4.6 Article

Synthesis and photovoltaic properties of organic dyes containing N-fluoren-2-yl dithieno[3,2-b:2′,3′-d]pyrrole and different donors

Journal

ORGANIC ELECTRONICS
Volume 26, Issue -, Pages 109-116

Publisher

ELSEVIER SCIENCE BV
DOI: 10.1016/j.orgel.2015.07.019

Keywords

Organic dyes; Dye-sensitized solar cells; Optical spectra; Theoretical calculations; Dithienopyrrole; Fluorene

Funding

  1. Department of Science and Technology, New Delhi, India [DST/TSG/PT/2013/09]
  2. UGC, New Delhi
  3. DST through FIST Grant

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New organic dyes containing fluorene appended dithienopyrrole as electron rich linker, different arylamine/ heterocyclic units as conjugating donors and cyanoacrylic acid as acceptor have been synthesized and characterized as sensitizers for dye-sensitized solar cells. The effect of different conjugated donors such as triarylamine, carbazole and phenothiazine on the photophysical, electrochemical and photovoltaic properties is investigated. The optical and electrochemical properties of the dyes are strongly influenced by conjugating donors. The dye containing phenothiazine donor exhibited longer wavelength absorption and low oxidation potential. The time dependent density functional calculations performed on the dye models reveal charge transfer character for the longer wavelength absorption. The dye-sensitized solar cells fabricated using a dye containing fluorenyldiphenylamine donor displayed highest power conversion efficiency (6.81%) in the series originating from the high short circuit current density (J(SC) = 14.01 mA cm (2)) and high open circuit voltage (V-OC = 738 mV). (C) 2015 Elsevier B.V. All rights reserved.

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