Search Results (40)

With the rapid development of Internet of Things (IoT) and bioscience technology, wearable smart devices are developing toward advanced trends such as flexibility, convenience and environmental-friendliness. Poly (p-styrenesulfonic acid) (PSS), as a common template and dispersant, is indispensable in the polymerization of conductive polymers. However, the doping amount of PSS has a significant effect on the electrical conductivity of the polymer. Herein, different molar quantities of PSS were used to assist the polymerization of 3,4-ethylenedioxythiophene (EDOT) monomer in a horseradish peroxidase/hydrogen peroxide (HRP/H₂O₂) low-temperature system to obtain conductive finishing solutions with more excellent electrical properties. Then, the polyester nonwoven fabric was immersed in the conductive finishing solution, and when the addition ratio of EDOT and PSS was 1:2, the conductive performance was optimal (3.27 KΩ cm⁻¹). Finally, the conductive fabric was assembled into a pressure sensor and a temperature sensor, which can transmit Morse code in the form of single-parameter (pressure response or temperature response) or collaboration. Overall, this research has great potential for production of poly(3,4-ethylenedioxythiophene) (PEDOT)-based composites and their applications in smart wearable device. Full article

Vitamins are crucial micro-nutrients for overall well-being, making continuous monitoring essential. There are demands to provide an alternative detection, especially using a portable detection or a point-of-care-testing (POCT) device. One promising approach is employing an in situ electro-polymerised MIP (eMIP), which offers a straightforward polymerisation technique on screen-printed electrodes (SPEs). Here, we report a review based on three databases (PubMed, Scopus, and Web of Science) from 2014 to 2024 using medical subject heading (MeSH) terms “electrochemical polymerisation” OR “electropolymerisation” crossed with the terms “molecularly imprinted polymer” AND “vitamin A” OR “vitamin D” OR “vitamin E” OR “vitamin K” OR “fat soluble vitamin” OR “vitamin B” OR “vitamin C” OR “water soluble vitamin”. The resulting 12 articles covered the detection of vitamins in ascorbic acid, riboflavin, cholecalciferol, calcifediol, and menadione using monomers of catechol (CAT), 3,4-ethylenedioxythiophene (EDOT), o-aminophenol (oAP), o-phenylenediamine (oPD), pyrrole, p-aminophenol (pAP), p-phenylenediamine (pPD), or resorcinol (RES), using common bare electrodes including graphite rod electrode (GRE), glassy carbon electrode (GCE), gold electrode (GE), and screen-printed carbon electrode (SPCE). The most common electrochemical detections were differential pulse voltammetry (DPV) and linear sweep voltammetry (LSV). The imprinting factor (IF) of the eMIP-modified electrodes were from 1.6 to 21.0, whereas the cross-reactivity was from 0.0% to 29.9%. Several types of food and biological samples were tested, such as supplement tablets, poultry and pharmaceutical drugs, soft drinks, beverages, milk, infant formula, human and calf serum, and human plasma. However, more discoveries and development of detection methods needs to be performed, especially for the vitamins that have not been studied yet. This will allow the improvement in the application of eMIPs on portable-based detection and POCT devices. Full article

The development of sensitive and selective methods for detecting pesticide residues has become paramount for ensuring food safety. In this work, a high-performance molecularly imprinted electrochemical sensor based on the composite of Cu-BTC- and FeCo-ZIF-derived N-doped carbon (FeCo@NC), synthesized by pyrolysis and electrodeposition, was developed for Benomyl (BN) detection. The materials were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). In this sensing system, the Cu-BTC/FeCo@NC composite used as the electrode substrate displayed a large specific surface area, high electronic conductivity, and rich active catalytic sites, demonstrating excellent electrocatalytic ability toward BN oxidation. Meanwhile, Cu-BTC, with its abundant surface functional groups, facilitated strong hydrogen bonding interactions with the imprinted template molecule of 3,4-ethylenedioxythiophene (EDOT), promoting the formation of a uniform molecularly imprinted membrane on the substrate material surface. The introduced MIP-PEDOT could enhance the selective recognition and enrichment of the target BN, leading to an amplified detection signal. Thanks to the synergistic effects between Cu-BTC/FeCo@NC and MIP-PEDOT, the proposed sensor achieved a low detection limit of 1.67 nM. Furthermore, the fabricated sensor exhibited high selectivity, reproducibility, and interference resistance in detecting BN. The method has been successfully applied to the determination of BN in vegetable and fruit samples, indicating its potential for use in practical applications. Full article

