Jung Hei ChoiMohamed E. El‐KhoulyTaehee KimYoun-Su KimUng Chan YoonShunichi FukuzumiKyungkon Kim
We fabricated solution-processed organic photovoltaic cells (OPVs) using substituted two sexithiophenes, a,w-bis(dimethyl- n -octylsilyl)sexithiophene ( DSi-6T ) and a,w-dihexylsexithiophene ( DH-6T ), as electron donors, and [6,6]-phenyl-C 61 -butyric acid methyl ester (PCBM) as an electron acceptor. Solution-processed OPVs using DH-6T and DSi-6T showed good photovoltaic properties in spite of their poor solubility. The best performance was observed on DSi-6T : PCBM 1 : 5 (w/w) blend cell with an open circuit voltage (Voc) of 0.63 V, short circuit current density (Jsc) of 1.34 mA/cm 2 , fill factor (FF) of 55%, and power conversion efficiency of 0.44% under AM 1.5 G illumination. Although DH-6T has higher hole mobility than DSi-6T , the DSi-6T : PCBM blend cell showed higher hole mobility than DH-6T : PCBM cell. Therefore, DSi-6T cell showed higher device performance than DH-6T cell due to its silyl substitutions, which lead to the increase of the solubility. The incorporation of solution-processed TiO 2 interfacial layer in the DSi-6T : PCBM devices significantly enhances FF due to the reduced charge recombination near active layer/Al interface.
Jianchang WuYuchao MaNa WuYi LinJian LinLilei WangChang‐Qi Ma
Bright WalkerChunki KimThuc‐Quyen Nguyen
Chang LiuKai WangPengcheng DuChao YiTianyu MengXiong Gong
P.C. Reshmi VarmaManoj A. G. Namboothiry