4.8 Article

Suppressing Dissolution of Pt-Based Electrocatalysts through the Electronic Metal-Support Interaction

期刊

ADVANCED ENERGY MATERIALS
卷 11, 期 38, 页码 -

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/aenm.202101050

关键词

electronic metal-support interaction; graphitic-N doping; oxygen reduction reaction; platinum; stability

资金

  1. Open Research Fund of Jiangsu Provincial Key Laboratory of Environmental Engineering [KF2018001]
  2. National Natural Science Foundation of China [21871008, 52072389]
  3. Shanghai Science and Technology Innovation Action Plan [20dz1204400]
  4. State Key Laboratory of ASIC System [2020KF002]
  5. Program of Shanghai Academic Research Leader [20XD1424300]

向作者/读者索取更多资源

In this study, the dissolution of Pt nanoparticles was successfully suppressed by adjusting the electronic structure of surface Pt atoms, leading to enhanced catalytic stability. The specially designed graphitic-N-doped carbon nanosheets effectively reduced the rate of Pt dissolution by anchoring Pt nanoparticles.
Suppressing the Pt dissolution still remains a big challenge in improving the long-term stability of Pt-based catalysts in electrochemical energy conversion. In this work, the degradation of Pt nanoparticles is successfully suppressed via weakening the Pt-O dipole effect by adjusting the electronic structure of surface Pt atoms. The specially designed graphitic-N-doped carbon nanosheets with balanced N content and graphitization degree as well as fewer defects are prepared for anchoring Pt nanoparticles to enhance the electronic metal-support interaction. This can accelerate the electron transfer from Pt to substrate, decrease the surface electron density of Pt, and attenuate the Pt-O interaction. As a result, the rate of Pt dissolution decreases by 95% compared to that of commercial Pt/C toward the oxygen reduction reaction and thus the catalytic stability is significantly improved in the electrochemical accelerated durability test. The theoretical simulation shows that the inhibition of surface Pt dissolution is attributed to the enhanced energy barrier in the initial relaxation process.

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