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dc.contributor.authorMelchionna, Michele
dc.contributor.authorCriado, Alejandro
dc.contributor.authorBonchio, Marcella
dc.contributor.authorFornasiero, Paolo
dc.contributor.authorPaolucci, Francesco
dc.contributor.authorPrato, Maurizio
dc.date.accessioned2024-08-07T10:05:32Z
dc.date.available2024-08-07T10:05:32Z
dc.date.issued2020-08-19
dc.identifier.citationACS Appl. Energy Mater. 2020, 3, 9, 8509–8518es_ES
dc.identifier.issn2574-0962 (eISSN)
dc.identifier.urihttp://hdl.handle.net/2183/38440
dc.description.abstract[Abstract]: The combination of multiwalled carbon nanotubes (MWCNTs) with undoped CeO2 na-noparticles (NPs) is effective for the direct electrocatalytic reduction of CO2 to formic acid (FA) at acidic pH (0.1 M HNO3), at overpotential as low as η = −0.02 V (vs RHE) with Faradic efficiency (FE) up to 65%. Exsitu and operando evidence identifies nons-toichiometric Ce4+/3+O2–x reduced sites as essential for the selective CO2 reduction reac-tion (CO2RR). The MWCNT-mediated electrochemical reduction of the CeO2 NPs of-fers a definite advantage with respect to the generally adopted thermochemical cycles (800–1500 °C) or deep hydrogenation pretreatments, thus presenting an interesting perspective for the engineering of CeO2 electrocatalysts.es_ES
dc.description.sponsorshipThis work was supported by the Italian Ministero dell’Istruzione, Universitàe Ricerca (PRIN prot. 2017PBXPN4), the H2020 - RIA-CE-NMBP-25 Program (Grant No. 862030), and Universities of Bologna and Trieste, INSTM; Dr. Matteo Crosera (University of Trieste) is acknowledged for the ICPOES analysis. M.P., as the recipient of the AXA Chair, is grateful to the AXA Research Fund for financial support. This work was performed under the Maria de Maeztu Units of Excellence Program from the Spanish State Research Agency (Grant No. MDM-2017-0720).es_ES
dc.language.isoenges_ES
dc.publisherAmerican Chemical Societyes_ES
dc.relationinfo:eu-repo/grantAgreement/MIUR/Progetti di Ricerca di Rilevante Interesse Nazionale 2017/2017PBXPN4/IT/es_ES
dc.relationinfo:eu-repo/grantAgreement/EC/H2020/862030es_ES
dc.relationinfo:eu-repo/grantAgreement/AEI/Plan Estatal de Investigación Científica y Técnica y de Innovación 2013-2016/MDM-2017-0720/ES/es_ES
dc.relation.urihttps://doi.org/10.1021/acsaem.0c01145es_ES
dc.rightsCopyright © 2020 American Chemical Society. This is an open access article published under an ACS AuthorChoice License (https://pubs.acs.org/page/policy/authorchoice_termsofuse.html), which permits copying and redistribution of the article or any adaptations for non-commercial purposes.es_ES
dc.subjectCarbon nanotubeses_ES
dc.subjectCerium oxidees_ES
dc.subjectCarbon dioxide reductiones_ES
dc.subjectElectrocatalytic hydrogenationes_ES
dc.subjectMetal oxide electrocatalystses_ES
dc.titleWater-Mediated ElectroHydrogenation of CO2 at Near-Equilibrium Potential by Carbon Nanotubes/Cerium Dioxide Nanohybridses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.accessinfo:eu-repo/semantics/openAccesses_ES
UDC.journalTitleACS Applied Energy Materialses_ES
UDC.volume3es_ES
UDC.issue9es_ES
UDC.startPage8509es_ES
UDC.endPage8518es_ES
dc.identifier.doi10.1021/acsaem.0c01145


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