Boosting alkaline hydrogen oxidation by tuning the interface of WO <sub>3</sub> ‐Ir

Abstract Interface engineering is a prospective method for improving electrochemical performance, while efficient interfacial tuning is still difficult. Here, a series of WO 3 ‐Ir catalysts with tuned interfaces were obtained from WO 3 support with different surface states. The prepared WO 3 ‐O‐Ir catalyst with higher interfacial oxygen content shows excellent hydrogen oxidation reaction activity with a mass activity of 54.04 A g Ir −1 for hydrogen oxidation reaction, which is superior to WO 3 ‐W‐Ir with higher tungsten content and even commercial Pt/C catalysts. Theoretical calculation and X‐ray photoelectron spectroscopy valence band spectrum analyses verify that the position of the d‐band center is directly proportional to the interfacial oxygen content. This modulates the electronic structure of the active phase, increasing the binding energy for OH species and enhancing their adsorption capacity, which boost the performance for hydrogen oxidation reaction.

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Publication Details

Journal
Rare Metals
Published
2025-05-08
DOI
https://doi.org/10.1007/s12598-025-03320-z
Citations
4
Primary Topic
Electrocatalysts for Energy Conversion
Type
article
Field-Weighted Citation Impact
1.45

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article

Boosting alkaline hydrogen oxidation by tuning the interface of WO 3 ‐Ir

Peng Yao, Bo Zhou, Zhenyuan Ji, Guoxing Zhu et al.
4 citations
Rare Metals
Electrocatalysts for Energy Conversion
1.45
article

Boosting alkaline hydrogen oxidation by tuning the interface of WO 3 ‐Ir

Peng Yao, Bo Zhou, Zhenyuan Ji, Guoxing Zhu, Albert Akeno Nyaaba, Yang Li, Yuanjun Liu, Junyi Liu, Hongbo Zhou, Yan Zhong
article en
4 citations

Abstract

Abstract Interface engineering is a prospective method for improving electrochemical performance, while efficient interfacial tuning is still difficult. Here, a series of WO 3 ‐Ir catalysts with tuned interfaces were obtained from WO 3 support with different surface states. The prepared WO 3 ‐O‐Ir catalyst with higher interfacial oxygen content shows excellent hydrogen oxidation reaction activity with a mass activity of 54.04 A g Ir −1 for hydrogen oxidation reaction, which is superior to WO 3 ‐W‐Ir with higher tungsten content and even commercial Pt/C catalysts. Theoretical calculation and X‐ray photoelectron spectroscopy valence band spectrum analyses verify that the position of the d‐band center is directly proportional to the interfacial oxygen content. This modulates the electronic structure of the active phase, increasing the binding energy for OH species and enhancing their adsorption capacity, which boost the performance for hydrogen oxidation reaction.

Rare MetalsVol. 44(9)
Jiangsu University (CN), Jiangsu University of Science and Technology (CN), Institute of New Materials (CN)
National Natural Science Foundation of China
Openalex Percentile: Top 19%
Electrocatalysts for Energy Conversion
1.45
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