Fast-charging and durable all-solid-state lithium-sulfur batteries enabled by pre-embedded solid-solid redox mediator
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Updated: Nov 7, 2026

Solid-state Graft Copolymer Electrolytes for Lithium Battery Applications
Published on: August 12, 2013
Huimin Song1, Ruizhuo Zhang2, Chenxi Zheng3
1Beijing Key Laboratory for Theory and Technology of Advanced Battery Materials, School of Materials Science and Engineering, Peking University, Beijing, China.
Abstract:
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 I2/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 I2/I- nano-network throughout the positive electrode, thereby enabling fast charging. The cell exhibits a specific capacity of 851.9 mA h g-1S/I when charged at 10 C, and 474.7 mA h g-1S/I at a charging rate of 24 C (1 C is defined as 945 mA g-1S/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.
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