期刊
CHEMISTRY OF MATERIALS
卷 24, 期 21, 页码 4123-4133出版社
AMER CHEMICAL SOC
DOI: 10.1021/cm3021929
关键词
conjugated polymers; hole mobility; organic field-effect transistors
资金
- Georgia Institute of Technology
- Center for Organic Photonics and Electronics (COPE) at Georgia Tech
- ACS Petroleum Research Fund [PRF 49158ND7]
- National Science Foundation [DMR-1207284]
- STC Program of the National Science Foundation [DMR-0120967]
- NSF through the MRSEC program
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [0848833] Funding Source: National Science Foundation
- Division Of Materials Research
- Direct For Mathematical & Physical Scien [1207284] Funding Source: National Science Foundation
A series of benzothiadiazole oligothiophene and oligo(thienylene vinylene) donor-acceptor (D-A) copolymers were synthesized and characterized. These low optical band gap materials (similar to 1.5 eV) are capable of absorbing photons in the range of 400-800 nm and exhibit good thermal stability. Their hole mobilities, determined using an organic field-effect transistor (OFET) architecture, vary over a range of 3 orders of magnitude and strongly correlate with the molecular ordering and morphology of the respective thin films. Spin-coated films of the poly(benzothiadiazole-sexithiophene) PBT6, which exhibits a highly crystalline lamellar pi-pi stacked edge-on orientation on the OFET substrate, possesses a hole mobility of ca. 0.2 cm(2)/V.s. Vinylene-containing analogs PBT6V2 and PBT6V2' are amorphous and exhibit very low mobilities. The molecular weight of PBT6 has a strong influence on the electronic properties: a sample with a lower molecular weight exhibits a mobility approximately 1 order of magnitude lower than the high molecular weight homologue, and the absorption maximum is appreciably blue-shifted. The hole mobility of PBT6 is further enhanced by a factor of ca. 3 through fabrication of the OFET by drop casting. OFETs fabricated by this process exhibit mobilities of up to 0.75 cm(2)/V.s and I-ON/OFF ratios in the range of 10(6)-10(7). These results demonstrate the potential of incorporating benzothiadiazole units into polythiophene derivatives to develop, high-mobility semiconducting polymers.
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