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 |
Zugehörige Links: | |
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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