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作 者:张大为[1] 袁华堂[1] 杨化滨[1] 周作祥[1] 张允什[1]
机构地区:[1]南开大学新能源材料化学研究所
出 处:《电化学》1997年第3期263-270,共8页Journal of Electrochemistry
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.
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