Effect of ionic conductivity of electrolyte on printed planar and vertical organic electrochemical transistors.

Conducting polymers with mixed electronic/ionic transport are attracting a great deal of interest for applications in organic electrochemical transistors (OECTs). Ions play a crucial role in OECT performance. The concentration and mobility of ions in the electrolyte influence the current flow in the OECT and its transconductance. This study examines the electrochemical properties and ionic conductivity of two semi-solid electrolytes, iongels, and organogels, with diverse ionic species and properties. Our results indicate that the organogels exhibited higher ionic conductivities than the iongels. Furthermore, the geometry of OECTs plays an important role in determining their transconductance. Thus, this study employs a novel approach for fabricating vertical-configuration OECTs with significantly shorter channel lengths planar devices. This is achieved through a printing method that offers advantages, such as design versatility, scalability, expedited production time, and reduced cost relative to traditional microfabrication methods. The transconductance values obtained for the vertical OECTs were significantly (approximately 50 times) higher than those of the planar devices because of their shorter channel lengths. Finally, the impact of different gating media on the performance of both planar and vertical OECTs was studied, and devices gated by organogels demonstrated improved transconductance and switching speed (almost two times higher) than those gated by iongels.

An intrinsically stretchable and bendable electrochromic device.

Stretchable electrochromic devices (ECDs) were fabricated from electrospun PEDOT:PSS (poly(3, 4-ethylenedioxythiophene):polystyrene sulfonate) fibers. Stretchable and transparent electrodes with a sheet resistance of 1200 Ω sq-1were prepared by depositing the conductive fibers on elastomeric substrates that were prepared from polydimethylsiloxane. The conductive substrates replaced the ITO coated glass electrodes that are typically used in ECDs. The functioning device was prepared from a flexible chitosan electrolytic gel and a 4, 7-bis(4-diphenylaminophenyl)-2, 1, 3-benzothiaziazole (TPA-BZT-TPA) electrochrome that were deposited on the streatchable transparent electrodes. The assembled device could be stretched to 150% its original length and bent to a curvature of 0.1. The device could be operated and switched between its yellow (off) and blue (on) states while being stretched and bent with a maximum contrast ΔT ≈ 30% at 805 nm and a coloration efficiency of 168 cm2C-1. The stretchable device had an electrochromic contrast that was 30% greater than its counterpart that was prepared from conventional ITO-glass electrodes. The critical composition required for making devices truly stretchable was possible by evaluating the performance of five types of devices consisting of different layers.

Titanyl phthalocyanine ambipolar thin film transistors making use of carbon nanotube electrodes.

The capability of efficiently injecting charge carriers into organic films and finely tuning their morphology and structure is crucial to improve the performance of organic thin film transistors (OTFTs). In this work, we investigate OTFTs employing carbon nanotubes (CNTs) as the source-drain electrodes and, as the organic semiconductor, thin films of titanyl phthalocyanine (TiOPc) grown by supersonic molecular beam deposition (SuMBD). While CNT electrodes have shown an unprecedented ability to improve charge injection in OTFTs, SuMBD is an effective technique to tune film morphology and structure. Varying the substrate temperature during deposition, we were able to grow both amorphous (low substrate temperature) and polycrystalline (high substrate temperature) films of TiOPc. Regardless of the film morphology and structure, CNT electrodes led to superior charge injection and transport performance with respect to benchmark Au electrodes. Vacuum annealing of polycrystalline TiOPc films with CNT electrodes yielded ambipolar OTFTs.

Electroconductive cardiac patch based on bioactive PEDOT:PSS hydrogels.

Engineering cardiac implants for treating myocardial infarction (MI) has advanced, but challenges persist in mimicking the structural properties and variability of cardiac tissues using traditional bioconstructs and conventional engineering methods. This study introduces a synthetic patch with a bioactive surface designed to swiftly restore functionality to the damaged myocardium. The patch combines a composite, soft, and conductive hydrogel-based on (3,4-ethylenedioxythiophene):polystyrene-sulfonate (PEDOT:PSS) and polyvinyl alcohol (PVA). This cardiac patch exhibits a reasonably high electrical conductivity (40 S/cm) and a stretchability up to 50% of its original length. Our findings reveal its resilience to 10% cyclic stretching at 1 Hz with no loss of conductivity over time. To mediate a strong cell-scaffold adhesion, we biofunctionalize the hydrogel with a N-cadherin mimic peptide, providing the cardiac patch with a bioactive surface. This modification promote increased adherence and proliferation of cardiac fibroblasts (CFbs) while effectively mitigating the formation of bacterial biofilm, particularly against Staphylococcus aureus, a common pathogen responsible for surgical site infections (SSIs). Our study demonstrates the successful development of a structurally validated cardiac patch possessing the desired mechanical, electrical, and biofunctional attributes for effective cardiac recovery. Consequently, this research holds significant promise in alleviating the burden imposed by myocardial infarctions.

