Photodegradation of methylene blue using crystalline titanosilicate quantum-confined semiconductor
- Autores
- Luca, Vittorio; Osborne, Michael; Sizgek, Devlet; Griffith, Christopher; Araujo, Paula Zulema
- Año de publicación
- 2006
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Synthetic sitinakite contains in its structure a discrete wire-like sublattice of linked TiO6 octahedra. This sublattice is held apart by silicate tetrahedra forming one-dimensional channels that run down the c axis. The optical properties of this structural arrangement have been studied and compared with other titanosilicate phases, the best known being ETS-10. Thus, sitinakite which has twice the titanate wire diameter of ETS-10 has a band gap of 4.07 eV compared with 3.87 eV. The reduced electron-hole effective mass of the sitinakite quantum-confined system has been calculated through use of the effective mass model and compared with that of other titanosilicate materials. The sitinakite phase has been shown to effectively photodegrade methylene blue (MB) dye at pH 7 using visible light excitation and displays a higher degradation rate than TiO2 (Degussa, P25) under the same experimental conditions. On the contrary, under UV excitation, the photodegradation rate obtained using P25 is much higher than that using sitinakite. Given that the band edge of sitinkaite is significantly blue shifted compared with that of P25, photodegradation of MB using sitinakite is attributed to sensitization of the MB cationic dye which is strongly adsorbed onto the negatively charged sitinakite surfaces.
Fil: Luca, Vittorio. Australian Nuclear Science and Technology Organisation; Australia
Fil: Osborne, Michael. Australian Nuclear Science and Technology Organisation; Australia
Fil: Sizgek, Devlet. Australian Nuclear Science and Technology Organisation; Australia
Fil: Griffith, Christopher. Australian Nuclear Science and Technology Organisation; Australia
Fil: Araujo, Paula Zulema. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina - Materia
-
X-Ray Absorption
Titanium Oxide
Photocatalysis
Ion-Exchange
Titosilicate - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- https://creativecommons.org/licenses/by-nc-sa/2.5/ar/
- Repositorio
- Institución
- Consejo Nacional de Investigaciones Científicas y Técnicas
- OAI Identificador
- oai:ri.conicet.gov.ar:11336/54100
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oai:ri.conicet.gov.ar:11336/54100 |
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spelling |
Photodegradation of methylene blue using crystalline titanosilicate quantum-confined semiconductorLuca, VittorioOsborne, MichaelSizgek, DevletGriffith, ChristopherAraujo, Paula ZulemaX-Ray AbsorptionTitanium OxidePhotocatalysisIon-ExchangeTitosilicatehttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Synthetic sitinakite contains in its structure a discrete wire-like sublattice of linked TiO6 octahedra. This sublattice is held apart by silicate tetrahedra forming one-dimensional channels that run down the c axis. The optical properties of this structural arrangement have been studied and compared with other titanosilicate phases, the best known being ETS-10. Thus, sitinakite which has twice the titanate wire diameter of ETS-10 has a band gap of 4.07 eV compared with 3.87 eV. The reduced electron-hole effective mass of the sitinakite quantum-confined system has been calculated through use of the effective mass model and compared with that of other titanosilicate materials. The sitinakite phase has been shown to effectively photodegrade methylene blue (MB) dye at pH 7 using visible light excitation and displays a higher degradation rate than TiO2 (Degussa, P25) under the same experimental conditions. On the contrary, under UV excitation, the photodegradation rate obtained using P25 is much higher than that using sitinakite. Given that the band edge of sitinkaite is significantly blue shifted compared with that of P25, photodegradation of MB using sitinakite is attributed to sensitization of the MB cationic dye which is strongly adsorbed onto the negatively charged sitinakite surfaces.Fil: Luca, Vittorio. Australian Nuclear Science and Technology Organisation; AustraliaFil: Osborne, Michael. Australian Nuclear Science and Technology Organisation; AustraliaFil: Sizgek, Devlet. Australian Nuclear Science and Technology Organisation; AustraliaFil: Griffith, Christopher. Australian Nuclear Science and Technology Organisation; AustraliaFil: Araujo, Paula Zulema. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaAmerican Chemical Society2006-12info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/54100Luca, Vittorio; Osborne, Michael; Sizgek, Devlet; Griffith, Christopher; Araujo, Paula Zulema; Photodegradation of methylene blue using crystalline titanosilicate quantum-confined semiconductor; American Chemical Society; Chemistry Of Materials; 18; 26; 12-2006; 6132-61380897-4756CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/abs/10.1021/cm052839pinfo:eu-repo/semantics/altIdentifier/doi/10.1021/cm052839pinfo:eu-repo/semantics/openAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-10-15T14:36:12Zoai:ri.conicet.gov.ar:11336/54100instacron:CONICETInstitucionalhttp://ri.conicet.gov.ar/Organismo científico-tecnológicoNo correspondehttp://ri.conicet.gov.ar/oai/requestdasensio@conicet.gov.ar; lcarlino@conicet.gov.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:34982025-10-15 14:36:12.475CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Photodegradation of methylene blue using crystalline titanosilicate quantum-confined semiconductor |
title |
Photodegradation of methylene blue using crystalline titanosilicate quantum-confined semiconductor |
spellingShingle |
Photodegradation of methylene blue using crystalline titanosilicate quantum-confined semiconductor Luca, Vittorio X-Ray Absorption Titanium Oxide Photocatalysis Ion-Exchange Titosilicate |
title_short |
