the quarry site. The dating results indicate the site to be the oldest known evidence for core-shell pigment processing. We show that the ochre mined at Lovas was exported from the site based on its characteristic signature at other archaeological sites in the region. Our discovery not only provides a methodological framework for future characterisation of ochre pigments, but also provides the earliest known evidence for "value-adding" of products for trade. PMID:26147808

  11. Energy-Cascaded Upconversion in an Organic Dye-Sensitized Core/Shell Fluoride Nanocrystal.

    PubMed

    Chen, Guanying; Damasco, Jossana; Qiu, Hailong; Shao, Wei; Ohulchanskyy, Tymish Y; Valiev, Rashid R; Wu, Xiang; Han, Gang; Wang, Yan; Yang, Chunhui; Ågren, Hans; Prasad, Paras N

    2015-11-11

    Lanthanide-doped upconversion nanoparticles hold promises for bioimaging, solar cells, and volumetric displays. However, their emission brightness and excitation wavelength range are limited by the weak and narrowband absorption of lanthanide ions. Here, we introduce a concept of multistep cascade energy transfer, from broadly infrared-harvesting organic dyes to sensitizer ions in the shell of an epitaxially designed core/shell inorganic nanostructure, with a sequential nonradiative energy transfer to upconverting ion pairs in the core. We show that this concept, when implemented in a core-shell architecture with suppressed surface-related luminescence quenching, yields multiphoton (three-, four-, and five-photon) upconversion quantum efficiency as high as 19% (upconversion energy conversion efficiency of 9.3%, upconversion quantum yield of 4.8%), which is about ~100 times higher than typically reported efficiency of upconversion at 800 nm in lanthanide-based nanostructures, along with a broad spectral range (over 150 nm) of infrared excitation and a large absorption cross-section of 1.47 × 10(-14) cm(2) per single nanoparticle. These features enable unprecedented three-photon upconversion (visible by naked eye as blue light) of an incoherent infrared light excitation with a power density comparable to that of solar irradiation at the Earth surface, having implications for broad applications of these organic-inorganic core/shell nanostructures with energy-cascaded upconversion. PMID:26487489

  12. Novel Organically Modified Core-Shell Clay for Epoxy Composites—“SOBM Filler 1”

    PubMed Central

    Iheaturu, Nnamdi Chibuike; Madufor, Innocent Chimezie

    2014-01-01

    Preparation of a novel organically modified clay from spent oil base drilling mud (SOBM) that could serve as core-shell clay filler for polymers is herein reported. Due to the hydrophilic nature of clay, its compatibility with polymer matrix was made possible through modification of the surface of the core clay sample with 3-aminopropyltriethoxysilane (3-APTES) compound prior to its use. Fourier transform infrared (FT-IR) spectroscopy was used to characterize clay surface modification. Electron dispersive X-ray diffraction (EDX) and scanning electron microscopy (SEM) were used to expose filler chemical composition and morphology, while electrophoresis measurement was used to examine level of filler dispersion. Results show an agglomerated core clay powder after high temperature treatment, while EDX analysis shows that the organically modified clay is composed of chemical inhomogeneities, wherein elemental compositions in weight percent vary from one point to the other in a probe of two points. Micrographs of the 3-APTES coupled SOBM core-shell clay filler clearly show cloudy appearance, while FT-IR indicates 25% and 5% increases in fundamental vibrations band at 1014 cm−1 and 1435 cm−1, respectively. Furthermore, 3-APTES coupled core-shell clay was used to prepare epoxy composites and tested for mechanical properties. PMID:27355022

  13. Nanowire-in-microtube structured core/shell fibers via multifluidic coaxial electrospinning.

    PubMed

    Chen, Hongyan; Wang, Nü; Di, Jiancheng; Zhao, Yong; Song, Yanlin; Jiang, Lei

    2010-07-01

    A multifluidic coaxial electrospinning approach is reported here to fabricate core/shell ultrathin fibers with a novel nanowire-in-microtube structure from more optional fluid pairs than routine coaxial electrospinning. The advantage of this approach lies in the fact that it introduces an extra middle fluid between the core and shell fluids of traditional coaxial electrospinning, which can work as an effective spacer to decrease the interaction of the other two fluids. Under the protection of a proper middle fluid, more fluid pairs, even mutually miscible fluids, can be operated to generate "sandwich"-structured ultrathin fibers with a sharp boundary between the core and shell materials. It thereby largely extends the scope of optional materials. Selectively removing the middle layer of the as-prepared fibers results in an interesting nanowire-in-microtube structure. Either homogeneous or heterogeneous fibers with well-tailored sandwich structures have been successfully fabricated. This method is an important extension of traditional co-electrospinning that affords a more universal avenue to preparing core/shell fibers; moreover, the special hollow cavity structure may introduce some extra properties into the conventional core/shell structure, which may find potential applications such as optical applications, microelectronics, and others. PMID:20337483

  14. Identification and characteristics of ZnO/MgO core-shell nanowires

    SciTech Connect

    Yang, S. Wang, L.; Wang, Y.; Li, L.; Wang, T.; Jiang, Z.

    2015-03-15

    In this paper, ZnO/MgO core-shell nanowires are synthesized based on a one-step chemical vapor deposition (CVD) method. The scanning electron microscopy (SEM) images of core-shell nanowires indicate that Mg addition has little influence on the morphology of the synthesizing products. High crystalline quality ZnO/MgO core-shell nanowires instead of ZnMgO ternary compounds are identified by X-ray diffraction (XRD) patterns, transmission electron microscopy (TEM) images, selected area electron diffraction (SAED) pattern and photoluminescence (PL) spectra. The experimental results show that the ultraviolet (UV) emission of these samples with MgO shell is 12 times higher than that of the corresponding bare ZnO nanowires, and the suppression of the green emission is only 1/45 of the bare ZnO nanowires. It is also found that PL properties are proportional to Mg ratio. The UV emission enhancement and green emission suppression are due to the passivation of surface defects and the improvement of ZnO crystalline quality. The results are very useful for the development of optical devices based on nanowires.

  15. Synthesis and characterization of core-shell Fe3O4-gold-chitosan nanostructure

    PubMed Central

    2012-01-01

    Background Fe3O4-gold-chitosan core-shell nanostructure can be used in biotechnological and biomedical applications such as magnetic bioseparation, water and wastewater treatment, biodetection and bioimaging, drug delivery, and cancer treatment. Results Magnetite nanoparticles with an average size of 9.8 nm in diameter were synthesized using the chemical co-precipitation method. A gold-coated Fe3O4 monotonous core-shell nanostructure was produced with an average size of 15 nm in diameter by glucose reduction of Au3+ which is then stabilized with a chitosan cross linked by formaldehyde. The results of analyses with X-ray diffraction (XRD), Fourier Transformed Infrared Spectroscopy (FTIR), Transmission Electron Microscopy (TEM), and Atomic Force Microscopy (AFM) indicated that the nanoparticles were regularly shaped, and agglomerate-free, with a narrow size distribution. Conclusions A rapid, mild method for synthesizing Fe3O4-gold nanoparticles using chitosan was investigated. A magnetic core-shell-chitosan nanocomposite, including both the supermagnetic properties of iron oxide and the optical characteristics of colloidal gold nanoparticles, was synthesized. PMID:22221555

  16. Vertically aligned P(VDF-TrFE) core-shell structures on flexible pillar arrays

    SciTech Connect

    Choi, Yoon-Young; Yun, Tae Gwang; Qaiser, Nadeem; Paik, Haemin; Roh, Hee Seok; Hong, Jongin; Hong, Seungbum; Han, Seung Min; No, Kwangsoo

    2015-06-04

    PVDF and P(VDF-TrFE) nano- and micro- structures are widely used due to their potential applications in several fields, including sensors, actuators, vital sign transducers, and energy harvesters. In this study, we developed vertically aligned P(VDF-TrFE) core-shell structures using high modulus polyurethane acrylate (PUA) pillars as the support structure to maintain the structural integrity. In addition, we were able to improve the piezoelectric effect by 1.85 times from 40 ± 2 to 74 ± 2 pm/V when compared to the thin film counterpart, which contributes to the more efficient current generation under a given stress, by making an effective use of the P(VDF-TrFE) thin top layer as well as the side walls. We attribute the enhancement of piezoelectric effects to the contributions from the shell component and the strain confinement effect, which was supported by our modeling results. We envision that these organic-based P(VDF-TrFE) core-shell structures will be used widely as 3D sensors and power generators because they are optimized for current generations by utilizing all surface areas, including the side walls of core-shell structures.

  17. Vertically aligned P(VDF-TrFE) core-shell structures on flexible pillar arrays

    DOE PAGESBeta

    Choi, Yoon-Young; Yun, Tae Gwang; Qaiser, Nadeem; Paik, Haemin; Roh, Hee Seok; Hong, Jongin; Hong, Seungbum; Han, Seung Min; No, Kwangsoo

    2015-06-04

    PVDF and P(VDF-TrFE) nano- and micro- structures are widely used due to their potential applications in several fields, including sensors, actuators, vital sign transducers, and energy harvesters. In this study, we developed vertically aligned P(VDF-TrFE) core-shell structures using high modulus polyurethane acrylate (PUA) pillars as the support structure to maintain the structural integrity. In addition, we were able to improve the piezoelectric effect by 1.85 times from 40 ± 2 to 74 ± 2 pm/V when compared to the thin film counterpart, which contributes to the more efficient current generation under a given stress, by making an effective use ofmore » the P(VDF-TrFE) thin top layer as well as the side walls. We attribute the enhancement of piezoelectric effects to the contributions from the shell component and the strain confinement effect, which was supported by our modeling results. We envision that these organic-based P(VDF-TrFE) core-shell structures will be used widely as 3D sensors and power generators because they are optimized for current generations by utilizing all surface areas, including the side walls of core-shell structures.« less

  18. Vertically aligned P(VDF-TrFE) core-shell structures on flexible pillar arrays.

    PubMed

    Choi, Yoon-Young; Yun, Tae Gwang; Qaiser, Nadeem; Paik, Haemin; Roh, Hee Seok; Hong, Jongin; Hong, Seungbum; Han, Seung Min; No, Kwangsoo

    2015-01-01

    PVDF and P(VDF-TrFE) nano- and micro- structures have been widely used due to their potential applications in several fields, including sensors, actuators, vital sign transducers, and energy harvesters. In this study, we developed vertically aligned P(VDF-TrFE) core-shell structures using high modulus polyurethane acrylate (PUA) pillars as the support structure to maintain the structural integrity. In addition, we were able to improve the piezoelectric effect by 1.85 times from 40 ± 2 to 74 ± 2 pm/V when compared to the thin film counterpart, which contributes to the more efficient current generation under a given stress, by making an effective use of the P(VDF-TrFE) thin top layer as well as the side walls. We attribute the enhancement of piezoelectric effects to the contributions from the shell component and the strain confinement effect, which was supported by our modeling results. We envision that these organic-based P(VDF-TrFE) core-shell structures will be used widely as 3D sensors and power generators because they are optimized for current generations by utilizing all surface areas, including the side walls of core-shell structures. PMID:26040539

  19. Core-Shell Processing of Natural Pigment: Upper Palaeolithic Red Ochre from Lovas, Hungary

    PubMed Central

    Sajó, István E.; Kovács, János; Fitzsimmons, Kathryn E.; Jáger, Viktor; Lengyel, György; Viola, Bence; Talamo, Sahra; Hublin, Jean-Jacques

    2015-01-01

    Ochre is the common archaeological term for prehistoric pigments. It is applied to a range of uses, from ritual burials to cave art to medications. While a substantial number of Palaeolithic paint mining pits have been identified across Europe, the link between ochre use and provenance, and their antiquity, has never yet been identified. Here we characterise the mineralogical signature of core-shell processed ochre from the Palaeolithic paint mining pits near Lovas in Hungary, using a novel integration of petrographic and mineralogical techniques. We present the first evidence for core-shell processed, natural pigment that was prepared by prehistoric people from hematitic red ochre. This involved combining the darker red outer shell with the less intensely coloured core to efficiently produce an economical, yet still strongly coloured, paint. We demonstrate the antiquity of the site as having operated between 14–13 kcal BP, during the Epigravettian period. This is based on new radiocarbon dating of bone artefacts associated with the quarry site. The dating results indicate the site to be the oldest known evidence for core-shell pigment processing. We show that the ochre mined at Lovas was exported from the site based on its characteristic signature at other archaeological sites in the region. Our discovery not only provides a methodological framework for future characterisation of ochre pigments, but also provides the earliest known evidence for “value-adding” of products for trade. PMID:26147808

  20. Controllable synthesis of a novel hedgehog-like core/shell structure

    NASA Astrophysics Data System (ADS)

    Wang, Shumin; Tian, Hongwei; Pei, Yanhui; Meng, Qingnan; Chen, Jianli; Wang, Huan; Zeng, Yi; Zheng, Weitao; Liu, Yichun

    2012-02-01

    A novel hedgehog-like core/shell structure, consisting of a high density of vertically aligned graphene sheets and a thin graphene shell/a copper core (VGs-GS/CC), has been synthesized via a simple one-step synthesis route using radio-frequency plasma-enhanced chemical vapor deposition (RF-PECVD). Scanning and transmission electron microscopy investigations show that the morphology of this core/shell material could be controlled by deposition time. For a short deposition time, only multilayer graphene shell tightly surrounds the copper particle, while as the deposition time is relative long, graphene sheets extend from the surface of GS/CC. The GS can protect CC particles from oxidation. The growth mechanism for the obtained GS/CC and VGs-GS/CC has been revealed. Compared to VGs, VGs-GS/CC material exhibits a better electron field emission property. This investigation opens a possibility for designing a core/shell structure of different carbon-metal hybrid materials for a wide variety of practical applications.

  1. Ablation characteristics of electrospun core-shell nanofiber by femtosecond laser.

    PubMed

    Park, ChangKyoo; Xue, Ruipeng; Lannutti, John J; Farson, Dave F

    2016-08-01

    This study examined the femtosecond laser ablation properties of core and shell polymers their relationship to the ablation characteristics of core-shell nanofibers. The single-pulse ablation threshold of bulk polycaprolactone (PCL) was measured to be 2.12J/cm(2) and that of bulk polydimethylsiloxane (PDMS) was 4.07J/cm(2). The incubation coefficients were measured to be 0.82±0.02 for PCL and 0.53±0.03 for PDMS. PDMS-PCL core-shell and pure PCL nanofibers were fabricated by electrospinning. The energy/volume of pure PCL and PDMS-PCL core-shell nanofiber ablation was investigated by measuring linear ablation grooves made at different scanning speeds. At large scanning speed, higher energy/volume was required for machining PDMS-PCL nanofiber than for PCL nanofiber. However, at small scanning speed, comparable energy/volume was measured for PDMS-PCL and PCL nanofiber ablation. Additionally, in linear scanned ablation of PDMS-PCL fibers at small laser pulse energy and large scanning speed, there were partially ablated fibers where the shell was ablated but the core remained. This was attributed to the lower ablation threshold of the shell material. PMID:27157748

  2. Exploring meso-/microporous composite molecular sieves with core-shell structures.

    PubMed

    Qian, Xufang F; Li, Bin; Hu, Yuanyuan Y; Niu, Guoxing X; Zhang, D Yahong H; Che, Renchao C; Tang, Yi; Su, Dangsheng S; Asiri, Abdullah M; Zhao, Dongyuan Y

    2012-01-16

    A series of core-shell-structured composite molecular sieves comprising zeolite single crystals (i.e., ZSM-5) as a core and ordered mesoporous silica as a shell were synthesized by means of a surfactant-directed sol-gel process in basic medium by using cetyltrimethylammonium bromide (CTAB) as a template and tetraethylorthosilicate (TEOS) as silica precursor. Through this coating method, uniform mesoporous silica shells closely grow around the anisotropic zeolite single crystals, the shell thickness of which can easily be tuned in the range of 15-100 nm by changing the ratio of TEOS/zeolite. The obtained composite molecular sieves have compact meso-/micropore junctions that form a hierarchical pore structure from ordered mesopore channels (2.4-3.0 nm in diameter) to zeolite micropores (≈0.51 nm). The short-time kinetic diffusion efficiency of benzene molecules within pristine ZSM-5 (≈7.88×10(-19)  m(2)  s(-1)) is almost retainable after covering with 75 nm-thick mesoporous silica shells (≈7.25×10(-19)  m(2)  s(-1)), which reflects the greatly opened junctions between closely connected mesopores (shell) and micropores (core). The core-shell composite shows greatly enhanced adsorption capacity (≈1.35 mmol  g(-1)) for large molecules such as 1,3,5-triisopropylbenzene relative to that of pristine ZSM-5 (≈0.4 mmol  g(-1)) owing to the mesoporous silica shells. When Al species are introduced during the coating process, the core-shell composite molecular sieves demonstrate a graded acidity distribution from weak acidity of mesopores (predominant Lewis acid sites) to accessible strong acidity of zeolite cores (Lewis and Brønsted acid sites). The probe catalytic cracking reaction of n-dodecane shows the superiority of the unique core-shell structure over pristine ZSM-5. Insight into the core-shell composite structure with hierarchical pore and graded acidity distribution show great potential for petroleum catalytic processes. PMID

  3. TEM Study of the Growth Mechanism, Phase Transformation, and Core/shell Structure of Semiconductor Nanowires

    NASA Astrophysics Data System (ADS)

    Wong, Tai Lun

    In this thesis, the fabrication and characterization of one-dimensional nanostructures have been studied systematically to understand the growth mechanism and structure transformation of one-dimensional nanostructures. The growth behavior of the ultrathin ZnSe nanowires with diameter less than 60 nm was found to be different from classical vapor-liquid-solid (VLS) process. The growth rate increases when the diameter of nanowires decreases, in contrast to the classical VLS process in which the growth rate increases with the diameter. The nucleation, initial growth, growth rates, defects, interface structures and growth direction of the nanowires were investigated by high resolution transmission electron microscopy (HRTEM). We found the structure and growth direction of ultra-thin nanowires are highly sensitive to growth temperatures and diameters of nanowires. At a low growth temperature (380°C), the growth direction for most nanowires is along <111>. Planar defects were found throughout the nanowires. At a high growth temperature (530°C), uniform nanowires with diameters around 10nm were grown along <110> and <112> directions, and the nanowires with diameters larger than 20nm were mainly grown along <111> direction. The possible growth mechanism of ultrathin nanowires was proposed by combining the solid catalytic growth with the interface diffusion theory, in order to explain how the growth temperature and the size of the catalysts influent the morphology, growth direction and growth rate of ultrathin nanowires. Structural and phase transformation of a nickel coated Si nanowire to NiSi2/SiC core-shell nanowire heterostructures has been investigated by the in-situ Transmission Electron Microscope (TEM). The phase transformation is a single-site nucleation process and therefore a single crystalline NiSi2 core resulted in the core-shell nanowire heterostructures. The transformation of the Si nanowire to NiSi2/SiC core-shell nanowire heterostructures was extremely

  4. Heteroaggregation assisted wet synthesis of core-shell silver-silica-cadmium selenide nanowires

    NASA Astrophysics Data System (ADS)

    Pita, Isabel A.; Singh, Shalini; Silien, Christophe; Ryan, Kevin M.; Liu, Ning

    2015-12-01

    A method has been developed for the wet solution synthesis of core shell heterogeneous nanowires. An ultrathin silica layer was first grown around plain silver nanowires to act as a suitable insulator. An outer nanoparticle layer was then attached through heteroaggregation by dispersing the un-functionalized nanowires in toluene solutions containing nanoparticles of CdSe or Au. Total coverage of nanoparticles on nanowires was found to increase with the nanoparticle size, which is attributed to the increase in the van der Waals interaction between the nanoparticles and the nanowire with the increasing size of nanoparticles. Using this method, we achieved over 79.5% coverage of CdSe nanoparticles (24 nm × 11 nm) on the nanowire surface. Although following the same trend, Au nanoparticles show an overall lower coverage than CdSe, with only 24.2% coverage at their largest particle size of 19 nm in diameter. This result is attributed to the increase in steric repulsion during attachment due to the increasing length of capping ligands. Investigation of the core-shell nanowire's optical properties yielded CdSe Raman peak enhancement by a factor of 2-3 due to the excitation of surface plasmon propagation. Our method can be applied to the attachment of a wide range of nanoparticles to nanowire materials in non-polar solution and the core-shell nanowires show great potential for incorporation into various microscopic and drug delivery applications.A method has been developed for the wet solution synthesis of core shell heterogeneous nanowires. An ultrathin silica layer was first grown around plain silver nanowires to act as a suitable insulator. An outer nanoparticle layer was then attached through heteroaggregation by dispersing the un-functionalized nanowires in toluene solutions containing nanoparticles of CdSe or Au. Total coverage of nanoparticles on nanowires was found to increase with the nanoparticle size, which is attributed to the increase in the van der Waals

  5. Single-step in situ synthesis of double bond-grafted yttrium-hydroxide nanotube core-shell structures.

    PubMed

    Li, Weijia; Wang, Xun; Li, Yadong

    2004-01-21

    Novel MMA-Y(OH)(3) nanotube core-shell structures have been successfully prepared with double bonds successfully grafted on the surface through a single-step in-situ hydrothermal method. PMID:14737530

  6. Core shell micron-scale composites of titanium oxide and carbide formed through controlled thermal-plasma oxidation

    NASA Astrophysics Data System (ADS)

    Li, Ya-Li; Ishigaki, Takamasa

    2003-01-01

    Core-shell structured micron-scale spheres of titanium oxide and carbide were prepared by the controlled in-flight oxidation of a powder of irregularly shaped titanium-carbide particles in an argon-oxygen thermal plasma. Mono-dispersed core-shell particles with rutile shells and TiC cores were formed by an intermediate-rate input of oxygen to the plasma gas. The partial oxidation of the TiC particles in the liquid phase was accompanied by spheroidization of the surface oxide melt, thus giving rise to a core-shell composite under rapid quenching. TiO 2-TiC core-shell composites have potential as new materials for roles such as light-scattering media, photo-catalysts, and electro-rheorogical fluids.

  7. One-pot synthesis of highly luminescent CdTe/CdS core/shell nanocrystals in aqueous phase

    NASA Astrophysics Data System (ADS)

    Gu, Zhenyu; Zou, Lei; Fang, Zheng; Zhu, Weihong; Zhong, Xinhua

    2008-04-01

    Surface passivation of nanocrystals with suitable organic or inorganic materials is key to improving the photoluminescence (PL) efficiency and stability of nanocrystals. Although the hot-injection organometallic approach is a powerful tool to achieve different kinds of core/shell structures, direct synthesis of such structures in aqueous phase, which bears many advantages such as biocompatibility, water-solubility, environment-friendliness, and cheapness, is less often reported. Herein we present a facile approach for the one-pot preparation of a water-soluble core/shell structure with CdTe cores packed in a CdS shell in aqueous phase. In comparison with plain CdTe nanocrystals, the PL efficiency of the obtained CdTe/CdS core/shell structure can approach about 75%. The stability of the core/shell structure to UV irradiation and oxidation is also improved.

  8. Highly Stretchable and Transparent Supercapacitor by Ag-Au Core-Shell Nanowire Network with High Electrochemical Stability.

    PubMed

    Lee, Habeom; Hong, Sukjoon; Lee, Jinhwan; Suh, Young Duk; Kwon, Jinhyeong; Moon, Hyunjin; Kim, Hyeonseok; Yeo, Junyeob; Ko, Seung Hwan

    2016-06-22

    Stretchable and transparent electronics have steadily attracted huge attention in wearable devices. Although Ag nanowire is the one of the most promising candidates for transparent and stretchable electronics, its electrochemical instability has forbidden its application to the development of electrochemical energy devices such as supercapacitors. Here, we introduce a highly stretchable and transparent supercapacitor based on electrochemically stable Ag-Au core-shell nanowire percolation network electrode. We developed a simple solution process to synthesize the Ag-Au core-shell nanowire with excellent electrical conductivity as well as greatly enhanced chemical and electrochemical stabilities compared to pristine Ag nanowire. The proposed core-shell nanowire-based supercapacitor still possesses fine optical transmittance and outstanding mechanical stability up to 60% strain. The Ag-Au core-shell nanowire can be a strong candidate for future wearable electrochemical energy devices. PMID:27285849

  9. When cubic cobalt sulfide meets layered molybdenum disulfide: a core-shell system toward synergetic electrocatalytic water splitting.

    PubMed

    Zhu, Han; Zhang, Junfeng; Yanzhang, Ruoping; Du, Mingliang; Wang, Qingfa; Gao, Guohua; Wu, Jiandong; Wu, Guangming; Zhang, Ming; Liu, Bo; Yao, Juming; Zhang, Xiangwen

    2015-08-26

    A new class of Co9 S8 @MoS2 core-shell structures formed on carbon nanofibers composed of cubic Co9 S8 as cores and layered MoS2 as shells is described. The core-shell design of these nanostructures allows the advantages of MoS2 and Co9 S8 to be combined, serving as a bifunctional electrocatalyst for H2 and O2 evolution. PMID:26179503

  10. A core-shell-structured molecularly imprinted polymer on upconverting nanoparticles for selective and sensitive fluorescence sensing of sulfamethazine.

    PubMed

    Tian, Jinghan; Bai, Jialei; Peng, Yuan; Qie, Zhiwei; Zhao, Yufeng; Ning, Baoan; Xiao, Dan; Gao, Zhixian

    2015-08-01

    A core-shell structured molecularly imprinted polymer on upconverting nanoparticles (UCNPs@MIP) was synthesized for the fluorescence (FL) sensing of sulfamethazine (SMZ). Hexagonal UCNPs were synthesized by the solvothermal method, then coated with a thin silica shell and modified with vinyl groups. Finally, surface polymerization was initiated among the vinyl groups, the functional monomers and cross-linking agents by the initiator. The MIP synthesized by this procedure was anchored on the surface of UCNPs, possessed better site accessibility and lower transfer resistance for the target molecule compared to bulk imprinted materials. The obtained UCNPs@MIP showed good binding capacity, fast response, high selectivity and specificity to the SMZ. The FL intensity of the UCNPs@MIP decreased sensitively with the increasing concentration of SMZ in the range of 50-700 ng mL(-1), the detection limit was 34 ng mL(-1) (S/N = 3). The UCNPs@MIP was successfully applied to the detection of SMZ in chicken samples. Thanks to the unique near-infrared (NIR) excitation nature of UCNPs, the chicken meat only needed some simple extraction procedures before FL detection, no complex purifications were required. The average recoveries ranged from 96.01% to 98.90%, with relative standard deviations (RSDs) below 4.5%. This work offers a novel sensing system that combined the advantages of upconverting nanotechnology and molecularly imprinted technology. PMID:26075380

  11. Demonstration of Confined Electron Gas and Steep-Slope Behavior in Delta-Doped GaAs-AlGaAs Core-Shell Nanowire Transistors.

    PubMed

    Morkötter, S; Jeon, N; Rudolph, D; Loitsch, B; Spirkoska, D; Hoffmann, E; Döblinger, M; Matich, S; Finley, J J; Lauhon, L J; Abstreiter, G; Koblmüller, G

    2015-05-13

    Strong surface and impurity scattering in III-V semiconductor-based nanowires (NW) degrade the performance of electronic devices, requiring refined concepts for controlling charge carrier conductivity. Here, we demonstrate remote Si delta (δ)-doping of radial GaAs-AlGaAs core-shell NWs that unambiguously exhibit a strongly confined electron gas with enhanced low-temperature field-effect mobilities up to 5 × 10(3) cm(2) V(-1) s(-1). The spatial separation between the high-mobility free electron gas at the NW core-shell interface and the Si dopants in the shell is directly verified by atom probe tomographic (APT) analysis, band-profile calculations, and transport characterization in advanced field-effect transistor (FET) geometries, demonstrating powerful control over the free electron gas density and conductivity. Multigated NW-FETs allow us to spatially resolve channel width- and crystal phase-dependent variations in electron gas density and mobility along single NW-FETs. Notably, dc output and transfer characteristics of these n-type depletion mode NW-FETs reveal excellent drain current saturation and record low subthreshold slopes of 70 mV/dec at on/off ratios >10(4)-10(5) at room temperature. PMID:25923841

  12. Upconversion-luminescent/magnetic dual-functional sub-20 nm core-shell SrF2:Yb,Tm@CaF2:Gd heteronanoparticles.

    PubMed

    Li, Ai-Hua; Lü, Mengyun; Yang, Jun; Chen, Lin; Cui, Xiaohong; Sun, Zhijun

    2016-04-01

    Sub-20 nm core-shell and water-soluble SrF2:Yb,Tm@CaF2:Gd heteronanoparticles with both upconversion luminescence (UCL) and magnetic resonance imaging (MRI) capabilities were designed and synthesized via a two-step hydrothermal method. In the design of the heteronanoparticles, SrF2:Yb,Tm nanoparticles with high UCL efficiency are chosen as the core material for strong UCL output; and by epitaxially coating the SrF2:Yb,Tm core particles with inert and biocompatible shells of CaF2:Gd, the core-shell heteronanoparticles are endowed with a magnetic capability (longitudinal relaxivity of 2.4 mM(-1) s(-1)) for MRI, as well as an enhancement of the near infrared (NIR) UCL by 9.2 times. The aqueous dispersion of SrF2:Yb,Tm@CaF2:Gd heteronanoparticles with a concentration of 2.6 wt% can emit NIR UCL so as to be easily detected with a fiber optical spectrometer under illumination of a 975 nm laser diode with a power density of 8.8 W cm(-2). Such a dispersion with a Gd(3+) concentration of 0.0143 mM in the shell region of the heteronanoparticles can also generate the detectable quickening of longitudinal relaxation. The results promise the strong potential of this nanomaterial for applications in bioimaging as a dual-functional probe. PMID:26934836

  13. A sensitive electrochemiluminescence immunosensor based on luminophore capped Pd@Au core-shell nanoparticles as signal tracers and ferrocenyl compounds as signal enhancers.

