电解质
材料科学
相间
正交晶系
化学工程
抗血小板
兴奋剂
快离子导体
离子键合
锂(药物)
电化学窗口
纳米技术
离子电导率
阳极
无机化学
电化学
不稳定性
工作(物理)
结构稳定性
分离器(采油)
离子
作者
Liyuan Qian,Yu Ye,Diancheng Chen,Dixing Ni,Haibin Lin,Xiaofei Wang,Liusuo Wu,Songbai Han,Jinlong Zhu,Yusheng Zhao
标识
DOI:10.1021/acsenergylett.6c00619
摘要
The development of solid-state lithium-metal batteries is hindered by interfacial instability at the Li metal–electrolyte interface and limited Li+ transport in inorganic electrolytes. Lithium-rich antiperovskites such as Li2OHCl are promising but suffer from unclear SEI chemistry and insufficient ionic conductivity. Herein, sulfur doping is introduced for the first time as a targeted strategy to engineer both the bulk structure and interfacial behavior of Li2OHCl. Partial substitution of O2– with S2– induces a transformation from orthorhombic to cubic structure, accompanied by lattice distortion and weakened Li–S bonding, which collectively reduce the Li+ migration barrier and enhance ionic conductivity. Furthermore, sulfur doping drives the formation of a Li2S-rich solid electrolyte interphase at the Li2OHCl/Li interface, enabling homogenized Li+ flux and effective suppression of lithium dendrite nucleation. This work provides a general heteroatom-doping strategy to optimize both bulk and interfacial characteristics in LiRAP electrolytes for advanced solid-state batteries.
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