阳极
电解质
卤化物
阴极
电池(电)
材料科学
储能
固态
快离子导体
大气压力
体积热力学
合金
能量密度
化学工程
纳米技术
冶金
工程物理
无机化学
化学
电极
电气工程
热力学
工程类
物理化学
功率(物理)
物理
海洋学
地质学
作者
Benjamin Hennequart,Maria Platonova,Ronan Chometon,Thomas Marchandier,Alessandro Benedetto,Elisa Quemin,Romain Dugas,Christophe Lethien,Jean‐Marie Tarascon
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2024-01-12
卷期号:9 (2): 454-460
被引量:6
标识
DOI:10.1021/acsenergylett.3c02513
摘要
All-solid-state batteries aim to provide increased safety and higher energy density for next-generation energy storage. However, challenges remain due to volume changes and inadequate contact between the cathode active material and solid electrolyte particles, leading to poor cyclability. This study investigates the use of the halide-based Li3YBr2Cl4 solid electrolyte to address these issues. Through experimental evaluations with the LiNi0.6Mn0.2Co0.2O2 cathode material, we demonstrate reliable operation down to 0.1 MPa against a LiIn alloy and 0.2 MPa against a Li metal anode, with limited capacity loss. Furthermore, we observe that pressures below 5 MPa do not hinder the rate capabilities, retaining 70% of the C/20 capacity even under 1C discharge rate. These findings underscore the potential of halide-based ASSBs for practical applications and Li metal integration, providing insights for developing reliable low-pressure all-solid-state battery systems.
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