Solution processable benzotriazole and fluorene containing copolymers for photovoltaic applications


KAYA E., APAYDIN D. H. , Yildiz D. E. , TOPPARE L. , Cirpan A.

SOLAR ENERGY MATERIALS AND SOLAR CELLS, vol.99, pp.321-326, 2012 (Journal Indexed in SCI) identifier identifier

  • Publication Type: Article / Article
  • Volume: 99
  • Publication Date: 2012
  • Doi Number: 10.1016/j.solmat.2011.12.021
  • Title of Journal : SOLAR ENERGY MATERIALS AND SOLAR CELLS
  • Page Numbers: pp.321-326

Abstract

2-Dodecyl benzotriazole and 9,9-dioctylfluorene containing alternating copolymers poly((9,9-dioctylfluorene)-2,7-diyl-(2-dodecyl-benzo[1,2,3]triazole)) (P1), poly((9,9-dioctylfluorene)-2,7-diyl-(4,7-bis(thien-2-yl) 2-dodecyl-benzo[1,2,3]triazole)) (P2), poly((9,9-dioctylfluorene)-2,7-diyl-(4,7-bis(3-hexylthien-5-yl) 2-dodecyl benzo[1,2,3]triazole)) (P3) were synthesized via a typical Suzuki coupling polymerization. UV-vis and electrochemical studies indicated that polymers have desirable HOMO-LUMO and band gap energy levels, enabling efficient electron transfer when blending them with fullerene derivatives. Photovoltaic properties of the copolymers mixed with [6,6] phenyl-C61-butyric acid methyl ester (PCBM), were investigated. P2 exhibited the best device performance with an open circuit voltage of 0.6 V. short circuit current of 3.4 mA/cm(2) and power conversion efficiency of 0.56% under Air mass 1.5 Global (AM 1.5G, 100 mW/cm(2)) illumination. Hole mobilities of the polymers were calculated using space charge limited current (SCLC) method and found to be in the order of 10(-5) for P1 and P2 and 10(-4) for P3. (C) 2012 Elsevier B.V. All rights reserved.