电解质
溶解度
阴极
电池(电)
卤化物
离子电导率
材料科学
无机化学
溶解
电导率
铜
箔法
化学工程
导电体
电化学窗口
离子
铝
快离子导体
离子键合
电流密度
沉积(地质)
化学
电极
电阻率和电导率
离子交换
作者
Yueyue Wang,Limin Wang,Xiaolong Yan,Yang Xu,Xing-Yu Wang,Xiangzhen Zhu,Yanlong Wu,Xu Han,Changtai Zhao,Congying Fang,Xiao-kang Tan,Mengying Zhang,Yinzhuang Fang,Yingying Jiang,Biwei Xiao,Xiaona Li,Jianwen Liang,Tao Mei
标识
DOI:10.1002/anie.202518966
摘要
Abstract The Cu cathode has great potential due to its low cost and high capacity. However, the limited ionic conductivity of the electrolyte for Cu ions and poor solubility of Cu species severely hinder the rapid development of Li–Cu batteries. Herein, we synthesized a Cu + halide solid electrolyte (Cu 2 ZrCl 6 , CZC) by mechanochemical method, which exhibited a high room‐temperature Cu + conductivity (about 14 mS cm −1 ) and high solubility of Cu species. The Cu||CZC||Cu symmetric battery demonstrated the ability to maintain stable Cu + plating/stripping over 1000 h at 0.1 mA cm −2 . We further constructed a model of the synergistic migration and ion exchange of Cu + and Li + in CZC and Li 2 ZrCl 6 electrolytes. Based on this, we assembled the first all‐solid‐state lithium–copper battery (ASSLCB), which delivered a high reversible specific capacity of 360 mAh g −1 (1.7–3.8 V versus Li⁺/Li, at 37 mA g −1 ) and exhibited outstanding cycling performance across 50 cycles at a current of 62.5 mA g −1 . Additionally, we designed a cathode‐free ASSLCB, utilizing aluminum foil as the current collector to demonstrate the deposition and dissolution of pure copper metal. This study provides a new design concept for Cu + conductors and lays a foundation for the future research of ASSLCBs.
科研通智能强力驱动
Strongly Powered by AbleSci AI