    PubMed

    Liu, Yuting; Wang, Haijun; Xiong, Chengyi; Yuan, Yali; Chai, Yaqin; Yuan, Ruo

    2016-07-15

    In this work, N-(aminobutyl)-N-(ethylisoluminol) (ABEI), an analogue of luminol, is served as both the reductant and luminescence reagent to synthesize ABEI capped Pd@Au core-shell nanoparticles (ABEI-Pd@AuNPs). The nanoparticles not only exhibit inherent electrochemiluminescence (ECL) property, but also possess advantages of noble-metal nanomaterials such as outstanding electronic property, high specific surface area and good biocompatibility. In order to enhance the luminescence efficiency, ferrocene monocarboxylic acid (Fc) as catalyzer is grafted on the surface of ABEI-Pd@AuNPs with the aid of l-cysteine (l-Cys). When the Fc is electrochemically oxidized to ferricinium cation species (Fc(+)), the decomposition of H2O2 which existed in detection solution can be catalyzed by Fc(+) to generate oxygen-related free radicals, resulting effective signal amplification for ABEI-H2O2 system. For potential applications, the Pd@Au core-shell nanoparticles bifunctionalized by ABEI and catalyzer are employed as nano-carriers to immobilize detection antibody (Ab2). Based on sandwiched immunoreactions, a "signal-on" ECL immunosensor is developed for detection of human collagen type IV (Col IV), a potential biomarker associated with diabetic nephropathy. Consequently, the proposed immunosensor provides a wide linear detection ranging from 1pgmL(-1) to 10ngmL(-1) with a relatively low detection limit of 0.3pgmL(-1) (S/N=3). PMID:26985586

  14. Silicon nanowire array/Cu2O crystalline core-shell nanosystem for solar-driven photocatalytic water splitting.

    PubMed

    Xiong, Zuzhou; Zheng, Maojun; Liu, Sida; Ma, Li; Shen, Wenzhong

    2013-07-01

    P-type Cu2O nanocrystals were deposited on n-type silicon nanowire arrays (Si NWs) to form core-shell heterojunction arrays structure via a simple electroless deposition technique. Scanning electron microscopy, transmission electron microscope and x-ray diffraction were utilized to characterize the morphology and structure of the core-shell nanosystem. The reflectivity of the obtained core-shell structure measured by UV/vis spectrometry showed a comparatively low reflectivity in the visible-light region, which implied good optical absorption performance. The water splitting performance of the obtained Si NWs, planar Si/Cu2O structure and Si NW/Cu2O core-shell nanosystem were studied. Owing to the large specific surface area, heterojunctions formed between Cu2O nanocrystallites and Si NWs and the light trapping effect of the NW array structure, the photocatalytic performance of the Si NW/Cu2O core-shell nanosystem increased markedly compared with that of pure silicon NWs and a planar Si/Cu2O structure, which means excellent hydrogen production capacity under irradiation with simulated sunlight. In addition, the photocatalytic performance of the core-shell nanosystem was improved obviously after platinum nanoparticles were electrodeposited on it. PMID:23733303

  15. Silicon nanowire array/Cu2O crystalline core-shell nanosystem for solar-driven photocatalytic water splitting

    NASA Astrophysics Data System (ADS)

    Xiong, Zuzhou; Zheng, Maojun; Liu, Sida; Ma, Li; Shen, Wenzhong

    2013-07-01

    P-type Cu2O nanocrystals were deposited on n-type silicon nanowire arrays (Si NWs) to form core-shell heterojunction arrays structure via a simple electroless deposition technique. Scanning electron microscopy, transmission electron microscope and x-ray diffraction were utilized to characterize the morphology and structure of the core-shell nanosystem. The reflectivity of the obtained core-shell structure measured by UV/vis spectrometry showed a comparatively low reflectivity in the visible-light region, which implied good optical absorption performance. The water splitting performance of the obtained Si NWs, planar Si/Cu2O structure and Si NW/Cu2O core-shell nanosystem were studied. Owing to the large specific surface area, heterojunctions formed between Cu2O nanocrystallites and Si NWs and the light trapping effect of the NW array structure, the photocatalytic performance of the Si NW/Cu2O core-shell nanosystem increased markedly compared with that of pure silicon NWs and a planar Si/Cu2O structure, which means excellent hydrogen production capacity under irradiation with simulated sunlight. In addition, the photocatalytic performance of the core-shell nanosystem was improved obviously after platinum nanoparticles were electrodeposited on it.

  16. Global optimization and oxygen dissociation on polyicosahedral Ag32Cu6 core-shell cluster for alkaline fuel cells

    NASA Astrophysics Data System (ADS)

    Zhang, N.; Chen, F. Y.; Wu, X. Q.

    2015-07-01

    The structure of 38 atoms Ag-Cu cluster is studied by using a combination of a genetic algorithm global optimization technique and density functional theory (DFT) calculations. It is demonstrated that the truncated octahedral (TO) Ag32Cu6 core-shell cluster is less stable than the polyicosahedral (pIh) Ag32Cu6 core-shell cluster from the atomistic models and the DFT calculation shows an agreeable result, so the newfound pIh Ag32Cu6 core-shell cluster is further investigated for potential application for O2 dissociation in oxygen reduction reaction (ORR). The activation energy barrier for the O2 dissociation on pIh Ag32Cu6 core-shell cluster is 0.715 eV, where the d-band center is -3.395 eV and the density of states at the Fermi energy level is maximal for the favorable absorption site, indicating that the catalytic activity is attributed to a maximal charge transfer between an oxygen molecule and the pIh Ag32Cu6 core-shell cluster. This work revises the earlier idea that Ag32Cu6 core-shell nanoparticles are not suitable as ORR catalysts and confirms that Ag-Cu nanoalloy is a potential candidate to substitute noble Pt-based catalyst in alkaline fuel cells.

  17. Global optimization and oxygen dissociation on polyicosahedral Ag32Cu6 core-shell cluster for alkaline fuel cells

    PubMed Central

    Zhang, N.; Chen, F. Y.; Wu, X.Q.

    2015-01-01

    The structure of 38 atoms Ag-Cu cluster is studied by using a combination of a genetic algorithm global optimization technique and density functional theory (DFT) calculations. It is demonstrated that the truncated octahedral (TO) Ag32Cu6 core-shell cluster is less stable than the polyicosahedral (pIh) Ag32Cu6 core-shell cluster from the atomistic models and the DFT calculation shows an agreeable result, so the newfound pIh Ag32Cu6 core-shell cluster is further investigated for potential application for O2 dissociation in oxygen reduction reaction (ORR). The activation energy barrier for the O2 dissociation on pIh Ag32Cu6 core-shell cluster is 0.715 eV, where the d-band center is −3.395 eV and the density of states at the Fermi energy level is maximal for the favorable absorption site, indicating that the catalytic activity is attributed to a maximal charge transfer between an oxygen molecule and the pIh Ag32Cu6 core-shell cluster. This work revises the earlier idea that Ag32Cu6 core-shell nanoparticles are not suitable as ORR catalysts and confirms that Ag-Cu nanoalloy is a potential candidate to substitute noble Pt-based catalyst in alkaline fuel cells. PMID:26148904

  18. Synthesis and optical study of green light emitting polymer coated CdSe/ZnSe core/shell nanocrystals

    SciTech Connect

    Tripathi, S.K.; Sharma, Mamta

    2013-05-15

    Highlights: ► Synthesis of Polymer coated core CdSe and CdSe/ZnSe core/shell NCs. ► From TEM image, the spherical nature of CdSe and CdSe/ZnSe is obtained. ► Exhibiting green band photoemission peak at 541 nm and 549 nm for CdSe core and CdSe/ZnSe core/shell NCs. ► The shell thickness has been calculated by using superposition of quantum confinement energy model. - Abstract: CdSe/ZnSe Core/Shell NCs dispersed in PVA are synthesized by chemical method at room temperature. This is characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), UV/Vis spectra and photoluminescence spectroscopy (PL). TEM image shows the spherical nature of CdSe/ZnSe core/shell NCs. The red shift of absorption and emission peak of CdSe/ZnSe core/shell NCs as compared to CdSe core confirmed the formation of core/shell. The superposition of quantum confinement energy model is used for calculation of thickness of ZnSe shell.

  19. Preparation and photocatalytic activity of eccentric Au-titania core-shell nanoparticles by block copolymer templates.

    PubMed

    Li, Xue; Fu, Xiaoning; Yang, Hui

    2011-02-21

    A novel route for a preparation of eccentric Au-titania core-shell nanoparticles using gold nanoparticles (AuNPs) with block copolymer shells as a template is reported. AuNPs with poly(2-vinyl pyridine)-block-poly(ethylene oxide) (PVP-b-PEO) block copolymer shells are first prepared by UV irradiation of the solution of PVP-b-PEO/HAuCl(4) complexes. Then the sol-gel reaction of titanium tetra-isopropoxide (TTIP) selectively on the surfaces of AuNPs leads to Au-titania core-shell composite nanoparticles. The eccentric Au-titania core-shell nanoparticles are obtained from the Au-titania core-shell composite nanoparticles by removal of organic interlayer by UV treatment. Photocatalytic activities of the resulting eccentric core-shell nanoparticles are investigated in terms of the degradation of methylene blue (MB). The results show that the eccentric core-shell structures endow the catalyst with greatly enhanced photocatalytic activity. PMID:21157597

  20. Engineering of Hollow Core-Shell Interlinked Carbon Spheres for Highly Stable Lithium-Sulfur Batteries.

    PubMed

    Sun, Qiang; He, Bin; Zhang, Xiang-Qian; Lu, An-Hui

    2015-08-25

    We report engineered hollow core-shell interlinked carbon spheres that consist of a mesoporous shell, a hollow void, and an anchored carbon core and are expected to be ideal sulfur hosts for overcoming the shortage of Li-S batteries. The hollow core-shell interlinked carbon spheres were obtained through solution synthesis of polymer spheres followed by a pyrolysis process that occurred in the hermetical silica shell. During the pyrolysis, the polymer sphere was transformed into the carbon core and the carbonaceous volatiles were self-deposited on the silica shell due to the blocking effect of the hermetical silica shell. The gravitational force and the natural driving force of lowering the surface energy tend to interlink the carbon core and carbon/silica shell, resulting in a core-shell interlinked structure. After the SiO2 shell was etched, the mesoporous carbon shell was generated. When used as the sulfur host for Li-S batteries, such a hierarchical structure provides access to Li(+) ingress/egress for reactivity with the sulfur and, meanwhile, can overcome the limitations of low sulfur loading and a severe shuttle effect in solid carbon-supported sulfur cathodes. Transmission electron microscopy and scanning transmission electron microscopy images provide visible evidence that sulfur is well-encapsulated in the hollow void. Importantly, such anchored-core carbon nanostructures can simultaneously serve as a physical buffer and an electronically connecting matrix, which helps to realize the full potential of the active materials. Based on the many merits, carbon-sulfur cathodes show a high utilization of sulfur with a sulfur loading of 70 wt % and exhibit excellent cycling stability (i.e., 960 mA h g(-1) after 200 cycles at a current density of 0.5 C). PMID:26182333

  1. A study of the compartmentalization of core-shell nanoparticles through fluorescence energy transfer of dopants.

    PubMed

    Chávez, Jorge L; Jiang, Hui; Duran, Randolph S

    2010-02-01

    Hybrid organic-inorganic templates and core-shell nanoparticles were used as models to study the communication between fluorescent probes placed inside nanoparticles. The hybrid templates were prepared on the basis of a mixed-surfactant system using octadecyltrimethoxysilane as a reactive amphiphile. The core-shell particles were obtained after coating of the templates with a siloxane shell, using the silanol groups on their surface. Atomic force microscopy imaging showed that the templates were made of a flexible material that flattened significantly after deposition on a substrate and evaporation of the solvent. Pyrene was sequestered by the templates in an aqueous suspension, which placed it in a nonpolar environment, as observed by its fluorescence response. Subsequently, double-doped templates were prepared by sequestering coumarin 153 (C153), with pyrene-doped hybrid templates. The communication between these probes was studied on the basis of their spectral properties, by means of fluorescence resonance energy transfer (FRET). Energy transfer between the dyes with efficiencies up to 55% was observed. Similarly, double-doped core-shell particles prepared on the basis of the hybrid templates were doped with this pair of dyes. Despite the presence of the shell, which was intended to increment the average separation between the probes, interaction of the dyes was observed, although with lower efficiencies. A similar study was performed with C153 and 4-(dicyanomethylene)-2-methyl-6-p-(dimethylamino)styryl-4H-pyran (DCM). FRET studies indicated that the probes were placed in proximity to each other. We confirmed these observations by means of fluorescence lifetime measurements, which showed a decrease in the lifetime of the donor upon addition of the acceptor. PMID:20023306

  2. Process-Dependent Properties in Colloidally Synthesized “Giant” Core/Shell Nanocrystal Quantum Dots

    SciTech Connect

    Hollingsworth, Jennifer A.; Ghosh, Yagnaseni; Dennis, Allison M.; Mangum, Benjamin D.; Park, Young-Shin; Kundu, Janardan; Htoon, Han

    2012-06-07

    Due to their characteristic bright and stable photoluminescence, semiconductor nanocrystal quantum dots (NQDs) have attracted much interest as efficient light emitters for applications from single-particle tracking to solid-state lighting. Despite their numerous enabling traits, however, NQD optical properties are frustratingly sensitive to their chemical environment, exhibit fluorescence intermittency ('blinking'), and are susceptible to Auger recombination, an efficient nonradiative decay process. Previously, we showed for the first time that colloidal CdSe/CdS core/shell nanocrystal quantum dots (NQDs) comprising ultrathick shells (number of shell monolayers, n, > 10) grown by protracted successive ionic layer adsorption and reaction (SILAR) leads to remarkable photostability and significantly suppressed blinking behavior as a function of increasing shell thickness. We have also shown that these so-called 'giant' NQDs (g-NQDs) afford nearly complete suppression of non-radiative Auger recombination, revealed in our studies as long biexciton lifetimes and efficient multiexciton emission. The unique behavior of this core/shell system prompted us to assess correlations between specific physicochemical properties - beyond shell thickness - and functionality. Here, we demonstrate the ability of particle shape/faceting, crystalline phase, and core size to determine ensemble and single-particle optical properties (quantum yield/brightness, blinking, radiative lifetimes). Significantly, we show how reaction process parameters (surface-stabilizing ligands, ligand:NQD ratio, choice of 'inert' solvent, and modifications to the SILAR method itself) can be tuned to modify these function-dictating NQD physical properties, ultimately leading to an optimized synthetic approach that results in the complete suppression of blinking. We find that the resulting 'guiding principles' can be applied to other NQD compositions, allowing us to achieve non-blinking behavior in the near

  3. Green synthesis and characterization of Au@Pt core-shell bimetallic nanoparticles using gallic acid

    NASA Astrophysics Data System (ADS)

    Zhang, Guojun; Zheng, Hongmei; Shen, Ming; Wang, Lei; Wang, Xiaosan

    2015-06-01

    In this study, we developed a facile and benign green synthesis approach for the successful fabrication of well-dispersed urchin-like Au@Pt core-shell nanoparticles (NPs) using gallic acid (GA) as both a reducing and protecting agent. The proposed one-step synthesis exploits the differences in the reduction potentials of AuCl4- and PtCl62-, where the AuCl4- ions are preferentially reduced to Au cores and the PtCl62- ions are then deposited continuously onto the Au core surface as a Pt shell. The as-prepared Au@Pt NPs were characterized by transmission electron microscope (TEM); high-resolution transmission electron microscope (HR-TEM); scanning electron microscope (SEM); UV-vis absorption spectra (UV-vis); X-ray diffraction (XRD); Fourier transmission infrared spectra (FT-IR). We systematically investigated the effects of some experimental parameters on the formation of the Au@Pt NPs, i.e., the reaction temperature, the molar ratios of HAuCl4/H2PtCl6, and the amount of GA. When polyvinylpyrrolidone K-30 (PVP) was used as a protecting agent, the Au@Pt core-shell NPs obtained using this green synthesis method were better dispersed and smaller in size. The as-prepared Au@Pt NPs exhibited better catalytic activity in the reaction where NaBH4 reduced p-nitrophenol to p-aminophenol. However, the results showed that the Au@Pt bimetallic NPs had a lower catalytic activity than the pure Au NPs obtained by the same method, which confirmed the formation of Au@Pt core-shell nanostructures because the active sites on the surfaces of the Au NPs were covered with a Pt shell.

  4. Synthesis of fly ash based core-shell composites for use as functional pigment in paints

    NASA Astrophysics Data System (ADS)

    Sharma, Richa; Tiwari, Sangeeta

    2016-04-01

    Fly ash is a combustion residue, mainly composed of silica, alumina and iron oxides. It is produced by the power industries in very large amounts and usually disposed in landfills, which have represented an environmental problem in recent years1. The need to generate a market for fly ash consumption is the main reason why alternative applications have been studied. It has been applied as an additive in construction materials like cement and pavements2. The present work describes the synthesis of Flyash-Titania core-shell particles by precipitation technique using Titanium tetra isopropoxide (TTIP) which can be used for variety of applications such as NIR reflecting materials for cool coatings, Photocatalysis etc. In this work, Fly ash is used in core and Nano -TiO2 is coated as shell on it. Surfactants are used to improve the adhesion of Nano Titania shell on fly ash core. Effect on adhesion of TiO2 on Fly ash is studied by using different types of surfactant. The preparation of core shells was carried out in absence of surfactant as well as using anionic and non-ionic surfactants. The percentage of surfactant was varied to study the effect of amount of surfactant on the uniformity and size of particles in the shell using Kubelka-Munk transformed reflectance spectra. The morphology of core shell structures was studied using SEM technique. Use of anionic surfactant results in more uniform coating with reduced particle size of the shell material. The composite particles prepared by using anionic surfactant are having good pigment properties and also shows good reflectance in Near Infrared region and hence can be used as a pigment in cool coatings.

  5. Preparation of hollow core/shell microspheres of hematite and its adsorption ability for samarium.

    PubMed

    Yu, Sheng-Hui; Yao, Qi-Zhi; Zhou, Gen-Tao; Fu, Sheng-Quan

    2014-07-01

    Hollow core/shell hematite microspheres with diameter of ca. 1-2 μm have been successfully achieved by calcining the precursor composite microspheres of pyrite and polyvinylpyrrolidone (PVP) in air. The synthesized products were characterized by a wide range of techniques including powder X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy (EDX), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC), and Brunauer-Emmett-Teller (BET) gas sorptometry. Temperature- and time-dependent experiments unveil that the precursor pyrite-PVP composite microspheres finally transform into hollow core/shell hematite microspheres in air through a multistep process including the oxidation and sulfation of pyrite, combustion of PVP occluded in the precursor, desulfation, aggregation, and fusion of nanosized hematite as well as mass transportation from the interior to the exterior of the microspheres. The formation of the hollow core/shell microspheres dominantly depends on the calcination temperature under current experimental conditions, and the aggregation of hematite nanocrystals and the core shrinking during the oxidation of pyrite are responsible for the formation of the hollow structures. Moreover, the adsorption ability of the hematite for Sm(III) was also tested. The results exhibit that the hematite microspheres have good adsorption activity for trivalent samarium, and that its adsorption capacity strongly depends on the pH of the solution, and the maximum adsorption capacity for Sm(III) is 14.48 mg/g at neutral pH. As samarium is a typical member of the lanthanide series, our results suggest that the hollow hematite microspheres have potential application in removal of rare earth elements (REEs) entering the water environment. PMID:24892188

  6. Core-shell electrospun polybutylene terephthalate/polypyrrole hollow nanofibers for micro-solid phase extraction.

    PubMed

    Bagheri, Habib; Rezvani, Omid; Banihashemi, Solmaz

    2016-02-19

    In the present work, a new micro-solid phase extraction (μ-SPE) sorbent as an extracting medium based on core-shell nanofibers was synthesized by electrospinning. The core-shell nanofibers of polyvinylpyrrolidone-Polybutylene terephthalate/polypyrrole (PVP-PBT/PPy) were electrospun and subsequently, modified hollow nanofibers were prepared by removing the central PVP moiety. Moreover, conventional PBT/PPy was also prepared for the comparison purposes. The homogeneity and the porous surface structure of the core-shell nanofibers were confirmed by scanning electron microscopy (SEM). The applicability of the fabricated nanofibers-coating was examined by immersed μ-SPE of some selected triazine herbicides from aqueous samples and wheat grains. Subsequently, the extracted analytes were transferred into a gas chromatography (GC) after solvent desorption. Influencing parameters on the morphology of nanofiber such as elctrospinning parameters and the weight ratio of components were optimized. In addition, effects of different parameters influencing the extraction efficiency including extraction temperature, extraction time, ionic strength, sample pH, desorption temperature, and desorption time were investigated and optimized. Eventually, the developed method was validated by gas chromatography-mass spectrometry (GC-MS). At the optimum conditions, the relative standard deviation values for real water samples spiked with the selected triazines at 1 ng mL(-1) were 4-8% (n=3) and the limits of detection for the studied compounds were between 50 and 90 ng L(-1). The calibration curves for the selected triazines were in the range of 0.3-500 ng mL(-1) and regression coefficients (R(2)) were between 0.9985 and 0.9996. PMID:26810808

  7. Structural optical correlated properties of SnO2/Al2O3 core@ shell heterostructure

    NASA Astrophysics Data System (ADS)

    Heiba, Zein K.; Imam, N. G.; Bakr Mohamed, Mohamed

    2016-07-01

    Nano size polycrystalline samples of the core@shell heterostructure of SnO2 @ xAl2O3 (x = 0, 25, 50, 75 wt.%) were synthesized by sol-gel technique. The resulting samples were characterized with fourier transform infrared spectroscopy (FT-IR), photoluminescence (PL) and X-ray powder diffraction (XRD). The XRD patterns manifest diffraction peaks of SnO2 as main phase with weak peaks corresponding to Al2O3 phase. The formation of core@ shell structure is confirmed by TEM images and Rietveld quantitative phase analysis which revealed that small part of Al2O3 is incorporated into the SnO2 lattice while the main part (shell) remains as a separate phase segregated on the grain boundary surface of SnO2 (core). It is found that the grain size of the mixed oxides SnO2 @ xAl2O3 is below 10 nm while for pure SnO2 it is over 41 nm, indicating that alumina can effectively prevent SnO2 from further growing up in the process of calcination. This is confirmed by the large increase in the specific surface area for mixed oxide samples. The PL emission showed great dependence on the structure properties analyzed by XRD and FTIR. The PL results recommend Al2O3@SnO2 core@shell heterostructure to be a promising short-wavelength luminescent optoelectronic devices for blue, UV, and laser light-emitting diodes.

  8. Synthesis and microwave-absorbing properties of Co3Fe7@C core-shell nanostructure

    NASA Astrophysics Data System (ADS)

    Guo, Xiao Dang; Qiao, Xiao Jing; Ren, Qing Guo; Wan, Xiang; Li, Wang Chang; Sun, Zhi Gang

    2015-07-01

    Co3Fe7@C core-shell nanoparticles with high performance of microwave-absorbing properties were prepared by hydrothermal method and heat treatment. The transformation of structural, morphological and magnetic properties among the carbon-encapsulated composites, which were annealed at three different temperatures, were investigated by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM) and vibrating sample magnetometer (VSM). XRD analysis indicated the phase composition of Co3Fe7/CoFe2O4, Fe3C/Co3Fe7 and pure Co3Fe7 at different annealing temperatures. TEM confirmed the Co3Fe7@graphite core-shell nanostructure with an average particle size of 180 nm. The saturation magnetization ( M s) increased monotonically with the increase in temperature, which was attributed to the crystal growth and purity of metallic core. Co3Fe7@graphite nanoparticles exhibited the hysteretic loops of soft ferromagnetic behavior with high M s of 222.85 emu g-1, weak remanent magnetization ( M r) and coercivity ( H c). For Co3Fe7@graphite nanomaterial, a reflection loss exceeding -20 dB was obtained between 2.8 and 10.2 GHz, which almost covering from S-band to X-band. The maximum reflection loss is -26.8 dB at 9 GHz with 1.8 mm thickness. The excellent microwave absorption properties result from the proper electromagnetic match in core-shell nanostructure and the strong natural ferromagnetic resonance.

  9. pH sensitive core-shell magnetic nanoparticles for targeted drug delivery in cancer therapy.

    PubMed

    Lungu, Iulia Ioana; Rădulescu, Marius; Mogoşanu, George Dan; Grumezescu, Alexandru Mihai

    2016-01-01

    In the last decade, nanobiotechnology has evolved rapidly with an extensive impact on biomedical area. In order to improve bioavailability and minimize adverse effects, drug delivery systems based on magnetic nanocomposites are under development mainly for cancer imaging and antitumor therapy. In this regard, pH sensitive core-shell magnetic nanoparticles (NPs) with accurate controlled size and shape are synthesized by various modern methods, such as homogeneous precipitation, coprecipitation, microemulsion or polyol approaches, high temperature and hydrothermal reactions, sol-gel reactions, aerosol÷vapor processes and sonolysis. Due to their unique combined physico-chemical and biological properties (such as higher dispensability, chemical and thermal stability, biocompatibility), pH responsive core-shell magnetic NPs are widely investigated for controlled release of cytostatic drugs into the tumor site by means of pH change: magnetite@silicon dioxide (Fe3O4@SiO2), Fe3O4@titanium dioxide (TiO2), β-thiopropionate-polyethylene glycol (PEG)-modified Fe3O4@mSiO2, Fe3O4 NPs core coated with SiO2 with an imidazole group modified PEG-polypeptide (mPEG-poly-L-Asparagine), polyacrylic acid (PAA) and folic acid (FA) coating of the iron oxide NP core, methoxy polyethylene glycol-block-polymethacrylic acid-block-polyglycerol monomethacrylate (MPEG-b-PMAA-b-PGMA) attached by a PGMA block to a Fe3O4 core, PEG-modified polyamidoamine (PAMAM) dendrimer shell with Fe3O4 core and mesoporous silica coated on Fe3O4, mostly coated with an anticancer drug. This review paper highlights the modern research directions currently employed to demonstrate the utility of the pH responsive core-shell magnetic NPs in diagnosis and treatment of oncological diseases. PMID:27151685

  10. Ising nanowires with simple core-shell structure; Their characteristic phenomena

    NASA Astrophysics Data System (ADS)

    Kaneyoshi, T.

    2016-09-01

    The phase diagrams and magnetizations of Ising nanowires with simple core-shell structure are investigated by the use of the effective field theory with correlations. A lot of characteristic behaviors observed in ferromagnetic and ferrimagnetic materials as well as novel phenomena have been obtained, although one section of the system is consisted of one spin-1/2 surface shell atom and one spin-1/2 core atom and they are coupled with a positive or a negative shell-core exchange interaction.

