Author
Listed:
- Wen-Xing Zheng
(Tianjin University of Technology)
- Xuan-Xuan Cheng
(Tianjin University of Technology)
- Ping-Ping Chen
(Tianjin University of Technology)
- Lin-Lin Wang
(Tianjin University of Technology)
- Ying Duan
(Tianjin University of Technology)
- Guo-Jin Feng
(Tianjin University of Technology)
- Xiao-Ran Wang
(Tianjin University of Technology)
- Jing-Jing Li
(Tianjin University of Technology)
- Chao Zhang
(Tianjin University of Technology)
- Zi-You Yu
(Tianjin University of Technology)
- Tong-Bu Lu
(Tianjin University of Technology)
Abstract
Ruthenium dioxide has attracted extensive attention as a promising catalyst for oxygen evolution reaction in acid. However, the over-oxidation of RuO2 into soluble H2RuO5 species results in a poor durability, which hinders the practical application of RuO2 in proton exchange membrane water electrolysis. Here, we report a confinement strategy by enriching a high local concentration of in-situ formed H2RuO5 species, which can effectively suppress the RuO2 degradation by shifting the redox equilibrium away from the RuO2 over-oxidation, greatly boosting its durability during acidic oxygen evolution. Therefore, the confined RuO2 catalyst can continuously operate at 10 mA cm–2 for over 400 h with negligible attenuation, and has a 14.8 times higher stability number than the unconfined RuO2 catalyst. An electrolyzer cell using the confined RuO2 catalyst as anode displays a notable durability of 300 h at 500 mA cm–2 and at 60 °C. This work demonstrates a promising design strategy for durable oxygen evolution reaction catalysts in acid via confinement engineering.
Suggested Citation
Wen-Xing Zheng & Xuan-Xuan Cheng & Ping-Ping Chen & Lin-Lin Wang & Ying Duan & Guo-Jin Feng & Xiao-Ran Wang & Jing-Jing Li & Chao Zhang & Zi-You Yu & Tong-Bu Lu, 2025.
"Boosting the durability of RuO2 via confinement effect for proton exchange membrane water electrolyzer,"
Nature Communications, Nature, vol. 16(1), pages 1-9, December.
Handle:
RePEc:nat:natcom:v:16:y:2025:i:1:d:10.1038_s41467-024-55747-0
DOI: 10.1038/s41467-024-55747-0
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