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Growth Dynamics and Processes Governing the Stability of Electrodeposited Size-Controlled Cubic Cu Catalysts

[Image: see text] The renewable energy-powered conversion of industrially generated CO(2) into useful chemicals and fuels is considered a promising technology for the sustainable development of our modern society. The electrochemical reduction of CO(2) (CO(2)RR) is one of the possible conversion pro...

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Autores principales: Grosse, Philipp, Yoon, Aram, Rettenmaier, Clara, Chee, See Wee, Cuenya, Beatriz Roldan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735016/
https://www.ncbi.nlm.nih.gov/pubmed/33335640
http://dx.doi.org/10.1021/acs.jpcc.0c09105
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author Grosse, Philipp
Yoon, Aram
Rettenmaier, Clara
Chee, See Wee
Cuenya, Beatriz Roldan
author_facet Grosse, Philipp
Yoon, Aram
Rettenmaier, Clara
Chee, See Wee
Cuenya, Beatriz Roldan
author_sort Grosse, Philipp
collection PubMed
description [Image: see text] The renewable energy-powered conversion of industrially generated CO(2) into useful chemicals and fuels is considered a promising technology for the sustainable development of our modern society. The electrochemical reduction of CO(2) (CO(2)RR) is one of the possible conversion processes that can be employed to close the artificial carbon cycle, mimicking nature’s photosynthesis. Nevertheless, to enable green catalytic processes, selectivity for the desired products must be achieved. In the case of CO(2)RR, the selectivity is strongly dependent on the electrocatalyst structure. Here, we explore the phase space of synthesis parameters required for the electrodeposition of Cu cubes with {100} facets on glassy carbon substrates and elucidate their influence on the size, shape, coverage, and uniformity of the cubes. We found that the concentration of Cl(–) ions in solution controls the cube size, shape, and coverage, whereas the ratio of the reduction versus oxidation time and number of cycles in the alternating potential electrodeposition protocol can be used to further tune the cube size. Cyclic voltammetry experiments were complemented with in situ electrochemical scanning electron microscopy to follow the growth dynamics and ex situ transmission electron microscopy and electron diffraction. Our results indicate that the cube growth starts from nuclei formed during the first cycle, followed by a layered deposition and partial dissolution of new material in subsequent cycles.
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spelling pubmed-77350162020-12-15 Growth Dynamics and Processes Governing the Stability of Electrodeposited Size-Controlled Cubic Cu Catalysts Grosse, Philipp Yoon, Aram Rettenmaier, Clara Chee, See Wee Cuenya, Beatriz Roldan J Phys Chem C Nanomater Interfaces [Image: see text] The renewable energy-powered conversion of industrially generated CO(2) into useful chemicals and fuels is considered a promising technology for the sustainable development of our modern society. The electrochemical reduction of CO(2) (CO(2)RR) is one of the possible conversion processes that can be employed to close the artificial carbon cycle, mimicking nature’s photosynthesis. Nevertheless, to enable green catalytic processes, selectivity for the desired products must be achieved. In the case of CO(2)RR, the selectivity is strongly dependent on the electrocatalyst structure. Here, we explore the phase space of synthesis parameters required for the electrodeposition of Cu cubes with {100} facets on glassy carbon substrates and elucidate their influence on the size, shape, coverage, and uniformity of the cubes. We found that the concentration of Cl(–) ions in solution controls the cube size, shape, and coverage, whereas the ratio of the reduction versus oxidation time and number of cycles in the alternating potential electrodeposition protocol can be used to further tune the cube size. Cyclic voltammetry experiments were complemented with in situ electrochemical scanning electron microscopy to follow the growth dynamics and ex situ transmission electron microscopy and electron diffraction. Our results indicate that the cube growth starts from nuclei formed during the first cycle, followed by a layered deposition and partial dissolution of new material in subsequent cycles. American Chemical Society 2020-11-26 2020-12-10 /pmc/articles/PMC7735016/ /pubmed/33335640 http://dx.doi.org/10.1021/acs.jpcc.0c09105 Text en © 2020 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Grosse, Philipp
Yoon, Aram
Rettenmaier, Clara
Chee, See Wee
Cuenya, Beatriz Roldan
Growth Dynamics and Processes Governing the Stability of Electrodeposited Size-Controlled Cubic Cu Catalysts
title Growth Dynamics and Processes Governing the Stability of Electrodeposited Size-Controlled Cubic Cu Catalysts
title_full Growth Dynamics and Processes Governing the Stability of Electrodeposited Size-Controlled Cubic Cu Catalysts
title_fullStr Growth Dynamics and Processes Governing the Stability of Electrodeposited Size-Controlled Cubic Cu Catalysts
title_full_unstemmed Growth Dynamics and Processes Governing the Stability of Electrodeposited Size-Controlled Cubic Cu Catalysts
title_short Growth Dynamics and Processes Governing the Stability of Electrodeposited Size-Controlled Cubic Cu Catalysts
title_sort growth dynamics and processes governing the stability of electrodeposited size-controlled cubic cu catalysts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7735016/
https://www.ncbi.nlm.nih.gov/pubmed/33335640
http://dx.doi.org/10.1021/acs.jpcc.0c09105
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