Please use this identifier to cite or link to this item: http://hdl.handle.net/1822/49650

TitleBenzothiadiazole derivatives functionalized with two different (hetero)aromatic donor groups: synthesis and evaluation as TiO2 sensitizers for DSSCs
Author(s)Fernandes, Sara Sofia Marques
Pereira, Ana
Ivanou, Dzmitry
Mendes, Adélio
Raposo, M. Manuela M.
KeywordsSynthesis
Heterocycles
5-Hexyl-2,2’-bithienyl electron donor group
Benzothiadiazole
Auxiliary donor or acceptor heterocycles
Cyanoacetic acid anchoring group
Co-adsorption
Dye-sensitized solar cells (DSSCs)
Thiophene
UV-visible spectroscopy
Fluorescence
Push-pull pi-conjugated systems
Dye-sensitized solar cells
Issue date2018
PublisherElsevier
JournalDyes and Pigments
CitationFernandes, S. S. M.; Pereira, A.; Ivanou, D.; Mendes, A.; Raposo, M. M. M. Benzothiadiazole derivatives functionalized with two different (hetero)aromatic donor groups: synthesis and evaluation as TiO2 sensitizers for DSSCs Dyes Pigments 2018, 151, 89-94
Abstract(s)A series of benzothiadiazole-based push-pull heterocyclic systems were synthesized and characterized in order to study the variations induced by different aromatic and heterocyclic donor groups in the optical, electronic and photovoltaic properties of DSSCs prepared with the respective cyanoacetic acid derivatives. The organic sensitizers bear a 5-hexyl-2,2’-bithienyl or N,N-diphenylanilino donor moieties conjugated with a thienyl-benzothiadiazole spacer functionalized with the electron acceptor/anchoring cyanoacetic acid group. The solar cell based on TiO2 sensitized with the novel dye bearing the 5-hexyl-2,2’-bithienyl donor, exhibited a power conversion efficiency of 0.95 % due the inefficient electron injection. Co-adsorption studies of the same dye resulted in enhanced photovoltaic conversion efficiency of 2.49 %, which represents an improvement of cell efficiency of 260 %. The sensitizer bearing the N,N-diphenylanilino donor exhibited 4.51 % power conversion efficiency, that was further enhanced by co-sensitization to 5.22 % efficiency.
TypeArticle
URIhttp://hdl.handle.net/1822/49650
DOI10.1016/j.dyepig.2017.10.038
ISSN0143-7208
e-ISSN1873-3743
Publisher versionhttps://doi.org/10.1016/j.dyepig.2017.10.038
Peer-Reviewedyes
AccessOpen access
Appears in Collections:CDQuim - Artigos (Papers)

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