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Monitoring the Effects of Illumination on the Structure of Conjugated Polymer Gels Using Neutron Scattering
Published on: December 21, 2017
Molecular Dispersion of Conjugated Polymers via Amine Containing Additives Facilitates Coating and Preserves Solid
Berfin Keleş1, Fatih Sema1, Yağmur Bozkurt2
1Department of Chemistry, İzmir Institute of Technology, Gülbahçe, Urla 35430, İzmir, Türkiye.
Abstract:
Conjugated polymers are promising for optoelectronic applications but suffer from aggregation-caused quenching (ACQ) in the solid state. We demonstrate that incorporating amine-based additives polyethylenimine (PEI), ethylenediamine (EDA), N-methylpyrrolidone (NMP), dimethylpiperazine (DMP), and 1-methylimidazole (1MI) into thiophene-based polymers significantly suppresses ACQ through noncovalent physical interactions. Comprehensive spectroscopic and morphological analyses reveal that amine additives enhance quantum yields up to 29.6% for P1-1MI and induce a 10-fold increase for P3-PEI, while radiative rate constants (kr) rise by factors of 3-6. Atomic force microscopy shows a dramatic reduction in surface roughness, with Ra decreasing from 549.8 nm in pristine P1 to 145.3 nm in P1-PEIFG, indicating improved film homogeneity and smoother morphologies. Raman spectroscopy and 2D mapping confirm enhanced chain ordering and reduced aggregation, with signal intensity increasing from ∼23,000 au in pristine P1 to ∼1.1 × 106 a.u. in P1-PEI. Additionally, time-dependent color evolution under varying environmental conditions sunlight, +4 °C, and -20 °C demonstrates the potential of these composites as stimuli-responsive coatings. This work presents a scalable, nondestructive strategy to tailor the optical, morphological, and environmental-response properties of conjugated polymer films, with direct implications for sensors, organic electronics, and smart coating applications. Collectively, these findings demonstrate that physically interacting amine-based additives effectively increase interchain spacing, weaken π-π interactions, and suppress aggregation in conjugated polymer solids. This research advances the current state of the art by achieving a 10-fold increase in solid-state quantum yield and establishing a quantitative mechanistic link between supramolecular organization and macroscopic homogeneity through Raman 2D mapping, while introducing dynamic stimuli responsiveness.
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