Heterophase RuO <sub>2</sub> oxygen evolution catalyst for durable proton exchange membrane water electrolysis

Dissolution of ruthenium (Ru) species under harsh anode operating conditions severely impedes the commercialization of non-iridium (Ir) proton exchange membrane water electrolyzers (PEMWEs). Here, we propose a catalyst design strategy that engineers phases beyond conventional atomic ordering, constructing a heterophase MoRuO<i><sub>x</sub></i> catalyst (AC-MoRuO<i><sub>x</sub></i>). This catalyst achieves 10 milliamperes per square centimeter in an acidic oxygen evolution reaction with merely 180-millivolt overpotential while operating stably for >3000 hours. In PEMWE devices, AC-MoRuO<i><sub>x</sub></i> delivers record durability at industrial current densities: ≥2000 hours at 1.0 ampere per square centimeter and 1000 hours at 1.5 amperes per square centimeter. We demonstrate that heterophase architecture and atomic arrangements reconfigure electronic structures and phase distribution, simultaneously optimizing active-site density and structural integrity. This breakthrough resolves the long-standing activity-stability trade-off in ruthenium-based catalysts.

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Publication Details

Journal
Science Advances
Published
2025-12-17
DOI
https://doi.org/10.1126/sciadv.aea4543
Citations
4
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
1.45

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article

Heterophase RuO 2 oxygen evolution catalyst for durable proton exchange membrane water electrolysis

Jingzhi Shang, Zechao Zhuang, Yunhu Han, Guanzhen Chen et al.
4 citations
Science Advances
Electrocatalysts for Energy Conversion
1.45
article

Heterophase RuO 2 oxygen evolution catalyst for durable proton exchange membrane water electrolysis

Jingzhi Shang, Zechao Zhuang, Yunhu Han, Guanzhen Chen, Ruihu Lu, Xintong Li, Yu Wang, Jian Wang, Ziyun Wang, Xuewen Zhang, Hao Fei, Tao Gan, Jiena Weng, Chao Ma
article en
4 citations

Abstract

Dissolution of ruthenium (Ru) species under harsh anode operating conditions severely impedes the commercialization of non-iridium (Ir) proton exchange membrane water electrolyzers (PEMWEs). Here, we propose a catalyst design strategy that engineers phases beyond conventional atomic ordering, constructing a heterophase MoRuO<i><sub>x</sub></i> catalyst (AC-MoRuO<i><sub>x</sub></i>). This catalyst achieves 10 milliamperes per square centimeter in an acidic oxygen evolution reaction with merely 180-millivolt overpotential while operating stably for >3000 hours. In PEMWE devices, AC-MoRuO<i><sub>x</sub></i> delivers record durability at industrial current densities: ≥2000 hours at 1.0 ampere per square centimeter and 1000 hours at 1.5 amperes per square centimeter. We demonstrate that heterophase architecture and atomic arrangements reconfigure electronic structures and phase distribution, simultaneously optimizing active-site density and structural integrity. This breakthrough resolves the long-standing activity-stability trade-off in ruthenium-based catalysts.

Science AdvancesVol. 11(51)
University of Auckland (NZ), City University of Hong Kong (HK), Northwestern Polytechnical University (CN), Chinese Academy of Sciences (CN), Nanjing University of Posts and Telecommunications (CN), Shanghai Advanced Research Institute (CN), Columbia University (US), Tsinghua University (CN)
Salt Science Research Foundation, Royal Society Te Apārangi, Natural Science Foundation of Shaanxi Province, Marsden Fund
Openalex Percentile: Top 17%
Electrocatalysts for Energy Conversion
1.45
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