Compatibility of Halide Electrolytes in Solid-State Li–S Battery Cathodes

作者：Shoma Yanagihara, Jan Huebner, Zheng Huang, Atsushi Inoishi, Hirofumi Akamatsu, Katsuro Hayashi, Saneyuki Ohno · 发表于：Chemistry of Materials · 年份：2024 · DOI：10.1021/acs.chemmater.4c02159 · 被引用次数：22 · 研究领域：Advanced Battery Materials and Technologies、Advancements in Battery Materials、Advanced Battery Technologies Research

High Resolution Image Download MS PowerPoint Slide The utilization of earth-abundant and high-capacity sulfur in solid-state batteries presents a promising strategy to circumvent the use of rare transition metals and enhance achievable specific energy. However, numerous challenges remain. The transport limitation within the cathode composite, particularly with sulfide electrolytes during charging, has been identified as a major degradation mechanism in solid-state Li–S batteries. This degradation is linked to electrolyte oxidation and a concomitant reduction in the effective ionic conductivity of the cathode composite. Inspired by the sufficiently high oxidation stability of halide-based electrolytes, we investigated their compatibility with solid-state Li–S batteries in this work. The electrochemical stability of halides in contact with conductive additives, the stability window of fast ion transport in the composite electrodes, and chemical compatibility with sulfur-active materials (e.g., S and Li 2 S), in addition to the cyclability of the halide-based composite electrodes, are explored. Three halides were employed as model electrolytes: Li 3 InCl 6, Li 3 YCl 6, and Li 3 YBr 6 . Despite its high oxidation stability, Li 3 InCl 6 exhibited rapid degradation due to electrolyte reduction. The composite with Li 3 YCl 6 lost its capacity because of chemical incompatibility, especially with Li 2 S, resulting in the formation of LiYS 2 at the interface. In contrast, Li 3 YBr 6 de...