Influence of pH of Colloidal Suspension on the Electrical Conductivity of SnO2 thin Films Deposited Via Sol-Gel-Dip-Coating

Detalhes bibliográficos
Autor(a) principal: Ravaro, Leandro Piaggi [UNESP]
Data de Publicação: 2011
Outros Autores: Scalvi, Luis Vicente de Andrade [UNESP]
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Institucional da UNESP
Texto Completo: http://dx.doi.org/10.1590/S1516-14392011005000010
http://hdl.handle.net/11449/8459
Resumo: Tin dioxide (SnO2) thin films are deposited by the dip-coating technique from colloidal suspensions prepared with distinct pH through the sol-gel method. The decrease of the pH contributes to the destruction of an electrical layer adjacent to particles in solution, leading to a high degree of aggregation among these particles due to the generation of cross-linked bonds (Sn-O-Sn) between them. The aggregation affects the electrical properties of films, because the pH variation produces particle with distinct sizes in the film. Undoped samples prepared from pH 6 leads to the highest conductivity among the investigated undoped samples, in agreement with X-ray diffractograms, which indicate higher crystallinity for lower pH. Arrhenius plot evaluated from temperature dependent conductivity data leads to activation energies of the deepest level between 67 to 140 meV, for the films prepared from suspensions with pH 6 to 11. The most probable explanation for this variation in the conductivity and activation energy is related to distinct potential barriers between grains, due to distinct packing caused by cross-linked bonds formed during suspension phase. Characterization of samples lightly doped with Er3+ confirms that acid pH leads to higher conductivity, but the highest conduction takes place at even lower pH when compared to undoped thin films.
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spelling Influence of pH of Colloidal Suspension on the Electrical Conductivity of SnO2 thin Films Deposited Via Sol-Gel-Dip-Coatingtin dioxidesol-gel-dip-coatingelectrical conductivitypHTin dioxide (SnO2) thin films are deposited by the dip-coating technique from colloidal suspensions prepared with distinct pH through the sol-gel method. The decrease of the pH contributes to the destruction of an electrical layer adjacent to particles in solution, leading to a high degree of aggregation among these particles due to the generation of cross-linked bonds (Sn-O-Sn) between them. The aggregation affects the electrical properties of films, because the pH variation produces particle with distinct sizes in the film. Undoped samples prepared from pH 6 leads to the highest conductivity among the investigated undoped samples, in agreement with X-ray diffractograms, which indicate higher crystallinity for lower pH. Arrhenius plot evaluated from temperature dependent conductivity data leads to activation energies of the deepest level between 67 to 140 meV, for the films prepared from suspensions with pH 6 to 11. The most probable explanation for this variation in the conductivity and activation energy is related to distinct potential barriers between grains, due to distinct packing caused by cross-linked bonds formed during suspension phase. Characterization of samples lightly doped with Er3+ confirms that acid pH leads to higher conductivity, but the highest conduction takes place at even lower pH when compared to undoped thin films.Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)UNESP State Univ São Paulo, Postgrad Program Mat Sci & Technol, Bauru, SP, BrazilUNESP State Univ São Paulo, Dept Phys, Bauru, SP, BrazilUNESP State Univ São Paulo, Postgrad Program Mat Sci & Technol, Bauru, SP, BrazilUNESP State Univ São Paulo, Dept Phys, Bauru, SP, BrazilUniversidade Federal de São Carlos (UFSCar), Dept Engenharia MaterialsUniversidade Estadual Paulista (Unesp)Ravaro, Leandro Piaggi [UNESP]Scalvi, Luis Vicente de Andrade [UNESP]2014-05-20T13:26:19Z2014-05-20T13:26:19Z2011-01-01info:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/article113-117http://dx.doi.org/10.1590/S1516-14392011005000010Materials Research-ibero-american Journal of Materials. São Carlos: Universidade Federal de São Carlos (UFSCar), Dept Engenharia Materials, v. 14, n. 1, p. 113-117, 2011.1516-1439http://hdl.handle.net/11449/845910.1590/S1516-14392011005000010S1516-14392011000100019WOS:000289856400019S1516-14392011000100019.pdf77307194764512320000-0001-5762-6424Web of Sciencereponame:Repositório Institucional da UNESPinstname:Universidade Estadual Paulista (UNESP)instacron:UNESPengMaterials Research-ibero-american Journal of Materials1.1030,398info:eu-repo/semantics/openAccess2024-04-25T17:39:40Zoai:repositorio.unesp.br:11449/8459Repositório InstitucionalPUBhttp://repositorio.unesp.br/oai/requestopendoar:29462024-04-25T17:39:40Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)false
