阴极
氧化还原
离子
降级(电信)
储能
溶解
材料科学
化学
硫系化合物
化学工程
纳米技术
计算机科学
光电子学
物理化学
物理
冶金
有机化学
功率(物理)
工程类
电信
量子力学
作者
Xuelian Qu,Aobing Du,Tao Wang,Qingyu Kong,Guodong Chen,Zhonghua Zhang,Jingwen Zhao,Xin Liu,Xinhong Zhou,Shanmu Dong,Guanglei Cui
标识
DOI:10.1002/anie.202204423
摘要
Chalcogenides have been viewed as important conversion-type Mg2+ -storage cathodes to fulfill the high volumetric energy density promise of magnesium (Mg) batteries. However, the low initial Columbic efficiency and the rapid capacity degradation remain challenges for the chalcogenide cathodes, as the clear Mg2+ -storage mechanism has yet to be clarified. Herein, we illustrate that the charge storage mechanism of the Cu2-x Se cathode is a reversible displacement reaction along with a polyselenide (PSe) mediated solution process of anion-compensation. The unique anion redox improves charge storage, while the dissolution of PSe also leads to performance degradation. To address this issue, we introduce Mo6 S8 into the Cu2-x Se cathode to immobilize PSe, which significantly improves performance, especially the reversible capacity (from 140 mAh g-1 to 220 mAh g-1 ). This work provides inspiration for the modification of the Mg2+ -storage cathode, which is a milestone for high-performance Mg batteries.
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