Search Results (42)

Organic-type solar cells containing an active layer of block copolymer donor PTB7-Fx (x = 0, 20, and 100), based on benzo [1,2-b:4,5-b’]dithiophene and variably fluorinated thieno [3,4-b]thiophene units, and fullerene acceptor [6,6]phenyl-C₇₁-methylbutyrate, were constructed. The active layer thin film of the solar cells was obtained from a dichlorobenzene solution at an established concentration via spin-coating of the donor–acceptor mixture in the presence of solvent additives such as 3% diiodooctane and 1% triethyl phosphate. Organic photovoltaic elements with normal device architecture were prepared on glass substrates using an indium tin oxide anode, a spin-coated hole transporting layer of poly(ethylene dioxythiophene):polystyrenesulfonate, the aforementioned active layer, followed by an electron transporting layer of zinc oxide nanoparticles, and finally a magnetron sputtered silver (Ag) top-electrode. The optical properties, thin film morphology, and the thickness of the active layers were investigated. Additionally, current density–voltage characteristics and impedance spectra of photovoltaic devices were measured. It was found that PTB7-Fx:PC₇₁BM-based solar cells processed in the presence of two types of solvent additives, diiodooctane and triethyl phosphate, with a sputtered Ag top-electrode display similar absorption and quantum efficiency spectra, as well as comparable current density–voltage characteristics and efficiencies to the same devices fabricated without additives. The diiodooctane solvent additive preferably dissolves the fullerene component and has a positive effect on fill factor enhancement, impedance spectra improvement, and amelioration in charge carrier transport and collection, whereas the triethyl phosphate solvent additive preferentially dissolves the copolymer donor and has a more pronounced impact on the refined morphology of the thin film active layers. Full article

Zinc(II) bis(8-hydroxyquinolinate) (Zn(HQ)₂) and 1,10-phenanthroline (phen) were combined to fabricate an organic semiconductor in a bulk heterojunction architecture and subsequently embedded in a poly 3,4-ethylene dioxythiophene–polystyrene sulfonate (PEDOT–PSS) matrix. The resulting Zn(HQ)₂-phen/PEDOT–PSS was deposited as a film upon tin-oxide-coated glass and graphite-covered Tetra Pak (TP)-recycled substrates for the manufacture of organic photoconductive devices. The topographical and micromechanical characteristics of the hybrid films were assessed by atomic force microscopy, with an average roughness of 5.6 nm, maximum tensile strength of 7.95 MPa, and Knoop microhardness of 14.7. The fundamental energy gap (E_g) was determined employing the Kubelka–Munk function, with E_g of 3.5–3.8 eV. These results were complemented with a computational DFT molecular orbital analysis of the species involved in the hybrid semiconductor. The devices were electrically characterized under UV irradiation conditions, obtaining the current–voltage and power–voltage relationships. The maximum current in the TP–graphite device is 1.8 × 10⁻² A and 1.1 × 10⁻² A in the device on glass–ITO. Zn(HQ)₂-phen/PEDOT–PSS film presents its own operating regimes relating to a photoconductor or flexible photoresistor. The power in the device on glass–ITO is 120 mW and 113 mW for shortwave and longwave, respectively, and in the device on TP–graphite, it is 198 mW and 139 mW. Full article

Polydimethylsiloxane (PDMS) and poly(3,4-ethylene dioxythiophene):poly(4-styrene-sulfonate) (PEDOT:PSS) composites were tested to determine their suitability for charging small-scale batteries in conjunction with a piezoelectric actuator as an energy harvester. Two different PEDOT:PSS patterns (zigzag and serpentine) were tested, and the maximum DC voltage of a system incorporating PEDOT:PSS was determined. The aim of this work is to study the effect of soft corners in the electrical routing of aircraft and IoT sensors. The zigzag and serpentine patterns were considered for this study because of their simplicity in design. Without the polymer, 2.3 V was produced by the actuator, while adding PEDOT:PSS resulted in the voltage being reduced to 1.7 V. The piezoelectric actuator was connected to a 3.6 V rechargeable Li-ion battery, and the battery’s voltage was recorded over 1 h. The voltage from the piezoelectric actuator was 3.8 V. Without PEDOT:PSS, the battery was charged to a maximum of 3 V. Adding the PEDOT:PSS to the circuit reduced the maximum charge to a voltage of 2 V. The results indicate that while PEDOT:PSS composites can be used in conjunction with piezoelectric energy harvesters, more work is still needed to optimize the system to increase efficiency and charging rates. Full article

