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Textile-based SrAl 2 O 4 (SAO): Eu2+, Dy3+ composite material offers functional, aesthetic, and safety benefits, making it a valuable innovation with diverse applications in various industries. The susceptibility of textile-based SAO: Eu2+, Dy3+ composite material is degraded with repeated washing, which can diminish its luminescent properties over time. Our major goal was to create a cloth with durable photoluminescent qualities by incorporating waterborne polyurethane (WPU) as a protective coating that could generate light constantly without a light source. Through a systematic approach involving the synthesis of photoluminescent SAO: Eu2+, Dy3+ particles and their integration into a cloth substrate with waterborne polyurethane, a durable cloth with enhanced durability, protection, and adhesion properties are achieved. Cotton fabric and a rotary screen-printing machine were used to apply a thin, translucent layer of glow-in-the-dark pigment to produce the photoluminescence characteristics of the developed cloth revealing efficient light absorption and emission behavior, with emission spectra centered around absorption wavelength between 560 nm and 880 nm, with a 500 nm emission peak, exhibiting of the presence of Eu2+ and Dy3+ activator ions. In addition, to assess the comfort of the treated cotton fabric, a fabroOmeter test was conducted, that provided insights into its overall comfort level. Furthermore, the cloth demonstrates excellent stability and longevity of photoluminescence under various environmental conditions, making it suitable for applications requiring high visibility, safety signage, decorative elements, and apparel wear. This research underscores the potential of polyurethane-enhanced photoluminescent textiles as versatile and sustainable solutions for diverse practical applications. [Display omitted] [ABSTRACT FROM AUTHOR]

The struggle against climate change necessitates innovative technologies for storing and utilizing renewable energy. Hydrogen is considered a promising solution for harnessing renewable energy in a wide range of applications. In addition to its application as a raw material in the steel and the chemical industry, hydrogen can also be utilized as an energy carrier in conjunction with fuel cells (e.g. with Polymer Electrolyte Membrane Fuel Cells PEMFC) for heavy-duty vehicles, emergency power supplies or the maritime sector. To achieve the required electrical voltages for these applications, several hundred cells are assembled to a stack. A crucial component of an individual cell alongside the Membrane Electrode Assembly (MEA) is the Bipolar Plate (BPP), consisting of two bonded Bipolar Half Plates (BPHP). The BPP enables an inflow of reactive media, the cooling of the cell and is also required for the electrical contacting of the stacked cells as well as the overall mechanical stability. According to previous studies, fully bonded BPPs, especially in the flow field, significantly improve both mechanical and electrical properties of the entire stack. The here presented innovative approach for adhesive deposition aims at bonding graphitic BPHPs to BPPs with a high throughput capability while maintaining high flexibility and process stability. The process is based on the conventional screen printing technique, which in this case is performed without a stencil, allowing for a high flexibility regarding the cell geometry. Furthermore, the range of usable adhesives can be expanded with minor adjustments, allowing for not only paste adhesives but also thermally activated powders. With the presented approach, the adhesive volume can be controlled precisely and applied uniformly by selecting a suitable screen. The feasibility of the approach was tested and initial parameter estimations for potential industrial implementation were determined. [ABSTRACT FROM AUTHOR]

This work demonstrates the fabrication, characterization, and energy storage capacity of high calcium-doped strontium titanate thick films (Sr0.60Ca0.40TiO3) for the first time. The thick films were fabricated using the screen-printing technique and densified using uniaxial pressing. The effect of densification on the structural, morphological, and surface chemical compositional of the materials was studied. The densified thick film revealed a notable frequency stability of dielectric permittivity (ε′) ≈ 198 with a low dielectric loss tangent (tanδ) in the order of 10− 3 between 100 Hz and 1 MHz and was characterized by slim P-E loops signifying its paraelectric nature. A high energy recovery density (Ue) of 4.1 J/cm3 and a high energy efficiency of 96% were simultaneously reached. [ABSTRACT FROM AUTHOR]

With the increasing demand for compact, lightweight, cost‐effective, and high‐performance radiofrequency (RF) devices, the development of low‐profile antennas becomes crucial. This article presents a study of a novel carbon–cellulose‐based paste intended for screen printing RF devices. The investigation specifically explores the application of high‐reactivity carbon mixture (HRCM) particles as conductive fillers. The results demonstrate that optimal electrical conductivity values and discrete electromagnetic dipole performances can be achieved at lower concentrations of solid conductive material compared to conventional pastes, for similar applications. This offers benefits in terms of total cost, material consumption, and environmental impact. The paste formulation showcases a complex non‐Newtonian behavior, where yielding flow and thixotropicity are found to be independent and dependent on preshear conditions, respectively. This behavior can be attributed to the network orientation and rearrangement of filler structures within the paste system, which in turn are responsible for filler pattern uniformity and overall printing quality. Compared to traditional conductive materials, HRCM pastes are proven to be a viable alternative for RF devices fabrication, including printed Wi‐Fi antennas. [ABSTRACT FROM AUTHOR]

Hydrogen sulfide (H2S) is a highly toxic and corrosive gas commonly found in industrial emissions and natural gas processing, posing serious risks to human health and environmental safety even at low concentrations. The early detection of H2S is therefore critical for preventing accidents and ensuring compliance with safety regulations. This study presents the development of porous ZnO/SnO2-nanocomposite gas sensors tailored for the ultrasensitive detection of H2S at sub-ppb levels. Utilizing a screen-printing method, we fabricated five different sensor compositions—ranging from pure SnO2 to pure ZnO—and characterized their structural and morphological properties through X-ray diffraction (XRD) and scanning electron microscopy (SEM). Among these, the SnO2/ZnO sensor with a composition-weight ratio of 3:4 demonstrated the highest response at 325 °C, achieving a low detection limit of 0.14 ppb. The sensor was evaluated for detecting H2S concentrations ranging from 5 ppb to 500 ppb under dry, humid air and N2 conditions. The relative concentration error was carefully calculated based on analytical sensitivity, confirming the sensor's precision in measuring gas concentrations. Our findings underscore the significant advantages of mixture nanocomposites in enhancing gas sensitivity, offering promising applications in environmental monitoring and industrial safety. This research paves the way for the advancement of highly effective gas sensors capable of operating under diverse conditions with high accuracy. [ABSTRACT FROM AUTHOR]

In recent years, third-generation solar cells have experienced a remarkable growth in efficiency, making them a highly promising alternative energy solution. Currently, high-efficiency solar cells often use top electrodes fabricated by thermal evaporation, which rely on high-cost and high energy-consumption vacuum equipment, raising significant concerns for mass production. This study develops a method for fabricating silver electrodes using the screen-printing process, aiming to achieve solar cell production through an all-solution coating process. By selecting appropriate blocking-layer materials and optimizing the process, we have achieved device efficiencies for organic photovoltaics (OPVs) with screen-printed silver electrodes comparable to those with silver electrodes fabricated by thermal evaporation. Furthermore, we developed a method to cure the silver ink using near-infrared (NIR) annealing, significantly reducing the curing time from 30 min with hot air annealing to just 5 s. Additionally, by employing sheet-to-sheet (S2S) slot-die coating, we scaled up the device area and completed module development, successfully verifying stability in ambient air. We have also extended the application of screen-printed silver electrodes to perovskite solar cells (PSCs). [ABSTRACT FROM AUTHOR]

