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W Doping in Ni(12)P(5) as a Platform to Enhance Overall Electrochemical Water Splitting

[Image: see text] Bifunctional electrocatalysts for efficient hydrogen generation from water splitting must overcome both the sluggish water dissociation step of the alkaline hydrogen evolution half-reaction (HER) and the kinetic barrier of the anodic oxygen evolution half-reaction (OER). Nickel pho...

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Detalles Bibliográficos
Autores principales: Ghosh, Sirshendu, Kadam, Sunil R., Kolatkar, ShayLee, Neyman, Alevtina, Singh, Chanderpratap, Enyashin, Andrey N., Bar-Ziv, Ronen, Bar-Sadan, Maya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2021
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8762645/
https://www.ncbi.nlm.nih.gov/pubmed/34963045
http://dx.doi.org/10.1021/acsami.1c16755
Descripción
Sumario:[Image: see text] Bifunctional electrocatalysts for efficient hydrogen generation from water splitting must overcome both the sluggish water dissociation step of the alkaline hydrogen evolution half-reaction (HER) and the kinetic barrier of the anodic oxygen evolution half-reaction (OER). Nickel phosphides are a promising catalysts family and are known to develop a thin active layer of oxidized Ni in an alkaline medium. Here, Ni(12)P(5) was recognized as a suitable platform for the electrochemical production of γ-NiOOH—a particularly active phase—because of its matching crystallographic structure. The incorporation of tungsten by doping produces additional surface roughness, increases the electrochemical surface area (ESCA), and reduces the energy barrier for electron-coupled water dissociation (the Volmer step for the formation of H(ads)). When serving as both the anode and cathode, the 15% W-Ni(12)P(5) catalyst provides an overall water splitting current density of 10 mA cm(–2) at a cell voltage of only 1.73 V with good durability, making it a promising bifunctional catalyst for practical water electrolysis.