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The design of smart photoelectrodes is used to modulate and control the spatio-temporal production of reactive oxygen species (ROS). In this work, we develop photoactive films with tunable nanostructured morphologies to favor ROS production photostimulation. To that aim, we synthesized graft copolymers, made of poly(3-hexylthiophene) (P3HT) and poly(ε-caprolactone) (PCL), P3HT--PCL, which were employed to fabricate compact films by drop casting. The films were further subjected to a thermo-oxidative treatment in the presence of HO at 42 °C. This led to nanostructured films with a porosity (∼500 nm diameter and ∼70 nm height) controlled at specific copolymer compositions, as determined by atomic force microscopy (AFM). The nanostructured P3HT films possess higher storage moduli (') than flat P3HT films, as determined by nanoindentation measurements. Finally, the performance of nanostructured P3HT films as photoelectrodes is assessed in a three-electrode electrochemical cell upon visible-light irradiation ( = 467 nm), leading to the spatiotemporal production of HO at non-cytotoxic levels for future non-invasive redox medicine applications.
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http://dx.doi.org/10.1039/d5nr00027k | DOI Listing |
Phys Chem Chem Phys
August 2025
Department of Chemistry and Biochemistry, Auburn University, Auburn, Alabama 36849, USA.
Charge carrier mobility is a key factor underlying the performance of conjugated polymers as conductive materials for flexible and lightweight electronics. Chemical doping is typically used to improve polymer conductivity by increasing the carrier density. However, doping consequently induces both morphological and electrostatic changes within the polymer that impact charge mobility, the extent to which remains unclear.
View Article and Find Full Text PDFACS Omega
August 2025
Solar Energy Institute, Ege University, 35000 Izmir, Turkey.
In this study, we explore the effect of halogen-light-assisted (LA) annealing on the crystallization of poly-(3-hexylthiophene) (P3HT) films and the morphology of P3HT:[6,6]-phenyl-C61-butyric acid methyl ester (PCBM) blends, along with their impact on organic solar cell performance. Samples were annealed at various temperatures (100-120 °C) and durations (5-15 min) using both conventional hot plate (HP) and LA methods. Structural analysis showed that LA annealing significantly enhanced the crystallinity of P3HT films through improved in-plane molecular stacking.
View Article and Find Full Text PDFACS Nano
August 2025
Department of Chemical Engineering, Pohang University of Science and Technology, Pohang 37673, Republic of Korea.
Doping of conjugated polymers, which offers precise control over energy levels and electrical conductivity, has faced setbacks because of its low doping efficiency. The majority of generated charge carriers become bound to dopant counterions through Coulomb interaction, leaving only a small fraction of free charges. Although the inherent energetic disorder in polymers may reduce the theoretically predicted Coulomb potential barrier and facilitate the release of bound charges to become mobile, this hypothesis has not been thoroughly quantified.
View Article and Find Full Text PDFJ Phys Chem B
July 2025
Aiiso Yufeng Li Family Department of Chemical and Nano Engineering, UC San Diego, La Jolla, California92093-0448, United States.
Electron delocalization between monomers in conjugated polymers influences both the charge transport and the mechanical properties of this class of materials. While this delocalization is generally understood to be maximized by coplanar monomer arrangements that enable π-orbital overlap, the precise geometric factors controlling delocalization remain incompletely characterized. Current molecular mechanics (MM) models of conjugated polymers primarily focus on intermonomer dihedral torsion, neglecting the potential effects of out-of-plane ("improper") torsion between monomers.
View Article and Find Full Text PDFMolecules
June 2025
Division of Applied Chemistry, Faculty of Engineering, Hokkaido University, Sapporo 060-8628, Hokkaido, Japan.
Conjugated polymer nanoparticles (CP NPs) attract attention as nanoscale materials used for a variety of applications. In relation to this, the internal structure of CP NPs is an important factor for their properties, and numerous investigations have been carried out to control their nanomorphology. Here, we report the formation of CP NPs from defect-free cyclic poly(3-hexylthiophene) (-P3HT) using a microfluidic device, and the effect of polymer topology on their structural and solvatochromic properties was investigated.
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