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Sample records for cdse obtenidas por

  1. Ab Initio Study on Atomic Structures and Physical Properties of CdSe Quantum Nanodots

    DTIC Science & Technology

    2009-11-25

    CdSe quantum dots , with magic number (( CdSe )13, ( CdSe )19, ( CdSe )33 and ( CdSe )34 ). Effects of organic ligand binding on the stability of CdSe as well...calculations of optical absorption spectra for CdSe quantum dots , with magic number (( CdSe )13, ( CdSe )19, ( CdSe )33 and ( CdSe )34 ), have been calculated in...1 AOARD-08-4037 Title of Proposed Project: Ab initio study on atomic structures and physical

  2. Amphoteric CdSe nanocrystalline quantum dots.

    PubMed

    Islam, Mohammad A

    2008-06-25

    The nanocrystal quantum dot (NQD) charge states strongly influence their electrical transport properties in photovoltaic and electroluminescent devices, optical gains in NQD lasers, and the stability of the dots in thin films. We report a unique electrostatic nature of CdSe NQDs, studied by electrophoretic methods. When we submerged a pair of metal electrodes, in a parallel plate capacitor configuration, into a dilute solution of CdSe NQDs in hexane, and applied a DC voltage across the pair, thin films of CdSe NQDs were deposited on both the positive and the negative electrodes. Extensive characterizations including scanning electron microscopy (SEM), atomic force microscopy (AFM), Fourier transform infrared (FTIR) and Raman studies revealed that the films on both the positive and the negative electrodes were identical in every respect, clearly indicating that: (1) a fraction (<1%) of the CdSe NQDs in free form in hexane solution are charged and, more importantly, (2) there are equal numbers of positive and negative CdSe NQDs in the hexane solution. Experiments also show that the number of deposited dots is at least an order of magnitude higher than the number of initially charged dots, indicating regeneration. We used simple thermodynamics to explain such amphoteric nature and the charging/regeneration of the CdSe NQDs.

  3. Shell deposition of CdSe nano dots and rods

    NASA Astrophysics Data System (ADS)

    Yang, Ping; Chen, Hsueh Shin; Zhang, Qiang; Shi, Ruixia; Wang, Junpeng; Che, Quande

    2014-08-01

    To investigate the shell deposited kinetics, CdSe quantum dots (QDs) and nanorods (NRs) with a maximum length of 17 nm were fabricated via organic synthesis routes. CdSe with a hexagonal crystal structure (wurtzite) favors epitaxial growth on the {002} surfaces when well-controlled conditions were used. The morphologies and sizes of CdSe samples depended strongly on chemicals and temperature. In the case of 320 °C, CdSe NRs with adjusted length of 7-17 nm were obtained from trioctylphosphine oxide (TOPO) and tetradecylphosphonic acid (TDPA). In contrast, short CdSe NRs (less than 10 nm) were created from octadecylphosphonic acid (ODPA) and trioctylamine (TOA). Spherical CdSe QDs were further fabricated using stearic acid (SA) and TOPO at 300 °C. CdSe cores were coated with Cd0.5Zn0.5S and CdTe shells. Anisotropic growth occurred during shell deposition because CdS shells grown preferentially on the {001} facet of the CdSe core. In the case of CdSe core prepared from TOPO and TDPA, CdSe/Cd0.5Zn0.5S core/shell samples prepared from long CdSe NRs (more than 10 nm) revealed a peanut morphology while the core/shell samples created from short ones (less than 10 nm) exhibited a spherical morphology. All of the CdSe/Cd0.5Zn0.5S core/shell samples revealed a similar length to that of the CdSe cores. This phenomenon was also observed for the core/shell samples fabricated using CdSe NRs prepared by ODPA and TOA. This is ascribed to the well-developed crystal structure of CdSe NRs fabricated using an organic synthesis at high temperature. In contrast, this anisotropic growth did not occur when spherical CdSe QDs prepared from SA and TOPO and the shell (Cd0.5Zn0.5S) coating carried out using SA and TOA. To indicate the shell depositing process, CdSe NRs fabricated using TDPA and TOPO were coated with a CdTe shell. CdTe monomers were deposited on the middle and tip parts of the CdSe NRs to form a tetrapod-like morphology at 220 °C. This is ascribed to the large difference of

  4. Anisotropy in CdSe quantum rods

    SciTech Connect

    Li, Liang-shi

    2003-01-01

    The size-dependent optical and electronic properties of semiconductor nanocrystals have drawn much attention in the past decade, and have been very well understood for spherical ones. The advent of the synthetic methods to make rod-like CdSe nanocrystals with wurtzite structure has offered us a new opportunity to study their properties as functions of their shape. This dissertation includes three main parts: synthesis of CdSe nanorods with tightly controlled widths and lengths, their optical and dielectric properties, and their large-scale assembly, all of which are either directly or indirectly caused by the uniaxial crystallographic structure of wurtzite CdSe. The hexagonal wurtzite structure is believed to be the primary reason for the growth of CdSe nanorods. It represents itself in the kinetic stabilization of the rod-like particles over the spherical ones in the presence of phosphonic acids. By varying the composition of the surfactant mixture used for synthesis we have achieved tight control of the widths and lengths of the nanorods. The synthesis of monodisperse CdSe nanorods enables us to systematically study their size-dependent properties. For example, room temperature single particle fluorescence spectroscopy has shown that nanorods emit linearly polarized photoluminescence. Theoretical calculations have shown that it is due to the crossing between the two highest occupied electronic levels with increasing aspect ratio. We also measured the permanent electric dipole moment of the nanorods with transient electric birefringence technique. Experimental results on nanorods with different sizes show that the dipole moment is linear to the particle volume, indicating that it originates from the non-centrosymmetric hexagonal lattice. The elongation of the nanocrystals also results in the anisotropic inter-particle interaction. One of the consequences is the formation of liquid crystalline phases when the nanorods are dispersed in solvent to a high enough

  5. Phonons in bulk CdSe and CdSe nanowires.

    PubMed

    Mohr, Marcel; Thomsen, Christian

    2009-03-18

    We present first-principles calculations for bulk CdSe and CdSe nanowires with diameters of up to 22 A. Their electronic and structural properties are presented and discussed. The vibrational properties of bulk CdSe and the zone-center vibrations of the nanowires are calculated and analyzed. An iterative, symmetry-based relaxation method is used that yields improved results for phonon frequencies. We find that the band gap varies with the surface termination and that strongly size-dependent and nearly constant vibrational modes exist in the nanowires, depending on the displacement directions. A strong shift in frequency for specific modes is found, stemming from surface contributions to the polarization, similar to that reported for thin slabs. A comparison with experimental data from Raman measurements is given.

  6. Biomolecular recognition in DNA tagged CdSe nanowires.

    PubMed

    Sarangi, S N; Goswami, K; Sahu, S N

    2007-06-15

    DNA template driven CdSe nanobeads (NBs) and nanowires (NWs) have been synthesized by an electrodeposition technique. The synthesis protocol has yielded randomly oriented cubic CdSe NBs with mean size approximately 3.0 nm in presence of single stranded DNA, poly G(30). Monocrystalline cubic CdSe NWs of width approximately 4.0 nm with string-like morphology have been achieved when synthesized in presence of both poly G(30) and its conjugate, poly C(30). Optical absorption of CdSe NBs show a blue shift of 0.8 eV and long wavelength tailing where as NWs show steep increase of absorption in shorter wavelength regime accompanied by a further blue shift. DNA tags to the NBs or NWs have been confirmed from Fourier transform infrared spectroscopy measurements. Biomolecular recognition with CdSe NWs have been established by photoluminescence measurements.

  7. Medición de placas astrométricas obtenidas con el telescopio Astrográfico de La Plata

    NASA Astrophysics Data System (ADS)

    di Sisto, R. P.; Orellana, R.

    El Observatorio de La Plata cuenta con un gran número de placas de asteroides y cometas obtenidas con el telescopio astrográfico, que cubren gran parte del cielo del hemisferio sur. En 1996 se recopilaron y clasificaron 2187 placas (Beca para estudiantes de la AAA 1996) de las cuales 2031 corresponden a asteroides. Los datos de cada placa se volcaron en una base de datos creada para facilitar su manejo y preservar la información. A partir de este trabajo se revisaron los MPC electrónicos y se identificaron aquellas placas de asteroides pertenecientes a nuestra base de datos cuyos resultados no fueron publicados en los mismos. De un total de 400 placas que no aparecían publicadas sobresalía un paquete constituído por 40 placas obtenidas en 1977. Estas últimas fueron reducidas utilizando las posiciones y movimientos propios de las estrellas de referencia obtenidas del catálogo SAO 2000 dadas para el sistema FK5. Las posiciones calculadas fueron enviadas y publicadas en los Minor Planet Circulars (MPC).

  8. Novel mechanical behaviors of wurtzite CdSe nanowires

    NASA Astrophysics Data System (ADS)

    Fu, Bing; Chen, Li; Xie, Yiqun; Feng, Jie; Ye, Xiang

    2015-09-01

    As an important semiconducting nanomaterial, CdSe nanowires have attracted much attention. Although many studies have been conducted in the electronic and optical properties of CdSe NWs, the mechanical properties of Wurtzite (WZ) CdSe nanowires remain unclear. Using molecular dynamics simulations, we have studied the tensile mechanical properties and behaviors of [0001]-oriented Wurtzite CdSe nanowires. By monitoring the stretching processes of CdSe nanowires, three distinct structures are found: the WZ wire, a body-centered tetragonal structure with four-atom rings (denoted as BCT-4), and a structure that consists of ten-atom rings with two four-atom rings (denoted as TAR-4) which is observed for the first time. Not only the elastic tensile characteristics are highly reversible under unloading, but a reverse transition between TAR-4 and BCT-4 is also observed. The stretching processes also have a strong dependence on temperature. A tubular structure similar to carbon nanotubes is observed at 150 K, a single-atom chain is formed at 300, 350 and 450 K, and a double-atom chain is found at 600 K. Our findings on tensile mechanical properties of WZ CdSe nanowires does not only provide inspiration to future study on other properties of CdSe nanomaterials but also help design and build efficient nanoscale devices.

  9. Reversible ultrafast melting in bulk CdSe

    SciTech Connect

    Wu, Wenzhi; He, Feng; Wang, Yaguo

    2016-02-07

    In this work, transient reflectivity changes in bulk CdSe have been measured with two-color femtosecond pump-probe spectroscopy under a wide range of pump fluences. Three regions of reflectivity change with pump fluences have been consistently revealed for excited carrier density, coherent phonon amplitude, and lattice temperature. For laser fluences from 13 to 19.3 mJ/cm{sup 2}, ultrafast melting happens in first several picoseconds. This melting process is purely thermal and reversible. A complete phase transformation in bulk CdSe may be reached when the absorbed laser energy is localized long enough, as observed in nanocrystalline CdSe.

  10. Synthesis and characterization of Cr doped CdSe nanoparticles

    NASA Astrophysics Data System (ADS)

    Majid, Abdul; Arshad, Humaira; Murtaza, Shahzad

    2015-09-01

    Chromium doped cadmium selenide (CdSe) nanoparticles were prepared via Chemical Co-precipitation Method. The effects of doping and doping concentration on structural and optical properties of the materials were studied. The structural characterization of samples carried out by using X-ray diffraction (XRD) indicated the formation of CdSe nanoparticles of zinc blend (cubic) polytype. It was also noted that lattice parameter decreases with increase in doping concentration. Fourier Transform Infrared Spectroscopy (FTIR) analysis of the samples shows the presence of several modes of vibration related to CdSe nanoparticles and the dopant.

  11. Magnetic study of Fe-doped CdSe nanomaterials

    NASA Astrophysics Data System (ADS)

    Das, Sayantani; Banerjee, Sourish; Sinha, T. P.

    2016-05-01

    Nanoparticles of pure and iron (50 %) doped cadmium selenide (CdSe) have been synthesized by soft chemical route. EDAX analysis supports the inclusion of Fe into CdSe nanoparticles. The average particle size of pure and doped CdSe is found to be ˜50 nm from scanning electron microscopy (SEM). Magnetization of the samples are measured under the field cooled (FC) and zero field cooled (ZFC) modes in the temperature range from 5K to 300K applying a magnetic field of 500Oe. Field dependent magnetization (M-H) measurement indicates presence of room temperature (RT) paramagnetism and low temperature (5K) ferromagnetism of the sample.

  12. Photoelectric processes in CdSe thin film solar cells

    SciTech Connect

    Rickus, E.

    1984-05-01

    Efficiencies exceeding 7 percent have been achieved with CdSe/ZnSe/Au thin film solar cells. The collection efficiency of carriers in highly oriented CdSe films is near unity, resulting in short circuit current densities comparable to values observed on single crystalline cells. Recombination of carriers at the CdSe/ZnSe interface plays a minor role. CdSe /SUB x/ Te /SUB 1-x/ cells show the potential of enhanced short circuit current densities. Crystallographic and chemical inhomogeneities have a major influence on their performance. The comparison of photoelectrochemical cells based on CdSe single crystals and on polycrystalline layers demonstrates the photovoltaic quality of our CdSe films.

  13. Dielectric relaxation of CdSe nanoparticles

    NASA Astrophysics Data System (ADS)

    Das, Sayantani; Dutta, Alo; Ghosh, Binita; Banerjee, Sourish; Sinha, T. P.

    2014-11-01

    Nanoparticles of cadmium selenide (CdSe) have been synthesized by soft chemical route using mercaptoethanol as a capping agent. X-ray diffraction and transmission electron microscope measurements show that the prepared sample belongs to sphalerite structure with the average particle size of 25 nm. The band gap of the material is found to be 2.1 eV. The photoluminescence (PL) emission spectra of the sample are measured at various excitation wavelengths. The PL spectra appear in the visible region, and the emission feature depends on the wavelength of the excitation. Impedance spectroscopy is applied to investigate the dielectric relaxation of the sample in a temperature range from 323 to 473 K and in a frequency range from 42 Hz to 1.1 MHz. The complex impedance plane plot has been analyzed by an equivalent circuit consisting of two serially connected R-CPE units, each containing a resistance (R) and a constant phase element (CPE). The dielectric relaxation of the sample is investigated in the electric modulus formalism. The temperature dependent relaxation times obey the Arrhenius law. The Havriliak-Negami model is used to investigate the dielectric relaxation mechanism in the sample. The frequency dependent conductivity spectra are found to obey the power law.

  14. Optics of colloidal quantum-confined CdSe nanoscrolls

    SciTech Connect

    Vasiliev, R B; Sokolikova, M S; Vitukhnovskii, A G; Ambrozevich, S A; Selyukov, A S; Lebedev, V S

    2015-09-30

    Nanostructures in the form of 1.2-nm-thick colloidal CdSe nanoplatelets rolled into scrolls are investigated. The morphology of these scrolls is analysed and their basic geometric parameters are determined (diameter 29 nm, longitudinal size 100 – 150 nm) by TEM microscopy. Absorption and photoluminescence spectra of these objects are recorded, and the luminescence decay kinetics is studied. It is shown that the optical properties of CdSe nanoscrolls differ significantly from the properties of CdSe quantum dots and that these nanoscrolls are attractive for nanophotonic devices due to large oscillator strengths of the transition, small widths of excitonic peaks and short luminescence decay times. Nanoscrolls can be used to design hybrid organic–inorganic pure-color LEDs with a high luminescence quantum yield and low operating voltages. (optics and technology of nanostructures)

  15. Electrodeposition and characterization of CdSe semiconducting nanowires.

    PubMed

    Yu-Zhang, K; Guo, D Z; Mallet, J; Molinari, M; Loualiche, A; Troyon, M

    2008-04-01

    In this paper, we present our work on the electrodeposited CdSe semiconducting nanowires. Using a low cost and low temperature approach by electrochemistry, CdSe nanowires were successfully grown using polycarbonate template. Depending on the host pore dimension of the substrate, wire diameter can be varied from 400 nm down to 30 nm and wire length from a few microns to tens microns. The as-deposited nanowires exhibit predominantly metastable zinc blende (ZB) structure but after the heat treatment they become wurtzite (W) structure. A combination of different characterization techniques, such as X-ray diffraction, SEM, TEM-HRTEM and EDXS, was used to investigate the growth morphology, crystalline structure and defects in the nanowires. The luminescent properties of CdSe nanowires have also been studied by means of photoluminescence.

  16. Piezo-phototronic effect of CdSe nanowires.

    PubMed

    Dong, Lin; Niu, Simiao; Pan, Caofeng; Yu, Ruomeng; Zhang, Yan; Wang, Zhong Lin

    2012-10-23

    The piezo-phototronic effect on transport properties of flexible CdSe NW devices is investigated. An optimum sensitivity of the flexible CdSe NW devices can be achieved by adjusting the applied strain and illumination intensity. The piezo-phototronic effect under compressive strain increases the internal electric field of the Schottky barrier, and assists the separation of the photo-excited electron-hole pairs, resulting in the increase of photocurrent. A trap-mediated mechanism is responsible for the decreased hole separation when the strain is larger than the critical strain.

  17. Scanning tunneling luminescence of individual CdSe nanowires.

    PubMed

    Lutz, Theresa; Kabakchiev, Alexander; Dufaux, Thomas; Wolpert, Christian; Wang, Zhe; Burghard, Marko; Kuhnke, Klaus; Kern, Klaus

    2011-08-22

    The local luminescence properties of individual CdSe nanowires composed of segments of zinc blende and wurtzite crystal structures are investigated by low-temperature scanning tunneling luminescence spectroscopy. Light emission from the wires is achieved by the direct injection of holes and electrons, without the need for coupling to tip-induced plasmons in the underlying metal substrate. The photon energy is found to increase with decreasing wire diameter due to exciton confinement. The bulk bandgap extrapolated from the energy versus diameter dependence is consistent with photon emission from the zinc blende-type CdSe sections.

  18. Laser cooling of CdSe quantum dots

    NASA Astrophysics Data System (ADS)

    Nemova, Galina; Kashyap, Raman

    2014-05-01

    We present a theoretical scheme for laser cooling of the colloidal cadmium selenide (CbSe) QDs. The laser cooling process is based on the anti-Stokes fluorescence observed in QDs. We have considered laser cooling in the system of identical CdSe QDs laser pumped with energy of photons less than mean fluorescence energy. The dependences of all parameters of the system on the temperature have been taken into account. Following to our simulation the laser cooling with temperature drop ~100K can be realised with well technologically developed today passivated CdSe QDs.

  19. VLS synthesis of disordered CdSe nanowires and optical properties of an individual CdSe nanowire

    NASA Astrophysics Data System (ADS)

    Xiao, Bin-bin; Xu, Yue-bing

    2011-12-01

    Disordered CdSe nanowires have been successfully grown on silicon substrates by Au-catalyzed vapor-liquid-solid (VLS) mechanism. Scanning electron microscopy (SEM) reveals that the as-prepared products consist of a large quantity of 1D nanowire disordered predominantly perpendicular to the surface of the substrate. A plausible formation mechanism of disordered CdSe nanowires is proposed here. X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM) confirm on their hexagonal wurtzite crystallite structure. An intense red near-band edge emission (702 nm) is observed based on room temperature photoluminescence measurements of individual nanowire. This kind of CdSe nanostructures may be used in optoelectronics devices in the near future.

  20. Current Oscillations in Doped Thin Films of CdSe.

    DTIC Science & Technology

    The previously unreported phenomenon of current oscillations in doped thin films of cadmium selenide was explored. It was concluded that, with...appropriate processing, devices made with thin films of CdSe will exhibit current oscillations when high electric fields and illumination are applied, and that these oscillations have frequencies of 5 to 8000 Hz. (Author)

  1. van der Waals epitaxy and photoresponse of two-dimensional CdSe plates

    NASA Astrophysics Data System (ADS)

    Zhu, Dan-Dan; Xia, Jing; Wang, Lei; Li, Xuan-Ze; Tian, Li-Feng; Meng, Xiang-Min

    2016-06-01

    Here we demonstrate the first growth of two-dimensional (2D) single-crystalline CdSe plates on mica substrates via van der Waals epitaxy. The as-synthesized 2D plates exhibit hexagonal, truncated triangular and triangular shapes with the lateral size around several microns. Photodetectors based on 2D CdSe plates present a fast response time of 24 ms, revealing that 2D CdSe is a promising building block for ultrathin optoelectronic devices.

  2. Compressive and Tensile Stress in CdSe Semiconductor Quantum Dots

    SciTech Connect

    Meulenberg, R W; Jennings, T; Strouse, G F

    2004-06-02

    Compressive and tensile stress in colloidal CdSe quantum dots (QDs) is examined using resonance Raman spectroscopy. We find that the dispersion of the longitudinal optical phonon mode with size does not follow theoretical calculations based on phonon confinement models. To account for these deviations, the presence of compressive or tensile stress in the QDs was proposed. We find that CdSe QDs prepared via a single source precursor (SSP) method exhibit compressive stress, while CdSe QDs prepared via high temperature lyothermal methods exhibit tensile stress. Evidence is provided that the SSP CdSe QDs stress is directly related to a surface effect.

  3. Direct Patterning of CdSe Quantum Dots into Sub-100 nm Structures

    SciTech Connect

    Hampton, Meredith J.; Templeton, Joseph L.; DeSimone, Joseph M.

    2010-03-02

    Ordered, two-dimensional cadmium selenide (CdSe) arrays have been fabricated on indium-doped tin oxide (ITO) electrodes using the pattern replication in nonwetting templates (PRINT) process. CdSe quantum dots (QDs) with an average diameter of 2.7 nm and a pyridine surface ligand were used for patterning. The PRINT technique utilizes a perfluoropolyether (PFPE) elastomeric mold that is tolerant of most organic solvents, thus allowing solutions of CdSe QDs in 4-picoline to be used for patterning without significant deformation of the mold. Nanometer-scale diffraction gratings have been successfully replicated with CdSe QDs.

  4. Electron-Phonon Coupling in a CdSe Nanowire

    NASA Astrophysics Data System (ADS)

    Barrett, Christopher; Wang, Lin-Wang

    2012-02-01

    It is important to calculate the coupling between phonons and electrons in realistic nanostructures, e.g. to understand carrier cooling and dynamics in a nanowire. In this talk, we will present results of phonon spectrum calculations using a customized valence force field (VFF) method. This customized VFF method is developed to be fittable to the results of any ab-initio calculations, with density functional theory (DFT) results being used in this work. By fitting many different DFT calculations on different motifs and their perturbations, we have obtained in the custom VFF a very efficient method that closely reproduces DFT phonons for CdSe nanowires with (10-10) surfaces having Cd-Se dimerization. We have also combined the results of these phonon spectrum calculations with electronic structure calculations to obtain the electron-phonon coupling. We will present this result and and show how the electron-phonon coupling affects the carrier dynamics in the nanowire.

  5. Phonon spectrum in a CdSe nanowire

    NASA Astrophysics Data System (ADS)

    Barrett, Chris; Wang, Lin-Wang

    2011-03-01

    It is important to calculate the phonon spectrum of realistic nanowires, e.g. to understand its thermo conductivity or to calculate the electron-phonon interaction. In this talk, we will present results of phonon spectrum calculation using valence force field (VFF) method. An important issue is to construct the VFF to describe the surface atomic displacement. We have developed a general VFF formalism to fit our VFF result with the density functional theory (DFT) calculated surface atom displacement energies. In particular, the (10-10) CdSe surface is modelled with Cd-Se dimerization. We will discuss the quality of such VFF model. The phonon spectrum of the nanowire will be presented, and its implication on the phonon transport and electron-phonon coupling will also be discussed. This work is supported by U.S. Department of Energy BES, office of science, under Contract No. DE-AC02-05CH11231.

  6. Deposition of CdSe by EC-ALE

    NASA Astrophysics Data System (ADS)

    Mathe, Mkhulu K.; Cox, Stephen M.; Flowers, Billy H.; Vaidyanathan, R.; Pham, Long; Srisook, Nattapong; Happek, Uwe; Stickney, John L.

    2004-10-01

    The optimization of a program for CdSe thin film deposition using electrochemical atomic layer epitaxy (EC-ALE) is reported. EC-ALE uses surface limited reactions, underpotential deposition, to form compound thin film deposits one atomic layer at a time on Au substrates. Cyclic voltammograms showing deposition of Cd and Se on the Au substrate were first performed to identify cycle potentials. CdSe thin films were formed using an automated flow deposition system, by alternately depositing Se and Cd atomic layers, forming a compound monolayer each cycle. In total, 200 cycle deposits were formed using a series of different potentials, to better optimize the deposition conditions. Electron probe microanalysis of the deposits showed Cd/Se ratio between 1.01 and 1.13. X-ray diffraction indicated the deposits were zinc blende, with a (1 1 1) preferred orientation. The thickness of the deposits were determined using ellipsometry, and found to be around 70 nm. AFM studies of the morphology of substrates and deposits indicated that conformal films were formed. The band gaps of the deposits was determined using UV-VIS absorption measurements, photoconductivity and reflection adsorption FTIR, and all suggested a value of 1.74 eV, consistent with literature values.

  7. CdSe nanowires grown by using chemical bath deposition

    NASA Astrophysics Data System (ADS)

    Gubur, H. Metin; Septekin, F.; Alpdogan, S.

    2015-10-01

    The Cadmium-selenide (CdSe) nanowire thin films were prepared on glass substrates by using chemical bath deposition (CBD) at 70 °C. Cadmium sulfate and sodium selenosulphate were used as Cd2+ and Se2- ion sources, respectively. The CdSe nanowire film was annealed in an air atmosphere at 573 K for 1 hour. X-ray diffraction (XRD) results showed that the nanowire films as-deposited and annealed had mixed cubic and hexagonal phase. Scanning electron microscopy (SEM) indicated that the CdSe nanowires had lengths ranging from 642 nm to 2.5 μm and diameters ranging from 46 nm to 211 nm. The optical properties of the as-deposited and the annealed nanowire films, an investigated by recording the transmission spectra by using an UV-visible spectrophotometer revealed that the energy band gap decreased (from 1.78 eV to 1.50 eV) upon annealing. The conductivity measurements made by using four-probe methods for both the annealed and the as-deposited films showed that the resistivity, conductivity and activation energy changed upon annealing.

  8. Ligand Induced Circular Dichroism and Circularly Polarized Luminescence in CdSe Quantum Dots

    PubMed Central

    Tohgha, Urice; Deol, Kirandeep K.; Porter, Ashlin G.; Bartko, Samuel G.; Choi, Jung Kyu; Leonard, Brian M.; Varga, Krisztina; Kubelka, Jan; Muller, Gilles; Balaz, Milan

    2014-01-01

    Chiral thiol capping ligands L- and D-cysteines induced modular chiroptical properties in achiral cadmium selenide quantum dots (CdSe QDs). Cys-CdSe prepared from achiral oleic acid capped CdSe by post-synthetic ligand exchange displayed size-dependent electronic circular dichroism (CD) and circularly polarized luminescence (CPL). Opposite CPL signals were measured for the CdSe QDs capped with D- and L-cysteine. The CD profile and CD anisotropy varied with size of CdSe nanocrystals with largest anisotropy observed for CdSe nanoparticles of 4.4 nm. Magic angle spinning solid state NMR (MAS ssNMR) experiments suggested bidentate interaction between cysteine and the surface of CdSe. Density functional theory (DFT) calculations verified that attachment of L- and D-cysteine to the surface of model (CdSe)13 nanoclusters induces measurable opposite CD signals for the exitonic band of the nanocluster. The chirality was induced by the hybridization of highest occupied CdSe molecular orbitals with those of the chiral ligand. PMID:24200288

  9. Low-temperature synthesis of CdSe nanocrystal quantum dots.

    PubMed

    Siy, Jacqueline T; Brauser, Eric M; Bartl, Michael H

    2011-01-07

    A method for fabricating colloidal CdSe nanocrystals at low reaction temperatures was developed. The transition from CdSe clusters to continuously-growing nanocrystals was found to be crucial in the formation of high-quality quantum dots with narrow size distribution and efficient, tunable optical properties.

  10. CdSe quantum dot internalization by Bacillus subtilis and Escherichia coli

    NASA Technical Reports Server (NTRS)

    Kloepfer, Jeremiah A.; Mielke, Randall E.; Nadeau, Jay L.

    2004-01-01

    Biological labeling has been demonstrated with CdSe quantum dots in a variety of animal cells, but bacteria are harder to label because of their cell walls. We discuss the challenges of using minimally coated, bare CdSe quantum dots as luminescent internal labels for bacteria.

  11. Influence of Surfactants and Charges on CdSe Quantum Dots

    SciTech Connect

    Yang, Ping; Tretiak, Sergei; Ivanov, Sergei

    2011-07-11

    The chemistry between CdSe quantum dots and common surface capping ligands is invested using density functional theory. We will discuss the electronic structures and optical properties of CdSe QDs controlled by the size of particle, self-organization, capping ligands, and positive charges. Charges on quantum dots have profound effects on their structures, binding energies, and optical properties.

  12. A Safer, Easier, Faster Synthesis for CdSe Quantum Dot Nanocrystals

    ERIC Educational Resources Information Center

    Boatman, Elizabeth M.; Lisensky, George C.; Nordell, Karen J.

    2005-01-01

    The synthesis for CdSe quantum dot nanocrystals that vary in color and are a visually engaging way to demonstrate quantum effects in chemistry is presented. CdSe nanocrystals are synthesized from CdO and elemental Se using a kinetic growth method where particle size depends on reaction time.

  13. Single-crystal CdSe nanowires prepared via vapor-phase growth assisted with silicon.

    PubMed

    Wang, Z Y; Zhang, L D; Ye, C H; Fang, X S; Xiao, Z D; Kong, M G

    2005-12-01

    Hexagonal cadmium selenide (CdSe) nanowires, with diameter around 20 nm, were synthesized using a simple vapor-phase growth. Silicon (Si) powder acts as a source material assisting the synthesis, which is very important to the formation of the CdSe nanowires. We also suggest that self-catalysis at the Cd-terminated (0001) surface, together with the assistance action of Si, leads to the formation of wire-like structures to be formed. Meanwhile, the assistance of Si is responsible for the fineness and uniformity of the CdSe nanowires. The possible growth mechanism of the CdSe nanowires is proposed, and the optical property of the as-grown CdSe nanowires is characterized.

  14. CdSe nanocrystals: controlled growth and diameter-dependent photoluminescence

    NASA Astrophysics Data System (ADS)

    Zhang, Qiang; Yang, Ping; Chen, Hsueh Shin; Huang, Baibiao; Shen, Jianxing

    2014-02-01

    Phosphonic and carboxylic acids were used as capping agents to fabricate CdSe nanocrystals (NCs) through organic synthesis, leading to a controlled growth of the NCs with adjustable morphologies from dots to rods. The binding energies and steric hindrance of ligands dramatically affected the growth kinetics of CdSe NCs, and therefore the resulting geometry of NCs. The detailed investigations of ligand effect on the growth of NCs and an efficient control over the NCs morphology were presented. CdSe nanorods (NRs) with various aspect ratios were created for studying relation between the diameter of NRs and photoluminescence (PL). Consequently, a synergic use of PL spectra and transmission electron microscopy images allowed us to systematically investigate the relationship between morphology and PL properties of as-prepared CdSe rods. The PL properties of CdSe NRs were finally found to be strongly diameter dependent and weakly related to their lengths.

  15. Synthesis of highly luminescent mercaptosuccinic acid-coated CdSe nanocrystals under atmospheric conditions.

    PubMed

    Dong, Meiting; Xu, Jingyi; Liu, Shuxian; Zhou, Ying; Huang, Chaobiao

    2014-11-01

    Here we report a facile one-pot method for the preparation of high-quality CdSe nanocrystals (NCs) in aqueous solution under an air atmosphere. Compared with the traditional use of NaHSe or H2 Se, the more stable sodium selenite is utilized as the Se source for preparing highly luminescent CdSe nanocrystals. By using mercaptosuccinic acid (MSA) as the capping agent and borate-citrate acid as the buffering solution, CdSe nanocrystals with high quantum yield (up to 70%) have been synthesized conveniently. The influence of different experimental parameters, such as the pH of the precursor solution, the molar ratio of Cd(2+) to Na2 SeO3 and Cd(2+) to MSA on the CdSe nanocrystals, has been systematically investigated. The prepared CdSe NCs were spherical with a size of ~ 5 nm.

  16. Optical properties of CdSe nanowires -- Experiment and theory

    NASA Astrophysics Data System (ADS)

    Vietmeyer, Felix

    CdSe nanowires are one-dimensional semiconductor nanostructures with unique properties. The wires studied in this work possess diameters on the nanometer scale while diameters are on the order of tens of microns. For CdSe structures this has the consequence that size quantization effects are at play along the radial dimension while longitudinal dimensions are outside the confinement regime. Physical and electrical properties are therefore expected to be diameter dependent, but not very sensitive to variations in length. Another important aspect to consider is that the diameters studied span a range from small (i.e. d˜3-5 nm) where wires show discrete transitions akin to quantum dots all the way up to large (i.e. d˜25 nm). At the largest size studied, the material does not show size quantization effects and its properties are similar to bulk CdSe. One of the key questions I would like to answer is what characterizes the transition from a regime controlled by quantum effects (i.e. small diameter nanowires) to bulk-like semiconductors (i.e. large diameter wires). The tools used to carry out the characterization include a number of steady-state and time-resolved spectroscopic techniques that are used to probe semiconductor nanowires both on the ensemble and single nanowire level. For single wire level measurements, the tool of choice is optical microscopy. Using microscopy, individual nanowires can be identified and studied using various excitation and emission wavelengths to characterize their properties. Using emission and absorption spectroscopies, the electronic structure of the nanowire as well as how charges interact is revealed. It, in turn, allows identifying signatures that belong to photogenerated charges that exist as coulombically bound electron-hole pairs (excitons) and distinguish them from free charges.

  17. CdSe film surface property changes during growth

    SciTech Connect

    Smyntyna, V.A.; Gerasyutenko, V.A.; Korneeva, S.A.

    1988-04-01

    The morphology changes as a cadmium selenide film grows, as indicated by transmission and scanning electron microscopes, and the microcomposition also alters, so the conductivity as a function of thickness and of substrate temperature is examined to relate the surface electronic properties to the measured adsorption sensitivity. Cadmium self-doping occurring during CdSe film growth is followed by excess cadmium atoms accumulating on the surface, which form clusters and give rise to a nonmonotone dependence of the conductivity and adsorption sensitivity on thickness.

  18. Sulforaphane Protects the Liver against CdSe Quantum Dot-Induced Cytotoxicity

    PubMed Central

    Wang, Wei; He, Yan; Yu, Guodong; Li, Baolong; Sexton, Darren W.; Wileman, Thomas; Roberts, Alexandra A.; Hamilton, Chris J.; Liu, Ruoxi; Chao, Yimin; Shan, Yujuan; Bao, Yongping

    2015-01-01

    The potential cytotoxicity of cadmium selenide (CdSe) quantum dots (QDs) presents a barrier to their use in biomedical imaging or as diagnostic and therapeutic agents. Sulforaphane (SFN) is a chemoprotective compound derived from cruciferous vegetables which can up-regulate antioxidant enzymes and induce apoptosis and autophagy. This study reports the effects of SFN on CdSe QD-induced cytotoxicity in immortalised human hepatocytes and in the livers of mice. CdSe QDs induced dose-dependent cell death in hepatocytes with an IC50 = 20.4 μM. Pre-treatment with SFN (5 μM) increased cell viability in response to CdSe QDs (20 μM) from 49.5 to 89.3%. SFN induced a pro-oxidant effect characterized by depletion of intracellular reduced glutathione during short term exposure (3–6 h), followed by up-regulation of antioxidant enzymes and glutathione levels at 24 h. SFN also caused Nrf2 translocation into the nucleus, up-regulation of antioxidant enzymes and autophagy. siRNA knockdown of Nrf2 suggests that the Nrf2 pathway plays a role in the protection against CdSe QD-induced cell death. Wortmannin inhibition of SFN-induced autophagy significantly suppressed the protective effect of SFN on CdSe QD-induced cell death. Moreover, the role of autophagy in SFN protection against CdSe QD-induced cell death was confirmed using mouse embryonic fibroblasts lacking ATG5. CdSe QDs caused significant liver damage in mice, and this was decreased by SFN treatment. In conclusion, SFN attenuated the cytotoxicity of CdSe QDs in both human hepatocytes and in the mouse liver, and this protection was associated with the induction of Nrf2 pathway and autophagy. PMID:26402917

  19. Sulforaphane Protects the Liver against CdSe Quantum Dot-Induced Cytotoxicity.

    PubMed

    Wang, Wei; He, Yan; Yu, Guodong; Li, Baolong; Sexton, Darren W; Wileman, Thomas; Roberts, Alexandra A; Hamilton, Chris J; Liu, Ruoxi; Chao, Yimin; Shan, Yujuan; Bao, Yongping

    2015-01-01

    The potential cytotoxicity of cadmium selenide (CdSe) quantum dots (QDs) presents a barrier to their use in biomedical imaging or as diagnostic and therapeutic agents. Sulforaphane (SFN) is a chemoprotective compound derived from cruciferous vegetables which can up-regulate antioxidant enzymes and induce apoptosis and autophagy. This study reports the effects of SFN on CdSe QD-induced cytotoxicity in immortalised human hepatocytes and in the livers of mice. CdSe QDs induced dose-dependent cell death in hepatocytes with an IC50 = 20.4 μM. Pre-treatment with SFN (5 μM) increased cell viability in response to CdSe QDs (20 μM) from 49.5 to 89.3%. SFN induced a pro-oxidant effect characterized by depletion of intracellular reduced glutathione during short term exposure (3-6 h), followed by up-regulation of antioxidant enzymes and glutathione levels at 24 h. SFN also caused Nrf2 translocation into the nucleus, up-regulation of antioxidant enzymes and autophagy. siRNA knockdown of Nrf2 suggests that the Nrf2 pathway plays a role in the protection against CdSe QD-induced cell death. Wortmannin inhibition of SFN-induced autophagy significantly suppressed the protective effect of SFN on CdSe QD-induced cell death. Moreover, the role of autophagy in SFN protection against CdSe QD-induced cell death was confirmed using mouse embryonic fibroblasts lacking ATG5. CdSe QDs caused significant liver damage in mice, and this was decreased by SFN treatment. In conclusion, SFN attenuated the cytotoxicity of CdSe QDs in both human hepatocytes and in the mouse liver, and this protection was associated with the induction of Nrf2 pathway and autophagy.

  20. Synthesis and applications of CdSe nanoparticles

    NASA Astrophysics Data System (ADS)

    Rao, M. C.; Ravindranadh, K.; Shekhawat, M. S.

    2013-06-01

    Polymer nanoparticle composite materials have attracted the interest of a number of researchers, due to their synergistic and hybrid properties derived from several components. Whether in solution or in bulk, these materials offer unique mechanical, electrical, optical and thermal properties. CdSe nanoparticles have been prepared at room temperature. Cadmium chloride 99 mM of 4 mL is added to 2.2g Poly vinyl alcohol. The volume of solution is made up to 50 mL by bi-distilled water and the solution is left for 24 hours at room temperature to swell. After that the solution is warmed up to 60°C and stirred for 4 hours until viscous transparent solution is obtained. One milliliter of Sodium Hydrogen Selenide is dropped into the solution with gentle stirring. Solution is casted on flat glass plate dishes. After the solvent evaporation, a thin film containing CdSe nanoparticles are obtained. The film is washed with de-ionized water to remove other soluble salts before measurements.

  1. Spontaneous emission enhancement of colloidal CdSe nanoplatelets

    NASA Astrophysics Data System (ADS)

    Yang, Zhili; Pelton, Matthew; Waks, Edo

    Colloidal CdS /CdSe/CdS nanoplatelets synthesized recently are high efficient nano-emitters and gain media for nanoscale lasers and other nonlinear optical devices. They are characterized as quantum well structure due to energy gap difference between core CdSe and shell CdS, of which the luminescent wavelength could be tuned precisely by their thickness of growth. However, the influence of environment on the material's optical properties and further enhancement of the emission to implement nanoscale systems remains to be investigated. Here we demonstrate spontaneous emission rate enhancement of these CdSe nanoplatelets coupled to a photonic crystal cavity. We show clearly the photoluminescent spectrum modification of the nanoplatelets emission and an averaged Purcell enhancement factor of 3.1 is achieved when they are coupled to carefully-designed nanobeam photonic crystal cavities compared to the ones on unpatterned surface in our experiment of lifetime measurement. Also the phenomenon of cavity quality factor increasing is observed when increasing intensity of pumping, which attributes to saturable absorption of the nanoplatelets. Our success in enhancement of emission from these nanoplatelets here paves the road to realize actual nanoscale integrated systems such as ultra-low threshold micro-cavity lasers.

  2. CdSe quantum dots synthesized by laser ablation in water and their photovoltaic applications

    NASA Astrophysics Data System (ADS)

    Horoz, Sabit; Lu, Liyou; Dai, Qilin; Chen, Jiajun; Yakami, Baichhabi; Pikal, J. M.; Wang, Wenyong; Tang, Jinke

    2012-11-01

    CdSe quantum dots (QDs) have been prepared by a facile and clean synthesis method--laser ablation in water. The structural and luminescent properties of the CdSe QDs have been investigated. The CdSe QDs of wurtzite crystal structure have an average particle size of about 5 nm. The QDs can be attached to ZnO nanowires making them ideal for applications in QD-sensitized nanowire solar cells. A uniqueness of the QDs attached to the ZnO nanowires by this laser ablation method is that they do not contain ligands, and the preparation avoids the complicated process of ligand exchange.

  3. Experimental Observation of Quantum Confinement in the Conduction Band of CdSe Quantum Dots

    SciTech Connect

    Lee, J I; Meulenberg, R W; Hanif, K M; Mattoussi, H; Klepeis, J E; Terminello, L J; van Buuren, T

    2006-12-15

    Recent theoretical descriptions as to the magnitude of effect that quantum confinement has on he conduction band (CB) of CdSe quantum dots (QD) have been conflicting. In this manuscript, we experimentally identify quantum confinement effects in the CB of CdSe QDs for the first time. Using X-ray absorption spectroscopy, we have unambiguously witnessed the CB minimum shift to higher energy with decreasing particle size and have been able to compare these results to recent theories. Our experiments have been able to identify which theories correctly describe the CB states in CdSe QDs. In particular, our experiments suggest that multiple theories describe the shifts in the CB of CdSe QDs and are not mutually exclusive.

  4. Optical absorption, induced bleaching, and photoluminescence of CdSe nanoplatelets grown in cadmium octanoate matrix.

    PubMed

    Lyashchova, Alina; Dmytruk, Andriy; Dmitruk, Igor; Klimusheva, Gertruda; Mirnaya, Tetyana; Asaula, Vitaliy

    2014-02-20

    CdSe nanoparticles (NPs) are chemically synthesized in thermotropic ionic liquid crystalline (LC) phase of cadmium octanoate that was used as a nanoreactor. The nanocomposite samples are obtained by the rapid cooling of the LC phase to room temperature. Observed doublet structure in absorption spectra of the nanocomposites is characteristic for the two-dimensional CdSe nanoplatelets (NPLs). The thicknesses of the CdSe NPLs are 1.6, 1.9 and 2.3 nm as determined from the absorption spectra, and correspond to 4, 5 and 6 CdSe monolayers, respectively. Induced simultaneous bleaching of the doublet components observed under femtosecond laser excitation, as well as photoluminescence spectra and their kinetics are found compatible with the model of excitons with heavy- and light-hole valence bands confined in nanoplatelets.

  5. Optical absorption, induced bleaching, and photoluminescence of CdSe nanoplatelets grown in cadmium octanoate matrix

    NASA Astrophysics Data System (ADS)

    Lyashchova, Alina; Dmytruk, Andriy; Dmitruk, Igor; Klimusheva, Gertruda; Mirnaya, Tetyana; Asaula, Vitaliy

    2014-02-01

    CdSe nanoparticles (NPs) are chemically synthesized in thermotropic ionic liquid crystalline (LC) phase of cadmium octanoate that was used as a nanoreactor. The nanocomposite samples are obtained by the rapid cooling of the LC phase to room temperature. Observed doublet structure in absorption spectra of the nanocomposites is characteristic for the two-dimensional CdSe nanoplatelets (NPLs). The thicknesses of the CdSe NPLs are 1.6, 1.9 and 2.3 nm as determined from the absorption spectra, and correspond to 4, 5 and 6 CdSe monolayers, respectively. Induced simultaneous bleaching of the doublet components observed under femtosecond laser excitation, as well as photoluminescence spectra and their kinetics are found compatible with the model of excitons with heavy- and light-hole valence bands confined in nanoplatelets.

  6. Tuning luminescence and reducing reabsorption of CdSe quantum disks for luminescent solar concentrators

    NASA Astrophysics Data System (ADS)

    Lin, Huichuan; Xie, Peng; Liu, Yong; Zhou, Xiang; Li, Baojun

    2015-08-01

    Cadmium selenide (CdSe) quantum disks (QDs) have been synthesized for application in luminescent solar concentrators (LSCs). Luminescence tuning and reabsorption reduction of the QDs were achieved by controlling their size using a hot injection method. The overlap of the absorption and photoluminescence spectra of the as-prepared CdSe QDs was negligible. The as-prepared CdSe QDs were incorporated into polymethylmethacrylate without aggregation and luminescence quenching. The obtained highly transparent composites with non-affecting light-emitting properties were used as LSCs. The placement of a CdSe QDs doped LSC prototype (10 × 1 × 0.1 cm) on a Si-cell resulted in a 201% increase in the electrical power output of the Si-cell compared with that of the bare Si-cell.

  7. Aqueous synthesis and characterization of TGA-capped CdSe quantum dots at freezing temperature.

    PubMed

    Sun, Qizhuang; Fu, Shasha; Dong, Tingmei; Liu, Shuxian; Huang, Chaobiao

    2012-07-11

    CdSe quantum dots (QDs) have traditionally been synthesized in organic phase and then transferred to aqueous solution by functionalizing their surface with silica, polymers, short-chain thiol ligands, or phospholipid micelles. However, a drastic increase in the hydrodynamic size and biotoxicity of QDs may hinder their biomedical applications. In this paper, the TGA-capped CdSe QDs are directly synthesized in aqueous phase at freezing temperature, and they prove to possess high QY (up to 14%).

  8. Synthesis of CdSe quantum dots for quantum dot sensitized solar cell

    SciTech Connect

    Singh, Neetu Kapoor, Avinashi; Kumar, Vinod; Mehra, R. M.

    2014-04-24

    CdSe Quantum Dots (QDs) of size 0.85 nm were synthesized using chemical route. ZnO based Quantum Dot Sensitized Solar Cell (QDSSC) was fabricated using CdSe QDs as sensitizer. The Pre-synthesized QDs were found to be successfully adsorbed on front ZnO electrode and had potential to replace organic dyes in Dye Sensitized Solar Cells (DSSCs). The efficiency of QDSSC was obtained to be 2.06 % at AM 1.5.

  9. Growth and Excitonic Emission of CdSe Ultra-Thin Quantum Wells Without Thickness Fluctuations

    NASA Astrophysics Data System (ADS)

    Alfaro-Martínez, Adrián; Hernández-Calderón, Isaac

    2007-04-01

    Due to the cation and anion surface reconstruction properties, one Cd-Se atomic layer epitaxy (ALE) cycle produces a coverage of 0.5 CdSe monolayers. In this work we demonstrate that even when an odd number of cycles are deposited to produce ultra-thin quantum wells, under the appropriate growth conditions, the photoluminescence spectrum indicates the absence of thickness fluctuations. A single excitonic peak is detected in the whole sample.

  10. Size and temperature dependence of the tensile mechanical properties of zinc blende CdSe nanowires

    NASA Astrophysics Data System (ADS)

    Fu, Bing; Chen, Na; Xie, Yiqun; Ye, Xiang; Gu, Xiao

    2013-11-01

    The effect of size and temperature on the tensile mechanical properties of zinc blende CdSe nanowires is investigated by all atoms molecular dynamic simulation. We found the ultimate tensile strength and Young's modulus will decrease as the temperature and size of the nanowire increase. The size and temperature dependence are mainly attributed to surface effect and thermally elongation effect. High reversibility of tensile behavior will make zinc blende CdSe nanowires suitable for building efficient nanodevices.

  11. White emission using mixtures of CdSe quantum dots and PMMA as a phosphor

    NASA Astrophysics Data System (ADS)

    Chung, Wonkeun; Park, Kwanhwi; Yu, Hong Jeong; Kim, Jihyun; Chun, Byung-Hee; Kim, Sung Hyun

    2010-02-01

    White light emitting diodes (LEDs) were fabricated using an InGaN 460 nm blue emission LED chip as the excitation source and CdSe quantum dots dispersed in PMMA as the phosphor. CdSe quantum dots were synthesized by the wet chemical method using CdO and Selenium powder as precursors. The three different size, 2.9, 3.4 and 4.3 nm in diameter, of CdSe quantum dots obtained using this method exhibited emission peaks at 555, 580 and 625 nm, respectively with a quantum yield of 10-30%. Mixed phosphors containing different weight ratio of CdSe and PMMA (1:0.1, 1:1, 1:5 and 1:10 wt%) were deposited on the LED chip to investigate the effects of different weight ratios of CdSe and PMMA on the performance of the white LEDs. The fabricated white LEDs that contained CdSe and PMMA weight ratio at 1:10 showed the best performance and the CIE color coordinates varied less with different applied currents. The luminous efficiency of single phosphor (580 nm CdSe) white LEDs was 5.62 lm/W with a CRI of 15.7, whereas the luminous efficiency of dual phosphors (555, 625 nm CdSe) white LEDs was 3.79 lm/W with a CRI of 61.4 at 20 mA. The CIE coordinates of single and dual phosphors white LEDs varied from (0.33, 0.28) to (0.29, 0.26) and from (0.39, 0.33) to (0.39, 0.32), respectively, when the working current ranged from 5 to 80 mA.

  12. Ultrashort light pulse selfdifraction in Si and CdSe single crystals

    NASA Astrophysics Data System (ADS)

    Baltramejunas, R.; Vaitkus, J.; Veleckas, D.

    1981-10-01

    Interaction of mode-locked neodyme-glass laser pulses with Si and CdSe single crystals has been investigated. The dependence of light induced diffraction on time is demonstrated in differently doped Si and CdSe. the possibility to use semiconductors for light-coherence measurement is discussed and necessary conditions are determined. The influence of thermal heating is discussed. the mechanisms of recombination at high excitation level was determined in both materials.

  13. Optical properties of two-dimensional (2D) CdSe nanostructures

    NASA Astrophysics Data System (ADS)

    Cherevkov, S. A.; Baranov, A. V.; Fedorov, A. V.; Litvin, A. P.; Artemyev, M. V.; Prudnikau, A. V.

    2013-09-01

    The resonant and off-resonant Raman spectra of optical phonons in two-dimensional CdSe nanocrystals of 5, 6, and 7 monolayers are analysed. The spectra are dominated by SO and LO phonon bands of CdSe, whose frequencies are thickness-independent in the off-resonant Raman scattering but demonstrate an evident thickness dependence in the case of the resonant Raman scattering.

  14. Efficient cw lasing in a Cr{sup 2+}:CdSe crystal

    SciTech Connect

    Akimov, V A; Kozlovskii, V I; Korostelin, Yu V; Landman, A I; Podmar'kov, Yu P; Skasyrsky, Ya K; Frolov, M P

    2007-11-30

    Continuous wave lasing in a Cr{sup 2+}:CdSe crystal is obtained for the first time. The Cr{sup 2+}:CdSe crystal pumped by a 1.908-{mu}m thulium fibre laser generated 1.07 W at 2.623 {mu}m with the quantum slope efficiency with respect to the absorbed power equal to 60%. (letters)

  15. Functional Si and CdSe quantum dots: synthesis, conjugate formation, and photoluminescence quenching by surface interactions.

    PubMed

    Sudeep, P K; Emrick, Todd

    2009-12-22

    Silicon quantum dots (QDs) were prepared with a corona of di-n-octyl phosphine oxides, by performing hydrosilylation chemistry on the surface of hydrogen-terminated Si QDs. These novel Si QDs proved well-suited to serve as "ligands" for other semiconductor QDs, such as CdSe, by interaction of the phosphine oxide corona with the CdSe surface. A pronounced photoluminescence quenching of CdSe quantum dots was observed upon introduction of the phosphine oxide functionalized Si QDs to a CdSe QD solution. Surface functionalization of the Si QDs proved critically important to observing these effects, as conventional (alkane-covered) Si QD samples gave no evidence of electronic interactions with TOPO-covered CdSe. In a comparative system, phosphine oxide terminated oligo(phenylene vinylene) molecules acting as CdSe QD ligands provide a similar fluorescence quenching, with exciton decay kinetics supporting the formation of an electronically interacting hybrid materials system.

  16. Intraband relaxation in CdSe quantum dots

    NASA Astrophysics Data System (ADS)

    Guyot-Sionnest, Philippe; Shim, Moonsub; Matranga, Chris; Hines, Margaret

    1999-07-01

    The relaxation of the 1P to 1S electronic states of CdSe semiconductor nanocrystals is followed by infrared pump-probe spectroscopy. Fast (1 ps) and slow (>200 ps) components are observed. Using different capping molecules to control the hole states, we show how the intraband relaxation slows down as the hole is in a shallow trap, a deep trap, or a charge-separated complex, providing strong support for an electron-hole Auger coupling. The slow component corresponds to an energy relaxation rate orders of magnitude slower than in bulk systems. It may be the first indication of the phonon bottleneck effect long expected in strongly confined quantum dots.

  17. Electrically driven light emission from individual CdSe nanowires.

    PubMed

    Doh, Yong-Joo; Maher, Kristin N; Ouyang, Lian; Yu, Chun L; Park, Hongkun; Park, Jiwoong

    2008-12-01

    We report electroluminescence (EL) measurements carried out on three-terminal devices incorporating individual n-type CdSe nanowires. Simultaneous optical and electrical measurements reveal that EL occurs near the contact between the nanowire and a positively biased electrode or drain. The surface potential profile, obtained by using Kelvin probe microscopy, shows an abrupt potential drop near the position of the EL spot, while the band profile obtained from scanning photocurrent microscopy indicates the existence of an n-type Schottky barrier at the interface. These observations indicate that light emission occurs through a hole leakage or an inelastic scattering induced by the rapid potential drop at the nanowire-electrode interface.

  18. Laser-induced charge separation in CdSe nanowires.

    PubMed

    Schäfer, Sebastian; Wang, Zhe; Zierold, Robert; Kipp, Tobias; Mews, Alf

    2011-07-13

    A combination of electrostatic force microscopy and optical microscopy was used to investigate the charge state of individual CdSe nanowires upon local illumination with a focused laser beam. The nanowires were found to be positively charged at the excitation spot and negatively charged at the distant end(s). For high laser powers, the amount of accumulated charges increases logarithmically with the laser power. These effects are described by a diffusion-based model where the results are in good agreement with the experimentally observed effects. On the basis of this model the charge imbalance along the nanowire should establish in the course of nanoseconds. The net charge separation within homogeneous nanowires upon local illumination is of importance for several electronic devices.

  19. Carrier recombination dynamics in individual CdSe nanowires

    NASA Astrophysics Data System (ADS)

    Vietmeyer, Felix; Frantsuzov, Pavel A.; Janko, Boldizsar; Kuno, Masaru

    2011-03-01

    Carrier dynamics in single CdSe nanowires (NWs) have been studied using various techniques. They include measurements of single wire emission intensities as a function of pump fluence, excitation intensity-dependent emission quantum yields, and excited-state lifetimes. Ensemble transient differential absorption studies of induced bleach dynamics have also been conducted. Results of these studies show superlinear growth of the emission intensity as a function of excitation intensity. This is corroborated by single nanowire emission quantum yields that vary as a function of excitation fluence and range from 0.1% to values over 10%. At the same time, measured emission lifetimes are short (<100 ps) while the nanowire band-edge bleach persists for over a nanosecond. To explain all of the abovementioned results, a kinetic model that accounts for both the nature of photogenerated carriers within the wires as well as their subsequent recombination dynamics has been developed.

  20. Structural and transport properties of CdSe nanorods

    SciTech Connect

    Das, Sayantani Banerjee, Sourish; Dutta, Alo; Ghosh, Binita; Sinha, T. P.

    2015-06-24

    The nanorods of cadmium selenide (CdSe) have been synthesized by soft chemical route. The selected area electron diffraction pattern, high resolution TEM and X-ray diffraction pattern indicate the cubic structure of the sample. The band gap of the sample is obtained using Tauc relation to UV-visible spectrum and found to be 1.92 eV. 1{sup st} order and 2{sup nd} order Raman bands are followed to investigate the behaviour of the phonon modes of the materials which is considered to be important to predict the potential of the material to microwave applications. Thermal behaviour of the sample is investigated using differential scanning calorimeter. Kissinger equation is used to calculate the activation energy of the sample, which is found to be 1.67 eV.

  1. Fluorescence quenching of CdSe quantum dots on graphene

    SciTech Connect

    Guo, Xi Tao; Hua Ni, Zhen Yan Nan, Hai; Hui Wang, Wen; Yan Liao, Chun; Zhang, Yan; Wei Zhao, Wei

    2013-11-11

    We studied systematically the fluorescence quenching of CdSe quantum dots (QDs) on graphene and its multilayers, as well as graphene oxide (GO) and reduced graphene oxide (rGO). Raman intensity of QDs was used as a quantitatively measurement of its concentration in order to achieve a reliable quenching factor (QF). It was found that the QF of graphene (∼13.1) and its multilayers is much larger than rGO (∼4.4), while GO (∼1.5) has the lowest quenching efficiency, which suggests that the graphitic structure is an important factor for quenching the fluorescence of QDs. It was also revealed that the QF of graphene is not strongly dependent on its thicknesses.

  2. Structural and transport properties of CdSe nanorods

    NASA Astrophysics Data System (ADS)

    Das, Sayantani; Dutta, Alo; Ghosh, Binita; Banerjee, Sourish; Sinha, T. P.

    2015-06-01

    The nanorods of cadmium selenide (CdSe) have been synthesized by soft chemical route. The selected area electron diffraction pattern, high resolution TEM and X-ray diffraction pattern indicate the cubic structure of the sample. The band gap of the sample is obtained using Tauc relation to UV-visible spectrum and found to be 1.92 eV. 1st order and 2nd order Raman bands are followed to investigate the behaviour of the phonon modes of the materials which is considered to be important to predict the potential of the material to microwave applications. Thermal behaviour of the sample is investigated using differential scanning calorimeter. Kissinger equation is used to calculate the activation energy of the sample, which is found to be 1.67 eV.

  3. Vertically aligned CdSe nanowire arrays for energy harvesting and piezotronic devices.

    PubMed

    Zhou, Yu Sheng; Wang, Kai; Han, Weihua; Rai, Satish Chandra; Zhang, Yan; Ding, Yong; Pan, Caofeng; Zhang, Fang; Zhou, Weilie; Wang, Zhong Lin

    2012-07-24

    We demonstrated the energy harvesting potential and piezotronic effect in vertically aligned CdSe nanowire (NW) arrays for the first time. The CdSe NW arrays were grown on a mica substrate by the vapor-liquid-solid process using a CdSe thin film as seed layer and platinum as catalyst. High-resolution transmission electron microscopy image and selected area electron diffraction pattern indicate that the CdSe NWs have a wurtzite structure and growth direction along (0001). Using conductive atomic force microscopy (AFM), an average output voltage of 30.7 mV and maximum of 137 mV were obtained. To investigate the effect of strain on electron transport, the current-voltage characteristics of the NWs were studied by positioning an AFM tip on top of an individual NW. By applying normal force/stress on the NW, the Schottky barrier between the Pt and CdSe was found to be elevated due to the piezotronic effect. With the change of strain of 0.12%, a current decreased from 84 to 17 pA at 2 V bias. This paper shows that the vertical CdSe NW array is a potential candidate for future piezo-phototronic devices.

  4. Thermal conductivity of zinc blende and wurtzite CdSe nanostructures.

    PubMed

    Yang, Juekuan; Tang, Hao; Zhao, Yang; Zhang, Yin; Li, Jiapeng; Ni, Zhonghua; Chen, Yunfei; Xu, Dongyan

    2015-10-14

    Many binary octet compounds including CdSe can be grown in either the wurtzite (WZ) or zinc blende (ZB) phase, which has aroused great interest among the research community in understanding the phase dependence of the thermal transport properties of these compounds. So far, it has been debatable whether the ZB phase possesses higher thermal conductivity than the WZ phase. In this work, we report on thermal conductivity measurements of CdSe nanowires/nanoribbons with both WZ and ZB phases via a suspended device method. At room temperature, the thermal conductivity of all the ZB CdSe nanostructures measured in this work is higher than the bulk thermal conductivity of the WZ CdSe reported in the literature, suggesting that the bulk thermal conductivity of the ZB CdSe is higher than that of the WZ phase. Our result is different from previous experimental results in the literature for InAs nanowires which suggest similar thermal conductivity values for the bulk ZB and WZ InAs crystals. The higher thermal conductivity of the ZB CdSe can be explained by its lower anharmonicity and a smaller number of atoms per unit cell compared to the WZ phase.

  5. In-situ material state monitoring using embedded CdSe quantum dots

    NASA Astrophysics Data System (ADS)

    Brubaker, Cole D.; Frecker, Talitha M.; Njoroge, Ian; Shane, Dylan O.; Smudde, Christine M.; Rosenthal, Sandra J.; Jennings, G. Kane; Adams, Douglas E.

    2016-04-01

    The development of new, smart materials capable of intrinsically detecting and communicating the occurrence of external loads and resultant damage present in a material will be crucial in the advancement of future structural health monitoring (SHM) and nondestructive evaluation (NDE) technologies. Traditionally, many SHM and NDE approaches have relied on the use of physical sensors to monitor a structure for damage, but are often hindered by their requirements for power consumption and large-scale data collection. In this work, we seek to evaluate the effectiveness of ultrasmall, white-light emitting Cadmium Selenide quantum dots (CdSe QDs) as an alternative to providing in-situ material state monitoring capabilities, while also aiming to reduce reliance on data collection and power consumption to effectively monitor a material and structure for damage. To achieve this goal, CdSe QDs are embedded in an optically clear epoxy composite matrix and exposed to external mechanical loadings. Initial results show a corresponding relationship between the shifts in observed emission spectra and external load for samples containing CdSe QDs. The effectiveness of CdSe QDs as a surface strain gauge on aluminum and fiberglass are also investigated in this paper. By monitoring changes in the emission spectra for materials containing CdSe QDs before, during and after the application of external loads, the effectiveness of CdSe QDs for communicating the occurrence of external loads acting on a material and detecting changes in material state is evaluated.

  6. High-conjugation-efficiency aqueous CdSe quantum dots.

    PubMed

    Au, Giang H T; Shih, Wan Y; Shih, Wei-Heng

    2013-11-12

    Quantum dots (QDs) are photoluminescent nanoparticles that can be directly or indirectly coupled with a receptor such as an antibody to specifically image a target biomolecule such as an antigen. Recent studies have shown that QDs can be directly made at room temperature and in an aqueous environment (AQDs) with 3-mercaptopropionic acid (MPA) as the capping ligand without solvent and ligand exchange typically required by QDs made by the organic solvent routes (OQDs). In this study, we have synthesized CdSe AQDs and compared their conjugation efficiency and imaging efficacy with commercial carboxylated OQDs in HT29 colon cancer cells using a primary antibody-biotinylated secondary antibody-streptavidin (SA) sandwich. We showed that the best imaging condition for AQDs occurred when one AQD was bound with 3 ± 0.3 SA with a nominal SA/AQD ratio of 4 corresponding to an SA conjugation efficiency of 75 ± 7.5%. In comparison, for commercial CdSe-ZnS OQDs to achieve 2.7 ± 0.4 bound SAs per OQD for comparable imaging efficacy a nominal SA/OQD ratio of 80 was needed corresponding to an SA conjugation efficiency of 3.4 ± 0.5% for CdSe-ZnS OQDs. The more than 10 times better SA conjugation efficiency of the CdSe AQDs as compared to that of the CdSe-ZnS OQDs was attributed to more capping molecules on the AQD surface as a result of the direct aqueous synthesis. More capping molecules on the AQD surface also allowed the SA-AQD conjugate to be stable in cell culture medium for more than three days without losing their staining capability in a flowing cell culture medium. In contrast, SA-OQD conjugates aggregated in cell culture medium and in phosphate buffer saline solution over time.

  7. Moléculas orgánicas obtenidas en simulaciones experimentales del medio interestelar.

    NASA Astrophysics Data System (ADS)

    Muñoz-Caro, Guillermo Manuel

    Las nubes moleculares son regiones de formación de estrellas, con temperaturas cinéticas entre 10-50 K y densidades de 103-106 átomos cm-3. Su materia está formada por gas y polvo interestelar. Estas partículas de polvo están cubiertas por una fina capa de hielo, de unos 0.01 μm, que contiene H2O y a menudo CO, CO2, CH3OH y NH3. El hielo es presumiblemente irradiado por fotones ultravioleta y rayos cósmicos en las zonas poco profundas de las nubes moleculares y las regiones circunestelares. En un sistema de vacío, P ˜ 10-7 mbar, simulamos la deposición de hielo a partir de 10 K y la irradiación ultravioleta por medio de una lámpara de descarga de hidrógeno activada con microondas. La evolución del hielo se observa por medio de un espectrómetro infrarrojo. De este modo es posible determinar la composición del hielo observado en el medio interestelar y predecir la presencia de moléculas aún no detectadas en el espacio, que han sido producto del procesamiento del hielo en nuestros experimentos. También es posible calentar el sistema hasta temperatura ambiente para sublimar el hielo depositado. Cuando el hielo ha sido previamente irradiado, se observa un residuo compuesto por moléculas orgánicas complejas, algunas prebióticas, como varios ácidos carboxílicos, aminas, amidas, ésteres y en menor proporción moléculas heterocíclicas y aminoácidos. Algunas de estas moléculas podrían detectarse en estado gaseoso por medio de observaciones milimétricas y de radio. También podrían estar presentes en el polvo cometario, cuyo análisis químico está planeado por las misiones Stardust y Rosetta. Mientras tanto, nuestro grupo está llevando a cabo el análisis de partículas de polvo interplanetario (IDPs), algunas de las cuales pueden ser de origen cometario. Al igual que ocurre con los productos obtenidos por irradiación del hielo en nuestros experimentos, algunas IDPs son ricas en material orgánico que contiene oxígeno.

  8. Enhanced photogenerated carrier collection in hybrid films of bio-templated gold nanowires and nanocrystalline CdSe.

    PubMed

    Haberer, Elaine D; Joo, John H; Hodelin, Juan F; Hu, Evelyn L

    2009-10-14

    Hybrid films of bio-templated gold nanowires and chemical bath deposited nanocrystalline CdSe were fabricated. The conductivity of the gold nanowires within the hybrid material was controlled by gold electroless deposition. Photocurrent measurements were taken on gold nanowire films, CdSe chemical bath deposited films, and hybrid films. The incorporation of gold nanowires within the hybrid material clearly increased the extraction of photogenerated carriers within the CdSe. Photocurrent showed a direct correlation with gold nanowire conductivity.

  9. Enhanced photogenerated carrier collection in hybrid films of bio-templated gold nanowires and nanocrystalline CdSe

    NASA Astrophysics Data System (ADS)

    Haberer, Elaine D.; Joo, John H.; Hodelin, Juan F.; Hu, Evelyn L.

    2009-10-01

    Hybrid films of bio-templated gold nanowires and chemical bath deposited nanocrystalline CdSe were fabricated. The conductivity of the gold nanowires within the hybrid material was controlled by gold electroless deposition. Photocurrent measurements were taken on gold nanowire films, CdSe chemical bath deposited films, and hybrid films. The incorporation of gold nanowires within the hybrid material clearly increased the extraction of photogenerated carriers within the CdSe. Photocurrent showed a direct correlation with gold nanowire conductivity.

  10. Multiple Exciton Generation Solar Cells Using CdSe Quantum Dots

    NASA Astrophysics Data System (ADS)

    Gebreselassie, Haftom Mesfin; Sharma, R. B.; Chander, Nikhil

    2011-10-01

    Experimental and Simulation works of Nanostructured Solar Cells Using CdSe Quantum Dots have been analyzed and investigated. CdSe quantum dots have been synthesized from non coordinating and high boiling solvent Octadecene and a series of increasing CdSe particle sizes are produced. The synthesized CdSe quantum dots are highly examined under a Transmission Electron Microscope and four images of different sizes of CdSe quantum dots (5.8 nm, 6.4 nm, 7.0 nm and 7.7 nm) have been obtained. A 1.1×1.1 cm2 TiO2 electrode is prepared using indium tin oxide conducting glass and TiO2 nanoparticles. The Oleic acid terminated CdSe quantum dots are separated from the octadecene by using 100% ethanol and centrifuge machine of spin about 4000 rpm until the shaking gave no longer suspension. The CdSe quantum dot (5.8 nm) was adsorbed on TiO2 photoelectrode and used as sensitizer. The relationship of Bandgap energy, Emission wavelength with respect to quantum dot size have been simulated and investigated. In this paper work, a sandwich type cell configuration which is made up of TiO2 photoelectrode, graphite coated counter electrode, an electrolyte of iodine and potassium iodide have been used. This sandwich type cell has been exposed to sun light and we have achieved 0.32 V and 0.2 mA cm-2 of potential difference and current respectively.

  11. Nonradiative energy transfer in colloidal CdSe nanoplatelet films

    NASA Astrophysics Data System (ADS)

    Guzelturk, Burak; Olutas, Murat; Delikanli, Savas; Kelestemur, Yusuf; Erdem, Onur; Demir, Hilmi Volkan

    2015-01-01

    Nonradiative energy transfer (NRET) has been extensively studied in colloidal nanocrystal (quantum dots) and nanorod (quantum wires) assemblies. In this work, we present the first account of spectroscopic evidence of NRET in solid thin films of CdSe based colloidal nanoplatelets (NPLs), also known as colloidal quantum wells. The NRET was investigated as a function of the concentration of two NPL populations with different vertical thicknesses via steady state and time resolved spectroscopy. NRET takes place from the NPLs with smaller vertical thickness (i.e., larger band gap) to the ones with a larger vertical thickness (i.e., smaller band gap) with efficiency up to ~60%. Here, we reveal that the NRET efficiency is limited in these NPL solid film assemblies due to the self-stacking of NPLs within their own population causing an increased distance between the donor-acceptor pairs, which is significantly different to previously studied colloidal quantum dot based architectures for nonradiative energy transfer.Nonradiative energy transfer (NRET) has been extensively studied in colloidal nanocrystal (quantum dots) and nanorod (quantum wires) assemblies. In this work, we present the first account of spectroscopic evidence of NRET in solid thin films of CdSe based colloidal nanoplatelets (NPLs), also known as colloidal quantum wells. The NRET was investigated as a function of the concentration of two NPL populations with different vertical thicknesses via steady state and time resolved spectroscopy. NRET takes place from the NPLs with smaller vertical thickness (i.e., larger band gap) to the ones with a larger vertical thickness (i.e., smaller band gap) with efficiency up to ~60%. Here, we reveal that the NRET efficiency is limited in these NPL solid film assemblies due to the self-stacking of NPLs within their own population causing an increased distance between the donor-acceptor pairs, which is significantly different to previously studied colloidal quantum dot based

  12. Quantum chemistry of the minimal CdSe clusters

    NASA Astrophysics Data System (ADS)

    Yang, Ping; Tretiak, Sergei; Masunov, Artëm E.; Ivanov, Sergei

    2008-08-01

    Colloidal quantum dots are semiconductor nanocrystals (NCs) which have stimulated a great deal of research and have attracted technical interest in recent years due to their chemical stability and the tunability of photophysical properties. While internal structure of large quantum dots is similar to bulk, their surface structure and passivating role of capping ligands (surfactants) are not fully understood to date. We apply ab initio wavefunction methods, density functional theory, and semiempirical approaches to study the passivation effects of substituted phosphine and amine ligands on the minimal cluster Cd2Se2, which is also used to benchmark different computational methods versus high level ab initio techniques. Full geometry optimization of Cd2Se2 at different theory levels and ligand coverage is used to understand the affinities of various ligands and the impact of ligands on cluster structure. Most possible bonding patterns between ligands and surface Cd/Se atoms are considered, including a ligand coordinated to Se atoms. The degree of passivation of Cd and Se atoms (one or two ligands attached to one atom) is also studied. The results suggest that B3LYP/LANL2DZ level of theory is appropriate for the system modeling, whereas frequently used semiempirical methods (such as AM1 and PM3) produce unphysical results. The use of hydrogen atom for modeling of the cluster passivating ligands is found to yield unphysical results as well. Hence, the surface termination of II-VI semiconductor NCs with hydrogen atoms often used in computational models should probably be avoided. Basis set superposition error, zero-point energy, and thermal corrections, as well as solvent effects simulated with polarized continuum model are found to produce minor variations on the ligand binding energies. The effects of Cd-Se complex structure on both the electronic band gap (highest occupied molecular orbital-lowest unoccupied molecular orbital energy difference) and ligand binding

  13. Sonochemical synthesis of CdS and CdSe nanowires.

    PubMed

    Jiang, Li-Ping; Xu, Shu; Miao, Jian-Jun; Wang, Hui; Zhu, Jun-Jie

    2006-08-01

    A convenient sonochemical route was developed to fabricate one-dimensional (1D) CdS or CdSe assemblies via a simple template method with two-steps: Firstly, the colloid one dimensional cadmium hydroxide particles were prepared as templates under sonication; then, the colloid particles were converted into 1D CdS or CdSe assemblies via a replacement reaction after the surface nucleation and crystal growth processes. The as-prepared CdS and CdSe nanowires were characterized by XRD, TEM, XPS, and UV-visible Spectroscopy. The effects of the ultrasonic irradiation were discussed. It is believed that the ultrasound irradiation played a positive role in both the assembly of the colloid cadmium hydroxide particles into the 1D structure and the growth of CdSe and CdS nanowires. The effects of pH on the morphologies of the cadmium hydroxide template were also discussed. The band gaps of the as-prepared 1D CdSe and CdS assemblies were calculated to be 3.1 eV and 4.9 eV, respectively, indicating the quantum size effect. The as-prepared products might have potential applications in nanodevices in future.