With the constant increase of electronic waste globally, society is demanding and governments are boosting the development of electronics with less pollutant materials and reduced environmental impact. One way to achieve this is to implement materials that are functional and structural at the same time, reducing material use and assembling parts. Further, printing techniques, such as screen printing, reduce considerably costs and time compared with conventional electronics; combined with methods to conform printed electronics to a 3D shape, such as thermoforming, allow to obtain nonplanar surface electronics simply and efficiently. Herein, screen‐printable inks made of styrene–ethylene/butylene–styrene and different aspect‐ratio carbon‐based materials for conformable electronics are reported. The inks are prepared with carbon black, carbon nanotubes, and reduced graphene oxide as conductive fillers, printed on a flexible substrate and thermoformed. Carbon black and carbon nanotube samples are functional after the process, with conductivities of 96 and 141 S m−1 for the best performing sample of each filler, respectively. Rheological, morphological, thermal, and electrical properties of the materials are also characterized. This study shows the influence of the filler's type and aspect ratio on the morphology and electrical conductivity of the printed materials before and after thermoforming. [ABSTRACT FROM AUTHOR]

Due to its superior reliability and performance, thick film technology is extensively employed in various applications, including automotive electronics, consumer electronics, communication engineering, and aerospace. However, a challenge arises from the mutual diffusion during the electronic paste production process, which leads to a decline in insulation performance and hinders the production of three-dimensional equipment. Inspired by the principles of low-temperature co-fired ceramic technology, a multi-layered ceramic structure has been successfully bonded using thick film technology by introducing a borosilicate glass-ceramics layer. To further enhance the properties of this multi-layered ceramic structure, approximately 8 wt% SiO 2 was incorporated into the borosilicate glass-ceramics. This addition effectively inhibits silver diffusion and reduces the diffusion depth within the glass-ceramic film. The key mechanisms behind this improvement are the increased activation energy for crystallization, resulting in a slower crystallization rate due to the addition of SiO 2. Moreover, the multi-layered ceramic with a sandwich structure exhibits remarkable properties. Notably, the dielectric strength of this system has been significantly enhanced to 13.9 kV/mm, accompanied by a high adhesion strength of 790 N. These enhanced properties of the optimized system indicate promising characteristics for multi-layer circuit applications. [ABSTRACT FROM AUTHOR]

This work presents the development of fully printed, large‐area, semi‐transparent Dye‐Sensitized Solar Cells (DSSCs) using TiO2 nanoparticles treated with TiCl4, a “D35” push‐pull dye sensitizer, and I3−/I− redox mediator. Cells with areas of 4 and 200 cm2 were printed using hexagonal, stripe, and standard designs, employing digital materials deposition (DMD) technology. The porous films printed via DMD, confirmed by scanning electron microscopy (SEM), improved solar cells performance by enhancing the Open Circuit Voltage (Voc) and fill factor (FF). The hexagonal design, in particular, facilitated better electrolyte impregnation in the TiO2 mesoporous structure, boosting current density. This design yielded a power conversion efficiency (PCE) of 7.05% for 4 cm2 DSSCs, surpassing the stripe (5.50%) and standard (5.48%) designs. Its higher performance can be attributed to lower interfacial charge recombination rates and improvedcharge transfer and collection efficiency. Photophysical measurements indicated faster charge transfer rates in hexagonal cells (≈ 1.3  ×  109s−1) compared to the stripe (9.8  ×  108 s−1) and standard (9.5  ×  108 s−1) designs. Hence, our work highlights the potential of hexagonal design to improve both efficiency and transparency while reducing material consumption, offering a promising approach for manufacturing semi‐transparent solar cells. [ABSTRACT FROM AUTHOR]

This study explores the intricate interaction between the properties of textile substrates and screen-printing parameters in shaping fabric circuits using silver conductive ink. Via analyzing key variables such as fabric type, mesh density, and the number of overprinted layers, the research revealed how the porous structure, large surface area, and fiber morphology of textile substrates influence ink absorption, ultimately enhancing the electrical connectivity of the printed circuits. Notably, the hydrophilic cotton staple fibers fabric effectively absorbed the conductive ink into the fabric substrate, demonstrating superior electrical performance compared with the hydrophobic polyester filament fabric after three overprinting, unlike the results observed after a single print. As mesh density decreased and the number of prints increased, the electrical resistance of the circuit gradually reduced, but ink bleeding on the fabric surface became more pronounced. Cotton fabric, via absorbing the ink deeply, exhibited less surface bleeding, while polyester fabric showed more noticeable ink spreading. These findings provide valuable insights for improving screen printing technology for textile circuits and contribute to the development of advanced fabric circuits that enhance the functionality of smart wearable technology. [ABSTRACT FROM AUTHOR]

This study presents the development of a novel screen printable quasi‐solid polymer electrolyte (p‐QSPE) for Electrochromic Displays (ECDs) applications. p‐QSPE is composed of three key components: polyvinylidene fluoride (PVDF), a high‐dielectric constant polymer that ensures high ionic conductivity in solid‐state; glyceril propoxy triacrylate (GPTA), a UV‐cross‐linkable monomer that provides structure and durability for overprinting; titanium dioxide (TiO₂) nanoparticles, which modulate the electrolyte's rheological properties for screen printing; reducing the solvent (PC:EC) content to only 35.90 wt.%. Electrochemical Impedance Spectroscopy (EIS) revealed that this well‐designed formulation achieved an ionic conductivity of 1.17 × 10−3 S cm−1 at room temperature, surpassing the threshold required for commercial applications. Moreover, p‐QSPE facilitated the production of fully screen printed ECDs in an industrial printing line, streamlining their production process and achieving an optimal balance between printability, overprint resilience, and device performance. Operational tests for the ECDs showed fast switching times (<6 s for t90 and <2 s for t75) across a wide temperature range (−20 °C to 80 °C). Additionally, the electrolyte demonstrated low charge consumption (2.10 ± 0.11 mC cm−2) and a lifespan exceeding 10 000 cycles. These results highlight the potential of p‐QSPE as a screen printable, high‐performance electrolyte, capable of advancing ECD manufacturing by enabling the production of fully screen‐printed, performing ECDs. [ABSTRACT FROM AUTHOR]

Within this work, we investigate the potential to optimize the screen‐printed front side metallization of silicon heterojunction (SHJ) solar cells. Three iterative experiments are conducted to evaluate the impact of the utilized fine mesh screen configurations and grid layout adaption (finger pitch) for the front side metallization on silver laydown and electrical performance of the solar cells. With respect to the screen configuration, we compare the performance of a fine‐mesh knotless screen to a conventionally angled screen demonstrating an additional gain of Δη = +0.1%abs due to reduced shading losses. Additionally, a grid layout is improved by increasing the number of contact fingers from 120 to 156. Furthermore, the current possibility to push the fine‐line printing process for low‐temperature pastes to the limit is investigated by reducing the nominal finger width wn to 20, 18, and 15 μm. It is shown that even the smallest nominal width of wn = 15 μm can be printed with high quality, leading to an additional efficiency gain of Δη = +0.15%abs as well as a reduction of silver paste laydown by −5 mg. Finally, a batch of champion cells is fabricated by applying the findings of the previous experiments, which results in a maximum efficiency of ηmax = 23.2%. Compared to the reference group without optimization, this corresponds to a gain of Δη = +0.17%abs, which comes along with an additional decrease of the silver paste laydown by approximately −2 mg. This emphasizes the significance of consistent optimization of the screen‐printing process in terms of cell performance and resource utilization for SHJ solar cells. [ABSTRACT FROM AUTHOR]

