Search Results (67)

Asymmetric micro-supercapacitors (AMSCs) with a small size and high energy density can be compatible with portable and wearable electronic devices and are capable of providing stable, long-term power supply, attracting great research interest in recent years. Here, we present a simple and rapid preparation method for AMSCs’ fabrication. By regulating the hydrophilicity and hydrophobicity of coplanar laser-induced graphene (LIG) through the adjustment of the laser parameters, two electrode materials with distinct hydrophilic–hydrophobic properties were selectively deposited by sequentially dip-coating. The LIGs serve as current collectors, with activated carbon and poly (3,4-ethylenedioxythiophene): poly (styrene sulfonate) as active materials. After coating the electrolytes and folding the two electrodes, a high-performance AMSC was achieved. The device exhibits a high areal capacitance of 85.88 mF cm⁻² at a current density of 0.4 mA cm⁻², along with an impressive energy density of 11.93 µWh cm⁻² and a good rate performance. Moreover, it is demonstrated to be highly stable in 500,000 cycles. Two AMSCs in series can supply power to an electronic clock and birthday card. The method of preparing asymmetric electrodes in the same plane greatly facilitates the large-area preparation of AMSCs and series–parallel connection, providing an excellent idea for developing high-performance miniature energy storage devices. Full article

Recent research on incorporating biomass resources into functional polymers has garnered significant attention. Poly(3,4-ethylenedioxythiophene)/poly(styrene sulfonate) (PEDOT:PSS) is the most commercially successful conducting polymer composed of over 70 wt% petroleum-derived PSS, which presents an opportunity for partial replacement with biomass-based resources. In this study, a complex of PEDOT and sulfated cellulose nanofiber (PEDOT:s-CNF) was synthesized, and the relationship between its conductivity and doping conditions was investigated. PEDOT was synthesized on s-CNF, which was used in place of PSS, and the results indicate that conductivity increases as PEDOT polymerization progresses; however, excessive polymerization reduces electrical conductivity. Based on X-ray photoelectron spectroscopy and zeta potential measurements, the doping concentration decreases as PEDOT polymerization progresses to an excess state. This decrease is attributed to the depletion of sulfate groups, which act as dopants on s-CNFs, occurring as a consequence of the addition of PEDOT monomers. Enhancing the degree of sulfate group substitution on s-CNFs and incorporating additional dopants containing sulfonic groups improved conductivity. Specifically, adding p-toluenesulfonic acid (PTSA) as a dopant increased conductivity, reaching approximately 10 mS cm⁻¹. However, at higher PTSA concentrations, the strong acidity of sulfonic groups reduced the degree of sulfate group dissociation, leading to a decline in doping efficiency. Full article

Wearable electronic devices have shown great application prospects in the fields of tactile sensing, electronic skin, and soft robots. However, the existing wearable electronic devices face limitations such as power supply challenges, lack of portability, and discomfort, which restrict their applications. The invention of triboelectric nanogenerators (TENGs) with dual functions of energy harvesting and sensing provides an innovative solution to address these issues. This study prepared a highly stretchable conductive hydrogel using doped conducting polymer poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) as a strain sensor, demonstrating high sensitivity (GF = 4.31), an ultra-wide sensing range (0–1690%), ultra-fast response speed (0.15 s), excellent durability, and repeatability. A high-performance triboelectric nanogenerator was constructed using the hydrogel as an electrode, achieving an output performance of up to 192 V. Furthermore, the TENG fixed in the hands, wrists, legs, and feet of the human body can be used as a wearable electronic device to monitor human motion, which is conducive to promoting the development of triboelectric nanogenerators based on conductive hydrogels in strain sensors and self-powered wearable devices. Full article

