Promoted Catalytic Activity of CoSx@MoSx/MoOx Supported on Carbon Papers for Electrocatalytic Hydrogen Evolution Reaction

Author:

Hong Sung Hyun1ORCID,Tekalgne Mahider Asmare1ORCID,Ryu Sangwoo2ORCID,Ahn Sang Hyun3ORCID,Kim Soo Young1ORCID

Affiliation:

1. Department of Materials Science and Engineering, Korea University, 145 Anam-ro, Seongbuk-gu, Seoul 02841, Republic of Korea

2. Department of Advanced Materials Engineering, Kyonggi University, Suwon 16227, Republic of Korea

3. School of Chemical Engineering and Materials Science, Chung-Ang University, 84 Heukseok-ro, Dongjak-gu, Seoul 06974, Republic of Korea

Abstract

Developing cost-effective and stable materials for the electrocatalysis of hydrogen evolution reaction (HER) remains challenging. In this study, efficient catalysts for HER were synthesized by integrating the cobalt and molybdenum oxides via electrodeposition, followed by subsequent sulfurization of the as-prepared oxides using chemical vapor deposition (CVD). This methodology allowed the incorporation of both cobalt and molybdenum components into the catalyst in a single step. The as-synthesized CoSx@MoSx/MoOx-based catalysts exhibited excellent hydrogen production performance in acidic media owing to the presence of Co-S and Mo-S bonds in the hybrid structure. Particularly, CoSx@MoSx/MoOx(90@360) and MoSx@CoOx(180@180) displayed the best HER performances with low overpotentials of 80 mV and 150 mV, respectively. The catalysts were highly stable, with their stability preserved for over 1000 cycles with marginal reduction in overall efficiency. Therefore, these findings suggest the potential of CoSx@MoSx/MoOx and MoSx@CoOx composites as ideal candidates for developing low-cost catalysts for electrochemical hydrogen production.

Funder

Korean government

Publisher

Hindawi Limited

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