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Electrocatalytic Oxygen Evolution Reaction (OER) on Ru, Ir, and Pt Catalysts: A Comparative Study of Nanoparticles and Bulk Materials
Abstract
A comparative investigation was performed to examine the intrinsic catalytic activity and durability of carbon supported Ru, Ir, and Pt nanoparticles and corresponding bulk materials for the electrocatalytic oxygen evolution reaction (OER). The electrochemical surface characteristics of nanoparticles and bulk materials were studied by surface-sensitive cyclic voltammetry. Although basically similar voltammetric features were observed for nanoparticles and bulk materials of each metal, some differences were uncovered highlighting the changes in oxidation chemistry. On the basis of the electrochemical results, we demonstrated that Ru nanoparticles show lower passivation potentials compared to bulk Ru material. Ir nanoparticles completely lost their voltammetric metallic features during the voltage cycling, in contrast to the corresponding bulk material. Finally, Pt nanoparticles show an increased oxophilic nature compared to bulk Pt. With regard to the OER performance, the most pronounced effects of nanoscaling were identified for Ru and Pt catalysts. In particular, the Ru nanoparticles suffered from strong corrosion at applied OER potentials and were therefore unable to sustain the OER. The Pt nanoparticles exhibited a lower OER activity from the beginning on and were completely deactivated during the applied OER stability protocol, in contrast to the corresponding bulk Pt catalyst. We highlight that the OER activity and durability were comparable for Ir nanoparticles and bulk materials. Thus, Ir nanoparticles provide a high potential as nanoscaled OER catalyst.
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Metadata
- Authors
- Reier, T., Oezaslan, M., & Strasser, P.
- Venue
- ACS Catalysis
- Publisher
- American Chemical Society (ACS)
- Published
- 2012-07-23
- Volume
- 2
- Issue
- 8
- Pages
- 1765-1772
- ISSN
- 2155-5435 (ISSN-L)
- OpenAlex
- W2332386396
- Cited by
- 2,589
- References
- 3
- FWCI
- 16.16
- Type
- journal article
- Language
- en
- Open access
- closed
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