RESUMEN

Neural electrodes have recently been developed with surface modifications of conductive polymers, in particular poly(3,4-ethylenedioxythiophene) (PEDOT), and extensively studied for their roles in recording and stimulation, aiming to improve their biocompatibility. In this work, the implications for the design of practical neural sensors are clarified, and systematic procedures for their preparation are reported. In particular, this study introduces the use of in vitro double electrode experiments to mimic the responses of neural electrodes with a focus on signal-recording electrodes modified with PEDOT. Specifically, potential steps on one unmodified electrode in an array are used to identify the responses for PEDOT doped with different anions and compared with that of a bare platinum (Pt) electrode. The response is shown to be related to the rearrangement of ions in solution near the detector electrode resulting from the potential step, with a current transient seen at the detector electrode. A rapid response for PEDOT doped with chloride (ca. 0.04 s) ions was observed and attributed to the fast movement of chloride ions in and out of the polymer film. In contrast, PEDOT doped with poly(styrenesulfonate) (PSS) responds much slower (ca. 2.2 s), and the essential immobility of polyanion constrains the direction of current flow.

RESUMEN

Organic electrochemical transistors (OECTs) employing conductive polymers (CPs) have gained remarkable prominence and have undergone extensive advancements in wearable and implantable bioelectronic applications in recent years. Among the diverse arrays of CPs, poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) is a common choice for the active-layer channel in p-type OECTs, showing a remarkably high transconductance for the high amplification of signals in biosensing applications. This investigation focuses on the novel engineering of PEDOT:PSS composite materials by seamlessly integrating several additives, namely, dimethyl sulfoxide (DMSO), (3-glycidyloxypropyl)trimethoxysilane (GOPS), and a nonionic fluorosurfactant (NIFS), to fine-tune their electrical conductivity, self-healing capability, and stretchability. To elucidate the intricate influences of the DMSO, GOPS, and NIFS additives on the formation of PEDOT:PSS composite films, theoretical calculations were performed, encompassing the solubility parameters and surface energies of the constituent components of the NIFS, PEDOT, PSS, and PSS-GOPS polymers. Furthermore, we conducted a comprehensive array of material analyses, which reveal the intricacies of the phase separation phenomenon and its interaction with the materials' characteristics. Our research identified the optimal composition for the PEDOT:PSS composite films, characterized by outstanding self-healing and stretchable capabilities. This composition has proven to be highly effective for constructing an active-layer channel in the form of OECT-based biosensors fabricated onto polydimethylsiloxane substrates for detecting dopamine. Overall, these findings represent significant progress in the application of PEDOT:PSS composite films in wearable bioelectronics and pave the way for the development of state-of-the-art biosensing technologies.

RESUMEN

Electric cell-substrate impedance sensing (ECIS) is an innovative approach for the label-free and real-time detection of cell morphology, growth, and apoptosis, thereby playing an essential role as both a viable alternative and valuable complement to conventional biochemical/pharmaceutical analysis in the field of diagnostics. Constant improvements are naturally sought to further improve the effective range and reliability of this technology. In this study, we developed poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS) conducting polymer (CP)-based bioelectrodes integrated into homemade ECIS cell-culture chamber slides for the simultaneous drug release and real-time biosensing of cancer cell viability under drug treatment. The CP comprised tailored PEDOT:PSS, poly(ethylene oxide) (PEO), and (3-glycidyloxypropyl)trimethoxysilane (GOPS) capable of encapsulating antitumor chemotherapeutic agents such as doxorubicin (DOX), docetaxel (DTX), and a DOX/DTX combination. This device can reliably monitor impedance signal changes correlated with cell viability on chips generated by cell adhesion onto a predetermined CP-based working electrode while simultaneously exhibiting excellent properties for both drug encapsulation and on-demand release from another CP-based counter electrode under electrical stimulation (ES) operation. Cyclic voltammetry curves and surface profile data of different CP-based coatings (without or with drugs) were used to analyze the changes in charge capacity and thickness, respectively, thereby further revealing the correlation between their drug-releasing performance under ES operation (determined using ultraviolet-visible (UV-vis) spectroscopy). Finally, antitumor drug screening tests (DOX, DTX, and DOX/DTX combination) were performed on MCF-7 and HeLa cells using our developed CP-based ECIS chip system to monitor the impedance signal changes and their related cell viability results.