  14. CdSe nanocrystals ingrained dielectric nanocomposites: synthesis and photoluminescence properties

    NASA Astrophysics Data System (ADS)

    Dey, Chirantan; Goswami, Madhumita; Karmakar, Basudeb

    2015-01-01

    Cadmium selenide (CdSe) nanocrystals ingrained dielectric nanocomposites in a B2O3-SiO2-Al2O3-Na2O-K2O borosilicate glass system were synthesized by a single step in situ melt quenching technique. The sizes of the nanocrystals as well as the band gap of the nanocomposites were controlled by both concentration of CdSe and post thermal treatment duration. The nanocomposites were characterized by different instrumental techniques including detailed photoluminescence studies. The sizes of the CdSe nanocrystals were found to alter in the range 4-16 nm as estimated from the effective mass approximation model and optical absorption spectroscopy. However, the TEM analysis revealed the generation of two different size ranges, 3-4 and 23-45 nm, of the particles within the dielectric matrix. Selected area diffraction (SAED) and x-ray diffraction (XRD) patterns authenticate the formation of hexagonal nanostructures of CdSe. These nanocomposites were found to be capable of exhibiting strong visible red luminescence around 715 nm on excitation at 446 nm. This has originated from the electron-hole recombination of CdSe nanocrystal and defects or traps related transitions. The properties of these nanocomposites advocate their significant applications as semiconductor based luminescent materials.

  15. The Optical Properties of CdSe Quantum Dots by Using Spray-Atomization Method

    NASA Astrophysics Data System (ADS)

    Rosmani, C. H.; Abdullah, S.; Rusop, M.

    2013-06-01

    Cadmium Selenide (CdSe) quantum dots (QDs) is inorganic material by using spray-atomization method which is the novelty to find out the optical properties for the CdSe QDs. The Selenium (Se) precursor and Cadmium (Cd) precursor were prepared first. Se precursor by using sodium sulfite aqueous was mixed with selenium (Se) powder. For Cd precursor was used cadmium chloride (CdCI) as the Cd precursor. From previous research, CdSe QDs was obtained by using capping agent such as tri-n-octylphosphine oxide (TOPO) and trioctylphosphine (TOP). These capping agent are hazardous to environment and human. By using spray-atomization method it is more safe and economically. The photoluminescence (PL) was used to investigate the optical properties and to investigate the energy band gap from PL result. The field emission scanning electron microscopy (FESEM) was used to know the surface morphology of CdSe QDs. By PL result, the energy band gap was calculate and the comparison was investigate between the size of particle and the energy band gap. This important in this paper is to investigate the optical properties of CdSe QDs by using sprays-atomization method and to relate with the particle size.

  16. Abundancias químicas de estrellas de Mercurio-Manganeso obtenidas con espectros EBASIM

    NASA Astrophysics Data System (ADS)

    Pintado, O. I.; Adelman, S. J.

    Se determinan las abundancias químicas de estrellas de HgMn usando espectros obtenidos con EBASIM en CASLEO en un rango de longitud de onda comprendido entre los 400 y 890 nm. Los valores iniciales de temperatura efectiva y gravedad superficial se calculan con la fotometría uvbyβ. Las abundancias se calculan usando WIDTH9 y SYNTHE. Los resultados se comparan análisis realizados por los autores usando espectros obtenidos con el espectrógrado REOSC del CASLEO, el espectrógrafo echelle del Telescopio Anglo-Australiano y el espectrógrafo Coudé del Dominion Astrophysical Observatory.

  17. First principles study of O defects in CdSe

    NASA Astrophysics Data System (ADS)

    T-Thienprasert, J.; Limpijumnong, S.; Du, M.-H.; Singh, D. J.

    2012-08-01

    Recently, the vibrational signatures related to oxygen defects in oxygen-doped CdSe were measured using ultrahigh resolution Fourier transform infrared (FTIR) spectroscopy by Chen et al.(2008) [1]. They observed two absorption bands centered at ∼1991.77 and 2001.3 cm-1, which they attributed to the LVMs of OCd, in the samples grown with the addition of CdO and excess Se. For the samples claimed to be grown with even more excess Se, three high-frequency modes (1094.11, 1107.45, and 1126.33) were observed and assigned to the LVMs of OSe-VCd complex. In this work, we explicitly calculated the vibrational signatures of OCd and OSe-VCd complex defects based on first principles approach. The calculated vibrational frequencies of OCd and OSe-VCd complex are inconsistent with the frequencies observed by Chen et al., indicating that their observed frequencies are from other defects. Potential defects that could explain the experimentally observed modes are suggested.

  18. Digital Doping in Magic-Sized CdSe Clusters.

    PubMed

    Muckel, Franziska; Yang, Jiwoong; Lorenz, Severin; Baek, Woonhyuk; Chang, Hogeun; Hyeon, Taeghwan; Bacher, Gerd; Fainblat, Rachel

    2016-07-26

    Magic-sized semiconductor clusters represent an exciting class of materials located at the boundary between quantum dots and molecules. It is expected that replacing single atoms of the host crystal with individual dopants in a one-by-one fashion can lead to unique modifications of the material properties. Here, we demonstrate the dependence of the magneto-optical response of (CdSe)13 clusters on the discrete number of Mn(2+) ion dopants. Using time-of-flight mass spectrometry, we are able to distinguish undoped, monodoped, and bidoped cluster species, allowing for an extraction of the relative amount of each species for a specific average doping concentration. A giant magneto-optical response is observed up to room temperature with clear evidence that exclusively monodoped clusters are magneto-optically active, whereas the Mn(2+) ions in bidoped clusters couple antiferromagnetically and are magneto-optically passive. Mn(2+)-doped clusters therefore represent a system where magneto-optical functionality is caused by solitary dopants, which might be beneficial for future solotronic applications.

  19. Optical Properties of CdSe Nanocrystalline Photoanodes

    NASA Astrophysics Data System (ADS)

    Lesar, Amanda; Garuthara, Rohana

    2015-03-01

    Cadmium selenide (CdSe) nanocrystalline photoanodes were prepared by chemical solution deposition, with deposition time varied from 24 hours to 120 hours. Photoluminescence (PL) spectroscopy, reflectance and transmittance spectra, and photoelectric current were measured to optically characterize each sample. Photoelectric current was measured in a liquid junction configuration, with sodium sulfide as the electrolyte and platinum foil as the electrode. The PL, reflectance, and transmittance spectra were measured for each sample from 79 K to room temperature. Chemical solution deposition should lead to quantum size effects, as longer deposition times form larger size nanocrystals. Quantum size effects were observed, as longer depositions times led to a shift towards lower energy in the peak of the PL spectra. The temperature dependence of the PL peak energy position was also analyzed; as the temperature increased, the peak shifted towards higher energy. Using the reflectance and transmittance spectra, the absorption coefficient α was calculated, and the Tauc`s plot of (αhν) 2 versus (hν) was graphed. A correlation between the observed absorption edge and the PL spectra was seen, as the absorption edge energy was approximately equal to the PL energy peak.

  20. Uncovering Hot Hole Dynamics in CdSe Nanocrystals.

    PubMed

    Liu, Cunming; Peterson, Jeffrey J; Krauss, Todd D

    2014-09-04

    Single and multiple exciton relaxation dynamics of CdSe/CdZnS nanocrystal quantum dots (QDs) monitored at the two lowest optical transitions, 1Se-1S3/2 and 1Se-2S3/2, have been examined using ultrafast transient absorption (TA) spectroscopy. For the CdSe/CdZnS QDs studied, the 1Se-1S3/2 and 1Se-2S3/2 transitions are widely separated (∼180 meV) compared to bare CdSe QDs (∼50-100 meV), allowing for clearly distinguishable TA signals attributable to hot hole relaxation. Holes depopulate from the 2S3/2 state with a lifetime of 7 ± 2 ps, which is consistent with the predictions for hole relaxation via a phonon coupling pathway to lower-energy hole states, with possible contributions from hole trapping as well. These results suggest that tuning the surface chemistry of semiconductor QDs is a viable route to measure and possibly control their hot hole relaxation dynamics.

  1. Serotonin-Labeled CdSe Nanocrystals: Applications for Neuroscience

    NASA Astrophysics Data System (ADS)

    Kippeny, Tadd; Adkins, Erika; Adams, Scott; Thomlinson, Ian; Schroeter, Sally; Defelice, Louis; Blakely, Randy; Rosenthal, Sandra

    2000-03-01

    Serotonin (5-hydroxytryptamine, 5-HT) is an important neurotransmitter which has been linked to the regulation of critical behaviors including sleep, appetite, and mood. The serotonin transporter (SERT) is a 12-transmembrane domain protein responsible for clearance of serotonin from extracellular spaces following release. In order to assess the potential for use of ligand-conjugated nanocrystals to target cell surface receptors, ion channels, and transporters we have measured the ability of serotonin-labeled CdSe nanocrystals (SNACs) to block the uptake of tritiated serotonin by the human and Drosophila serotonin transporters (hSERT and dSERT). Estimated Ki values, the SNAC concentration at which half of the serotonin transport activity is blocked, were determined by nonlinear regression to be Ki (hSERT ) = 74uM and Ki (dSERT ) = 29uM. These values and our inability to detect free serotonin indicate that SNACs selectively interact with the serotonin recognition site of the transporter. We have also exposed the SNACs to cells containing ionotropic serotonin receptors and have measured the electrical response of the cell using a two microelectrode voltage clamp. We find that serotonin receptors do respond to the SNACs and we measure currents similar to the free serotonin response. These results indicate that ligand-conjugated nanocrystals can be used to label both receptor and transporter proteins. Initial fluorescence labeling experiments will be discussed.

  2. Preparation and characterization of CdSe colloidal quantum dots by pptical spectroscopy and 2D DOSY NMR

    NASA Astrophysics Data System (ADS)

    Geru, I.; Bordian, O.; Culeac, I.; Turta, C.; Verlan, V.; Barba, A.

    2015-02-01

    We present experimental results on preparation and characterization of colloidal CdSe quantum dots (QD) in organic solvent. CdSe QDs were synthesized following a modified literature method and have been characterized by UV-Vis absorption and photoluminescent (PL) spectroscopy, as well as by 2D Diffusion Ordered Spectroscopy (DOSY) NMR. The average CdSe particles size estimated from the UV-Vis absorption spectra was found to be in the range 2.28 - 2.92 nm, which correlates very well with the results obtained from NMR measurements. The PL spectrum for CdSe nanodots can be characterized by a narrow emission band with the peak maximum shifting from 508 to 566 nm in dependence of the CdSe nanoparticle size. The PL is dominated by a near-band-edge emission, accompanied by a weak broad band in the near IR, related to the surface shallow trap emission.

  3. Van der Waals materials for the passivation of monolayer closed-packed films of CdSe quantum dots

    NASA Astrophysics Data System (ADS)

    Wang, Dennis Zi-Ren; Zhang, Datong; Creswell, Richard; Lu, Chenguang; Hu, Jiayang; Herman, Irving P.

    2015-03-01

    Van der Waals (vdW) materials are shown to protect CdSe quantum dots (QDs) from oxidization. Few-layer vdW materials, e.g. graphene and MoS2, were transferred onto a monolayer closed-packed CdSe quantum dots and were examined by photoluminescence (PL) after different time periods. By comparing the PL of CdSe QDs in uncovered areas and those covered by different numbers of layers of graphene and MoS2, we saw that vdW encapsulation slows down the aging of CdSe QDs dramatically. PL mapping results clearly showed better protection of the CdSe QDs under the central part of the vdW material compared to that at the edge; this can be explained by the diffusion of oxygen and water vapor from the edge of the vdW materials.

  4. Growth and properties of CdSe thin films by a new process of electrochemical selenization of Cd metal layers

    SciTech Connect

    Rastogi, A.C.; Balakrishnan, K.S.; Jain, K.

    1999-06-01

    Growth and properties of cadmium selenide semiconductor thin films prepared by a new electrochemical selenization process (ECS) are described. The as-formed CdSe thin films have large ({approximately}1 {micro}m) crystallites in hexagonal modification. The differential selenization kinetics in the intra- and intergrain regions causes the formation of stoichiometric CdSe film to be highly dependent on time. CdSe composition is independent of selenization parameters. Two direct optical band gaps at 2.09 and 1.44 eV, as opposed to a single gap at 1.7 eV, are observed in CdSe film selenized at 0.6 and 0.4 mA/cm{sup 2} current densities, respectively. A mechanism of selenization based on Cd ionization by oxygen reduction and reaction with cathodically released Se ions is proposed for the CdSe film formation.

  5. Structural Characterization Of CdSe and ZnSe Nanostructures

    NASA Astrophysics Data System (ADS)

    Bhattacharyya, B.; Kalita, P. K.; Datta, P.

    2010-10-01

    Chemically bath deposited CdSe and ZnSe powder possesses mixed type structures whereas it is hexagonal wurtzite type in thin film form. SEM images of CdSe symmetrically exhibit the growth of spherical, rod and the rose(flower) type microstructures. ZnSe shows fine grain structures. The growth of microstructures in these selenides according to the growth direction along c-axis of hexagonal wurtzite crystal. Photoluminescence shows strong blue luminescence at 414 and 437 nm in CdSe nanoparticles. ZnSe shows strong PL at 650 nm that is attributed to the strong d-native traps. The blue shifted band gap luminescence at 392 nm shows the quantum confinement in ZnSe nanoparticles.

  6. Simple synthesis of luminescent CdSe quantum dots from ascorbic acid and selenium dioxide.

    PubMed

    Wang, Yilin; Yu, Meihua; Yang, Kun; Lu, Jianping; Chen, Linqing

    2015-12-01

    A simple, low-cost and convenient method was developed for the synthesis of highly luminescent CdSe quantum dots (QDs) in an aqueous medium. Compared with previous methods, this synthesis was carried out in one pot using ascorbic acid (C6H8O6) to replace NaBH4 or N2H4·H2O as a reductant, and selenium dioxide to replace selenium or its other hazardous, expensive and unstable compounds as a precursor. The mechanism of CdSe QDs formation was elucidated. The influence of various experimental variables, including refluxing time, Cd/MSA and Cd/Se molar ratios, on the luminescent properties of the QDs were systematically investigated. X-Ray powder diffraction and transmission electron microscopy characterization indicated that the QDs had a pure cubic zinc-blended structure with a spherical shape.

  7. Tuning the emission of CdSe quantum dots by controlled trap enhancement.

    PubMed

    Baker, David R; Kamat, Prashant V

    2010-07-06

    Ligand exchange with 3-mercaptopropionic acid (MPA) has been successfully used to tune the emission intensity of trioctylphosphineoxide/dodecylamine-capped CdSe quantum dots. Addition of 3-mercaptopropionic acid (MPA) to CdSe quantum dot suspension enhances the deep trap emission with concurrent quenching of the band edge emission. The smaller sized quantum dots, because of larger surface/volume ratio, create a brighter trap emission and are more easily tuned. An important observation is that the deep trap emission which is minimal after synthesis is brightened to have a quantum yield of 1-5% and can be tuned based on the concentration of MPA in solution with the quantum dots. Photoluminescence decay and transient absorption measurements reveal the role of surface bound MPA in altering the photophysical properties of CdSe quantum dots.

  8. Strain Effect on the Electronic and Optical Properties of CdSe Nanowires.

    PubMed

    Huan, Hao; Chen, Li; Ye, Xiang

    2017-12-01

    First-principles density functional theory (DFT) simulations were carried out to study the strain dependence on the electronic and optical properties of cadmium selenide (CdSe) nanowires (NWs). The band structures, effective masses of electron and holes, dielectric properties, and other optical properties (such as extinction coefficient, optical reflectivity, and absorption coefficient) were calculated under both compressive and tensile uniaxial strains. Size-dependence was also discussed by comparing results among CdSe wires with various diameters. Simulation results show that an interesting band-switch behavior occurs at the valence bands regardless of size. The cause and the consequences of such band-switch behavior were also studied. Further strain dependence on corresponding electronic and optical properties were examined as well. Our results provide insights to possible mechanical tuning via strain on the electronic and optical properties of CdSe NWs.

  9. Photogeneration of hydrogen from water using CdSe nanocrystals demonstrating the importance of surface exchange

    PubMed Central

    Das, Amit; Han, Zhiji; Haghighi, Mohsen Golbon; Eisenberg, Richard

    2013-01-01

    Unique tripodal S-donor capping agents with an attached carboxylate are found to bind tightly to the surface of CdSe nanocrystals (NCs), making the latter water soluble. Unlike that in similarly solubilized CdSe NCs with one-sulfur or two-sulfur capping agents, dissociation from the NC surface is greatly reduced. The impact of this behavior is seen in the photochemical generation of H2 in which the CdSe NCs function as the light absorber with metal complexes in aqueous solution as the H2-forming catalyst and ascorbic acid as the electron donor source. This precious-metal–free system for H2 generation from water using [Co(bdt)2]− (bdt, benzene-1,2-dithiolate) as the catalyst exhibits excellent activity with a quantum yield for H2 formation of 24% at 520 nm light and durability with >300,000 turnovers relative to catalyst in 60 h. PMID:24082134

  10. The direct observation of charge separation dynamics in CdSe quantum dots/cobaloxime hybrids

    SciTech Connect

    Huang, J.; Tang, Y.; Mulfort, Karen L.; Zhang, Xiaoyi

    2016-02-14

    In this work, we investigated photoinduced charge separation dynamics in a CdSe quantum dot/cobaloxime molecular catalyst hybrid using the combination of transient optical (OTA) and X-ray absorption (XTA) spectroscopy. We show that ultrafast charge separation occurs through electron transfer (ET) from CdSe QDs to cobaloxime. In addition to the enhanced 1S exciton bleach recovery in CdSe QDs due to the presence of cobaloxime, the direct evidence for ET process, i.e. the formation of the transient charge separated state, is captured by XTA. These results not only demonstrate the capability of XTA to capture the transient species during the photoinduced reactions in hybrid nanostructures but also enhance our understanding of charge separation dynamics in semiconductor nanocrystal/molecular catalyst hybrid

  11. Pulsed laser deposition of Mn doped CdSe quantum dots for improved solar cell performance

    SciTech Connect

    Dai, Qilin; Wang, Wenyong E-mail: jtang2@uwyo.edu; Tang, Jinke E-mail: jtang2@uwyo.edu; Sabio, Erwin M.

    2014-05-05

    In this work, we demonstrate (1) a facile method to prepare Mn doped CdSe quantum dots (QDs) on Zn{sub 2}SnO{sub 4} photoanodes by pulsed laser deposition and (2) improved device performance of quantum dot sensitized solar cells of the Mn doped QDs (CdSe:Mn) compared to the undoped QDs (CdSe). The band diagram of photoanode Zn{sub 2}SnO{sub 4} and sensitizer CdSe:Mn QD is proposed based on the incident-photon-to-electron conversion efficiency (IPCE) data. Mn-modified band structure leads to absorption at longer wavelengths than the undoped CdSe QDs, which is due to the exchange splitting of the CdSe:Mn conduction band by the Mn dopant. Three-fold increase in the IPCE efficiency has also been observed for the Mn doped samples.

  12. Synchronously pumped CdSe optical parametric oscillator in the 9-10 microm region.

    PubMed

    Watson, M A; O'Connor, M V; Shepherd, D P; Hanna, D C

    2003-10-15

    Continuous mode-locked operation of a singly resonant, synchronously pumped optical parametric oscillator (SPOPO) based on CdSe has produced idler output tuned over the range of 9.1-9.7 microm, the longest wavelength generated so far to our knowledge from a SPOPO. Average idler powers as high as approximately 70 mW are generated in the crystal. Tandem pumping with a diffraction-grating-tuned parametric oscillator in periodically poled lithium niobate provides a convenient and agile means of tuning the noncritically phase-matched CdSe device. The absence of any detrimental thermal effects in the CdSe crystal suggests that significant further power scaling should be possible, with idler tuning ranges extendable to cover 8-12 microm.

  13. Surface states and photovoltaic effects in CdSe quantum dot films

    SciTech Connect

    Kronik, L.; Ashkenasy, N.; Leibovitch, M.; Fefer, E.; Shapira, Y.; Gorer, S.; Hodes, G.

    1998-05-01

    Photovoltaic effects in CdSe quantum dot (QD) films have been studied using surface photovoltage spectroscopy and complementary methods. The results show that, contrary to previous studies, nonnegligible electric fields can exist in QD films. As a result, driftlike currents must be considered, in addition to the well-known diffusion like currents. However, it is found that the specific case of photovoltage sign reversal, observed after etching highly quantized CdSe QD films, is governed by diffusion like transport. The latter is highly influenced by preferential trapping of one type of charge carrier. The preferential trapping is shown to be surface localized and is strongly ambient dependent. It is shown that the photovoltaic properties of these CdSe QD films are dominated by their surface state distribution.

  14. Identification of fullerene-like CdSe nanoparticles from optical spectroscopy calculations

    NASA Astrophysics Data System (ADS)

    Botti, Silvana; Marques, Miguel A. L.

    2007-01-01

    Semiconducting nanoparticles are the building blocks of optical nanodevices as their electronic states, and therefore light absorption and emission, can be controlled by modifying their size and shape. CdSe is perhaps the most studied of these nanoparticles, due to the efficiency of its synthesis, the high quality of the resulting samples, and the fact that the optical gap is in the visible range. In this article, we study light absorption of CdSe nanostructures with sizes up to 1.5nm within density functional theory. We study both bulk fragments with wurtzite symmetry and fullerene-like core-cage structures. The comparison with recent experimental optical spectra allows us to confirm the synthesis of these fullerene-like CdSe clusters.

  15. Strain Effect on the Electronic and Optical Properties of CdSe Nanowires

    NASA Astrophysics Data System (ADS)

    Huan, Hao; Chen, Li; Ye, Xiang

    2017-03-01

    First-principles density functional theory (DFT) simulations were carried out to study the strain dependence on the electronic and optical properties of cadmium selenide (CdSe) nanowires (NWs). The band structures, effective masses of electron and holes, dielectric properties, and other optical properties (such as extinction coefficient, optical reflectivity, and absorption coefficient) were calculated under both compressive and tensile uniaxial strains. Size-dependence was also discussed by comparing results among CdSe wires with various diameters. Simulation results show that an interesting band-switch behavior occurs at the valence bands regardless of size. The cause and the consequences of such band-switch behavior were also studied. Further strain dependence on corresponding electronic and optical properties were examined as well. Our results provide insights to possible mechanical tuning via strain on the electronic and optical properties of CdSe NWs.

  16. The study of CdSe colloidal quantum dots synthesized in aqueous and organic media

    NASA Astrophysics Data System (ADS)

    Mikhailov, I. I.; Tarasov, S. A.; Solomonov, A. V.; Aleksandrova, O. A.; Matyushkin, L. B.; Mazing, D. S.

    2014-12-01

    The samples of CdSe colloidal quantum dots (CQDs) synthesized in aqueous and organic media are studied. The possibility of luminescence peak position control depending on nanoparticle growth process is demonstrated. The samples synthesized in organic medium revealed the luminescence color variation effect with nanoparticle growth. The relation of this effect with processes of nucleation and defect formation in nanoparticles is considered. The CQDs of CdSe coated with CdS shell are fabricated. The use of inorganic shell can provide a double increase of the luminescence quantum yield.

  17. Luminescence blue-shift of CdSe nanowires beyond the quantum confinement regime

    NASA Astrophysics Data System (ADS)

    Yan, Yuan; Liao, Zhi-Min; Bie, Ya-Qing; Wu, Han-Chun; Zhou, Yang-Bo; Fu, Xue-Wen; Yu, Da-Peng

    2011-09-01

    Photoluminescence (PL) properties of individual CdSe nanowires with diameters beyond the quantum confinement regime have been studied. A blue-shift in the PL spectra was observed with decreasing nanowire diameter. We attribute the blue-shift to band-filling effect. Carrier density induced by surface vacancy doping and laser excitation is found to be high enough to meet the criterion of the band-filling effect and increases with decreasing nanowire diameter. Temperature dependent PL analysis and characterizations of a single CdSe nanowire based field-effect transistor were also performed.

  18. Blue luminescence and superstructures from magic size clusters of CdSe.

    PubMed

    Riehle, Frank S; Bienert, Roland; Thomann, Ralf; Urban, Gerald A

    2009-02-01

    In this letter, we present a low-temperature synthesis route revealing a new type of ultrasmall CdSe nanoparticle family with exceptional narrow blue emissions between 437 and 456 nm and full width at half-maxima below 20 nm. Transmission electron microscopy characterization shows the uniformity of the nanoparticles, which have a diameter of 1.6 nm. After surface modification, the spherical particles assemble into nanowires, demonstrating their potential as building blocks for the generation of highly ordered superstructures. They can also be used as single source precursors for the synthesis of CdSe nanocrystals.

  19. Enhanced random lasing from a colloidal CdSe quantum dot-Rh6G system

    NASA Astrophysics Data System (ADS)

    Augustine, Anju K.; Radhakrishnan, P.; Nampoori, V. P. N.; Kailasnath, M.

    2015-02-01

    In this letter, we report random laser action in a system where optical amplification is provided by colloidal CdSe quantum dots (CQDs) triggered by the emission from Rhodamine 6G. The laser emission from CdSe QDs is optically excited by Rh-6G which in turn is photo-pumped by a frequency-doubled Q-switched Nd : YAG laser system at an excitation wavelength of 532 nm. At intensities greater than the threshold value, laser emission is characterized by narrowing peaks.

  20. Highly luminescent two dimensional excitons in atomically thin CdSe nanosheets

    NASA Astrophysics Data System (ADS)

    Halder, O.; Pradhani, A.; Sahoo, P. K.; Satpati, B.; Rath, S.

    2014-05-01

    Atomically thin Cadmium Selenide (CdSe) nanosheets have been synthesized using a surfactant mediated growth technique. The transmission electron microscopy studies confirm the presence of single layered nanosheets with thickness 1.31 nm and their stacking structures which are complemented by the small angle x-ray scattering measurements. The strongly bound and polarized character of two dimensional excitonic states with enhanced oscillator strength yielding distinct narrow blue luminescence has been observed from the CdSe nanosheets using room temperature based optical studies.

  1. Highly luminescent two dimensional excitons in atomically thin CdSe nanosheets

    SciTech Connect

    Halder, O.; Pradhani, A.; Rath, S.; Sahoo, P. K.; Satpati, B.

    2014-05-05

    Atomically thin Cadmium Selenide (CdSe) nanosheets have been synthesized using a surfactant mediated growth technique. The transmission electron microscopy studies confirm the presence of single layered nanosheets with thickness 1.31 nm and their stacking structures which are complemented by the small angle x-ray scattering measurements. The strongly bound and polarized character of two dimensional excitonic states with enhanced oscillator strength yielding distinct narrow blue luminescence has been observed from the CdSe nanosheets using room temperature based optical studies.

  2. An oleic acid-capped CdSe quantum-dot sensitized solar cell

    SciTech Connect

    Chen Jing; Song, J. L.; Deng, W. Q.; Sun, X. W.; Jiang, C. Y.; Lei, W.; Huang, J. H.; Liu, R. S.

    2009-04-13

    In this letter, we report an oleic acid (OA)-capped CdSe quantum-dot sensitized solar cell (QDSSC) with an improved performance. The TiO{sub 2}/OA-CdSe photoanode in a two-electrode device exhibited a photon-to-current conversion efficiency of 17.5% at 400 nm. At AM1.5G irradiation with 100 mW/cm{sup 2} light intensity, the QDSSCs based on OA-capped CdSe showed a power conversion efficiency of about 1%. The function of OA was to increase QD loading, extend the absorption range and possibly suppress the surface recombination.

  3. Investigation of size dependent structural and optical properties of thin films of CdSe quantum dots

    SciTech Connect

    Sharma, Madhulika; Sharma, A.B.; Mishra, N.; Pandey, R.K.

    2011-03-15

    Research highlights: {yields} CdSe q-dots have been synthesized using simple chemical synthesis route. {yields} Thin film of CdSe quantum dots exhibited self-organized growth. {yields} Size dependent blue shift observed in the absorption edge of CdSe nanocrystallites. {yields} PL emission band corresponds to band edge luminescence and defect luminescence. {yields} Organized growth led to enhancement in luminescence yield of smaller size Q-dots. -- Abstract: Cadmium selenide (CdSe) quantum dots were grown on indium tin oxide substrate using wet chemical technique for possible application as light emitting devices. The structural, morphological and luminescence properties of the as deposited thin films of CdSe Q-dot have been investigated, using X-ray diffraction, transmission electron microscopy, atomic force microscopy and optical and luminescence spectroscopy. The quantum dots have been shown to deposit in an organized array on ITO/glass substrate. The as grown Q-dots exhibited size dependent blue shift in the absorption edge. The effect of quantum confinement also manifested as a blue shift of photoluminescence emission. It is shown that the nanocrystalline CdSe exhibits intense photoluminescence as compared to the large grained polycrystalline CdSe films.

  4. Precisión de las velocidades radiales obtenidas con el REOSC

    NASA Astrophysics Data System (ADS)

    González, J. F.; Lapasset, E.

    Complementando una línea de trabajo iniciada con anterioridad discutimos la estabilidad del espectrógrafo REOSC de CASLEO en DC para la medición de velocidades radiales en base al análisis de observaciones realizadas en enero y abril de 1997. En esas oportunidades obtuvimos 26 espectros de estrellas patrones y 27 espectros de 3 estrellas usadas como estrellas de referencia en nuestro programa de cúmulos abiertos. Además tomamos 26 espectros de crepúsculo con el telescopio en posiciones cubriendo el rango H=-4,+4 y δ =-90,+30. Mediante correlaciones cruzadas derivamos la velocidad de 19 órdenes en cada uno de estos espectros. En base a un análisis estadístico de los datos obtenidos discutimos la contribución de los distintos factores que afectan a la dispersión de lectura observada. En particular, la flexión del instrumento no introduciría errores significativos cuando se observa con masas de aire menores que 2.0. La dispersión de los valores de velocidad medidos para espectros de alta relación S/N de una misma estrella resultó del orden de 0.5 km/s. La comparación con los valores de velocidad publicados por distintos autores para las estrellas patrones no permite distinguir ninguna diferencia sistemática apreciable de las velocidades de CASLEO, siendo la media cuadrática de los residuos del orden de 1.0 km/s.

  5. Probing metabolic stability of CdSe nanoparticles: alkaline extraction of free cadmium from liver and kidney samples of rats exposed to CdSe nanoparticles

    PubMed Central

    Arslan, Zikri; Ates, Mehmet; McDuffy, Wanaki; Agachan, M. Sabri; Farah, Ibrahim O.; Yu, W. William; Bednar, Anthony J.

    2011-01-01

    Cadmium selenide nanoparticles (CdSe NPs) exhibit novel optoelectronic properties for potential biomedical applications. However, their metabolic stability is not fully understood because of the difficulties in measurement of free Cd from biological tissues of exposed individuals. In this study, alkaline dissolution with tetramethylammonium hydroxide (TMAH) is demonstrated for selective determination of free Cd and intact NPs from liver and kidney samples of animals that were exposed to thiol-capped CdSe NPs. Aqueous suspensions of CdSe NPs (3.2 nm) were used to optimize the conditions for extracting free Cd without affecting NPs. Nanoparticles were found to aggregate when heated in TMAH without releasing any significant Cd to solution. Performance of the method in discriminating free Cd and intact NPs were verified by Dogfish Liver (DOLT-4) certified reference material. The samples from the animals were digested in 4 mL TMAH at 70 °C to extract free Cd followed by analysis of aqueous phase by ICP-MS. Both liver and kidney contained significant levels of free Cd. Total Cd was higher in the liver, while kidney accumulated mostly free Cd such that up to 47.9% of total Cd in the kidney was free Cd when NPs were exposed to UV-light before injection. PMID:21700388

  6. Guided CdSe Nanowires Parallelly Integrated into Fast Visible-Range Photodetectors

    PubMed Central

    2016-01-01

    One-dimensional semiconductor nanostructures, such as nanowires (NWs), have attracted tremendous attention due to their unique properties and potential applications in nanoelectronics, nano-optoelectronics, and sensors. One of the challenges toward their integration into practical devices is their large-scale controlled assembly. Here, we report the guided growth of horizontal CdSe nanowires on five different planes of sapphire. The growth direction and crystallographic orientation are controlled by the epitaxial relationship with the substrate as well as by a graphoepitaxial effect of surface nanosteps and grooves. CdSe is a promising direct-bandgap II–VI semiconductor active in the visible range, with potential applications in optoelectronics. The guided CdSe nanowires were found to have a wurtzite single-crystal structure. Field-effect transistors and photodetectors were fabricated to examine the nanowire electronic and optoelectronic properties, respectively. The latter exhibited the fastest rise and fall times ever reported for CdSe nanostructures as well as a relatively high gain, both features being essential for optoelectronic applications. PMID:28032987

  7. HPVB AND HPVZM SHAPED GROWTH OF CDZNTE, CDSE AND ZNSE CRYSTALS.

    SciTech Connect

    KOLESNIKOV,N.N.; JAMES,R.B.; BERZIGIAROVA,N.S.; KULAKOV,M.P.

    2002-07-07

    High-pressure Bridgman (HPVB) and vertical zone melting (HPVZM) growth processes have been applied for the manufacturing of Cd{sub 1-x}Zn{sub x}Te (x = 0.04-0.2), CdSe and ZnSe crystal tapes with sizes up to 120 x 120 x 12 mm. The influences of the technological parameters describing the growth processes on the crystal quality and some selected material properties are discussed. The dependence of the inclusion (bubbles) content on the deviation from melt stoichiometry is determined. A method for growing plates with low content of inclusions is described. High-resistivity crystal tapes of undoped CdZnTe (10{sup 10} Ohm x cm), CdSe (10{sup 11} Ohm x cm) and ZnSe (>10{sup 11} Ohm x cm) were prepared. The possibility of tape growth on oriented seeds is shown for the example of CdSe. The primary differences between HPVB and HPVZM results are described. The main HPVZM advantage for II-VI compound crystal growth is the possibility of obtaining crystals with more stoichiometric composition or with a controlled deviation from stoichiometry. Hence, HPVZM is preferable for growing high-resistivity II-VI crystals with low inclusion content and possibly with better transport properties. Keywords for this report are: Crystal growth, shaped crystal growth, ZnSe, CdSe, CdZnTe, CZT, HPVB, Bridgman, HPVZM, zone melting, radiation detectors.

  8. Photoluminescence of patterned CdSe quantum dot for anti-counterfeiting label on paper

    NASA Astrophysics Data System (ADS)

    Isnaeni, Yulianto, Nursidik; Suliyanti, Maria Margaretha

    2016-03-01

    We successfully developed a method utilizing colloidal CdSe nanocrystalline quantum dot for anti-counterfeiting label on a piece of glossy paper. We deposited numbers and lines patterns of toluene soluble CdSe quantum dot using rubber stamper on a glossy paper. The width of line pattern was about 1-2 mm with 1-2 mm separation between lines. It required less than one minute for deposited CdSe quantum dot on glossy paper to dry and become invisible by naked eyes. However, patterned quantum dot become visible using long-pass filter glasses upon excitation of UV lamp or blue laser. We characterized photoluminescence of line patterns of quantum dot, and we found that emission boundaries of line patterns were clearly observed. The error of line size and shape were mainly due to defect of the original stamper. The emission peak wavelength of CdSe quantum dot was 629 nm. The emission spectrum of deposited quantum dot has full width at half maximum (FWHM) of 30-40 nm. The spectra similarity between deposited quantum dot and the original quantum dot in solution proved that our stamping method can be simply applied on glossy paper without changing basic optical property of the quantum dot. Further development of this technique is potential for anti-counterfeiting label on very important documents or objects.

  9. Guided CdSe Nanowires Parallelly Integrated into Fast Visible-Range Photodetectors.

    PubMed

    Shalev, Erga; Oksenberg, Eitan; Rechav, Katya; Popovitz-Biro, Ronit; Joselevich, Ernesto

    2017-01-24

    One-dimensional semiconductor nanostructures, such as nanowires (NWs), have attracted tremendous attention due to their unique properties and potential applications in nanoelectronics, nano-optoelectronics, and sensors. One of the challenges toward their integration into practical devices is their large-scale controlled assembly. Here, we report the guided growth of horizontal CdSe nanowires on five different planes of sapphire. The growth direction and crystallographic orientation are controlled by the epitaxial relationship with the substrate as well as by a graphoepitaxial effect of surface nanosteps and grooves. CdSe is a promising direct-bandgap II-VI semiconductor active in the visible range, with potential applications in optoelectronics. The guided CdSe nanowires were found to have a wurtzite single-crystal structure. Field-effect transistors and photodetectors were fabricated to examine the nanowire electronic and optoelectronic properties, respectively. The latter exhibited the fastest rise and fall times ever reported for CdSe nanostructures as well as a relatively high gain, both features being essential for optoelectronic applications.

  10. Nonvolatile multibit Schottky memory based on single n-type Ga doped CdSe nanowires.

    PubMed

    Wu, Di; Jiang, Yang; Yu, Yongqiang; Zhang, Yugang; Li, Guohua; Zhu, Zhifeng; Wu, Chunyan; Wang, Li; Luo, Linbao; Jie, Jiansheng

    2012-12-07

    Nonvolatile resistive switching has been observed for the first time in CdSe nanowire (NW)/Au Schottky barrier diodes, where a Schottky contact electrode and an Ohmic contact electrode were formed at the Au/CdSe NW and CdSe NW/In interfaces, respectively. The CdSe NWs Schottky devices were found to possess multibit storage ability in an individual nanowire, and exhibited excellent memory characteristics, with a resistance on/off ratio exceeding four orders of magnitude, a long retention time of over 10(4) s and a lower operating voltage of 2 V. By replacing the SiO(2)/Si substrate with a poly ethylene terephthalate substrate, flexible and transparent memory devices with superior stability under strain were realized. The resistive switching of CdSe NW/Au Schottky devices is understood by electron trapping and detrapping in the interfacial oxide layer. Our findings provide a viable way to create new functional high-density nonvolatile multibit memory devices compatible with simple processing techniques for normal one-dimensional nanomaterials.

  11. Nonvolatile multibit Schottky memory based on single n-type Ga doped CdSe nanowires

    NASA Astrophysics Data System (ADS)

    Wu, Di; Jiang, Yang; Yu, Yongqiang; Zhang, Yugang; Li, Guohua; Zhu, Zhifeng; Wu, Chunyan; Wang, Li; Luo, Linbao; Jie, Jiansheng

    2012-12-01

    Nonvolatile resistive switching has been observed for the first time in CdSe nanowire (NW)/Au Schottky barrier diodes, where a Schottky contact electrode and an Ohmic contact electrode were formed at the Au/CdSe NW and CdSe NW/In interfaces, respectively. The CdSe NWs Schottky devices were found to possess multibit storage ability in an individual nanowire, and exhibited excellent memory characteristics, with a resistance on/off ratio exceeding four orders of magnitude, a long retention time of over 104 s and a lower operating voltage of 2 V. By replacing the SiO2/Si substrate with a poly ethylene terephthalate substrate, flexible and transparent memory devices with superior stability under strain were realized. The resistive switching of CdSe NW/Au Schottky devices is understood by electron trapping and detrapping in the interfacial oxide layer. Our findings provide a viable way to create new functional high-density nonvolatile multibit memory devices compatible with simple processing techniques for normal one-dimensional nanomaterials.

  12. Resonant and Nonresonant Nonlinear Optical Spectroscopy of CDSE Quantum Dots for Nonlinear Photonic Applications

    DTIC Science & Technology

    2006-11-01

    excitations. 1. INTRODUCTION Colloidal semiconductor nanocrystals have drawn significant attention because of their distinct roles in nonlinear... colloidal semiconductor nanoscale materials significantly changes with resonant and nonresonant excitation processes. The processes leading to non...2. EXPERIMENT CdSe colloidal quantum-dot nanocrystals for Z- scan and DFWM spectroscopy were prepared by injecting Se solution (a mixture of

  13. A Biphasic Ligand Exchange Reaction on Cdse Nanoparticles: Introducing Undergraduates to Functionalizing Nanoparticles for Solar Cells

    ERIC Educational Resources Information Center

    Zemke, Jennifer M.; Franz, Justin

    2016-01-01

    Semiconductor nanoparticles, including cadmium selenide (CdSe) particles, are attractive as light harvesting materials for solar cells. In the undergraduate laboratory, the size-tunable optical and electronic properties can be easily investigated; however, these nanoparticles (NPs) offer another platform for application-based tunability--the NP…

  14. Application of CdSe quantum dots for the direct detection of TNT.

    PubMed

    Yi, Kui-Yu

    2016-02-01

    CdSe quantum dots were synthesized through a simple, green organic-phase method. Paraffin was used as the reaction solvent and a reducing agent, oleic acid was the reaction ligand, and oleyl amine was the stabilizer. Based on the phenomenon of TNT quenched oil-soluble CdSe quantum dot fluorescence, a simple, fast, and direct method of TNT detection was established. Under optimum conditions, the degree of fluorescence quenching of oil-soluble CdSe quantum dots had a good linear correlation with TNT concentration in the 1.0×10(-7)-5.0×10(-5) mol/L range, and the correlation coefficient was 0.9990. TNT detection limit was 2.1×10(-8)mol/L. The method was successfully used to determine TNT-explosion dust samples, results were satisfactory. The fluorescence quenching mechanism of oil-soluble CdSe quantum dots by TNT was also discussed.

  15. Size effect on the electronic and optical band gap of CdSe QD

    SciTech Connect

    Sisodia, Namita

    2014-04-24

    Present paper deals with a critical and comprehensive analysis of the dependence of photo emission (PE) electronic band gap and optical absorption (OA) excitonic band gap on the size of CdSe QD, via connecting it with excitonic absorbance wavelength. Excitonic absorbance wavelength is determined through an empirical fit of established experimental evidences. Effective excitonic charge and Bohr radius is determined as a function of size. Increase in size of the CdSe QD results in greater Bohr radius and smaller effective excitonic charge. Excitonic binding energy as a degree of size of QD is also calculated which further relates with the difference in PE electronic and OA optical band gaps. It is also shown that with increase in size of CdSe QD, the excitonic binding energy decreases which consequently increases differences in two band gaps. Our results are very well comparable with the established results. Explanation for the origin of the unusual optical properties of CdSe QD has been also discussed.

  16. Femtosecond time-resolved energy transfer from CdSe nanoparticles to phthalocyanines

    NASA Astrophysics Data System (ADS)

    Dayal, S.; Królicki, R.; Lou, Y.; Qiu, X.; Berlin, J. C.; Kenney, M. E.; Burda, C.

    2006-07-01

    The first real-time observation of the early events during energy transfer from a photoexcited CdSe nanoparticle to an attached phthalocyanine molecule are presented in terms of a femtosecond spectroscopic pump-probe study of the energy transfer in conjugates of CdSe nanoparticles (NPs) and silicon phthalocyanines (Pcs) with 120 fs time resolution. Four different silicon phthalocyanines have been conjugated to CdSe NPs. All of these have proven potential for photodynamic therapy (PDT). In such NP-Pc conjugates efficient energy transfer (ET) from CdSe NPs to Pcs occurs upon selective photoexcitation of the NP moiety. Spectral analysis as well as time-resolved fluorescence up-conversion measurements revealed the structure and dynamics of the investigated conjugates. Femtosecond transient differential absorption (TDA) spectroscopy was used for the investigation of the non-radiative carrier and ET dynamics. The formation of excitons, trapped carriers states, as well as stimulated emission was monitored in the TDA spectra and the corresponding lifetimes of these states were recorded. The time component for energy transfer was found to be between 15 and 35 ps. The ET efficiencies are found to be 20-70% for the four Pc conjugates, according to fluorescence quenching experiments. Moreover, as a result of the conjugation between NP and the Pcs the photoluminescence efficiency of the Pc moieties in the conjugates do not strictly follow the quantum yields of the bare phthalocyanines.

  17. Ligand-assisted fabrication of hollow CdSe nanospheres viaOstwald ripening and their microwave absorption properties

    NASA Astrophysics Data System (ADS)

    Cao, Minhua; Lian, Huiqin; Hu, Changwen

    2010-12-01

    Hollow CdSe nanospheres were successfully synthesized by a ligand-assisted solvothermal method based on an Ostwald ripening mechanism. The hollow CdSe nanospheres were synthesized in benzyl alcohol under solvothermal conditions using Cd(Ac)2 and Se as the precursors, and tryptophan as a ligand. The resulting hollow structures consisted of small nanocrystallite building blocks. More importantly, the hollow CdSe nanospheres could be used as an excellent microwave absorber for cm- and mm-wave absorption, depending on the thickness of the absorber.

  18. Solution-based stoichiometric control over charge transport in nanocrystalline CdSe devices.

    PubMed

    Kim, David K; Fafarman, Aaron T; Diroll, Benjamin T; Chan, Silvia H; Gordon, Thomas R; Murray, Christopher B; Kagan, Cherie R

    2013-10-22

    Using colloidal CdSe nanowire (NW) field-effect transistors (FETs), we demonstrated the dependence of carrier transport on surface stoichiometry by chemically manipulating the atomic composition of the NW surface. A mild, room-temperature, wet-chemical process was devised to introduce cadmium, selenium, or sulfur adatoms at the surface of the NWs in completed devices. Changes in surface composition were tested for by energy dispersive spectroscopy and inductively coupled plasma-atomic emission spectroscopy and through the use of the vibrational reporter thiocyanate. We found that treatment with cadmium acetate enhances electron currents, while treatment with sodium selenide or sodium sulfide suppressed them. The efficacy of doping CdSe NWs through subsequent thermal diffusion of indium was highly dependent on the surface composition. While selenium-enriched CdSe NW FETs were characterized by little to no electron currents, when combined with indium, they yielded semimetallic devices. Sulfur-enriched, indium-doped devices also displayed dramatically enhanced electron currents, but to a lesser extent than selenium and formed FETs with desirable ION/IOFF >10(6). The atomic specificity of the electronic behavior with different surface chalcogens suggested indium was bound to chalcogens at the NW surface, indicating commonalities with and implications for indium-containing CdSe nanocrystal films. Low temperature measurements of indium-doped CdSe NW FETs showed no evidence of impurity scattering, further supporting the existence of an indium-chalcogen interaction at the surface rather than in the core of the NW.

  19. Study of optical and structural properties of CdSe quantum dot embedded in PVA polymer matrix

    NASA Astrophysics Data System (ADS)

    Tyagi, Chetna; Sharma, Ambika

    2015-08-01

    To enhance the properties and applicability of devices it is essential to incorporate semiconductor nanoparticles into polymer matrix. This introduces a new branch of science which includes device fabrications such as gas sensors, nonlinear optics, catalysis etc. Herein, we have synthesized CdSe/PVA nanocomposite (NC) material using wet chemical synthesis technique. The XRD studies revealed the formation of crystalline structure of CdSe nanoparticles (NP's) and PVA NC's with an average size of 100 nm and 5 nm respectively. Energy band gap is determined using UV-VIS Spectroscopy. A red shift in the absorption edge of CdSe/PVA NC is observed with respect to CdSe Np's, The photoluminescence spectra also show red shift for CdSe/PVA NC as compared to CdSe NP's Thus the use of CdSe/PVA for solar cell application would be more preferable than CdSe NP's.

  20. Controlled assembling of CdSe nanoparticles into the mesopores of SBA-15 via hot soap method

    NASA Astrophysics Data System (ADS)

    Bao, J.; Shen, Y.; Sun, Y.; Wu, J.; Chen, X.; Dai, N.; Zhang, J. C.

    2008-02-01

    We describe a hot soap method for assembling CdSe nanoparticles inside the channels of mesoporous SBA-15 materials. X-ray diffraction (XRD), transmission electron microscopy (TEM), energy dispersive spectrometry (EDS), UV-vis absorption spectra, and fluorescence spectra have been successfully used to characterize the structure and the optical properties of the mesoporous materials. EDS analysis carried out on the pores of composite mesoporous silica shows strong Cd and Se signals, confirming the formation of CdSe nanoparticles inside the SBA-15 pores. TEM image shows that the CdSe nanoparticles are about 4-5 nm in sizes and uniformly dispersed inside the pores of mesoporous silica. In the UV-vis absorption spectra of the CdSe nanoparticles inside the SBA-15 hosts, a significant blue shift is detected and attributed to the confinement of channels of SBA-15.

  1. Optical properties of water soluble CdSe quantum dots modified by a novel biopolymer based on sodium alginate

    NASA Astrophysics Data System (ADS)

    Bardajee, Ghasem Rezanejade; Hooshyar, Zari

    2013-10-01

    Water soluble CdSe quantum dots (QDs) were modified using a novel biopolymer based on the graft copolymerization of poly (acrylic acid) as a monomer onto sodium alginate as a backbone at room temperature. The obtained CdSe QDs were characterized by Fourier transform infrared spectrometer, thermo-gravimetry analysis, transmission electron microscopy, and dynamic light scattering. Optical properties of the prepared CdSe QDs were investigated by absorption and fluorescence spectra. It was found that the resultant QDs incredibly exhibited high fluorescence intensity and quantum yields. Lastly, the influence of the aging time on the fluorescence intensity of the modified CdSe QDs was studied by their fluorescence spectra. Due to the optical behavior of this modified QDs; it could be of potential interest in biological systems.

  2. Influence of nanocrystalline size on optical band gap in CdSe thin films prepared by DC sputtering

    NASA Astrophysics Data System (ADS)

    Khalaf, Mohammed Khammass; ALhilli, Baha A. M.; Khudiar, Ausama I.; Alzahra, Anwar Abd

    2016-01-01

    Cadmium selenide CdSe thin films have been deposited on glass substrate by using plasma sputtering at room temperature with different times of sputtering. The CdSe thin films are characterized using XRD. The crystallite size of the film is calculated from XRD data, which is found as 12.65 nm as-deposited. It is also found that crystallite size of CdSe thin films increased with thin films thickness. The optical properties concerning the absorption spectra were studied for the prepared thin films. The energy band gaps were found to be in the range of 2.21 eV to 1.8 eV. On varying the film thickness in the range of 350 nm to 600 nm, it was found that the optical band gap increased due to the nanocrystalline size of the CdSe thin films decreased.

  3. Nonlinear optical switching and optical limiting in colloidal CdSe quantum dots investigated by nanosecond Z-scan measurement

    NASA Astrophysics Data System (ADS)

    Valligatla, Sreeramulu; Haldar, Krishna Kanta; Patra, Amitava; Desai, Narayana Rao

    2016-10-01

    The semiconductor nanocrystals are found to be promising class of third order nonlinear optical materials because of quantum confinement effects. Here, we highlight the nonlinear optical switching and optical limiting of cadmium selenide (CdSe) quantum dots (QDs) using nanosecond Z-scan measurement. The intensity dependent nonlinear absorption and nonlinear refraction of CdSe QDs were investigated by applying the Z-scan technique with 532 nm, nanosecond laser pulses. At lower intensities, the nonlinear process is dominated by saturable absorption (SA) and it is changed to reverse saturable absorption (RSA) at higher intensities. The SA behaviour is attributed to the ground state bleaching and the RSA is ascribed to free carrier absorption (FCA) of CdSe QDs. The nonlinear optical switching behaviour and reverse saturable absorption makes CdSe QDs are good candidate for all-optical device and optical limiting applications.

  4. A facile method to synthesis high-quality CdSe quantum dots for large and tunable nonlinear absorption

    NASA Astrophysics Data System (ADS)

    Cao, Yawan; Wang, Chong; Zhu, Baohua; Gu, Yuzong

    2017-04-01

    The CdSe nanocrystals (NCs) were synthesized by a hot injection method in the atmospheric environment without any protective gas. The size of CdSe NC was tuned by controlling the growth time and the NCs' high-quality was confirmed by UV-visible spectroscopy, photoluminescence spectroscopy, X-ray diffraction and transmission electron microscopy. A large third-order nonlinear optical (NLO) absorption of CdSe NCs was obtained by using Z-scan technique with 30 ps excitation at 532 nm, which was tunable with variable size and the energy difference between the first exciton absorption peak and the laser wavelength. The NLO susceptibility of CdSe NCs can reach as high as 1.81 × 10-10 esu at the size of 3.3 nm and at resonance absorption peak.

  5. CdSe magic-sized nuclei, magic-sized nanoclusters and regular nanocrystals: monomer effects on nucleation and growth.

    PubMed

    Yu, Kui

    2012-02-21

    Colloidal semiconductor quantum dots (QDs) have been well appreciated for their potential in nanophotonics with an unprecedented impact in various areas, including light emitting diodes (LEDs) and solar cells. There is an outstanding demand on the control of size and size distribution for the various applications, with rational design supported by fundamental understanding of nucleation and growth. This Research News introduces recent advances in the synthesis of colloidal CdSe magic-sized nuclei (MSN) exhibiting sharp bandgap emission, with a model proposed to illustrate the nature of monomers and their degree of supersaturation (DS) affecting the formation of various CdSe MSN, magic-sized nanoclusters (MSCs), and regular nanocrystals (RNCs). Also, this model addresses tuning the CdSe RNCs into the CdSe MSN with the presence of cadmium acetate (Cd(OAc)2) affecting the nature of the monomers.

  6. Synthesis of CdSe quantum dots using selenium dioxide as selenium source and its interaction with pepsin.

    PubMed

    Wang, Yilin; Mo, Yunchuan; Zhou, Liya

    2011-09-01

    A novel method has been developed for the synthesis of thioglycolic acid (TGA)-capped CdSe quantum dots (QDs) in an aqueous medium when selenium dioxide worked as a selenium source and sodium borohydride acted as a reductant. The interaction between CdSe QDs and pepsin was investigated by fluorescence spectroscopy. It was proved that the fluorescence quenching of pepsin by CdSe QDs was mainly a result of the formation of CdSe-pepsin complex. Based on the fluorescence quenching results, the Stern-Volmer quenching constant (Ksv), binding constant (KA) and binding sites (n) were calculated. According to the Foster's non-radiative energy transfer theory, the binding distance (r) between pepsin and CdSe QDs was obtained. The influence of CdSe QDs on the conformation of pepsin has been analyzed by synchronous fluorescence spectra, which provided that the secondary structure of pepsin has been changed by the interaction of CdSe QDs with pepsin.

  7. Synthesis of CdSe quantum dots using various long-chain fatty acids and their phase transfer.

    PubMed

    Zhang, Qiang; Zhang, Aiyu; Yang, Ping; Shen, Jianxing

    2013-06-01

    Monodispersed colloidal photoluminescent CdSe quantum dots (QDs) were synthesized via an organic approach by using cadmium oxide and elemental selenium as precursors, and long-chain fatty acids as surface ligands. The hydrocarbon chain length of the fatty acid was adjusted to investigate the effect on CdSe QDs. The fatty acid ligands with different hydrocarbon chain lengths showed an apparent effect on the nanocrystal nucleation and growth which is the key controlling the size, size distribution and crystal structure of resulting CdSe QDs. This effect was attributable to the steric hindrance of different hydrocarbon length of the fatty acids, which affected the reactivity of the monomers and nanocrystals during the nanocrystal nucleation and growth. The water-soluble CdSe QDs were obtained by encapsulating the CdSe ODs in oil phase with amphiphilic poly(styrene-co-maleic anhydride) (PSMA)-ethanolamine (EA) polymers, which made it possible for further applications of the CdSe QDs in aqueous environment such as surface functionalization for biological labeling and application in photocatalysis and photosensitization.

  8. Synthesis of CdSe quantum dots using selenium dioxide as selenium source and its interaction with pepsin

    NASA Astrophysics Data System (ADS)

    Wang, Yilin; Mo, Yunchuan; Zhou, Liya

    2011-09-01

    A novel method has been developed for the synthesis of thioglycolic acid (TGA)-capped CdSe quantum dots (QDs) in an aqueous medium when selenium dioxide worked as a selenium source and sodium borohydride acted as a reductant. The interaction between CdSe QDs and pepsin was investigated by fluorescence spectroscopy. It was proved that the fluorescence quenching of pepsin by CdSe QDs was mainly a result of the formation of CdSe-pepsin complex. Based on the fluorescence quenching results, the Stern-Volmer quenching constant ( Ksv), binding constant ( KA) and binding sites ( n) were calculated. According to the Foster's non-radiative energy transfer theory, the binding distance ( r) between pepsin and CdSe QDs was obtained. The influence of CdSe QDs on the conformation of pepsin has been analyzed by synchronous fluorescence spectra, which provided that the secondary structure of pepsin has been changed by the interaction of CdSe QDs with pepsin.

  9. CdSe quantum dot-fullerene hybrid nanocomposite for solar energy conversion: electron transfer and photoelectrochemistry.

    PubMed

    Bang, Jin Ho; Kamat, Prashant V

    2011-12-27

    The development of organic/inorganic hybrid nanocomposite systems that enable efficient solar energy conversion has been important for applications in solar cell research. Nanostructured carbon-based systems, in particular C(60), offer attractive strategies to collect and transport electrons generated in a light harvesting assembly. We have assembled CdSe-C(60) nanocomposites by chemically linking CdSe quantum dots (QDs) with thiol-functionalized C(60). The photoinduced charge separation and collection of electrons in CdSe QD-C(60) nanocomposites have been evaluated using transient absorption spectroscopy and photoelectrochemical measurements. The rate constant for electron transfer between excited CdSe QD and C(60) increased with the decreasing size of the CdSe QD (7.9 × 10(9) s(-1) (4.5 nm), 1.7 × 10(10) s(-1) (3.2 nm), and 9.0 × 10(10) s(-1) (2.6 nm)). Slower hole transfer and faster charge recombination and transport events were found to dominate over the forward electron injection process, thus limiting the deliverance of maximum power in CdSe QD-C(60)-based solar cells. The photoinduced charge separation between CdSe QDs and C(60) opens up new design strategies for developing light harvesting assemblies.

  10. Quantum confinement effect of CdSe induced by nanoscale solvothermal reaction.

    PubMed

    Lee, Jin-Wook; Im, Jeong-Hyuk; Park, Nam-Gyu

    2012-10-21

    We report a novel method, nanoscale solvothermal reaction (NSR), to induce the quantum confinement effect of CdSe on nanostructured TiO(2) by solvothermal route. The time-dependent growth of CdSe is observed in solution at room temperature, which is found to be accomplished instantly by heat-treatment in the presence of solvent at 1 atm. However, no crystal growth occurs upon heat-treatment in the absence of solvent. The nanoscale solvothermal growth of CdSe quantum dot is realized on the nanocrystalline oxide surface, where Cd(NO(3))(2)·4H(2)O and Na(2)SeSO(3) solutions are sequentially spun on nanostructured TiO(2), followed by heat-treatment at temperatures ranging from 100 °C to 250 °C. Size of CdSe increases from 4.4 nm to 5.3 nm, 8.7 nm and 14.8 nm, which results in decrease in optical band gap from 2.19 eV to, 1.95 eV, 1.74 eV and 1.75 eV with increasing the NSR temperature from 100 °C to 150 °C, 200 °C and 250 °C, respectively, which is indicative of the quantum confinement effect. Thermodynamic studies reveal that increase in the size of CdSe is related to increase in enthalpy, for instance, from 3.77 J mg(-1) for 100 °C to 8.66 J mg(-1) for 200 °C. Quantum confinement effect is further confirmed from the CdSe-sensitized solar cell, where onset wavelength in external quantum efficiency spectra is progressively shifted from 600 nm to 800 nm as the NSR temperature increases, which leads to a significant improvement of power conversion efficiency by a factor of more than four. A high photocurrent density of 13.7 mA cm(-2) is obtained based on CdSe quantum dot grown by NSR at 200 °C.

  11. Bovine serum albumin-directed synthesis of biocompatible CdSe quantum dots and bacteria labeling.

    PubMed

    Wang, Qisui; Ye, Fangyun; Fang, Tingting; Niu, Wenhan; Liu, Peng; Min, Xinmin; Li, Xi

    2011-03-01

    A simple method was developed for preparing CdSe quantum dots (QDs) using a common protein (bovine serum albumin (BSA)) to sequester QD precursors (Cd(2+)) in situ. Fluorescence (FL) and absorption spectra showed that the chelating time between BSA and Cd(2+), the molar ratio of BSA/Cd(2+), temperature, and pH are the crucial factors for the quality of QDs. The average QD particle size was estimated to be about 5 nm, determined by high-resolution transmission electron microscopy. With FL spectra, Fourier transform infrared spectra, and thermogravimetric analysis, an interesting mechanism was discussed for the formation of the BSA-CdSe QDs. The results indicate that there might be conjugated bonds between CdSe QDs and -OH, -NH, and -SH groups in BSA. In addition, fluorescence imaging suggests that the QDs we designed can successfully label Escherichia coli cells, which gives us a great opportunity to develop biocompatible tools to label bacteria cells.

  12. Film formation of CdSe quantum dot embedded phosphate glass on an FTO glass substrate

    NASA Astrophysics Data System (ADS)

    Han, Karam; Kim, Yoon Hwa; Im, Won Bin; Chung, Woon Jin

    2015-07-01

    A thick film with CdSe quantum dot (QD) embedded glass was formed on a fluorine-doped tin oxide (FTO) glass substrate. Phosphate glasses with different CdO and ZnSe concentrations were synthesized, and the heat treatment conditions were varied to determine the appropriate QD and film formation conditions. Phosphate glass with 1 mol. % CdO and 1.5 mol. % ZnSe showed controlled crystallization of CdSe QDs when they were heat treated at 550℃ for 1 hr. Absorption spectra and Raman spectroscopy identified the QD formation. Precursor glass was ground into powder and pasted onto FTO only and TiO2/FTO glass substrates via the screen printing method. Glass film embedded with QDs was successfully formed after sintering, thus demonstrating its potential for film applications. [Figure not available: see fulltext.

  13. Morphology of ultrathin CdSe quantum confinement layers in ZnSe matrices

    NASA Astrophysics Data System (ADS)

    Chinyama, K. G.; O'Donnell, K. P.; Rosenauer, A.; Gerthsen, D.

    1999-06-01

    Using a combination of transmission electron microscopy (TEM), high resolution TEM (HRTEM), digital analysis of lattice images (DALI), and correspondence analysis (CA) we present at near-atomic resolution the morphology of a nominal 2 monolayer (ML) cadmium selenide (CdSe) quantum well (QW) between ZnSe barriers. We reveal the presence of ˜10 ML zinc cadmium selenide (Zn xCd 1- xSe) alloy insertion layer of varying composition in a ZnSe matrix. A spotty pattern in the plane of the layer indicates the presence of self-assembled clusters or islands similar to the structures commonly referred to as quantum dots. Further analysis indicates that these clusters, of less than 10 nm in lateral extent, themselves contain sites highly saturated with CdSe. Analysis of photoluminescence (PL) spectra suggests that the emission originates predominantly from excitons trapped in these islands.

  14. Fingerprint detection and using intercalated CdSe nanoparticles on non-porous surfaces.

    PubMed

    Algarra, Manuel; Radotić, Ksenija; Kalauzi, Aleksandar; Mutavdžić, Dragosav; Savić, Aleksandar; Jiménez-Jiménez, José; Rodríguez-Castellón, Enrique; da Silva, Joaquim C G Esteves; Guerrero-González, Juan José

    2014-02-17

    A fluorescent nanocomposite based on the inclusion of CdSe quantum dots in porous phosphate heterostructures, functionalized with amino groups (PPH-NH2@CdSe), was synthesized, characterized and used for fingerprint detection. The main scopes of this work were first to develop a friendly chemical powder for detecting latent fingerprints, especially in non-porous surfaces; their further intercalation in PPH structure enables not to spread the fluorescent nanoparticles, for that reason very good fluorescent images can be obtained. The fingerprints, obtained on different non-porous surfaces such as iron tweezers, mobile telephone screen and magnetic band of a credit card, treated with this powder emit a pale orange luminescence under ultraviolet excitation. A further image processing consists of contrast enhancement that allows obtaining positive matches according to the information supplied from a police database, and showed to be more effective than that obtained with the non-processed images. Experimental results illustrate the effectiveness of proposed methods.

  15. CdSe nanorods dominate photocurrent of hybrid CdSe-P3HT photovoltaic cell.

    PubMed

    Schierhorn, Martin; Boettcher, Shannon W; Peet, Jeffrey H; Matioli, Elison; Bazan, Guillermo C; Stucky, Galen D; Moskovits, Martin

    2010-10-26

    Photovoltaic devices based on organic semiconductors require charge-separating networks (bulk heterojunctions) for optimal performance. Here we report on the fabrication of organic-inorganic photovoltaic devices with tailored (n-type) CdSe nanorod arrays aligned perpendicularly to the substrate. The nanorod lengths varied from 58 ± 12 to 721 ± 15 nm, while the diameters and inter-rod spacings were kept constant at 89.5 ± 7.5 and 41.3 ± 9.9 nm, respectively. Short-circuit densities improved linearly with nanorod length, resulting in power conversion efficiencies of up to 1.38% for cells with nanorods 612 ± 46 nm long. Notably, the cell's efficiency was dominated by exciton generation in the CdSe nanorods.

  16. Electric field-induced emission enhancement and modulation in individual CdSe nanowires.

    PubMed

    Vietmeyer, Felix; Tchelidze, Tamar; Tsou, Veronica; Janko, Boldizsar; Kuno, Masaru

    2012-10-23

    CdSe nanowires show reversible emission intensity enhancements when subjected to electric field strengths ranging from 5 to 22 MV/m. Under alternating positive and negative biases, emission intensity modulation depths of 14 ± 7% are observed. Individual wires are studied by placing them in parallel plate capacitor-like structures and monitoring their emission intensities via single nanostructure microscopy. Observed emission sensitivities are rationalized by the field-induced modulation of carrier detrapping rates from NW defect sites responsible for nonradiative relaxation processes. The exclusion of these states from subsequent photophysics leads to observed photoluminescence quantum yield enhancements. We quantitatively explain the phenomenon by developing a kinetic model to account for field-induced variations of carrier detrapping rates. The observed phenomenon allows direct visualization of trap state behavior in individual CdSe nanowires and represents a first step toward developing new optical techniques that can probe defects in low-dimensional materials.

  17. Optical quenching of photoconductivity in CdSe single nanowires via waveguiding excitation.

    PubMed

    Gu, Fuxing; Wang, Pan; Yu, Huakang; Guo, Bing; Tong, Limin

    2011-05-23

    We demonstrate broadband optical quenching of photoconductivity in CdSe single nanowires with low excitation power. Using 1550-nm-wavelength light with 10-nW power for waveguiding excitation, we observe a typical responsivity of 0.5 A/W for quenching the photoconductivity established by 10-µW 660-nm-wavelength background light in a 403-nm-diameter CdSe nanowire, with detectable limit of the quenching power down to pW level at room temperature, which is several orders of magnitude lower than those reported previously. This large quenching effect originates from the enhanced light-defect interaction in the nanowires via waveguiding excitation. These results open new opportunities for noninvasive characterization of deep-level defect states in low-dimensional semiconductor nanomaterials, and novel optoelectronic applications of semiconductor nanowires such as high-sensitive broadband photodetection.

  18. Light-gated single CdSe nanowire transistor: photocurrent saturation and band gap extraction

    NASA Astrophysics Data System (ADS)

    Zhang, Yang; Chakraborty, Ritun; Kudera, Stefan; Krahne, Roman

    2015-11-01

    CdSe nanowires are popular building blocks for many optoelectronic devices mainly owing to their direct band gap in the visible range of the spectrum. Here we investigate the optoelectronic properties of single CdSe nanowires fabricated by colloidal synthesis, in terms of their photocurrent-voltage characteristics and photoconductivity spectra recorded at 300 and 18 K. The photocurrent is identified as the secondary photocurrent, which gives rise to a photoconductive gain of 35. We observe a saturation of the photocurrent beyond a certain voltage bias that can be related to the finite drift velocity of electrons. From the photoconductivity spectra, we determine the band gap energy of the nanowires as 1.728 eV, and we resolve low-energy peaks that can be associated with sub-bandgap states.

  19. Improved solar cell based on ZnO nanowires and CdSe quantum dots

    NASA Astrophysics Data System (ADS)

    Nadarajah, Athavan; Word, Robert C.; Konenkamp, Rolf

    2010-03-01

    We report a solar cell nanostructure that incorporates CdSe quantum dots embedded in a ZnO nanowire film and a hole-conducting polymer layer. This arrangement allows for enhanced light absorption and efficient collection of the carriers. Microscopic studies show the conversion of CdSe quantum dots into an inter-connected and continuous polycrystalline thin film upon annealing in cadmium chloride ambient. This structural change of the quantum dot layer destroys the quantum confinement and improves the charge transport in the layer significantly. It also provides for improved charge transfer to the adjacent contacting layers. The optimized solar cell exhibits an external quantum efficiency of 65 percent and an energy conversion efficiency above 2 percent.

  20. Ultrafast spectroscopy of quantum confined states in a single CdSe nanowire.

    PubMed

    Schumacher, Thorsten; Giessen, Harald; Lippitz, Markus

    2013-04-10

    We measure for the first time transient absorption spectra of individual CdSe nanowires with about 10 nm diameter. Confinement of the carrier wave functions leads to discrete states which can be described by a six-band effective mass model. Combining transient absorption and luminescence spectroscopy allows us to track the excitation dynamics in the visible and near-infrared spectral range. About 10% of all absorbed photons lead to an excitation of the lowest energy state. Of these excitations, less than 1% lead to a photon in the optical far-field. Almost all emission is reabsorbed by other parts of the nanowire. These findings might explain the low overall quantum efficiency of CdSe nanowires.

  1. Ultrathin CdSe in Plasmonic Nanogaps for Enhanced Photocatalytic Water Splitting

    PubMed Central

    2015-01-01

    Enhanced plasmonic fields are a promising way to increase the efficiency of photocatalytic water splitting. The availability of atomically thin materials opens up completely new opportunities. We report photocatalytic water splitting on ultrathin CdSe nanoplatelets placed in plasmonic nanogaps formed by a flat gold surface and a gold nanoparticle. The extreme field intensity created in these gaps increases the electron–hole pair production in the CdSe nanoplatelets and enhances the plasmon-mediated interfacial electron transfer. Compared to individual nanoparticles commonly used to enhance photocatalytic processes, gap-plasmons produce several orders of magnitude higher field enhancement, strongly localized inside the semiconductor sheet thus utilizing the entire photocatalyst efficiently. PMID:25937870

  2. Reassignment of the OSe-VCd complex in CdSe

    NASA Astrophysics Data System (ADS)

    Bastin, Dirk; Lavrov, E. V.; Weber, J.

    2014-02-01

    An IR absorption study of CdSe single crystals is presented. The as-received material revealed three absorption lines at 1094.2, 1107.5, and 1126.3 cm-1, which were previously assigned to the OSe-VCd complex [G. Chen et al., Phys. Rev. Lett. 101, 195502 (2008)] We show that each of the lines is accompanied by a number of weaker satellites with intensities which match the natural abundances of sulfur isotopes. In contrast to the original identification it is suggested that these peaks are local vibrational modes of a SOn complex. The three modes correspond to different orientations of the complex in the CdSe lattice. Arguments are presented in favor of 2 oxygen atoms (n = 2) in the complex. Measurements with uniaxial stress applied to the samples revealed defect symmetries and activation energies for the defect reorientation. The complex was found to be stable up to 750 °C.

  3. Study of sub band gap absorption of Sn doped CdSe thin films

    NASA Astrophysics Data System (ADS)

    Kaur, Jagdish; Rani, Mamta; Tripathi, S. K.

    2014-04-01

    The nanocrystalline thin films of Sn doped CdSe at different dopants concentration are prepared by thermal evaporation technique on glass substrate at room temperature. The effect of Sn doping on the optical properties of CdSe has been studied. A decrease in band gap value is observed with increase in Sn concentration. Constant photocurrent method (CPM) is used to study the absorption coefficient in the sub band gap region. Urbach energy has been obtained from CPM spectra which are found to increase with amount of Sn dopants. The refractive index data calculated from transmittance is used for the identification of oscillator strength and oscillator energy using single oscillator model which is found to be 7.7 and 2.12 eV, 6.7 and 2.5 eV for CdSe:Sn 1% and CdSe:Sn 5% respectively.

  4. Synthesis of CdSe nanoparticles in the presence of aminodextran as stabilizing and capping agent.

    PubMed

    Sondi, Ivan; Siiman, Olavi; Matijević, Egon

    2004-07-15

    Water-dispersible Amdex-CdSe nanoparticle complexes with sufficient luminescence intensity were prepared at room temperature by rapidly mixing aqueous solutions of either sodium selenide or selenourea with those of cadmium chloride in the presence of amino-derivatized polysaccharides (Amdex) as stabilizing agent. It was shown that the size of CdSe crystallites decreased with increasing content of the polymer in the precipitation process. When present in a sufficient amount, Amdex was found to be an effective stabilizing and capping agent, producing CdSe nanocrystals of weak-to-medium luminescence intensity (maximum room temperature quantum yields of 15-16%). Furthermore, Amdex has proven to be an effective protective agent against photochemical degradation.

  5. Generation of fluorescent CdSe nanocrystals by short-pulse laser fragmentation

    NASA Astrophysics Data System (ADS)

    Zholudov, Yu. T.; Sajti, C. L.; Slipchenko, N. N.; Chichkov, B. N.

    2015-12-01

    A simple liquid-phase laser fragmentation approach, resulting in the rapid transformation of CdSe microcrystals into colloidal quantum dots (QDs), is presented. Laser fragmentation is achieved by irradiating a CdSe suspension in dimethylformamide with intense infrared, picosecond laser pulses followed by surface passivation with oleylamine or different types of phosphines. The generated QDs reveal perfect colloidal stability preventing agglomeration and precipitation, and show characteristic QD absorption and fluorescence characteristics, whereas their emission properties strongly depend on the surface states and applied capping ligands. These QDs show distinct photoemission under 405-nm single-photon and 800-nm multi-photon excitations in the 560- to 610-nm spectral region corresponding to the QDs size of about 1.5-2 nm in diameter which is confirmed by transmission electron microscopy.

  6. Photoelectrochemical properties of CdSe /SUB x/ Te /SUB 1-x/ semiconducting solid solutions

    SciTech Connect

    Kolbasov, G.Y.; Karpov, I.I.; Khanat, L.N.; Pavelets, A.M.

    1986-03-01

    This paper studies the photoelectrochemical properties of polycrystalline films of CdSe /SUB x/ Te /SUB 1-x/ solid solutions at x between 0.5 and 0.8. The spectral dependence of photolectro-chemical current is shown measured with a constant number of light quanta striking CdSe /SUB x/ Te /SUP 1-x/ electrodes with compositions. The results obtained indicate that there is no change in potential drop across the Helmholtz layer when the intensity of the light striking the sample is varied, and that ohmic losses at the photoelectrode are low for the light intensities used. Recombination-type losses of the photogenerated carriers which increae with decreasing superficial band bending are chiefly responsible for the decrease in photocurrent.

  7. Direct growth of CdSe semiconductor quantum dots in glass matrix by femtosecond laser beam

    NASA Astrophysics Data System (ADS)

    Bell, G.; Filin, A. I.; Romanov, D. A.; Levis, R. J.

