4.8 Article

New Insight of Pyrrole-Like Nitrogen for Boosting Hydrogen Evolution Activity and Stability of Pt Single Atoms

Journal

SMALL
Volume 17, Issue 16, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/smll.202004453

Keywords

atomic layer deposition; density functional theory calculations; hydrogen evolution reaction; platinum; single atoms; XAS analysis

Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC)
  2. Canada Research Chair (CRC) Program
  3. Canada Foundation for Innovation (CFI)
  4. University of Western Ontario
  5. Science Challenge Project [TZ2018004]
  6. Fundamental Research Funds for the Central Universities
  7. National Natural Science Foundation of China [51861130360, 51572016, 11974037, 22075203, 21802065, U1530401]
  8. Newton Advanced Fellowships [NAF\R1\180242]
  9. Beijing Computational Science Research Center (CSRC)

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This study investigates the enhanced mechanisms between Pt single atoms and different types of nitrogen-doped support materials. The Pt catalyst shows improved hydrogen evolution reaction activity with an increase in pyrrole-like nitrogen content in the carbon nanotube support. The superior performance of the Pt single atom catalysts is attributed to the interaction between dyz and s orbitals of hydrogen and sp(3) hybrid orbital of nitrogen.
Single atomic Pt catalysts exhibit particularly high hydrogen evolution reaction (HER) activity compared to conventional nanomaterial-based catalysts. However, the enhanced mechanisms between Pt and their coordination environment are not understood in detail. Hence, a systematic study examining the different types of N in the support is essential to clearly demonstrate the relationship between Pt single atoms and N-doped support. Herein, three types of carbon nanotubes with varying types of N (pyridine-like N, pyrrole-like N, and quaternary N) are used as carbon support for Pt single atom atomic layer deposition. The detailed coordination environment of the Pt single atom catalyst is carefully studied by electron microscope and X-ray absorption spectra (XAS). Interestingly, with the increase of pyrrole-like N in the CNT support, the HER activity of the Pt catalyst also improves. First principle calculations results indicate that the interaction between the dyz and s orbitals of H and sp(3) hybrid orbital of N should be the origin of the superior HER performance of these Pt single atom catalysts (SACs).

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