화학공학소재연구정보센터
Macromolecules, Vol.49, No.16, 5788-5795, 2016
Alkoxyl Side Chain Substituted Thieno[3,4-c]pyrrole-4,6-dione To Enhance Photovoltaic Performance with Low Steric Hindrance and High Dipole Moment
A series of N-OR substituted thieno[3,4-c]pyrrole-4,6-dione (TPD) and benzo[1,2-b:4,5-b']dithiophene (BDT) based copolymers are systematically investigated. The replacing CH2 with smaller size oxygen atom not only reduces the steric hindrance but also enhances the dipole moment (Delta mu(ge)), which is in favor of charge separation. while the optical and electrochemical properties almost remain unchanged due to the alkoxyl chain on TPD unit not conjugated with the backbone. Consequently, the PBT-O8 based solar cell devices yield a remarkable short-circuit current density (J(SC)) of up to 14.3 mA/cm(2) and power conversion efficiency (PCE) of 8.22%, which exhibits an increase of 10% in comparison with that of PBT-C8 (PCE 7.50%). Furthermore, the PCEs increase almost linearly with decreasing side chain length from 012 to 010 to 08. Apart from the novel TPD analogues reported here, this work also provides a new insight into the ingenious use of alkoxyl side chain to improve the photovoltaic performance.