宽量程高时间分辨扫描变像管

 为改善大偏转角度的偏转像质,设计了一种高时间分辨、大扫描长度的扫描变像管电子光学和行波偏转系统。对变像管后加速技术进行了实验研究,结合图像外增强技术,解决了大面积扫描图像的探测灵敏度问题,达到了同时扩展扫描变像管的时间量程和提高时间分辨力的目的,研制出了宽时间量程、高时间分辨力的扫描变像管。初步实验表明,在量程为5 ns时,时间分辨力达到5 ps,也就是时间分辨力与时间量程之比达到1/1 000。     

超导量子比特中的量子跳跃方法

量子力学自建立以来很长一段时间被当作是描述系综运动的理论。但是上世纪80年代对囚禁离子和原子的研究观测到了量子跳跃现象,迫使人们发展了一些能够用于单量子系统的方法,其中之一就是量子跳跃方法。本文总结了我们近来把量子跳跃方法应用到以约瑟夫森隧道结为基础的超导量子比特的工作。我们不但实验观测到宏观量子系统中的量子跳跃,还可以利用量子跳跃现象来研究固体中普遍存在的两能级系统及其引起的超导量子比特中的退相干。     

纳米结构电学性质的静电力显微镜研究方法

纳米尺度的材料具有许多不同于宏观体材料的奇特的物理和化学特性.了解纳米结构的物性随材料尺寸及形状的变化关系,对于设计和合成具有特定功能的纳米材料有重要的指导意义.静电力显微镜技术为研究微纳米尺度下材料的电学特性提供了强有力的工具.文章介绍了这种测量技术的基本原理,并列举了几种在静电力显微镜基础上发展起来的纳米材料电学性...     

基于对比态原理的常压气体黏度关联式

本文依据对比态原理.通过关联常压下气态物质的无量纲黏度ηr与对比温度Tr以及临界压缩因子Zc,分别建立了适用于单原子气体、双原子气体、碳氢化合物气体以及卤代烃类气态物质的常压下黏度关联式.选用40种物质常压黏度数据对上述关联式分别进行了验证.与文献数据相比,气体黏度计算的相对偏差绝对平均值分别为:0.47%、0.45%...     

疏水介孔SiO2的制备与性能表征

以廉价的工业级正硅酸乙酯为原料,经过酸碱两步催化制备二氧化硅凝胶,以三甲基氯硅烷/六甲基二硅氧烷混合液对凝胶进行直接表面改性,常压干燥下得到高比表面积疏水性二氧化硅气凝胶.用SEM、IR、N2吸脱附、TG-DTA、接触角的测定等分析方法对二氧化硅化学成分、结构形貌、比表面积、热稳定性和疏水性能进行了研究.结果表明,经改...     

Fabrication of hollow silica microspheres utilizing a hydrothermal approach

Hollow silica microspheres(HSMSs) have been successfully fabricated via a facile hydrothermal route using D-glucose as the sacrificial template and sodium silicate powder as the silica precursor.The resulting silica hollow particles were characterized by scanning electron microscopy(SEM),transmission electron microscopy(TEM),X-ray diffraction(XRD),and infrared spectroscopy(IR).The surface area was determined using the BET method.SEM and TEM images exhibited micro-sized silica hollow particles with a size of ~1.5μm.     

Synthesis and electrochemical performance of LiNi0.6Co0.2Mn0.2O2 as a concentration-gradient cathode material for lithium batteries

A well-ordered and spherical LiNi0.6Co0.2Mn0.2O2 cathode material was successfully synthesized from Ni and Mn concentration-gradient precursors via co-precipitation. The crystal structure, morphology and electrochemical properties of LiNi0.6Co0.2Mn0.2O2 were characterized by X-ray diffraction, scanning electron microscopy, energy-dispersive spectroscopy, and charge-discharge tests. The material delivered an initial discharge capacity of 174.3 mAh/g at 180 mA/g （1 C rate） between 2.8 and 4.3 V and more than 93.1% of that was retained after 100 cycles. In addition, it also exhibited excellent rate capability, high cut-off voltage and temperature performance.     

Coking-resistant Ni-ZrO2/A1203 catalyst for CO methanation

Highly coke-resisting ZrO2-decorated Ni/A1203 catalysts for CO methanation were prepared by a two-step process. The support was first loaded with NiO by impregnating method and then modified with ZrO2 by deposition-precipitation method （IM-DP）. Nitrogen adsorption- desorption, X-ray diffraction, scanning electron microscopy, transmission electron microscopy, thermogravimetdc analysis, H2 temperature- programmed reduction and desorption, NH3 temperature-programmed desorption, and zeta potential analysis were employed to characterize the samples. The results revealed that, compared with the catalysts with the same composition prepared by co-impregnation （CI） and sequential impregnation （SI） methods, the Ni/A1203 catalyst prepared by IM-DP showed much enhanced catalytic performance for syngas methanation under the condition of atmospheric pressure and a high weight hourly space velocity of 120000 mL.g-1 .h-1. In a 80 h life time test under the condition of 300-600 ~C and 3.0 MPa, this catalyst showed high stability and resistance to coking, and the amount of deposited carbon was only 0.4 wt%. On the contrary, the deposited carbon over the catalyst without ZrO2 reached 1.5 wt% after a 60 h life time test. The improved catalytic performance was attributed to the selective deposition of ZrO2 nanoparticles on the surface of NiO rather than A1203, which could he well controlled via changing the electrostatic interaction in the DP procedure. This unique structure could enhance the dissociation of CO2 and generate surface oxygen intermediates, thus preventing carbon deposition on the Ni particles in syngas methanation.     

多壁碳纳米管修饰玻碳电极测定铜离子

以多壁碳纳米管(MWCNTs)修饰玻碳电极为工作电极,采用阳极溶出线性扫描法研究了铜离子的电化学测定方法。探讨了MWCNTs修饰层数、富集电位、富集时间、溶液pH、支持电解质对峰电流的影响。实验表明,铜离子浓度在1.0×10-8~1.0×10-5mol·L-1范围内与峰电流呈良好的线性关系,检测限为2.0×10-9mol·L-1,且该电极具有良好的稳定性和抗干扰能力。     

Partially crystallized Pd nanoparticles decorated TiO2 prepared by atmospheric-pressure cold plasma and its enhanced photocatalytic performance

TiO2 decorated with partially crystallized Pd nanoparticles （Pd/TiO2-P） was successfully prepared by atmospheric-pressure dielectric barrier discharge cold plasma. The XRD and XPS analyses proved that Pd ions were reduced to partially crystallized metallic Pd nanoparticles in Pd/TiO2-P. The XPS spectra also indicated that an enhanced metal-support interaction was formed due to the existence of partially crystallized Pd nanoparticles with lower coordination number in Pd/TiO2-P. Photocatalytic activity of Pd/TiO2-P was much higher than that of TiO2 samples decorated with well crystallized Pd nanoparticles.