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 language | English |
|---|---|
| Pages (from-to) | 11023-11029 |
| Number of pages | 7 |
| Journal | Journal of Materials Chemistry A |
| Volume | 4 |
| Issue number | 28 |
| DOIs | |
| Publication status | Published - 2016 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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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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