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作 者:李安铭[1] 呼梦娟[1] 刘宝忠[1] 范燕平[1] 张宝庆[1] 张志[1]
机构地区:[1]河南理工大学材料科学与工程学院,河南焦作454000
出 处:《河南理工大学学报(自然科学版)》2012年第3期334-339,共6页Journal of Henan Polytechnic University(Natural Science)
基 金:国家自然科学基金资助项目(51001043);中国博士后特别资助项目(201104390);中国博士后基金资助项目(20100470990);包头市科技发展计划(2011J1003);河南理工大学博士基金资助项目(B2010-13)
摘 要:采用真空电弧熔炼和热处理方法制备了La1-xCexNi3.54Co0.78Mn0.35Al0.32(x=0.1,0.2,0.3,0.4,0.5,0.6)贮氢合金.X射线衍射(XRD)分析表明,合金含有单一CaCu5型六方结构相.电化学性能测试表明,随着x的增加,合金的最大放电容量从348.1mAh/g(x=0.1)单调地减小到310.1 mAh/g(x=0.6);HRD1200先从28.6%(x=0.1)增加到65.4%(x=0.5)然后降低到60.1%(x=0.6),归因于合金表面的电催化活性和合金体内氢原子扩散速率均随x的增大先增大后减小.The hydrogen storage alloys La1- x Ce Ni3.54 Coo. 78 Mn0 35 A10.32 ( x = 0. 1,0.2,0. 3,0.4,0.5,0.6 ) were synthesized by induction melting and heat treatment. XRD analysis indicated that the alloys consisted of a single CaCu5 -type phase. The electrochemical performance test showed that with increasing x value, the maximum discharge capacity decreased monotonically from 348.1 to 310. 1 mAh/g. For the discharge current density of 1200 mA/g, the HRD of the alloy electrode first increased from 28.6% (x = O. 1 ) to 65.4% (x = 0.5) , and then decreased to 60. 1% (x = O. 6). This was mainly attributed to the electrocatalytic activity for charge - transfer reaction at the electrode/electrolyte interface and the hydrogen diffusion in the bulk of alloys, which increased first and then decreased.
分 类 号:TG132.25[一般工业技术—材料科学与工程]
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