高温高压下CeTbO3合成过程中电阻的动态测试研究

 在0.5 GPa、4.0 GPa的压力下，从室温到800 ℃的温度范围内测量了氧化物CeTbO₃、单稀土氧化物Tb₄O₇、CeO₂和摩尔比维4∶1配比的混合物CeO₂+Tb₄O₇等的电阻随温度变化关系。对这四种物质均反映出电阻随温度增加而减小的半导体特征。在压力维0.5 GPa，温度高于600 ℃时发现了混合物CeO₂+Tb₄O₇、氧化物Tb₄O₇中电阻变化的起伏。X射线衍射谱表明，对应这一电阻变化，在结构上出现了变化。结果分析表明，这一变化与Tb⁴⁺→Tb³⁺的价态变化密切相联。     

Li2O-B2O3-P2O5系统非晶态混合骨架效应的NMR研究

用核磁共振对非晶态中B³⁺离子的微观结构进行了测定,结合Raman光谱的研究,对Li₂O-B₂O₃-P₂O₅系统非晶态的性能(电导率、密度等)在P₂O₅/B₂O₃比约等于1时产生极值的原因从理论上作了阐明。     

透射光栅的实验标定和衍射效率的理论模拟

透射光栅广泛应用于软X射线能谱测量.为了获得用于惯性约束聚变研究的透射光栅的各级衍射效率及其他参数,在北京同步辐射源上200—1600 eV能量范围内对其进行了标定,获得了透射光栅衍射效率的实验结果.扩展了透射光栅衍射效率的计算方法,提出了7边准梯形截面衍射效率计算模型.分析拟合了实验数据,理论结果与实验结果很好符合.得到了7边准梯形的透射光栅栅线截面结构. 关键词： 透射光栅 衍射效率 实验标定 光栅模型     

Synthesis of single-crystalline wurtzite aluminum nitride nanowires by direct arc discharge

High-density hexagonal aluminum nitride (h-AlN) nanowires were synthesized through the direct reaction of Al with nitrogen gas without catalyst and template using a direct arc discharge method. The as-grown AlN nanowires were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and Raman spectroscopy. The h-AlN nanowires have a diameter in the range 20–70 nm and a length of several tens of micrometers. Vapor–solid growth mechanisms can be employed to explain the formation of the h-AlN nanowires. PACS 81.05.Ea; 81.10.Bk; 81.16.Dn; 68.65.-k; 81.16.-c     

脉冲激光偏振方向对氮分子高次谐波的影响——基于含时密度泛函理论的模拟

采用含时密度泛函方法,结合赝势模型和电子交换相关作用的广义梯度近似,模拟了氮分子在超强飞秒激光脉冲作用下的高次谐波产生现象,并研究了激光脉冲偏振方向对氮分子高次谐波的影响.结果表明氮分子的高次谐波谱具有典型原子谐波谱的特征;谐波谱强度随着θ(激光偏振方向与分子轴向夹角)的增大而减小.这与J.Itatanl在Nature上报道的实验结果基本一致.     

基于固体腔扫描法布里-珀罗干涉仪的大气温度绝对探测方法研究

大气温度是描述大气状态的重要基本特征参量之一.目前,基于Rayleigh散射的大气温度探测方法多应用于大气温度的相对探测,即温度反演时需要响应函数和校准程序.本文提出了利用固体腔扫描式法布里-珀罗干涉仪进行大气Rayleigh散射谱型的精细探测方法和残余米散射信号的抑制方法.根据Rayleigh散射谱特点,针对固体腔扫描式法布里-珀罗干涉仪的自由光谱区、固体腔几何长度、腔体介质类型、半高全宽、腔体反射率、扫描间隔等参数进行了优化设计.利用优化参数的固体腔扫描式法布里-珀罗干涉仪获取Rayleigh散射谱上离散点信息,并采用多项式插值方法获得拟合谱型,与根据标准大气模型和S6模型获得的理论谱型进行比对,大气温度探测不确定度小于0.8 K.当信噪比为10时,白天与夜晚的探测距离分别为4.5和7.9 km.该方法可实现大气温度廓线的全天时和高精度绝对探测,并对同类高光谱激光雷达分光系统研究具有借鉴意义,为我国高光谱激光雷达陆基及星载应用提供了一套可行的分光系统解决方案.     