Hybrid organohalide perovskites have received considerable attention due to their exceptional photovoltaic (PV) conversion efficiencies in optoelectronic devices. In this study, we report the development of a highly sensitive, self-powered perovskite-based photovoltaic photodiode (PVPD) fabricated by incorporating a poly(amic acid)-polyimide (PAA-PI) copolymer as an interfacial layer between a methylammonium lead iodide (CH₃NH₃PbI₃, MAPbI₃) perovskite light-absorbing layer and a poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonate) (PEDOT: PSS) hole injection layer. The PAA-PI interfacial layer effectively suppresses carrier recombination at the interfaces, resulting in a high power conversion efficiency (PCE) of 11.8% compared to 10.4% in reference devices without an interfacial layer. Moreover, applying the PAA-PI interfacial layer to the MAPbI₃ PVPD significantly improves the photodiode performance, increasing the specific detectivity by 49 times to 7.82 × 10¹⁰ Jones compared to the corresponding results of reference devices without an interfacial layer. The PAA-PI-passivated MAPbI₃ PVPD also exhibits a wide linear dynamic range of ~103 dB and fast response times, with rise and decay times of 61 and 18 µs, respectively. The improved dynamic response of the PAA-PI-passivated MAPbI₃ PVPD enables effective weak-light detection, highlighting the potential of advanced interfacial engineering with PAA-PI interfacial layers in the development of high-performance, self-powered perovskite photovoltaic photodetectors for a wide range of optoelectronic applications. Full article

Electrically conductive polymeric materials have recently garnered significant interest from researchers due to their potential applications in the biomedical field, including medical implants, tissue engineering, flexible electronic devices, and biosensors. Poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) is considered the most successful conducting polymer due to its higher electrical conductivity and chemical stability, but it suffers from limited solubility in common organic solvents, poor mechanical properties, and low biocompatibility. An area of tremendous interest is in combining PEDOT:PSS with another polymer to form a blend or composite material in order to access the beneficial properties of both materials. However, the hydrophilic nature of PEDOT:PSS makes it difficult to produce composites with non-polar polymers. In order to overcome these problems, we have specifically designed and synthesized two new sulfonated polyurethanes (PUS) with high sulfonic acid functionality. The two polyurethanes, one water-soluble (PUS1) and one water-insoluble (PUS2), were used to make blends with two commercially available PEDOT:PSS formulations (Clevios^TM FET and PH1000). Solvent cast films on glass substrates were made from water-soluble PEDOT:PSS/PUS1 blends while free-standing films of PEDOT:PSS/PUS2 blends were fabricated by compression-moulding. Ethylene glycol was used as conductivity enhancer, which showed an increase in the conductivity by several orders of magnitude in most of the compositions investigated. The highest conductivity of 438 S cm⁻¹ was achieved for the blend with 80 wt% of PEDOT:PSS (PH1000) in PUS1. Full article

Poly(3,4-ethylenedioxythiophene)-poly(styrenesulfonate) (PEDOT:PSS) is a commonly used conductive polymer in organic optoelectronic devices. The conductivity and work function of the PEDOT:PSS are two important parameters that significantly determine the performance of the associated optoelectronic device. Traditionally, some solvents were doped in PEDOT:PSS solution or soaked in PEDOT:PSS film to improve its electrical conductivity, but they damaged the integrity of PEDOT:PSS and reduce the film’s work function. Herein, for the first time, we use femtosecond laser irradiation to modify the electrical conductivity and work function of PEDOT:PSS film. We proposed that the femtosecond laser irradiation could selectively remove the superficial insulative PSS, thereby improving the electrical conductivity of the film. The femtosecond laser-irradiated PEDOT:PSS film was further employed as a hole injection layer within cutting-edge perovskite light-emitting diodes (PeLEDs). A maximum luminosity of 950 cd/m² was obtained in PeLEDs irradiated by femtosecond laser light in thin films, which is five times higher than that of the controlled device. Moreover, the external quantum efficiency of the devices was also increased from 4.6% to 6.3%. This work paved a cost-effective way to regulate the electrical properties of the PEDOT:PSS film. Full article

