Hybridized heterostructure of CoS and MoS2 nanoparticles for highly-efficient and robust bifunctional water electrolysis
- Authors
- Ahmed, Abu Talha Aqueel; Lee, Chi Ho; Ansari, Abu Saad; Pawar, S. M.; Han, Jonghoon; Park, Sunjung; Shin, Giho; Yeon, Seungun; Cho, Sangeun; Seol, Jaehun; Lee, Sang Uck; Kim, Hyungsang; Im, Hyunsik
- Issue Date
- Aug-2022
- Publisher
- Elsevier BV
- Keywords
- CoS/MoS2 nanoparticle heterostructure; Hydrothermal growth; Electrocatalyst; Bifunctional activity; Density functional theory
- Citation
- Applied Surface Science, v.592, pp 1 - 13
- Pages
- 13
- Indexed
- SCIE
SCOPUS
- Journal Title
- Applied Surface Science
- Volume
- 592
- Start Page
- 1
- End Page
- 13
- URI
- https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/111344
- DOI
- 10.1016/j.apsusc.2022.153196
- ISSN
- 0169-4332
1873-5584
- Abstract
- For industrial hydrogen production, it is beneficial to develop highly-efficient, earth-abundant, and bifunctional electrocatalysts which exhibit compatibility between oxygen evolution reaction (OER) or hydrogen evolution reaction (HER) activity and stability in the same electrolyte. Herein, we report a bifunctional hybrid CoS/MoS2 nanoparticle electrocatalyst in 1 M KOH, fulfilling desirable industrial criteria for water electrolysis. The CoS/MoS2 catalyst exhibits excellent OER and HER activities with very low overpotentials as well as outstanding stability for more than 100 h, even at a high current density of 250 mA cm(-2). The bifunctional CoS/MoS2 catalyst-based water-electrolyzer exhibits a low cell voltage of 1.52 V at 10 mA cm(-2) (1.714 V at 100 mA cm(-2)) with long-term stability. Density functional theory calculations reveal that the hybrid CoS/MoS2 electrocatalyst shows one-way electron transfer that can activate both oxidative/reductive reactions. Therefore, it exhibits superior OER and HER activities, outperforming the state-of-the-art noble-metal-free catalysts.
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Collections - COLLEGE OF SCIENCE AND CONVERGENCE TECHNOLOGY > DEPARTMENT OF CHEMICAL AND MOLECULAR ENGINEERING > 1. Journal Articles

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