Self-healing, stretchable and recyclable polyurethane-PEDOT:PSS conductive blends.

Future electronics call for materials with mechanical toughness, flexibility, and stretchability. Moreover, self-healing and recyclability are highly desirable to mitigate the escalating environmental threat of electronic waste (e-waste). Herein, we report a stretchable, self-healing, and recyclable material based on a mixture of the conductive polymer poly(3,4-ethylenedioxythiophene) doped with polystyrene sulfonate (PEDOT:PSS) with a custom-designed polyurethane (PU) and polyethylene glycol (PEG). This material showed excellent elongation at brake (∼350%), high toughness (∼24.6 MJ m-3), moderate electrical conductivity (∼10 S cm-1), and outstanding mechanical and electrical healing efficiencies. In addition, it demonstrated exceptional recyclability with no significant loss in the mechanical and electrical properties after being recycled 20 times. Based on these properties, as a proof of principle for sustainable electronic devices, we demonstrated that electrocardiogram (ECG) electrodes and pressure sensors based on this material could be recycled without significant performance loss. The development of multifunctional electronic materials that are self-healing and fully recyclable is a promising step toward sustainable electronics, offering a potential solution to the e-waste challenge.

Advances in Electrode Materials for Scalp, Forehead, and Ear EEG: A Mini-Review.

Electroencephalogram (EEG) records the electrical activity of neurons in the cerebral cortex and is used extensively to diagnose, treat, and monitor psychiatric and neurological conditions. Reliable contact between the skin and the electrodes is essential for achieving consistency and for obtaining electroencephalographic information. There has been an increasing demand for effective equipment and electrodes to overcome the time-consuming and cumbersome application of traditional systems. Recently, ear-centered EEG has met with growing interest since it can provide good signal quality due to the proximity of the ear to the brain. In addition, it can facilitate mobile and unobtrusive usage due to its smaller size and ease of use, since it can be used without interfering with the patient's daily activities. The purpose of this mini-review is to first introduce the broad range of electrodes used in conventional (scalp) EEG and subsequently discuss the state-of-the-art literature about around- and in-the-ear EEG.

All-printed and stretchable organic electrochemical transistors using a hydrogel electrolyte.

Stretchable electronic devices are expected to play an important role in wearable electronics. Solution-processable conducting materials are desirable because of their versatile processing. Herein, we report the fabrication of fully stretchable organic electrochemical transistors (OECTs) by printing all components of the device. To achieve the stretchability of the whole body of the devices, a printed planar gate electrode and polyvinyl alcohol (PVA) hydrogel electrolyte were employed. Stretchable silver paste provided a soft feature to drain/source, gate and interconnect, without any additional strategies needed to improve the stretchability of the metallic components. The resulting OECTs showed a performance comparable to inkjet or screen-printed OECTs. The maximum transconductance and on/off ratio were 1.04 ± 0.13 mS and 830, respectively. The device was stable for 50 days and stretched up to 110% tensile strain, which makes it suitable for withstanding the mechanical deformation expected in wearable electronics. This work paves the way for all-printed and stretchable transistors in wearable bioelectronics.

Fabrication of Curli Fiber-PEDOT:PSS Biomaterials with Tunable Self-Healing, Mechanical, and Electrical Properties.

Poly(3,4-ethylenedioxythiophene) polystyrenesulfonate (PEDOT:PSS) is a highly conductive, easily processable, self-healing polymer. It has been shown to be useful in bioelectronic applications, for instance, as a biointerfacing layer for studying brain activity, in biosensitive transistors, and in wearable biosensors. A green and biofriendly method for improving the mechanical properties, biocompatibility, and stability of PEDOT:PSS involves mixing the polymer with a biopolymer. Via structural changes and interactions with PEDOT:PSS, biopolymers have the potential to improve the self-healing ability, flexibility, and electrical conductivity of the composite. In this work, we fabricated novel protein-polymer multifunctional composites by mixing PEDOT:PSS with genetically programmable amyloid curli fibers produced byEscherichia coli bacteria. Curli fibers are among the stiffest protein polymers and, once isolated from bacterial biofilms, can form plastic-like thin films that heal with the addition of water. Curli-PEDOT:PSS composites containing 60% curli fibers exhibited a conductivity 4.5-fold higher than that of pristine PEDOT:PSS. The curli fibers imbued the biocomposites with an immediate water-induced self-healing ability. Further, the addition of curli fibers lowered the Young's and shear moduli of the composites, improving their compatibility for tissue-interfacing applications. Lastly, we showed that genetically engineered fluorescent curli fibers retained their ability to fluoresce within curli-PEDOT:PSS composites. Curli fibers thus allow to modulate a range of properties in conductive PEDOT:PSS composites, broadening the applications of this polymer in biointerfaces and bioelectronics.

