
Journal of Materials Chemistry C p. 15597 - 15602 (2020)
Update date:2022-08-29
Topics:
Chen, Mingxi
Dang, Yangyang
Dong, Huanli
Hu, Wenping
Hu, Yongxu
Ji, Deyang
Li, Jie
Li, Liqiang
Liu, Jinyu
Qin, Zhengsheng
Sun, Yajing
Zhen, Yonggang
By introducing the naphthyl group into the 2,6-positions of anthracene, two different anthracene derivatives, 2,6-di(2-naphthyl)anthracene (2,6-di(2-Na)Ant) and 2,6-di(1-naphthyl)anthracene (2,6-di(1-Na)Ant) were synthesized. The tiny change in the substitution site of the naphthyl group leads to a significant difference in the molecular packing and further exerts a great impact on their optoelectronic properties. Thin film field-effect transistors for 2,6-di(2-Na)Ant show charge transport mobility up to 2.1 cm2 V-1 s-1, while 2,6-di(1-Na)Ant demonstrates no mobility. Moreover, thin film phototransistors of 2,6-di(2-Na)Ant show a photoresponsivity of 6.9 × 103 A W-1, a high photosensitivity of 2.6 × 106 and an excellent detectivity of 3.4 × 1016 Jones, which is one of the highest performances of thin film organic phototransistors reported to date. This journal is
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