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Title

Modification of the electronic properties of the π-spacer of chromophores linked to calix[4]arene platform for DSSCs applications

AuthorsColom, E.; Andrés-Castán, J. M.; Barrios, Daniel; Duerto, Isolda; Franco, Santiago; Garín, Javier; Orduna, Jesús; Villacampa, Belén; Blesa, María Jesús
KeywordsMetal-free sensitizer
Multichromophore
Aggregation
Benzothiadiazole
Issue Date2019
PublisherElsevier
CitationDyes and Pigments 164: 43-53 (2019)
AbstractWe have developed two novel dyes based on p-tert-butyl-calix[4]arene in order to evaluate their behavior as sensitizer in photovoltaic devices. These dyes consist in a difunctionalized calix[4]arene with triphenylamine (TPA)-donor, a heteroaromatic π-conjugated spacer, thiophene and benzothiadiazole-phenyl ring, respectively and cyanoacetic acid as acceptor group. The effect of the π-spacer has been studied by UV–vis spectroscopy and Differential Pulse Voltammetry and the models compounds have been theoretically investigated. The dye bearing phenylbenzothiadiazole results in a bathochromic shifted absorption and an adequate efficiency to transfer charge from D to A. The considerable increase of the photocurrent density results in a better efficiency of the devices prepared with these novel dyes with respect to the p-tert-butyl-calix[4]arene derivatives bearing TPA dye. In particular, p-tert-butyl-calix[4]arene derivative based on phenylbenzothiadiazole has reached an efficiency value of 5.84% which means an increase of 33% of the efficiency over those calix[4]arene derivatives with TPA dye.
Publisher version (URL)https://doi.org/10.1016/j.dyepig.2018.12.066
URIhttp://hdl.handle.net/10261/181610
DOI10.1016/j.dyepig.2018.12.066
ISSN0143-7208
E-ISSN1873-3743
Appears in Collections:(ICMA) Artículos
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