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
CONICET Digital (CONICET)
Institución
Consejo Nacional de Investigaciones Científicas y Técnicas
OAI Identificador
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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