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991.
Vikram Sen Neeraj Panwar G.L. Bhalla 《Journal of Physics and Chemistry of Solids》2007,68(9):1685-1691
We report here the structural, magnetotransport and morphological studies of Sb-doped La2/3Ba1/3Mn1−xSbxO3 perovskite manganites. Pristine material La2/3Ba1/3MnO3 (LBMO) shows two insulator-metal (I-M) transitions in the electrical resistivity-temperature (ρ-T) behavior. While the higher temperature transition (TP1) at ∼340 K is reminiscent of the usual I-M transition in manganites, the lower temperature transition (TP2) at ∼250 K has been ascribed to the grain boundary (GB) effects arising out of the ionic size mismatch between the ions present at the rare-earth site (La3+ and Ba2+). With Sb-doping TP1 shifts to lower temperatures while TP2 remains invariant up to 3% and shifts to lower temperature for 5%. Room temperature electrical resistivity and the peak values also increase successively with Sb-doping. Scanning electron micrographs of the samples exhibit a gradual increase in their grain sizes with Sb indicating a gradual decrease in the GB density. Shift of TP1 with doping is explained on the basis of a competition between double-exchange and super-exchange mechanisms. The overall electrical resistivity increases and the shift in the electrical resistivity hump (TP2) with Sb-doping is found related to be gradually decreasing GB density and the ensuing lattice strain increase at the GBs. The intrinsic magnetoresistance (MR) gets suppressed and extrinsic MR gets enhanced with Sb-doping. At T>TP1, the electrical resistivity is found to follow the adiabatic polaron hopping model whereas the electron-magnon scattering is found to dominate in the metallic regime (T<TP1). 相似文献
992.
We report on near-field scanning optical microscopy measurements on randomly textured ZnO thin films. These films are commonly used as transparent conducting oxide in thin-film solar cells. Textured interfaces are used to increase the scattering of light, which leads to a better light trapping in the solar cell. Here, both the topography and the local transmission are measured with a tapered fiber tip with very high spatial resolution. By varying the distance of the tip and the wavelength of the incident light, the optical profile is visualized and reveals a strong confinement of light on a subwavelength scale which corresponds to ridges in the surface structure. The confinement of light results from guided optical modes in the ZnO which are accompanied by a modulated evanescent field in air. No corresponding structure to this modulation is found in the topography. These results give new insight for further improvement of light trapping in solar cells. 相似文献
993.
Density functional theory study on LaNi4.5Al0.5 hydride phase: electronic properties and sites occupation* 下载免费PDF全文
In this paper the crystal structure, electronic structure and hydrogen site occupation of LaNi4.5Al0.5Hy hydride phase (y = 5.0, 6.0) have been investigated by using full-potential linearized augmented plane wave method. The hydrogen atoms were found to prefer the 6m, 12o and 12n sites, while no 4h sites were occupied. A narrowed Ni-d band is found due to the lattice expansion, the total density of states at EF increases with y, which indicates that the compounds become less stable. The interaction between Al and Ni, H plays a dominant role in the stability of LaNi4.5Al0.5 hydride phase. The smaller the shift of EF towards the higher energy region, the more stable the compounds will be. The obtained results are compared with experimental data and discussed in the light of previous works. 相似文献
994.
用密度泛函B3LYP/6-31G**计算方法,对不同碳链长度和不同氧化态( V2 +/V+.)紫罗碱二硫醇的平衡几何构型及相应电子结构的研究表明,两种氧化态在吡啶环共面性和前线轨道电子集居上的差异与特征,导致氧化态V2 +成为紫罗碱亲合金原子形成Au-S-nVn-S-Au结构的关键组分,自由基V+.则在该结构的氧化还原电子传导中发挥核心作用.S-S核间距与前线轨道能隙的计算结果表明,在紫罗碱二硫醇单分子电导的测量中,亚甲基数n达到12的分子长度是有效的. 相似文献
995.
地球同步轨道二维扫描像移补偿技术建模与分析 总被引:2,自引:0,他引:2
在建立二维扫描观测模型的基础上,提出了基于椭球体地球模型的二维扫描像移补偿方案,给出了任意空间观测到的目标位置的快速迭代算法,并以真实轨道和仿真姿态数据验证了像移补偿模型的实际性能。仿真结果表明,对于长周期(大于一个东西方向扫描行周期)轨道和姿态偏差,可以通过调整仪器坐标系内的扫描轨迹来实现像移补偿;同时,在现有轨道测量和控制条件下,轨道因素引起的瞬时方位角和俯仰角补偿量在0.01°~0.1°量级,且随轨道位置不同而变化。FY-2C卫星在轨偏航轴姿态失配修正实例证实了上述模型的有效性。 相似文献
996.
