Search Results (143)

Some common conductive polymers are polyfuran, polyacetylene, polythiophene, and poly-pyrrole. Since their discovery, many researchers have been exploring and evaluating their conductive and electronic properties. Various applications have been developed for conductive materials. Their biocompatibility offers a new alternative for studying and solving complex problems, such as cellular activity, or, more recently, for use as neural implants and as an alternative to spinal cord regenerative tissue. This is particularly true for the use of poly pyrrole. The main obstacle lies in estimating some of the mechanical properties, such as Young’s or shear modulus values for poly pyrrole, since these vary depending on the type of synthesis used. This article outlines a composite methodology for characterizing the elastic modulus according to ASTM D882 and the shear modulus according to E143 standards. It is specifically designed and applied for 3D composite samples involving PLA and PPy, where the PPy was processed by plasma oxidation. As a result, an increase of 360.11 MPa in the modulus of elasticity is observed on samples coated with poly pyrrole. The results are evaluated through a numerical test using COMSOL Multiphysics software 6.2 version, finding a similar behavior in the elastic zone, as indicated by the stress–strain diagram. The statistical analysis yields consistent data for tensile and shear results, with low to moderate variability. Full article

A novel process for the synthesis of binder-free, porous nickel/polythiophene-functionalized sulfur (Ni/S-PTh) composite cathodes for lithium–sulfur (Li–S) batteries is introduced in this paper. Initially, a polyvinyl butyl polymer scaffold is 3D printed, then coated with a graphite-based conducting layer, and, finally, it is pulse-plated for nickel deposition to produce a high-surface-area, mechanically stable current collector. S-PTh particles are afterwards co-deposited into the Ni matrix through composite electrodeposition. After the dissolution of the polymer template, the resulting self-standing electrodes still maintain porous structure with uniform sulfur distribution and a distinct transition between the dense Ni layer and the Ni/S-PTh composite layer. Electrochemical characterization of the Ni/S-PTh composite cathodes by galvanostatic cycling at C/10 rate results in an initial specific discharge capacity of ~1120 mAh·g⁻¹ and a specific capacity of ~910 mAh·g⁻¹ after 200 cycles, resulting in a high capacity retention of ~81 %. For our novel approach, no steps at high temperatures or toxic solvents are involved and the need for polymer binders and conductive additives is avoided. These results demonstrate the potential of composite electrodeposition in combination with 3D printing for producing sustainable, high-performance sulfur cathodes with tunable architecture. Full article

Polybenzoxazine (PBz)-based conducting materials have gained significant attention due to their unique combination of thermal stability, mechanical strength, and electrical conductivity. These polymers integrate the inherent advantages of polybenzoxazines—such as low water absorption, high glass transition temperature, and excellent chemical resistance—with the electrical properties of conducting polymers like polyaniline, polypyrrole, and polythiophene. The incorporation of conductive elements in polybenzoxazine networks can be achieved through blending, in situ polymerization, or hybridization with nanostructures such as graphene, carbon nanotubes, or metallic nanoparticles. These modifications enhance their charge transport properties, making them suitable for applications in flexible electronics, energy storage devices, sensors, and electromagnetic shielding materials. Furthermore, studies highlight that polybenzoxazine matrices can improve the processability and environmental stability of conventional conducting polymers while maintaining high conductivity. The structure–property relationships of polybenzoxazine-based composites demonstrate that tailoring monomer composition and polymerization conditions can significantly influence their conductivity, thermal stability, and mechanical properties. This review summarizes recent advancements in PBz composites, focusing on their synthesis, structural modifications, conductivity mechanisms, and potential applications in advanced energy storage systems. Full article

In this work, conductive polymers, i.e., polyaniline (PANI) and its copolymers with polypyrrole (PPy), polythiophene (PTh), and poly (3,4-ethylenedioxythiophene) (PEDOT) were synthesized following chemical oxidative polymerization methods and used in the construction of supercapacitor devices. These conductive copolymers were characterized by structural (FTIR, XRD), morphological (FESEM), electrochemical (CV and GCD), and impedance spectroscopy studies. The PANI-PPy copolymer showed higher sp. capacitance of 420 F/g and cyclic capacitive retention of 97.8% compared to the other copolymers. Additionally, Tafel extrapolation studies demonstrated that the PANI-PEDOT had the lowest corrosion rate. To further assess performance, asymmetric supercapacitor devices (ASDs) were fabricated using prepared materials. GCD analysis demonstrated that the PANI-PTh//AC device achieved a sp. capacitance of 81 F/g and power density of 550 W/kg, while the PANI-PPy//AC device exhibited a capacitance of 69 F/g. PANI-PTh//AC device shows superior performance over other electrode configurations. Full article

