Feng Yutong, Yu Xiaoyu, Wang Boya, Zhang Tengsheng, Zhou Wanhai, Wang Yifeng, Li Xinran, Zhao Jian, Zhao Jingwen, Li Wei, Ma Chenyan, Zhao Dongyuan, Chao Dongliang
Laboratory of Advanced Materials, Aqueous Battery Center, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, State Key Laboratory of Molecular Engineering of Polymers, and Faculty of Chemistry and Materials, Fudan University, Shanghai, 200433, P. R. China.
School of Chemistry and Chemical Engineering, Liaoning Normal University, Dalian, 116029, P. R. China.
Angew Chem Int Ed Engl. 2025 Feb 17;64(8):e202420514. doi: 10.1002/anie.202420514. Epub 2024 Dec 4.
Sulfur-based aqueous batteries (SABs) are regarded as promising candidates for safe, low-cost, and high-energy storage. However, the sluggish redox kinetics of polysulfides pose a significant challenge to the practical performance of SABs. Herein, we report a unique redox regulation strategy that leverages thiosulfate-mediated ligand-chain interaction to accelerate the polysulfide redox process (S/S). The SO species in the electrolyte can induce the rapid reduction of polysulfide through a spontaneous chemical reaction with sulfur species, while facilitating the reversible oxidation of short-chain sulfides. Moreover, the thiosulfate redox pair (SO /SO ) within the KSO electrolyte contributes additional capacity at higher potential (E >0 V vs SHE). Consequently, the elaborate SAB delivers an unprecedented K storage capacity of 2470 mAh g , coupled with a long cycling life exceeding 1000 cycles. Remarkably, thiosulfate-mediated SAB achieves an energy density of 616 Wh kg , surpassing both organic K-S batteries and conventional aqueous battery systems. This work elucidates the mechanism underlying the thiosulfate-mediated polysulfide redox process, thereby opening a pathway for the development of high-energy aqueous batteries.
基于硫的水系电池(SABs)被视为安全、低成本和高能量存储的有前途的候选者。然而,多硫化物缓慢的氧化还原动力学对SABs的实际性能构成了重大挑战。在此,我们报告了一种独特的氧化还原调节策略,该策略利用硫代硫酸盐介导的配体-链相互作用来加速多硫化物氧化还原过程(S/S)。电解质中的SO 物种可以通过与硫物种的自发化学反应诱导多硫化物的快速还原,同时促进短链硫化物的可逆氧化。此外,KSO电解质中的硫代硫酸盐氧化还原对(SO /SO )在较高电位(E >0 V vs SHE)下贡献额外的容量。因此,精心设计的SAB提供了前所未有的2470 mAh g的钾存储容量,同时具有超过1000次循环的长循环寿命。值得注意的是,硫代硫酸盐介导的SAB实现了616 Wh kg的能量密度,超过了有机钾硫电池和传统水系电池系统。这项工作阐明了硫代硫酸盐介导的多硫化物氧化还原过程的机制,从而为高能水系电池的开发开辟了一条途径。