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  Improved CO2 Electroreduction Performance on Plasma-Activated Cu Catalysts via Electrolyte Design: Halide Effect

Gao, D., Scholten, F., & Roldan Cuenya, B. (2017). Improved CO2 Electroreduction Performance on Plasma-Activated Cu Catalysts via Electrolyte Design: Halide Effect. ACS Catalysis, 7(8), 5112-5120. doi:10.1021/acscatal.7b01416.

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 Urheber:
Gao, Dunfeng1, Autor
Scholten, Fabian1, Autor
Roldan Cuenya, Beatriz1, 2, Autor           
Affiliations:
1Department of Physics, Ruhr-University Bochum, 44780 Bochum, Germany, ou_persistent22              
2Interface Science, Fritz Haber Institute, Max Planck Society, ou_2461712              

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 Zusammenfassung: As a sustainable pathway for energy storage and to close the carbon cycle, CO2 electroreduction has recently gained significant interest. We report here the role of the electrolyte, in particular of halide ions, on O2 electroreduction over plasma-oxidized polycrystalline Cu foils. It was observed that halide ions such as I can induce significant nanostructuring of the oxidized Cu surface, even at open circuit potential, including the formation of Cu crystals with welldefined
shapes. Furthermore, the presence of Cl, Br, and I was found to lower the overpotential and to increase the CO2 electroreduction rate on plasma-activated preoxidized Cu
catalyst in the order Cl, Br < I, without sacrificing their intrinsically high C2−C3 product selectivity (∼65% total Faradaic efficiency at −1.0 V vs RHE). This enhancement in catalytic performance is mainly attributed to the specific adsorption of halides with a higher coverage on our oxidized Cu surface during the reaction, which have been previously reported to facilitate the formation and stabilization of the carboxyl (*COOH)
intermediate by partial charge donation from the halide ions to CO2.

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Sprache(n): eng - English
 Datum: 2017-06-162017-05-012017-06-202017-08-04
 Publikationsstatus: Erschienen
 Seiten: 9
 Ort, Verlag, Ausgabe: -
 Inhaltsverzeichnis: -
 Art der Begutachtung: Expertenbegutachtung
 Identifikatoren: DOI: 10.1021/acscatal.7b01416
 Art des Abschluß: -

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Titel: ACS Catalysis
  Kurztitel : ACS Catal.
Genre der Quelle: Zeitschrift
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Affiliations:
Ort, Verlag, Ausgabe: Washington, DC : ACS
Seiten: 9 Band / Heft: 7 (8) Artikelnummer: - Start- / Endseite: 5112 - 5120 Identifikator: Anderer: 2155-5435
CoNE: https://pure.mpg.de/cone/journals/resource/2155-5435