    2016-02-01

    Controllable, spatially inhomogeneous distributions of CdSe nanocrystals smaller than the exciton Bohr radius are grown in a glass matrix under combined action of sample heating (below the transformation temperature) and focused high-repetition femtosecond (fs) laser beam. Selective quantum dot precipitation is evidenced by position-dependent absorption and Raman spectra. The particle size is estimated as r = 2.1 ± 0.3 nm by comparing the measured absorption and Raman spectra with those obtained from the samples grown in glass by traditional heat-treatment procedure. Direct growth of CdSe quantum dots in glass is enabled by nonlinear excitation using a focused fs duration laser beam (as differentiated from other methods), and this opens an avenue for adjustable selective growth patterns.

  8. Enhancement of Photoluminescence Intensity of CdSe Nanorods Doped in Cholesteric Liquid Crystals

    NASA Astrophysics Data System (ADS)

    Huang, Chiu-Chang; Chou, Tsu-Ruey; Chen, Jun-Wei; Chao, Chih-Yu

    2015-02-01

    The enhancement of photoluminescence (PL) signals of CdSe nanorods caused by embedding in the cholesteric liquid crystals (CLCs) is demonstrated in this article. Three kinds of different CLCs have been used in this experiment, and the results have shown that the phenomenon of PL enhancement generally occurs in each sample. Moreover, the relations between the enhancement and the pitch of CLCs have been analyzed as well. It displays an inversely proportional property, that is, a greater enhancement of the PL signal is achieved in the samples with shorter pitches of CLCs. The highest PL amplification acquired in this study is 3.31 times. The enhancement phenomenon is attributed to the presence of oily streaks in CLCs, which possess advantages due to the excitation of CdSe nanorods. With the versatile properties that CLC have, this study suggests that the method could provide a potential way for PL signal manipulation in many optical fields.

  9. Direct observation of electron-to-hole energy transfer in CdSe quantum dots.

    PubMed

    Hendry, E; Koeberg, M; Wang, F; Zhang, H; de Mello Donegá, C; Vanmaekelbergh, D; Bonn, M

    2006-02-10

    We independently determine the subpicosecond cooling rates for holes and electrons in CdSe quantum dots. Time-resolved luminescence and terahertz spectroscopy reveal that the rate of hole cooling, following photoexcitation of the quantum dots, depends critically on the electron excess energy. This constitutes the first direct, quantitative measurement of electron-to-hole energy transfer, the hypothesis behind the Auger cooling mechanism proposed in quantum dots, which is found to occur on a 1 +/- 0.15 ps time scale.

  10. A mirage study of CdSe colloidal quantum dot films, Urbach tail, and surface states.

    PubMed

    Guyot-Sionnest, Philippe; Lhuillier, Emmanuel; Liu, Heng

    2012-10-21

    Thermal deflection spectroscopy allows to measure very small absorption and uncovers absorption tails extending well below the bulk bandgap energy for CdSe quantum dots films after ligand exchange by sulfide. In this monodispersed system, the redshift, the broadening, and the absorption tails cannot be solely attributed to electronic coupling between the dots. Instead, mixing of hole states from the quantum dot and surface is proposed to dominate the changes of the interband spectra at the absorption edge.

  11. A mirage study of CdSe colloidal quantum dot films, Urbach tail, and surface states

    NASA Astrophysics Data System (ADS)

    Guyot-Sionnest, Philippe; Lhuillier, Emmanuel; Liu, Heng

    2012-10-01

    Thermal deflection spectroscopy allows to measure very small absorption and uncovers absorption tails extending well below the bulk bandgap energy for CdSe quantum dots films after ligand exchange by sulfide. In this monodispersed system, the redshift, the broadening, and the absorption tails cannot be solely attributed to electronic coupling between the dots. Instead, mixing of hole states from the quantum dot and surface is proposed to dominate the changes of the interband spectra at the absorption edge.

  12. Understanding the isothermal growth kinetics of cdse quantum dots through microfluidic reactor assisted combinatorial synthesis

    NASA Astrophysics Data System (ADS)

    Swain, Basudev; Hong, Myung Hwan; Kang, Lee-Seung; Lee, Chan Gi

    2016-11-01

    With the use of a microfluidic-assisted combinatorial reactor, the synthesis of CdSe quantum dots was optimized by varying one parameter at a time, and the isothermal growth kinetics of CdSe quantum dots using various models was analyzed. To understand precisely the nucleation and growth characteristics of CdSe quantum dots (QDs), we synthesized the CdSe QDs using various experimental conditions. Different model equations, like acceleratory growth-time curves, sigmoidal growth-time curves or Johnson-Mehl-Avrami-Kolmogorov (JMAK), acceleratory growthtime curves based on diffusion, geometric model growth-time curves, and nth order growth-time curves were fitted. Among all growth models, the JMAK model with α = 1 - {e^{ - {{(kt)}^n}}}, and n = 1 was the best fitting model with the MATLAB interactive curve-fitting procedure were used. Errors associated with the best-fitting model and statistics for the goodness of fit were analyzed. Most of the models were not as good as the other than the proposed model. The errors associated with the proposed model were minimal, and the growth kinetics and other associated statistical factors are very similar, for all the variables investigated. The minimal error associated with the reproducibility and the similar data for growth kinetics for all studied parameters indicated that microfluidic-assisted combinatorial synthesis can be used in the industrial production of QDs. By using the proposed model to obtain an understanding of growth of QDs, their size and properties can be managed and simulated.

  13. Excitation enhancement of CdSe quantum dots by single metal nanoparticles

    NASA Astrophysics Data System (ADS)

    Chen, Yeechi; Munechika, Keiko; Jen-La Plante, Ilan; Munro, Andrea M.; Skrabalak, Sara E.; Xia, Younan; Ginger, David S.

    2008-08-01

    We study plasmon-enhanced fluorescence from CdSe /CdS/CdZnS/ZnS core/shell quantum dots near a variety of Ag and Au nanoparticles. The photoluminescence excitation (PLE) spectrum of quantum dots closely follows the localized surface plasmon resonance (LSPR) scattering spectrum of the nanoparticles. We measure excitation enhancement factors of ˜3 to 10 for different shapes of single metal nanoparticles.

  14. Wire-supported CdSe nanowire array photoelectrochemical solar cells.

    PubMed

    Zhang, Luhui; Shi, Enzheng; Li, Zhen; Li, Peixu; Jia, Yi; Ji, Chunyan; Wei, Jinquan; Wang, Kunlin; Zhu, Hongwei; Wu, Dehai; Cao, Anyuan

    2012-03-14

    Previous fiber-shaped solar cells are based on polymeric materials or dye-sensitized wide band-gap oxides. Here, we show that efficient fiber solar cells can be made from semiconducting nanostructures (e.g. CdSe) with smaller band-gap as the light absorption material. We directly grow a vertical array of CdSe nanowires uniformly around a core metal wire and make the device by covering the top of nanowires with a carbon nanotube (CNT) film as the porous transparent electrode. The CdSe-CNT fiber solar cells show power conversion efficiencies of 1-2% under AM 1.5 illumination after the nanowires are infiltrated with redox electrolyte. We do not use a secondary metal wire (e.g. Pt) as in conventional fiber-shaped devices, instead, the end part of the CNT film is condensed into a conductive yarn to serve as the secondary electrode. In addition, our CdSe nanowire-based photoelectrochemical fiber solar cells maintain good flexibility and stable performance upon rotation and bending to large angles.

  15. Photosensitization of ZnO nanowires with CdSe quantum dots for photovoltaic devices.

    PubMed

    Leschkies, Kurtis S; Divakar, Ramachandran; Basu, Joysurya; Enache-Pommer, Emil; Boercker, Janice E; Carter, C Barry; Kortshagen, Uwe R; Norris, David J; Aydil, Eray S

    2007-06-01

    We combine CdSe semiconductor nanocrystals (or quantum dots) and single-crystal ZnO nanowires to demonstrate a new type of quantum-dot-sensitized solar cell. An array of ZnO nanowires was grown vertically from a fluorine-doped tin oxide conducting substrate. CdSe quantum dots, capped with mercaptopropionic acid, were attached to the surface of the nanowires. When illuminated with visible light, the excited CdSe quantum dots injected electrons across the quantum dot-nanowire interface. The morphology of the nanowires then provided the photoinjected electrons with a direct electrical pathway to the photoanode. With a liquid electrolyte as the hole transport medium, quantum-dot-sensitized nanowire solar cells exhibited short-circuit currents ranging from 1 to 2 mA/cm2 and open-circuit voltages of 0.5-0.6 V when illuminated with 100 mW/cm2 simulated AM1.5 spectrum. Internal quantum efficiencies as high as 50-60% were also obtained.

  16. Photocatalytic Hydrogen Generation Efficiencies in One-Dimensional CdSe Heterostructures.

    PubMed

    Tongying, Pornthip; Plashnitsa, Vladimir V; Petchsang, Nattasamon; Vietmeyer, Felix; Ferraudi, Guillermo J; Krylova, Galyna; Kuno, Masaru

    2012-11-01

    To better understand the role nanoscale heterojunctions play in the photocatalytic generation of hydrogen, we have designed several model one-dimensional (1D) heterostructures based on CdSe nanowires (NWs). Specifically, CdSe/CdS core/shell NWs and Au nanoparticle (NP)-decorated core and core/shell NWs have been produced using facile solution chemistries. These systems enable us to explore sources for efficient charge separation and enhanced carrier lifetimes important to photocatalytic processes. We find that visible light H2 generation efficiencies in the produced hybrid 1D structures increase in the order CdSe < CdSe/Au NP < CdSe/CdS/Au NP < CdSe/CdS with a maximum H2 generation rate of 58.06 ± 3.59 μmol h(-1) g(-1) for CdSe/CdS core/shell NWs. This is 30 times larger than the activity of bare CdSe NWs. Using femtosecond transient differential absorption spectroscopy, we subsequently provide mechanistic insight into the role nanoscale heterojunctions play by directly monitoring charge flow and accumulation in these hybrid systems. In turn, we explain the observed trend in H2 generation rates with an important outcome being direct evidence for heterojunction-influenced charge transfer enhancements of relevant chemical reduction processes.

  17. Radial Electron Momentum Densities of Colloidal CdSe Nanocrystals Determined by Positron Beam Analysis

    SciTech Connect

    Denison, A B; Meulenberg, R; Eijt, S W H; Van Veen, A; Mijnarends, P E; Barbiellini, B; Bansil, A; Fischer, C; Weber, M H; Lynn, K G

    2003-07-31

    We present depth-resolved positron 2D angular correlation of annihilation radiation (2DACAR) experiments on CdSe quantum dots in the diameter range from 2.5 to 6 nm, deposited as micrometer thin layers. The average radial distribution of the valence electron momentum density (EMD) of CdSe quantum dots has been extracted, which reveals a systematic dependence upon particle size. The quantum confinement related changes and their size scaling observable at the Jones zone momentum of {approx}0.8 a.u. seem to agree with the previous coincidence Doppler study. In addition, the average radial EMD shows an increase in the low-momentum range (<0.6 a.u.) and a reduction in the high-momentum range (>1.6 a.u.) with respect to that measured on a bulk CdSe single crystal. Possible origins of these are described. First-principles calculations based on the Korringa-Kohn-Rostoker (KKR) method were performed to gain a better insight.

  18. Interaction of the CdSe quantum dots with plant cell walls.

    PubMed

    Djikanović, Daniela; Kalauzi, Aleksandar; Jeremić, Milorad; Xu, Jianmin; Mićić, Miodrag; Whyte, Jeffrey D; Leblanc, Roger M; Radotić, Ksenija

    2012-03-01

    There is an increasing application of quantum dots (QDs) in plant science, as markers for the cells or their cell walls (CWs). In a plant cell the CW is a first target place for external agents. We studied interaction of CdSe QDs with CWs isolated from a conifer -Picea omorika (Panč) Purkynĕ branch. Binding of CdSe QDs was followed by using fluorescence microscopy, fluorescence and FT-IR spectroscopy. The aim of the study was to see whether the QDs induce structural changes in the CW, as well as to find out which kind of interactions between QDs and CWs occur and to which particular constituent polymers QDs preferably bind. The isolated CW is an appropriate object for study of the interactions with nanoparticles. The results show that in the CW, CdSe predominantly binds to cellulose, via OH groups and to lignin, via the conjugated CC/C-C chains. The differences in interaction of wet and dry CWs with QDs/chloroform were also studied. In the reaction of the dry CW sample with QDs/chloroform, hydrophobic interactions are dominant. When water was added after QDs/chloroform, hydrophilic interactions enable a partial reconstruction of the CC chains. The results have an implication on the use of the QDs in plant bio-imaging.

  19. Conduction band offset determination between strained CdSe and ZnSe layers using DLTS

    NASA Astrophysics Data System (ADS)

    Rangel-Kuoppa, Victor-Tapio

    2013-12-01

    The conduction band offset between strained CdSe layers embedded in unintentionally n-type doped ZnSe is measured and reported. Two samples, consisting of thirty Ultra Thin Quantum Wells (UTQWs) of CdSe embedded in ZnSe, grown by Atomic Layer Epitaxy, are used for this study. The thicknesses of the UTQWs are one and three monolayers (MLs) in each sample, respectively. As expected, the sample with one ML UTQWs does not show any energy level in the UTQWs due to the small thickness of the UTQWs, while the thickness of the sample with 3 ML UTQWs is large enough to form an energy level inside the UTQWs. This energy level appears as a majority trap with an activation energy of 223.58 ± 9.54 meV. This corresponds to UTQWs with barrier heights (the conduction band offset) between 742 meV and 784 meV. These values suggest that the band gap misfit between strained CdSe and ZnSe is around 70.5 to 74 % in the conduction band.

  20. Large stokes shift of Ag doped CdSe quantum dots via aqueous route.

    PubMed

    Huang, Jian; Jiang, Yang; Duan, Hongyan; Liu, Chao; Mi, Longfei; Lan, Xinzheng; Zhou, Hongyang; Zhong, Honghai

    2013-10-01

    Monodispersed and luminescent Ag-doped CdSe semiconductor quantum dots (d-dots) were synthesized by an aqueous route assisted with electrochemical preparation of Se source with 3-mercaptopropionic acid as stabilizer. The silver dopants were incorporated into the host crystals via cation-exchange mechanism. X-ray diffraction patterns revealed that the as-synthesized CdSe:Ag d-dots were well retained in the zinc blende structure. The CdSe:Ag d-dots that exhibited uniform size distribution and good crystallnity could be observed by High-resolution transmission electron microscopy (HRTEM), with average diameter of 2.7 nm. Successful doping was confirmed by X-ray photoelectron spectroscopy survey spectra. The peculiar Ag-related photoluminescence showed strong intensity, and at the same time, intrinsic band-edge exciton emission of CdSe QDs was suppressed. The dopant emission exhibited larger Stockes shift of - 0.51 eV than that of the band-gap emission, and varied from 546 to 583 nm by changing electrolytic time. Possible radiative recombination mechanism of the aqueous Ag-doped CdSe d-dots was discussed. The results demonstrated that doping can be an effective way to manipulate the optical properties of semiconductor nanocrystals.

  1. Conduction band offset determination between strained CdSe and ZnSe layers using DLTS

    SciTech Connect

    Rangel-Kuoppa, Victor-Tapio

    2013-12-04

    The conduction band offset between strained CdSe layers embedded in unintentionally n-type doped ZnSe is measured and reported. Two samples, consisting of thirty Ultra Thin Quantum Wells (UTQWs) of CdSe embedded in ZnSe, grown by Atomic Layer Epitaxy, are used for this study. The thicknesses of the UTQWs are one and three monolayers (MLs) in each sample, respectively. As expected, the sample with one ML UTQWs does not show any energy level in the UTQWs due to the small thickness of the UTQWs, while the thickness of the sample with 3 ML UTQWs is large enough to form an energy level inside the UTQWs. This energy level appears as a majority trap with an activation energy of 223.58 ± 9.54 meV. This corresponds to UTQWs with barrier heights (the conduction band offset) between 742 meV and 784 meV. These values suggest that the band gap misfit between strained CdSe and ZnSe is around 70.5 to 74 % in the conduction band.

  2. Analysis of the effects of surface chemistry on the XAS spectra of CdSe nanomaterials

    NASA Astrophysics Data System (ADS)

    Whitley, Heather; Prendergast, David; Ogitsu, Tadashi; Schwegler, Eric

    2010-03-01

    X-ray absorption spectroscopy (XAS) is an element-specific probe of local electronic structure, and is an ideal method to analyze chemical bonding. We investigate the consistency of theoretically predicted structures of CdSe nanomaterials with recently measured XAS via ab initio calculations. Using plane-wave DFT, the x-ray absorption cross-section for the Cd L3-edge of small CdSe clusters with a variety of surface ligands is calculated. We also highlight the importance of including excitonic effects in our simulations of core excitation spectra. We compare our simulations to existing experimental data on the ligand dependence of XAS for ligated quantum dots up to ˜3nm in diameter. Based on the favorable comparison of our theoretical spectra with experimental measurements, we infer the validity of our DFT-derived structure and surface passivation for these quantum dots and its relevance to understanding optoelectronic properties of solution-synthesized CdSe nanocrystals. Prepared by LLNL under Contract DE-AC52-07NA27344.

  3. Atomistic Analysis of Room Temperature Quantum Coherence in Two-Dimensional CdSe Nanostructures.

    PubMed

    Pal, Sougata; Nijjar, Parmeet; Frauenheim, Thomas; Prezhdo, Oleg V

    2017-03-02

    Recent experiments on CdSe nanoplatelets synthesized with precisely controlled thickness that eliminates ensemble disorder have allowed accurate measurement of quantum coherence at room temperature. Matching exactly the CdSe cores of the experimentally studied particles and considering several defects, we establish the atomistic origins of the loss of coherence between heavy and light hole excitations in two-dimensional CdSe and CdSe/CdZnS core/shell structures. The coherence times obtained using molecular dynamics based on tight-binding density functional theory are in excellent agreement with the measured values. We show that a long coherence time is a consequence of both small fluctuations in the energy gap between the excited state pair, which is much less than thermal energy, and a slow decay of correlation between the energies of the two states. Anionic defects at the core/shell interface have little effect on the coherence lifetime, while cationic defects strongly perturb the electronic structure, destroying the experimentally observed coherence. By coupling to the same phonon modes, the heavy and light holes synchronize their energy fluctuations, facilitating long-lived coherence. We further demonstrate that the electronic excitations are localized close to the surface of these narrow nanoscale systems, and therefore, they couple most strongly to surface acoustic phonons. The established features of electron-phonon coupling and the influence of defects, surfaces, and core/shell interfaces provide important insights into quantum coherence in nanoscale materials in general.

  4. Optical properties of P3HT:tributylphosphine oxide-capped CdSe nanocomposites

    NASA Astrophysics Data System (ADS)

    Benchaabane, A.; Ben Hamed, Z.; Lahmar, A.; Sanhoury, M. A.; Kouki, F.; Zellama, K.; Zeinert, A.; Bouchriha, H.

    2016-08-01

    The optical properties of nanocomposite layers prepared by incorporation of tributylphosphine oxide (TBPO)-capped CdSe nanocrystals (NCs) in a P3HT polymer matrix are studied using different nanocrystal concentrations. Reflection spectra analyzed through Kim oscillator model lead to the determination of optical constants such as refractive index n, extinction coefficient k, dielectric permittivity ɛ and absorption coefficient α.Using the common Cauchy, Drude-Lorentz, Tauc and single-effective-oscillator theoretical models, we have determined the values of static refractive index n s and permittivity ɛ s, plasma frequency ω_{{p}}, carrier density N, optical band gap E g and oscillator and dispersion energies E0 and E d, respectively. It is found that TBPO-capped CdSe NCs concentration affects the optoelectronic parameters of the nanocomposite thin films. Moreover, the disorder of this hybrid system is also studied by the determination of Urbach energy, which increases with TBPO-capped CdSe concentration.

  5. Electrochemiluminescent detection of Pb2+ by graphene/gold nanoparticles and CdSe quantum dots

    NASA Astrophysics Data System (ADS)

    Lu, Liping; Guo, Linqing; Li, Jiao; Kang, Tianfang; Cheng, Shuiyuan

    2016-12-01

    A highly sensitive electrochemiluminescent detection method for lead ions (Pb(II)) was fabricated based on the distance-dependent quenching of the electrochemiluminescence from CdSe quantum dots by nanocomposites of graphene and gold nanoparticles. Graphene/gold nanoparticles were electrochemically deposited onto a glassy carbon electrode through the constant potential method. Thiol-labeled DNA was then assembled on the surface of the electrode via gold-sulfur bonding, following which the amino-labeled terminal of the DNA was linked to carboxylated CdSe quantum dots by the formation of amide bonds. The 27-base aptamer was designed with two different domains: the immobilization and detection sequences. The immobilization sequence was paired with 12 complementary bases and immobilized on the gold electrode; the single-stranded detection sequence, rich in G bases, formed a G-quadruplex (G4) structure in the presence of Pb2+. The formation of G4 shortens the distance between the CdSe quantum dots and the Au electrode, which decreases the electrochemiluminescent intensity in a linear fashion, proportional to the concentration of Pb(II). The linear range of the sensor was 10-10 to 10-8 mol/L (R = 0.9819) with a detection limit of 10-10 mol/L. This sensor detected Pb(II) in real water samples with satisfactory results.

  6. Cytotoxicity and fluorescence studies of silica-coated CdSe quantum dots for bioimaging applications

    NASA Astrophysics Data System (ADS)

    Vibin, Muthunayagam; Vinayakan, Ramachandran; John, Annie; Raji, Vijayamma; Rejiya, Chellappan S.; Vinesh, Naresh S.; Abraham, Annie

    2011-06-01

    The toxicological effects of silica-coated CdSe quantum dots (QDs) were investigated systematically on human cervical cancer cell line. Trioctylphosphine oxide capped CdSe QDs were synthesized and rendered water soluble by overcoating with silica, using aminopropyl silane as silica precursor. The cytotoxicity studies were conducted by exposing cells to freshly synthesized QDs as a function of time (0-72 h) and concentration up to micromolar level by Lactate dehydrogenase assay, MTT [3-(4,5-Dimethylthiazol-2-yl)-2,5-Diphenyltetrazolium Bromide] assay, Neutral red cell viability assay, Trypan blue dye exclusion method and morphological examination of cells using phase contrast microscope. The in vitro analysis results showed that the silica-coated CdSe QDs were nontoxic even at higher loadings. Subsequently the in vivo fluorescence was also demonstrated by intravenous administration of the QDs in Swiss albino mice. The fluorescence images in the cryosections of tissues depicted strong luminescence property of silica-coated QDs under biological conditions. These results confirmed the role of these luminescent materials in biological labeling and imaging applications.

  7. Detection of CdSe quantum dot photoluminescence for security label on paper

    SciTech Connect

    Isnaeni, Sugiarto, Iyon Titok; Bilqis, Ratu; Suseno, Jatmiko Endro

    2016-02-08

    CdSe quantum dot has great potential in various applications especially for emitting devices. One example potential application of CdSe quantum dot is security label for anti-counterfeiting. In this work, we present a practical approach of security label on paper using one and two colors of colloidal CdSe quantum dot, which is used as stamping ink on various types of paper. Under ambient condition, quantum dot is almost invisible. The quantum dot security label can be revealed by detecting emission of quantum dot using photoluminescence and cnc machine. The recorded quantum dot emission intensity is then analyzed using home-made program to reveal quantum dot pattern stamp having the word ’RAHASIA’. We found that security label using quantum dot works well on several types of paper. The quantum dot patterns can survive several days and further treatment is required to protect the quantum dot. Oxidation of quantum dot that occurred during this experiment reduced the emission intensity of quantum dot patterns.

  8. Electrogenerated chemiluminescence from a CdSe nanocrystal film and its sensing application in aqueous solution.

    PubMed

    Zou, Guizheng; Ju, Huangxian

    2004-12-01

    Electrogenerated chemiluminescence (ECL) of semiconductor quantum dots in aqueous solutions and its first sensing application were studied by depositing CdSe nanocrystals (NCs) on a paraffin-impregnated graphite electrode (PIGE). The CdSe nanocrystal thin film exhibited two ECL peaks at -1.20 (ECL-1) and -1.50 V (ECL-2) in pH 9.3, 0.1 M PBS during the cyclic sweep between 0 and -1.8 V at 20 mV s(-1). The electron-transfer reaction between individual electrochemically reduced nanocrystal species and oxidant coreactants such as H(2)O(2) and reduced dissolved oxygen led to ECL-1. When mass NCs packed densely in the film were reduced electrochemically, assembly of reduced nanocrystal species could react with coreactants to produce another ECL signal, ECL-2. ECL-1 showed higher sensitivity to the concentration of oxidant coreactants than ECL-2 and thus was used for ECL detection of coreactant, H(2)O(2). A linear response of ECL-1 to H(2)O(2) was observed in the concentration range of 2.5 x 10(-7)-6 x 10(-5) M with a detection limit of 1.0 x10(-7) M. The fabrication of 10 CdSe nanocrystal thin-film modified PIGEs displayed an acceptable reproducibility with a RSD of 1.18% obtained at H(2)O(2) level of 10 microM.

  9. Inverted organic solar cells using a solution-processed TiO2/CdSe electron transport layer to improve performance

    NASA Astrophysics Data System (ADS)

    Ma, Xiaoxiao; Xiong, Zhicheng; Wang, Wen; Zhang, Luming; Wu, Sujuan; Lu, Xubing; Gao, Xingsen; Shui, Lingling; Liu, Jun-Ming

    2016-04-01

    In the present work, cadmium selenide (CdSe) nanoparticles are deposited directly on TiO2 film to fabricate the TiO2/CdSe interlayer by a chemical bath deposition method. The inverted organic solar cells using poly(3-hexylthiophene) (P3HT) and [6,6]-phenyl C61 butyric acid methyl ester (PCBM) bulk heterojunction as an active layer and TiO2/CdSe interlayer as an electron transport layer (ETL) are fabricated in air. A series of microstructural, photo-electronic, and electrochemical characterizations on these cells are performed. The TiO2/CdSe structure with respect to either the TiO2 layer or the CdSe layer as the ETL exhibits significantly enhanced external quantum efficiency (EQE) in the visible region. The photoluminescence (PL) measurement shows that the exciton dissociation in the TiO2/CdSe structure is more effective than that in either the TiO2 or CdSe structure. The Nyquist plots obtained from electrochemical impedance spectroscopy (EIS) implies that the charge recombination in the TiO2/CdSe structure can be suppressed with respect to that in either the CdSe or TiO2 structure. The photovoltaic performances of the cells with the TiO2/CdSe ETL are clearly improved compared with the reference cells only with the TiO2 layer or CdSe layer as the ETL.

  10. Electrochemical synthesis of morphology-controlled segmented CdSe nanowires.

    PubMed

    Shpaisman, Nava; Givan, Uri; Patolsky, Fernando

    2010-04-27

    Morphology, that is, the study of form comprising shape, size, and structure, is important for materials research in general. For nanostructured materials, popularly known as nanomaterials, morphology has a special significance since form, in this case, dictates physical and chemical properties. Unlike bulk materials, properties of nanomaterials are strongly correlated to form. Here, we present a novel strategy for the synthesis of morphology-controlled segmented CdSe semiconductor nanowires based on a straightforward sweep voltammetry approach of preprogrammed characteristics. It was found here that, by simply and simultaneously modulating the basic parameters of each cyclic voltammetry cycle during the nanowire growth process, scan rate, and cycle potential range, we can achieve a precise control over the morphology of the semiconductor material segment, density, and dimensions, obtained after each voltammetric cycle. The morphology of CdSe segments was found to be controlled by the extent of co-deposition of metal cadmium together with the deposition of CdSe. Thus "dense" CdSe segments and "nondense" segments can be achieved in the absence and presence of cadmium metal co-deposition, respectively. Accompanied by the density modulation achieved by the potential range applied, it was also observed that a fine control over each segment's length, varying between few tenths to few hundred nanometers, can be achieved by simple altering the scan rate of each cycle along the wire. Also, we propose a simple mechanism that accounts for the formation of segments of controlled morphology. This is the first report on the synthesis of "segmented" CdSe nanowires of controlled morphology, density, and length of each segment, by simple single-step cycle voltammetry preprogrammed sequences from a single electrodeposition solution. In addition, this novel strategy may be applied for the synthesis of additional analogue semiconductor materials of importance (e.g., CdS, CdTe, etc

  11. Green route synthesis of high quality CdSe quantum dots for applications in light emitting devices

    SciTech Connect

    Bera, Susnata; Singh, Shashi B.; Ray, S.K.

    2012-05-15

    Investigation was made on light emitting diodes fabricated using CdSe quantum dots. CdSe quantum dots were synthesized chemically using olive oil as the capping agent, instead of toxic phosphine. Room temperature photoluminescence investigation showed sharp 1st excitonic emission peak at 568 nm. Bi-layer organic/inorganic (P3HT/CdSe) hybrid light emitting devices were fabricated by solution process. The electroluminescence study showed low turn on voltage ({approx}2.2 V) .The EL peak intensity was found to increase by increasing the operating current. - Graphical abstract: Light emitting diode was fabricated using CdSe quantum dots using olive oil as the capping agent, instead of toxic phosphine. Bi-layer organic/inorganic (P3HT/CdSe) hybrid light emitting device shows strong electroluminescence in the range 630-661 nm. Highlights: Black-Right-Pointing-Pointer CdSe Quantum dots were synthesized using olive oil as the capping agent. Black-Right-Pointing-Pointer Light emitting device was fabricated using CdSe QDs/P3HT polymer heterojunction. Black-Right-Pointing-Pointer The I-V characteristics study showed low turn on voltage at {approx}2.2 V. Black-Right-Pointing-Pointer The EL peak intensity increases with increasing the operating current.

  12. Chemically synthesized CdSe quantum dots inhibit growth of human lung carcinoma cells via ROS generation

    PubMed Central

    Jigyasu, Aditya Kumar; Siddiqui, Sahabjada; Lohani, Mohatashim; Khan, Irfan Ali; Arshad, Md

    2016-01-01

    Quantum dots (QDs), semiconducting materials have potential applications in the field of electronic and biomedical applications including cancer therapy. In present study, cadmium selenide (CdSe) QDs were synthesized by chemical method. Octadecene was used as non-coordinating solvent which facilitated the formation of colloidal solutions of nanoparticles. CdSe QDs were characterized by UV-vis spectrometer and transmission electron microscope (TEM). The size measured by TEM was varied between 2-5 nm depending upon temperature. The cytotoxic activity of QDs was monitored by MTT assay, nuclear condensation, ROS activity and DNA fragmentation assay on human lung epithelial A549 cell line. Cells were treated with different concentrations of varying size of CdSe QDs for 24 h. CdSe QDs induced significant (p < 0.05) dose dependent cytotoxicity and this was comparable to the sizes of particles. Smaller particles were more cytotoxic to the large particles. Fluorescence microscopic analysis revealed that QDs induced oxidative stress generating significant ROS level and consequently, induced nuclear condensation and DNA fragmentation. Study suggested the cytotoxicity of CdSe QDs via ROS generation and DNA fragmentation depending upon particles size. PMID:27047318

  13. Effect of surface passivating ligand on structural and optoelectronic properties of polymer : CdSe quantum dot composites

    NASA Astrophysics Data System (ADS)

    Kumari, Kusum; Kumar, Umesh; Sharma, Shailesh N.; Chand, Suresh; Kakkar, Rita; Vankar, V. D.; Kumar, Vikram

    2008-12-01

    We demonstrate the effect of surface passivation of cadmium selenide quantum dots (CdSe QDs) (~5-7 nm) by tri-n-octylphosphene-oxide (TOPO) and oleic acid (OA) on the structural and optoelectronic properties of their respective polymer : CdSe composites by dispersing them in poly(2-methoxy-5(2-ethylhexyloxy)-1,4-phenylinevinylene) and poly(3-hexylthiophene) polymers. It has been found that OA passivated-QDs (~7 nm), as compared with TOPO passivated CdSe QDs (~5 nm), are of (i) high quality that provide better steric stability against coagulation, homogeneity and photostability to their respective polymer : CdSe composites, (ii) show low value of Stern-Volmer quenching constant (KSV) calculated from photoluminescence quenching measurements. These effects have been attributed to (i) CdSe(OA) (~7 nm) particles having relatively smaller surface energies compared with CdSe(TOPO) (~5 nm) particles thus showing lesser quenching capabilities (ii) dominance of respective processes of photoinduced Förster energy transfer between host polymer (donors) and guest CdSe nanocrystals (acceptors) in polymer : CdSe(OA) composites and charge transfer in polymer : CdSe(TOPO) composites.

  14. Controlling the cytotoxicity of CdSe magic-sized quantum dots as a function of surface defect density.

    PubMed

    Silva, Anielle Christine Almeida; Silva, Marcelo José Barbosa; da Luz, Felipe Andrés Cordero; Silva, Danielle Pereira; de Deus, Samantha Luara Vieira; Dantas, Noelio Oliveira

    2014-09-10

    Quantum dots are potentially very useful as fluorescent probes in biological systems. However, they are inherently cytotoxic because of their constituents. We controlled the cytotoxicity of CdSe magic-sized quantum dots (MSQDs) as a function of surface defect density by altering selenium (Se) concentration during synthesis. Higher Se concentrations reduced the cytotoxicity of the CdSe MSQDs and diminished mRNA expression of methallothionein because of the low cadmium ions (Cd(2+)) concentration adsorbed on the surface of the MSQDs. These results agree with luminescence spectra, which show that higher Se concentrations decrease the density of surface defects. Therefore, our results describe for the first time a simple way of controlling the cytotoxicity of CdSe MSQDs and making them safer to use as fluorescence probes in biological systems.

  15. Comparative behavior of CdS and CdSe quantum dots in poly(3-hexylthiophene) based nanocomposites

    SciTech Connect

    Sonar, Prashant . E-mail: sonar@mat.ethz.ch; Sreenivasan, K.P.; Madddanimath, Trupti; Vijayamohanan, K. . E-mail: viji@ems.ncl.res.in

    2006-01-05

    CdS and CdSe nanoparticles have been prepared using conducting poly(3-hexylthiophene) (P3HT) matrix with an objective to understand the effect of nanoparticles on the polymer matrix using electrochemical and spectroscopic techniques. The spectroscopic results reveal that the electronic structure of polymer is strongly influenced by the characteristics of embedded semiconducting nanoparticles. SEM and TEM images show the ordered morphology of the CdS and CdSe nanoparticles in presence of the polymer matrix. Cyclic voltammetry performed both in the presence and absence of light enables us to understand the redox changes in P3HT due to CdS and CdSe quantum dots such as the generation of free radical in the excited state and their electrochemical band gaps.

  16. Electronic structure and optical absorption spectra of CdSe covered with ZnSe and ZnS epilayers

    NASA Astrophysics Data System (ADS)

    Yun, So Jeong; Lee, Geunsik; Kim, Jai Sam; Shin, Seung Koo; Yoon, Young-Gui

    2006-02-01

    Using the first-principles methods we compute the electronic structure and the absorption spectra for a wurtzite CdSe (0001) slab covered with zincblende ZnSe and ZnS epilayers. For each structure we compute the DOS and the imaginary part of the dielectric function. We find that the semiconductor passivation shifts the 'near Fermi-level' states of the bare CdSe slab down to lower energy levels. The migration suggests the decrease of surface effects and energy loss. We observe the substantial reduction of the abnormal peaks in the absorption spectra of the bare CdSe slab, which seems to be a consequence of the DOS migration. This is consistent with the experimental results that a proper passivation enhance the luminescence efficiency. We also study the case that the epilayer surface is terminated with PH 3 and find the PH 3 passivation also reduces the surface state to some extent.

  17. Diameter- and current-density-dependent growth orientation of hexagonal CdSe nanowire arrays via electrodeposition.

    PubMed

    Sun, Hongyu; Li, Xiaohong; Chen, Yan; Guo, Defeng; Xie, Yanwu; Li, Wei; Liu, Baoting; Zhang, Xiangyi

    2009-10-21

    Controlling the growth orientation of semiconductor nanowire arrays is of vital importance for their applications in the fields of nanodevices. In the present work, hexagonal CdSe nanowire arrays with various preferential growth orientations have been successfully yielded by employing the electrodeposition technique using porous alumina as templates (PATs). We demonstrate by experimental and theoretical efforts that the growth orientation of the CdSe nanowires can be effectively manipulated by varying either the nanopore diameter of the PATs or the deposited current density, which has significant effects on the optical properties of the CdSe nanowires. The present study provides an alternative approach to tuning the growth direction of electrodeposited nanowires and thus is of importance for the fabrication of nanodevices with controlled functional properties.

  18. Diameter- and current-density-dependent growth orientation of hexagonal CdSe nanowire arrays via electrodeposition

    NASA Astrophysics Data System (ADS)

    Sun, Hongyu; Li, Xiaohong; Chen, Yan; Guo, Defeng; Xie, Yanwu; Li, Wei; Liu, Baoting; Zhang, Xiangyi

    2009-10-01

    Controlling the growth orientation of semiconductor nanowire arrays is of vital importance for their applications in the fields of nanodevices. In the present work, hexagonal CdSe nanowire arrays with various preferential growth orientations have been successfully yielded by employing the electrodeposition technique using porous alumina as templates (PATs). We demonstrate by experimental and theoretical efforts that the growth orientation of the CdSe nanowires can be effectively manipulated by varying either the nanopore diameter of the PATs or the deposited current density, which has significant effects on the optical properties of the CdSe nanowires. The present study provides an alternative approach to tuning the growth direction of electrodeposited nanowires and thus is of importance for the fabrication of nanodevices with controlled functional properties.

  19. Advanced Architecture for Colloidal PbS Quantum Dot Solar Cells Exploiting a CdSe Quantum Dot Buffer Layer.

    PubMed

    Zhao, Tianshuo; Goodwin, Earl D; Guo, Jiacen; Wang, Han; Diroll, Benjamin T; Murray, Christopher B; Kagan, Cherie R

    2016-09-22

    Advanced architectures are required to further improve the performance of colloidal PbS heterojunction quantum dot solar cells. Here, we introduce a CdI2-treated CdSe quantum dot buffer layer at the junction between ZnO nanoparticles and PbS quantum dots in the solar cells. We exploit the surface- and size-tunable electronic properties of the CdSe quantum dots to optimize its carrier concentration and energy band alignment in the heterojunction. We combine optical, electrical, and analytical measurements to show that the CdSe quantum dot buffer layer suppresses interface recombination and contributes additional photogenerated carriers, increasing the open-circuit voltage and short-circuit current of PbS quantum dot solar cells, leading to a 25% increase in solar power conversion efficiency.

  20. A novel toxicity mechanism of CdSe nanoparticles to Saccharomyces cerevisiae: enhancement of vacuolar membrane permeabilization (VMP).

    PubMed

    Sun, Meiqing; Yu, Qilin; Liu, Ming; Chen, Xiaoyan; Liu, Zhe; Zhou, Hao; Yuan, Yingjin; Liu, Lu; Li, Mingchun; Zhang, Chengdong

    2014-09-05

    Cadmium selenide (CdSe) nanoparticles are implemented in a wide range of applications, but their potential risk to the ecosystem, especially to the organisms essential for the maintenance of ecosystem homeostasis, such as fungal populations, plants and bacteria, remains to be elucidated. In this study, we investigated their toxicity to one of the most important fungal model organisms, Saccharomyces cerevisiae. Growth inhibition assays revealed that the synthesized CdSe nanoparticles with the sizes of 20-30 nm had strong inhibitory effect on yeast growth (IC50=80 ppm). This toxicity was not attributed to mitochondrial dysfunction and autophagy, but was dependent on End3-mediated endocytosis, and was associated with reactive oxygen species (ROS) accumulation and an enhancement of vacuolar membrane permeabilization (VMP). These results reveal a key role of the vacuole during the interaction between CdSe nanoparticles and yeast cells.

  1. Photocurrent enhancement of SiNW-FETs by integrating protein-shelled CdSe quantum dots

    NASA Astrophysics Data System (ADS)

    Moh, Sang Hyun; Kulkarni, Atul; San, Boi Hoa; Lee, Jeong Hun; Kim, Doyoun; Park, Kwang Su; Lee, Min Ho; Kim, Taesung; Kim, Kyeong Kyu

    2016-01-01

    We proposed a new strategy to increase the photoresponsivity of silicon NW field-effect transistors (FETs) by integrating CdSe quantum dots (QDs) using protein shells (PSs). CdSe QDs were synthesized using ClpP, a bacterial protease, as protein shells to control the size and stability of QD and to facilitate the mounting of QDs on SiNWs. The photocurrent of SiNW-FETs in response to light at a wavelength of 480 nm was enhanced by a factor of 6.5 after integrating CdSe QDs because of the coupling of the optical properties of SiNWs and QDs. As a result, the photoresponsivity to 480 nm light reached up to 3.1 × 106, the highest value compared to other SiNW-based devices in the visible light range.We proposed a new strategy to increase the photoresponsivity of silicon NW field-effect transistors (FETs) by integrating CdSe quantum dots (QDs) using protein shells (PSs). CdSe QDs were synthesized using ClpP, a bacterial protease, as protein shells to control the size and stability of QD and to facilitate the mounting of QDs on SiNWs. The photocurrent of SiNW-FETs in response to light at a wavelength of 480 nm was enhanced by a factor of 6.5 after integrating CdSe QDs because of the coupling of the optical properties of SiNWs and QDs. As a result, the photoresponsivity to 480 nm light reached up to 3.1 × 106, the highest value compared to other SiNW-based devices in the visible light range. Electronic supplementary information (ESI) available: Materials and methods. See DOI: 10.1039/c5nr07901b

  2. CdSe white quantum dots-based white light-emitting diodes with high color rendering index

    NASA Astrophysics Data System (ADS)

    Su, Yu-Sheng; Hsiao, Chih-Chun; Chung, Shu-Ru

    2016-09-01

    A white light emission CdSe quantum dots (QDs) can be prepared by chemical route under 180°C. An organic oleic acid (OA) is used to react with CdO to form Cd-OA complex. Hexadecylamine (HDA) and 1-Octadecene (ODE) were used as co-surfactants. By controlling the reaction time, a white light emission CdSe QDs can be obtained after reacts for 3 to 10 min. The luminescence spectra compose two obvious emission peaks and entire visible light ranges from 400 to 650 nm. Based on TEM measurement result, spherical morphologies with particle size 2.39+/-0.27 nm can be obtained. The quantum yields (QYs) of white CdSe QD are between 20 and 60 %, which depends on reaction time. A white CdSe QDs were mixed with UV cured gel (OPAS-226) with weight ratios 50.0 wt. %, and putted the mixture into reflective cup (3020, 13 mil) as convert type. The white LEDs have controllable CIE coordinates and correlated color temperature (CCT). The luminous efficacy of the device is less than 3 lm/W, but the color rendering index (CRI) for all devices are higher than 80. Since the luminous efficacy of hybrid devices has a direct dependence on the external QY of the UV-LED as well, the luminous efficacy can be improved by well dispersion of CdSe QDs in UV gel matrix and using optimized LED chips. Therefore, in this study, we provide a new and simple method to prepare high QY of white CdSe QDs and its have a potential to applicate in solid-state lighting.

  3. Theoretical calculations of structural, electronic, and elastic properties of CdSe1-x Te x : A first principles study

    NASA Astrophysics Data System (ADS)

    M, Shakil; Muhammad, Zafar; Shabbir, Ahmed; Muhammad Raza-ur-rehman, Hashmi; M, A. Choudhary; T, Iqbal

    2016-07-01

    The plane wave pseudo-potential method was used to investigate the structural, electronic, and elastic properties of CdSe1-x Te x in the zinc blende phase. It is observed that the electronic properties are improved considerably by using LDA+U as compared to the LDA approach. The calculated lattice constants and bulk moduli are also comparable to the experimental results. The cohesive energies for pure CdSe and CdTe binary and their mixed alloys are calculated. The second-order elastic constants are also calculated by the Lagrangian theory of elasticity. The elastic properties show that the studied material has a ductile nature.

  4. Synthesis and optical characterisation of triphenylamine-based hole extractor materials for CdSe quantum dots.

    PubMed

    Planells, Miquel; Reynolds, Luke X; Bansode, Umesh; Chhatre, Shraddha; Ogale, Satishchandra; Robertson, Neil; Haque, Saif A

    2013-05-28

    We report the synthesis and optical characterisation of different triphenylamine-based hole capture materials able to anchor to CdSe quantum dots (QDs). Cyclic voltammetry studies indicate that these materials exhibit reversible electrochemical behaviour. Photoluminescence and transient absorption spectroscopy techniques are used to study interfacial charge transfer properties of the triphenylamine functionalized CdSe QDs. Specifically, we show that the functionalized QDs based on the most easily oxidised triphenylamine display efficient hole-extraction and long-lived charge separation. The present findings should help identify new strategies to control charge transfer QD-based optoelectronic devices.

  5. Dislocation-driven growth of porous CdSe nanorods from CdSe.(ethylenediamine)0.5 nanorods

    NASA Astrophysics Data System (ADS)

    Kim, Hyung-Bae; Jang, Du-Jeon

    2015-12-01

    Porous CdSe nanorods having a novel flute-like morphology have been prepared facilely via the hydrothermal treatment of CdSe.(en)0.5 (en = ethylenediamine) nanorods as sacrificial templates. During the hydrothermal process, various crystalline imperfections such as stacking faults and twinning planes appear due to lattice mismatches between orthorhombic CdSe.(en)0.5 and hexagonal wurtzite porous CdSe nanorods and subsequently disappear to release mismatched strains. In the self-healing process of defects, due to the imbalance of in-and-out atomic diffusion, point defects of atomic vacancies are heavily generated in CdSe nanorods to produce volume defects of voids eventually. The photoluminescence of CdSe nanorods shifts to the red region and decreases in intensity with the increase of the hydrolysis time as surface states and selenium vacancies increase. The mean lifetime of photoluminescence increases with the increase of the hydrothermal-treatment time as the fractional amplitude of the surface-state-related component increases.Porous CdSe nanorods having a novel flute-like morphology have been prepared facilely via the hydrothermal treatment of CdSe.(en)0.5 (en = ethylenediamine) nanorods as sacrificial templates. During the hydrothermal process, various crystalline imperfections such as stacking faults and twinning planes appear due to lattice mismatches between orthorhombic CdSe.(en)0.5 and hexagonal wurtzite porous CdSe nanorods and subsequently disappear to release mismatched strains. In the self-healing process of defects, due to the imbalance of in-and-out atomic diffusion, point defects of atomic vacancies are heavily generated in CdSe nanorods to produce volume defects of voids eventually. The photoluminescence of CdSe nanorods shifts to the red region and decreases in intensity with the increase of the hydrolysis time as surface states and selenium vacancies increase. The mean lifetime of photoluminescence increases with the increase of the hydrothermal

  6. Multicolored silica coated CdSe core/shell quantum dots

    NASA Astrophysics Data System (ADS)

    Goftman, Valentina V.; Markin, Alexey V.; De Saeger, Sarah; Goryacheva, Irina Y.

    2016-04-01

    Silanization is a convenient route to provide water-solubility to the quantum dots (QDs) with different structure. Green, orange and red emitting CdSe-based QDs were synthesized by varying of number and material of wider-band gap shells and fluorescent properties of QDs were characterized before and after silanization. It was shown that structure of the QD influences on the quantum yield of the silanized QDs: the better CdSe core is protected with wider-band gap semiconductor shells, the more fluorescence properties remain after silica coated QD possess. Hence silica coated QDs have a great perspectives for the multiplex analysis.

  7. Diameter scaling of the optical band gap in individual CdSe nanowires.

    PubMed

    Myalitsin, Anton; Strelow, Christian; Wang, Zhe; Li, Zhen; Kipp, Tobias; Mews, Alf

    2011-10-25

    The diameter dependence of the optical band gap of single CdSe nanowires (NWs) is investigated by a combination of atomic force microscopy, scanning fluorescence microscopy, and transmission electron microscopy. We find a good congruence of the experimental data to calculations within the effective mass approximation taking into account quantization, exciton Coulomb interaction, and dielectric mismatch. The experimental data are furthermore compared to different theoretical approaches. We discuss the influence of alternating wurtzite and zinc blende segments along the NWs on their optical properties.

  8. Hot spot assisted blinking suppression of CdSe quantum dots

    NASA Astrophysics Data System (ADS)

    Lu, Liu; Tong, Xuan; Zhang, Xu; Ren, Naifei; Jiang, Bo; Lu, Haifei

    2016-05-01

    This work compares the blinking of CdSe QDs on glass, single silver nanowire, and double aligned nanowires. The corresponding on-time fractions of these three cases are 50%, 70% and 85% respectively, which indicates that aligned double nanowires shows more efficient suppression than that of single nanowire. This phenomenon is attributed to the higher concentration of hot electron from hot spot between nanowires. Occupation of the non-radiative recombination centers by hot electrons from silver nanowires can be explained for the suppressed blinking behavior. The result has provided a novel pathway of suppressing the blinking behavior of QDs through plasmonic hot spot.

  9. Determination of the Exciton Binding Energy in CdSe Quantum Dots

    SciTech Connect

    Meulenberg, R; Lee, J; Wolcott, A; Zhang, J; Terminello, L; van Buuren, T

    2009-10-27

    The exciton binding energy (EBE) in CdSe quantum dots (QDs) has been determined using x-ray spectroscopy. Using x-ray absorption and photoemission spectroscopy, the conduction band (CB) and valence band (VB) edge shifts as a function of particle size have been determined and combined to obtain the true band gap of the QDs (i.e. without and exciton). These values can be compared to the excitonic gap obtained using optical spectroscopy to determine the EBE. The experimental EBE results are compared with theoretical calculations on the EBE and show excellent agreement.

  10. Selenium Redox Reactivity on Colloidal CdSe Quantum Dot Surfaces

    PubMed Central

    2016-01-01

    Understanding the structural and compositional origins of midgap states in semiconductor nanocrystals is a longstanding challenge in nanoscience. Here, we report a broad variety of reagents useful for photochemical reduction of colloidal CdSe quantum dots, and we establish that these reactions proceed via a dark surface prereduction step prior to photoexcitation. Mechanistic studies relying on the specific properties of various reductants lead to the proposal that this surface prereduction occurs at oxidized surface selenium sites. These results demonstrate the use of small-molecule inorganic chemistries to control the physical properties of colloidal QDs and provide microscopic insights into the identities and reactivities of their localized surface species. PMID:27518320

  11. Electrical conduction mechanism in annealed and light soaked silver doped CdSe thin films

    NASA Astrophysics Data System (ADS)

    Kaur, Jagdish; Tripathi, S. K.

    2015-08-01

    Thin films of silver (Ag) doped CdSe are prepared on glass substrates by thermal evaporation technique in inert gas atmosphere. SEM micrograph reveals uniform and homogenous distribution of nanoparticles on the glass substrates. The composition of the film is investigated by EDX analysis. Thin films are thermally annealed and light soaked to study the thermally and optically induced effect. Electrical conduction in annealed thin films exhibits different conduction mechanisms in low and high temperature region while conduction in light soaked thin films is single thermally activated process. The activation energies for dark and photoconductivities are also investigated.

  12. Anisotropy of optical transitions in ordered ensemble of CdSe quantum rods.

    PubMed

    Mukhina, Maria V; Maslov, Vladimir G; Baranov, Alexander V; Artemyev, Mikhail V; Orlova, Anna O; Fedorov, Anatoly V

    2013-09-01

    We report on the observation of spectral dependence of absorption anisotropy in a CdSe quantum rod (QR) ensemble, which is aligned in a polymer film with a nanocrystal concentration of 2×10(-5) M. The experimental data on the polarization direction and anisotropy factor were obtained for the lowest excitonic transition and the second group of transitions in the QR. The nonzero constant value of anisotropy was investigated for the high-energy transitions, and is evidence of the one-dimensional confinement in the QR.

  13. (Time-resolved fluorescence studies of surface recombination in CdSe electrodes)

    SciTech Connect

    Not Available

    1991-01-01

    The long range goal of our investigations is to understand the dynamics of heterogeneous electron transfer reactions. The primary method we use to monitor the carrier dynamics is the fluorescence of the bandgap emission. This all optical approach circumvents the limitations of photopotential and photocurrent methods. Before such studies on a reactive system can be informative, it is necessary to understand the dynamics of the photogenerated carriers under nonreactive conditions. Presently we are concentrating on carrier dynamics in the materials, cadmium selenide (CdSe) and cadmium sulfide (CdS). Under these conditions the carriers recombine either directly or through intragap electronic states. 2 refs., 1 fig.

  14. Optimal packing size of non-ligated CdSe nanoclusters for microstructure synthesis

    SciTech Connect

    Tefera, Anteneh G.; Mochena, Mogus D.; Johnson, Elijah; Dickerson, James

    2014-09-14

    Structural and electrostatic properties of nanoclusters of CdSe of diameter 1–2 nm are studied with first principle calculations to determine the optimal size for synthesizing microstructures. Based on robustness of the core structure, i.e., the retention of tetrahedral geometry, hexagonal ring structure, and overall wu{sup ¨}rtzite structure to surface relaxations, we conclude that nanoclusters of ~2 nm diameter are the best candidates to form a dense microstructure with minimal interstitial space. Se-terminated surfaces retain a zigzag structure as Se atoms are pulled out and Cd atoms are pulled in due to relaxation, therefore, are best suited for inter-nanocluster formations.

  15. Construction of dentate bonded TiO2-CdSe heterostructures with enhanced photoelectrochemical properties: versatile labels toward photoelectrochemical and electrochemical sensing.

    PubMed

    Gao, Picheng; Ma, Hongmin; Yan, Tao; Wu, Dan; Ren, Xiang; Yang, Jiaojiao; Du, Bin; Wei, Qin

    2015-01-14

    A facile synthetic route for TiO2-CdSe heterostructures was proposed based on dentate binding of TiO2 to carboxyl. Carboxyl functionalized CdSe quantum dots (CF-CdSe QDs) were successfully bonded onto TiO2 nanoparticles (NPs), which could significantly improve the photoelectrochemical (PEC) properties of TiO2 NPs. This is ascribed to the fact that CdSe QDs with a narrow band gap could be stimulated under visible light irradiation, and the energy levels of TiO2 NPs and CF-CdSe QDs are aligned with an electrolyte solution. High resolution transmission electron microscopy images revealed the heterostructures of the TiO2-CdSe composites. Ultraviolet visible spectroscopy, photoluminescence emission spectroscopy and electrochemical impedance spectroscopy analysis exhibited that the prepared TiO2-CdSe heterostructures have improved light absorption, charge separation efficiency and electron transfer ability in the visible light region. TiO2-CdSe heterostructures were used as versatile labels for fabrication of PEC and electrochemical immunosensors, and human immune globulin G (HIgG) was used as a model analyte. The immunosensor showed high sensitivity, a low detection limit and a wide linear range, which could be applied in practical serum sample analysis. The constructed TiO2-CdSe heterostructures would have potential applications in photocatalysis, aptasensors, cytosensors and other areas of nanotechnology.

  16. Effect of deposition temperature on the structural and optical properties of CdSe QDs thin films deposited by CBD method

    SciTech Connect

    Laatar, F.; Harizi, A.; Smida, A.; Hassen, M.; Ezzaouia, H.

    2016-06-15

    Highlights: • Synthesis of CdSe QDs with L-Cysteine capping agent for applications in nanodevices. • The films of CdSe QDs present uniform and good dispersive particles at the surface. • Effect of bath temperature on the structural and optical properties of CdSe QDs thin films. • Investigation of the optical constants and dispersion parameters of CdSe QDs thin films. - Abstract: Cadmium selenide quantum dots (CdSe QDs) thin films were deposited onto glass substrates by a chemical bath deposition (CBD) method at different temperatures from an aqueous solution containing L-Cysteine (L-Cys) as capping agent. The evolution of the surface morphology and elemental composition of the CdSe films were studied by AFM, SEM, and EDX analyses. Structural and optical properties of CdSe thin films were investigated by XRD, UV–vis and PL spectroscopy. The dispersion behavior of the refractive index is described using the single oscillator Wemple-DiDomenico (W-D) model, and the physical dispersion parameters are calculated as a function of deposition temperature. The dispersive optical parameters such as average oscillator energy (E{sub o}), dispersion energy (E{sub d}), and static refractive index (n{sub o}) were found to vary with the deposition temperature. Besides, the electrical free carrier susceptibility (χ{sub e}) and the carrier concentration of the effective mass ratio (N/m*) were evaluated according to the Spitzer-Fan model.

  17. Anisotropy of electron-phonon interaction in nanoscale CdSe platelets as seen via off-resonant and resonant Raman spectroscopy

    NASA Astrophysics Data System (ADS)

    Cherevkov, S. A.; Fedorov, A. V.; Artemyev, M. V.; Prudnikau, A. V.; Baranov, A. V.

    2013-07-01

    The off-resonant and resonant Raman spectra of optical phonons in colloidal CdSe nanoplatelets (NPLs) with the thickness of 4, 5, and 6 CdSe monolayers are analyzed. These spectra are dominated by SO and LO phonon bands of CdSe whose frequencies are thickness independent in the off-resonant Raman but demonstrate evident thickness dependence similar to that observed for confined optical phonons in CdSe quantum dots in the resonant Raman. The results show that conventional optical phonons propagating along the NPL lateral planes contribute mainly to the off-resonant Raman while confined optical phonons propagating in the perpendicular direction dominate the Raman spectra excited in the resonance with confined exciton transitions of CdSe NPLs. An anisotropic electron-phonon interaction is proposed to be responsible for this effect in the CdSe NPLs. A formation of Cd-S monolayer on the surface of CdSe NPLs treated by thiol-containing ligands is also detected in Raman spectra.

  18. Effect of air-annealing on the morphological, microstructural and optical properties of CdSe NCs grown into porous anodic alumina template

    NASA Astrophysics Data System (ADS)

    Laatar, F.; Hassen, M.; Smida, A.; Riahi, R.; Bel Haj Mohamed, N.; Ezzaouia, H.

    2015-07-01

    In this work, cadmium selenide nanocrystals (CdSe NCs) were embedded into porous anodic alumina (PAA) template by simple immersion in aqueous solution containing L-cysteine (Cys) functionalized CdSe NCs and water. The prepared samples were heat treated at different temperatures between 150 and 300 °C during 30 min under air. The effect of thermal treatment under air on the CdSe NCs/PAA has been shown from morphological, microstructural and optical studies. Several characterization techniques such as scanning electron microscopy (SEM), atomic force microscopy (AFM), and X-ray diffraction (XRD) spectroscopy were used to investigate the surface morphology and microstructural properties of CdSe nanoparticles on the PAA template as function of air-annealing temperature. XRD study shows the transformation phase of deposited CdSe nanoparticles on the PAA template from cubic structure to hexagonal structure at 300 °C. The morphology of CdSe nanorods array which are into the PAA surface were exhibited by AFM scan. Optical properties of CdSe NCs into PAA have been studied at different air-annealing temperatures using optical absorption and photoluminescence (PL) spectroscopy. The results showed that the crystal quality was significantly improved with the annealing temperature increase, bringing about an enhancement in PL and a decrease in optical band gap from 2.44 to 2.2 eV exhibiting a red shift.

  19. The Magic-Size Nanocluster (CdSe)34 as a Low-Temperature Nucleant for Cadmium Selenide Nanocrystals; Room-Temperature Growth of Crystalline Quantum Platelets.

    PubMed

    Wang, Yuanyuan; Zhang, Ying; Wang, Fudong; Giblin, Daryl E; Hoy, Jessica; Rohrs, Henry W; Loomis, Richard A; Buhro, William E

    2014-04-08

    Reaction of Cd(OAc)2·2H2O and selenourea in primary-amine/secondary-amine cosolvent mixtures affords crystalline CdSe quantum platelets at room temperature. Their crystallinity is established by X-ray diffraction analysis (XRD), high-resolution transmission electron microscopy (TEM), and their sharp extinction and photoluminescence spectra. Reaction monitoring establishes the magic-size nanocluster (CdSe)34 to be a key intermediate in the growth process, which converts to CdSe quantum platelets by first-order kinetics with no induction period. The results are interpreted to indicate that the critical crystal-nucleus size for CdSe under these conditions is in the range of (CdSe)34 to (CdSe)68. The nanocluster is obtained in isolated form as [(CdSe)34(n-octylamine)16(di-n-pentylamine)2], which is proposed to function as crystal nuclei that may be stored in a bottle.

  20. Surface control of CdSe nanocrystals by UV-exposure in air and successive thermal treatment under ultra high vacuum

    NASA Astrophysics Data System (ADS)

    Choi, Hyun-Ju; Wang, Seok-Joo; Kim, Hyuncheol; Park, Hyung-Ho; Chang, Ho Jung; Jeon, Hyeongtag

    2008-08-01

    Colloidal CdSe nanocrystals were synthesized through a solution process. The CdSe nanocrystals coated on Si(1 0 0) wafers were UV-exposed in either an air or argon atmosphere to distinguish the effect of generated ozone from UV-radiation at 365 nm on the removal of surface capping pyridine molecules. The pyridine on the CdSe nanocrystal's surface could be effectively removed by the ozone generated during UV-exposure with an accompanying highly oxidized surface state of the CdSe nanocrystals. For the removal of surface oxides of CdSe nanocrystals, a successive thermal treatment under ultra high vacuum (UHV) was adopted. The optical energy bandgap measured by using UV-vis absorption spectroscopy showed a red shift with treatment with an increase of annealing temperature. The electronic energy structure of UHV-annealed CdSe nanocrystals film was analyzed in situ using X-ray absorption and photoelectron spectroscopy. A great resemblance was found between the values of the optical and electron energy bandgaps of effectively surface-treated CdSe nanocrystals film after UHV-annealing at 400 °C.

  1. Magneto-optical spectrum and the effective excitonic Zeeman splitting energies of Mn and Co-doped CdSe nanowires

    SciTech Connect

    Xiong, Wen; Chen, Wensuo

    2013-12-21

    The electronic structure of Mn and Co-doped CdSe nanowires are calculated based on the six-band k·p effective-mass theory. Through the calculation, it is found that the splitting energies of the degenerate hole states in Mn-doped CdSe nanowires are larger than that in Co-doped CdSe nanowires when the concentration of these two kinds of magnetic ions is the same. In order to analysis the magneto-optical spectrum of Mn and Co-doped CdSe nanowires, the four lowest electron states and the four highest hole states are sorted when the magnetic field is applied, and the 10 lowest optical transitions between the conduction subbands and the valence subbands at the Γ point in Mn and Co-doped CdSe nanowires are shown in the paper, it is found that the order of the optical transitions at the Γ point almost do not change although two different kinds of magnetic ions are doped in CdSe nanowires. Finally, the effective excitonic Zeeman splitting energies at the Γ point are found to increase almost linearly with the increase of the concentration of the magnetic ions and the magnetic field; meanwhile, the giant positive effective excitonic g factors in Mn and Co-doped CdSe nanowires are predicted based on our theoretical calculation.

  2. Effect of Ligands on Characteristics of (CdSe)13 Quantum Dot

    SciTech Connect

    Gao, Yang; Zhou, Bo; Kang, Seung-gu; Xin, Minsi; Yang, Ping; Dai, Xing; Wang, Zhigang; Zhou, Ruhong

    2014-01-01

    The widespread applications of quantum dots (QDs) have spurred an increasing interest in the study of their coating ligands, which can not only protect the electronic structures of the central QDs, but also control their permeability through biological membranes with both size and shape. In this work, we have used density functional theory (DFT) to investigate the electronic structures of (CdSe)13 passivated by OPMe2(CH2)nMe ligands with different lengths and various numbers of branches (Me=methyl group, n = 0, 1-3). Our results show that the absorption peak in the ultraviolet-visible (UV-vis) spectra displays a clear blue-shift, on the scale of ~100 nm, upon the binding of ligands. Once the total number of ligands bound with (CdSe)13 reached a saturated number (9 or 10), no more blue-shift occurred in the absorption peak in the UV-vis spectra. On the other hand, the aliphatic chain length of ligands has a negligible effect on the optical properties of the QD core. Analyses of the bonding characteristics confirm that optical transitions are dominantly governed by the central QD core rather than the organic passivation. Interestingly, the density of states (DOS) share similar characteristics as vibrational spectra, even though there is no coordination vibration mode between the ligands and the central QD. These findings might provide insights on the material design for the passivation of quantum dots for biomedical applications.

  3. Dislocation-driven CdS and CdSe nanowire growth.

    PubMed

    Wu, Haoyu; Meng, Fei; Li, Linsen; Jin, Song; Zheng, Gengfeng

    2012-05-22

    We report the synthesis of CdS and CdSe nanowires (NWs) and nanoribbons (NRs) with gold catalysts by H(2)-assisted chemical vapor deposition. Nanopods and nanocones were obtained without catalysts at higher system pressure. Transmission electron microscopy (TEM) studies, including two-beam TEM and displaced-aperture dark-field TEM characterization, were used to investigate the NW growth mechanism. Dislocation contrast and twist contours have been routinely observed within the synthesized one-dimensional (1D) CdS and CdSe NWs, suggesting the operation of the dislocation-driven NW growth mechanism under our experimental conditions. The Burgers vectors of dislocations and the associated Eshelby twists were measured and quantified. We hypothesize that gold nanoparticles provide nucleation sites to initiate the growth of CdS/CdSe NWs and lead to the formation of dislocations that continue to drive and sustain 1D growth at a low supersaturation level. Our study suggests that the dislocation-driven mechanism may also contribute to the growth of other 1D nanomaterials that are commonly considered to grow via the vapor-liquid-solid mechanism.

  4. Direct Measurement of Single CdSe Nanowire Extinction Polarization Anisotropies.

    PubMed

    McDonald, Matthew P; Vietmeyer, Felix; Kuno, Masaru

    2012-08-16

    The origin of sizable absorption polarization anisotropies (ρabs) in one-dimensional (1D) semiconductor nanowires (NWs) has been debated. Invoked explanations employ either classical or quantum mechanical origins, where the classical approach suggests dielectric constant mismatches between the NW and its surrounding environment as the predominant source of observed polarization sensitivities. At the same time, the confinement-influenced mixing of states suggests a sizable contribution from polarization-sensitive transition selection rules. Sufficient evidence exists in the literature to support either claim. However, in all cases, these observations stem from excitation polarization anisotropy (ρexc) studies, which only indirectly measure ρabs. In this manuscript, we directly measure the band edge extinction polarization anisotropies (ρext) of individual CdSe NWs using single NW extinction spectroscopy. Observed polarization anisotropies possess distinct spectral features and wavelength dependencies that correlate well with theoretical transition selection rules derived from a six-band k·p theory used to model the electronic structure of CdSe NWs.

  5. Experimental determination of single CdSe nanowire absorption cross sections through photothermal imaging.

    PubMed

    Giblin, Jay; Syed, Muhammad; Banning, Michael T; Kuno, Masaru; Hartland, Greg

    2010-01-26

    Absorption cross sections ((sigma)abs) of single branched CdSe nanowires (NWs) have been measured by photothermal heterodyne imaging (PHI). Specifically, PHI signals from isolated gold nanoparticles (NPs) with known cross sections were compared to those of individual CdSe NWs excited at 532 nm. This allowed us to determine average NW absorption cross sections at 532 nm of (sigma)abs = (3.17 +/- 0.44) x 10(-11) cm2/microm (standard error reported). This agrees well with a theoretical value obtained using a classical electromagnetic analysis ((sigma)abs = 5.00 x 10(-11) cm2/microm) and also with prior ensemble estimates. Furthermore, NWs exhibit significant absorption polarization sensitivities consistent with prior NW excitation polarization anisotropy measurements. This has enabled additional estimates of the absorption cross section parallel ((sigma)abs) and perpendicular ((sigma)abs(perpendicular) to the NW growth axis, as well as the corresponding NW absorption anisotropy ((rho)abs). Resulting values of (sigma)abs = (5.6 +/- 1.1) x 10(-11) cm2/microm, (sigma)abs(perpendicular) = (1.26 +/- 0.21) x 10(-11) cm2/microm, and (rho)abs = 0.63+/- 0.04 (standard errors reported) are again in good agreement with theoretical predictions. These measurements all indicate sizable NW absorption cross sections and ultimately suggest the possibility of future direct single NW absorption studies.

  6. Photoluminescence enhancement of CdSe quantum dots: a case of organogel-nanoparticle symbiosis.

    PubMed

    Wadhavane, Prashant D; Galian, Raquel E; Izquierdo, M Angeles; Aguilera-Sigalat, Jordi; Galindo, Francisco; Schmidt, Luciana; Burguete, M Isabel; Pérez-Prieto, Julia; Luis, Santiago V

    2012-12-19

    Highly fluorescent organogels (QD-organogel), prepared by combining a pseudopeptidic macrocycle and different types of CdSe quantum dots (QDs), have been characterized using a battery of optical and microscopic techniques. The results indicate that the presence of the QDs not only does not disrupt the supramolecular organization of the internal fibrillar network of the organogel to a significant extent, but it also decreases the critical concentration of gelator needed to form stable and thermoreversible organogels. Regarding the photophysical properties of the QDs, different trends were observed depending on the presence of a ZnS inorganic shell around the CdSe core. Thus, while the core-shell QDs preserve their photophysical properties in the organogel medium, a high to moderate increase of the fluorescence intensity (up to 528%) and the average lifetime (up to 1.7), respectively, was observed for the core QDs embedded in the organogel. The results are relevant for the development of luminescent organogels based on quantum dots, which have potential applications as advanced hybrid materials in different fields.

  7. Templating growth of gold nanostructures with a CdSe quantum dot array.

    PubMed

    Paul, Neelima; Metwalli, Ezzeldin; Yao, Yuan; Schwartzkopf, Matthias; Yu, Shun; Roth, Stephan V; Müller-Buschbaum, Peter; Paul, Amitesh

    2015-06-07

    In optoelectronic devices based on quantum dot arrays, thin nanolayers of gold are preferred as stable metal contacts and for connecting recombination centers. The optimal morphology requirements are uniform arrays with precisely controlled positions and sizes over a large area with long range ordering since this strongly affects device performance. To understand the development of gold layer nanomorphology, the detailed mechanism of structure formation are probed with time-resolved grazing incidence small-angle X-ray scattering (GISAXS) during gold sputter deposition. Gold is sputtered on a CdSe quantum dot array with a characteristic quantum dot spacing of ≈7 nm. In the initial stages of gold nanostructure growth, a preferential deposition of gold on top of quantum dots occurs. Thus, the quantum dots act as nucleation sites for gold growth. In later stages, the gold nanoparticles surrounding the quantum dots undergo a coarsening to form a complete layer comprised of gold-dot clusters. Next, growth proceeds dominantly via vertical growth of gold on these gold-dot clusters to form an gold capping layer. In this capping layer, a shift of the cluster boundaries due to ripening is found. Thus, a templating of gold on a CdSe quantum dot array is feasible at low gold coverage.

  8. Cellular uptake induced biotoxicity of surface-modified CdSe quantum dots

    NASA Astrophysics Data System (ADS)

    Sanwlani, Shilpa; Rawat, Kamla; Pal, Meena; Bohidar, Himadri B.; Verma, Anita Kamra

    2014-05-01

    Cellular uptake of quantum dots (QDs) by cells is of utmost importance for establishing QDs as biostable fluorescent markers that facilitate early diagnosis and detection of cancer. The surface states of QDs are critical to enhance the cellular uptake. Biocompatible CDSe QDs were synthesized using mercaptopropionic acid, amino-ethanethiol HCl, cyltrimethylammonium bromide, dodecyltrimethylammonium bromide, tetrabutylammonium iodide (TBAI), and sodium dodecyl sulfate were functionalized using ligand-exchange method. Cytocompatibility and cellular uptake of QDs were evaluated in human embryonic kidney cells (HEK-29), and breast cancer cells (MCF-7) as reduced cytotoxicity is desirable for biological applications. Approximately, 60 % cytotoxicity was observed in all surface-coated QDs and QD100 in 72 h in both the cell lines, except TBAI that indicated 30 % cytotoxicity in 72 h, and only 10 % in 24 h. Glutathione, the detoxifying molecule, is detrimental for understanding the oxidative stress of the cell. The QDs showed enhanced Glutathione- S-transferase (GST) activity in the MCF-7 cell line. In HEK, CdSe per se was also able to induce a high level of GST. QDs toxicity may either be related to the induction of reactive oxygen species or the direct release of metal ions. Optimization of QDs in terms of quantification and DNA damage is imperative for realistic biological applications.

  9. Tuning luminescent properties of CdSe nanoclusters by phosphine surface passivation

    NASA Astrophysics Data System (ADS)

    Lysova, Iryna; Anton, Halina; Dmitruk, Igor; Mely, Yves

    2016-12-01

    Appropriate surface ligands are required for tuning the physicochemical and photophysical properties of nanoclusters (NCs). These surface ligands are especially critical for passivating the small (CdSe)33,34 NCs where the majority of atoms are at the NC surface. In this study, triphenylphosphine (TPP), trioctylphosphine (TOP) and tris(pentafluorophenyl)phosphine (TPFP) have been tested as capping agents for alkylamine-coated CdSe NCs. TPP and TOP compounds are found to increase the quantum yield of photoluminescence (PL) from 0.15% to 0.6% and 0.53%, respectively, and to preserve this increased PL with time, probably by preventing charge leakage as a result of their binding to Se atoms. Since no dramatic change in the shape of NCs’ PL spectrum occurs after surface treatment, both the exciton band and the low-energy broad band in magic NCs are thought to describe the intrinsic luminescence properties of the NCs. As a result, the PL increase due to Se passivation is thought to be mainly caused by a decrease in the efficiency of the NC nonradiative pathways.

  10. Hard-disk behavior and beyond in Langmuir films of CdSe nanoparticles.

    PubMed

    Ozturk, Birol; Behin-Aein, Ghazal; Flanders, Bret N

    2005-05-10

    Harnessing the spontaneous behavior of a population of particles is an attractive approach to the fabrication of targeted nanostructures. Underlying this goal is the interparticle potential, as it dictates the spontaneous behavior of the system. To this end, we present methodology for using quantitative film balance studies of trioctylphosphine oxide (TOPO) stabilized CdSe nanoparticles to determine their effective interparticle potential on the air-water interface. A simple protocol for reducing the quantity of excess TOPO to negligible levels of surface activity is established. In studying clean populations of 2.08, 2.22, 2.36, 2.49, 2.63, and 2.91 nm nanoparticles, quantitative agreement between their pressure-area isotherms and the Carnahan-Starling hard-disk equation of state is achieved. This analysis indicates that CdSe nanoparticles of a given diameter behave how hard disks with significantly smaller diameters would behave. This finding suggests that an attractive contribution to the interparticle potential, such as the dipolar potential, plays a significant role in the spontaneous organization of these particles.

