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A Bifunctional Nonprecious Metal Catalyst for Oxygen Reduction and Water Oxidation

Gorlin, Yelena, Jaramillo, Thomas F.·2010·Journal of the American Chemical Society

Abstract

There is a growing interest in oxygen electrochemistry as conversions between O(2) and H(2)O play an important role in a variety of renewable energy technologies. The goal of this work is to develop active bifunctional catalyst materials for water oxidation and oxygen reduction. Drawing inspiration from a cubane-like CaMn(4)O(x), the biological catalyst found in the oxygen evolving center (OEC) in photosystem II, nanostructured manganese oxide surfaces were investigated for these reactions. Thin films of nanostructured manganese oxide were found to be active for both oxygen reduction and water oxidation, with similar overall oxygen electrode activity to the best known precious metal nanoparticle catalysts: platinum, ruthenium, and iridium. Physical and chemical characterization of the nanostructured Mn oxide bifunctional catalyst reveals an oxidation state of Mn(III), akin to one of the most commonly observed Mn oxidation states found in the OEC.

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Metadata

Authors
Gorlin, Y., & Jaramillo, T. F.
Venue
Journal of the American Chemical Society
Published
2010-09-14
Volume
132
Issue
39
Pages
13612-13614
ISSN
  • 0002-7863 (ISSN-L)
  • 1520-5126
OpenAlex
W2020893927
Cited by
1,566
References
1
FWCI
18.38
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: A Bifunctional Nonprecious Metal Catalyst for Oxygen Reduction and Water Oxidation. https://app.cochat.ai/papers/10.1021/ja104587v
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Gorlin, Y., & Jaramillo, T. F. (2010). A Bifunctional Nonprecious Metal Catalyst for Oxygen Reduction and Water Oxidation. Journal of the American Chemical Society. https://doi.org/10.1021/ja104587v

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Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.