4.5 Article

RuP Nanoparticles Supported on N, O Codoped Porous Hollow Carbon for Efficient Hydrogen Oxidation Reaction

Journal

ADVANCED MATERIALS INTERFACES
Volume 9, Issue 9, Pages -

Publisher

WILEY
DOI: 10.1002/admi.202102193

Keywords

DFT calculations; electrocatalysis; HOR; hydroxyl binding energy; reaction mechanisms

Funding

  1. National Natural Science Foundation of China [51772283, 22072140, 22102169]
  2. Fundamental Research Funds for the Central Universities [WK2060000032]

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In this study, a highly active and low-cost anodic HOR electrocatalyst was prepared, which plays a significant role in the large-scale application of AEMFCs. The catalyst exhibited high catalytic activity, achieving a mass activity 13 times higher than that of traditional Ru/NOC catalyst and even superior to that of Pt/C catalyst.
Highly active and low-cost anodic hydrogen oxidation reaction (HOR) catalysts play a significant role in the large-scale application of anion exchange membrane fuel cells (AEMFCs). Herein, a novel anodic HOR electrocatalyst with RuP nanoparticles loaded on N, O codoped porous hollow carbon (RuP/NOC) is prepared. The catalyst exhibits high catalytic activity toward HOR, achieving a kinetic mass activity of 3.25 mA mu g(PGM)(-1) at 50 mV, 13 times higher than that of Ru/NOC and even superior to that of Pt/C. Density functional theory (DFT) calculations demonstrate that the transfer of electrons from ruthenium to phosphorus shifts down the d-band center of Ru, weakening the hydroxyl binding energy and decreasing the reaction energy barrier for HOR, thus enhancing the catalytic activity of Ru.

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