Recent Progress on Self-Healable Conducting Polymers.

Materials able to regenerate after damage have been the object of investigation since the ancient times. For instance, self-healing concretes, able to resist earthquakes, aging, weather, and seawater have been known since the times of ancient Rome and are still the object of research. During the last decade, there has been an increasing interest in self-healing electronic materials, for applications in electronic skin (E-skin) for health monitoring, wearable and stretchable sensors, actuators, transistors, energy harvesting, and storage devices. Self-healing materials based on conducting polymers are particularly attractive due to their tunable high conductivity, good stability, intrinsic flexibility, excellent processability and biocompatibility. Here recent developments are reviewed in the field of self-healing electronic materials based on conducting polymers, such as poly 3,4-ethylenedioxythiophene (PEDOT), polypyrrole (PPy), and polyaniline (PANI). The different types of healing, the strategies adopted to optimize electrical and mechanical properties, and the various possible healing mechanisms are introduced. Finally, the main challenges and perspectives in the field are discussed.

Self-healing, stretchable, and highly adhesive hydrogels for epidermal patch electrodes.

Flexible, self-healing and adhesive conductive materials with Young's modulus matching biological tissues are highly desired for applications in bioelectronics. Here, we report self-healing, stretchable, highly adhesive and conductive hydrogels obtained by mixing polyvinyl alcohol, sodium tetraborate and a screen printing paste containing the conducting polymer Poly (3,4-ethylenedioxythiophene) doped with polystyrene sulfonate (PEDOT:PSS) and diol additives. The as prepared hydrogels exhibited modelling ability, high adhesion on pig skin (1.96 N/cm2), high plastic stretchability (>10000%), a moderate conductivity, a low compressive modulus (0.3-3.7 KPa), a good strain sensitivity (gauge factor = 3.88 at 500% strain), and remarkable self-healing properties. Epidermal patch electrodes prepared using one of our hydrogels demonstrated high-quality recording of electrocardiography (ECG) and electromyography (EMG) signal. Because of their straightforward fabrication, outstanding mechanical properties and possibility to combine the electrode components in a single material, hydrogels based on PVA, borax and PEDOT:PSS are highly promising for applications in bioelectronics and wearable electronics. STATEMENT OF SIGNIFICANCE: Soft materials with electrical conductivity are investigated for healthcare applications, such as electrodes to measure vital signs that can easily adapt to the shape and the movements of human skin. Conductive hydrogels (i.e. gels containing water) are ideal materials for this purpose due softness and flexibility. In this this work, we report hydrogels obtained mixing an electrically conductive polymer, a water-soluble biocompatible polymer and a salt. These materials show high adhesion on skin, electrical conductivity and ability to self-repair after a mechanical damage. These hydrogels were successfully used to fabricate electrode to measure cardiac and muscular electrical signals.

Tailoring the Self-Healing Properties of Conducting Polymer Films.

The conducting polymer polyethylenedioxythiophene doped with polystyrene sulfonate (PEDOT:PSS) has received great attention in the field of wearable bioelectronics due to its tunable high electrical conductivity, air stability, ease of processability, biocompatibility, and recently discovered self-healing ability. It has been observed that blending additives with PEDOT:PSS or post-treatment permits the tailoring of intrinsic polymer properties, though their effects on the water-enabled self-healing property have not previously been established. Here, it is demonstrated that the water-enabled healing behavior of conducting polymers is decreased by crosslinkers or by acid post-treatment. Organic dopants of PEDOT have high water swelling ratios and lead to water-enabled healing, while inorganic dopants fail in the healing of PEDOT. The water-enabled healing of two isolated PEDOT:PSS squares with a 5 µm width gap and a thickness less than 1 µm is shown. This work will help pave the way for the further development of conducting polymer-based self-healable bioelectronics and flexible and stretchable electronics.

