Preparation of poly(3‐hexylthiophene) conjugated polymer brush films from amine‐terminated surfaces

Abstract Conjugated polymer brush (CPB) films are more robust and exhibit more vertically aligned polymer chains than their spun‐cast analogs. We prepare CPB films of poly(3‐hexylthiophene) (P3HT) by coupling an amine‐terminated surface (ATS) formed from (3‐aminopropyl)triethoxysilane (APTES) on Si/SiO 2 to 4‐bromobenzoic acid using standard, inexpensive peptide coupling reagents. The resulting terminal bromobenzene is reacted with Pd(P t Bu 3 ) 2 and immersed in the monomer solution. X‐ray photoelectron spectroscopy, spectroscopic ellipsometry and static water contact angle measurements confirm the surface chemistry at each stage of P3HT CPB preparation. Atomic force microscopy(AFM) and UV–vis spectrophotometry indicate that the CPB films prepared by this method exhibit similar morphology and optical properties to those produced from other methods of poly(3‐alkylthiophene) CPB film preparation. Variations of the standard approach, such as using a pre‐synthesized silane counterpart or with (11‐aminoundecyl)triethoxysilane, show comparable film morphologies by AFM. This method is used to produce the first CPB film of poly(3‐dodecylthiophene), showing its utility for exploring CPB films of more sterically demanding polymers. Peptide coupling is used to prepare an analogous functionalized thiol for initiating P3HT CPB film growth from Au surfaces, and microcontact printing with this thiol allows preparation of the first patterned CPB film of P3HT.

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Publication Details

Journal
Journal of Polymer Science
Published
2024-09-05
DOI
https://doi.org/10.1002/pol.20240377
Citations
2
Primary Topic
Molecular Junctions and Nanostructures
Type
article
Field-Weighted Citation Impact
0.42

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article

Preparation of poly(3‐hexylthiophene) conjugated polymer brush films from amine‐terminated surfaces

K Campbell, Ruth J. Augustine, Robert D. Geil, Brian H. Augustine et al.
2 citations
Journal of Polymer Science
Molecular Junctions and Nanostructures
0.42
article

Preparation of poly(3‐hexylthiophene) conjugated polymer brush films from amine‐terminated surfaces

K Campbell, Ruth J. Augustine, Robert D. Geil, Brian H. Augustine, Pamela M. Lundin, Shobha Mantripragada, Grace C. Parizek, Olivia J. Armendarez, Sadie M. Flagg, Evan J. Silver, Isabella P. Diaz, T. Kaz
article en
2 citations

Abstract

Abstract Conjugated polymer brush (CPB) films are more robust and exhibit more vertically aligned polymer chains than their spun‐cast analogs. We prepare CPB films of poly(3‐hexylthiophene) (P3HT) by coupling an amine‐terminated surface (ATS) formed from (3‐aminopropyl)triethoxysilane (APTES) on Si/SiO 2 to 4‐bromobenzoic acid using standard, inexpensive peptide coupling reagents. The resulting terminal bromobenzene is reacted with Pd(P t Bu 3 ) 2 and immersed in the monomer solution. X‐ray photoelectron spectroscopy, spectroscopic ellipsometry and static water contact angle measurements confirm the surface chemistry at each stage of P3HT CPB preparation. Atomic force microscopy(AFM) and UV–vis spectrophotometry indicate that the CPB films prepared by this method exhibit similar morphology and optical properties to those produced from other methods of poly(3‐alkylthiophene) CPB film preparation. Variations of the standard approach, such as using a pre‐synthesized silane counterpart or with (11‐aminoundecyl)triethoxysilane, show comparable film morphologies by AFM. This method is used to produce the first CPB film of poly(3‐dodecylthiophene), showing its utility for exploring CPB films of more sterically demanding polymers. Peptide coupling is used to prepare an analogous functionalized thiol for initiating P3HT CPB film growth from Au surfaces, and microcontact printing with this thiol allows preparation of the first patterned CPB film of P3HT.

Journal of Polymer ScienceVol. 62(23)
High Point University (US), University of North Carolina at Chapel Hill (US), North Carolina Agricultural and Technical State University (US), Furman University (US)
National Science Foundation, North Carolina Biotechnology Center, High Point University, National Nanotechnology Coordinating Office, Division of Materials Research, Division of Electrical, Communications and Cyber Systems, Division of Chemistry
Openalex Percentile: Top 38%
Molecular Junctions and Nanostructures
0.42
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