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Influence of Support Material on the Structural Evolution of Copper during Electrochemical CO2 Reduction

Koh, Ezra S. ; Geiger, Simon ; Gunnarson, Alexander ; Imhof, Timo ; Meyer, Gregor M. ; Paciok, Paul ; Etzold, Bastian J. M. ; Rose, Marcus ; Schüth, Ferdi ; Ledendecker, Marc (2023)
Influence of Support Material on the Structural Evolution of Copper during Electrochemical CO2 Reduction.
In: ChemElectroChem, 2023, 10 (5)
doi: 10.26083/tuprints-00024529
Artikel, Zweitveröffentlichung, Verlagsversion

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Kurzbeschreibung (Abstract)

The copper-catalyzed electrochemical CO2 reduction reaction represents an elegant pathway to reduce CO2 emissions while producing a wide range of valuable hydrocarbons. The selectivity for these products depends strongly on the structure and morphology of the copper catalyst. However, continued deactivation during catalysis alters the obtained product spectrum. In this work, we report on the stabilizing effect of three different carbon supports with unique pore structures. The influence of pore structure on stability and selectivity was examined by high-angle annular dark field scanning transmission electron microscopy and gas chromatography measurements in a micro-flow cell. Supporting particles into confined space was found to increase the barrier for particle agglomeration during 20 h of chronopotentiometry measurements at 100 mA cm−2 resembling long-term CO2 reduction conditions. We propose a catalyst design preventing coalescence and agglomeration in harsh electrochemical reaction conditions, exemplarily demonstrated for the electrocatalytic CO2 reduction. With this work, we provide important insights into the design of stable CO2 electrocatalysts that can potentially be applied to a wide range of applications.

Typ des Eintrags: Artikel
Erschienen: 2023
Autor(en): Koh, Ezra S. ; Geiger, Simon ; Gunnarson, Alexander ; Imhof, Timo ; Meyer, Gregor M. ; Paciok, Paul ; Etzold, Bastian J. M. ; Rose, Marcus ; Schüth, Ferdi ; Ledendecker, Marc
Art des Eintrags: Zweitveröffentlichung
Titel: Influence of Support Material on the Structural Evolution of Copper during Electrochemical CO2 Reduction
Sprache: Englisch
Publikationsjahr: 20 November 2023
Ort: Darmstadt
Publikationsdatum der Erstveröffentlichung: 1 März 2023
Ort der Erstveröffentlichung: Weinheim
Verlag: Wiley
Titel der Zeitschrift, Zeitung oder Schriftenreihe: ChemElectroChem
Jahrgang/Volume einer Zeitschrift: 10
(Heft-)Nummer: 5
Kollation: 8 Seiten
DOI: 10.26083/tuprints-00024529
URL / URN: https://tuprints.ulb.tu-darmstadt.de/24529
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Herkunft: Zweitveröffentlichungsservice
Kurzbeschreibung (Abstract):

The copper-catalyzed electrochemical CO2 reduction reaction represents an elegant pathway to reduce CO2 emissions while producing a wide range of valuable hydrocarbons. The selectivity for these products depends strongly on the structure and morphology of the copper catalyst. However, continued deactivation during catalysis alters the obtained product spectrum. In this work, we report on the stabilizing effect of three different carbon supports with unique pore structures. The influence of pore structure on stability and selectivity was examined by high-angle annular dark field scanning transmission electron microscopy and gas chromatography measurements in a micro-flow cell. Supporting particles into confined space was found to increase the barrier for particle agglomeration during 20 h of chronopotentiometry measurements at 100 mA cm−2 resembling long-term CO2 reduction conditions. We propose a catalyst design preventing coalescence and agglomeration in harsh electrochemical reaction conditions, exemplarily demonstrated for the electrocatalytic CO2 reduction. With this work, we provide important insights into the design of stable CO2 electrocatalysts that can potentially be applied to a wide range of applications.

Status: Verlagsversion
URN: urn:nbn:de:tuda-tuprints-245298
Sachgruppe der Dewey Dezimalklassifikatin (DDC): 500 Naturwissenschaften und Mathematik > 540 Chemie
Fachbereich(e)/-gebiet(e): 07 Fachbereich Chemie
07 Fachbereich Chemie > Ernst-Berl-Institut > Fachgebiet Technische Chemie
Hinterlegungsdatum: 20 Nov 2023 11:24
Letzte Änderung: 21 Nov 2023 07:03
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