Self-powered ultraviolet photodetectors hold significant potential for diverse applications across both military and civilian fields. Owing to its wide bandgap, high electron mobility, and adaptability to various substrates, gallium oxide (Ga₂O₃) serves as a crucial material for fabricating self-powered ultraviolet photodetectors. Photodetectors based on p-n heterojunctions of conductive polymers and gallium oxide have great application potential benefiting from unique advantages of conductive polymers. This review provides an extensive overview of typical ultraviolet photodetectors based on conductive polymer/gallium oxide heterojunctions, focusing on the physical structure, fabrication process, and photoelectric properties of heterojunction devices formed by Ga₂O₃ with conductive polymers like polythiophene, polyaniline, and polycarbazole, etc. Different conductive polymers yield varying performance improvements in the fabricated devices: polythiophene/Ga₂O₃ devices exhibit high conductivity and flexible bandgap tuning to meet diverse wavelength detection needs; PANI/Ga₂O₃ devices feature simple fabrication and low cost, with doping control to enhance charge carrier transport efficiency; polycarbazole/Ga₂O₃ devices offer high thermal stability and efficient hole transport. Among them, the polythiophene/Ga₂O₃ device demonstrates the most superior overall performance, making it the ideal choice for high-performance Ga₂O₃-based photodetectors and a representative of such research. This review identifies the existing technical challenges and provides valuable insights for designing more efficient Ga₂O₃/conductive polymer heterojunction photodetectors. Full article

Thin films of monomeric species polythiophene (PTh), poly-(3,4-ethylenedioxythiophene) (PEDOT), and the copolymer PTh/PEDOT were prepared through electropolymerization and deposited above fluorine-doped tin oxide (FTO) substrates. The functional groups of the monomeric species (PTh, PEDOT) and polymeric species (PTh/PEDOT) were characterized by Fourier-transform infrared spectroscopy, while morphological properties were evaluated using scanning electron microscopy, optical microscopy, and atomic force microscopy. The analysis showed that monomers films exhibited less material deposition; otherwise, the copolymer PTh/PEDOT showed better deposition on substrate. In addition, the electrochemical characterization showed that the materials that resulted from copolymerization presented an improvement in electrochemical properties relating to monomer properties. The effect of overoxidation of the monomers applied during the electropolymerization process is also known. Full article

Conducting polymers (CPs) have emerged as promising materials for gas sensors due to their organic nature coupled with unique and versatile optical, electrical, chemical, and electrochemical properties. This review provides a comprehensive overview of the latest developments in conducting polymer-based gas sensors. First, the fundamental gas sensing mechanisms in CPs-based sensors are elucidated, covering diverse transduction modes including electrochemical, chemiresistive, optical, piezoelectric, and field-effect transistor-based sensing. Next, the various types of conducting polymers employed in gas sensors, such as polypyrrole, polyaniline, polythiophene, and their composites are introduced, with emphasis on their synthesis methods, structural characteristics, and gas sensing response properties. Finally, the wide range of applications of these sensors is discussed, spanning industrial process control, environmental monitoring, food safety, biomedical diagnosis, and other fields, as well as existing issues such as long-term stability and humidity interference, and a summary of the biocompatibility and regulatory standards of these conductive polymers is provided. By integrating insights from sensing mechanisms, materials, and applications, this review offers a holistic understanding of CPs-based gas sensors. It also highlights future research directions, including device miniaturization, AI-assisted gas identification, multifunctional integrated sensing systems, wearable and flexible sensor platforms, and enhanced sensitivity, selectivity, and on-site detection capabilities. Full article

