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Morphological Changes in PEDOT:PSS under Electrolytes, Dopamine, and PEG-400 Exposure: A Molecular Simulation Perspective

Amali G. Guruge, Hesam Makki, Alessandro Troisi

Research output: Contribution to journalArticlepeer-review

Abstract

Poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) is a widely used conducting polymer, whose conductivity can be enhanced by incorporation of specific chemical components, whereas diffusion of water into the material can reduce its conductivity. These changes are typically linked to morphological changes in lamella crystallite size, π–π stacking, chain orientation, and interlamella connectivity. However, an atomistic-level understanding of how specific chemical components influence these properties remains limited, particularly in relation to experimentally observed conductivity trends. In this study, molecular dynamics (MD) simulations are employed to investigate the effects of electrolytes, dopamine, and poly(ethylene glycol) 400 (PEG-400) on PEDOT:PSS morphology and relate the findings to experimental observations. All chemical components were found to screen electrostatic interactions between PEDOT and PSS, potentially affecting the conductivity. Dopamine tends to reduce conductivity by intercalating between PEDOT and PSS, disrupting interdomain connectivity. In contrast, PEG-400 enhances conductivity by improving interlamellar connectivity without altering PEDOT chain conformation, challenging conventional explanations and suggesting an alternative mechanism. CuCl2 enhances conductivity via PEDOT conformational changes associated with partial PSS loss, whereas NaCl shows minimal morphological changes, in agreement with established explanations. Overall, MD simulations confirm the established trends, provide alternative insights, and challenge commonly accepted explanations, demonstrating their utility in validating, refining, and reinterpreting molecular mechanisms in complex polymer systems.

Original languageEnglish
Pages (from-to)1752-1762
Number of pages11
JournalMacromolecules
Volume59
Issue number3
Early online date27 Jan 2026
DOIs
Publication statusPublished - 10 Feb 2026

Acknowledgements

This work made use of the Barkla High-Performance Computing facilities at the University of Liverpool.

Funding

The authors thank support from the European Research Council (Grant No. 101020369).

ASJC Scopus subject areas

  • Organic Chemistry
  • Polymers and Plastics
  • Inorganic Chemistry
  • Materials Chemistry

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