Activating RuOCo Interaction on the a-Co(OH)2 @Ru Interface for Accelerating the Volmer Step of Alkaline Hydrogen Evolution.

Abstract

The state-of-the-art active hydrogen evolution reaction (HER) catalysts in acid electrolytes generally lose considerable catalytic performance in alkaline electrolytes mainly due to the additional water dissociation step. Designing composite materials is an effective strategy to accelerate alkaline water electrolysis by optimizing the electronic structure of materials. Here, different phases of Co(OH)2 -supported Ru clusters (α/β-Co(OH)2 @Ru) are prepared for enabling a highly efficient electrocatalytic HER performance in alkaline solution. The prepared α-Co(OH)2 nanosheets facilitate the loading of uniform and high-density Ru clusters and the formed highly active RuOCo bonds at the interface. The synergistic interaction endows the hybrid catalyst with low overpotential of 33mV at 10mA cm-2 . Moreover, the homemade anion exchange membrane water electrolysis cell based on α-Co(OH)2 @Ru affords a cell voltage of 2V to drive a current density of 270mA cm-2 and performs stably during continuous operation for over 100h. Density functional theory calculations demonstrate that active RuOCo bonds in α-Co(OH)2 @Ru optimize the energy barriers for H2 O dissociation and OH- desorption to facilitate the Volmer reaction step. This work offers a strategy for designing interfacial chemical bonds for high electrocatalytic activity.