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Heterostructured CeO2-M (M = Co, Cu, Mn, Fe, Ni) oxide nanocatalysts for the visible-light photooxidation of pinene to aroma oxygenates

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dc.contributor.author Mavuso, MA
dc.contributor.author Makgwane, Peter R
dc.contributor.author Ray, Suprakas S
dc.date.accessioned 2020-07-13T11:27:53Z
dc.date.available 2020-07-13T11:27:53Z
dc.date.issued 2020-04
dc.identifier.citation Mavuso, M.A., Makgwane, P.R. and Ray, S.S. 2020. Heterostructured CeO2-M (M = Co, Cu, Mn, Fe, Ni) oxide nanocatalysts for the visible-light photooxidation of pinene to aroma oxygenates. ACS Omega, v5(17), 9775-9788. en_US
dc.identifier.issn 2470-1343
dc.identifier.uri https://pubs.acs.org/doi/10.1021/acsomega.9b04396?goto=supporting-info&
dc.identifier.uri https://dx.doi.org/10.1021/acsomega.9b04396
dc.identifier.uri http://hdl.handle.net/10204/11470
dc.description Copyright: 2020 American Chemical Society. This is an open access article published under a Creative Commons Attribution (CC-BY) License, which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. en_US
dc.description.abstract Herein, we report the enhanced photocatalytic activity of heterostructured CeO2 nanocatalysts interfaced with Cu, Co, Ni, Mn, and Fe metal oxides. The CeO2 catalysts exhibited an enhanced red shift in the visible-light response compared to CeO2. This improved absorption range effectively suppressed electron (e-)/hole (+h) recombination by forming localized energy bands associated with defect oxygen vacancies (Vo) induced by the Mn+ ions incorporated in CeO2. Under visible-light irradiation, CeO2 catalysts are active for a-pinene oxidation to the aroma oxygenates, pinene oxide, verbenol, and verbenone. Both Fe2O3-CeO2 and NiO- CeO2 gave the highest pinene conversions of 71.3 and 53.1%, respectively, with corresponding pinene oxide selectivities of 57.3 and 58.2%. The enhanced photocatalytic performance of the heterostructured CeO2 catalysts compared to CeO2 is attributed to their enhanced visible-light absorption range and efficient suppression of e-/+h recombination. The Fe2O3- CeO2 catalyst was highly recyclable and did not show any significant loss of its photoactivity. en_US
dc.language.iso en en_US
dc.publisher American Chemical Society en_US
dc.relation.ispartofseries Worklist;23560
dc.subject CeO2 en_US
dc.subject Biomass-derived terpene compounds en_US
dc.subject Photocatalysis en_US
dc.title Heterostructured CeO2-M (M = Co, Cu, Mn, Fe, Ni) oxide nanocatalysts for the visible-light photooxidation of pinene to aroma oxygenates en_US
dc.type Article en_US
dc.identifier.apacitation Mavuso, M., Makgwane, P. R., & Ray, S. S. (2020). Heterostructured CeO2-M (M = Co, Cu, Mn, Fe, Ni) oxide nanocatalysts for the visible-light photooxidation of pinene to aroma oxygenates. http://hdl.handle.net/10204/11470 en_ZA
dc.identifier.chicagocitation Mavuso, MA, Peter R Makgwane, and Suprakas S Ray "Heterostructured CeO2-M (M = Co, Cu, Mn, Fe, Ni) oxide nanocatalysts for the visible-light photooxidation of pinene to aroma oxygenates." (2020) http://hdl.handle.net/10204/11470 en_ZA
dc.identifier.vancouvercitation Mavuso M, Makgwane PR, Ray SS. Heterostructured CeO2-M (M = Co, Cu, Mn, Fe, Ni) oxide nanocatalysts for the visible-light photooxidation of pinene to aroma oxygenates. 2020; http://hdl.handle.net/10204/11470. en_ZA
dc.identifier.ris TY - Article AU - Mavuso, MA AU - Makgwane, Peter R AU - Ray, Suprakas S AB - Herein, we report the enhanced photocatalytic activity of heterostructured CeO2 nanocatalysts interfaced with Cu, Co, Ni, Mn, and Fe metal oxides. The CeO2 catalysts exhibited an enhanced red shift in the visible-light response compared to CeO2. This improved absorption range effectively suppressed electron (e-)/hole (+h) recombination by forming localized energy bands associated with defect oxygen vacancies (Vo) induced by the Mn+ ions incorporated in CeO2. Under visible-light irradiation, CeO2 catalysts are active for a-pinene oxidation to the aroma oxygenates, pinene oxide, verbenol, and verbenone. Both Fe2O3-CeO2 and NiO- CeO2 gave the highest pinene conversions of 71.3 and 53.1%, respectively, with corresponding pinene oxide selectivities of 57.3 and 58.2%. The enhanced photocatalytic performance of the heterostructured CeO2 catalysts compared to CeO2 is attributed to their enhanced visible-light absorption range and efficient suppression of e-/+h recombination. The Fe2O3- CeO2 catalyst was highly recyclable and did not show any significant loss of its photoactivity. DA - 2020-04 DB - ResearchSpace DP - CSIR KW - CeO2 KW - Biomass-derived terpene compounds KW - Photocatalysis LK - https://researchspace.csir.co.za PY - 2020 SM - 2470-1343 T1 - Heterostructured CeO2-M (M = Co, Cu, Mn, Fe, Ni) oxide nanocatalysts for the visible-light photooxidation of pinene to aroma oxygenates TI - Heterostructured CeO2-M (M = Co, Cu, Mn, Fe, Ni) oxide nanocatalysts for the visible-light photooxidation of pinene to aroma oxygenates UR - http://hdl.handle.net/10204/11470 ER - en_ZA


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