  11. Blue and green electroluminescence from CdSe nanocrystal quantum-dot-quantum-wells

    SciTech Connect

    Lu, Y. F.; Cao, X. A.

    2014-11-17

    CdS/CdSe/ZnS quantum dot quantum well (QDQW) nanocrystals were synthesized using the successive ion layer adsorption and reaction technique, and their optical properties were tuned by bandgap and strain engineering. 3-monolayer (ML) CdSe QWs emitted blue photoluminescence at 467 nm with a spectral full-width-at-half-maximum of ∼30 nm. With a 3 ML ZnS cladding layer, which also acts as a passivating and strain-compensating layer, the QDQWs acquired a ∼35% quantum yield of the QW emission. Blue and green electroluminescence (EL) was obtained from QDQW light-emitting devices with 3–4.5 ML CdSe QWs. It was found that as the peak blueshifted, the overall EL was increasingly dominated by defect state emission due to poor hole injection into the QDQWs. The weak EL was also attributed to strong field-induced charge separation resulting from the unique QDQW geometry, weakening the oscillator strength of optical transitions.

  12. Hydrophilic CdSe thin films by low cost spray pyrolysis technique and annealing effects

    NASA Astrophysics Data System (ADS)

    Logu, T.; Sankarasubramanian, K.; Soundarrajan, P.; Sethuraman, K.

    2015-03-01

    Cadmium selenide (CdSe) thin films were deposited on glass substrates at 200°C by homemade chemical spray pyrolysis technique. The as-deposited films were annealed in air atmosphere for 3 hrs, at two different temperatures (350 and 450°C). The as-deposited film has been observed to possess uniform surface with crystalline sphalerite cubic structure and optical band gap of E g = 2.4 eV. It is worth noting that after annealing, metastable cubic sphalerite phase transforms into stable well crystalline hexagonal wurtzite phase. The optical band gap was found to decrease from 2.4 eV to 1.75 eV. The average surface roughness is 1.5 nm for the as-deposited film which rises to 4.2 nm after annealing the film in air atmosphere. The contact angle was found to vary from 94° ± 1° to 81° ± 1° with annealing temperature. In addition, from Wenzel's relation it is concluded that CdSe thin film is hydrophilic in nature. [Figure not available: see fulltext.

  13. Efficient intranuclear gene delivery by CdSe aqueous quantum dots electrostatically-coated with polyethyleneimine

    NASA Astrophysics Data System (ADS)

    Au, Giang H. T.; Y Shih, Wan; Shih, Wei-Heng

    2015-01-01

    Quantum dots (QDs) are semiconducting nanoparticles with photoluminescence properties that do not photobleach. Due to these advantages, using QDs for non-viral gene delivery has the additional benefit of being able to track the delivery of the genes in real time as it happens. We investigate the efficacy of mercaptopropionic acid (MPA)-capped CdSe aqueous quantum dots (AQDs) electrostatically complexed with branched polyethyleneimine (PEI) both as a non-viral gene delivery vector and as a fluorescent probe for tracking the delivery of genes into nuclei. The MPA-capped CdSe AQDs that were completely synthesized in water were the model AQDs. A nominal MPA:Cd:Se = 4:3:1 was chosen for optimal photoluminescence and zeta potential. The gene delivery study was carried out in vitro using a human colon cancer cell line, HT29 (ATCC). The model gene was a plasmid DNA (pDNA) that can express red fluorescent protein (RFP). Positively charged branched PEI was employed to provide a proton buffer to the AQDs to allow for endosomal escape. It is shown that by using a PEI-AQD complex with a PEI/AQD molar ratio of 300 and a nominal pDNA/PEI-AQD ratio of 6, we can achieve 75 ± 2.6% RFP expression efficiency with cell vitality remaining at 78 ± 4% of the control.

  14. High-Temperature Microfluidic Synthesis of CdSe Nanocrystals inNanoliter Droplets

    SciTech Connect

    Chan, Emory M.; Alivisatos, A. Paul; Mathies, Richard A.

    2005-06-09

    The high-temperature synthesis of CdSe nanocrystals innanoliter-volume droplets flowing in a perfluorinated carrier fluidthrough a microfabricated reactor is presented. A flow-focusing nanojetstructure with a step increase in channel height reproducibly generatedoctadecene droplets in Fomblin Y 06/6 perfluorinated polyether atcapillary numbers up to 0.81 and with a droplet:carrier fluid viscosityratio of 0.035. Cadmium and selenium precursors flowing in octadecenedroplets through a high-temperature (240-300 degrees C) glassmicroreactor produced high quality CdSe nanocrystals, as verified byoptical spectroscopy and transmission electron microscopy. Isolating thereaction solution in droplets prevented particle deposition andhydrodynamic dispersion, allowing the reproducible synthesis ofnanocrystals at three different temperatures and four different residencetimes in the span of four hours. Our synthesis of a wide range ofnanocrystals at high temperatures, high capillary numbers, and lowviscosity ratio illustrates the general utility of droplet-basedmicrofluidic reactors to encapsulate nanoliter volumes of organic oraqueous solutions and to precisely control chemical or biochemicalreactions.

  15. Opto-electrical energy conversion by thin electrolytic CdSe films on Ni substrates

    NASA Astrophysics Data System (ADS)

    Glenis, G. X.; Athanassopoulou, M. D.; Argyropoulos, Th G.; Dervos, C. T.

    2015-02-01

    Thin-films (300 nm) of zinc-blende (cubic structure) CdSe (111) electrolytically deposited on nickel substrates had their surface characteristics investigated by XRD, SEM, and profilometry scans. A metal-CdSe-metal structure was formed by positioning a Au electrode on top of CdSe and the I-V characteristics of the resulting device were investigated in the dark and under low intensities (≤0.2 mW cm-2) of diffused solar radiation. The experimental results show that the illuminated structure is an active device that produces electric power in the 2nd quadrant of the I-V curve. This response may be related to the Ni-to-CdSe interface, where carriers are effectively generated as a result of deep energy level formations, spatially confined in the interfacial region of the depletion layer width of the Ni-CdSe junction. A potential energy diagram is proposed to present the spatially and energetically confined deep-level parameters, the operation principles (carrier generation and transport processes) across the structure and link them to the obtained I-V response. A mathematical modeling based on the Schokley-Read-Hall recombination theory confirms the experimentally obtained current profiles of illuminated junctions. Such opto-electrical tranducers might be implemented in multilayer photovoltaic hetero-structures to enhance their conversion efficiencies and reduce their operating temperatures.

  16. Structural and optical properties of solvothermal synthesized nearly monodispersed CdSe nanocrystals

    NASA Astrophysics Data System (ADS)

    Shahi, A. K.; Pandey, B. K.; Singh, B. P.; Gopal, R.

    2016-09-01

    Water soluble nearly monodisperse CdSe nanocrystals have been successfully synthesized via aqueous phase solvothermal route in non ionic surfactant glycolic acid ethoxylate 4-non phenyl ether (GAEPE). X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) are used to determine the phase, structural parameters such as lattice constants, strain, x-ray density and specific surface area, morphology, shape and size distribution, respectively, whereas optical properties are studied by UV-visible absorption and photoluminescence (PL) spectroscopy. All the diffraction peaks of XRD pattern indexed to wurtzite phase of hexagonal system of CdSe and crystallite sizes estimated to be 13-29 nm along some stronger and narrower peaks which is also consistent with TEM measurement while crystallinity and defects have been analyzed with selective area electron diffraction (SAED) pattern. Optical absorption spectrum shows that the as prepared sample exhibits primary and secondary absorption band centered at 2.15 eV and 1.82 eV, respectively, which is blue shifted as compared to bulk value (1.74 eV) of band gap due to quantum confinement effect. Photoluminescence spectrum shows sharp excitonic emission band centered at 583 nm which is nearer to primary band gap energy.

  17. Controlled synthesis of CdSe quantum dots by a microwave-enhanced process: a green approach for mass production.

    PubMed

    Ayele, Delele Worku; Chen, Hung-Ming; Su, Wei-Nien; Pan, Chun-Jern; Chen, Liang-Yih; Chou, Hung-Lung; Cheng, Ju-Hsiang; Hwang, Bing-Joe; Lee, Jyh-Fu

    2011-05-09

    A method that does not employ hot-injection techniques has been developed for the size-tunable synthesis of high-quality CdSe quantum dots (QDs) with zinc blende structure. In this environmentally benign synthetic route, which uses less toxic precursors, solvents, and capping ligands, CdSe QDs that absorb visible light are obtained. The size of the as-prepared CdSe QDs and thus their optical properties can be manipulated by changing the microwave reaction conditions. The QDs were characterized by XRD, TEM, UV/Vis, FTIR, time-resolved fluorescence spectroscopy, and fluorescence spectrophotometry. In this approach, the reaction is conducted in open air and at a much lower temperature than in hot-injection techniques. The use of microwaves in this process allows for a highly reproducible and effective synthesis protocol that is fully adaptable for mass production and can be easily employed to synthesize a variety of semiconductor QDs with the desired properties. Possible applications of the CdSe QDs were assessed by deposition on TiO(2) films.

  18. Incidence of the core composition on the stability, the ROS production and the toxicity of CdSe quantum dots.

    PubMed

    Kauffer, Florence-Anaïs; Merlin, Christophe; Balan, Lavinia; Schneider, Raphaël

    2014-03-15

    Mercaptosuccinic acid-capped CdSe and alloyed CdSe(S) QDs were prepared in aqueous solution at 100 and 170°C, respectively. These dots were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), and UV-vis and photoluminescence spectroscopies. The dots were found to be of similar size (ca. 2nm) but differ in their composition and surface chemistry. The photostability of the QDs was found to correlate with their ability to produce reactive oxygen species (ROS) upon light activation. CdSe QDs produce hydroxyl radicals immediately after irradiation due to their modest photostability, while CdSe(S) QDs start to generate the hydroxyl radicals only once they start to be bleached (ca. 30min). Cytotoxicity experiments conducted on Escherichia coli cells revealed that CdSe QDs were the more toxic despite being the least loaded in cadmium. In addition, consistent with ROS assays, the cytotoxicity of the CdSe QDs appeared light-dependent and is in accordance with a light-dependent oxidative stress observed with an oxyR-based whole cell biosensor. Our results demonstrate the crucial role played by nanoparticles synthesis process on their PL properties, their stability and their toxicity.

  19. Study of the Spectral Properties of Nanocomposites with CdSe Quantum Dots in a Wide Range of Low Temperatures

    NASA Astrophysics Data System (ADS)

    Magaryan, K. A.; Eremchev, I. Y.; Karimullin, K. R.; Knyazev, M. V.; Mikhailov, M. A.; Vasilieva, I. A.; Klimusheva, G. V.

    2015-09-01

    Luminescence spectra of the colloidal solution of CdSe quantum dots (in toluene) were studied in a wide range of low temperatures. Samples were synthesized in the liquid crystal matrix of cadmium octanoate (CdC8). A comparative analysis of the obtained data with previous results was performed.

  20. Study of optical and structural properties of CdSe quantum dot embedded in PVA polymer matrix

    SciTech Connect

    Tyagi, Chetna Sharma, Ambika

    2015-08-28

    To enhance the properties and applicability of devices it is essential to incorporate semiconductor nanoparticles into polymer matrix. This introduces a new branch of science which includes device fabrications such as gas sensors, nonlinear optics, catalysis etc. Herein, we have synthesized CdSe/PVA nanocomposite (NC) material using wet chemical synthesis technique. The XRD studies revealed the formation of crystalline structure of CdSe nanoparticles (NP’s) and PVA NC’s with an average size of 100 nm and 5 nm respectively. Energy band gap is determined using UV-VIS Spectroscopy. A red shift in the absorption edge of CdSe/PVA NC is observed with respect to CdSe Np’s, The photoluminescence spectra also show red shift for CdSe/PVA NC as compared to CdSe NP’s Thus the use of CdSe/PVA for solar cell application would be more preferable than CdSe NP’s.

  1. CdSe nanocrystal sensitized anatase TiO2 (001) tetragonal nanosheet-array films for photovoltaic application.

    PubMed

    Feng, Shuanglong; Yang, Junyou; Liu, Ming; Liu, Yong

    2013-02-01

    CdSe nanocrystal sensitized TiO2 nanosheet array heterostructure films were fabricated by a two-step method. Firstly, a single crystalline anatase TiO2 tetragonal nanosheet-array film on a transparent conductive fluorine-doped tin oxide (FTO) substrate was successfully prepared by hydrothermal method. Then, CdSe nanocrystalline sensitizers were deposited on the TiO2 nanosheet array by CBD method. The products were characterized with XRD, SEM, TEM and UV-vis absorption spectroscopy. The effect of the CdSe nanocrystal deposition time and the length of the TiO2 sheet on the photovoltaic performance of the resulting CdSe/TiO2 nanosheet array electrodes were also investigated. In comparison with the non-sensitized TiO2 nanosheet array, the photocurrent of CdSe sensitized TiO2 nanosheet has a great enhancement, which gives some insight to the fundamental mechanism of the performance improvement.

  2. Controlled synthesis and optical properties of tunable CdSe quantum dots and effect of pH

    SciTech Connect

    Ratnesh, R. K.; Mehata, Mohan Singh

    2015-09-15

    Cadmium selenide (CdSe) quantum dots (Q-dots) were prepared by using non-coordinating solvent octadecene instead of coordinating agent trioctylphosphine oxide (TOPO). Reaction processes were carried out at various temperatures of 240°, 260°, 280° and 300° C under nitrogen atmosphere. The prepared CdSe Q-dots which are highly stable show uniform size distribution and tunable optical absorption and photoluminescence (PL). The growth temperature significantly influenced the particle size; spectral behavior, energy band gap and PL intensity and the full width at half maxima (FWHM). Three different methods were employed to determine the particle size and the average particle size of the CdSe Q-dots is 3.2 - 4.3 nm, grown at different temperatures. In addition, stable and mono-dispersed water soluble CdSe Q-dots were prepared by the ligand exchange technique. Thus, the water soluble Q-dots, which are sensitive to the basic pH may be important for biological applications.

  3. Effects of culture conditions of Pseudomonas aeruginosa strain RB on the synthesis of CdSe nanoparticles.

    PubMed

    Ayano, Hiroyuki; Kuroda, Masashi; Soda, Satoshi; Ike, Michihiko

    2015-04-01

    Cadmium selenide (CdSe) was synthesized by Pseudomonas aeruginosa strain RB in a culture containing lactic acid as a carbon source, 1 mM selenite, and 1 mM cadmium under various conditions. High purity (1.02-1.16 of the atomic ratio of Se to Cd) and efficient synthesis of biogenic CdSe nanoparticles were observed at 25-30°C, 0.05-10 g L(-1) NaCl, and neutral pH conditions compared with other tested conditions. However, the size and shape of synthesized CdSe nanoparticles were not changed by changing culture conditions. The contents of S and Se in the particles respectively increased under alkaline and weak acidic conditions. Furthermore, high temperature (>37°C), high salinity (>10 g L(-1) NaCl), and alkaline pH affected the CdSe-synthesizing rate by strain RB. This report is the first optimizing the culture conditions for synthesizing biogenic CdSe nanoparticles in a batch processing.

  4. Controlled synthesis and optical properties of tunable CdSe quantum dots and effect of pH

    NASA Astrophysics Data System (ADS)

    Ratnesh, R. K.; Mehata, Mohan Singh

    2015-09-01

    Cadmium selenide (CdSe) quantum dots (Q-dots) were prepared by using non-coordinating solvent octadecene instead of coordinating agent trioctylphosphine oxide (TOPO). Reaction processes were carried out at various temperatures of 240°, 260°, 280° and 300° C under nitrogen atmosphere. The prepared CdSe Q-dots which are highly stable show uniform size distribution and tunable optical absorption and photoluminescence (PL). The growth temperature significantly influenced the particle size; spectral behavior, energy band gap and PL intensity and the full width at half maxima (FWHM). Three different methods were employed to determine the particle size and the average particle size of the CdSe Q-dots is 3.2 - 4.3 nm, grown at different temperatures. In addition, stable and mono-dispersed water soluble CdSe Q-dots were prepared by the ligand exchange technique. Thus, the water soluble Q-dots, which are sensitive to the basic pH may be important for biological applications.

  5. Green synthesis of highly efficient CdSe quantum dots for quantum-dots-sensitized solar cells

    SciTech Connect

    Gao, Bing; Shen, Chao; Zhang, Mengya; Yuan, Shuanglong; Yang, Yunxia E-mail: grchen@ecust.edu.cn; Chen, Guorong E-mail: grchen@ecust.edu.cn; Zhang, Bo

    2014-05-21

    Green synthesis of CdSe quantum dots for application in the quantum-dots-sensitized solar cells (QDSCs) is investigated in this work. The CdSe QDs were prepared with glycerol as the solvent, with sharp emission peak, full width at half maximum around 30 nm, and absorption peak from 475 nm to 510 nm. The reaction is environmental friendly and energy saving. What's more, the green synthesized CdSe QDs are coherence to the maximum remittance region of the solar spectrum and suitable as sensitizers to assemble onto TiO{sub 2} electrodes for cell devices application. What's more, the dynamic procedure of the carriers' excitation, transportation, and recombination in the QDSCs are discussed. Because the recombination of the electrons from the conduction band of TiO{sub 2}'s to the electrolyte affects the efficiency of the solar cells greatly, 3-Mercaptopropionic acid capped water-dispersible QDs were used to cover the surface of TiO{sub 2}. The resulting green synthesized CdSe QDSCs with Cu{sub 2}S as the electrode show a photovoltaic performance with a conversion efficiency of 3.39%.

  6. Synthesis of Tapered CdS Nanobelts and CdSe Nanowires with Good Optical Property by Hydrogen-Assisted Thermal Evaporation.

    PubMed

    Wang, Min; Fei, Guangtao

    2009-07-10

    The tapered CdS nanobelts and CdSe nanowires were prepared by hydrogen-assisted thermal evaporation method. Different supersaturation leads to two different kinds of 1D nanostructures. The PL measurements recorded from the as-prepared tapered CdS nanobelts and CdSe nanowires show only a bandgap emission with relatively narrow full-width half maximum, which means that they possess good optical property. The as-synthesized high-quality tapered CdS nanobelts and CdSe nanowires may be excellent building blocks for photonic devices.

  7. Measuring photoluminescence spectra of self-assembly array nanowire of colloidal CdSe quantum dots using scanning near-field optics microscopy

    NASA Astrophysics Data System (ADS)

    Bai, Zhongchen; Hao, Licai; Zhang, Zhengping; Qin, Shuijie

    2016-05-01

    A novel periodic array CdSe nanowire is prepared on a substrate of the porous titanium dioxide by using a self-assembly method of the colloidal CdSe quantum dots (QDs). The experimental results show that the colloidal CdSe QDs have renewedly assembled on its space scale and direction in process of losing background solvent and form the periodic array nanowire. The main peak wavelength of Photoluminescence (PL) spectra, which is measured by using a 100-nm aperture laser beam spot on a scanning near-field optics microscopy, has shifted 60 nm with compared to the colloidal CdSe QDs. Furthermore, we have measured smaller ordered nanometer structure in thin QDs area as well, a 343-nm periodic nanowire in thick QDs area and the colloidal QDs in edge of well-ordered nanowire.

  8. Nanocrystal Size-Dependent Efficiency of Quantum Dot Sensitized Solar Cells in the Strongly Coupled CdSe Nanocrystals/TiO2 System.

    PubMed

    Yun, Hyeong Jin; Paik, Taejong; Diroll, Benjamin; Edley, Michael E; Baxter, Jason B; Murray, Christopher B

    2016-06-15

    Light absorption and electron injection are important criteria determining solar energy conversion efficiency. In this research, monodisperse CdSe quantum dots (QDs) are synthesized with five different diameters, and the size-dependent solar energy conversion efficiency of CdSe quantum dot sensitized solar cell (QDSSCs) is investigated by employing the atomic inorganic ligand, S(2-). Absorbance measurements and transmission electron microscopy show that the diameters of the uniform CdSe QDs are 2.5, 3.2, 4.2, 6.4, and 7.8 nm. Larger CdSe QDs generate a larger amount of charge under the irradiation of long wavelength photons, as verified by the absorbance results and the measurements of the external quantum efficiencies. However, the smaller QDs exhibit faster electron injection kinetics from CdSe QDs to TiO2 because of the high energy level of CBCdSe, as verified by time-resolved photoluminescence and internal quantum efficiency results. Importantly, the S(2-) ligand significantly enhances the electronic coupling between the CdSe QDs and TiO2, yielding an enhancement of the charge transfer rate at the interfacial region. As a result, the S(2-) ligand helps improve the new size-dependent solar energy conversion efficiency, showing best performance with 4.2-nm CdSe QDs, whereas conventional ligand, mercaptopropionic acid, does not show any differences in efficiency according to the size of the CdSe QDs. The findings reported herein suggest that the atomic inorganic ligand reinforces the influence of quantum confinement on the solar energy conversion efficiency of QDSSCs.

  9. Surface structure of CdSe Nanorods revealed by combined X-rayabsorption fine structure measurements and ab-initio calculations

    SciTech Connect

    Aruguete, Deborah A.; Marcus, Matthew A.; Li, Liang-shi; Williamson, Andrew; Fakra, Sirine; Gygi, Francois; Galli, Giulia; Alivisatos, A. Paul

    2006-01-27

    We report orientation-specific, surface-sensitive structural characterization of colloidal CdSe nanorods with extended X-ray absorption fine structure spectroscopy and ab-initio density functional theory calculations. Our measurements of crystallographically-aligned CdSe nanorods show that they have reconstructed Cd-rich surfaces. They exhibit orientation-dependent changes in interatomic distances which are qualitatively reproduced by our calculations. These calculations reveal that the measured interatomic distance anisotropy originates from the nanorod surface.

  10. Synthesis and Characterizations of Pb-modified CdSe Aqueous Quantum Dots and Their Applications in Quantum Dot-Sensitized Solar Cells

    NASA Astrophysics Data System (ADS)

    Lu, Cheng-Hsin

    Quantum Dots (QDs) are semiconductor nanocrystals with typical size ranges around 1-20 nm. They exhibit distinctive size-dependent photoluminescence (PL) properties due to the quantum confinement effect. QDs have great potentials in display, lighting, lasing, bioimaging, fluorescent label, sensor, photodetector, and photovoltaic applications, and have been widely studied in the past decades. Cadmium selenide (CdSe) QDs have been synthesized using an environmentally friendly, aqueous method under low temperature. While traditional QDs synthesized by hot injection method using organic solvent generally exhibit edge-state emission with narrow peaks, aqueous quantum dots (AQDs) tend to have trap-state emissions with broad peaks. The objective of this thesis is to investigate how Pb modifications in CdSe AQDs synthesis can affect the optoelectronic properties of the QDs and how these modifications affect their corresponding photovoltaic performance in quantum dot-sensitized solar cell (QDSSC) applications. Lead (Pb) precursor has been introduced either during the synthesis or after the synthesis of CdSe AQDs forming either Pb-doped or Pb-coated CdSe QDs, respectively. Pb-doped CdSe QDs exhibit red-shift in both absorption and emission spectra while Pb-coated CdSe QDs exhibit blue-shift in both absorption and emission spectra along with the generation of more surface defects. Although blue-shifted absorption indicating a narrower absorption range and the surface defects providing undesired recombination pathways are detrimental to solar cell performance, however surprisingly, we found that QDSSCs made from Pb-coated CdSe QDs actually had better solar cell performance than that made from Pb-doped CdSe QDs. We attributed this finding to a protection/passivation layer formed in-situ when the coated Pb react with the iodide/triiodide electrolyte during solar cell operation resulting in QDSSCs with better charge injection and stability.

  11. Optical and Phonon Characterization of Ternary CdSe x S1- x Alloy Quantum Dots

    NASA Astrophysics Data System (ADS)

    Thi, L. A.; Cong, N. D.; Dang, N. T.; Nghia, N. X.; Quang, V. X.

    2016-05-01

    Ternary CdSe x S1- x alloy quantum dots (QDs) were synthesized using a wet chemical method. Their morphology, particle size, structural, optical, and vibrational properties were investigated using transmission electron microscopy, x-ray diffraction, UV-Vis, fluorescence and Raman spectroscopy, respectively. The optical and vibrational properties of the QDs can be controlled by adjusting the Se/S molar ratio. The absorption and emission peaks shift to a longer wavelength range when increasing the Se content. The presence of two CdSe-like and CdS-like longitudinal optical phonon modes was observed. The dependencies of the optical and phonon modes on the Se content are discussed in detail.

  12. Characterization of defects in colloidal CdSe nanocrystals by the modified thermostimulated luminescence technique

    SciTech Connect

    Katsaba, A. V. Fedyanin, V. V.; Ambrozevich, S. A.; Vitukhnovsky, A. G.; Lobanov, A. N.; Selyukov, A. S.; Vasiliev, R. B.; Samatov, I. G.; Brunkov, P. N.

    2013-10-15

    The temperature dependencies of the luminescence spectra of 5-nm-diameter CdSe semiconductor nanocrystals synthesized by colloidal-chemistry methods are investigated. The two bands observed in these spectra around 2.01 and 1.37 eV correspond to band-to-band transitions and luminescence of defect states, respectively. A model explaining the temperature behavior of the luminescence band intensities both upon cooling and heating is put forward. A new modification of spectrally resolved thermostimulated luminescence technique making it possible to determine the activation energies and the character of traps responsible for the temperature dependence of the luminescence intensities is suggested. This technique is used to obtain the activation energies of the emission and capture of electrons at traps (190 and 205 meV, respectively) and to determine the depth of the electron level (57 meV) responsible for luminescence in the 1.37-eV region.

  13. Persistent Inter-Excitonic Quantum Coherence in CdSe Quantum Dots

    PubMed Central

    Caram, Justin R.; Zheng, Haibin; Dahlberg, Peter D.; Rolczynski, Brian S.; Griffin, Graham B.; Fidler, Andrew F.; Dolzhnikov, Dmitriy S.; Talapin, Dmitri V.; Engel, Gregory S.

    2014-01-01

    The creation and manipulation of quantum superpositions is a fundamental goal for the development of materials with novel optoelectronic properties. In this letter, we report persistent (~80 fs lifetime) quantum coherence between the 1S and 1P excitonic states in zinc-blende colloidal CdSe quantum dots at room temperature, measured using Two-Dimensional Electronic Spectroscopy. We demonstrate that this quantum coherence manifests as an intradot phenomenon, the frequency of which depends on the size of the dot excited within the ensemble of QDs. We model the lifetime of the coherence and demonstrate that correlated interexcitonic fluctuations preserve relative phase between excitonic states. These observations suggest an avenue for engineering long-lived interexcitonic quantum coherence in colloidal quantum dots. PMID:24719679

  14. Electronic structure of cobalt doped CdSe quantum dots using soft X-ray spectroscopy

    SciTech Connect

    Joshua T. Wright; Su, Dong; van Buuren, Tony; Meulenberg, Robert W.

    2014-08-21

    The electronic structure and magnetic properties of cobalt doped CdSe quantum dots (QDs) are studied using electron microscopy, soft X-ray spectroscopy, and magnetometry. Magnetometry measurements suggest these QDs are superparamagnetic, contrary to a spin-glass state observed in the bulk analogue. Moreover, the electron microscopy shows well formed QDs, but with cobalt existing as doped into the QD and as unreacted species not contained in the QD. X-ray absorption measurements at the Co L3-edge suggest that changes in spectra features as a function of particle size can be described considering combination of a cobalt ion in a tetrahedral crystal field and an octahedrally coordinated (impurity) phase. With decreasing particle sizes, the impurity phase increases, suggesting that small QDs can be difficult to dope.

  15. Aqueous synthesis and characterization of Ni, Zn co-doped CdSe QDs

    NASA Astrophysics Data System (ADS)

    Thirugnanam, N.; Govindarajan, D.

    2016-01-01

    Ni, Zn co-doped CdSe quantum dots (QDs) were synthesized by chemical precipitation method through aqueous route. The prepared QDs were characterized by X-ray diffraction (XRD) technique, UV-Vis absorption spectroscopy, photoluminescence (PL) spectroscopy and high resolution transmission electron microscopy (HRTEM). XRD technique results indicate that the prepared samples have a zinc blende cubic phase. From UV-Vis absorption spectroscopy technique, the prepared samples were blue shifted with respect to their bulk counter part due to quantum confinement effect. Among different doping ratios examined, a maximum PL emission intensity was observed for CdSe:Ni(1 %):Zn(1 %) QDs. HRTEM pictures show that the prepared QDs were in spherical shape.

  16. Generation of Rashba spin-orbit coupling in CdSe nanowire by ionic liquid gate.

    PubMed

    Zhang, Shan; Tang, Ning; Jin, Weifeng; Duan, Junxi; He, Xin; Rong, Xin; He, Chenguang; Zhang, Lisheng; Qin, Xudong; Dai, Lun; Chen, Yonghai; Ge, Weikun; Shen, Bo

    2015-02-11

    Spintronic devices rely on the spin degree of freedom (DOF), and spin orbit coupling (SOC) is the key to manipulate spin DOF. Quasi-one-dimensional structures, possessing marked anisotropy gives more choice for the manipulation of the spin DOF since the concrete SOC form varies along with crystallographic directions. The anisotropy of the Dresselhaus SOC in cadmium selenide (CdSe) nanobelt and nanowire was studied by circular photogalvanic effect. It was demonstrated that the Dresselhaus SOC parameter is zero along the [0001] crystallographic direction, which suppresses the spin relaxation and increases the spin diffusion length, and thus is beneficial to the spin manipulation. To achieve a device structure with Rashba SOC presence and Dresselhaus SOC absence for manipulating the spin DOF, an ionic liquid gate was produced on a nanowire grown along the [0001] crystallographic direction, and the Rashba SOC was induced by gating, as expected.

  17. Broad spectral photocurrent enhancement in Au-decorated CdSe nanowires.

    PubMed

    Chakraborty, Ritun; Greullet, Fanny; George, Chandramohan; Baranov, Dmitry; Di Fabrizio, Enzo; Krahne, Roman

    2013-06-21

    Metal-semiconductor hybrid nanostructures promise improved photoconductive performance due to plasmonic properties of the metal portions and intrinsic electric fields at the metal-semiconductor interface that possibly enhance charge separation. Here we report gold decorated CdSe nanowires as a novel functional material and investigate the influence of gold decoration on the lateral facets on the photoconductive properties. Gold decorated nanowires show typically an at least ten-fold higher photocurrent as compared to their bare counterparts. Interestingly, the photocurrent enhancement is wavelength independent, although the plasmon resonance related to the gold particles appears in the absorption spectra. Our experiments show that light scattering and Schottky fields associated with the metal-semiconductor interface are at the origin of the photocurrent enhancement.

  18. Exciton recombination dynamics in CdSe nanowires: bimolecular to three-carrier Auger kinetics.

    PubMed

    Robel, István; Bunker, Bruce A; Kamat, Prashant V; Kuno, Masaru

    2006-07-01

    Ultrafast relaxation dynamics of charge carriers in CdSe quantum wires with diameters between 6 and 8 nm are studied as a function of carrier density. At high electron-hole pair densities above 10(19) cm(-3) the dominant process for carrier cooling is the "bimolecular" Auger recombination of one-dimensional (1D) excitons. However, below this excitation level an unexpected transition from a bimolecular (exciton-exciton) to a three-carrier Auger relaxation mechanism occurs. Thus, depending on excitation intensity, electron-hole pair relaxation dynamics in the nanowires exhibit either 1D or 0D (quantum dot) character. This dual nature of the recovery kinetics defines an optimal intensity for achieving optical gain in solution-grown nanowires given the different carrier-density-dependent scaling of relaxation rates in either regime.

  19. Silver nanowires-based signal amplification for CdSe quantum dots electrochemiluminescence immunoassay.

    PubMed

    Huang, Tingyu; Meng, Qingmin; Jie, Guifen

    2015-04-15

    A novel silver-cysteine hybrid nanowires (SCNWs) with many reactive carboxyl and amine groups were prepared, which enable them to be used as idea signal amplifying labels in bioassays. A large number of CdSe quantum dots (QDs) were loaded on the SCNWs to develop amplified SCNWs-QDs electrochemiluminescence (ECL) signal probe. The PAMAM dendrimer-SCNWs nanohybrids covered on the electrode constructed an effective antibody immobilization matrix and made the immobilized biomolecules hold high stability and bioactivity. Based on the specific sandwich immunoreaction strategy, the detection antibody (Ab2)-SCNWs-QDs ECL signal probe was applied to the sensitive signal-on ECL immunoassay of human IgG. The SCNWs-QDs ECL not only opens promising new ECL emitting species, but also promotes the development of novel ECL signal-transition platforms for biosensing devices.

  20. Quantum-confined emission and fluorescence blinking of individual exciton complexes in CdSe nanowires.

    PubMed

    Franz, Dennis; Reich, Aina; Strelow, Christian; Wang, Zhe; Kornowski, Andreas; Kipp, Tobias; Mews, Alf

    2014-11-12

    One-dimensional semiconductor nanostructures combine electron mobility in length direction with the possibility of tailoring the physical properties by confinement effects in radial direction. Here we show that thin CdSe quantum nanowires exhibit low-temperature fluorescence spectra with a specific universal structure of several sharp lines. The structure strongly resembles the pattern of bulk spectra but show a diameter-dependent shift due to confinement effects. Also the fluorescence shows a pronounced complex blinking behavior with very different blinking dynamics of different emission lines in one and the same spectrum. Time- and space-resolved optical spectroscopy are combined with high-resolution transmission electron microscopy of the very same quantum nanowires to establish a detailed structure-property relationship. Extensive numerical simulations strongly suggest that excitonic complexes involving donor and acceptor sites are the origin of the feature-rich spectra.

  1. Microwave synthesis of CdSe and CdTe nanocrystals in nonabsorbing alkanes.

    PubMed

    Washington, Aaron L; Strouse, Geoffrey F

    2008-07-16

    Controlling nanomaterial growth via the "specific microwave effect" can be achieved by selective heating of the chalcogenide precursor. The high polarizability of the precursor allows instantaneous activation and subsequent nucleation leading to the synthesis of CdSe and CdTe in nonmicrowave absorbing alkane solvents. Regardless of the desired size, narrow dispersity nanocrystals can be isolated in less than 3 min with high quantum efficiencies and elliptical morphologies. The reaction does not require a high temperature injection step, and the alkane solvent can be easily removed. In addition, batch-to-batch variance in size is 4.2 +/- 0.14 nm for 10 repeat experimental runs. The use of a stopped-flow reactor allows near continuous automation of the process leading to potential industrial benefits.

  2. Interaction of Globular Plasma Proteins with Water-Soluble CdSe Quantum Dots.

    PubMed

    Pathak, Jyotsana; Rawat, Kamla; Sanwlani, Shilpa; Bohidar, H B

    2015-06-08

    The interactions between water-soluble semiconductor quantum dots [hydrophilic 3-mercaptopropionic acid (MPA)-coated CdSe] and three globular plasma proteins, namely, bovine serum albumin (BSA), β-lactoglobulin (β-Lg) and human serum albumin (HSA), are investigated. Acidic residues of protein molecules form electrostatic interactions with these quantum dots (QDs). To determine the stoichiometry of proteins bound to QDs, we used dynamic light scattering (DLS) and zeta potential techniques. Fluorescence resonance energy transfer (FRET) experiments revealed energy transfer from tryptophan residues in the proteins to the QD particles. Quenching of the intrinsic fluorescence of protein molecules was noticed during this binding process (hierarchy HSA<β-Lg

  3. Auger-Limited Carrier Recombination and Relaxation in CdSe Colloidal Quantum Wells.

    PubMed

    Baghani, Erfan; O'Leary, Stephen K; Fedin, Igor; Talapin, Dmitri V; Pelton, Matthew

    2015-03-19

    Using time-resolved photoluminescence spectroscopy, we show that two-exciton Auger recombination dominates carrier recombination and cooling dynamics in CdSe nanoplatelets, or colloidal quantum wells. The electron-hole recombination rate depends only on the number of electron-hole pairs present in each nanoplatelet, and is consistent with a two-exciton recombination process over a wide range of exciton densities. The carrier relaxation rate within the conduction and valence bands also depends only on the number of electron-hole pairs present, apart from an initial rapid decay, and is consistent with the cooling rate being limited by reheating due to Auger recombination processes. These Auger-limited recombination and relaxation dynamics are qualitatively different from the carrier dynamics in either colloidal quantum dots or epitaxial quantum wells.

  4. Photoinduced fluorescence enhancement in CdSe /ZnS quantum dot monolayers: Influence of substrate

    NASA Astrophysics Data System (ADS)

    Uematsu, Takafumi; Maenosono, Shinya; Yamaguchi, Yukio

    2006-07-01

    Photoinduced fluorescence enhancement (PFE) of CdSe /ZnS core/shell quantum dot (QD) films on SiOx substrates was investigated. The fluorescence intensity of the QD film on SiO1.9 was greatly enhanced by continuous irradiation in vacuum, while the same QD film on SiO0.6 showed a small enhancement of the fluorescence intensity. After irradiation, the rate of fluorescence decay of the QD film on SiO0.6 was smaller than that of the QD film on SiO1.9. Our results suggest that the origin of PFE derives from the photoejection of electrons into the substrate, and that the oxygen-excess-related defects work as trap sites for the electrons.

  5. Optical characterization of CdSe quantum dots with metal chalcogenide ligands in solutions and solids

    NASA Astrophysics Data System (ADS)

    Zhang, Y. Q.; Cao, X. A.

    2011-07-01

    The exchange of the original organic ligands of colloidal CdSe core and CdSe/CdS/ZnS core/multishell quantum dots (QDs) with inorganic metal chalcogenide ligands (SnS44-) resulted in carrier delocalization in solutions and enhanced inter-QD electronic coupling in solids, as inferred from peak redshift and broadening of the absorption and photoluminescence (PL) spectra. The SnS4-capped QDs retained strong excitonic absorption but suffered significant PL quenching. Mild thermal treatment below 350 °C transformed the SnS4 ligands into a more conductive phase, leading to stronger coupling yet complete PL quenching. These findings suggest that QD solids with metal chalcogenide ligands may have high quantum yields of photocurrent generation and can be used as functional blocks in thin-film solar cells for efficient solar energy conversion.

  6. Spin Selective Charge Transport through Cysteine Capped CdSe Quantum Dots.

    PubMed

    Bloom, Brian P; Kiran, Vankayala; Varade, Vaibhav; Naaman, Ron; Waldeck, David H

    2016-07-13

    This work demonstrates that chiral imprinted CdSe quantum dots (QDs) can act as spin selective filters for charge transport. The spin filtering properties of chiral nanoparticles were investigated by magnetic conductive-probe atomic force microscopy (mCP-AFM) measurements and magnetoresistance measurements. The mCP-AFM measurements show that the chirality of the quantum dots and the magnetic orientation of the tip affect the current-voltage curves. Similarly, magnetoresistance measurements demonstrate that the electrical transport through films of chiral quantum dots correlates with the chiroptical properties of the QD. The spin filtering properties of chiral quantum dots may prove useful in future applications, for example, photovoltaics, spintronics, and other spin-driven devices.

  7. Understanding the features in the ultrafast transient absorption spectra of CdSe quantum dots

    NASA Astrophysics Data System (ADS)

    Zhang, Cheng; Do, Thanh Nhut; Ong, Xuanwei; Chan, Yinthai; Tan, Howe-Siang

    2016-12-01

    We describe a model to explain the features of the ultrafast transient absorption (TA) spectra of CdSe core type quantum dots (QDs). The measured TA spectrum consists of contributions by the ground state bleach (GSB), stimulated emission (SE) and excited state absorption (ESA) processes associated with the three lowest energy transition of the QDs. We model the shapes of the GSB, SE and ESA spectral components after fits to the linear absorption. The spectral positions of the ESA components take into account the biexcitonic binding energy. In order to obtain the correct weightage of the GSB, SE and ESA components to the TA spectrum, we enumerate the set of coherence transfer pathways associated with these processes. From our fits of the experimental TA spectra of 65 Å diameter QDs, biexcitonic binding energies for the three lowest energy transitions are obtained.

  8. Thickness dependent optical and electrical properties of CdSe thin films

    NASA Astrophysics Data System (ADS)

    Purohit, A.; Chander, S.; Nehra, S. P.; Lal, C.; Dhaka, M. S.

    2016-05-01

    The effect of thickness on the optical and electrical properties of CdSe thin films is investigated in this paper. The films of thickness 445 nm, 631 nm and 810 nm were deposited on glass and ITO coated glass substrates using thermal evaporation technique. The deposited thin films were thermally annealed in air atmosphere at temperature 100°C and were subjected to UV-Vis spectrophotometer and source meter for optical and electrical analysis respectively. The absorption coefficient is observed to increase with photon energy and found maximum in higher photon energy region. The extinction coefficient and refractive index are also calculated. The electrical analysis shows that the electrical resistivity is observed to be decreased with thickness.

  9. Hot-electron luminescence in aged electrodeposited CdSe liquid-junction solar cell

    SciTech Connect

    Silberstein, R.P.; Tomkiewicz, M.

    1983-01-01

    We have utilized Raman spectroscopy and scanning Auger electron spectroscopy (AES) to probe the surface of polycrystalline, electrodeposited CdSe photoelectrodes which have been aged in a polysulfide electrolyte under illumination and in darkness. We have observed characteristic ''hot-electron'' luminescence at multiples of ..omega../sub LO/ (CdS) = 305 cm/sup -1/ in the light-aged electrode, indicating that a surface layer of CdS has been formed. AES profiling shows that extensive substitution of S for Se has occurred, in the light-aged electrode alone, to a depth of approx.600 A. Measurements at 300 K suggest that Raman scattering can be a useful, in situ, contactless, nondestructive probe of CdS formation.

  10. Ordered structures based on self-organized Au and CdSe nanoparticles

    SciTech Connect

    Zaporozhets, M. A.; Savilov, S. V.; Zhigalina, O. M.; Sul'yanov, S. N.; Volkov, V. V.; Nikolaichik, V. I.; Gubin, S. P.; Avilov, A. S.

    2012-05-15

    Methods for obtaining cadmium selenide and gold nanoparticles have been developed. The sizes of the nanoparticles are determined and the morphology, structure, and chemical composition of these nanoparticles and their ensembles are studied by a complex of structural methods: electron diffraction, X-ray diffraction, energy-dispersive X-ray analysis, high-resolution transmission electron microscopy, and small-angle X-ray scattering. Gold nanoparticles are mainly spherical and have an average size of 10 nm. They are single-phase and have an fcc crystal structure. Samples of synthesized CdSe nanoparticles contain monodisperse spherical particles 12 nm in size with a wurtzite structure. The deposition of nanoparticles on a carbon substrate is accompanied by their self-organization into a closely packed two-dimensional structure with a pronounced texture in which all nanoparticles are oriented in the [001] direction perpendicularly to the carbon substrate plane.

  11. Selective recognition of dysprosium(III) ions by enhanced chemiluminescence CdSe quantum dots.

    PubMed

    Hosseini, Morteza; Ganjali, Mohammad R; Vaezi, Zahra; Faridbod, Farnoush; Arabsorkhi, Batool; Sheikhha, Mohammad H

    2014-01-01

    The intensity of emitted light from CdSe quantum dots (QDs)-H2O2 is described as a novel chemiluminescence (CL) reaction for determination of dysprosium. This reaction is based on the catalytic effect of Dy(3+) ions, causing a significant increase in the light emission, as a result of the reaction of quantum dots (QDs) with hydrogen peroxide. In the optimum conditions, this method was satisfactorily described by linear calibration curve in the range of 8.3×10(-7)-5.0×10(-6)M, the detection limit of 6.0×10(-8)M, and the relative standard deviation for five determinations of 2.5×10(-6)M Dy(3+) 3.2%. The main experimental advantage of the proposed method is its selective to Dy(3+) ions compared with common coexisting cations, therefore, it was successfully applied for the determination of dysprosium ions in water samples.

  12. Parameters influencing the performance and stability of CdSe MIS solar cells

    SciTech Connect

    Rickus, E.

    1982-09-01

    CdSe MIS solar cells with ZnSe as ''I-layer'' are very insensitive to oxidative ambients and to humidity even in the unsealed state. They show lower sensitivity to ''I-film'' thickness-variations than native-oxide devices. The use of wide-bandgap semiconductor as ''I-film'' opens new ways to influence the energetic position of the potential barrier caused by the ''I-layer''. Expecially doping of the ZnSe-film results in a distinct enhancement of the fill factor. AM 1-efficiencies of 6.6 percent on 1 cm/sup 2/ active area have been achieved with relatively low effort. Further optimizations will enhance the efficiency of this simple, economic solar cell.

  13. Transient charge technique investigation of HgI/sub 2/ and CdSe nuclear detectors

    SciTech Connect

    Roth, M.; Burger, A.; Nissenbaum, J.; Schieber, M.

    1987-02-01

    The use of the Transient Charge Technique (TCT) for the evaluation of high resistivity Mercuric Iodide and Cadmium Selenide nuclear radiation detectors is suggested. It has been shown that the real values of mobilities and trapping times of electrons and holes in HgI/sub 2/ can be easily obtained from the analysis of the voltage transient response to drift of charge carriers created by alpha particles. This allows one to evaluate the bulk transport properties of the material and, additionally, to estimate accurately the surface recombination velocity of the carriers. Preliminary results on the shape of voltage transients in CdSe are also reported, and the limitations of the use of the TCT for characterization of both materials are discussed.

  14. Radiative rate modification in CdSe quantum dot-coated microcavity

    SciTech Connect

    Veluthandath, Aneesh V.; Bisht, Prem B.

    2015-12-21

    Whispering gallery modes (WGMs) of the microparticles with spherical or cylindrical symmetry have exceptionally high quality factors and small mode volume. Quantum dots (QDs) are zero dimensional systems with variable band gap as well as luminescent properties with applications in photonics. In this paper, the WGMs have been observed in the luminescence spectra of CdSe QD-coated single silica microspheres. Theoretical estimations of variation of resonance frequency, electric field, and Q-values have been done for a multilayer coating of QDs on silica microspheres. Observed WGMs have been identified for their mode number and polarization using Mie theory. Broadening of modes due to material absorption has been observed. Splitting of WGMs has also been observed due to coherent coupling of counter propagating waves in the microcavity due to the presence of QDs. At room temperature, the time-resolved study indicates the modification of the radiative rate due to coupling of WGMs of the microcavity-QD hybrid system.

  15. CdTe and CdSe Quantum Dots Cytotoxicity: A Comparative Study on Microorganisms

    PubMed Central

    Gomes, Suzete A.O.; Vieira, Cecilia Stahl; Almeida, Diogo B.; Santos-Mallet, Jacenir R.; Menna-Barreto, Rubem F. S.; Cesar, Carlos L.; Feder, Denise

    2011-01-01

    Quantum dots (QDs) are colloidal semiconductor nanocrystals of a few nanometers in diameter, being their size and shape controlled during the synthesis. They are synthesized from atoms of group II–VI or III–V of the periodic table, such as cadmium telluride (CdTe) or cadmium selenium (CdSe) forming nanoparticles with fluorescent characteristics superior to current fluorophores. The excellent optical characteristics of quantum dots make them applied widely in the field of life sciences. Cellular uptake of QDs, location and translocation as well as any biological consequence, such as cytotoxicity, stimulated a lot of scientific research in this area. Several studies pointed to the cytotoxic effect against micoorganisms. In this mini-review, we overviewed the synthesis and optical properties of QDs, and its advantages and bioapplications in the studies about microorganisms such as protozoa, bacteria, fungi and virus. PMID:22247686

  16. Magnetic polaron on dangling-bond spins in CdSe colloidal nanocrystals.

    PubMed

    Biadala, Louis; Shornikova, Elena V; Rodina, Anna V; Yakovlev, Dmitri R; Siebers, Benjamin; Aubert, Tangi; Nasilowski, Michel; Hens, Zeger; Dubertret, Benoit; Efros, Alexander L; Bayer, Manfred

    2017-03-13

    Non-magnetic colloidal nanostructures can demonstrate magnetic properties typical for diluted magnetic semiconductors because the spins of dangling bonds at their surface can act as the localized spins of magnetic ions. Here we report the observation of dangling-bond magnetic polarons (DBMPs) in 2.8-nm diameter CdSe colloidal nanocrystals (NCs). The DBMP binding energy of 7 meV is measured from the spectral shift of the emission lines under selective laser excitation. The polaron formation at low temperatures occurs by optical orientation of the dangling-bond spins (DBSs) that result from dangling-bond-assisted radiative recombination of spin-forbidden dark excitons. Modelling of the temperature dependence of the DBMP-binding energy and emission intensity shows that the DBMP is composed of a dark exciton and about 60 DBSs. The exchange integral of one DBS with the electron confined in the NC is ∼0.12 meV.

  17. Persistent Inter-Excitonic Quantum Coherence in CdSe Quantum Dots.

    PubMed

    Caram, Justin R; Zheng, Haibin; Dahlberg, Peter D; Rolczynski, Brian S; Griffin, Graham B; Fidler, Andrew F; Dolzhnikov, Dmitriy S; Talapin, Dmitri V; Engel, Gregory S

    2014-01-02

    The creation and manipulation of quantum superpositions is a fundamental goal for the development of materials with novel optoelectronic properties. In this letter, we report persistent (~80 fs lifetime) quantum coherence between the 1S and 1P excitonic states in zinc-blende colloidal CdSe quantum dots at room temperature, measured using Two-Dimensional Electronic Spectroscopy. We demonstrate that this quantum coherence manifests as an intradot phenomenon, the frequency of which depends on the size of the dot excited within the ensemble of QDs. We model the lifetime of the coherence and demonstrate that correlated interexcitonic fluctuations preserve relative phase between excitonic states. These observations suggest an avenue for engineering long-lived interexcitonic quantum coherence in colloidal quantum dots.

  18. Influence of acid and alkaline sources on optical, structural and photovoltaic properties of CdSe nanoparticles precipitated from aqueous solution

    NASA Astrophysics Data System (ADS)

    Coria-Monroy, C. Selene; Sotelo-Lerma, Mérida; Hu, Hailin

    2016-06-01

    CdSe is a widely researched material for photovoltaic applications. One of the most important parameters of the synthesis is the pH value, since it determines the kinetics and the mechanism of the reaction and in consequence, the optical and morphological properties of the products. We present the synthesis of CdSe in solution with strict control of pH and the comparison of ammonia and KOH as alkaline sources and diluted HCl as acid medium. CdSe formation was monitored with photoluminescence emission spectra (main peak in 490 nm, bandgap of CdSe nanoparticles). XRD patterns indicated that CdSe nanoparticles are mainly of cubic structure for ammonia and HCl, but the hexagonal planes appear with KOH. Product yield decreases with pH and also decreases with KOH at constant pH value since ammonia has a double function, as complexing agent and alkaline source. Changes in morphology were observed in SEM images as well with the different alkaline source. The effect of alkaline sources on photovoltaic performance of hybrid organic solar cells with CdSe and poly(3-hexylthiophene) as active layers was clearly observed, indicating the importance of synthesis conditions on optoelectronic properties of promising semiconductor nanomaterials for solar cell applications.

  19. Surface Passivation of CdSe Quantum Dots in All Inorganic Amorphous Solid by Forming Cd1−xZnxSe Shell

    PubMed Central

    Xia, Mengling; Liu, Chao; Zhao, Zhiyong; Wang, Jing; Lin, Changgui; Xu, Yinsheng; Heo, Jong; Dai, Shixun; Han, Jianjun; Zhao, Xiujian

    2017-01-01

    CdSe quantum dots (QDs) doped glasses have been widely investigated for optical filters, LED color converter and other optical emitters. Unlike CdSe QDs in solution, it is difficult to passivate the surface defects of CdSe QDs in glass matrix, which strongly suppress its intrinsic emission. In this study, surface passivation of CdSe quantum dots (QDs) by Cd1−xZnxSe shell in silicate glass was reported. An increase in the Se/Cd ratio can lead to the partial passivation of the surface states and appearance of the intrinsic emission of CdSe QDs. Optimizing the heat-treatment condition promotes the incorporation of Zn into CdSe QDs and results in the quenching of the defect emission. Formation of CdSe/Cd1−xZnxSe core/graded shell QDs is evidenced by the experimental results of TEM and Raman spectroscopy. Realization of the surface passivation and intrinsic emission of II-VI QDs may facilitate the wide applications of QDs doped all inorganic amorphous materials. PMID:28169376

  20. Surface Passivation of CdSe Quantum Dots in All Inorganic Amorphous Solid by Forming Cd1‑xZnxSe Shell

    NASA Astrophysics Data System (ADS)

    Xia, Mengling; Liu, Chao; Zhao, Zhiyong; Wang, Jing; Lin, Changgui; Xu, Yinsheng; Heo, Jong; Dai, Shixun; Han, Jianjun; Zhao, Xiujian

    2017-02-01

    CdSe quantum dots (QDs) doped glasses have been widely investigated for optical filters, LED color converter and other optical emitters. Unlike CdSe QDs in solution, it is difficult to passivate the surface defects of CdSe QDs in glass matrix, which strongly suppress its intrinsic emission. In this study, surface passivation of CdSe quantum dots (QDs) by Cd1‑xZnxSe shell in silicate glass was reported. An increase in the Se/Cd ratio can lead to the partial passivation of the surface states and appearance of the intrinsic emission of CdSe QDs. Optimizing the heat-treatment condition promotes the incorporation of Zn into CdSe QDs and results in the quenching of the defect emission. Formation of CdSe/Cd1‑xZnxSe core/graded shell QDs is evidenced by the experimental results of TEM and Raman spectroscopy. Realization of the surface passivation and intrinsic emission of II-VI QDs may facilitate the wide applications of QDs doped all inorganic amorphous materials.

  1. Comparative experiments of graphene covalently and physically binding CdSe quantum dots to enhance the electron transport in flexible photovoltaic devices.

    PubMed

    Jung, Mi-Hee; Chu, Moo-Jung

    2014-08-07

    In this research, we prepared composite films via covalent coupling of CdSe quantum dots (QDs) to graphene through the direct binding of aryl radicals to the graphene surface. To compare the carrier transport with the CdSe aryl binding graphene film, we prepared CdSe pyridine capping graphene films through the pi-pi interactions of noncovalent bonds between the graphene and pyridine molecules. The photovoltaic devices were fabricated from the two hybrid films using the electrophoretic deposition method on flexible substrates. Even though the two hybrid films have the same amount of QDs and graphene, time-resolved fluorescence emission decay results show that the emission lifetime of the CdSe aryl group binding graphene film is significantly shorter than that of the pyridine capping CdSe-graphene. The quantum efficiency and photocurrent density of the device fabricated from CdSe aryl binding graphene were also higher than those of the device fabricated from pyridine capping CdSe-graphene. These results indicated that the carrier transport of the QD-graphene system is not related to the additive effect from the CdSe and graphene components but rather is a result of the unique interactions between the graphene and QDs. We could expect that these results can be useful in designing QD-graphene composite materials, which are applied in photovoltaic devices.

  2. Resonant surface-enhanced Raman scattering by optical phonons in a monolayer of CdSe nanocrystals on Au nanocluster arrays

    NASA Astrophysics Data System (ADS)

    Milekhin, Alexander G.; Sveshnikova, Larisa L.; Duda, Tatyana A.; Rodyakina, Ekaterina E.; Dzhagan, Volodymyr M.; Sheremet, Evgeniya; Gordan, Ovidiu D.; Himcinschi, Cameliu; Latyshev, Alexander V.; Zahn, Dietrich R. T.

    2016-05-01

    Here we present the results on an investigation of resonant Stokes and anti- Stokes surface-enhanced Raman scattering (SERS) by optical phonons in colloidal CdSe nanocrystals (NCs) homogeneously deposited on arrays of Au nanoclusters using the Langmuir-Blodgett technology. The thickness of deposited NCs, determined by transmission and scanning electron microscopy, amounts to approximately 1 monolayer. Special attention is paid to the determination of the localized surface plasmon resonance (LSPR) energy in the arrays of Au nanoclusters as a function of the nanocluster size by means of micro-ellipsometry. SERS by optical phonons in CdSe NCs shows a significant enhancement factor with a maximal value of 2 × 103 which depends resonantly on the Au nanocluster size and thus on the LSPR energy. The deposition of CdSe NCs on the arrays of Au nanocluster dimers enabled us to study the polarization dependence of SERS. It was found that a maximal SERS signal is observed for the light polarization along the dimer axis. Finally, SERS by optical phonons was observed for CdSe NCs deposited on the structures with a single Au dimer. A difference of the LO phonon energy is observed for CdSe NCs on different single dimers. This effect is explained as the confinement-induced shift which depends on the CdSe nanocrystal size and indicates quasi-single NC Raman spectra being obtained.

  3. Study of binary and ternary organic hybrid CdSe quantum dot photodetector

    NASA Astrophysics Data System (ADS)

    Ramar, M.; Kajal, S.; Pal, Prabir; Srivastava, R.; Suman, C. K.

    2015-09-01

    The hybrid binary and ternary photodetectors (PDs) were fabricated from P3HT-PC71BM with CdSe quantum dot (QD) materials. The absorption spectra of P3HT:PC71BM (named as B1), P3HT:CdSe (B2) and P3HT:CdSe:PC71BM (T) active blended material were analyzed in the wavelength range from 350 to 800 nm. The current density-voltage characteristics of the device were measured in dark and under illumination for study of detector detectivities and the contact with electrode. The ratio at -0.5 V for PDs B1, B2 and T is 1.1 × 102, 1.9 × 102 and 1.8 × 103, respectively. The values of detectivity for B1, B2 and T are 1 × 1010, 2 × 1010 and 7 × 1011 Jones, respectively. The for PD T is ten times in comparison with B1 and B2 PDs. The linear dynamic range (LDR) value for ternary device is more than double to both binary PDs. The absorption by CdSe QD increases the photon efficiency in the ternary detector, and at the same time the ternary detectors have high detectivity in broad spectral range. The responsivity of current to the light intensity exponent θ for detector B1, B2 and T is ~0.55, 0.55 and 0.62, respectively, which represents a complex process of electron hole generation, recombination and trapping within active material.

  4. Computational insights into CdSe quantum dots' interactions with acetate ligands.

    PubMed

    Tamukong, Patrick K; Peiris, Wadumesthrige D N; Kilina, Svetlana

    2016-07-27

    Using density functional theory (DFT) and time-dependent DFT (TDDFT), we investigate the effects of carboxylate groups on the electronic and optical properties of CdSe quantum dots (QDs). We specifically focus on the mechanisms of the binding of the acetate anion to the QD surface with and without excess of Cd(2+) cations. Our calculations show that the most stable ligated conformations are those where an acetate is attached to extra Cd(2+) ion forming a [Cd(2+)(CH3COO(-))] at the QD's surface, while also accompanied by an acetate attached nearby at the surface balancing the overall neutral charge of the system. In contrast, formation of a neutral metal-acetate complex [Cd(2+)(CH3COO(-))2] at the QD surface is found to be the least energetically preferable. A strength of the QD-ligand interaction depends on the solvent, the facet of the QD to which the ligands are attached, and the binding mode - with the bridging mode found to be the most stable conformation for both acetate and cadmium acetate ligands. The cadmium acetate ligands introduce electron trap states at the edge of the conduction band - unoccupied orbitals predominately localized on Cd(2+) ion - that are extremely sensitive to the ligand position and the solvent polarity. Polar solvents like acetonitrile delocalize the electronic density over the entire system and, thus, eliminate trap states. As a result, mixed passivation of the CdSe QDs by pairs of cadmium acetate and acetate ligands provides optimal optical properties with minimal contributions of the ligand-related trap states and optically bright lowest energy transitions.

  5. Orbital alignment at the internal interface of arylthiol functionalized CdSe molecular hybrids

    NASA Astrophysics Data System (ADS)

    Li, Zhi; Mazzio, Katherine A.; Okamoto, Ken; Luscombe, Christine K.; Schlaf, Rudy

    2015-04-01

    Organic-inorganic nanoparticle molecular hybrid materials are interesting candidates for improving exciton separation in organic solar cells. The orbital alignment at the internal interface of cadmium selenide (ArS-CdSe) hybrid materials functionalized with covalently attached arylthiolate moieties was investigated through X-ray photoemission spectroscopy (XPS) and ultraviolet photoemission spectroscopy (UPS). A physisorbed interface between arylthiol (ArSH) ligands and CdSe nanoparticles was also investigated for comparison. This interface was created via a multi-step thin film deposition procedure in-vacuo, where the surface was characterized after each experimental step. This enabled the direct comparison of ArSH/CdSe interfaces produced via physisorption and ArS-CdSe covalently attached hybrid materials, which rely on a chemical reaction for their synthesis. All material depositions were performed using an electrospray deposition, which enabled the direct injection of solution-originating molecular species into the vacuum system. This method allows XPS and UPS measurements to be performed immediately after deposition without exposure to the atmosphere. Transmission electron microscopy was used to determine the morphology and particle size of the deposited materials. Ultraviolet-visible spectroscopy was used to estimate the optical band gap of the CdSe nanoparticles and the HOMO-LUMO gap of the ArSH ligands. These experiments showed that hybridization via covalent bonds results in an orbital realignment at the ArSH/CdSe interface in comparison to the physisorbed interface. The orbital alignment within the hybrid caused a favorable electron injection barrier, which likely facilitates exciton-dissociation while preventing charge-recombination.

  6. Orbital alignment at the internal interface of arylthiol functionalized CdSe molecular hybrids

    SciTech Connect

    Li, Zhi; Schlaf, Rudy; Mazzio, Katherine A.; Okamoto, Ken; Luscombe, Christine K.

    2015-04-21

    Organic-inorganic nanoparticle molecular hybrid materials are interesting candidates for improving exciton separation in organic solar cells. The orbital alignment at the internal interface of cadmium selenide (ArS-CdSe) hybrid materials functionalized with covalently attached arylthiolate moieties was investigated through X-ray photoemission spectroscopy (XPS) and ultraviolet photoemission spectroscopy (UPS). A physisorbed interface between arylthiol (ArSH) ligands and CdSe nanoparticles was also investigated for comparison. This interface was created via a multi-step thin film deposition procedure in-vacuo, where the surface was characterized after each experimental step. This enabled the direct comparison of ArSH/CdSe interfaces produced via physisorption and ArS-CdSe covalently attached hybrid materials, which rely on a chemical reaction for their synthesis. All material depositions were performed using an electrospray deposition, which enabled the direct injection of solution-originating molecular species into the vacuum system. This method allows XPS and UPS measurements to be performed immediately after deposition without exposure to the atmosphere. Transmission electron microscopy was used to determine the morphology and particle size of the deposited materials. Ultraviolet-visible spectroscopy was used to estimate the optical band gap of the CdSe nanoparticles and the HOMO-LUMO gap of the ArSH ligands. These experiments showed that hybridization via covalent bonds results in an orbital realignment at the ArSH/CdSe interface in comparison to the physisorbed interface. The orbital alignment within the hybrid caused a favorable electron injection barrier, which likely facilitates exciton-dissociation while preventing charge-recombination.

  7. Electrochemical photovoltaic cells CdSe thin film electrodes. Final report, June 1979-June 1980

    SciTech Connect

    Russak, M.A.; Reichman, J.; DeCarlo, J.; Creter, C.

    1980-07-01

    Progress on developing stable, thin-film CdSe electrodes with sunlight conversion efficiency of 10% for use with aqueous polysulfide electrolytes in frontwall and backwall illuminated EPCs is reported. The main effort has been directed towards establishing the relationships among thin-film processing, resultant electronic properties and I-V performance in order to produce electrodes with maximum power conversion efficiency. The most encouraging results have been obtained with CdSe thin-film electrodes produced in two ways for frontwall cells. Films were deposited on titanium at approximately 100/sup 0/C with a high Se/Cd ratio and then heat treated in air at 350 to 400/sup 0/C. These films usually have a very fine grained microstructure after heat treatment and the resultant electrodes exhibit fairly square I-V characteristics with fill factors of 0.6 or greater and high current output. The overall power efficiency of these electrodes is limited by relatively low output voltages. At present, power conversion efficiencies of 3 to 5% can be obtained reproducibly at simulated AM2 conditions with electrodes processed in this manner. The second type of film that has yielded very promising results is deposited on titanium at substrate temperatures greater than 400/sup 0/C. The interesting feature of these electrodes is their increased open circuit voltage. However, the current output and fill factor are lower. As a result, the power conversion efficiency of these electrodes is 3 to 4%. Backwall electrodes with an efficiency of greater than 4% and short circuit densities near theoretical for AM2 conditions have been produced.

  8. Electrochemical preparation of vertically aligned, hollow CdSe nanotubes and their p-n junction hybrids with electrodeposited Cu2O

    NASA Astrophysics Data System (ADS)

    Debgupta, Joyashish; Devarapalli, Ramireddy; Rahman, Shakeelur; Shelke, Manjusha V.; Pillai, Vijayamohanan K.

    2014-07-01

    Vertically aligned, hollow nanotubes of CdSe are grown on fluorine doped tin oxide (FTO) coated glass substrates by ZnO nanowire template-assisted electrodeposition technique, followed by selective removal of the ZnO core using NH4OH. A detailed mechanism of nucleation and anisotropic growth kinetics of nanotubes have been studied by a combination of characterization tools such as chronoamperometry, SEM and TEM. Interestingly, ``as grown'' CdSe nanotubes (CdSe NTs) on FTO coated glass plates behave as n-type semiconductors exhibiting an excellent photo-response (with a generated photocurrent density value of ~470 μA cm-2) while in contact with p-type Cu2O (p-type semiconductor, grown separately on FTO plates) because of the formation of a n-p heterojunction (type II). The observed photoresponse is 3 times higher than that of a similar device prepared with electrodeposited CdSe films (not nanotubes) and Cu2O on FTO. This has been attributed to the hollow 1-D nature of CdSe NTs, which provides enhanced inner and outer surface areas for better absorption of light and also assists faster transport of photogenerated charge carriers.Vertically aligned, hollow nanotubes of CdSe are grown on fluorine doped tin oxide (FTO) coated glass substrates by ZnO nanowire template-assisted electrodeposition technique, followed by selective removal of the ZnO core using NH4OH. A detailed mechanism of nucleation and anisotropic growth kinetics of nanotubes have been studied by a combination of characterization tools such as chronoamperometry, SEM and TEM. Interestingly, ``as grown'' CdSe nanotubes (CdSe NTs) on FTO coated glass plates behave as n-type semiconductors exhibiting an excellent photo-response (with a generated photocurrent density value of ~470 μA cm-2) while in contact with p-type Cu2O (p-type semiconductor, grown separately on FTO plates) because of the formation of a n-p heterojunction (type II). The observed photoresponse is 3 times higher than that of a similar

  9. Ligand capping effect for dye solar cells with a CdSe quantum dot sensitized ZnO nanorod photoanode.

    PubMed

    Sun, Xiao Wei; Chen, Jing; Song, Jun Ling; Zhao, De Wei; Deng, Wei Qiao; Lei, Wei

    2010-01-18

    We report a quantum dot sensitized solar cell (QDSSC) with a thioglycolic acid (TGA) capped CdSe quantum dot (QD) sensitized ZnO nanorod photoanode. As revealed by UV-Vis absorption spectrum and transmission electron microscopy, the quantum dots can be effectively adsorbed onto ZnO nanorods. By studying the emission decay, the quenching of the CdSe QDs by ZnO nanorod was verified, and an electron transfer (from QD to ZnO) rate constant of 1 x 10(8) s(-1) was obtained. The efficiency of the as-prepared QDSSC was 0.66% and an incident power conversion efficiency of 22% at 400 nm was achieved.

  10. Thiolated DAB dendrimers and CdSe quantum dots nanocomposites for Cd(II) or Pb(II) sensing.

    PubMed

    Algarra, M; Campos, B B; Alonso, B; Miranda, M S; Martínez, A M; Casado, C M; Esteves da Silva, J C G

    2012-01-15

    Four different generation of thiol-DAB dendrimers were synthesized, S-DAB-G(x) (x=1, 2, 3 and 5), and coupled with CdSe quantum dots, to obtain fluorescent nanocomposites as metal ions sensing. Cd(II) and Pb(II) showed the higher enhancement and quenching effects respectively towards the fluorescence of S-DAB-G(5)-CdSe nanocomposite. The fluorescence enhancement provoked by Cd(II) can be linearized using a Henderson-Hasselbalch type equation and the quenching provoked by Pb(II) can be linearized by a Stern-Volmer equation. The sensor responds to Cd(II) ion in the 0.05-0.7μM concentration range and to Pb(II) ion in the 0.01-0.15mM concentration range with a LOD of 0.06mM. The sensor has selectivity limitations but its dendrimer configuration has analytical advantages.

  11. Polarization-sensitive nanowire photodetectors based on solution-synthesized CdSe quantum-wire solids.

    PubMed

    Singh, Amol; Li, Xiangyang; Protasenko, Vladimir; Galantai, Gabor; Kuno, Masaru; Xing, Huili Grace; Jena, Debdeep

    2007-10-01

    Polarization-sensitive photodetectors are demonstrated using solution-synthesized CdSe nanowire (NW) solids. Photocurrent action spectra taken with a tunable white light source match the solution linear absorption spectra of the NWs, showing that the NW network is responsible for the device photoconductivity. Temperature-dependent transport measurements reveal that carriers responsible for the dark current through the nanowire solids are thermally excited across CdSe band gap. The NWs are aligned using dielectrophoresis between prepatterned electrodes using conventional optical photolithography. The photocurrent through the NW solid is found to be polarization-sensitive, consistent with complementary absorption (emission) measurements of both single wires and their ensembles. The range of solution-processed semiconducting NW materials, their facile synthesis, ease of device fabrication, and compatibility with a variety of substrates make them attractive for potential nanoscale polarization-sensitive photodetectors.

  12. Fortification of CdSe quantum dots with graphene oxide. Excited state interactions and light energy conversion.

    PubMed

    Lightcap, Ian V; Kamat, Prashant V

    2012-04-25

    Graphene based 2-D carbon nanostructures provide new opportunities to fortify semiconductor based light harvesting assemblies. Electron and energy transfer rates from photoexcited CdSe colloidal quantum dots (QDs) to graphene oxide (GO) and reduced graphene oxide (RGO) were isolated by analysis of excited state deactivation lifetimes as a function of degree of oxidation and charging in (R)GO. Apparent rate constants for energy and electron transfer determined for CdSe-GO composites were 5.5 × 10(8) and 6.7 × 10(8) s(-1), respectively. Additionally, incorporation of GO in colloidal CdSe QD films deposited on conducting glass electrodes was found to enhance the charge separation and electron conduction through the QD film, thus allowing three-dimensional sensitization. Photoanodes assembled from CdSe-graphene composites in quantum dot sensitized solar cells display improved photocurrent response (~150%) over those prepared without GO.

  13. Cd/Hg cationic substitution in magic-sized CdSe clusters: Optical characterization and theoretical studies

    NASA Astrophysics Data System (ADS)

    Antanovich, Artsiom; Prudnikau, Anatol; Gurin, Valerij; Artemyev, Mikhail

    2015-07-01

    We examine conversion of magic-sized CdSe clusters (MSCs) into HgSe ones by means of Cd/Hg cation exchange. With this procedure Cd8Cd17- and Cd32-selenide clusters can be converted into corresponding Hg8-, Hg17- and Hg32-selenide ones. Upon cationic exchange MSCs behavior differs from that of bulkier counterparts - larger (2-3 nm) quantum dots. Unlike CdSe colloidal quantum dots, magic-sized clusters are converted in fast and complete manner without a formation of intermediate mixed CdxHg1-x compounds that was established on the basis of optical absorption spectroscopy and chemical composition analysis. These assumptions were supported by DFT quantum chemical calculations performed for Cd8-, Cd17- and Hg8-, Hg17-selenide model clusters. Energies of experimental and calculated optical transitions were compared in order to prove the isostructural character of cationic substitution in magic-sized clusters.

  14. Vacuum evaporated CdSe /SUB 1-x/ Te /SUB x/ thin films for electrochemical photovoltaic cells

    SciTech Connect

    Russak, M.A.; Creter, C.

    1984-03-01

    CdSe /SUB 1-x/ Te /SUB x/ thin films have been produced over a wide range of x values by concurrent vacuum evaporation of the constituent elements. The most consistent results in terms of producing single-phase material were obtained when substrate temperatures were in the range of 350/sup 0/-450/sup 0/C. Photoelectrochemical evaluation of the resultant thin films indicated postdeposition heat-treatment and surface etching were necessary to maximize photovoltaic outputs. A dependence of photoelectrochemical behavior, bandgap, and efficiency on x value was also found. The maximum efficiency recorded was 7.4% for a CdSe /SUB 0.8/ Te /SUB 0.2/ composition under simulated AM2 conditions.

  15. Temperature- and field-dependent energy transfer in CdSe nanocrystal aggregates studied by magneto-photoluminescence spectroscopy.

    PubMed

    Blumling, Daniel E; Tokumoto, Takahisa; McGill, Stephen; Knappenberger, Kenneth L

    2012-08-21

    The influence of temperature and applied magnetic fields on photoluminescence (PL) emission and electronic energy transfer (ET) of both isolated and aggregated CdSe nanocrystals was investigated. Following 400-nm excitation, temperature-dependent, intensity-integrated and energy-resolved PL measurements were used to quantify the emission wavelength and amplitude of isolated CdSe nanocrystals. The results indicated an approximately three-fold increase in PL intensity upon decreasing the temperature from 300 K to 6 K; this was attributed to a reduction of charge carrier access to nanocrystal surface trap states and suppression of thermal loss channels. Temperature-dependent PL measurements of aggregated CdSe nanocrystals, which included both energy-donating and -accepting particles, were analyzed using a modified version of Förster theory. Temperature-dependent ET efficiency increased from 0.55 to 0.75 upon decreasing the sample temperature from 225 K to 6 K, and the ET data contained the same trend observed for the PL of isolated nanoclusters. The application of magnetic fields to increase nanocrystal ET efficiency was studied using magneto-photoluminescence measurements recorded at a sample temperature of 1.6 K. We demonstrated that the exciton fine structure population of the donor was varied using applied magnetic fields, which in turn dictated the PL yield and the resultant ET efficiency of the CdSe nanocrystal aggregate system. The experimental data indicated an ET efficiency enhancement of approximately 7%, which was limited by the random orientation of the spherical nanocrystals in the thin film.

