1998
DOI: 10.1021/ma980632u
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Inhomogeneity of Spin-Coated and Cast Non-Regioregular Poly(3-hexylthiophene) Films. Structures and Electrical and Photophysical Properties

Abstract: We report structures and electrical and photophysical properties of spin-coated and cast non-regioregular poly(3-hexylthiophene) (P3HT) films. Large differences of the properties are found in these films prepared from different conditions. Results of optical absorption, electron spin resonance, and X-ray diffraction measurements show that the extent of conjugation of P3HT is homogeneous in the spin-coated film, whereas it is inhomogeneous in the cast film. The existence of relatively strong distorted segments … Show more

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Cited by 87 publications
(70 citation statements)
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References 25 publications
(56 reference statements)
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“…Furthermore, a shoulder peak appeared around 600 nm, which can be assigned to vibronic structure with a 0-0 transition (-Ã transition originated fromelectron orbital overlap between adjacent thiophene rings). 2,19 Such a spectral profile is in agreement with that of P3HT colloidal dispersions in various solvents, [12][13][14][15] indicating thatstacking interaction caused by aggregation of polymer chains would take place in the particle. Figure 3 also shows that the increased polymer concentrations led to a larger red shift and a broader spectrum, suggesting that interchain interaction would be stronger as the concentration became higher.…”
supporting
confidence: 72%
“…Furthermore, a shoulder peak appeared around 600 nm, which can be assigned to vibronic structure with a 0-0 transition (-Ã transition originated fromelectron orbital overlap between adjacent thiophene rings). 2,19 Such a spectral profile is in agreement with that of P3HT colloidal dispersions in various solvents, [12][13][14][15] indicating thatstacking interaction caused by aggregation of polymer chains would take place in the particle. Figure 3 also shows that the increased polymer concentrations led to a larger red shift and a broader spectrum, suggesting that interchain interaction would be stronger as the concentration became higher.…”
supporting
confidence: 72%
“…P3HT has been widely studied in the past and is well known as being an effective hole transport polymer, with higher hole mobility than many other conjugated polymers, including the poly(phenylenevinylene)s. 2 Initially, however, rather low hole mobilities were reported for regiorandom P3HT. 3 However, when head-to-tail regioregularly substituted P3HT became available, the hole mobilities were found to be dramatically improved. [4][5][6] The increase in mobility was related to side-chain-induced self-organization into a well-ordered twodimensional lamellar structure.…”
mentioning
confidence: 99%
“…Impurities and defects in the film will generate trapping and localization of charges, thus decreasing the mobility. Typical values for the mobility are 10 -6 -10 -3 cm 2 s -1 V -1 , [16] but by increasing the order of the film it can be greatly improved to values reaching 0.6 cm 2 s -1 V -1 and above. [17,18] It is also possible to have regions within the same film with different structural order, having high mobility in certain domains surrounded by larger amorphous areas with relatively lower mobility.…”
Section: Charge Transportmentioning
confidence: 99%