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dc.contributor.author Ali, Shahzad -
dc.contributor.author Razzaq, Abdul -
dc.contributor.author Kim, Hwapyong -
dc.contributor.author In, Su-Il -
dc.date.accessioned 2021-10-17T13:00:03Z -
dc.date.available 2021-10-17T13:00:03Z -
dc.date.created 2021-10-07 -
dc.date.issued 2022-02 -
dc.identifier.issn 1385-8947 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/15566 -
dc.description.abstract Cu-based photocatalysts are widely used for the photocatalytic reduction of CO2 owing to their non-toxicity, earth abundance, extended light absorption, suppressed charge recombination, and good catalytic performance. In addition to low cost, abundant availability, and the ease of synthesis, they exhibit unique features, such as broad optical absorption, reaction intermediates stabilization, and C–C coupling ability, which lead to the formation of C2 + products. The photocatalytic activity of Cu-based photocatalysts is essentially linked to the optical absorption and interfacial charge transfer at the junction of Cu and the semiconductor substrate. However, the poor resistance of Cu to oxidation seriously perturbs the effective utilization of its unique features in practical applications. To date, various approaches, such as the use of metal/non-metal co-catalysts, Z-scheme heterostructures, and hole scavengers, have been proposed to improve its photocatalytic performance and maintain its stability in prolonged reactions. In addition to these approaches, as single metal atom catalysts, atomically dispersed Cu photocatalysts have gained immense attention because they can regain the desired oxidation state, and hence exhibit good stability. The designation of suitable oxidation states of Cu for various CO2 reduction reaction steps is challenging because of the rapid change in its oxidation states under ambient/irradiated environments. However, in situ spectroscopic analyses have nominated Cu2+ for CO2 adsorption, Cu1+ for the photoreduction reaction, and Cu0 for effective charge separation. In this review, the recent advancements in the photocatalytic activity, selectivity, and stability of Cu-based photocatalysts are discussed systematically. Certain concepts and mechanisms related to the photocatalytic performance of Cu-based catalysts have also been discussed. Finally, the future research directions are discussed based on the available relevant literature. © 2021 Elsevier B.V. -
dc.language English -
dc.publisher Elsevier BV -
dc.title Activity, selectivity, and stability of earth-abundant CuO/Cu2O/Cu0-based photocatalysts toward CO2 reduction -
dc.type Article -
dc.identifier.doi 10.1016/j.cej.2021.131579 -
dc.identifier.wosid 000729803500006 -
dc.identifier.scopusid 2-s2.0-85115618650 -
dc.identifier.bibliographicCitation Chemical Engineering Journal, v.429 -
dc.description.isOpenAccess FALSE -
dc.subject.keywordAuthor Photocatalytic activity -
dc.subject.keywordAuthor Plasmonic photocatalysts -
dc.subject.keywordAuthor Selectivity -
dc.subject.keywordAuthor Stability -
dc.subject.keywordAuthor C2+ products -
dc.subject.keywordAuthor CO2 photoreduction -
dc.subject.keywordAuthor Cu-based photocatalyst -
dc.subject.keywordAuthor Heterostructured photocatalyst -
dc.subject.keywordAuthor Interfacial charge transfer -
dc.subject.keywordPlus Charge transfer -
dc.subject.keywordPlus Copper -
dc.subject.keywordPlus Copper oxides -
dc.subject.keywordPlus Light absorption -
dc.subject.keywordPlus Oxidation -
dc.subject.keywordPlus Photocatalytic activity -
dc.subject.keywordPlus Reaction intermediates -
dc.subject.keywordPlus Spectroscopic analysis -
dc.subject.keywordPlus Stability -
dc.subject.keywordPlus Substrates -
dc.subject.keywordPlus C2+ product -
dc.subject.keywordPlus CO2 photoreduction -
dc.subject.keywordPlus Cu-based -
dc.subject.keywordPlus Cu-based photocatalyst -
dc.subject.keywordPlus Heterostructured photocatalyst -
dc.subject.keywordPlus Interfacial charge transfer -
dc.subject.keywordPlus Oxidation state -
dc.subject.keywordPlus Photo reduction -
dc.subject.keywordPlus Plasmonic photocatalysts -
dc.subject.keywordPlus Selectivity -
dc.subject.keywordPlus Carbon dioxide -
dc.citation.title Chemical Engineering Journal -
dc.citation.volume 429 -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.relation.journalResearchArea Engineering -
dc.relation.journalWebOfScienceCategory Engineering, Environmental; Engineering, Chemical -
dc.type.docType Article -
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Department of Energy Science and Engineering Green and Renewable Energy for Endless Nature(GREEN) Lab 1. Journal Articles

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