Strain sensors from conducting polymer hydrogel have been widely employed in various wearable devices, electronic skins, and biomedical applications. These sensors provide outstanding flexibility and high sensitivity by integrating conducting polymer with hydrogels, making them particularly suitable for monitoring human motion and physiological signals like heart rate or muscle activity. Despite their extensive application potential, conducting polymer hydrogel face several technical challenges in practical use, including poor mechanical properties, lack of long‐term stability, and difficulty in customizable design. This work introduces a method for fabricating a multipedal strain sensor using poly(3,4‐ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS)/polyvinyl alcohol (PVA) dimethyl sulfoxide (DMSO)hydrogels through screen printing and demonstrates its application in human motion monitoring. The multipedal strain sensor demonstrates a low Young's modulus (200 kPa), high stretchability (400%), and excellent mechanical cyclic stability (3000 cycles). Furthermore, this strain sensor is further applied to detect human movements such as chewing, smiling, fist clenching, arm bending, and carotid pulse monitoring. Comparative analysis between the multipedal‐designed sensor and the non‐designed sensor highlights the enhanced sensing capabilities of the multipedal sensor. The design of this multipedal sensor holds the potential to broaden the design concepts for strain sensors and offers new insights for wearable devices and electronic skins. [ABSTRACT FROM AUTHOR]

The rheological behavior and printing characteristics of the screen-printing slurry for Nd-Fe-B grain boundary diffusion are key factors that determine the quality of printing and magnetic performance. However, few studies have focused on the organic medium, a crucial material for slurry. In this paper, the rheology, thixotropy, and thermal decomposition behavior of the organic vehicle in Nd-Fe-B screen printing slurry were studied. The results show that the organic vehicle formed by terpineol and polyvinyl butyral (PVB) exhibits typical non-Newtonian fluid characteristics, with excellent rheology and thixotropy, ensuring that the slurry prepared from it has excellent static stability and printing consistency. Additionally, the carbon residue of the organic vehicle formed by terpineol and PVB is less than 0.1% at 900 °C, avoiding excessive carbon entering the magnet during the diffusion process. Moreover, studying the rheology and thixotropy of the organic vehicle through a rheometer can quickly screen the slurry system. This work provides valuable guidance for designing an organic vehicle for screen-printing slurry for Nd-Fe-B grain boundary diffusion in future research. [ABSTRACT FROM AUTHOR]

A homogenous and well-packed electron transport layer (ETL) is crucial in attaining high-performance perovskite solar cells (PSCs). Two vital tasks are carried out by ETL: excellent electron collection, and proficiently prevents the recombination of charge carriers. Hole transport layer (HTL) free screen-printed carbon-based perovskite solar cells (SP-C-PSCs) are particularly favored within the realm of PSCs due to their exceptional scalability, durability, and affordability. Titanium dioxide (TiO2) has been widely used as the ETL in these SP-C-PSCs due to its suitable band energy structure, ease of production, and low cost; nevertheless, it must be of high quality and uniformly deposited. Here experimental analytical study of PSCs was conducted, employed surface passivation to compact titania (c-TiO2) ETL using TiCl4 passivation agent through two different deposition techniques. This passivation is applied to lower its surface roughness, improve electron transport capability, increase crystallinity, reduce micro pores, exhibit better energy level alignment, and to reduce the recombination sites. Consequently, the device with surface passivation enhances the power conversion efficiency (PCE) and long-term ambient stability of PSCs by maximizing the c-TiO2 ETL electrical characteristics. It is also discovered that the passivated c-TiO2 layer has increased hydrophobicity and reduced the RMS surface roughness from 28.8 to 27.3 nm. The PCE of the fabricated SP-C-PSCs is improved by 32.34% through applying spin-coating TiCl4 passivation, and 21.74% enhancement is recorded by applying dip-coating TiCl4 passivation. Furthermore, after 1344 h of storage under ambient conditions without encapsulation, the device passivated with spin-coating retained 84.27%, the device passivated with dip-coating maintained 85.50%, while the reference device reserved just 75.84% PCE. [ABSTRACT FROM AUTHOR]

Our research addresses the pressing need for environmental sensors capable of large-scale, on-site detection of a wide array of heavy metals with highly accurate sensor metrics. We present a novel approach using electrochemically polished (ECP) carbon screen-printed electrodes (cSPEs) for high-sensitivity detection of cadmium and lead. By applying a range of techniques, including scanning electron microscopy, energy-dispersive spectroscopy, Raman spectroscopy, electrochemical impedance spectroscopy, and cyclic voltammetry, we investigated the impact of the electrochemical potential scan range, scan rate, and the number of cycles on electrode response and its ability to detect cadmium and lead. Our findings reveal a 41 ± 1.2% increase in voltammogram currents and a 51 ± 1.6% decrease in potential separations (n = 3), indicating a significantly improved active electrode area and kinetics. The impedance model elucidates the microstructural and electrochemical property changes in the ECP-treated electrodes, showing an 88 ± 2% (n = 3) decrease in the charge transfer resistance, leading to enhanced electrode electrical conductivity. A bismuth-reduced graphene oxide nanocomposite-modified, ECP-treated electrode demonstrated a higher cadmium and lead sensitivity of up to 5 ± 0.1 μAppb−1cm−2 and 2.7 ± 0.1 μAppb−1cm−2 (n = 3), respectively, resulting in sub-ppb limits of detection in spiked deionized water samples. Our study underscores the potential of optimally ECP-activated electrodes as a foundation for designing ultrasensitive heavy metal sensors for a wide range of real-world heavy metal-contaminated waters. [ABSTRACT FROM AUTHOR]

Abstract Environmental concerns and climate protection are gaining increasing emphasis nowadays. A growing number of industries and scientific fields are involved in this trend. Sustainable electronics is an emerging research strand. Environmentally friendly and biodegradable or biobased raw materials can be used for the development of green flexible electronic devices, which may serve to reduce the pollution generated by plastics and electronics waste. In this work, we present cytocompatible, electrically conductive structures of nanocarbon water-soluble composites based on starch films. To accomplish this goal, potato starch-based films with glycerol as a plasticiser were developed along with a water-soluble vehicle for nanocarbon-based electroconductive pastes specifically dedicated to screen printing technology. Films were characterized by optical microscopy, scanning electron microscopy (SEM) mechanical properties and surface free energy.