Hexahydro-1,3,5-trinitro-1,3,5-triazine (RDX), a typical representative of energetic materials, is widely applied in military and industrial fields with its high energy density and excellent detonation performances. However, when used as a raw material for propellants and rocket propellants, RDX poses certain safety concerns due to its high sensitivity to external stimuli such as electrostatic discharge, impact, and friction, which limits its further application. Herein, to reduce the RDX electrostatic spark and mechanical sensitivities and improve safety performances, a conductive polymer of poly(3,4-ethylene-dioxythiophene)–poly(styrenesulfonate) (PEDOT:PSS) was introduced into the energetic material system based on a simple suction filtration method. RDX-based energetic composites with varying PEDOT:PSS mass fractions were prepared by both micron-sized RDX and nanosized RDX. The RDX-based energetic composites were characterized, and their response characteristics and performances were tested and compared. The results demonstrated that the conductive interfaces constructed by PEDOT:PSS on the RDX surface significantly reduced the electrostatic spark and mechanical sensitivity. The electrostatic spark sensitivity of μ-RDX-based energetic composites decreased by 40%, while the impact sensitivity and friction sensitivity decreased by 76.47% and 50%, respectively. Compared to micron-sized RDX-based energetic composites, the nano-sized RDX-based energetic composites desensitization effect on electrostatic spark sensitivity was more pronounced. For n-RDX-based energetic composites, the electrostatic spark sensitivity decreased by 66.4%. Furthermore, the assembly and desensitization mechanism of the RDX-based energetic composites were thoroughly investigated. This study not only provides a simple and reliable assembly method for the safe application of RDX but also offers corresponding data and experimental support for future research, which is of significant importance for the application of energetic materials. Full article

The aim of this paper is to investigate the influence of the molecules of conducting polymers on the properties of potentiometric sensors. Two conducting polymers, poly(3-octylthiophene-2,5-diyl) and poly(3,4-ethylene-1,4-dioxythiophene), were compared in the context of the design of ion-selective electrodes. This study offers a comparison of the most popular conducting polymers in the context of the design of potentiometric sensors. Firstly, the properties of both materials, such as their microstructure, electrical performance, wettability, and thermic properties, were examined. Subsequently, conducting polymers were applied as transducer layers in potassium-selective sensors. The properties of both groups of sensors were evaluated using the potentiometry method. Research has shown that the presence of poly(3-octylthiophene-2,5-diyl) (POT) in the transducer layer makes it superhydrophobic, leading to a long lifetime of sensors. On the other hand, the addition of poly(3,4-ethylene-1,4-dioxythiophene) polystyrene sulfonate (PEDOT:PSS) allows for the enhancement of electrical capacitance parameter values, which beneficially influence the stability of the potentiometric response of sensors. Both examined conducting polymers turned out to be perfect materials for transducer layers in potentiometric sensors, each being responsible for enhancing different properties of electrodes. Full article

In this work, we present the innovative synthesis of salophen (acetaminosalol) derivatives in a solvent-free environment by high-speed ball milling, using a non-conventional activation method, which allowed obtaining compounds in a shorter time and with a better yield. Furthermore, for the first time, the salophen derivatives were deposited as composite films, using a matrix of poly 3,4-ethylene dioxythiophene:polystyrene sulfonate (PEDOT:PSS) polymer. Significant findings include the transformation from the benzoid to the quinoid form of PEDOT post-IPA treatment, as evidenced by Raman spectroscopy. SEM analysis revealed the formation of homogeneous films, and AFM provided insights into the changes in surface roughness and morphology post-IPA treatment, which may be crucial for understanding potential applications in electronics. The optical bandgap ranges between 2.86 and 3.2 eV for PEDOT:PSS-salophen films, placing them as organic semiconductors. The electrical behavior of the PEDOT:PSS-salophen films undergoes a transformation with the increase in voltage, from ohmic to space charge-limited conduction, and subsequently to constant current, with a maximum of 20 mA. These results suggest the possible use of composite films in organic electronics. Full article