Asunto(s)

Doxorrubicina , Humanos , Impedancia Eléctrica , Células HeLa , Liberación de Fármacos , Reproducibilidad de los Resultados , Doxorrubicina/farmacología

RESUMEN

In this work, poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS)/poly(vinylidene fluoride) (PVDF) nanofiber-web-based transparent conducting electrodes (TCEs) were fabricated for use in dye-sensitized photovoltaic textiles. The PEDOT:PSS solution was mixed with dimethyl sulfoxide (DMSO) solvent, and the PEDOT:PSS/DMSO mixture was applied on the PVDF nanofiber web using a simple brush-painting technique to prepare ultrathin and -lightweight, highly transparent TCEs. When the PVDF nanofiber web was treated with a 3:7 PEDOT:PSS and DMSO mixture (P3D7 sample), it exhibited ∼84% transmittance at a wavelength of 550 nm with an average sheet resistance of ∼1.5 kΩ/sq. In addition, it showed a figure of merit (FOM) of 0.104 × 10-3 Ω-1. In the trial test, the P3D7 TCE-based photovoltaic textile exhibited an average voltage of 73.20 mV and an average current of 0.44 mA/cm2.

RESUMEN

Highly conductive nylon 6 nanofiber webs, incorporating poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) and dimethyl sulfoxide (DMSO), were prepared for textile-based signal transmission lines. To improve the electrical performance of the textiles, they were optimized by the number of coating cycles and the solvent treatment step. The nanofiber web coated four times with PEDOT:PSS showed a six-times reduction in sheet resistance compared to that of once. In addition, the sample treated with both adding and dipping of DMSO showed a significant decrease of 83 times in sheet resistance compared to the sample without treatment of DMSO. Using samples with excellent electrical conductivity, the waveforms of the signal in the time domain were analyzed and shown to have an amplitude and phase almost identical to that of the conventional copper wire. As a result of the S21 characteristic curve, selected textiles were available up to the 15 MHz frequency bandwidth. In the FE-SEM image, it was observed that the surface of the coated sample was generally covered with PEDOT:PSS, which was distinguished from the untreated sample. These results demonstrate that the nanofiber web treated with the optimized conditions of PEDOT:PSS and DMSO can be applied as promising textile-based signal transmission lines for smart clothing.

RESUMEN

A novel capacitive sensor for measuring the water-level and monitoring the water quality has been developed in this work by using an enhanced screen printing technology. A commonly used environment-friendly conductive polymer poly(3,4-ethylenedioxythiophene):poly (styrenesulfonate) (PEDOT:PSS) for conductive sensors has a limited conductivity due to its high sheet resistance. A physical treatment performed during the printing process has reduced the sheet resistance of printed PEDOT:PSS on polyethylenterephthalat (PET) substrate from 264.39 Ω/sq to 23.44 Ω/sq. The adhesion bonding force between printed PEDOT:PSS and the substrate PET is increased by using chemical treatment and tested using a newly designed adhesive peeling force test. Using the economical conductive ink PEDOT:PSS with this new physical treatment, our capacitive sensors are cost-efficient and have a sensitivity of up to 1.25 pF/mm.