Flexible wearable electronics are in urgent need of advanced micro‐energy storage devices. MXenes are widely used in supercapacitors because of their excellent conductivity and hydrophilicity. Nevertheless, MXene‐based supercapacitors typically exhibit low capacitance and unsatisfied rate performance, particularly in the solid compact MXene film electrode with limited porosity and/or ion diffusion paths. Here, the synthesis of MXene inks with enlarged interlayer spacing for facilitated ion diffusion kinetics by intercalating lithium ions is reported. The ion‐intercalated MXene inks are further screen‐printed for scalable production of MXene‐based micro‐supercapacitors (MSCs). Benefiting from such an electrode architecture design, as well as the wide voltage window of 21 m bis(trifluoromethane)sulfonimide lithium (LiTFSI) water‐in‐salt electrolyte, the device exhibits impressive areal capacitance (252 mF cm−2), much‐improved rate performance (capacitance retention rate as high as 80%), excellent cyclic stability (retains 98.4% of initial capacitance after 10 000 cycles) and flexibility, showing great potential in the field of wearable intelligent electronics. [ABSTRACT FROM AUTHOR]

Environmental concerns and climate protection are gaining increasing emphasis nowadays. A growing number of industries and scientific fields are involved in this trend. Sustainable electronics is an emerging research strand. Environmentally friendly and biodegradable or biobased raw materials can be used for the development of green flexible electronic devices, which may serve to reduce the pollution generated by plastics and electronics waste. In this work, we present cytocompatible, electrically conductive structures of nanocarbon water-soluble composites based on starch films. To accomplish this goal, potato starch-based films with glycerol as a plasticiser were developed along with a water-soluble vehicle for nanocarbon-based electroconductive pastes specifically dedicated to screen printing technology. Films were characterized by optical microscopy, scanning electron microscopy (SEM) mechanical properties and surface free energy. [ABSTRACT FROM AUTHOR]

La0.6Sr0.4CoO3 (LSC) coatings with a thickness of 50–100 µm were deposited on Fe-25Cr ferritic stainless steel (DIN 50049) via screen printing. The required suspension had been prepared using fine LSC powders synthesised using EDTA gel processes. In its bulk form, the LSC consisted entirely of the rhombohedral phase with space group R-3c, and it exhibited high electrical conductivity (~144 S·cm−1). LSC-coated steel was oxidised in air at 1073 K, i.e., under conditions corresponding to SOFC cathode operation, for times of up to 144 h. The in situ electrical resistance of the steel/La0.6Sr0.4CoO3 layered system during oxidation was measured. The products formed on the samples after the oxidation reaction resulting from exposure to the corrosive medium were investigated using XRD, SEM-EDS, and TEM-SAD. The microstructural, nanostructural, phase, and chemical analysis of films was performed with a focus on the film/substrate interface. It was determined that the LSC coating interacts with the oxidised steel in the applied conditions, and a multi-layer interfacial zone is formed. Detailed TEM-SAD observations indicated the formation of a main layer consisting of SrCrO4, which was the reaction product of (La,Sr)CoO3, and the Cr2O3 scale formed on the metal surface. The formation of the SrCrO4 phase resulted in improved electrical conductivity of the investigated metal/ceramics layered composite material, as demonstrated by the low area-specific resistance values of 5 mΩ·cm2, thus making it potentially useful as a SOFC interconnect material operating at the tested temperature. In addition, the evaporation rate of chromium measured for the uncoated steel and the steel/La0.6Sr0.4CoO3 layered system likewise indicates that the coating is capable of acting as an effective barrier against the formation of volatile compounds of chromium. [ABSTRACT FROM AUTHOR]

Flexible thermoelectric materials have drawn significant attention from researchers due to their potential applications in wearable electronics and the Internet of Things. Despite many reports on these materials, it remains a significant challenge to develop cost-effective methods for large-scale, patterned fabrication of materials that exhibit both excellent thermoelectric performance and remarkable flexibility. In this study, we have developed an Ag2Se-based ink with excellent printability that can be used to fabricate flexible thermoelectric films by screen printing and low-temperature sintering. The printed films exhibit a Seebeck coefficient of −161 μV/K and a power factor of 3250.9 μW/m·K2 at 400 K. Moreover, the films demonstrate remarkable flexibility, showing minimal changes in resistance after being bent 5000 times at a radius of 5 mm. Overall, this research offers a new opportunity for the large-scale patterned production of flexible thermoelectric films. [ABSTRACT FROM AUTHOR]

This manuscript describes the synthesis of green long afterglow nanophosphors SrAl2O4:Eu2+, Nd3+ using the combustion process. The study encompassed the photoluminescence behavior, elemental composition, chemical valence, morphology, and phase purity of SrAl2O4:Eu2+, Nd3+ nanoparticles. The results demonstrate that after introducing Eu2+ into the matrix lattice, it exhibits an emission band centered at 508 nm when excited by 365 nm ultraviolet light, which is induced by the 4f65d1→4f7 transition of Eu2+ ions. The optimal doping concentrations of Eu2+ and Nd3+ were determined to be 2% and 1%, respectively. Based on X-ray diffraction (XRD) analysis, we have found that the physical phase was not altered by the doping of Eu2+ and Nd3+. Then, we analyzed and compared the quantum yield, fluorescence lifetime, and afterglow decay time of the samples; the co-doped ion Nd3+ itself does not emit light, but it can serve as an electron trap center to collect a portion of the electrons produced by the excitation of Eu2+, which gradually returns to the ground state after the excitation stops, generating an afterglow luminescence of about 15 s. The quantum yields of SrAl2O4:Eu2+ and SrAl2O4:Eu2+, Nd3+ phosphors were 41.59% and 10.10% and the fluorescence lifetimes were 404 ns and 76 ns, respectively. In addition, the Eg value of 4.98 eV was determined based on the diffuse reflectance spectra of the material, which closely matches the calculated bandgap value of SrAl2O4. The material can be combined with polyacrylic acid to create optical anti-counterfeiting ink, and the butterfly and ladybug patterns were effectively printed through screen printing; this demonstrates the potential use of phosphor in the realm of anti-counterfeiting printing. [ABSTRACT FROM AUTHOR]

Printing techniques hold great potential in the manufacture of electronics such as sensors, micro-supercapacitors, and flexible electronics. However, developing large-scale functional conductive inks with appropriate rheological properties and active components still remains a challenge. Herein, through optimizing the formulations of ink, iron single sites supported N-doped carbon black (Fe1-NC) inks can serve as both conductive electrodes and high-reactive catalysts to realize convenient glucose detection, which pronouncedly reduces the dosage of enzyme and simplifies the sensors preparation. In detail, utilizing in-situ pyrolysis method, Fe1-NC single-atom catalysts (SACs) are prepared in bulk (dekagram-level). The batched Fe1-NC SACs materials can be uniformly mixed with modulated ink to realize the screen printing with high resolution and uniformity. Also, the whole scalable preparation and ink-functional process can be extended to various metals (including Co, Ni, Cu, and Mn). The introduction of highly active Fe1-NC sites reduces the amount of enzyme used in glucose detection by at least 50%, contributing to the cost reduction of sensors. The strategy in harnessing the SACs onto the carbon inks thus provides a broad prospect for the low-cost and large-scale printing of sensitive sensing devices. [ABSTRACT FROM AUTHOR]

