Synthesis of Zn(1-x)Cd(x)S:Mn/ZnS quantum dots and their application to light-emitting diodes

3.6?nm sized Mn-doped Zn(1-x)Cd(x)S quantum dots (QDs) with the composition (x) of 1, 0.5, 0.2 and 0 were synthesized by a reverse micelle approach. The bandgap energy of Zn(1-x)Cd(x)S:Mn QDs was tuned to a higher energy by increasing the Zn content, and the actual composition of alloyed Zn(1-x)Cd(x)S:Mn QDs was found to be different from the solution composition. Consecutive overcoating of the Zn(1-x)Cd(x)S:Mn QD surface by a ZnS shell was done, and the core/shell structured QDs exhibited quantum yields of 14-30%, depending on the composition of the core QDs. Using CdS:Mn/ZnS QDs, orange and white light-emitting diodes (LEDs) pumped by a near-UV and blue LED chips, respectively, were fabricated and their optical properties are described.     

Arrays of ZnO/Zn(x)Cd(1-x)Se nanocables: band gap engineering and photovoltaic applications

Arrays of ZnO/Zn(x)Cd(1-x)Se (0 ≤ x ≤ 1) core/shell nanocables with shells of tunable compositions have been synthesized on fluorine-doped tin oxide glass substrates via a simple ion-exchange approach. Through the effects of stoichiometry and type II heterojunction, optical absorptions of the nanocable arrays can be controllably tuned to cover almost the entire visible spectrum. Lattice parameters and band gaps of the ternary Zn(x)Cd(1-x)Se shells were found to have respectively linear and quadratic relationships with the Zn content (x). These ZnO/Zn(x)Cd(1-x)Se nanocable arrays are further demonstrated to be promising photoelectrodes for photoelectrochemical solar cells, giving a maximum power conversion efficiency up to 4.74%.     

Effect of shell layers on luminescence of colloidal CdSe/Zn(0.5)Cd(0.5)Se/ZnSe/ZnS core/multishell quantum dots

Colloidal CdSe/Zn(0.5)Cd(0.5)Se/ZnSe/ZnS core/multishell quantum dots (QDs) were synthesized by using the well developed successive ion layer adsorption and reaction (SILAR) technique. The UV-vis and PL spectra, TEM, X-ray diffraction and Raman measurement were performed to investigate the structure and optical properties of prepared QDs during the growth of shell layers, which indicated that the stress in CdSe core became stronger with the increasing shell thickness. Due to the gradual adjustment of the lattice parameters in the radial direction and the radial increase of the respective valence- and conduction-band offsets, the optical measurements show a significant enhancement in the photoluminescence quantum yield (QY) and an expedited radiative decay in QDs overcoated with thicker shell. The temperature-dependent optical spectra were measured, and the relation between the microstructure and the optical properties of these core/multishell quantum dots was discussed.     

水热法合成N-乙酰-L-半胱氨酸稳定的Cd_xZn_（1-x）Se合金量子点

采用了N-乙酰-L-半胱氨酸为稳定剂,通过水热法制备了荧光发射峰可调、粒径均匀且结晶性能良好的ZnxCd1-xSe合金量子点,并采用紫外-可见光吸收光谱（UV-Vis）、荧光光谱（PL）、X射线衍射（XRD）、高分辨透射电镜（HRTEM）等对其结构和性能进行了表征。重点研究了Cd2＋/Zn2＋比值、初始溶液pH值、水热反应温度和时间等实验条件对ZnxCd1-xSe量子点荧光性能的影响。研究表明所制备的量子点荧光量子产率高（35%）,荧光发射谱半峰宽窄（FWHM〈50nm）,有望作为生物荧光标记物。     

Birefringence of Zn(x)Cd(1-x)S near the isotropic point

The birefringence of the mixed crystal Zn0.14Cd0.86S has been measured near its isotropic point and found to be highly dispersive. The region of strong dispersion shifts to shorter wavelengths than observed in pure CdS, and its magnitude near the isotropic point is larger. These results are highly significant for the development of narrowband dispersive birefringent filters in the blue-green region of the spectrum.     

Highly luminescent (Zn,Cd)Te/CdSe colloidal heteronanowires with tunable electron-hole overlap

We report the synthesis of ultranarrow (Zn,Cd)Te/CdSe colloidal heteronanowires, using ZnTe magic size clusters as seeds. The wire formation starts with a partial Zn for Cd cation exchange, followed by self-organization into segmented heteronanowires. Further growth occurs by inclusion of CdSe. The heteronanowires emit in the 530 to 760 nm range with high quantum yields. The electron-hole overlap decreases with increasing CdSe volume fraction, allowing the optical properties to be controlled by adjusting the heteronanowire composition.     

