摘要
在密封的电池体系中(即贫液状态),包铜储氢合金电极具有较好的抗氧化能力;而在强碱性溶液中(即富液状态),铜在电极工作的电位范围内(-1.1~-0.4V)具有一定的稳定性,但当扩展扫描范围(-1.1~-0.2V),将出现铜的氧化还原反应.随着充放电循环的进行,铜被氧化成Cu2O,进而形成CuO2-2进入电解质(KOH)溶液中,充电时又以Cu的形式于电极表面析出.针对这一现象,本文利用电位阶跃实验研究了CuO2-2离子在镍电极上的电沉积过程。
Negative electrode made from Cu microencapsulated hydrogen storage alloy was studied by using cyclic voltammetry method. The results showed that copper as a coating material was of a certain stability in 5 mol/L KOH solution within the range of charge and discharge voltage. But when expanding the sweep voltage, the CV curve showed a pair of distinct oxidation reduction current peaks of Cu 2O formation at E =-0.3 V and Cu 2O reduction at E =-0.6 V. With charging discharging cycles, copper is liable to be oxidized to Cu 2O and further oxidized into CuO 2- 2. When charged again, CuO 2- 2 anion is reduced and Cu is electrodeposited on the sufrace of electroce. In respond to this phenomenon, the electrodeposition process of CuO 2- 2 on the smooth Ni electrode was studied by constant potential step technique. The results showed that the deposition process of copper followed the two dimension instantaneous mechanism.
出处
《电化学》
CAS
CSCD
1997年第3期263-270,共8页
Journal of Electrochemistry
关键词
储氢合金
表面包覆
铜
电沉积
镍电极
Hydrogen storage alloy, Microencapsulation, Copper, Cyclic voltammetry, Constant potential step technique, Electrodeposition