In battery systems, there are several established form factors targeting mass market applications, like D, C, AA, AAA series, lithium round cells, and coin cells. Besides these standardized batteries, in printed electronics, there are several approaches to realize flat batteries of different material systems fabricating primary and secondary battery types. For a dedicated application in agriculture, a sensor system requires a degradable primary battery. In this paper, the development of a dedicated zinc–carbon battery is described, supplying the sensor application with 4.5 Vnom. The battery has a 170 mm length and a 23 mm outer diameter. while the inner core is open for the antenna system of the application. The active area is up to 161 cm2. The design and manufacturing aspects are described. The rolled-up battery system is fully charged after manufacturing and ready to operate. It may remain inside the degradable sensor system after use in the field. [ABSTRACT FROM AUTHOR]

The sustainable use of natural resources is becoming an increasingly important issue today. Stone paper, produced as an alternative to cellulose-based paper from the forest, is rich in minerals and produced without cellulose and water. This study focuses on the behavior of screen-printing ink on two different papers, stone paper and coated sticker paper. Properties such as ink adhesion, rubbing resistance, optical printing ink density, ink consumption, and lightfastness were measured on these surfaces. Solvent- and UV-based inks were used, and printing was carried out on cellulose-based (coated sticker paper) and mineral-based (stone paper) paper layers using three different mesh counts (90, 120, and 140 tpc). The rubbing resistance and lightfastness of the papers were also measured. The present findings revealed that stone paper had the same printability properties as cellulose-based paper. The study concluded that using a 140 tpc mesh with both types of ink results in a high-lightfastness ink layer and lower ink consumption. UV-based inks exhibited high rub resistance across all mesh counts. Additionally, when printing with stone paper, there will be a reduction in ink consumption, thereby achieving cost savings. Based on the present findings, it was concluded that water- and oil-resistant stone paper can be considered an essential alternative in many fields, including the printing industry. [ABSTRACT FROM AUTHOR]

Measurements of Young's modulus and residual stresses of screen‐printed ink layers using a bulge test on coated polyimide‐based membranes are proposed in this work. The applied bulge test monitors the deflection of membranes under pressure with interferometry. The obtained Young's modulus ranges from 6 to 8 GPa for a carbon blend‐based ink and is around 12 GPa for a silver nanoparticle ink. These values are compared with standard nanoindentation and show good agreement. Besides, the residual stresses range from −4 to 8 MPa for the carbon blend‐based ink, while the silver ink is measured around −10 MPa. The use of the membrane‐based method underlines the influence of exact deposition and curing conditions on the ink film material properties. The impact of the substrate on the ink layer properties, such as the thickness and its uniformity, is discussed, especially with regard to the heat treatment of the membrane. [ABSTRACT FROM AUTHOR]

This study investigates the potential of the dye extracted from the fruits of the alien invasive plant staghorn sumac (lat. Rhus typhina) as a sustainable and environmentally friendly colorant. By using a range of solvents, including distilled water, methanol, ethanol, propanol, acetonitrile, acetone, and dichloromethane, this study aims to determine the optimum solvent for the extraction of anthocyanin dyes from the fruit of staghorn sumac for the formulation of printing inks and for screen printing on paper and cotton fabric. The colors of the prints made with different dye extracts varied between more or less intense brownish-yellow hues, with the exception of the dye extracts in methanol and ethanol, which gave more brownish-orange hues. All prints showed excellent resistance to rubbing on cotton fabrics as well as to wet ironing. The light fastness of prints made with inks containing dyes extracted from all organic solvents was very good. Good wash fastness of prints on cotton fabrics was only achieved with inks made with dyes extracted in propanol and dichloromethane. The ink made from the dye extracted in propanol proved to be the best choice for printing on cotton fabric due to its uniform, intense, and resilient prints, while the inks made from the dyes extracted in distilled water and ethanol were also a good choice for printing on paper. [ABSTRACT FROM AUTHOR]

Wearable sweat sensors can noninvasively, in real time, and continuously monitor various physiological markers in sweat at the molecular level, which has a wide range of application prospects in the fields of health management, healthcare, and clinical diagnosis. However, effective sweat sampling remains a great challenge. Here, we prepared Janus fabric sweat glucose sensors, which were made by electrospinning hydrophobic polyurethane (PU) on a super hydrophilic gauze that can unidirectionally transport sweat from the skin (hydrophobic side) to the electrode (hydrophilic side). The screen-printed electrode modified by glucose oxidase has a good linear response to glucose. On-body experiments show that the sensor can detect glucose levels in sweat in real-time. The Janus fabric glucose sensor with its in situ monitoring capability and unidirectional liquid transport, and requires very low production costs, is expected to facilitate the development of smart textile sensors, opening new possibilities for exploring precise and controllable platforms for body fluid collection and sensing. [ABSTRACT FROM AUTHOR]

As part of the evolving Industry 4.0 landscape, machine learning-based visual inspection plays a key role in enhancing production efficiency. Screen printing, a versatile and cost-effective manufacturing technique, is widely applied in industries like electronics, textiles, and automotive. However, the production of complex multilayered designs is error-prone, resulting in a variety of defect appearances and classes. These defects can be characterized as small in relation to large sample areas and weakly pronounced. Sufficient defect visualization and robust defect detection methods are essential to address these challenges, especially considering the permitted design variability. In this work, we present a novel automatic visual inspection system for surface defect detection on decorated foil plates. Customized optical modalities, integrated into a sequential inspection procedure, enable defect visualization of production-related defect classes. The introduced patch-wise defect detection methods, designed to leverage less labeled data, prove effective for industrial defect detection, meeting the given process requirements. In this context, we propose an industry-applicable and scalable data preprocessing workflow that minimizes the overall labeling effort while maintaining high detection performance, as known in supervised settings. Moreover, the presented methods, not relying on any labeled defective training data, outperformed a state-of-the-art unsupervised anomaly detection method in terms of defect detection performance and inference speed. [ABSTRACT FROM AUTHOR]

Redesigning anode structures in Li‐ion batteries (LIBs) has been a focus of research aimed at surpassing the energy density of conventional LIBs. Although anode‐free LIBs present a promising architecture, their low Coulombic efficiency is a major drawback. This paper introduces a novel hybrid anode that integrates the current collector (CC) and active materials into a single, cohesive porous structure, which supports both de/intercalation and de/plating reactions. The hybrid anode consists of a porous Cu matrix with embedded ZrO2 powders and graphite; the quantity of graphite is only a third of that present in a traditional graphite anode. The porous structure and additives enhance the electrochemical performance of the hybrid anode by minimizing the Li–electrolyte interactions, forming a stable solid–electrolyte interface and Li4Zr3O8 passivation layer, and reducing the nucleation overpotential. Especially, the unique surface morphology, characterized by a negative curvature between sintered Cu particles, lowers the diffusion potential, which further reduces the nucleation overpotential. Additionally, the periodic mesh‐imprinted top surface, created via screen printing, promotes uniform Li plating. The results demonstrate that the cycling performance and energy density offered by the fabricated hybrid anode are superior to those of conventional graphite anodes. [ABSTRACT FROM AUTHOR]

