Scalable production of foam-like nickel-molybdenum coatings via plasma spraying as bifunctional electrocatalysts for water splitting

Foam-like NiMo coatings were produced from an inexpensive mixture of Ni, Al, and Mo powders atmospheric plasma spraying. The coatings were deposited onto stainless-steel meshes forming a highly porous network mainly composed of nanostructured Ni and highly active Ni Mo. High material loading (200 mg...

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Published inPhysical chemistry chemical physics : PCCP Vol. 25; no. 31; pp. 20794 - 20807
Main Authors Wu, Xiuyu, Piñeiro-García, Alexis, Rafei, Mouna, Boulanger, Nicolas, Canto-Aguilar, Esdras Josué, Gracia-Espino, Eduardo
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 09.08.2023
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Summary:Foam-like NiMo coatings were produced from an inexpensive mixture of Ni, Al, and Mo powders atmospheric plasma spraying. The coatings were deposited onto stainless-steel meshes forming a highly porous network mainly composed of nanostructured Ni and highly active Ni Mo. High material loading (200 mg cm ) with large surface area (1769 cm per cm ) was achieved without compromising the foam-like characteristics. The coatings exhibited excellent activity towards both hydrogen evolution (HER) and oxygen evolution (OER) reactions in alkaline media. The HER active coating required an overpotential of 42 mV to reach a current density of -50 mA cm with minimum degradation after a 24 h chronoamperometry test at -10 mA cm . Theoretical simulations showed that several crystal surfaces of Ni Mo exhibit near optimum hydrogen adsorption energies and improved water dissociation that benefit the HER activity. The OER active coating also consisting of nanostructured Ni and Ni Mo required only 310 mV to achieve a current density of 50 mA cm . The OER activity was maintained even after 48 h of continuous operation. We envisage that the development of scalable production techniques for Ni Mo alloys will greatly benefit its usage in commercial alkaline water electrolysers.
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ISSN:1463-9076
1463-9084
1463-9084
DOI:10.1039/d3cp01444d