Formation of Ordered Mesostructured TiO 2 Thin Film: A Soft Coarse-Grained Simulation Study
- Autores
- Tang, Qiyun; Angelome, Paula Cecilia; Soler-Illia, Galo Juan de Avila Arturo; Müller, Marcus
- Año de publicación
- 2017
- Idioma
- inglés
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Ordered mesostructured TiO2 thin films are employed in diverse applications ranging from catalysis and sensing, to photovoltaic and lithium-ion batteries. Experimentally these mesostructured thin films are fabricated via a sol-gel process coupled with evaporation-induced self-assembly of a supramolecular template, where the concentration of hydrogen chloride (HCl) and water play vital roles. We employ a soft, coarse-grained model of the amphiphilic template Brij58 and spherical particles, representing titanium-oxo clusters, to study the role of HCl and water on the formation of mesostructured TiO2 thin films. The template-cluster and cluster-cluster interactions are re-flected in the interaction terms δNBP and εP P , respectively. The results show that the decrease of HCl (increase of εP P ) leads to the formation of large mesopores due to the strong attraction between particles, giving rise to a high dispersity index (low order) of the thin films. However, the decrease of water (increase of δNBP ) will compensate the entropic attraction between particles, resulting in thin films with low dispersity index (high order). The variation of the dispersity index in the δNBP -εP P plane provides an intuitive understanding that the slow evaporation of HCl could drive the film towards uniform mesoporous state whereas fast evaporation pushes the film through a non-uniform phase. These results indicate that even if the mass proportion of the surfactantsBrij58 and titanium precursors is the same in the initial solution, the final mesoporous structures could be diverse, which was confirmed by the controlled experiments. We also confirm the postprocessing-towards-order strategy by making the particle?s rearrangement available by weakening the εP P . The outlined procedure paves the way of soft, coarse-grained models to understand thecomplex co-assembly of transition metal clusters and amphiphilic surfactants towards the rational design of highly ordered mesoporous structures.
Fil: Tang, Qiyun. Universität Göttingen; Alemania
Fil: Angelome, Paula Cecilia. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Soler-Illia, Galo Juan de Avila Arturo. Universidad Nacional de San Martin. Instituto de Nanosistemas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina
Fil: Müller, Marcus. Universität Göttingen; Alemania - Materia
-
COARSE GRAINED
TIO2
BRIJ 58
MESOPOROUS - Nivel de accesibilidad
- acceso embargado
- 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:11336/41657
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oai:ri.conicet.gov.ar:11336/41657 |
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network_name_str |
CONICET Digital (CONICET) |
spelling |
Formation of Ordered Mesostructured TiO 2 Thin Film: A Soft Coarse-Grained Simulation StudyTang, QiyunAngelome, Paula CeciliaSoler-Illia, Galo Juan de Avila ArturoMüller, MarcusCOARSE GRAINEDTIO2BRIJ 58MESOPOROUShttps://purl.org/becyt/ford/1.4https://purl.org/becyt/ford/1Ordered mesostructured TiO2 thin films are employed in diverse applications ranging from catalysis and sensing, to photovoltaic and lithium-ion batteries. Experimentally these mesostructured thin films are fabricated via a sol-gel process coupled with evaporation-induced self-assembly of a supramolecular template, where the concentration of hydrogen chloride (HCl) and water play vital roles. We employ a soft, coarse-grained model of the amphiphilic template Brij58 and spherical particles, representing titanium-oxo clusters, to study the role of HCl and water on the formation of mesostructured TiO2 thin films. The template-cluster and cluster-cluster interactions are re-flected in the interaction terms δNBP and εP P , respectively. The results show that the decrease of HCl (increase of εP P ) leads to the formation of large mesopores due to the strong attraction between particles, giving rise to a high dispersity index (low order) of the thin films. However, the decrease of water (increase of δNBP ) will compensate the entropic attraction between particles, resulting in thin films with low dispersity index (high order). The variation of the dispersity index in the δNBP -εP P plane provides an intuitive understanding that the slow evaporation of HCl could drive the film towards uniform mesoporous state whereas fast evaporation pushes the film through a non-uniform phase. These results indicate that even if the mass proportion of the surfactantsBrij58 and titanium precursors is the same in the initial solution, the final mesoporous structures could be diverse, which was confirmed by the controlled experiments. We also confirm the postprocessing-towards-order strategy by making the particle?s rearrangement available by weakening the εP P . The outlined procedure paves the way of soft, coarse-grained models to understand thecomplex co-assembly of transition metal clusters and amphiphilic surfactants towards the rational design of highly ordered mesoporous structures.Fil: Tang, Qiyun. Universität Göttingen; AlemaniaFil: Angelome, Paula Cecilia. