| Version | Summary | Created by | Modification | Content Size | Created at | Operation |
|---|---|---|---|---|---|---|
| 1 | Jack Zhong | -- | 137 | 2026-10-21 09:41:26 | | | |
| 2 | Jack Zhong | -11 word(s) | 126 | 2026-10-21 09:42:53 | | |
Polythiophene is a conjugated polymer built from thiophene rings linked at the 2- and 5-positions. The overlap of the pi orbitals along the chain gives it an extended conjugation, and oxidation or reduction produces mobile charge carriers [1]. The unsubstituted polymer is insoluble and infusible, so alkyl side chains are attached to the 3-position to make it processable [2]. The regioregularity of those side chains controls how the chains stack, and a head-to-tail arrangement gives the highest conductivity [3]. Doping shifts the absorption from the visible into the near infrared, which underlies the electrochromic behaviour [4]. The conductivity falls on exposure to air because the doped state is oxidatively unstable, so encapsulation is needed for a stable device [5].