河南理工大学学报:自然科学版
河南理工大學學報:自然科學版
하남리공대학학보:자연과학판
JOURNAL OF HENAN POLYTECHNIC UNIVERSITY
2012年
3期
334-339
,共6页
李安铭%呼梦娟%刘宝忠%范燕平%张宝庆%张志
李安銘%呼夢娟%劉寶忠%範燕平%張寶慶%張誌
리안명%호몽연%류보충%범연평%장보경%장지
贮氢合金%电化学性能%动力学性能
貯氫閤金%電化學性能%動力學性能
저경합금%전화학성능%동역학성능
Hydregen storage alloy%electrochemical performance%kinetics performance
采用真空电弧熔炼和热处理方法制备了La1-x Cex Ni3.54 CO0.78 Mn0.35 A10.32(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-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310.1mAh/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z的增大先增大后减小.
採用真空電弧鎔煉和熱處理方法製備瞭La1-x Cex Ni3.54 CO0.78 Mn0.35 A10.32(x=0.1,0.2,0.3,0.4,0.5,0.6)貯氫閤金.x射線衍射(XRD)分析錶明,閤金含有單-CaCu5型六方結構相.電化學性能測試錶明,隨著x的增加,閤金的最大放電容量從348.1mAh/g(x=0.1)單調地減小到310.1mAh/g(x=0.6);HRD1200先從28.6%(x=0.1)增加到65.4%(x=0.5)然後降低到60.1%(x=0.6),歸因于閤金錶麵的電催化活性和閤金體內氫原子擴散速率均隨z的增大先增大後減小.
채용진공전호용련화열처리방법제비료La1-x Cex Ni3.54 CO0.78 Mn0.35 A10.32(x=0.1,0.2,0.3,0.4,0.5,0.6)저경합금.x사선연사(XRD)분석표명,합금함유단-CaCu5형륙방결구상.전화학성능측시표명,수착x적증가,합금적최대방전용량종348.1mAh/g(x=0.1)단조지감소도310.1mAh/g(x=0.6);HRD1200선종28.6%(x=0.1)증가도65.4%(x=0.5)연후강저도60.1%(x=0.6),귀인우합금표면적전최화활성화합금체내경원자확산속솔균수z적증대선증대후감소.
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.