阴极
水溶液
阳极
氧化还原
电池(电)
化学工程
材料科学
有机自由基电池
电极
导电体
相(物质)
电化学
双水相体系
无机化学
四氰基对醌二甲烷
动力学
化学
纳米技术
电流密度
电压
锂离子电池的纳米结构
作者
Mingyi Ning,Jinshu Zhang,Jianxue Wu,Yantuo Li,Yang Yang,Bingjie Ma,Liang Liu,Wei Liu
标识
DOI:10.1002/batt.202500722
摘要
Aqueous copper‐ion batteries are attractive for their cost, safety, and sustainability but are limited by a narrow voltage window and modest rate performance. A coupled‐redox strategy is proposed in which the organic molecular cathode 7,7,8,8‐ tetracyanoquinodimethane (TCNQ) and Cu 2+ each accept one electron to form TCNQ – and Cu + , which then coordinate into a conductive CuTCNQ phase formed in situ. This phase accelerates charge transport and stabilizes the redox process, delivering a specific capacity of 171 mAh g −1 at 0.5 A g −1 . Owing to the fast kinetics of CuTCNQ, the cell retains a specific capacity of 82 mAh g −1 after 700 cycles at a high current density of 5 A g −1 . Extending the concept to a decoupled Zn//TCNQ aqueous battery with a TCNQ cathode and Zn anode yields an operating voltage of 1.32 V. These results show that pairing an organic‐molecule with Cu 2+ to form a conductive coordination phase is an effective route to high‐rate, long‐life aqueous copper‐ion storage and broadens the role of organic electrodes in aqueous batteries.
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