Kwon Jiseok, Choi Seunggun, Sun Jooheon, Jo Seonghan, Kim Jeongheon, Yoo Hee Eun, Paik Ungyu, Song Taeseup
Department of Energy Engineering, Hanyang University, 222 Wangsimni-ro, Seongdong-gu, Seoul, 04763, Republic of Korea.
Department of Materials Science and Engineering, Carnegie Mellon University, Pittsburgh, Pennsylvania, 15213, USA.
Small Methods. 2025 Aug;9(8):e2500199. doi: 10.1002/smtd.202500199. Epub 2025 May 15.
Hydrogen evolution reaction (HER) under alkaline conditions is determined by the water dissociation process. Strengthening the adsorption ability of the electrocatalyst is crucial to promoting water dissociation in the alkaline HER, whereas too-intense adsorption will poison the active sites. Herein, the adsorption ability of NiFeP is modulated by nonmetal F doping for an efficient and durable alkaline HER. F incorporation in NiFeP (NiFePF) tailors the electronic structure of Ni, Fe, and P, optimizing the adsorption of OH/H on the active sites. The balanced OH/H adsorption facilitates the water dissociation and hydrogen evolution of NiFePF, exhibiting the smaller overpotential of 233 mV at 100 mA cm. Furthermore, NiFePF achieves 1 A cm at an overpotential of only 231 mV under 30 wt% KOH. The balanced OH/H adsorption ability in NiFePF facilitates the desorption of OH and alleviates the poisoning active center, limiting the surface hydroxylation of NiFePF to a few nanometers. This enables NiFePF to remain stable for 360 h, demonstrating its commercial potential.
碱性条件下的析氢反应(HER)由水的解离过程决定。增强电催化剂的吸附能力对于促进碱性HER中的水离解至关重要,而吸附过强会使活性位点中毒。在此,通过非金属F掺杂来调节NiFeP的吸附能力,以实现高效且耐用的碱性HER。F掺入NiFeP(NiFePF)中可调整Ni、Fe和P的电子结构,优化活性位点上OH/H的吸附。平衡的OH/H吸附促进了NiFePF的水离解和析氢,在100 mA cm时表现出233 mV的较小过电位。此外,在30 wt% KOH条件下,NiFePF在仅231 mV的过电位下即可达到1 A cm。NiFePF中平衡的OH/H吸附能力有助于OH的解吸并减轻中毒活性中心,将NiFePF的表面羟基化限制在几纳米。这使得NiFePF能够保持360小时的稳定性,展现出其商业潜力。