Molybdenum-Enriched Mo<sub>0.5</sub>Ru<sub>0.5</sub>O<sub>2</sub> Nanoparticles for Efficient and Stable Oxygen Evolution Reaction.
basic_science · Level V
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- Record sourced from PubMed, PMID 41362270.
- Also identified by DOI 10.1002/adma.202520210.
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Abstract
Ruthenium dioxide (RuO<sub>2</sub>) shows excellent activity toward the acidic oxygen evolution reaction (OER); however, its practical application is limited by poor long-term stability. Herein, a single-phase Mo<sub>0.5</sub>Ru<sub>0.5</sub>O<sub>2</sub> nanoparticle catalyst is reported with a high Mo content, synthesized via high-temperature thermal shock treatment under an oxygen atmosphere (HTSO), exhibiting high activity and stability in OER. The HTSO technique involves rapidly heating the precursor to ≈1200 °C for ≈0.05 s in oxygen, followed by immediate quenching at a rate of ≈10<sup>4</sup> °C s<sup>-1</sup>. The resulting nanoparticles exhibit a uniform size of ≈10 nm and homogeneous elemental mixing, overcoming the thermodynamic barriers that typically lead to phase separation in conventional synthesis methods. The Mo<sub>0.5</sub>Ru<sub>0.5</sub>O<sub>2</sub> catalyst achieves an overpotential of 210 mV at 10 mA cm<sup>-2</sup> and maintains stable performance over 300 h at 50 mA cm<sup>-2</sup> in OER, significantly surpassing the stability of RuO<sub>2</sub> and other reported high-metal-content doped RuO<sub>2</sub> catalysts. High-valence Mo, with its multiple accessible oxidation states and compatible ionic radius, serves as an ideal dopant for RuO<sub>2</sub>, enabling stable lattice substitution, effective electron donation, and ultimately suppressing Ru over-oxidation while enhancing stability. This approach enhances catalyst stability and Ru utilization, providing a versatile platform for synthesizing other metal-doped RuO<sub>2</sub> systems toward cost-effective and stable OER catalysts.