4.7 Article

Ultrathin Co3O4-Pt core-shell nanoparticles coupled with three-dimensional graphene for oxygen reduction reaction

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 46, Issue 17, Pages 10303-10311

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2020.12.137

Keywords

Co3O4-Pt; Core shell; High Pt utilization; Electrocatalyst; Oxygen reduction reaction

Funding

  1. National Natural Science Foundation of China [U1705252]
  2. National Natural Science Foundation of Fujian Province [U1705252]
  3. National Basic Research Program of China [21972027]
  4. Guangxi Science and Technology Project [AA17204083, AB16380030]
  5. Natural Science Founda-tion of Guangdong Province [2015A030312007]

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The study demonstrates that ultrathin Co(OH)(2) nanoparticles can be converted into Co3O4-Pt core-shell nanoparticles with high Pt utilization through thermal annealing and controlled replacement reaction on 3D graphene. This nanostructure shows optimized mass activity and specific activity, significantly outperforming traditional Pt/C catalysts.
Design and synthesis of platinum catalysts within atomic level are of great significance for the practical application of fuel cells. We found that the ultrathin Co(OH)(2) nanoparticles can be converted into Co3O4-Co core-shell nanostructures through a thermal annealing process in reducing atmosphere, which are uniformly distributed on the surface of 3D graphene (3DG). The Co3O4-Co core-shell nanoparticles have been successfully transformed into Co3O4-Pt core-shell nanoparticles via a controlled replacement reaction. The Co3O4-Pt @3DG contains only a few atomic layers of Pt shell, and presents a high Pt utilization nanostructure. Besides, the 3D graphene serves as a catalysts carrier with open structure, and offers a three-dimensional molecular accessibility and conducive to mass transfer. Significantly, the optimized mass activity and specific activity of 1.018 A/mgPt and 2.17 mA/cm(2) have been achieved on Co3O4-Pt @3DG at 0.9 V vs RHE, which are 7.6and 8.1 times higher than those of Pt/C (0.134 A/mgPt and 0.266 mA/cm(2)), respectively. The high activity is mainly attributed to the ultrathin core-shell structure with an ultrahigh Pt utilization, and the interaction between the near-surface Co3O4 and the surface Pt shell with a tensile strain to surface Pt shell, and the electrons transfer from Co to Pt. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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