  11. Converging sequences in the ab initio no-core shell model

    SciTech Connect

    Forssen, C.; Vary, J. P.; Caurier, E.; Navratil, P.

    2008-02-15

    We demonstrate the existence of multiple converging sequences in the ab initio no-core shell model. By examining the underlying theory of effective operators, we expose the physical foundations for the alternative pathways to convergence. This leads us to propose a revised strategy for evaluating effective interactions for A-body calculations in restricted model spaces. We suggest that this strategy is particularly useful for applications to nuclear processes in which states of both parities are used simultaneously, such as for transition rates. We demonstrate the utility of our strategy with large-scale calculations in light nuclei.

  12. Widely tuning optical properties of nanoporous gold-titania core-shells.

    PubMed

    Qian, Lihua; Shen, Bo; Qin, Gaowu W; Das, Biswajit

    2011-01-01

    Widely shifting localized surface plasmon resonance (LSPR) bands of nanoporous metals is essential for light manipulation within small volumes. In this work, nanoporous gold-titania core-shells fabricated by atomic layer deposition exhibit tunable LSPR of gold skeletons in comparison with nanoporous gold-alumina developed before. Extremely large red-shift of LSPR band in nanoporous gold-titania from 537 to 751 nm results from high refractive index of titania and its dielectric medium dependence of LSPR, and the well-controlled thickness of titania shell at the nanometer scale will benefit to integrate optical nanodevices with supreme performances. PMID:21219020

  13. Multifunctional core-shell-corona-type polymeric micelles for anticancer drug-delivery and imaging.

    PubMed

    Bastakoti, Bishnu Prasad; Wu, Kevin C-W; Inoue, Masamichi; Yusa, Shin-ichi; Nakashima, Kenichi; Yamauchi, Yusuke

    2013-04-01

    We have developed core-shell-corona-type polymeric micelles that can integrate multiple functions in one system, including the capability of accommodating hydrophobic dyes into core and hydrophilic drug into the shell, as well as pH-triggered drug-release. The neutral and hydrophilic corona sterically stabilizes the multifunctional polymeric micelles in aqueous solution. The mineralization of calcium phosphate (CaP) on the PAA domain not only enhances the diagnostic efficacy of organic dyes, but also works as a diffusion barrier for the controlled release. PMID:23417774

  14. Tunable two types of Fano resonances in metal-dielectric core-shell nanoparticle clusters

    NASA Astrophysics Data System (ADS)

    Yang, Zhong-Jian; Wang, Qu-Quan; Lin, Hai-Qing

    2013-09-01

    We demonstrate that two types of Fano resonances could be observed in metal-dielectric core-shell nanoparticle heptamer clusters. The first kind of Fano resonance is caused by the coupling between electric dipolar plasmon modes. It still remains with high refractive index shells even though metal cores are separated by them. The second one is caused by the interference between scattering electromagnetic modes of dielectric shell and modified plasmon modes. The energy and line shape of these Fano resonances are highly tunable with shell index and particle geometry, which could find applications in nanophotonics.

  15. Core-shell polymeric microcapsules with superior thermal and solvent stability.

    PubMed

    Kang, Sen; Baginska, Marta; White, Scott R; Sottos, Nancy R

    2015-05-27

    A protective polydopamine (PDA) coating is applied to core-shell microcapsule surfaces by the polymerization of dopamine monomers. A neutral aqueous solution and the addition of an oxidant (i.e., ammonium persulfate) are crucial for microcapsule survival and the initiation of PDA polymerization, respectively. The resulting PDA coating is a dense and uniform layer approximately 50 nm thick. The PDA protective coating significantly increases capsule stability at an elevated temperature (180 °C) and in a variety of organic solvents and acidic/basic solutions that otherwise lead to deflation and loss of the core content of uncoated microcapsules. PMID:25923539

  16. Probing inhomogeneous composition in core/shell nanowires by Raman spectroscopy

    SciTech Connect

    Amaduzzi, F.; Alarcón-Lladó, E.; Russo-Averchi, E.; Matteini, F.; Heiß, M.; Tütüncüoglu, G.; Conesa-Boj, S.; Fontcuberta i Morral, A.; Mata, M. de la; Arbiol, J.

    2014-11-14

    Due to its non-destructive and its micro-spatial resolution, Raman spectroscopy is a powerful tool for a rapid structural and compositional characterization of nanoscale materials. Here, by combining the compositional dependence of the Raman peaks with the existence of photonic modes in the nanowires, we address the composition inhomogeneities of Al{sub x}Ga{sub 1−x}As/GaAs core/shell structures. The experimental results are validated with complementary chemical composition maps of the nanowire cross-sections and finite-difference time-domain simulations of the photonic modes.

  17. Longitudinal versus polar wrinkling of core-shell fibers with anisotropic size mismatches

    NASA Astrophysics Data System (ADS)

    Patrício, P.; Teixeira, P. I. C.; Trindade, A. C.; Godinho, M. H.

    2014-01-01

    We consider a fiber made of a soft elastic material, encased in a stiff elastic shell (core-shell geometry). If the core and shell dimensions are mismatched, e.g., because the core shrinks while the shell does not, but the two remain attached, then an elastic instability is triggered whereby wrinkles may appear on the shell. The wrinkle orientation may be longitudinal (along the fiber axis), polar (along the fiber perimeter), or a mixture of both, depending on the fiber's geometrical and material parameters. Here we investigate under what conditions longitudinal or polar wrinkling will occur.

  18. Hybrid Ag@TiO2 core-shell nanostructures with highly enhanced photocatalytic performance.

    PubMed

    Yang, X H; Fu, H T; Wong, K; Jiang, X C; Yu, A B

    2013-10-18

    A new synthetic approach has been developed to prepare silver@titanium dioxide (Ag@TiO2) core-shell nanostructures with controllable size, shape, crystal phase and function at ambient conditions (e.g. in water, ≤100 ° C). This approach shows a few unique features, including short reaction time (a few minutes) for forming core-shell nanostructures, no requirement of high temperature calcinations for generating TiO2 (e.g. at ~100 ° C in our case), tunable TiO2 shell thickness, high yield and good reproducibility. The experimental results show that the Ag@TiO2 core-shell nanostructures exhibit excellent photocatalytic activity compared to the commercial TiO2 (P25) and Ag-doped TiO2 nanocomposite in the degradation of organic dye molecules (e.g. methyl orange) with ultraviolet (UV) irradiation. This could be attributed to the large surface area of TiO2 nanoparticles for maximum harvesting of UV light, mixed anatase and rutile crystalline phases in the TiO2 shell and the effective charge separation between Ag and TiO2 that can reduce the possible recombination of electron-hole (e(-)-h(+)) pairs within TiO2 generated under UV radiation. To further understand the charge separation situation within Ag-TiO2 composites, theoretical simulation (e.g. density functional theory, DFT) was employed in this study. The DFT simulation results indicate that for the Ag@TiO2 core-shell nanostructures, photo-generated electrons transfer readily from the external TiO2 layer to the internal Ag layer with heavy accumulation compared to those doping Ag on TiO2 surfaces, which may reduce the recombination of e(-)-h(+) pairs and thus enhance the photocatalytic efficiency. The findings may open a new strategy to synthesize TiO2-based photocatalysts with highly enhanced efficiency for environmental remediation applications. PMID:24045164

  19. Hybrid Ag@TiO2 core-shell nanostructures with highly enhanced photocatalytic performance

    NASA Astrophysics Data System (ADS)

    Yang, X. H.; Fu, H. T.; Wong, K.; Jiang, X. C.; Yu, A. B.

    2013-10-01

    A new synthetic approach has been developed to prepare silver@titanium dioxide (Ag@TiO2) core-shell nanostructures with controllable size, shape, crystal phase and function at ambient conditions (e.g. in water, ≤100 ° C). This approach shows a few unique features, including short reaction time (a few minutes) for forming core-shell nanostructures, no requirement of high temperature calcinations for generating TiO2 (e.g. at ˜100 ° C in our case), tunable TiO2 shell thickness, high yield and good reproducibility. The experimental results show that the Ag@TiO2 core-shell nanostructures exhibit excellent photocatalytic activity compared to the commercial TiO2 (P25) and Ag-doped TiO2 nanocomposite in the degradation of organic dye molecules (e.g. methyl orange) with ultraviolet (UV) irradiation. This could be attributed to the large surface area of TiO2 nanoparticles for maximum harvesting of UV light, mixed anatase and rutile crystalline phases in the TiO2 shell and the effective charge separation between Ag and TiO2 that can reduce the possible recombination of electron-hole (e--h+) pairs within TiO2 generated under UV radiation. To further understand the charge separation situation within Ag-TiO2 composites, theoretical simulation (e.g. density functional theory, DFT) was employed in this study. The DFT simulation results indicate that for the Ag@TiO2 core-shell nanostructures, photo-generated electrons transfer readily from the external TiO2 layer to the internal Ag layer with heavy accumulation compared to those doping Ag on TiO2 surfaces, which may reduce the recombination of e--h+ pairs and thus enhance the photocatalytic efficiency. The findings may open a new strategy to synthesize TiO2-based photocatalysts with highly enhanced efficiency for environmental remediation applications.

  20. Optimal design of hollow core-shell structural active materials for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Jiang, Wenjuan; Li, Tingting; Ma, Zengsheng; Lin, Jianguo; Lu, Chunsheng

    To mitigate mechanical and chemical degradation of active materials, hollow core-shell structures have been applied in lithium ion batteries. Without embedding of lithium ions, the rigid coating shell can constrain the inward volume deformation. In this paper, optimal conditions for the full use of inner hollow space are identified in terms of the critical ratio of shell thickness and inner size and the state of charge. It is shown that the critical ratios are 0.10 and 0.15 for Si particle and tube (0.12 and 0.18 for Sn particle and tube), and above which there is lack of space for further lithiation.

  1. No-Core Shell Model Calculations in Light Nuclei with Three-Nucleon Forces

    SciTech Connect

    Barrett, B R; Vary, J P; Nogga, A; Navratil, P; Ormand, W E

    2004-01-08

    The ab initio No-Core Shell Model (NCSM) has recently been expanded to include nucleon-nucleon (NN) and three-nucleon (3N) interactions at the three-body cluster level. Here it is used to predict binding energies and spectra of p-shell nuclei based on realistic NN and 3N interactions. It is shown that 3N force (3NF) properties can be studied in these nuclear systems. First results show that interactions based on chiral perturbation theory lead to a realistic description of {sup 6}Li.

  2. Preparation and optical properties of silica@Ag Cu alloy core-shell composite colloids

    NASA Astrophysics Data System (ADS)

    Zhang, Jianhui; Liu, Huaiyong; Wang, Zhenlin; Ming, Naiben

    2007-04-01

    The silica@Ag-Cu alloy core-shell composite colloids have been successfully synthesized by an electroless plating approach to explore the possibility of modifying the plasmon resonance at the nanoshell surface by varying the metal nanoshell composition for the first time. The surface plasmon resonance of the composite colloids increases in intensity and shifts towards longer, then shorter wavelengths as the Cu/Ag ratio in the alloy shell is increased. The variations in intensity of the surface plasmon resonance with the Cu/Ag ratio obviously affect the Raman bands of the silica colloid core. The report here may supply a new technique to effectively modify the surface plasmon resonance.

  3. Shape evolution of a core-shell spherical particle under hydrostatic pressure.

    PubMed

    Colin, Jérôme

    2012-03-01

    The morphological evolution by surface diffusion of a core-shell spherical particle has been investigated theoretically under hydrostatic pressure when the shear modulii of the core and shell are different. A linear stability analysis has demonstrated that depending on the pressure, shear modulii, and radii of both phases, the free surface of the composite particle may be unstable with respect to a shape perturbation. A stability diagram finally emphasizes that the roughness development is favored in the case of a hard shell with a soft core. PMID:22587137

  4. Metal enhanced fluorescence in rare earth doped plasmonic core-shell nanoparticles

    NASA Astrophysics Data System (ADS)

    Derom, S.; Berthelot, A.; Pillonnet, A.; Benamara, O.; Jurdyc, A. M.; Girard, C.; Colas des Francs, G.

    2013-12-01

    We theoretically and numerically investigate metal enhanced fluorescence of plasmonic core-shell nanoparticles doped with rare earth (RE) ions. Particle shape and size are engineered to maximize the average enhancement factor (AEF) of the overall doped shell. We show that the highest enhancement (11 in the visible and 7 in the near-infrared) is achieved by tuning either the dipolar or the quadrupolar particle resonance to the rare earth ion’s excitation wavelength. Additionally, the calculated AEFs are compared to experimental data reported in the literature, obtained in similar conditions (plasmon mediated enhancement) or when a metal-RE energy transfer mechanism is involved.

  5. First-Principles Study on β-SiC/BNNT Core/shell Nanocable

    NASA Astrophysics Data System (ADS)

    Zou, X. C.; Ouyang, J.; Wu, M. S.; Liu, G.; Lei, X. L.; Ouyang, C. Y.; Xu, B.

    2013-09-01

    In this paper, we studied the structural and electronic properties of core/shell nanocables composed of cubic silicon carbide nanowires (β-SiCNW) and boron nitride nanotubes (BNNT) using first-principles pseudopotential plane wave method within density functional theory. Our results show that the β-SiC/BNNT heterojunction structures are metallic, which primarily originates from the contributions of the BNNTs and the surfaces of SiCNWs. The BNNTs exhibit metallic characters after the SiC nanowires are inserted. The transition of the BNNTs is attributed to the charge transfer between BNNTs and SiCNWs.

  6. Au@Pd core-shell nanobricks with concave structures and their catalysis of ethanol oxidation.

    PubMed

    Wang, Wenjin; Zhang, Jie; Yang, Shengchun; Ding, Bingjun; Song, Xiaoping

    2013-10-01

    Au@Pd core-shell nanobricks (CNBs) with concave surfaces and Pd shells with a thickness of approximately 5 nm were synthesized by co-reduction of HAuCl4 and H2 PdCl4 in the presence of Au seeds and Ag ions. These as-synthesized concave CNBs exhibit significantly enhanced catalytic activity for the electrooxidation of ethanol in alkaline media compared to the commercially-used Pd black. The improved performance of the Au@Pd CNBs can be attributed to the exposed stepped surfaces, high-index facets, and the synergistic effects of the core and shell metals. PMID:23929810

  7. Multilevel memristor effect in metal-semiconductor core-shell nanoparticles tested by scanning tunneling spectroscopy

    NASA Astrophysics Data System (ADS)

    Chakrabarti, Sudipto; Pal, Amlan J.

    2015-05-01

    We have grown gold (Au) and copper-zinc-tin-sulfide (CZTS) nanocrystals and Au-CZTS core-shell nanostructures, with gold in the core and the semiconductor in the shell layer, through a high-temperature colloidal synthetic approach. Following usual characterization, we formed ultrathin layers of these in order to characterize the nanostructures in an ultrahigh-vacuum scanning tunneling microscope. Scanning tunneling spectroscopy of individual nanostructures showed the memristor effect or resistive switching from a low- to a high-conducting state upon application of a suitable voltage pulse. The Au-CZTS core-shell nanostructures also show a multilevel memristor effect with the nanostructures undergoing two transitions in conductance at two magnitudes of voltage pulse. We have studied the reproducibility, reversibility, and retentivity of the multilevel memristors. From the normalized density of states (NDOS), we infer that the memristor effect is correlated to a decrease in the transport gap of the nanostructures. We also infer that the memristor effect occurs in the nanostructures due to an increase in the density of available states upon application of a voltage pulse.We have grown gold (Au) and copper-zinc-tin-sulfide (CZTS) nanocrystals and Au-CZTS core-shell nanostructures, with gold in the core and the semiconductor in the shell layer, through a high-temperature colloidal synthetic approach. Following usual characterization, we formed ultrathin layers of these in order to characterize the nanostructures in an ultrahigh-vacuum scanning tunneling microscope. Scanning tunneling spectroscopy of individual nanostructures showed the memristor effect or resistive switching from a low- to a high-conducting state upon application of a suitable voltage pulse. The Au-CZTS core-shell nanostructures also show a multilevel memristor effect with the nanostructures undergoing two transitions in conductance at two magnitudes of voltage pulse. We have studied the reproducibility

  8. Jacobi no-core shell model for p-shell nuclei

    NASA Astrophysics Data System (ADS)

    Liebig, S.; Meißner, U.-G.; Nogga, A.

    2016-04-01

    We introduce an algorithm to obtain coefficients of fractional parentage for light p-shell nuclei. The coefficients enable one to use Jacobi coordinates in no-core shell model calculations separating off the center-of-mass motion. Fully antisymmetrized basis states are given together with recoupling coefficients that allow one to apply two- and three-nucleon operators. As an example, we study the dependence on the harmonic oscillator frequency of 3H, 4He, 6He, 6Li and 7Li and extract their binding and excitation energies. The coefficients will be made openly accessible as HDF5 data files.

  9. Surface-engineered core-shell nano-size ferrites and their antimicrobial activity

    SciTech Connect

    Baraliya, Jagdish D. Joshi, Hiren H.

    2014-04-24

    We report the results of biological study on core-shell structured MFe{sub 2}O{sub 4} (where M = Co, Mn, Ni) nanoparticles and influence of silica- DEG dual coating on their antimicrobial activity. Spherical MFe{sub 2}O{sub 4} nanoparticles were prepared via a Co-precipitation method. The microstructures and morphologies of these nanoparticles were studied by x-ray diffraction and FTIR. The antimicrobial activity study carried out in nutrient agar medium with addition of antimicrobial synthesis compound which is tested for its activity against different types of bacteria.

  10. Controllable synthesis of concave cubic gold core-shell nanoparticles for plasmon-enhanced photon harvesting.

    PubMed

    Bai, Yang; Butburee, Teera; Yu, Hua; Li, Zhen; Amal, Rose; Lu, G Q Max; Wang, Lianzhou

    2015-07-01

    Well-defined core-shell nanoparticles (NPs) containing concave cubic Au cores and TiO2 shells (CA@T) were synthesized in colloidal suspension. These CA@T NPs exhibit Localized Surface Plasmon Resonance (LSPR) absorption in the NIR region, which provides a unique property for utilizing the low energy range of the solar spectrum. In order to evaluate the plasmonic enhancement effect, a variety of CA@T NPs were incorporated into working electrodes of dye-sensitized solar cells (DSSCs). By adjusting the shell thickness of CA@T NPs, the plasmonic property can be tuned to achieve maximum photovoltaic improvement. Furthermore, the DSSC cells fabricated with the CA@T NPs exhibit a remarkably plasmonic assisted conversion efficiency enhancement (23.3%), compared to that (14.8%) of the reference cells assembled with spherical Au@TiO2 core-shell (SA@T) NPs under similar conditions. Various characterizations reveal that this performance improvement is attributed to the much stronger electromagnetic field generated at the hot spots of CA@T NPs, resulting in significantly higher light harvesting and more efficient charge separation. This study also provides new insights into maximizing the plasmonic enhancement, offering great potential in other applications including light-matter interaction, photocatalytic energy conversion and new-generation solar cells. PMID:25498878

  11. No-Core Shell Model for 48-Ca, 48-Sc and 48-Ti

    SciTech Connect

    Popescu, S; Stoica, S; Vary, J P; Navratil, P

    2004-10-26

    The authors report the first no-core shell model results for {sup 48}Ca, {sup 48}Sc and {sup 48}Ti with derived and modified two-body Hamiltonians. We use an oscillator basis with a limited {bar h}{Omega} range around 40/A{sup 1/3} = 11 MeV and a limited model space up to 1 {bar h}{Omega}. No single-particle energies are used. They find that the charge dependence of the bulk binding energy of eight A = 48 nuclei is reasonably described with an effective Hamiltonian derived from the CD-Bonn interaction while there is an overall underbinding by about 0.4 MeV/nucleon. However, resulting spectra exhibit deficiencies that are anticipated due to: (1) basis space limitations and/or the absence of effective many-body interactions; and, (2) the absence of genuine three-nucleon interactions. They introduce phenomenological modifications to obtain fits to total binding and low-lying spectra. The resulting no-core shell model opens a path for applications to experiments such as the double-beta ({beta}{beta}) decay process.

  12. Mechanisms of morphological evolution on faceted core-shell nanowire surfaces

    NASA Astrophysics Data System (ADS)

    Zhang, Qian; Aqua, Jean-Noël; Voorhees, Peter W.; Davis, Stephen H.

    2016-06-01

    Core-shell nanowires with radial heterostructures hold great promise in photonic and electronic applications and controlling the formation of these heterostructures in the core-shell conguration remains a challenge. Recently, GaAs nanowires have been used as substrates to create AlGaAs shells. The deposition of the AlGaAs layer leads to the spontaneous formation of Al-rich stripes along certain crystallographic directions and quantum dots near the apexes of the shell. A general two-dimensional model has been developed for the motion of the faceted solid-vapor interfaces for pure materials that accounts for capillarity and deposition. With this model, the growth processes and morphological evolution of shells of nanowires around hexagonal cores (six small facets {112} in the corners of six equivalent facets {110}) are investigated in detail both analytically and numerically. It is found that deposition can yield facets that are not present on the Wulff shape. These small facets can have slowly time-varying sizes that can lead to stripe structures and quantum dots depending on the balances between diffusion and deposition. The effects of deposition rates and polarity (or asymmetry) on planes {112} on the development of the configurations of nanowires are discussed. The numerical results are compared with experimental results giving almost quantitative agreement, despite the fact that only pure materials are treated herein whereas the experiments deal with alloys.

  13. Synthesis and characterization of Fe3O4-TiO2 core-shell nanoparticles

    NASA Astrophysics Data System (ADS)

    Stefan, M.; Pana, O.; Leostean, C.; Bele, C.; Silipas, D.; Senila, M.; Gautron, E.

    2014-09-01

    Composite core-shell nanoparticles may have morpho-structural, magnetic, and optical (photoluminescence (PL)) properties different from each of the components considered separately. The properties of Fe3O4-TiO2 nanoparticles can be controlled by adjusting the titania amount (shell thinness). Core-shell nanoparticles were prepared by seed mediated growth of semiconductor (TiO2) through a modified sol-gel process onto preformed magnetite (Fe3O4) cores resulted from the co-precipitation method. The structure and morphology of samples were characterized by X-ray diffraction, transmission electron microscopy (TEM), and high resolution-TEM respectively. X-ray photoelectron spectroscopy was correlated with ICP-AES. Magnetic measurements, optical absorption spectra, as well as PL spectroscopy indicate the presence of a charge/spin transfer from the conduction band of magnetite into the band gap of titania nanocrystals. The process modifies both Fe3O4 and TiO2 magnetic and optical properties, respectively.

  14. Mechanical Fracturing of Core-Shell Undercooled Metal Particles for Heat-Free Soldering

    PubMed Central

    Çınar, Simge; Tevis, Ian D.; Chen, Jiahao; Thuo, Martin

    2016-01-01

    Phase-change materials, such as meta-stable undercooled (supercooled) liquids, have been widely recognized as a suitable route for complex fabrication and engineering. Despite comprehensive studies on the undercooling phenomenon, little progress has been made in the use of undercooled metals, primarily due to low yields and poor stability. This paper reports the use of an extension of droplet emulsion technique (SLICE) to produce undercooled core-shell particles of structure; metal/oxide shell-acetate (‘/’ = physisorbed, ‘-’ = chemisorbed), from molten Field’s metal (Bi-In-Sn) and Bi-Sn alloys. These particles exhibit stability against solidification at ambient conditions. Besides synthesis, we report the use of these undercooled metal, liquid core-shell, particles for heat free joining and manufacturing at ambient conditions. Our approach incorporates gentle etching and/or fracturing of outer oxide-acetate layers through mechanical stressing or shearing, thus initiating a cascade entailing fluid flow with concomitant deformation, combination/alloying, shaping, and solidification. This simple and low cost technique for soldering and fabrication enables formation of complex shapes and joining at the meso- and micro-scale at ambient conditions without heat or electricity. PMID:26902483

  15. Engineering of Superparamagnetic Core-Shell Iron Oxide/N-Chloramine Nanoparticles for Water Purification.

    PubMed

    Haham, Hai; Natan, Michal; Gutman, Ori; Kolitz-Domb, Michal; Banin, Ehud; Margel, Shlomo

    2016-07-20

    In this study, we describe the synthesis and characterization of superparamagnetic core-shell iron oxide (IO)/N-halamine antibacterial nanoparticles (NPs). For this purpose, superparamagnetic IO core NPs were coated with cross-linked polymethacrylamide (PMAA) by surfactant-free dispersion copolymerization of methacrylamide and N,N-methylenebis(acrylamide) in an aqueous continuous phase. The effect of the polymerization process on the chemical composition, size, shape, crystallinity, and magnetic properties of the IO/PMAA NPs was elucidated. Conversion of the core-shell IO/PMAA NPs into their N-halamine form, IO/PMAA-Cl, was accomplished using a chlorination reaction with sodium hypochlorite. The influence of chlorination on the shape, crystallinity, and magnetic properties of the IO/PMAA NPs was studied. The IO/PMAA-Cl NPs demonstrated excellent antibacterial activity against Gram-negative and Gram-positive bacteria. Finally, the chlorination recharging capabilities of the NPs and their potential for use in the purification of water containing bacteria were demonstrated with magnetic columns packed with the IO/PMAA-Cl NPs. PMID:27348740

  16. Intrinsically core-shell plasmonic dielectric nanostructures with ultrahigh refractive index

    PubMed Central

    Yue, Zengji; Cai, Boyuan; Wang, Lan; Wang, Xiaolin; Gu, Min

    2016-01-01

    Topological insulators are a new class of quantum materials with metallic (edge) surface states and insulating bulk states. They demonstrate a variety of novel electronic and optical properties, which make them highly promising electronic, spintronic, and optoelectronic materials. We report on a novel conic plasmonic nanostructure that is made of bulk-insulating topological insulators and has an intrinsic core-shell formation. The insulating (dielectric) core of the nanocone displays an ultrahigh refractive index of up to 5.5 in the near-infrared frequency range. On the metallic shell, plasmonic response and strong backward light scattering were observed in the visible frequency range. Through integrating the nanocone arrays into a-Si thin film solar cells, up to 15% enhancement of light absorption was predicted in the ultraviolet and visible ranges. With these unique features, the intrinsically core-shell plasmonic nanostructure paves a new way for designing low-loss and high-performance visible to infrared optical devices. PMID:27051869

  17. Synthesis of zirconium tungstate-zirconia core-shell composite particles

    SciTech Connect

    Khazeni, Nasser; Mavis, Bora; Guenduez, Guengoer; Colak, Uner

    2011-11-15

    Highlights: {yields} ZrW{sub 2}O{sub 8}-ZrO{sub 2} core-shell particles to offer solutions for sintering problems. {yields} Core synthesis by a precursor based on tungstic acid and zirconium acetate. {yields} Shell phase by urea hydrolysis in the presence of zirconium ions. {yields} [Urea]/[ZrOCl{sub 2}] ratio controls the rate of shell precursor precipitation. -- Abstract: In this work, ZrW{sub 2}O{sub 8}-ZrO{sub 2} core-shell composite particles were synthesized. ZrW{sub 2}O{sub 8} that was used in the core is a material with negative coefficient of thermal expansion, and it was synthesized from a high-pH precursor based on use of tungstic acid and zirconium acetate. Shell layer was composed of ZrO{sub 2} nanocrystallites and precipitated from an aqueous solution by urea hydrolysis. While volume of the shell was effectively controlled by the initial zirconium ion concentration in the solutions, the rate of precipitation was a function of the ratio of initial concentrations of urea to zirconium ions. It is hypothesized that isolation of the ZrW{sub 2}O{sub 8} within a layer of ZrO{sub 2}, will be a key element in solving problems associated with reactivity of ZrW{sub 2}O{sub 8} towards other components in sintering of ceramic-ceramic composites with tuned or zero thermal expansion coefficient.

