Electrolyte Structure of Lithium Polysulfides with Anti-Reductive Solvent Shells for Practical Lithium-Sulfur Batteries

被引:151
作者
Zhang, Xue-Qiang [1 ]
Jin, Qi [2 ]
Nan, Yi-Ling [3 ]
Hou, Li-Peng [1 ]
Li, Bo-Quan [4 ]
Chen, Xiang [1 ]
Jin, Zhe-Hui [3 ]
Zhang, Xi-Tian [2 ]
Huang, Jia-Qi [4 ]
Zhang, Qiang [1 ]
机构
[1] Tsinghua Univ, Beijing Key Lab Green Chem React Engn & Technol, Dept Chem Engn, Beijing 100084, Peoples R China
[2] Harbin Normal Univ, Key Lab Photon & Elect Bandgap Mat, Minist Educ, Sch Phys & Elect Engn, Harbin 150025, Heilongjiang, Peoples R China
[3] Univ Alberta, Sch Min & Petr Engn, Dept Civil & Environm Engn, Edmonton, AB T6G 1H9, Canada
[4] Beijing Inst Technol, Adv Res Inst Multidisciplinary Sci, Beijing 100081, Peoples R China
基金
中国国家自然科学基金; 加拿大自然科学与工程研究理事会;
关键词
electrolyte structure; lithium metal anode; lithium-sulfur batteries; polysulfide encapsulation; solvent shell; NUCLEAR-MAGNETIC-RESONANCE; HIGH-ENERGY DENSITY; LIQUID ELECTROLYTE; METAL ANODE; PERFORMANCE; INTERPHASE; MECHANISM; CATHODE;
D O I
10.1002/anie.202103470
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The lithium-sulfur (Li-S) battery is regarded as a promising secondary battery. However, constant parasitic reactions between the Li anode and soluble polysulfide (PS) intermediates significantly deteriorate the working Li anode. The rational design to inhibit the parasitic reactions is plagued by the inability to understand and regulate the electrolyte structure of PSs. Herein, the electrolyte structure of PSs with anti-reductive solvent shells was unveiled by molecular dynamics simulations and nuclear magnetic resonance. The reduction resistance of the solvent shell is proven to be a key reason for the decreased reactivity of PSs towards Li. With isopropyl ether (DIPE) as a cosolvent, DIPE molecules tend to distribute in the outer solvent shell due to poor solvating power. Furthermore, DIPE is more stable than conventional ether solvents against Li metal. The reactivity of PSs is suppressed by encapsulating PSs into anti-reductive solvent shells. Consequently, the cycling performance of working Li-S batteries was significantly improved and a pouch cell of 300 Wh kg(-1) was demonstrated. The fundamental understanding in this work provides an unprecedented ground to understand the electrolyte structure of PSs and the rational electrolyte design in Li-S batteries.
引用
收藏
页码:15503 / 15509
页数:7
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