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Soler-Illia, Galo Juan de Avila Arturo. Universidad Nacional de San Martin. Instituto de Nanosistemas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; ArgentinaFil: Müller, Marcus. Universität Göttingen; AlemaniaRoyal Society of Chemistry2017-10info:eu-repo/date/embargoEnd/2018-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfapplication/pdfhttp://hdl.handle.net/11336/41657Tang, Qiyun; Angelome, Paula Cecilia; Soler-Illia, Galo Juan de Avila Arturo; Müller, Marcus; Formation of Ordered Mesostructured TiO 2 Thin Film: A Soft Coarse-Grained Simulation Study; Royal Society of Chemistry; Physical Chemistry Chemical Physics; 19; 41; 10-2017; 28249-282621463-9076CONICET DigitalCONICETenginfo:eu-repo/semantics/altIdentifier/doi/10.1039/C7CP05304Einfo:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2017/CP/C7CP05304Einfo:eu-repo/semantics/embargoedAccesshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/reponame:CONICET Digital (CONICET)instname:Consejo Nacional de Investigaciones Científicas y Técnicas2025-09-03T09:56:00Zoai:ri.conicet.gov.ar:11336/41657instacron: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:34982025-09-03 09:56:01.064CONICET Digital (CONICET) - Consejo Nacional de Investigaciones Científicas y Técnicasfalse |
dc.title.none.fl_str_mv |
Formation of Ordered Mesostructured TiO 2 Thin Film: A Soft Coarse-Grained Simulation Study |
title |
Formation of Ordered Mesostructured TiO 2 Thin Film: A Soft Coarse-Grained Simulation Study |
spellingShingle |
Formation of Ordered Mesostructured TiO 2 Thin Film: A Soft Coarse-Grained Simulation Study Tang, Qiyun COARSE GRAINED TIO2 BRIJ 58 MESOPOROUS |
title_short |
Formation of Ordered Mesostructured TiO 2 Thin Film: A Soft Coarse-Grained Simulation Study |
title_full |
Formation of Ordered Mesostructured TiO 2 Thin Film: A Soft Coarse-Grained Simulation Study |
title_fullStr |
Formation of Ordered Mesostructured TiO 2 Thin Film: A Soft Coarse-Grained Simulation Study |
title_full_unstemmed |
Formation of Ordered Mesostructured TiO 2 Thin Film: A Soft Coarse-Grained Simulation Study |
title_sort |
Formation of Ordered Mesostructured TiO 2 Thin Film: A Soft Coarse-Grained Simulation Study |
dc.creator.none.fl_str_mv |
Tang, Qiyun Angelome, Paula Cecilia Soler-Illia, Galo Juan de Avila Arturo Müller, Marcus |
author |
Tang, Qiyun |
author_facet |
Tang, Qiyun Angelome, Paula Cecilia Soler-Illia, Galo Juan de Avila Arturo Müller, Marcus |
author_role |
author |
author2 |
Angelome, Paula Cecilia Soler-Illia, Galo Juan de Avila Arturo Müller, Marcus |
author2_role |
author author author |
dc.subject.none.fl_str_mv |
COARSE GRAINED TIO2 BRIJ 58 MESOPOROUS |
topic |
COARSE GRAINED TIO2 BRIJ 58 MESOPOROUS |
purl_subject.fl_str_mv |
https://purl.org/becyt/ford/1.4 https://purl.org/becyt/ford/1 |
dc.description.none.fl_txt_mv |
Ordered mesostructured TiO2 thin films are employed in diverse applications ranging from catalysis and sensing, to photovoltaic and lithium-ion batteries. Experimentally these mesostructured thin films are fabricated via a sol-gel process coupled with evaporation-induced self-assembly of a supramolecular template, where the concentration of hydrogen chloride (HCl) and water play vital roles. We employ a soft, coarse-grained model of the amphiphilic template Brij58 and spherical particles, representing titanium-oxo clusters, to study the role of HCl and water on the formation of mesostructured TiO2 thin films. The template-cluster and cluster-cluster interactions are re-flected in the interaction terms δNBP and εP P , respectively. The results show that the decrease of HCl (increase of εP P ) leads to the formation of large mesopores due to the strong attraction between particles, giving rise to a high dispersity index (low order) of the thin films. However, the decrease of water (increase of δNBP ) will compensate the entropic attraction between particles, resulting in thin films with low dispersity index (high order). The variation of the dispersity index in the δNBP -εP P plane provides an intuitive understanding that the slow