  16. Synthesis, Surface Studies, Composition and Structural Characterization of CdSe, Core/Shell, and Biologically Active Nanocrystals

    PubMed Central

    Rosenthal, Sandra J.; McBride, James; Pennycook, Stephen J.; Feldman, Leonard C.

    2011-01-01

    Nanostructures, with their very large surface to volume ratio and their non-planar geometry, present an important challenge to surface scientists. New issues arise as to surface characterization, quantification and interface formation. This review summarizes the current state of the art in the synthesis, composition, surface and interface control of CdSe nanocrystal systems, one of the most studied and useful nanostructures. PMID:21479151

  17. HPVB and HPVZM shaped growth of CdZnTe, CdSe, and ZnSe crystals

    NASA Astrophysics Data System (ADS)

    Kolesnikov, Nikolai N.; James, Ralph B.; Berzigiarova, Nadejda S.; Kulakov, Mihail P.

    2003-01-01

    High-pressure Bridgman (HPVB) and vertical zone melting (HPVZM) growth has been applied for manufacturing Cd1-xZnxTe (x = 0.04 - 0.2), CdSe and ZnSe crystal tapes with sizes up to 120×120×12 mm. The influence of the technological parameters of the growth process on the crystal quality and some properties is discussed. The dependence of the inclusion (bubbles) content on deviation from the melt stoichiometry is determined. The method for growing plates with low content of the inclusions is described. High-resistivity crystal tapes of undoped CdZnTe (1010 Ohm×cm), CdSe (1011 Ohm×cm) and ZnSe (>1011 Ohm×cm) were prepared. Possibility of the tape growth on the oriented seed is shown on example of CdSe. The difference between HPVB and HPVZM results is described. Main HPVZM advantage for II-VI compound crystal growth is possibility of obtaining crystals with stoichiometric composition or with controlled deviation from stoichiometry. Hence HPVZM is preferable for growing high-resistivity II-VI crystals with low inclusion content.

  18. Phosphine-free synthesis of CdSe quantum dots in a new co-capping ligand system.

    PubMed

    Wang, Chun; Jiang, Yang; Zhang, Zhongping; Li, Guohua; Chen, Lanlan; Jie, Jiansheng

    2009-08-01

    High-quality CdSe quantum dots with zinc blende structure were successfully synthesized via a new cheaper, greener phosphine-free route, using environmentally friendly N,N-dimethyl-oleoyl amide as the solvent of Se. The process eliminates trioctylphoshine from the synthesis, using oleic acid (OA) as a primary capping ligand and benzophenone (BP) as a secondary ligand in the noncoordinating solvent. It has been found that the addition of BP can improve the size distribution (below 10%) of as-synthesized CdSe quantum dots greatly, and the nucleation and growth process can also be well-separated. Moreover, a comprehensive examination on the control of particle size and size distribution was performed by systematically varying the BP/OA molar ratio. The phosphine-free route enables us to obtain high-quality CdSe quantum dots with sharp UV-vis absorption peak, size ranging from 2.8 to 6.8 nm, and narrow full width of half-maximum between 27 and 35 nm with purely band-edge luminescence, and without any post-synthesis processing.

  19. Improving the sensitivity of indirect-type organic X-ray detector by blending with CdSe quantum dots

    NASA Astrophysics Data System (ADS)

    Kim, B.; Lee, J.; Kang, J.

    2017-01-01

    In this study, The blending effect of CdSe quantum dots (QDs) dispersed in a poly(3-hexylthiophene) (P3HT):phenyl-C61-butyric acid methyl ester (PCBM) active layer was investigated to improve the sensitivity of indirect-type X-ray detectors. 3 different sizes of CdSe QDs (5, 7, and 9 nm) were blended in P3HT:PCBM (weight ratio of 1:1) layers. The 5 nm-QD blended condition showed relatively high short circuit current density (Jsc), power conversion efficiency (PCE), and sensitivity. The optimal amount of 5nm-QDs in the P3HT:PCBM layer was also investigated in the range of 0 to 4 mg. As the final outcome, the detector fabricated with 3 mg of 5 nm-QDs in the active layer showed the highest sensitivity of 220.08 nC/mR·cm2, which was 28% higher than the sensitivity of the pristine P3HT:PCBM detector. Through the addition of the optimal amount of CdSe QDs to the P3HT:PCBM layer, the sensitivity of the X-ray detector was enhanced due to the increment of photon-absorption and charge transport.

  20. A dry method to synthesize dendritic Ag2Se nanostructures utilizing CdSe quantum dots and Ag thin films

    NASA Astrophysics Data System (ADS)

    Hu, Lian; Zhang, Bingpo; Xu, Tianning; Li, Ruifeng; Wu, Huizhen

    2015-01-01

    Dendritic Ag2Se nanostructures are synthesized in a dry environment by UV irradiating the hybrids composed of CdSe quantum dots (QDs) and silver (Ag). UV irradiation on CdSe QDs induces a photooxidation effect on the QD surface and leads to the formation of SeO2 components. Then SeO2 reacts with the Ag atoms in either Ag film or QD layer to produce the Ag2Se. The growth mechanism of Ag2Se dendrites on solid Ag films is explored and explained by a diffusion limited aggregation model in which the QD layer provides enough freedom for Ag2Se motion. Since the oxidation of the CdSe QDs is the critical step for the Ag2Se dendrites formation this dry chemical interaction between QDs and Ag film can be applied in the study of the QD surface chemical properties. With this dry synthesis method, the Ag2Se dendrites can also be facilely formed at the designed area on Ag substrates.

  1. Porous networks of CdSe nanocrystal chains from ultrafine Cd(OH)2 nanowires and their composite materials.

    PubMed

    Ko, Sungwook; Kim, Jeong Won; Moon, Geon Dae; Shim, Hee-Sang; Kim, Won Bae; Jeong, Unyong

    2010-03-16

    Long ultrathin Cd(OH)(2) nanowires have been selectively grown on silica colloids in a basic aqueous condition. The Cd(OH)(2) nanowires could be detached from the surface of the silica colloids by simply applying ultrasonication and then transformed into isolated CdSe nanocrystal chains. When the transformation into CdSe was conducted without detaching the Cd(OH)(2) nanowires, nanoporous CdSe shells composed of wire-like nanocrystal chains were produced. The good solubility of the Cd(OH)(2) nanowires in both hydrophilic and hydrophobic solvents facilitated the formation of composites with quantum dots, magnetic particles, organic molecules, and polymers. Embedding premade quantum dots possessed broad light absorption range and enhanced photoluminescence. Large amount of superparamagnetic particles endowed a fast magnetic response in addition to the fluorescence. Composites of organic/nanocrystal chains were readily fabricated by employing the electrostatic attraction between the positively charged Cd(OH)(2) nanowires and negatively charged polymers or small molecules.

  2. Understanding the electronic structure of CdSe quantum dot-fullerene (C60) hybrid nanostructure for photovoltaic applications

    NASA Astrophysics Data System (ADS)

    Sarkar, Sunandan; Rajbanshi, Biplab; Sarkar, Pranab

    2014-09-01

    By using the density-functional tight binding method, we studied the electronic structure of CdSe quantum dot(QD)-buckminsterfullerene (C60) hybrid systems as a function of both the size of the QD and concentration of the fullerene molecule. Our calculation reveals that the lowest unoccupied molecular orbital energy level of the hybrid CdSeQD-C60 systems lies on the fullerene moiety, whereas the highest occupied molecular orbital (HOMO) energy level lies either on the QD or the fullerene depending on size of the CdSe QD. We explored the possibility of engineering the energy level alignment by varying the size of the CdSe QD. With increase in size of the QD, the HOMO level is shifted upward and crosses the HOMO level of the C60-thiol molecule resulting transition from the type-I to type-II band energy alignment. The density of states and charge density plot support these types of band gap engineering of the CdSe-C60 hybrid systems. This type II band alignment indicates the possibility of application of this nanohybrid for photovoltaic purpose.

  3. A dry method to synthesize dendritic Ag2Se nanostructures utilizing CdSe quantum dots and Ag thin films.

    PubMed

    Hu, Lian; Zhang, Bingpo; Xu, Tianning; Li, Ruifeng; Wu, Huizhen

    2015-01-09

    Dendritic Ag2Se nanostructures are synthesized in a dry environment by UV irradiating the hybrids composed of CdSe quantum dots (QDs) and silver (Ag). UV irradiation on CdSe QDs induces a photooxidation effect on the QD surface and leads to the formation of SeO2 components. Then SeO2 reacts with the Ag atoms in either Ag film or QD layer to produce the Ag2Se. The growth mechanism of Ag2Se dendrites on solid Ag films is explored and explained by a diffusion limited aggregation model in which the QD layer provides enough freedom for Ag2Se motion. Since the oxidation of the CdSe QDs is the critical step for the Ag2Se dendrites formation this dry chemical interaction between QDs and Ag film can be applied in the study of the QD surface chemical properties. With this dry synthesis method, the Ag2Se dendrites can also be facilely formed at the designed area on Ag substrates.

  4. Ab Initio Study of the Effects of Surface Chemistry and Size on Xray Absorption Spectra of CdSe Nanoparticles

    NASA Astrophysics Data System (ADS)

    Whitley, Heather; Prendergast, David; Ogitsu, Tadashi; Schwegler, Eric

    2009-03-01

    The specificity of their opto-electronic properties with respect to size, shape, and surface chemistry, as well as cost-effective solution based methods of synthesis, make CdSe nanoparticles a material of choice for use in novel opto-electronic devices, such as photovoltaics and field effect transistors. Developing methods by which these nanomaterials can be systematically engineered to meet specific device goals is largely dependent on understanding how surface passivation and reconstruction affect the properties of a given nanomaterial. Xray absorption spectroscopy (XAS) is an ideal method for structural analysis, but its application to studying nanomaterial surfaces is nontrivial due to the convolution of the absorption of surface atoms with those within the nanomaterial. We utilize ab initio methods to investigate the dependence of the Cd L-edge xray absorption cross-section on the size and passivation for Cd atoms both at the surface and within the core of CdSe nanomaterials. We aim to enable routine surface characterization of CdSe nanomaterials via XAS. Prepared by LLNL under Contract DE-AC52 07NA27344.

  5. Bioinspired, direct synthesis of aqueous CdSe quantum dots for high-sensitive copper(II) ion detection.

    PubMed

    Bu, Xiaohai; Zhou, Yuming; He, Man; Chen, Zhenjie; Zhang, Tao

    2013-11-21

    Luminescent CdSe semiconductor quantum dots (QDs), which are coated with a denatured bovine serum albumin (dBSA) shell, have been directly synthesized via a bioinspired approach. The dBSA coated CdSe QDs are ultrasmall (d < 2.0 nm) with a narrow size distribution and exhibit a strong green fluorescent emission at about 525 nm. They can be stored for months at room temperature and possess excellent stability against ultraviolet irradiation, high salt concentration, and a wide physiological range of pH. Systematic experimental investigations have shown the contribution of dBSA with free cysteine residues for both their effective ion chelating and surface passivating interactions during the formation and stabilization of CdSe QDs. The luminescent QDs are used for copper(II) ion detection due to their highly sensitive and selective fluorescence quenching response to Cu(2+). The concentration dependence of the quenching effect can be best described by the typical Stern-Volmer equation in a linearly proportional concentration of Cu(2+) ranging from 10 nM to 7.5 μM with a detection limit of 5 nM. As confirmed by various characterization results, a possible quenching mechanism is given: Cu(2+) ions are first reduced to Cu(+) by the dBSA shell and then chemical displacement between Cu(+) and Cd(2+) is performed at the surface of the ultrasmall metallic core to impact the fluorescence performance.

  6. Surface-enhanced Raman scattering by colloidal CdSe nanocrystal submonolayers fabricated by the Langmuir–Blodgett technique

    PubMed Central

    Sveshnikova, Larisa L; Duda, Tatyana A; Rodyakina, Ekaterina E; Dzhagan, Volodymyr M; Gordan, Ovidiu D; Veber, Sergey L; Himcinschi, Cameliu; Latyshev, Alexander V; Zahn, Dietrich R T

    2015-01-01

    Summary We present the results of an investigation of surface-enhanced Raman scattering (SERS) by optical phonons in colloidal CdSe nanocrystals (NCs) homogeneously deposited on both arrays of Au nanoclusters and Au dimers using the Langmuir–Blodgett technique. The coverage of the deposited NCs was less than one monolayer, as determined by transmission and scanning electron microscopy. SERS by optical phonons in CdSe nanocrystals showed a significant enhancement that depends resonantly on the Au nanocluster and dimer size, and thus on the localized surface plasmon resonance (LSPR) energy. The deposition of CdSe nanocrystals on the Au dimer nanocluster arrays enabled us to study the polarization dependence of SERS. The maximal SERS signal was observed for light polarization parallel to the dimer axis. The polarization ratio of the SERS signal parallel and perpendicular to the dimer axis was 20. The SERS signal intensity was also investigated as a function of the distance between nanoclusters in a dimer. Here the maximal SERS enhancement was observed for the minimal distance studied (about 10 nm), confirming the formation of SERS “hot spots”. PMID:26734529

  7. Reconstructing a solid-solid phase transformation pathway in CdSe nanosheets with associated soft ligands

    PubMed Central

    Wang, Zhongwu; Wen, Xiao-Dong; Hoffmann, Roald; Son, Jae Sung; Li, Ruipeng; Fang, Chia-Chen; Smilgies, Detlef-M.; Hyeon, Taeghwan

    2010-01-01

    Integrated single-crystal-like small and wide-angle X-ray diffraction images of a CdSe nanosheet under pressure provide direct experimental evidence for the detailed pathway of transformation of the CdSe from a wurtzite to a rock-salt structure. Two consecutive planar atomic slips [(001) 〈110〉 in parallel and (102) with a distortion angle of ∼40°] convert the wurtzite-based nanosheet into a saw-like rock-salt nanolayer. The transformation pressure is three times that in the bulk CdSe crystal. Theoretical calculations are in accord with the mechanism and the change in transformation pressure, and point to the critical role of the coordinated amines. Soft ligands not only increase the stability of the wurtzite structure, but also improve its elastic strength and fracture toughness. A ligand extension of 2.3 nm appears to be the critical dimension for a turning point in stress distribution, leading to the formation of wurtzite (001)/zinc-blende (111) stacking faults before rock-salt nucleation. PMID:20855580

  8. Effect of Different Ligands on Carrier Dynamics of CdSe Quatum Dots for Solar Cells Applications

    NASA Astrophysics Data System (ADS)

    Yakami, Baichhabi R.; Togha, Urice; Mahat, Meg; Nandyala, Shashank R.; Balaz, Milan; Pikal, Jon M.; Department of Electrical; Computer Engineering Team; Department of Chemistry Team; Department of Physics Team

    2015-03-01

    We have carried out steady state absorption and photoluminescence (PL), as well as time resolved PL and ultrafast transient absorption (TA) studies of CdSe quantum dots (QD) with five different capping ligands: trioctylphosphine oxide (TOPO), oleic acid (OA), dodecanethiol (DDT), mercaptopropionic acid (MPA), and L-cysteine (Cys). These ligands have different chemical structures and which effects the optical properties of the QDs. Measurements were conducted on QD sizes ranging from Ø = 2.5nm to 4.6nm with smaller QDs showing an excitonic PL and a broad surface trap state PL. The ligand exchange of OA CdSe QDs with MPA, DDT and Cys leads to quenching of excitonic PL intensity accompanied by a larger surface trap state to excitonic PL intensity ratio. This is consistent with the TRPL measurements, which show faster exciton PL decays for CdSe QDs with MPA, DDT and Cys ligands compared to OA and TOPO. The PL decay shows multi-exponential behavior with the average lifetime decreasing with increasing QD size. Data from TA experiments using a white light probe is also used to study the picosecond carrier dynamics. These measurements shed light on the role of capping ligands on the carrier dynamics of the QD used as sensitizers in solar cells. U.S. Department of Energy.

  9. Continuous-flow synthesis of CdSe quantum dots: a size-tunable and scalable approach.

    PubMed

    Mirhosseini Moghaddam, Mojtaba; Baghbanzadeh, Mostafa; Sadeghpour, Amin; Glatter, Otto; Kappe, C Oliver

    2013-08-26

    In recent years, continuous-flow/microreactor processing for the preparation of colloidal nanocrystals has received considerable attention. The intrinsic advantages of microfluidic reactors have opened new opportunities for the size-controlled synthesis of nanocrystals either in the laboratory or on a large scale. Herein, an experimentally simple protocol for the size-tunable continuous-flow synthesis of rather monodisperse CdSe quantum dots (QDs) is presented. CdSe QDs are manufactured by using cadmium oleate as cadmium source, selenium dioxide as selenium precursor, and 1-octadecene as solvent. Exploiting selenium dioxide as selenium source and 1-octadecene as solvent allows execution of the complete process in open air without any requirement for air-free manipulations using a glove box or Schlenk line. Continuous-flow processing is performed with a stainless steel coil of 1.0 mm inner diameter pumping the combined precursor solution through the reactor by applying a standard HPLC pump. The effect of different reaction parameters, such as temperature, residence time, and flow rate, on the properties of the resulting CdSe QDs was investigated. A temperature increase from 240 to 260 °C or an extension of the residence time from 2 to 20 min affords larger nanocrystals (range 3-6 nm) whereas the size distribution does not change significantly. Longer reaction times and higher temperatures result in QDs with lower quantum yields (range 11-28 %). The quality of the synthesized CdSe QDs was confirmed by UV/Vis and photoluminescence spectroscopy, small-angle X-ray scattering, and high-resolution transmission electron microscopy. Finally, the potential of this protocol for large-scale manufacturing was evaluated and by operating the continuous-flow process for 87 min it was possible to produce 167 mg of CdSe QDs (with a mean diameter of 4 nm) with a quantum yield of 28 %.

  10. Optical and Surface Characterization Studies of CdSe Quantum Dots Undergoing Photooxidation

    NASA Astrophysics Data System (ADS)

    Powell, Lauren C. J.

    Realization of the potential of Quantum Dots (QDs) for biological, energy-efficient lighting and energy harvesting applications requires that their long-term photostability be improved, especially with regards to protection from photooxidation. The overarching objective of this project was the determination of the chemical and physical mechanisms of photooxidation of CdSe QDs. Pittsburgh-based Crystalplex, Inc. provided CdSe QDs with different organic ligands for this research. Three integrated in situ and ex situ characterization techniques were used to observe changes in optical behavior, QD morphology, and surface chemistry during photooxidation conditions. Single-molecule fluorescence microscopy experiments were used to observe real-time changes in the photoluminescence (PL) behavior of single QDs with oleic and lauric acid ligands. The QDs are exposed to 1 atm of pure O2, dry Ar, Ar bubbled through DI water, or air in an environmental chamber and excited with a 488 nm light. Changes in PL intensities were analyzed with respect to the periods of exposure to controlled atmospheres and light. Samples illuminated continuously exhibited strong photoenhancement effects, while those kept in the dark showed atmospheric-dependent PL loss. Microstructural and chemical identification was performed with aberration-corrected transmission electron microscopy (TEM). Ex situ exposures of QD samples to air, dry O2, and dry Ar revealed changes in surface oxide growth with respect to exposure length, illumination, and column vacuum pressure. Samples exposed to air and light exhibited the most extensive photooxidation. Quantum dots with oleic acid ligands were treated with UV/ozone plasma, and extensive degradation of QDs was observed. X-ray photoemission spectroscopy (XPS) measurements at CMU were used to identify the chemical and bonding states of the surface species before and after photooxidation. Analysis of the acquired spectra showed that exposure to below-bandgap light

  11. Electrochemical preparation of vertically aligned, hollow CdSe nanotubes and their p-n junction hybrids with electrodeposited Cu2O.

    PubMed

    Debgupta, Joyashish; Devarapalli, Ramireddy; Rahman, Shakeelur; Shelke, Manjusha V; Pillai, Vijayamohanan K

    2014-08-07

    Vertically aligned, hollow nanotubes of CdSe are grown on fluorine doped tin oxide (FTO) coated glass substrates by ZnO nanowire template-assisted electrodeposition technique, followed by selective removal of the ZnO core using NH4OH. A detailed mechanism of nucleation and anisotropic growth kinetics of nanotubes have been studied by a combination of characterization tools such as chronoamperometry, SEM and TEM. Interestingly, "as grown" CdSe nanotubes (CdSe NTs) on FTO coated glass plates behave as n-type semiconductors exhibiting an excellent photo-response (with a generated photocurrent density value of ∼ 470 μA cm(-2)) while in contact with p-type Cu2O (p-type semiconductor, grown separately on FTO plates) because of the formation of a n-p heterojunction (type II). The observed photoresponse is 3 times higher than that of a similar device prepared with electrodeposited CdSe films (not nanotubes) and Cu2O on FTO. This has been attributed to the hollow 1-D nature of CdSe NTs, which provides enhanced inner and outer surface areas for better absorption of light and also assists faster transport of photogenerated charge carriers.

  12. Fe2+-doped CdSe single crystal: growth, spectroscopic and laser properties, potential use as a 6 µm broadband amplifier

    NASA Astrophysics Data System (ADS)

    Frolov, M. P.; Gordienko, V. M.; Korostelin, Yu V.; Kozlovsky, V. I.; Podmar'kov, Yu P.; Potemkin, F. V.; Skasyrsky, Ya K.

    2017-02-01

    We report on the successful growth of single crystals of Fe2+:CdSe by seeded physical vapor transport (SPVT) technique with doping within the growing process and subsequent annealing in Se vapor. Luminescence lifetime measurements, spectroscopic studies of 5E-5T2 transition of Fe2+ in CdSe, and laser experiments were performed. The lifetime of the 5T2 energy level was measured to be 20  ±  5 ns at a room temperature (RT) of 290 K. At liquid nitrogen (LN) temperature, luminescence kinetics displayed a non-exponential decay, which can be fitted to a bi-exponential function with time constants τ 1  =  6 µs and τ 2  =  29 µs. As much as 3.2 mJ of output energy at 5.2 µm with 27% absorbed pump energy slope efficiency of an Fe2+:CdSe laser was achieved at RT under 2.94 µm nanosecond Er:YAG laser pumping. The Fe2+:CdSe laser was tuned from 4.63 to 6.10 µm. Obtained characteristics of Fe2+:CdSe indicate that the crystal can be considered a promising medium for amplification of femtosecond pulses in the middle infrared range up to 6 µm.

  13. Effects of morphology, diameter and periodic distance of the Ag nanoparticle periodic arrays on the enhancement of the plasmonic field absorption in the CdSe quantum dots

    NASA Astrophysics Data System (ADS)

    Kohnehpoushi, Saman; Eskandari, Mehdi; Ahmadi, Vahid; Yousefirad, Mansooreh; Nabavi, Elham

    2016-09-01

    In this work, the numerical calculations of plasmonic field absorption of Ag nanoparticles (Ag NPs) periodic arrays in the CdSe quantum dot (QD) film are investigated by the three-dimensional finite difference time domain (FDTD). Diameter (D), periodic distance (P), and morphology effects of Ag NPs are investigated on the improvement of the plasmonic field absorption in CdSe QD film. Results show that plasmonic field absorption in CdSe QD film is enhanced with reduction of D of Ag NPs until 5 nm and reduces thereafter. It is observed that with raising D of Ag NPs, optimum plasmonic field absorption in CdSe QD film is shifted toward the higher P. Moreover, with varying morphology of Ag NPs from spherical to cylindrical, cubic, ringing and pyramid, the plasmonic field absorption is considerably enhanced in CdSe QD film and position of quadrupole plasmon mode (QPPM) is shifted toward further wavelength. For cylindrical Ag NPs, the QPPM intensity increased with raising height (H) until 15 nm and reduces thereafter.

  14. Size Dependence of Fluorescence Blinking Statistics from CdSe Nanorods

    NASA Astrophysics Data System (ADS)

    Wang, Siying; Querner, Claudia; Emmons, Thomas; Drndic, Marija; Crouch, Catherine

    2007-03-01

    We report fluorescence blinking statistics measured from single CdSe nanorods (NRs) of seven different sizes with aspect ratios ranging from 3 to 11. The off-times follow a power-law probability distribution; on-times follow a truncated power law distribution, P(τon)˜τon^-αe^-τon/τc. At fixed excitation intensity, the truncation rate 1/τc increases with increasing aspect ratio. For a particular sample, 1/τc increases gradually with increasing excitation intensity. Examining 1/τc vs. single-particle photon absorption rate for all samples indicates that the shape dependence of the absorption cross-section does not fully account for the observed variation in crossover time τc. Surprisingly, we observe no significant difference between core and core/shell nanorods or core rods with different surface ligands. Our results suggest that NR internal structural defects or degree of quantum confinement may contribute to the shape dependence of the crossover time.

  15. Synthesis and characterization of CdSe quantum dots dispersed in PVA matrix by chemical route

    NASA Astrophysics Data System (ADS)

    Khan, Zubair M. S. H.; Ganaie, Mohsin; Khan, Shamshad A.; Husain, M.; Zulfequar, M.

    2016-05-01

    CdSe quantum dots using polyvinyl alcohol as a capping agent have been synthesized via a simple heat induced thermolysis technique. The structural analysis of CdSe/PVA thin film was studied by X-ray diffraction, which confirms crystalline nature of the prepared film. The surface morphology and particle size of the prepared sample was studied by Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM). The SEM studies of CdSe/PVA thin film shows the average size of particles in the form of clusters of several quantum dots in the range of 10-20 nm. The morphology of CdSe/PVA thin film was further examined by TEM. The TEM image shows the fringes of tiny dots with average sizes of 4-7 nm. The optical properties of CdSe/PVA thin film were studied by UV-VIS absorption spectroscopy. The CdSe/PVA quantum dots follow the role of direct transition and the optical band gap is found to be 4.03 eV. From dc conductivity measurement, the observed value of activation energy was found to be 0.71 eV.

  16. Direct Observation of Photoexcited Hole Localization in CdSe Nanorods

    SciTech Connect

    Yang, Ye; Wu, Kaifeng; Shabaev, Andrew; Efros, Alexander L.; Lian, Tianquan; Beard, Matthew C.

    2016-07-08

    Quantum-confined 1D semiconductor nanostructures are being investigated for hydrogen generation photocatalysts. In the photoreaction, after fast electron transfer, holes that remain in the nanostructure play an important role in the total quantum yield of hydrogen production. Unfortunately, knowledge of hole dynamics is limited due to lack of convenient spectroscopic signatures. Here, we directly probe hole localization dynamics within CdSe nanorods (NRs) by combining transient absorption (TA) and time-resolved terahertz (TRTS) spectroscopy. We show that when methylene blue is used as an electron acceptor, the resulting electron transfer occurs with a time constant of 3.5 +/- 0.1 ps and leaves behind a delocalized hole. However, the hole quickly localizes in the Coulomb potential well generated by the reduced electron acceptor near the NR surface with time constant of 11.7 +/- 0.2 ps. Our theoretical investigation suggests that the hole becomes confined to a ~ +/-0.8 nm region near the reduced electron acceptor and the activation energy to detrap the hole from the potential well can be as large as 235 meV.

  17. Picosecond energy transfer and multiexciton transfer outpaces Auger recombination in binary CdSe nanoplatelet solids

    NASA Astrophysics Data System (ADS)

    Rowland, Clare E.; Fedin, Igor; Zhang, Hui; Gray, Stephen K.; Govorov, Alexander O.; Talapin, Dmitri V.; Schaller, Richard D.

    2015-05-01

    Fluorescence resonance energy transfer (FRET) enables photosynthetic light harvesting, wavelength downconversion in light-emitting diodes (LEDs), and optical biosensing schemes. The rate and efficiency of this donor to acceptor transfer of excitation between chromophores dictates the utility of FRET and can unlock new device operation motifs including quantum-funnel solar cells, non-contact chromophore pumping from a proximal LED, and markedly reduced gain thresholds. However, the fastest reported FRET time constants involving spherical quantum dots (0.12-1 ns; refs , , ) do not outpace biexciton Auger recombination (0.01-0.1 ns; ref. ), which impedes multiexciton-driven applications including electrically pumped lasers and carrier-multiplication-enhanced photovoltaics. Few-monolayer-thick semiconductor nanoplatelets (NPLs) with tens-of-nanometre lateral dimensions exhibit intense optical transitions and hundreds-of-picosecond Auger recombination, but heretofore lack FRET characterizations. We examine binary CdSe NPL solids and show that interplate FRET (˜6-23 ps, presumably for co-facial arrangements) can occur 15-50 times faster than Auger recombination and demonstrate multiexcitonic FRET, making such materials ideal candidates for advanced technologies.

  18. The role of ligands in the optical and electronic spectra of CdSe nanoclusters

    SciTech Connect

    Kilina, Svletana; Sergei, Ivanov A; Victor, Klimov I; Sergei, Tretiak

    2008-01-01

    We investigate the impact of ligands on morphology, electronic structure, and optical response of the Cd33Se33 cluster, which already overlapps in size with the smallest synthesized CdSe quantum dots (QDs). Our Density Functional Theory (DFT) calculations demonstrate significant surface reorganization both for the bare cluster and for the cluster capped by amine and phosphine oxide ligand models. We observe strong surface-ligand interactions leading to substantial charge redistribution and polarization effects on the surface. This effect results in the appearance of hybridized states, where the electronic density is spread over the cluster and the ligands. Neither the ligand's nor hybridized molecular orbitals appear as trap states inside or near the band gap of the QD. Instead, being optically dark, dense hybridized states from the edges of the valence and the conduction bands could open new relaxation channels for high energy photoexcitations. Comparing quantum dots passivated by different ligands, we found that hybridized states are denser in at the edge of the conduction band of the cluster ligated with phosphine oxide molecules than that with primary amines. Such a different manifestation of ligand binding may potentially lead to the faster electron relaxation in dots passivated by phosphine oxide than by amine ligands, which is in agreement with experimental data.

  19. Contactless microwave study of dispersive transport in thin film CdSe

    NASA Astrophysics Data System (ADS)

    Grabtchak, Serguei Yu; Cocivera, Michael

    1996-01-01

    The contactless microwave technique was used to measure light-induced transients in the power absorbed by thin films of polycrystalline CdSe. Because the rise time of the microwave cavity was 60 ns, the analysis was limited to 100 ns or longer. Measurement of these transients at a number of fixed frequencies across the ``dark'' resonance frequency made reconstruction of the difference signal possible. This signal, which represents the difference between the ``dark'' and ``light'' Lorentz resonance curves, was determined at various times during the decay. Analysis of these signals provided the time dependence for the changes in the real and imaginary parts of the dielectric constant, which correspond to the densities of the trapped and free electrons. The decays of these parameters were characterized by three time domains. At the shortest times, the two parameters did not have the same time dependence. At intermediate times, the densities of both the trapped and free electrons had the same time dependence characterized by a power law decay, and a mechanism consistent with these results involves rapid equilibration between the free electrons and those in the shallow traps. Decay in this region was consistent with a dispersive transport mechanism. Intensity effects indicate saturation of the shallow traps. The third region occurred at the break in the power law dependence indicating a bimolecular recombination process. Measurements at higher temperatures indicate a change from a bimolecular to a monomolecular recombination mechanism.

  20. CdSe quantum-dot-sensitized solar cell with ∼100% internal quantum efficiency.

    PubMed

    Fuke, Nobuhiro; Hoch, Laura B; Koposov, Alexey Y; Manner, Virginia W; Werder, Donald J; Fukui, Atsushi; Koide, Naoki; Katayama, Hiroyuki; Sykora, Milan

    2010-11-23

    We have constructed and studied photoelectrochemical solar cells (PECs) consisting of a photoanode prepared by direct deposition of independently synthesized CdSe nanocrystal quantum dots (NQDs) onto a nanocrystalline TiO(2) film (NQD/TiO(2)), aqueous Na(2)S or Li(2)S electrolyte, and a Pt counter electrode. We show that light harvesting efficiency (LHE) of the NQD/TiO(2) photoanode is significantly enhanced when the NQD surface passivation is changed from tri-n-octylphosphine oxide (TOPO) to 4-butylamine (BA). In the PEC the use of NQDs with a shorter passivating ligand, BA, leads to a significant enhancement in both the electron injection efficiency at the NQD/TiO(2) interface and charge collection efficiency at the NQD/electrolyte interface, with the latter attributed mostly to a more efficient diffusion of the electrolyte through the pores of the photoanode. We show that by utilizing BA-capped NQDs and aqueous Li(2)S as an electrolyte, it is possible to achieve ∼100% internal quantum efficiency of photon-to-electron conversion, matching the performance of dye-sensitized solar cells.

  1. Probing Interfacial Electronic States in CdSe Quantum Dots using Second Harmonic Generation Spectroscopy

    DOE PAGES

    Doughty, Benjamin L.; Ma, Yingzhong; Shaw, Robert W

    2015-01-07

    Understanding and rationally controlling the properties of nanomaterial surfaces is a rapidly expanding field of research due to the dramatic role they play on the optical and electronic properties vital to light harvesting, emitting and detection technologies. This information is essential to the continued development of synthetic approaches designed to tailor interfaces for optimal nanomaterial based device performance. In this work, closely spaced electronic excited states in model CdSe quantum dots (QDs) are resolved using second harmonic generation (SHG) spectroscopy, and the corresponding contributions from surface species to these states are assessed. Two distinct spectral features are observed in themore » SHG spectra, which are not readily identified in linear absorption and photoluminescence excitation spectra. These features include a weak band at 395 6 nm, which coincides with transitions to the 2S1/2 1Se state, and a much more pronounced band at 423 4 nm arising from electronic transitions to the 1P3/2 1Pe state. Chemical modification of the QD surfaces through oxidation resulted in disappearance of the SHG band corresponding to the 1P3/2 1Pe state, indicating prominent surface contributions. Signatures of deep trap states localized on the surfaces of the QDs are also observed. We further find that the SHG signal intensities depend strongly on the electronic states being probed and their relative surface contributions, thereby offering additional insight into the surface specificity of SHG signals from QDs.« less

  2. Interaction of β-cyclodextrin-capped CdSe quantum dots with inorganic anions and cations.

    PubMed

    Shang, Zhuo Bin; Hu, Shuang; Wang, Yu; Jin, Wei Jun

    2011-01-01

    A facile method was developed for the preparation of water soluble β-Cyclodextrin (β-CD)-modified CdSe quantum dots (QDs) (β-CD-QDs) by directly replacing the oleic acid ligands on the QDs surface with β-CD in an alkaline aqueous solution. The as-prepared QDs show good stability in aqueous solution for several months. Oxoanions, including phosphoric acid ion, sulphite acid ion and carbonic acid ion, affect the fluorescence of β-CD-QDs. Among them, H(2)PO(4)(-) exhibited the largest quenching effect. For the polyprotic acids (HO)(3)AO, the effect of acidic anions on the fluorescence of β-CD-QDs was in the order: monoanion (HO)(2)AO(2)(-) > dianion (HO)AO(3)(2-) > trianion AO(4)(3-). After photoactivation for several days in the presence of anions at alkaline pH, the β-CD-QDs exhibited strong fluorescence emission. The effect of various heavy and transition metal ions on the fluorescence properties of the β-CD-QDs was investigated further. It was found that Ag(+), Hg(2+) and Co(2+) have significant quenching effect on the fluorescence of the β-CD-QDs. The Stern-Volmer quenching constants increased in the order: Hg(2+) < Co(2+)

  3. Bent Polytypic ZnSe and CdSe Nanowires Probed by Photoluminescence.

    PubMed

    Kim, Yejin; Im, Hyung Soon; Park, Kidong; Kim, Jundong; Ahn, Jae-Pyoung; Yoo, Seung Jo; Kim, Jin-Gyu; Park, Jeunghee

    2017-03-15

    Nanowires (NWs) have witnessed tremendous development over the past two decades owing to their varying potential applications. Semiconductor NWs often contain stacking faults due to the presence of coexisting phases, which frequently hampers their use. Herein, it is investigated how stacking faults affect the optical properties of bent ZnSe and CdSe NWs, which are synthesized using the vapor transport method. Polytypic zinc blende-wurtzite structures are produced for both these NWs by altering the growth conditions. The NWs are bent by the mechanical buckling of poly(dimethylsilioxane), and micro-photoluminescence (PL) spectra were then collected for individual NWs with various bending strains (0-2%). The PL measurements show peak broadening and red shifts of the near-band-edge emission as the bending strain increases, indicating that the bandgap decreases with increasing the bending strain. Remarkably, the bandgap decrease is more significant for the polytypic NWs than for the single phase NWs. This work provides insights into flexible electronic devices of 1D nanostructures by engineering the polytypic structures.

  4. Electron hopping between Wurtzite CdSe Quantum Dots Linked by Molecules

    NASA Astrophysics Data System (ADS)

    Chu, Iek-Heng; Radulaski, Marina; Vukmirovic, Nenad; Cheng, Hai-Ping; Wang, Lin-Wang

    2011-03-01

    Recent experimental results show that the transport properties of quantum dot (QD) arrays will be tremendously improved after attached by cross-linking molecules. Here, we present an ab initio study on the electron hopping rates between wurtzite CdSe QDs connected by Sn 2 S6 molecules. The conduction band minima (CBM) transports among connected QDs are calculated. The charge patching method (CPM) is used to construct the charge density of the QDs and the connected systems. The folded spectrum method (FSM) was applied to find the band edge states and the electronic coupling between the neighboring QDs. Electron-phonon couplings are calculated to yield the reorganization energy. The electron hopping rate is then calculated by Marcus theory and its corresponding quantum treatments. Hopping rates for three different sizes of QDs, and two different types of molecular attachments are also presented here for comparison. Supported by DOE/BES-DE-FG02-02ER45995, DOE/BES-DE-AC02-05CH11231 and NSF/DMR-0804407, and computers from NERSC.

  5. Enhancement in the photorefractive performance of organic composites photosensitized with functionalized CdSe quantum dots

    NASA Astrophysics Data System (ADS)

    Liang, Yichen; Wang, Wei; Moon, Jong-Sik; Winiarz, Jeffrey G.

    2016-08-01

    Enhancement in the photorefractive (PR) performance of organic composites photosensitized by CdSe quantum dots (QCdSe) passivated with the charge-transport ligands, sulfonated triphenyldiamine (STPD), is reported. This enhancement is primarily attributed to the ability of the passivating ligand, STPD, to facilitate the charge-transfer process between the QCdSe and the triphenyldiamine (TPD) charge-transport matrix. The PR composites exhibited a maximum photocharge-generation efficiency of 0.9% and two-beam coupling gain coefficient of 110 cm-1. These figures of merit represent a significant improvement over similar composites photosensitized with more conventional trioctylphosphine oxide-passivated QCdSe (TQCdSe). Moreover, composites photosensitized with SQCdSe had a faster response time of τ = 128 ms at an electric field of 60 V/μm compared with τ = 982 ms for those containing TQCdSe. Because of the molecular similarity between the STPD passivating groups and the TPD-based charge-transport matrix, concentrations of up to 1.4 wt% of SQCdSe are achieved in PR composites without any detectable phase separation, a considerable improvement over the 0.7 wt% for TQCdSe.

  6. Probing Interfacial Electronic States in CdSe Quantum Dots using Second Harmonic Generation Spectroscopy

    SciTech Connect

    Doughty, Benjamin L.; Ma, Yingzhong; Shaw, Robert W

    2015-01-07

    Understanding and rationally controlling the properties of nanomaterial surfaces is a rapidly expanding field of research due to the dramatic role they play on the optical and electronic properties vital to light harvesting, emitting and detection technologies. This information is essential to the continued development of synthetic approaches designed to tailor interfaces for optimal nanomaterial based device performance. In this work, closely spaced electronic excited states in model CdSe quantum dots (QDs) are resolved using second harmonic generation (SHG) spectroscopy, and the corresponding contributions from surface species to these states are assessed. Two distinct spectral features are observed in the SHG spectra, which are not readily identified in linear absorption and photoluminescence excitation spectra. These features include a weak band at 395 6 nm, which coincides with transitions to the 2S1/2 1Se state, and a much more pronounced band at 423 4 nm arising from electronic transitions to the 1P3/2 1Pe state. Chemical modification of the QD surfaces through oxidation resulted in disappearance of the SHG band corresponding to the 1P3/2 1Pe state, indicating prominent surface contributions. Signatures of deep trap states localized on the surfaces of the QDs are also observed. We further find that the SHG signal intensities depend strongly on the electronic states being probed and their relative surface contributions, thereby offering additional insight into the surface specificity of SHG signals from QDs.

  7. Structure and Ultrafast Dynamics of White-Light-Emitting CdSe Nanocrystals

    SciTech Connect

    Bowers, Michael J; McBride, James; Garrett, Maria Danielle; Sammons, Jessica A.; Dukes, Albert; Schreuder, Michael A.; Watt, Tony L.; Lupini, Andrew R; Pennycook, Stephen J; Rosenthal, Sandra

    2009-01-01

    White-light emission from ultrasmall CdSe nanocrystals offers an alternative approach to the realization of solid-state lighting as an appealing technology for consumers. Unfortunately, their extremely small size limits the feasibility of traditional methods for nanocrystal characterization. This paper reports the first images of their structure, which were obtained using aberration-corrected atomic number contrast scanning transmission electron microscopy (Z-STEM). With subangstrom resolution, Z-STEM is one of the few available methods that can be used to directly image the nanocrystal's structure. The initial images suggest that they are crystalline and approximately four lattice planes in diameter. In addition to the structure, for the first time, the exciton dynamics were measured at different wavelengths of the white-light spectrum using ultrafast fluorescence upconversion spectroscopy. The data suggest that a myriad of trap states are responsible for the broad-spectrum emission. It is hoped that the information presented here will provide a foundation for the future development and improvement of white-light-emitting nanocrystals.

  8. Nanodomain fragmentation and local rearrangements in CdSe under pressure

    PubMed Central

    Leoni, Stefano; Ramlau, Reiner; Meier, Katrin; Schmidt, Marcus; Schwarz, Ulrich

    2008-01-01

    Structural transformations in extended solids result from local atomic rearrangements and phase growth mechanisms. A broad class of technologically relevant properties critically depends on local structural issues connected with domain sizes, domain boundary geometries, and defects. However, a precise understanding of structural transformation mechanisms and domain formation is still an open question. Here, we demonstrate the feasibility of very detailed mechanistic investigations in real materials as a prerequisite for intelligent property control. We address the problem of domain fragmentation in bulk CdSe under pressure, jointly by molecular dynamics simulations, high-pressure experiments, and HR-TEM imaging. We show that domain fragmentation is taking place in the high-pressure regime, where nucleation events generate both zinc blende (B3) and wurtzite (B4) structural motifs and, in turn, cause the final lamellar appearance observable by high-resolution TEM. A changed nucleation pattern and a modified B3/B4 ratio represents the system's response to modified external stress conditions. PMID:19052229

  9. Size dependent tunnel diode effects in gold tipped CdSe nanodumbbells

    NASA Astrophysics Data System (ADS)

    Saraf, Deepashri; Kumar, Ashok; Kanhere, Dilip; Kshirsagar, Anjali

    2017-02-01

    We report simulation results for scanning tunneling spectroscopy of gold-tipped CdSe nanodumbbells of lengths ˜27 Å and ˜78 Å. Present results are based on Bardeen, Tersoff, and Hamann formalism that takes inputs from ab initio calculations. For the shorter nanodumbbell, the current-voltage curves reveal negative differential conductance, the characteristic of a tunnel diode. This behaviour is attributed to highly localized metal induced gap states that rapidly decay towards the center of the nanodumbbell leading to suppression in tunneling. In the longer nanodumbbell, these gap states are absent in the central region, as a consequence of which zero tunneling current is observed in that region. The overall current-voltage characteristics for this nanodumbbell are observed to be largely linear near the metal-semiconductor interface and become rectifying at the central region, the nature being similar to its parent nanorod. The cross-sectional heights of these nanodumbbells also show bias-dependence where we begin to observe giant Stark effect features in the semiconducting central region of the longer nanodumbbell.

  10. Effect of oxygen on the properties of encapsulated polycrystalline CdSe films

    SciTech Connect

    Lee, M.J.; Langford, R.M.; Wright, S.W.; Judge, C.P.; Chater, R.J.

    2000-04-01

    This paper presents a comprehensive study of the effects of annealing silicon dioxide encapsulated CdSe films in oxygen on the microstructure, resistivity, photosensitivity and energy levels. The energy levels were investigated by using the independent methods of thermally stimulated current, photocurrent spectral response, and Hall measurements. The film structure is wurtzite with grains of average size 0.25 {micro}m, which extend through the thickness of the films. Annealing the films in oxygen at 450 C increases the resistivity from 10 ohm cm to 10{sup 6} ohm cm. The electron mobility, which has an activation energy of 0.08 eV, remains constant at about 100 cm{sup 2}V{sup {minus}1}s{sup {minus}1} during the anneal steps. The change in the resistivity is due to a combination of thermal rearrangement and oxygen diffusing uniformly into the films. Various energy levels ranging from 0.11 eV to 1.3 eV were detected and the density of all these decreased on annealing.

  11. Directed energy transfer in films of CdSe quantum dots: beyond the point dipole approximation.

    PubMed

    Zheng, Kaibo; Žídek, Karel; Abdellah, Mohamed; Zhu, Nan; Chábera, Pavel; Lenngren, Nils; Chi, Qijin; Pullerits, Tõnu

    2014-04-30

    Understanding of Förster resonance energy transfer (FRET) in thin films composed of quantum dots (QDs) is of fundamental and technological significance in optimal design of QD based optoelectronic devices. The separation between QDs in the densely packed films is usually smaller than the size of QDs, so that the simple point-dipole approximation, widely used in the conventional approach, can no longer offer quantitative description of the FRET dynamics in such systems. Here, we report the investigations of the FRET dynamics in densely packed films composed of multisized CdSe QDs using ultrafast transient absorption spectroscopy and theoretical modeling. Pairwise interdot transfer time was determined in the range of 1.5 to 2 ns by spectral analyses which enable separation of the FRET contribution from intrinsic exciton decay. A rational model is suggested by taking into account the distribution of the electronic transition densities in the dots and using the film morphology revealed by AFM images. The FRET dynamics predicted by the model are in good quantitative agreement with experimental observations without adjustable parameters. Finally, we use our theoretical model to calculate dynamics of directed energy transfer in ordered multilayer QD films, which we also observe experimentally. The Monte Carlo simulations reveal that three ideal QD monolayers can provide exciton funneling efficiency above 80% from the most distant layer. Thereby, utilization of directed energy transfer can significantly improve light harvesting efficiency of QD devices.

  12. Electronic Structure of Ligated CdSe Clusters: Dependence on DFT Methodology

    SciTech Connect

    Albert, VV; Ivanov, SA; Tretiak, S; Kilina, SV

    2011-07-07

    Simulations of ligated semiconductor quantum dots (QDs) and their physical properties, such as morphologies, QD-ligand interactions, electronic structures, and optical transitions, are expected to be very sensitive to computational methodology. We utilize Density Functional Theory (DFT) and systematically study how the choice of density functional, atom-localized basis set, and a solvent affects the physical properties of the Cd{sub 33}Se{sub 33} cluster ligated with a trimethyl phosphine oxide ligand. We have found that qualitative performance of all exchange-correlation (XC) functionals is relatively similar in predicting strong QD-ligand binding energy ({approx}1 eV). Additionally, all functionals predict shorter Cd-Se bond lengths on the QD surface than in its core, revealing the nature and degree of QD surface reconstruction. For proper modeling of geometries and QD-ligand interactions, however, augmentation of even a moderately sized basis set with polarization functions (e.g., LANL2DZ* and 6-31G*) is very important. A polar solvent has very significant implications for the ligand binding energy, decreasing it to 0.2-0.5 eV. However, the solvent model has a minor effect on the optoelectronic properties, resulting in persistent blue shifts up to {approx}0.3 eV of the low-energy optical transitions. For obtaining reasonable energy gaps and optical transition energies, hybrid XC functionals augmented by a long-range Hartree-Fock orbital exchange have to be applied.

  13. Size dependent tunnel diode effects in gold tipped CdSe nanodumbbells.

    PubMed

    Saraf, Deepashri; Kumar, Ashok; Kanhere, Dilip; Kshirsagar, Anjali

    2017-02-07

    We report simulation results for scanning tunneling spectroscopy of gold-tipped CdSe nanodumbbells of lengths ∼27 Å and ∼78 Å. Present results are based on Bardeen, Tersoff, and Hamann formalism that takes inputs from ab initio calculations. For the shorter nanodumbbell, the current-voltage curves reveal negative differential conductance, the characteristic of a tunnel diode. This behaviour is attributed to highly localized metal induced gap states that rapidly decay towards the center of the nanodumbbell leading to suppression in tunneling. In the longer nanodumbbell, these gap states are absent in the central region, as a consequence of which zero tunneling current is observed in that region. The overall current-voltage characteristics for this nanodumbbell are observed to be largely linear near the metal-semiconductor interface and become rectifying at the central region, the nature being similar to its parent nanorod. The cross-sectional heights of these nanodumbbells also show bias-dependence where we begin to observe giant Stark effect features in the semiconducting central region of the longer nanodumbbell.

  14. LETTER TO THE EDITOR: Photoluminescence properties of single CdSe quantum dots in ZnSe obtained by self-organized growth

    NASA Astrophysics Data System (ADS)

    Shen, M. Y.; Goto, T.; Kurtz, E.; Zhu, Z.; Yao, T.

    1998-03-01

    The photoluminescence of single CdSe quantum dots in ZnSe grown by molecular beam epitaxy and that of the same system grown by atomic layer epitaxy were investigated. The spectral diffusion and on/off behaviour of single CdSe quantum dots were observed, and the spectral diffusion range was only about 1 meV. The spectral peak shifting became quicker as the temperature rose. The spectral change from blue-shift to red-shift (or vice versa) was much quicker than that found in CdSe quantum dots synthesized as colloids. The phenomena are qualitatively explained by a Stark effect which originated from an Auger ionization process. The spectral diffusion may be a common property among single quantum dots.

  15. A simple and facile synthesis of MPA capped CdSe and CdSe/CdS core/shell nanoparticles

    NASA Astrophysics Data System (ADS)

    Sukanya, D.; Sagayaraj, P.

    2015-06-01

    II-VI semiconductor nanostructures, in particular, CdSe quantum dots have drawn a lot of attention because of their promising potential applications in biological tagging, photovoltaic, display devices etc. due to their excellent optical properties, high emission quantum yield, size dependent emission wavelength and high photostability. In this paper, we describe the synthesis and properties of mercaptopropionic acid capped CdSe and CdSe/CdS nanoparticles through a simple and efficient co-precipitation method followed by hydrothermal treatment. The growth process, characterization and the optical absorption as a function of wavelength for the synthesized MPA capped CdSe and CdSe/CdS nanoparticles have been determined using X-ray diffraction study (XRD), Ultraviolet-Visible spectroscopy (UV-Vis), Fourier transform infrared spectroscopy (FT-IR) and High Resolution Transmission Electron Microscopy (HRTEM).

  16. Direct Observation of sp-d Exchange Interactions in Colloidal Mn2+- and Co2+-Doped CdSe Quantum Dots

    SciTech Connect

    Archer, Paul I.; Santangelo, Steven A.; Gamelin, Daniel R.

    2007-03-23

    The defining attribute of a diluted magnetic semiconductor (DMS) is the existence of dopant-carrier magnetic exchange interactions. In this letter, we report the first direct observation of such exchange interactions in colloidal doped CdSe nanocrystals. Doped CdSe quantum dots were synthesized by thermal decomposition of (Me4N)2[Cd4(SePh)10] in the presence of TMCl2 (TM2+ ) Mn2+ or Co2+) in hexadecylamine and were characterized by several analytical and spectroscopic techniques. Using magnetic circular dichroism spectroscopy, successful doping and the existence of giant excitonic Zeeman splittings in both Mn2+- and Co2+-doped wurtzite CdSe quantum dots are demonstrated unambiguously.

  17. A simple and facile synthesis of MPA capped CdSe and CdSe/CdS core/shell nanoparticles

    SciTech Connect

    Sukanya, D.; Sagayaraj, P.

    2015-06-24

    II-VI semiconductor nanostructures, in particular, CdSe quantum dots have drawn a lot of attention because of their promising potential applications in biological tagging, photovoltaic, display devices etc. due to their excellent optical properties, high emission quantum yield, size dependent emission wavelength and high photostability. In this paper, we describe the synthesis and properties of mercaptopropionic acid capped CdSe and CdSe/CdS nanoparticles through a simple and efficient co-precipitation method followed by hydrothermal treatment. The growth process, characterization and the optical absorption as a function of wavelength for the synthesized MPA capped CdSe and CdSe/CdS nanoparticles have been determined using X-ray diffraction study (XRD), Ultraviolet-Visible spectroscopy (UV-Vis), Fourier transform infrared spectroscopy (FT-IR) and High Resolution Transmission Electron Microscopy (HRTEM)

  18. The influence of sequential ligand exchange and elimination on the performance of P3HT: CdSe quantum dot hybrid solar cells.

    PubMed

    Lee, Donggu; Lim, Jaehoon; Park, Myeongjin; Kim, Jun Young; Song, Jiyun; Kwak, Jeonghun; Lee, Seonghoon; Char, Kookheon; Lee, Changhee

    2015-11-20

    We report on a sequential ligand exchange and elimination process for the fast and easy surface modification of CdSe quantum dots (QDs) in order to improve the electronic interaction between poly(3-hexylthiophene) (P3HT) and CdSe QDs in P3HT:CdSe hybrid solar cells. We systematically investigated the influence of surface treatment on the insulating ligand shell of CdSe QDs using (1)H-NMR analysis, and correlated their influence on the photovoltaic properties of P3HT:CdSe hybrid solar cells. A decrease in the average thickness of the ligand shells directly improved carrier transport properties. Moreover, the presence of remnant 1-hexylamine ligands provided efficient surface trap passivation. As a result, overall solar cell performance (especially fill factor and power conversion efficiency) was enhanced and the recombination mechanism was dominated by monomolecular recombination due to enhanced carrier collection length (l(C0)).

  19. ZnO nanosheets decorated with CdSe and TiO2 for the architecture of dye-sensitized solar cells.

    PubMed

    Kim, Young Tae; Park, Mi Yeong; Choi, Kang Ho; Tai, Wei Sheng; Shim, Won Hyun; Park, Sun-Young; Kang, Jae-Wook; Lee, Kyu Hwan; Jeong, Yongsoo; Kim, Young Dok; Lim, Dong Chan

    2011-03-01

    Pure and TiO2- and CdSe-deposited ZnO nanosheets aligned vertically to the surface of ITO (Indium tin oxide) are prepared using electrodeposition, which is used for building blocks of dye sensitized solar cell. A significant improvement in the photovoltaic efficiency can be obtained by depositing TiO2 or CdSe on ZnO. Photoluminescence spectra show that the TiO2 and CdSe nanostructures suppress the recombination of the electron-hole pair of ZnO. We suggest that the interface charge transfer at TiO2-ZnO and CdSe-ZnO should be responsible for the suppression of the electron-hole pair recombination and enhanced solar cell efficiency by TiO2 and CdSe nanostructures.

  20. Enhancing the conversion efficiency of red emission by spin-coating CdSe quantum dots on the green nanorod light-emitting diode.

    PubMed

    Lee, Ya-Ju; Lee, Chia-Jung; Cheng, Chun-Mao

    2010-11-08

    A hybrid structure of CdSe quantum dots (QDs) (λ = 640 nm) spin-coated on the indium gallium nitride (InGaN) nanorod light-emitting diode (LED, λ = 525 nm) is successfully fabricated. Experimental results indicate that the randomness and the minuteness of nanorods scatter the upcoming green light into the surrounding CdSe QDs efficiently, subsequently alleviating the likelihood of the emitted photons of red emission being recaptured by the CdSe QDs (self-absorption effect), and that increases the coupling probability of emission lights and the overall conversion efficiency. Moreover, the revealed structure with high color stability provides an alternative solution for general lighting applications of next generation.

  1. The properties of vacuum-evaporated CdS and CdSe double layered films doping with copper and chlorine

    SciTech Connect

    Gu, P.F.; Li, H.F.; Zhu, Z.C.; Tang, J.F.

    1993-12-31

    The effect of doping with copper and chlorine on various properties of vacuum-evaporated CdS and CdSe double layers has been studied. The properties specifically studied were: (1) the dark conductivity and photoconductivity as functions of the doping concentration and the ratio of copper to chlorine, (2) the response time of various photoconductive films and (3) the optical absorption and spectral response. It was found that the dark conductivity decreases and the photoconductivity increases significantly if the ratio of Cu to Cl is suitable. The response time was about 5--10 ms for doping films and more than 100 ms for undoping ones. The optical absorption increases and the spectral response moves to a longer wavelength as the concentration of CdSe increases. The response wavelength can be changed by adjusting the thickness ratio of CdS to CdSe.

  2. Optically enhanced SnO{sub 2}/CdSe core/shell nanostructures grown by sol-gel spin coating method

    SciTech Connect

    Kumar, Vijay Goswami, Y. C.; Rajaram, P.

    2015-08-28

    Synthesis of SnO{sub 2}/CdSe metal oxide/ chalcogenide nanostructures on glass micro slides using ultrasonic sol-gel process followed by spin coating has been reported. Stannous chloride, cadmium chloride and selenium dioxide compounds were used for Sn, Cd and Se precursors respectively. Ethylene glycol was used as complexing agent. The samples were characterized by XRD, SEM, AFM and UV-spectrophotometer. All the peaks shown in diffractograms are identified for SnO{sub 2}. Peak broadening observed in core shell due to stress behavior of CdSe lattice. Scanning electron microscope and AFM exhibits the conversion of cluster in to nanorods structures forms. Atomic force microscope shows the structures in nanorods form and a roughness reduced 1.5194 nm by the deposition of CdSe. Uv Visible spectra shows a new absorption edge in the visible region make them useful for optoelectronic applications.

  3. Structural and optical characterization of electrodeposited CdSe in mesoporous anatase TiO2 for regenerative quantum-dot-sensitized solar cells.

    PubMed

    Sauvage, Frédéric; Davoisne, Carine; Philippe, Laetitia; Elias, Jamil

    2012-10-05

    We investigated CdSe-sensitized TiO(2) solar cells by means of electrodeposition under galvanostatic control. The electrodeposition of CdSe within the mesoporous film of TiO(2) gives rise to a uniform, thickness controlled, conformal layer of nanostructured CdSe particles intimately wrapping the anatase TiO(2) nanoparticles. This technique has the advantage of providing not only a fast method for sensitization ( < 5 min) but also being easily scalable to the sensitization of large-area panels. XRD together with SAED analysis highlight that the deposit of CdSe is exclusively constituted of the hexagonal polymorph. In addition, hierarchical growth has also been shown, starting from the formation of a TiO(2)-CdSe core-shell structure followed by the growth of an assembly of CdSe nanoparticles resembling cauliflowers. This assembly exhibits at its core a mosaic texture with crystallites of about 3 nm in size, in contrast to a shell composed of well-crystallized single crystals between 5 and 10 nm in size. Preliminary results on the photovoltaic performance of such a nanostructured composite of TiO(2) and CdSe show 0.8% power conversion efficiency under A.M.1.5 G conditions-100 mW cm(-2) in association with a new regenerative redox couple based on cobalt(+III/+II) polypyridil complex (V(oc ) = 485 mV, J(sc ) = 4.26 mA cm (-2), ff=0.37).

  4. Effect of CdSe nanoparticles on the fluorescence spectra of conjugate polymer P3HT: An experimental and theoretical study

    NASA Astrophysics Data System (ADS)

    Mastour, Nouha; Bouchriha, Habib

    2016-11-01

    In this work we have investigated the effect of CdSe nanoparticles (Nps) on the fluorescence spectra of conjugate polymer Poly(3-hexylthiophene-2,5-diyl) (P3HT). The fluorescence intensity is significantly decreased in both solution and solid films by the incorporation of CdSe Nps. This observed effect in the nanocomposite P3HT-CdSe is analyzed by using the Franck-Condon theory which reproduces correctly the decrease of the fluorescence with the Nps concentration and permits to reach the Huang-Rhys factor and the relaxation energy which are shown efficient to explain the fluorescence quenching.

  5. CdSe-CdS nanoheteroplatelets with efficient photoexcitation of central CdSe region through epitaxially grown CdS wings.

    PubMed

    Prudnikau, Anatol; Chuvilin, Andrey; Artemyev, Mikhail

    2013-10-02

    We synthesized a new type of optically active semiconductor nanoheterostructure based on CdSe nanoplatelets with epitaxially grown CdS flat branches or wings. CdS branches work as efficient photonic antenna in the blue spectral region, enhancing the excitation of CdSe band edge emission. The formation of CdSe-CdS nanoheteroplatelets instead of CdSe/CdS core-shell nanoplatelets was achieved using short-chain Cd ethylhexanoate and sulfur in octadecene as precursors for CdS overgrowth in the presence of acetate salt.

  6. Synthesis of CdSe quantum dots with luminescence in the violet region of the solar spectrum.

    PubMed

    Shukla, Nisha; Nigra, Michael M

    2010-01-01

    We have designed a simple, one-step synthesis of CdSe quantum dots with photoluminescence frequencies ranging from the red through to the violet region of the solar spectrum. The photoluminescence peaks have FWHM of 30 nm indicating absorption over a narrow range of wavelengths. The effect of solvent type and solvent boiling point on the physical and photoluminescence properties of the quantum dots has been studied. High boiling point, non-polar solvents shift the photoluminescence peak to longer wavelengths and low boiling point, polar solvents shift the photoluminescence peak to shorter wavelengths.

  7. Temperature and Wavelength Dependence of Energy Transfer Process Between Quantized States and Surface States in CdSe Quantum Dots.

    PubMed

    Zhang, Lei; Xu, Qinfeng; Liu, Mingliang; Kong, Lingbin; Jiao, Mengmeng; Mu, Haifeng; Wang, Dehua; Wang, Honggang; Chen, Jiannong; Yang, Chuanlu

    2017-12-01

    Temperature and wavelength dependence of energy transfer (ET) process between quantized states and surface trap states of CdSe quantum dots was investigated, respectively. The experimental results demonstrate that the photoluminescence (PL) intensity of the quantized states decreases with respect to the trap state emission, especially at lower temperatures. The observed ET process between quantized states and trap states which is influenced by the thermal population behavior. At the same temperature, the silver films can greatly enhance the energy transfer (ET) rate from the quantized states to trap states due to surface plasmonic coupling effect.

  8. Properties of electrospun CdS and CdSe filled poly(methyl methacrylate) (PMMA) nanofibres

    SciTech Connect

    Mthethwa, T.P.; Moloto, M.J.; De Vries, A.; Matabola, K.P.

    2011-04-15

    Graphical abstract: SEM images of CdS/PMMA showing coiling as loading of CdS nanoparticles is increased. Thermal stability is increased with increase in %loading of both CdS and CdSe nanoparticles. Research highlights: {yields} TOPO-capped CdS and HDA-capped CdSe nanoparticles were synthesized and fully characterized. {yields} The nanoparticles were mixed with the polymer, PMMA using electrospinning technique using 2, 5 and 10% weight loadings. {yields} The mixture was spun to produce fibres with optical and thermal properties showing significant change and also the increase in loading causing bending or spiraling. {yields} Both TEM images for nanoparticles and SEM for fibres shows the morphology and sizes of the particles. -- Abstract: Electrospinning technique was used to fabricate poly(methyl methacrylate) (PMMA) fibres incorporating CdS and CdSe quantum dots (nanoparticles). Different nanoparticle loadings (2, 5 and 10 wt% with respect to PMMA) were used and the effect of the quantum dots on the properties of the fibres was studied. The optical properties of the hybrid composite fibres were investigated by photoluminescence and UV-vis spectrophotometry. Scanning electron microscopy (SEM), X-ray diffraction and FTIR spectrophotometry were also used to investigate the morphology and structure of the fibres. The optical studies showed that the size-tunable optical properties can be achieved in the polymer fibres by addition of quantum dots. SEM images showed that the morphologies of the fibres were dependent on the added amounts of quantum dots. A spiral type of morphology was observed with an increase in the concentration of CdS and CdSe nanoparticles. Less beaded structures and bigger diameter fibres were obtained at higher quantum dot concentrations. X-ray diffractometry detected the amorphous peaks of the polymer and even after the quantum dots were added and the FTIR analysis shows that there was no considerable interaction between the quantum dots and the

  9. Luminescence of CdSe quantum dots near a layer of silver nanoparticles ion-synthesized in sapphire

    NASA Astrophysics Data System (ADS)

    Galyametdinov, Yu. G.; Shamilov, R. R.; Nuzhdin, V. I.; Valeev, V. F.; Stepanov, A. L.

    2016-11-01

    We study the characteristics of the luminescence of composite films based on polymethyl methacrylate with CdSe quantum dots deposited from solution onto the surface of a sapphire substrate containing a preliminarily formed layer with ion-synthesized silver nanoparticles. The sapphire layer with silver nanoparticles exhibits selective plasmon absorption in the visible spectral range with a peak at 463 nm. Enhancement in the exciton luminescence intensity of quantum dots with a peak at 590 nm is observed upon excitation at wavelengths lying in the region of plasmon resonance of metal nanoparticles, as well as luminescence quenching for quantum dots located in the vicinity of silver nanoparticles.

  10. Raman analysis of chemical substitution of Cd atoms by Hg in CdSe quantum dots and rods

    NASA Astrophysics Data System (ADS)

    Cherevkov, Sergei A.; Baranov, Alexander V.; Ushakova, Elena V.; Litvin, Alexander P.; Fedorov, Anatoly V.; Prudnikau, Anatol V.; Artemyev, Mikhail V.

    2016-01-01

    We investigate nanocrystals of ternary compounds CdXHg1-XSe with 0CdSe NCs used for Cd/Hg substitution, either zinc blende or wurtzite, strongly affects the structural properties of the resultant CdXHg1-XSe quantum dots and rods.

  11. Competition effects among size, dimensionality and pressure on modulating bandgap of CdSe and ZnO nanocrystals

    NASA Astrophysics Data System (ADS)

    Jiang, Xiao Bao; Sheng, Hong Chao; Gu, Xiao Yan; Shi, Ming Xiao

    2015-12-01

    Size, dimensionality and pressure play important roles on modulating band gap (Eg) of semiconductor nanocrystals, and have attracted extensive attention in recent years. In this letter, a simple thermodynamic model is developed and the competition relation among size, dimensionality and pressure effects on Eg is discussed. The accuracy of our prediction is confirmed by the experimental data and simulation results of CdSe and ZnO nanocrystals. This model provides a new insight into the size, dimensionality and pressure effects on Eg and guides the optimal selection as design quantum devices.

  12. Determination of dispersive optical constants of nanocrystalline CdSe (nc-CdSe) thin films

    SciTech Connect

    Sharma, Kriti; Al-Kabbi, Alaa S.; Saini, G.S.S.; Tripathi, S.K.

    2012-06-15

    Highlights: ► nc-CdSe thin films are prepared by thermal vacuum evaporation technique. ► TEM analysis shows NCs are spherical in shape. ► XRD reveals the hexagonal (wurtzite) crystal structure of nc-CdSe thin films. ► The direct optical bandgap of nc-CdSe is 2.25 eV in contrast to bulk (1.7 eV). ► Dispersion of refractive index is discussed in terms of Wemple–DiDomenico single oscillator model. -- Abstract: The nanocrystalline thin films of CdSe are prepared by thermal evaporation technique at room temperature. These thin films are characterized by transmission electron microscopy (TEM), scanning electron microscopy (SEM), energy dispersive X-ray analysis (EDX), X-ray diffraction (XRD) and photoluminescence spectroscopy (PL). The transmission spectra are recorded in the transmission range 400–3300 nm for nc-CdSe thin films. Transmittance measurements are used to calculate the refractive index (n) and absorption coefficient (α) using Swanepoel's method. The optical band gap (E{sub g}{sup opt}) has been determined from the absorption coefficient values using Tauc's procedure. The optical constants such as extinction coefficient (k), real (ε{sub 1}) and imaginary (ε{sub 2}) dielectric constants, dielectric loss (tan δ), optical conductivity (σ{sub opt}), Urbach energy (E{sub u}) and steepness parameter (σ) are also calculated for nc-CdSe thin films. The normal dispersion of refractive index is described using Wemple–DiDomenico single-oscillator model. Refractive index dispersion is further analysed to calculate lattice dielectric constant (ε{sub L}).

  13. Structural, optical and electrical characterization of vacuum-evaporated nanocrystalline CdSe thin films for photosensor applications

    NASA Astrophysics Data System (ADS)

    Kumar, Vipin; Sharma, D. K.; Sharma, Kapil; Dwivedi, D. K.

    2016-11-01

    II-VI nanocrystalline semiconductors offer a wide range of applications in electronics, optoelectronics and photonics. Thin films of CdSe were deposited onto ultra-clean glass substrates by vacuum evaporation method. The as-deposited films were annealed in vacuum at 350 K. The structural, elemental, morphological, optical and electrical investigations of annealed films were carried out. The X-ray diffraction pattern of the films shows that films were polycrystalline in nature having hexagonal structure with preferential orientation of grains along (002) plane. SEM image indicates that the films were uniform and well covered to the glass substrate. EDAX analysis confirms the stoichiometric composition of the film. Raman spectra were used to observe the characteristic vibrational modes of CdSe. The energy band gap of these films was obtained by absorption spectra. The films were found to have a direct type of transition of band gap occurring at 1.75 eV. The dark electrical conductivity and photoconductivity reveals that the films were semiconducting in nature indicating the suitability of these films for photosensor applications. The Hall effect measurement reveals that the films have n-type electrical conductivity.

  14. Asymmetric tunneling rates for electrons and holes at CdSe quantum dot/carbon nanotube interfaces

    NASA Astrophysics Data System (ADS)

    Ismail-Beigi, Sohrab; Jiang, Jie

    2014-03-01

    Decorating carbon nanotubes with CdSe quantum dots (QDs) is one potential approach for creating high efficiency photovoltaics. Our collaborators at Yale recently produced a ligand-free covalent attachment of CdSe QDs to carbon nanotubes through an organic ligand exchange mechanism. Our prior first principles work described the energetics of the various binding processes and rationalized the experimental growth methodology. After a brief review of the system, we will describe our intriguing finding that excited electrons and holes tunnel with different rates out of the QD and into the carbon nanotubes. The asymmetric tunneling rate itself can, in principle, boost the separation of photo-excited charge at the interface even if there are insufficient band energy differences across the interface. We describe our results for the tunneling rates computed using (i) a brute force approach with increasing simulation cell size to remove periodic effects, and (ii) a Green's function method that directly connects the QD to a thermodynamically large electron reservoir (e.g., a very long pristine nanotube). Supported by NSF SOLAR DMR 0934520.

  15. Characterization and polymerization of thienylphenyl and selenylphenyl amines and their interaction with CdSe quantum dots.

    PubMed

    Lana-Villarreal, Teresa; Font-Sanchis, Enrique; Sastre-Santos, Angela; Fernández-Lázaro, Fernando; Gómez, Roberto

    2011-04-18

    Hybrid quantum-dot-sensitized solar cells show promising novel optoelectronic properties. An adequate design of such cells requires a deep understanding of the characteristics of each component, including their interactions. In this context, the electrochemical properties of two different hole-transporting materials (HTMs) and their chemical interactions with trioctylphosphine-capped CdSe quantum dots are investigated to evaluate their potential use in hybrid quantum-dot-sensitized solar cells. Tris[4-(thien-2-yl)phenyl]amine (TTPA) and tris[4-(selen-2-yl)phenyl]amine (TSePA) are studied in the solid state as thin films deposited on a conducting substrate. Spectroelectrochemical studies evidence both solid-state electropolymerization and doping. Upon addition of TSePA or partially polymerized TTPA to a colloidal solution of trioctylphosphine-capped CdSe quantum dots, the steady-state photoluminescence is quenched. This suggests that the quantum dots and the HTM strongly interact, probably through an excited-state charge-transfer mechanism. The combination of all these pieces of information indicates that polymerized TTPA and TSePA are potential candidates as HTMs for hybrid quantum-dot-sensitized solar cells.

  16. Self-powered flexible and transparent photovoltaic detectors based on CdSe nanobelt/graphene Schottky junctions.

    PubMed

    Gao, Zhiwei; Jin, Weifeng; Zhou, Yu; Dai, Yu; Yu, Bin; Liu, Chu; Xu, Wanjin; Li, Yanping; Peng, Hailin; Liu, Zhongfan; Dai, Lun

    2013-06-21

    Flexible and transparent electronic and optoelectronic devices have attracted more and more research interest due to their potential applications in developing portable, wearable, low-cost, and implantable devices. We have fabricated and studied high-performance flexible and transparent CdSe nanobelt (NB)/graphene Schottky junction self-powered photovoltaic detectors for the first time. Under 633 nm light illumination, typical photosensitivity and responsivity of the devices are about 1.2 × 10(5) and 8.7 A W(-1), respectively. Under 3500 Hz switching frequency, the response and recovery times of them are about 70 and 137 μs, respectively, which, to the best of our knowledge, are the best reported values for nanomaterial based Schottky junction photodetectors up to date. The detailed properties of the photodetectors, such as the influences of incident light wavelength and light intensity on the external quantum efficiency and speed, are also investigated. Detailed discussions are made in order to understand the observed phenomena. Our work demonstrates that the self-powered flexible and transparent CdSe NB/graphene Schottky junction photovoltaic detectors have a bright application prospect.

  17. Mechanism for strong binding of CdSe quantum dots to multiwall carbon nanotubes for solar energy harvesting.

    PubMed

    Azoz, Seyla; Jiang, Jie; Keskar, Gayatri; McEnally, Charles; Alkas, Alp; Ren, Fang; Marinkovic, Nebojsa; Haller, Gary L; Ismail-Beigi, Sohrab; Pfefferle, Lisa D

    2013-08-07

    As hybrid nanomaterials have myriad of applications in modern technology, different functionalization strategies are being intensely sought for preparing nanocomposites with tunable properties and structures. Multi-Walled Carbon Nanotube (MWNT)/CdSe Quantum Dot (QD) heterostructures serve as an important example for an active component of solar cells. The attachment mechanism of CdSe QDs and MWNTs is known to affect the charge transfer between them and consequently to alter the efficiency of solar cell devices. In this study, we present a novel method that enables the exchange of some of the organic capping agents on the QDs with carboxyl functionalized MWNTs upon ultrasonication. This produces a ligand-free covalent attachment of the QDs to the MWNTs. EXAFS characterization reveals direct bond formation between the CdSe QDs and the MWNTs. The amount of oleic acid exchanged is quantified by temperature-programmed decomposition; the results indicate that roughly half of the oleic acid is removed from the QDs upon functionalized MWNT addition. Additionally, we characterize the optical and structural properties of the QD-MWNT heterostructures and investigate how these properties are affected by the attachment. The steady state photoluminescence response of QDs is completely quenched. The lifetime of the PL of the QDs measured with time resolved photoluminescence shows a significant decrease after they are covalently bonded to functionalized MWNTs, suggesting a fast charge transfer between QDs and MWNTs. Our theoretical calculations are consistent with and support these experimental findings and provide microscopic models for the QD binding mechanisms.

