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Fast-charging and durable all-solid-state lithium-sulfur batteries enabled by pre-embedded solid-solid redox mediator

Journal 2026 · IF 18.1 · 发表于 2026 年 10 月 9 日
作者: Song Huimin,Zhang Ruizhuo,Zheng Chenxi,Münch Konrad,Shen Kaier,Liu Fang,Hong Xufeng,Wang Hong,Meng Jiashen,Yan Yingjing,Shi Weize,He Mengxue,Ma Yue,Li Yitao,Xiao Zhitong,Shafqat Muhammad Burhan,Gao Xin,Wu Jinsong,Luo Mingchuan,Song Tinglu,Ma Chenyan,Zheng Lei,Gao Peng,Safari Mohammadhosein,Wang Yu,Henkel Philip,Janek Jürgen,Brezesinski Torsten,Pang Quanquan
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摘要

All-solid-state lithium-sulfur batteries promise high specific energy and low cost. However, they are challenged by poor rate capability and cycling stability owing to the slow solid-solid sulfur redox reactions. Here, we present fast-charging and durable all-solid-state lithium-sulfur batteries enabled by a pre-embedded solid-solid redox mediator using an amorphous sulfur/iodine nano-eutectic positive electrode. The iodine, intimately homogenized with sulfur owing to carbon mesopore encapsulation, undergoes rapid I 2 /I − redox reaction, mediating solid-solid sulfur reactions by promoting electron transfer across the boundaries. The iodine within the carbon and on its surface reacts in situ with the sulfide catholyte to form a globally distributed I 2 /I − nano-network throughout the positive electrode, thereby enabling fast charging. The cell exhibits a specific capacity of 851.9 mA h g −1 S/I when charged at 10 C, and 474.7 mA h g −1 S/I at a charging rate of 24 C (1 C is defined as 945 mA g −1 S/I ). The high reversibility of the redox-mediated reaction enables durable cycling for 9,000 cycles over 9 months at 2 C and 2,800 cycles over 17 months at 0.5 C. This strategy represents a perspective for developing solid-state conversion electrodes that are plagued by sluggish reactions.