Optimizing the Electronic Structure of Ruthenium Oxide by Neodymium Doping for Enhanced Acidic Oxygen Evolution Catalysis

It is a great challenge to design active and durable oxygen evolution reaction (OER) electrocatalysts for proton exchange membrane (PEM) electrolyzer due to the high dissolution of electrocatalysts in acidic solution. Herein, the Nd-doped RuO2 (Nd0.1RuOx) is developed for enhanced oxygen evolution in 0.5 m H2SO4 solution with an overpotential of 211 mV to achieve 10 mA cm(-2). The theoretical calculation reveals that the improved activity of Nd0.1RuOx is due to the moderate decrease of d-band center energy, which balances the adsorption and desorption of oxygen intermediates. Moreover, the formation of more high valence state Ru4+ in Nd0.1RuOx is beneficial to the chemical stability of Ru species during the OER process, indicating that the introduction of Nd can effectively suppress the dissolution of Ru in acidic electrolytes. In addition, the PEM electrolyzer using Nd0.1RuOx/CC as the anode can be operated at 10 mA cm(-2) stably for 50 h. This study sheds new light on the design of the OER catalysts in acid by engineering the electronic structure of RuO2.

Automated summary

By engineering the electronic structure of Nd0.1RuOx, the oxygen evolution activity in acidic solution can be enhanced, and the dissolution of ruthenium can be effectively suppressed, thus providing a design strategy for active and durable catalysts in proton exchange membrane electrolyzers.