4.2 Article

Design, synthesis of organic sensitizers containing carbazole and triphenylamine π-bridged moiety for dye-sensitized solar cells

Journal

JOURNAL OF THE IRANIAN CHEMICAL SOCIETY
Volume 16, Issue 9, Pages 1923-1937

Publisher

SPRINGER
DOI: 10.1007/s13738-019-01663-w

Keywords

Carbazole; Chemical synthesis; Dye-sensitized solar cells; Photoconversion efficiency; Thermal stability; Triphenylamine

Funding

  1. Department of Science and Technology, SERB, Extramural Major Research Project [EMR/2015/000969]
  2. Department of Science and Technology, CERI, New Delhi, India [DST/TM/CERI/C130(G)]
  3. University Grants Commission, New Delhi, India [41-215/2012 (SR)]

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A series of novel push-pull-based D-pi-A-containing organic dyes have been synthesized using triphenylamine and carbazole act as pi-conjugated donor and cyanoacrylic acid acceptor as well as anchoring group for application of dye-sensitized solar cells. These organic dyes D1, D2 and D3 exhibited excellent photophysical, electrochemical properties, superior stoke shift, high thermal stabilities and sufficient HOMO-LUMO energy levels, which is facilitated to dye regeneration and effective injection of electron from the excited state of the dyes into the conduction band (TiO2). Our results suggested that carbazole pi-bridge has an important role in the photovoltaic performance. The D1 and D2 dyes are planar linear structure, longer pi-conjugated bridging units, when compared to the starburst structure of D3 organic dye. Moreover, the carbazole pi-bridged conjugated D1 dye showed promising photovoltaic conversion efficiency (eta) of 1.4%, V-oc = 735 mV, J(sc) = 2.7 mA/cm(2), ff = 0.73 (fill factor), when compared with the conventional N719 and D5 organic dyes.

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