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Reducing Overpotential of Solid-State Sulfide Conversion in Potassium-Sulfur Batteries.
Ye, Chao; Shan, Jieqiong; Li, Huan; Kao, Chun-Chuan; Gu, Qinfen; Qiao, Shi-Zhang.
  • Ye C; School of Chemical Engineering and Advanced Materials, The University of Adelaide, Adelaide, SA, 5005, Australia.
  • Shan J; School of Chemical Engineering and Advanced Materials, The University of Adelaide, Adelaide, SA, 5005, Australia.
  • Li H; School of Chemical Engineering and Advanced Materials, The University of Adelaide, Adelaide, SA, 5005, Australia.
  • Kao CC; School of Chemical Engineering and Advanced Materials, The University of Adelaide, Adelaide, SA, 5005, Australia.
  • Gu Q; Australian Synchrotron, ANSTO, 800 Blackburn Rd., Clayton, VIC, 3168, Australia.
  • Qiao SZ; School of Chemical Engineering and Advanced Materials, The University of Adelaide, Adelaide, SA, 5005, Australia.
Angew Chem Int Ed Engl ; 62(22): e202301681, 2023 May 22.
Article en En | MEDLINE | ID: mdl-36975137
Improving kinetics of solid-state sulfide conversion in sulfur cathodes can enhance sulfur utilization of metal-sulfur batteries. However, fundamental understanding of the solid-state conversion remains to be achieved. Here, taking potassium-sulfur batteries as a model system, we for the first time report the reducing overpotential of solid-state sulfide conversion via the meta-stable S3 2- intermediates on transition metal single-atom sulfur hosts. The catalytic sulfur host containing Cu single atoms demonstrates high capacities of 1595 and 1226 mAh g-1 at current densities of 335 and 1675 mA g-1 , respectively, with stable Coulombic efficiency of ≈100 %. Combined spectroscopic characterizations and theoretical computations reveal that the relatively weak Cu-S bonding results in low overpotential of solid-state sulfide conversion and high sulfur utilization. The elucidation of solid-state sulfide conversion mechanism can direct the exploration of highly efficient metal-sulfur batteries.
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Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Idioma: En Año: 2023 Tipo del documento: Article