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Microwave-Assisted Synthesis of Carbon-Based (N, Fe)-Codoped TiO(2) for the Photocatalytic Degradation of Formaldehyde
A microwave-assisted sol–gel method was used to synthesize (N, Fe)-codoped activated carbon (AC)/TiO(2) photocatalyst for enhanced optical absorption in the visible light region. The prepared samples were characterized via X-ray diffraction, scanning electron microscopy, transmission electron micros...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573084/ https://www.ncbi.nlm.nih.gov/pubmed/26377213 http://dx.doi.org/10.1186/s11671-015-1061-6 |
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author | Tian, Fei Wu, Zhansheng Tong, Yanbin Wu, Zhilin Cravotto, Giancarlo |
author_facet | Tian, Fei Wu, Zhansheng Tong, Yanbin Wu, Zhilin Cravotto, Giancarlo |
author_sort | Tian, Fei |
collection | PubMed |
description | A microwave-assisted sol–gel method was used to synthesize (N, Fe)-codoped activated carbon (AC)/TiO(2) photocatalyst for enhanced optical absorption in the visible light region. The prepared samples were characterized via X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, Brunauer–Emmett–Teller analysis, ultraviolet–visible light spectroscopy, X-ray photoelectron spectroscopy, and photoluminescence spectroscopy. The results showed no significant difference in the surface area of AC/TiO(2) (approximately 500 m(2)/g) after doping. TiO(2) was uniformly distributed on the surface of AC, which exhibited coexisting anatase and rutile structures with a mean crystallite diameter of approximately 20 nm. N and Fe monodoping on AC/TiO(2) reduced the energy band gap of TiO(2) to 2.81 and 2.79 eV, respectively, which mainly attributed to the impurity energy formed in the energy gap of TiO(2). In (N, Fe)-codoped AC/TiO(2), N and Fe are incorporated into the TiO(2) framework and narrow the band gap of TiO(2) to 2.58 eV, thereby causing a large redshift. Codoping of N and Fe enhanced the production of hydroxyl radicals (⋅OH) and improved the photocatalytic activity of the resultant AC/TiO(2) compared with those of undoped and N- or Fe-monodoped AC/TiO(2). N-Fe-AC/TiO(2) degraded 93 % of the formaldehyde under Xe-lamp irradiation. Moreover, the photocatalyst was easily recyclable. In summary, a novel and efficient method to mineralize low concentrations of HCHO in wastewater was discovered. |
format | Online Article Text |
id | pubmed-4573084 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-45730842015-09-24 Microwave-Assisted Synthesis of Carbon-Based (N, Fe)-Codoped TiO(2) for the Photocatalytic Degradation of Formaldehyde Tian, Fei Wu, Zhansheng Tong, Yanbin Wu, Zhilin Cravotto, Giancarlo Nanoscale Res Lett Nano Commentary A microwave-assisted sol–gel method was used to synthesize (N, Fe)-codoped activated carbon (AC)/TiO(2) photocatalyst for enhanced optical absorption in the visible light region. The prepared samples were characterized via X-ray diffraction, scanning electron microscopy, transmission electron microscopy, Fourier transform infrared spectroscopy, Brunauer–Emmett–Teller analysis, ultraviolet–visible light spectroscopy, X-ray photoelectron spectroscopy, and photoluminescence spectroscopy. The results showed no significant difference in the surface area of AC/TiO(2) (approximately 500 m(2)/g) after doping. TiO(2) was uniformly distributed on the surface of AC, which exhibited coexisting anatase and rutile structures with a mean crystallite diameter of approximately 20 nm. N and Fe monodoping on AC/TiO(2) reduced the energy band gap of TiO(2) to 2.81 and 2.79 eV, respectively, which mainly attributed to the impurity energy formed in the energy gap of TiO(2). In (N, Fe)-codoped AC/TiO(2), N and Fe are incorporated into the TiO(2) framework and narrow the band gap of TiO(2) to 2.58 eV, thereby causing a large redshift. Codoping of N and Fe enhanced the production of hydroxyl radicals (⋅OH) and improved the photocatalytic activity of the resultant AC/TiO(2) compared with those of undoped and N- or Fe-monodoped AC/TiO(2). N-Fe-AC/TiO(2) degraded 93 % of the formaldehyde under Xe-lamp irradiation. Moreover, the photocatalyst was easily recyclable. In summary, a novel and efficient method to mineralize low concentrations of HCHO in wastewater was discovered. Springer US 2015-09-16 /pmc/articles/PMC4573084/ /pubmed/26377213 http://dx.doi.org/10.1186/s11671-015-1061-6 Text en © Tian et al. 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. |
spellingShingle | Nano Commentary Tian, Fei Wu, Zhansheng Tong, Yanbin Wu, Zhilin Cravotto, Giancarlo Microwave-Assisted Synthesis of Carbon-Based (N, Fe)-Codoped TiO(2) for the Photocatalytic Degradation of Formaldehyde |
title | Microwave-Assisted Synthesis of Carbon-Based (N, Fe)-Codoped TiO(2) for the Photocatalytic Degradation of Formaldehyde |
title_full | Microwave-Assisted Synthesis of Carbon-Based (N, Fe)-Codoped TiO(2) for the Photocatalytic Degradation of Formaldehyde |
title_fullStr | Microwave-Assisted Synthesis of Carbon-Based (N, Fe)-Codoped TiO(2) for the Photocatalytic Degradation of Formaldehyde |
title_full_unstemmed | Microwave-Assisted Synthesis of Carbon-Based (N, Fe)-Codoped TiO(2) for the Photocatalytic Degradation of Formaldehyde |
title_short | Microwave-Assisted Synthesis of Carbon-Based (N, Fe)-Codoped TiO(2) for the Photocatalytic Degradation of Formaldehyde |
title_sort | microwave-assisted synthesis of carbon-based (n, fe)-codoped tio(2) for the photocatalytic degradation of formaldehyde |
topic | Nano Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4573084/ https://www.ncbi.nlm.nih.gov/pubmed/26377213 http://dx.doi.org/10.1186/s11671-015-1061-6 |
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