电解质
材料科学
阴极
化学工程
离子键合
相间
储能
纳米技术
硫化物
金属
离子电导率
阳极
半电池
离子液体
纳米颗粒
悬挂(拓扑)
电极
电化学
化学稳定性
离子强度
沉积(地质)
电化学窗口
作者
Wenting Fan,Yijiao Wang,Xiuying Jin,Yugen Zhang,Xiang Zhang,Tengfei Zhang
标识
DOI:10.1021/acssuschemeng.5c11416
摘要
Sulfide-based solid-state electrolytes (SSEs) are attractive candidates for high-energy all-solid-state lithium-ion batteries due to their high ionic conductivity. However, the intrinsic chemical instability against Li metal leads to continuous interfacial degradation. Herein, we design a gradient hybrid electrolyte by introducing a borohydride-based interfacial buffer to achieve complete anode-electrolyte isolation without sacrificing energy density. The borohydride component, with its intrinsic reducibility and deformability, facilitates the formation of a stable solid electrolyte interphase (SEI) while maintaining ionic transport comparable to pristine sulfide SSEs. Benefiting from this interfacial stabilization, the hybrid SSE enables long-term cycling over 2000 h and delivers a high specific capacity of 516.3 mAh g–1 at 10 C with selenium cathode featuring dual-electron reactions. This study demonstrates that borohydride-mediated interfaces effectively suppress parasitic reactions and provide a universal and scalable strategy to unlock the potential of sulfide-based solid-state batteries.
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