This study explores the potential of copper-doped nickel oxide (Cu:NiO) as a hole transport layer (HTL) in flexible photovoltaic (PV) devices using a combined first-principles and finite element analysis approach. Density functional theory (DFT) calculations reveal that Cu doping introduces additional states in the valence band of NiO, leading to enhanced charge transport. Notably, Cu:NiO exhibits a direct band gap (reduced from 3.04 eV in NiO to 1.65 eV in the stable supercell structure), facilitating the efficient hole transfer from the active layer. Furthermore, the Fermi level shifts towards the valence band in Cu:NiO, promoting hole mobility. This translates to an improved photovoltaic performance, with Cu:NiO-based HTLs achieving ~18% and ~9% power conversion efficiencies (PCEs) in perovskite and poly 3-hexylthiophene: 1-3-methoxycarbonyl propyl-1-phenyl 6,6 C 61 butyric acid methyl ester (P3HT:PCBM) polymer solar cells, respectively. Finally, a finite element analysis demonstrates the potential of these composite HTLs with Poly 3,4-ethylene dioxythiophene)—polystyrene sulfonate (PEDOT:PSS) in flexible electronics design and the optimization of printing processes. Overall, this work highlights Cu:NiO as a promising candidate for high-performance and flexible organic–inorganic photovoltaic cells. Full article

Flexible thermoelectric generators (FTEGs), which can overcome the energy supply limitations of wearable devices, have received considerable attention. However, the use of toxic Te-based materials and fracture-prone electrodes constrains the application of FTEGs. In this study, a novel Ag₂Se and Poly (3,4-ethylene dioxythiophene): poly (styrene sulfonate) (PEDOT:PSS)/multi-walled carbon nanotube (MWCNT) FTEG with a high output performance and good flexibility is developed. The thermoelectric columns formulated in the work are environmentally friendly and reliable. The key enabler of this work is the use of embedded EGaIn electrodes, which increase the temperature difference collected by the thermoelectric column, thereby improving the FTEG output performance. Additionally, the embedded EGaIn electrodes could be directly printed on polydimethylsiloxane (PDMS) molds without wax paper, which simplifies the preparation process of FTEGs and enhances the fabrication efficiency. The FTEG with embedded electrodes exhibits the highest output power density of 25.83 μW/cm² and the highest output power of 10.95 μW at ΔT = 15 K. The latter is 31.6% higher than that of silver-based FTEGs and 2.5% higher than that of covered EGaIn-based FTEGs. Moreover, the prepared FTEG has an excellent flexibility (>1500 bends) and output power stability (>30 days). At high humidity and high temperature, the prepared FTEG maintains good performance. These results demonstrate that the prepared FTEGs can be used as a stable and environmentally friendly energy supply for wearable devices. Full article

This study aims to develop a microelectrode array-based neural probe that can record dopamine activity with high stability and sensitivity. To mimic the high stability of the gold standard method (carbon fiber electrodes), the microfabricated platinum microelectrode is coated with carbon-based nanomaterials. Carboxyl-functionalized multi-walled carbon nanotubes (COOH-MWCNTs) and carbon quantum dots (CQDs) were selected for this purpose, while a conductive polymer like poly (3-4-ethylene dioxythiophene) (PEDOT) or polypyrrole (PPy) serves as a stable interface between the platinum of the electrode and the carbon-based nanomaterials through a co-electrodeposition process. Based on our comparison between different conducting polymers and the addition of CQD, the CNT–CQD–PPy modified microelectrode outperforms its counterparts: CNT–CQD–PEDOT, CNT–PPy, CNT–PEDOT, and bare Pt microelectrode. The CNT–CQD–PPy modified microelectrode has a higher conductivity, stability, and sensitivity while achieving a remarkable limit of detection (LOD) of 35.20 ± 0.77 nM. Using fast-scan cyclic voltammetry (FSCV), these modified electrodes successfully measured dopamine’s redox peaks while exhibiting consistent and reliable responses over extensive use. This electrode modification not only paves the way for real-time, precise dopamine sensing using microfabricated electrodes but also offers a novel electrochemical sensor for in vivo studies of neural network dynamics and neurological disorders. Full article