Chemiresistive sensors integrated with functionalized conductive polymers have emerged as promising candidates for wearable applications, offering adequate protection against highly toxic and widely prevalent organophosphate compounds, due to their high sensitivity, room-temperature operation, and straightforward fabrication process. However, these chemiresistive sensors exhibit poor resistance to water vapor due to the intrinsic properties of these conducting polymers, likely leading to false sensor alarms. In this study, we engineered a series of water-vapor-resistant, yet organophosphate-sensitive, conducting polymers by electro-copolymerizing hexafluoroisopropanol (HFIP)-grafted 3,4-ethylenedioxythiophene (EDOT-HFIP) with EDOT comonomers bearing hydrophobic alkyl groups of varying lengths (ethyl, butyl, and hexyl). The typical results indicated that increasing the alkyl length and alkyl-bearing EDOT comonomer composition significantly enhanced the water resistance of the EDOT-HFIP copolymers and the copolymer-integrated chemiresistive sensor, but this improvement came at the unacceptable cost of compromising the organophosphate sensitivity. To address this issue, we developed a surface-driven phase-segregation strategy to enrich the alkyl chains on the surface while concentrating the HFIP groups beneath it by treating the silica substrates using oxygen plasma before polymer spin coating, thus decoupling and optimizing the two mutually competing characteristics. Finally, the chemiresistive sensor integrated with the EDOT-HFIP copolymer containing 10% hexyl-grafted EDOT comonomer exhibited an organophosphate (DMMP) resistive response 657 times higher than that to water vapor, and more than two times that of a PEDOT-HFIP sensor, while preserving the original specific sensitivity of the PEDOT-HFIP sensor. Furthermore, it demonstrated a markedly improved shelf storage stability, being directly exposed to air for 14 days without any special protection. We envision that this surface-driven phase-segregation strategy could offer a promising solution to the significant challenge of air moisture interference in highly sensitive polymer sensors, promoting their practical use in real-world applications. Full article

In this investigation, electrochemical deposition procedures were reported to synthesize a novel composite polymer, 3-methylpyrrole-dodecyl sulfate sodium/3,4-ethylenedioxythiophene (3MPY-SDS/EDOT) coatings, on OL 37 samples for anticorrosion protection. The anionic surfactant dodecyl sulfate sodium used in deposition can have a relevant action on the protective capacity. These coatings were considered by cyclic voltammetry (CV), Fourier transform infrared (FT-IR) spectroscopy, and scanning electron microscopy (SEM) methods. The protective attributes of OL 37 coated with P3MPY-SDS/PEDOT have been examined by potentiostatic and potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) procedures in 0.5 M H₂SO₄. The corrosion rate of the P3MPY-SDS/PEDOT-coated OL 37 sample was found to be approximately nine times lower than that of the uncoated sample. The protective layers of these composites demonstrate an effectiveness of over 90%. The optimal efficiency is obtained by electrochemical deposition of P3MPY-SDS/PEDOT, performed at applied potentials of 1.0 V, 1.2 V, and 1.4 V, with current densities of 3 mA/cm² and 5 mA/cm² and a molar ratio of 5:3 at 20 min. The influence of electrochemical polymerization parameters—applied potential, current density, scan rate, cycle number, and monomer ratio—on the protective behavior of P3MPY-SDS/PEDOT layers was analyzed, identifying optimal synthesis conditions. Corrosion examinations confirmed that P3MPY-SDS/PEDOT coatings provide effective protection for OL 37 in a corrosive environment. 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

