材料科学
电解质
盐(化学)
硼
锂(药物)
金属锂
金属
离子
无机化学
导电聚合物
化学工程
聚合物
电极
有机化学
化学
复合材料
冶金
医学
物理化学
工程类
内分泌学
作者
Changxing Han,Lixin Qiao,Gaojie Xu,Guansheng Chen,Kai Chen,Shenghang Zhang,Jun Ma,Shanmu Dong,Xinhong Zhou,Yongqin Han,Zili Cui,Guanglei Cui
标识
DOI:10.1021/acsami.3c15703
摘要
Polymer electrolytes (PEs) with excellent flexibility and superior compatibility toward lithium (Li) metal anodes have been deemed as one of the most promising alternatives to liquid electrolytes. However, conventional lithium bis(trifluoromethanesulfonyl)imide (LiTFSI)-based dual-ion PEs suffer from a low Li ion transference number and notorious Li dendrite growth. Here, a single-ion conducting polyborate salt without any fluorinated groups, polymeric lithium dihydroxyterephthalic acid borate (PLDPB), is presented for addressing the issues of Li metal batteries. Owing to a nearly immovable bulky anion and the presence of a rigid benzene structure, the PLDPB@poly(ethylene oxide) (PEO) PE exhibits an ultrahigh Li ion transference number (0.94) and excellent mechanical strength, which could significantly restrict the growth of Li dendrites. Postmortem analysis reveals that a fluorine-free solid electrolyte interphase (SEI) enriched with B-O and benzene-containing species is formed on the surface of the Li metal anode, thereby facilitating elimination of excessive parasitic reactions and simultaneously suppressing the formation of Li dendrites. Consequently, the LiFePO
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