4.8 Article

Dynamic transformation of cubic copper catalysts during CO2 electroreduction and its impact on catalytic selectivity

Journal

NATURE COMMUNICATIONS
Volume 12, Issue 1, Pages -

Publisher

NATURE PORTFOLIO
DOI: 10.1038/s41467-021-26743-5

Keywords

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Funding

  1. European Research Council under grant ERC-OPERANDOCAT [ERC-725915]
  2. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) [SPP 2080-406944504, CRC 1316]
  3. Deutsche Forschungsgemeinschaft (DFG, German Research Foundation) under Germany's Excellence Strategy [EXC 2008/1 (UniSysCat)-390540038]
  4. Max-Planck-EPFL-Center for Molecular Nanoscience and Technology
  5. Alexander von Humboldt Foundation
  6. IMPRS Functional Interfaces in Physics and Chemistry

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To design effective and stable catalysts for energy conversion applications, it is essential to understand how they transform under reaction conditions and reveal the structure-property relationships, especially for catalysts used in the electroreduction of carbon dioxide. Real-time electrochemical studies show the restructuring of copper(I) oxide cubes during reaction and its impact on catalyst selectivity. Understanding the changes in catalysts during reaction is crucial for rational design, with studies linking structural transformations of cubic copper oxide catalysts with their selectivity.
To rationally design effective and stable catalysts for energy conversion applications, we need to understand how they transform under reaction conditions and reveal their underlying structure-property relationships. This is especially important for catalysts used in the electroreduction of carbon dioxide where product selectivity is sensitive to catalyst structure. Here, we present real-time electrochemical liquid cell transmission electron microscopy studies showing the restructuring of copper(I) oxide cubes during reaction. Fragmentation of the solid cubes, re-deposition of new nanoparticles, catalyst detachment and catalyst aggregation are observed as a function of the applied potential and time. Using cubes with different initial sizes and loading, we further correlate this dynamic morphology with the catalytic selectivity through time-resolved scanning electron microscopy measurements and product analysis. These comparative studies reveal the impact of nanoparticle re-deposition and detachment on the catalyst reactivity, and how the increased surface metal loading created by re-deposited nanoparticles can lead to enhanced C2+ selectivity and stability. Understanding the changes that occur in catalysts during reaction are key to the rational design. Here, the authors use electrochemical transmission electron microscopy and time-resolved product analysis to unveil how cubic copper oxide catalysts evolve during electrochemical CO2 reduction, linking their structural transformations with their selectivity.

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