电解质
碳酸乙烯酯
阳极
枝晶(数学)
材料科学
电化学
腐蚀
锂(药物)
极化(电化学)
金属
环氧乙烷
碳酸二甲酯
无机化学
化学工程
化学
冶金
复合材料
甲醇
有机化学
电极
聚合物
医学
共聚物
几何学
数学
物理化学
工程类
内分泌学
作者
Chenglong Deng,Binbin Yang,Yaohui Liang,Yi Zhao,Boshun Gui,Chuanyu Hou,Yanxin Shang,Jinxiang Zhang,Tinglu Song,Xuzhong Gong,Nan Chen,Feng Wu,Renjie Chen
标识
DOI:10.1002/anie.202400619
摘要
Abstract The unstable interface between Li metal and ethylene carbonate (EC)‐based electrolytes triggers continuous side reactions and uncontrolled dendrite growth, significantly impacting the lifespan of Li metal batteries (LMBs). Herein, a bipolar polymeric protective layer (BPPL) is developed using cyanoethyl (−CH 2 CH 2 C≡N) and hydroxyl (−OH) polar groups, aiming to prevent EC‐induced corrosion and facilitating rapid, uniform Li + ion transport. Hydrogen‐bonding interactions between −OH and EC facilitates the Li + desolvation process and effectively traps free EC molecules, thereby eliminating parasitic reactions. Meanwhile, the −CH 2 CH 2 C≡N group anchors TFSI − anions through ion‐dipole interactions, enhancing Li + transport and eliminating concentration polarization, ultimately suppressing the growth of Li dendrite. This BPPL enabling Li|Li cell stable cycling over 750 cycles at 10 mA cm −2 for 2 mAh cm −2 . The Li|LiNi 0.8 Mn 0.1 Co 0.1 O 2 and Li|LiFePO 4 full cells display superior electrochemical performance. The BPPL provides a practical strategy to enhanced stability and performance in LMBs application.
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