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Electron beam (EB) irradiation, a powerful method for electronic and molecular structure regulation of polymer materials, has been proven to be an effective strategy to boost the electrical conductivity (σ) of PEDOT: PSS. However, the irradiation damage from chain scission and cross-linking has an adverse effect on the mechanical and thermal performance. Herein, we propose a convenient approach to enhance irradiation resistance property by adding a chemical oxidant, ammonium persulfate (APS), into PEDOT: PSS, in which irradiation-induced fragmentations can be reaggregated via initiating free radical polymerization through APS. The PEDOT: PSS films doped with 5 wt % APS were exposed to 10 MeV EB irradiation at doses ranging from 2.5 to 20 kGy. The electrical conductivity of PEDOT: PSS-APS films reached 596 S cm at a dose of 2.5 kGy, 2 orders of magnitude higher than that of pure PEDOT: PSS films (4.94 S cm), while the Seebeck coefficient remained nearly constant. An optimal thermoelectric power factor (PF) of 16.75 μW m K was achieved. The 1000-fold increase in carrier concentration () can elucidate the enhancement in the PF despite the deterioration of carrier mobility. During irradiation, more effective cross-linking occurred in PEDOT: PSS-APS films than in pure PEDOT: PSS. Structural characterization and DFT computational results implied that the imine or protonated amine brought by APS could not only improve the molecular structure but also narrow the band gap, which helped charge transport. The chain fragments caused by chain scission during irradiation could be polymerized via APS into new molecular chains, which influenced the transportation of charge carriers and resulted in enhanced thermal stability and mechanical properties of PEDOT: PSS-APS films. This work provides a simple and innovative treatment to improve both the thermoelectric property and the irradiation resistance of conducting polymers.
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http://dx.doi.org/10.1021/acsami.5c04618 | DOI Listing |
Macromol Biosci
September 2025
IMEM-BRT Group, Departament d'Enginyeria Química, EEBE, Universitat Politècnica de Catalunya, Barcelona, Spain.
This study investigates a multifunctional hydrogel system integrating carboxymethyl cellulose (CMC) in a 3D-printed limonene (LIM) scaffold coated with poly(3,4-ethylenedioxythiophene): polystyrene sulfonate (PEDOT:PSS). The system allows to enhance wound healing, prevent infections, and monitor the healing progress. CMC is crosslinked with citric acid (CA) to form the hydrogel matrix (CMC-CA), while the 3D-printed limonene (LIM) scaffold is embedded within the hydrogel to provide mechanical support.
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August 2025
Department of Chemistry and Biochemistry, Auburn University Auburn Alabama 36849 USA
Organic mixed ionic-electronic conducting polymers remain at the forefront of materials development for bioelectronic device applications. During electrochemical operation, structural dynamics and variations in electrostatic interactions in the polymer occur, which affect dual transport of the ions and electronic charge carriers. Such effects remain unclear due to a lack of spectroscopic methods capable of capturing these dynamics, which hinders the rational design of higher-performance polymers.
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September 2025
Dept. of Electrical and Electronic Engineering, Noakhali Science and Technology University, Noakhali 3814, Bangladesh.
Perovskite solar cells (PSCs) are rapidly advancing due to their high power conversion efficiencies (PCEs) and low fabrication costs. However, their commercialization is hindered by lead toxicity and the use of expensive materials, such as Spiro-OMeTAD and gold electrodes. This study presents a comprehensive SCAPS-1D simulation-based analysis of 14 perovskite absorber materials, spanning both Pb-based and lead-free compounds, under a unified device architecture using low-cost, nontoxic components: ZnO as the electron transport material (ETM), PEDOT:PSS + WO as a dual hole transport material, and nickel as the back contact.
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August 2025
Department of Industrial Systems Engineering and Design, Universitat Jaume I, Castelló de la Plana, Valencian Community, 12006, Spain.
Background: Thermoelectric (TE) materials can directly convert heat into electricity, which is beneficial for energy sustainability. Organic conducting polymers are TE materials that have drawn significant attention owing to different favorable properties, such as good processability, availability, flexibility, and intrinsically low thermal conductivity. Among the organic TEs, poly(3,4-ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) is the most extensively investigated material because of its stability and high electrical conductivity.
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August 2025
Laboratoire Matériaux Avancés et Phénomènes Quantiques, Faculté des Sciences de Tunis, Université de Tunis El Manar, Campus Universitaire, Tunis 2092, Tunisia.
This paper reports the use of P18-8, a novel conjugated polymer combining poly-(1,4-phenylene-ethynylene) and poly-(1,4-phenylene-vinylene), in the fabrication of an organic diode with the structure ITO/PEDOT:PSS/P18-8/LiF/Al. The electrical properties of the fabricated device were characterized using impedance spectroscopy across a frequency range of 100 Hz to 1 MHz at various applied voltages. The current density-voltage (-) characteristic exhibited ohmic behavior at low applied voltages, while at higher voltages, it conformed to the space charge limited current (SCLC) theory.
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