Carbon Monoxide as a Promoter of Atomically Dispersed Platinum Catalyst in 
Electrochemical Hydrogen Evolution Reaction

Kwon, Han Chang; Kim, Minho; Grote, Jan-Philipp; Cho, Sung June; Chung, Min Wook; Kim, Haesol; Won, Dahye; Žeradjanin, Aleksandar R.; Mayrhofer, Karl Johann Jakob; Choi, Minkee; Kim, Hyungjun; Choi, Chang Hyuck

doi:10.1021/jacs.8b09211

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Carbon Monoxide as a Promoter of Atomically Dispersed Platinum Catalyst in Electrochemical Hydrogen Evolution Reaction

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Grote, Jan-Philipp
Electrocatalysis, Interface Chemistry and Surface Engineering, Max-Planck-Institut für Eisenforschung GmbH, Max Planck Society;

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Žeradjanin, Aleksandar R.
Electrocatalysis, Interface Chemistry and Surface Engineering, Max-Planck-Institut für Eisenforschung GmbH, Max Planck Society;
Helmholtz-Institute Erlangen-Nuremberg for Renewable Energy (IEK-11), Forschungszentrum Jülich, Egerlandstrasse 3, 91058 Erlangen, Germany;

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Mayrhofer, Karl Johann Jakob
Department of Chemical and Biological Engineering, Friedrich-Alexander-Universität Erlangen-Nürnberg, 91058 Erlangen, Germany;
Electrocatalysis, Interface Chemistry and Surface Engineering, Max-Planck-Institut für Eisenforschung GmbH, Max Planck Society;
Helmholtz-Institute Erlangen-Nuremberg for Renewable Energy (IEK-11), Forschungszentrum Jülich, Egerlandstrasse 3, 91058 Erlangen, Germany;

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Zitation

Kwon, H. C., Kim, M., Grote, J.-P., Cho, S. J., Chung, M. W., Kim, H., et al. (2018). Carbon Monoxide as a Promoter of Atomically Dispersed Platinum Catalyst in Electrochemical Hydrogen Evolution Reaction. Journal of the American Chemical Society, 140(47), 16198-16205. doi:10.1021/jacs.8b09211.

Zitierlink: https://hdl.handle.net/21.11116/0000-0002-D081-0

Zusammenfassung

Carbon monoxide is widely known to poison Pt during heterogeneous catalysis owing to its strong donor-acceptor binding ability. Herein, we report a counterintuitive phenomenon of this general paradigm when the size of Pt decreases to an atomic level, namely, the CO-promoting Pt electrocatalysis toward hydrogen evolution reactions (HER). Compared to pristine atomic Pt catalyst, reduction current on a CO-modified catalyst increases significantly. Operando mass spectroscopy and electrochemical analyses demonstrate that the increased current arises due to enhanced H2 evolution, not additional CO reduction. Through structural identification of catalytic sites and computational analysis, we conclude that CO-ligation on the atomic Pt facilitates Hads formation via water dissociation. This counterintuitive effect exemplifies the fully distinct characteristics of atomic Pt catalysts from those of bulk Pt, and offers new insights for tuning the activity of similar classes of catalysts. Copyright © 2018 American Chemical Society.