To scale carbon dioxide reduction (CO2R), establishing a structure-property-performance relationship of the catalyst under the reaction conditions is a priority. Particularly in membrane electrode assembly (MEA) electrolyzers, knowledge about the valence state and coordination environment of the catalyst is of value yet limited. We developed an MEA electrolyzer that utilizes X-ray absorption spectroscopy to investigate the structural evolution of Cu2O-derived catalysts under CO2R and compare the same catalysts in a flow cell. Additionally, we study the influence of CO reduction and incorporating Ag on the reconstruction of the catalyst. We find that the strong reduction environment in the MEA and feeding CO leads to reconstruction of Cu2O particles, favoring higher coordination and lower oxidation states, which coincides with a shift in the reaction selectivity from C2+ to hydrogen. Conversely, incorporating small amounts of Ag in the catalyst restricts the reconstruction. These findings advocate for in situ studies in zero-gap electrolyzers.

Zero-Gap Electrolyzers Accelerate Reconstruction of Cu2O-Derived Catalysts under CO2 Reduction / J. Abed, I. Grigioni, T. Kose, W. Alnoush, S. Park, A. Polo, B. Lee, D. Sinton, D. Higgins, E.H. Sargent. - In: ACS ENERGY LETTERS. - ISSN 2380-8195. - 9:12(2024 Dec), pp. 6225-6232. [10.1021/acsenergylett.4c02634]

Zero-Gap Electrolyzers Accelerate Reconstruction of Cu2O-Derived Catalysts under CO2 Reduction

I. Grigioni
Co-primo
;
A. Polo;
2024

Abstract

To scale carbon dioxide reduction (CO2R), establishing a structure-property-performance relationship of the catalyst under the reaction conditions is a priority. Particularly in membrane electrode assembly (MEA) electrolyzers, knowledge about the valence state and coordination environment of the catalyst is of value yet limited. We developed an MEA electrolyzer that utilizes X-ray absorption spectroscopy to investigate the structural evolution of Cu2O-derived catalysts under CO2R and compare the same catalysts in a flow cell. Additionally, we study the influence of CO reduction and incorporating Ag on the reconstruction of the catalyst. We find that the strong reduction environment in the MEA and feeding CO leads to reconstruction of Cu2O particles, favoring higher coordination and lower oxidation states, which coincides with a shift in the reaction selectivity from C2+ to hydrogen. Conversely, incorporating small amounts of Ag in the catalyst restricts the reconstruction. These findings advocate for in situ studies in zero-gap electrolyzers.
Settore CHEM-02/A - Chimica fisica
Settore CHEM-04/A - Chimica industriale
   Photoelectrochemical Solar Light Conversion into Fuels on Colloidal Quantum Dots Based Photoanodes (QuantumSolarFuels)
   QuantumSolarFuels
   EUROPEAN COMMISSION
   H2020
   846107

   Chasing Long Hydrocarbon Chains via CO2 Reduction
   CLHC
   UNIVERSITA' DEGLI STUDI DI MILANO
dic-2024
https://pubs.acs.org/doi/10.1021/acsenergylett.4c02634#
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1139436
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