Free-standing films based on conducting polymers, such as poly(3,4-ethylenedioxythiophene): poly(styrene sulfonate) (PEDOT:PSS), offer many benefits over traditional metal electrodes for applications in flexible electronics. However, to ensure structural integrity when contacting aqueous environments and high levels of electrical conductivity, solution-processed polymers require additives that act as crosslinking agents and conductivity enhancers. In this work, a new approach is presented to fabricate water-resistant free-standing films of PEDOT:PSS and simultaneously increase their conductivity, using an oxetane compound as an additive. It is shown that at moderate temperatures, oxetane polymerizes within the PEDOT:PSS acidic medium, forming hydroxymethyl-substituted polyether compounds that form a network upon crosslinking with PSS. The polymer composite films show self-sustainability, structural stability in aqueous environments, and enhanced conductivity. Finally, the potential of the free-standing films as health-monitoring electrodes, specifically for human electrocardiography, is explored. Full article

Substrate-free electrodes are promising dry electrodes for long-term physiological electrical signal monitoring due to their ultra-thinness, conformal contact, and stable skin–electrode impedance. However, the response of substrate-free electrodes to various disturbances during electrocardiogram (ECG) monitoring and the corresponding optimization needs to be investigated. This paper investigates the specific effects of various influencing factors on skin–electrode impedance and ECG during electrocardiogram (ECG) detection. The research utilizes substrate-free poly(3,4-ethylenedioxythiophene)/poly(styrene-sulfonate) (PEDOT:PSS) electrodes. The investigation employs several methods, including skin–electrode impedance comparison, ECG waveform analysis, spectrum analysis, and signal-to-noise ratio (SNR) evaluation. To avoid the impact of physiological state differences in subjects at different times, relevant data were only compared with the same group of experiments conducted in the same period. The results demonstrate that the substrate-free conformal contact PEDOT:PSS electrode has more stable skin–electrode impedance and could obtain a more stable ECG than partial contact electrodes (the SNR of the partial contact and conformal contact electrodes are 1.2768 ± 4.0299 dB and 7.2637 ± 1.4897 dB, respectively). Furthermore, the ECG signal quality of the substrate-free conformal contact PEDOT:PSS electrode was independent of the electrode area and shape (the SNRs of the large, medium, and small electrodes are 4.0447 ± 0.4616 dB, 3.9115 ± 0.5885 dB, and 4.1556 ± 0.5557 dB, respectively; the SNRs of the circular, square, and triangular electrodes are 9.2649 ± 0.6326 dB, 9.2471 ± 0.6806 dB, and 9.1514 ± 0.6875 dB, respectively), showing high signal acquisition capability that is the same as microneedle electrodes and better than fabric electrodes. The results of clothing friction effects show that skin–electrode impedance stability was important for ECG stability, while the impedance value was not (the SNRs of friction and non-friction electrodes are 2.4128 ± 7.0784 dB and 9.2164 ± 0.6696 dB, respectively). Moreover, the skin–electrode impedance maintains stability even at a high breathing frequency, but the ECG signal fluctuates at a high breathing frequency. This experiment demonstrates that even when the skin–electrode impedance remains stable, the ECG signal can still be susceptible to interference from other factors. This study suggests that substrate-free PEDOT:PSS that could form conformal contact with the skin has higher skin–electrode impedance stability and could measure a high ECG signal even with a small electrode area, demonstrating its potential as dry ECG electrodes, but the interference from other physiological electrical signals may require better circuit design. Full article

All-inorganic metal halide perovskite is promising for highly efficient and thermally stable perovskite light-emitting diodes (PeLEDs). However, there is still great room for improvement in the film quality, including low coverage and high trap density, which play a vital role in achieving high-efficiency PeLEDs. In this work, lead acetate (Pb(Ac)₂) was introduced into the perovskite precursor solution as an additive. Experimental results show that perovskite films deposited from a one-step anti-solvent free solution process with increased surface coverage and reduced trap density were obtained, leading to enhanced photoluminescence (PL) intensity. More than that, the valence band maximum (VBM) of perovskite films was reduced, bringing about a better energy level matching the work function of the hole-injection layer (HIL) poly (3,4-ethylenedioxythiophene)-poly (styrene sulfonate) (PEDOT: PSS), which is facilitated for the hole injection, leading to a decrease in the turn-on voltage (V_th) of PeLEDs from 3.4 V for the control device to 2.6 V. Finally, the external quantum efficiency (EQE) of the sky blue PeLEDs (at 484 nm) increased from 0.09% to 0.66%. The principles of Pb(Ac)₂ were thoroughly investigated by using X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR). This work provides a simple and effective strategy for improving the morphology of perovskite and therefore the performance of PeLEDs. Full article

