纳米片
电化学
硫化物
铜
镁
兴奋剂
硫化铜
材料科学
阴极
氧化还原
无机化学
化学工程
冶金
电极
化学
纳米技术
光电子学
物理化学
工程类
作者
Xin Liu,Youqi Zhu,Changliang Du,Jiachen Tian,Lifen Yang,Xiuyun Yao,Zhitao Wang,Xilan Ma,Jianhua Hou,Chuanbao Cao
标识
DOI:10.1016/j.cej.2023.142433
摘要
Sluggish kinetics and inferior redox reversibility have limited the further development of the CuS cathode material in advanced rechargeable magnesium batteries. Herein, a cation-doping strategy is reported to regulate the electrochemical Mg2+ storage behaviors of Co-doped CuS nanosheet cathodes via an effective microwave assisted synthesis technique. With cationic Co-doping, the fast electrochemical diffusion kinetics and optimized reversible redox reaction could be achieved over Co-doped CuS nanosheet cathodes. Specifically, the optimized Co-doped CuS nanosheet cathodes deliver excellent reversible capacity of 297 mAh g−1 under 200 mA g−1, outstanding rate capabilities of 143.4 mAh g−1 at 1.0 A g−1, and enhanced long-term cyclic life with 0.0722 % capacity decay of per cycle at 1.0 A g−1. The enriched electrochemical performance of Co-doped CuS nanosheet cathodes can be attributed to the cation-doping effect that could efficiently shield the strong Coulombic effect among magnesium ions and host anions to accelerate Mg2+ diffusion kinetics. Therefore, the cationic Co-doping strategy provides a novel avenue to regulate the favorable cathode reaction for rapid magnesium storage.
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