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Heterostructure CoS2/MoS2 Nanosheets as a Dual-Active Electrocatalyst for the Oxygen Evolution Reaction.
Li, Yang; Du, Qi-Xuan; Cui, Jian; Yang, Hong-Wei; Qian, Hua.
Afiliação
  • Li Y; School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, China.
  • Du QX; School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, China.
  • Cui J; School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, China.
  • Yang HW; School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, China.
  • Qian H; School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing 210094, China.
Inorg Chem ; 63(4): 1954-1961, 2024 Jan 29.
Article em En | MEDLINE | ID: mdl-38214970
ABSTRACT
Cost-effective and earth-abundant oxygen evolution reaction (OER) electrocatalysts are an incredible research hotspot in numerous energy storage and conversion technology fields. Herein, CoS2/MoS2 nanosheets supported by carbon cloth as a dual-active CC@CoS2/MoS2 heterostructure electrocatalyst is prepared through a simple solvothermal method. The catalyst demonstrates admirable OER performance in 1 M KOH solution with a low overpotential of 243 mV at a current density of 10 mA cm-2 and a minor Tafel slope of 109 mV dec-1, displaying honorable stability after 1000 cyclic voltammetry (CV) cycles and long-term robustness over 60 h. Theoretical calculations further ascertain that the rate-determining step of the electrocatalytic course of the CC@CoS2/MoS2 heterostructure is the conversion *O + OH- → *OOH + e- with a lower energy barrier of 1.49 eV due to the heterojunction established by CoS2 and MoS2, which can promote the OER performance of electrocatalysts. The actual identification of the catalytic mechanism in the heterostructure is conducive to the improvement of electrocatalysis applications in the OER.

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article