  18. Se EXAFS study of the elevated wurtzite to rock salt structural phase transition in CdSe nanocrystals

    SciTech Connect

    Tolbert, S.H.; Alivisatos, A.P. |

    1993-09-01

    High pressure Se EXAFS data has been obtained on 2.7 nm radius CdSe semiconductor nanocrystals. This system is observed to undergo a solid-solid phase transition at 6.5 GPa which is approximately twice the reported value for bulk CdSe. In combination with high pressure optical absorption experiments, EXAFS data can be used to identify the high-pressure phase structure as rock salt. EXAFS data can be fit with equations of state to yield pressure volume curves. Resultant values of bulk modulus and its derivative with respect to pressure are B{sub o} = 37 {plus_minus} 5 GPa and B{sub o}{prime} = 11 {plus_minus} 3. A thermodynamic model for the data is presented in which the internal energy in each phase is modified by a surface energy term. Differences in surface energy are used to explain the elevation in phase transition pressure. The model can be used to estimate a value for the surface energy in the rock salt phase; 1.9 {plus_minus} 0.3 N/m is obtained in comparison to 0.9 {plus_minus} 0. 1 N/m for the wurtzite phase.

  19. Reassignment of the O{sub Se}−V{sub Cd} complex in CdSe

    SciTech Connect

    Bastin, Dirk; Lavrov, E. V.; Weber, J.

    2014-02-21

    An IR absorption study of CdSe single crystals is presented. The as-received material revealed three absorption lines at 1094.2, 1107.5, and 1126.3 cm{sup −1}, which were previously assigned to the O{sub Se}−V{sub Cd} complex [G. Chen et al., Phys. Rev. Lett. 101, 195502 (2008)] We show that each of the lines is accompanied by a number of weaker satellites with intensities which match the natural abundances of sulfur isotopes. In contrast to the original identification it is suggested that these peaks are local vibrational modes of a SO{sub n} complex. The three modes correspond to different orientations of the complex in the CdSe lattice. Arguments are presented in favor of 2 oxygen atoms (n = 2) in the complex. Measurements with uniaxial stress applied to the samples revealed defect symmetries and activation energies for the defect reorientation. The complex was found to be stable up to 750 °C.

  20. Linear and nonlinear optical properties of functionalized CdSe quantum dots prepared by plasma sputtering and wet chemistry.

    PubMed

    Humbert, Christophe; Dahi, Abdellatif; Dalstein, Laetitia; Busson, Bertrand; Lismont, Marjorie; Colson, Pierre; Dreesen, Laurent

    2015-05-01

    We develop an innovative manufacturing process, based on radio-frequency magnetron sputtering (RFMS), to prepare neat CdSe quantum dots (QDs) on glass and silicon substrates and further chemically functionalize them. In order to validate the fabrication protocol, their optical properties are compared with those of QDs obtained from commercial solutions and deposited by wet chemistry on the substrates. Firstly, AFM measurements attest that nano-objects with a mean diameter around 13 nm are located on the substrate after RFMS treatment. Secondly, the UV-Vis absorption study of this deposited layer shows a specific optical absorption band, located at 550 nm, which is related to a discrete energy level of QDs. Thirdly, by using two-color sum-frequency generation (2C-SFG) nonlinear optical spectroscopy, we show experimentally the functionalization efficiency of the RFMS CdSe QDs layer with thiol derived molecules, which is not possible on the QDs layer prepared by wet chemistry due to the surfactant molecules from the native solution. Finally, 2C-SFG spectroscopy, performed at different visible wavelengths, highlights modifications of the vibration mode shape whatever the QDs deposition method, which is correlated to the discrete energy level of the QDs.

  1. Dimensionality of nanoscale TiO2 determines the mechanism of photoinduced electron injection from a CdSe nanoparticle

    DOE PAGES

    Tafen, De Nyago; Long, Run; Prezhdo, Oleg V.

    2014-03-10

    Assumptions about electron transfer (ET) mechanisms guide design of catalytic, photovoltaic, and electronic systems. We demonstrate that the mechanism of ET from a CdSe quantum dot (QD) into nanoscale TiO2 depends on TiO2 dimensionality. The injection into a TiO2 QD is adiabatic due to strong donor–acceptor coupling, arising from unsaturated chemical bonds on the QD surface, and low density of acceptor states. In contrast, the injection into a TiO2 nanobelt (NB) is nonadiabatic, because the state density is high, the donor–acceptor coupling is weak, and multiple phonons accommodate changes in the electronic energy. The CdSe adsorbant breaks symmetry of delocalizedmore » TiO2 NB states, relaxing coupling selection rules, and generating more ET channels. Both mechanisms can give efficient ultrafast injection. Furthermore, the dependence on system properties is very different for the two mechanisms, demonstrating that the fundamental principles leading to efficient charge separation depend strongly on the type of nanoscale material.« less

  2. Magnetic-field-dependent spin decoherence and dephasing in room-temperature CdSe nanocrystal quantum dots

    NASA Astrophysics Data System (ADS)

    Fumani, A. Khastehdel; Berezovsky, J.

    2013-10-01

    We perform and analyze a series of time-resolved Faraday rotation measurements of coherent spin dynamics in a room-temperature ensemble of CdSe nanocrystal quantum dots (NCQDs) to study the decoherence and dephasing mechanisms that limit the transverse spin lifetime. Coherent spin lifetimes on the order of nanoseconds have been previously observed in CdSe NCQDs, but the presence of multiple components with distinct dynamics and strong inhomogeneous dephasing have made it difficult to study the relevant spin decay mechanisms quantitatively. Here, we obtain reliable fitting results by ensuring that cross-correlations between model parameters are minimized for the parameters of interest. Furthermore, we characterize the morphological inhomogeneity of the NCQD ensemble using transmission electron microscopy to constrain the model parameters that specify inhomogeneous dephasing. We find that g-factor inhomogeneity-induced dephasing (gID) is not sufficient to explain the magnetic-field-dependent decay of the spin signal. We propose an additional decoherence mechanism arising from rapid transitions between the fine structure states of the exciton referred to as fine-structure decoherence (FSD). By including both gID and FSD in the model, excellent fits are obtained to the data, including a prominent short-time-scale feature, which has typically been excluded from the fits in previous work.

  3. Ligand-controlled rates of photoinduced electron transfer in hybrid CdSe nanocrystal/poly(viologen) films.

    PubMed

    Tagliazucchi, Mario; Tice, Daniel B; Sweeney, Christina M; Morris-Cohen, Adam J; Weiss, Emily A

    2011-12-27

    This paper describes a study of the rates of photoinduced electron transfer (PET) from CdSe quantum dots (QDs) to poly(viologen) within thin films, as a function of the length of the ligands passivating the QDs. Ultrafast (<10 ps), quantitative PET occurs from CdSe QDs coated with HS-(CH(2))(n)-COOH for n = 1, 2, 5, and 7 to viologen units. The observed decrease in the magnitude of the PET rate constant with n is weaker than that expected from the decay of the electron tunneling probability across extended all-trans mercaptocarboxylic acids but well-described by electron tunneling across a collapsed ligand shell. The PET rate constants for films with n = 10 and 15 are much slower than those expected based on the trend for n = 1-7; this deviation is ascribed to the formation of bundles of ligands on the surface of the QD that make the tunneling process prohibitively slow by limiting access of the viologen units to the surfaces of the QDs. This study highlights the importance of molecular-level morphology of donor and acceptor materials in determining the rate and yield of interfacial photoinduced electron transfer in thin films.

  4. Charge separation in type II tunneling structures of close-packed CdTe and CdSe nanocrystals.

    PubMed

    Gross, Dieter; Susha, Andrei S; Klar, Thomas A; Da Como, Enrico; Rogach, Andrey L; Feldmann, Jochen

    2008-05-01

    We report on charge separation between type II aligned CdTe and CdSe nanocrystals. Two types of electrostatically bound nanocrystal structures have been studied: first, clusters of nanocrystals hold together by Ca(II) ions in aqueous solution and, second, thin film structures of nanocrystals created with layer-by-layer deposition in combination with polyelectrolytes. In both types of structures, short interparticle distances of less than 1 nm have been achieved, whereby the isolating organic ligands on the nanocrystal surfaces and/or the polymer monolayers act as tunneling barriers between nanocrystals. We have observed an efficient quenching of photoluminescence and a reduced emission lifetime for CdTe nanocrystals in both types of type II heterostructures. This result is explained by a spatial charge separation of the photoexcited electron-hole pairs due to tunneling of charge carriers through the thin organic layer between CdTe and CdSe nanocrystals. Type II heterostructures demonstrated here may find future applications in photovoltaics.

  5. Graphene oxide based CdSe photocatalysts: Synthesis, characterization and comparative photocatalytic efficiency of rhodamine B and industrial dye

    SciTech Connect

    Ghosh, Trisha; Lee, Jeong-Ho; Meng, Ze-Da; Ullah, Kefayat; Park, Chong-Yeon; Nikam, Vikram; Oh, Won-Chun

    2013-03-15

    Highlights: ► CdSe–graphene is synthesized by hydrothermal method. ► Three molar solutions of CdSe were used making three different composites. ► RhB and Texbrite MST-L were used as sample dye solutions. ► Texbrite MST-L is photo degraded in visible light. ► UV-spectroscopic analysis was done to measure degradation. - Abstract: CdSe–graphene composites were prepared using simple “hydrothermal method” where the graphene surface was modified using different molar solutions of cadmium selenide (CdSe) in aqueous media. The characterization of CdSe–graphene composites were studied by X-ray diffraction (XRD), energy dispersive X-ray (EDX), scanning electron microscope (SEM), and with transmission electron microscope (TEM). The catalytic activities of CdSe-composites were evaluated by degradation of rhodamine B (RhB) and commercial industrial dye “Texbrite MST-L (TXT-MST)” with fixed concentration. The degradation was observed by the decrease in the absorbance peak studied by UV spectrophotometer. The decrease in the dye concentration indicated catalytic degradation effect by CdSe–graphene composites.

  6. Shell-dependent electroluminescence from colloidal CdSe quantum dots in multilayer light-emitting diodes

    NASA Astrophysics Data System (ADS)

    Jing, Pengtao; Zheng, Jinju; Zeng, Qinghui; Zhang, Youlin; Liu, Xiaomin; Liu, Xueyan; Kong, Xianggui; Zhao, Jialong

    2009-02-01

    We report electroluminescence (EL) of colloidal CdSe/CdS, CdSe/ZnS, and CdSe/CdS/CdZnS/ZnS core/shell quantum dots (QDs) in multilayer light-emitting diodes (LEDs) fabricated by spin coating a near monolayer of the core/shell QDs on cross-linkable hole transporting layers. It is found that CdSe/CdS QD-LEDs exhibit a faster decrease in EL quantum efficiency (˜2% at a brightness of 100 cd/m2) with increasing current density and lower maximum brightness than those of CdSe/ZnS QD-LEDs. A more significant redshift and spectral broadening of the EL observed in CdSe core/shell QDs with a CdS or CdS/CdZnS/ZnS shell than with a ZnS shell indicate that the electron wave function can penetrate into the shell under electric field. The difference in device performance and EL spectra results from conduction band offsets between the CdSe cores and CdS or ZnS shells, suggesting the existence of the exciton ionization in the QD-LEDs.

  7. Annealing-induced optical and sub-band-gap absorption parameters of Sn-doped CdSe thin films

    NASA Astrophysics Data System (ADS)

    Kaur, Jagdish; Tripathi, S. K.

    2016-01-01

    Thin films of Sn-doped CdSe were prepared by thermal evaporation onto glass substrates in an argon gas atmosphere and annealed at different temperatures. Structural evaluation of the films was carried out using X-ray diffraction and their stoichiometry studied by energy-dispersive X-ray analysis. The films exhibit a preferred orientation along the hexagonal direction of CdSe. The optical transmittance of the films shows a red shift of the absorption edge with annealing. The fundamental absorption edge corresponds to a direct energy gap with a temperature coefficient of 3.34 × 10-3 eV K-1. The refractive index, optical conductivity and real and imaginary parts of the dielectric constants were found to increase after annealing. The sub-band gap absorption coefficient was evaluated using the constant photocurrent method. It varies exponentially with photon energy. The Urbach energy, the density of defect states, and the steepness of the density of localized states were evaluated from the sub-band-gap absorption.

  8. Hybrid solar cells of micro/mesoporous Zn( and its graphite composites sensitized by CdSe quantum dots

    NASA Astrophysics Data System (ADS)

    Islam, SM Z.; Gayen, Taposh; Tint, Naing; Shi, Lingyan; Ebrahim, Amani M.; Seredych, Mykola; Bandosz, Teresa J.; Alfano, Robert

    2014-01-01

    Quantum efficiencies (QEs) of innovative hybrid solar cells fabricated using micro/mesoporous zinc (hydr)oxide and its graphite-based composites sensitized by semiconductor quantum dots (SQDs) are reported. High absorption coefficient of CdSe SQDs and the wide band gap of zinc (hydr)oxide and its composites with graphite oxide (GO) are essential to achieve solar cells of higher QEs. Hybrid solar cells are fabricated from zinc (hydr)oxide and its composites (with 2 and 5 wt.% of graphite oxides, termed as, ZnGO-2 and ZnGO-5, respectively) while using potassium iodide or perovskite as an electrolyte. A two-photon fluorescence (TPF) imaging technique was used to determine the internal structure of the solar cell device. The photocurrent and current-voltage measurements were used to measure short-circuit current and open-circuit voltage to calculate the fill factor and QE of these solar cells. The highest QE (up to ˜10.62%) is realized for a ZnGO-2-based solar cell using potassium iodide as its electrolyte and the CdSe quantum dot as its sensitizer.

  9. The use of heat transfer fluids in the synthesis of high-quality CdSe quantum dots, core/shell quantum dots, and quantum rods.

    PubMed

    Asokan, Subashini; Krueger, Karl M; Alkhawaldeh, Ammar; Carreon, Alessandra R; Mu, Zuze; Colvin, Vicki L; Mantzaris, Nikos V; Wong, Michael S

    2005-10-01

    Fluorescent semiconductor nanoparticles, or quantum dots, have potential uses as an optical material, in which the optoelectronic properties can be tuned precisely by particle size. Advances in chemical synthesis have led to improvements in size and shape control, cost, and safety. A limiting step in large-scale production is identified to be the raw materials cost, in which a common synthesis solvent, octadecene, accounts for most of the materials cost for a batch of CdSe quantum dots. Thus, less expensive solvents are needed. In this paper, we identify heat transfer fluids, a class of organic liquids commonly used in chemical process industries to transport heat between unit operations, as alternative solvents for quantum dot synthesis. We specifically show that two heat transfer fluids can be used successfully in the synthesis of CdSe quantum dots with uniform particle sizes. We show that the synthesis chemistry for CdSe/CdS core/shell quantum dots and CdSe quantum rods can also be performed in heat transfer fluids. With the aid of a population balance model, we interpret the effect of different HT fluids on QD growth kinetics in terms of solvent effects, i.e., solvent viscosity, CdSe bulk solubility in the solvent, and surface free energy.

  10. High performance of Mn-doped CdSe quantum dot sensitized solar cells based on the vertical ZnO nanorod arrays

    NASA Astrophysics Data System (ADS)

    Hou, Juan; Zhao, Haifeng; Huang, Fei; Jing, Qun; Cao, Haibin; Wu, Qiang; Peng, Shanglong; Cao, Guozhong

    2016-09-01

    Doping transition metal ions Mn2+ to semiconductor quantum dots (QDs) are extremely interesting for the development of photovoltaic devices. Quantum dot sensitized solar cells (QDSCs) are able to show promising power conversion efficiencies (PCE) by employing Mn2+ doped QDs. Herein we achieve effective CdS/Mnsbnd CdSe/ZnS QDs co-sensitized vertical ZnO nanorod arrays film that provides an appreciable enhancement in photovoltaic performance. The measured PCE of the solar cells with Mn2+ doped CdSe QDs is 4.14%, which is higher than the efficiency of 2.91% for the solar cells without Mn2+ or a ∼42% increase. The improvement in PCE is ascribed to a higher open-circuit voltage (Voc = 0.74 V) and a superior short-circuit current density (Jsc = 12.6 mA cm-2) with the introduction of Mn2+ into CdSe QDs. The enhancement seen with Mn2+ doped CdSe QDs are investigated and explained by the fact that the enhanced light absorption and reduced charge recombination by the formation of Mnsbnd CdSe passivation layer covering the QDs.

  11. Efficient CdSe quantum dot-sensitized solar cells prepared by an improved successive ionic layer adsorption and reaction process.

    PubMed

    Lee, Hyojoong; Wang, Mingkui; Chen, Peter; Gamelin, Daniel R; Zakeeruddin, Shaik M; Grätzel, Michael; Nazeeruddin, Md K

    2009-12-01

    In pursuit of efficient quantum dot (QD)-sensitized solar cells based on mesoporous TiO(2) photoanodes, a new procedure for preparing selenide (Se(2-)) was developed and used for depositing CdSe QDs in situ over TiO(2) mesopores by the successive ionic layer adsorption and reaction (SILAR) process in ethanol. The sizes and density of CdSe QDs over TiO(2) were controlled by the number of SILAR cycles applied. After some optimization of these QD-sensitized TiO(2) films in regenerative photoelectrochemical cells using a cobalt redox couple [Co(o-phen)(3)(2+/3+)], including addition of a final layer of CdTe, over 4% overall efficiencies were achieved at 100 W/m(2) with about 50% IPCE at its maximum. Light-harvesting properties and transient voltage decay/impedance measurements confirmed that CdTe-terminated CdSe QD cells gave better charge-collection efficiencies and kinetic parameters than corresponding CdSe QD cells. In a preliminary study, a CdSe(Te) QD-sensitized TiO(2) film was combined with an organic hole conductor, spiro-OMeTAD, and shown to exhibit a promising efficiency of 1.6% at 100 W/m(2) in inorganic/organic hybrid all-solid-state cells.

  12. Cadmium telluride (CdTe) and cadmium selenide (CdSe) leaching behavior and surface chemistry in response to pH and O2.

    PubMed

    Zeng, Chao; Ramos-Ruiz, Adriana; Field, Jim A; Sierra-Alvarez, Reyes

    2015-05-01

    Cadmium telluride (CdTe) and cadmium selenide (CdSe) are increasingly being applied in photovoltaic solar cells and electronic components. A major concern is the public health and ecological risks associated with the potential release of toxic cadmium, tellurium, and/or selenium species. In this study, different tests were applied to investigate the leaching behavior of CdTe and CdSe in solutions simulating landfill leachate. CdTe showed a comparatively high leaching potential. In the Toxicity Characteristic Leaching Procedure (TCLP) and Waste Extraction Test (WET), the concentrations of cadmium released from CdTe were about 1500 and 260 times higher than the regulatory limit (1 mg/L). In contrast, CdSe was relatively stable and dissolved selenium in both leaching tests was below the regulatory limit (1 mg/L). Nonetheless, the regulatory limit for cadmium was exceeded by 5- to 6- fold in both tests. Experiments performed under different pH and redox conditions confirmed a marked enhancement in CdTe and CdSe dissolution both at acidic pH and under aerobic conditions. These findings are in agreement with thermodynamic predictions. Taken as a whole, the results indicate that recycling of decommissioned CdTe-containing devices is desirable to prevent the potential environmental release of toxic cadmium and tellurium in municipal landfills.

  13. Isolation of a selenite-reducing and cadmium-resistant bacterium Pseudomonas sp. strain RB for microbial synthesis of CdSe nanoparticles.

    PubMed

    Ayano, Hiroyuki; Miyake, Masaki; Terasawa, Kanako; Kuroda, Masashi; Soda, Satoshi; Sakaguchi, Toshifumi; Ike, Michihiko

    2014-05-01

    Bacteria capable of synthesizing CdSe from selenite and cadmium ion were enriched from a soil sample. After repeated transfer of the soil-derived bacterial cultures to a new medium containing selenite and cadmium ion 42 times (during 360 days), an enrichment culture that can simultaneously remove selenite and cadmium ion (1 mM each) from the liquid phase was obtained. The culture's color became reddish-brown, indicating CdSe nanoparticle production, as confirmed by energy-dispersive x-ray spectra (EDS). As a result of isolation operations, the bacterium that was the most responsible for synthesizing CdSe, named Pseudomonas sp. RB, was obtained. Transmission electron microscopy and EDS revealed that this strain accumulated nanoparticles (10-20 nm) consisting of selenium and cadmium inside and on the cells when cultivated in the same medium for the enrichment culture. This report is the first describing isolation of a selenite-reducing and cadmium-resistant bacterium. It is useful for CdSe nanoparticle synthesis in the simple one-vessel operation.

  14. Tuning Hole and Electron Transfer from Photo-excited CdSe Quantum Dot to Phenol Derivatives: Effect of Electron Donating and Withdrawing Moiety.

    PubMed

    Ghosh, Hirendra Nath; Debnath, Tushar; Sebastian, Deepa; Maiti, Sourav

    2017-03-27

    Charge transfer processes from photo-excited CdSe QDs to phenol derivatives with electron donating (4-methoxy) and electron withdrawing (4-nitro) moiety have been demonstrated by using steady state and time-resolved emission and femto-second transient absorption spectroscopy. Steady state and time-resolved emission studies suggest that in presence of both 4-nitro phenol (4NP) and 4-methoxy phenol (4MP) CdSe QDs luminescence gets quenched. Stern-Volmer analysis suggests both static and dynamic mechanisms are active for both the QD/phenol composites. Cyclic volatmetric analysis recommends that photo-excited CdSe QDs can donate electron to 4NP and hole to 4MP. To reconfirm both electron and hole transfer mechanism CdSe/CdS quasi type-II and CdSe/CdTe type-II core-shell NC were synthesized and the photoluminescence quenching were monitored in absence and in presence of both 4NP and 4MP where systematically hole and electron transfer were restricted. Our studies suggest that indeed electron and hole transfer take place from photo-excited CdSe to 4NP and 4MP respectively. To monitor the charge transfer dynamics in both the systems in early time scale, we have employed femtosecond transient absorption (TA) spectroscopic techniques. Both electron and hole transfer and charge recombination dynamics have been discussed and effect of electron donating and withdrawing group has been demonstrated.

  15. Microwave-assisted synthesis of CdSe quantum dots: can the electromagnetic field influence the formation and quality of the resulting nanocrystals?

    PubMed

    Moghaddam, Mojtaba Mirhosseini; Baghbanzadeh, Mostafa; Keilbach, Andreas; Kappe, C Oliver

    2012-12-07

    Microwave-assisted syntheses of colloidal nanocrystals (NCs), in particular CdSe quantum dots (QDs), have gained considerable attention due to unique opportunities provided by microwave dielectric heating. The extensive use of microwave heating and the frequently suggested specific microwave effects, however, pose questions about the role of the electromagnetic field in both the formation and quality of the produced QDs. In this work a one-pot protocol for the tunable synthesis of monodisperse colloidal CdSe NCs using microwave dielectric heating under carefully controlled conditions is introduced. CdSe QDs are fabricated using selenium dioxide as a selenium precursor, 1-octadecene as a solvent and reducing agent, cadmium alkyl carboxylates or alkyl phosphonates as cadmium sources, 1,2-hexadecanediol to stabilize the cadmium complex and oleic acid to stabilize the resulting CdSe QDs. Utilizing the possibilities of microwave heating technology in combination with accurate online temperature control the influence of different reaction parameters such as reaction temperature, ramp and hold times, and the timing and duration of oleic acid addition have been carefully investigated. Optimum results were obtained by performing the reaction at 240 °C applying a 5 min ramp time, 2 min hold time before oleic acid addition, 90 s for oleic acid addition, and a 5 min hold time after oleic acid addition (8.5 min overall holding at 240 °C). By using different cadmium complexes in the microwave protocol CdSe QDs with a narrow size distribution can be obtained in different sizes ranging from 0.5-4 nm by simply changing the cadmium source. The QDs were characterized by TEM, HRTEM, UV-Vis, and photoluminescence methods and the size distribution was monitored by SAXS. Control experiments involving conventional conductive heating under otherwise identical conditions ensuring the same heating and cooling profiles, stirring rates, and reactor geometries demonstrate that the

  16. 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

  17. Effect of lateral size and thickness on the electronic structure and optical properties of quasi two-dimensional CdSe and CdS nanoplatelets

    NASA Astrophysics Data System (ADS)

    Bose, Sumanta; Song, Zhigang; Fan, W. J.; Zhang, D. H.

    2016-04-01

    The effect of lateral size and vertical thickness of CdSe and CdS nanoplatelets (NPLs) on their electronic structure and optical properties are investigated using an effective-mass envelope function theory based on the 8-band k ṡ p model with valence force field considerations. Volumetrically larger NPLs have lower photon emission energy due to limited quantum confinement, but a greater transition matrix element (TME) due to larger electron-hole wavefunction overlap. The optical gain characteristics depend on several factors such as TME, Fermi factor, carrier density, NPL dimensions, material composition, and dephasing rate. There is a red shift in the peak position, more so with an increase in thickness than lateral size. For an increasing carrier density, the gain spectrum undergoes a slight blue shift due to band filling effect. For a fixed carrier density, the Fermi factor is higher for volumetrically larger NPLs and so is the difference between the quasi-Fermi level separation and the effective bandgap. The transparency injection carrier density (and thus input current density threshold) is dimension dependent and falls for volumetrically larger NPLs, as they can attain the requisite exciton count for transparency with a relatively lower density. Between CdSe and CdS, CdSe has lower emission energy due to smaller bandgap, but a higher TME due to lower effective mass. CdS, however, has a higher so hole contribution due to a lower spin-orbit splitting energy. Both CdSe and CdS NPLs are suitable candidates for short-wavelength LEDs and lasers in the visible spectrum, but CdSe is expected to exhibit better optical performance.

  18. Vectorial electron transfer for improved hydrogen evolution by mercaptopropionic-acid-regulated CdSe quantum-dots-TiO2 -Ni(OH)2 assembly.

    PubMed

    Yu, Shan; Li, Zhi-Jun; Fan, Xiang-Bing; Li, Jia-Xin; Zhan, Fei; Li, Xu-Bing; Tao, Ye; Tung, Chen-Ho; Wu, Li-Zhu

    2015-02-01

    A visible-light-induced hydrogen evolution system based on a CdSe quantum dots (QDs)-TiO2 -Ni(OH)2 ternary assembly has been constructed under an ambient environment, and a bifunctional molecular linker, mercaptopropionic acid, is used to facilitate the interaction between CdSe QDs and TiO2 . This hydrogen evolution system works effectively in a basic aqueous solution (pH 11.0) to achieve a hydrogen evolution rate of 10.1 mmol g(-1)  h(-1) for the assembly and a turnover frequency of 5140 h(-1) with respect to CdSe QDs (10 h); the latter is comparable with the highest value reported for QD systems in an acidic environment. X-ray photoelectron spectroscopy, X-ray absorption spectroscopy, and control experiments demonstrate that Ni(OH)2 is an efficient hydrogen evolution catalyst. In addition, inductively coupled plasma optical emission spectroscopy and the emission decay of the assembly combined with the hydrogen evolution experiments show that TiO2 functions mainly as the electron mediator; the vectorial electron transfer from CdSe QDs to TiO2 and then from TiO2 to Ni(OH)2 enhances the efficiency for hydrogen evolution. The assembly comprises light antenna CdSe QDs, electron mediator TiO2 , and catalytic Ni(OH)2 , which mimics the strategy of photosynthesis exploited in nature and takes us a step further towards artificial photosynthesis.

  19. Upconversion Nanoparticles for Security Printing and CdSe QDs for Drug Delivery Applications

    NASA Astrophysics Data System (ADS)

    Baride, Aravind

    demonstrated NIR light induced release of a target molecule, coumarin, from functionalized quantum dots. Coumarin, a model drug molecule, is released upon NIR two-photon excitation of cinnamate capped CdSe QDs. Electron transfer from the excited QD to the cinnamate ligand induces the release of coumarin. The electron transfer across the QD to the cinnamate ligand is confirmed by evaluation of uncaging activity in the cinnamate capped CdSe/ZnS core-shell QDs.

  20. Contactless microwave study of shallow traps in thin-film CdSe

    NASA Astrophysics Data System (ADS)

    Grabtchak, Serguei Yu.; Cocivera, Michael

    1994-12-01

    The contactless microwave technique was used to measure light-induced transients in the power absorption by thin films of polycrystalline CdSe. Because the rise time of the detector was 500 ns, the analysis was limited 1 μsec or longer. Measurement of these transients at a number of fixed frequencies across the ``dark'' resonance frequency made reconstruction of the difference signal possible. This signal, which represents the difference between the ``dark'' and ``light'' Lorentz resonance curves, was determined at various times during the decay. Analysis of these signals provided the changes in the real and imaginary parts of the dielectric constant as a function of time. The decays of these parameters were characterized by the sum of two exponential terms: τ1=16.9 μsec and τ2=261.5 μsec for the change in the imaginary part, and τ1=18.5 μsec and τ2=283 μsec for the change in the real part. The close agreement of these values indicates the simultaneous presence of both trapped and free electrons having identical decay times. A mechanism consistent with these results involves rapid equilibration between the free electrons and those in the two shallow traps. Decay from each trap is the rate limiting step, and the time to reach thermodynamic equilibrium must be less than 500 ns. The initial electron densities in the two traps were 2.1×1018 and 1.0×1018 cm-3, and the corresponding concentrations of the free electrons were 3.6×1017 and 1.4×1017 cm-3. For the free electrons, the values for the drift mobility were 2.1 and 1.8 cm2/V s, respectively. Using the harmonic-oscillator model for trapped electrons, the trap energies were 0.096 eV for the fast decay and 0.152 eV for the slower decay. The initial changes in a real part of the dielectric constant were 44.9 and 11.9, respectively. Thus, the photoinduced concentrations of electrons in naturally existing shallow traps are sufficient to effect large changes in the dielectric constant on a short time scale.

  1. CdTe and CdSe quantum dots: synthesis, characterizations and applications in agriculture

    NASA Astrophysics Data System (ADS)

    Dieu Thuy Ung, Thi; Tran, Thi Kim Chi; Nga Pham, Thu; Nghia Nguyen, Duc; Khang Dinh, Duy; Liem Nguyen, Quang

    2012-12-01

    This paper highlights the results of the whole work including the synthesis of highly luminescent quantum dots (QDs), characterizations and testing applications of them in different kinds of sensors. Concretely, it presents: (i) the successful synthesis of colloidal CdTe and CdSe QDs, their core/shell structures with single- and/or double-shell made by CdS, ZnS or ZnSe/ZnS; (ii) morphology, structural and optical characterizations of the synthesized QDs; and (iii) testing examples of QDs as the fluorescence labels for agricultural-bio-medical objects (for tracing residual pesticide in agricultural products, residual clenbuterol in meat/milk and for detection of H5N1 avian influenza virus in breeding farms). Overall, the results show that the synthesized QDs have very good crystallinity, spherical shape and strongly emit at the desired wavelengths between ˜500 and 700 nm with the luminescence quantum yield (LQY) of 30-85%. These synthesized QDs were used in fabrication of the three testing fluorescence QD-based sensors for the detection of residual pesticides, clenbuterol and H5N1 avian influenza virus. The specific detection of parathion methyl (PM) pesticide at a content as low as 0.05 ppm has been realized with the biosensors made from CdTe/CdS and CdSe/ZnSe/ZnS QDs and the acetylcholinesterase (AChE) enzymes. Fluorescence resonance energy transfer (FRET)-based nanosensors using CdTe/CdS QDs conjugated with 2-amino-8-naphthol-6-sulfonic acid were fabricated that enable detection of diazotized clenbuterol at a content as low as 10 pg ml-1. For detection of H5N1 avian influenza virus, fluorescence biosensors using CdTe/CdS QDs bound on the surface of chromatophores extracted and purified from bacteria Rhodospirillum rubrum were prepared and characterized. The specific detection of H5N1 avian influenza virus in the range of 3-50 ng μl-1 with a detection limit of 3 ng μL-1 has been performed based on the antibody-antigen recognition.

  2. Probing structure-induced optical behavior in a new class of self-activated luminescent 0D/1D CaWO₄ metal oxide – CdSe nanocrystal composite heterostructures

    SciTech Connect

    Han, Jinkyu; McBean, Coray; Wang, Lei; Hoy, Jessica; Jaye, Cherno; Liu, Haiqing; Li, Zhuo-Qun; Sfeir, Matthew Y.; Fischer, Daniel A.; Taylor, Gordon T.; Misewich, James A.; Wong, Stanislaus S.

    2015-01-30

    In this report, we synthesize and characterize the structural and optical properties of novel heterostructures composed of (i) semiconducting nanocrystalline CdSe quantum dot (QDs) coupled with (ii) both one and zero-dimensional (1D and 0D) motifs of self-activated luminescence CaWO₄ metal oxides. Specifically, ~4 nm CdSe QDs have been anchored onto (i) high-aspect ratio 1D nanowires, measuring ~230 nm in diameter and ~3 μm in length, as well as onto (ii) crystalline 0D nanoparticles (possessing an average diameter of ~ 80 nm) of CaWO₄ through the mediation of 3-mercaptopropionic acid (MPA) as a connecting linker. Composite formation was confirmed by complementary electron microscopy and spectroscopy (i.e. IR and Raman) data. In terms of luminescent properties, our results show that our 1D and 0D heterostructures evince photoluminescence (PL) quenching and shortened PL lifetimes of CaWO₄ as compared with unbound CaWO₄. We propose that a photo-induced electron transfer process occurs from CaWO₄ to CdSe QDs, a scenario which has been confirmed by NEXAFS measurements and which highlights a decrease in the number of unoccupied orbitals in the conduction bands of CdSe QDs. By contrast, the PL signature and lifetimes of MPA-capped CdSe QDs within these heterostructures do not exhibit noticeable changes as compared with unbound MPA-capped CdSe QDs. The striking difference in optical behavior between CaWO₄ nanostructures and CdSe QDs within our heterostructures can be correlated with the relative positions of their conduction and valence energy band levels. In addition, the PL quenching behaviors for CaWO₄ within the heterostructure configuration were examined by systematically varying (i) the quantities and coverage densities of CdSe QDs as well as (ii) the intrinsic morphology (and by extension, the inherent crystallite size) of CaWO₄ itself.

  3. Structure and Composition of Cu Doped CdSe Nanocrystals Using Soft X-ray Absorption Spectroscopy

    SciTech Connect

    Meulenberg, R W; van Buuren, T; Hanif, K M; Willey, T M; Strouse, G F; Terminello, L J

    2004-06-04

    The local structure and composition of Cu ions dispersed in CdSe nanocrystals is examined using soft x-ray absorption near edge spectroscopy (XANES). Using Cu L-edge XANES and X-ray photoelectron measurements (XPS), we find that the Cu ions exist in the Cu(I) oxidation state. We also find that the observed Cu L-edge XANES signal is directly proportional to the molar percent of Cu present in our final material. Se L-edge XANES indicates changes in the Se density of states with Cu doping, due to a chemical bonding effect, and supports a statistical doping mechanism. Photoluminescence (PL) measurements indicate the Cu ions may act as deep electron traps. We show that XANES, XPS, and PL are a powerful combination of methods to study the electronic and chemical structure of dopants in nanostructured materials.

  4. Fiber and fabric solar cells by directly weaving carbon nanotube yarns with CdSe nanowire-based electrodes.

    PubMed

    Zhang, Luhui; Shi, Enzheng; Ji, Chunyan; Li, Zhen; Li, Peixu; Shang, Yuanyuan; Li, Yibin; Wei, Jinquan; Wang, Kunlin; Zhu, Hongwei; Wu, Dehai; Cao, Anyuan

    2012-08-21

    Electrode materials are key components for fiber solar cells, and when combined with active layers (for light absorption and charge generation) in appropriate ways, they enable design and fabrication of efficient and innovative device structures. Here, we apply carbon nanotube yarns as counter electrodes in combination with CdSe nanowire-grafted primary electrodes (Ti wire) for making fiber and fabric-shaped photoelectrochemical cells with power conversion efficiencies in the range 1% to 2.9%. The spun-twist long nanotube yarns possess both good electrical conductivity and mechanical flexibility compared to conventional metal wires or carbon fibers, which facilitate fabrication of solar cells with versatile configurations. A unique feature of our process is that instead of making individual fiber cells, we directly weave single or multiple nanotube yarns with primary electrodes into a functional fabric. Our results demonstrate promising applications of semiconducting nanowires and carbon nanotubes in woven photovoltaics.

  5. Insertion of CdSe quantum dots in ZnSe nanowires: MBE growth and microstructure analysis

    NASA Astrophysics Data System (ADS)

    den Hertog, M.; Elouneg-Jamroz, M.; Bellet-Amalric, E.; Bounouar, S.; Bougerol, C.; André, R.; Genuist, Y.; Poizat, J. P.; Kheng, K.; Tatarenko, S.

    2011-05-01

    ZnSe nanowire growth has been successfully achieved on ZnSe (1 0 0) and (1 1 1)B buffer layers deposited on GaAs substrates. Cubic [1 0 0] oriented ZnSe nanowires or [0 0 0 1] oriented hexagonal NWs are obtained on (1 0 0) substrates while [1 1 1] oriented cubic mixed with [0 0 0 1] oriented hexagonal regions are obtained on (1 1 1)B substrates. Most of the NWs are perpendicular to the surface in the last case. CdSe quantum dots were successfully incorporated in the ZnSe NWs as demonstrated by transmission electron microscopy, energy filtered TEM and high angle annular dark field scanning TEM measurements.

  6. On-surface formation of metal nanowire transparent top electrodes on CdSe nanowire array-based photoconductive devices.

    PubMed

    Azulai, Daniel; Givan, Uri; Shpaisman, Nava; Belenkova, Tatyana Levi; Gilon, Hagit; Patolsky, Fernando; Markovich, Gil

    2012-06-27

    A simple wet chemical approach was developed for a unique on-surface synthesis of transparent conductive films consisting of ultrathin gold/silver nanowires directly grown on top of CdSe nanowire array photoconductive devices enclosed in polycarbonate membranes. The metal nanowire film formed an ohmic contact to the semiconductor nanowires without additional treatment. The sheet resistance and transparency of the metal nanowire arrays could be controlled by the number of metal nanowire layers deposited, ranging from ∼98-99% transmission through the visible range and several kOhm/sq sheet resistance for a single layer, to 80-85% transmission and ∼100 Ohm/sq sheet resistance for 4 layers.

  7. Exciton-phonon coupling efficiency in CdSe quantum dots embedded in ZnSe nanowires

    NASA Astrophysics Data System (ADS)

    Bounouar, S.; Morchutt, C.; Elouneg-Jamroz, M.; Besombes, L.; André, R.; Bellet-Amalric, E.; Bougerol, C.; den Hertog, M.; Kheng, K.; Tatarenko, S.; Poizat, J. Ph.

    2012-01-01

    Exciton luminescence of a CdSe quantum dot (QD) inserted in a ZnSe nanowire is strongly influenced by the dark exciton states. Because of the small size of these QDs (2-5 nm), exchange interaction between hole and electron is highly enhanced and we measured large energy splitting between bright and dark exciton states (ΔE∈[4,9.2] meV) and large spin-flip rates between these states. Statistics on many QDs showed that this splitting depends on the QD size. Moreover, we measured an increase of the spin-flip rate to the dark states with increasing energy splitting. We explain this observation with a model, taking into account the fact that the exciton-phonon interaction depends on the bright to dark exciton energy splitting, as well as on the size and shape of the exciton wave function. It also has consequences on the exciton line intensity at high temperature.

  8. Fluorescence modulation of single CdSe nanowires by charge injection through the tip of an atomic-force microscope.

    PubMed

    Schäfer, Sebastian; Wang, Zhe; Kipp, Tobias; Mews, Alf

    2011-09-23

    We demonstrate a direct correlation between the charge state and photoluminescence (PL) intensity of individual CdSe nanowires by actively charging them and performing electrostatic force microscopy and PL measurements simultaneously. While the injection of positive charges leads to an immediate PL quenching, a small amount of injected electrons can lead to an increase of the PL intensity. We directly observed the migration of excess charges into the substrate, which leads to a recovery of the PL. Further, we show that the PL of individual NWs can be actively switched between on and off states by charging with the atomic-force microscope tip. We propose a model based on charge trapping and migration into the substrate to explain our results.

  9. Fast monolayer adsorption and slow energy transfer in CdSe quantum dot sensitized ZnO nanowires.

    PubMed

    Zheng, Kaibo; Žídek, Karel; Abdellah, Mohamed; Torbjörnsson, Magne; Chábera, Pavel; Shao, Shuyan; Zhang, Fengling; Pullerits, Tõnu

    2013-07-25

    A method for CdSe quantum dot (QD) sensitization of ZnO nanowires (NW) with fast adsorption rate is applied. Photoinduced excited state dynamics of the quantum dots in the case of more than monolayer coverage of the nanowires is studied. Transient absorption kinetics reveals an excitation depopulation process of indirectly attached quantum dots with a lifetime of ~4 ns. Photoluminescence and incident photon-to-electron conversion efficiency show that this process consists of both radiative e-h recombination and nonradiative excitation-to-charge conversion. We argue that the latter occurs via interdot energy transfer from the indirectly attached QDs to the dots with direct contact to the nanowires. From the latter, fast electron injection into ZnO occurs. The energy transfer time constant is found to be around 5 ns.

  10. Investigation of light induced effect on density of states of Pb doped CdSe thin films

    NASA Astrophysics Data System (ADS)

    Kaur, Jagdish; Singh, Baljinder; Tripathi, S. K.

    2016-05-01

    Thin films of Pb doped CdSe are deposited on the glass substrates by thermal evaporation technique using inert gas condensation method. The prepared thin films are light soaked under vacuum of 2×10-3 mbar for two hour. The absorption coefficient in the sub-band gap region has been studied using Constant Photocurrent Method (CPM). The absorption coefficient in the sub-band gap region follows an exponential Urbach tail. The value of Urbach energy and number density of defect states have been calculated from the absorption coefficient in the sub-band gap region and found to increase after light soaking treatment. The energy distribution of the occupied density of states below Fermi level has been evaluated using derivative procedure of the absorption coefficient.

  11. Thermally induced effect on sub-band gap absorption in Ag doped CdSe thin films

    NASA Astrophysics Data System (ADS)

    Kaur, Jagdish; Sharma, Kriti; Bharti, Shivani; Tripathi, S. K.

    2015-05-01

    Thin films of Ag doped CdSe have been prepared by thermal evaporation using inert gas condensation (IGC) method taking Argon as inert gas. The prepared thin films are annealed at 363 K for one hour. The sub-band gap absorption spectra in the as deposited and annealed thin films have been studied using constant photocurrent method (CPM). The absorption coefficient in the sub-band gap region is described by an Urbach tail in both as deposited and annealed thin films. The value of Urbach energy and number density of trap states have been calculated from the absorption coefficient in the sub-band gap region which have been found to increase after annealing treatment indicating increase in disorderness in the lattice. The energy distribution of the occupied density of states below Fermi level has also been studied using derivative procedure of absorption coefficient.

  12. New transient absorption observed in the spectrum of colloidal CdSe nanoparticles pumped with high-power femtosecond pulses

    SciTech Connect

    Burda, C.; Link, S.; Green, T.C.; El-Sayed, M.A.

    1999-12-09

    The power dependence of the transient absorption spectrum of CdSe nanoparticle colloids with size distribution of 4.0 {+-} 0.4 nm diameter is studied with femtosecond pump-probe techniques. At the lowest pump laser power, the absorption bleaching (negative spectrum) characteristic of the exciton spectrum is observed with maxima at 560 and 480 nm. As the pump laser power increases, two new transient absorptions at 510 and 590 nm with unresolved fast rise (<100 fs) and long decay times ({much{underscore}gt}150 ps) are observed. The energy of each of the positive absorption is red shifted from that of the bleach bands by {approximately}120 MeV. The origin of this shift is discussed in terms of the effect of the internal electric field of the many electron-hole pairs formed within the quantum dot at the high pump intensity, absorption from a metastable excited state or the formation of biexcitons.

  13. Fiber and fabric solar cells by directly weaving carbon nanotube yarns with CdSe nanowire-based electrodes

    NASA Astrophysics Data System (ADS)

    Zhang, Luhui; Shi, Enzheng; Ji, Chunyan; Li, Zhen; Li, Peixu; Shang, Yuanyuan; Li, Yibin; Wei, Jinquan; Wang, Kunlin; Zhu, Hongwei; Wu, Dehai; Cao, Anyuan

    2012-07-01

    Electrode materials are key components for fiber solar cells, and when combined with active layers (for light absorption and charge generation) in appropriate ways, they enable design and fabrication of efficient and innovative device structures. Here, we apply carbon nanotube yarns as counter electrodes in combination with CdSe nanowire-grafted primary electrodes (Ti wire) for making fiber and fabric-shaped photoelectrochemical cells with power conversion efficiencies in the range 1% to 2.9%. The spun-twist long nanotube yarns possess both good electrical conductivity and mechanical flexibility compared to conventional metal wires or carbon fibers, which facilitate fabrication of solar cells with versatile configurations. A unique feature of our process is that instead of making individual fiber cells, we directly weave single or multiple nanotube yarns with primary electrodes into a functional fabric. Our results demonstrate promising applications of semiconducting nanowires and carbon nanotubes in woven photovoltaics.Electrode materials are key components for fiber solar cells, and when combined with active layers (for light absorption and charge generation) in appropriate ways, they enable design and fabrication of efficient and innovative device structures. Here, we apply carbon nanotube yarns as counter electrodes in combination with CdSe nanowire-grafted primary electrodes (Ti wire) for making fiber and fabric-shaped photoelectrochemical cells with power conversion efficiencies in the range 1% to 2.9%. The spun-twist long nanotube yarns possess both good electrical conductivity and mechanical flexibility compared to conventional metal wires or carbon fibers, which facilitate fabrication of solar cells with versatile configurations. A unique feature of our process is that instead of making individual fiber cells, we directly weave single or multiple nanotube yarns with primary electrodes into a functional fabric. Our results demonstrate promising applications

  14. Low temperature synthesis of ZnS and CdZnS shells on CdSe quantum dots.

    PubMed

    Zhu, Huiguang; Prakash, Arjun; Benoit, Denise N; Jones, Christopher J; Colvin, Vicki L

    2010-06-25

    Methods for synthesizing quantum dots generally rely on very high temperatures to both nucleate and grow core and core-shell semiconductor nanocrystals. In this work, we generate highly monodisperse ZnS and CdZnS shells on CdSe semiconductor nanocrystals at temperatures as low as 65 degrees C by enhancing the precursor solubility. Relatively small amounts of trioctylphosphine and trioctylphosphine oxide have marked effects on the solubility of the metal salts used to form shells; their inclusion in the precursor solutions, which use thiourea as a sulfur source, can lead to homogeneous and fully dissolved solutions. Upon addition to suspensions of quantum dot cores, these precursors deposit as uniform shells; the lowest temperature for shell growth (65 degrees C) yields the thinnest shells (d < 1 nm) while the same process at higher temperatures (180 degrees C) forms thicker shells (d approximately 1-2 nm). The growth of the shell structures, average particle size, size distribution, and shape were examined using optical spectroscopy, transmission electron microscopy, x-ray diffraction, and transmittance small angle x-ray scattering. The photoluminescence quantum yield (QY) of the as-prepared CdSe/ZnS quantum dots ranged from 26% to 46% as compared to 10% for the CdSe cores. This method was further generalized to CdZnS shells by mixing cadmium and zinc acetate precursors. The CdSe/CdZnS nanocrystals have a thicker shell and higher QY (40% versus 36%) as compared to the CdSe/ZnS prepared under similar conditions. These low temperature methods for shell growth are readily amenable to scale-up and can provide a route for economical and less energy intensive production of quantum dots.

  15. Facile and green synthesis of CdSe quantum dots in protein matrix: tuning of morphology and optical properties.

    PubMed

    Ahmed, M; Guleria, A; Rath, M C; Singh, A K; Adhikari, S; Sarkar, S K

    2014-08-01

    Herein, we have demonstrated a facile and green approach for the synthesis of Cadmium selenide (CdSe) quantum dots (QDs). The process was mediated by bovine serum albumin (BSA) and it was found that BSA plays the dual role of reducing agent as well as a stabilizing agent. The QDs exhibited sharp excitonic absorption features at ~500 nm and subsequently showed reasonably good photoluminescence (PL) at room temperature. The PL is seen to be strongly dependent on the concentration of the precursors and hence, the luminescence of these QDs could be conveniently tuned across the visible spectrum simply by varying molar ratio of the precursors. It can be envisaged from the fact that a red-shift of about 100 nm in the PL peak position was observed when the molar ratio of the precursors ([Cd2+]:[Se2-], in mM) was varied from 10:5 to 10:40. Subsequently, the charge carrier relaxation dynamics associated with the different molar ratio of precursors has been investigated and very interesting information regarding the energy level structures of these QDs were revealed. Most importantly, in conjunction with the optical tuning, the nanomorphology of these nanoparticles was found to vary with the change in molar ratios of Se and Cd precursors. This aspect can provide a new direction of controlling the shape of CdSe nanoparticles. The possible mechanism of the formation as well as for the shape variation of these nanoparticles with the molar ratios of precursors has been proposed, taking into account the role of amino acid residues (present in BSA). Moreover, the QDs were water soluble and possessed fairly good colloidal stability therefore, can have potential applications in catalysis and bio-labeling. On the whole, the present methodology of protein assisted synthesis is relatively new especially for semiconducting nanomaterials and may provide some unique and interesting aspects to control and fine tune the morphology vis-à-vis, their optical properties.

  16. Low temperature synthesis of ZnS and CdZnS shells on CdSe quantum dots

    NASA Astrophysics Data System (ADS)

    Zhu, Huiguang; Prakash, Arjun; Benoit, Denise N.; Jones, Christopher J.; Colvin, Vicki L.

    2010-06-01

    Methods for synthesizing quantum dots generally rely on very high temperatures to both nucleate and grow core and core-shell semiconductor nanocrystals. In this work, we generate highly monodisperse ZnS and CdZnS shells on CdSe semiconductor nanocrystals at temperatures as low as 65 °C by enhancing the precursor solubility. Relatively small amounts of trioctylphosphine and trioctylphosphine oxide have marked effects on the solubility of the metal salts used to form shells; their inclusion in the precursor solutions, which use thiourea as a sulfur source, can lead to homogeneous and fully dissolved solutions. Upon addition to suspensions of quantum dot cores, these precursors deposit as uniform shells; the lowest temperature for shell growth (65 °C) yields the thinnest shells (d < 1 nm) while the same process at higher temperatures (180 °C) forms thicker shells (d ~ 1-2 nm). The growth of the shell structures, average particle size, size distribution, and shape were examined using optical spectroscopy, transmission electron microscopy, x-ray diffraction, and transmittance small angle x-ray scattering. The photoluminescence quantum yield (QY) of the as-prepared CdSe/ZnS quantum dots ranged from 26% to 46% as compared to 10% for the CdSe cores. This method was further generalized to CdZnS shells by mixing cadmium and zinc acetate precursors. The CdSe/CdZnS nanocrystals have a thicker shell and higher QY (40% versus 36%) as compared to the CdSe/ZnS prepared under similar conditions. These low temperature methods for shell growth are readily amenable to scale-up and can provide a route for economical and less energy intensive production of quantum dots.

  17. Nanoscale connectivity in a TiO2/CdSe quantum dots/functionalized graphene oxide nanosheets/Au nanoparticles composite for enhanced photoelectrochemical solar cell performance.

    PubMed

    Narayanan, Remya; Deepa, Melepurath; Srivastava, Avanish Kumar

    2012-01-14

    Electron transfer dynamics in a photoactive coating made of CdSe quantum dots (QDs) and Au nanoparticles (NPs) tethered to a framework of ionic liquid functionalized graphene oxide (FGO) nanosheets and mesoporous titania (TiO(2)) was studied. High resolution transmission electron microscopy analyses on TiO(2)/CdSe/FGO/Au not only revealed the linker mediated binding of CdSe QDs with TiO(2) but also, surprisingly, revealed a nanoscale connectivity between CdSe QDs, Au NPs and TiO(2) with FGO nanosheets, achieved by a simple solution processing method. Time resolved fluorescence decay experiments coupled with the systematic quenching of CdSe emission by Au NPs or FGO nanosheets or by a combination of the latter two provide concrete evidences favoring the most likely pathway of ultrafast decay of excited CdSe in the composite to be a relay mechanism. A balance between energetics and kinetics of the system is realized by alignment of conduction band edges, whereby, CdSe QDs inject photogenerated electrons into the conduction band of TiO(2), from where, electrons are promptly transferred to FGO nanosheets and then through Au NPs to the current collector. Conductive-atomic force microscopy also provided a direct correlation between the local nanostructure and the enhanced ability of composite to conduct electrons. Point contact I-V measurements and average photoconductivity results demonstrated the current distribution as well as the population of conducting domains to be uniform across the TiO(2)/CdSe/FGO/Au composite, thus validating the higher photocurrent generation. A six-fold enhancement in photocurrent and a 100 mV increment in photovoltage combined with an incident photon to current conversion efficiency of 27%, achieved in the composite, compared to the inferior performance of the TiO(2)/CdSe/Au composite imply that FGO nanosheets and Au NPs work in tandem to promote charge separation and furnish less impeded pathways for electron transfer and transport. Such a

  18. Coexpression of CdSe and CdSe/CdS quantum dots in live cells using molecular hyperspectral imaging technology.

    PubMed

    Li, Qingli; Peng, Hui; Wang, Jing; Wang, Yiting; Guo, Fangmin

    2015-11-01

    A direct spatial and spectral observation of CdSe and CdSe/CdS quantum dots (QDs) as probes in live cells is performed by using a custom molecular hyperspectral imaging (MHI) system. Water-soluble CdSe and CdSe/CdS QDs are synthesized in aqueous solution under the assistance of high-intensity ultrasonic irradiation and incubated with colon cancer cells for bioimaging. Unlike the traditional fluorescence microscopy methods, MHI technology can identify QD probes according to their spectral signatures and generate coexpression and stain titer maps by a clustering method. The experimental results show that the MHI method has potential to unmix biomarkers by their spectral information, which opens up a pathway of optical multiplexing with many different QD probes.

  19. Non-volatile resistive memory device fabricated from CdSe quantum dot embedded in thermally grown In2O3 nanostructure by oblique angle deposition

    NASA Astrophysics Data System (ADS)

    Kannan, V.; Kim, Hyun-Seok; Park, Hyun-Chang

    2016-11-01

    In this paper we report In2O3/CdSe quantum dot based non-volatile resistive memory device with ON/OFF ratio ∼1000. Indium nanostructures were grown by oblique angle deposition technique in a thermal evaporator. Indium oxide nanostructures had size ranging from 20 nm to 100 nm as observed from TEM and AFM methods. The facile device fabricated with a layer of CdSe quantum dot on indium oxide film exhibited excellent endurance characteristics over 100,000 switching cycles. Retention tests showed good stability for over 4000 s. Memory operating mechanism is proposed based on charge trapping/de-trapping in quantum dots with indium oxide acting as barrier leading to Coulomb blockade. The mechanism is supported by negative differential resistance (NDR) observed exclusively in the ON state.

  20. Effect of CdSe nanoparticle addition on nanostructuring of PS-b-P4VP copolymer via solvent vapor exposure.

    PubMed

    Etxeberria, Haritz; Fernandez, Raquel; Zalakain, Iñaki; Mondragon, Iñaki; Eceiza, Arantxa; Kortaberria, Galder

    2014-02-15

    The surface morphology of poly(styrene-b-4 vinyl pyridine) (PS-b-P4VP) diblock copolymer thin films after solvent vapor annealing has been studied. Morphological features can be switched upon exposure to vapors of a solvent selective for one of the blocks. Self-assembled nanostructures such as hexagonal or striped morphologies were obtained varying vapor exposure time. In addition, the effect of the presence of CdSe nanoparticles located in the P4VP block on obtained nanostructures was analyzed. Atomic force microscopy (AFM) was used for morphological characterization of the block copolymer and the nanocomposites. AFM images showed that nanostructuring was different depending on the amount of CdSe nanoparticles, due to the decrease in P4VP chain mobility.

  1. Synthesis of CdSe -- TiO2 Nanocomposites and Their Applications to TiO2 Sensitized Solar Cells

    SciTech Connect

    Kim, J. Y.; Choi, S. B.; Noh, J. H.; HunYoon, S.; Lee, S.; Noh, T. H.; Frank, A. J.; Hong, K. S.

    2009-01-01

    CdSe-TiO{sub 2} nanocomposites were synthesized via aminolysis of Ti-oleate complexes in the presence of CdSe nanocrystals, and their application as sensitizers for TiO{sub 2} solar cells was investigated. The formation of CdSe-TiO{sub 2} nanocomposites was confirmed using transmission electron microscopy and Raman spectroscopy. The emission spectrum of CdSe-TiO{sub 2} nanocomposites revealed photoinduced charge separation at the CdSe-TiO{sub 2} interface of the composite. The photocurrent-voltage properties of CdSe-TiO{sub 2}-sensitized TiO{sub 2} particle films compared favorably with those of CdSe-sensitized TiO{sub 2} films. Evidence was also found indicating that the TiO{sub 2} component of the composite protects CdSe against degradation during film annealing.

  2. Study of optical nonlinearity of CdSe and CdSe@ZnO core-shell quantum dots in nanosecond regime

    NASA Astrophysics Data System (ADS)

    Deepika; Dhar, Rakesh; Mohan, Devendra

    2015-12-01

    Thioglycolic acid capped cadmium selenide (CdSe) and CdSe@ZnO core-shell quantum dots have been synthesized in aqueous phase. The sample was characterized by UV-vis spectrophotometer, TEM and Z-scan technique. The nonlinear optical parameters viz. nonlinear absorption coefficient (β), nonlinear refractive index (n2) and third-order nonlinear susceptibilities (χ3) of quantum dots have been estimated using second harmonic of Nd:YAG laser. The study predicts that CdSe@ZnO quantum dots exhibits strong nonlinearity as compared to core CdSe quantum dots. The nonlinearity in quantum dots is attributed to the presence of resonant excitation and free optical processes. The presence of RSA in these nanoparticles makes them a potential material for the development of optical limiter.

  3. Coexpression of CdSe and CdSe/CdS quantum dots in live cells using molecular hyperspectral imaging technology

    NASA Astrophysics Data System (ADS)

    Li, Qingli; Peng, Hui; Wang, Jing; Wang, Yiting; Guo, Fangmin

    2015-11-01

    A direct spatial and spectral observation of CdSe and CdSe/CdS quantum dots (QDs) as probes in live cells is performed by using a custom molecular hyperspectral imaging (MHI) system. Water-soluble CdSe and CdSe/CdS QDs are synthesized in aqueous solution under the assistance of high-intensity ultrasonic irradiation and incubated with colon cancer cells for bioimaging. Unlike the traditional fluorescence microscopy methods, MHI technology can identify QD probes according to their spectral signatures and generate coexpression and stain titer maps by a clustering method. The experimental results show that the MHI method has potential to unmix biomarkers by their spectral information, which opens up a pathway of optical multiplexing with many different QD probes.

  4. Photoelectron Spectroscopy of CdSe Nanocrystals in the Gas Phase: A Direct Measure of the Evanescent Electron Wave Function of Quantum Dots

    DTIC Science & Technology

    2013-01-01

    Spectroscopy of CdSe Nanocrystals in the Gas Phase: A Direct Measure of the Evanescent Electron Wave Function of Quantum Dots Wei Xiong...the fraction of evanescent electron wave function that extends outside of the quantum dot . This work shows that gas-phase photoelectron spectroscopy ...function. KEYWORDS: Quantum dots , ultrafast, electronic structure, aerodynamic lens, gas phase photoelectron spectroscopy , velocity map imaging Quantum

  5. The effect of semiconducting CdSe and ZnSe nanoparticles on the fluorescence of Sm3+ in lead borate glasses

    NASA Astrophysics Data System (ADS)

    Mallur, Saisudha; Fatokun, Stephen; Babu, P. K.

    2015-03-01

    We studied the fluorescence spectra of Sm3+ doped lead borate glasses containing zinc selenide (ZnSe) and cadmium selenide (CdSe) nanoparticles with the following compositions (x PbO: 96.5-x B2O3:0.5 Sm2O3:3ZnSe/CdSe, x =36.5 and 56.5 mol%). These glass samples are prepared using the melt-quenching technique. Each sample is annealed just below the glass transition temperature at 400°C for 3 hrs and 6 hrs. We have chosen PbO-B2O3 glasses to incorporate Sm3+ ions because they have large glass forming region, high refractive index, and good physical and thermal stability. Fluorescence spectra of these samples are obtained with the excitation wavelength at 477 nm. Four fluorescence transitions are observed at 563 nm, 598 nm, 646 nm and 708 nm. The transition at 646 nm is found to be a hypersensitive transition that strongly depends on the covalency of the Sm-O bond and the asymmetry of the crystal field at Sm site. The 646 nm/598 nm fluorescence intensity ratio has been studied for different annealing times and PbO concentration for both ZnSe and CdSe samples. The presence of CdSe nanoparticles is seen to produce the greatest influence on the fluorescence intensity ratio. This could be due to the size of the CdSe nanoparticles and covalency of the Sm-O bond.

  6. Anodic Electrogenerated Chemiluminescence of Ru(bpy)32+ with CdSe Quantum Dots as Coreactant and Its Application in Quantitative Detection of DNA

    PubMed Central

    Dong, Yong-Ping; Gao, Ting-Ting; Zhou, Ying; Jiang, Li-Ping; Zhu, Jun-Jie

    2015-01-01

    In the present paper, we report that CdSe quantum dots (QDs) can act as the coreactant of Ru(bpy)32+ electrogenerated chemiluminescence (ECL) in neutral condition. Strong anodic ECL signal was observed at ~1.10 V at CdSe QDs modified glassy carbon electrode (CdSe/GCE), which might be mainly attributed to the apparent electrocatalytic effect of QDs on the oxidation of Ru(bpy)32+. Ru(bpy)32+ can be intercalated into the loop of hairpin DNA through the electrostatic interaction to fabricate a probe. When the probe was bound to the CdSe QDs modified on the GCE, the intense ECL signal was obtained. The more Ru(bpy)32+ can be intercalated when DNA loop has larger diameter and the stronger ECL signal can be observed. The loop of hairpin DNA can be opened in the presence of target DNA to release the immobilized Ru(bpy)32+, which can result in the decrease of ECL signal. The decreased ECL signal varied linearly with the concentration of target DNA, which showed the ECL biosensor can be used in the sensitive detection of DNA. The proposed ECL biosensor showed an excellent performance with high specificity, wide linear range and low detection limit. PMID:26472243

  7. Photogenerated excitons in plain core CdSe nanocrystals with unity radiative decay in single channel: the effects of surface and ligands.

    PubMed

    Gao, Yuan; Peng, Xiaogang

    2015-04-01

    A systematic and reproducible method was developed to study the decay dynamics of an exciton, a photogenerated electron-hole pair, in semiconductor nanocrystals in solution. Results revealed that the excitons in plain core CdSe nanocrystals in either zinc-blende or wurtzite or mixed lattice structures could be reproducibly prepared to decay radiatively in unity quantum yield and in single channel. The single-channel lifetime was found to increase monotonically by increasing size of the CdSe nanocrystals, with zinc-blende ones increasing in a relatively slow pace. Surface inorganic stoichiometry was found to be a sensitive parameter to affect the exciton decay dynamics for all crystal structures with different sizes. Excess Se (Cd) sites on the surface were found to induce short (long) lifetime channels for the excitons. Both types of traps reduced the quantum yield of the radiative decay of the excitons, and the hole traps associated with Se sites were nearly not emissive. With optimal surface inorganic stoichiometry, primary amines were identified as "ideal" organic ligands for CdSe core nanocrystals to achieve unity radiative decay of excitons in single channel in comparison to other types of neutral ligands commonly applied in the field.

  8. Secondary coordination sphere accelerates hole transfer for enhanced hydrogen photogeneration from [FeFe]-hydrogenase mimic and CdSe QDs in water.

    PubMed

    Wen, Min; Li, Xu-Bing; Jian, Jing-Xin; Wang, Xu-Zhe; Wu, Hao-Lin; Chen, Bin; Tung, Chen-Ho; Wu, Li-Zhu

    2016-07-15

    Achieving highly efficient hydrogen (H2) evolution via artificial photosynthesis is a great ambition pursued by scientists in recent decades because H2 has high specific enthalpy of combustion and benign combustion product. [FeFe]-Hydrogenase ([FeFe]-H2ase) mimics have been demonstrated to be promising catalysts for H2 photoproduction. However, the efficient photocatalytic H2 generation system, consisting of PAA-g-Fe2S2, CdSe QDs and H2A, suffered from low stability, probably due to the hole accumulation induced photooxidation of CdSe QDs and the subsequent crash of [FeFe]-H2ase mimics. In this work, we take advantage of supramolecular interaction for the first time to construct the secondary coordination sphere of electron donors (HA(-)) to CdSe QDs. The generated secondary coordination sphere helps realize much faster hole removal with a ~30-fold increase, thus leading to higher stability and activity for H2 evolution. The unique photocatalytic H2 evolution system features a great increase of turnover number to 83600, which is the highest one obtained so far for photocatalytic H2 production by using [FeFe]-H2ase mimics as catalysts.

  9. Anodic Electrogenerated Chemiluminescence of Ru(bpy)32+ with CdSe Quantum Dots as Coreactant and Its Application in Quantitative Detection of DNA

    NASA Astrophysics Data System (ADS)

    Dong, Yong-Ping; Gao, Ting-Ting; Zhou, Ying; Jiang, Li-Ping; Zhu, Jun-Jie

    2015-10-01

    In the present paper, we report that CdSe quantum dots (QDs) can act as the coreactant of Ru(bpy)32+ electrogenerated chemiluminescence (ECL) in neutral condition. Strong anodic ECL signal was observed at ~1.10 V at CdSe QDs modified glassy carbon electrode (CdSe/GCE), which might be mainly attributed to the apparent electrocatalytic effect of QDs on the oxidation of Ru(bpy)32+. Ru(bpy)32+ can be intercalated into the loop of hairpin DNA through the electrostatic interaction to fabricate a probe. When the probe was bound to the CdSe QDs modified on the GCE, the intense ECL signal was obtained. The more Ru(bpy)32+ can be intercalated when DNA loop has larger diameter and the stronger ECL signal can be observed. The loop of hairpin DNA can be opened in the presence of target DNA to release the immobilized Ru(bpy)32+, which can result in the decrease of ECL signal. The decreased ECL signal varied linearly with the concentration of target DNA, which showed the ECL biosensor can be used in the sensitive detection of DNA. The proposed ECL biosensor showed an excellent performance with high specificity, wide linear range and low detection limit.

  10. Anodic Electrogenerated Chemiluminescence of Ru(bpy)3(2+) with CdSe Quantum Dots as Coreactant and Its Application in Quantitative Detection of DNA.

    PubMed

    Dong, Yong-Ping; Gao, Ting-Ting; Zhou, Ying; Jiang, Li-Ping; Zhu, Jun-Jie

    2015-10-16

    In the present paper, we report that CdSe quantum dots (QDs) can act as the coreactant of Ru(bpy)3(2+) electrogenerated chemiluminescence (ECL) in neutral condition. Strong anodic ECL signal was observed at ~1.10 V at CdSe QDs modified glassy carbon electrode (CdSe/GCE), which might be mainly attributed to the apparent electrocatalytic effect of QDs on the oxidation of Ru(bpy)3(2+). Ru(bpy)3(2+) can be intercalated into the loop of hairpin DNA through the electrostatic interaction to fabricate a probe. When the probe was bound to the CdSe QDs modified on the GCE, the intense ECL signal was obtained. The more Ru(bpy)3(2+) can be intercalated when DNA loop has larger diameter and the stronger ECL signal can be observed. The loop of hairpin DNA can be opened in the presence of target DNA to release the immobilized Ru(bpy)3(2+), which can result in the decrease of ECL signal. The decreased ECL signal varied linearly with the concentration of target DNA, which showed the ECL biosensor can be used in the sensitive detection of DNA. The proposed ECL biosensor showed an excellent performance with high specificity, wide linear range and low detection limit.

  11. Current matching using CdSe quantum dots to enhance the power conversion efficiency of InGaP/GaAs/Ge tandem solar cells.

    PubMed

    Lee, Ya-Ju; Yao, Yung-Chi; Tsai, Meng-Tsan; Liu, An-Fan; Yang, Min-De; Lai, Jiun-Tsuen

    2013-11-04

    A III-V multi-junction tandem solar cell is the most efficient photovoltaic structure that offers an extremely high power conversion efficiency. Current mismatching between each subcell of the device, however, is a significant challenge that causes the experimental value of the power conversion efficiency to deviate from the theoretical value. In this work, we explore a promising strategy using CdSe quantum dots (QDs) to enhance the photocurrent of the limited subcell to match with those of the other subcells and to enhance the power conversion efficiency of InGaP/GaAs/Ge tandem solar cells. The underlying mechanism of the enhancement can be attributed to the QD's unique capacity for photon conversion that tailors the incident spectrum of solar light; the enhanced efficiency of the device is therefore strongly dependent on the QD's dimensions. As a result, by appropriately selecting and spreading 7 mg/mL of CdSe QDs with diameters of 4.2 nm upon the InGaP/GaAs/Ge solar cell, the power conversion efficiency shows an enhancement of 10.39% compared to the cell's counterpart without integrating CdSe QDs.

  12. Chemical bath deposition of photosensitive CdS and CdSe thin films and their conversion to n-type for solar cell applications

    SciTech Connect

    Nair, M.T.S.; Nair, P.K.; Zingaro, R.A.; Meyers, E.A.

    1995-12-31

    Methods for preparing good quality CdS and CdSe thin films of 0.1--0.7 {micro}m thickness from solutions at 24--50 C containing citratocadmium(II) ions and thiourea (for CdS) or N,N-dimethyl selenourea (for CdSe) are presented. The as prepared CdS thin films are photosensitive showing photo- to dark-conductivity ratio (S) of > 10{sup 6} under AM-2 illumination. Annealing of these films at 400--450 C for a few minutes converts them to n-type through partial conversion of the films to non stoichiometric CdO. In the case of CdSe, such annealing improves the photosensitivity of the films from S = 10 (as prepared) to > 10{sup 7} (after annealing) under AM-2 illumination. Either film can be converted to n-type with dark conductivities of > 1 {Omega}{sup {minus}1} cm{sup {minus}1} and S = 1 to 10 under AM-2 illumination using a post deposition treatment in dilute (0.01--0.05 M) HgCl{sub 2} solution followed by heating at 200 C.

  13. Shape control of cadmium hydroxides (Cd(OH)2) sensitive to pH quenching depth and massive production of CdSe nanocrystals by their chemical transformation.

    PubMed

    Ko, Sungwook; Moon, Geon Dae; Lee, Jung-Pil; Park, Soojin; Jeong, Unyong

    2011-08-05

    This study demonstrates that the structure of cadmium hydroxides (Cd(OH)(2)) precipitated from a basic cadmium nitrate solution can be finely controlled by adjusting the pH of the precursor solution. The synthesis process involves only pouring the saturated solution into pure water to quench the pH and the total process is finished within 30 s. At a shallow pH quenching, the unstable nanoparticles turned into microparticles via a ripening process. Cd(OH)(2) was precipitated in the form of one-dimensional nanowires and then two-dimensional plates as the pH quenching was increased. At a large pH quenching, porous aggregates of Cd(OH)(2) were obtained due to the too fast precipitation. The ultrafine Cd(OH)(2) nanowires were readily transformed into CdSe chain-like nanocrystals. The transformation was quick and gave 100% yield, facilitating massive production of CdSe nanocrystals in an aqueous condition. The Cd(OH)(2) nanowires were directly grown on Si nanowires and transformed into CdSe chain-like nanocrystals, decorating the surface of each Si nanowire.

  14. Shape control of cadmium hydroxides (Cd(OH)2) sensitive to pH quenching depth and massive production of CdSe nanocrystals by their chemical transformation

    NASA Astrophysics Data System (ADS)

    Ko, Sungwook; Moon, Geon Dae; Lee, Jung-Pil; Park, Soojin; Jeong, Unyong

    2011-08-01

    This study demonstrates that the structure of cadmium hydroxides (Cd(OH)2) precipitated from a basic cadmium nitrate solution can be finely controlled by adjusting the pH of the precursor solution. The synthesis process involves only pouring the saturated solution into pure water to quench the pH and the total process is finished within 30 s. At a shallow pH quenching, the unstable nanoparticles turned into microparticles via a ripening process. Cd(OH)2 was precipitated in the form of one-dimensional nanowires and then two-dimensional plates as the pH quenching was increased. At a large pH quenching, porous aggregates of Cd(OH)2 were obtained due to the too fast precipitation. The ultrafine Cd(OH)2 nanowires were readily transformed into CdSe chain-like nanocrystals. The transformation was quick and gave 100% yield, facilitating massive production of CdSe nanocrystals in an aqueous condition. The Cd(OH)2 nanowires were directly grown on Si nanowires and transformed into CdSe chain-like nanocrystals, decorating the surface of each Si nanowire.

  15. Electronic band structure of zinc blende CdSe and rock salt PbSe semiconductors with silicene-type honeycomb geometry

    NASA Astrophysics Data System (ADS)

    Delerue, Christophe; Vanmaekelbergh, D.

    2015-09-01

    We report on the electronic band structure of 2D CdSe and PbSe semiconductors that have a silicene-type honeycomb geometry. Atomistic tight-binding calculations are performed on several model systems that bear a strong resemblance to the silicene-type honeycomb structures that were recently obtained by nanocrystal self-assembly. The calculated band structures are compared both to those of 2D quantum wells and graphene-type honeycomb structures. It is found that in silicene type CdSe honeycomb structures, the lowest electron conduction bands (derived from S-type nanocrystal wave functions) form a Dirac-type dispersion, very similar as in graphene. The P-type bands are usually more complex. However, when the hybridization between S- and P-type bands increases, a second Dirac cone and a genuine non-trivial flat band is observed, similar as in the case of graphene-type honeycomb structures of CdSe. There is a strong non-trivial gap between the first and second valence band, hosting the quantum spin Hall effect. Silicene-type PbSe structures show Dirac features in their bands, which however can be clouded due to the multi-valley character of PbSe.

