电解质
阳极
电化学
金属锂
聚合物
乙醚
金属
极化(电化学)
化学工程
锂(药物)
材料科学
枝晶(数学)
碳酸乙烯酯
无机化学
化学
电极
有机化学
复合材料
冶金
物理化学
内分泌学
工程类
医学
数学
几何学
作者
Tuoya Naren,Gui‐Chao Kuang,Ruheng Jiang,Piao Qing,Hao Yang,Jialin Lin,Yuejiao Chen,Weifeng Wei,Xiaobo Ji,Libao Chen
标识
DOI:10.1002/anie.202305287
摘要
Lithium (Li) metal anodes have the highest theoretical capacity and lowest electrochemical potential making them ideal for Li metal batteries (LMBs). However, Li dendrite formation on the anode impedes the proper discharge capacity and practical cycle life of LMBs, particularly in carbonate electrolytes. Herein, we developed a reactive alternative polymer named P(St-MaI) containing carboxylic acid and cyclic ether moieties which would in situ form artificial polymeric solid electrolyte interface (SEI) with Li. This SEI can accommodate volume changes and maintain good interfacial contact. The presence of carboxylic acid and cyclic ether pendant groups greatly contribute to the induction of uniform Li ion deposition. In addition, the presence of benzyl rings makes the polymer have a certain mechanical strength and plays a key role in inhibiting the growth of Li dendrites. As a result, the symmetric Li||Li cell with P(St-MaI)@Li layer can stably cycle for over 900 h under 1 mA cm-2 without polarization voltage increasing, while their Li||LiFePO4 full batteries maintain high capacity retention of 96 % after 930 cycles at 1C in carbonate electrolytes. The innovative strategy of artificial SEI is broadly applicable in designing new materials to inhibit Li dendrite growth on Li metal anodes.
科研通智能强力驱动
Strongly Powered by AbleSci AI