In Situ Construction of Built-In Opposite Electric Field Balanced Surface Adsorption for Hydrogen Evolution Reaction

Achieving a balance between H-atom adsorption and binding with H desorption is crucial for catalyzing hydrogen evolution reaction (HER). In this study, the feasibility of designing and implementing built-in opposite electric fields (OEF) is demonstrated to enable optimal H atom adsorption and H deso...

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Veröffentlicht in:Small (Weinheim an der Bergstrasse, Germany) Germany), 2024-05, Vol.20 (19), p.e2309249-e2309249
Hauptverfasser: Xu, Tianyi, Tian, Fuyu, Jiao, Dongxu, Fan, Jinchang, Jin, Zhaoyong, Zhang, Lei, Zhang, Wei, Zheng, Lirong, Singh, David J, Zhang, Lijun, Zheng, Weitao, Cui, Xiaoqiang
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Sprache:eng
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Zusammenfassung:Achieving a balance between H-atom adsorption and binding with H desorption is crucial for catalyzing hydrogen evolution reaction (HER). In this study, the feasibility of designing and implementing built-in opposite electric fields (OEF) is demonstrated to enable optimal H atom adsorption and H desorption using the Ni (BO ) /Ni P heterostructure as an example. Through density functional theory calculations of planar averaged potentials, it shows that opposite combinations of inward and outward electric fields can be achieved at the interface of Ni (BO ) /Ni P , leading to the optimization of the H adsorption free energy (ΔG ) near electric neutrality (0.05 eV). Based on this OEF concept, the study experimentally validated the Ni (BO ) /Ni P system electrochemically forming Ni (BO ) through cyclic voltammetry scanning of B-doped Ni P . The surface of Ni (BO ) undergoes reconstruction, as characterized by Grazing Incidence Wide-Angle X-ray Scattering (GIWAXS) and in situ Raman spectroscopy. The resulting catalyst exhibits excellent HER activity in alkaline media, with a low overpotential of 33 mV at 10 mA cm and stability maintained for over 360 h. Therefore, the design strategy of build-in opposite electric field enables the development of high-performance HER catalysts and presents a promising approach for electrocatalyst advancement.
ISSN:1613-6810
1613-6829
DOI:10.1002/smll.202309249