Heterostructured NiMo-sulfide micro-pillar arrays for advanced alkaline electrocatalytic clean hydrogen production via overall water splitting
- Authors
- Mujawar, Sarfraj H.; Salunke, Amol S.; Deokate, Ramesh J.; Salunke, Shrikrishna T.; Shrestha, Nabeen K.; Im, Hyunsik; Inamdar, Akbar I.
- Issue Date
- Jul-2024
- Publisher
- Elsevier BV
- Keywords
- Electrocatalysis; Green hydrogen generation; Hydrogen evolution reaction; Overall water splitting
- Citation
- Applied Surface Science, v.661, pp 1 - 9
- Pages
- 9
- Indexed
- SCIE
SCOPUS
- Journal Title
- Applied Surface Science
- Volume
- 661
- Start Page
- 1
- End Page
- 9
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/26095
- DOI
- 10.1016/j.apsusc.2024.160081
- ISSN
- 0169-4332
1873-5584
- Abstract
- Transition metals doped molybdenum sulfide/oxide present themselves as capable for hydrogen evolution reaction (HER), because of their exceptional chemical and physical properties. In this study, we introduce a strategy for synthesizing molybdenum-based binary sulfide/oxide heterostructures using a hydrothermal method. An electrochemical investigation revealed the pivotal role of NiMo-sulfide in achieving remarkable bifunctional electrocatalytic activity, resulting in a current density of −50 mA cm−2 at an overpotential of 174 mV for HER. The excellent reaction kinetics were evident from the low Tafel slope of 116.8 mVdec−1. The electrolyzer showcased outstanding performance, with the best-performing NiMo-sulfide and benchmark RuO2 at the anode. It achieved a low cell potential of 1.60 V to reach 10 mA cm−2, exhibited remarkable durability for 100 h, and demonstrated promise for water splitting with a Faradaic efficiency of 94 and 89 % for O2 and H2 evolution respectively. Furthermore, the electrolyzer displayed potential for large-scale hydrogen production by attaining an industrially appropriate current density of 800 mA cm−2 at a cell potential of 2.24 V. This study also highlights the latest advancements in electrodialysis to enhance the catalytic activity of electrode materials. © 2024 Elsevier B.V.
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Collections - College of Advanced Convergence Engineering > Division of System Semiconductor > 1. Journal Articles

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