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Hexylthiophene-Functionalized Carbazole Dyes for Efficient Molecular Photovoltaics: Tuning of Solar-Cell Performance by Structural Modification
634
Citations
62
References
2008
Year
EngineeringOrganic ElectronicsOrganic Solar CellSolar-cell PerformanceMolecule-based MaterialPhoto-electrochemical CellPhotovoltaic DevicesChemistryHexylthiophene-functionalized Carbazole DyesPhotovoltaicsChemical EngineeringThiophene MoietiesSolar Cell StructuresThiophene GroupsMk DyesHybrid MaterialsMaterials SciencePhotochemistrySolar PowerMolecular EngineeringOrganic Charge-transfer CompoundConjugated PolymerStructural ModificationSolar CellsSolar Cell Materials
The performance of DSSCs using MK dyes depends strongly on the number and position of n‑hexyl chains and thiophene units. The study designed and synthesized MK dyes with carbazole donors and cyanoacrylic acid acceptors linked via n‑hexyl‑substituted oligothiophenes for use in dye‑sensitized solar cells. Adding n‑hexyl chains to thiophene groups retards charge recombination, extending electron lifetime, while the dye loading and aggregate thickness on TiO₂, governed by hexyl chain number, further influences DSSC performance. Incorporating n‑hexyl chains increased Voc and efficiency, with MK‑2 achieving 8.3 % η (Jsc = 15.22 mA cm⁻², Voc = 0.73 V, FF = 0.75) under AM1.5G, while higher dye loading extended electron lifetime but lowered Jsc and FF.
Novel organic dyes (MK dyes), which have a carbazole derivative as an electron donor and a cyanoacrylic acid moiety (═C(—C≡N)COOH) as an electron acceptor and an anchoring group, connected with n-hexyl-substituted oligothiophenes as a π-conjugated system, were designed and synthesized for application in dye-sensitized solar cells (DSSCs), which are one of the promising molecular photovoltaics. The photovoltaic performance of the DSSCs based on MK dyes markedly depends on the molecular structure of the dyes in terms of the number and position of n-hexyl chains and the number of thiophene moieties. Retardation of charge recombination caused by the existence of n-hexyl chains linked to the thiophene groups resulted in an increase in electron lifetime. As a consequence, an improvement of open-circuit photovoltage (Voc) and hence the solar-to-electric power conversion efficiency (η) of DSSCs was achieved upon addition of n-hexyl chains to the thiophene groups. In addition, the adsorption condition (amount of dye molecules and/or dye aggregate thickness) on the nanoporous TiO2 electrode, depending on the number of hexyl chains, strongly affected the performance of DSSCs. A larger amount and/or thicker aggregate of dye molecules brought about longer electron lifetime, which resulted in higher Voc, and slower diffusion of I3− ions in the nanoporous TiO2 electrode, which led to lower short-circuit photocurrent (Jsc) and fill factor (FF). In the result of thorough investigation on the series of MK dyes, a DSSC based on MK-2 consisting of n-hexyl-substituted quarter-thiophene produced 8.3% of η (Jsc = 15.22 mA cm−2, Voc = 0.73 V, and FF = 0.75) under 100 mW cm−2 simulated AM1.5G solar irradiation.
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