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Catalytically altering the redox pathway of sulfur in propylene carbonate electrolyte using dual-nitrogen/oxygen-containing carbon

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Chinese Journal of Catalysis 2024年第8期63卷 224-233页

作者： Linghui Yu Heng Zhang luyuan paul wang.samuel jun hoong ong Shibo Xi Bo Chen Rui Guo Ting wang Yonghua Du Wei Chen Ovadia Lev Zhichuan J.Xu School of Chemistry and Chemical Engineering Wuhan Textile UniversityWuhan 430200HubeiChina School of Materials Science and Engineering Nanyang Technological UniversitySingapore 639798Singapore Hubei Key Laboratory of Biomass Fibers&Eco-Dyeing&Finishing Wuhan Textile UniversityWuhan 430200HubeiChina Institute of Sustainability for Chemicals Energy and Environment(ISCE2)Agency for ScienceTechnology and Research in Singapore(A*STAR)1 Pesek RoadJurong Island 627833Singapore Department of Chemistry National University of SingaporeSingapore 117543Singapore College of the Environment&Ecology Xiamen UniversityXiamen 361102FujianChina National Synchrotron Light Source II Brookhaven National LaboratoryUptonNY 11973USA The Institute of Chemistry The Hebrew University of JerusalemJerusalem 9190401Israel Singapore-HUJ Alliance for Research and Enterprise NEW-CREATE Phase IICampus for Research Excellence and Technological Enterprise(CREATE)Singapore138602Singapore Energy Research Institute@NTU ERI@NInterdisciplinary Graduate SchoolNanyang Technological UniversitySingapore 639798Singapore

Carbonate electrolytes are one of the most desirable electrolytes for high-energy lithium-sulfur batteries(LSBs)because of their successful implementation in commercial Li-ion *** low-polysulfide-solubility feature of some carbonate solvents also makes them very promising for overcoming the shuttle effects of ***,regular sulfur electrodes experience undesired electrochemical mechanisms in carbonate electrolytes due to side *** this study,we report a catalytic redox mechanism of sulfur in propylene carbonate(PC)electrolyte based on a compari-son *** catalytic mechanism is characterized by the interactions between polysulfides and dual N/O functional groups on the host carbon,which largely prevents side reactions between pol-ysulfides and the carbonate *** a mechanism coupled with the low-polysulfide-solubility feature leads to stable cycling of LSBs in PC *** dual N/O functional groups are identified via a density functional theory *** work provides an alternative route for enabling LSBs in carbonate electrolytes.

关键词： Energy storage Lithium-sulfur battery Catalytic redox reaction Porous carbon Carbonate electrolyte

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