Layered oxides exhibit interesting performance as positive electrodes for commercial sodium-ion batteries. Nevertheless, the replacement of low-sustainable nickel with more abundant iron would be desirable. Although it can be achieved in P2-Na_2/3Ni_2/9Fe_2/9Mn_5/9O₂, its performance still requires further improvement. Many imaginative strategies such as surface modification have been proposed to minimize undesirable interactions at the cathode–electrolyte interface while facilitating sodium insertion in different materials. Here, we examine four different approaches based on the use of the electron-conductive polymer poly(3,4-ethylene dioxythiophene) (PEDOT) as an additive: (i) electrochemical in situ polymerization of the monomer, (ii) manual mixing with the active material, (iii) coating the current collector, and (iv) a combination of the latter two methods. As compared with pristine layered oxide, the electrochemical performance shows a particularly effective way of increasing cycling stability by using electropolymerization. Contrarily, the mixtures show less improvement, probably due to the heterogeneous distribution of oxide and polymer in the samples. In contrast with less conductive polyanionic cathode materials such as phosphates, the beneficial effects of PEDOT on oxide cathodes are not as much in rate performance as in inhibiting cycling degradation, due to the compactness of the electrodes without loss of electrical contact between active particles. Full article

Molecularly imprinted polymers (MIPs) have garnered significant attention as a promising material for engineering specific biological receptors with superior chemical complementarity to target molecules. In this study, we present an electrochemical biosensing platform incorporating MIP films for the selective detection of the interleukin-1β (IL-1β) biomarker, particularly suitable for mobile point-of-care testing (POCT) applications. The IL-1β-imprinted biosensors were composed of poly(eriochrome black T (EBT)), including an interlayer of poly(3,4-ethylene dioxythiophene) and a 4-aminothiophenol monolayer, which were electrochemically polymerized simultaneously with template proteins (i.e., IL-1β) on custom flexible screen-printed carbon electrodes (SPCEs). The architecture of the MIP films was designed to enhance the sensor sensitivity and signal stability. This approach involved a straightforward sequential-electropolymerization process and extraction for leaving behind cavities (i.e., rebinding sites), resulting in the efficient production of MIP-based biosensors capable of molecular recognition for selective IL-1β detection. The electrochemical behaviors were comprehensively investigated using cyclic voltammograms and electrochemical impedance spectroscopy responses to assess the imprinting effect on the MIP films formed on the SPCEs. In line with the current trend in in vitro diagnostic medical devices, our simple and effective MIP-based analytical system integrated with mobile POCT devices offers a promising route to the rapid detection of biomarkers, with particular potential for periodontitis screening. Full article

The progression of Alzheimer’s disease (AD) is positively correlated with the phosphorylation damage of Tau-441 protein, which is the marker with the most potential for the early detection of AD. The low content of Tau-441 in human serum is a major difficulty for the realization of content detection. Herein, we prepared an electrochemical immunosensor modified with Poly(3,4-ethylene-dioxythiophene)-poly (styrene sulfonate) (PEDOT: PSS)/Carboxylated multi-walled carbon nanotube (MWCNTs-COOH) nanocomposites based on electrochemical immunoassay technology for the low-concentration detection of Tau-441. The immunosensor based on the nanocomposite can take advantage of the characteristics of conductive polymers to achieve electrical signal amplification and use MWCNTs-COOH to increase the contact area of the active site and bond with the Tau-441 antibodies on the electrode. The physicochemical and electrical properties of PEDOT: PSS/MWCNTs-COOH were studied by in situ characterization techniques and electrochemical characterization methods, indicating that the immunosensor has high selectivity and sensitivity to the Tau-441 immune reaction. Under optimized optimal conditions, the electrochemical immunosensor detected a range of concentrations of Tau-441 to obtain a low detection of limit (0.0074 ng mL⁻¹) and demonstrated good detection performance through actual human serum sample testing experiments. Therefore, the study provides an effective reference value for the early diagnosis of AD. Full article

