Surface reconstruction on silver nanoparticles decorated trimetallic hydroxide nanosheets to generate highly active oxygen-deficient (oxy) hydroxide layer for high-efficient water oxidation

The transition-metal (oxy)hydroxides have been considered as one of the promising electrocatalysts for oxygen evolution reaction (OER). Therefore, it is necessary to have in-depth study on the origin behind their favorable inherent OER activity and further improve their catalytic performance. Herein, nickel-cobalt-vanadium trimetallic (oxy)hydroxide nanosheets decorated with silver nanoparticles (Ag NPs) (Ag@NiV0.2Co0.2) are fabricated for OER by a simple spontaneous redox reaction. The Ag@NiV0.2Co0.2 can deliver an overpotential of only 255 mV at 10 mA cm(-2) and a small Tafel slope of 38.3 mV dec(-1) in alkaline solution. We accredit the outstanding catalytic performance to the following aspects: (1) the active (oxy)hydroxide layer on the surface of Ag@NiV0.2Co0.2 generated through the surface reconstruction, (2) the optimal local coordination induced by the interaction between Ag NPs and trimetallic system, (3) the extensively exposed active sites, and (4) the significantly improved charge-transfer ability due to the incorporation of Ag NPs. Our findings may provide deep understanding on the mechanism of OER and offers a novel strategy to design electrocatalysts with superior OER activity.

Automated summary

The study fabricates nickel-cobalt-vanadium trimetallic (oxy)hydroxide nanosheets decorated with silver nanoparticles for oxygen evolution reaction, showing outstanding catalytic performance with an overpotential of only 255 mV and a small Tafel slope of 38.3 mV dec(-1) in alkaline solution. The exceptional catalytic performance is attributed to the active (oxy)hydroxide layer on the surface, optimal local coordination induced by interaction between Ag NPs and trimetallic system, extensively exposed active sites, and significantly improved charge-transfer ability due to the incorporation of Ag NPs.