Effects of Methyl-Substituted Phenanthrolines on the Performance of Ruthenium(II) Dye-Sensitizers
Autor(a) principal: | |
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Data de Publicação: | 2015 |
Outros Autores: | , , , , , |
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=S0103-50532015001102224 |
Resumo: | Tris-heteroleptic ruthenium(II) cis-[Ru(Me4-phen)(dcbH2)(NCS)2], where Me4-phen = 3,4,7,8-tetramethyl-1,10-phenanthroline, dcbH2 = 4,4'-dicarboxylic acid 2,2'-bipyridine, was synthesized, purified and characterized. Its characteristics were compared with those determined for cis-[Ru(Me2-phen)(dcbH2)(NCS)2] and cis-[Ru(phen)(dcbH2)(NCS)2] aiming to evaluate the effect of the number of methyl groups on the properties of the compounds. Changes in the Fourier transform infrared (FTIR) and 1H nuclear magnetic resonance (NMR) spectra indicated a modification in the electronic distribution of the complex because of the presence of methyl groups at the 3 and 8 positions of 1,10-phenanthroline. These changes also modified the excited state properties and resulted in a blue shift of the absorption and emission spectra. The complex was incorporated onto TiO2 to prepare dye-sensitized solar cells, achieving up to JSC = 11.9 mA cm–2, VOC = 0.627 V, ff = 0.67 and η = 5.0%. |
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Effects of Methyl-Substituted Phenanthrolines on the Performance of Ruthenium(II) Dye-Sensitizersruthenium(II) polypyridyl dyesdye-sensitized solar cellsenergy conversionTris-heteroleptic ruthenium(II) cis-[Ru(Me4-phen)(dcbH2)(NCS)2], where Me4-phen = 3,4,7,8-tetramethyl-1,10-phenanthroline, dcbH2 = 4,4'-dicarboxylic acid 2,2'-bipyridine, was synthesized, purified and characterized. Its characteristics were compared with those determined for cis-[Ru(Me2-phen)(dcbH2)(NCS)2] and cis-[Ru(phen)(dcbH2)(NCS)2] aiming to evaluate the effect of the number of methyl groups on the properties of the compounds. Changes in the Fourier transform infrared (FTIR) and 1H nuclear magnetic resonance (NMR) spectra indicated a modification in the electronic distribution of the complex because of the presence of methyl groups at the 3 and 8 positions of 1,10-phenanthroline. These changes also modified the excited state properties and resulted in a blue shift of the absorption and emission spectra. The complex was incorporated onto TiO2 to prepare dye-sensitized solar cells, achieving up to JSC = 11.9 mA cm–2, VOC = 0.627 V, ff = 0.67 and η = 5.0%.Sociedade Brasileira de Química2015-11-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532015001102224Journal of the Brazilian Chemical Society v.26 n.11 2015reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20150208info:eu-repo/semantics/openAccessMüller,Andressa V.Mendonça,Poliana S.Parant,StéphaneDuchanois,ThibautGros,Philippe C.Beley,MarcPolo,André S.eng2015-11-24T00:00:00Zoai:scielo:S0103-50532015001102224Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2015-11-24T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false |
dc.title.none.fl_str_mv |
Effects of Methyl-Substituted Phenanthrolines on the Performance of Ruthenium(II) Dye-Sensitizers |
title |
Effects of Methyl-Substituted Phenanthrolines on the Performance of Ruthenium(II) Dye-Sensitizers |
spellingShingle |
Effects of Methyl-Substituted Phenanthrolines on the Performance of Ruthenium(II) Dye-Sensitizers Müller,Andressa V. ruthenium(II) polypyridyl dyes dye-sensitized solar cells energy conversion |
title_short |
Effects of Methyl-Substituted Phenanthrolines on the Performance of Ruthenium(II) Dye-Sensitizers |
title_full |
Effects of Methyl-Substituted Phenanthrolines on the Performance of Ruthenium(II) Dye-Sensitizers |
title_fullStr |
Effects of Methyl-Substituted Phenanthrolines on the Performance of Ruthenium(II) Dye-Sensitizers |
title_full_unstemmed |
Effects of Methyl-Substituted Phenanthrolines on the Performance of Ruthenium(II) Dye-Sensitizers |
title_sort |
Effects of Methyl-Substituted Phenanthrolines on the Performance of Ruthenium(II) Dye-Sensitizers |
author |
Müller,Andressa V. |
author_facet |
Müller,Andressa V. Mendonça,Poliana S. Parant,Stéphane Duchanois,Thibaut Gros,Philippe C. Beley,Marc Polo,André S. |
author_role |
author |
author2 |
Mendonça,Poliana S. Parant,Stéphane Duchanois,Thibaut Gros,Philippe C. Beley,Marc Polo,André S. |
author2_role |
author author author author author author |
dc.contributor.author.fl_str_mv |
Müller,Andressa V. Mendonça,Poliana S. Parant,Stéphane Duchanois,Thibaut Gros,Philippe C. Beley,Marc Polo,André S. |
dc.subject.por.fl_str_mv |
ruthenium(II) polypyridyl dyes dye-sensitized solar cells energy conversion |
topic |
ruthenium(II) polypyridyl dyes dye-sensitized solar cells energy conversion |
description |
Tris-heteroleptic ruthenium(II) cis-[Ru(Me4-phen)(dcbH2)(NCS)2], where Me4-phen = 3,4,7,8-tetramethyl-1,10-phenanthroline, dcbH2 = 4,4'-dicarboxylic acid 2,2'-bipyridine, was synthesized, purified and characterized. Its characteristics were compared with those determined for cis-[Ru(Me2-phen)(dcbH2)(NCS)2] and cis-[Ru(phen)(dcbH2)(NCS)2] aiming to evaluate the effect of the number of methyl groups on the properties of the compounds. Changes in the Fourier transform infrared (FTIR) and 1H nuclear magnetic resonance (NMR) spectra indicated a modification in the electronic distribution of the complex because of the presence of methyl groups at the 3 and 8 positions of 1,10-phenanthroline. These changes also modified the excited state properties and resulted in a blue shift of the absorption and emission spectra. The complex was incorporated onto TiO2 to prepare dye-sensitized solar cells, achieving up to JSC = 11.9 mA cm–2, VOC = 0.627 V, ff = 0.67 and η = 5.0%. |
publishDate |
2015 |
dc.date.none.fl_str_mv |
2015-11-01 |
dc.type.driver.fl_str_mv |
info:eu-repo/semantics/article |
dc.type.status.fl_str_mv |
info:eu-repo/semantics/publishedVersion |
format |
article |
status_str |
publishedVersion |
dc.identifier.uri.fl_str_mv |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532015001102224 |
url |
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532015001102224 |
dc.language.iso.fl_str_mv |
eng |
language |
eng |
dc.relation.none.fl_str_mv |
10.5935/0103-5053.20150208 |
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.26 n.11 2015 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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1750318177825325056 |