Contact printing of compositionally graded CdS(x)Se(1-x) nanowire parallel arrays for tunable photodetectors

Spatially composition-graded CdS(x)Se(1-x) (x = 0-1) nanowires are grown and transferred as parallel arrays onto Si/SiO(2) substrates by a one-step, directional contact printing process. Upon subsequent device fabrication, an array of tunable-wavelength photodetectors is demonstrated. From the spectral photoconductivity measurements, the cutoff wavelength for the device array, as determined by the bandgap, is shown to cover a significant portion of the visible spectrum. The ability to transfer a collection of crystalline semiconductor nanowires while preserving the spatially graded composition may enable a wide range of applications, such as tunable lasers and photodetectors, efficient photovoltaics, and multiplexed chemical sensors.     

(Ag2Se)1-x(Bi2Se3)x的热电性能研究

具有本征低晶格热导率的I-V-VI₂族三元硫属化合物在热电领域引起了广泛关注。AgBiSe₂作为这类化合物中少有的n型半导体, 成为一种有潜力的热电材料。本工作系统研究了AgBiSe₂的热电性能。基于Ag₂Se-Bi₂Se二元相图, 单相的(Ag₂Se)_1-x(Bi₂Se₃)_x的成分在x=0.4~0.62范围可调, 使得该材料载流子浓度具有可调性。结果表明, 通过组分调控获得了较宽范围的载体浓度1.0×10¹⁹~5.7×10¹⁹ cm^-3, 并基于声学声子散射的单一抛物带模型对其电传输性能进行了综合评估。本研究获得的最高载流子浓度接近理论最优值, 在700 K实现了最高ZT值0.5。本研究有助于深入理解AgBiSe₂的传输特性和决定热电性能的基本物理参数。     

Tailoring the composition of self-assembled Si(1-x)C(x) quantum dots: simulation of plasma/ion-related controls

Precise control of composition and internal structure is essential for a variety of novel technological applications which require highly tailored binary quantum dots (QDs) with predictable optoelectronic and mechanical properties. The delicate balancing act between incoming flux and substrate temperature required for the growth of compositionally graded (Si(1-x)C(x); x varies throughout the internal structure), core-multishell (discrete shells of Si and C or combinations thereof) and selected composition (x set) QDs on low-temperature plasma/ion-flux-exposed Si(100) surfaces is investigated via a hybrid numerical simulation. Incident Si and C ions lead to localized substrate heating and a reduction in surface diffusion activation energy. It is shown that by incorporating ions in the influx, a steady-state composition is reached more quickly (for selected composition QDs) and the composition gradient of a Si(1-x)C(x) QD may be fine tuned; additionally (with other deposition conditions remaining the same), larger QDs are obtained on average. It is suggested that ionizing a portion of the influx is another way to control the average size of the QDs, and ultimately, their internal structure. Advantages that can be gained by utilizing plasma/ion-related controls to facilitate the growth of highly tailored, compositionally controlled quantum dots are discussed as well.     

Fabrication, structural characterization and photoluminescence of single-crystal Zn(x)Cd(1-x)S zigzag nanowires

Large-scale synthesis of ternary Zn(x)Cd(1-x)S zigzag nanowires was achieved in a one-step metal-organic chemical vapour deposition (MOCVD) process with co-fed single precursors of ZnS and CdS. Their morphologies, structures and optical properties were characterized and confirmed by scanning electron microscopy, high-resolution transmission electron microscopy, x-ray spectroscopy, and photoluminescence. The Zn(x)Cd(1-x)S zigzag nanowires are single crystalline, with axis [001], by changing the growth direction from [Formula: see text] to [Formula: see text]. Regarding the formation of zigzag nanowires, we suggest that the shear strain and slight fluctuation of the reaction conditions may be the major factors that make the nanowires change growth direction. In addition, because of the lower temperature and versatility, this new fabrication method might present a new and facile way to form other ternary nanomaterials. Furthermore, the green emission of the nanowires may have potential applications in electronic/optical nanodevices.     

Composition and temperature dependence of the optical properties of Zn(1-x) Cd(x)Se (0 < or = x < or = 0.34) below the fundamental bandgap

The II-VI ternary semiconductor alloy system Zn(1-x) Cd(x) Se with 0 < or = x < or = 0.2 has important applications as the active material in blue-green light-emitting diodes and lasers. For the wavelength and temperature ranges over which these devices are designed to operate, a knowledge of the optical properties of the alloys is important. We report the results of spectroscopic ellipsometry measurements of the real part of the dielectric function epsilon1 for Zn-rich Zn(1-x) Cd(x) Se layers deposited epitaxially on (100) GaAs. We derive compact expressions that allow one to calculate accurate epsilon1 spectra from 1.5 eV, the low-energy limit of our ellipsometer, to E0-0.05 eV, where E0 is the fundamental bandgap energy, for any composition and temperature within the ranges 0 < or = x < or = 0.34 and 25 < or = T < 260 degrees C. Furthermore, we expect that the results can also be extrapolated to cover the substrate temperature range typically used for the growth of these films (250-300 degrees C). Hence the results presented here are also useful in future real-time spectroscopic ellipsometry studies of Zn(1-x) Cd(x) Se film growth.     

