Published March 9, 2022 | Version Published
Journal article Open

Electrosynthesis of Biocompatible Free-Standing PEDOT Thin Films at a Polarised Liquid|Liquid Interface

  • 1. The Bernal Institute and Department of Chemical Sciences, School of Natural Sciences, University of Limerick (UL), Limerick V94 T9PX, Ireland
  • 2. The Bernal Institute and Department of Physics School of Natural Sciences, University of Limerick (UL), Limerick V94 T9PX, Ireland
  • 3. The Bernal Institute, University of Limerick (UL), Limerick V94 T9PX, Ireland
  • 4. School of Mathematics and Physics, Queen's University Belfast (QUB), Belfast BT71 NN, UK

Description

Conducting polymers (CPs) find applications in energy conversion and storage, sensor, and biomedical technologies, once processed into thin films. Hydrophobic CPs, like poly(3,4-ethylenedioxythiophene) (PEDOT), typically require surfactant additives, such as poly(styrenesulfonate) (PSS), to aid their aqueous processability as thin films. However, excess PSS diminishes CP electrochemical performance, biocompatibility, and device stability. Here, we report the electrosynthesis of PEDOT thin films at a polarised liquid|liquid interface, a method non-reliant on conductive solid substrates that produces free-standing, additive-free, biocompatible, easily transferrable, and scalable 2D PEDOT thin films of any shape or size in a single-step at ambient conditions. Electrochemical control of thin film nucleation and growth at the polarised liquid|liquid interface allows control over the morphology, transitioning from 2D (flat on both sides with thickness <50 nm) to “Janus” 3D (with a flat and rough side, each showing distinct physical properties, and thickness >850 nm) films. The PEDOT thin films were p-doped (approaching the theoretical limit), showed high π-π conjugation, were processed directly as thin films without insulating PSS, and were thus highly conductive without post-processing. This work demonstrates that interfacial electrosynthesis directly produces PEDOT thin films with distinctive molecular architectures inaccessible in bulk solution or at solid electrode-electrolyte interfaces and emergent properties that facilitate technological advances. In this regard, we demonstrate the PEDOT thin film’s superior biocompatibility as scaffolds for cellular growth, opening immediate applications in organic electrochemical transistor (OECT) devices for monitoring cell behaviour over extended time periods, bio-scaffolds and medical devices, without needing physiologically unstable and poorly biocompatible PSS.

Notes

A.G.-Q. and A.H. acknowledge funding received from Irish Research Council (IRC) Government of Ireland Postdoctoral Fellowship Awards (Grant Numbers GOIPD/2018/252 and GOIPD/2020/821, respectively). R.A.L. and S.M acknowledge funding received from IRC Government of Ireland Postgraduate scholarships (Grant Numbers GOIPG/2018/2132 and GOIPG/2019/3693).

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Additional details

Funding

Designing Reactive Functionalised Soft Interfaces _ Self-healing soft materials for solar energy conversion, energy storage, and sustainable low cost hydrogen production 13/SIRG/2137
Science Foundation Ireland
SOFT-PHOTOCONVERSION – Solar Energy Conversion without Solid State Architectures: Pushing the Boundaries of Photoconversion Efficiencies at Self-healing Photosensitiser Functionalised Soft Interfaces 716792
European Commission