Density functional theory predicts lanthanide doping enhances OER in RuO2 catalysts, suggesting improved efficiency.
Regulating the reaction pathway of the oxygen evolution reaction (OER) is pivotal in enhancing the activity and stability of RuO₂-based catalysts. However, it remains challenging to achieve the desired oxide pathway mechanism (OPM) for RuO₂-based catalysts. Herein, we use density functional theory calculations to predict that Sm doping can tune the OER pathway of RuO₂ toward the OPM. We successfully synthesize various lanthanide-doped RuO₂ catalysts and demonstrate an overpotential as low as 184 mV at 10 mA cm⁻² for Sm-doped RuO₂ supported on reduced graphene oxide (Sm-RuO₂/rGO). Sm-RuO₂/rGO exhibits a stable operation for over 200 h at 500 mA cm⁻². In situ characterizations confirm the functionality of incorporated Sm atoms in triggering an OPM pathway for RuO₂. Our work demonstrates an effective strategy to regulate the OER pathway of RuO₂-based catalysts, enabling highly efficient and durable OER under acidic conditions and showing great promise for industrial applications.
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Yang et al. (2026) studied this question.
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