  18. Carboxymethyl chitosan-poly(amidoamine) dendrimer core-shell nanoparticles for intracellular lysozyme delivery.

    PubMed

    Zhang, Xiaoyang; Zhao, Jun; Wen, Yan; Zhu, Chuanshun; Yang, Jun; Yao, Fanglian

    2013-11-01

    Intracellular delivery of native, active proteins is challenging due to the fragility of most proteins. Herein, a novel polymer/protein polyion complex (PIC) nanoparticle with core-shell structure was prepared. Carboxymethyl chitosan-grafted-terminal carboxyl group-poly(amidoamine) (CM-chitosan-PAMAM) dendrimers were synthesized by amidation and saponification reactions. (1)H NMR was used to characterize CM-chitosan-PAMAM dendrimers. The TEM images and results of lysozyme loading efficiency indicated that CM-chitosan-PAMAM dendrimers could self-assemble into core-shell nanoparticles, and lysozyme was efficiently encapsulated inside the core of CM-chitosan-PAMAM dendrimer nanoparticles. Activity of lysozyme was completely inhibited by CM-chitosan-PAMAM Dendrimers at physiological pH, whereas it was released into the medium and exhibited a significant enzymatic activity in an acidic intracellular environment. Moreover, the CM-chitosan-PAMAM dendrimer nanoparticles did not exhibit significant cytotoxicity in the range of concentrations below 3.16 mg/ml. The results indicated that these CM-chitosan-PAMAM dendrimers have excellent properties as highly potent and non-toxic intracellular protein carriers, which would create opportunities for novel applications in protein delivery. PMID:24053810

  19. Fast-dissolving core-shell composite microparticles of quercetin fabricated using a coaxial electrospray process.

    PubMed

    Li, Chen; Yu, Deng-Guang; Williams, Gareth R; Wang, Zhuan-Hua

    2014-01-01

    This study reports on novel fast-dissolving core-shell composite microparticles of quercetin fabricated using coaxial electrospraying. A PVC-coated concentric spinneret was developed to conduct the electrospray process. A series of analyses were undertaken to characterize the resultant particles in terms of their morphology, the physical form of their components, and their functional performance. Scanning and transmission electron microscopies revealed that the microparticles had spherical morphologies with clear core-shell structure visible. Differential scanning calorimetry and X-ray diffraction verified that the quercetin active ingredient in the core and sucralose and sodium dodecyl sulfate (SDS) excipients in the shell existed in the amorphous state. This is believed to be a result of second-order interactions between the components; these could be observed by Fourier transform infrared spectroscopy. In vitro dissolution and permeation studies showed that the microparticles rapidly released the incorporated quercetin within one minute, and had permeation rates across the sublingual mucosa around 10 times faster than raw quercetin. PMID:24643072

  20. Design of Gas-phase Synthesis of Core-Shell Particles by Computational Fluid - Aerosol Dynamics.

    PubMed

    Buesser, B; Pratsinis, S E

    2011-11-01

    Core-shell particles preserve the bulk properties (e.g. magnetic, optical) of the core while its surface is modified by a shell material. Continuous aerosol coating of core TiO2 nanoparticles with nanothin silicon dioxide shells by jet injection of hexamethyldisiloxane precursor vapor downstream of titania particle formation is elucidated by combining computational fluid and aerosol dynamics. The effect of inlet coating vapor concentration and mixing intensity on product shell thickness distribution is presented. Rapid mixing of the core aerosol with the shell precursor vapor facilitates efficient synthesis of hermetically coated core-shell nanoparticles. The predicted extent of hermetic coating shells is compared to the measured photocatalytic oxidation of isopropanol by such particles as hermetic SiO2 shells prevent the photocatalytic activity of titania. Finally the performance of a simpler, plug-flow coating model is assessed by comparisons to the present detailed CFD model in terms of coating efficiency and silica average shell thickness and texture. PMID:23729817

  1. Magnetic proximity effect in ferrimagnetic-ferromagnetic core-shell Prussian blue analogues molecular magnet

    NASA Astrophysics Data System (ADS)

    Bhatt, Pramod; Kumar, Amit; Meena, S. S.; Mukadam, M. D.; Yusuf, S. M.

    2016-05-01

    A magnetic proximity effect has been observed in core-shell structure of molecular magnet, Mn1.5[Cr(CN)6]·mH2O@Ni1.5[Cr(CN)6]·nH2O, synthesized using a ferrimagnetic core of Mn1.5[Cr(CN)6]·7.5H2O surrounded by a ferromagnetic shell of Ni1.5[Cr(CN)6]·7.5H2O. The values of Curie temperature (TC) are found to be of ∼65 and ∼60 K for the bare-core and bare-shell compounds, respectively. However, an enhanced TC (∼70 K) has been observed for the core-shell structure. The proximity effect (due to presence of interface exchange coupling) between core and shell is responsible for the observed enhancement of TC. A neutron depolarization study also confirms finite depolarization below ∼70 K.

  2. Effects of Nonlocal Exact Exchange on Electrons in Core/Shell Nanowires

    NASA Astrophysics Data System (ADS)

    Wong, Bryan; Long, Andrew

    2013-03-01

    The unique properties of semiconducting heterostructure nanowires hold great promise for their incorporation in next-generation transistors, circuits, and nanoscale devices. The reduction in dimensionality produced by confining electrons in these heterostructure nanowires results in a dramatic change in their electronic structure, leading to novel properties such as ballistic transport and conductance quantization. In order to understand the formation of electron gases in core-shell nanowires, we developed a new pseudospectral approach for incorporating many-body, nonlocal exact exchange interactions within a self-consistent Schrodinger-Poisson formalism. Our approach is efficiently implemented in the open-source software package PAMELA (Pseudospectral Analysis Method with Exchange & Local Approximations) that can calculate electronic energies, densities, wavefunctions, and band-bending diagrams. Furthermore, in order to present a general-purpose set of tools that both experimentalists and theorists can easily use to predict electron gas formation in core-shell nanowires, we document and provide our efficient and user-friendly PAMELA source code that is freely available at http://alum.mit.edu/www/usagi.

  3. Multilevel memristor effect in metal-semiconductor core-shell nanoparticles tested by scanning tunneling spectroscopy.

    PubMed

    Chakrabarti, Sudipto; Pal, Amlan J

    2015-06-01

    We have grown gold (Au) and copper-zinc-tin-sulfide (CZTS) nanocrystals and Au-CZTS core-shell nanostructures, with gold in the core and the semiconductor in the shell layer, through a high-temperature colloidal synthetic approach. Following usual characterization, we formed ultrathin layers of these in order to characterize the nanostructures in an ultrahigh-vacuum scanning tunneling microscope. Scanning tunneling spectroscopy of individual nanostructures showed the memristor effect or resistive switching from a low- to a high-conducting state upon application of a suitable voltage pulse. The Au-CZTS core-shell nanostructures also show a multilevel memristor effect with the nanostructures undergoing two transitions in conductance at two magnitudes of voltage pulse. We have studied the reproducibility, reversibility, and retentivity of the multilevel memristors. From the normalized density of states (NDOS), we infer that the memristor effect is correlated to a decrease in the transport gap of the nanostructures. We also infer that the memristor effect occurs in the nanostructures due to an increase in the density of available states upon application of a voltage pulse. PMID:25966930

  4. Intrinsically core-shell plasmonic dielectric nanostructures with ultrahigh refractive index.

    PubMed

    Yue, Zengji; Cai, Boyuan; Wang, Lan; Wang, Xiaolin; Gu, Min

    2016-03-01

    Topological insulators are a new class of quantum materials with metallic (edge) surface states and insulating bulk states. They demonstrate a variety of novel electronic and optical properties, which make them highly promising electronic, spintronic, and optoelectronic materials. We report on a novel conic plasmonic nanostructure that is made of bulk-insulating topological insulators and has an intrinsic core-shell formation. The insulating (dielectric) core of the nanocone displays an ultrahigh refractive index of up to 5.5 in the near-infrared frequency range. On the metallic shell, plasmonic response and strong backward light scattering were observed in the visible frequency range. Through integrating the nanocone arrays into a-Si thin film solar cells, up to 15% enhancement of light absorption was predicted in the ultraviolet and visible ranges. With these unique features, the intrinsically core-shell plasmonic nanostructure paves a new way for designing low-loss and high-performance visible to infrared optical devices. PMID:27051869

  5. Stabilization of Palladium Nanoparticles on Nanodiamond-Graphene Core-Shell Supports for CO Oxidation.

    PubMed

    Zhang, Liyun; Liu, Hongyang; Huang, Xing; Sun, Xueping; Jiang, Zheng; Schlögl, Robert; Su, Dangsheng

    2015-12-21

    Nanodiamond-graphene core-shell materials have several unique properties compared with purely sp(2) -bonded nanocarbons and perform remarkably well as metal-free catalysts. In this work, we report that palladium nanoparticles supported on nanodiamond-graphene core-shell materials (Pd/ND@G) exhibit superior catalytic activity in CO oxidation compared to Pd NPs supported on an sp(2) -bonded onion-like carbon (Pd/OLC) material. Characterization revealed that the Pd NPs in Pd/ND@G have a special morphology with reduced crystallinity and are more stable towards sintering at high temperature than the Pd NPs in Pd/OLC. The electronic structure of Pd is changed in Pd/ND@G, resulting in weak CO chemisorption on the Pd NPs. Our work indicates that strong metal-support interactions can be achieved on a non-reducible support, as exemplified for nanocarbon, by carefully tuning the surface structure of the support, thus providing a good example for designing a high-performance nanostructured catalyst. PMID:26568172

  6. Supported Core@Shell Electrocatalysts for Fuel Cells: Close Encounter with Reality

    PubMed Central

    Hwang, Seung Jun; Yoo, Sung Jong; Shin, Jungho; Cho, Yong-Hun; Jang, Jong Hyun; Cho, Eunae; Sung, Yung-Eun; Nam, Suk Woo; Lim, Tae-Hoon; Lee, Seung-Cheol; Kim, Soo-Kil

    2013-01-01

    Core@shell electrocatalysts for fuel cells have the advantages of a high utilization of Pt and the modification of its electronic structures toward enhancement of the activities. In this study, we suggest both a theoretical background for the design of highly active and stable core@shell/C and a novel facile synthetic strategy for their preparation. Using density functional theory calculations guided by the oxygen adsorption energy and vacancy formation energy, Pd3Cu1@Pt/C was selected as the most suitable candidate for the oxygen reduction reaction in terms of its activity and stability. These predictions were experimentally verified by the surfactant-free synthesis of Pd3Cu1/C cores and the selective Pt shell formation using a Hantzsch ester as a reducing agent. In a similar fashion, Pd@Pd4Ir6/C catalyst was also designed and synthesized for the hydrogen oxidation reaction. The developed catalysts exhibited high activity, high selectivity, and 4,000 h of long-term durability at the single-cell level. PMID:23419683

  7. Employing Core-Shell Quantum Dots as Triplet Sensitizers for Photon Upconversion.

    PubMed

    Okumura, Keisuke; Mase, Kazuma; Yanai, Nobuhiro; Kimizuka, Nobuo

    2016-06-01

    A new family of surface-functionalized CdSe/ZnS core-shell quantum dots (csQD) has been developed, which work as triplet sensitizers for triplet-triplet annihilation-based photon upconversion (TTA-UC). The surface modification of csQD with acceptor molecules plays a key role in the efficient relay of the excited energy of csQD to emitter molecules in the bulk solution, where the generated emitter triplets undergo triplet-triplet annihilation that leads to photon upconversion. Interestingly, improved UC properties were achieved with the core-shell QDs compared with core-only CdSe QDs (cQD). The threshold excitation intensity, which is defined as the necessary irradiance to achieve efficient TTA process, decreases by more than a factor of four. Furthermore, the total UC quantum yield is enhanced more than 50-fold. These enhancements should be derived from better optical properties of csQD, in which the non-radiative surface recombination sites are passivated by the shell layer with wider bandgap. PMID:27121225

  8. Core/Shell and High Aspect Ratio Magnetic Oxide Nanoparticles for Antenna Applications

    NASA Astrophysics Data System (ADS)

    Ekiert, Thomas F., Jr.; O'Malley, Matthew; Yocum, Brandon; Lippold, Jennifer; Lyle, Mallory; Griner, Angela; Flynn, Cory; Nickel, Anna; Alexander, Max D., Jr.

    2012-02-01

    Improved antenna gain, reduced antenna aperture size, and improved bandwidth are of interest to an increasingly mobile world. To obtain these improvements our efforts are directed at developing new magnetic oxide nanoparticle/polymer composites with modifiable permeability and permittivity and low electrical losses. Our approach consists of producing core/shell and shape controlled magnetic nanoparticles. Methods of synthesis utilize microwave and traditional heating to perform hydrothermal and solvothermal reactions. Decomposition of metal acetylacetonates is performed using various alcohols resulting in spherical nanoparticles with diameters of 8-16 nm and 3-7 nm for Fe3O4 and CoFe2O4, respectively. Microwave methods result in similar particles, but are produced in an hour or less as compared to 48 hrs via the traditional solvothermal method. Successive growths are used to produce larger monolithic particles as well as core/shell systems where exchange coupling between the core and shell is observed. Hexaferrite particles have been produced via hydrothermal synthesis, while high aspect ratio Fe3O4 nanoparticles ( 10-100 nm) produced via hydrothermal synthesis result in nanoneedles with high μr.

  9. A theoretical study on the advantage of core-shell particles with radially-oriented mesopores.

    PubMed

    Deridder, Sander; Catani, Martina; Cavazzini, Alberto; Desmet, Gert

    2016-07-22

    We report on a first-principles numerical study explaining the potential advantage of core-shell particles with strictly radially-oriented mesopores. Comparing the efficiency of these particles with fully porous and core-shell particles with a conventional (i.e., randomly oriented) mesopore network, the present numerical study shows a similar strong reduction in minimal reduced plate height (hmin) as was very recently observed in an experimental study by Wei et al. (respectively a hmin-reduction on the order of about 1 and 0.5 reduced plate height-units). As such, the present work provides a theoretical basis to understand and confirm their experimental findings and quantifies the general advantage of "radial-diffusion-only" particles. Determining the effective longitudinal diffusion (B-term contribution) in a series of dedicated, independent simulations, it was found that this contribution can be described by a very simple, yet fully exact mathematical expression for the case of "radial- diffusion-only" particles. Using this expression, the significant increase in efficiency of these particles can be fully attributed to their much smaller B-term band broadening, while their C-term band broadening (representing the mass transfer resistance) remains unaffected. PMID:27317003

  10. Core-Shell Coating Silicon Anode Interfaces with Coordination Complex for Stable Lithium-Ion Batteries.

    PubMed

    Zhou, Jinqiu; Qian, Tao; Wang, Mengfan; Xu, Na; Zhang, Qi; Li, Qun; Yan, Chenglin

    2016-03-01

    In situ core-shell coating was used to improve the electrochemical performance of Si-based anodes with polypyrrole-Fe coordination complex. The vast functional groups in the organometallic coordination complex easily formed hydrogen bonds when in situ modifying commercial Si nanoparticles. The incorporation of polypyrrole-Fe resulted in the conformal conductive coating surrounding each Si nanoparticle, not only providing good electrical connection to the particles but also promoting the formation of a stable solid-electrolyte-interface layer on the Si electrode surface, enhancing the cycling properties. As an anode material for Li-ion batteries, modified silicon powders exhibited high reversible capacity (3567 mAh/g at 0.3 A/g), good rate property (549.12 mAh/g at 12 A/g), and excellent cycling performance (reversible capacity of 1500 mAh/g after 800 cycles at 1.2 A/g). The constructed novel concept of core-shell coating Si particles presented a promising route for facile and large-scale production of Si-based anodes for extremely durable Li-ion batteries, which provided a wide range of applications in the field of energy storage of the renewable energy derived from the solar energy, hydropower, tidal energy, and geothermal heat. PMID:26863089

  11. Photosensitive and biomimetic core-shell nanofibrous scaffolds as wound dressing.

    PubMed

    Jin, Guorui; Prabhakaran, Molamma P; Ramakrishna, Seeram

    2014-01-01

    Tissue engineered skin grafts that mimic the native extracellular matrix of skin has gained huge popularity among clinicians since they increase the survival rate of the patients. Phototherapy shows promising results with respect to acute and chronic pain relief, treatment of inflammatory conditions and promotion of wound healing. Here, we encapsulated a photosensitive polymer poly (3-hexylthiophene) (P3HT) and epidermal growth factor in the core-shell-structured Gelatin/poly(L-lactic acid)-co-poly-(ε-caprolactone) nanofibers [Gel/PLLCL/P3GF(cs)] by coaxial spinning and studied the potential application of the Gel/PLLCL/P3GF(cs) nanofibrous scaffold as a novel skin graft. The proliferation of fibroblasts was significantly improved on Gel/PLLCL/P3GF(cs) under light stimulation compared to fibroblasts on the same scaffold under dark condition. Studies on the in vitro wound healing ability of Gel/PLLCL/P3GF(cs) showed complete closure of wound after 9 days under "light stimulation" too. Furthermore, the potential of adipose-derived stem cells (ASCs) to differentiate to epidermal cells on Gel/PLLCL/P3GF(cs) was evaluated. The differentiated ASCs with keratinocytes morphology were only found on the light stimulated Gel/PLLCL/P3GF(cs). Our results suggest that the photosensitive core-shell Gel/PLLCL/P3GF(cs) nanofibers could be a novel substrate to aid in the reestablishment of skin architecture. PMID:24417712

  12. Quantitative analysis of core-shell catalyst nanoparticles for industrial applications

    NASA Astrophysics Data System (ADS)

    E, H.; Nellist, P. D.; Lozano-Perez, S.; Ozkaya, D.

    2012-07-01

    Pd@Pt core-shell designed nanoparticle catalysts have been shown to dramatically increase the activity and selectivity of the oxygen reduction reaction in fuel cells. Aberration corrected electron microscopy offers the spatial resolution and chemical sensitivity to unlock these structures at the atomic scale. Understanding the particle size, shape and the exact nature of the shell coverage (whether it is full, partial or whether the particle is alloyed) is vital to understanding their behaviour. This paves the way for even more effective catalyst designs. We present a semi-statistical investigation into the size, morphology and bimetallic content of various core-shell particle designs, pre- and post- fuel cell cycling, using high resolution HAADF STEM and EDX. In addition, careful quantitative analysis of our datasets will allow us to extract information, not only of the morphology, but also the thickness and coverage of the particle shells. We compare this with chemical findings about activity and selectivity to understand how shell coverage and content affect catalytic activity.

  13. Magnetic behavior of Joule-heated magnetic core-shell nanowires with positive magnetostrictive core material

    NASA Astrophysics Data System (ADS)

    Dumitru, Ioan; Astefanoaei, Iordana; Cimpoesu, Dorin; Stancu, Alexandru

    2015-10-01

    Temperature field is an important parameter to be known and controlled in the magnetization process of the core-shell nanowires. The paper analyzes the temperature dependence of hysteretic process in a core-shell nanowire subjected to a dc Joule heating process. An electrical current that passes through the wire induces a temperature and a thermal stress field in the system. Spatial and temporal evolution of the temperature in system was analyzed using a model based on time-dependent heat conduction equation. The stresses determined by thermal gradients and different expansion characteristics of core and shell materials were computed. The temperature and stress depend on the size parameters of the system, dc Joule current and the initial temperature of the system. The magnetic behavior of the nanowire was analyzed using the Micromag application. The magnetic state of the core is influenced by the temperature field induced by a dc current applied to the system. For core materials with positive magnetostriction coefficient the coercive field increases at the increase of dc current intensity passed through the system.

  14. Size effects in bimagnetic CoO/CoFe2O4 core/shell nanoparticles.

    PubMed

    Lavorato, Gabriel C; Lima, Enio; Tobia, Dina; Fiorani, Dino; Troiani, Horacio E; Zysler, Roberto D; Winkler, Elin L

    2014-09-01

    The control of the size of bimagnetic nanoparticles represents an important step toward the study of fundamental properties and the design of new nanostructured magnetic materials. We report the synthesis and the structural and magnetic characterization of bimagnetic CoO/CoFe2O4 core/shell nanoparticles. The material was fabricated by a seed-mediated growth high-temperature decomposition method with sizes in the range of 5-11 nm. We show that the core/shell morphology favours the crystallinity of the shell phase, and the reduction of the particle size leads to a remarkable increase of the magnetic hardening. When the size is reduced, the coercive field at 5 K increases from 21.5 kOe to 30.8 kOe, while the blocking temperature decreases from 388 K to 167 K. The size effects on the magnetic behaviour are described through a phenomenological model for strongly ferri-/antiferromagnetic coupled phases. PMID:25120018

  15. Mechanical Fracturing of Core-Shell Undercooled Metal Particles for Heat-Free Soldering.

    PubMed

    Çınar, Simge; Tevis, Ian D; Chen, Jiahao; Thuo, Martin

    2016-01-01

    Phase-change materials, such as meta-stable undercooled (supercooled) liquids, have been widely recognized as a suitable route for complex fabrication and engineering. Despite comprehensive studies on the undercooling phenomenon, little progress has been made in the use of undercooled metals, primarily due to low yields and poor stability. This paper reports the use of an extension of droplet emulsion technique (SLICE) to produce undercooled core-shell particles of structure; metal/oxide shell-acetate ('/' = physisorbed, '-' = chemisorbed), from molten Field's metal (Bi-In-Sn) and Bi-Sn alloys. These particles exhibit stability against solidification at ambient conditions. Besides synthesis, we report the use of these undercooled metal, liquid core-shell, particles for heat free joining and manufacturing at ambient conditions. Our approach incorporates gentle etching and/or fracturing of outer oxide-acetate layers through mechanical stressing or shearing, thus initiating a cascade entailing fluid flow with concomitant deformation, combination/alloying, shaping, and solidification. This simple and low cost technique for soldering and fabrication enables formation of complex shapes and joining at the meso- and micro-scale at ambient conditions without heat or electricity. PMID:26902483

  16. Interfacial strain effect on type-I and type-II core/shell quantum dots

    NASA Astrophysics Data System (ADS)

    Gheshlaghi, Negar; Pisheh, Hadi Sedaghat; Karim, M. Rezaul; Malkoc, Derya; Ünlü, Hilmi

    2016-09-01

    A comparative experimental and theoretical study on the calculation of capped core diameter in ZnSe/ZnS, CdSe/Cd(Zn)S type-I and ZnSe/CdS type-II core/shell nanocrystals is presented. The lattice mismatch induced interface strain between core and shell was calculated from continuum elastic theory and applied in effective mass approximation method to obtain the corresponding capped core diameter. The calculated results were compared with diameter of bare cores (CdSe and ZnSe) from transmission electron microscopy images to obtain the amount of the stretched or squeezed core after deposition of tensile or compressive shells. The result of the study showed that the core is squeezed in ZnSe/ZnS and CdSe/Cd(Zn)S after compressive shell and stretched in ZnSe/CdS after tensile shell deposition. The stretched and squeezed amount of the capped core found to be in proportion with lattice mismatch amount in the core/shell structure.

  17. Synthesis of core-shell bioaffinity chitosan-TiO₂ composite and its environmental applications.

    PubMed

    Xiao, Gang; Su, Haijia; Tan, Tianwei

    2015-01-01

    Based on the coupling of molecular imprinting, chitosan biosorption, and nano TiO2 photocatalysis technologies, a novel core-shell organic-inorganic hybrid material of surface imprinted chitosan-TiO2 composite (SICT) was prepared with methyl orange as the template. SEM, EDS, AFM, pore size analysis, and FTIR characterization results illustrated that TiO2 nano powder was successfully coated on the surface of chitosan microparticles via intermolecular hydrogen bonds to form the core-shell organic-inorganic composites with rough and porous surface morphology. SICT showed enhanced photocatalytic selectivity for methyl orange (M.O.) compared with the non-imprinted chitosan-TiO2 composites because of the existing of more suitable sites generated by surface molecular imprinting. The removal of M.O. by SICT was mainly from the photocatalytic degradation rather than simple adsorption. SICT could be reused directly without further desorption and regeneration for 10 cycles with preserving 60% of its photocatalytic efficiency. The reusability of SICT would be beneficial for the simplification of the operating steps and the cost reduction which facilitated its practical applications in wastewater treatment concerning environmental organic pollutants. PMID:25464333

  18. Strain-Mediated Interfacial Dynamics during Au-PbS Core-Shell Nanostructure Formation.

    PubMed

    Niu, Kai-Yang; Liu, Miao; Persson, Kristin A; Han, Yu; Zheng, Haimei

    2016-06-28

    An understanding of the hierarchical nanostructure formation is of significant importance for the design of advanced functional materials. Here, we report the in situ study of lead sulfide (PbS) growth on gold (Au) nanorod seeds using liquid cell transmission electron microscopy (TEM). By tracking the formation dynamics of Au-PbS core-shell nanoparticles, we found the preferential heterogeneous nucleation of PbS on the ends of a Au nanorod prior to the development of a complete PdS shell. During PbS shell growth, drastic sulfidation of Au nanorod was observed, leading to large volume shrinkage (up to 50%) of the initial Au nanorod seed. We also captured intriguing wavy interfacial behavior, which can be explained by our DFT calculation results that the local strain gradient at the core-shell interface facilitates the mass transport and mediates reversible phase transitions of Au ↔ Au2S during the PbS shell growth. PMID:27214625

  19. Renewable Decyl-alcohol Templated Synthesis of Si-Cu Core-Shell Nanocomposite

    NASA Astrophysics Data System (ADS)

    Salim, M. A.; >H Misran, S. Z.; Shah, N. N. H.; Razak, N. A. A.; >A Manap,

    2013-06-01

    Monodispersed silica spheres with particles size of ca. 450 nm were successfully synthesized using a modified Stöber method. The synthesized monodispersed silica spheres were successfully coated with copper using modified sol-gel method employing nonsurfactant surface modifiers and catalyst. A renewable palm oil based decyl-alcohol (C10) as nonsurfactant surface modifiers and catalyst were used to modify the silica surfaces prior to coating with copper. The X-ray diffraction patterns of Si-Cu core-shell exhibited a broad peak corresponding to amorphous silica networks and monoclinic CuO phase. It was found that samples modified in the presence of 1 ml catalyst exhibited homogeneous deposition. The surface area of core materials (SiO2) was at ca. 7.04 m2/g and Si-Cu core-shell was at ca. 8.21 m2/g. The band gap of samples prepared with and without catalyst was calculated to be ca. 2.45 eV and ca. 3.90 eV respectively based on the UV-vis absorption spectrum of the product.

  20. Synthesis and Characterization of Au@Cu Core-Shell Nanoparticles

    NASA Astrophysics Data System (ADS)

    Khanal, Subarna; Velazquez-Salazar, Jesus; Yacaman, Miguel Jose

    2011-10-01

    The synthesis of bimetallic nanoparticles has become so important in present times due to its diverse applications of nanotechnology. Particularly most of the bimetallic nanoparticles are focused to use in catalysis, plasmonic, magnetic, sensors, and many other applications. In Au/Cu case, the bulk Au and Cu are soluble at all compositions. But the structure of Au/Cu nanoparticles depends on the preparation methods. The structure might be the core shell, alloys or other morphology. Au- Cu core-shell nanocrystals were prepared using a two-step polyol reduction method. First, Au core seeds were prepared by reducing HAuCl4. 4H2O in ethylene glycol (EG) using oil-bath heating in the presence of polyvinylpyrrolidone (PVP) as a polymer surfactant. Then Cu shells were overgrown on Au core seeds by reducing Cu2(OAc)4 in EG with PVP again using oil-bath heating. The morphology is studied by STEM HITACHI S-5500.The resultant crystal structures were characterized using TEM, high-resolution (HR)-TEM and the STEM were using for the study of micro analysis.

  1. Synthesis, structural characterization and magnetic properties of Fe/Pt core-shell nanoparticles

    NASA Astrophysics Data System (ADS)

    Pisane, K. L.; Singh, Sobhit; Seehra, M. S.

    2015-05-01

    Structural and magnetic properties of Fe/Pt core-shell nanostructure prepared by a sequential reduction process are reported. Transmission electron microscopy shows nearly spherical particles fitting a lognormal size distribution with Do = 3.0 nm and distribution width λD = 0.31. In x-ray diffraction, Bragg lines only from the Pt shell are clearly identified with line-widths yielding crystallite size = 3.1 nm. Measurements of magnetization M vs. T (2 K-350 K) in magnetic fields up to 90 kOe show a blocking temperature TB = 13 K below which hysteresis loops are observed with coercivity HC increasing with decreasing T reaching HC = 750 Oe at 2 K. Temperature dependence of the ac susceptibilities at frequencies fm = 10 Hz-5 kHz is measured to determine the change in TB with fm using the Vogel-Fulcher law. This analysis shows the presence of significant interparticle interaction, the Neel-Brown relaxation frequency fo = 5.3 × 1010 Hz and anisotropy constant Ka = 3.6 × 106 ergs/cm3. A fit of the M vs. H data up to H = 90 kOe for T > TB to the modified Langevin function taking particle size distribution into account yields magnetic moment per particle consistent with the proposed core-shell structure; Fe core of 2.2 nm diameter and Pt shell of 0.4 nm thickness.

