Surface-localized phase mediation accelerates quasi-solid-state reaction kinetics in sulfur batteries

被引:10
作者
Liu, Yatao [1 ,2 ]
An, Yun [1 ]
Fang, Chi [3 ]
Ye, Yaokun [3 ]
An, Yifeng [1 ]
He, Mengxue [1 ]
Jia, Yongfeng [1 ]
Hong, Xufeng [1 ]
Liu, Yumei [1 ]
Gao, Song [1 ]
Hao, Yizhou [4 ]
Chen, Jianhao [4 ]
Zheng, Jiaxin [3 ]
Lu, Yunfeng [2 ,5 ]
Zou, Ruqiang [1 ]
Pang, Quanquan [1 ]
机构
[1] Peking Univ, Sch Mat Sci & Engn, Beijing Key Lab Theory & Technol Adv Battery Mat, Beijing, Peoples R China
[2] Beijing Univ Chem Technol, Coll Chem Engn, State Key Lab Organ Inorgan Composites, Beijing, Peoples R China
[3] Peking Univ, Sch Adv Mat, Shenzhen Grad Sch, Shenzhen, Peoples R China
[4] Peking Univ, Int Ctr Quantum Mat, Sch Phys, Beijing, Peoples R China
[5] Beijing Univ Chem Technol, Beijing Adv Innovat Ctr Soft Matter Sci & Engn, Beijing, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金; 北京市自然科学基金; 国家重点研发计划;
关键词
LI-S BATTERIES; ENERGY DENSITY; LITHIUM; ELECTROLYTES; SOLVENT; CATHODES;
D O I
10.1038/s41557-025-01735-w
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Lithium-sulfur batteries promise high energy density storage but show poor stabilities owing to uncontrolled polysulfide dissolution. Although limiting polysulfide solvation to establish quasi-solid-state sulfur reaction can decouple electrode reactions from the electrolyte volume, this approach suffers from slow reaction kinetics. Here we propose a surface-localized polysulfide-solvation strategy to mediate the reaction of 'quasi-solid' polysulfide by leveraging an organic phase mediator with a weakly solvating electrolyte. This electrolyte restricts polysulfide dissolution globally while the phase mediator complexes with the surface polysulfide, promoting polysulfide solvation at the surface and facilitating fast surface-localized solution-phase sulfur reactions. Lithium-sulfur batteries using surface-localized phase mediation show excellent rate performance with 494 mA h g-1-sulfur at 16 C and stabilized cycling for 300 cycles with 90.2% capacity retention. The strategy enables steady operation of a 2.4 Ah 331 Wh kg-1 pouch cell. Our work highlights the advantages of surface phase mediation in controlling electrode reaction pathways and kinetics via electrolyte rational design.
引用
收藏
页码:614 / 623
页数:13
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