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dc.contributor.authorUsman, M
dc.contributor.authorHumayun, M
dc.contributor.authorGarba, MD
dc.contributor.authorUllah, L
dc.contributor.authorZeb, Z
dc.contributor.authorHelal, A
dc.contributor.authorSuliman, MH
dc.contributor.authorAlfaifi, BY
dc.contributor.authorIqbal, N
dc.contributor.authorAbdinejad, M
dc.contributor.authorTahir, AA
dc.contributor.authorUllah, H
dc.date.accessioned2022-07-01T12:43:05Z
dc.date.issued2021-08-09
dc.date.updated2022-07-01T11:16:50Z
dc.description.abstractElectrochemical CO2 reduction reaction (CO2RR) provides a promising approach to curbing harmful emissions contributing to global warming. However, several challenges hinder the commercialization of this technology, including high overpotentials, electrode instability, and low Faradic efficiencies of desirable products. Several materials have been developed to overcome these challenges. This mini-review discusses the recent performance of various cobalt (Co) electrocatalysts, including Co-single atom, Co-multi metals, Co-complexes, Co-based metal-organic frameworks (MOFs), Co-based covalent organic frameworks (COFs), Co-nitrides, and Co-oxides. These materials are reviewed with respect to their stability of facilitating CO2 conversion to valuable products, and a summary of the current literature is highlighted, along with future perspectives for the development of efficient CO2RR.en_GB
dc.description.sponsorshipEngineering and Physical Sciences Research Council (EPSRC)en_GB
dc.description.sponsorshipSaudi Aramco Chair Programmeen_GB
dc.format.extent2029-
dc.format.mediumElectronic
dc.identifier.citationVol. 11(8), article 2029en_GB
dc.identifier.doihttps://doi.org/10.3390/nano11082029
dc.identifier.grantnumberEP/V049046/1en_GB
dc.identifier.grantnumberEP/T025875en_GB
dc.identifier.grantnumberORCP2390en_GB
dc.identifier.urihttp://hdl.handle.net/10871/130119
dc.identifierORCID: 0000-0003-1985-6127 (Tahir, Asif Ali)
dc.identifierScopusID: 10439744200 | 57201834379 (Tahir, Asif Ali)
dc.identifierResearcherID: A-2515-2014 | C-3609-2014 (Tahir, Asif Ali)
dc.identifierORCID: 0000-0001-9290-0265 (Ullah, Habib)
dc.identifierScopusID: 6701392760 (Ullah, Habib)
dc.language.isoenen_GB
dc.publisherMDPIen_GB
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pubmed/34443860en_GB
dc.rights© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).en_GB
dc.subjectCO2 conversionen_GB
dc.subjectECO2RRen_GB
dc.subjectMOFsen_GB
dc.subjectcobalt catalystsen_GB
dc.subjectelectrocatalystsen_GB
dc.titleElectrochemical Reduction of CO2: A Review of Cobalt Based Catalysts for Carbon Dioxide Conversion to Fuelsen_GB
dc.typeArticleen_GB
dc.date.available2022-07-01T12:43:05Z
dc.identifier.issn2079-4991
exeter.article-numberARTN 2029
exeter.place-of-publicationSwitzerland
dc.descriptionThis is the final version. Available on open access from MDPI via the DOI in tis recorden_GB
dc.identifier.eissn2079-4991
dc.identifier.journalNanomaterialsen_GB
dc.relation.ispartofNanomaterials (Basel), 11(8)
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_GB
dcterms.dateAccepted2021-08-05
dc.rights.licenseCC BY
rioxxterms.versionVoRen_GB
rioxxterms.licenseref.startdate2021-08-09
rioxxterms.typeJournal Article/Reviewen_GB
refterms.dateFCD2022-07-01T12:40:56Z
refterms.versionFCDVoR
refterms.dateFOA2022-07-01T12:43:14Z
refterms.panelBen_GB
refterms.dateFirstOnline2021-08-09


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© 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
Except where otherwise noted, this item's licence is described as © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).