The electrochemical hydrogen storage properties of Mg67-xPdxCo33 (x=1, 3, 5, 7) electrodes with BCC phase

被引:4
|
作者
Zhan, Leyu [1 ,2 ]
Zhang, Yao [1 ,2 ]
Zhu, Yunfeng [3 ]
Zhuang, Xiangyang [1 ,2 ]
Dong, Jun [4 ]
Guo, Xinli [1 ]
Chen, Jian [1 ]
Wang, Zengmei [1 ]
Li, Liquan [3 ]
机构
[1] Southeast Univ, Sch Mat Sci & Engn, Nanjing 211189, Jiangsu, Peoples R China
[2] Jiangsu Key Lab Adv Metall Mat, Nanjing 211189, Jiangsu, Peoples R China
[3] Nanjing Tech Univ, Coll Mat Sci & Engn, Nanjing 210009, Jiangsu, Peoples R China
[4] Southeast Univ, Sch Informat Sci & Engn, Nanjing 210096, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
Mg-Co-based electrode alloys; Ball milling; Body-centered cubic structure; Electrochemical performances; Substitution; ALLOYS; CO; PERFORMANCES; SUBSTITUTION; ABSORPTION; DESORPTION; MG50CO50; BEHAVIOR; NICKEL; FE;
D O I
10.1016/j.jallcom.2015.12.068
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The ternary Mg67-xPdxCo33 (x = 1, 3, 5, 7) alloys were prepared and served as anode materials for the Ni-MH battery system. Pd facilitates the formation of a full body-centered cubic (BCC) phase in binary Mg67Co33. All Mg67-xPdxCo33 (x = 1, 3, 5, 7) alloys possess BCC structure in nano-crystalline, which were observed by XRD and TEM analyses. In addition, their lattice parameters increase with the augmentation of Pd content. The chargeedischarge experiments show that Mg64Pd3Co33 owns the maximum discharge capacity of 624 mAh g(-1) among Mg67-xPdxCo33 (x = 1, 3, 5, 7) electrodes, which was greatly enhanced from our previously studied binary Mg-Co and ternary Mg-Co-Pd electrodes. All electrochemical kinetics e. g. exchange current density, hydrogen atomic diffusion capability were improved by substituting Pd for Mg, which were also relevant with the increment of Pd amount in the alloys. X-ray photoelectric spectroscopy (XPS) and Inductively Coupled Plasma-Mass Spectrometry (ICP-MS) demonstrated that Pd relieved the severe corrosions and capacity degradations of the electrodes. (C) 2015 Elsevier B. V. All rights reserved.
引用
收藏
页码:396 / 403
页数:8
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