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

机译:钙钛矿型氧化物LaGaO3作为Ni-MH二次电池新型负极材料的电化学性能研究

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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.
机译:本文采用溶胶-凝胶法合成了钙钛矿型氧化物LaGaO3,提出了一种新型的二次电池负极材料。使用计时电位法,电位动力学极化法和计时电流单体技术在328 K的温度下分析了氧化物的电化学性能。在前三个充电/放电循环中,氧化物LaGaO3的放电容量在220 mAh g(-1)时达到最大值,然后降低。氧化物的循环稳定性的降低可以通过电极的腐蚀行为来解释,这是由于电化学反应随循环的电活性表面积的减少。动力学结果表明,活化后,阳极的交流电流密度I-0和氢扩散系数DH随电荷状态的增加而降低,这可以归因于从α相转变为β相时电极表面的变化。 。电极的整个电化学反应受两个重要过程控制:电极表面的电荷转移反应和氢原子在电极主体内的扩散。 (C)2016 Elsevier Ltd和Techna Group S.r.l.版权所有。

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