  2. Synthesis of Core-shell Structured Amorphous Si Nanoparticles by Induction Thermal Plasmas

    NASA Astrophysics Data System (ADS)

    Okamoto, Daisuke; Kageyama, Takuya; Tanaka, Manabu; Sone, Hirotaka; Watanabe, Takayuki

    2015-09-01

    Core-shell structured amorphous Si nanoparticles were synthesized by induction thermal plasma. Crystalline Si powder with 3 μm of average diameter was injected into the induction thermal plasma at 4 MHz. The Si raw materials immediately evaporate in the high temperature plasma region and nanoparticles were produced through the quenching process. Counterflow quenching gas was injected from downstream of the torch with its direction against the plasma flow. The effect of the operating parameter such as flow rate of quenching gas and input power was investigated. Collected particles were characterized by X-ray diffraction, transmission electron microscopy, electron energy-loss spectroscopy, and Raman spectroscopy. Obtained results indicate that amorphization degree of the synthesized nanoparticles is more than 90% when additional quenching gas of 20 L/min is injected. The quenching rate of the prepared nanoparticles in the growth region have an important role on determining the amorphization degree. Moreover, EELS and Raman analyses showed the synthesized nanoparticles were coated by the SiO2 shell with thickness of 2-4 nm. These findings indicated that amorphous Si/SiO2 core-shell structured nanoparticles were successfully synthesized by induction thermal plasma in single step.

  3. The multifunctional wound dressing with core-shell structured fibers prepared by coaxial electrospinning

    NASA Astrophysics Data System (ADS)

    Wei, Qilin; Xu, Feiyang; Xu, Xingjian; Geng, Xue; Ye, Lin; Zhang, Aiying; Feng, Zengguo

    2016-04-01

    The non-woven wound dressing with core-shell structured fibers was prepared by coaxial electrospinning. The polycaprolactone (PCL) was electrospun as the fiber's core to provide mechanical strength whereas collagen was fabricated into the shell in order to utilize its good biocompatibility. Simultaneously, the silver nanoparticles (Ag- NPs) as anti-bacterial agent were loaded in the shell whereas the vitamin A palmitate (VA) as healing-promoting drug was encapsulated in the core. Resulting from the fiber's core-shell structure, the VA released from the core and Ag-NPs present in the shell can endow the dressing both heal-promoting and anti-bacteria ability simultaneously, which can greatly enhance the dressing's clinical therapeutic effect. The dressing can maintain high swelling ratio of 190% for 3 d indicating its potential application as wet dressing. Furthermore, the dressing's anti-bacteria ability against Staphylococcus aureus was proved by in vitro anti-bacteria test. The in vitro drug release test showed the sustainable release of VA within 72 h, while the cell attachment showed L929 cells can well attach on the dressing indicating its good biocompatibility. In conclusion, the fabricated nanofibrous dressing possesses multiple functions to benefit wound healing and shows promising potential for clinical application.

  4. Core-Shell Composite Hydrogels for Controlled Nanocrystal Formation and Release of Hydrophobic Active Pharmaceutical Ingredients.

    PubMed

    Badruddoza, Abu Zayed Md; Godfrin, P Douglas; Myerson, Allan S; Trout, Bernhardt L; Doyle, Patrick S

    2016-08-01

    Although roughly 40% of pharmaceuticals being developed are poorly water soluble, this class of drugs lacks a formulation strategy capable of producing high loads, fast dissolution kinetics, and low energy input. In this work, a novel bottom-up approach is developed for producing and formulating nanocrystals of poorly water-soluble active pharmaceutical ingredients (APIs) using core-shell composite hydrogel beads. Organic phase nanoemulsion droplets stabilized by polyvinyl alcohol (PVA) and containing a model hydrophobic API (fenofibrate) are embedded in the alginate hydrogel matrix and subsequently act as crystallization reactors. Controlled evaporation of this composite material produces core-shell structured alginate-PVA hydrogels with drug nanocrystals (500-650 nm) embedded within the core. Adjustable loading of API nanocrystals up to 83% by weight is achieved with dissolution (of 80% of the drug) occurring in as little as 30 min. A quantitative model is also developed and experimentally validated that the drug release patterns of the fenofibrate nanocrystals can be modulated by controlling the thickness of the PVA shell and drug loading. Thus, these composite materials offer a "designer" drug delivery system. Overall, our approach enables a novel means of simultaneous controlled crystallization and formulation of hydrophobic drugs that circumvents energy intensive top-down processes in traditional manufacturing. PMID:27249402

  5. The multifunctional wound dressing with core-shell structured fibers prepared by coaxial electrospinning

    NASA Astrophysics Data System (ADS)

    Wei, Qilin; Xu, Feiyang; Xu, Xingjian; Geng, Xue; Ye, Lin; Zhang, Aiying; Feng, Zengguo

    2016-06-01

    The non-woven wound dressing with core-shell structured fibers was prepared by coaxial electrospinning. The polycaprolactone (PCL) was electrospun as the fiber's core to provide mechanical strength whereas collagen was fabricated into the shell in order to utilize its good biocompatibility. Simultaneously, the silver nanoparticles (Ag-NPs) as anti-bacterial agent were loaded in the shell whereas the vitamin A palmitate (VA) as healing-promoting drug was encapsulated in the core. Resulting from the fiber's core-shell structure, the VA released from the core and Ag-NPs present in the shell can endow the dressing both heal-promoting and anti-bacteria ability simultaneously, which can greatly enhance the dressing's clinical therapeutic effect. The dressing can maintain high swelling ratio of 190% for 3 d indicating its potential application as wet dressing. Furthermore, the dressing's anti-bacteria ability against Staphylococcus aureus was proved by in vitro anti-bacteria test. The in vitro drug release test showed the sustainable release of VA within 72 h, while the cell attachment showed L929 cells can well attach on the dressing indicating its good biocompatibility. In conclusion, the fabricated nanofibrous dressing possesses multiple functions to benefit wound healing and shows promising potential for clinical application.

  6. Formation mechanism of monodispersed spherical core-shell ceria/polymer hybrid nanoparticles

    SciTech Connect

    Izu, Noriya; Uchida, Toshio; Matsubara, Ichiro; Itoh, Toshio; Shin, Woosuck; Nishibori, Maiko

    2011-08-15

    Graphical abstract: The formation mechanism for core-shell nanoparticles is considered to be as follows: nucleation and particle growth occur simultaneously (left square); very slow particle growth occurs (middle square). Highlights: {yields} The size of the resultant nanoparticles was strongly and complicatedly dependent on the set temperature used during reflux heating and the PVP molecular weight. {yields} The size of the nanoparticles increased by a 2-step process as the reflux heating time increased. {yields} The IR spectral changes with increasing reflux time indicated the increase in the number of cross-linked polymers in the shell. -- Abstract: Very unique core-shell ceria (cerium oxide)/polymer hybrid nanoparticles that have monodispersed spherical structures and are easily dispersed in water or alcohol without the need for a dispersant were reported recently. The formation mechanism of the unique nanoparticles, however, was not clear. In order to clarify the formation mechanism, these nanoparticles were prepared using a polyol method (reflux heating) under varied conditions of temperature, time, and concentration and molecular weight of added polymer (poly(vinylpyrrolidone)). The size of the resultant nanoparticles was strongly and complicatedly dependent on the set temperature used during reflux heating and the poly(vinylpyrrolidone) molecular weight. Furthermore, the size of the nanoparticles increased by a 2-step process as the reflux heating time increased. The IR spectral changes with increasing reflux time indicated the increase in the number of cross-linked polymers in the shell. From these results, the formation mechanism was discussed and proposed.

  7. Dual-responsive magnetic core-shell nanoparticles for nonviral gene delivery and cell separation.

    PubMed

    Majewski, Alexander P; Schallon, Anja; Jérôme, Valérie; Freitag, Ruth; Müller, Axel H E; Schmalz, Holger

    2012-03-12

    We present the synthesis of dual-responsive (pH and temperature) magnetic core-shell nanoparticles utilizing the grafting-from approach. First, oleic acid stabilized superparamagnetic maghemite (γ-Fe(2)O(3)) nanoparticles (NPs), prepared by thermal decomposition of iron pentacarbonyl, were surface-functionalized with ATRP initiating sites bearing a dopamine anchor group via ligand exchange. Subsequently, 2-(dimethylamino)ethyl methacrylate (DMAEMA) was polymerized from the surface by ATRP, yielding dual-responsive magnetic core-shell NPs (γ-Fe(2)O(3)@PDMAEMA). The attachment of the dopamine anchor group on the nanoparticle's surface is shown to be reversible to a certain extent, resulting in a grafting density of 0.15 chains per nm(2) after purification. Nevertheless, the grafted NPs show excellent long-term stability in water over a wide pH range and exhibit a pH- and temperature-dependent reversible agglomeration, as revealed by turbidimetry. The efficiency of γ-Fe(2)O(3)@PDMAEMA hybrid nanoparticles as a potential transfection agent was explored under standard conditions in CHO-K1 cells. Remarkably, γ-Fe(2)O(3)@PDMAEMA led to a 2-fold increase in the transfection efficiency without increasing the cytotoxicity, as compared to polyethyleneimine (PEI), and yielded on average more than 50% transfected cells. Moreover, after transfection with the hybrid nanoparticles, the cells acquired magnetic properties that could be used for selective isolation of transfected cells. PMID:22296556

  8. Carbon-Supported IrNi Core-Shell Nanoparticles: Synthesis Characterization and Catalytic Activity

    SciTech Connect

    K Sasaki; K Kuttiyiel; L Barrio; D Su; A Frenkel; N Marinkovic; D Mahajan; R Adzic

    2011-12-31

    We synthesized carbon-supported IrNi core-shell nanoparticles by chemical reduction and subsequent thermal annealing in H{sub 2}, and verified the formation of Ir shells on IrNi solid solution alloy cores by various experimental methods. The EXAFS analysis is consistent with the model wherein the IrNi nanoparticles are composed of two-layer Ir shells and IrNi alloy cores. In situ XAS revealed that the Ir shells completely protect Ni atoms in the cores from oxidation or dissolution in an acid electrolyte under elevated potentials. The formation of Ir shell during annealing due to thermal segregation is monitored by time-resolved synchrotron XRD measurements, coupled with Rietveld refinement analyses. The H{sub 2} oxidation activity of the IrNi nanoparticles was found to be higher than that of a commercial Pt/C catalyst. This is predominantly due to Ni-core-induced Ir shell contraction that makes the surface less reactive for IrOH formation, and the resulting more metallic Ir surface becomes more active for H{sub 2} oxidation. This new class of core-shell nanoparticles appears promising for application as hydrogen anode fuel cell electrocatalysts.

  9. Atrazine adsorption removal with nylon6/polypyrrole core-shell nanofibers mat: possible mechanism and characteristics

    NASA Astrophysics Data System (ADS)

    Yang, Bi-Yi; Cao, Yang; Qi, Fei-Fei; Li, Xiao-Qing; Xu, Qian

    2015-05-01

    A functionalized nylon6/polypyrrole core-shell nanofibers mat (PA6/PPy NFM) was prepared via situ polymerization on nylon6 electrospun nanofibers mat (PA6 NFM) template and used as an adsorbent to remove atrazine from aqueous solutions. The core-shell structure of PA6/PPy NFM can be clearly proved under scanning electron microscope (SEM), transmission electron microscopy (TEM), and X-ray photoelectron spectroscopy (XPS). The effects of initial solution pH and ionic strength, as well as the comparison of the adsorption capacity of functionalized (PA6/PPy NFM) and non-functionalized (PA6 NFM) adsorbent, were examined to reveal the possible adsorption mechanism. The results indicated that π-π interaction and electrostatic interaction should play a key role in the adsorption process. The kinetics and thermodynamics studies also further elucidated the detailed adsorption characteristics of atrazine removal by PA6/PPy NFM. The adsorption of atrazine could be well described by the pseudo-second-order equation. The adsorption equilibrium data was well fitted with the Freundlich isotherm model with a maximum adsorption capacity value of 14.8 mg/g. In addition, the increase of adsorption rate caused by a temperature increase could be felicitously explained by the endothermic reaction. The desorption results showed that the adsorption capacity remained almost unchanged after six adsorption/desorption cycles. These results suggest that PA6/PPy NFM could be employed as an efficient adsorbent for removing atrazine from contaminated water sources.

  10. Magnetic properties of fluffy Fe@α-Fe2O3 core-shell nanowires

    PubMed Central

    2013-01-01

    Novel fluffy Fe@α-Fe2O3 core-shell nanowires have been synthesized using the chemical reaction of ferrous sulfate and sodium borohydride, as well as the post-annealing process in air. The coercivity of the as-synthesized nanowires is above 684 Oe in the temperature range of 5 to 300 K, which is significantly higher than that of the bulk Fe (approximately 0.9 Oe). Through the annealing process in air, the coercivity and the exchange field are evidently improved. Both the coercivity and the exchange field increase with increasing annealing time (TA) and reach their maximum values of 1,042 and 78 Oe, respectively, at TA = 4 h. The magnetic measurements show that the effective anisotropy is increased with increasing the thickness of theα-Fe2O3 by annealing. The large values of coercivity and exchange field, as well as the high surface area to volume ratio, may make the fluffy Fe@α-Fe2O3 core-shell nanowire a promising candidate for the applications of the magnetic drug delivery, electrochemical energy storage, gas sensors, photocatalysis, and so forth. PMID:24134440

  11. Direct Fabrication of Monodisperse Silica Nanorings from Hollow Spheres - A Template for Core-Shell Nanorings.

    PubMed

    Zhong, Kuo; Li, Jiaqi; Liu, Liwang; Brullot, Ward; Bloemen, Maarten; Volodin, Alexander; Song, Kai; Van Dorpe, Pol; Verellen, Niels; Clays, Koen

    2016-04-27

    We report a new type of nanosphere colloidal lithography to directly fabricate monodisperse silica (SiO2) nanorings by means of reactive ion etching of hollow SiO2 spheres. Detailed TEM, SEM, and AFM structural analysis is complemented by a model describing the geometrical transition from hollow sphere to ring during the etching process. The resulting silica nanorings can be readily redispersed in solution and subsequently serve as universal templates for the synthesis of ring-shaped core-shell nanostructures. As an example we used silica nanorings (with diameter of ∼200 nm) to create a novel plasmonic nanoparticle topology, a silica-Au core-shell nanoring, by self-assembly of Au nanoparticles (<20 nm) on the ring's surface. Spectroscopic measurements and finite difference time domain simulations reveal high quality factor multipolar and antibonding surface plasmon resonances in the near-infrared. By loading different types of nanoparticles on the silica core, hybrid and multifunctional composite nanoring structures could be realized for applications such as MRI contrast enhancement, catalysis, drug delivery, plasmonic and magnetic hyperthermia, photoacoustic imaging, and biochemical sensing. PMID:27031364

  12. Effects of Cryogenic Temperature on Fracture Toughness of Core-Shell Rubber (CSR) Toughened Epoxy Nanocomposites

    NASA Technical Reports Server (NTRS)

    Wang, J.; Cannon, S. A.; Magee, D.; Schneider, J. A.

    2008-01-01

    This study investigated the effects of core-shell rubber (CSR) nanoparticles on the mechanical properties and fracture toughness of an epoxy resin at ambient and liquid nitrogen (LN2) temperatures. Varying amounts of Kane Ace MX130 toughening agent were added to a commercially available EPON 862/Epikure W epoxy resin. Elastic modulus was calculated using quasi-static tensile data. Fracture toughness was evaluated by the resulting breaking energy measured in Charpy impact tests conducted on an instrumented drop tower. The size and distribution of the CSR nanoparticles were characterized using Transmission Electron Microscopy (TEM) and Small Angle X-ray Scattering (SAXS). Scanning Electron Microscopy (SEM) was used to study the fracture surface morphology. The addition of the CSR nanoparticles increased the breaking energy with negligible change in elastic modulus and ultimate tensile stress (UTS). At ambient temperature the breaking energy increased with increasing additions of the CSR nanoparticles, while at LN2 temperatures, it reached a maximum at 5 wt% CSR concentration. KEY WORDS: liquid nitrogen (LN2) properties, fracture toughness, core-shell rubber (CSR).

  13. Polymer Assisted Core-shell Ag-C nanoparticles Synthesis via Green hydrothermal Technique

    NASA Astrophysics Data System (ADS)

    Williams, James; Mishra, Sanjay

    2009-03-01

    Core-Shell Ag-C nanoparticles were synthesized in the presence of glucose through a one-pot green hydrothermal wet chemical process. An aqueous solution of glucose and Ag nitrate was hydrothermally treated to produce porous carbonaceous shell over silver core nanoparticles. The growth of carbon shells was regulated by either of the polymers (poly) vinyl pyrrolidone (PVP) or poly vinyl alcohol (PVA). The two polymers were compared to take a measure of different tunable sizes of cores, and shells. The effects of hydrothermal temperature, time, and concentration of reagents on the final formation of nanostructures were studied using UV-vis extinction spectra, transmission electron microscope, and Raman spectroscopy. The polymer molecules were found to be incorporated into carbonaceous shell. The resulting opacity of the shell was found to be hydrothermal time and temperature dependent. The shell structure was found to be more uniform with PVP than PVA. Furthermore, the polymer concentration was found to influence size and shape of the core-silver particles as well. The core-shelled nanoparticles have surfaces with organic groups capable of assembling with different reagents that could be useful in drug-delivery, optical nanodevices or biochemistry.

  14. Huge enhancement of upconversion luminescence by broadband dye sensitization of core/shell nanocrystals.

    PubMed

    Yin, Dongguang; Liu, Yumin; Tang, Jingxiu; Zhao, Feifei; Chen, Zhiwen; Zhang, Tingting; Zhang, Xinyu; Chang, Na; Wu, Chenglong; Chen, Dongwei; Wu, Minghong

    2016-09-14

    Upconversion nanocrystals (UCNCs) hold promise for bioimaging, solar cells, photocatalysis and volumetric displays. However, their upconversion luminescence intensities are usually low due to the weak and narrowband near-infrared absorption of lanthanide ions. Herein, we introduce and validate a strategy to hugely enhance upconversion luminescence intensity by using an organic near-infrared dye as an antenna to sensitize core/shell UCNCs. The dye can increase absorptivity and broaden the absorption spectrum of the UCNCs. Such dye sensitization, in combination with a core/shell structure, can tremendously enhance the upconversion luminescence (UCL) intensity of the UCNCs. The UCL intensity of dye-sensitized UCNCs excited at 820 nm is 800-folds higher than that of pure UCNCs excited at 980 nm. Further enhancement can be obtained by optimization of the dye emission and UCNC absorption spectral overlap. Moreover, the proposed approach can be extended to cover any part of the solar spectrum by using a set of dyes. This work provides new insights into the efficient enhancement of upconversion luminescence of the UCNCs and facilitates their applications. PMID:27484165

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

    PubMed

    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

    2015-01-01

    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. PMID:26133469

  16. Tegafur loading and release properties of magnetite/poly(alkylcyanoacrylate) (core/shell) nanoparticles.

    PubMed

    Arias, José L; Ruiz, M Adolfina; Gallardo, Visitación; Delgado, Angel V

    2008-01-01

    In this work, we describe a reproducible method to prepare polymeric colloidal nanospheres of poly(ethyl-2-cyanoacrylate), poly(butylcyanoacrylate), poly(hexylcyanoacrylate) and poly(octylcyanoacrylate) with a magnetite core, and loaded with the anticancer drug Tegafur. The method is based on the emulsion polymerization procedure, often used in the synthesis of poly(alkylcyanoacrylate) nanospheres for drug delivery. The heterogeneous structure of the particles confer them both magnetic-field responsiveness and potential applicability as drug carriers. In order to investigate to what extent is this target achieved, we compare the surface electrical properties of the core/shell particles with those of both the nucleus and the coating material. The hysteresis cycles of both magnetite and composite particles demonstrate that the polymer shell reduces the magnetic responsiveness of the particles, but keeps their soft ferrimagnetic character unchanged. A detailed investigation of the capabilities of the core/shell particles to load this drug is shown. We found, by means of spectrophotometric and electrophoretic measurements, the existence of two drug loading mechanisms: absorption or entrapment in the polymeric network, and surface adsorption. The type of polymer, the pH and the drug concentration are the main factors determining the drug incorporation to the nanoparticles. The release studies showed a biphasic profile affected by the type of polymeric shell, the type of drug incorporation and the amount of drug loaded. PMID:17949844

  17. Preparation and electromagnetic properties of core/shell polystyrene@polypyrrole@nickel composite microspheres.

    PubMed

    Li, Wenzhe; Qiu, Teng; Wang, Leilei; Ren, Shanshan; Zhang, Jiangru; He, Lifan; Li, Xiaoyu

    2013-02-01

    Through a novel method, we successfully synthesized electromagnetic (EM) functional polystyrene@polypyrrole@nickel (PS@PPy@Ni) composite microspheres. The PS@PPy spheres with well-defined core/shell structure have been synthesized via an in situ chemical oxidative copolymerization of pyrrole (Py) and N-2-carboxyethylpyrrole (PyCOOH) templated by PS microspheres. The reaction was carried out under heterophase conditions using the mixture of ethanol and water as the continuous phase. Tailored by the carboxyl groups on the surface of microspheres, magnetic nickel layer has been steady deposited onto the P(Py-PyCOOH) layer of the microspheres through an activation-electroless plating technology. The fine PS@P(Py-PyCOOH)@Ni core/shell structures could be obtained with the PyCOOH content up to 50 wt % in the P(Py-PyCOOH) layer. Moreover, the as-prepared PS@P(Py-PyCOOH)@Ni composites are ferromagnetic materials and behave as a good electromagnetic (EM) absorption material due to the coating of Ni layer around the PS@P(Py-PyCOOH) spheres. The PS@P(Py-PyCOOH)@Ni composite spheres show the remarkable EM wave absorption property with the maximum reflection loss (around -20.06 dB) at 10.69 GHz. The EM wave absorption can retained lower than -10 dB within a broad frequency range from 9.16 to 13.75 GHz. PMID:23277287

  18. Charge carrier identification in tunneling spectroscopy of core-shell nanocrystals

    NASA Astrophysics Data System (ADS)

    Nguyen, T. H.; Habinshuti, J.; Justo, Y.; Gomes, R.; Mahieu, G.; Godey, S.; Nys, J. P.; Carrillo, S.; Hens, Z.; Robbe, O.; Turrell, S.; Grandidier, B.

    2011-11-01

    Semiconductor PbSe/CdSe core-shell nanocrystals (NCs) in a double barrier tunnel junction have been investigated by means of scanning tunneling spectroscopy at low temperature. From the analysis of the differential conductance peak position as a function of the potential distribution in both potential barriers, we demonstrate a unipolar transport regime for a large amount of NCs. The same charge carriers are injected on both sides of the zero-conductance gap, and the peaks observed at higher energy arise from the charging of the NCs. Similar results are obtained for CdSe/CdS dot-in-rod NCs, indicating that the addition of a shell favors transitions between different charge states rather than single particle excited states. Further characterization of the PbSe/CdSe core-shell NCs by x-ray photoemission spectroscopy reveals that the variations in the transport properties from NC to NC are explained by the occurrence of unprotected PbSe facets that have different orientations in the junction.

  19. Preparation of gold/titania core-shell nanocomposites with a tunable shell thickness.

    PubMed

    Kanda, Takashi; Komata, Kazuyoshi; Torigoe, Kanjiro; Endo, Takeshi; Sakai, Kenichi; Abe, Masahiko; Sakai, Hideki

    2014-01-01

    Gold/titania nanocomposites with a core-shell structure were prepared by sol-gel reaction of titanium tetrabutoxide (TTBO) with gold nanoparticles, core-stabilized with cetyltrimethylammonium bromide (CTAB), using a ternary mixture of alcohol/acetonitrile/water as solvent. TEM characterization of the resulting constructs revealed spherical nanocomposites, each containing a single gold core. The mean diameter of the gold cores was 13 nm, while the thicknesses of titania shells were readily tuned in the range 4-30 nm by varying the alkyl chain length of the alcohol. In addition, the gold nanoparticles exhibited a deep red color, with an intense extinction peak at 527 nm, owing to their surface plasmon resonance (SPR) properties. When the Au nanoparticles were coated with a titania shell, their color changed to purple and the SPR peak shifted to a higher wavelength of 537 nm. Furthermore, the core-shell nanocomposites were found to display photocatalytic activity for the oxidation of 2-propanol under illumination by visible light (λ=500-560 nm). PMID:24717542

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

    DOE PAGESBeta

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

    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 bemore » 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.« less

  1. Mechanical Fracturing of Core-Shell Undercooled Metal Particles for Heat-Free Soldering

    NASA Astrophysics Data System (ADS)

    Çınar, Simge; Tevis, Ian D.; Chen, Jiahao; Thuo, Martin

    2016-02-01

    Phase-change materials, such as meta-stable undercooled (supercooled) liquids, have been widely recognized as a suitable route for complex fabrication and engineering. Despite comprehensive studies on the undercooling phenomenon, little progress has been made in the use of undercooled metals, primarily due to low yields and poor stability. This paper reports the use of an extension of droplet emulsion technique (SLICE) to produce undercooled core-shell particles of structure; metal/oxide shell-acetate (‘/’ = physisorbed, ‘-’ = chemisorbed), from molten Field’s metal (Bi-In-Sn) and Bi-Sn alloys. These particles exhibit stability against solidification at ambient conditions. Besides synthesis, we report the use of these undercooled metal, liquid core-shell, particles for heat free joining and manufacturing at ambient conditions. Our approach incorporates gentle etching and/or fracturing of outer oxide-acetate layers through mechanical stressing or shearing, thus initiating a cascade entailing fluid flow with concomitant deformation, combination/alloying, shaping, and solidification. This simple and low cost technique for soldering and fabrication enables formation of complex shapes and joining at the meso- and micro-scale at ambient conditions without heat or electricity.

  2. Core-shell nanostructures for ultrasensitive detection of α-thrombin

    NASA Astrophysics Data System (ADS)

    Chen, Xia; Liu, Hongli; Zhou, Xiaodong; Hu, Jiming

    2010-12-01

    We have synthesized a stable, sensitive and specific surface-enhanced Raman tag, and demonstrated its application in human α-thrombin detection. The tag consists of aptamer-modified core-shell nanoparticles with hydrophobic Au@Ag as core and silica as shell encapsulating Raman active molecules. By taking advantage of the Raman signal enhancement effect by metallic nanostructures, high stability and robustness of glass-coated core-shell nanostructures and the recognition capabilities of aptamers, we designed a sandwich detection for protein identification with high selectivity and sensitivity. In this way, we realized the ultrasensitive detection of α-thrombin. GDNs (glass-coated, dye-tagged nanoparticles), which were conjugated with oligonucleotides or antibodies, were extremely soluble in water, and had mechanical and chemical stability, easily controllable-size distribution and friendly biocompatibility. Specifically, the glass coating renders the particles amenable to use in many solvents without altering the Raman spectral response and makes agglomeration a nonfactor. All these merits open the door of the real applications in diagnostics or medical investigations in complex biofluids, such as human plasma and serum. Using the aptamer-modified GDNs as Raman tags, we successfully performed the detection of α-thrombin in human plasma. Furthermore, the overall method have been proved effective and selective, and may be implemented for multiplex target analysis simultaneously.

