4.8 Article

Stable Pd-Cu Hydride Catalyst for Efficient Hydrogen Evolution

Journal

NANO LETTERS
Volume 22, Issue 3, Pages 1391-1397

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.1c04840

Keywords

Pd-based catalysts; Pd-Cu hydrides; hydrogen evolution reaction; electrocatalysis; hydrogen adsorption free energy

Funding

  1. National Natural Science Foundation of China [22109043]
  2. Shanghai Risingstar Program [20QA1402400]
  3. Fundamental Research Funds for the Central Universities
  4. Ministry of Science and Technology, Taiwan [MOST 110-2221-E-008-061-MY3]
  5. Program of Introducing Talents of Discipline to Universities [B16017]
  6. Frontiers Science Center for Materiobiology and Dynamic Chemistry at East China University of Science and Technology
  7. Feringa Nobel Prize Scientist Joint Research Center at East China University of Science and Technology
  8. Shanghai Municipal Science and Technology [2018SHZDZX03]

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In this study, a stable Pd-Cu hydride catalyst was designed and synthesized, which combines the advantages of Pd-M and PdHx structures to improve the stability and durability of the hydrogen evolution reaction.
Pd has been regarded as one of the alternatives to Pt as a promising hydrogen evolution reaction (HER) catalyst. Strategies including Pd-metal alloys (Pd-M) and Pd hydrides (PdHx) have been proposed to boost HER performances. However, the stability issues, e.g., the dissolution in Pd-M and the hydrogen releasing in PdHx, restrict the industrial application of Pd-based HER catalysts. We here design and synthesize a stable Pd-Cu hydride (PdCu0.2H0.43) catalyst, combining the advantages of both Pd-M and PdHx structures and improving the HER durability simultaneously. The hydrogen intercalation is realized under atmospheric pressure (1.0 atm) following our synthetic approach that imparts high stability to the Pd-Cu hydride structure. The obtained PdCu0.2H0.43 catalyst exhibits a small overpotential of 28 mV at 10 mA/cm(2), a low Tafel slope of 23 mV/dec, and excellent HER durability due to its appropriate hydrogen adsorption free energy and alleviated metal dissolution rate.

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