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锆基纳米复合储氢材料HTQAB2.1/Mg的微结构与电化学性能

The Microstructure and Electrochemical Performance of HTQAB2.1/Mg Zr-Based Nanocomposite Hydrogen Storage Materials

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【作者】 陈东马常祥陈廉陈德敏

【Author】 CHEN Dong1, MA Changxiang1, CHEN Lian2, CHEN Demin2(1. School of Science, Northeastern University, Shenyang 110004, China; 2. Institute of Metal Research, Chinese Academy of Sciences, Shenyang 110016, China.

【机构】 东北大学理学院东北大学理学院中国科学院金属研究所中国科学院金属研究所 辽宁沈阳 110004辽宁沈阳 110004辽宁沈阳 110016辽宁沈阳 110016

【摘要】 采用球磨复合+烧结处理(BMS)及机械复合+烧结处理(MMS)两种方法制备了Zr0.9Ti0.1(Ni0.57V0.10Mn0.28Co0.05)2.1 X%Mg(X=10,20)锆基纳米复合储氢材料·经XRD、TEM SAED分析表明,BMS和MMS的复合储氢材料皆由MgCu2型立方结构的单一C15 Laves相Zr基合金和密排六方结构的Mg金属构成,未发现两者之间的合金化效应·电化学测试表明,在60mA/g电流密度下,复合材料(MMS、BMS)活化性能好·MMS电极的最大放电容量为410mAh/g(X=20),而BMS的放电容量为360mAh/g(X=20)·在大电流密度下(≥3000mA/g),BMS电极的容量明显高于MMS电极,以BMS(HTQAB2 1 10%Mg)电极的大电流放电性能为最好·因此,HTQAB2 1锆基纳米复合材料不仅适用于高能量型NiMH动力电池而且更适用于高功率型NiMH动力电池·

【Abstract】 The Zrbased nanocomposite hydrogen storage materials Zr09Ti01(Ni055V012Mn028Co005)21X%Mg(X=10,20) were prepared by two ways: ballmilling+sintering treatment (BMS) and mechanical alloying+sintering treatment(MMS). XRD and TEMSAED examinations show that microstructure of the materials is composed of MgCu5type cubic structure C15Laves phase and hexagonal structure Mg. Their electrochemical performance tests show that the composite electrodes (MMS,BMS) have good activation properties at 60?mA/g current density. The maximum discharge capacity of MMS electrodes is 410?mAh/g(x=20),while BMS electrodes is 360?mAh/g(x=20). At high current density(≥3?000?mA/g),the discharge capacity of BMS electrodes is obviously higher than those of the MMS eletrodes. The BMS(HTQAB2110%Mg) electrode shows the best current density discharge performance. Therefore,HTQAB2.1 type Zrbased nanocomposite materials are suitable for not only highenergy NiMH batteries but also highpower NiMH batteries.

【基金】 国家"八六三"高技术计划资助项目(715 004 0233);国家重点基础研究发展规划项目(G2000026403)·
  • 【文献出处】 东北大学学报 ,JOURNAL OF NORTHEASTERN UNIVERSITY , 编辑部邮箱 ,2003年01期
  • 【分类号】TG139.8
  • 【被引频次】5
  • 【下载频次】145
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