Jian XIE
材料科学技术（英文）
Li-storage intermetallic compound FeSb2 was prepared by solvothermal method and was studied as a promising anode material for secondary lithium-ion batteries. The as-prepared powder was characterized by X-ray diffraction (XRD) and field emission scanning electron microscopy (FESEM). The electrochemical Li-storage performances of this intermetallic anode were evaluated in a two-electrode cell Li/LiPF6(EC+DMC)/FeSb2. It was found that the particle size of FeSb2 powder is in nanoscale and this intermetallic anode exhibited enhanced cycling behavior comparing to its microscaled counterpart prepared by levitation-melting/ball-milling route.
关键词:
FeSb2
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null
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null
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null
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null
Jian XIE
材料科学技术（英文）
The polyaniline (PAni)/polyvinylidene fluoride (PVDF) hybrid was served as a novel binder for CoSb3-based alloy electrode. The effect of PAni content on the electrochemical performances of the alloy electrode was investigated. It was found that the CoSb3 electrode using the binary PAni/PVDF binder exhibits higher reversible capacity than that using the single PVDF binder, especially in the initial cycles. As a result, the PAni/PVDF hybrid could be a promising binder for the alloy electrode.
关键词:
PAni/PVDF binder
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null
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null
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null
Jian XIE
,
Xinbing ZHAO
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Gaoshao CAO
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Mingjian ZHAO
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Yaodong ZHONG
材料科学技术（英文）
Some transition metal antimonides were prepared by levitation melting and subsequent ball-milling. The electrochemical behaviors of these materials as new candidate negative electrode materials in lithium ion secondary batteries were investigated. It was found that they exhibited significantly larger volumetric capacity than carbon-based materials. The formation and composition of solid electrolyte interface (SEI) film were characterized by electrochemical impedance spectroscopy (EIS) and Fourier transform infra-red (FTIR) spectroscopy.
关键词:
Antimonide
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null
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null
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null
徐菊良
,
邓博
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孙涛
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李劲
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蒋益明
金属学报
doi:10.3724/SP.J.1037.2009.00598
利用Thermo-Calc软件并结合金相显微镜,定性研究了2205双相不锈钢在800℃下敏化不同时间后的微观组织演变过程.通过研究扫描速率、介质成分、介质温度和试样表面状态优化了双环电化学动电位再活化法(DL-EPR),并用该优化方法研究了2205双相不锈钢晶间腐蚀敏感性.结果表明:DL-EPR法能定量评价σ相对2205双相不锈钢晶间腐蚀敏感性的影响,随敏化时间延长,σ相含量增多,晶jian 腐蚀敏感性也随之增加.腐蚀形貌的观测验证了这一规律,
关键词:
2205双相不锈钢
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DL-EPR
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晶间腐蚀敏感性
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σ相
刘建国
,
安振涛
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张倩
,
杜仕国
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姚凯
,
王金
材料导报
doi:10.11896/j.issn.1005-023X.2017.04.030
为评估氧化剂硝酸羟胺的热稳定性,使用标准液体铝皿于3 K/min、4 K/min、5 K/min加热速率下进行热分析.借助非等温DSC曲线的参数值,应用Kissinger法和Ozawa法求得热分解反应的表观活化能和指前因子,根据Zhang-Hu-Xie-Li公式、Hu-Yang-Liang-Xie公式、Hu-Zhao-Gao公式以及Zhao-Hu-Gao公式,计算硝酸羟胺的自加速分解温度和热爆炸临界温度,并对热分解机理函数进行了研究.设计了7条热分解反应路径,采用密度泛函理论B3LYP/6-311++G(d,p)方法对硝酸羟胺的热分解进行了动力学和热力学计算.计算结果表明,硝酸羟胺热分解的自加速分解温度TsADT=370.05 K,热爆炸临界温度Te0=388.68K,Tbp0=397.54 K,热分解最可几机理函数的微分形式为f(a) =17×(1-α)18/17.硝酸羟胺热分解各路径中,动力学优先支持路径Path 6、Path 5、Path 4和Path 1生成NO和NO2,其次是Path 2、Path 7和Path 3生成N2和N2O.温度在373 K以下时,Path 1'反应无法自发进行,硝酸羟胺无法进行自发的热分解.从热力学的角度来看,硝酸羟胺在370.05K以下储存是安全的.
关键词:
硝酸羟胺
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热分析
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热稳定性
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热分解机理
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密度泛函理论
