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The structure-dependent enhancement of the oxygen reduction reaction performance of Co-based low Pt catalysts through Au addition

  • Zi Jun Lin
  • , Tsung Fu Chou
  • , Chen Wei Liu
  • , Po Hsiang Huang
  • , Yao Zhang Guo
  • , Jeng Han Wang*
  • , Kuan Wen Wang
  • *Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

Abstract

In this study, we have investigated the oxygen reduction reaction (ORR) activity and durability of Co-based catalysts mechanistically. CoPt/C catalysts with a Pt loading of 7 wt% and Au modification have been prepared and shown excellent ORR performance. The various as-prepared CoPt/C and CoPtAu/C catalysts have about 2.6-9.2 times higher mass activity than commercial Pt/C. The mechanistic insight obtained by density functional theory calculations has shown that the enhanced activity is attributable to the fact that Co-based catalysts can easily dissociate surface O2∗ without the high-barrier protonation step and efficiently remove the dissociated O∗. The improved stability, 1000th decay = 14.6%, corresponds to the fact that the core Au can resist the shrinkage of surface Pt during the accelerated durability test.

Original languageEnglish
Pages (from-to)11023-11029
Number of pages7
JournalJournal of Materials Chemistry A
Volume4
Issue number28
DOIs
Publication statusPublished - 2016

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 7 - Affordable and Clean Energy
    SDG 7 Affordable and Clean Energy

ASJC Scopus subject areas

  • General Chemistry
  • Renewable Energy, Sustainability and the Environment
  • General Materials Science

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