Study of electrochemical performances of perovskite-type oxide LaGaO3 for application as a novel anode material for Ni-MH secondary batteries

被引:16
作者
Kaabi, A. [1 ]
Tliha, M. [1 ,2 ]
Dhahri, A. [3 ]
Khaldi, C. [1 ]
Lamloumi, J. [1 ]
机构
[1] Univ Tunis, Lab Mech Mat & Proc, Grp Met Hydrides, ENSIT Ex ESSTT, Tunis, Tunisia
[2] Umm Alqura Univ, Univ Fac, Dept Phys, Al Qunfudah, Saudi Arabia
[3] Univ Monastir, Lab Phys Chem Mat, Monastir, Tunisia
关键词
Perovskite-type electrode; Electrochemical properties; Hydrogen absorbing materials; Hydrogen insertion; Hydrogen batteries; METAL HYDRIDE ELECTRODES; HYDROGEN-STORAGE; DIFFUSION-COEFFICIENT; NEGATIVE ELECTRODE; AL SUBSTITUTION; ALLOY; TI; NICKEL; COBALT;
D O I
10.1016/j.ceramint.2016.04.082
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
In this paper, the perovskite-type oxide LaGaO3, which is proposed as a novel anode material for secondary batteries, was synthesized by the sol-gel method. The electrochemical performance of the oxide was analyzed at temperature 328 K using chronopotentiometry, potentiodynamic polarization and chronoamperomertry techniques. During the first three of charge/discharge cycles, the discharge capacity of the oxide LaGaO3 reaches its maximum value at 220 mAh g(-1) and thereafter decreases. The degradation of cycling stability of the oxide can be explained by the corrosion behavior of the electrode as a result of the decrease in the electroactive surface area of the electrochemical reaction with cycling. The kinetic results showed that both the exchange current density I-0 and the hydrogen diffusion coefficient D-H of the anode decrease with increasing state of charge, after activation, which can be ascribed to the change in the electrode surface when transforming from alpha to beta phase. The whole electrochemical reactions of the electrode are governed by two important processes: charge-transfer reaction on the electrode surface and hydrogen atom diffusion within the bulk of the electrode. (C) 2016 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:11682 / 11686
页数:5
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