Intrinsic sensitivity of Cd/sub 1-x/Zn/sub x/Te semiconductors for digital radiographic imaging

The intrinsic sensitivity of cadmium zinc telluride (Cd/sub 1-x/Zn/sub x/Te) semiconductor detectors has been experimentally measured, within the X-ray diagnostic energy range. The results of this study indicate that the intrinsic efficiency of Cd/sub 1-x/Zn/sub x/Te can be increased by optimizing geometrical and physical detection parameters such as X-ray irradiation geometry, detector thickness, and applied electric field. These results indicate that Cd/sub 1-x/Zn/sub x/Te is a suitable candidate for digital imaging applications.     

Thermal and optical properties of Cd1-x Zn x S thin films by photoacoustics

Ternary compounds Cd_1-x Zn _x S for various Zn concentration in thin films are synthesized by spray pyrolysis and studied by photoacoustics technique for thermal and optical properties. The thermal diffusivity as a function of the alloy composition measured by photoacoustics shows a maximum at x = 0.6. The optical band gap increases with zinc concentration and the continuous change indicates the formation of solid solution.     

Growth and properties of Zn(1-x)CdxO and Zn(1-x)CdxO/ZnO core/shell nanoparticles

Octylamine capped Zn(1-x)CdxO alloys and Zn(1-x)CdxO/ZnO core/shell nanoparticles have been grown by the thermal decomposing of zinc and cadmium cupferronates in organic solvents. Zn(1-x)CdxO alloys incorprated with different concentration of Cd have been grown by quickly injecting of their precursors at 200 degrees C. Zn(1-x)CdxO/ZnO core/shell nanoparticles are performed by slowly injecting of shell precursors at 180 degrees C. The prepared nanoparticles are characterized by X-ray diffraction, absorption spectrometer, Mirco-Raman spectrometer and transmission electron microscopy. The band gap of ZnCdO alloys shrinks linearly and the crystal lattice expands with an increase of Cd concentration. The growth of ZnO shells on ZnCdO cores enhances the core luminescence dramatically and results in a red shift in the absorption and emission of Zn(1-x)CdxO cores.     

Characterization of Cd1−x Zn x Se thin films deposited at low temperature by chemical route

Optoelectronic technologically important pseudo-binary Cd_1−x Zn _x Se thin films with a variable composition (0 < x < 1) has been developed by chemical bath deposition method. The objective to study growth kinetics, physical, microscopic, compositional, optical, electrical and structural changes. Cd_1−x Zn _x Se have been deposited on non-conducting glass substrate in tartarate bath containing Cd⁺² and Zn⁺² ions with sodium selenosulphate with an aqueous alkaline medium at 278 K. The quality and the thickness of the films are depends upon deposition temperature, deposition time and pH, etc. X-ray diffraction (XRD), atomic absorption spectroscopy, optical absorption, scanning electron microscopy and thermoelectric technique characterized the films. The XRD study indicates the polycrystalline nature in single cubic phase over whole range of composition. Analysis of absorption spectra gave direct type band gap, the magnitude of which increases non-linearly as zinc content in the film is increased and dc electrical conductivity at room temperature was found to decreases from 10⁻⁷ to 10⁻⁸ (Ω cm)⁻¹. All the films show n-type conductivity. The promising features observed are the formation of continuous solid solutions in a single cubic phase.     

Microstructure and magnetic properties of Fe(x)Ni(1-x) alloy nanoplatelets

Plate-like nanoparticles (or nanoplatelets) of Fe(x)Ni(1-x) (x = 0.1, 0.2, 0.3, 0.4, 0.5, and 0.6) alloy were successfully synthesized through a simple sonochemical method. The shapes of the alloy nanoplatelets with different Fe atom contents are almost same. Their average diameters are about 50 nm, and their average thicknesses are several nanometers. The obtained Fe(x)Ni(1-x) alloy nanoplatelets are single-phased and have a face-centered cubic (FCC) crystal structure. The lattice constants of the alloy nanoplatelets are larger than the corresponding bulk value and increase with increasing Fe content. The surface oxidation of the alloy nanoplatelets leads to the lattice expansion. The alloy nanoplatelet powders are all ferromagnetic, and their saturation magnetizations are slightly lower than the corresponding bulk value. The saturation magnetic field and the coercivity increase with increasing Fe content. Magnetic hysteresis loops along the directions deviating different angles from the nanoplatelets plane are obviously different, indicating that the easy-axis is in the in-plane direction and the magnetization reversal is incoherent mode. The micromagnetic simulation results for the array composed of thirty-six Fe0.6Ni0.4 alloy nanoplatelets fit well with the measured data.     