In this article, a series of novel conducting copolymers P(FuPy-co-EDOT) are prepared via cyclic voltammetry electropolymerization method by using N-furfuryl pyrrole (FuPy) and 3,4-ethylenedioxythiophene (EDOT) as comonomers. The molecular structure, surface morphology, electrochemical, and optical properties of the resulting copolymers are characterized in detail upon varying the feed ratios of FuPy/EDOT in the range of 1/1 to 1/9. The results demonstrate that the prepared P(FuPy-co-EDOT) copolymers with a higher proportion of EDOT units (FuPy/EDOT: 2/8~1/9) possess good redox activity, tunable optical absorption performances, and low band gaps (1.75~1.86 eV). Spectroelectrochemistry studies indicate that the resulting copolymers with increased EDOT units show strengthened electrochromic characteristics, exhibiting a red-to-green-to-blue multicolor reversible transition, especially for the P(FuPy₁-co-EDOT₉) copolymer films. They also show increased optical contrast (9~34%), fast response time (0.8~2.4 s), and good coloring efficiency (110~362 cm² C⁻¹). Additionally, the complementary bilayer P(FuPy-co-EDOT)/PEDOT electrochromic devices (ECDs) are also assembled and evaluated to hold excellent electrochromic switching performances with relatively high optical contrast (25%), rapid response time (0.9 s), and satisfactory coloring efficiency (416 cm² C⁻¹). Together with the superior open circuit memory and cycling stability, they can be used as a new type of electrochromic material and have considerable prospects as promising candidates for electrochromic devices. Full article

Electropolymerization is a convenient way to obtain conducting polymers (CPs) directly adhered to an electrode surface. CPs are well-known for their various application fields in photovoltaic cells, chemical sensors, and electronics. By implementing chirality into a CP, the application possibilities will spread further onto chiral sensors or optoelectronics. In this work, we introduce a new inherently chiral polymer based on a macrocyclic 3,4-ethylenedioxythiophene-diketopyrrolopyrrole-3,4-ethylenedioxythiophene triad (EDOT-DPP-EDOT) fused by 1,4-phenylene groups, which was prepared via oxidative electropolymerization directly on the electrode surface. The investigation of the chiroptical properties was performed by circular dichroism spectroscopy in the solid state. The enantiomeric pure polymer films obtained showed dissymmetry factors of up to −2.71 × 10⁻⁴, whereby linear dichroism contributions can be widely excluded. Full article

In the field of contemporary epidermal bioelectronics, there is a demand for energy supplies that are safe, lightweight, flexible and robust. In this work, double-network polymer hydrogels were synthesized by polymerization of 3,4-ethylenedioxythiophene (EDOT) into a poly(vinyl alcohol)/poly(ethylene glycol diacrylate) (PVA/PEGDA) double-network hydrogel matrix. The PEDOT-PVA/PEGDA double-network hydrogel shows both excellent mechanical and electrochemical performance, having a strain up to 498%, electrical conductivity as high as 5 S m⁻¹ and specific capacitance of 84.1 ± 3.6 mF cm⁻². After assembling two PEDOT-PVA/PEGDA double-network hydrogel electrodes with the free-standing boron cross-linked PVA/KCl hydrogel electrolyte, the formed supercapacitor device exhibits a specific capacitance of 54.5 mF cm⁻² at 10 mV s⁻¹, with an energy density of 4.7 μWh cm⁻². The device exhibits excellent electrochemical stability with 97.6% capacitance retention after 3000 charging–discharging cycles. In addition, the hydrogel also exhibits great sensitivity to strains and excellent antifouling properties. It was also found that the abovementioned hydrogel can achieve stable signals under both small and large deformations as a flexible sensor. The flexible and antifouling PEDOT-PVA/PEGDA double-network hydrogel-based supercapacitor is a promising power storage device with potential applications in wearable electronics. Full article

