Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/98953
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Title: Hollow porous carbon-confined atomically ordered PtCo3 intermetallics for an efficient oxygen reduction reaction
Authors: Hu, Y 
Guo, X 
Shen, T
Zhu, Y 
Wang, D
Issue Date: 6-May-2022
Source: ACS catalysis, 6 May 2022, v. 12, no. 9, p. 5380-5387
Abstract: PtM3alloys have demonstrated superior oxygen reduction reaction (ORR) activity due to the strong strain effect caused by non-noble metal cores. However, the serious corrosion of non-noble metals in acid solutions is still challenging. Herein, a hollow porous N-doped carbon sphere-encapsulated PtCo3intermetallic electrocatalyst (O-PtCo3@HNCS) is successfully prepared through Co pre-embedding and the subsequent impregnation-reduction method. The Co pre-embedding step is responsible for the formation of abundant mesopores, and the subsequent impregnation-reduction process leads to Pt-Co ordering and carbon encapsulation. Benefiting from the accelerated mass transfer process, enhanced metal interaction, and physical confinement effect, O-PtCo3@HNCS exhibits excellent ORR activity and durability with negligible half-wave loss after long-term stability test in acid solutions. The ordered PtCo3nanoparticles tightly anchored in the carbon matrix without obvious aggregation, sintering, and agglomeration, responsible for the superior durability. The strategy for the carbon confinement in this work paves the way for achieving highly efficient catalysts with low Pt content, which can be used in various energy-related systems.
Keywords: Atomically ordered structure
Carbon encapsulation
Fuel cells
Hollow porous structure
Intermetallic electrocatalyst
Publisher: American Chemical Society
Journal: ACS catalysis 
EISSN: 2155-5435
DOI: 10.1021/acscatal.2c01541
Rights: © 2022 American Chemical Society
This document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Catalysis, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acscatal.2c01541.
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