Electrochemical and electrochromic properties of poly(4,4" dimethoxy 3'-methyl 2,2':5',2" terthiophene)

Detalhes bibliográficos
Autor(a) principal: Dias,Bruna L.
Data de Publicação: 2005
Outros Autores: Girotto,Emerson M., Matos,Roberto de, Santos,Marcos J. L., De Paoli,Marco-A., Gazotti,Wilson A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000500009
Resumo: This work describes the electrochemical, spectroelectrochemical and electrochromic properties of poly(4,4" dimethoxy 3'-methyl 2,2':5',2" terthiophene) thin films. The effect of temperature on the electropolymerization was studied by cyclic voltammetry measured in situ. The temperatures used were -10, 0, 10, 20, and 40 ºC. Results indicate that the electropolymerization temperature directly affect the degree of chain organization. The optical response time for bleaching was 0.8 s and for coloring 0.3 s (for films synthesized at 40 ºC, 60 nm thick). After 1400 electrochromic cycles, the chromatic contrast at 570 nm changes from 31 to 14%. The coloration efficiency was enhanced as a function of redox cycling. This was probably caused by a decrease in the injected charge necessary for the color change, suggesting that the electroactive losses occurring during the cycles are related to sites not responsible for electrochromic contrast.
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spelling Electrochemical and electrochromic properties of poly(4,4" dimethoxy 3'-methyl 2,2':5',2" terthiophene)thiophene derivativeselectrochromic propertieselectro polymerizationelectrochromismconducting polymerThis work describes the electrochemical, spectroelectrochemical and electrochromic properties of poly(4,4" dimethoxy 3'-methyl 2,2':5',2" terthiophene) thin films. The effect of temperature on the electropolymerization was studied by cyclic voltammetry measured in situ. The temperatures used were -10, 0, 10, 20, and 40 ºC. Results indicate that the electropolymerization temperature directly affect the degree of chain organization. The optical response time for bleaching was 0.8 s and for coloring 0.3 s (for films synthesized at 40 ºC, 60 nm thick). After 1400 electrochromic cycles, the chromatic contrast at 570 nm changes from 31 to 14%. The coloration efficiency was enhanced as a function of redox cycling. This was probably caused by a decrease in the injected charge necessary for the color change, suggesting that the electroactive losses occurring during the cycles are related to sites not responsible for electrochromic contrast.Sociedade Brasileira de Química2005-08-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000500009Journal of the Brazilian Chemical Society v.16 n.4 2005reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.1590/S0103-50532005000500009info:eu-repo/semantics/openAccessDias,Bruna L.Girotto,Emerson M.Matos,Roberto deSantos,Marcos J. L.De Paoli,Marco-A.Gazotti,Wilson A.eng2005-08-25T00:00:00Zoai:scielo:S0103-50532005000500009Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2005-08-25T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv Electrochemical and electrochromic properties of poly(4,4" dimethoxy 3'-methyl 2,2':5',2" terthiophene)
title Electrochemical and electrochromic properties of poly(4,4" dimethoxy 3'-methyl 2,2':5',2" terthiophene)
spellingShingle Electrochemical and electrochromic properties of poly(4,4" dimethoxy 3'-methyl 2,2':5',2" terthiophene)
Dias,Bruna L.
thiophene derivatives
electrochromic properties
electro polymerization
electrochromism
conducting polymer
title_short Electrochemical and electrochromic properties of poly(4,4" dimethoxy 3'-methyl 2,2':5',2" terthiophene)
title_full Electrochemical and electrochromic properties of poly(4,4" dimethoxy 3'-methyl 2,2':5',2" terthiophene)
title_fullStr Electrochemical and electrochromic properties of poly(4,4" dimethoxy 3'-methyl 2,2':5',2" terthiophene)
title_full_unstemmed Electrochemical and electrochromic properties of poly(4,4" dimethoxy 3'-methyl 2,2':5',2" terthiophene)
title_sort Electrochemical and electrochromic properties of poly(4,4" dimethoxy 3'-methyl 2,2':5',2" terthiophene)
author Dias,Bruna L.
author_facet Dias,Bruna L.
Girotto,Emerson M.
Matos,Roberto de
Santos,Marcos J. L.
De Paoli,Marco-A.
Gazotti,Wilson A.
author_role author
author2 Girotto,Emerson M.
Matos,Roberto de
Santos,Marcos J. L.
De Paoli,Marco-A.
Gazotti,Wilson A.
author2_role author
author
author
author
author
dc.contributor.author.fl_str_mv Dias,Bruna L.
Girotto,Emerson M.
Matos,Roberto de
Santos,Marcos J. L.
De Paoli,Marco-A.
Gazotti,Wilson A.
dc.subject.por.fl_str_mv thiophene derivatives
electrochromic properties
electro polymerization
electrochromism
conducting polymer
topic thiophene derivatives
electrochromic properties
electro polymerization
electrochromism
conducting polymer
description This work describes the electrochemical, spectroelectrochemical and electrochromic properties of poly(4,4" dimethoxy 3'-methyl 2,2':5',2" terthiophene) thin films. The effect of temperature on the electropolymerization was studied by cyclic voltammetry measured in situ. The temperatures used were -10, 0, 10, 20, and 40 ºC. Results indicate that the electropolymerization temperature directly affect the degree of chain organization. The optical response time for bleaching was 0.8 s and for coloring 0.3 s (for films synthesized at 40 ºC, 60 nm thick). After 1400 electrochromic cycles, the chromatic contrast at 570 nm changes from 31 to 14%. The coloration efficiency was enhanced as a function of redox cycling. This was probably caused by a decrease in the injected charge necessary for the color change, suggesting that the electroactive losses occurring during the cycles are related to sites not responsible for electrochromic contrast.
publishDate 2005
dc.date.none.fl_str_mv 2005-08-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
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dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000500009
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532005000500009
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.1590/S0103-50532005000500009
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.16 n.4 2005
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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