Spectroelectrochemical Study of CO2 Reduction on TiO2 Electrodes in Acetonitrile

Please use this identifier to cite or link to this item: http://hdl.handle.net/10045/101210
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dc.contributorGrupo de Espectroelectroquímica y Modelización (GEM)es_ES
dc.contributorGrupo de Fotoquímica y Electroquímica de Semiconductores (GFES)es_ES
dc.contributor.authorMendieta-Reyes, Néstor E.-
dc.contributor.authorCheuquepán, William-
dc.contributor.authorRodes, Antonio-
dc.contributor.authorGómez, Roberto-
dc.contributor.otherUniversidad de Alicante. Departamento de Química Físicaes_ES
dc.contributor.otherUniversidad de Alicante. Instituto Universitario de Electroquímicaes_ES
dc.date.accessioned2020-01-14T12:00:39Z-
dc.date.available2020-01-14T12:00:39Z-
dc.date.issued2019-11-06-
dc.identifier.citationACS Catalysis. 2020, 10(1): 103-113. doi:10.1021/acscatal.9b02932es_ES
dc.identifier.issn2155-5435-
dc.identifier.urihttp://hdl.handle.net/10045/101210-
dc.description.abstractOne of the main current goals of humanity is the CO2 conversion into high energy compounds for facilitating both a diminution of the CO2 atmospheric levels and the development of energy storage strategies. In many studies, TiO2 has been successfully used as a photocatalyst for CO2 reduction, but there is still a lack of understanding of its catalytic behavior. In this context, CO2 reduction has been studied on nanoporous TiO2 electrodes in acetonitrile media by means of (spectro) electrochemical methods (ATR-IR and UV–vis). Importantly, the onset of the cathodic Faradaic processes related with CO2 reduction on TiO2 electrodes is located at −0.81 V versus SHE, which is less negative than that observed for metal electrodes under similar conditions. UV–vis spectroelectrochemical results indicate that the electrocatalytic behavior of TiO2 is related to the generation of oxygen vacancies and Ti3+ sites at its surface and promoted by electrolytes with nonintercalating cations in agreement with recent results on WO3 electrodes. ATR-IR spectroelectrochemical measurements allow for monitoring of the TiO2/solution interfacial state as reduction proceeds. Specifically, IR bands for carbon monoxide and carbonyl groups related with carbonate and oxalate are observed. Additionally, a chromatographic analysis shows CO and oxalate as main products. With controlled water addition (0.5 M), methanol and CO were found to be the main products. Based on these results, a mechanism for CO2 reduction on TiO2 electrodes is presented in which the regeneration of the TiO2 surface by oxide electrodissolution/deposition is a critical step.es_ES
dc.description.sponsorshipWe are grateful for the financial support of the Ministerio de Ciencia, Innovación y Universidades through projects MAT2015-71727-R and RTI2018-102061-B-I00 (FONDOS FEDER).es_ES
dc.languageenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.rights© 2019 American Chemical Societyes_ES
dc.subjectCO2 reductiones_ES
dc.subjectTiO2 electrodeses_ES
dc.subjectATR-IR spectroelectrochemistryes_ES
dc.subjectUV−vis spectroelectrochemistryes_ES
dc.subjectElectrochromismes_ES
dc.subjectElectrocatalysises_ES
dc.subject.otherQuímica Físicaes_ES
dc.titleSpectroelectrochemical Study of CO2 Reduction on TiO2 Electrodes in Acetonitrilees_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.peerreviewedsies_ES
dc.identifier.doi10.1021/acscatal.9b02932-
dc.relation.publisherversionhttps://doi.org/10.1021/acscatal.9b02932es_ES
dc.rights.accessRightsinfo:eu-repo/semantics/embargoedAccesses_ES
dc.date.embargoEndinfo:eu-repo/date/embargoEnd/2020-11-07es_ES
Appears in Collections:INV - GEM - Artículos de Revistas
INV - GFES - Artículos de Revistas

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