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

被引:0
|
作者
Feng, Yutong [1 ]
Wang, Boya [1 ]
Zhou, Wanhai [1 ]
Jin, Hongrun [1 ]
Yu, Xiaoyu [1 ]
Zhang, Tengsheng [1 ]
Zhao, Jian [2 ]
Li, Hongpeng [1 ]
Zhao, Jingwen [3 ]
Li, Wei [1 ]
Ma, Chenyan [4 ]
Chao, Dongliang [1 ]
Zhao, Dongyuan [1 ]
机构
[1] Fudan Univ, Lab Adv Mat, Shanghai Key Lab Mol Catalysis & Innovat Mat, Coll Chem & Mat, Shanghai 200433, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, CAS Key Lab Sci & Technol Appl Catalysis, Dalian 116023, Peoples R China
[3] Chinese Acad Sci, Qingdao Inst Bioenergy & Bioproc Technol, Qingdao Ind Energy Storage Res Inst, Qingdao 266101, Peoples R China
[4] Chinese Acad Sci, Beijing Synchrotron Radiat Facil BSRF, Inst High Energy Phys, Beijing 100049, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
CATHODE; OXYGEN;
D O I
10.1021/jacs.4c10159
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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 = -0.51 V vs SHE) of low-valent polysulfide redox (S2-/S-0). Here, instead of relying on traditional aqueous polysulfide redox, for the first time, we demonstrate a high-valent thiosulfate redox (S2O32-/S4O62-) electrochemistry, exhibiting positive redox potential (E-0 > 0 V vs SHE) and reversible cation storage in aqueous environment. Operando X-ray absorption fine structure spectroscopy, in situ 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-1, 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.
引用
收藏
页码:25343 / 25349
页数:7
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