Molybdenum/selenium based heterostructure catalyst for efficient hydrogen evolution: Effects of ionic dissolution and repolymerization on catalytic performance

• Published in: Journal of colloid and interface science Vol. 658; pp. 32 - 42
• Main Authors: Yang, Mameng, Bao, Weiwei, Zhang, Junjun, Ai, Taotao, Han, Jie, Li, Yan, Liu, Jiangying, Zhang, Pengfei, Feng, Liangliang
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 15.03.2024
• Subjects: Heterojunction structure; Hydrogen evolution; In situ Raman; Surface reconstruction; Transition metal selenides; Heterojunction structure; In situ Raman; Surface reconstruction; Transition metal selenides; Hydrogen evolution
• ISSN: 0021-9797; 1095-7103
• DOI: 10.1016/j.jcis.2023.12.033

The dynamic evolution of Mo and Se during hydrogen evolution and their effects on the catalytic performance of HER were revealed by using interface engineering to construct MoSe2@CoSe2 heterostructure. [Display omitted] Transition metal chalcogenides (TMCs) are recognized as highly efficient electrocatalysts and have wide applications in the field of hydrogen production by electrolysis of water, but the real catalytic substances and catalytic processes of these catalysts are not clear. The species evolution of Mo and Se during alkaline hydrogen evolution was investigated by constructing MoSe2@CoSe2 heterostructure. The real-time evolution of Mo and Se in MoSe2@CoSe2 was monitored using in situ Raman spectroscopy to determine the origin of the activity. Mo and Se in MoSe2@CoSe2 were dissolved in the form of MoO42- and SeO32-, respectively, and subsequently re-adsorbed and polymerized on the electrode surface to form new species Mo2O72- and SeO42-. Theoretical calculations show that adsorption of Mo2O72- and SeO42- can significantly enhance the HER catalytic activity of Co(OH)2. The addition of additional MoO42- and SeO32- to the electrolyte with Co(OH)2 electrodes both enhances its HER activity and promotes its durability. This study helps to deepen our insight into mechanisms involved in the structural changes of catalyst surfaces and offers a logical basis for revealing the mechanism of the influence of species evolution on catalytic performance.