The stunning thermoelectric behavior of inorganic/organic hybrids and the lack of information on screen-printed flexible thermoelectric generators based on Cu 3 Se 2 and Polyaniline for low-temperature applications have motivated this work. The synergic influence of various acid dopants, concentration, and annealing temperature of polyaniline on the power density of Cu 3 Se 2 /PANI ink-based flexible thermoelectric generator is explored. The presence of 1.5 wt% of H 2 SO 4 -PANI, annealed at 60 °C, decreased the bandgap and electrical resistance of Cu 3 Se 2 by 11.96 % and 29.4 %, respectively. As a result, an increase of 46.06 % in the Seebeck coefficient and 242 % in the power output is achieved, which is many folds higher than the few reported works using novel materials. In addition, the Cu 3 Se 2 /H 2 SO 4 -PANI ink-based flexible thermoelectric generator with eight legs exhibited a maximum power output, power density, and power factor of 25.69 nW, 23.79 mW/m2, and 0.77 nW/m2K2 at ΔT = 100 °C, respectively under external load. [ABSTRACT FROM AUTHOR]

Polydimethylsiloxane (PDMS) with multiwalled carbon nanotubes (MWCNT) fillers is a piezoresistive nanocomposite which is conformable, printable, and biocompatible. It is widely employed as a sensing layer in flexible pressure sensors, electronic skin (e-skin) of humanoid robots and as wearable sensors. Piezoresistive nanocomposites show significant increase in their electrical conductivity above a certain percolation threshold. In this work, PDMS + MWCNT-based sensing layers with different nanofiller MWCNT concentrations (2, 4 and 7 wt.%) are screen-printed and their electrical, mechanical, and percolation threshold responses are verified. The static I–V characteristics of the samples for a biasing DC voltage of 0-6 V are studied. The tensile test confirms maximum elongation of more than 50 mm. The change in resistance was minimal for 2 wt.% sample as the MWCNT's are sparsely distributed and no conducting channels are formed; for the 7 wt.% sensing layer, negligible change in resistance was observed as the conducting channels are broken. The highest change in resistance of 2.4 MΩ was observed after the percolation threshold value of 4 wt.% of the nanofiller concentration was reached. Overall, the 4 wt.% screen-printed piezoresistive nanocomposite layer showed highest sensitivity with a gauge factor of 4.76 and a linear response suitable for industrial applications. [ABSTRACT FROM AUTHOR]

Hybrid organic‐inorganic perovskite solar cells (PSCs) have rapidly advanced in the new generation of photovoltaic devices. As the demand for energy continues to grow, the pursuit of more stable, highly efficient, and cost‐effective solar cells has intensified in both academic research and the industry. Consequently, the development of scalable fabrication techniques that yield a uniform and dense perovskite absorber layer with optimal crystallization plays a crucial role to enhance stability and higher efficiency of perovskite solar modules. This review provides a comprehensive summary of recent advancements, comparison, and future prospects of scalable deposition techniques for perovskite photovoltaics. We discuss various techniques, including solution‐based and physical methods such as blade coating, inkjet printing (IJP), screen printing, slot‐die coating, physical vapor deposition, and spray coating that have been employed for fabrication of perovskite modules. The advantages and challenges associated with these techniques, such as contactless and maskless deposition, scalability, and compatibility with roll‐to‐roll processes, have been thoroughly examined. Finally, the integration of multiple subcells in perovskite solar modules is explored using different scalable deposition techniques. [ABSTRACT FROM AUTHOR]

In synergy with constructing a sustainable environment, facile reuse of carbon-rich biowastes as inexpensive precursors for the synthesis of value-added functional carbon dots (CDs) has garnered fruitful outcomes. Pistachio shells comprising cellulose, hemicellulose, and lignin were successfully utilized as a carbon source for the synthesis of CDs through carbonization and subsequent hydrothermal method. The methanolic fraction with desirable fluorescence in the visible region obtained after column purification of CDs was further characterized using TEM, EDS, SAED, FTIR, XPS, RS, XRD, and TCSPC techniques. The blue and green emitting CDs were used as colorants to prepare a water-based ink for screen printing. The screen prints on UV dull paper substrate exhibited good colorimetric and density values. The UV-induced yellow fluorescence of the ink film can be used as a security feature to authenticate genuine document/products and data storage. [ABSTRACT FROM AUTHOR]

[Display omitted] • Use of a university two-step strategy to construct 3D VO 2 /CNT@PANI with core–shell architecture. • Taking full advantage of the synergistic effect, the optimal VO 2 /CNT@PANI exhibits superior electrochemical performances. • Fabrication of a full-printable in-planar symmetric supercapacitor with a remarkable areal energy density and cycling life. • Great potential application prospects in the field of portable/wearable electronics. As a progressive electronic energy storage device, the flexible supercapacitor holds tremendous promise for powering wearable/portable electronic products. Of various pseudocapacitor materials, vanadium dioxide (VO 2) has garnered extensive attention due to its impressive theoretical capacitance. However, the challenges of inferior cycling life and lower energy density to be addressed. Herein, we prepare VO 2 nanorods with winding carbon nanotubes (CNT) via a facile solvothermal route, followed by in situ polymerization of polyaniline (PANI) shell. Taking full advantage of the synergistic effect, the VO 2 /CNT@PANI composite delivers a high specific capacitance of 354.2F/g at 0.5 A/g and a long cycling life of ∼ 88.2 % over 5000 cycles resulting from the enhanced conductivity of CNT and stabilization of PANI shell. By screen printing the formulated inks with outstanding rheological behaviours, we manufacture an in-planar VO 2 /CNT@PANI symmetric supercapacitor (VO 2 /CNT@PANI SSC) device featuring an orderly arrangement structure. This device yields a remarkable areal energy density of 99.57 μWh/cm2 at a power density of 387.5 μW/cm2 while retaining approximately ∼ 87.6 % of its initial capacitance after prolonged use. Furthermore, we successfully powered a portable game machine for more than 2 min using two SSCs connected in series with ease. Therefore, this work presents a universal strategy that utilises combination and coating to boost electrochemical performance for flexible high-performance supercapacitors. [ABSTRACT FROM AUTHOR]

In this study, Silicon Carbide (SiC) nanoparticle-based serigraphic printing inks were formulated to fabricate highly sensitive and wide temperature range printed thermistors. Inter-digitated electrodes (IDEs) were screen printed onto Kapton® substrate using commercially avaiable silver ink. Thermistor inks with different weight ratios of SiC nanoparticles were printed atop the IDE structures to form fully printed thermistors. The thermistors were tested over a wide temperature range form 25 °C to 170 °C, exhibiting excellent repeatability and stability over 15 h of continuous operation. Optimal device performance was achieved with 30 wt.% SiC-polyimide ink. We report highly sensitive devices with a TCR of −0.556%/°C, a thermal coefficient of 502 K (β -index) and an activation energy of 0.08 eV. Further, the thermistor demonstrates an accuracy of ±1.35 °C, which is well within the range offered by commercially available high sensitivity thermistors. SiC thermistors exhibit a small 6.5% drift due to changes in relative humidity between 10 and 90%RH and a 4.2% drift in baseline resistance after 100 cycles of aggressive bend testing at a 40° angle. The use of commercially available low-cost materials, simplicity of design and fabrication techniques coupled with the chemical inertness of the Kapton® substrate and SiC nanoparticles paves the way to use all-printed SiC thermistors towards a wide range of applications where temperature monitoring is vital for optimal system performance. [ABSTRACT FROM AUTHOR]

