期刊
CHEMCATCHEM
卷 10, 期 23, 页码 5505-5510出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cctc.201801408
关键词
heterogeneous catalysis; homogeneous catalysis; metal-porphycenes; oxygen reduction reaction; electrocatalysis
资金
- Toyota Research Institute
It has been a long-standing goal to find alternative, cost effective catalysts for oxygen reduction reaction (ORR) in fuel cells. Molecular complexes capable of efficiently catalyzing ORR, when supported on a conducting solid surface could provide interesting hybrid materials combining the best of homogeneous and heterogeneous catalysis. We use density functional theory to study the ORR activity of molecular (unsupported) and gold supported 3d metal (II)-porphycenes (MPc). All the 3d metal-porphycenes adsorb strongly on the Au(111) support with negative free energy of formation ranging from 1.0-3.0eV while solvation lowers the energy of molecular MPc by only 0.5eV compared to the gas phase. These indicate that the 3d MPc are stable and anchored firmly to the gold surface under ORR conditions. Based on our analysis, the gold support enhances the ORR activity in some of the examined MPc systems. We find that the molecular MnPc and FePc are the best ORR electrocatalysts with theoretical overpotentials of 0.44V and 0.36V. This work highlights the important role of the support in preserving/increasing the activity of molecular catalyst.
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