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Ion-sharing interface and directional doping synergize N-MoS2/Se-CoS2 catalyst for efficient hydrogen evolution

  • Meng Nie
  • , Qian Yang
  • , Yan Jin
  • , Congcong Ning
  • , Shuaifeng Lou
  • , Chaozhong Guo
  • , Jiajun Wang
  • , Xiangnan Gong
  • , Baoshan Hu*
  • *Corresponding author for this work
  • Chongqing University
  • National-Municipal Joint Engineering
  • Chongqing University of Science and Technology
  • School of Chemistry and Chemical Engineering, Harbin Institute of Technology
  • Chongqing University of Arts and Science

Research output: Contribution to journalArticlepeer-review

Abstract

Interfacing and doping can effectively harmonize the electronic and coordination states of active centers in the electrocatalysts. Herein, we prepare heterostructured N-MoS2/Se-CoS2 electrocatalyst with ion-sharing interfaces and directional doping to activate inert basal phases for hydrogen evolution reaction (HER). Based on experimental and theoretical results, their synergistic effects on electron redistribution, electronic structure and coordination chemistry are investigated; furthermore, roles of each component and bridged Mo-S-Co sites at the phase interfaces as active sites in optimizing the adsorption/desorption of essential reaction intermediates H* and OH, as well as the free energies of unit reaction steps in the HER, are elucidated in depth. The N-MoS2/Se-CoS2 catalyst needs only 37 mV to give current density of 10 mA cm−2 with a low Tafel slope of 49.4 mV dec−1; more importantly, the catalyst delivers a long-term durability for HER in alkaline condition and comparable performance with commercial RuO2||Pt/C system in a two-electrode assembled electrolyzer. This work provides more insights into the design and preparation of high-performance heterostructured electrocatalysts.

Original languageEnglish
Pages (from-to)9-21
Number of pages13
JournalJournal of Catalysis
Volume424
DOIs
StatePublished - Aug 2023
Externally publishedYes

Keywords

  • Directional doping
  • Heterogeneous interfaces
  • Hydrogen evolution
  • Synergistic mechanism
  • Transition metal dichalcogenide

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