Minimizing the impact of electromagnetic radiation (EMR) holds paramount importance in safeguarding individuals who frequently utilize electrical and electronic devices. Electrically conductive textiles, which possess specialized EMR shielding features, present a promising solution to mitigate the risks related to EMR. Furthermore, these textile-based shielding materials could find application as radar-absorbing materials in stealth technology, emphasizing the need for substantial absorption capabilities in shielding mechanisms. In this study, various textile-based materials with an electrically conductive coating that contain the conjugated polymer system poly(3,4-ethylene-dioxythiophene)-polystyrene sulfonate (PEDOT:PSS) were prepared and investigated. The influence of the textile substrate structural parameters, coating deposit, and coating method on their microwave properties—transmission, reflection, and absorption—was investigated. Reflection and transmission measurements were conducted within a frequency range of 2 to 18 GHz. These measurements revealed that, for the tested samples, the shielding properties are determined by the combined effect of reflection and absorption. However, the role of these two parameters varies across the tested frequency range. It was defined that for fabrics coated on one side, better reflection reduction is obtained when the shielding effectiveness (SE) is below |20| dB. It was found that by controlling the coating deposition on the fabric, it is possible to fine-tune the electrical properties to a certain extent, thereby influencing the microwave properties of the coated fabrics. The studies of prepared samples have shown that reflection and transmission parameters depend not only on the type and quantity of conductive paste applied to the fabric but also on the fabric’s construction parameters and the coating technique used. It was found that the denser the substrate used for coating, the more conductive paste solidifies on the surface, forming a thicker coat on the top. For conductive fabrics with the same substrate to achieve a particular SE value using the knife-over-roll coating technology, the required coating deposit amount is considerably lower as compared with the deposit necessary in the case of screen printing: for the knife-over-roll-coated sample to reach SE 15 dB, the required deposit is approximately 14 g/m²; meanwhile, for a sample coated via screen printing, this amount rises to 23 g/m². Full article

The accurate mimicking of the fibrillary structure of the extracellular matrix represents one of the critical aspects of tissue engineering, playing a significant role in cell behavior and functions during the regenerative process. This work proposed the design of PVA-based multi-component membranes as a valuable and highly versatile strategy to support in vitro regeneration of different tissues. PVA can be successfully processed through electrospinning processes, allowing for the integration of other organic/inorganic materials suitable to confer additive bio-functional properties to the fibers to improve their biological response. It was demonstrated that adding polyethylene oxide (PEO) improves fiber processability; moreover, SEM analyses confirmed that blending PVA with PEO or gelatin enables the reduction of fiber size from 1.527 ± 0.66 μm to 0.880 ± 0.30 μm and 0.938 ± 0.245 μm, respectively, also minimizing defect formation. Furthermore, in vitro tests confirmed that gelatin integration allows the formation of bioactive nanofibers with improved biological response in terms of L929 adhesion and proliferation. Lastly, the processability of PVA fibers with conductive phases such as polyvinylpyrrolidone (PVP) or poly(3,4-ethylene dioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) has also been verified. From this perspective, they could be promisingly used to design electroactive composite fibers able to support the regeneration process of electrically stimulated tissues such as nerves or muscles. Full article

In this paper, we propose a novel tactile sensor with a “fingerprint” design, named due to its spiral shape and dimensions of 3.80 mm × 3.80 mm. The sensor is duplicated in a four-by-four array containing 16 tactile sensors to form a “SkinCell” pad of approximately 45 mm by 29 mm. The SkinCell was fabricated using a custom-built microfabrication platform called the NeXus which contains additive deposition tools and several robotic systems. We used the NeXus’ six-degrees-of-freedom robotic platform with two different inkjet printers to deposit a conductive silver ink sensor electrode as well as the organic piezoresistive polymer PEDOT:PSS-Poly (3,4-ethylene dioxythiophene)-poly(styrene sulfonate) of our tactile sensor. Printing deposition profiles of 100-micron- and 250-micron-thick layers were measured using microscopy. The resulting structure was sintered in an oven and laminated. The lamination consisted of two different sensor sheets placed back-to-back to create a half-Wheatstone-bridge configuration, doubling the sensitivity and accomplishing temperature compensation. The resulting sensor array was then sandwiched between two layers of silicone elastomer that had protrusions and inner cavities to concentrate stresses and strains and increase the detection resolution. Furthermore, the tactile sensor was characterized under static and dynamic force loading. Over 180,000 cycles of indentation were conducted to establish its durability and repeatability. The results demonstrate that the SkinCell has an average spatial resolution of 0.827 mm, an average sensitivity of 0.328 $\mathsf{m}\mathsf{\Omega }/\mathsf{\Omega }/\mathsf{N}$, expressed as the change in resistance per force in Newtons, an average sensitivity of 1.795 µV/N at a loading pressure of 2.365 PSI, and a dynamic response time constant of 63 ms which make it suitable for both large area skins and fingertip human–robot interaction applications. Full article