2009
DOI: 10.1002/pola.23246
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Linking polythiophene chains with vinylene‐bridges: A way to improve charge transport in polymer field‐effect transistors

Abstract: A series of novel branched polythiophene derivatives bearing different densities of vinylene-bridges as linking chains were synthesized by a general synthetic strategy. The organic field-effect transistors, which were fabricated by spincoating the polymer solutions onto octadecyltrichlorosilane-modified SiO 2 /Si substrates with top-contact configuration, afforded a high mobility of 8.0 Â 10 À3 cm 2 V À1 s À1 with an on/off ratio greater than 10 4 and a threshold voltage of about À3 V in saturation regime. The… Show more

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Cited by 13 publications
(7 citation statements)
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“…Compound 9 was purchased from Sigma‐Aldrich and used without further purification. The starting materials and some intermediates (Compounds 1 ,27 2 ,28 4 ,29 6 ,30 7 ,31 8 ,32 M5 ,33 and M6 21) were synthesized according to the literature procedures. Other reagents were obtained from Sinopharm Chemical Reagent (Shanghai, China).…”
Section: Methodsmentioning
confidence: 99%
“…Compound 9 was purchased from Sigma‐Aldrich and used without further purification. The starting materials and some intermediates (Compounds 1 ,27 2 ,28 4 ,29 6 ,30 7 ,31 8 ,32 M5 ,33 and M6 21) were synthesized according to the literature procedures. Other reagents were obtained from Sinopharm Chemical Reagent (Shanghai, China).…”
Section: Methodsmentioning
confidence: 99%
“…Conjugated polymers, especially thiophene‐containing polymers, have been widely used in polymer solar cells (PSCs),1–8 polymer light‐emitting diodes (PLEDs),9, 10 and organic field‐effect transistors (OFETs) 11–13. Among the organic optoelectronic devices, OFETs are under active development and got a great progress over the past decade,14–16 because of their promising applications in electronic paper, radio frequency identification tags, smart cards, memories, sensors and active matrix displays.…”
Section: Introductionmentioning
confidence: 99%
“…Other variations on the reaction conditions are also reported. [9][10][11][12][13] When 2-alkylthiophenes are used as the starting compounds, bromination occurs at the 5-position first (as in 12,14) and then at the 3-position (as in10) (Scheme 4). 5,8,14 D'Aleo et al proposed an alternate method to obtain bromo-substituted alkylthiophenes using ammonium bromide in the presence of hydrogen peroxide in aqueous acetic acid to selectively access the monobromo 7 or the dibromo 8 derivative (Scheme 5).…”
Section: General Preparation Of Halo-substituted Alkylthiophenesmentioning
confidence: 99%