The facile synthesis of efficient non-precious-metal-based bifunctional catalysts for overall water splitting is highly desirable from both industrial and environmental perspectives. This study reports the electrodeposition and characterization of a transition-metal (Mo, Fe)-codoped nickel phosphide (Ni3P:FeMo) bifunctional catalyst for enhanced overall water splitting in an alkaline medium. The Ni3P:FeMo catalyst exhibited outstanding electrocatalytic performance for both the hydrogen evolution reaction and oxygen evolution reaction with low overpotentials of −103 and 290 mV, respectively, at a high current density of 100 mA/cm2 along with fast electrocatalytic kinetics. A full water-splitting electrolyzer consisting of a bifunctional Ni3P:FeMo catalyst required a low cell voltage of 1.48 V to attain a current density of 10 mA/cm2 with excellent stability for more than 50 h. Density functional theory calculations provided insights into the microscopic mechanism of the effective modulation of the p- and d-band centers of the P and Ni active sites by the Mo and Fe codoping of Ni3P, thereby enhancing the bifunctional catalytic activity of Ni3P.
|Original language||English (US)|
|Journal||ACS Applied Energy Materials|
|State||Published - Dec 2 2021|
Bibliographical noteKAUST Repository Item: Exported on 2022-01-27
Acknowledgements: This work was supported by the Basic Science Research Program of the National Research Foundation of Korea (grant nos. 2018R1D1A1B07049046 and 2021R1A2B5B01002879) and the Creative Materials Discovery Program on Creative Multilevel Research Center (2018M3D1A1057844).