首页|Lithium cation-doped tungsten oxide as a bidirectional nanocatalyst for lithium-sulfur batteries with high areal capacity

Lithium cation-doped tungsten oxide as a bidirectional nanocatalyst for lithium-sulfur batteries with high areal capacity

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Lithium-sulfur(Li-S)batteries are promising for high energy-storage applications but suffer from sluggish conversion reaction kinetics and substantial lithium sulfide(Li2S)oxidation barrier,especially under high sulfur loadings.Here,we report a Li cation-doped tungsten oxide(LixWOx)electrocatalyst that efficiently accelerates the S↔Li2S interconversion kinetics.The incorporation of Li dopants into WOx cationic vacan-cies enables bidirectional electrocatalytic activity for both polysulfide reduction and Li2S oxidation,along with enhanced Li+diffusion.In conjunction with theoretical calculations,it is discovered that the improved electrocatalytic activity originates from the Li dopant-induced geometric and electronic struc-tural optimization of the LixWOx,which promotes the anchoring of sulfur species at favourable adsorp-tion sites while facilitating the charge transfer kinetics.Consequently,Li-S cells with the LixWOx bidirectional electrocatalyst show stable cycling performance and high sulfur utilization under high sul-fur loadings.Our approach provides insights into cation engineering as an effective electrocatalyst design strategy for advancing high-performance Li-S batteries.

Cation engineeringElectrocatalysisPolysulfide conversionLithium sulfide oxidationLithium-sulfur batteries

Biying Wang、Ke Chen、Jieying Liang、Zhichun Yu、Da-Wei Wang、Ruopian Fang

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School of Chemical Engineering,The University of New South Wales,Sydney,NSW 2052,Australia

Faculty of Materials Science and Energy Engineering,Shenzhen University of Advanced Technology,Shenzhen 518055,Guangdong,China

Institute of Technology for Carbon Neutrality,Shenzhen Institute of Advanced Technology,Chinese Academy of Sciences,Shenzhen 518055,Guangdong,China

2024

能源化学
中国科学院大连化学物理研究所 中国科学院成都有机化学研究所

能源化学

CSTPCDEI
影响因子:0.654
ISSN:2095-4956
年,卷(期):2024.98(11)