Annealing effects on structural and electrochemical properties of (LaPrNdZr)0.83Mg0.17(NiCoAlMn)3.3 alloy

被引:98
作者
Li, F. [1 ]
Young, K. [1 ]
Ouchi, T. [1 ]
Fetcenko, M. A. [1 ]
机构
[1] Ovon Battery Co, Energy Convers Devices Inc, Rochester Hills, MI 48309 USA
关键词
Hydrogen absorbing materials; Transition metal alloys and compounds; Metal hydride; Electrochemical reactions; HYDROGEN STORAGE ALLOYS; METAL HYDRIDE ELECTRODES; NI/MH BATTERIES; INTERMETALLIC HYDRIDES; SLOPING PLATEAUS; CO; LA; PHASE; MICROSTRUCTURE; SUBSTITUTION;
D O I
10.1016/j.jallcom.2008.03.084
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
Rare-earth magnesium nickel based alloys (La0.205Pr0.392Nd0.392Zr0.012)(0.83)Mg0.17Ni2.97Co0.1Al0.2Mn0.03 were studied with various annealing conditions. The phase structures of the alloys before and after electrochemical cycling were examined by x-ray diffraction and Rietveld analysis. The alloys mainly consisted of two or more phases from the group of Ce2Ni7-, CaCu5-, Ce5Co19-, or CeNi3- type phases. Phase abundance drastically changed with different annealing temperatures. As the annealing temperature increased, hydrogen storage capacity first increased and then decreased as indicated by the pressure-concentration isotherms. The electrochemical test showed a similar trend, resulting in a maximum discharge capacity which started at 339 mAh/g (1173 K), increased to 345 mAh/g (1198K) and then decreased to 312 mAh/g (1273 K). The addition of Pr and Nd created a new AB3 phase with a CeNi3 structure after annealing, which contributed to better high rate dischargeability due to both a lower transferring resistance at the surface/electrolyte interface and a higher bulk diffusion coefficient. (c) 2008 Elsevier B. V. All rights reserved.
引用
收藏
页码:371 / 377
页数:7
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