Herein, we report the enhanced photocatalytic activity of heterostructured CeO nanocatalysts interfaced with Cu, Co, Ni, Mn, and Fe metal oxides. The CeO catalysts exhibited an enhanced red shift in the visible-light response compared to CeO. This improved absorption range effectively suppressed electron (e)/hole (h) recombination by forming localized energy bands associated with defect oxygen vacancies ( ) induced by the M ions incorporated in CeO. Under visible-light irradiation, CeO catalysts are active for α-pinene oxidation to the aroma oxygenates, pinene oxide, verbenol, and verbenone. Both FeO-CeO and NiO-CeO 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 CeO catalysts compared to CeO is attributed to their enhanced visible-light absorption range and efficient suppression of e/h recombination. The FeO-CeO catalyst was highly recyclable and did not show any significant loss of its photoactivity.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7203698 | PMC |
http://dx.doi.org/10.1021/acsomega.9b04396 | DOI Listing |
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