4.6 Article

Palladium Nanoparticles/Defective Graphene Composites as Oxygen Reduction Electrocatalysts: A First-Principles Study

期刊

JOURNAL OF PHYSICAL CHEMISTRY C
卷 116, 期 4, 页码 2710-2719

出版社

AMER CHEMICAL SOC
DOI: 10.1021/jp2096983

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资金

  1. King Abdullah University of Science and Technology
  2. NSFC of China [11174045, 21103015]
  3. Chinese Scholarship Council [2009606533]
  4. Dalian University of Technology [1000-893238, 1000-893374]
  5. Fundamental Research Funds for the Central Universities [DUT11LK19]

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The impact of graphene substrate-Pd nanoparticle interaction on the O, OH, and OOH adsorption that is directly related to the electrocatalytic performance of these composites in oxygen reduction reaction (ORR) has been investigated by first-principles-based calculations. The calculated binding energy of a Pd-13 nanoparticle on a single vacancy graphene is as high as -6.10 eV, owing to the hybridization between the dsp states of the Pd particles with the sp(2) dangling bonds at the defect sites. The strong interaction results in the averaged d-band center of the deposited Pd nanoparticles shifted away from the Fermi level from -1.02 to -1.45 eV. Doping the single vacancy graphene with B or N will further tune the average d-band center and also the activity of the composite toward O, OH, and OOH adsorption. The adsorption energies of O, OH, and OOH are reduced from -4.78, -4.38, and -1.56 eV on the freestanding Pd-13 nanopartide to -4.57, -2.66, and -1.39 eV on Pd-13/single vacancy graphene composites, showing that the defective graphene substrate will not only stabilize the Pd nanoparticles but also reduce the adsorption energies of the O-containing species to the Pd particle, and so as the poisoning of the ORR active sites.

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