一种基于双波长的光声测温技术

光声测温是一种利用光声效应来进行温度监控的新方法,具有非侵入式、高灵敏度和探测深度较深等优点.但现有的单波长光声测温方法极易受到系统及测量环境干扰而导致测量精度降低.为了解决这一问题,本文提出了一种双波长光声温度测量方法.在光声测温理论的基础上,分析推导了双波长光声测温的基本原理,并进行了仿体及离体组织样品的双波长光声测温实验.实验结果显示,与传统单波长模式相比,双波长模式下的光声温度测量误差明显减小,测量精度平均提高35%以上.研究结果表明双波长光声测温方法能够有效提高光声温度测量的精度和稳定性,可作为一种更精准的光声温度监控方法应用于医疗手术等领域.     

Ionic liquid-based electrolyte with dual-functional LiDFOB additive toward high-performance LiMn<Subscript>2</Subscript>O<Subscript>4</Subscript> batteries

Manganese oxide-based cathodes are one of the most promising lithium-ion battery (LIB) cathode materials due to their cost-effectiveness, high discharge voltage plateau (above 4.0 V vs. Li/Li⁺), superior rate capability, and environmental benignity. However, these batteries using conventional LiPF₆-based electrolytes suffer from Mn dissolution and poor cyclic capability at elevated temperature. In this paper, the ionic liquid (IL)-based electrolytes, consisting of 1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfon)imidate (PYR_1,4-TFSI), propylene carbonate (PC), lithium bis(trifluoromethanesulfon)imide (LiTFSI), and lithium oxalyldifluoroborate (LiDFOB) additive, were explored for improving the high temperature performance of the LiMn₂O₄ batteries. It was demonstrated that LiTFSI-ILs/PC electrolyte associated with LiDFOB addition possessed less Mn dissolution and Al corrosion at the elevated temperature in LiMn₂O₄/Li batteries. Cyclic voltammetry and electrochemical impedance spectroscopy implied that this kind of electrolyte also contributed to the formation of a highly stable solid electrolyte interface (SEI), which was in accordance with the polarization measurement and the Li deposition morphology of the symmetric lithium metal cell, thus beneficial for improving the cycling performance of the LiMn₂O₄ batteries at the elevated temperature. Cyclic voltammetry and electrochemical impedance spectroscopy implied that the cells using this kind of electrolyte exhibited better interfacial stability, which was further verified by the polarization measurement and the Li deposition morphology of the symmetric lithium metal cell, thus beneficial for improving the cycling performance of the LiMn₂O₄ batteries at the elevated temperature. These unique characteristics would endow this kind of electrolyte a very promising candidate for the manganese oxide-based batteries.     

Effects of different precipitants on LiNi<Subscript>0.5</Subscript>Mn<Subscript>1.5</Subscript>O<Subscript>4</Subscript> for lithium ion batteries prepared by modified co-precipitation method

Effects of two different precipitants of Na₂CO₃ and Na₂C₂O₄ on LiNi_0.5Mn_1.5O₄ (LNMO) cathode materials, which are prepared by a modified co-precipitation method, have been investigated. Various measurements have been applied to characterize the physical and electrochemical performances of LNMO. Compared with the LNMO prepared by the oxalate co-precipitation (LNMO2), the material synthesized by the carbonate co-precipitation (LNMO1) not only shows more uniform porosity and smaller particles but also has a better rate capability and cycling performance. In addition, the sample prepared by carbonate has a stable spherical structure, due to the fact that carbonate co-precipitation with less gas release during calcination can prevent the destruction of the as-prepared LNMO material structure and promote the formation of regular particle and aperture. Based on the electrochemical test results, LNMO1 shows greatly enhanced electrochemical performance of a high initial discharge capacity of 125.6 mAh g^?1 at 0.25 °C, as well as a preferably capacity retention of 96.5% after 100 cycles at 0.5 °C. And even at a high rate of 10 °C, the discharge capacity of LNMO1-based cell still approaches 83.1 mAh g^?1.