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dc.contributor.author
Morin Caamano, Tatiana  
dc.contributor.author
Houache, Mohamed S. E.  
dc.contributor.author
Sandoval, Mario German  
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Couillard, Martin  
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Weck, Arnaud  
dc.contributor.author
Baranova, Elena. A.  
dc.contributor.author
Abu Lebdeh, Yaser  
dc.date.available
2024-12-02T16:06:11Z  
dc.date.issued
2023-04-05  
dc.identifier.citation
Morin Caamano, Tatiana; Houache, Mohamed S. E.; Sandoval, Mario German; Couillard, Martin; Weck, Arnaud; et al.; Tuning the Polarity of Dinitrile-Based Electrolyte Solutions for CO2 Electroreduction on Copper Catalysts; American Chemical Society; Journal of Physical Chemistry C; 127; 15; 5-4-2023; 7230-7238  
dc.identifier.issn
1932-7447  
dc.identifier.uri
http://hdl.handle.net/11336/249174  
dc.description.abstract
The development of carbon dioxide electrochemical reduction (CO2ER) has mainly focused on aqueous electrolytes. However, the low solubility of apolar CO2 in polar water negatively impacts the electrochemical process, especially mass transport. Organic-based electrolytes, such as methanol, acetonitrile, and dimethylformamide, have been explored as an alternative due to increased CO2 solubility. Yet, insights into other organic electrolytes are scarce. Dinitrile solvents have decreased polarity in comparison to the mononitrile solvent acetonitrile and thus can potentially further increase CO2 solubility and advance the reaction’s performance. Herein, the novelty of dinitrile-based electrolytes for the application of CO2ER is explored. Acetonitrile, adiponitrile, and sebaconitrile were used to study the effects of a secondary nitrile group addition and the length of the aliphatic, nonpolar chain on salt solubility, electrolyte conductivity, and CO2 solubility. Electrochemical effects were evaluated through cyclic voltammetry (CV) and chronoamperometry (CA) measurements with copper (Cu) and copper oxide (CuO) commercial nanoparticle catalysts. DFT calculations were employed to further explore the CO2 interactions with the selected solvents. Finally, it was found that tuning the polarity of the nitrile solvent results in a profound effect on the physiochemical properties of the electrolyte solutions, markedly CO2 solubility and the CO2ER.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
American Chemical Society  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by/2.5/ar/  
dc.subject
Catalysts  
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Electrical conductivity  
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Electrolytes  
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Solubility  
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Solvents  
dc.subject.classification
Física de los Materiales Condensados  
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Ciencias Físicas  
dc.subject.classification
CIENCIAS NATURALES Y EXACTAS  
dc.title
Tuning the Polarity of Dinitrile-Based Electrolyte Solutions for CO2 Electroreduction on Copper Catalysts  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2024-11-25T12:34:43Z  
dc.journal.volume
127  
dc.journal.number
15  
dc.journal.pagination
7230-7238  
dc.journal.pais
Estados Unidos  
dc.journal.ciudad
Washington  
dc.description.fil
Fil: Morin Caamano, Tatiana. University of Ottawa; Canadá  
dc.description.fil
Fil: Houache, Mohamed S. E.. No especifíca;  
dc.description.fil
Fil: Sandoval, Mario German. University of Ottawa; Canadá. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro Científico Tecnológico Conicet - Bahía Blanca. Instituto de Física del Sur. Universidad Nacional del Sur. Departamento de Física. Instituto de Física del Sur; Argentina  
dc.description.fil
Fil: Couillard, Martin. No especifíca;  
dc.description.fil
Fil: Weck, Arnaud. University of Ottawa; Canadá  
dc.description.fil
Fil: Baranova, Elena. A.. University of Ottawa; Canadá  
dc.description.fil
Fil: Abu Lebdeh, Yaser. University of Ottawa; Canadá  
dc.journal.title
Journal of Physical Chemistry C  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/http://dx.doi.org/10.1021/acs.jpcc.3c00819  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/https://pubs.acs.org/doi/10.1021/acs.jpcc.3c00819?ref=PDF#