Molybdenum‐Enriched Mo <sub>0.5</sub> Ru <sub>0.5</sub> O <sub>2</sub> Nanoparticles for Efficient and Stable Oxygen Evolution Reaction

K Kaizhu Zeng I In Gyeom Kim (Energy and Environment Directorate Pacific Northwest National Laboratory 3335 Innovation Blvd. Richland WA 99354 USA) F Fangyuan Liu P Peiyuan Gao (Pacific Northwest National Laboratory) L Litao Yan (Energy and Environment Directorate) B Bhuvana Modachur Sivakumar (Energy and Environment Directorate Pacific Northwest National Laboratory 3335 Innovation Blvd. Richland WA 99354 USA) T Thomas W Wietsma (Energy and Environment Directorate Pacific Northwest National Laboratory 3335 Innovation Blvd. Richland WA 99354 USA) Y Yiheng Du (Department of Electrical and Computer Engineering Yale University New Haven CT 06511 USA) Q Qian Zhang C Chong Yang Y Yang Hu T Tangyuan Li (Department of Electrical and Computer Engineering Yale University New Haven CT 06511 USA) S Shu Hu (Department of Chemical and Environmental Engineering, Yale University) Y Yuyan Shao (Energy and Environment Directorate) L Liangbing Hu (Department of Electrical and Computer Engineering Yale University New Haven CT 06511 USA)

Abstract

Abstract Ruthenium dioxide (RuO 2 ) 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 0.5 Ru 0.5 O 2 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 4   °C s −1 . 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 0.5 Ru 0.5 O 2 catalyst achieves an overpotential of 210 mV at 10 mA cm −2 and maintains stable performance over 300 h at 50 mA cm −2 in OER, significantly surpassing the stability of RuO 2 and other reported high‐metal‐content doped RuO 2 catalysts. High‐valence Mo, with its multiple accessible oxidation states and compatible ionic radius, serves as an ideal dopant for RuO 2 , 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 2 systems toward cost‐effective and stable OER catalysts.

Article Details

Volume / Issue Vol. 38, Issue 19
Published April 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (15)

K

Kaizhu Zeng

I

In Gyeom Kim

Energy and Environment Directorate Pacific Northwest National Laboratory 3335 Innovation Blvd. Richland WA 99354 USA

F

Fangyuan Liu

P

Peiyuan Gao

Pacific Northwest National Laboratory

L

Litao Yan

Energy and Environment Directorate

B

Bhuvana Modachur Sivakumar

Energy and Environment Directorate Pacific Northwest National Laboratory 3335 Innovation Blvd. Richland WA 99354 USA

T

Thomas W Wietsma

Energy and Environment Directorate Pacific Northwest National Laboratory 3335 Innovation Blvd. Richland WA 99354 USA

Y

Yiheng Du

Department of Electrical and Computer Engineering Yale University New Haven CT 06511 USA

Q

Qian Zhang

C

Chong Yang

Y

Yang Hu

T

Tangyuan Li

Department of Electrical and Computer Engineering Yale University New Haven CT 06511 USA

S

Shu Hu

Department of Chemical and Environmental Engineering, Yale University

Y

Yuyan Shao

Energy and Environment Directorate

L

Liangbing Hu

Department of Electrical and Computer Engineering Yale University New Haven CT 06511 USA