In this research, two polymers of P1 and P2 based on monomers consisting of thiophene, 3,4-Ethylenedioxythiophene (EDOT) and diketopyrrolopyrrole (DPP) are designed and obtained via Stille coupling polycondensation. The material shows excellent coplanarity and structural regularity due to the fine planarity of DPP itself and the weak non-covalent bonding interactions existing between the three units. Two different lengths of non-conjugated side chains are introduced and this has an effect on the intermolecular chain stacking, causing the film absorption to display different characteristic properties. On the other hand, the difference in the side chains does not have a significant effect on the thermal stability and the energy levels of the frontier orbitals of the materials, which is related to the fact that the materials both feature extremely high conjugation lengths and specific molecular compositions. Microscopic investigations targeting the side chains provide a contribution to the further design of organic semiconductor materials that meet device requirements. Tests based on organic transistors show a slight difference in conductivity between the two polymers, with P2 having better hole mobility than P1. This study highlights the importance of the impact of side chains on device performance, especially in the field of organic electronics. Full article

Therapeutic solutions for injuries in the peripheral nervous system are limited and not existing in the case of the central nervous system. The electrical stimulation of cells through a cell-supporting conductive scaffold may contribute to new therapeutic solutions for nerve regeneration. In this work, biocompatible Polylactic acid (PLA) fibrous scaffolds incorporating Fe(III)Tosylate (FeTos) were produced by electrospinning a mixture of PLA/FeTos solutions towards a rotating cylinder, inducing fiber alignment. Fibers were coated with the conductive polymer Poly(3,4 ethylenedioxythiophene) (PEDOT) formed by vapor-phase polymerization of EDOT at 70 °C for 2 h. Different solvents (ETH, DMF and THF) were used as FeTos solvents to investigate the impact on the scaffold’s conductivity. Scaffold conductivity was estimated to be as high as 1.50 × 10⁻¹ S/cm when FeTos was dissolved in DMF. In vitro tests were performed to evaluate possible scaffold cytotoxicity, following ISO 10993-5, revealing no cytotoxic effects. Differentiation and growth of cells from the neural cell line SH-SY5Y seeded on the scaffolds were also assessed, with neuritic extensions observed in cells differentiated in neurons with retinoic acid. These extensions tended to follow the preferential alignment of the scaffold fibers. Full article

An industrial submicron-sized Fe₂O₃ with no special shape was decorated by a multi-layer coating of oxygen-deficient TiO_2−x and conducting polymer PEDOT (poly 3,4-ethylenedioxythiophene). A facile sol–gel method followed by an EDOT polymerization process was adopted to synthesize the hierarchical coating composite. The microstructure and phase composition were characterized using an X-ray diffraction analysis (XRD), scanning electron microscopy (SEM), and transmission electron microscopy (TEM). In particular, the existence state of PEDOT was determined using Fourier transform infrared (FT-IR) and a thermogravimetric (TG) analysis. The characterization results indicated the dual phase was well-coated on the Fe₂O₃ and its thickness was nano scale. Electrochemical characterization indicated that the multi-layer coating was helpful for significantly enhancing the cycle stability of the Fe₂O₃, and its electrochemical performance was even better than that of the single-layer coating samples. The synergistic effects of the ceramic phase and conducting polymer were demonstrated to be useful for improving electrochemical properties. The obtained FTP-24 sample exhibited a specific discharge capacity of 588.9 mAh/g after 360 cycles at a current density of 100 mA/g, which effectively improved the intrinsic cycling performance of the Fe₂O₃, with a corresponding discharge capacity of 50 mAh/g after 30 cycles. Full article