evaporation of HCl could drive the film towards uniform mesoporous state whereas fast evaporation pushes the film through a non-uniform phase. These results indicate that even if the mass proportion of the surfactantsBrij58 and titanium precursors is the same in the initial solution, the final mesoporous structures could be diverse, which was confirmed by the controlled experiments. We also confirm the postprocessing-towards-order strategy by making the particle?s rearrangement available by weakening the εP P . The outlined procedure paves the way of soft, coarse-grained models to understand thecomplex co-assembly of transition metal clusters and amphiphilic surfactants towards the rational design of highly ordered mesoporous structures. Fil: Tang, Qiyun. Universität Göttingen; Alemania Fil: Angelome, Paula Cecilia. Comisión Nacional de Energía Atómica. Centro Atómico Constituyentes; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Soler-Illia, Galo Juan de Avila Arturo. Universidad Nacional de San Martin. Instituto de Nanosistemas; Argentina. Consejo Nacional de Investigaciones Científicas y Técnicas; Argentina Fil: Müller, Marcus. Universität Göttingen; Alemania |
description |
Ordered mesostructured TiO2 thin films are employed in diverse applications ranging from catalysis and sensing, to photovoltaic and lithium-ion batteries. Experimentally these mesostructured thin films are fabricated via a sol-gel process coupled with evaporation-induced self-assembly of a supramolecular template, where the concentration of hydrogen chloride (HCl) and water play vital roles. We employ a soft, coarse-grained model of the amphiphilic template Brij58 and spherical particles, representing titanium-oxo clusters, to study the role of HCl and water on the formation of mesostructured TiO2 thin films. The template-cluster and cluster-cluster interactions are re-flected in the interaction terms δNBP and εP P , respectively. The results show that the decrease of HCl (increase of εP P ) leads to the formation of large mesopores due to the strong attraction between particles, giving rise to a high dispersity index (low order) of the thin films. However, the decrease of water (increase of δNBP ) will compensate the entropic attraction between particles, resulting in thin films with low dispersity index (high order). The variation of the dispersity index in the δNBP -εP P plane provides an intuitive understanding that the slow evaporation of HCl could drive the film towards uniform mesoporous state whereas fast evaporation pushes the film through a non-uniform phase. These results indicate that even if the mass proportion of the surfactantsBrij58 and titanium precursors is the same in the initial solution, the final mesoporous structures could be diverse, which was confirmed by the controlled experiments. We also confirm the postprocessing-towards-order strategy by making the particle?s rearrangement available by weakening the εP P . The outlined procedure paves the way of soft, coarse-grained models to understand thecomplex co-assembly of transition metal clusters and amphiphilic surfactants towards the rational design of highly ordered mesoporous structures. |
publishDate |
2017 |
dc.date.none.fl_str_mv |
2017-10 info:eu-repo/date/embargoEnd/2018-11-01 |
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/11336/41657 Tang, Qiyun; Angelome, Paula Cecilia; Soler-Illia, Galo Juan de Avila Arturo; Müller, Marcus; Formation of Ordered Mesostructured TiO 2 Thin Film: A Soft Coarse-Grained Simulation Study; Royal Society of Chemistry; Physical Chemistry Chemical Physics; 19; 41; 10-2017; 28249-28262 1463-9076 CONICET Digital CONICET |
url |
http://hdl.handle.net/11336/41657 |
identifier_str_mv |
Tang, Qiyun; Angelome, Paula Cecilia; Soler-Illia, Galo Juan de Avila Arturo; Müller, Marcus; Formation of Ordered Mesostructured TiO 2 Thin Film: A Soft Coarse-Grained Simulation Study; Royal Society of Chemistry; Physical Chemistry Chemical Physics; 19; 41; 10-2017; 28249-28262 1463-9076 CONICET Digital CONICET |
dc.language.none.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
info:eu-repo/semantics/altIdentifier/doi/10.1039/C7CP05304E info:eu-repo/semantics/altIdentifier/url/http://pubs.rsc.org/en/Content/ArticleLanding/2017/CP/C7CP05304E |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/embargoedAccess https://creativecommons.org/licenses/by-nc-sa/2.5/ar/ |
eu_rights_str_mv |
embargoedAccess |
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 |
Royal Society of Chemistry |
publisher.none.fl_str_mv |
Royal Society of Chemistry |
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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1842269377845526528 |
score |
13.13397 |