Highlighting the electrochemical performance of AB4-type single-phase La0.60Sm0.22Mg0.18Ni4.09Al0.09Mn0.10 hydrogen storage alloy for nickel metal hydride batteries

被引:0
|
作者
Zhang, Ning [1 ]
Lu, Hang [1 ]
Wang, Wen-Feng [1 ]
Jia, Qiu-Yue [1 ]
Zhang, An-Yi [1 ]
Li, Yuan [1 ]
Xi, Ning [2 ]
Han, Shu-Min [1 ,2 ]
Zhang, Lu [1 ,2 ]
机构
[1] Yanshan Univ, Hebei Key Lab Appl Chem, State Key Lab Metastable Mat Sci & Technol, Qinhuangdao 066004, Peoples R China
[2] Baotou Zhongke Xuanda New Energy Technol Co LTD, Baotou 014030, Peoples R China
来源
RARE METALS | 2025年
关键词
Nickel metal hydride batteries; RE-Mg-Ni-based alloys; Hydrogen storage alloys; AB(4)-type superlattice structure; Cyclic stability; High rate discharge ability; NI-BASED ALLOYS; CYCLING STABILITY; MN CONTENT; AS-CAST; LA; MG; A(2)B(7); RE; SM; MICROSTRUCTURE;
D O I
10.1007/s12598-024-03118-5
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Rare earth-Mg-Ni-based superlattice structure alloys have garnered recognition as promising materials for hydrogen storage. However, their application is impeded by suboptimal cycling longevity. The novel AB(4)-type alloy emerges as an attractive candidate, distinguished by its good structure stability, high rate capability, and long-term durability. Herein, we designed an AB(4)-type La0.60Sm0.22Mg0.18Ni4.09Al0.09Mn0.10 alloy that manifests superior electrochemical performance. The obtained AB(4)-type single-phase alloy delivers a high discharge capacity of 375.2 mAh<middle dot>g(-1) and features outstanding discharge ability at high rates, maintaining 121 mAh<middle dot>g(-1) even at a discharge rate of 6C. The excellent high-rate discharge performance can be attributed to its fast charge transfer and hydrogen diffusion kinetics. Moreover, the AB(4)-type alloy maintains a capacity retention of 84.5% after 200 cycles and retains 55.7% of its capacity retention even after 500 cycles. This work provides a good alternative to hydrogen storage alloy with high power and long cycling durability performance for nickel metal hydride batteries.
引用
收藏
页码:3392 / 3404
页数:13
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