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Synthesis and photovoltaic performance of dibenzofulvene-based organic sensitizers for DSSC

Authors :
Antonio Cardone
Giuseppe Ciccarella
L. De Marco
Agostina Lina Capodilupo
Roberto Giannuzzi
Giuseppina Anna Corrente
Eduardo Fabiano
Giuseppe Gigli
Capodilupo, A. L.
Giannuzzi, Riccardo
Corrente, GIUSEPPINA ANNA
DE MARCO, Luisa
Fabiano, Eduardo
Cardone, A.
Gigli, Giuseppe
Ciccarella, Giuseppe
Source :
Tetrahedron (Oxf., Online) 72 (2016): 5788–5797. doi:10.1016/j.tet.2016.08.006, info:cnr-pdr/source/autori:Capodilupo A.-L.; Giannuzzi R.; Corrente G.A.; De Marco L.; Fabiano E.; Cardone A.; Gigli G.; Ciccarella G./titolo:Synthesis and photovoltaic performance of dibenzofulvene-based organic sensitizers for DSSC/doi:10.1016%2Fj.tet.2016.08.006/rivista:Tetrahedron (Oxf., Online)/anno:2016/pagina_da:5788/pagina_a:5797/intervallo_pagine:5788–5797/volume:72
Publication Year :
2016
Publisher :
Elsevier BV, 2016.

Abstract

Three novel 2D-π-A metal-free organic dyes TK 7 – 9 containing a dibenzofulvene ( DBF ) linked to two thiophene units as the π-bridge, diarylamines with and without alkoxy chains as donor groups and the cyanoacrylic acid moiety as the acceptor and anchoring group were synthesized. The new dyes TK were characterized by optical and electrochemical measurements and density functional theory calculations and were used as sensitizers in liquid dye-sensitized solar cells. The effects of alkoxy-functionalization of donor moiety and of hexyl chain insertion onto one thienyl ring of π-linker on dye properties and performances were investigated. The results discover the dye TK7 , bearing two simple diphenylamine groups without alkoxy chains, exhibits the best behavior in terms of light absorption and cell performance (PCE of 7.9% and photovoltaic parameters of J sc of 17.82 mA cm −2 , V oc of 670 mV and FF of 0.66). Lower power conversion efficiencies of 6.3% and 6.1% were found for TK8 and TK9 , respectively, as a consequence of the presence of the alkoxy chains.

Details

ISSN :
00404020
Volume :
72
Database :
OpenAIRE
Journal :
Tetrahedron
Accession number :
edsair.doi.dedup.....90421532b52bc12a2b7950e79f028bba