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21.
Vineet Singh 《Journal of Physics and Chemistry of Solids》2009,70(7):1074-1079
In the present study we have synthesized CdS semiconducting quantum dots by the chemical precipitation method using Thioglycerol as the capping agent. X-ray powder diffraction (XRD) and transmission electron microscopy (TEM) are employed to characterize the size, morphology and crystalline structure of the as-prepared material. The synthesized QPs have a mixture of cubical and hexagonal crystal symmetry with 12 nm average diameter. Ultraviolet-visible (UV-vis) absorption spectroscopy is used to calculate the band gap of the material and blue shift in absorption edge. Confinement of the optical phonon modes in the QPs is studied by Raman spectroscopy, while FTIR for identification of chemical bonds in the nanomaterial. Multiple cadmium and sulphur defects were observed by employing the photoluminescence (PL) method. 相似文献
22.
This paper deals with ultrasound medical image processing, particularly to filter the noise while preserving the edges and
structures of information. The mathematical processing consists in solving by a numerical way a nonlinear evolutive boundary
value problem. Several numerical semi-implicit time marching schemes are considered and analyzed. At each time step, parallel
synchronous or asynchronous Schwarz alternating methods are used to solve the linear system and its convergence is studied.
Lastly, the results of sequential and parallel simulations are presented.
相似文献
23.
In this work, we reported the effect of Li2CO3 addition on the structural, optical, ferroelectric properties and electric-field-induced strain of Bi0.5(Na,K)0.5TiO3 (BNKT) solid solution with CaZrO3 ceramics. Both rhombohedral and tetragonal structures were distorted after adding Lithium (Li). The band gap values decreased from 2.91 to 2.69 eV for 5 mol% Li-addition. The maximum polarization and remanent polarization decreased from 49.66 μC/cm2 to 27.11 μC/cm2 and from 22.93 μC/cm2 to 5.35 μC/cm2 for un-doped and 5 mol% Li- addition BNKT ceramics, respectively. The maximum Smax/Emax value was 567 pm/V at 2 mol% Li2CO3 access. We expected this work will help to understand the role of A-site dopant in lead-free ferroelectric BNKT materials. 相似文献
24.
Linear dextran and helix amylose were covalently bonded with nonlinear optical (NLO) chromophores. The influence of the conformation of the polymer matrix on the NLO behavior of the supramolecular structure has been studied. The second order hyperpolarizability depends not only on the secondary structure of the biopolymer, but also on the position of the chromophore towards the polymeric backbone. Functionalization of NLO-phores with biopolymers led to increased thermo- and photostability. 相似文献
25.
We have investigated the effect of axial magnetic field on the band structure, dipole matrix elements and absorption spectrum in different energy ranges, using tight binding approximation. It is found that magnetic field breaks the degeneracy in the band structure and creates new allowed transitions in the dipole matrix which leads to creation of new peaks in the absorption spectrum. It is found that, unlike to CNTs which show metallic–semiconductor transition, the BNNTs remain semiconductor in any magnetic field strength. By calculation the diameter dependence of peak positions, we found that the positions of three first peaks in the lower energy region (E <5.3 eV) are proportional to n−2. In the middle energy region (7 < E < 7.5 eV) all (n, 0) zigzag BNNTs, with even and odd nanotube index, have two distinct peaks in the absence of magnetic field which these peaks may be used to identify zigzag BNNTs from other tube chiralities. For odd (even) tubes, in the middle energy region, applying the magnetic field leads to splitting of these two peaks into three (five) distinct peaks. 相似文献
26.
