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Time-resolved operando insights into the tunable selectivity of Cu–Zn nanocubes during pulsed CO2 electroreduction

MPG-Autoren
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Herzog,  Antonia       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Rüscher,  Martina
Interface Science, Fritz Haber Institute, Max Planck Society;

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Jeon,  Hyosang
Interface Science, Fritz Haber Institute, Max Planck Society;

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Timoshenko,  Janis       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Rettenmaier,  Clara       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Hejral,  Uta       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Davis,  Earl       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Haase,  Felix       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Kordus,  David       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Kühl,  Stefanie
Interface Science, Fritz Haber Institute, Max Planck Society;

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Frandsen,  Wiebke
Interface Science, Fritz Haber Institute, Max Planck Society;

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Bergmann,  Arno       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Roldan Cuenya,  Beatriz       
Interface Science, Fritz Haber Institute, Max Planck Society;

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Zitation

Herzog, A., Rüscher, M., Jeon, H., Timoshenko, J., Rettenmaier, C., Hejral, U., et al. (2024). Time-resolved operando insights into the tunable selectivity of Cu–Zn nanocubes during pulsed CO2 electroreduction. Energy & Environmental Science, 17(19), 7081-7096. doi:10.1039/D4EE02308K.


Zitierlink: https://hdl.handle.net/21.11116/0000-000F-C427-8
Zusammenfassung
Pulsed electrochemical CO2 reduction (CO2RR) has emerged as a facile way to alter the product selectivities toward desired multicarbon products, but so far, it has been mainly applied to monometallic Cu-based electrodes, which suffer from stability issues. Here, ZnO-decorated Cu2O nanocubes were exposed to various pulsed CO2RR treatments to uncover the effect of the redox transitions of both metals on the dynamic catalyst structure and composition and its link to their catalytic function. Here, an increase in the ethanol selectivity was observed once pulsed into the oxidation regime of zinc, while the parasitic hydrogen evolution drastically increased once pulsed into the oxidation regime of Cu. By employing time-resolved operando X-ray absorption spectroscopy, X-ray diffraction, and surface-enhanced Raman spectroscopy, we could follow the dynamically induced interplay between Zn oxide, CuZn alloy, metallic Zn and metallic Cu formation, and the coverage of co-adsorbed hydroxide and *CO. Our study highlights the relevance of zinc oxide and an increased OH coverage for the enhancement of the catalyst selectivity toward ethanol.