Mg/sub x/Zn/sub 1-x/O: a new piezoelectric material

Piezoelectric ZnO thin films have been successfully used for multilayer surface acoustic wave (SAW) and bulk acoustic wave (BAW) devices. Magnesium zinc oxide (Mg/sub x/Zn/sub 1-x/O) is a new piezoelectric material, which is formed by alloying ZnO and MgO. Mg/sub x/Zn/sub 1-x/O allows for flexibility in thin film SAW device design, as its piezoelectric properties can be tailored by controlling the Mg composition, as well as by using Mg/sub x/Zn/sub 1-x/O/ZnO multilayer structures. We report the metal-organic chemical vapor deposition (MOCVD) growth, structural characterization and SAW evaluation of piezoelectric Mg/sub x/Zn/sub 1-x/O (x<0.35) thin films grown on (011~2) r-plane sapphire substrates. The primary axis of symmetry, the c-axis, lies on the Mg/sub x/Zn/sub 1-x/O growth plane, resulting in the in-plane anisotropy of piezoelectric properties. SAW test devices for Rayleigh and Love wave modes, propagating parallel and perpendicular to the c-axis, were designed and fabricated. Their SAW properties, including velocity dispersion and piezoelectric coupling, were characterized. It has been found that the acoustic velocity increases, whereas the piezoelectric coupling decreases with increasing Mg composition in piezoelectric Mg/sub x/Zn/sub 1-x/O films.     

Growth of Zn(1_x)Mg(x)O and Zn(1_x)Cd(x)O nanowires and the application in light emitting devices

Magnesium and Cadmium doped ZnO nanowires were successfully grown by Chemical Vapor deposition method in a tube furnance. Photoluminescence spectra show that the band gap of ZnO nanowire has been tuned from 4.00 eV to 2.08 eV by Magnesium and Cadmium doping. Transmission Electron Microscopy and X-ray diffraction characterization analysis indicate that most of the formed nanowires are single crystalline with good quality. Zn(1-x)Cd(x)O nanowire sample was used for heterojunctional light emitting diode fabrication. Electroluminescence measurement yields a strong emission peak at 553 nm from the Zn(1-x)Cd(x)O nanowire.     

Low-temperature noninjection approach to homogeneously-alloyed PbSe(x)S(1-x) colloidal nanocrystals for photovoltaic applications

Homogeneously alloyed PbSe(x)S(1-x) nanocrystals (NCs) with their excitonic absorption peaks in wavelength shorter than 1200 nm were developed for photovoltaic (PV) applications. Schottky-type solar cells fabricated with our PbSe?.?S?.? NCs as their active materials reached a high power conversion efficiency (PCE) of 3.44%, with an open circuit voltage (V(oc)) of 0.49 V, short circuit photocurrent (J(sc)) of 13.09 mA/cm2, and fill factor (FF) of 0.54 under Air Mass 1.5 global (AM 1.5G) irradiation of 100 mW/cm2. The syntheses of the small-sized colloidal PbSe(x)S(1-x) NCs were carried out at low temperature (60 °C) with long growth periods (such as 45 min) via a one-pot noninjection-based approach in 1-octadecene (ODE), featuring high reaction yield, high product quality, and high synthetic reproducibility. This low-temperature approach employed Pb(oleate)? as a Pb precursor and air-stable low-cost thioacetamide (TAA) as a S source instead of air-sensitive high-cost bis(trimethylsilyl)sulfide ((TMS)?S), with n-tributylphosphine selenide (TBPSe) as a Se precursor instead of n-trioctylphosphine selenide (TOPSe). The reactivity difference of TOPSe made from commercial TOP 90% and TBPSe made from commercial TBP 97% and TBP 99% was addressed with in situ observation of the temporal evolution of NC absorption and with 31P nuclear magnetic resonance (NMR). Furthermore, the addition of a strong reducing/nucleation agent diphenylphosphine (DPP) promoted the reactivity of the Pb precursor through the formation of a Pb-P complex, which is much more reactive than Pb(oleate)?. Thus, the reactivity of TBPSe was increased more than that of TAA. The larger the DPP-to-Pb feed molar ratio, the more the Pb-P complex, the higher the Se amount in the resulting homogeneously alloyed PbSe(x)S(1-x) NCs. Therefore, the use of DPP allowed reactivity match of the Se and S precursors and led to sizable nucleation at low temperature so that long growth periods became feasible. The present study brings insight into the formation mechanism of monomers, nucleation/growth of colloidal composition-tunable NCs, and materials design and synthesis for next-generation low-cost and high-efficiency solar cells.