Plasmonic-enhanced photocatalysis reactions using gold nanostructured films

This work shows the enhancement of the visible photocatalytic activity of TiO 2 NPs film using the localized surface plasmonic resonance of Au nanostructures. We adopted a simple yet effective surface treatment to tune the size distribution, and plasmonic resonance spectrum of Au nanostructured film...

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Bibliographic Details
Published inRSC advances Vol. 1; no. 38; pp. 22324 - 2233
Main Authors Ibrahem, Mohammed A, Rasheed, Bassam G, Mahdi, Rahman I, Khazal, Taha M, Omar, Maryam M, O'Neill, Mary
Format Journal Article
LanguageEnglish
Published England Royal Society of Chemistry 10.06.2020
The Royal Society of Chemistry
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Summary:This work shows the enhancement of the visible photocatalytic activity of TiO 2 NPs film using the localized surface plasmonic resonance of Au nanostructures. We adopted a simple yet effective surface treatment to tune the size distribution, and plasmonic resonance spectrum of Au nanostructured films on glass substrates, by hot plate annealing in air at low temperatures. A hybrid photocatalytic film of TiO 2 :Au is utilized to catalyse a selective photodegradation reaction of Methylene Blue in solution. Irradiation at the plasmonic resonance wavelength of the Au nanostructures provides more effective photodegradation compared to broadband artificial sunlight of significantly higher intensity. This improvement is attributed to the active contribution of the plasmonic hot electrons injected into the TiO 2 . The broadband source initiates competing photoreactions in the photocatalyst, so that carrier transfer from the catalyst surface to the solution is less efficient. The proposed hybrid photocatalyst can be integrated with a variety of device architectures and designs, which makes it highly attractive for low-cost photocatalysis applications. This work shows the enhancement of the visible photocatalytic activity of TiO 2 NPs film using the localized surface plasmonic resonance of Au nanostructures.
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ISSN:2046-2069
2046-2069
DOI:10.1039/d0ra03858j