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The development of durable and conductive coatings on polyethylene terephthalate (PET) yarns is critical for smart textiles but has remained limited by weak interfacial adhesion and coating uniformity. We introduced a Tris/N-Methyl-2-pyrrolidone (NMP) co-solvent (80:20 v/v) that controlled polydopamine (PDA) interlayer formation on hydrophobic PET and produced a smooth, chemically stable coating (∼139 nm within 10 h). Pure NMP does not support PDA polymerization, whereas Tris alone induces rapid aggregation and irregular deposits; the mixed solvent balances reaction rate and interfacial wetting, thereby enabling uniform PDA growth. Subsequent in-situ polymerization of polypyrrole (PPy) on PDA-modified PET produces compact, adherent coatings at oxidant-to-monomer molar ratio is 1:1. The optimized composite yarns exhibit a practical baseline resistance of 1.69 kΩ and improved electromechanical stability over 100 stretch-recovery cycles, with a resistance change (ΔR/R 0 ) of +102.1% compared with +225.8% for the PDA-free control (F0). This approach shortened PDA deposition time by > 50% relative to typical aqueous routes while enhancing interfacial robustness and cyclic durability. The co-solvent design provides a general pathway to fabric-compatible, reliable conductive yarns for wearable electronics and stretchable sensing.
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Rho et al. (2026) studied this question.
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