A Model for the pH-Dependent Selectivity of the Oxygen Reduction Reaction Electrocatalyzed by N‑Doped Graphitic Carbon
Nitrogen-doped graphitic carbon materials have been extensively studied as potential replacements for Pt-based electrocatalysts for the oxygen reduction reaction (ORR). However, little is known about the catalytic mechanisms, including the parameters that determine the selectivity of the reaction. B...
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Published in | Journal of the American Chemical Society Vol. 138; no. 42; pp. 13923 - 13929 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Chemical Society
26.10.2016
American Chemical Society (ACS) |
Subjects | |
Online Access | Get full text |
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Summary: | Nitrogen-doped graphitic carbon materials have been extensively studied as potential replacements for Pt-based electrocatalysts for the oxygen reduction reaction (ORR). However, little is known about the catalytic mechanisms, including the parameters that determine the selectivity of the reaction. By comparing theoretical calculations of the ORR selectivity at a well-defined graphene nanostructure with experimental results, we propose a model based on interfacial solvation to explain the observed preference for the four-electron pathway in alkaline electrolytes. The hydrophobic environment around the active sites, as in enzymatic catalysis, restricts the access of water and destabilizes small ionic species such as peroxide, the product of the two-electron pathway. This model, when applied to acidic electrolytes, shows the ORR preferring the two-electron pathway, consistent with the well-known pH-dependent ORR selectivity catalyzed by graphitic carbon materials. Because of the similarity between more complex N-doped graphitic carbon materials and our model system, we can extend this model to the former and rationalize nearly all of the previously reported experimental results on the selectivity of ORR catalyzed by these materials. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 FG02-07ER15889 USDOE Office of Science (SC) |
ISSN: | 0002-7863 1520-5126 |
DOI: | 10.1021/jacs.6b06778 |