Song DongHoon, Roh Jeonghan, Choi Jungwoo, Lee Hyein, Koh Gyungmo, Kwon YongKeun, Kim HyoWon, Lee Hyuck Mo, Kim MinJoong, Cho EunAe
Department of Materials Science and Engineering, Korea Advanced Institute of Science and Technology (KAIST), 291 Daehak-ro, Yuseong-gu, Daejeon, 34141, Republic of Korea.
Hydrogen Research Department, Korea Institute of Energy Research (KIER), 152 Gajeong-ro, Yuseong-gu, Daejeon, 34129, Republic of Korea.
Adv Sci (Weinh). 2024 Oct;11(39):e2403752. doi: 10.1002/advs.202403752. Epub 2024 Aug 19.
Herein, a heterogeneous structure of Ni-Mo catalyst comprising NiMo nanoalloys decorated on a MoO matrix via electrodeposition is introduced. This catalyst exhibits remarkable hydrogen evolution reaction (HER) activity across a range of pH conditions. The heterogeneous Ni-Mo catalyst showed low overpotentials only of 24 and 86, 21 and 60, and 37 and 168 mV to produce a current density of 10 and 100 mA cm (η and η) in alkaline, acidic, and neutral media, respectively, which represents one of the most active catalysts for the HER. The enhanced activity is attributed to the hydrogen spillover effect, where hydrogen atoms migrate between the NiMo alloys and the MoO matrix, forming hydrogen molybdenum bronze as additional active sites. Additionally, the NiMo facilitated the water dissociation process, which helps the Volmer step in the alkaline/neutral HER. Through electrochemical analysis, in situ Raman spectroscopy, and density functional theory calculations, the fast HER mechanism is elucidated.
在此,介绍了一种通过电沉积在MoO基体上装饰NiMo纳米合金的Ni-Mo催化剂的异质结构。该催化剂在一系列pH条件下均表现出显著的析氢反应(HER)活性。这种异质Ni-Mo催化剂在碱性、酸性和中性介质中,分别仅需24和86、21和60以及37和168 mV的低过电位即可产生10和100 mA cm²的电流密度(η10和η100),这代表了用于HER的最具活性的催化剂之一。活性增强归因于氢溢流效应,其中氢原子在NiMo合金和MoO基体之间迁移,形成氢钼青铜作为额外的活性位点。此外,NiMo促进了水的解离过程,这有助于碱性/中性HER中的Volmer步骤。通过电化学分析、原位拉曼光谱和密度泛函理论计算,阐明了快速HER机制。