材料科学
电解质
锂(药物)
电化学
化学工程
储能
离子电导率
快离子导体
准固态
纳米技术
电极
物理化学
热力学
化学
医学
功率(物理)
物理
工程类
内分泌学
色素敏化染料
作者
Kun Zhang,Feng Wu,Xinran Wang,Suting Weng,Xiaoyu Yang,Huichun Zhao,Ruiqi Guo,Yuheng Sun,Wenbin Zhao,Tinglu Song,Xuefeng Wang,Ying Bai,Chuan Wu
标识
DOI:10.1002/aenm.202200368
摘要
Abstract All‐solid‐state lithium batteries (ASSLBs), as the next‐generation energy storage system, potentially bridge the gap between high energy density and operational safety. However, the application of ASSLBs is technically handicapped by the extremely weak interfacial contact and dendrite growth that is prone to unstabilize solid electrolyte interphase (SEI) with limited electrochemical performance. In this contribution, air‐stable and interface‐compatible solid electrolyte/lithium integration is proposed by in situ copolymerization of poly(ethylene glycol methacrylate)‐Li 1.5 Al 0.5 Ge 1.5 (PO 4 ) 3 ‐lithium (PEGMA‐LAGP‐Li). The first‐of‐this‐kind hierarchy provides a promising synergy of flexibility‐rigidity (Young's modulus 3 GPa), high ionic conductivity (2.37 × 10 −4 S cm −1 ), high lithium‐ion transfer number ( t Li+ = 0.87), and LiF‐rich SEI, all contributing to homogenized lithium‐ion flux, significantly prolonged cycle stability ( > 3500 h) and obvious dendrite suppression for high‐performance ASSLBs. Furthermore, the integration protects lithium from air corrosion, providing insights into a novel interface‐enhancement paradigm and realizing the first ASSLBs assembly in ambient conditions without any loss of specific capacity.
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