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Title: H 2 Dissociation on Noble Metal Single Atom Catalysts Adsorbed on and Doped into CeO 2 (111)

Abstract

In this study, we used density functional theory (DFT) calculations to investigate the dissociation of H 2 on an Ag single atom catalyst adsorbed on the pristine CeO 2 (111) surface (Ag/CeO 2), or substituting a surface Ce atom on the reduced (Ag:CeO 2-x) and partially hydrogenated (Ag:H–CeO 2) surfaces. The initial state of the H 2 dissociation reaction in the different investigated models corresponds to distinct oxidation states, +1, +2, or +3, of the Ag atom, thus allowing us to examine the influence of the charge transfers between the noble metal, the oxide, and the hydrogen atoms on the reaction pathway and activation energy. In all investigated models, the computed barrier of H 2 dissociation is lowered by about 0.6 eV in comparison to that on metal-free CeO 2. On Ag/CeO 2 and Ag:CeO 2-x, also the energy of H 2 dissociative adsorption is smaller than that on metal-free ceria. These results suggest that CeO 2 modified with dispersed Ag atoms is a promising anode material for proton exchange membrane fuel cells. Lastly, further comparison of our results for Ag to analogous calculations for Cu and Au single atom catalysts reveals trends in the computed barriers that can bemore » related to the change of the metal oxidation state in the reaction.« less

Authors:
ORCiD logo [1];  [1]; ORCiD logo [2]
  1. University of Modena and Reggio-Emilia, Modena, Emilia-Romagna (Italy); CNR-S3 Institute of Nanoscience, Modena (Italy)
  2. Princeton Univ., NJ (United States)
Publication Date:
Research Org.:
Princeton Univ., NJ (United States)
Sponsoring Org.:
USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22). Chemical Sciences, Geosciences & Biosciences Division
OSTI Identifier:
1506607
Grant/Contract Number:  
SC0007347
Resource Type:
Accepted Manuscript
Journal Name:
Journal of Physical Chemistry. C
Additional Journal Information:
Journal Name: Journal of Physical Chemistry. C; Journal ID: ISSN 1932-7447
Publisher:
American Chemical Society
Country of Publication:
United States
Language:
English
Subject:
37 INORGANIC, ORGANIC, PHYSICAL, AND ANALYTICAL CHEMISTRY; 36 MATERIALS SCIENCE

Citation Formats

Righi, Giulia, Magri, Rita, and Selloni, Annabella. H2 Dissociation on Noble Metal Single Atom Catalysts Adsorbed on and Doped into CeO2 (111). United States: N. p., 2019. Web. doi:10.1021/acs.jpcc.9b00609.
Righi, Giulia, Magri, Rita, & Selloni, Annabella. H2 Dissociation on Noble Metal Single Atom Catalysts Adsorbed on and Doped into CeO2 (111). United States. doi:10.1021/acs.jpcc.9b00609.
Righi, Giulia, Magri, Rita, and Selloni, Annabella. Thu . "H2 Dissociation on Noble Metal Single Atom Catalysts Adsorbed on and Doped into CeO2 (111)". United States. doi:10.1021/acs.jpcc.9b00609.
@article{osti_1506607,
title = {H2 Dissociation on Noble Metal Single Atom Catalysts Adsorbed on and Doped into CeO2 (111)},
author = {Righi, Giulia and Magri, Rita and Selloni, Annabella},
abstractNote = {In this study, we used density functional theory (DFT) calculations to investigate the dissociation of H2 on an Ag single atom catalyst adsorbed on the pristine CeO2 (111) surface (Ag/CeO2), or substituting a surface Ce atom on the reduced (Ag:CeO2-x) and partially hydrogenated (Ag:H–CeO2) surfaces. The initial state of the H2 dissociation reaction in the different investigated models corresponds to distinct oxidation states, +1, +2, or +3, of the Ag atom, thus allowing us to examine the influence of the charge transfers between the noble metal, the oxide, and the hydrogen atoms on the reaction pathway and activation energy. In all investigated models, the computed barrier of H2 dissociation is lowered by about 0.6 eV in comparison to that on metal-free CeO2. On Ag/CeO2 and Ag:CeO2-x, also the energy of H2 dissociative adsorption is smaller than that on metal-free ceria. These results suggest that CeO2 modified with dispersed Ag atoms is a promising anode material for proton exchange membrane fuel cells. Lastly, further comparison of our results for Ag to analogous calculations for Cu and Au single atom catalysts reveals trends in the computed barriers that can be related to the change of the metal oxidation state in the reaction.},
doi = {10.1021/acs.jpcc.9b00609},
journal = {Journal of Physical Chemistry. C},
number = ,
volume = ,
place = {United States},
year = {2019},
month = {3}
}

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This content will become publicly available on March 28, 2020
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