Issue 15, 2013

Electrografting onto ITO substrates of poly(thiophene)-based micelles decorated by acrylate groups

Abstract

We report on a simple process for the chemisorption of poly(thiophene)-based block copolymers onto ITO substrates. Two poly(thiophene) block copolymers functionalized by acrylates on the second block are prepared by the Grignard Metathesis (GRIM) process. The first block is composed of poly(3-hexylthiophene) (P3HT) and the second block is either a polythiophene bearing an acrylate group on each monomer unit (PAcET), or a polythiophene bearing both acrylate and poly(ethylene glycol) side chains (P(AcET-co-PEGET)). After characterizing their macromolecular parameters and optical properties, we investigate their ability to self-assemble into micelles in DMF solutions. This solvent is required for the electrografting procedure that is used for strongly anchoring the polymer to ITO. These micelles are expected to be formed by a P3HT core and a PAcET or P(AcET-co-PEGET) shell. When PEG side chains are present in the second block, the copolymer nicely self-assembles into micelles decorated by acrylates. Cathodic polarization of ITO induces chemisorption and polymerization of acrylate groups, leading to an adherent organized film of poly(thiophene)-based micelles. The optical absorption spectra show that the electrografted polymer chains have a degree of π-electron conjugation similar to that of crystalline P3HT films. In the absence of the PEG chains, the copolymer does not organize into micelles, due to the low stabilizing ability of the second block in DMF.

Graphical abstract: Electrografting onto ITO substrates of poly(thiophene)-based micelles decorated by acrylate groups

Supplementary files

Article information

Article type
Paper
Submitted
22 Apr 2013
Accepted
08 May 2013
First published
09 May 2013

Polym. Chem., 2013,4, 4151-4161

Electrografting onto ITO substrates of poly(thiophene)-based micelles decorated by acrylate groups

F. Ouhib, S. Desbief, R. Lazzaroni, S. Melinte, C. A. Duţu, C. Jerôme and C. Detrembleur, Polym. Chem., 2013, 4, 4151 DOI: 10.1039/C3PY00511A

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