  3. Modulation of protein release from biodegradable core-shell structured fibers prepared by coaxial electrospinning.

    PubMed

    Jiang, Hongliang; Hu, Yingqian; Zhao, Pengcheng; Li, Yan; Zhu, Kangjie

    2006-10-01

    Biodegradable core-shell structured fibers with poly(epsilon-caprolactone) as shell and bovine serum albumin (BSA)-containing dextran as core were prepared by coaxial electrospinning for incorporation and controlled release of proteins. BSA loading percent in the fibers and its release rate could be conveniently varied by the feed rate of the inner dope during electrospinning. With the increase in the feed rate of the inner dope, there was an associated increase in the loading percent and accelerated release of BSA. Poly(ethylene glycol) (PEG) was added to the shell section of the fibers to further finely modulate the release behavior of BSA. It was revealed that the release rate of BSA increased with the PEG percent in the shell section. By varying the feed rate of the inner dope and PEG content, most of BSA could be released from the core-shell structured fibers within the period of time ranging from 1 week to more than 1 month. The effect of the feed rate of the inner dope and addition of PEG into the shell section on the fiber morphology was also examined by scanning electron microscope. PMID:16544305

  4. Fast-Dissolving Core-Shell Composite Microparticles of Quercetin Fabricated Using a Coaxial Electrospray Process

    PubMed Central

    Li, Chen; Yu, Deng-Guang; Williams, Gareth R.; Wang, Zhuan-Hua

    2014-01-01

    This study reports on novel fast-dissolving core-shell composite microparticles of quercetin fabricated using coaxial electrospraying. A PVC-coated concentric spinneret was developed to conduct the electrospray process. A series of analyses were undertaken to characterize the resultant particles in terms of their morphology, the physical form of their components, and their functional performance. Scanning and transmission electron microscopies revealed that the microparticles had spherical morphologies with clear core-shell structure visible. Differential scanning calorimetry and X-ray diffraction verified that the quercetin active ingredient in the core and sucralose and sodium dodecyl sulfate (SDS) excipients in the shell existed in the amorphous state. This is believed to be a result of second-order interactions between the components; these could be observed by Fourier transform infrared spectroscopy. In vitro dissolution and permeation studies showed that the microparticles rapidly released the incorporated quercetin within one minute, and had permeation rates across the sublingual mucosa around 10 times faster than raw quercetin. PMID:24643072

  5. Focused ion beam fabrication of novel core-shell nanowire structures.

    PubMed

    He, Li; Johansson, Jonas; Murayama, Mitsuhiro; Hull, Robert

    2008-11-01

    A novel method of indirect deposition by means of a focused ion beam (FIB) is utilized to develop metal/insulator/semiconductor nanowire core-shell structures. This method is based upon depositing an annular pattern centered on a nanowire, with secondary deposition then coating the wire. Typical cross-sectional deposition area increments as a function of ion doses are 1.3 × 10(-2) µm(2) nC(-1) for Pt and 3.5 × 10(-2) µm(2) nC(-1) for SiO(2). The structures are examined with a transmission electron microscope (TEM) using a new nanowire TEM sample preparation method that allows direct examinations of individually selected core-shell nanowires fabricated under different indirect FIB deposition conditions. Elemental analyses by means of energy dispersive x-ray spectroscopy and electron energy filtered TEM imaging verify the deposition of SiO(2) and Pt layers. Relatively uniform Pt and SiO(2) coatings on individual GaP nanowires can be achieved with overall thickness deviation of about 10% for deposition up to 25-30 nm thick Pt or SiO(2) shells. It should be possible to extend this approach to any nanowire/nanotube system, and to a wide range of coatings in any desired layer sequences. PMID:21832742

  6. Exciton spin dynamics and photoluminescence polarization of CdSe/CdS dot-in-rod nanocrystals in high magnetic fields

    NASA Astrophysics Data System (ADS)

    Siebers, B.; Biadala, L.; Yakovlev, D. R.; Rodina, A. V.; Aubert, T.; Hens, Z.; Bayer, M.

    2015-04-01

    The exciton spin dynamics and polarization properties of the related emission are investigated in colloidal CdSe/CdS dot-in-rod (DiR) and spherical core/shell nanocrystal (NC) ensembles by magneto-optical photoluminescence (PL) spectroscopy in magnetic fields up to 15 T. It is shown that the degree of circular polarization (DCP) of the exciton emission induced by the magnetic field is affected by the NC geometry as well as the exciton fine structure and can provide information on nanorod orientation. A theory to describe the circular and linear polarization properties of the NC emission in a magnetic field is developed. It takes into account phonon mediated coupling between the exciton fine structure states as well as the dielectric enhancement effect resulting from the anisotropic shell of DiR NCs. This theoretical approach is used to model the experimental results and allows us to explain most of the measured features. The spin dynamics of the dark excitons is investigated in magnetic fields by time-resolved photoluminescence. The results highlight the importance of confined acoustic phonons in the spin relaxation of dark excitons. The bare core surface as well as the core/shell interface give rise to an efficient spin-relaxation channel, while the surface of core/shell NCs seems to play only a minor role.

  7. Microstructure-dependent mechanical properties of electrospun core-shell scaffolds at multi-scale levels.

    PubMed

    Horner, Christopher B; Ico, Gerardo; Johnson, Jed; Zhao, Yi; Nam, Jin

    2016-06-01

    Mechanical factors among many physiochemical properties of scaffolds for stem cell-based tissue engineering significantly affect tissue morphogenesis by controlling stem cell behaviors including proliferation and phenotype-specific differentiation. Core-shell electrospinning provides a unique opportunity to control mechanical properties of scaffolds independent of surface chemistry, rendering a greater freedom to tailor design for specific applications. In this study, we synthesized electrospun core-shell scaffolds having different core composition and/or core-to-shell dimensional ratios. Two independent biocompatible polymer systems, polyetherketoneketone (PEKK) and gelatin as the core materials while maintaining the shell polymer with polycaprolactone (PCL), were utilized. The mechanics of such scaffolds was analyzed at the microscale and macroscales to determine the potential implications it may hold for cell-material and tissue-material interactions. The mechanical properties of individual core-shell fibers were controlled by core-shell composition and structure. The individual fiber modulus correlated with the increase in percent core size ranging from 0.55±0.10GPa to 1.74±0.22GPa and 0.48±0.12GPa to 1.53±0.12GPa for the PEKK-PCL and gelatin-PCL fibers, respectively. More importantly, it was demonstrated that mechanical properties of the scaffolds at the macroscale were dominantly determined by porosity under compression. The increase of scaffold porosity from 70.2%±1.0% to 93.2%±0.5% by increasing the core size in the PEKK-PCL scaffold resulted in the decrease of the compressive elastic modulus from 227.67±20.39kPa to 14.55±1.43kPa while a greater changes in the porosity of gelatin-PCL scaffold from 54.5%±4.2% to 89.6%±0.4% resulted in the compressive elastic modulus change from 484.01±30.18kPa to 17.57±1.40kPa. On the other hand, the biphasic behaviors under tensile mechanical loading result in a range from a minimum of 5.42±1.05MPa to a maximum

  8. Unlocking the Origin of Superior Performance of a Si-Ge Core-Shell Nanowire Quantum Dot Field Effect Transistor.

    PubMed

    Dhungana, Kamal B; Jaishi, Meghnath; Pati, Ranjit

    2016-07-13

    The sustained advancement in semiconducting core-shell nanowire technology has unlocked a tantalizing route for making next generation field effect transistor (FET). Understanding how to control carrier mobility of these nanowire channels by applying a gate field is the key to developing a high performance FET. Herein, we have identified the switching mechanism responsible for the superior performance of a Si-Ge core-shell nanowire quantum dot FET over its homogeneous Si counterpart. A quantum transport approach is used to investigate the gate-field modulated switching behavior in electronic current for ultranarrow Si and Si-Ge core-shell nanowire quantum dot FETs. Our calculations reveal that for the ON state, the gate-field induced transverse localization of the wave function restricts the carrier transport to the outer (shell) layer with the pz orbitals providing the pathway for tunneling of electrons in the channels. The higher ON state current in the Si-Ge core-shell nanowire FET is attributed to the pz orbitals that are distributed over the entire channel; in the case of Si nanowire, the participating pz orbital is restricted to a few Si atoms in the channel resulting in a smaller tunneling current. Within the gate bias range considered here, the transconductance is found to be substantially higher in the case of a Si-Ge core-shell nanowire FET than in a Si nanowire FET, which suggests a much higher mobility in the Si-Ge nanowire device. PMID:27280769

  9. The synthesis and properties of bifunctional and intelligent Fe3O4@titanium oxide core/shell nanoparticles.

    PubMed

    Yin, Yichao; Liu, Chenjie; Wang, Baoxiang; Yu, Shoushan; Chen, Kezheng

    2013-05-21

    A simple, one-pot solvothermal method has been demonstrated for the preparation of bifunctional Fe3O4@titanium oxide core/shell nanoparticles. In a typical procedure, tetraalkoxyl titanium Ti(OC4H9)4 and FeCl3 as precursors were added into ethylene glycol and further solvothermal treatment was used to synthesize the core/shell particles. The core/shell particles were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray diffraction (XRD), SQUID MPMS and rheometry. The morphological results showed titanium oxide nanorods with 100-200 nm length and 10-20 nm diameter coated on the surface of 200-300 nm Fe3O4 submicrospheres. Reaction time, the titanium source, the barium salt etc. have an influence on the morphology of core/shell particles. The core/shell particles can not only respond to an external magnetic field, but also to an electric field--a novel application of electrorheological fluid. PMID:23532087

  10. Preparation and photocatalytic properties of magnetically reusable Fe3O4@ZnO core/shell nanoparticles

    NASA Astrophysics Data System (ADS)

    Wang, Jian; Yang, Jinghai; Li, Xiuyan; Wang, Dandan; Wei, Bing; Song, Hang; Li, Xuefei; Fu, Siwei

    2016-01-01

    Fe3O4@ZnO binary nanoparticles were synthesized by a simple two-step chemical method and characterized using various analytical instruments. TEM result proved the binary nanoparticles have core/shell structures and average particle size is 60 nm. Photocatalytic investigation of Fe3O4@ZnO core/shell nanoparticles was carried out using rhodamine B (RhB) solution under UV light. Fe3O4@ZnO core/shell nanoparticles showed enhanced photocatalytic performance in comparison with the as prepared ZnO nanoparticles. The enhanced photocatalytic activity for Fe3O4@ZnO might be resulting from the higher concentration of surface oxygen vacancies and the suppressing effect of the Fe3+ ions on the recombination of photoinduced electron-hole pairs. Magnetization saturation value (5.96 emu/g) of Fe3O4@ZnO core/shell nanoparticles is high enough to be magnetically removed by applying a magnetic field. The core/shell photocatalyst can be easily separated by using a commercial magnet and almost no decrease in photocatalytic efficiency was observed even after recycling six times.

  11. Fuel cell performance of palladium-platinum core-shell electrocatalysts synthesized in gram-scale batches

    DOE PAGESBeta

    Khateeb, Siddique; Su, Dong; Guerreo, Sandra; Darling, Robert M.; Protsailo, Lesia V.; Shao, Minhua

    2016-05-03

    This article presents the performance of palladium-platinum core-shell catalysts (Pt/Pd/C) for oxygen reduction synthesized in gram-scale batches in both liquid cells and polymer-electrolyte membrane fuel cells. Core-shell catalyst synthesis and characterization, ink fabrication, and cell assembly details are discussed. The Pt mass activity of the Pt/Pd core-shell catalyst was 0.95 A mg–1 at 0.9 V measured in liquid cells (0.1 M HClO4), which was 4.8 times higher than a commercial Pt/C catalyst. The performances of Pt/Pd/C and Pt/C in large single cells (315 cm2) were assessed under various operating conditions. The core-shell catalyst showed consistently higher performance than commercial Pt/Cmore » in fuel cell testing. A 20–60 mV improvement across the whole current density range was observed on air. Sensitivities to temperature, humidity, and gas composition were also investigated and the core-shell catalyst showed a consistent benefit over Pt under all conditions. However, the 4.8 times activity enhancement predicated by liquid cell measurements was not fully realized in fuel cells.« less

  12. Quantitative characterizations of styrene butadiene core shell latexes by TOF-SIMS and pyrolysis GC/MS

    NASA Astrophysics Data System (ADS)

    Maekawa, Toshihiko

    2006-07-01

    We have established a characterization method of a 100 nm sized core-shell latexes composed of styrene-butadiene co-polymer. The core-shell structure was revealed by TEM observation of the latex film after modification with OsO 4 vapor. Pyrolysis gas chromatography combined with mass spectrometry (Py-GC/MS) of the latexes showed the average chemical composition of the core-shell latexes. TOF-SIMS of the latex film gave the characteristic peak for styrene and butadiene. The peak intensities changed in accordance with the chemical composition of the latexes. Surface composition of the latex film, which corresponds to the composition of the shell part of the latexes, was estimated from this peak intensity ratio. From the combined analysis of Py-GC/MS and TOF-SIMS of the latexes, we successfully evaluated the chemical composition of both the core part and the shell part of latexes individually. As the results of characterization of some core-shell latex, it was revealed that the high degree of cross-linking is needed to synthesize the tailored core-shell latex.

  13. Magnetically self-assembled SrFe12O19/Fe-Co core/shell particles

    SciTech Connect

    Xu, X; Park, J; Hong, YK; Lane, AM

    2015-02-15

    Epitaxial growth to synthesize core/shell-structured materials is limited because large lattice mismatches are common between materials. Magnetically hard/soft, core/shell-structured materials can be potentially used for rare-earth free permanent magnets, but their synthesis presents a challenge. We report a wet chemistry method to synthesize core/shell structured particles consisting of a magnetically hard SrFe12O19 core and a soft Fe-Co shell, with a lattice mismatch of similar to 100%, which cannot be achieved by conventional epitaxial growth or other alternative methods. When decreasing the size of the magnetically soft Fe-Co nanoclusters to below 5 nm, we show that they can be magnetically attracted by the hard SrFe12O19 to form core/shell structured particles. An AC demagnetization experiment demonstrates the formation mechanism of the core/shell particles, and their magnetic hysteresis loop shows potential for use as rare-earth free permanent magnets. Published by Elsevier B.V.

  14. A colorimetric assay for measuring iodide using Au@Ag core-shell nanoparticles coupled with Cu(2+).

    PubMed

    Zeng, Jingbin; Cao, Yingying; Lu, Chun-Hua; Wang, Xu-Dong; Wang, Qianru; Wen, Cong-Ying; Qu, Jian-Bo; Yuan, Cunguang; Yan, Zi-Feng; Chen, Xi

    2015-09-01

    Au@Ag core-shell nanoparticles (NPs) were synthesized and coupled with copper ion (Cu(2+)) for the colorimetric sensing of iodide ion (I(-)). This assay relies on the fact that the absorption spectra and the color of metallic core-shell NPs are sensitive to their chemical ingredient and dimensional core-to-shell ratio. When I(-) was added to the Au@Ag core-shell NPs-Cu(2+) system/solution, Cu(2+) can oxidize I(-) into iodine (I2), which can further oxidize silver shells to form silver iodide (AgI). The generated Au@AgI core-shell NPs led to color changes from yellow to purple, which was utilized for the colorimetric sensing of I(-). The assay only took 10 min with a lowest detectable concentration of 0.5 μM, and it exhibited excellent selectivity for I(-) over other common anions tested. Furthermore, Au@Ag core-shell NPs-Cu(2+) was embedded into agarose gels as inexpensive and portable "test strips", which were successfully used for the semi-quantitation of I(-) in dried kelps. PMID:26388386

  15. Facile synthesis of water-soluble luminescent mesoporous Tb(OH)3@SiO2 core-shell nanospheres

    PubMed Central

    2013-01-01

    Luminescent mesoporous Tb(OH)3@SiO2 core-shell nanospheres were synthesized through W/O microemulsion process at ambient temperature. The negatively charged silica favors a coating of the positively charged Tb3+ composite. Thus, silicon layer was adsorbed on the surface of Tb(OH)3 groups to form Tb-O-Si through electrostatic interaction. X-ray diffraction, field emission transmission electron microscopy (FE-TEM), energy-dispersive X-ray spectrometry, and Fourier transform infrared, UV/Visible, and photoluminescence spectroscopies were applied to examine the phase purity, crystallinity, surface morphology, and optical properties of the core-shell nanospheres. The FE-TEM results have revealed typically ordered mesoporous characteristics of the material with monodisperse spherical morphology in a narrow size distribution. The luminescent mesoporous core-shell nanospheres exposed remarkable splitting with broadening in the emission transition 5D4 → 7F5 (543 nm). In addition, the luminescent mesoporous core-shell nanospheres emit strong green fluorescence (from Tb3+) in the middle of the visible region under 325 nm (3.8) excitation. The luminescent mesoporous Tb(OH)3@SiO2 core-shell nanospheres can therefore be exploited as fluorescent probes in biomarkers or biolabeling, optical sensing, and drug delivery system. Further, these nanospheres could have potential use as scattering layers in dye-sensitized solar cells. PMID:23574757

  16. Au@SiO2 core-shell structure involved with methotrexate: Fabrication, biodegradation process and bioassay explore.

    PubMed

    Huo, Xiaolei; Dai, Chaofan; Tian, Deying; Li, Shuping; Li, Xiaodong

    2015-12-30

    A new strategy is proposed to synthesize a kind of Au@SiO2 core-shell structure with methotrexate (MTX) loaded within it. Firstly, MTX molecules are attracted to the surface and vicinity of Au nanoparticles (NPs). Then the enriched MTX molecules on the surface of Au NPs have a good chance to be wrapped into the core-shell structure when SiO2 is uniformly deposited on the Au core. Secondly, the effect of Au amount and MTX content on the drug-loading capacity is emphatically studied and the result shows that core-shell structure plays a vital role in drug loading. In addition, the biodegradation process is also examined in phosphate buffer solution (PBS) at 37°C. The results show that the biodegradation of Au-MTX@SiO2 core-shell structure can be divided into two stages: the release of drug together with the fragmentation of core-shell structure and the subsequent dissolution of SiO2 layers. Lastly, in vitro bioassay tests give the evidence that obvious tumor inhibition can be achieved in presence of Au-MTX@SiO2 NPs even at low concentration and the efficacy can be greatly enhanced by the photothermal therapy on Au cores. PMID:26516099

  17. Facile synthesis of water-soluble luminescent mesoporous Tb(OH)3@SiO2 core-shell nanospheres

    NASA Astrophysics Data System (ADS)

    Ansari, Anees A.; Labis, Joselito; Aldwayyan, Abdullah S.; Hezam, Mahmoud

    2013-04-01

    Luminescent mesoporous Tb(OH)3@SiO2 core-shell nanospheres were synthesized through W/O microemulsion process at ambient temperature. The negatively charged silica favors a coating of the positively charged Tb3+ composite. Thus, silicon layer was adsorbed on the surface of Tb(OH)3 groups to form Tb-O-Si through electrostatic interaction. X-ray diffraction, field emission transmission electron microscopy (FE-TEM), energy-dispersive X-ray spectrometry, and Fourier transform infrared, UV/Visible, and photoluminescence spectroscopies were applied to examine the phase purity, crystallinity, surface morphology, and optical properties of the core-shell nanospheres. The FE-TEM results have revealed typically ordered mesoporous characteristics of the material with monodisperse spherical morphology in a narrow size distribution. The luminescent mesoporous core-shell nanospheres exposed remarkable splitting with broadening in the emission transition 5D4 → 7F5 (543 nm). In addition, the luminescent mesoporous core-shell nanospheres emit strong green fluorescence (from Tb3+) in the middle of the visible region under 325 nm (3.8) excitation. The luminescent mesoporous Tb(OH)3@SiO2 core-shell nanospheres can therefore be exploited as fluorescent probes in biomarkers or biolabeling, optical sensing, and drug delivery system. Further, these nanospheres could have potential use as scattering layers in dye-sensitized solar cells.

  18. Growth and characterization of ZnO/ZnTe core/shell nanowire arrays on transparent conducting oxide glass substrates

    PubMed Central

    2012-01-01

    We report the growth and characterization of ZnO/ZnTe core/shell nanowire arrays on indium tin oxide. Coating of the ZnTe layer on well-aligned vertical ZnO nanowires has been demonstrated by scanning electron microscope, tunneling electron microscope, X-ray diffraction pattern, photoluminescence, and transmission studies. The ZnO/ZnTe core/shell nanowire arrays were then used as the active layer and carrier transport medium to fabricate a photovoltaic device. The enhanced photocurrent and faster response observed in ZnO/ZnTe, together with the quenching of the UV emission in the PL spectra, indicate that carrier separation in this structure plays an important role in determining their optical response. The results also indicate that core/shell structures can be made into useful photovoltaic devices. PMID:22804871

  19. Design of Core-Shell Heterostructure Nanofibers with Different Work Function and Their Sensing Properties to Trimethylamine.

    PubMed

    Li, Feng; Gao, Xing; Wang, Rui; Zhang, Tong; Lu, Geyu; Barsan, Nicolae

    2016-08-01

    The metal oxide semiconductor (MOS) core-shell heterostructure nanofibers (NFs) have been successfully synthesized via an environmentally friendly coaxial electrospinning approach. To demonstrate the potential applications of the as-prepared samples, sensors based on MOS core-shell heterostructure NFs have been fabricated and their gas sensing properties were investigated. Results show that the sensors exhibit an advanced gas sensing property to trimethylamine (TMA) including the outstanding selectivity and rapid response/recovery processes in comparison with the sensors based on single MOS NFs. These phenomena are closely associated with the electron flow caused by the work function difference between MOS of the core and the shell. The approach proposed in this study may contribute to the realization of more sensitive MOS core-shell heterostructure sensors. PMID:27403999

  20. Alloy Cu3Pt nanoframes through the structure evolution in Cu-Pt nanoparticles with a core-shell construction

    PubMed Central

    Han, Lin; Liu, Hui; Cui, Penglei; Peng, Zhijian; Zhang, Suojiang; Yang, Jun

    2014-01-01

    Noble metal nanoparticles with hollow interiors and customizable shell compositions have immense potential for catalysis. Herein, we present an unique structure transformation phenomenon for the fabrication of alloy Cu3Pt nanoframes with polyhedral morphology. This strategy starts with the preparation of polyhedral Cu-Pt nanoparticles with a core-shell construction upon the anisotropic growth of Pt on multiply twinned Cu seed particles, which are subsequently transformed into alloy Cu3Pt nanoframes due to the Kirkendall effect between the Cu core and Pt shell. The as-prepared alloy Cu3Pt nanoframes possess the rhombic dodecahedral morphology of their core-shell parents after the structural evolution. In particular, the resulting alloy Cu3Pt nanoframes are more effective for oxygen reduction reaction but ineffective for methanol oxidation reaction in comparison with their original Cu-Pt core-shell precursors. PMID:25231376

  1. Core-shell hematite nanorods: a simple method to improve the charge transfer in the photoanode for photoelectrochemical water splitting.

    PubMed

    Gurudayal; Chee, Png Mei; Boix, Pablo P; Ge, Hu; Yanan, Fang; Barber, James; Wong, Lydia Helena

    2015-04-01

    We report a simple method to produce a stable and repeatable photoanode for water splitting with a core-shell hematite (α-Fe2O3) nanorods system by combining spray pyrolysis and hydrothermal synthesis. Impedance spectroscopy revealed passivation of the surface states by the shell layer, which results in an increase of the charge injection through the hematite conduction band. In pristine hematite more holes are accumulated on the surface and the charge transfer to the electrolyte occurs through surface states, whereas in the core-shell hematite photoanode the majority of hole transfer process occurs through the valence band. As a result the photoactivity of the core-shell nanorods, 1.2 mA cm(-2), at 1.23 V vs RHE, is twice that of pristine hematite nanorods. The alteration of the interface energetics is supported by TEM, showing that the crystallinity of the surface has been improved by the deposition of the shell. PMID:25790720

  2. Exchange coupled SrFe12O19/Fe-Co core/shell particles with different shell thickness

    NASA Astrophysics Data System (ADS)

    Xu, Xia; Hong, Yang-Ki; Park, Jihoon; Lee, Woncheol; Lane, Alan M.

    2015-11-01

    SrFe12O19/Fe-Co core/shell particles with different shell thickness were synthesized by polyol reduction of Fe and Co ions at 180°C with SrFe12O19 particles dispersed in solvent. The core/shell structure is formed by magnetic self-assembly due to the remanent magnetization of SrFe12O19 particles. Within a limited concentration range, the shell thickness could be controlled by regulating the concentration of Fe and Co ions. Core/shell structured SrFe12O19/Fe-Co particles showed more effective exchange coupling effects between hard and soft phases than physically mixed SrFe12O19 and Fe-Co particles. [Figure not available: see fulltext.

  3. An electrostatic nanogenerator based on ZnO/ZnS core/shell electrets with stabilized quasi-permanent charge

    SciTech Connect

    Wang, Chao; Cai, Liang; Feng, Yajuan; Chen, Lin; Yan, Wensheng E-mail: zhsun@ustc.edu.cn; Liu, Qinghua; Yao, Tao; Hu, Fengchun; Pan, Zhiyun; Sun, Zhihu E-mail: zhsun@ustc.edu.cn; Wei, Shiqiang

    2014-06-16

    ZnO-based nanogenerators with excellent performance and convenient functionalization are particularly desirable for self-powered technology, which is however difficult to achieve simultaneously in traditional piezoelectric ZnO nanogenerators. Here, we report a design of electrostatic ZnO nanogenerator by virtue of a type-II ZnO/ZnS core/shell nanostructure electrets, which can turn acoustic waves into electric power with an energy conversion efficiency of 2.2%. The ZnO/ZnS core/shell electrets are charged by ultraviolet irradiation with a long-term stability of the electrostatic charges under ambient condition. The electronic and atomic structure evolution in the charged ZnO/ZnS core/shell electrets are also discussed by detailed experimental and theoretical investigations. This design opens up an alternative path for fabricating robust ZnO-based nanogenerator for future nanotechnology application.

  4. Synthesis of large uniform gold and core-shell gold-silver nanoparticles: Effect of temperature control

    NASA Astrophysics Data System (ADS)

    Tiunov, I. A.; Gorbachevskyy, M. V.; Kopitsyn, D. S.; Kotelev, M. S.; Ivanov, E. V.; Vinokurov, V. A.; Novikov, A. A.

    2016-01-01

    The temperatures of nucleation and growth for gold and silver nanoparticles are quite close to each other in citrate-based seeded-growth synthesis. Hence, thorough temperature control during the synthesis of gold and gold-silver core-shell nanoparticles is expected to improve the yield of uniform non-aggregated nanoparticles suitable for selective contrasting of surface defects. Gold and gold-silver core-shell nanoparticles of size ranging from 20 to 160 nm were synthesized using various means of temperature control. The synthesized nanoparticles were characterized by transmission electron microscopy (TEM), dynamic light scattering (DLS) and UV-Vis spectroscopy. Model nanocracks were milled on pipeline steel specimen by focused ion beam (FIB). It was found that to produce large uniform core-shell nanoparticles, thorough temperature control is required during formation of the gold seeds and the silver shell. Moreover, the synthesized nanoparticles were used for selective contrasting of defects on metal surface.

  5. Alloy Cu3Pt nanoframes through the structure evolution in Cu-Pt nanoparticles with a core-shell construction

    NASA Astrophysics Data System (ADS)

    Han, Lin; Liu, Hui; Cui, Penglei; Peng, Zhijian; Zhang, Suojiang; Yang, Jun

    2014-09-01

    Noble metal nanoparticles with hollow interiors and customizable shell compositions have immense potential for catalysis. Herein, we present an unique structure transformation phenomenon for the fabrication of alloy Cu3Pt nanoframes with polyhedral morphology. This strategy starts with the preparation of polyhedral Cu-Pt nanoparticles with a core-shell construction upon the anisotropic growth of Pt on multiply twinned Cu seed particles, which are subsequently transformed into alloy Cu3Pt nanoframes due to the Kirkendall effect between the Cu core and Pt shell. The as-prepared alloy Cu3Pt nanoframes possess the rhombic dodecahedral morphology of their core-shell parents after the structural evolution. In particular, the resulting alloy Cu3Pt nanoframes are more effective for oxygen reduction reaction but ineffective for methanol oxidation reaction in comparison with their original Cu-Pt core-shell precursors.

  6. Realization of defect-free epitaxial core-shell GaAs/AlGaAs nanowire heterostructures

    SciTech Connect

    Tambe, Michael J.; Lim, Sung Keun; Smith, Matthew J.; Gradecak, Silvija; Allard, Lawrence F.

    2008-10-13

    We report the controlled growth of vertically aligned GaAs/AlGaAs core-shell nanowires. By optimizing the shell deposition temperature and catalyst density we maintain high temperature stability and achieve defect-free epitaxial AlGaAs shell deposition with high aluminum incorporation. Energy dispersive x-ray analysis determines the shell composition to be Al{sub 0.9}Ga{sub 0.1}As and measures the uniformity of the shell thickness. Lattice-resolved high-angle annular dark-field scanning transmission electron microscopy images confirm the core-shell interface to be defect-free, epitaxial, and atomically sharp. The ability to realize GaAs/AlGaAs core-shell nanowires with precise control over the morphology and composition is essential to the development of nanowire-based high mobility electronics.