In the evolving landscape of portable electronics, there is a critical demand for components that meld stretchability with optical transparency, especially in supercapacitors. Traditional materials fall short in harmonizing conductivity, stretchability, transparency, and capacity. Although poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) stands out as an exemplary candidate, further performance enhancements are necessary to meet the demands of practical applications. This study presents an innovative and effective method for enhancing electrochemical properties by homogeneously incorporating Ru(III) into PEDOT:PSS. These Ru(III) PEDOT:PSS complexes are readily synthesized by dipping PEDOT:PSS films in RuCl₃ solution for no longer than one minute, leveraging the high specific capacitance of Ru(III) while minimizing interference with transmittance. The supercapacitor made with this Ru(III) PEDOT:PSS complex demonstrated an areal capacitance of 1.62 mF cm⁻² at a transmittance of 73.5%, which was 155% higher than that of the supercapacitor made with PEDOT:PSS under comparable transparency. Notably, the supercapacitor retained 87.8% of its initial capacitance even under 20% tensile strain across 20,000 cycles. This work presents a blueprint for developing stretchable and transparent supercapacitors, marking a significant stride toward next-generation wearable electronics. Full article

Third-generation biosensors use enzymes capable of direct electron transfer (DET) to the sensor surface. They are of interest for continuous glucose monitoring in blood or interstitial fluid, but they are rarely investigated. One reason is the hindered DET of the enzymes to the metallic electrodes. In this publication, a novel method for the immobilization of cellobiose dehydrogenase (CDH) DET enzymes employing conductive poly(3,4-ethylenedioxythiophene)-poly (styrene sulfonate) (PEDOT:PSS) inks and a protective polyethylene glycol dimethacrylate (PEG-DMA) hydrogel layer on gold electrodes is reported. This layer stack showed a glucose-specific current response for voltages between −0.2 and 0.4 V in physiological PBS buffer, and enabled interference-less sensing in a solution of acetaminophen, ascorbic acid, dopamine, and uric acid at 0 V. A Michaelis–Menten fit led to a maximum current density (I_max) of 257 ± 7.9 nA/mm² and a Michaelis–Menten constant (K_m) of 28.4 ± 2.2 mM, with a dynamic range of 0.1–20 mM glucose and a limit of detection of 0.1 mM. After 16 h of continuous measurement of 20 mM glucose, the signal decreased to 60% of its initial value. Storage stability was successfully verified until up to 10 days. In summary, this paper shows a simplified approach for the fabrication of third-generation biosensors using CDH-PEDOT:PSS and PEG-DMA hydrogel inks. Full article

Epilepsy is a chronic neurological disorder characterized by recurrent seizures resulting from abnormal neuronal hyperexcitability. In the case of pharmacoresistant epilepsy requiring resection surgery, the identification of the Epileptogenic Zone (EZ) is critical. Fast Ripples (FRs; 200–600 Hz) are one of the promising biomarkers that can aid in EZ delineation. However, recording FRs requires physically small electrodes. These microelectrodes suffer from high impedance, which significantly impacts FRs’ observability and detection. In this study, we investigated the potential of a conductive polymer coating to enhance FR observability. We employed biophysical modeling to compare two types of microelectrodes: Gold (Au) and Au coated with the conductive polymer poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonate) (Au/PEDOT:PSS). These electrodes were then implanted into the CA1 hippocampal neural network of epileptic mice to record FRs during epileptogenesis. The results showed that the polymer-coated electrodes had a two-order lower impedance as well as a higher transfer function amplitude and cut-off frequency. Consequently, FRs recorded with the PEDOT:PSS-coated microelectrode yielded significantly higher signal energy compared to the uncoated one. The PEDOT:PSS coating improved the observability of the recorded FRs and thus their detection. This work paves the way for the development of signal-specific microelectrode designs that allow for better targeting of pathological biomarkers. Full article