This review examines the distinct advantages of organic semiconductors over conventional insulating polymers as optically active materials in photonic applications. We analyze the fundamental principles governing their unique optical and electronic properties, from basic conjugated polymer systems to advanced molecular architectures. The review systematically explores key material classes, including polyfluorenes, polyphenylene vinylenes, and polythiophenes, highlighting their dual electrical–optical functionality unavailable in passive polymer systems. Particular attention is given to polymer blends, composites, and hybrid organic–inorganic systems, demonstrating how semiconductor properties enable enhanced performance through materials engineering. We contrast passive components with active photonic devices, illustrating how the semiconductor nature of these polymers facilitates novel functionalities beyond simple light guiding. The review explores emerging applications in neuromorphic photonics, quantum systems, and bio-integrated devices, where the combined electronic–optical properties of organic semiconductors create unique capabilities impossible with insulating polymers. Finally, we discuss design strategies for optimizing these distinctive properties and present perspectives on future developments. This review establishes organic semiconductors as transformative materials for advancing photonic technologies through their combined electronic–optical functionality. Full article

Microbial fuel cell (MFC) is a bioelectrochemical device for biomass power generation, and the anode material determines the performance of the MFC. In this study, a novel anode material, which is a combination of graphite oxide/polythiophene (GO/Pth), was prepared on a carbon felt (CF) substrate and exhibited excellent capacitive performance. The MFC equipped with the CF/GO/Pth anode achieved a significant increase in power density, reaching a maximum value of 2.9 W/m³, which is a 3.32-fold increase in power density compared to that of the CF anode. Meanwhile, the CF/GO/Pth anode stored charge Q_t value was as high as 11,258.68 C/m², which was 4.13 times higher than that of the CF anode (2727.66 C/m²). High-throughput analysis showed that the percentage of charge-producing bacteria on the surface of the CF/GO/Pth anode was more than 90%, which was significantly higher than that of the charge-producing bacteria attached to the CF anode. This further confirms the significant enhancement of MFC performance by materials such as GO and Pth coated on the CF surface. In this study, CF/GO/Pth anode materials were prepared to successfully enhance the power output and charge storage capacity of MFC, and they also showed broad application prospects in the degradation of polluted waste liquids. Full article

The field of wearable sensors has evolved with operating devices capable of measuring biomechanics and biometrics, and detecting speech. The transduction, being the conversion of the biosignal to a measurable and quantifiable electrical signal, is governed by a conductive organic polymer. Meanwhile, the conformality of skin to the substrate is quintessential. Both the substrate and the conductive polymer must work in concert to reversibly deform with the user’s movements for motion tracking. While polydimethylsiloxane shows mechanical compliance as a sensor substrate, it is of environmental interest to replace it with sustainable and degradable alternatives. As both the bulk of the weight and area of the sensor consist of the substrate, using renewable and biodegradable materials for its preparation would be an important step toward improving the lifecycle of wearable sensors. This review highlights wearable resistive sensors that are prepared from naturally occurring polymers that are both sustainable and biodegradable. Conductive polythiophenes are also presented, as well as how they are integrated into the biopolymer for sensors showing mechanical compliance with skin. This polymer is highlighted because of its structural conformality, conductivity, and processability, ensuring it fulfils the requirements for its use in sensors without adversely affecting the overall sustainability and biodegradability of resistive sensors. Different sustainable resistive sensors are also presented, and their performance is compared to conventional sensors to illustrate the successful integration of the biosourced polymers into sensors without comprising the desired elasticity and sensitivity to movement. The current state-of-the-art in sustainable resistive sensors is presented, along with knowledge of how biopolymers from different fields can be leveraged in the rational design of the next generation of sustainable sensors that can potentially be composted after their use. Full article

This study presents an effective method to remove organic dyes from wastewater, using a composite of few-layered porous (FLP) Ti₃C₂T_x MXene and polythiophene (PTh) nanospheres. The FLP MXene, which was pre-synthesized by a series of intercalation, heat-induced TiO₂ formation, and its selective etching, was combined with PTh nanospheres via a simple solution method. The composite effectively removed various organic dyes, but its efficiency was altered depending on the type of dye. Particularly, the removal efficiency of methylene blue reached 91.3% and 97.8% after irradiation for 10 min and 1 h, respectively. The high dye removal efficiency was attributed to the large surface area (32.01 m²/g) of the composite, strong electrostatic interaction between the composite and dye molecules, and active photodegradation process. The strong electrostatic interaction and large surface area could facilitate the adsorption of dye molecules, while photocatalytic activity further enhance dye removal under light. These results are indicative that the PTh/FLP MXene composite may be a promising material for environmental remediation through synergistic processes of adsorption and photocatalysis. Full article

