4.8 Article

Fe-Regulated Amorphous-Crystal Ni(Fe)P-2 Nanosheets Coupled with Ru Powerfully Drive Seawater Splitting at Large Current Density

Journal

SMALL
Volume 19, Issue 36, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202300030

Keywords

amorphous-crystal structures; density functional theory; large current density; metal phosphide; water splitting

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This research reports a unique bifunctional catalyst consisting of Ru nanocrystals coupled with amorphous-crystalline Ni(Fe)P-2 nanosheets (Ru-Ni(Fe)P-2/NF). The catalyst exhibits excellent performance for oxygen and hydrogen evolution reactions in alkaline water and seawater, respectively, surpassing commercial Pt/C/NF and RuO2/NF catalysts. It also maintains stable performance at high current densities, making it a promising candidate for industrial-scale seawater splitting.
Water electrolysis is an ideal method for industrial green hydrogen production. However, due to increasing scarcity of freshwater, it is inevitable to develop advanced catalysts for electrolyzing seawater especially at large current density. This work reports a unique Ru nanocrystal coupled amorphous-crystal Ni(Fe)P-2 nanosheet bifunctional catalyst (Ru-Ni(Fe)P-2/NF), caused by partial substitution of Fe to Ni atoms in Ni(Fe)P-2, and explores its electrocatalytic mechanism by density functional theory (DFT) calculations. Owing to high electrical conductivity of crystalline phases, unsaturated coordination of amorphous phases, and couple of Ru species, Ru-Ni(Fe)P-2/NF only requires overpotentials of 375/295 and 520/361 mV to drive a large current density of 1 A cm(-2) for oxygen/hydrogen evolution reaction (OER/HER) in alkaline water/seawater, respectively, significantly outperforming commercial Pt/C/NF and RuO2/NF catalysts. In addition, it maintains stable performance at large current density of 1 A cm(-2) and 600 mA cm(-2) for 50 h in alkaline water and seawater, respectively. This work provides a new way for design of catalysts toward industrial-level seawater splitting.

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