Although electrochemical water splitting is an effective and green approach to produce oxygen and hydrogen, the realization of efficient bifunctional catalysts that are stable in variable electrolytes is still a significant challenge. Herein, we report a three-dimensional hierarchical assembly structure composed of an ultrathin Ru shell and a Ru-Ni alloy core as a catalyst functioning under universal pH conditions. Compared with the typical Ir/C-Pt/C system, superior catalytic performances and excellent durability of the overall water splitting under universal pH have been demonstrated. The introduction of Ni downshifts the d-band center of the Ru-Ni electrocatalysts, modulating the surface electronic environment. Density functional theory results reveal that the mutually restrictive d-band interaction lowers the binding of (Ru, Ni) and (H, O) for easier O-O and H-H formation. The structure-induced eg-dz2 misalignment leads to minimization of surface Coulomb repulsion to achieve a barrier-free water-splitting process.
Keywords: Catalysis; Energy Materials; Materials Science.
Copyright © 2019 The Author(s). Published by Elsevier Inc. All rights reserved.