Electropolymerized Poly(3,4-ethylenedioxythiophene) (PEDOT) Coatings for Implantable Deep-Brain-Stimulating Microelectrodes.

Conducting polymers have been widely explored as coating materials for metal electrodes to improve neural signal recording and stimulation because of their mixed electronic-ionic conduction and biocompatibility. In particular, the conducting polymer poly(3,4-ethylenedioxythiophene) (PEDOT) is one of the best candidates for biomedical applications due to its high conductivity and good electrochemical stability. Coating metal electrodes with PEDOT has shown to enhance the electrode's performance by decreasing the impedance and increasing the charge storage capacity. However, PEDOT-coated metal electrodes often have issues with delamination and stability, resulting in decreased device performance and lifetime. In this work, we were able to electropolymerize PEDOT coatings on sharp platinum-iridium recording and stimulating neural electrodes and demonstrated its mechanical and electrochemical stability. Electropolymerization of PEDOT:tetrafluoroborate was carried out in three different solvents: propylene carbonate, acetonitrile, and water. The stability of the coatings was assessed via ultrasonication, phosphate buffer solution soaking test, autoclave sterilization, and electrical pulsing. Coatings prepared with propylene carbonate or acetonitrile possessed excellent electrochemical stability and survived autoclave sterilization, prolonged soaking, and electrical stimulation without major changes in electrochemical properties. Stimulating microelectrodes were implanted in rats and stimulated daily, for 7 and 15 days. The electrochemical properties monitored in vivo demonstrated that the stimulation procedure for both coated and uncoated electrodes decreased the impedance.

Poly(3,4-ethylenedioxythiophene) (PEDOT) Coatings for High-Quality Electromyography Recording.

Conducting polymer coatings on metal electrodes are an efficient solution to improve neural signal recording and stimulation, due to their mixed electronic-ionic conduction and biocompatibility. To date, only a few studies have been reported on conducting polymer coatings on metallic wire electrodes for muscle signal recording. Chronic muscle signal recording of freely moving animals can be challenging to acquire with coated electrodes, due to muscle movement around the electrode that can increase instances of coating delamination and device failure. The poor adhesion of conducting polymers to some inorganic substrates and the possible degradation of their electrochemical properties after harsh treatments, such as sterilization, or during implantation limits their use for biomedical applications. Here, we demonstrate the mechanical and electrochemical stability of the conducting polymer, poly(3,4-ethylenedioxythiophene) (PEDOT) doped with LiClO4, deposited on stainless steel multistranded wire electrodes for invasive muscle signal recording in mice. The mechanical and electrochemical stability was achieved by tuning the electropolymerization conditions. PEDOT-coated and bare stainless steel electrodes were implanted in the neck muscle of five mice for electromyographic (EMG) activity recording over a period of 6 weeks. The PEDOT coating improved the electrochemical properties of the stainless steel electrodes, lowering the impedance, resulting in an enhanced signal-to-noise ratio during in vivo EMG recording compared to bare electrodes.

Two-dimensional nanotemplates as surface cues for the controlled assembly of organic molecules.

Controlled two-dimensional assembly of organic molecules can be successfully realized by meansof surface nanotemplates that provide surface cues for assembly upon adsorption. Examples of suchtemplates are nanostructured surfaces and organic porous networks. In this review, we discuss theformation and use of such templates for controlled molecular assembly. The formation of the organicporous network is typically based on non-covalent interactions, e.g., hydrogen bonds, dipole-dipoleinteractions, metal-organic coordination bonds together with substrate-mediated molecular interactions.The pores of the network can act as hosts for specific organic molecules. The chemical structureof the molecular building blocks of the porous network has a primary effect on the shape, size,and chemical reactivity of the cavities. Long-range mesoscale reconstructions can also be employedas surface nanotemplates based on the selective adsorption of atomic or molecular species at specificsurface sites. Scanning tunneling microscopy is the key tool to study the formation of the nanotemplatesas well as the effect of the template in the growth of the ordered organic structures. The reportedstudies contribute to build the rationale in the design and fabrication of two-dimensional organicnetworks. The topic covered in this review represents an important challenge in nanotechnology sincethese findings might have a wide range of applications, e.g., in electronics, sensing, and bio-recognition.

Heterocirculenes as a new class of organic semiconductors.

We report a fabrication of field-effect transistors using the new organic semiconductors octathio[8]circulene and tetrathiotetraseleno[8]circulene . The maximum hole mobility of 9 x 10(-3) cm(2) V(-1) s(-1) is, most likely, limited by one-dimensional growth of and in thin films.