Development of Synergistically Efficient Ni–Co Pair Catalytic Sites for Enhanced Polysulfide Conversion in Lithium–Sulfur Batteries

Author:

Zhao Chongchong12,Huo Feng234,Yang Yi25,Ruan Jingjing2,Chai Fengtao2,Xu Hui2,Liu Yanxia23,Zhang Lan3,Cabot Andreu67,Sun Zixu5ORCID,Zhang Yatao1

Affiliation:

1. School of Chemical Engineering Zhengzhou University Zhengzhou 450000 China

2. Henan Key Laboratory of Energy Storage Materials and Processes Zhengzhou Institute of Emerging Industrial Technology Zhengzhou 450003 China

3. Beijing Key Laboratory of Ionic Liquids Clean Process CAS Key Laboratory of Green Process and Engineering State Key Laboratory of Multiphase Complex Systems Institute of Process Engineering Chinese Academy of Sciences Beijing 100190 China

4. Longzihu New Energy Laboratory Zhengzhou 450000 China

5. Key Lab for Special Functional Materials of Ministry of Education School of Materials Science and Engineering Henan University Kaifeng 475004 China

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

7. Catalan Institution for Research and Advanced Studies – ICREA Pg. Lluís Companys 23 Barcelona 08010 Spain

Abstract

AbstractThe performance of Lithium–sulfur (Li–S) batteries is constrained by the migration of lithium polysulfide (LiPS), the slow conversion of LiPS, and the significant reaction barrier encountered during the precipitation/dissolution of Li2S throughout the discharge/charge cycle. In this contribution, the study presents Ni–Co dual‐atom catalytic sites on hollow nitrogen‐doped carbon (NiCoNC). Theoretical calculations and experimental data reveal that the dual‐atom catalysts (DACs) accelerate the kinetic conversion of LiPSs and facilitate the formation/decomposition of Li2S during discharging and charging, which minimizes LiPS migration. Consequently, the utilization of S/NiCoNC cathodes manifests a substantial initial capacity of 1348.5 mAh g−1 at 0.1 C, exceptional cycling stability with an average capacity degradation rate of 0.028% per cycle over 900 cycles at 0.5 C, and noteworthy rate capability with a capacity of 626 mAh g−1 at 2 C. Electrodes with a higher sulfur loading of 4.5 mg cm−2 and a low electrolyte/sulfur ratio of 8 µL mg−1 exhibit exceptional specific capacities of up to 1236 mAh g−1 at 0.1 C, as well as noteworthy capacity retention of 494.2 mAh g−1 after 200 cycles at 0.2 C. This study effectively showcases the potential of DACs as catalysts for sulfur cathodes, thereby enhancing the overall performance of Li–S batteries.

Funder

National Natural Science Foundation of China

National Key Research and Development Program of China

Generalitat de Catalunya

Natural Science Foundation of Henan Province

Publisher

Wiley

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