TY - JOUR
T1 - Anthracene-based semiconductors for organic field-effect transistors
AU - Chen, Mengyun
AU - Yan, Lijia
AU - Zhao, Yang
AU - Murtaza, Imran
AU - Meng, Hong
AU - Huang, Wei
N1 - Publisher Copyright:
© The Royal Society of Chemistry 2018.
PY - 2018
Y1 - 2018
N2 - Organic field-effect transistors (OFETs), reported for the first time in 1986, with favourable flexible potential and easy-fabrication properties, are complementary to traditional inorganic field-effect transistors. In fact, OFETs not only afford promising applications in flexible, lightweight circuits and displays, like radio frequency identification devices (RFIDs) and portable screens, they are also useful tools for understanding the charge transport in molecular solids. Anthracene, as a building block for the active layer in OFETs, has the noteworthy advantages of strong intermolecular interaction, due to its planar structure, and high air stability owing to its appropriate energy levels. In this review, 150 anthracene derivatives with substituents at peri- and end-positions are discussed, from the aspects of physicochemical properties, thin film morphology, crystalline characteristics, and charge mobility in OFETs. Particularly, we shed light on the analysis of molecular packing structures, through the investigation of single crystals and molecular modelling, and underline the extraordinary application of anthracene derivatives in organic light-emitting transistors.
AB - Organic field-effect transistors (OFETs), reported for the first time in 1986, with favourable flexible potential and easy-fabrication properties, are complementary to traditional inorganic field-effect transistors. In fact, OFETs not only afford promising applications in flexible, lightweight circuits and displays, like radio frequency identification devices (RFIDs) and portable screens, they are also useful tools for understanding the charge transport in molecular solids. Anthracene, as a building block for the active layer in OFETs, has the noteworthy advantages of strong intermolecular interaction, due to its planar structure, and high air stability owing to its appropriate energy levels. In this review, 150 anthracene derivatives with substituents at peri- and end-positions are discussed, from the aspects of physicochemical properties, thin film morphology, crystalline characteristics, and charge mobility in OFETs. Particularly, we shed light on the analysis of molecular packing structures, through the investigation of single crystals and molecular modelling, and underline the extraordinary application of anthracene derivatives in organic light-emitting transistors.
UR - http://www.scopus.com/inward/record.url?scp=85050388922&partnerID=8YFLogxK
U2 - 10.1039/c8tc01865k
DO - 10.1039/c8tc01865k
M3 - 文献综述
AN - SCOPUS:85050388922
SN - 2050-7534
VL - 6
SP - 7416
EP - 7444
JO - Journal of Materials Chemistry C
JF - Journal of Materials Chemistry C
IS - 28
ER -