The lithium ion conducting solid polymer electrolytes (SPE) based on PVAc-LiClO4 of various compositions were prepared by solution casting technique. Structure and surface morphology characterization were studied by X-ray diffraction (XRD) analysis and scanning electron microscopy (SEM) measurements, respectively. Thermal and conductivity behavior of polymer-salt complexes were studied by employing differential scanning calorimetry (DSC) and ac impedance measurements, respectively. XRD and SEM analyses indicate the amorphous nature of the polymer-salt complexes. DSC measurements show decrease in Tg with the increase in LiClO4 concentrations. The bulk conductivity of the PVAc:LiClO4 polymer electrolytes was found to vary between 7.6×10−7 and 6.2×10−5 S cm−1 at 303 K with the increase in salt concentration. The temperature dependence of the polymer electrolyte complexes appear to obey Arrhenius law. 相似文献
997.
The microstructure of a Fe–Mn–Si–Al twinning-induced plasticity (TWIP) steel exhibiting remarkable work hardening rate under uniaxial tensile deformation was investigated using transmission electron microscopy to uncover the mechanism(s) controlling the nucleation and growth of the mechanically induced twins. The results show that the stair-rod cross-slip deviation mechanism is necessary for the formation of the twins, while large extrinsic stacking faults homogenously distributed within the grains could act as preferential sources for the activation of the deviation process. The influence of such features on the thickness and strength of the twins and the resulting mechanical behaviour is discussed and compared to similar works recently performed on Fe–Mn–C TWIP steels. 相似文献
998.
Zhi-Peng Li Toshiyuki Mori Jin Zou John Drennan 《Journal of solid state chemistry》2011,184(9):2458-2461
Analytical transmission electron microscopy, in particular with the combination of energy dispersive X-ray spectroscopy (EDX) and electron energy-loss spectroscopy (EELS), has been performed to investigate the microstructure and microchemistry of the interfacial region between the cathode (La0.6Sr0.4Co0.8Fe0.2O3, LSCF) and the electrolyte (Gd-doped ceria, GDC). Two types of diffusions, mutual diffusion between cathode and electrolyte as well as the diffusion along grain boundaries, have been clarified. These diffusions suggest that the chemical stability of LSCF and GDC are not as good as previously reported. The results are more noteworthy if we take into consideration the fact that such interdiffusions occur even during the sintering process of cell preparation. 相似文献
999.
Nelly Durand Bruno Ameduri Bernard Boutevin 《Journal of polymer science. Part A, Polymer chemistry》2011,49(1):82-92
The synthesis and characterizations of fluorinated telomers based on vinylidene fluoride (VDF) by iodine transfer polymerization (ITP) are presented. These telomers were prepared in the presence of ω‐iodoperfluorinated functional chain transfer agents, C6F13I or C4F9I. ITPs were initiated by thermal decomposition of bis(4‐tert‐butylcyclohexyl) peroxydicarbonate (BBCHPDC), in solution (in the presence of acetonitrile). The obtained telomers were characterized by different analyses such as elemental analyses, nuclear magnetic resonance (NMR), Fourier transform infrared spectroscopy, size exclusion chromatography, X‐ray diffraction (XRD), and finally by thermal analyses such as differential scanning calorimetry (DSC) and thermogravimetric analyses. These technical analyses enabled one to assess their chemical structures, various thermal properties, and their crystalline forms. The assignments of the characteristic signals obtained by 19F NMR spectroscopy enabled one to calculate the average degrees of polymerization (DPn) and percentages of ? CH2CF2I end group functionalities that depend on the initiator and the fractionation process after reaction. A good control of polymerization was shown by the absence of reversed ? CH2CF2? CF2CH2? (VDF–VDF dyads) and narrow polydispersity indices (<1.2). The XRD and DSC evidenced the influence of the chain length of the telomers on the crystallinity rate (>70%) and indicated two crystalline forms, α and β, that depended on DPn values. © 2010 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2010 相似文献
1000.
Yuepeng Xing Yiwang Chen Xiaohui He 《Journal of polymer science. Part A, Polymer chemistry》2011,49(20):4425-4432
Copolymerization of norbornene (NB) with methoxycarbonylnorbornene (NB‐COOCH3) was carried out with catalytic system of Ni{CF3C(O)CHC[N(naphthyl)]CH3}2 and B(C6F5)3 in toluene. The catalytic system exhibited higher activity 2.69 × 105 (gpolymer/mol Ni h) for copolymerization of norbornene and methoxycarbonylnorbornene. The influence results of the comonomer feed content on the polymerization showed that the NB‐COOCH3 has a very high insertion ratio in all copolymers, and the NB‐COOCH3 content in copolymers can be controlled to be 7.9–77.6 mol % at content of 10–90 mol % of the NB‐COOCH3 in the monomer feeds ratios. The reactivity ratios, rNB‐COOCH3 = 0.578 and rNB = 0.859, were determined by the Kelen–TÜdÕs method. Copolymers were processed by solution casting method, dry/wet phase inversion technique, and electrospinning. The films prepared by solution casting method showed good transparency in the visible region. The membranes processed by dry/wet phase inversion technique were microporous structures. The fibers diameters fabricated by electrospinning were about 3 μm. © 2011 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem, 2011 相似文献