镍
循环伏安法
氧化还原
材料科学
电化学
钴
电池(电)
阳极
阴极
化学工程
共晶体系
电极
沉积(地质)
无机化学
过渡金属
水溶液
选择性
金属
深共晶溶剂
阴极保护
资源回收
动力学
作者
Zhi Yi Leong,Jintao Zhang,Yu Li,Yongtai Xu,Zhaolin Liu,Yunhe Hou,Tiande Mo,Hui Ying Yang
标识
DOI:10.1021/acs.est.6c02921
摘要
Growing demand for electric vehicles has intensified the need for sustainable recovery of critical metals from end-of-life lithium-ion batteries (LIBs). A specific challenge is the separation of Ni and Co due to nearly identical coordination chemistry and redox potentials. Here, we report a bipolar pulsed electrodeposition strategy in reline deep eutectic solvent (DES) that enables selective separation of Ni and Co without the use of aqueous acids or organic extractants. Spectroscopic analyses reveal that Ni2+ and Co2+ exist predominantly as tetrahedral [NiCl4]2- and [CoCl4]2- complexes in reline, while cyclic voltammetry shows distinct redox kinetics that can be temporally modulated through alternating cathodic and anodic pulses. This dynamic control drives preferential Ni deposition and rapid Co stripping, producing progressively Ni-enriched films with tunable morphologies. COMSOL simulations reproduce the periodic current response and confirm that selectivity arises from kinetic asymmetry rather than equilibrium speciation. These findings establish the use of bipolar pulsed electrodeposition for targeted separation of Ni and Co, offering a green perspective for green electrochemical metal recovery and circular battery resource management.
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