Photodegradation of methylene blue using crystalline titanosilicate quantum-confined semiconductor |
title_full |
Photodegradation of methylene blue using crystalline titanosilicate quantum-confined semiconductor |
title_fullStr |
Photodegradation of methylene blue using crystalline titanosilicate quantum-confined semiconductor |
title_full_unstemmed |
Photodegradation of methylene blue using crystalline titanosilicate quantum-confined semiconductor |
title_sort |
Photodegradation of methylene blue using crystalline titanosilicate quantum-confined semiconductor |
dc.creator.none.fl_str_mv |
Luca, Vittorio Osborne, Michael Sizgek, Devlet Griffith, Christopher Araujo, Paula Zulema |
author |
Luca, Vittorio |
author_facet |
Luca, Vittorio Osborne, Michael Sizgek, Devlet Griffith, Christopher Araujo, Paula Zulema |
author_role |
author |
author2 |
Osborne, Michael Sizgek, Devlet Griffith, Christopher Araujo, Paula Zulema |
author2_role |
author author author author |
dc.subject.none.fl_str_mv |
X-Ray Absorption Titanium Oxide Photocatalysis Ion-Exchange Titosilicate |
topic |
X-Ray Absorption Titanium Oxide Photocatalysis Ion-Exchange Titosilicate |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Synthetic sitinakite contains in its structure a discrete wire-like sublattice of linked TiO6 octahedra. This sublattice is held apart by silicate tetrahedra forming one-dimensional channels that run down the c axis. The optical properties of this structural arrangement have been studied and compared with other titanosilicate phases, the best known being ETS-10. Thus, sitinakite which has twice the titanate wire diameter of ETS-10 has a band gap of 4.07 eV compared with 3.87 eV. The reduced electron-hole effective mass of the sitinakite quantum-confined system has been calculated through use of the effective mass model and compared with that of other titanosilicate materials. The sitinakite phase has been shown to effectively photodegrade methylene blue (MB) dye at pH 7 using visible light excitation and displays a higher degradation rate than TiO2 (Degussa, P25) under the same experimental conditions. On the contrary, under UV excitation, the photodegradation rate obtained using P25 is much higher than that using sitinakite. Given that the band edge of sitinkaite is significantly blue shifted compared with that of P25, photodegradation of MB using sitinakite is attributed to sensitization of the MB cationic dye which is strongly adsorbed onto the negatively charged sitinakite surfaces. Fil: Luca, Vittorio. Australian Nuclear Science and Technology Organisation; Australia Fil: Osborne, Michael. Australian Nuclear Science and Technology Organisation; Australia Fil: Sizgek, Devlet. Australian Nuclear Science and Technology Organisation; Australia Fil: Griffith, Christopher. Australian Nuclear Science and Technology Organisation; Australia Fil: Araujo, Paula Zulema. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina |
description |
Synthetic sitinakite contains in its structure a discrete wire-like sublattice of linked TiO6 octahedra. This sublattice is held apart by silicate tetrahedra forming one-dimensional channels that run down the c axis. The optical properties of this structural arrangement have been studied and compared with other titanosilicate phases, the best known being ETS-10. Thus, sitinakite which has twice the titanate wire diameter of ETS-10 has a band gap of 4.07 eV compared with 3.87 eV. The reduced electron-hole effective mass of the sitinakite quantum-confined system has been calculated through use of the effective mass model and compared with that of other titanosilicate materials. The sitinakite phase has been shown to effectively photodegrade methylene blue (MB) dye at pH 7 using visible light excitation and displays a higher degradation rate than TiO2 (Degussa, P25) under the same experimental conditions. On the contrary, under UV excitation, the photodegradation rate obtained using P25 is much higher than that using sitinakite. Given that the band edge of sitinkaite is significantly blue shifted compared with that of P25, photodegradation of MB using sitinakite is attributed to sensitization of the MB cationic dye which is strongly adsorbed onto the negatively charged sitinakite surfaces. |
publishDate |
2006 |
dc.date.none.fl_str_mv |
2006-12 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
http://hdl.handle.net/11336/54100 Luca, Vittorio; Osborne, Michael; Sizgek, Devlet; Griffith, Christopher; Araujo, Paula Zulema; Photodegradation of methylene blue using crystalline titanosilicate quantum-confined semiconductor; American Chemical Society; Chemistry Of Materials; 18; 26; 12-2006; 6132-6138 0897-4756 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/54100 |
identifier_str_mv |
Luca, Vittorio; Osborne, Michael; Sizgek, Devlet; Griffith, Christopher; Araujo, Paula Zulema; Photodegradation of methylene blue using crystalline titanosilicate quantum-confined semiconductor; American Chemical Society; Chemistry Of Materials; 18; 26; 12-2006; 6132-6138 0897-4756 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/url/http://pubs.acs.org/doi/abs/10.1021/cm052839p info:eu-repo/semantics/altIdentifier/doi/10.1021/cm052839p |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
dc.format.none.fl_str_mv |
application/pdf application/pdf |
dc.publisher.none.fl_str_mv |
American Chemical Society |
publisher.none.fl_str_mv |
American Chemical Society |
dc.source.none.fl_str_mv |
reponame:CONICET Digital (CONICET) instname:Consejo Nacional de Investigaciones Científicas y Técnicas |
reponame_str |
CONICET Digital (CONICET) |
collection |
CONICET Digital (CONICET) |
instname_str |
Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.name.fl_str_mv |
CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicas |
repository.mail.fl_str_mv |
dasensio@conicet.gov.ar; lcarlino@conicet.gov.ar |
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1846082826568466432 |
score |
13.22299 |