Pyrene (Pr) was used to improve the electrochemical and electrochromic properties of polythiophene copolymerized with 3,4-ethylenedioxythiophene (EDOT). The corresponding product, poly(3,4-ethylenedioxythiophene-co-Pyrene) (P(EDOT-co-Pr)), was successfully synthesized by electrochemical polymerization with different monomer concentrations in propylene carbonate solution containing 0.1 M lithium perchlorate (LiClO₄/PC (0.1 M)). The homopolymer and copolymer films were analyzed by Fourier transform infrared spectroscopy (FT-IR), color-coordinate and colorimetric methods, cyclic voltammetry (CV), spectroelectrochemistry (SEC), and UV–visible spectroscopy (UV-Vis). Homopolymer poly(3,4-ethylenedioxythiophene) (PEDOT) and the P(EDOT-co-Pr) copolymer were investigated, which included examining their colorimetric, electrochemical, and electrochromic characteristics. The color shifts resulting from redox reactions of the polymers were also observed. The copolymers with different monomer concentrations achieved multicolor shifts, such as light purple, dark blue, dark red, green, and earthy yellow. Moreover, P(EDOT-co-Pr) had a small optical bandgap (1.74–1.83 eV), excellent optical contrast (31.68–45.96%), and high coloring efficiency (350–507 cm² C⁻¹). In particular, P(EDOT1-co-Pr3) exhibited outstanding cycling stability, retaining 91% of its initial optical contrast after cycling for 10,000 s, and it is expected to be a promising candidate copolymer for electrochromic applications. Full article

The electrochromic phenomenon of conducting polymer is mainly dominated by the π-π* band transition. The π conjugation is influenced by the coplanarity between polymer units, deviations from which can lead to an increased ionization potential and band gap values. In order to investigate the effect of plane distortion angle on electrochromic color in the main chain structure of polymerization, high-performance poly(3,3′-dimethyl-2,2′-bithiophene) (PDMeBTh) with a large plane distortion angle is successfully synthesized in boron trifluoride diethyl etherate (BFEE) by the electrochemical anodic oxidation method. The electrochemical and thermal properties of PDMeBTh prepared from BFEE and ACN/TBATFB are compared. The electrochromic properties of PDMeBTh are systematically investigated. The PDMeBTh shows a different color change (orange-yellow in the neutral state) compared to poly (3-methylthiophene) (light-red in the neutral state) due to the large torsion angle between thiophene rings of the main polymer chain. The optical contrast, response time, and coloring efficiency (CE) of the prepared PDMeBTh are also studied, which shows good electrochromic properties. For practical applications, an electrochromic device is fabricated by the PDMeBTh and PEDOT. The color of the device can be reversibly changed between orange-yellow and dark blue. The light contrast of the device is 27% at 433 nm and 61% at 634 nm. The CE value of the device is 403 cm² C⁻¹ at 433 nm and 577 cm² C⁻¹ at 634 nm. The constructed device also has good open circuit memory and electrochromic stability, showing good potential for practical applications. Full article

In the development of wearable electronic devices, the composite modification of conductive polymers and single-walled carbon nanotubes (SWCNTs) has become a burgeoning research area. This study presents the synthesis of a novel polythiophene derivative, poly(3-alkoxythiophene) (P3(TEG)T), with alkoxy side chains. Different molecular weight variants of P3(TEG)T (P1–P4) were prepared and combined with SWCNTs to form composite materials. Density functional theory (DFT) calculations revealed a reduced bandgap for P3(TEG)T. Raman spectroscopy demonstrated π-π interactions between P3(TEG)T and SWCNTs, facilitating the dispersion of single-walled carbon nanotubes and the formation of a continuous conductive network. Among the composite films, P4/SWCNTs-0.9 exhibited the highest thermoelectric performance, with a power factor (PF) value of 449.50 μW m⁻¹ K⁻². The fabricated flexible thermoelectric device achieved an output power of 3976.92 nW at 50 K, with a tensile strength of 59.34 MPa for P4/SWCNTs. Our findings highlight the strong interfacial interactions between P3(TEG)T and SWCNTs in the composite material, providing an effective charge transfer pathway. Furthermore, an improvement in the tensile performance was observed with an increase in the molecular weight of the polymer used in the composite, offering a viable platform for the development of high-performance flexible organic thermoelectric materials. Full article