RESUMEN

Piezoresistive pressure sensors have garnered significant attention because of their wide applications in automobiles, intelligent buildings, and biomedicine. For in vivo testing, the size of pressure sensors is a vital factor to monitor the pressure of specific portions of a human body. Therefore, the primary focus of this study is to miniaturize piezoresistive pressure sensors with graphene oxide (GO)-incorporated poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) composite films on a flexible substrate for biomedical applications. Prior to the fabrication of pressure sensors, a comprehensive material analysis was applied to identify the horizontal placement of GO flakes within the PEDOT:PSS copolymers, revealing a reduction in variable range hopping distance and an enhancement in carrier mobility. For devices scaled to 0.2 cm, the sensitivity of PEDOT:PSS pressure sensors was conspicuously decreased owing to the late response, which can be effectively solved by GO incorporation. Using technology computer-aided design simulations, the current crowded at the PEDOT:PSS film surface and in the vicinity of an indium-tin-oxide electrode corner was found to be responsible for the changes in piezoresistive behaviors of the scaled devices. The miniaturized flexible piezoresistive pressure sensors with PEDOT:PSS/GO composite films are capable of monitoring the brain pressure of intracranial surgery of a rat and discerning different styles of music for a potential application in hearing aids.

RESUMEN

Ionic electroactive polymers (IEAPs) have received considerable attention for their flexibility, lightweight composition, large displacement, and low-voltage activation. Recently, many metal-nonmetal composite electrodes have been actively studied. Specifically, graphene oxide-silver nanowire (GO-Ag NW) composite electrodes offer advantages among IEAPs with metal-nonmetal composite electrodes. However, GO-Ag NW composite electrodes still show a decrease in displacement owing to low stability and durability during driving. Therefore, the durability and stability of the IEAPs with metal-nonmetal composite electrodes must be improved. One way to improve the device durability is coating the electrode surface with a protective layer. This layer must have enough flexibility and suitable electrical properties such that it does not hinder the IEAPs' driving. Herein, a poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS) protective layer and 4-(1,1,3,3-tetramethylbutyl)phenyl-polyethylene glycol (Triton X-100) are applied to improve driving performance. Triton X-100 is a nonionic surfactant that transforms the PEDOT:PSS capsule into a nanofibril structure. In this study, a mixed Triton X-100/PEDOT:PSS protective layer at an optimum weight ratio was coated onto the GO-Ag NW composite-electrode-based IEAPs under various conditions. The IEAP actuators based on GO-Ag NW composite electrodes with a protective layer of PEDOT:PSS treated with Triton X-100 showed the best stability and durability.

RESUMEN

Poly(9,9-dioctylfluorene) (PFO) has attracted significant interests owing to its versatility in electronic devices. However, changes in its optical properties caused by its various phases and the formation of oxidation defects limit the application of PFO in light-emitting diodes (LEDs). We investigated the effects of the addition of Triton X-100 (hereinafter shortened as TX) in poly(3,4-ethylenedioxythiophene):poly(styrenesulfonate) (PEDOT:PSS) to induce interlayer diffusion between PEDOT:PSS and PFO to enhance the stability of the PFO phase and suppress its oxidation. Photoluminescence (PL) measurement on PFO/TX-mixed PEDOT:PSS layers revealed that, upon increasing the concentration of TX in the PEDOT:PSS layer, the ß phase of PFO could be suppressed in favor of the glassy phase and the wide PL emission centered at 535 nm caused by ketone defects formed by oxidation was decreased considerably. LEDs were then fabricated using PFO as an emission layer, TX-mixed PEDOT:PSS as hole-transport layer, and zinc oxide (ZnO) nanorods as electron-transport layer. As the TX concentration reached 3 wt %, the devices exhibited dramatic increases in current densities, which were attributed to the enhanced hole injection due to TX addition, along with a shift in the dominant emission wavelength from a green electroluminescence (EL) emission centered at 518 nm to a blue EL emission centered at 448 nm. The addition of TX in PEDOT:PSS induced a better hole injection in the PFO layer, and through interlayer diffusion, stabilized the glassy phase of PFO and limited the formation of oxidation defects.