As a π-conjugated conductive polymer, poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) is recognized as a promising environmentally friendly thermoelectric material. However, its low conductivity has limited applications in the thermoelectric field. Although thermoelectric efficiency can be significantly enhanced through post-treatment doping, these processes often involve environmentally harmful organic solvents or reagents. In this study, a novel and environmentally benign method using purified water (including room temperature water and subsequent warm water) to treat PEDOT:PSS film has been developed, resulting in improved thermoelectric performance. The morphology data, chemical composition, molecular structure, and thermoelectric performance of the films before and after treatment were characterized and analyzed using a scanning electron microscope (SEM), Raman spectrum, XRD pattern, X-ray photoelectron spectroscopy (XPS), and a thin film thermoelectric measurement system. The results demonstrate that the water treatment effectively removes nonconductive PSS from PEDOT:PSS composites, significantly enhancing their conductivity. Treated films exhibit improved thermoelectric properties, particularly those treated only 15 times with room temperature water, achieving a high electrical conductivity of 62.91 S/cm, a Seebeck coefficient of 14.53 μV K⁻¹, and an optimal power factor of 1.3282 µW·m^–1·K^–2. In addition, the subsequent warm water treatment can further enhance the thermoelectric properties of the film sample. The underlying mechanism of these improvements is also discussed. Full article

This work investigates the optimization of carbon-based electrodes employed in bio-electrochemical systems (BES) through the deposition of nanostructured layers of poly(3,4-ethylene-dioxy-thiophene) poly(styrene-sulfonate) (PEDOT:PSS) on commercial carbon paper electrodes via ultrasonic spray coating (USC). This innovative application of USC demonstrated that uniform and controlled depositions of PEDOT:PSS can be successfully performed on carbon-based electrodes. To this end, the morphology and spatial uniformity of depositions were verified via scanning electron microscopy and Raman spectroscopy. Electrochemical characterizations of fabricated electrodes demonstrated a more than two-fold increase in the electrochemical active surface area with respect to bare carbon paper. A lab-scale experiment on BES was performed, selecting microbial fuel cells (MFCs) as the reference devices. Devices featuring USC-deposited PEDOT:PSS electrodes showed a three-fold-higher energy recovery with respect to control cells, reaching a maximum value of (13 ± 2) J·m⁻³. Furthermore, the amount of PEDOT:PSS required to optimize MFCs’ performance is in line with values reported in the literature for other deposition methods. In conclusion, this work demonstrates that USC is a promising technique for application in BES. Full article

As a remarkable multifunctional material, ferroferric oxide (Fe₃O₄) exhibits considerable potential for applications in many fields, such as energy storage and conversion technologies. However, the poor electronic and ionic conductivities of classical Fe₃O₄ restricts its application. To address this challenge, Fe₃O₄ nanoparticles are combined with graphene oxide (GO) via a typical hydrothermal method, followed by a conductive wrapping using poly(3,4-ethylenedioxythiophene):poly(styrene sulfonic sulfonate) (PEDOT:PSS) for the fabrication of composite films. Upon acid treatment, a highly conductive porous Fe₃O₄@RGO/PEDOT:PSS hybrid is successfully constructed, and each component exerts its action that effectively facilitates the electron transfer and subsequent performance improvement. Specifically, the Fe₃O₄@RGO/PEDOT:PSS porous film achieves a high specific capacitance of 244.7 F g⁻¹ at a current of 1 A g⁻¹. Furthermore, due to the facial fabrication of the highly conductive networks, the free-standing film exhibits potential advantages in flexible thermoelectric (TE) materials. Notably, such a hybrid film shows a high electric conductivity (σ) of 507.56 S cm⁻¹, a three times greater value than the Fe₃O₄@RGO component, and achieves an optimized Seebeck coefficient (S) of 13.29 μV K⁻¹ at room temperature. This work provides a novel route for the synthesis of Fe₃O₄@RGO/PEDOT:PSS multifunctional films that possess promising applications in energy storage and conversion. Full article