Two poly(3,4-ethylenedioxythiophene) polyrotaxanes (PEDOT∙TMe-βCD and PEDOT∙TMe-γCD) end-capped by pyrene (Py) were synthesized by oxidative polymerization of EDOT encapsulated into TMe-βCD or TMe-γCD cavities with iron (III) chloride (FeCl₃) in water and chemically characterized. The effect of TMe-βCD or TMe-γCD encapsulation of PEDOT backbones on the molecular weight, thermal stability, and solubility were investigated in depth. UV–vis absorption, fluorescence (F_L), phosphorescence (P_H), quantum efficiencies, and lifetimes in water and acetonitrile were also explored, together with their surface morphology and electrical properties. Furthermore, dynamic light scattering was used to study the hydrodynamic diameter (DH) and z-potential (ZP-ζ) of the water soluble fractions of PEDOT∙TMe-βCD and PEDOT∙TMe-γCD. PEDOT∙TMe-βCD and PEDOT∙TMe-γCD exhibited a sharp monodisperse peak with a DH of 55 ± 15 nm and 122 ± 32 nm, respectively. The ZP-ζ value decreased from −31.23 mV for PEDOT∙TMe-βCD to −20.38 mV for PEDOT∙TMe-γCD, indicating that a negatively charged layer covers their surfaces. Surface pressure–area isotherms and Brewster angle microscopy (BAM) studies revealed the capability of the investigated compounds to organize into sizeable and homogeneous 2D supramolecular assemblies at the air–water interface. The control of the 2D monolayer organization through the thermodynamic parameters of PEDOT∙TMe-βCD and PEDOT∙TMe-γCD suggests potential for a wide range of optoelectronic applications. Full article

The molecular engineering of conjugated systems has proven to be an effective method for understanding structure–property relationships toward the advancement of optoelectronic properties and biosensing characteristics. Herein, a series of three thieno[3,4-c]pyrrole-4,6-dione (TPD)-based conjugated monomers, modified with electron-rich selenophene, 3,4-ethylenedioxythiophene (EDOT), or both building blocks (Se-TPD, EDOT-TPD, and EDOT-Se-TPD), were synthesized using Stille cross-coupling and electrochemically polymerized, and their electrochromic properties and applications in a glucose biosensing platform were explored. The influence of structural modification on electrochemical, electronic, optical, and biosensing properties was systematically investigated. The results showed that the cyclic voltammograms of EDOT-containing materials displayed a high charge capacity over a wide range of scan rates representing a quick charge propagation, making them appropriate materials for high-performance supercapacitor devices. UV-Vis studies revealed that EDOT-based materials presented wide-range absorptions, and thus low optical band gaps. These two EDOT-modified materials also exhibited superior optical contrasts and fast switching times, and further displayed multi-color properties in their neutral and fully oxidized states, enabling them to be promising materials for constructing advanced electrochromic devices. In the context of biosensing applications, a selenophene-containing polymer showed markedly lower performance, specifically in signal intensity and stability, which was attributed to the improper localization of biomolecules on the polymer surface. Overall, we demonstrated that relatively small changes in the structure had a significant impact on both optoelectronic and biosensing properties for TPD-based donor–acceptor polymers. Full article

In this work, the effect of iron(III) in the preparation of a conductive porous composite using a biomass waste-based starch template was evaluated. Biopolymers are obtained from natural sources, for instance, starch from potato waste, and its conversion into value-added products is highly significant in a circular economy. The biomass starch-based conductive cryogel was polymerized via chemical oxidation of 3,4-ethylenedioxythiophene (EDOT) using iron(III) p-toluenesulfonate as a strategy to functionalize porous biopolymers. Thermal, spectrophotometric, physical, and chemical properties of the starch template, starch/iron(III), and the conductive polymer composites were evaluated. The impedance data of the conductive polymer deposited onto the starch template confirmed that at a longer soaking time, the electrical performance of the composite was improved, slightly modifying its microstructure. The functionalization of porous cryogels and aerogels using polysaccharides as raw materials is of great interest for applications in electronic, environmental, and biological fields. Full article