Benzotriazole and benzothiadiazole containing conjugated copolymers for organic solar cell applications
Citation
Karakus, M., Apaydın, D. H., Yıldız, D. E., Toppare, L., & Cirpan, A. (2012). Benzotriazole and benzothiadiazole containing conjugated copolymers for organic solar cell applications. Polymer, 53(6), 1198-1202.Abstract
2-Dodecyl benzotriazole (BTz) and benzothiadiazole (BTd) containing copolymers poly(4-(2-dodecyl-2H-benzo[d][1,2,3]triazol-4-yl)benzo[c][1,2,5] thiadiazole (P1), poly(4-(5-(2-dodecyl-7-(thiophen-2yl)-2H-benzo[d][1,2,3] triazol-4-yl)thiophen-2-yl)benzo[c][1,2,5] thiadiazole (P2) and poly(4-(5-(2-dodecyl-7-(4-hexylthiophen-2-yl)-2H-benzo[d] [1,2,3]triazol-4-yl)- 3-hexylthiophen-2-yl) benzo[c][1,2,5] thiadiazole (P3) were synthesized via Suzuki polycondensation. We report the application of conjugated copolymers in bulk heterojunction photovoltaic devices. When the copolymers were blended with [6,6]phenyl-C61-butyric acid methyl ester (PCBM), P2 showed the best performance with an open circuit voltage (Voc), a short-circuit current density (Jsc) and a power conversion efficiency (PCE) of 0.45 V, 3.48 mA cm-2 and 0.45%, respectively, under AM 1.5G illumination conditions (100 mW cm-2). The hole mobilities of the devices were calculated from J-V curves using Space Charge Limited Current (SCLC) method and the maximum mobility value was found to be 3.15 × 10-5 cm 2 V-1 s-1 for the P2:PCBM blend. © 2012 Published by Elsevier Ltd.
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PolymerVolume
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