Nitrogen-sensitized dual phase titanate/titania for visible-light driven phenol degradation

A dual-phase material (DP-160) comprising hydrated titanate (H2Ti3O7·xH2O) and anatase (TiO2) was synthesized in a low-temperature one-pot process in the presence of triethylamine (TEA) as the N-source. The unique structure exhibits strong visible light absorption. The chromophore is linked to Ti–N...

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Main Authors: Schreyer, Martin K., Cheng, Yu Hua, Subramaniam, Vishnu-Priya, Gong, Dangguo, Tang, Yuxin, Highfield, James, Pehkonen, Simo Olavi, Pichat, Pierre, Chen, Zhong
Other Authors: School of Materials Science & Engineering
Format: Article
Language:English
Published: 2013
Online Access:https://hdl.handle.net/10356/95829
http://hdl.handle.net/10220/11274
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Institution: Nanyang Technological University
Language: English
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spelling sg-ntu-dr.10356-958292020-06-01T10:21:11Z Nitrogen-sensitized dual phase titanate/titania for visible-light driven phenol degradation Schreyer, Martin K. Cheng, Yu Hua Subramaniam, Vishnu-Priya Gong, Dangguo Tang, Yuxin Highfield, James Pehkonen, Simo Olavi Pichat, Pierre Chen, Zhong School of Materials Science & Engineering A dual-phase material (DP-160) comprising hydrated titanate (H2Ti3O7·xH2O) and anatase (TiO2) was synthesized in a low-temperature one-pot process in the presence of triethylamine (TEA) as the N-source. The unique structure exhibits strong visible light absorption. The chromophore is linked to Ti–N bonds derived from both surface sensitization and sub-surface (bulk) doping. From transmission electron microscope (TEM) and textural studies by N2 physisorption, the composite exists as mesoporous particles with a grain size of ∼20 nm and mean pore diameter of 3.5 nm, responsible for the high surface area (∼180 m2/g). DP-160 demonstrated photocatalytic activity in the degradation of phenol under visible light (λ>420 nm). The activity of the composite was further enhanced by a small addition (0.001 M) of H2O2, which also gave rise to some visible light activity in the control samples. This effect is believed to be associated with the surface peroxo-titanate complex. GC–MS analyses showed that the intermediate products of phenol degradation induced by visible light irradiation of DP-160 did not differ from those obtained by UV (band-gap) irradiation of TiO2. The overall performance of the composite is attributed to efficient excitation via inter-band states (due to N-doping), surface sensitization, improved adsorptive properties of aromatic compounds due to the N-carbonaceous overlayer, and the presence of heterojunctions that are known to promote directional charge transfer in other mixed-phase titanias like Degussa P25. 2013-07-12T02:56:28Z 2019-12-06T19:22:06Z 2013-07-12T02:56:28Z 2019-12-06T19:22:06Z 2012 2012 Journal Article Cheng, Y. H., Subramaniam, V.-P., Gong, D., Tang, Y., Highfield, J., Pehkonen, S. O., et al. (2012). Nitrogen-sensitized dual phase titanate/titania for visible-light driven phenol degradation. Journal of solid state chemistry, 196, 518-527. 0022-4596 https://hdl.handle.net/10356/95829 http://hdl.handle.net/10220/11274 10.1016/j.jssc.2012.07.011 en Journal of solid state chemistry © 2012 Elsevier Inc.
institution Nanyang Technological University
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description A dual-phase material (DP-160) comprising hydrated titanate (H2Ti3O7·xH2O) and anatase (TiO2) was synthesized in a low-temperature one-pot process in the presence of triethylamine (TEA) as the N-source. The unique structure exhibits strong visible light absorption. The chromophore is linked to Ti–N bonds derived from both surface sensitization and sub-surface (bulk) doping. From transmission electron microscope (TEM) and textural studies by N2 physisorption, the composite exists as mesoporous particles with a grain size of ∼20 nm and mean pore diameter of 3.5 nm, responsible for the high surface area (∼180 m2/g). DP-160 demonstrated photocatalytic activity in the degradation of phenol under visible light (λ>420 nm). The activity of the composite was further enhanced by a small addition (0.001 M) of H2O2, which also gave rise to some visible light activity in the control samples. This effect is believed to be associated with the surface peroxo-titanate complex. GC–MS analyses showed that the intermediate products of phenol degradation induced by visible light irradiation of DP-160 did not differ from those obtained by UV (band-gap) irradiation of TiO2. The overall performance of the composite is attributed to efficient excitation via inter-band states (due to N-doping), surface sensitization, improved adsorptive properties of aromatic compounds due to the N-carbonaceous overlayer, and the presence of heterojunctions that are known to promote directional charge transfer in other mixed-phase titanias like Degussa P25.
author2 School of Materials Science & Engineering
author_facet School of Materials Science & Engineering
Schreyer, Martin K.
Cheng, Yu Hua
Subramaniam, Vishnu-Priya
Gong, Dangguo
Tang, Yuxin
Highfield, James
Pehkonen, Simo Olavi
Pichat, Pierre
Chen, Zhong
format Article
author Schreyer, Martin K.
Cheng, Yu Hua
Subramaniam, Vishnu-Priya
Gong, Dangguo
Tang, Yuxin
Highfield, James
Pehkonen, Simo Olavi
Pichat, Pierre
Chen, Zhong
spellingShingle Schreyer, Martin K.
Cheng, Yu Hua
Subramaniam, Vishnu-Priya
Gong, Dangguo
Tang, Yuxin
Highfield, James
Pehkonen, Simo Olavi
Pichat, Pierre
Chen, Zhong
Nitrogen-sensitized dual phase titanate/titania for visible-light driven phenol degradation
author_sort Schreyer, Martin K.
title Nitrogen-sensitized dual phase titanate/titania for visible-light driven phenol degradation
title_short Nitrogen-sensitized dual phase titanate/titania for visible-light driven phenol degradation
title_full Nitrogen-sensitized dual phase titanate/titania for visible-light driven phenol degradation
title_fullStr Nitrogen-sensitized dual phase titanate/titania for visible-light driven phenol degradation
title_full_unstemmed Nitrogen-sensitized dual phase titanate/titania for visible-light driven phenol degradation
title_sort nitrogen-sensitized dual phase titanate/titania for visible-light driven phenol degradation
publishDate 2013
url https://hdl.handle.net/10356/95829
http://hdl.handle.net/10220/11274
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