Visible-Light-Driven Antibacterial Activity of Poly(3hexylthiophene-2,5-diyl) Nanoparticles

Abstract

Sterilisation using photocatalysts does not lead to the development of drug-resistant bacteria and has therefore attracted significant attention. Particularly, organic semiconductors typically comprise earth-abundant elements and allow facile tuning of their material properties through organic synthesis. A representative organic semiconductor, poly(3hexylthiophene-2,5-diyl) (P3HT), exhibits visible-light absorption and efficient charge-transport properties owing to its πconjugated structure, emphasising its potential for visible-light-driven photocatalysis. However, the hydrophobic nature of P3HT makes it difficult to employ in aqueous environments conducive to bacterial growth while maintaining its chemical structure. In this work, to investigate the antibacterial activity of hydrophobic organic semiconductors in aqueous environments, P3HT nanoparticles (NPs) with diameters ranging approximately 40-100 nm were prepared via reprecipitation, enabling stable dispersion in aqueous solution while maintaining the molecular structure of P3HT. P3HT NPs with higher regioregularity and larger specific surface areas generate greater amounts of reactive oxygen species and exhibit an enhanced antibacterial activity. P3HT NPs with 99% regioregularity and an average particle diameter of 42 nm achieved a sterilisation rate of 99% against E. coli after 6 h of visible-light irradiation. This work demonstrates that predominantly hydrophobic organic semiconductors can be developed as photocatalysts capable of sterilisation in aqueous environments through NP formation.

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Article information

Article type
Paper
Submitted
09 Nov 2025
Accepted
18 Mar 2026
First published
19 Apr 2026
This article is Open Access
Creative Commons BY license

Nanoscale, 2026, Accepted Manuscript

Visible-Light-Driven Antibacterial Activity of Poly(3hexylthiophene-2,5-diyl) Nanoparticles

T. Ishikawa, A. Shibata, H. Kasai and K. Oka, Nanoscale, 2026, Accepted Manuscript , DOI: 10.1039/D5NR04734J

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