  16. Understanding the electronic structure of CdSe quantum dot-fullerene (C{sub 60}) hybrid nanostructure for photovoltaic applications

    SciTech Connect

    Sarkar, Sunandan; Rajbanshi, Biplab; Sarkar, Pranab

    2014-09-21

    By using the density-functional tight binding method, we studied the electronic structure of CdSe quantum dot(QD)-buckminsterfullerene (C{sub 60}) hybrid systems as a function of both the size of the QD and concentration of the fullerene molecule. Our calculation reveals that the lowest unoccupied molecular orbital energy level of the hybrid CdSeQD-C{sub 60} systems lies on the fullerene moiety, whereas the highest occupied molecular orbital (HOMO) energy level lies either on the QD or the fullerene depending on size of the CdSe QD. We explored the possibility of engineering the energy level alignment by varying the size of the CdSe QD. With increase in size of the QD, the HOMO level is shifted upward and crosses the HOMO level of the C{sub 60}-thiol molecule resulting transition from the type-I to type-II band energy alignment. The density of states and charge density plot support these types of band gap engineering of the CdSe-C{sub 60} hybrid systems. This type II band alignment indicates the possibility of application of this nanohybrid for photovoltaic purpose.

  17. Secondary coordination sphere accelerates hole transfer for enhanced hydrogen photogeneration from [FeFe]-hydrogenase mimic and CdSe QDs in water

    PubMed Central

    Wen, Min; Li, Xu-Bing; Jian, Jing-Xin; Wang, Xu-Zhe; Wu, Hao-Lin; Chen, Bin; Tung, Chen-Ho; Wu, Li-Zhu

    2016-01-01

    Achieving highly efficient hydrogen (H2) evolution via artificial photosynthesis is a great ambition pursued by scientists in recent decades because H2 has high specific enthalpy of combustion and benign combustion product. [FeFe]-Hydrogenase ([FeFe]-H2ase) mimics have been demonstrated to be promising catalysts for H2 photoproduction. However, the efficient photocatalytic H2 generation system, consisting of PAA-g-Fe2S2, CdSe QDs and H2A, suffered from low stability, probably due to the hole accumulation induced photooxidation of CdSe QDs and the subsequent crash of [FeFe]-H2ase mimics. In this work, we take advantage of supramolecular interaction for the first time to construct the secondary coordination sphere of electron donors (HA−) to CdSe QDs. The generated secondary coordination sphere helps realize much faster hole removal with a ~30-fold increase, thus leading to higher stability and activity for H2 evolution. The unique photocatalytic H2 evolution system features a great increase of turnover number to 83600, which is the highest one obtained so far for photocatalytic H2 production by using [FeFe]-H2ase mimics as catalysts. PMID:27417065

  18. Secondary coordination sphere accelerates hole transfer for enhanced hydrogen photogeneration from [FeFe]-hydrogenase mimic and CdSe QDs in water

    NASA Astrophysics Data System (ADS)

    Wen, Min; Li, Xu-Bing; Jian, Jing-Xin; Wang, Xu-Zhe; Wu, Hao-Lin; Chen, Bin; Tung, Chen-Ho; Wu, Li-Zhu

    2016-07-01

    Achieving highly efficient hydrogen (H2) evolution via artificial photosynthesis is a great ambition pursued by scientists in recent decades because H2 has high specific enthalpy of combustion and benign combustion product. [FeFe]-Hydrogenase ([FeFe]-H2ase) mimics have been demonstrated to be promising catalysts for H2 photoproduction. However, the efficient photocatalytic H2 generation system, consisting of PAA-g-Fe2S2, CdSe QDs and H2A, suffered from low stability, probably due to the hole accumulation induced photooxidation of CdSe QDs and the subsequent crash of [FeFe]-H2ase mimics. In this work, we take advantage of supramolecular interaction for the first time to construct the secondary coordination sphere of electron donors (HA‑) to CdSe QDs. The generated secondary coordination sphere helps realize much faster hole removal with a ~30-fold increase, thus leading to higher stability and activity for H2 evolution. The unique photocatalytic H2 evolution system features a great increase of turnover number to 83600, which is the highest one obtained so far for photocatalytic H2 production by using [FeFe]-H2ase mimics as catalysts.

  19. Photocatalytic H2 production using a hybrid assembly of an [FeFe]-hydrogenase model and CdSe quantum dot linked through a thiolato-functionalized cyclodextrin.

    PubMed

    Cheng, Minglun; Wang, Mei; Zhang, Shuai; Liu, Fengyuan; Yang, Yong; Wan, Boshun; Sun, Licheng

    2017-03-07

    It is a great challenge to develop iron-based highly-efficient and durable catalytic systems for the hydrogen evolution reaction (HER) by understanding and learning from [FeFe]-hydrogenases. Here we report photocatalytic H2 production by a hybrid assembly of a sulfonate-functionalized [FeFe]-hydrogenase mimic (1) and CdSe quantum dot (QD), which is denoted as 1/β-CD-6-S-CdSe (β-CD-6-SH = 6-mercapto-β-cyclodextrin). In this assembly, thiolato-functionalized β-CD acts not only as a stabilizing reagent of CdSe QDs but also as a host compound for the diiron catalyst, so as to confine CdSe QDs to the space near the site of diiron catalyst. In addition, another two reference systems comprising MAA-CdSe QDs (HMAA = mercaptoacetic acid) and 1 in the presence and absence of β-CD, denoted as 1/β-CD/MAA-CdSe and 1/MAA-CdSe, were studied for photocatalytic H2 evolution. The influences of β-CD and the stabilizing reagent β-CD-6-S(-) on the stability of diiron catalyst, the fluorescence lifetime of CdSe QDs, the apparent electron transfer rate, and the photocatalytic H2-evolving efficiency were explored by comparative studies of the three hybrid systems. The 1/β-CD-6-S-CdSe system displayed a faster apparent rate for electron transfer from CdSe QDs to the diiron catalyst compared to that observed for MAA-CdSe-based systems. The total TON for visible-light driven H2 evolution by the 1/β-CD-6-S-CdSe QDs in water at pH 4.5 is about 2370, corresponding to a TOF of 150 h(-1) in the initial 10 h of illumination, which is 2.7- and 6.6-fold more than the amount of H2 produced from the reference systems 1/β-CD/MAA-CdSe and 1/MAA-CdSe. Additionally, 1/β-CD-6-S-CdSe gave 2.4-5.1 fold enhancement in the apparent quantum yield and significantly improved the stability of the system for photocatalytic H2 evolution.

  20. Exploring size and state dynamics in CdSe quantum dots using two-dimensional electronic spectroscopy

    SciTech Connect

    Caram, Justin R.; Zheng, Haibin; Rolczynski, Brian S.; Griffin, Graham B.; Engel, Gregory S.; Dahlberg, Peter D.; Dolzhnikov, Dmitriy S.; Talapin, Dmitri V.

    2014-02-28

    Development of optoelectronic technologies based on quantum dots depends on measuring, optimizing, and ultimately predicting charge carrier dynamics in the nanocrystal. In such systems, size inhomogeneity and the photoexcited population distribution among various excitonic states have distinct effects on electron and hole relaxation, which are difficult to distinguish spectroscopically. Two-dimensional electronic spectroscopy can help to untangle these effects by resolving excitation energy and subsequent nonlinear response in a single experiment. Using a filament-generated continuum as a pump and probe source, we collect two-dimensional spectra with sufficient spectral bandwidth to follow dynamics upon excitation of the lowest three optical transitions in a polydisperse ensemble of colloidal CdSe quantum dots. We first compare to prior transient absorption studies to confirm excitation-state-dependent dynamics such as increased surface-trapping upon excitation of hot electrons. Second, we demonstrate fast band-edge electron-hole pair solvation by ligand and phonon modes, as the ensemble relaxes to the photoluminescent state on a sub-picosecond time-scale. Third, we find that static disorder due to size polydispersity dominates the nonlinear response upon excitation into the hot electron manifold; this broadening mechanism stands in contrast to that of the band-edge exciton. Finally, we demonstrate excitation-energy dependent hot-carrier relaxation rates, and we describe how two-dimensional electronic spectroscopy can complement other transient nonlinear techniques.

  1. Exploring size and state dynamics in CdSe quantum dots using two-dimensional electronic spectroscopy

    PubMed Central

    Caram, Justin R.; Zheng, Haibin; Dahlberg, Peter D.; Rolczynski, Brian S.; Griffin, Graham B.; Dolzhnikov, Dmitriy S.; Talapin, Dmitri V.; Engel, Gregory S.

    2014-01-01

    Development of optoelectronic technologies based on quantum dots depends on measuring, optimizing, and ultimately predicting charge carrier dynamics in the nanocrystal. In such systems, size inhomogeneity and the photoexcited population distribution among various excitonic states have distinct effects on electron and hole relaxation, which are difficult to distinguish spectroscopically. Two-dimensional electronic spectroscopy can help to untangle these effects by resolving excitation energy and subsequent nonlinear response in a single experiment. Using a filament-generated continuum as a pump and probe source, we collect two-dimensional spectra with sufficient spectral bandwidth to follow dynamics upon excitation of the lowest three optical transitions in a polydisperse ensemble of colloidal CdSe quantum dots. We first compare to prior transient absorption studies to confirm excitation-state-dependent dynamics such as increased surface-trapping upon excitation of hot electrons. Second, we demonstrate fast band-edge electron-hole pair solvation by ligand and phonon modes, as the ensemble relaxes to the photoluminescent state on a sub-picosecond time-scale. Third, we find that static disorder due to size polydispersity dominates the nonlinear response upon excitation into the hot electron manifold; this broadening mechanism stands in contrast to that of the band-edge exciton. Finally, we demonstrate excitation-energy dependent hot-carrier relaxation rates, and we describe how two-dimensional electronic spectroscopy can complement other transient nonlinear techniques. PMID:24588185

  2. Quantitative assessment of Tn antigen in breast tissue micro-arrays using CdSe aqueous quantum dots.

    PubMed

    Au, Giang H T; Mejias, Linette; Swami, Vanlila K; Brooks, Ari D; Shih, Wan Y; Shih, Wei-Heng

    2014-03-01

    In this study, we examined the use of CdSe aqueous quantum dots (AQDs) each conjugated to three streptavidin as a fluorescent label to image Tn antigen expression in various breast tissues via a sandwich staining procedure where the primary monoclonal anti-Tn antibody was bound to the Tn antigen on the tissue, a biotin-labeled secondary antibody was bound to the primary anti-Tn antibody, and finally the streptavidin-conjugated AQDs were bound to the biotin on the secondary antibody. We evaluated the AQD staining of Tn antigen on tissue microarrays consisting of 395 cores from 115 cases including three tumor cores and one normal-tissue core from each breast cancer case and three tumor cores from each benign case. The results indicated AQD-Tn staining was positive in more than 90% of the cells in the cancer cores but not the cells in the normal-tissue cores and the benign tumor cores. As a result, AQD-Tn staining exhibited 95% sensitivity and 90% specificity in differentiating breast cancer against normal breast tissues and benign breast conditions. These results were better than the 90% sensitivity and 80% specificity exhibited by the corresponding horse radish peroxidase (HRP) staining using the same antibodies on the same tissues and those of previous studies that used different fluorescent labels to image Tn antigen. In addition to sensitivity and specificity, the current AQD-Tn staining with a definitive threshold was quantitative.

  3. Cytotoxic effects of CdSe quantum dots on maturation of mouse oocytes, fertilization, and fetal development.

    PubMed

    Hsieh, Ming-Shu; Shiao, Nion-Heng; Chan, Wen-Hsiung

    2009-05-14

    Quantum dots (QDs) are useful novel luminescent markers, but their embryonic toxicity is yet to be fully established, particularly in oocyte maturation and sperm fertilization. Earlier experiments by our group show that CdSe-core QDs have cytotoxic effects on mouse blastocysts and are associated with defects in subsequent development. Here, we further investigate the influence of CdSe-core QDs on oocyte maturation, fertilization, and subsequent pre- and postimplantation development. CdSe-core QDs induced a significant reduction in the rates of oocyte maturation, fertilization, and in vitro embryo development, but not ZnS-coated CdSe QDs. Treatment of oocytes with 500 nM CdSe-core QDs during in vitro maturation (IVM) led to increased resorption of postimplantation embryos and decreased placental and fetal weights. To our knowledge, this is the first study to report the negative impact of CdSe-core QDs on mouse oocyte development. Moreover, surface modification of CdSe-core QDs with ZnS effectively prevented this cytotoxicity.

  4. CdSe Nanowire-Based Flexible Devices: Schottky Diodes, Metal-Semiconductor Field-Effect Transistors, and Inverters.

    PubMed

    Jin, Weifeng; Zhang, Kun; Gao, Zhiwei; Li, Yanping; Yao, Li; Wang, Yilun; Dai, Lun

    2015-06-24

    Novel CdSe nanowire (NW)-based flexible devices, including Schottky diodes, metal-semiconductor field-effect transistors (MESFETs), and inverters, have been fabricated and investigated. The turn-on voltage of a typical Schottky diode is about 0.7 V, and the rectification ratio is larger than 1 × 10(7). The threshold voltage, on/off current ratio, subthreshold swing, and peak transconductance of a typical MESFET are about -0.3 V, 4 × 10(5), 78 mV/dec, and 2.7 μS, respectively. The inverter, constructed with two MESFETs, exhibits clear inverting behavior with the gain to be about 28, 34, and 38, at the supply voltages (V(DD)) of 3, 5, and 7 V, respectively. The inverter also shows good dynamic behavior. The rising and falling times of the output signals are about 0.18 and 0.09 ms, respectively, under 1000 Hz square wave signals input. The performances of the flexible devices are stable and reliable under different bending conditions. Our work demonstrates these flexible NW-based Schottky diodes, MESFETs, and inverters are promising candidate components for future portable transparent nanoelectronic devices.

  5. A new route to produce efficient surface-enhanced Raman spectroscopy substrates: gold-decorated CdSe nanowires

    NASA Astrophysics Data System (ADS)

    Das, Gobind; Chakraborty, Ritun; Gopalakrishnan, Anisha; Baranov, Dmitry; Di Fabrizio, Enzo; Krahne, Roman

    2013-05-01

    Surface-enhanced Raman spectroscopy is a popular tool for the detection of extremely small quantities of target molecules. Au nanoparticles have been very successful in this respect due to local enhancement of the light intensity caused by their plasmon resonance. Furthermore, Au nanoparticles are biocompatible, and target substances can be easily attached to their surface. Here, we demonstrate that Au-decorated CdSe nanowires when employed as SERS substrates lead to an enhancement as large as 105 with respect to the flat Au surfaces. In the case of hybrid metal-CdSe nanowires, the Au nucleates preferably on lattice defects at the lateral facets of the nanowires, which leads to a homogeneous distribution of Au nanoparticles on the nanowire, and to an efficient quenching of the nanowire luminescence. Moreover, the size of the Au nanoparticles can be well controlled via the AuCl3 concentration in the fabrication process. We demonstrate the effectiveness of our SERS substrates with two target substances, namely, cresyl-violet and rhodamine-6G. Au-decorated nanowires can be easily fabricated in large quantities at low cost by wet-chemical synthesis. Furthermore, their deposition onto various substrates, as well as the functionalization of these wires with the target substances, is as straightforward as with the traditional markers.

  6. a Design of Rainbow Solar Cell:. AN Orderly Gradient of Cds-Cdse Sensitized Zno Solar Cell

    NASA Astrophysics Data System (ADS)

    Hu, Xiaoyan; Tang, Yiwen

    2012-08-01

    A rainbow solar cell configuration based on CdS-CdSe quantum dots (QDs) orderly assembled onto ZnO nanowire (NW) was designed. The rainbow configuration involves alternate cycles of ZnO NW growth and orderly deposition of CdS and CdSe on the different ZnO layer. As a demonstration, in the assembly of ZnO NW bilayer, the presence of CdS shell on the first ZnO NW layer can effectively avoid the fusion of the first ZnO NW layer at the root. Thus the internal surface area of the bilayer assembly is largely enhanced. When the bilayer assemblies were used to fabricate quantum-dotsensitized solar cells (QD-SSCs), a power conversion efficiency (η) of 0.197% was obtained which was higher than that of conventional ZnO/CdS based QDSSCs. Such a rainbow QD-SSC allows one to couple high electron injection rate of QDs and wide absorption range effectively.

  7. Effect of CdSe Nanoparticles on the Growth of Te Nanowires: Greater Length and Tortuosity and Nonmonotonic Concentration Effect

    SciTech Connect

    Lilly, G. Daniel; Chen, Yanbin; Pan, Xiaoqing; Kotov, Nicholas A.

    2010-01-22

    Improved control over nanowire (NW) geometry and composition offers multiple benefits for design material and devices, including uses in complex nanoelectronic circuits, facilitating their organization on substrates, providing more efficient charge transport over large distances, and greater mechanical strength. Te NWs have many interesting thermoelectric, piezoelectric, conducting, and photoconducting properties and are highly reactive with numerous chemicals, allowing Te NWs to be used as templates for NWs of other compositions. Te NWs are made in this work from CdTe nanoparticles (NPs) by slow oxidation. Te NWs with average lengths of 6.63 ± 1.07 μm and aspect ratios of 50 were initially formed. Unexpectedly, the presence of CdSe NPs results in a drastic increase in the length, aspect ratio, and tortuosity of the Te NWs. We believe that Se2- is being incorporated into the Te seeds as elemental Se, fouling them and reducing the number of viable Te seeds, which allows longer Te NWs to form. Excessive amount of CdTe NPs stops the growth of Te NWs completely making the concentration dependence strongly nonmonotonic. The longest tortuous NWs grown in this fashion have lengths of 15.56 ± 4.16 μm and aspect ratios 103. This work reveals a novel process taking place between growing NW and NPs. These finding indicate advantages of using NPs for reaction control for preparation of NW with high practical relevance.

  8. Origins of low energy-transfer efficiency between patterned GaN quantum well and CdSe quantum dots

    SciTech Connect

    Xu, Xingsheng

    2015-03-02

    For hybrid light emitting devices (LEDs) consisting of GaN quantum wells and colloidal quantum dots, it is necessary to explore the physical mechanisms causing decreases in the quantum efficiencies and the energy transfer efficiency between a GaN quantum well and CdSe quantum dots. This study investigated the electro-luminescence for a hybrid LED consisting of colloidal quantum dots and a GaN quantum well patterned with photonic crystals. It was found that both the quantum efficiency of colloidal quantum dots on a GaN quantum well and the energy transfer efficiency between the patterned GaN quantum well and the colloidal quantum dots decreased with increases in the driving voltage or the driving time. Under high driving voltages, the decreases in the quantum efficiency of the colloidal quantum dots and the energy transfer efficiency can be attributed to Auger recombination, while those decreases under long driving time are due to photo-bleaching and Auger recombination.

  9. Electron relaxation in the CdSe quantum dot - ZnO composite: prospects for photovoltaic applications

    PubMed Central

    Žídek, Karel; Abdellah, Mohamed; Zheng, Kaibo; Pullerits, Tõnu

    2014-01-01

    Quantum dot (QD)-metal oxide composite forms a “heart” of the QD-sensitized solar cells. It maintains light absorption and electron-hole separation in the system and has been therefore extensively studied. The interest is largely driven by a vision of harvesting the hot carrier energy before it is lost via relaxation. Despite of importance of the process, very little is known about the carrier relaxation in the QD-metal oxide composites. In order to fill this gap of knowledge we carry out a systematic study of initial electron dynamics in different CdSe QD systems. Our data reveal that QD attachment to ZnO induces a speeding-up of transient absorption onset. Detailed analysis of the onset proves that the changes are caused by an additional relaxation channel dependent on the identity of the QD-ZnO linker molecule. The faster relaxation represents an important factor for hot carrier energy harvesting, whose efficiency can be influenced by almost 50%. PMID:25430684

  10. Size and Temperature Dependence of Electron Transfer between CdSe Quantum Dots and a TiO 2 Nanobelt

    DOE PAGES

    Tafen, De Nyago; Prezhdo, Oleg V.

    2015-02-24

    Understanding charge transfer reactions between quantum dots (QD) and metal oxides is fundamental for improving photocatalytic, photovoltaic and electronic devices. The complexity of these processes makes it difficult to find an optimum QD size with rapid charge injection and low recombination. We combine time-domain density functional theory with nonadiabatic molecular dynamics to investigate the size and temperature dependence of the experimentally studied electron transfer and charge recombination at CdSe QD-TiO2 nanobelt (NB) interfaces. The electron injection rate shows strong dependence on the QD size, increasing for small QDs. The rate exhibits Arrhenius temperature dependence, with the activation energy of themore » order of millielectronvolts. The charge recombination process occurs due to coupling of the electronic subsystem to vibrational modes of the TiO2 NB. Inelastic electron-phonon scattering happens on a picosecond time scale, with strong dependence on the QD size. Our simulations demonstrate that the electron-hole recombination rate decreases significantly as the QD size increases, in excellent agreement with experiments. The temperature dependence of the charge recombination rates can be successfully modeled within the framework of the Marcus theory through optimization of the electronic coupling and the reorganization energy. Our simulations indicate that by varying the QD size, one can modulate the photoinduced charge separation and charge recombination, fundamental aspects of the design principles for high efficiency devices.« less

  11. Electronic structures in a CdSe spherical quantum dot in a magnetic field: Diagonalization method and variational method

    NASA Astrophysics Data System (ADS)

    Wu, Shudong; Wan, Li

    2012-03-01

    The electronic structures of a CdSe spherical quantum dot in a magnetic field are obtained by using an exact diagonalization method and a variational method within the effective-mass approximation. The dependences of the energies and wave functions of electron states, exciton binding energy, exciton transition energy, and exciton diamagnetic shift on the applied magnetic field are investigated theoretically in detail. It is observed that the degeneracy of magnetic quantum number m is removed due to the Zeeman effect when the magnetic field is present. For the states with m ≥ 0, the electron energies increase as the magnetic field increases. However, for the states with m < 0, the electron energies decrease to a minimum, and then increase with increasing the magnetic field. The energies and wave functions of electron states obtained from the variational method based on the variational functions we proposed are in excellent agreement with the results obtained from the exact diagonalization method we presented. A comparison between the results obtained from the variational functions proposed by us and Xiao is also verified.

  12. Correlation between CdSe QD Synthesis, Post-Synthetic Treatment, and BHJ Hybrid Solar Cell Performance

    PubMed Central

    Eck, Michael; Krueger, Michael

    2016-01-01

    In this publication we show that the procedure to synthesize nanocrystals and the post-synthetic nanocrystal ligand sphere treatment have a great influence not only on the immediate performance of hybrid bulk heterojunction solar cells, but also on their thermal, long-term, and air stability. We herein demonstrate this for the particular case of spherical CdSe nanocrystals, post-synthetically treated with a hexanoic acid based treatment. We observe an influence from the duration of this post-synthetic treatment on the nanocrystal ligand sphere size, and also on the solar cell performance. By tuning the post-synthetic treatment to a certain degree, optimal device performance can be achieved. Moreover, we show how to effectively adapt the post-synthetic nanocrystal treatment protocol to different nanocrystal synthesis batches, hence increasing the reproducibility of hybrid nanocrystal:polymer bulk-heterojunction solar cells, which usually suffers due to the fluctuations in nanocrystal quality of different synthesis batches and synthesis procedures. PMID:28335243

  13. Direct electro-optical pumping for hybrid CdSe nanocrystal/III-nitride based nano-light-emitting diodes

    NASA Astrophysics Data System (ADS)

    Mikulics, M.; Arango, Y. C.; Winden, A.; Adam, R.; Hardtdegen, A.; Grützmacher, D.; Plinski, E.; Gregušová, D.; Novák, J.; Kordoš, P.; Moonshiram, A.; Marso, M.; Sofer, Z.; Lüth, H.; Hardtdegen, H.

    2016-02-01

    We propose a device concept for a hybrid nanocrystal/III-nitride based nano-LED. Our approach is based on the direct electro-optical pumping of nanocrystals (secondary excitation) by electrically driven InGaN/GaN nano-LEDs as the primary excitation source. To this end, a universal hybrid optoelectronic platform was developed for a large range of optically active nano- and mesoscopic structures. The advantage of the approach is that the emission of the nanocrystals can be electrically induced without the need of contacting them. The proof of principal was demonstrated for the electro-optical pumping of CdSe nanocrystals. The nano-LEDs with a diameter of 100 nm exhibit a very low current of ˜8 nA at 5 V bias which is several orders of magnitude smaller than for those conventionally used. The leakage currents in the device layout were typically in the range of 8 pA to 20 pA/cm2 at 5 V bias. The photon-photon down conversion efficiency was determined to be 27%. Microphotoluminescence and microelectroluminescence characterization demonstrate the potential for future optoelectronics and highly secure "green" information technology applications.

  14. Exploring size and state dynamics in CdSe quantum dots using two-dimensional electronic spectroscopy.

    PubMed

    Caram, Justin R; Zheng, Haibin; Dahlberg, Peter D; Rolczynski, Brian S; Griffin, Graham B; Dolzhnikov, Dmitriy S; Talapin, Dmitri V; Engel, Gregory S

    2014-02-28

    Development of optoelectronic technologies based on quantum dots depends on measuring, optimizing, and ultimately predicting charge carrier dynamics in the nanocrystal. In such systems, size inhomogeneity and the photoexcited population distribution among various excitonic states have distinct effects on electron and hole relaxation, which are difficult to distinguish spectroscopically. Two-dimensional electronic spectroscopy can help to untangle these effects by resolving excitation energy and subsequent nonlinear response in a single experiment. Using a filament-generated continuum as a pump and probe source, we collect two-dimensional spectra with sufficient spectral bandwidth to follow dynamics upon excitation of the lowest three optical transitions in a polydisperse ensemble of colloidal CdSe quantum dots. We first compare to prior transient absorption studies to confirm excitation-state-dependent dynamics such as increased surface-trapping upon excitation of hot electrons. Second, we demonstrate fast band-edge electron-hole pair solvation by ligand and phonon modes, as the ensemble relaxes to the photoluminescent state on a sub-picosecond time-scale. Third, we find that static disorder due to size polydispersity dominates the nonlinear response upon excitation into the hot electron manifold; this broadening mechanism stands in contrast to that of the band-edge exciton. Finally, we demonstrate excitation-energy dependent hot-carrier relaxation rates, and we describe how two-dimensional electronic spectroscopy can complement other transient nonlinear techniques.

  15. Chirality Inversion of CdSe and CdS Quantum Dots without Changing the Stereochemistry of the Capping Ligand.

    PubMed

    Choi, Jung Kyu; Haynie, Benjamin E; Tohgha, Urice; Pap, Levente; Elliott, K Wade; Leonard, Brian M; Dzyuba, Sergei V; Varga, Krisztina; Kubelka, Jan; Balaz, Milan

    2016-03-22

    L-cysteine derivatives induce and modulate the optical activity of achiral cadmium selenide (CdSe) and cadmium sulfide (CdS) quantum dots (QDs). Remarkably, N-acetyl-L-cysteine-CdSe and L-homocysteine-CdSe as well as N-acetyl-L-cysteine-CdS and L-cysteine-CdS showed "mirror-image" circular dichroism (CD) spectra regardless of the diameter of the QDs. This is an example of the inversion of the CD signal of QDs by alteration of the ligand's structure, rather than inversion of the ligand's absolute configuration. Non-empirical quantum chemical simulations of the CD spectra were able to reproduce the experimentally observed sign patterns and demonstrate that the inversion of chirality originated from different binding arrangements of N-acetyl-L-cysteine and L-homocysteine-CdSe to the QD surface. These efforts may allow the prediction of the ligand-induced chiroptical activity of QDs by calculating the specific binding modes of the chiral capping ligands. Combined with the large pool of available chiral ligands, our work opens a robust approach to the rational design of chiral semiconducting nanomaterials.

  16. Portable exhausters POR-004 SKID B, POR-005 SKID C, POR-006 SKID D storage plan

    SciTech Connect

    Nelson, O.D.

    1997-09-04

    This document provides a storage plan for portable exhausters POR-004 SKID B, POR-005 SKID C, AND POR-006 SKID D. The exhausters will be stored until they are needed by the TWRS (Tank Waste Remediation Systems) Saltwell Pumping Program. The storage plan provides criteria for portable exhauster storage, periodic inspections during storage, and retrieval from storage.

  17. CdSe quantum dot-functionalized TiO2 nanohybrids as a visible light induced photoelectrochemical platform for the detection of proprotein convertase subtilisin/kexin type 6.

    PubMed

    Pang, Xuehui; Pan, Jihong; Wang, Lin; Ren, Wei; Gao, Picheng; Wei, Qin; Du, Bin

    2015-09-15

    Proprotein convertase subtilisin/kexin type 6 (PCSK6) plays a major role in promoting the progression of rheumatoid arthritis to a higher aggressive status. A novel highly sensitive photoelectrochemical platform was developed for the detection of PCSK6 by using CdSe quantum dots (QDs)-functionalized TiO2 nanoparticles (NPs) nanohybrids (TiO2@CdSe) as the photo-to-electron conversion medium. TiO2@CdSe showed excellent visible-light absorbency, and much higher photoelectrochemical activity than both CdSe QDs and TiO2 NPs. The 5' and 3' primers of PCSK6 ssDNA acted as capture probes to realize the detection of PCSK6 ssDNA by the specific recognition. The capture probes can be fixed by poly-l-lysine (PLL) through positively strong electrostatic attraction and the carboxyl group of TiO2@CdSe nanohybrids. PLL was electropolymerized on ITO electrode by cyclic voltammetry (CV). Simultaneously, the amino group of PLL can interact with the carboxyl group of TiO2@CdSe nanohybrids to enhance the stability of the photoelectrochemical signal. The fabricated aptsensor exhibited excellent performance towards PCSK6 with a wide linear range (0.5 pg/mL to 80.0 ng/mL) and a detection limit of 0.1 fg/mL. This work opens up a new detection platform for PCSK6 with good sensitivity, reproducibility and stability.

  18. Experimental determination of the absorption cross-section and molar extinction coefficient of CdSe and CdTe nanowires.

    PubMed

    Protasenko, Vladimir; Bacinello, Daniel; Kuno, Masaru

    2006-12-21

    Absorption cross-sections and corresponding molar extinction coefficients of solution-based CdSe and CdTe nanowires (NWs) are determined. Chemically grown semiconductor NWs are made via a recently developed solution-liquid-solid (SLS) synthesis, employing low melting Au/Bi bimetallic nanoparticle "catalysts" to induce one-dimensional (1D) growth. Resulting wires are highly crystalline and have diameters between 5 and 12 nm as well as lengths exceeding 10 microm. Narrow diameters, below twice the corresponding bulk exciton Bohr radius of each material, place CdSe and CdTe NWs within their respective intermediate to weak confinement regimes. Supporting this are solution linear absorption spectra of NW ensembles showing blue shifts relative to the bulk band gap as well as structure at higher energies. In the case of CdSe, the wires exhibit band edge emission as well as strong absorption/emission polarization anisotropies at the ensemble and single-wire levels. Analogous photocurrent polarization anisotropies have been measured in recently developed CdSe NW photodetectors. To further support fundamental NW optical/electrical studies as well as to promote their use in device applications, experimental absorption cross-sections are determined using correlated transmission electron microscopy, UV/visible extinction spectroscopy, and inductively coupled plasma atomic emission spectroscopy. Measured CdSe NW cross-sections for 1 microm long wires (diameters, 6-42 nm) range from 6.93 x 10(-13) to 3.91 x 10(-11) cm2 at the band edge (692-715 nm, 1.73-1.79 eV) and between 3.38 x 10(-12) and 5.50 x 10(-11) cm2 at 488 nm (2.54 eV). Similar values are obtained for 1 microm long CdTe NWs (diameters, 7.5-11.5 nm) ranging from 4.32 x 10(-13) to 5.10 x 10(-12) cm2 at the band edge (689-752 nm, 1.65-1.80 eV) and between 1.80 x 10(-12) and 1.99 x 10(-11) cm2 at 2.54 eV. These numbers compare well with previous theoretical estimates of CdSe/CdTe NW cross-sections far to the blue of the

  19. Probing structure-induced optical behavior in a new class of self-activated luminescent 0D/1D CaWO₄ metal oxide – CdSe nanocrystal composite heterostructures

    DOE PAGES

    Han, Jinkyu; McBean, Coray; Wang, Lei; ...

    2015-01-30

    In this report, we synthesize and characterize the structural and optical properties of novel heterostructures composed of (i) semiconducting nanocrystalline CdSe quantum dot (QDs) coupled with (ii) both one and zero-dimensional (1D and 0D) motifs of self-activated luminescence CaWO₄ metal oxides. Specifically, ~4 nm CdSe QDs have been anchored onto (i) high-aspect ratio 1D nanowires, measuring ~230 nm in diameter and ~3 μm in length, as well as onto (ii) crystalline 0D nanoparticles (possessing an average diameter of ~ 80 nm) of CaWO₄ through the mediation of 3-mercaptopropionic acid (MPA) as a connecting linker. Composite formation was confirmed by complementarymore » electron microscopy and spectroscopy (i.e. IR and Raman) data. In terms of luminescent properties, our results show that our 1D and 0D heterostructures evince photoluminescence (PL) quenching and shortened PL lifetimes of CaWO₄ as compared with unbound CaWO₄. We propose that a photo-induced electron transfer process occurs from CaWO₄ to CdSe QDs, a scenario which has been confirmed by NEXAFS measurements and which highlights a decrease in the number of unoccupied orbitals in the conduction bands of CdSe QDs. By contrast, the PL signature and lifetimes of MPA-capped CdSe QDs within these heterostructures do not exhibit noticeable changes as compared with unbound MPA-capped CdSe QDs. The striking difference in optical behavior between CaWO₄ nanostructures and CdSe QDs within our heterostructures can be correlated with the relative positions of their conduction and valence energy band levels. In addition, the PL quenching behaviors for CaWO₄ within the heterostructure configuration were examined by systematically varying (i) the quantities and coverage densities of CdSe QDs as well as (ii) the intrinsic morphology (and by extension, the inherent crystallite size) of CaWO₄ itself.« less

  20. Optimization of structural and dielectric properties of CdSe loaded poly(diallyl dimethyl ammonium chloride) polymer in a desired frequency and temperature window

    SciTech Connect

    Tyagi, Chetna Sharma, Ambika

    2016-01-07

    In the present paper, investigations of CdSe loaded poly(diallyl dimethyl ammonium chloride) (PDADMAC) nanocomposites and pure PDADMAC synthesized by wet chemical technique have been carried out. Fourier transform infrared and X-ray diffraction analysis have been performed to reveal the structural details of pure polymer and polymer nanocomposite (PNC). The dielectric behavior of pure polymer and PNC has been recorded, which results in higher value of the real and imaginary part of dielectric constant for PNC, as compared with pure PDADMAC. The increase is attributed to the addition of CdSe quantum dots to the pure polymer. The contribution of ionic and electronic polarization has been observed at higher frequency. The theoretical fitting of Cole-Cole function to the experimental data of dielectric constant of PNC and pure PDADMAC results in the determination of relaxation time and conductivity of space charge carriers. The CdSe loaded polymer nanocomposite has been used as an electrolyte in the battery fabrication with configuration Al/PNC/Ag{sub 2}O. The ac conductivity measurements have been carried out for both samples in a frequency window of 1 kHz–5 MHz and at different temperatures varying from 298 K to 523 K. Activation energy (E{sub a}) has been determined for pure polymer as well as PNC and is found to be less for PNC, as compared with pure polymer. Further, impedance measurement at different temperatures results in two frequency ranges corresponding to ionic conduction and blocking electrode effect. The value of bulk resistance for pure polymer and PNC has been found to be 3660 Ω and 442 Ω, respectively, at 298 K temperature. Electric modulus has been determined and is observed to support the dielectric constant data; it further reveals the deviation from Debye behavior at a higher frequency.

  1. Atomistic Description of Thiostannate-Capped CdSe Nanocrystals: Retention of Four-Coordinate SnS4 Motif and Preservation of Cd-Rich Stoichiometry

    PubMed Central

    2016-01-01

    Colloidal semiconductor nanocrystals (NCs) are widely studied as building blocks for novel solid-state materials. Inorganic surface functionalization, used to displace native organic capping ligands from NC surfaces, has been a major enabler of electronic solid-state devices based on colloidal NCs. At the same time, very little is known about the atomistic details of the organic-to-inorganic ligand exchange and binding motifs at the NC surface, severely limiting further progress in designing all-inorganic NCs and NC solids. Taking thiostannates (K4SnS4, K4Sn2S6, K6Sn2S7) as typical examples of chalcogenidometallate ligands and oleate-capped CdSe NCs as a model NC system, in this study we address these questions through the combined application of solution 1H NMR spectroscopy, solution and solid-state 119Sn NMR spectroscopy, far-infrared and X-ray absorption spectroscopies, elemental analysis, and by DFT modeling. We show that through the X-type oleate-to-thiostannate ligand exchange, CdSe NCs retain their Cd-rich stoichiometry, with a stoichiometric CdSe core and surface Cd adatoms serving as binding sites for terminal S atoms of the thiostannates ligands, leading to all-inorganic (CdSe)core[Cdm(Sn2S7)yK(6y-2m)]shell (taking Sn2S76– ligand as an example). Thiostannates SnS44– and Sn2S76– retain (distorted) tetrahedral SnS4 geometry upon binding to NC surface. At the same time, experiments and simulations point to lower stability of Sn2S64– (and SnS32–) in most solvents and its lower adaptability to the NC surface caused by rigid Sn2S2 rings. PMID:25597625

  2. Double-sided CdS and CdSe quantum dot co-sensitized ZnO nanowire arrays for photoelectrochemical hydrogen generation.

    PubMed

    Wang, Gongming; Yang, Xunyu; Qian, Fang; Zhang, Jin Z; Li, Yat

    2010-03-10

    We report the design and characterization of a novel double-sided CdS and CdSe quantum dot cosensitized ZnO nanowire arrayed photoanode for photoelectrochemical (PEC) hydrogen generation. The double-sided design represents a simple analogue of tandem cell structure, in which the dense ZnO nanowire arrays were grown on an indium-tin oxide substrate followed by respective sensitization of CdS and CdSe quantum dots on each side. As-fabricated photoanode exhibited strong absorption in nearly the entire visible spectrum up to 650 nm, with a high incident-photon-to-current-conversion efficiency (IPCE) of approximately 45% at 0 V vs Ag/AgCl. On the basis on a single white light illumination of 100 mW/cm(2), the photoanode yielded a significant photocurrent density of approximately 12 mA/cm(2) at 0.4 V vs Ag/AgCl. The photocurrent and IPCE were enhanced compared to single quantum dot sensitized structures as a result of the band alignment of CdS and CdSe in electrolyte. Moreover, in comparison to single-sided cosensitized layered structures, this double-sided architecture that enables direct interaction between quantum dot and nanowire showed improved charge collection efficiency. Our result represents the first double-sided nanowire photoanode that integrates uniquely two semiconductor quantum dots of distinct band gaps for PEC hydrogen generation and can be possibly applied to other applications such as nanostructured tandem photovoltaic cells.

  3. Role of ZnS shell on stability, cytotoxicity, and photocytotoxicity of water-soluble CdSe semiconductor quantum dots surface modified with glutathione

    NASA Astrophysics Data System (ADS)

    Ibrahim, Salwa Ali; Ahmed, Wafaa; Youssef, Tareq

    2014-09-01

    Biomedical applications of quantum dots (QDs) have become a subject of a considerable concern in the past few decades. The present study examines the stability and cytotoxicity of two QDs systems in cell culture medium in the presence and absence of a thin layer of ZnS shell. The two systems were built from core, CdSe QDs, surface modified with glutathione (GSH), named CdSe˜GSH and CdSe/ZnS˜GSH. Our results demonstrated that 0.7 nm layer of ZnS shell played a significant role in the stability of CdSe/ZnS~GSH QDs in supplemented cell culture medium (RPMI). Also, a significant improvement in the physicochemical properties of the core CdSe QDs was shown by maintaining their spectroscopic characteristics in RPMI medium due to the wide band gap of ZnS shell. Both systems showed insignificant reduction in cell viability of HFB-4 or MCF-7 cell lines in the dark which was attributed to the effective GSH coating. Following photoirradiation with low laser power (irradiance 10 mW cm-2), CdSe~GSH QDs showed a significant decrease in cell viability after 60 min irradiation which may result from detachment of GSH molecules. Under the same irradiation condition, CdSe/ZnS~GSH QDs showed insignificant decrease in cell viability or after 2 h incubation from laser irradiation which was attributed to the strong binding between ZnS and GSH coatings. It can be concluded that the stability of CdSe core QDs was significantly improved in cell culture medium by encapsulation with a thin layer of ZnS shell whereas their cytotoxicity and photo-cytotoxicity are highly dependent on surface modification.

  4. Comparison of Toxicity of CdSe: ZnS Quantum Dots on Male Reproductive System in Different Stages of Development in Mice

    PubMed Central

    Amiri, Gholamreza; Valipoor, Akram; Parivar, Kazem; Modaresi, Mehrdad; Noori, Ali; Gharamaleki, Hamideh; Taheri, Jafar; Kazemi, Ali

    2016-01-01

    Background Quantum dots (QDs) are new types of fluorescent materials for biological labeling. QDs toxicity study is an essential requirement for future clinical applications. Therefore, this study aimed to evaluate cytotoxic effects of CdSe: ZnS QDs on male reproductive system. Materials and Methods In this experimental study, the different concentrations of CdSe: ZnS QDs (10, 20 and 40 mg/kg) were injected to 32 male mice (adult group) and 24 pregnant mice (embryo group) on day 8 of gestation. The histological changes of testis and epididymis were studied by a light microscopy, and the number of seminiferous tubules between two groups was compared. One-way analysis of variance (one-way Anova) using the Statistical Package for the Social Sciences (SPSS, SPSS Inc., USA) version 16 were performed for statistical analysis. Results In adult group, histological studies of testis tissues showed a high toxicity of CdSe: ZnS in 40 mg/kg dose followed by a decrease in lamina propria; destruction in interstitial tissue; deformation of seminiferous tubules; and a reduction in number of spermatogonia, spermatocytes, and spermatids. However, there was an interesting result in fetal testis development, meaning there was no significant effect on morphology and structure of the seminiferous tubules and number of sperm stem cells. Also histological study of epididymis tissues in both groups (adult and embryo groups) showed no significant effect on morphology and structure of tubule and epithelial cells, but there was a considerable reduction in number of spermatozoa in the lumen of the epididymal duct in 40 mg/kg dose of adult group. Conclusion The toxicity of QDs on testicular tissue of the mice embryo and adult are different before and after puberty. Due to lack of research in this field, this study can be an introduction to evaluate the toxicity of QDs on male reproduction system in different stages of development. PMID:26985339

  5. Optimization of structural and dielectric properties of CdSe loaded poly(diallyl dimethyl ammonium chloride) polymer in a desired frequency and temperature window

    NASA Astrophysics Data System (ADS)

    Tyagi, Chetna; Sharma, Ambika

    2016-01-01

    In the present paper, investigations of CdSe loaded poly(diallyl dimethyl ammonium chloride) (PDADMAC) nanocomposites and pure PDADMAC synthesized by wet chemical technique have been carried out. Fourier transform infrared and X-ray diffraction analysis have been performed to reveal the structural details of pure polymer and polymer nanocomposite (PNC). The dielectric behavior of pure polymer and PNC has been recorded, which results in higher value of the real and imaginary part of dielectric constant for PNC, as compared with pure PDADMAC. The increase is attributed to the addition of CdSe quantum dots to the pure polymer. The contribution of ionic and electronic polarization has been observed at higher frequency. The theoretical fitting of Cole-Cole function to the experimental data of dielectric constant of PNC and pure PDADMAC results in the determination of relaxation time and conductivity of space charge carriers. The CdSe loaded polymer nanocomposite has been used as an electrolyte in the battery fabrication with configuration Al/PNC/Ag2O. The ac conductivity measurements have been carried out for both samples in a frequency window of 1 kHz-5 MHz and at different temperatures varying from 298 K to 523 K. Activation energy (Ea) has been determined for pure polymer as well as PNC and is found to be less for PNC, as compared with pure polymer. Further, impedance measurement at different temperatures results in two frequency ranges corresponding to ionic conduction and blocking electrode effect. The value of bulk resistance for pure polymer and PNC has been found to be 3660 Ω and 442 Ω, respectively, at 298 K temperature. Electric modulus has been determined and is observed to support the dielectric constant data; it further reveals the deviation from Debye behavior at a higher frequency.

  6. Index of refraction and its temperature coefficient in CdSe0.18Te0.82 at 10.2 µm wavelength

    NASA Astrophysics Data System (ADS)

    Cohen, S.; Weil, R.; Muranevich, E.

    1994-07-01

    The index of refraction and its temperature dependence were measured at 10.22 μm on CdSe0.18Te0.82 grown by the Bridgman technique. The results are n=2.67±0.02 (different than the value expected from Vegard's law), and (1/n)(dn/dt)=(3.89±0.07)10-5 °C-1. The absorption coefficient of the sample has also been measured, α=(0.79±0.05) cm-1.

  7. Synthesis of water-soluble CdSe quantum dots with various fluorescent properties and their application in immunoassay for determination of C-reactive protein.

    PubMed

    Gasparyan, V K

    2014-09-01

    Effects of various factors on synthesis and fluorescent properties of CdSe quantum dots were studied. It was shown that variation of pH, stabilizer and concentration of precursors brings to obtaining of quantum dots with various fluorescent properties. The nanoparticles prepared were conjugated with rabbit antibodies to C-Reactive protein and C-Reactive protein for competitive immunoassay for determination of CRP. It was shown that interaction of these dots as a result of antigen-antibody reaction brings to resonance energy transfer and these changes in fluorescence spectra correlate with concentration of CRP. This approach permits to determine CRP in range between 4-100 ng.

  8. Tailoring the optical properties of poly(diallyl dimethyl ammonium chloride) polyelectrolyte by incorporation of 2-mercaptoethanol capped CdSe nanoparticles

    NASA Astrophysics Data System (ADS)

    Tyagi, Chetna; Sharma, Ambika

    2016-10-01

    The present work deals with the preparation and characterization of 2-mercaptoethanol capped cadmium selenide (CdSe) nanoparticles, dispersed in poly(diallyl dimethyl ammonium chloride) (PDADMAC) polyelectrolyte aqueous solution. X-ray diffraction spectra, scanning electron microscopy and energy-dispersive x-ray have been used to determine the structure, particle size (d), surface morphology and composition of various constituents. The absorption spectra of pure PDADMAC and the CdSe/PDADMAC polymer nanocomposite (PNC) are analyzed to determine the values of the absorption coefficient (α) and energy band gap (E g) which are found to be 4 eV and 3.26 eV respectively. A red shift in the spectrum of the PNC, as compared to the pure polymer, has been observed. With the addition of CdSe nanoparticles in the PDADMAC polyelectrolyte, a remarkable change in the optical parameters of the pure polymer has been observed. The refractive index (n) obtained by using Swanepoel’s method decreases in the case of the PNC as compared to the pure polymer. The value of the static refractive index (n 0) is found to be 4.29 for the pure polymer and 1.52 for the PNC. The extinction coefficient, dielectric constants, optical conductivity and relaxation time have been evaluated. The Wemple-DiDomenico model has been used to evaluate the dispersion parameters such as the average energy gap (E 0) and dispersion energy (E d). The values of the nonlinear refractive index (n 2) of the pure polymer and PNC have been determined using the theoretical approaches suggested by Boling and Tichy and Ticha. n 2 increases in the case of PNC, which relates to the decreased energy band gap. Photoluminescence (PL) spectra have been studied to explore the energy band structure and interaction between CdSe nanoparticles and PDADMAC. The PL peaks obtained at 437 nm and 461 nm correspond to the pure polymer whereas the peak at 577 nm is attributed to CdSe.

  9. Utilizing Electrical Characteristics of Individual Nanotube Devices to Study the Charge Transfer between CdSe Quantum Dots and Double-Walled Nanotubes

    DOE PAGES

    Zhu, Yuqi; Zhou, Ruiping; Wang, Lei; ...

    2017-03-02

    To study the charge transfer between cadmium selenide (CdSe) quantum dots (QDs) and double-walled nanotubes (DWNTs), various sizes of CdSe-ligand-DWNT structures are synthesized, and field-effect transistors (FETs) from individual functionalized DWNTs rather than networks of the same are fabricated. From the electrical measurements, two distinct electron transfer mechanisms from the QD system to the nanotube are identified. By the formation of the CdSe-ligand-DWNT heterostructure, an effectively n-doped nanotube is created due to the smaller work function of CdSe as compared with the nanotube. In addition, once the QD-DWNT system is exposed to laser light, further electron transfer from the QDmore » through the ligand, i.e. 4-mercaptophenol (MTH), to the nanotube occurs and a clear QD-size dependent tunneling process is observed. Furthermore, the detailed analysis of a large set of devices and the particular methodology employed here for the first time allowed for extracting a wavelength and quantum dot size dependent charge transfer efficiency – a quantity that is evaluated for the first time through electrical measurement.« less

  10. Photophysical Properties of Colloidal Mn(II)-Doped CdSe Nanoparticles: Exchange Fields, Exciton Storage, and Light-Induced Spontaneous Magnetization

    NASA Astrophysics Data System (ADS)

    Beaulac, Remi

    2010-03-01

    An attractive approach to controlling spin effects in semiconductor nanostructures for applications in electronics is to use light to generate, manipulate, or read out spins. The main focus of this presentation will be on the recent demonstration of spontaneous photoinduced polarization of Mn(II) spins in doped colloidal CdSe quantum dots, an effect due to the formation of excitonic magnetic polarons. Photoexcitation generates large dopant-carrier exchange fields, enhanced by strong spatial confinement, that lead to giant Zeeman splittings of the semiconductor band structure in the absence of applied magnetic fields. These internal exchange fields allow spontaneous magnetic saturation of the Mn(II) spins to be achieved at zero external magnetic field up to ca. 50 K, and photomagnetic effects are observed all the way up to room temperature. The factors that allow this fascinating effect to be observed in colloidal Mn(II)-doped CdSe nanoparticles will be discussed. Relevant Publications: 1) Beaulac, Schneider, Archer, Bacher, and Gamelin. Science, 325, 973 (2009) 2) Beaulac, Archer, Ochsenbein, and Gamelin, Adv. Funct. Mat., 18, 3873 (2008)

  11. Mercaptoethanol capped CdSe quantum dots and CdSe/ZnS core/shell: synthesis, characterization and cytotoxicity evaluation.

    PubMed

    Painuly, Diksha; Bhatt, Anugya; Krishnan, V Kalliyana

    2013-02-01

    CdSe Quantum dots (Q-dots) and CdSe/ZnS core/shell have been synthesized by wet chemical route using mercaptoethanol (ME) as cappant. The synthesized Q-dots and core/shell were characterized using X-ray diffraction (XRD), Transmission electron microscopy (TEM), Energy dispersive X-ray analysis (EDS), Dynamic Light Scattering (DLS), Optical absorption and luminescence spectroscopy. The core/shell formation was confirmed by both XRD and TEM analysis. The luminescence was shown to be considerably enhanced in the core/shell sample. Effect of dialysis process on the optical properties of the Q-dots and core/shell has also been discussed. Cytotoxicity studies have been carried out for Q-dots and core/shell. CdSe/ZnS core/shell was found to be non-cytotoxic as compared to CdSe Q-dots up to a certain concentration range. Polyethylene glycol (PEG) coating enhances the non-cytotoxic nature of CdSe/ZnS core/shell when compared with bare core/shell.

  12. Investigation of biocompatible and protein sensitive highly luminescent quantum dots/nanocrystals of CdSe, CdSe/ZnS and CdSe/CdS.

    PubMed

    Ratnesh, R K; Mehata, Mohan Singh

    2017-02-16

    The size and shape dependent semiconductor quantum dots (0D nanoparticles) with color tunability demonstrating significant influence in a biological system and considered as ideal probes. Here, a non-coordinated colloidal approach was used for the synthesis of CdSe, CdSe/ZnS and CdSe/CdS core-shell quantum dots (QDs) of 3-4nm. The synthesized nanocrystals show a high crystallinity, examined by X-ray diffraction (XRD) and high-resolution electron microscopy (HRTEM). The core-shell semiconductor QDs exhibit stronger photoluminescence (PL) as compared to the core QDs. The strong PL with small full-width half maximum (FWHM) indicates that the prepared QDs have a nearly uniform size distribution and well dispersibility. The quantum yield (QY) of core-shell QDs increases due to the surface passivation. Further, the PL of BSA is quenched strongly by the presence of core-shell QDs and follows the well-known Stern-Volmer (S-V) relation, whereas the PL lifetime does not follow the S-V relation, demonstrating that the observed quenching is predominantly static in nature. Among CdSe core, CdSe/ZnS and CdSe/CdS core-shell QDs, the CdSe/ZnS QDs shows the least cytotoxicity and most biocompatibility. Thus, the prepared core-shell QDs are biocompatible and exhibit strong sensing ability.

  13. Architectural control syntheses of CdS and CdSe nanoflowers, branched nanowires, and nanotrees via a solvothermal approach in a mixed solution and their photocatalytic property.

    PubMed

    Yao, Wei-Tang; Yu, Shu-Hong; Liu, Shu-Juan; Chen, Jun-Peng; Liu, Xian-Ming; Li, Fan-Qing

    2006-06-22

    Wurtzite CdS and CdSe nanostructures with complex morphologies such as urchin-like CdS nanoflowers, branched nanowires, and fractal nanotrees can be produced via a facile solvothermal approach in a mixed solution made of diethylenetriamine (DETA) and deionized water (DIW). The morphologies of CdS and CdSe nanocrystals can be easily controlled via tuning the volume ratio of DETA and DIW. Urchin-like CdS nanoflowers made of CdS nanorods are in a form of highly ordered hierarchical structures, while the nanowires are branched nanowires, and the fractal CdS nanotrees are a buildup of branched nanopines. The results demonstrated that solvothermal reaction in a mixed amine/water can access a variety of complex morphologies of semiconductor materials. The photocatalytic activity of CdS particles with different morphologies has been tested by the degradation of acid fuchsine under both UV and visible light, showing that the as-prepared branched CdS nanowires exhibit high photocatalytic activity for degradation of acid fuchsine.

  14. Differences in soil mobility and degradability between water-dispersible CdSe and CdSe/ZnS quantum dots.

    PubMed

    Navarro, Divina A; Banerjee, Sarbajit; Watson, David F; Aga, Diana S

    2011-08-01

    The relative leaching potential and degradation of water-dispersible CdSe and CdSe/ZnS quantum dots (QDs) were evaluated using small-scale soil columns. The potential of QDs to release toxic Cd(2+) and/or Se(2-)/SeO(3)(2-) ions upon degradation is of environmental concern and warrants investigation. Both classes of QDs exhibited limited soil mobility in CaCl(2), with more than 70% of the total Cd and Se species from QDs retained in the top soil after passing 10 column volumes of solution through the soil column. However, mobilization of Cd- and Se-species was observed when EDTA was used as the leaching solution. Approximately 98% of the total Cd(2+) loaded leached out from the Cd(2+)-spiked soil, while only 30% and 60% leached out from the CdSe and CdSe/ZnS QD-spiked soils, respectively. Soil column profiles and analysis of leachates suggest that intact QDs leached through the soil. Longer incubation (15 days) in soil prior to leaching indicated some degradation and/or surface modification of both QDs. These results suggest that chelating agents in the environment can enhance the soil mobility of intact and degraded QDs. It is apparent that QDs in soil, including the polymer-coated CdSe/ZnS QDs that are generally assumed to possess a higher degree of environmental stability, can undergo chemical transformations, which subsequently dictate their overall mobility.

  15. Performances of some low-cost counter electrode materials in CdS and CdSe quantum dot-sensitized solar cells

    PubMed Central

    2014-01-01

    Different counter electrode (CE) materials based on carbon and Cu2S were prepared for the application in CdS and CdSe quantum dot-sensitized solar cells (QDSSCs). The CEs were prepared using low-cost and facile methods. Platinum was used as the reference CE material to compare the performances of the other materials. While carbon-based materials produced the best solar cell performance in CdS QDSSCs, platinum and Cu2S were superior in CdSe QDSSCs. Different CE materials have different performance in the two types of QDSSCs employed due to the different type of sensitizers and composition of polysulfide electrolytes used. The poor performance of QDSSCs with some CE materials is largely due to the lower photocurrent density and open-circuit voltage. The electrochemical impedance spectroscopy performed on the cells showed that the poor-performing QDSSCs had higher charge-transfer resistances and CPE values at their CE/electrolyte interfaces. PMID:24512605

  16. Dimensionality of nanoscale TiO2 determines the mechanism of photoinduced electron injection from a CdSe nanoparticle

    SciTech Connect

    Tafen, De Nyago; Long, Run; Prezhdo, Oleg V.

    2014-03-10

    Assumptions about electron transfer (ET) mechanisms guide design of catalytic, photovoltaic, and electronic systems. We demonstrate that the mechanism of ET from a CdSe quantum dot (QD) into nanoscale TiO2 depends on TiO2 dimensionality. The injection into a TiO2 QD is adiabatic due to strong donor–acceptor coupling, arising from unsaturated chemical bonds on the QD surface, and low density of acceptor states. In contrast, the injection into a TiO2 nanobelt (NB) is nonadiabatic, because the state density is high, the donor–acceptor coupling is weak, and multiple phonons accommodate changes in the electronic energy. The CdSe adsorbant breaks symmetry of delocalized TiO2 NB states, relaxing coupling selection rules, and generating more ET channels. Both mechanisms can give efficient ultrafast injection. Furthermore, the dependence on system properties is very different for the two mechanisms, demonstrating that the fundamental principles leading to efficient charge separation depend strongly on the type of nanoscale material.

  17. CdSe magic-sized quantum dots incorporated in biomembrane models at the air-water interface composed of components of tumorigenic and non-tumorigenic cells.

    PubMed

    Goto, Thiago E; Lopes, Carla C; Nader, Helena B; Silva, Anielle C A; Dantas, Noelio O; Siqueira, José R; Caseli, Luciano

    2016-07-01

    Cadmium selenide (CdSe) magic-sized quantum dots (MSQDs) are semiconductor nanocrystals with stable luminescence that are feasible for biomedical applications, especially for in vivo and in vitro imaging of tumor cells. In this work, we investigated the specific interaction of CdSe MSQDs with tumorigenic and non-tumorigenic cells using Langmuir monolayers and Langmuir-Blodgett (LB) films of lipids as membrane models for diagnosis of cancerous cells. Surface pressure-area isotherms and polarization modulation reflection-absorption spectroscopy (PM-IRRAS) showed an intrinsic interaction between the quantum dots, inserted in the aqueous subphase, and Langmuir monolayers constituted either of selected lipids or of tumorigenic and non-tumorigenic cell extracts. The films were transferred to solid supports to obtain microscopic images, providing information on their morphology. Similarity between films with different compositions representing cell membranes, with or without the quantum dots, was evaluated by atomic force microscopy (AFM) and confocal microscopy. This study demonstrates that the affinity of quantum dots for models representing cancer cells permits the use of these systems as devices for cancer diagnosis.

  18. Self-assembly of CdSe quantum dots and colloidal titanium dioxide on copolymer microspheres (PS) for CdSe/PS and TiO2/CdSe/PS sub-microspheres with yolk-shell structure

    NASA Astrophysics Data System (ADS)

    Zhao, Qingchun

    2015-07-01

    Semiconductor nanocrystals serve as the building blocks for designing next generation solar cells, chemical/biological sensors, and metal chalcogenides (e.g., CdS, CdSe, PbS, and PbSe) are particularly useful for harnessing size-dependent optical and electronic properties in nanostructures. In this paper, relying on the interaction including van der Waals forces and hydrogen bond, CdSe/PS sub-microspheres composite and TiO2/CdSe/PS sub-microspheres with yolk-shell structure were prepared via self-assembly of CdSe quantum dots and colloidal titanium dioxide on modified PS surface. The morphology, structure and composition obtained products were investigated by scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM) and energy disperse X-ray spectroscopy (EDX). Transmission electron microscopy (TEM) investigations show the CdSe quantum dots and colloidal titanate were assembled on the surface of PS sub-microspheres. CdSe QD-polymer sub-microspheres composites in which the QDs retain their original emission efficiency can be obtained. TiO2/CdSe/PS sub-microspheres with yolk-shell structure can improve the efficiency of charge separation.

  19. A novel immunosensing platform for highly sensitive prostate specific antigen detection based on dual-quenching of photocurrent from CdSe sensitized TiO2 electrode by gold nanoparticles decorated polydopamine nanospheres.

    PubMed

    Dong, Yu-Xiang; Cao, Jun-Tao; Liu, Yan-Ming; Ma, Shu-Hui

    2017-05-15

    Herein, a novel photoelectrochemical (PEC) immunosensing platform for highly sensitive detection of prostate specific antigen (PSA) was constructed based on dual-quenching of photocurrent from CdSe sensitized TiO2 electrode by gold nanoparticles decorated dopamine-melanin nanospheres (AuNPs-Dpa-melanin CNSs). In this proposal, CdSe sensitized TiO2 was used as photoelectrochemical matrix and the functional AuNPs-Dpa-melanin CNSs were used as signal quenching element. The dual quenching of the gold nanoparticles decorated Dpa-melanin CNSs to the CdSe sensitized TiO2 was achieved as follows: (i) the strong energy transfer between the CdSe quantum dots (QDs) and Au NPs diminishes the photocurrent signal of CdSe QDs; (ii) the steric hindrance of AuNPs-Dpa-melanin CNSs partly obstructs the diffusion of the electron donor, i.e. ascorbic acid, to the surface of photoelectrode, which make the depleting efficiency of the photogenerated holes decrease, leading to a declined photocurrent intensity. On the basis of the dual quenching effect of AuNPs-Dpa-melanin CNSs, a competitive immunosensing platform for PSA was designed upon the specific binding of anti-PSA to PSA and PSA functionalized AuNPs-Dpa-melanin CNSs conjugates. This proposed immunosensor possesses wide linear range from 1.0×10(-11)gmL(-1) to 1.0×10(-7)gmL(-1) with the detection limit of 2.7pgmL(-1). Moreover, the applicability of the present method was demonstrated in the determination of PSA in human serum. The strategy creates new paradigms for PSA and other tumor markers detection and demonstrates high sensitivity, good specificity, and satisfied applicability in complex biological samples.

  20. A CdSe thin film: a versatile buffer layer for improving the performance of TiO2 nanorod array:PbS quantum dot solar cells

    NASA Astrophysics Data System (ADS)

    Tan, Furui; Wang, Zhijie; Qu, Shengchun; Cao, Dawei; Liu, Kong; Jiang, Qiwei; Yang, Ying; Pang, Shan; Zhang, Weifeng; Lei, Yong; Wang, Zhanguo

    2016-05-01

    To fully utilize the multiple exciton generation effects in quantum dots and improve the overall efficiency of the corresponding photovoltaic devices, nanostructuralizing the electron conducting layer turns out to be a feasible strategy. Herein, PbS quantum dot solar cells were fabricated on the basis of morphologically optimized TiO2 nanorod arrays. By inserting a thin layer of CdSe quantum dots into the interface of TiO2 and PbS, a dramatic enhancement in the power conversion efficiency from 4.2% to 5.2% was realized and the resulting efficiency is one of the highest values for quantum dot solar cells based on nanostructuralized buffer layers. The constructed double heterojunction with a cascade type-II energy level alignment is beneficial for promoting photogenerated charge separation and reducing charge recombination, thereby responsible for the performance improvement, as revealed by steady-state analyses as well as ultra-fast photoluminescence and photovoltage decays. Thus this paper provides a good buffer layer to the community of quantum dot solar cells.To fully utilize the multiple exciton generation effects in quantum dots and improve the overall efficiency of the corresponding photovoltaic devices, nanostructuralizing the electron conducting layer turns out to be a feasible strategy. Herein, PbS quantum dot solar cells were fabricated on the basis of morphologically optimized TiO2 nanorod arrays. By inserting a thin layer of CdSe quantum dots into the interface of TiO2 and PbS, a dramatic enhancement in the power conversion efficiency from 4.2% to 5.2% was realized and the resulting efficiency is one of the highest values for quantum dot solar cells based on nanostructuralized buffer layers. The constructed double heterojunction with a cascade type-II energy level alignment is beneficial for promoting photogenerated charge separation and reducing charge recombination, thereby responsible for the performance improvement, as revealed by steady

  1. The influence of CdSe and ZnSe nanoparticles on the optical properties of Sm3+ ions in lead borate glasses

    NASA Astrophysics Data System (ADS)

    Mallur, Saisudha B.; Heidorn, William D.; Fatokun, Stephen O.; Joshi, Krishna D.; Bista, Sandip S.; Babu, Panakkattu K.

    2017-03-01

    The effect of glass composition and the presence of CdSe/ZnSe nanoparticles (NPs) on the optical absorption and fluorescence of Sm-doped lead borate glasses are studied. Three sets of glass samples xPbO:(99.5-x) B2O3:0.5Sm2O3, x = 29.5-69.5 mol%, xPbO:(96.5-x) B2O3:0.5Sm2O3: 3CdSe/ZnSe, x = 36.5, and 56.5 mol% are prepared. NPs are grown by annealing these glasses just below the glass transition temperature. Average size of both types of NPs increases with annealing time; however, CdSe NPs grew to a larger size range (2 to 20 nm) compared to ZnSe NPs (1 to 16 nm). We analyzed the hypersensitive transition, intensity parameters, radiative transition probability, stimulated emission cross section (σp), and the area ratio of the electric dipole/magnetic dipole transitions of Sm3+. The intensity parameters show a minimum at 11 h annealing for 36.5 mol% and a maximum for the same annealing duration in 56.5 mol% PbO containing CdSe NPs. The σp for 56.5 mol% of PbO with CdSe NPs is found to be a maximum when the average NP size is around 14 nm. ZnSe NPs containing glasses also show significant changes in σp when the average particle size is 16 nm, for 36.5 mol% PbO. Our results suggest that the optical properties of Sm3+ in lead borate glasses are sensitive to its electronic environment which can be modified by varying the base glass composition and/or incorporating large NPs of CdSe/ZnSe. The large σp values that we observe for some of the glass compositions make them attractive materials for photonic devices and photovoltaic applications.

  2. Valence-band mixing effects in the upper-excited-state magneto-optical responses of colloidal Mn2+-doped CdSe quantum dots.

    PubMed

    Fainblat, Rachel; Muckel, Franziska; Barrows, Charles J; Vlaskin, Vladimir A; Gamelin, Daniel R; Bacher, Gerd

    2014-12-23

    We present an experimental study of the magneto-optical activity of multiple excited excitonic states of manganese-doped CdSe quantum dots chemically prepared by the diffusion doping method. Giant excitonic Zeeman splittings of each of these excited states can be extracted for a series of quantum dot sizes and are found to depend on the radial quantum number of the hole envelope function involved in each transition. As seven out of eight transitions involve the same electron energy state, 1Se, the dominant hole character of each excitonic transition can be identified, making use of the fact that the g-factor of the pure heavy-hole component has a different sign compared to pure light hole or split-off components. Because the magnetic exchange interactions are sensitive to hole state mixing, the giant Zeeman splittings reported here provide clear experimental evidence of quantum-size-induced mixing among valence-band states in nanocrystals.

  3. Giant Excitonic Exchange Splittings at Zero Field in Single Colloidal CdSe Quantum Dots Doped with Individual Mn(2+) Impurities.

    PubMed

    Fainblat, Rachel; Barrows, Charles J; Hopmann, Eric; Siebeneicher, Simon; Vlaskin, Vladmir A; Gamelin, Daniel R; Bacher, Gerd

    2016-09-28

    Replacing a single atom of a host semiconductor nanocrystal with a functional dopant can introduce completely new properties potentially valuable for "solotronic" information-processing applications. Here, we report successful doping of colloidal CdSe quantum dots with a very small number of manganese ions-down to the ultimate limit of one. Single-particle spectroscopy reveals spectral fingerprints of the spin-spin interactions between individual dopants and quantum-dot excitons. Spectrally well-resolved emission peaks are observed that can be related to the discrete spin projections of individual Mn(2+) ions. In agreement with theoretical predictions, the exchange splittings are enhanced by more than an order of magnitude in these quantum dots compared to their epitaxial counterparts, opening a path for solotronic applications at elevated temperatures.

  4. Correlation between the band gap, elastic modulus, Raman shift and melting point of CdS, ZnS, and CdSe semiconductors and their size dependency

    NASA Astrophysics Data System (ADS)

    Yang, C.; Zhou, Z. F.; Li, J. W.; Yang, X. X.; Qin, W.; Jiang, R.; Guo, N. G.; Wang, Y.; Sun, C. Q.

    2012-02-01

    With structural miniaturization down to the nanoscale, the detectable quantities of solid materials no longer remain constant but become tunable. For the II-VI semiconductors example, the band gap expands, the elastic modulus increases, the melting point drops, and the Raman optical phonons experience red shift associated with creation of low frequency Raman acoustic modes that undergo blue shift with decreasing the dimensional scale. In order to understand the common origin of the size dependency of these seemingly irrelevant properties, we formulated these quantities for CdS, ZnS, and CdSe semiconductors from the perspectives of bond order-length-strength correlation and the local bond averaging approach. Consistency between the theory predictions and the measured size dependence of these quantities clarified that the undercoordination-induced local strain and quantum entrapment and the varied fraction of undercoordinated atoms of the entire solid correlate these quantities and dominate their size effect.

  5. Light emission from conductive paths in nanocrystalline CdSe embedded Zr-doped HfO2 high-k stack

    NASA Astrophysics Data System (ADS)

    Lin, Chi-Chou; Kuo, Yue

    2015-03-01

    Electrical and optical properties of the solid state incandescent light emitting devices made of zirconium doped hafnium oxide high-k films with and without an embedded nanocrystalline CdSe layer on the p-type Si wafer have been studied. The broad band white light was emitted from nano sized conductive paths through the thermal excitation mechanism. Conductive paths formed from the dielectric breakdown have been confirmed from scanning electron microscopic and atomic force microscopic images and the secondary ion mass spectrometric elemental profiles. Si was diffused from the wafer to the device surface through the conductive path during the high temperature light emission process. There are many potential applications of this type of device.

  6. First-principles Investigation of CdSe Nanowires using Wannier functions:Effects of Surface and Confinement on dielectric properties

    NASA Astrophysics Data System (ADS)

    Kanai, Yosuke; Grossman, Jeffrey; Cicero, Giancarlo

    2010-03-01

    Understanding how the electronic properties of a material change at the nanoscale is important for a wide range of technological applications as well as for basic science. One-dimensional nano-structures such as nanowires hold great promise for their potential application in opto-electronic devices. In this work, we investigate the electronic polarity behavior and transverse polarizability of hexagonal Cadmium Selenide (CdSe) nanowires of up to 3 nm in diameter, using a Wannier function description from density functional theory calculations. We address effects of quantum confinement and surfactant molecules on these nanowire properties via a local property analysis using the Wannier functions, revealing a few interesting insights in terms of local polarity changes. Interestingly, the transverse polarizability is enhanced and deviates significantly from the classical model for a dielectric cylinder at this scale. We will discuss our observation in terms of surface and confinement effects.

  7. Pulsed laser deposition of CdSe Quantum dots on Zn2SnO4 nanowires and their photovoltaic applications.

    PubMed

    Dai, Qilin; Chen, Jiajun; Lu, Liyou; Tang, Jinke; Wang, Wenyong

    2012-08-08

    In this work we report a physical deposition-based, one-step quantum dot (QD) synthesis and assembly on ternary metal oxide nanowires for photovoltaic applications. Typical solution-based synthesis of colloidal QDs for QD sensitized solar cells involves nontrivial ligand exchange processing and toxic wet chemicals, and the effect of the ligands on carrier transport has not been fully understood. In this research using pulsed laser deposition, CdSe QDs were coated on Zn(2)SnO(4) nanowires without ligand molecules, and the coverage could be controlled by adjusting the laser fluence. Growth of QDs in dense nanowire network structures was also achieved, and photovoltaic cells fabricated using this method exhibited promising device performance. This approach could be further applied for the assembly of QDs where ligand exchange is difficult and could possibly lead to reduced fabrication cost and improved device performance.

  8. Distant- and Shape-Dependent Excitation Energy Transfer in Nanohybrid Systems: Computations on a Pheophorbide-α CdSe Nanocrystal Complex.

    PubMed

    Ziemann, Dirk; May, Volkhard

    2014-04-03

    The combination of semiconductor nanocrystals (NCs) and molecules for efficient electronic excitation energy transfer is expected to be a promising ingredient of novel hybrid photovoltaic devices. Here energy transfer from a CdSe NC to the tetrapyrrole-type Pheophorbide-a molecule (Pheo) is studied theoretically. The rate expression accounts for the correct NC-Pheo transfer coupling, for the multitude of NC single exciton levels as well as their thermal distribution, and for the electron-vibrational Pheo states. A spherical Cd1159Se1450 NC is compared with a similar large NC of pyramidal and hemisphere shape. Because of the different exciton energies and wave functions, the transfer rates differ somewhat. For all three types of NC, however, the Coulomb correlation essentially determines the magnitude of the transfer coupling and the exciton energy. In any case, the energy-transfer coupling is below 1 meV, excluding hybrid-state formation.

  9. Structural Disorder in Colloidal InAs and CdSe Nanocrystals Observed by X-Ray Absorption Near-Edge Spectroscopy

    SciTech Connect

    Hamad, K.S.; Hamad, K.S.; Roth, R.; Roth, R.; Rockenberger, J.; Rockenberger, J.; Alivisatos, A.P.; Alivisatos, A.P.; van Buuren, T.