  7. Core-shell biopolymer nanoparticle delivery systems: synthesis and characterization of curcumin fortified zein-pectin nanoparticles.

    PubMed

    Hu, Kun; Huang, Xiaoxia; Gao, Yongqing; Huang, Xulin; Xiao, Hang; McClements, David Julian

    2015-09-01

    Biopolymer core-shell nanoparticles were fabricated using a hydrophobic protein (zein) as the core and a hydrophilic polysaccharide (pectin) as the shell. Particles were prepared by coating cationic zein nanoparticles with anionic pectin molecules using electrostatic deposition (pH 4). The core-shell nanoparticles were fortified with curcumin (a hydrophobic bioactive molecule) at a high loading efficiency (>86%). The resulting nanoparticles were spherical, relatively small (diameter ≈ 250 nm), and had a narrow size distribution (polydispersity index ≈ 0.24). The encapsulated curcumin was in an amorphous (rather than crystalline form) as detected by differential scanning calorimetry (DSC). Fourier transform infrared (FTIR) and Raman spectra indicated that the encapsulated curcumin interacted with zein mainly through hydrophobic interactions. The nanoparticles were converted into a powdered form that had good water-dispersibility. These core-shell biopolymer nanoparticles could be useful for incorporating curcumin into functional foods and beverages, as well as dietary supplements and pharmaceutical products. PMID:25842338

  8. Fabrication of In2O3@In2S3 core-shell nanocubes for enhanced photoelectrochemical performance

    NASA Astrophysics Data System (ADS)

    Li, Haohua; Chen, Cong; Huang, Xinyou; Leng, Yang; Hou, Mengnan; Xiao, Xiaogu; Bao, Jie; You, Jiali; Zhang, Wenwen; Wang, Yukun; Song, Juan; Wang, Yaping; Liu, Qinqin; Hope, Gregory A.

    2014-02-01

    Herein, we report the facile synthesis of In2O3@In2S3 core-shell nanocubes and their improved photoelectrochemical property. In2O3@In2S3 core-shell nanocubes are grown on a F-doped SnO2 (FTO) glass substrate by a two-step process, which involves the electrodeposition of In2O3 nanocubes and a subsequent ion-exchange treatment. The improved light-harvesting ability and the suitable band alignment of the In2O3@In2S3 core-shell nanocubes generate a remarkable photocurrent density of 6.19 mA cm-2 (at 0 V vs. Ag/AgCl), which is substantially higher than the pristine In2O3 nanocubes. These results provide a new insight into the design of a high-performance photoanode for photoelectrochemical water splitting.

  9. Absorption spectra of CdSe-ZnS core-shell quantum dots at high photon energies: Experiment and modeling

    NASA Astrophysics Data System (ADS)

    Mukherjee, Amlan; Ghosh, Sandip

    2014-11-01

    Absorption spectra of CdSe-ZnS core-shell quantum dot (QD) ensembles, with average core diameters ranging from 2.6 nm to 7.2 nm have been obtained using both transmission and photoluminescence excitation measurements. In agreement with previous reports, the absorption coefficient at energies ≃1 eV above the effective bandgap increases monotonically as in bulk solids. A simple effective-mass spherical core-shell potential model cannot explain the relatively high absorption at higher energies. The calculated electron and hole radial envelope wavefunctions show asymmetry due to the core-shell structure. It leads to normally symmetry-disallowed transitions acquiring a weak oscillator strength, with their number and strength increasing with energy. A phenomenological model that invokes normally disallowed transitions in general is shown to reproduce the absorption spectrum at higher energies quite well. The oscillator strength scaling factor for such transitions increases with decrease in QD size, consistent with expectations.

  10. Fluorescence relaxation dynamics of CdSe and CdSe/CdS core/shell quantum dots

    SciTech Connect

    Kaur, Gurvir; Kaur, Harmandeep; Tripathi, S. K.

    2014-04-24

    Time-resolved fluorescence spectra for colloidal CdSe and CdSe/CdS core/shell quantum dots have been investigated to know their electron relaxation dynamics at the maximum steady state fluorescence intensity. CdSe core and CdSe/CdS type I core-shell materials with different shell (CdS) thicknesses have been synthesized using mercaptoacetic acid as a capping agent. Steady state absorption and emission studies confirmed successful synthesis of CdSe and CdSe/CdS core-shell quantum dots. The fluorescence shows a tri-exponential decay with lifetimes 57.39, 7.82 and 0.96 ns for CdSe quantum dots. The lifetime of each recombination decreased with growth of CdS shell over the CdSe core, with maximum contribution to fluorescence by the fastest transition.

  11. Optical properties of plasmonic light-emitting diodes based on flip-chip III-nitride core-shell nanowires.

    PubMed

    Nami, Mohsen; Feezell, Daniel F

    2014-12-01

    In this work, we utilize the finite difference time domain (FDTD) method to investigate the Purcell factor, light extraction efficiency (EXE), and cavity quality parameter (Q), and to predict the modulation response of Ag-clad flip-chip GaN/InGaN core-shell nanowire light-emitting diodes (LEDs) with the potential for electrical injection. We consider the need for a pn-junction, the effects of the substrate, and the limitations of nanoscale fabrication techniques in the evaluation. The investigated core-shell nanowire consists of an n-GaN core, surrounded by nonpolar m-plane quantum wells, p-GaN, and silver cladding layers. The core-shell nanowire geometry exhibits a Purcell factor of 57, resulting in a predicted limit of 30 GHz for the 3dB modulation bandwidth. PMID:25606879

  12. Strain distribution of confined Ge/GeO2 core/shell nanoparticles engineered by growth environments

    NASA Astrophysics Data System (ADS)

    Wei, Wenyan; Yuan, Cailei; Luo, Xingfang; Yu, Ting; Wang, Gongping

    2016-02-01

    The strain distributions of Ge/GeO2 core/shell nanoparticles confined in different host matrix grown by surface oxidation are investigated. The simulated results by finite element method demonstrated that the strains of the Ge core and the GeO2 shell strongly depend on the growth environments of the nanoparticles. Moreover, it can be found that there is a transformation of the strain on Ge core from tensile to compressive strain during the growth of Ge/GeO2 core/shell nanoparticles. And, the transformation of the strain is closely related with the Young's modulus of surrounding materials of Ge/GeO2 core/shell nanoparticles.

  13. Size-controlled, magnetic, and core-shell nanoparticles synthesized by inert-gas condensation

    NASA Astrophysics Data System (ADS)

    Koten, Mark A.

    Interest in nanoparticles (2 to 100 nm in diameter) and clusters of atoms (0.5 to 2 nm in diameter) has heightened over the past two and a half decades on both fundamental and functional levels. Nanoparticles and clusters of atoms are an exciting branch of materials science because they do not behave like normal bulk matter, nor do they act like molecules. They can have shockingly different physical, chemical, optical, or magnetic properties from the same material at a larger scale. In the case of nanoparticles, the surface-to-volume ratio can change fundamental properties like melting temperature, binding energy, or electron affinity. The definitions of markers used to distinguish between metallic, semiconducting, and insulating bulk condensed matter, such as the band gap and polarizability, can even be blurred or confused on the nanoscale. Similarly, clusters of atoms can form in structures that are only stable at finite sizes, and do not translate to bulk condensed matter. Thermodynamics of finite systems changes dramatically in nanovolumes such as wires, rods, cubes, and spheres, which can lead to complex core-shell and onion-like nanostructures. Consequently, these changes in properties and structure have led to many new possibilities in the field of materials engineering. Inert-gas condensation (IGC) is a well-established method of producing nanoparticles that condense from the gas phase. Its first use dates back to the early 1990s, and it has been used to fabricate nanoparticles both commercially and in research and development for applications in magnetism, biomedicine, and catalysts. In this dissertation, IGC was used to produce a wide variety of nanoparticles. First, control over the size distributions of Cu nanoparticles and how it relates to the plasma properties inside the nucleation chamber was investigated. Next, the formation of phase pure WFe2 nanoparticles revealed that this Laves phase is ferromagnetic instead of non-magnetic. Finally, core-shell

  14. Carbon coated MnO@Mn3N2 core-shell composites for high performance lithium ion battery anodes.

    PubMed

    Wu, Yongmin; Liu, Mengjia; Feng, Hongbin; Li, Jinghong

    2014-12-21

    Carbon coated MnO@Mn(3)N(2) core-shell composites (MnO@Mn(3)N(2)/C) were synthesized in a simple approach by calcining MnO(2) nanowires with urea at 800 °C under an ammonia atmosphere. Urea derived carbon nanosheets were partially coated on pure phase MnO@Mn(3)N(2) core-shell composites. Electrochemical measurements reveal that the MnO@Mn(3)N(2)/C displayed high discharge capacities, an excellent high-rate capability and an enhanced cycling performance. PMID:25384358

  15. Core-shell polymer nanoparticles for prevention of GSH drug detoxification and cisplatin delivery to breast cancer cells.

    PubMed

    Surnar, Bapurao; Sharma, Kavita; Jayakannan, Manickam

    2015-11-14

    Platinum drug delivery against the detoxification of cytoplasmic thiols is urgently required for achieving efficacy in breast cancer treatment that is over expressed by glutathione (GSH, thiol-oligopeptide). GSH-resistant polymer-cisplatin core-shell nanoparticles were custom designed based on biodegradable carboxylic functional polycaprolactone (PCL)-block-poly(ethylene glycol) diblock copolymers. The core of the nanoparticle was fixed as 100 carboxylic units and the shell part was varied using various molecular weight poly(ethylene glycol) monomethyl ethers (MW of PEGs = 100-5000 g mol(-1)) as initiator in the ring-opening polymerization. The complexation of cisplatin aquo species with the diblocks produced core-shell nanoparticles of 75 nm core with precise size control the particles up to 190 nm. The core-shell nanoparticles were found to be stable in saline solution and PBS and they exhibited enhanced stability with increase in the PEG shell thickness at the periphery. The hydrophobic PCL layer on the periphery of the cisplatin core behaved as a protecting layer against the cytoplasmic thiol residues (GSH and cysteine) and exhibited <5% of drug detoxification. In vitro drug-release studies revealed that the core-shell nanoparticles were ruptured upon exposure to lysosomal enzymes like esterase at the intracellular compartments. Cytotoxicity studies were performed both in normal wild-type mouse embryonic fibroblast cells (Wt-MEFs), and breast cancer (MCF-7) and cervical cancer (HeLa) cell lines. Free cisplatin and polymer drug core-shell nanoparticles showed similar cytotoxicity effects in the HeLa cells. In MCF-7 cells, the free cisplatin drug exhibited 50% cell death whereas complete cell death (100%) was accomplished by the polymer-cisplatin core-shell nanoparticles. Confocal microscopic images confirmed that the core-shell nanoparticles were taken up by the MCF-7 and HeLa cells and they were accumulated both at the cytoplasm as well at peri

  16. Large enhanced dielectric permittivity in polyaniline passivated core-shell nano magnetic iron oxide by plasma polymerization

    SciTech Connect

    Joy, Lija K.; Sooraj, V.; Sethulakshmi, N.; Anantharaman, M. R.; Sajeev, U. S.; Nair, Swapna S.; Narayanan, T. N.; Ajayan, P. M.

    2014-03-24

    Commercial samples of Magnetite with size ranging from 25–30 nm were coated with polyaniline by using radio frequency plasma polymerization to achieve a core shell structure of magnetic nanoparticle (core)–Polyaniline (shell). High resolution transmission electron microscopy images confirm the core shell architecture of polyaniline coated iron oxide. The dielectric properties of the material were studied before and after plasma treatment. The polymer coated magnetite particles exhibited a large dielectric permittivity with respect to uncoated samples. The dielectric behavior was modeled using a Maxwell–Wagner capacitor model. A plausible mechanism for the enhancement of dielectric permittivity is proposed.

  17. Sn(78)Ge(22)@carbon core-shell nanowires as fast and high-capacity lithium storage media.

    PubMed

    Lee, Hyojin; Cho, Jaephil

    2007-09-01

    Branched Sn78Ge22@carbon core-shell nanowires were prepared by thermal annealing of butyl-capped Sn78Ge22 clusters at 600 degrees C in a vacuum. The first discharge and charge capacities are 1250 and 1107 mA h/g, showing a Coulombic efficiency of 88%. Such a one-dimensional core-shell design exploits the benefits of the Sn78Ge22 nanowire to produce an exceptional high rate lithium reactivity (93% Coulombic efficiency at 8C (=6400 mA/g) rate) as well as excellent capacity retention after extended cycles (capacity retention of 94%). PMID:17661523

  18. Tiny Pd@Co core-shell nanoparticles confined inside a metal-organic framework for highly efficient catalysis.

    PubMed

    Chen, Yu-Zhen; Xu, Qiang; Yu, Shu-Hong; Jiang, Hai-Long

    2015-01-01

    A new strategy to pre-incorporate metal precursors followed by their in situ reduction is established to prepare tiny core-shell nanoparticles (NPs) stabilized by a metal-organic framework (MOF). The obtained Pd@Co core-shell NPs of ∼2.5 nm confined in the pores of a mesoporous MOF, MIL-101, exhibit synergistic and superior catalytic performance in hydrolytic dehydrogenation of NH3 BH3 under mild conditions compared to their monometallic and alloy counterparts as well as Pd@Co NPs located on a MOF surface. PMID:25201445

  19. Core-shell heterostructured metal oxide arrays enable superior light-harvesting and hysteresis-free mesoscopic perovskite solar cells

    NASA Astrophysics Data System (ADS)

    Mahmood, Khalid; Swain, Bhabani Sankar; Amassian, Aram

    2015-07-01

    To achieve highly efficient mesoscopic perovskite solar cells (PSCs), the structure and properties of an electron transport layer (ETL) or material (ETM) have been shown to be of supreme importance. Particularly, the core-shell heterostructured mesoscopic ETM architecture has been recognized as a successful electrode design, because of its large internal surface area, superior light-harvesting efficiency and its ability to achieve fast charge transport. Here we report the successful fabrication of a hysteresis-free, 15.3% efficient PSC using vertically aligned ZnO nanorod/TiO2 shell (ZNR/TS) core-shell heterostructured ETMs for the first time. We have also added a conjugated polyelectrolyte polymer into the growth solution to promote the growth of high aspect ratio (AR) ZNRs and substantially improve the infiltration of the perovskite light absorber into the ETM. The PSCs based on the as-synthesized core-shell ZnO/TiO2 heterostructured ETMs exhibited excellent performance enhancement credited to the superior light harvesting capability, larger surface area, prolonged charge-transport pathways and lower recombination rate. The unique ETM design together with minimal hysteresis introduces core-shell ZnO/TiO2 heterostructures as a promising mesoscopic electrode approach for the fabrication of efficient PSCs.To achieve highly efficient mesoscopic perovskite solar cells (PSCs), the structure and properties of an electron transport layer (ETL) or material (ETM) have been shown to be of supreme importance. Particularly, the core-shell heterostructured mesoscopic ETM architecture has been recognized as a successful electrode design, because of its large internal surface area, superior light-harvesting efficiency and its ability to achieve fast charge transport. Here we report the successful fabrication of a hysteresis-free, 15.3% efficient PSC using vertically aligned ZnO nanorod/TiO2 shell (ZNR/TS) core-shell heterostructured ETMs for the first time. We have also added a

  20. A multifunctional core-shell nanoparticle for dendritic cell-based cancer immunotherapy

    NASA Astrophysics Data System (ADS)

    Cho, Nam-Hyuk; Cheong, Taek-Chin; Min, Ji Hyun; Wu, Jun Hua; Lee, Sang Jin; Kim, Daehong; Yang, Jae-Seong; Kim, Sanguk; Kim, Young Keun; Seong, Seung-Yong

    2011-10-01

    Dendritic cell-based cancer immunotherapy requires tumour antigens to be delivered efficiently into dendritic cells and their migration to be monitored in vivo. Nanoparticles have been explored as carriers for antigen delivery, but applications have been limited by the toxicity of the solvents used to make nanoparticles, and by the need to use transfection agents to deliver nanoparticles into cells. Here we show that an iron oxide-zinc oxide core-shell nanoparticle can deliver carcinoembryonic antigen into dendritic cells while simultaneously acting as an imaging agent. The nanoparticle-antigen complex is efficiently taken up by dendritic cells within one hour and can be detected in vitro by confocal microscopy and in vivo by magnetic resonance imaging. Mice immunized with dendritic cells containing the nanoparticle-antigen complex showed enhanced tumour antigen specific T-cell responses, delayed tumour growth and better survival than controls.

  1. Pressure-controlled formation of crystalline, Janus, and core-shell supraparticles.

    PubMed

    Kister, Thomas; Mravlak, Marko; Schilling, Tanja; Kraus, Tobias

    2016-07-21

    Binary mixtures of nanoparticles self-assemble in the confinement of evaporating oil droplets and form regular supraparticles. We demonstrate that moderate pressure differences on the order of 100 kPa change the particles' self-assembly behavior. Crystalline superlattices, Janus particles, and core-shell particle arrangements form in the same dispersions when changing the working pressure or the surfactant that sets the Laplace pressure inside the droplets. Molecular dynamics simulations confirm that pressure-dependent interparticle potentials affect the self-assembly route of the confined particles. Optical spectrometry, small-angle X-ray scattering and electron microscopy are used to compare experiments and simulations and confirm that the onset of self-assembly depends on particle size and pressure. The overall formation mechanism reminds of the demixing of binary alloys with different phase diagrams. PMID:27340805

  2. Functionalized magnetic iron oxide/alginate core-shell nanoparticles for targeting hyperthermia.

    PubMed

    Liao, Shih-Hsiang; Liu, Chia-Hung; Bastakoti, Bishnu Prasad; Suzuki, Norihiro; Chang, Yung; Yamauchi, Yusuke; Lin, Feng-Huei; Wu, Kevin C-W

    2015-01-01

    Hyperthermia is one of the promising treatments for cancer therapy. However, the development of a magnetic fluid agent that can selectively target a tumor and efficiently elevate temperature while exhibiting excellent biocompatibility still remains challenging. Here a new core-shell nanostructure consisting of inorganic iron oxide (Fe3O4) nanoparticles as the core, organic alginate as the shell, and cell-targeting ligands (ie, D-galactosamine) decorated on the outer surface (denoted as Fe3O4@Alg-GA nanoparticles) was prepared using a combination of a pre-gel method and coprecipitation in aqueous solution. After treatment with an AC magnetic field, the results indicate that Fe3O4@Alg-GA nanoparticles had excellent hyperthermic efficacy in a human hepatocellular carcinoma cell line (HepG2) owing to enhanced cellular uptake, and show great potential as therapeutic agents for future in vivo drug delivery systems. PMID:26005343

  3. Vibrational modes of metal nanoshells and bimetallic core-shell nanoparticles

    PubMed Central

    Kirakosyan, Arman S.; Shahbazyan, Tigran V.

    2008-01-01

    We theoretically study the spectrum of radial vibrational modes in composite metal nanostructures such as bimetallic core-shell particles and metal nanoshells with dielectric core in an environment. We calculate frequencies and damping rates of fundamental (breathing) modes for these nanostructures along with those of two higher-order modes. For metal nanoshells, we find that the breathing mode frequency is always lower than the one for solid particles of the same size, while the damping is higher and increases with a reduction in the shell thickness. We identify two regimes that can be characterized as weakly damped and overdamped vibrations in the presence of external medium. For bimetallic particles, we find periodic dependence of frequency and damping rate on the shell thickness with period being determined by the mode number. For both types of nanostructures, the frequency of higher modes is nearly independent of the environment, while the damping rate shows a strong sensitivity to the outside medium. PMID:18647039

  4. Conductance oscillations of core-shell nanowires in transversal magnetic fields

    NASA Astrophysics Data System (ADS)

    Manolescu, Andrei; Nemnes, George Alexandru; Sitek, Anna; Rosdahl, Tomas Orn; Erlingsson, Sigurdur Ingi; Gudmundsson, Vidar

    2016-05-01

    We analyze theoretically electronic transport through a core-shell nanowire in the presence of a transversal magnetic field. We calculate the conductance for a variable coupling between the nanowire and the attached leads and show how the snaking states, which are low-energy states localized along the lines of the vanishing radial component of the magnetic field, manifest their existence. In the strong-coupling regime they induce flux periodic, Aharonov-Bohm-like, conductance oscillations, which, by decreasing the coupling to the leads, evolve into well-resolved peaks. The flux periodic oscillations arise due to interference of the snaking states, which is a consequence of backscattering at either the contacts with leads or magnetic or potential barriers in the wire.

  5. Germanium-silicon alloy and core-shell nanocrystals by gas phase synthesis

    NASA Astrophysics Data System (ADS)

    Mehringer, Christian; Kloner, Christian; Butz, Benjamin; Winter, Benjamin; Spiecker, Erdmann; Peukert, Wolfgang

    2015-03-01

    In this work we present a novel route to synthesize well defined germanium-silicon alloy (GexSi1-x) and core-shell nanocrystals (NCs) employing monosilane (SiH4) and monogermane (GeH4) as precursors in a continuously operated two-stage hot-wall aerosol reactor setup. The first hot-wall reactor stage (HWR I) is used to produce silicon (Si) seed particles from SiH4 pyrolysis in Argon (Ar). The resulting seeding aerosol is fed into the second reactor stage (HWR II) and a mixture of SiH4 and GeH4 is added. The ratio of the precursors in the feed, their partial pressures, the synthesis temperature in HWR II and the overall pressure are varied depending on the desired morphology and composition. Alloy particle production is achieved in the heterogeneous surface reaction regime, meaning that germanium (Ge) and Si are deposited on the seed surface simultaneously. The NCs can be synthesized with any desired composition, whilst maintaining a mean diameter around 30 nm with a geometric standard deviation (GSD) around 1.25. The absorption behavior and the related fundamental optical band gap energy in dependence on the alloy composition are exemplarily presented. They prove the possibility to tailor NC properties for electronical and opto-electronical applications. In the homogeneous gas phase reaction regime facetted Ge-Si core-shell structures are accessible. The Ge deposition on the seeds precedes the Si deposition due to different gas phase reaction kinetics of the precursors. The Si layer grows epitaxially on the Ge core and is around 5 nm thick.In this work we present a novel route to synthesize well defined germanium-silicon alloy (GexSi1-x) and core-shell nanocrystals (NCs) employing monosilane (SiH4) and monogermane (GeH4) as precursors in a continuously operated two-stage hot-wall aerosol reactor setup. The first hot-wall reactor stage (HWR I) is used to produce silicon (Si) seed particles from SiH4 pyrolysis in Argon (Ar). The resulting seeding aerosol is fed into

  6. CTMP-based cellulose fibers modified with core-shell latex for reinforcing biocomposites.

    PubMed

    Pan, Yuanfeng; Xiao, Huining; Zhao, Yi; Wang, Zhuang

    2013-06-01

    The toughening of cellulose fiber reinforced polypropylene (PP) was performed via adsorbing the cationic latex with core-shell structure onto chemithermomechanical pulp (CTMP) fibers as reinforcements, which is a novel approach for rendering the surface of cellulose fibers elastomeric. The mechanical, morphological and thermal properties of the resulting biocomposites, containing 40% (wt) of the modified fibers, were investigated. The results showed that with the increasing of the latex dosage up to 2% (wt on dry CTMP fibers), the impact, tensile and flexural strengths of the modified CTMP/PP biocomposites were significantly increased. The toughening mechanism was discussed based on the retarding of crack propagation and the promoting of crystallization of PP matrix (as revealed by DSC characterization). The overall performance of the biocomposite demonstrated that cationic latex-modified CTMP fiber is very effective in reinforcing thermoplastic-based biocomposites along with the synergetic effect on enhancing crystallinity of polymer matrix. PMID:23618289

  7. Synthesis of Ge/Si core/shell nanowires with suppression of branch formation

    NASA Astrophysics Data System (ADS)

    Noguchi, Tomohiro; Simanullang, Marolop; Xu, Zhengyu; Usami, Koichi; Kodera, Tetsuo; Oda, Shunri

    2016-05-01

    Ge/Si core/shell nanowires (Ge/Si-NWs) are promising materials for applications such as transistors, sensors, and thermoelectric devices. A major problem in the synthesis of Ge/Si-NWs using Au catalysts in conjunction with vapor–liquid–solid chemical vapor deposition is the formation of branched Si nanowires on the surface of Ge nanowires because of the migration of Au nanoparticles that serve as seeds. Based on an analysis of the Au–Ge phase diagram, we propose a method to mitigate this issue. By introducing Ge-rich conditions during the temperature-increase step between the formation of the Ge core and the Si shell, we have successfully eliminated Au nanoparticles on Ge surfaces, and thus fabricated Ge/Si-NWs without Si nanowires.

  8. Investigation into Photoconductivity in Single CNF/TiO2-Dye Core-Shell Nanowire Devices

    NASA Astrophysics Data System (ADS)

    Li, Zhuangzhi; Rochford, Caitlin; Javier Baca, F.; Liu, Jianwei; Li, Jun; Wu, Judy

    2010-09-01

    A vertically aligned carbon nanofiber array coated with anatase TiO2 (CNF/TiO2) is an attractive possible replacement for the sintered TiO2 nanoparticle network in the original dye-sensitized solar cell (DSSC) design due to the potential for improved charge transport and reduced charge recombination. Although the reported efficiency of 1.1% in these modified DSSC’s is encouraging, the limiting factors must be identified before a higher efficiency can be obtained. This work employs a single nanowire approach to investigate the charge transport in individual CNF/TiO2 core-shell nanowires with adsorbed N719 dye molecules in dark and under illumination. The results shed light on the role of charge traps and dye adsorption on the (photo) conductivity of nanocrystalline TiO2 CNF’s as related to dye-sensitized solar cell performance.

  9. Infrared length scale and extrapolations for the no-core shell model

    DOE PAGESBeta

    Wendt, K. A.; Forssén, C.; Papenbrock, T.; Sääf, D.

    2015-06-03

    In this paper, we precisely determine the infrared (IR) length scale of the no-core shell model (NCSM). In the NCSM, the A-body Hilbert space is truncated by the total energy, and the IR length can be determined by equating the intrinsic kinetic energy of A nucleons in the NCSM space to that of A nucleons in a 3(A-1)-dimensional hyper-radial well with a Dirichlet boundary condition for the hyper radius. We demonstrate that this procedure indeed yields a very precise IR length by performing large-scale NCSM calculations for 6Li. We apply our result and perform accurate IR extrapolations for bound statesmore » of 4He, 6He, 6Li, and 7Li. Finally, we also attempt to extrapolate NCSM results for 10B and 16O with bare interactions from chiral effective field theory over tens of MeV.« less

  10. Nanothermochromics with VO2-based core-shell structures: Calculated luminous and solar optical properties

    NASA Astrophysics Data System (ADS)

    Li, S.-Y.; Niklasson, G. A.; Granqvist, C. G.

    2011-06-01

    Composites including VO2-based thermochromic nanoparticles are able to combine high luminous transmittance Tlum with a significant modulation of the solar energy transmittance ΔTsol at a "critical" temperature in the vicinity of room temperature. Thus nanothermochromics is of much interest for energy efficient fenestration and offers advantages over thermochromic VO2-based thin films. This paper presents calculations based on effective medium theory applied to dilute suspensions of core-shell nanoparticles and demonstrates that, in particular, moderately thin-walled hollow spherical VO2 nanoshells can give significantly higher values of ΔTsol than solid nanoparticles at the expense of a somewhat lowered Tlum. This paper is a sequel to a recent publication [S.-Y. Li, G. A. Niklasson, and C. G. Granqvist, J. Appl. Phys. 108, 063525 (2010)].

