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用于先进硫基水系电池的高价硫代硫酸盐氧化还原电化学

High-Valent Thiosulfate Redox Electrochemistry for Advanced Sulfur-Based Aqueous Batteries.

作者信息

Feng Yutong, Wang Boya, Zhou Wanhai, Jin Hongrun, Yu Xiaoyu, Zhang Tengsheng, Zhao Jian, Li Hongpeng, Zhao Jingwen, Li Wei, Ma Chenyan, Chao Dongliang, Zhao Dongyuan

机构信息

Laboratory of Advanced Materials, Shanghai Key Laboratory of Molecular Catalysis and Innovative Materials, College of Chemistry and Materials, Fudan University, Shanghai 200433, PR China.

CAS Key Laboratory of Science and Technology on Applied Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian 116023, PR China.

出版信息

J Am Chem Soc. 2024 Sep 11;146(36):25343-25349. doi: 10.1021/jacs.4c10159. Epub 2024 Aug 28.

Abstract

Sulfur-based aqueous batteries (SABs) are promising for safe, low-cost, and high-capacity energy storage. However, the low output voltage of sulfur cannot meet the demands of high-energy cathode applications due to its intrinsic negative potential (E = -0.51 V vs SHE) of low-valent polysulfide redox (S/S). Here, instead of relying on traditional aqueous polysulfide redox, for the first time, we demonstrate a high-valent thiosulfate redox (SO/SO) electrochemistry, exhibiting positive redox potential (E > 0 V vs SHE) and reversible cation storage in aqueous environment. X-ray absorption fine structure spectroscopy, Raman spectroscopy, and density functional theory calculations reveal the high reversibility and dynamic charge transfer process of high-valent thiosulfate redox. Significantly, the aqueous thiosulfate redox exhibits a high operating voltage of approximately 1.4 V, a reversible capacity of 193 Ah L, and a long cycling life of over 1000 cycles (99.6% capacity retention). This work provides new insights into the high-valent S-based electrochemistry and opens a new pathway to achieve energetic aqueous batteries.

摘要

硫基水系电池(SABs)在安全、低成本和高容量储能方面具有广阔前景。然而,由于低价多硫化物氧化还原(S/S)的固有负电位(E = -0.51 V vs SHE),硫的低输出电压无法满足高能量阴极应用的需求。在此,我们首次展示了一种高价硫代硫酸盐氧化还原(SO/SO)电化学,而不是依赖传统的水系多硫化物氧化还原,该电化学在水性环境中表现出正的氧化还原电位(E > 0 V vs SHE)和可逆的阳离子存储。X射线吸收精细结构光谱、拉曼光谱和密度泛函理论计算揭示了高价硫代硫酸盐氧化还原的高可逆性和动态电荷转移过程。值得注意的是,水系硫代硫酸盐氧化还原表现出约1.4 V的高工作电压、193 Ah L的可逆容量和超过1000次循环的长循环寿命(容量保持率99.6%)。这项工作为高价硫基电化学提供了新的见解,并开辟了一条实现高能水系电池的新途径。

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