塔菲尔方程
电解质
腐蚀
电化学
合金
介电谱
电极
极化(电化学)
材料科学
氢气储存
氧化物
化学工程
分析化学(期刊)
无机化学
化学
冶金
物理化学
色谱法
工程类
作者
Chengyuan Ni,Huaiying Zhou,Zhongmin Wang,Qingrong Yao,Lanying Lu
标识
DOI:10.1016/s1452-3981(23)07935-x
摘要
The effect of electrolytes on the electrochemical properties of MmNi3.68Co0.72Mn0.43Al0.17 hydrogen storage alloy electrodes has been investigated at 303 K and 273 K. Three electrolytes (EL1, EL2, EL3) were obtained by adding 2 wt%, 4 wt% and 6 wt% LiOH into the original electrolyte EO (6 M/L KOH), respectively. The results indicate that the addition of LiOH improves the discharge capacity and cycle life at 303 K and 273 K. The highest maximum capacity and capacity retention (after 50th cycles) have been observed in electrolyte EL2. However, the high-rate dischargeability (HRD) decreases gradually from EO to EL3 at the two temperatures because of the addition of LiOH. The corrosion current Icorr from Tafel Polarization curves (TP) and the resistance of the oxide layer Rol from electrochemical impedance spectroscopy (EIS) indicates that the alloy electrode worked in EL1 has a better anti-corrosion ability. The real surface area of the electrodes estimated with EIS analysis, decrease from 51.95 cm2 in EO to 15.6 cm2 in EL2, but increase to 31.59 cm2 in EL3 after being fully activated. The additional LiOH improves the anti-pulverization ability of alloy powders, delay the loss of active elements within the alloy electrode, resulting in an inproved capacity retention of alloy electrode. Meanwhile, the electrochemical kinetics analysis suggests that the charge-transfer reaction at the interface of electrode surface and electrolyte is the rate-determining step when tested at 303 K and 273 K.
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