This paper reports the development of a facile and effective approach, based on the use of Zr-based metal-organic frameworks (UiO-66) sensor with micropores geometry, shape and particle morphology for the visual detection and removal of ultra-traces of some toxic metal ions such as Bi(III), Zn(II), Pb(II), Hg(II) and Cd(II). UiO-66 was used as selective carriers for accommodating hydrophobic chromophore probes such as dithizone (DZ) without coupling agent for sensitive and selective discrimination of trace level of toxic analytes. The developed UiO-66 sensor was utilized for the detection of ultra-traces of some toxic metal ions with the naked eye. The new sensor displays high sensitivity and selectivity of a wide range of detectable metals analytes up to 10−10 mol dm−3 in solution, in a rapid analyte uptake response (seconds). The developed sensor is stable, cost effective, easy to prepare, and would be useful for rapid detection and removal of ultra-traces of toxic metal ions in water samples. 相似文献
27.
Jiaying Yan Yaqing FengXiao Peng Yuanchao LiNuonuo Zhang Xianggao LiBao Zhang 《Tetrahedron letters》2013
Four π-extended, β,β′ aromatic ring fused porphyrins including mono- and opp-dibenzoporphyrins bearing two carboxyl groups at only one fused benzo group were synthesized. The optical results by UV–vis spectroscopy indicate that when compared with the absorption spectra of monobenzoporphyrins, greater light-harvesting capabilities can be realized for opp-dibenzoporphyrins with two benzo group at the opposite β,β′ positions of the porphyrin. The photovoltaic properties of these π-extended porphyrins were examined for the first time and the highest conversion efficiency of 1.62% was realized for opp-dibenzoporphyrin 8a-sensitized solar cell, which is ∼60% higher than that of monobenzoporphyrin 4a based solar cell indicating the effect of an extra aromatic π conjugation on the light-harvesting capabilities of π-extended porphyrins. Subsequent DFT calculation results supported our results obtained in the optical and photovoltaic studies. 相似文献
28.
We have found a correlation between ZnS nanocomposite nonlinear optical features and technological processing using electrolytic method. In the earlier researches this factor was neglected. However, it may open a new stage for operation by photovoltaic features of the well known semiconductors within a wide range of magnitudes. The titled nanostructured zinc sulfide (ZnS) was synthesized by electrolytic method. The obtained ZnS nano-crystallites possessed nano-particles sizes varying within 1.6 nm…1.8 nm. The titled samples were analyzed by XRD, HR-TEM, STEM, and nonlinear optical methods such as photo-induced two-photon absorption (TPA) and second harmonic generation (SHG). For this reason the nano-powders were embedded into the photopolymer poly(vinyl) alcohol (PVA) matrices. Role of aggregation in the mentioned properties is discussed. Possible origin of the such correlations are discussed. 相似文献
29.
30.
In this study, we developed a facile and benign green synthesis approach for the successful fabrication of well-dispersed urchin-like Au@Pt core–shell nanoparticles (NPs) using gallic acid (GA) as both a reducing and protecting agent. The proposed one-step synthesis exploits the differences in the reduction potentials of AuCl4− and PtCl62−, where the AuCl4− ions are preferentially reduced to Au cores and the PtCl62− ions are then deposited continuously onto the Au core surface as a Pt shell. The as-prepared Au@Pt NPs were characterized by transmission electron microscope (TEM); high-resolution transmission electron microscope (HR-TEM); scanning electron microscope (SEM); UV-vis absorption spectra (UV-vis); X-ray diffraction (XRD); Fourier transmission infrared spectra (FT-IR). We systematically investigated the effects of some experimental parameters on the formation of the Au@Pt NPs, i.e., the reaction temperature, the molar ratios of HAuCl4/H2PtCl6, and the amount of GA. When polyvinylpyrrolidone K-30 (PVP) was used as a protecting agent, the Au@Pt core–shell NPs obtained using this green synthesis method were better dispersed and smaller in size. The as-prepared Au@Pt NPs exhibited better catalytic activity in the reaction where NaBH4 reduced p-nitrophenol to p-aminophenol. However, the results showed that the Au@Pt bimetallic NPs had a lower catalytic activity than the pure Au NPs obtained by the same method, which confirmed the formation of Au@Pt core–shell nanostructures because the active sites on the surfaces of the Au NPs were covered with a Pt shell. 相似文献