  11. A facile one-pot method to synthesize ultrasmall core-shell superparamagnetic and upconversion nanoparticles.

    PubMed

    Cheng, Qian; Guo, Hongxuan; Li, Yu; Liu, Shouxin; Sui, Jiehe; Cai, Wei

    2016-08-01

    Ultrasmall core-shell Fe3O4@NaYF4:Yb(3+)/Er(3+) nanoparticles with bifunctional properties have been successfully synthesized via one pot thermolysis method using oleylamine as both solvent and stabilizer. X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR), upconversion (UC) luminescence spectra and the physical properties measurement system (PPMS) were used to characterize the resulting samples. The synthesized samples have uniform morphology with a mean size of 14.5nm and excellent dispersibility. Moreover, these nanoparticles exhibit superparamagnetic behaviour with saturation magnetization of 8.45emμ/g and efficient up-conversion emission with a two-photon induced process when excited by a 980nm laser. These results suggest that the synthesized ultrasmall bifunctional nanoparticles may find many biomedical applications, such as clinical diagnosis and treatment of cancers. PMID:27135942

  12. Galvanic Exchange in Colloidal Metal/Metal-Oxide Core/Shell Nanocrystals

    PubMed Central

    2016-01-01

    While galvanic exchange is commonly applied to metallic nanoparticles, recently its applicability was expanded to metal-oxides. Here the galvanic exchange is studied in metal/metal-oxide core/shell nanocrystals. In particular Sn/SnO2 is treated by Ag+, Pt2+, Pt4+, and Pd2+. The conversion dynamics is monitored by in situ synchrotron X-ray diffraction. The Ag+ treatment converts the Sn cores to the intermetallic AgxSn (x ∼ 4) phase, by changing the core’s crystal structure. For the analogous treatment by Pt2+, Pt4+, and Pd2+, such a galvanic exchange is not observed. This different behavior is caused by the semipermeability of the naturally formed SnO2 shell, which allows diffusion of Ag+ but protects the nanocrystal cores from oxidation by Pt and Pd ions.

  13. Electronic and optical properties of core-shell nanowires in a magnetic field.

    PubMed

    Ravi Kishore, V V; Partoens, B; Peeters, F M

    2014-03-01

    The electronic and optical properties of zincblende nanowires are investigated in the presence of a uniform magnetic field directed along the [001] growth direction within the k · p method. We focus our numerical study on core-shell nanowires consisting of the III-V materials GaAs, Al(x)Ga(1-x)As and (Al(y)Ga(1-y))₀.₅₁In₀.₄₉P. Nanowires with electrons confined in the core exhibit a Fock-Darwin-like spectrum, whereas nanowires with electrons confined in the shell show Aharonov-Bohm oscillations. Thus, by properly choosing the core and the shell materials of the nanowire, the optical properties in a magnetic field can be tuned in very different ways. PMID:24521608

  14. Angle-dependent magnetotransport in GaAs/InAs core/shell nanowires

    NASA Astrophysics Data System (ADS)

    Haas, Fabian; Wenz, Tobias; Zellekens, Patrick; Demarina, Nataliya; Rieger, Torsten; Lepsa, Mihail; Grützmacher, Detlev; Lüth, Hans; Schäpers, Thomas

    2016-04-01

    We study the impact of the direction of magnetic flux on the electron motion in GaAs/InAs core/shell nanowires. At small tilt angles, when the magnetic field is aligned nearly parallel to the nanowire axis, we observe Aharonov–Bohm type h/e flux periodic magnetoconductance oscillations. These are attributed to transport via angular momentum states, formed by electron waves within the InAs shell. With increasing tilt of the nanowire in the magnetic field, the flux periodic magnetoconductance oscillations disappear. Universal conductance fluctuations are observed for all tilt angles, however with increasing amplitudes for large tilt angles. We record this evolution of the electron propagation from a circling motion around the core to a diffusive transport through scattering loops and give explanations for the observed different transport regimes separated by the magnetic field orientation.

  15. Plasmonic luminescent core-shell nanocomposites-enhanced chemiluminescence arising from the decomposition of peroxomonosulfite

    NASA Astrophysics Data System (ADS)

    Chen, Hui; Xue, Wei; Lu, Chao; Li, Hai-fang; Zheng, Yongzan; Lin, Jin-Ming

    2013-12-01

    A core-shell structure of plasmonic luminescent nanocomposite, Ni@SiO2@FITC@SiO2 (NSFS) combining the stable luminescence of fluorophore with the excellent plasmonic property of metal nanomaterials, has been synthesized through layer-by-layer assembly. The effect of NSFS on the ultraweak chemiluminescence (CL) reaction of hydrogen peroxide (H2O2) and sodium bisulfite (NaHSO3) was explored for the first time. It was found that the CL intensity from the decomposition of peroxomonosulfite was significantly enhanced by NSFS. The mechanism of the nanocomposite-enhanced CL was revealed as the coupling of chemically induced excited states of fluorescein isothiocyanate (FITC) with surface plasmons of Ni nanoparticles based on studies of CL emission spectra, electron spin resonance spectra, extinction spectra and fluorescence spectra. The work sheds new light on the characteristics of the versatile materials and gives us new insight into the optical properties of fluorophores.

  16. Tuning the reactivity of energetic nanoparticles by creation of a core-shell nanostructure.

    PubMed

    Prakash, A; McCormick, A V; Zachariah, M R

    2005-07-01

    This article presents a novel method for tuning the reactivity of nanoenergetic materials by coating a strong oxidizer nanoparticle (potassium permanganate; approximately 150 nm) with a layer of a relatively mild oxidizer (iron oxide). The measured reactivity for a nano-Al/composite oxidizer could be varied by more than a factor of 10, as measured by the pressurization rate in a closed vessel (psl/micros), by changing the coating thickness of the iron oxide. The composite oxidizer nanoparticles were synthesized by a new aerosol approach in which the nonwetting interaction between iron oxide and molten potassium permanganate aids the phase segregation of a nanocomposite droplet into a core-shell structure. PMID:16178238

  17. CuGaS2 hollow spheres from Ga-CuS core-shell nanoparticles.

    PubMed

    Cha, Ji-Hyun; Jung, Duk-Young

    2014-05-01

    A liquid gallium emulsion was prepared as a starting material using ultrasound treatment in ethylene glycol. Core-shell particles of Ga@CuS were successfully synthesized by deposition of a CuS layer on gallium droplets through sonochemical deposition of copper ions and thiourea in an alcohol media. The core and shell of Ga@CuS products were composed of amorphous gallium metal and covellite phase CuS, which transformed into chalcopyrite CuGaS2 hollow spheres after sulfurization at 450°C, which was the lowest crystallization temperature. The formation of hollow nanostructures was ascribed to the Kirkendall mechanism, in which liquid gallium particles play an important role as reactive templates. In conclusion, we obtained CuGaS2 hollow spheres with a 430 nm outer diameter and 120 nm shell thickness that had the same crystal structure and electrical properties as bulk CuGaS2. PMID:24365224

  18. Biodegradable and magnetic core-shell composite particle prepared by emulsion solvent diffusion method

    NASA Astrophysics Data System (ADS)

    Oka, Chiemi; Ushimaru, Kazunori; Horiishi, Nanao; Tsuge, Takeharu; Kitamoto, Yoshitaka

    2016-02-01

    The present paper describes optimization of preparation conditions of a core-shell composite particle, and its heat generation by alternating magnetic fields. The composite particles are prepared with a modified emulsion solvent diffusion method, which is combined with Pickering emulsion stabilized by magnetic nanoparticles. In this method, the magnetic nanoparticles act as an emulsifier, and its amount and size are crucial to morphology of the composite particles. The magnetic nanoparticles of 8-9 nm would be strongly adsorbed at a liquid-liquid interface rather than the larger nanoparticles. At the optimized concentration of the magnetic nanoparticle’s suspension for the preparation, small and uniform composite particles are obtained since the amount of the nanoparticles is enough to prevent coalescence of droplets during the formation of the composites. The heat generation by alternating magnetic fields emerged certainly. This result suggests the composite particles have a property as a heat-generating carrier for hyperthermia treatment.

  19. Ag@poly(m-phenylenediamine) core-shell nanoparticles for highly selective, multiplex nucleic acid detection.

    PubMed

    Zhang, Yingwei; Wang, Lei; Tian, Jingqi; Li, Hailong; Luo, Yonglan; Sun, Xuping

    2011-03-15

    In this letter, we report on the one-step synthesis of Ag@poly(m-phenylenediamine) core-shell nanoparticles (APCSNPs), carried out by direct mixing of aqueous silver nitrate and m-phenylenediamine solutions at room temperature. We further demonstrate the use of APCSNP as a novel fluorescent sensing platform for nucleic acid detection. In this regard, the detection of DNA is accomplished in two steps. First, APCSNP absorbs and quenches the fluorescence of dye-labeled single-stranded DNA (ssDNA) as a probe. Second, hybridizing of the probe with its target produces a double-stranded DNA (dsDNA) that detaches from APCSNP, resulting in the recovery of dye fluorescence. It suggests that this sensing system has a high selectivity down to single-base mismatch, and the results exhibit good reproducibility. Furthermore, we also demonstrate its application for the multiplex detection of nucleic acid sequences. PMID:21302954

  20. Size-Tunable and Functional Core-Shell Structured Silica Nanoparticles for Drug Release

    SciTech Connect

    Chi, Fangli; Guo, Ya Nan; Liu, Jun; Liu, Yunling; Huo, Qisheng

    2010-02-18

    Size-tunable silica cross-linked micellar core-shell nanoparticles (SCMCSNs) were successfully synthesized from a Pluronic nonionic surfactant (F127) template system with organic swelling agents such as 1,3,5-trimethylbenzene (TMB) and octanoic acid at room temperature. The size and morphology of SCMCSNs were directly evidenced by TEM imaging and DLS measurements (up to ~90 nm). Pyrene and coumarin 153 (C153) were used as fluorescent probe molecules to investigate the effect and location of swelling agent molecules. Papaverine as a model drug was used to measure the loading capacity and release property of nanoparticles. The swelling agents can enlarge the nanoparticle size and improve the drug loading capacity of nanoparticles. Moreover, the carboxylic acid group of fatty acid can adjust the release behavior of the nanoparticles.

  1. Strained GaAs/InGaAs Core-Shell Nanowires for Photovoltaic Applications

    NASA Astrophysics Data System (ADS)

    Moratis, K.; Tan, S. L.; Germanis, S.; Katsidis, C.; Androulidaki, M.; Tsagaraki, K.; Hatzopoulos, Z.; Donatini, F.; Cibert, J.; Niquet, Y.-M.; Mariette, H.; Pelekanos, N. T.

    2016-04-01

    We report on the successful growth of strained core-shell GaAs/InGaAs nanowires on Si (111) substrates by molecular beam epitaxy. The as-grown nanowires have a density in the order of 108 cm-2, length between 3 and 3.5 μm, and diameter between 60 and 160 nm, depending on the shell growth duration. By applying a range of characterization techniques, we conclude that the In incorporation in the nanowires is on average significantly smaller than what is nominally expected based on two-dimensional growth calibrations and exhibits a gradient along the nanowire axis. On the other hand, the observation of sharp dot-like emission features in the micro-photoluminescence spectra of single nanowires in the 900-1000-nm spectral range highlights the co-existence of In-rich enclosures with In content locally exceeding 30 %.

  2. Spectroscopic characterization of magnetic Fe3O4@Au core shell nanoparticles.

    PubMed

    Fouad, Dina M; El-Said, Waleed A; Mohamed, Mona B

    2015-04-01

    The magnetic nanoparticles iron oxide (Fe3O4) nanoparticles and iron oxide/gold core-shell (Fe3O4/Au) nanoparticles were synthesized and their catalytic photo-degradation activity towards malathion as example of organophosphorus pesticides were reported. Iron oxide (Fe3O4) magnetic nanoparticle was successfully prepared through co-precipitation method by the reduction of ferric chloride (FeCl3) using ascorbic acid. The morphology of the prepared nanoparticles was characterized by the TEM and XRD (X-ray diffraction) techniques. Degradation of 10 ppm of malathion in the presence of these nanoparticles under UV radiation was monitored using (HPLC) and UV-visible spectra. Fe3O4/Au nanoparticles showed higher efficiency in photo-degradation of malathion than Fe3O4 ones. PMID:25617979

  3. Core-shell-corona-structured polyelectrolyte brushes-grafting magnetic nanoparticles for water harvesting.

    PubMed

    Liu, Guoqiang; Cai, Meirong; Wang, Xiaolong; Zhou, Feng; Liu, Weimin

    2014-07-23

    A novel superhydrophilic material, charged polymer brushes-grafted magnetic core-shell-corona composite nanoparticles (Fe3O4@SiO2@PSPMA), was developed to harvest water through the hydration effect. Because of both the strong hydration capability and the good swelling performance, the negatively charged polymer brushes, PSPMA brushes, endow the composite nanoparticles with superhydrophilicity and a good water-absorbing performance like a sponge, while the magnetic Fe3O4 cores allow easy separation of Fe3O4@SiO2@PSPMA nanoparticles with absorbed water from oil/water mixture under an external magnetic field. The functional particles have the capability of harvesting water droplets whether floating on an oil surface or in the oil. This water-absorbing material uses selective wettability to harvest water and achieve oil-water separation and may be useful in finding novel approaches for recycling water from sewage and removing water in the petroleum industry. PMID:24955817

  4. Scattering of core-shell nanowires with the interference of electric and magnetic resonances.

    PubMed

    Liu, Wei; Miroshnichenko, Andrey E; Oulton, Rupert F; Neshev, Dragomir N; Hess, Ortwin; Kivshar, Yuri S

    2013-07-15

    We study the scattering of normally incident waves by core-shell nanowires, which support both electric and magnetic resonances. Within such nanowires, for p-polarized incident waves, each electric resonance corresponds to two degenerate scattering channels while the magnetic resonance corresponds to only one channel. Consequently, when the electric dipole (ED) and magnetic dipole (MD) are tuned to overlap spectrally, the magnitude of the ED is twice that of the magnetic one, leading to a pair of angles of vanishing scattering. We further demonstrate that the scattering features of nanowires are polarization dependent, and vanishing scattering angles also can be induced by Fano resonances due to the interference of higher-order electric modes with the broad MD mode. PMID:23939129

  5. Nickel- and platinum-containing core@shell catalysts for hydrogen generation of aqueous hydrazine borane

    NASA Astrophysics Data System (ADS)

    Clémençon, D.; Petit, J. F.; Demirci, U. B.; Xu, Q.; Miele, P.

    2014-08-01

    Nickel and platinum were used to prepare a series of core@shell structures to be studied as catalysts for the dehydrogenation of aqueous hydrazine borane N2H4BH3 at 50 °C. The challenge was especially to get a maximum of 3 mol of gas by decomposition of the N2H4 moiety. In our conditions, the most efficient Ni@Pt was found to be the structure constituted of 5 atoms of nickel for 1 atom of platinum. This catalyst permits to generate up to 4.5 mol H2 + N2. Surface characterizations showed that the efficiency of this catalyst is due to the presence of both metals on the surface, suggesting therefore that the structure would be rather Ni@NiPt. Our main results are reported herein.

  6. Strained GaAs/InGaAs Core-Shell Nanowires for Photovoltaic Applications.

    PubMed

    Moratis, K; Tan, S L; Germanis, S; Katsidis, C; Androulidaki, M; Tsagaraki, K; Hatzopoulos, Z; Donatini, F; Cibert, J; Niquet, Y-M; Mariette, H; Pelekanos, N T

    2016-12-01

    We report on the successful growth of strained core-shell GaAs/InGaAs nanowires on Si (111) substrates by molecular beam epitaxy. The as-grown nanowires have a density in the order of 10(8) cm(-2), length between 3 and 3.5 μm, and diameter between 60 and 160 nm, depending on the shell growth duration. By applying a range of characterization techniques, we conclude that the In incorporation in the nanowires is on average significantly smaller than what is nominally expected based on two-dimensional growth calibrations and exhibits a gradient along the nanowire axis. On the other hand, the observation of sharp dot-like emission features in the micro-photoluminescence spectra of single nanowires in the 900-1000-nm spectral range highlights the co-existence of In-rich enclosures with In content locally exceeding 30 %. PMID:27037927

  7. Angle-dependent magnetotransport in GaAs/InAs core/shell nanowires

    PubMed Central

    Haas, Fabian; Wenz, Tobias; Zellekens, Patrick; Demarina, Nataliya; Rieger, Torsten; Lepsa, Mihail; Grützmacher, Detlev; Lüth, Hans; Schäpers, Thomas

    2016-01-01

    We study the impact of the direction of magnetic flux on the electron motion in GaAs/InAs core/shell nanowires. At small tilt angles, when the magnetic field is aligned nearly parallel to the nanowire axis, we observe Aharonov–Bohm type h/e flux periodic magnetoconductance oscillations. These are attributed to transport via angular momentum states, formed by electron waves within the InAs shell. With increasing tilt of the nanowire in the magnetic field, the flux periodic magnetoconductance oscillations disappear. Universal conductance fluctuations are observed for all tilt angles, however with increasing amplitudes for large tilt angles. We record this evolution of the electron propagation from a circling motion around the core to a diffusive transport through scattering loops and give explanations for the observed different transport regimes separated by the magnetic field orientation. PMID:27091000

  8. Cross-sectional aspect ratio modulated electronic properties in Si/Ge core/shell nanowires

    SciTech Connect

    Liu, Nuo; Lu, Ning; Yao, Yong-Xin; Zhang, Gui-Ping; Wang, Cai-Zhuang; Ho, Kai-Ming

    2013-02-28

    Electronic structures of (4, n) and (m, 4) (the NW has m layers parallel to the {1 1 1} facet and n layers parallel to {1 1 0}) Si/Ge core/shell nanowires (NWs) along the [1 1 2] direction with cross-sectional aspect ratio (m/n) from 0.36 to 2.25 are studied by first-principles calculations. An indirect to direct band gap transition is observed as m/n decreases, and the critical values of m/n and diameter for the transition are also estimated. The size of the band gap also depends on the aspect ratio. These results suggest that m/n plays an important role in modulating the electronic properties of the NWs.

  9. Infrared length scale and extrapolations for the no-core shell model

    NASA Astrophysics Data System (ADS)

    Wendt, K. A.; Forssén, C.; Papenbrock, T.; Sääf, D.

    2015-06-01

    We precisely determine the infrared (IR) length scale of the no-core shell model (NCSM). In the NCSM, the A -body Hilbert space is truncated by the total energy, and the IR length can be determined by equating the intrinsic kinetic energy of A nucleons in the NCSM space to that of A nucleons in a 3 (A -1 ) -dimensional hyper-radial well with a Dirichlet boundary condition for the hyper radius. We demonstrate that this procedure indeed yields a very precise IR length by performing large-scale NCSM calculations for 6Li. We apply our result and perform accurate IR extrapolations for bound states of 4He,6He,6Li , and 7Li . We also attempt to extrapolate NCSM results for 10B and 16O with bare interactions from chiral effective field theory over tens of MeV.

  10. Intrinsic dipole-field-driven mesoscale crystallization of core-shell ZnO mesocrystal microspheres.

    PubMed

    Liu, Z; Wen, X D; Wu, X L; Gao, Y J; Chen, H T; Zhu, J; Chu, P K

    2009-07-01

    Novel uniform-sized, core-shell ZnO mesocrystal microspheres have been synthesized on a large scale using a facile one-pot hydrothermal method in the presence of the water-soluble polymer poly(sodium 4-styrenesulfonate). The mesocrystal forms via a nonclassical crystallization process. The intrinsic dipole field introduced by the nanoplatelets as a result of selective adsorption of the polyelectrolyte on some polar surfaces of the nanoparticles acts as the driving force. In addition, it plays an important role throughout the mesoscale assembly process from the creation of the bimesocrystalline core to the apple-like structure and finally the microsphere. Our calculation based on a dipole model confirms the dipole-field-driven mechanism forming the apple-like structure. PMID:19518047

  11. Effective Operators Within the Ab Initio No-Core Shell Model

    SciTech Connect

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

    2004-11-30

    We implement an effective operator formalism for general one- and two-body operators, obtaining results consistent with the no-core shell model (NCSM) wave functions. The Argonne V8' nucleon-nucleon potential was used in order to obtain realistic wave functions for {sup 4}He, {sup 6}Li and {sup 12}C. In the NCSM formalism, we compute electromagnetic properties using the two-body cluster approximation for the effective operators and obtain results which are sensitive to the range of the bare operator. To illuminate the dependence on the range, we employ a Gaussian two-body operator of variable range, finding weak renormalization of long range operators (e.g., quadrupole) in a fixed model space. This is understood in terms of the two-body cluster approximation which accounts mainly for short-range correlations. Consequently, short range operators, such as the relative kinetic energy, will be well renormalized in the two-body cluster approximation.

  12. Platinum-tin oxide core-shell catalysts for efficient electro-oxidation of ethanol.

    PubMed

    Du, Wenxin; Yang, Guangxing; Wong, Emily; Deskins, N Aaron; Frenkel, Anatoly I; Su, Dong; Teng, Xiaowei

    2014-08-01

    Platinum-tin (Pt/Sn) binary nanoparticles are active electrocatalysts for the ethanol oxidation reaction (EOR), but inactive for splitting the C-C bond of ethanol to CO2. Here we studied detailed structure properties of Pt/Sn catalysts for the EOR, especially CO2 generation in situ using a CO2 microelectrode. We found that composition and crystalline structure of the tin element played important roles in the CO2 generation: non-alloyed Pt46-(SnO2)54 core-shell particles demonstrated a strong capability for C-C bond breaking of ethanol than pure Pt and intermetallic Pt/Sn, showing 4.1 times higher CO2 peak partial pressure generated from EOR than commercial Pt/C. PMID:25033229

  13. Ab Initio No-Core Shell Model Calculations Using Realistic Two- and Three-Body Interactions

    SciTech Connect

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

    2004-11-30

    There has been significant progress in the ab initio approaches to the structure of light nuclei. One such method is the ab initio no-core shell model (NCSM). Starting from realistic two- and three-nucleon interactions this method can predict low-lying levels in p-shell nuclei. In this contribution, we present a brief overview of the NCSM with examples of recent applications. We highlight our study of the parity inversion in {sup 11}Be, for which calculations were performed in basis spaces up to 9{Dirac_h}{Omega} (dimensions reaching 7 x 10{sup 8}). We also present our latest results for the p-shell nuclei using the Tucson-Melbourne TM three-nucleon interaction with several proposed parameter sets.

  14. Hybrid silica-gold core-shell nanoparticles for fluorescence enhancement

    NASA Astrophysics Data System (ADS)

    Grzelak, J.; Krajewska, A.; Krajnik, B.; Jamiola, D.; Choma, J.; Jankiewicz, B.; Piątkowski, D.; Nyga, P.; Mackowski, S.

    2016-06-01

    We demonstrate that SiO2 nanoparticles coated with a gold island film (GIF) provide an efficient plasmonic platform for enhancing fluorescence intensity of chlorophyll-containing photosynthetic complexes. Fluorescence images obtained for single SiO2-Au coreshell nanoparticles mixed with photosynthetic complexes reveal very uniform emission patterns of a circular shape, similarly as observed for bare SiO2 nanoparticles. The fluorescence enhancement of chlorophyll emission for SiO2-Au nanostructures is up to four-fold compared to bare SiO2 nanoparticles and shortening of fluorescence decay indicates its plasmonic origin. For doublets or triplets of core-shell SiO2-Au nanoparticles, the intensity of emission is further increased as a result of hot-spot formation at the interfaces of such assemblies.

  15. The synthesis and modification of CdTe/CdS core shell quantum dots.

    PubMed

    Chen, Jianqiu; Xiao, An; Zhang, Zhengwei; Yu, Yan; Yan, Zhengyu

    2015-12-01

    A simple and economical synthesis method of CdTe quantum dots (QDs) has been developed using glutathione as a modifier in an aqueous system. The fluorescent properties of as-prepared CdTe QDs at different reaction times were studied to optimize the synthesis conditions. CdTe/CdS QDs with core-shell structure was obtained by modifying as-synthesized CdTe QDs with refluxing and microwave method, respectively. The properties of the CdTe/CdS QDs were thoroughly investigated by photoluminescence (PL) and inverted fluorescence microscope, and exhibited high fluorescence intensity and good optical property. The study also shows that the microwave synthesis of CdTe/CdS QDs had more dispersed particle size and higher fluorescence intensity. PMID:26162337

  16. Spectral Tuning of Plasmon Resonance in a Core/Shell (Au)Ag Nanocomposite

    NASA Astrophysics Data System (ADS)

    Panarin, A. Yu.; Abakshonok, A. V.; Agabekov, V. E.; Eryomin, A. N.; Terekhov, S. N.

    2015-01-01

    A bimetallic (Au)Ag nanocomposite with a core/shell structure was synthesized in aqueous solution and a H2O/EtOH mixture (1:1) containing polymers (carboxymethylcellulose, sodium polystyrenesulfonate, polyvinylpyrrolidone, dextran). Its structure and optical properties were characterized. The shape and position of scattering bands of colloidal noble-metal nanoparticles with optical density <0.1 were undistorted by solvent absorption. Scattering spectra had to be corrected for solutions of greater optical density. A method for correcting the resonant lightscattering spectra of Au and (Au)Ag nanoparticles was proposed for a single-beam apparatus. The possibility of surface plasmon resonance tuning for (Au)Ag with a short-wavelength shift of ~150 nm for the absorption band maximum and of ~84 nm for the resonant scattering band was demonstrated by varying the AgNO3 concentration during formation of the silver shell on the gold core.

  17. Robust Pb2+ sensor based on flexible ZnO/ZnS core-shell nanoarrays

    NASA Astrophysics Data System (ADS)

    Zhao, Zhenfu; Jiang, Chunyan; Pu, Xiong; Du, Chunhua; Li, Linxuan; Ma, Bei; Hu, Weiguo

    2016-04-01

    We designed a flexible robust sensor with ZnO/ZnS core-shell nanoarrays to detect Pb2+ ions. This device is powered by electrical energy transferred from the environmental mechanical energy and senses Pb2+ ions with the cation exchange reaction between ZnS shell and Pb2+ ions (ZnS (s) + Pb2+ (aq) ↔ PbS (s) + Zn2+(aq)). The high density intrinsic carriers in PbS diffuse into the ZnO core to partly screen the piezopotential, which results in an exponential relationship between the concentrations of Pb2+ ions and the piezo-voltages. The detected limit is as low as 1 ppm. This sensor also exhibits a very high selectivity towards Pb2+ ions due to the limitation of energy band and solubility, which has potential applications in environmental protection and pollutant surveillance.

  18. Preparation TiO2 core-shell nanospheres and application as efficiency drug detection sensor

    PubMed Central

    2014-01-01

    In this paper, we report the facile preparation of monodisperse titanium dioxide-diltiazem/tetrachlorobismuth core-shell nanospheres (TiO2@DTMBi), in which, diltiazem (DTM)/tetrachlorobismuth (BiCl4) complexes were employed as electroactive materials. The morphology, size, formation, and structure of the obtained TiO2@DTMBi spheres were investigated by transmission electron microscopy, scanning electron microscopy, dynamic light scattering, Fourier transform infrared spectroscopy, and X-ray diffraction. The optimal condition of obtained monodisperse 40-nm TiO2@DTMBi spheres was researched. The results of using TiO2@DTMBi nanospheres as proposed drug sensor indicate a wide linear range (10-7 to 10-1 M) and a very low detection limit of 0.20 μg/mL. PMID:25246870

  19. Hole mobility in Ge/Si core/shell nanowires: What could be the optimum?

    SciTech Connect

    Li, Jing; Niquet, Yann-Michel; Jomaa, Narjes; Said, Moncef; Delerue, Christophe

    2014-12-08

    Recent experimental works have shown that Ge/Si core/shell nanowires (NWs) are very attractive for nanoelectronics and for low-temperature quantum devices, thanks to the confinement of holes in the Ge core. Reported hole mobilities of the order of 200 cm{sup 2}/V/s are promising for high-performance field-effect transistors. However, we demonstrate that mobilities more than ten times higher, up to 8000 cm{sup 2}/V/s, could be reached in Ge/Si NWs. Atomistic calculations reveal the considerable influence of the strains induced by the Si shell on the hole transport, whatever the NW orientation. The enhancement of electron-phonon interactions by confinement, which usually degrades the mobility in NWs, is therefore outbalanced by the effect of strains.

  20. Open structure ZnO/CdSe core/shell nanoneedle arrays for solar cells

    PubMed Central

    2012-01-01

    Open structure ZnO/CdSe core/shell nanoneedle arrays were prepared on a conducting glass (SnO2:F) substrate by solution deposition and electrochemical techniques. A uniform CdSe shell layer with a grain size of approximately several tens of nanometers was formed on the surface of ZnO nanoneedle cores after annealing at 400°C for 1.5 h. Fabricated solar cells based on these nanostructures exhibited a high short-circuit current density of about 10.5 mA/cm2 and an overall power conversion efficiency of 1.07% with solar illumination of 100 mW/cm2. Incident photo-to-current conversion efficiencies higher than 75% were also obtained. PMID:22995031