Promoting Oxygen Evolution Reaction Induced by Synergetic Geometric and Electronic Effects of IrCo Thin-Film Electrocatalysts
Kyu‐Su Kim, Shinae Park, Hyun Dong Jung, Sang‐Mun Jung, Hyunje Woo, Docheon Ahn, Sarah S. Park, Seoin Back, Yong‐Tae Kim
Abstract
The advancement of water electrolysis technology has seemingly plateaued. Further advances require new strategies to address the key limitations of the oxygen evolution reaction: high overpotential and low stability of electrode materials. Herein, we designed a nanoporous Ir3Co-core@IrO2-shell electrocatalyst with 5 and 3 times higher mass activity and 6 and 2 times higher activity–stability factors than conventional IrO2 nanoparticles and Ir nanoporous electrocatalysts, respectively. The origin of the performance enhancement in the Ir3Co-core@IrO2-shell electrocatalyst was revealed in computational density functional theory calculations. The residual Co after the dealloying process resulted in a down-shift of the d-band center position, thus weakening the −OH* adsorption energy. In addition, the electronic conductivity was enhanced by the three-dimensionally interconnected structure. Under high-current-density operating conditions, the Ohmic losses were reduced by the ultrafast charge transfer pathway provided by the metallic IrCo core.