    1999-10-01

    We report the observation of size dependent structural disorder by x-ray absorption near-edge spectroscopy (XANES) in InAs and CdSe nanocrystals 17{endash}80thinspthinsp{Angstrom} in diameter. XANES of the In and Cd M{sub 4,5} edges yields features that are sharp for the bulk solid but broaden considerably as the size of the particle decreases. FEFF7 multiple-scattering simulations reproduce the size dependent broadening of the spectra if a bulklike surface reconstruction of a spherical nanocrystal model is included. This illustrates that XANES is sensitive to the structure of the entire nanocrystal including the surface. {copyright} {ital 1999} {ital The American Physical Society }

  10. Light emission from conductive paths in nanocrystalline CdSe embedded Zr-doped HfO{sub 2} high-k stack

    SciTech Connect

    Lin, Chi-Chou; Kuo, Yue

    2015-03-23

    Electrical and optical properties of the solid state incandescent light emitting devices made of zirconium doped hafnium oxide high-k films with and without an embedded nanocrystalline CdSe layer on the p-type Si wafer have been studied. The broad band white light was emitted from nano sized conductive paths through the thermal excitation mechanism. Conductive paths formed from the dielectric breakdown have been confirmed from scanning electron microscopic and atomic force microscopic images and the secondary ion mass spectrometric elemental profiles. Si was diffused from the wafer to the device surface through the conductive path during the high temperature light emission process. There are many potential applications of this type of device.

  11. Electrochemiluminescence sensors for scavengers of hydroxyl radical based on its annihilation in CdSe quantum dots film/peroxide system.

    PubMed

    Jiang, Hui; Ju, Huangxian

    2007-09-01

    This work elucidated the detailed electrochemiluminescence (ECL) process of the thioglycolic acid-capped CdSe quantum dots (QDs) film/peroxide aqueous system. The QDs were first electrochemically reduced to form electrons-injected QDs approximately -1.1 V, which then reduced hydrogen peroxide to produce OH* radical. The intermediate OH* radical was a key species for producing holes-injected QDs. The ECL emission with a peak at -1.114 V was demonstrated to come from the 1Se-1Sh transition emission. Using thiol compounds as the model molecules to annihilate the OH* radical, their quenching effects on ECL emission were studied. This effect led to a novel strategy for ECL sensing of the scavengers of hydroxyl radical. The detection results of thiol compounds showed high sensitivity, good precision, and acceptable accuracy, suggesting the promising application of the proposed method for quick detection of both scavengers and generators of hydroxyl radical in different fields.

  12. Temperature dependence of the energy gap of zinc-blende CdSe and Cd1 - xZnxSe epitaxial layers

    NASA Astrophysics Data System (ADS)

    Lunz, U.; Kuhn, J.; Goschenhofer, F.; Schüssler, U.; Einfeldt, S.; Becker, C. R.; Landwehr, G.

    1996-12-01

    The temperature dependence of the energy gap of zinc-blende CdSe and Cd1-xZnxSe has been determined over the entire range of composition from optical transmission and reflection measurements at temperatures between 5 and 300 K. The experimental results can be expressed by the following modified empirical Varshni formula, whose parameters are functions of the composition x: Eg(x,T)=Eg(x,0)-β(x)T2/[T+γ(x)]. Eg(x,0) exhibits a nonlinear dependence on composition, according to Eg=Eg(0,0)(1-x)+Eg(1,0)x-ax(1-x). The parameters β(x) and γ(x) can be expressed by β(x)=β(0)(1-x)+β(1)x+bx(1-x) and γ(x)=γ(0)(1-x)+γ(1)x.

  13. Combining ligand-induced quantum-confined stark effect with type II heterojunction bilayer structure in CdTe and CdSe nanocrystal-based solar cells.

    PubMed

    Yaacobi-Gross, Nir; Garphunkin, Natalia; Solomeshch, Olga; Vaneski, Aleksandar; Susha, Andrei S; Rogach, Andrey L; Tessler, Nir

    2012-04-24

    We show that it is possible to combine several charge generation strategies in a single device structure, the performance of which benefits from all methods used. Exploiting the inherent type II heterojunction between layered structures of CdSe and CdTe colloidal quantum dots, we systematically study different ways of combining such nanocrystals of different size and surface chemistry and with different linking agents in a bilayer solar cell configuration. We demonstrate the beneficial use of two distinctly different sizes of NCs not only to improve the solar spectrum matching but also to reduce exciton binding energy, allowing their efficient dissociation at the interface. We further make use of the ligand-induced quantum-confined Stark effect in order to enhance charge generation and, hence, overall efficiency of nanocrystal-based solar cells.

  14. Genotoxicity evaluation of nanomaterials: dna damage, micronuclei, and 8-hydroxy-2-deoxyguanosine induced by magnetic doped CdSe quantum dots in male mice.

    PubMed

    Khalil, W K B; Girgis, E; Emam, A N; Mohamed, M B; Rao, K V

    2011-05-16

    Quantum dots (QDs) are a novel class of inorganic fluorophores which are gaining widespread recognition as a result of their exceptional photophysical properties and their applications as a biomarker and in molecular biomedical imaging. The aim of this study was to evaluate the in vivo genotoxicity in mice exposed to CdSe quantum dots of average size 5.0 ± 0.2 nm and CdSe doped with 1% cobalt ions of similar size. The quantum dots are surface modified using mercaptoacetic acid (MAA) in order to be biocompatible and water-soluble. The MAA-QDs were given to the mice orally at doses of 500, 1000, and 2000 mg/kg by weight of MAA-QDs. Bone marrow and liver samples were collected after two and seven days of treatment. The results indicated that after two days of treatment, the high dose of doped MAA-QDs was significantly able to induce DNA damage, formation of micronuclei (MNs), and generation of DNA adduct (8-hydroxy-2-deoxyguanosine, 8-OHdG). However, increasing DNA damage and the frequency of MNs formation as well as the generation of DNA adducts were observed with both the undoped MAA-QDs (2000 mg/kg) and doped MAA-QDs (1000 and 2000 mg/kg) after seven days of treatment. The results of our study indicate that exposure to high doses of pure MAA-QDs or MAA-QDs doped with cobalt has the potential to cause indirect in vivo genetic damage, which may be attributed to free radical-induced oxidative stress in mice.

  15. Ultrasensitive sandwich-type photoelectrochemical immunosensor based on CdSe sensitized La-TiO2 matrix and signal amplification of polystyrene@Ab2 composites.

    PubMed

    Fan, Dawei; Ren, Xiang; Wang, Haoyuan; Wu, Dan; Zhao, Di; Chen, Yucheng; Wei, Qin; Du, Bin

    2017-01-15

    A novel and sensitive sandwich-type photoelectrochemical (PEC) sensor was fabricated using signal amplification strategy for the quantitative detection of the prostate specific antigen (PSA). CdSe nanoparticles (NPs) sensitized lanthanum-doped titanium dioxide (La-TiO2) composites were used to bind the primary antibodies (Ab1). The doping of lanthanum promoted the visible light absorption of TiO2 and remarkably enhanced the photocurrent. Moreover, 0.3%La-TiO2 displayed the highest photocurrent in the La-TiO2 composites, which was twice as much as that of undoped TiO2. Carboxyl modified CdSe NPs were assembled onto La-TiO2 composites via the dentate binding between -COOH and Ti atom in TiO2 NPs, which dramatically promoted the photocurrent intensity by approximately 2.1 times. Carboxyl functionalized polystyrene (PS) microspheres were coated with the secondary antibodies (Ab2). Owing to the better insulation property and steric hindrance of the prepared polystyrene@Ab2 (PS@Ab2) composites, the significant reduction of the photocurrent signal was achieved after the specific immune recognition. Under the optimum experimental conditions, the fabricated PEC sensor realized ultrasensitive detection of PSA in the range of 0.05-100pgmL(-1) with a detection limit of 17fgmL(-1). Moreover, this well-designed PEC immunoassay exhibited ideal reproducibility, stability, and selectivity, which is a promising platform for the detection of other important tumor targets.

  16. Non-injection and one-pot approach to CdSe: Eu3+ hybrid nanocrystals with tunable photoluminescence from green to red

    NASA Astrophysics Data System (ADS)

    Kong, Lingcan; Chu, Xuefeng; Wang, Chuanxi; Yang, Xiaotian; Zhou, Lei

    2017-01-01

    Europium ion-doped CdSe hybrid nanocrystals (CdSe:Eu3+ NCs) as a class of new luminescent materials have drawn increasing attention in recent years owing to their remarkable optical properties. In this paper, we report a facile method to prepare CdSe:Eu3+ NCs using oleic acid (OA) as the capping agent. With this non-injection and one-pot synthesized approach, the formation and surface passivation of CdSe:Eu3+ NCs are performed simultaneously and result in intrinsic luminescence. The as-prepared CdSe:Eu3+ NCs are characterized by transmission electron microscopy, X-ray diffraction, and energy-dispersive X-ray spectroscopy (EDX). Their optical properties are also studied by UV-vis and photoluminescence spectra. Moreover, the effects of feed ratios and reaction temperatures on the optical properties are further investigated. The results show that the luminescent spectra of CdSe:Eu3+ NCs are tunable from green (490 nm) to red (630 nm) and gradually redshift with the increase of the nanoparticle size from 2.5 to 4.4 nm. Upon decoration with 2-thenoyltrifluoroacetone (TTA), the luminescence of europium ion drastically increases and efficient energy transfer from CdSe host to the europium ion is proposed. In addition, an MTT and apoptosis assay show CdSe:Eu3+ NCs have low cellular toxicity and could be used as fluorescence imaging for human epithelial type 2 (Hep-2) cells. These properties make CdSe:Eu3+ NCs a potential candidate for biological labeling, immunoassays, and optical sensing.

  17. Novel electrochemical biosensor based on PVP capped CoFe2O4@CdSe core-shell nanoparticles modified electrode for ultra-trace level determination of rifampicin by square wave adsorptive stripping voltammetry.

    PubMed

    Asadpour-Zeynali, Karim; Mollarasouli, Fariba

    2017-06-15

    This work introduces a new electrochemical sensor based on polyvinyl pyrrolidone capped CoFe2O4@CdSe core-shell modified electrode for a rapid detection and highly sensitive determination of rifampicin (RIF) by square wave adsorptive stripping voltammetry. The new PVP capped CoFe2O4@CdSe with core-shell nanostructure was synthesized by a facile synthesis method for the first time. PVP can act as a capping and etching agent for protection of the outer surface nanoparticles and formation of a mesoporous shell, respectively. Another important feature of this work is the choice of the ligand (1,10-phenanthroline) for precursor cadmium complex that works as a chelating agent in order to increase optical and electrical properties and stability of prepared nanomaterial. The nanoparticles have been characterized by field emission scanning electron microscopy (FESEM), transmission electron microscope (TEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), UV-vis, photoluminescence (PL) spectroscopy, FT-IR, and cyclic voltammetry techniques. The PL spectroscopy study of CoFe2O4@CdSe has shown significant PL quenching by the formation of CoFe2O4 core inside CdSe, this shows that CoFe2O4 NPs are efficient electron acceptors with the CdSe. It is clearly observed that the biosensor can significantly enhance electrocatalytic activity towards the oxidation of RIF, under the optimal conditions. The novelty of this work arises from the new synthesis method for the core-shell of CoFe2O4@CdSe. Then, the novel electrochemical biosensor was fabricated for ultra-trace level determination of rifampicin with very low detection limit (4.55×10(-17)M) and a wide linear range from 1.0×10(-16) to 1.0×10(-7)M. The fabricated biosensor showed high sensitivity and selectivity, good reproducibility and stability. Therefore, it was successfully applied for the determination of ultra-trace RIF amounts in biological and pharmaceutical samples with satisfactory recovery data.

  18. Detección y estudio mediante Fluorescencia Inducida por Láser de radicales libres formados por Disociación Multifotónica Infrarroja

    NASA Astrophysics Data System (ADS)

    Santos, M.; Díaz, L.; Torresano, J. A.; Rubio, L.; Samoudi, B.

    Una de las principales aplicaciones actuales de los procesos de disociación multifotónica inducidos por radiación láser infrarroja (DMI) es la producción de radiales libres, con el fin de estudiar sus propiedades cinéticas y espectroscópicas. La disociación de moléculas poliatómicas en el IR con láseres de CO2 tiene lugar desde la superficie de energía molecular mas baja y conduce generalmente a la formación de fragmentos en el estado electrónico fundamental, con diversos grados de excitación vibracional. En el Grupo de Procesos Multifotónicos del Instituto de Estructura de la Materia del C.S.I.C. hemos puesto a punto la técnica de Fluorescencia Inducida por Láser (LIF) para la detección y análisis en tiempo real de los fragmentos producidos en la DMI inducida mediante uno o dos campos láseres de diferentes longitudes de onda. Objetivos de nuestro trabajo han sido el estudio de los canales de disociación mayoritarios y de las especies transitoria producidas, así como de la distribución de energía interna con que éstas son generadas. En particular hemos detectado mediante LIF las especies: C2, CF, CH, SiH2, CF2, CH2, SiHCl, y CF3 a partir de la disociación de, entre otras, las siguientes moléculas: C2H3Br, C3F6, C4H8Si, C2H5ClSi y CH5ClSi. En este trabajo presentamos algunos de los resultados obtenidos mediante el estudio por LIF de estos radicales: estudio temporal de la señal LIF obtenida con determinación de tiempos de vida, espectros de excitación y fluorescencia, temperaturas vibracionales de formación, variación de la intensidad LIF con el tiempo de retraso entre los láseres de disociación y prueba, etc.

  19. A strategy to boost the cell performance of CdSexTe1-x quantum dot sensitized solar cells over 8% by introducing Mn modified CdSe coating layer

    NASA Astrophysics Data System (ADS)

    Wang, Guoshuai; Wei, Huiyun; Luo, Yanhong; Wu, Huijue; Li, Dongmei; Zhong, Xinhua; Meng, Qingbo

    2016-01-01

    CdSexTe1-x alloyed colloidal quantum dots show great potential application on quantum dot-sensitized solar cells (QDSCs) due to its relatively wide light absorption range and high chemical stability. In this respect, a thin Mn modified CdSe layer is introduced into TiO2/CdSexTe1-x alloyed QDs surface via a simple chemical bath deposition method (CBD) in order to further improve the cell performance. The power conversion efficiency of CdSexTe1-x QDSCs has been improved to 8.14%. Detailed investigation on the influence of this modification toward the TiO2/CdSexTe1-x interface on the cell performance reveals that introduction of Mn into CdSe QDs is found to facilitate the Mn-doped CdSe deposition and improve the light absorption of the device. In the meantime, the existence of the (Mn-)CdSe layer can also work as a passivation layer to reduce charge recombination.

  20. The influence of surface passivation on electronic energy relaxation dynamics of CdSe and CdSe/CdS nanocrystals studied using visible and near infrared transient absorption spectroscopy.

    PubMed

    Yi, Chongyue; Knappenberger, Kenneth L

    2015-03-19

    Charge carrier relaxation dynamics of electronically excited CdSe and CdSe/CdS core/shell nanocrystals (NCs) were studied using femtosecond time-resolved transient absorption spectroscopy, employing both visible and near-infrared (NIR) probe laser pulses. Following 400 nm excitation, the combination of visible and NIR laser probe pulses were used to determine the influence of surface passivation on electronic relaxation dynamics for nanocrystals overcoated with either organic ligands or inorganic semiconductors. In particular, low-energy NIR photons were used to isolate transient absorption signals due to either electron and hole intraband transitions. Four relaxation components were detected for CdSe NCs passivated by organic molecules: (1) picosecond hole relaxation; (2) electron deep trapping; (3) electron surface trapping; and (4) exciton radiative recombination. Based on TA data collected over a broad energy range, electron deep trapping at Se(2-) sites was suppressed for CdSe NCs passivated by inorganic (CdS) semiconducting materials. By comparing the time-dependent transient absorption data of a series of CdSe/CdS NCs with different shell thicknesses, evidence for the transition from Type-I to quasi Type-II NCs was obtained. These data illustrate the sensitivity of femtosecond time-resolved transient absorption measurements carried out over visible and near infrared probe energies for determining the influence of nanocrystal structure on electronic relaxation dynamics.

  1. Analysis of the electrodeposition and surface chemistry of CdTe, CdSe, and CdS thin films through substrate-overlayer surface-enhanced Raman spectroscopy.

    PubMed

    Gu, Junsi; Fahrenkrug, Eli; Maldonado, Stephen

    2014-09-02

    The substrate-overlayer approach has been used to acquire surface enhanced Raman spectra (SERS) during and after electrochemical atomic layer deposition (ECALD) of CdSe, CdTe, and CdS thin films. The collected data suggest that SERS measurements performed with off-resonance (i.e. far from the surface plasmonic wavelength of the underlying SERS substrate) laser excitation do not introduce perturbations to the ECALD processes. Spectra acquired in this way afford rapid insight on the quality of the semiconductor film during the course of an ECALD process. For example, SERS data are used to highlight ECALD conditions that yield crystalline CdSe and CdS films. In contrast, SERS measurements with short wavelength laser excitation show evidence of photoelectrochemical effects that were not germane to the intended ECALD process. Using the semiconductor films prepared by ECALD, the substrate-overlayer SERS approach also affords analysis of semiconductor surface adsorbates. Specifically, Raman spectra of benzenethiol adsorbed onto CdSe, CdTe, and CdS films are detailed. Spectral shifts in the vibronic features of adsorbate bonding suggest subtle differences in substrate-adsorbate interactions, highlighting the sensitivity of this methodology.

  2. Directional charge transfer mediated by mid-gap states: A transient absorption spectroscopy study of CdSe quantum dot/β-Pb0.33V2O5 heterostructures

    DOE PAGES

    Milleville, Christopher C.; Pelcher, Kate E.; Sfeir, Matthew Y.; ...

    2016-02-15

    For solar energy conversion, not only must a semiconductor absorb incident solar radiation efficiently but also its photoexcited electron—hole pairs must further be separated and transported across interfaces. Charge transfer across interfaces requires consideration of both thermodynamic driving forces as well as the competing kinetics of multiple possible transfer, cooling, and recombination pathways. In this work, we demonstrate a novel strategy for extracting holes from photoexcited CdSe quantum dots (QDs) based on interfacing with β-Pb0.33V2O5 nanowires that have strategically positioned midgap states derived from the intercalating Pb2+ ions. Unlike midgap states derived from defects or dopants, the states utilized heremore » are derived from the intrinsic crystal structure and are thus homogeneously distributed across the material. CdSe/β-Pb0.33V2O5 heterostructures were assembled using two distinct methods: successive ionic layer adsorption and reaction (SILAR) and linker-assisted assembly (LAA). Transient absorption spectroscopy measurements indicate that, for both types of heterostructures, photoexcitation of CdSe QDs was followed by the transfer of electrons to the conduction band of β-Pb0.33V2O5 nanowires and holes to the midgap states of β-Pb0.33V2O5 nanowires. Holes were transferred on time scales less than 1 ps, whereas electrons were transferred more slowly on time scales of ~2 ps. In contrast, for analogous heterostructures consisting of CdSe QDs interfaced with V2O5 nanowires (wherein midgap states are absent), only electron transfer was observed. Interestingly, electron transfer was readily achieved for CdSe QDs interfaced with V2O5 nanowires by the SILAR method; however, for interfaces incorporating molecular linkers, electron transfer was observed only upon excitation at energies substantially greater than the bandgap absorption threshold of CdSe. Furthermore, transient absorbance decay traces reveal longer excited-state lifetimes (1–3

  3. Rapid and One-Pot Synthesis of Self-Assembled CdSe Quantum Dots Functionalized with β-Cyclodextrin: Reduced Cytotoxicity and Band Gap Engineering.

    PubMed

    Guleria, Apurav; Rath, Madhab C; Singh, Ajay K; Adhikari, Soumyakanti

    2015-12-01

    We report a simple, rapid and one step method for the synthesis and in situ functionalization of CdSe quantum dots (QDs) with β-cyclodextrin (β-CD) in aqueous solution via electron beam (EB) irradiation technique. A probable mechanism has been elucidated for the formation of the QDs using pulse radiolysis technique. The average size of the QDs was found to be in the range of 2-3 nm with a size distribution of -14%. XPS measurements indicate that the -OH groups of the β-CD molecules binds predominantly with the Cd atoms present on the surface of the QDs. These QDs displayed broad photoluminescence (PL) with two emission peaks at 525 nm and 600 nm, which could be tuned by varying the experimental parameters. The broad PL spectrum has been attributed to the polydispersity in the density and the distribution of trap/defects states. Time resolved PL decay measurements further substantiated the domination of surface state originated carrier relaxation processes in the overall PL decay dynamics of QDs synthesized at higher doses and dose rates. The present study reveals that β-CD passivate the QDs by a non-inclusion complex, induces the self-assembling process into a networking architecture and simultaneously reduces their cytotoxicity as compared to the bare nanoparticles. The methodology described in this article may provide unique and interesting aspects to regulate and fine tune the formation of superstructures of nanomaterials vis-à-vis their optoelectronic properties.

  4. Gamma-radiation synthesis of silk fibroin coated CdSe quantum dots and their biocompatibility and photostability in living cells.

    PubMed

    Chang, Shu-Quan; Dai, Yao-Dong; Kang, Bin; Han, Wei; Chen, Da

    2009-10-01

    Silk fibroin coated CdSe quantum dots (SF-CdSe QDs) were successfully synthesized via a one-step gamma-radiation route in an aqueous system at room temperature. The as prepared products were characterized by transmission electron microscope (TEM), energy dispersion spectrum (EDS), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectrometer (FT-IR), X-ray diffraction (XRD), ultraviolet-visible spectroscopy (UV-vis) and photoluminescence spectrum (PL). The SF-CdSe QDs were about 5 nm in diameter and exhibited excellent water-solubility and photoluminescence properties. The cellular distribution, photostability and cytotoxicity of SF-CdSe QDs with different amount of SF coatings were also investigated by laser scanning confocal microscope (LSCM) and MTT assays in human pancreatic carcinoma (PANC-1) cells. All the results reveal that these QDs could be easily internalized by cells and localized in cytoplasm around nuclei. Moreover, SF-CdSe QDs were proved to be low cytotoxicity (the concentration of QDs < 5 microg mL(-1)) and high photostability (the illumination energy density < 2 x 10(-5) W microm(-2)) within PANC-1 cells, which was mainly due to the biocompatible silk fibroin. The resulted SF-CdSe QDs might have many potential applications in tumor imaging and therapy. And the synthesis strategy could be easily extended to fabrication of other nanoparticles coated with silk fibroin.

  5. Synthesis of 2-Mercaptonicotinic Acid-Capped CdSe Quantum Dots and its Application to Spectrofluorometric Determination of Cr(VI) in Water Samples.

    PubMed

    Hosseini, Mohammad Saeid; Khorashahi, Somayeh; Hosseini, Navid

    2016-05-01

    The CdSe quantum dots (QDs) capped with 2-mercaptonicotinic acid (H2MN) were prepared through a controllable process at 80 °C. The prepared QDs were characterized by XRD, TEM, IR, UV-Vis and fluorescence (FL) techniques. It was found that the QDs were nearly mono-disperse with the diameters in the range of 8-10 nm. These QDs are capable to exhibit strong FL even in concentrated acidic media. They exhibit an enhanced fluorescence in the presence of Cr(VI), which was used for the determination of Cr(VI) in water samples. The linear range was found to be 1 × 10(-7)-6.0 × 10(-6) M with the RSD and DL of 0.92 % and 5 × 10(-8) M, respectively. Except that Ca(2+) and Fe(3+) which can be eliminated through a simple precipitation process, the other co-existent ions present in natural water were not interfered. The recoveries obtained for the added amounts of Cr(VI) were in the range of 96.9-103.2 %, which denote on application of the method, satisfactorily.

  6. Controllable in situ photo-assisted chemical deposition of CdSe quantum dots on ZnO/CdS nanorod arrays and its photovoltaic application

    NASA Astrophysics Data System (ADS)

    Wang, Xinwei; Liu, Hong; Shen, Wenzhong

    2016-02-01

    Compound semiconductors have been widely applied in the energy field as light-harvesting materials, conducting substrates and other functional parts. Nevertheless, to effectively grow them in various forms toward objective applications, limitations have often been met to achieving high growth rate, simplicity of method and controllability of growing processes simultaneously. In this work, we have grown a uniform CdSe layer on ZnO/CdS nanorod arrays by a novel in situ photo-assisted chemical deposition method. The morphology and quality of the as-formed material could be significantly influenced by tuning the optical parameters of the injected light. Due to the effect of injected light on the key reactions during the growth, a modified natural light with removal of the UV and IR components seems to be more suitable than monochromic light. An efficiency of 3.59% was achieved without any additional treatment, significantly higher than the efficiency of 2.88% of the sample by conventional CBD method under similar conditions with growth rate one order of magnitude higher. In general, the result has suggested its potential importance for other compound materials and opto-electronic devices.

  7. Transient photoconductivity in CdSe nanoparticles and nanocrystalline TiO2 as measured by time-resolved terahertz spectroscopy

    NASA Astrophysics Data System (ADS)

    Schmuttenmaer, Charles A.; Turner, Gordon M.; Beard, Matthew C.

    2003-12-01

    The transient photoconductivity of dye-sensitized nanocrystalline colloidal TiO2 has been measured time-resolved THz spectroscopy (TRTS), a non-contact electrical probe with sub-picosecond temporal resolution. The photoconductivity deviates strongly from Drude behavior and is explained by disorder-induced carrier localization and/or backscattering of the photogenerated carriers. In addition, the carriers are found to thermally equilibrate with the lattice in roughly 300 femtoseconds. The size-dependent photoconductivity of CdSe nanoparticles ranging from 2.54 nm up to >25 nm has also been measured using TRTS. The measured change in the frequency-dependent optical density and change in phase of the transmitted THz pulse fall into three distinct groupings as a function of size and can be classified for diameters smaller than the Bohr exciton radius, diameters greater than the Bohr exciton radius but smaller than the bulk mean free path, and diameters greater than the bulk mean free path. The underlying cause of the grouping is a size-dependent mobility (or carrier scattering rate).

  8. Factors determining the photovoltaic performance of a CdSe quantum dot sensitized solar cell: the role of the linker molecule and of the counter electrode.

    PubMed

    Mora-Seró, Iván; Giménez, Sixto; Moehl, Thomas; Fabregat-Santiago, Francisco; Lana-Villareal, Teresa; Gómez, Roberto; Bisquert, Juan

    2008-10-22

    Colloidal CdSe quantum dots (QDs) of different sizes, prepared by a solvothermal route, have been employed as sensitizers of nanostructured TiO(2) electrode based solar cells. Three different bifunctional linker molecules have been used to attach colloidal QDs to the TiO(2) surface: mercaptopropionic acid (MPA), thioglycolic acid (TGA), and cysteine. The linker molecule plays a determinant role in the solar cell performance, as illustrated by the fact that the incident photon to charge carrier generation efficiency (IPCE) could be improved by a factor of 5-6 by using cysteine with respect to MPA. The photovoltaic properties of QD sensitized electrodes have been characterized for both three-electrode and closed two-electrode solar cell configurations. For three-electrode measurement a maximum power conversion efficiency near 1% can be deduced, but this efficiency is halved in the closed cell configuration mainly due to the decrease of the fill factor (FF).

  9. Controlled electrodeposition of bismuth nanocatalysts for the solution-liquid-solid synthesis of CdSe nanowires on transparent conductive substrates.

    PubMed

    Reim, Natalia; Littig, Alexander; Behn, Dino; Mews, Alf

    2013-12-11

    Semiconductor nanowires (NWs) composed of cadmium selenide (CdSe) have been directly grown on transparent conductive substrates via the solution-liquid-solid (SLS) approach using electrodeposited bismuth nanoparticles (Bi NPs) as catalyst. Bi NPs were fabricated on indium tin oxide (ITO) surfaces from a bismuth trichloride solution using potentiostatic double-pulse techniques. The size and density of electrodeposited Bi NPs were controlled by the pulse parameters. Since the NW diameter is governed by the dimension of the Bi catalyst, the electrodeposition is a reliable method to synthesize nanowires directly on substrates with a desired size and density. We show that the density can be adjusted from individual NWs on several square micrometer to very dense NW networks. The diameter can be controlled between thick nanowires above 100 nm to very thin NW of 7 nm in diameter, which is well below the respective exciton dimension. Hence, especially the thinnest NWs exhibit diameter-dependent photoluminescence energies as a result of quantum confinement effects in the radial dimension.

  10. Direct spectroscopic evidence of ultrafast electron transfer from a low band gap polymer to CdSe quantum dots in hybrid photovoltaic thin films.

    PubMed

    Couderc, Elsa; Greaney, Matthew J; Brutchey, Richard L; Bradforth, Stephen E

    2013-12-11

    Ultrafast transient absorption spectroscopy is used to study charge transfer dynamics in hybrid films composed of the low band gap polymer PCPDTBT and CdSe quantum dots capped with tert-butylthiol ligands. By selectively exciting the polymer, a spectral signature for electrons on the quantum dots appears on ultrafast time scales (≲ 65 fs), which indicates ultrafast electron transfer. From this time scale, the coupling between the polymer chains and the quantum dots is estimated to be J ≳ 17 meV. The reduced quantum dot acceptors exhibit an unambiguous spectral bleach signature, whose amplitude allows for the first direct calculation of the absolute electron transfer yield in a hybrid solar cell (82 ± 5%). We also show that a limitation of the hybrid system is rapid and measurable geminate recombination due to the small separation of the initial charge pair. The fast recombination is consistent with the internal quantum efficiency of the corresponding solar cell. We therefore have identified and quantified a main loss mechanism in this type of third generation solar cell.

  11. Size and Temperature Dependence of Electron Transfer between CdSe Quantum Dots and a TiO 2 Nanobelt

    SciTech Connect

    Tafen, De Nyago; Prezhdo, Oleg V.

    2015-02-24

    Understanding charge transfer reactions between quantum dots (QD) and metal oxides is fundamental for improving photocatalytic, photovoltaic and electronic devices. The complexity of these processes makes it difficult to find an optimum QD size with rapid charge injection and low recombination. We combine time-domain density functional theory with nonadiabatic molecular dynamics to investigate the size and temperature dependence of the experimentally studied electron transfer and charge recombination at CdSe QD-TiO2 nanobelt (NB) interfaces. The electron injection rate shows strong dependence on the QD size, increasing for small QDs. The rate exhibits Arrhenius temperature dependence, with the activation energy of the order of millielectronvolts. The charge recombination process occurs due to coupling of the electronic subsystem to vibrational modes of the TiO2 NB. Inelastic electron-phonon scattering happens on a picosecond time scale, with strong dependence on the QD size. Our simulations demonstrate that the electron-hole recombination rate decreases significantly as the QD size increases, in excellent agreement with experiments. The temperature dependence of the charge recombination rates can be successfully modeled within the framework of the Marcus theory through optimization of the electronic coupling and the reorganization energy. Our simulations indicate that by varying the QD size, one can modulate the photoinduced charge separation and charge recombination, fundamental aspects of the design principles for high efficiency devices.

  12. Electronic structure and properties of Cd4As2Br3 and Cd4Sb2I3, analogues of CdSe and CdTe

    NASA Astrophysics Data System (ADS)

    Roy, Anand; Suchitra; Manjunath, K.; Ahmad, Tokeer; Waghmare, Umesh V.; Rao, C. N. R.

    2017-04-01

    Substitution of aliovalent anions in metal oxides and chalcogenides significantly affects the electronic structure and properties of the materials. Thus, substitution of P3- and Cl- in CdS decreases the band gap and favorably influences the photocatalytic activity. Complete substitution of a trivalent (A3-) and a monovalent (B-) anions in a cadmium chalcogenides, CdX, should give rise to a material of the composition Cd A0.5B0.5 or Cd2AB, but a compound with the composition Cd4P2Cl3 (or Cd2PCl1.5) is obtained in the case of CdS. We have investigated the analogous compounds, Cd4As2Br3 and Cd4Sb2I3, wherein the anions in CdSe and CdTe are substituted by As, Br and Sb, I respectively. These compounds are direct band gap semiconductors with a band gap of 1.8-1.9 eV and a photoluminescence band in the visible region. First-principles calculations show both Cd4As2Br3 and Cd4Sb2I3 to be direct band gap semiconductors. The arsenic bromide is predicted to be photochemically more active for HER than the antimony iodide.

  13. Charge carrier resolved relaxation of the first excitonic state in CdSe quantum dots probed with near-infrared transient absorption spectroscopy.

    PubMed

    McArthur, Eric A; Morris-Cohen, Adam J; Knowles, Kathryn E; Weiss, Emily A

    2010-11-18

    This manuscript describes a global regression analysis of near-infrared (NIR, 900-1300 nm) transient absorptions (TA) of colloidal CdSe quantum dots (QDs) photoexcited to their first (1S(e)1S(3/2)) excitonic state. Near-IR TA spectroscopy facilitates charge carrier-resolved analysis of excitonic decay of QDs because signals in the NIR are due exclusively to absorptions of photoexcited electrons and holes, as probe energies in this region are not high enough to induce absorptions across the optical bandgap that crowd the visible TA spectra. The response of each observed component of the excitonic decay to the presence of a hole-trapping ligand (1-octanethiol) and an electron-accepting ligand (1,4-benzoquinone), and comparison of time constants to those for recovery of the ground state bleaching feature in the visible TA spectrum, allow for the assignment of the components to (i) a 1.6 ps hole trapping process, (ii) 19 ps and 274 ps surface-mediated electron trapping processes, and (iii) a ∼5 ns recombination of untrapped electrons.

  14. Controlled growth of high-density CdS and CdSe nanorod arrays on selective facets of two-dimensional semiconductor nanoplates

    NASA Astrophysics Data System (ADS)

    Wu, Xue-Jun; Chen, Junze; Tan, Chaoliang; Zhu, Yihan; Han, Yu; Zhang, Hua

    2016-05-01

    The rational synthesis of hierarchical three-dimensional nanostructures with specific compositions, morphologies and functionalities is important for applications in a variety of fields ranging from energy conversion and electronics to biotechnology. Here, we report a seeded growth approach for the controlled epitaxial growth of three types of hierarchical one-dimensional (1D)/two-dimensional (2D) nanostructures, where nanorod arrays of II-VI semiconductor CdS or CdSe are grown on the selective facets of hexagonal-shaped nanoplates, either on the two basal facets of the nanoplate, or on one basal facet, or on the two basal facets and six side facets. The seed engineering of 2D hexagonal-shaped nanoplates is the key factor for growth of the three resulting types of 1D/2D nanostructures. The wurtzite- and zinc-blende-type polymorphs of semiconductors are used to determine the facet-selective epitaxial growth of 1D nanorod arrays, resulting in the formation of different hierarchical three-dimensional (3D) nanostructures.

  15. Directional charge transfer mediated by mid-gap states: A transient absorption spectroscopy study of CdSe quantum dot/β-Pb0.33V2O5 heterostructures

    SciTech Connect

    Milleville, Christopher C.; Pelcher, Kate E.; Sfeir, Matthew Y.; Banerjee, Sarbajit; Watson, David F.

    2016-02-15

    For solar energy conversion, not only must a semiconductor absorb incident solar radiation efficiently but also its photoexcited electron—hole pairs must further be separated and transported across interfaces. Charge transfer across interfaces requires consideration of both thermodynamic driving forces as well as the competing kinetics of multiple possible transfer, cooling, and recombination pathways. In this work, we demonstrate a novel strategy for extracting holes from photoexcited CdSe quantum dots (QDs) based on interfacing with β-Pb0.33V2O5 nanowires that have strategically positioned midgap states derived from the intercalating Pb2+ ions. Unlike midgap states derived from defects or dopants, the states utilized here are derived from the intrinsic crystal structure and are thus homogeneously distributed across the material. CdSe/β-Pb0.33V2O5 heterostructures were assembled using two distinct methods: successive ionic layer adsorption and reaction (SILAR) and linker-assisted assembly (LAA). Transient absorption spectroscopy measurements indicate that, for both types of heterostructures, photoexcitation of CdSe QDs was followed by the transfer of electrons to the conduction band of β-Pb0.33V2O5 nanowires and holes to the midgap states of β-Pb0.33V2O5 nanowires. Holes were transferred on time scales less than 1 ps, whereas electrons were transferred more slowly on time scales of ~2 ps. In contrast, for analogous heterostructures consisting of CdSe QDs interfaced with V2O5 nanowires (wherein midgap states are absent), only electron transfer was observed. Interestingly, electron transfer was readily achieved for CdSe QDs interfaced with V2O5 nanowires by the SILAR method; however, for interfaces incorporating molecular linkers, electron transfer was observed only upon

  16. Lattice location and local magnetism of recoil implanted Fe impurities in wide and narrow band semiconductors CdTe, CdSe, and InSb: Experiment and theory

    SciTech Connect

    Mohanta, S. K.; Mishra, S. N.

    2014-05-07

    Employing the time differential perturbed angular distribution method, we have measured local susceptibility and spin relaxation rate of {sup 54}Fe nuclei implanted in III-V and II-VI semiconductors, CdTe, CdSe, and InSb. The magnetic response of Fe, identified to occupy the metal as well as the semi-metal atom sites, exhibit Curie-Weiss type susceptibility and Korringa like spin relaxation rate, revealing the existence of localized moments with small spin fluctuation temperature. The experimental results are supported by first principle electronic structure calculations performed within the frame work of density functional theory.

  17. Electron beam induced and microemulsion templated synthesis of CdSe quantum dots: tunable broadband emission and charge carrier recombination dynamics

    NASA Astrophysics Data System (ADS)

    Guleria, Apurav; Singh, Ajay K.; Rath, Madhab C.; Adhikari, Soumyakanti

    2015-04-01

    CdSe quantum dots (QDs) were synthesized by a rapid and one step templated approach inside the water pool of AOT (sodium bis(2-ethylhexyl) sulfosuccinate) based water-in-oil microemulsions (MEs) via electron beam (EB) irradiation technique with high dose rate, which favours high nucleation rate. The interplay of different experimental parameters such as precursor concentration, absorbed dose and {{W}0} values (aqueous phase to surfactant molar ratio) of MEs were found to have interesting consequences on the morphology, photoluminescence (PL), surface composition and carrier recombination dynamics of as-grown QDs. For instance, highly stable ultrasmall (∼1.7 nm) bluish-white light emitting QDs were obtained with quantum efficiency (η) of ∼9%. Furthermore, QDs were found to exhibit tunable broadband light emission extending from 450 to 750 nm (maximum FWHM ∼180 nm). This could be realized from the CIE (Commission Internationale d’Eclairage) chromaticity co-ordinates, which varied across the blue region to the orange region thereby, conferring their potential application in white light emitting diodes. Additionally, the average PL lifetime ≤ft( ≤ft< τ \\right> \\right) values could be varied from 18 ns to as high as 74 ns, which reflect the role of surface states in terms of their density and distribution. Another interesting revelation was the self-assembling of the initially formed QDs into nanorods with high aspect ratios ranging from 7 to 20, in correspondence with the {{W}0} values. Besides, the fundamental roles of the chemical nature of water pool and the interfacial fluidity of AOT MEs in influencing the photophysical properties of QDs were investigated by carrying out a similar study in CTAB (cetyltrimethylammonium bromide; cationic surfactant) based MEs. Surprisingly, very profound and contrasting results were observed wherein ≤ft< τ \\right> and η of the QDs in case of CTAB MEs were found to be at least three times lower as compared to

  18. Seed-mediated synthesis, properties and application of {gamma}-Fe{sub 2}O{sub 3}-CdSe magnetic quantum dots

    SciTech Connect

    Lin, Alex W.H.; Ang, Chung Yen; Patra, Pranab K.; Han Yu; Gu Hongwei; Le Breton, Jean-Marie; Juraszek, Jean; Chiron, Hubert; Papaefthymiou, Georgia C.; Tamil Selvan, Subramanian; Ying, Jackie Y.

    2011-08-15

    Seed-mediated growth of fluorescent CdSe quantum dots (QDs) around {gamma}-Fe{sub 2}O{sub 3} magnetic cores was performed at high temperature (300 deg. C) in the presence of organic surfactants. Bi-functional magnetic quantum dots (MQDs) with tunable emission properties were successfully prepared. The as-synthesized MQDs were characterized by high-resolution transmission electron microscopy (HRTEM) and dynamic light scattering (DLS), which confirmed the assembly of heterodimers. When a longer growth period was employed, a homogeneous dispersion of QDs around a magnetic nanoparticle was obtained. The magnetic properties of these nanocomposites were examined. The MQDs were superparamagnetic with a saturation magnetization of 0.40 emu/g and a coercivity of 138 Oe at 5 K. To demonstrate their potential application in bio-labeling, these MQDs were coated with a thin silica shell, and functionalized with a polyethylene glycol (PEG) derivative. The functionalized MQDs were effectively used for the labeling of live cell membranes of 4T1 mouse breast cancer cells and HepG2 human liver cancer cells. - Graphical abstract: (a) HRTEM image of oleic acid capped MPs. The size of MPs ranges from 8 to 10 nm. (b) XRD pattern of {gamma}-Fe{sub 2}O{sub 3} MPs. Highlights: > The fabrication of MQDs through a seed-mediated approach has been demonstrated. > The formation and assembly of these bi-functional nanocomposites have been elucidated. > The MQDs exhibit superparamagnetism and tunable emissions characteristic of the components. > MQDs with thin silica coating were successfully employed in the labeling of cancer cell membranes.

  19. Structural and size effects on the spectroscopic and redox properties of CdSe nanocrystals in solution: the role of defect states.

    PubMed

    Amelia, Matteo; Impellizzeri, Stefania; Monaco, Simone; Yildiz, Ibrahim; Silvi, Serena; Raymo, Françisco M; Credi, Alberto

    2011-08-22

    Two series of CdSe quantum dots (QDs) with different diameters are prepared, according to frequently used protocols of the same synthetic procedure. For each sample the photophysical properties and the potentials for the first reduction and oxidation processes in organic solution are determined. The band gap obtained from electrochemical experiments is compared with that determined from the absorption and luminescence spectra. While the optical band gap decreases upon increasing the nanocrystal diameter, as expected on the basis of quantum confinement, the redox potentials and the electrochemical band gap are not monotonously related to the QD size. For both series, the smallest and largest QDs are both easier to oxidize and reduce than mid-sized QDs. In fact, the latter samples exhibit very broad voltammetric profiles, which suggests that the heterogeneous electron-transfer processes from/to the electrode are kinetically hindered. Conversely, the electrochemical band gap for the smallest and largest particles of each series is somewhat smaller than the optical band gap. These results indicate that, while the optical band gap depends on the actual electron-hole recombination within the nanocrystal, and therefore follows the size dependence expected from the particle-in-a-box model, the electrochemical processes of these QDs are strongly affected by other factors, such as the presence of surface defects. The investigations suggest that the influence of these defects on the potential values is more important for the smallest and largest QDs of each series, as confirmed by the respective luminescence bands and quantum yields. An interpretation for the size-dependent evolution of the surface defects in these nanocrystals is proposed based on the mechanism of their formation and growth.

  20. The in vivo biodistribution and fate of CdSe quantum dots in the murine model: a laser ablation inductively coupled plasma mass spectrometry study.

    PubMed

    Wang, TsingHai; Hsieh, HuiAn; Hsieh, YiKong; Chiang, ChiShiun; Sun, YuhChang; Wang, ChuFang

    2012-12-01

    Understanding the cytotoxicity of quantum dots strongly relies upon the development of new analytical techniques to gather information about various aspects of the system. In this study, we demonstrate the in vivo biodistribution and fate of CdSe quantum dots in the murine model by means of laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). By comparing the hot zones of each element acquired from LA-ICP-MS with those in fluorescence images, together with hematoxylin and eosin-stained images, we are able to perceive the fate and in vivo interactions between quantum dots and rat tissues. One hour after intravenous injection, we found that all of the quantum dots had been concentrated inside the spleen, liver and kidneys, while no quantum dots were found in other tissues (i.e., muscle, brain, lung, etc.). In the spleen, cadmium-114 signals always appeared in conjunction with iron signals, indicating that the quantum dots had been filtered from main vessels and then accumulated inside splenic red pulp. In the liver, the overlapped hot zones of quantum dots and those of phosphorus, copper, and zinc showed that these quantum dots have been retained inside hepatic cells. Importantly, it was noted that in the kidneys, quantum dots went into the cortical areas of adrenal glands. At the same time, hot zones of copper appeared in proximal tubules of the cortex. This could be a sign that the uptake of quantum dots initiates certain immune responses. Interestingly, the intensity of the selenium signals was not proportional to that of cadmium in all tissues. This could be the result of the decomposition of the quantum dots or matrix interference. In conclusion, the advantage in spatial resolution of LA-ICP-MS is one of the most powerful tools to probe the fate, interactions and biodistribution of quantum dots in vivo.

  1. Low cost Schottky barrier solar cells fabricated on CdSe and Sb[sub 2]S[sub 3] films chemically deposited with silicotungstic acid

    SciTech Connect

    Savadogo, O.; Mandal, K.C. . Dept. of Metallurgie et de Genie des Materiaux)

    1994-10-01

    A novel method for fabricating high efficiency metal (Pt, Au, and Ni)/(CdSe or Sb[sub 2]S[sub 3]) Schottky barrier solar cells is reported. The method is based on the fabrication of n-CdSe or Sb[sub 2]S[sub 3] thin films chemically deposited with and without silicotungstic acid (STA). The performances of the Schottky junctions fabricated with the films deposited with STA, CdSe(STA), or Sb[sub 2]S[sub 3](STA), are significantly higher than those deposited without STA. Under AM1 illumination, the photovoltaic properties of the improved Pt/CdSe(STA) diode showed V[sub oc] = 0.72 V, J[sub sc] = 14.1 mA/cm[sup 2], FF [approx equal] 0.70, and efficiency [eta] [approx equal] 7.2%. Analogous results are obtained on Pt/n-Sb[sub 2]S[sub 3](STA), where the photovoltaic response of the improved diode showed V[sub oc] = 0.63 V, J[sub sc] = 11.3 mA/cm[sup 2], FF [approx equal] 0.63, and [eta] [approx equal] 5.5%. The ideality factor (n) and saturation current density (J[sub 0]) were also significantly improved. C-V measurements at 1 MHz showed that the barrier height ([phi][sub b]) of the fabricated diodes are 0.62 and 0.59 eV for Pt/CdSe and Pt-Sb[sub 2]S[sub 3] junctions, respectively, and 0.81 and 0.80 eV for Pt/CdSe(STA) and Pt-Sb[sub 2]S[sub 3](STA) junctions, respectively. It is also observed that the [phi][sub b] values are independent of the metal work functions (W). This is attributed to the Fermi level pinning of CdSe or Sb[sub 2]S[sub 3] films deposited with and without STA.

  2. Structural Insights into the PorK and PorN Components of the Porphyromonas gingivalis Type IX Secretion System

    PubMed Central

    Gorasia, Dhana G.; Veith, Paul D.; Hanssen, Eric G.; Glew, Michelle D.; Sato, Keiko; Yukitake, Hideharu; Nakayama, Koji; Reynolds, Eric C.

    2016-01-01

    The type IX secretion system (T9SS) has been recently discovered and is specific to Bacteroidetes species. Porphyromonas gingivalis, a keystone pathogen for periodontitis, utilizes the T9SS to transport many proteins including the gingipain virulence factors across the outer membrane and attach them to the cell surface via a sortase-like mechanism. At least 11 proteins have been identified as components of the T9SS including PorK, PorL, PorM, PorN and PorP, however the precise roles of most of these proteins have not been elucidated and the structural organization of these components is unknown. In this study, we purified PorK and PorN complexes from P. gingivalis and using electron microscopy we have shown that PorN and the PorK lipoprotein interact to form a 50 nm diameter ring-shaped structure containing approximately 32–36 subunits of each protein. The formation of these rings was dependent on both PorK and PorN, but was independent of PorL, PorM and PorP. PorL and PorM were found to form a separate stable complex. PorK and PorN were protected from proteinase K cleavage when present in undisrupted cells, but were rapidly degraded when the cells were lysed, which together with bioinformatic analyses suggests that these proteins are exposed in the periplasm and anchored to the outer membrane via the PorK lipid. Chemical cross-linking and mass spectrometry analyses confirmed the interaction between PorK and PorN and further revealed that they interact with the PG0189 outer membrane protein. Furthermore, we established that PorN was required for the stable expression of PorK, PorL and PorM. Collectively, these results suggest that the ring-shaped PorK/N complex may form part of the secretion channel of the T9SS. This is the first report showing the structural organization of any T9SS component. PMID:27509186

  3. Structural Insights into the PorK and PorN Components of the Porphyromonas gingivalis Type IX Secretion System.

    PubMed

    Gorasia, Dhana G; Veith, Paul D; Hanssen, Eric G; Glew, Michelle D; Sato, Keiko; Yukitake, Hideharu; Nakayama, Koji; Reynolds, Eric C

    2016-08-01

    The type IX secretion system (T9SS) has been recently discovered and is specific to Bacteroidetes species. Porphyromonas gingivalis, a keystone pathogen for periodontitis, utilizes the T9SS to transport many proteins including the gingipain virulence factors across the outer membrane and attach them to the cell surface via a sortase-like mechanism. At least 11 proteins have been identified as components of the T9SS including PorK, PorL, PorM, PorN and PorP, however the precise roles of most of these proteins have not been elucidated and the structural organization of these components is unknown. In this study, we purified PorK and PorN complexes from P. gingivalis and using electron microscopy we have shown that PorN and the PorK lipoprotein interact to form a 50 nm diameter ring-shaped structure containing approximately 32-36 subunits of each protein. The formation of these rings was dependent on both PorK and PorN, but was independent of PorL, PorM and PorP. PorL and PorM were found to form a separate stable complex. PorK and PorN were protected from proteinase K cleavage when present in undisrupted cells, but were rapidly degraded when the cells were lysed, which together with bioinformatic analyses suggests that these proteins are exposed in the periplasm and anchored to the outer membrane via the PorK lipid. Chemical cross-linking and mass spectrometry analyses confirmed the interaction between PorK and PorN and further revealed that they interact with the PG0189 outer membrane protein. Furthermore, we established that PorN was required for the stable expression of PorK, PorL and PorM. Collectively, these results suggest that the ring-shaped PorK/N complex may form part of the secretion channel of the T9SS. This is the first report showing the structural organization of any T9SS component.

  4. The higher excited electronic states and spin-orbit splitting of the valence band in three-dimensional assemblies of close-packed ZnSe and CdSe quantum dots in thin film form

    SciTech Connect

    Pejova, Biljana

    2008-08-15

    Optical properties of as-deposited and annealed thin films composed of three-dimensional arrays of sphalerite-type ZnSe and CdSe quantum dots (QDs), synthesized by chemical deposition, were investigated. Neglecting the S-D mixing of hole states, the lowest 'band to band' transitions in very small nanoclusters and in bulk-like clusters may be assigned as 1S{yields}1S and 1S{sub {delta}}{yields}1S, and are split by spin-orbit (SO) splitting energy of the bulk material-{delta}. The splitting energy between these transitions was found to be insensitive to QD size variations, which could be explained assuming that 1S hole states arising from valence band {gamma}{sub 7} and {gamma}{sub 8} components do not mix with higher angular momentum states and shift together to higher energies coupled via the isotropic hole mass. This implies significant difference between the SO splitting energies in the two semiconductors. Accounting for S-D mixing of hole states, the observed transitions may be attributed to the fundamental ground state-(1S{sub 3/2}, 1S{sub e}) and the ground state-(1S{sub 1/2}, 1S{sub e}) ones. The observed 'splittings' thus do not correspond exactly to SO splitting energy in both semiconductors, but are complex functions of it, as exact position of each hole energy level depends, besides on {delta}, also on other material-characteristic parameters. - Graphical abstract: Accounting for S-D mixing of hole states, the observed optical transitions in very small sphalerite-type ZnSe and CdSe nanoclusters are attributed to the ground state-(1S{sub 3/2}, 1S{sub e}) and the ground state-(1S{sub 1/2}, 1S{sub e}). The 'splittings' do not correspond to SO splitting energy, but are complex functions of it.

  5. Uniform Thin Films of CdSe and CdSe(ZnS) Core(shell) Quantum Dots by Sol-Gel Assembly: Enabling Photoelectrochemical Characterization and Electronic Applications

    PubMed Central

    Korala, Lasantha; Wang, Zhijie; Liu, Yi; Maldonado, Stephen; Brock, Stephanie L.

    2013-01-01

    Optoelectronic properties of quantum dot (QD) films are limited by (1) poor interfacial chemistry and (2) non-radiative recombination due to surface traps. To address these performance issues, sol-gel methods are applied to fabricate thin films of CdSe and core(shell) CdSe(ZnS) QDs. High-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) imaging with chemical analysis confirms that the surface of the QDs in the sol-gel thin films are chalcogen-rich, consistent with an oxidative-induced gelation mechanism in which connectivity is achieved by formation of dichalcogenide covalent linkages between particles. The ligand removal and assembly process is probed by thermogravimetric, spectroscopic and microscopic studies. Further enhancement of inter-particle coupling via mild thermal annealing, which removes residual ligands and reinforces QD connectivity, results in QD sol-gel thin films with superior charge transport properties, as shown by a dramatic enhancement of electrochemical photocurrent under white light illumination relative to thin films composed of ligand-capped QDs. A more than 2-fold enhancement in photocurrent, and a further increase in photovoltage can be achieved by passivation of surface defects via overcoating with a thin ZnS shell. The ability to tune interfacial and surface characteristics for the optimization of photophysical properties suggests that the sol-gel approach may enable formation of QD thin films suitable for a range of optoelectronic applications. PMID:23350924

  6. Intracellular Biosynthesis of Fluorescent CdSe Quantum Dots in Bacillus subtilis: A Strategy to Construct Signaling Bacterial Probes for Visually Detecting Interaction Between Bacillus subtilis and Staphylococcus aureus.

    PubMed

    Yan, Zheng-Yu; Ai, Xiao-Xia; Su, Yi-Long; Liu, Xin-Ying; Shan, Xiao-Hui; Wu, Sheng-Mei

    2016-02-01

    In this work, fluorescent Bacillus subtilis (B. subtilis) cells were developed as probes for imaging applications and to explore behaviorial interaction between B. subtilis and Staphylococcus aureus (S. aureus). A novel biological strategy of coupling intracellular biochemical reactions for controllable biosynthesis of CdSe quantum dots by living B. subtilis cells was demonstrated, through which highly luminant and photostable fluorescent B. subtilis cells were achieved with good uniformity. With the help of the obtained fluorescent B. subtilis cells probes, S. aureus cells responded to co-cultured B. subtilis and to aggregate. The degree of aggregation was calculated and nonlinearly fitted to a polynomial model. Systematic investigations of their interactions implied that B. subtilis cells inhibit the growth of neighboring S. aureus cells, and this inhibition was affected by both the growth stage and the amount of surrounding B. subtilis cells. Compared to traditional methods of studying bacterial interaction between two species, such as solid culture medium colony observation and imaging mass spectrometry detection, the procedures were more simple, vivid, and photostable due to the efficient fluorescence intralabeling with less influence on the cells' surface, which might provide a new paradigm for future visualization of microbial behavior.

  7. Effets de l'interaction avec l'oxygène sur le comportement de couches semi-conductrices de ZnO, SnO{2} et CdSe

    NASA Astrophysics Data System (ADS)

    Ain-Souya, A.; Ghers, M.; Haddad, A.; Tebib, W.; Rehamnia, R.; Messsalhi, A.; Bounouala, M.; Djouama, M. C.

    2005-05-01

    Les propriétés superficielles des matériaux solides diffèrent de celles du volume. A la surface, des défauts de différentes natures peuvent être présents. Ils permettent à la surface d'être interactive avec le milieu ambiant. Les multiples interactions entre les états de surface et des éléments du milieu extérieur peuvent modifier les propriétés superficielles. Ce travail étudie la régénération de couches semi-conductrices après adsorption isotherme d'oxygène à différentes températures effectuées entre 20 ° C et 300 ° C. Les matériaux qui ont servi à l'étude sont des couches de ZnO, SnO{2} et CdSe. Celles de CdSe ont été obtenues par co-évaporation, sous vide, de cadmium et de sélénium. Les échantillons de ZnO et SnO{2} ont été élaborés par oxydation, à des températures respectives de 450 ° C et 200 ° , de Zn et Sn déposés par électrolyse et par évaporation sous vide. Les matériaux évaporés ont été déposés sur des plaquettes en verre, les autres ont été électrodéposés sur des substrats métalliques. Les variations des propriétés électriques des couches ont été suivies par mesure de leur résistance électrique superficielle R. Les courbes LogR = f (103 /T (K)), relevées sous vide à différentes températures, sont caractéristiques d'un comportement de semi-conducteur. Des essais d'adsorption d'O{2} à différentes températures montrent des variations considérables de R. En effet, la chimisorption forte d'un gaz par une surface semi-conductrice est telle que l'échange électronique entre adsorbant et adsorbat provoque la formation d'une zone de charge d'espace modifiant la conduction superficielle. Les résultats mettent en évidence des domaines de température de plus haute sensibilité à l'oxygène. Pour le CdSe, certaines désorptions isothermes ont été suffisantes pour une régénération totale des échantillons. Les couches de ZnO ont souvent nécessité des désorptions programm

  8. The PorX Response Regulator of the Porphyromonas gingivalis PorXY Two-Component System Does Not Directly Regulate the Type IX Secretion Genes but Binds the PorL Subunit

    PubMed Central

    Vincent, Maxence S.; Durand, Eric; Cascales, Eric

    2016-01-01

    The Type IX secretion system (T9SS) is a versatile multi-protein complex restricted to bacteria of the Bacteriodetes phylum and responsible for the secretion or cell surface exposition of diverse proteins that participate to S-layer formation, gliding motility or pathogenesis. The T9SS is poorly characterized but a number of proteins involved in the assembly of the secretion apparatus in the oral pathogen Porphyromonas gingivalis have been identified based on genome substractive analyses. Among these proteins, PorY, and PorX encode typical two-component system (TCS) sensor and CheY-like response regulator respectively. Although the porX and porY genes do not localize at the same genetic locus, it has been proposed that PorXY form a bona fide TCS. Deletion of porX in P. gingivalis causes a slight decrease of the expression of a number of other T9SS genes, including sov, porT, porP, porK, porL, porM, porN, and porY. Here, we show that PorX and the soluble cytoplasmic domain of PorY interact. Using electrophoretic mobility shift, DNA-protein co-purification and heterologous host expression assays, we demonstrate that PorX does not bind T9SS gene promoters and does not directly regulate expression of the T9SS genes. Finally, we show that PorX interacts with the cytoplasmic domain of PorL, a component of the T9SS membrane core complex and propose that the CheY-like PorX protein might be involved in the dynamics of the T9SS. PMID:27630829

  9. System design description for portable 1,000 CFM exhauster Skids POR-007/Skid E and POR-008/Skid F

    SciTech Connect

    Nelson, O.D.

    1998-07-25

    The primary purpose of the two 1,000 CFM Exhauster Skids, POR-007-SKID E and POR-008-SKID F, is to provide backup to the waste tank primary ventilation systems for tanks 241-C-106 and 241-AY-102, and the AY-102 annulus in the event of a failure during the sluicing of tank 241-C-106 and subsequent transfer of sluiced waste to 241-AY-102. This redundancy is required since both of the tank ventilation systems have been declared as Safety Class systems.

  10. Click-chemistry approach to study mycoloylated proteins: Evidence for PorB and PorC porins mycoloylation in Corynebacterium glutamicum.

    PubMed

    Issa, Hanane; Huc-Claustre, Emilie; Reddad, Thamila; Bonadé Bottino, Nolwenn; Tropis, Maryelle; Houssin, Christine; Daffé, Mamadou; Bayan, Nicolas; Dautin, Nathalie

    2017-01-01

    Protein mycoloylation is a recently identified, new form of protein acylation. This post-translational modification consists in the covalent attachment of mycolic acids residues to serine. Mycolic acids are long chain, α-branched, β-hydroxylated fatty acids that are exclusively found in the cell envelope of Corynebacteriales, a bacterial order that includes important genera such as Mycobacterium, Nocardia or Corynebacterium. So far, only 3 mycoloylated proteins have been identified: PorA, PorH and ProtX from C. glutamicum. Whereas the identity and function of ProtX is unknown, PorH and PorA associate to form a membrane channel, the activity of which is dependent upon PorA mycoloylation. However, the exact role of mycoloylation and the generality of this phenomenon are still unknown. In particular, the identity of other mycoloylated proteins, if any, needs to be determined together with establishing whether such modification occurs in Corynebacteriales genera other than Corynebacterium. Here, we tested whether a metabolic labeling and click-chemistry approach could be used to detect mycoloylated proteins. Using a fatty acid alkyne analogue, we could indeed label PorA, PorH and ProtX and determine ProtX mycoloylation site. Importantly, we also show that two other porins from C. glutamicum, PorB and PorC are mycoloylated.

  11. Click-chemistry approach to study mycoloylated proteins: Evidence for PorB and PorC porins mycoloylation in Corynebacterium glutamicum

    PubMed Central

    Issa, Hanane; Huc-Claustre, Emilie; Reddad, Thamila; Bonadé Bottino, Nolwenn; Tropis, Maryelle; Houssin, Christine; Daffé, Mamadou; Bayan, Nicolas

    2017-01-01

    Protein mycoloylation is a recently identified, new form of protein acylation. This post-translational modification consists in the covalent attachment of mycolic acids residues to serine. Mycolic acids are long chain, α-branched, β-hydroxylated fatty acids that are exclusively found in the cell envelope of Corynebacteriales, a bacterial order that includes important genera such as Mycobacterium, Nocardia or Corynebacterium. So far, only 3 mycoloylated proteins have been identified: PorA, PorH and ProtX from C. glutamicum. Whereas the identity and function of ProtX is unknown, PorH and PorA associate to form a membrane channel, the activity of which is dependent upon PorA mycoloylation. However, the exact role of mycoloylation and the generality of this phenomenon are still unknown. In particular, the identity of other mycoloylated proteins, if any, needs to be determined together with establishing whether such modification occurs in Corynebacteriales genera other than Corynebacterium. Here, we tested whether a metabolic labeling and click-chemistry approach could be used to detect mycoloylated proteins. Using a fatty acid alkyne analogue, we could indeed label PorA, PorH and ProtX and determine ProtX mycoloylation site. Importantly, we also show that two other porins from C. glutamicum, PorB and PorC are mycoloylated. PMID:28199365

  12. Por La Vida intervention model for cancer prevention in Latinas.

    PubMed

    Navarro, A M; Senn, K L; Kaplan, R M; McNicholas, L; Campo, M C; Roppe, B

    1995-01-01

    Our goal was to describe the development and implementation of an intervention on cancer prevention for Latinas in San Diego, Calif. Thirty-six lay community workers ("consejeras") were recruited and trained to conduct educational group sessions. Each consejera recruited approximately 14 peers from the community to participate in the program (total number = 512). Half of the consejeras were randomly assigned to a control group, in which they participated in an equally engaging program entitled "Community Living Skills." Implementation of the intervention was assessed by qualitative and quantitative methods. Preintervention and postintervention self-report information was obtained from project participants on access to health care services, cancer knowledge, preventive measures, and previous cancer-screening examinations. Base-line data suggest that lack of knowledge, costs of cancer-screening tests, and the lack of a regular health care provider are the major obstacles against obtaining cancer-screening tests. Predisposing factors, such as fear and embarrassment, also constitute barriers to getting regular cervical cancer screening. Preliminary analysis indicates that the Por La Vida intervention increases use of cancer-screening tests in comparison to a community living skills control group. Universal access to health care would remove some of the major financial barriers to cancer screening. The Por La Vida program attempts to overcome the substantial barriers by reaching out to low-income Latinas and by providing information regarding the availability, acceptability, and preventive nature of cancer-screening tests.

  13. Compton imaging with the PorGamRays spectrometer

    NASA Astrophysics Data System (ADS)

    Judson, D. S.; Boston, A. J.; Coleman-Smith, P. J.; Cullen, D. M.; Hardie, A.; Harkness, L. J.; Jones, L. L.; Jones, M.; Lazarus, I.; Nolan, P. J.; Pucknell, V.; Rigby, S. V.; Seller, P.; Scraggs, D. P.; Simpson, J.; Slee, M.; Sweeney, A.; PorGamRays Collaboration

    2011-10-01

    The PorGamRays project aims to develop a portable gamma-ray detection system with both spectroscopic and imaging capabilities. The system is designed around a stack of thin Cadmium Zinc Telluride (CZT) detectors. The imaging capability utilises the Compton camera principle. Each detector is segmented into 100 pixels which are read out through custom designed Application Specific Integrated Circuits (ASICs). This device has potential applications in the security, decommissioning and medical fields. This work focuses on the near-field imaging performance of a lab-based demonstrator consisting of two pixelated CZT detectors, each of which is bonded to a NUCAM II ASIC. Measurements have been made with point 133Ba and 57Co sources located ˜35 mm from the surface of the scattering detector. Position resolution of ˜20 mm FWHM in the x and y planes is demonstrated.

  14. Gliding motility and Por secretion system genes are widespread among members of the phylum bacteroidetes.

    PubMed

    McBride, Mark J; Zhu, Yongtao

    2013-01-01

    The phylum Bacteroidetes is large and diverse, with rapid gliding motility and the ability to digest macromolecules associated with many genera and species. Recently, a novel protein secretion system, the Por secretion system (PorSS), was identified in two members of the phylum, the gliding bacterium Flavobacterium johnsoniae and the nonmotile oral pathogen Porphyromonas gingivalis. The components of the PorSS are not similar in sequence to those of other well-studied bacterial secretion systems. The F. johnsoniae PorSS genes are a subset of the gliding motility genes, suggesting a role for the secretion system in motility. The F. johnsoniae PorSS is needed for assembly of the gliding motility apparatus and for secretion of a chitinase, and the P. gingivalis PorSS is involved in secretion of gingipain protease virulence factors. Comparative analysis of 37 genomes of members of the phylum Bacteroidetes revealed the widespread occurrence of gliding motility genes and PorSS genes. Genes associated with other bacterial protein secretion systems were less common. The results suggest that gliding motility is more common than previously reported. Microscopic observations confirmed that organisms previously described as nonmotile, including Croceibacter atlanticus, "Gramella forsetii," Paludibacter propionicigenes, Riemerella anatipestifer, and Robiginitalea biformata, exhibit gliding motility. Three genes (gldA, gldF, and gldG) that encode an apparent ATP-binding cassette transporter required for F. johnsoniae gliding were absent from two related gliding bacteria, suggesting that the transporter may not be central to gliding motility.

  15. An investigation of exploitation versus exploration in GBEA optimization of PORS 15 and 16 Problems

    SciTech Connect

    Koch, Kaelynn

    2012-01-01

    It was hypothesized that the variations in time to solution are driven by the competing mechanisms of exploration and exploitation.This thesis explores this hypothesis by examining two contrasting problems that embody the hypothesized tradeoff between exploration and exploitation. Plus one recall store (PORS) is an optimization problem based on the idea of a simple calculator with four buttons: plus, one, store, and recall. Integer addition and store are classified as operations, and one and memory recall are classified as terminals. The goal is to arrange a fixed number of keystrokes in a way that maximizes the numerical result. PORS 15 (15 keystrokes) represents the subset of difficult PORS problems and PORS 16 (16 keystrokes) represents the subset of PORS problems that are easiest to optimize. The goal of this work is to examine the tradeoff between exploitation and exploration in graph based evolutionary algorithm (GBEA) optimization. To do this, computational experiments are used to examine how solutions evolve in PORS 15 and 16 problems when solved using GBEAs. The experiment is comprised of three components; the graphs and the population, the evolutionary algorithm rule set, and the example problems. The complete, hypercube, and cycle graphs were used for this experiment. A fixed population size was used.

  16. Crystallographic analysis of Neisseria meningitidis PorB extracellular loops potentially implicated in TLR2 recognition

    PubMed Central

    Kattner, Christof; Toussi, Deana; Zaucha, Jan; Wetzler, Lee M.; Rüppel, Nadine; Zachariae, Ulrich; Massari, Paola; Tanabe, Mikio

    2014-01-01

    Among all Neisseriae species, N. meningitidis and N. gonorrhoeae are the only human pathogens, causative agents of bacterial meningitis and gonorrhoea, respectively. PorB, a pan-Neisseriae trimeric porin that mediates diffusive transport of essential molecules across the bacterial outer membrane, is also known to activate host innate immunity via Toll-like receptor 2 (TLR2)-mediated signaling. The molecular mechanism of PorB binding to TLR2 is not known, but it has been hypothesized that electrostatic interactions contribute to ligand/receptor binding. Strain-specific sequence variability in the surface-exposed loops of PorB which are potentially implicated in TLR2 binding, may explain the difference in TLR2-mediated cell activation in vitro by PorB homologs from the commensal N. lactamica and the pathogen N. meningitidis. Here, we report a comparative structural analysis of PorB from N. meningitidis serogroup B strain 8765 (63% sequence homology with PorB from N. meningitidis serogroup W135) and a mutant in which amino acid substitutions in the extracellular loop 7 lead to significantly reduced TLR2-dependent activity in vitro. We observe that this mutation both alters the loop conformation and causes dramatic changes of electrostatic surface charge, both of which may affect TLR2 recognition and signalling. PMID:24361688

  17. Por Secretion System-Dependent Secretion and Glycosylation of Porphyromonas gingivalis Hemin-Binding Protein 35

    PubMed Central

    Shoji, Mikio; Sato, Keiko; Yukitake, Hideharu; Kondo, Yoshio; Narita, Yuka; Kadowaki, Tomoko; Naito, Mariko; Nakayama, Koji

    2011-01-01

    The anaerobic Gram-negative bacterium Porphyromonas gingivalis is a major pathogen in severe forms of periodontal disease and refractory periapical perodontitis. We have recently found that P. gingivalis has a novel secretion system named the Por secretion system (PorSS), which is responsible for secretion of major extracellular proteinases, Arg-gingipains (Rgps) and Lys-gingipain. These proteinases contain conserved C-terminal domains (CTDs) in their C-termini. Hemin-binding protein 35 (HBP35), which is one of the outer membrane proteins of P. gingivalis and contributes to its haem utilization, also contains a CTD, suggesting that HBP35 is translocated to the cell surface via the PorSS. In this study, immunoblot analysis of P. gingivalis mutants deficient in the PorSS or in the biosynthesis of anionic polysaccharide-lipopolysaccharide (A-LPS) revealed that HBP35 is translocated to the cell surface via the PorSS and is glycosylated with A-LPS. From deletion analysis with a GFP-CTD[HBP35] green fluorescent protein fusion, the C-terminal 22 amino acid residues of CTD[HBP35] were found to be required for cell surface translocation and glycosylation. The GFP-CTD fusion study also revealed that the CTDs of CPG70, peptidylarginine deiminase, P27 and RgpB play roles in PorSS-dependent translocation and glycosylation. However, CTD-region peptides were not found in samples of glycosylated HBP35 protein by peptide map fingerprinting analysis, and antibodies against CTD-regions peptides did not react with glycosylated HBP35 protein. These results suggest both that the CTD region functions as a recognition signal for the PorSS and that glycosylation of CTD proteins occurs after removal of the CTD region. Rabbits were used for making antisera against bacterial proteins in this study. PMID:21731719

  18. Molecular characterisation of Porcine rubulavirus (PorPV) isolates from different outbreaks in Mexico.

    PubMed

    Cuevas-Romero, S; Rivera-Benítez, J F; Blomström, A-L; Ramliden, M; Hernández-Baumgarten, E; Hernández-Jáuregui, P; Ramírez-Mendoza, H; Berg, M

    2016-02-01

    Since the report of the initial outbreak of Porcine rubulavirus (PorPV) infection in pigs, only one full-length genome from 1984 (PorPV-LPMV/1984) has been characterised. To investigate the overall genetic variation, full-length gene nucleotide sequences of current PorPV isolates were obtained from different clinical cases of infected swine. Genome organisation and sequence analysis of the encoded proteins (NP, P, F, M, HN and L) revealed high sequence conservation of the NP protein and the expression of the P and V proteins in all PorPV isolates. The V protein of one isolate displayed a mutation that has been implicated to antagonise the antiviral immune responses of the host. The M protein indicated a variation in a short region that could affect the electrostatic charge and the interaction with the membrane. One PorPV isolate recovered from the lungs showed a mutation at the cleavage site (HRKKR) of the F protein that could represent an important factor to determine the tissue tropism and pathogenicity of this virus. The HN protein showed high sequence identity through the years (up to 2013). Additionally, a number of sequence motifs of very high amino acid conservation among the PorPV isolates important for polymerase activity of the L protein have been identified. In summary, genetic comparisons and phylogenetic analyses indicated that three different genetic variants of PorPV are currently spreading within the swine population, and a new generation of circulating virus with different characteristics has begun to emerge.

  19. In silico studies of outer membrane of Neisseria meningitidis por a: its expression and immunogenic properties.

    PubMed

    Behrouzi, Ava; Bouzari, Saeid; Siadat, Seyed Davar; Irani, Shiva

    2014-01-01

    Neisseria meningitidis is a major causative agent of bacterial septicemia and meningitis in humans. Currently, there are no vaccines to prevent disease caused by strains of N.meningitidis serogroup B. The Class 1 Outer Membrane Protein (OMP) has been named porA which is a cation selective transmembrane protein of 45 KDa that forms trimeric pore in the meningococcal outer membrane. PorA from serogroup B N. meningitidis was cloned into prokaryotic expression vector pBAD-gIIIA. Recombinant protein was expressed with arabinose and affinity purified by Ni-NTA agarose, SDS-PAGE and western blotting were performed for protein determination and verification. BALB/c mice were immunized subcutaneously with purified rPorA together with alum adjuvant. Serum antibody responses to serogroups B N.meningitidis were determined by ELISA. Serum IgG response significantly increased in the group immunized with rPorA together with alum adjuvant in comparison with control groups. These results suggest that rPorA can be a potential vaccine candidate for serogroup B N.meningitidis.

  20. In Silico Studies of Outer Membrane of Neisseria Meningitidis Por A: Its Expression and Immunogenic Properties

    PubMed Central

    Behrouzi, Ava; Bouzari, Saeid; Siadat, Seyed Davar; Irani, Shiva

    2014-01-01

    Neisseria meningitidis is a major causative agent of bacterial septicemia and meningitis in humans. Currently, there are no vaccines to prevent disease caused by strains of N.meningitidis serogroup B. The Class 1 Outer Membrane Protein (OMP) has been named porA which is a cation selective transmembrane protein of 45 KDa that forms trimeric pore in the meningococcal outer membrane. PorA from serogroup B N. meningitidis was cloned into prokaryotic expression vector pBAD-gIIIA. Recombinant protein was expressed with arabinose and affinity purified by Ni-NTA agarose, SDS-PAGE and western blotting were performed for protein determination and verification. BALB/c mice were immunized subcutaneously with purified rPorA together with alum adjuvant. Serum antibody responses to serogroups B N.meningitidis were determined by ELISA. Serum IgG response significantly increased in the group immunized with rPorA together with alum adjuvant in comparison with control groups. These results suggest that rPorA can be a potential vaccine candidate for serogroup B N.meningitidis. PMID:25317403