Direct Monitoring of Li2S2 Evolution and Its Influence on the Reversible Capacities of Lithium‐Sulfur Batteries

Author:

Luo Yufeng12ORCID,Fang Zhenhan1,Duan Shaorong3,Wu Hengcai13,Liu Haitao4,Zhao Yuxing1,Wang Ke5,Li Qunqing1367,Fan Shoushan1367,Zheng Zijian2,Duan Wenhui367ORCID,Zhang Yuegang136,Wang Jiaping136ORCID

Affiliation:

1. Tsinghua-Foxconn Nanotechnology Research Center Tsinghua University Beijing 100084 China

2. Laboratory for Advanced Interfacial Materials and Devices School of Fashion and Textiles The Hong Kong Polytechnic University Hong Kong SAR 99077 China

3. Department of Physics Tsinghua University Beijing 100084 China

4. Laboratory of Computational Physics Institute of Applied Physics and Computational Mathematics Beijing 100088 China

5. School of Materials Science and Technology China University of Geosciences Beijing 100083 China

6. Frontier Science Center for Quantum Information Tsinghua University Beijing 100084 China

7. State Key Laboratory of Low-Dimensional Quantum Physics Tsinghua University Beijing 100084 China

Abstract

AbstractThe polysulfide (PS) dissolution and low conductivity of lithium sulfides (Li2S) are generally considered the main reasons for limiting the reversible capacity of the lithium‐sulfur (Li‐S) system. However, as the inevitable intermediate between PSs and Li2S, lithium disulfide (Li2S2) evolutions are always overlooked. Herein, Li2S2 evolutions are monitored from the operando measurements on the pouch cell level. Results indicate that Li2S2 undergoes slow electrochemical reduction and chemical disproportionation simultaneously during the discharging process, leading to further PS dissolution and Li2S generation without capacity contribution. Compared with the fully oxidized Li2S, Li2S2 still residues at the end of the charging state. Therefore, instead of the considered Li2S and PSs, slow electrochemical conversions and side chemical reactions of Li2S2 are the determining factors in limiting the sulfur utilization, corresponding to the poor reversible capacity of Li‐S batteries.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

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