材料科学
化学工程
锂(药物)
无机化学
化学
储能
电池(电)
锂离子电池的纳米结构
盐(化学)
能量密度
阴极
阳极
作者
Yuta Ito,Misae Otoyama,Yushi Fujita,Toyoki Okumura,Kazuki Yoshii
标识
DOI:10.1021/acsenergylett.6c01044
摘要
Abstract All-solid-state batteries (ASSBs) are next-generation energy storage systems with potential advantages in energy density and safety. However, loss of physical contact at the cathode−electrolyte interface during cycling leads to capacity fading. Here, we demonstrate that a supercooled, low-melting lithium salt enables a strategy for stabilizing cathode−electrolyte interfaces in sulfide-based ASSBs. The lithium salt, referred to as a single-cation ionic liquid (SCIL), exhibits a melting point of 76 °C and maintains a supercooled liquid state over periods. Through solvent-free processing at 90 °C, molten SCIL infiltrates interparticle voids without undesirable decomposition reactions, maintaining an ionic conductivity of 1.0 mS cm−1. When applied to composite cathodes, SCIL improves the initial Coulombic efficiency (from 76.8 to 85.2%), capacity retention (from 89.8 to 94.9% after 100 cycles), and rate capability (from 70 to 104 mAh g−1 at 1C). These findings demonstrate that supercooled lithium salts provide an interfacial stabilization strategy for sulfide-based ASSBs.
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