材料科学
锂(药物)
固态
图层(电子)
硫黄
化学工程
纳米技术
光电子学
无机化学
物理化学
化学
冶金
医学
内分泌学
工程类
作者
Hao Li,Lianmeng Cui,Fanglin Wu,J Wang,Yapeng Cheng,Canhuang Li,Jiangping Song,Yafeng Li,Dan Liu,Andreu Cabot,Chaoqi Zhang,Haolin Tang
标识
DOI:10.1002/aenm.202501259
摘要
Abstract Inadequate ionic transport across the electrode/electrolyte interface hampers the lithium‐sulfur reaction kinetics, thereby limiting the electrochemical performance of all‐solid‐state lithium‐sulfur batteries (ASSLSBs). Herein, a kinetically‐enhanced gradient modulator layer (KEGML) is proposed and fabricated via potential modulation. In situ/ex situ analyses reveal the optimal modulated potential difference driving the chemical reaction between Li ions and the P 2 S 5 pre‐interphase product for stabilized KEGML and maintained full‐sulfur conversion. Cryo‐focused ion beam‐scanning electron microscopy characterization and ab‐initio molecular dynamics confirm the interfacial reinforcement by gradient uniformization of ion transport and enhanced interface stability by efficiently avoiding the side effects between sulfur/sulfides solid electrolyte/carbon, respectively. As a result, an eightfold increase in ionic transport capability is achieved with KEGML at the end of the 200 cycles. Impressively, KEGML‐based ASSLSBs not only accelerate the redox conversions but also display an exceptional cycling stability of a specific capacity of 1578.9 mAh g −1 for ≈1.5 years with a 99.9% capacity retention and a high areal capacity of 13 mAh cm −2 over 200 cycles, which is among the record‐level. Even in the ambient environment from 60 °C to as low as −30 °C, it exhibits excellent adaptivity attributed to the fast kinetics, shedding light on future practical applications.
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