dc.title.none.fl_str_mv Influence of pH of Colloidal Suspension on the Electrical Conductivity of SnO2 thin Films Deposited Via Sol-Gel-Dip-Coating
title Influence of pH of Colloidal Suspension on the Electrical Conductivity of SnO2 thin Films Deposited Via Sol-Gel-Dip-Coating
spellingShingle Influence of pH of Colloidal Suspension on the Electrical Conductivity of SnO2 thin Films Deposited Via Sol-Gel-Dip-Coating
Ravaro, Leandro Piaggi [UNESP]
tin dioxide
sol-gel-dip-coating
electrical conductivity
pH
title_short Influence of pH of Colloidal Suspension on the Electrical Conductivity of SnO2 thin Films Deposited Via Sol-Gel-Dip-Coating
title_full Influence of pH of Colloidal Suspension on the Electrical Conductivity of SnO2 thin Films Deposited Via Sol-Gel-Dip-Coating
title_fullStr Influence of pH of Colloidal Suspension on the Electrical Conductivity of SnO2 thin Films Deposited Via Sol-Gel-Dip-Coating
title_full_unstemmed Influence of pH of Colloidal Suspension on the Electrical Conductivity of SnO2 thin Films Deposited Via Sol-Gel-Dip-Coating
title_sort Influence of pH of Colloidal Suspension on the Electrical Conductivity of SnO2 thin Films Deposited Via Sol-Gel-Dip-Coating
author Ravaro, Leandro Piaggi [UNESP]
author_facet Ravaro, Leandro Piaggi [UNESP]
Scalvi, Luis Vicente de Andrade [UNESP]
author_role author
author2 Scalvi, Luis Vicente de Andrade [UNESP]
author2_role author
dc.contributor.none.fl_str_mv Universidade Estadual Paulista (Unesp)
dc.contributor.author.fl_str_mv Ravaro, Leandro Piaggi [UNESP]
Scalvi, Luis Vicente de Andrade [UNESP]
dc.subject.por.fl_str_mv tin dioxide
sol-gel-dip-coating
electrical conductivity
pH
topic tin dioxide
sol-gel-dip-coating
electrical conductivity
pH
description Tin dioxide (SnO2) thin films are deposited by the dip-coating technique from colloidal suspensions prepared with distinct pH through the sol-gel method. The decrease of the pH contributes to the destruction of an electrical layer adjacent to particles in solution, leading to a high degree of aggregation among these particles due to the generation of cross-linked bonds (Sn-O-Sn) between them. The aggregation affects the electrical properties of films, because the pH variation produces particle with distinct sizes in the film. Undoped samples prepared from pH 6 leads to the highest conductivity among the investigated undoped samples, in agreement with X-ray diffractograms, which indicate higher crystallinity for lower pH. Arrhenius plot evaluated from temperature dependent conductivity data leads to activation energies of the deepest level between 67 to 140 meV, for the films prepared from suspensions with pH 6 to 11. The most probable explanation for this variation in the conductivity and activation energy is related to distinct potential barriers between grains, due to distinct packing caused by cross-linked bonds formed during suspension phase. Characterization of samples lightly doped with Er3+ confirms that acid pH leads to higher conductivity, but the highest conduction takes place at even lower pH when compared to undoped thin films.
publishDate 2011
dc.date.none.fl_str_mv 2011-01-01
2014-05-20T13:26:19Z
2014-05-20T13:26:19Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://dx.doi.org/10.1590/S1516-14392011005000010
Materials Research-ibero-american Journal of Materials. São Carlos: Universidade Federal de São Carlos (UFSCar), Dept Engenharia Materials, v. 14, n. 1, p. 113-117, 2011.
1516-1439
http://hdl.handle.net/11449/8459
10.1590/S1516-14392011005000010
S1516-14392011000100019
WOS:000289856400019
S1516-14392011000100019.pdf
7730719476451232
0000-0001-5762-6424
url http://dx.doi.org/10.1590/S1516-14392011005000010
http://hdl.handle.net/11449/8459
identifier_str_mv Materials Research-ibero-american Journal of Materials. São Carlos: Universidade Federal de São Carlos (UFSCar), Dept Engenharia Materials, v. 14, n. 1, p. 113-117, 2011.
1516-1439
10.1590/S1516-14392011005000010
S1516-14392011000100019
WOS:000289856400019
S1516-14392011000100019.pdf
7730719476451232
0000-0001-5762-6424
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Materials Research-ibero-american Journal of Materials
1.103
0,398
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv 113-117
dc.publisher.none.fl_str_mv Universidade Federal de São Carlos (UFSCar), Dept Engenharia Materials
publisher.none.fl_str_mv Universidade Federal de São Carlos (UFSCar), Dept Engenharia Materials
dc.source.none.fl_str_mv Web of Science
reponame:Repositório Institucional da UNESP
instname:Universidade Estadual Paulista (UNESP)
instacron:UNESP
instname_str Universidade Estadual Paulista (UNESP)
instacron_str UNESP
institution UNESP
reponame_str Repositório Institucional da UNESP
collection Repositório Institucional da UNESP
repository.name.fl_str_mv Repositório Institucional da UNESP - Universidade Estadual Paulista (UNESP)
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