The ITHfO slurry was prepared by doping HfO 2 into ITO, and In 2 O 3 -ITHfO thermocouples were fabricated using screen printing on Al 2 O 3 ceramic substrates. These thermocouples exhibit a temperature limit of 1600 ℃. Post-annealing at 1250 °C resulted in more crystalline films with increased particle size. During this process, Sn2+ in the films oxidised to Sn4+, and the valence of Hf increased. The high-temperature volatilisation of Sn led to a decrease in carrier concentration. However, Hf4+ can substitute for In3+, thereby providing a free electron. This substitution mitigates the reduction in carrier concentration and enhances the upper-temperature measurement capability of the thermocouple. These experimental findings offer a novel approach to doping ITO, aimed at improving the electrical performance of ceramic thermocouples. • Preparation of In 2 O 3 /ITHfO thermocouples by doping HfO 2 in ITO to test electrical performance. • In 2 O 3 /ITHfO thermocouple have a high temperature limit of 1600 ℃. • The temperature drift of In 2 O 3 /ITHfO thermocouples is smaller than that of ordinary In 2 O 3 -ITO thermocouples. [ABSTRACT FROM AUTHOR]

Energy‐harvesting technologies offer a sustainable, maintenance‐free alternative to conventional energy‐storage solutions in distributed low‐power applications. Flexible thermoelectric generators (TEGs) can generate electric power from a temperature gradient, even on complex surfaces. Organic materials are ideal candidates for flexible TEGs due to their good solution‐processability, natural abundance, low weight, and flexibility. Electronic and thermoelectric properties of organic materials have steadily progressed, while device architectures leveraging their advantages are largely missing. Here, a design and fabrication method are proposed for producing fully screen‐printed, flexible monolithic organic TEGs scalable up to m2, compatible with any screen‐printable ink. This approach is validated, along with its scalability, by printing TEGs composed of two different active inks, in three configurations, with up to 800 thermoelements, with performances well matching simulations based on materials parameters. It is demonstrated that by using an additive‐free graphene ink, a remarkable power density of 15 nW cm−2 at ΔT = 29.5 K can be achieved, with an estimated weight‐normalized power output of 1 µW g−1, highlighting a strong potential in portability. Owing to such power density, only limited areas are required to generate microwatts, sufficient for operating low‐power electronic devices such as sensors, and wearables. [ABSTRACT FROM AUTHOR]

Printed conductive polymer composites allow for the bespoke manufacture of products with complicated geometries, which is critical for rapid prototyping and adaptability of flexible electrical devices. However, it is still challenging to prepare environmentally friendly and sustainable conductive polymer composites with aqueous solvent systems which accomplish excellent printing and electromechanical properties at the same time. In this work, the effect of composite components on performance was explored, and orthogonal tests were utilized to discover the precise formulation of new green aqueous conductive polymer composites with superior performance. The printing accuracy of the conductive polymer composites was enhanced (printed circuit burrs less than 20 μm) and the dependability of the printed circuits as well as the failure mechanism during electrochemical migration (ECM) were thoroughly investigated. As a proof of concept, ultrahigh frequency (UHF) flexible linearly polarized antennae with read range forward surpassing 10 m was designed and printed. [ABSTRACT FROM AUTHOR]

In this work, ZnO thick films were synthesized via two simple and easy methods, mechanochemical synthesis and screen-printing deposition. The ZnO powders were obtained through milling at low temperature with milling times of 20, 40, and 60 min. The ZnO thick films were fabricated by depositing 10 cycles of ZnO inks onto glass substrates. The characterization of ZnO thick films revealed a thickness ranging from 4.9 to 5.4 µm with a surface roughness between 85 and 88 nm. The structural analysis confirmed a hexagonal wurtzite crystalline structure of ZnO, both in powders and in thick films, with a preferred orientation on the (002) and (101) planes. Nanostructures with sizes ranging from 36 to 46 nm were observed, exhibiting irregular agglomerated shapes, with an energy band found between 2.77 and 3.02 eV. A static experimental set up was fabricated for gas sensing tests with continuous UV-LED illumination. The ZnO thick films, well adhered to the glass substrate, demonstrated high sensitivity and selectivity to H2S gas under continuous UV-LED illumination at low operating temperatures ranging from 35 to 80 °C. The sensitivity was directly proportional, ranging from 3.93% to 22.40%, when detecting H2S gas concentrations from 25 to 600 ppm. [ABSTRACT FROM AUTHOR]

With the increasing demand for compact, lightweight, cost‐effective, and high‐performance radiofrequency (RF) devices, the development of low‐profile antennas becomes crucial. This article presents a study of a novel carbon–cellulose‐based paste intended for screen printing RF devices. The investigation specifically explores the application of high‐reactivity carbon mixture (HRCM) particles as conductive fillers. The results demonstrate that optimal electrical conductivity values and discrete electromagnetic dipole performances can be achieved at lower concentrations of solid conductive material compared to conventional pastes, for similar applications. This offers benefits in terms of total cost, material consumption, and environmental impact. The paste formulation showcases a complex non‐Newtonian behavior, where yielding flow and thixotropicity are found to be independent and dependent on preshear conditions, respectively. This behavior can be attributed to the network orientation and rearrangement of filler structures within the paste system, which in turn are responsible for filler pattern uniformity and overall printing quality. Compared to traditional conductive materials, HRCM pastes are proven to be a viable alternative for RF devices fabrication, including printed Wi‐Fi antennas.

Surface interactions of the materials during and after the printing process are extremely important for understanding and optimizing the process of graphic reproduction. In screen printing on porous and absorbent substrates, mesh type and ink composition significantly influence the properties of the printed product. To protect the absorbent printing substrates such as board from moisture penetration and to ensure the optimal interaction of the printed ink layer and the substrate, board substrates can be coated with protective primers before printing. In this research, biodegradable primers made of poly(ɛ‐caprolactone) and poly(lactic acid) were applied on the board substrate which was then screen-printed using two screen rulings of the mesh and two different types of water-based printing inks on unprimed and primed board substrates. Printed ink layer thickness, surface roughness, water vapor transmission rate, surface free energy and adhesion parameters were measured/calculated on all produced samples. Microscopy of the printed elements was performed to visualize the influence of the primers on the printed line edge. Results of the research have shown that the primers influence the roughness reduction of the printed ink layer. Furthermore, thickness of the printed ink layers increased when the primers were applied on the substrate, pointing to the decreased permeability of the board, which was confirmed by the reduced water vapor transmission rate of the primed and printed substrates. The surface free energies of the tested surfaces and the adhesion parameters between biodegradable primers and prepared printing inks differed depending on the type of the ink and primer, pointing to the optimal combination of the primer and ink for the favorable acceptance of printing ink on the substrate. Results of this research have enabled the optimization of the quality of screen-printed board product.

