n-Type thiophene semiconductors
View Patent ↗The new fluorocarbon-functionalized and/or heterocycle-modified polythiophenes, in particular, α,ω-diperfluorohexylsexithiophene DFH-6T can be straightforwardly prepared in high yield and purity. Introduction of such modifications to a thiophene core affords enhanced thermal stability and volatility, and increased electron affinity versus the unmodified compositions of the prior art. Evaporated films behave as n-type semiconductors, and can be used to fabricate thin film transistors with FET mobilities ˜0.01 cm 2 Vs—some of the highest reported to date for n-type organic semiconductors.
1. An n-type polythiophene composition having the structural formula
wherein R 1 , R 2 and R 3 are selected from the substituent group consisting of fluoroalkyl moieties, C n H 2n+1 and where n is about 1–12, H, F and (CH 2 ) a X and where a is about 1–12 and X is selected from the group consisting of amino, hydroxy and carboxylic acid functionalities; x is an integer selected from the group of integers consisting of 1 and integers greater than 1; and y is an integer selected from the group consisting of 0 and integers greater than 0, providing said composition comprises at least one perfluorophenyl component; and z is an integer selected from the group of integers consisting of 0 and integers greater than 0.
2. The n-type polythiophene composition of claim 1 wherein said fluoroalkyl moiety is selected from the group consisting of linear fluoroalkyl substituents, branched fluoroalkyl substituents and cyclic fluoroalkyl substituents.
3. The n-type polythiophene composition of claim 2 wherein said fluoroalkyl moiety has the structural formula C n F 2n+1 , where n is about 1–8.
4. The n-type polythiophene composition of claim 1 wherein x is about 1–4; y is about 1–8, and z is about 0–12.
5. The n-type polythiophene composition of claim 4 wherein said fluoroalkyl moiety has the structural formula C n F 2n+1 , where n is about 1–8.