<p>Interface engineering is a prospective method for improving electrochemical performance, while efficient interfacial tuning is still difficult. Here, a series of WO<sub>3</sub>-Ir catalysts with tuned interfaces were obtained from WO<sub>3</sub> support with different surface states. The prepared WO<sub>3</sub>-O-Ir catalyst with higher interfacial oxygen content shows excellent hydrogen oxidation reaction activity with a mass activity of 54.04 A g<sub>Ir</sub><sup>−1</sup> for hydrogen oxidation reaction, which is superior to WO<sub>3</sub>-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.</p> Graphical Abstract <p></p>

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Boosting alkaline hydrogen oxidation by tuning the interface of WO3-Ir

  • Yao Peng,
  • Albert Akeno Nyaaba,
  • Jun-Yi Liu,
  • Li Yang,
  • Yuan-Jun Liu,
  • Hong-Bo Zhou,
  • Zhen-Yuan Ji,
  • Bo Zhou,
  • Yan Zhong,
  • Guo-Xing Zhu

摘要

Interface engineering is a prospective method for improving electrochemical performance, while efficient interfacial tuning is still difficult. Here, a series of WO3-Ir catalysts with tuned interfaces were obtained from WO3 support with different surface states. The prepared WO3-O-Ir catalyst with higher interfacial oxygen content shows excellent hydrogen oxidation reaction activity with a mass activity of 54.04 A gIr−1 for hydrogen oxidation reaction, which is superior to WO3-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.

Graphical Abstract