The use of plant-based materials as alternatives to the hazardous synthetic chemicals traditionally employed in textile production can help create a more sustainable society; however, such materials have not been explored in sufficient detail. Herein, cotton fabrics were screen-printed with pastes containing Aronia berry extract (AE) and chitosan (CS), dried, cured, and washed. Subsequently, the printed fabrics were investigated in terms of their color, mechanical properties, and antibacterial and antioxidant activities. The obtained results revealed that AE and CS played distinctive functional roles as finishing agents in the cotton fabric treatment. The AE content in the pastes was positively correlated with a* and b* but negatively correlated with L*, and the presence of CS improved colorfastness against washing and light exposure. The fabrics printed with pastes containing ≥ 20% (w/v) AE and 2% (w/v) CS demonstrated significant antibacterial activity against Klebsiella pneumoniae and Staphylococcus aureus, while CS increased the activity resistance to washing. The fabrics printed with a paste containing 40% (w/v) AE exhibited an antioxidant capacity of ~ 70%. Thus, this study contributes to the field of sustainable textile functionalization and the use of plant extract – CS blends for screen printing.

Ensuring the long-term stability of screen-printed (SP) reference electrodes (REs) is increasingly essential because a major technical challenge in fabricating electrochemical sensors using screen printing is preparing an RE with a stable potential as it scales down in size. In this study, we fabricated SP electrodes that exhibit long-term stability in voltammetric and potentiometric experiments. The SP electrodes consisted of carbon working electrodes, a carbon counter electrode, an Ag/AgCl RE, and an ion-selective electrode (ISE) for detecting nitrate ions. The Ag/AgCl RE featured an electrolyte layer, a hydrophobic junction layer, and a small hole, collectively contributing to its long-term stability. This design achieved potential stability with minimal drift over extended periods in both 0.01 M PBS (pH 7.4) and 0.1 M Bis-tris (pH 6.5) buffer solutions. Additionally, the SP Ag/AgCl RE exhibited relatively low potential drift in the presence of various chemicals and different pH solutions. We analyzed the electrochemical behavior of two redox species, Fe(CN)63-/4− and Ru(NH3)62+/3+, using cyclic voltammetry and electrochemical impedance spectroscopy techniques at the SP electrodes. Potentiometric experiments confirmed the sensitivity, long-term stability, and selectivity of the SP ISE for nitrate ion detection, even in the presence of interfering ions.

This work provides a method for the development of conductive water-based printing inks for gravure, flexography and screen-printing incorporating commercial resins that are already used in the printing industry. The development of the respective conductive materials/pigments is based on the simultaneous (in one step) reduction of silver salts and graphene oxide in the presence of 2,5-diaminobenzenesulfonic acid that is used for the first time as the common in-situ reducing agent for these two reactions. The presence of aminophenylsulfonic derivatives is essential for the reduction procedure and in parallel leads to the enrichment of the graphene surface with aminophenylsulfonic groups that provide a high hydrophilicity to the final materials/pigments. [ABSTRACT FROM AUTHOR]

Wearable antennas are important in many areas of our lives, including the Internet of Things (IoT), health care, sports, the automobile industry, security, and entertainment. Wearable antennas should be designed with a compact size in order to be readily integrated and conform to the body shape, as well as a high performance to withstand mechanical and environmental changes. 5 G and 6 G technologies offer sufficient solutions for wearable antennas utilized for wireless body area networks (WBANs) and IoT applications in terms of high reliability, high gain, compactness, low cost, and high performance. In this work, we present for the first time a comprehnsive review of 5 G and 6 G wearable antennas discussing their significance, types, applications, and design issues in detail. A state-of-the-art for the recent 5 G wearable antenna reviews is also outlined. The main contribution of this work is explaining the compactness and performance enhancement methods at both bands in ascending order starting from low frequency, sub 6 GHz, 5 G mmWave, up to 6 G (high mmWavw and THz wave), so the reader will differentiate between the antennas' design requirements and challenges for different bands easily. The impacts of flexibility, bending, and on-body/off-body on antenna performance as well as specific absorption rate (SAR) calculation are also taken into account. This review can be considered a valuable tool for designers and researchers in designing many types of wearable antennas at 5 G and 6 G frequency bands for various applications by understanding the antenna's design problems, topologies, and types of substrate and conductive materials. [ABSTRACT FROM AUTHOR]

Summary: A dual‐band, wearable coplanar microstrip patch antenna (CPW) integrated with electromagnetic bandgap structure (EBG) to operate dual wireless bands at 2.48 GHz industrial, scientific, and medical band (ISM) and 5.2 GHz WLAN. The proposed textile wearable antenna and EBG structure are screen‐printed using silver conductive ink on the cotton polyester substrate (εr = 1.6) for flexible wearable applications. A 3 × 3 EBG array is realized by a concentric square patch surrounded by the annular square ring to reduce back radiation and increase the forward gain and front‐back ratio. The proposed EBG‐backed antenna, compared with the conventional CPW‐fed antenna, improves forward gain from 2.18 to 6.59 dB at 2.48 GHz and 3.5 to 7.03 dB at 5.2 GHz. Moreover, the EBG array is used to isolate the human body from the antenna and reduces the specific absorption rate (SAR). The antenna is performed with a human phantom tissue model, which exhibits a specific absorption rate of 0.12 W/kg, and 0.260 W/kg for 1 g tissue at 2.48 GHz and 5.2 GHz, respectively. [ABSTRACT FROM AUTHOR]

Flexible electronics, also referred to as printable electronics, represent an interesting technology for implementing electronic circuits via depositing electronic devices onto flexible substrates, boosting their possible applications. Among all flexible electronics, interdigitated electrodes (IDEs) are currently being used for different sensor applications since they offer significant benefits beyond their functionality as capacitors, like the generation of high output voltage, fewer fabrication steps, convenience of application of sensitive coatings, material imaging capability and a potential of spectroscopy measurements via electrical excitation frequency variation. This review examines the role of IDEs in printed and flexible electronics since they are progressively being incorporated into a myriad of applications, envisaging that the growth pattern will continue in the next generations of flexible circuits to come. [ABSTRACT FROM AUTHOR]

In stealth applications, there is a growing emphasis on the development of radar-absorbing structures that are efficient, flexible, and optically transparent. This study proposes a screen-printed metamaterial absorber (MMA) on polyethylene terephthalate (PET) substrates using indium tin oxide (ITO) as the grounding layer, which achieves both optical transparency and flexibility. These materials and methods enhance the overall flexibility and transparency of MMA. To address the limited transparency caused by the silver nanoparticle ink for the top pattern, a metal mesh was incorporated to reduce the area ratio of the printed patterns, thereby enhancing transparency. By incrementing the fractal order of the structure, we optimized the operating frequency to target the X-band, which is most commonly used in radar detection. The proposed MMA demonstrates remarkable performance, with a measured absorption of 91.99% at 8.85 GHz and an average optical transmittance of 46.70% across the visible light spectrum (450 to 700 nm), indicating its potential for applications in transparent windows or drone stealth. [ABSTRACT FROM AUTHOR]