Highly Conductive Quasi‐1D Hexagonal Chalcogenide Perovskite Sr8Ti7S21 with Efficient Polysulfide Regulation in Lithium‐Sulfur Batteries

Author:

Yang Dawei1ORCID,Han Yanbing2,Li Mengyao2,Li Canhuang34,Bi Wei1,Gong Qianhong1,Zhang Jie1,Zhang Jinglu2,Zhou Yingtang5,Gao Han2,Arbiol Jordi67,Shi Zhifeng2,Zhou Guangmin8,Cabot Andreu47ORCID

Affiliation:

1. Henan Province Key Laboratory of Photovoltaic Materials School of Future Technology Henan University Kaifeng 475004 P. R. China

2. Key Laboratory of Materials Physics of Ministry of Education School of Physics and Microelectronics Zhengzhou University Daxue Road 75 Zhengzhou 450052 P. R. China

3. Department of Chemistry Universitat de Barcelona Barcelona 08028 Spain

4. Catalonia Institute for Energy Research – IREC Sant Adrià de Besòs Barcelona 08930 Spain

5. National Engineering Research Center for Marine Aquaculture Marine Science and Technology College Zhejiang Ocean University Zhoushan Zhejiang Province 316004 China

6. Catalan Institute of Nanoscience and Nanotechnology (ICN2) Campus UAB, Bellaterra Barcelona Catalonia 08193 Spain

7. ICREA Pg. Lluís Companys 23 Barcelona 08010 Spain

8. Tsinghua‐Berkeley Shenzhen Institute & Tsinghua Shenzhen International Graduate School Tsinghua University Shenzhen 518055 P. R. China

Abstract

AbstractLithium‐sulfur batteries (LSBs) are regarded as one of the most promising candidates for next‐generation energy storage systems. However, the commercialization of LSBs is still hindered by several technical issues, including the notorious polysulfide migration from the cathode to the anode and the sluggish sulfur conversion kinetics. Herein, a quasi‐1D hexagonal chalcogenide perovskite, Sr8Ti7S21, is demonstrated as an efficient sulfur host able to overcome these limitations. Experimental results and density functional theory calculations show Sr8Ti7S21 to offer strong lithium polysulfides (LiPS) binding through multiple bond formation. Besides, Sr8Ti7S21 effectively facilitates the kinetics of the LiPS redox reaction. As a result, S@Sr8Ti7S21‐based cathodes exhibit excellent initial capacities up to 1315 mAh g−1 at 0.2C, impressive cycling stability with an average capacity decay rate of 0.08% per cycle over 400 cycles at 1C, and a high areal capacity of 6.58 mAh cm−2 under a high sulfur loading of 6.5 mg cm−2. This work reveals the potential capabilities and promising prospects of chalcogenide perovskites in advancing LSBs technology.

Funder

National Natural Science Foundation of China

Generalitat de Catalunya

Publisher

Wiley

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