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Catalytic mechanism and bonding analyses of Au-Pd single atom alloy (SAA): CO oxidation reaction
Single-atom catalysts (SACs), including metal-metal-bonded bimetallic ones named single-atom alloys (SAAs), have aroused significant interest in catalysis. In this article, the catalytic mechanism and bonding analysis of CO oxidation reaction on bimetallic gold-palladium (Au-Pd) model of single atom...
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Published in: | Science China materials 2020-06, Vol.63 (6), p.993-1002 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Single-atom catalysts (SACs), including metal-metal-bonded bimetallic ones named single-atom alloys (SAAs), have aroused significant interest in catalysis. In this article, the catalytic mechanism and bonding analysis of CO oxidation reaction on bimetallic gold-palladium (Au-Pd) model of single atom alloy Au
37
Pd
1
are investigated by using quantum chemical calculations. The molecular geometries and adsorbate/substrate binding energies of CO@Au-Pd, O
2
@Au-Pd and CO/O
2
@Au-Pd configurations are identified. The core-shell structure is confirmed to be the most stable structure for Au-Pd SAA, where the Pd atom prefers to situate at the core site. Charge transfer from the Pd atom to the Au atoms has been confirmed to stabilize the structure. According to the binding energy and chemical bonding analysis, both CO and O
2
prefer to bind to the Pd atom at the hex site with low coordination number. The formation of new co-adsorption species is identified, in which vertical and parallel bridging adsorptions of CO and O
2
on the Au-Pd bonds are observed. CO oxidation on Au-Pd SAA is found to be feasible with low energy barriers and follows the Langmuir-Hinshewood (L-H) mechanism. Our work offers insights into the significant role of single atom of the SAAs in catalytic reactions and can provide evidence for designing new SAAs with high-performance catalytic activities. |
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ISSN: | 2095-8226 2199-4501 |
DOI: | 10.1007/s40843-019-1257-x |