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Graphene Quantum Dot-TiO(2) Photonic Crystal Films for Photocatalytic Applications
Photonic crystal structuring has emerged as an advanced method to enhance solar light harvesting by metal oxide photocatalysts along with rational compositional modifications of the materials’ properties. In this work, surface functionalization of TiO(2) photonic crystals by blue luminescent graphen...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766274/ https://www.ncbi.nlm.nih.gov/pubmed/33371303 http://dx.doi.org/10.3390/nano10122566 |
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author | Apostolaki, Maria-Athina Toumazatou, Alexia Antoniadou, Maria Sakellis, Elias Xenogiannopoulou, Evangelia Gardelis, Spiros Boukos, Nikos Falaras, Polycarpos Dimoulas, Athanasios Likodimos, Vlassis |
author_facet | Apostolaki, Maria-Athina Toumazatou, Alexia Antoniadou, Maria Sakellis, Elias Xenogiannopoulou, Evangelia Gardelis, Spiros Boukos, Nikos Falaras, Polycarpos Dimoulas, Athanasios Likodimos, Vlassis |
author_sort | Apostolaki, Maria-Athina |
collection | PubMed |
description | Photonic crystal structuring has emerged as an advanced method to enhance solar light harvesting by metal oxide photocatalysts along with rational compositional modifications of the materials’ properties. In this work, surface functionalization of TiO(2) photonic crystals by blue luminescent graphene quantum dots (GQDs), n–π* band at ca. 350 nm, is demonstrated as a facile, environmental benign method to promote photocatalytic activity by the combination of slow photon-assisted light trapping with GQD-TiO(2) interfacial electron transfer. TiO(2) inverse opal films fabricated by the co-assembly of polymer colloidal spheres with a hydrolyzed titania precursor were post-modified by impregnation in aqueous GQDs suspension without any structural distortion. Photonic band gap engineering by varying the inverse opal macropore size resulted in selective performance enhancement for both salicylic acid photocatalytic degradation and photocurrent generation under UV–VIS and visible light, when red-edge slow photons overlapped with the composite’s absorption edge, whereas stop band reflection was attenuated by the strong UVA absorbance of the GQD-TiO(2) photonic films. Photoelectrochemical and photoluminescence measurements indicated that the observed improvement, which surpassed similarly modified benchmark mesoporous P25 TiO(2) films, was further assisted by GQDs electron acceptor action and visible light activation to a lesser extent, leading to highly efficient photocatalytic films. |
format | Online Article Text |
id | pubmed-7766274 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-77662742020-12-28 Graphene Quantum Dot-TiO(2) Photonic Crystal Films for Photocatalytic Applications Apostolaki, Maria-Athina Toumazatou, Alexia Antoniadou, Maria Sakellis, Elias Xenogiannopoulou, Evangelia Gardelis, Spiros Boukos, Nikos Falaras, Polycarpos Dimoulas, Athanasios Likodimos, Vlassis Nanomaterials (Basel) Article Photonic crystal structuring has emerged as an advanced method to enhance solar light harvesting by metal oxide photocatalysts along with rational compositional modifications of the materials’ properties. In this work, surface functionalization of TiO(2) photonic crystals by blue luminescent graphene quantum dots (GQDs), n–π* band at ca. 350 nm, is demonstrated as a facile, environmental benign method to promote photocatalytic activity by the combination of slow photon-assisted light trapping with GQD-TiO(2) interfacial electron transfer. TiO(2) inverse opal films fabricated by the co-assembly of polymer colloidal spheres with a hydrolyzed titania precursor were post-modified by impregnation in aqueous GQDs suspension without any structural distortion. Photonic band gap engineering by varying the inverse opal macropore size resulted in selective performance enhancement for both salicylic acid photocatalytic degradation and photocurrent generation under UV–VIS and visible light, when red-edge slow photons overlapped with the composite’s absorption edge, whereas stop band reflection was attenuated by the strong UVA absorbance of the GQD-TiO(2) photonic films. Photoelectrochemical and photoluminescence measurements indicated that the observed improvement, which surpassed similarly modified benchmark mesoporous P25 TiO(2) films, was further assisted by GQDs electron acceptor action and visible light activation to a lesser extent, leading to highly efficient photocatalytic films. MDPI 2020-12-21 /pmc/articles/PMC7766274/ /pubmed/33371303 http://dx.doi.org/10.3390/nano10122566 Text en © 2020 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 (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Apostolaki, Maria-Athina Toumazatou, Alexia Antoniadou, Maria Sakellis, Elias Xenogiannopoulou, Evangelia Gardelis, Spiros Boukos, Nikos Falaras, Polycarpos Dimoulas, Athanasios Likodimos, Vlassis Graphene Quantum Dot-TiO(2) Photonic Crystal Films for Photocatalytic Applications |
title | Graphene Quantum Dot-TiO(2) Photonic Crystal Films for Photocatalytic Applications |
title_full | Graphene Quantum Dot-TiO(2) Photonic Crystal Films for Photocatalytic Applications |
title_fullStr | Graphene Quantum Dot-TiO(2) Photonic Crystal Films for Photocatalytic Applications |
title_full_unstemmed | Graphene Quantum Dot-TiO(2) Photonic Crystal Films for Photocatalytic Applications |
title_short | Graphene Quantum Dot-TiO(2) Photonic Crystal Films for Photocatalytic Applications |
title_sort | graphene quantum dot-tio(2) photonic crystal films for photocatalytic applications |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7766274/ https://www.ncbi.nlm.nih.gov/pubmed/33371303 http://dx.doi.org/10.3390/nano10122566 |
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