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Enhancing Conversion Kinetics through Electron Density Dual-Regulation of Catalysts and Sulfur toward Room-/Subzero-Temperature Na-S Batteries.
Luo, Sainan; Ruan, Jiafeng; Wang, Yan; Chen, Min; Wu, Limin.
Afiliación
  • Luo S; Department of Materials Science, Fudan University, Shanghai, 200433, P. R. China.
  • Ruan J; School of Materials and Chemistry, University of Shanghai for Science and Technology, Shanghai, 200093, P. R. China.
  • Wang Y; Department of Materials Science, Fudan University, Shanghai, 200433, P. R. China.
  • Chen M; Department of Materials Science, Fudan University, Shanghai, 200433, P. R. China.
  • Wu L; Department of Materials Science, Fudan University, Shanghai, 200433, P. R. China.
Adv Sci (Weinh) ; 11(21): e2308180, 2024 Jun.
Article en En | MEDLINE | ID: mdl-38594907
ABSTRACT
Room-temperature sodium-sulfur (RT Na/S) batteries have received increasing attention for the next generation of large-scale energy storage, yet they are hindered by the severe dissolution of polysulfides, sluggish redox kinetic, and incomplete conversion of sodium polysulfides (NaPSs). Herein, the study proposes a dual-modulating strategy of the electronic structure of electrocatalyst and sulfur to accelerate the conversion of NaPSs. The selenium-modulated ZnS nanocrystals with electron rearrangement in hierarchical structured spherical carbon (Se-ZnS/HSC) facilitate Na+ transport and catalyze the conversion between short-chain sulfur and Na2S. And the in situ introduced Se within S can enhance conductivity and form an S─Se bond, suppressing the "polysulfides shuttle". Accordingly, the S@Se-ZnS/HSC cathode exhibits a specific capacity of as high as 1302.5 mAh g-1 at 0.1 A g-1 and ultrahigh-rate capability (676.9 mAh g-1 at 5.0 A g-1). Even at -10 °C, this cathode still delivers a high reversible capacity of 401.2 mAh g-1 at 0.05 A g-1 and 94% of the original capacitance after 50 cycles. This work provides a novel design idea for high-performance Na/S batteries.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Adv Sci (Weinh) Año: 2024 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Revista: Adv Sci (Weinh) Año: 2024 Tipo del documento: Article