New insights into self-modification of mesoporous titania nanoparticles for enhanced photoactivity: effect of microwave power density on formation of oxygen vacancies and Ti3+ defects

Mesoporous titania nanoparticles (MTN) were successfully prepared by a microwave (MW)-assisted method under various power densities. The catalysts were characterized by XRD, FT-IR, surface area analysis, TEM, and ESR. The characterization data indicated that higher power density increased the crysta...

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Main Authors: Jaafar, N. F., Jalil, A. A., Triwahyono, Sugeng, Shamsuddin, N.
Format: Article
Published: Royal Society of Chemistry 2015
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Online Access:http://eprints.utm.my/id/eprint/58640/
http://dx.doi.org/10.1039/c5ra15120a
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spelling my.utm.586402021-08-01T01:39:13Z http://eprints.utm.my/id/eprint/58640/ New insights into self-modification of mesoporous titania nanoparticles for enhanced photoactivity: effect of microwave power density on formation of oxygen vacancies and Ti3+ defects Jaafar, N. F. Jalil, A. A. Triwahyono, Sugeng Shamsuddin, N. QD Chemistry Mesoporous titania nanoparticles (MTN) were successfully prepared by a microwave (MW)-assisted method under various power densities. The catalysts were characterized by XRD, FT-IR, surface area analysis, TEM, and ESR. The characterization data indicated that higher power density increased the crystallinity and surface area of the MTN while decreasing the particle size and band-gap energy of the TiO2. Significantly, MW heating played an important role in formation of oxygen vacancies (OV) and Ti3+ site defects (TSD). The MTN (T1-T3) with 0.12, 0.37, and 0.56 W g-1 power density were found to degrade 84%, 88%, and 96% of 2-chlorophenol (2-CP) under visible light, respectively, compared to 69% by commercial TiO2. Besides narrowing the band gap, the OV and TSD also acted as electron acceptors that hindered the electron-hole recombination, as well as facilitated the charge carrier migration. The kinetics study over T3 showed that adsorption was the controlling step in the 2-CP degradation, which followed a pseudo-first-order Langmuir-Hinshelwood model. The photocatalytic reaction was still stable, even after five cycle runs without severe catalyst deactivation. This study demonstrates that the uniform heat distribution provided by MW is able to produce MTN that are rich with OV and TSD that are effective under visible light irradiation. Royal Society of Chemistry 2015 Article PeerReviewed Jaafar, N. F. and Jalil, A. A. and Triwahyono, Sugeng and Shamsuddin, N. (2015) New insights into self-modification of mesoporous titania nanoparticles for enhanced photoactivity: effect of microwave power density on formation of oxygen vacancies and Ti3+ defects. Rsc Advances, 5 (110). pp. 90991-91000. ISSN 2046-2069 http://dx.doi.org/10.1039/c5ra15120a DOI:10.1039/c5ra15120a
institution Universiti Teknologi Malaysia
building UTM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Malaysia
content_source UTM Institutional Repository
url_provider http://eprints.utm.my/
topic QD Chemistry
spellingShingle QD Chemistry
Jaafar, N. F.
Jalil, A. A.
Triwahyono, Sugeng
Shamsuddin, N.
New insights into self-modification of mesoporous titania nanoparticles for enhanced photoactivity: effect of microwave power density on formation of oxygen vacancies and Ti3+ defects
description Mesoporous titania nanoparticles (MTN) were successfully prepared by a microwave (MW)-assisted method under various power densities. The catalysts were characterized by XRD, FT-IR, surface area analysis, TEM, and ESR. The characterization data indicated that higher power density increased the crystallinity and surface area of the MTN while decreasing the particle size and band-gap energy of the TiO2. Significantly, MW heating played an important role in formation of oxygen vacancies (OV) and Ti3+ site defects (TSD). The MTN (T1-T3) with 0.12, 0.37, and 0.56 W g-1 power density were found to degrade 84%, 88%, and 96% of 2-chlorophenol (2-CP) under visible light, respectively, compared to 69% by commercial TiO2. Besides narrowing the band gap, the OV and TSD also acted as electron acceptors that hindered the electron-hole recombination, as well as facilitated the charge carrier migration. The kinetics study over T3 showed that adsorption was the controlling step in the 2-CP degradation, which followed a pseudo-first-order Langmuir-Hinshelwood model. The photocatalytic reaction was still stable, even after five cycle runs without severe catalyst deactivation. This study demonstrates that the uniform heat distribution provided by MW is able to produce MTN that are rich with OV and TSD that are effective under visible light irradiation.
format Article
author Jaafar, N. F.
Jalil, A. A.
Triwahyono, Sugeng
Shamsuddin, N.
author_facet Jaafar, N. F.
Jalil, A. A.
Triwahyono, Sugeng
Shamsuddin, N.
author_sort Jaafar, N. F.
title New insights into self-modification of mesoporous titania nanoparticles for enhanced photoactivity: effect of microwave power density on formation of oxygen vacancies and Ti3+ defects
title_short New insights into self-modification of mesoporous titania nanoparticles for enhanced photoactivity: effect of microwave power density on formation of oxygen vacancies and Ti3+ defects
title_full New insights into self-modification of mesoporous titania nanoparticles for enhanced photoactivity: effect of microwave power density on formation of oxygen vacancies and Ti3+ defects
title_fullStr New insights into self-modification of mesoporous titania nanoparticles for enhanced photoactivity: effect of microwave power density on formation of oxygen vacancies and Ti3+ defects
title_full_unstemmed New insights into self-modification of mesoporous titania nanoparticles for enhanced photoactivity: effect of microwave power density on formation of oxygen vacancies and Ti3+ defects
title_sort new insights into self-modification of mesoporous titania nanoparticles for enhanced photoactivity: effect of microwave power density on formation of oxygen vacancies and ti3+ defects
publisher Royal Society of Chemistry
publishDate 2015
url http://eprints.utm.my/id/eprint/58640/
http://dx.doi.org/10.1039/c5ra15120a
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