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用于锂金属电池的自支撑单离子硼酸盐基聚合物电解质

Self-Standing Single-Ion Borate Salt-Based Polymer Electrolyte for Lithium Metal Batteries.

作者信息

Han Changxing, Qiao Lixin, Xu Gaojie, Chen Guansheng, Chen Kai, Zhang Shenghang, Ma Jun, Dong Shanmu, Zhou Xinhong, Han Yongqin, Cui Zili, Cui Guanglei

机构信息

Department of Polymer Material, College of Materials Science and Engineering, Shandong University of Science and Technology, Qingdao 266510, P. R. China.

Qingdao Industrial Energy Storage Research Institute, Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao 266101, China.

出版信息

ACS Appl Mater Interfaces. 2024 Sep 18;16(37):48792-48802. doi: 10.1021/acsami.3c15703. Epub 2023 Dec 27.

Abstract

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/Li cells with PLDPB@PEO PEs show an improved long-term cycling performance and high capacity retention (90.0%) and Coulombic efficiency (99.9%) after 500 cycles. This work may inspire new ideas to boost the development of single-ion conducting salts for dendrite-free Li metal batteries.

摘要

具有出色柔韧性且与锂金属阳极具有优异兼容性的聚合物电解质(PEs),被视为液体电解质最有前景的替代品之一。然而,传统的基于双(三氟甲磺酰)亚胺锂(LiTFSI)的双离子聚合物电解质存在锂离子迁移数低和锂枝晶生长严重的问题。在此,提出了一种不含任何氟基团的单离子导电聚硼酸盐,聚对苯二甲酸二羟基锂硼酸酯(PLDPB),以解决锂金属电池的问题。由于存在几乎不动的大体积阴离子和刚性苯结构,PLDPB@聚环氧乙烷(PEO)聚合物电解质表现出超高的锂离子迁移数(0.94)和优异的机械强度,这可以显著抑制锂枝晶的生长。死后分析表明,在锂金属阳极表面形成了富含B-O和含苯物种的无氟固体电解质界面(SEI),从而有助于消除过多的寄生反应,同时抑制锂枝晶的形成。因此,采用PLDPB@PEO聚合物电解质的LiFePO/Li电池在500次循环后表现出改善的长期循环性能、高容量保持率(90.0%)和库仑效率(99.9%)。这项工作可能会激发新的思路,以推动用于无枝晶锂金属电池的单离子导电盐的发展。

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