期刊文献+

Donor-Acceptor Oligomers and Polymers Composed of Benzothiadiazole and 3-Hexylthiophene: Effect of Chain Length and Regioregularity 被引量:1

Donor-Acceptor Oligomers and Polymers Composed of Benzothiadiazole and 3-Hexylthiophene: Effect of Chain Length and Regioregularity
原文传递
导出
摘要 A series of donor-acceptor oligomer OBTThn (n = 1- 7) and polymer PBTThl and PBTTh2 composed of al- ternative 2,1,3-benzothiadiazole and 3-hexylthiophene have been designed and synthesized for the purpose of in- vestigation on the effect of chain length and side-chain regioregularity on their basic properties and photovoltaic performance. In the OBTThn oligomers and PBTThl polymer, all the hexyl side chains on thienyl units orient to- ward the same direction. Upon elongation of the chain length, the intramolecular charge transfer (ICT) absorption band in solution gradually redshifts from 398 nm for OBTThl to 505 nm for OBTThT, then to 512 nm for PBTThl polymer. Meanwhile, the HOMO energy level increases from -5.45 eV (OBTTh0 to -5.08 eV (OBTThT) and -5.09 eV (PBTThl), and the LUMO energy level decreases from -3.11 eV (OBTTh0 to -3.30 eV (OBTThT) and -3.33 eV (PBTThl), thus giving a smaller and smaller energy bandgap for higher oligomers and polymers. Theo- retical calculation suggests straight line-like backbone geometry for this series of oligomers and polymer. On the other hand, polymer PBTTh2 possesses a different side-chain regioregularity, in which every two neighbor hexyl side chains are arranged in different orienting direction. It is theoretically suggested to have curved line-like back- bone geometry. In solution, it shows similar photophysical and electrochemical properties as PBTThl. However in film state, it displays a less redshift in the ICT band as refer to that in solution than PBTThl. In combination with [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM), these oligomers and polymers were used as donor material to fabricate organic bulk heterojunction solar cells. Again, chain length-dependent device photovoltaic performance was observed. The device based on OBTTh4 showed a power conversion efficiency of 0.16%, while it increased to 0.36% and 0.49% for the devices based on OBTTh6 and PBTThb respectively. However, the side-chain regio- regularity has less influence on the device photovoltaic output since the device based on PBTTh~ displayed an effi- ciency of 0.52%, comparable to that of PBTThl. A series of donor-acceptor oligomer OBTThn (n = 1- 7) and polymer PBTThl and PBTTh2 composed of al- ternative 2,1,3-benzothiadiazole and 3-hexylthiophene have been designed and synthesized for the purpose of in- vestigation on the effect of chain length and side-chain regioregularity on their basic properties and photovoltaic performance. In the OBTThn oligomers and PBTThl polymer, all the hexyl side chains on thienyl units orient to- ward the same direction. Upon elongation of the chain length, the intramolecular charge transfer (ICT) absorption band in solution gradually redshifts from 398 nm for OBTThl to 505 nm for OBTThT, then to 512 nm for PBTThl polymer. Meanwhile, the HOMO energy level increases from -5.45 eV (OBTTh0 to -5.08 eV (OBTThT) and -5.09 eV (PBTThl), and the LUMO energy level decreases from -3.11 eV (OBTTh0 to -3.30 eV (OBTThT) and -3.33 eV (PBTThl), thus giving a smaller and smaller energy bandgap for higher oligomers and polymers. Theo- retical calculation suggests straight line-like backbone geometry for this series of oligomers and polymer. On the other hand, polymer PBTTh2 possesses a different side-chain regioregularity, in which every two neighbor hexyl side chains are arranged in different orienting direction. It is theoretically suggested to have curved line-like back- bone geometry. In solution, it shows similar photophysical and electrochemical properties as PBTThl. However in film state, it displays a less redshift in the ICT band as refer to that in solution than PBTThl. In combination with [6,6]-phenyl-C61-butyric acid methyl ester (PC61BM), these oligomers and polymers were used as donor material to fabricate organic bulk heterojunction solar cells. Again, chain length-dependent device photovoltaic performance was observed. The device based on OBTTh4 showed a power conversion efficiency of 0.16%, while it increased to 0.36% and 0.49% for the devices based on OBTTh6 and PBTThb respectively. However, the side-chain regio- regularity has less influence on the device photovoltaic output since the device based on PBTTh~ displayed an effi- ciency of 0.52%, comparable to that of PBTThl.
出处 《Chinese Journal of Chemistry》 SCIE CAS CSCD 2013年第11期1367-1379,共13页 中国化学(英文版)
基金 the National Natural Science Foundation of China,Chinese Academy of Sciences,and Shanghai Science and Technology Commission
关键词 conjugated polymers organic solar cells REGIOREGULARITY DONOR-ACCEPTOR OLIGOMERS conjugated polymers, organic solar cells, regioregularity, donor-acceptor, oligomers
  • 相关文献

参考文献53

  • 1(a) Roncali, J. Cheni. Rev. 1997, 97, 173.
  • 2van Mullekom, H. A. M.; Vekemans, J. A. J. M.; Havinga, E. E.; Meijer, E. W. Mater. Sci. Eng., R 2001, 32, 1.
  • 3(a) Gunes, S.; Neugebauer, H.; Sariciftci, N. S. Chem. Rev. 2007, 107, 13248.
  • 4Cheng, Y.-J.; Yang, S.-H.; Hsu, C.-S. Chem. Rev.2009, 109, 5868.
  • 5Chen, J.; Cao, Y. Acc. Chem. Res. 2009, 42, 17098.
  • 6Li, G.; Zhu, R.; Yang, Y. Nat. Photonics 2012, 6, 153.
  • 7Chen, L.; Shen, X.; Chen, Y. Chin. J. Chem. 2012, 30, 2219.
  • 8Qian, D.; Ma, W.; Li, Z.; Guo, X.; Zhang, S.; Ye, L.; Ade, H.; Tan, Z.; Hou, J. J. Am. Chem. Soc. 2013, 135, 8464.
  • 9Chen, C.-P.; Chen, Y.-C.; Yu, C.-Y. Polym. Chem. 2013, 4, 1161.
  • 10(a) Liang, Y.; Xu, Z.; Xia, J.; Tsai, S.-T.; Wu, Y.; Li, G.; Ray, C.; Yu, L. Adv. Mater. 2010, 22, E135.

同被引文献4

引证文献1

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部