Development of stretchable microneedle arrays via single-step digital light-processing printing for delivery of rhodamine B into skin tissue.

This paper introduces a novel approach for loading and releasing Rhodamine B (RhB) into the skin using minimally-invasive microneedle technology developed through digital light-processing (DLP) printing. Notably, this process involves the direct 3D fabrication of rigid microneedle arrays affixed to a flexible patch, marking a pioneering application of DLP printing in this context. The stretchable and durable design of the microneedle substrate enables it to adapt to dynamic movements associated with human activities. Moreover, the microneedle features a pore on each side of the pyramid needle, effectively optimizing its drug-loading capabilities. Results indicate that the microneedle patch can withstand up to 50 % strain without failure and successfully penetrates rat skin. In vitro drug release profiles, conducted through artificial and rat skin, were observed over a 70 h period. This study establishes the potential of a simple manufacturing process for the creation of pore-designed microneedle arrays with a stretchable substrate, showcasing their viability in transdermal drug delivery applications.

Recent research trends in textile-based temperature sensors: a mini review.

In this review, the current state of research on textile-based temperature sensors is explored by focusing on their potential use in various applications. The textile-based sensors show various advantages including flexibility, conformability and seamlessness for the wearer. Integration of the textile-based sensors into clothes or fabric-based products enables continuous and sensitive monitoring of change in temperature, which can be used for various medical and fitness applications. However, there are lacks of comprehensive review on the textile-based temperature sensors. This review introduces various types of textile-based temperature sensors, including resistive, thermoelectric and fibre-optical sensors. In addition, the challenges that need to be addressed to fully realise their potential, which include improving sensitivity and accuracy, integrating wireless communication capabilities, and developing low-cost fabrication techniques. The technological advances in textile-based temperature sensors to overcome the limitations will revolutionize wearable devices requiring function of temperature monitoring.

Self-poled and transparent polyvinylidene fluoride-co-hexafluoropropylene-based piezoelectric devices for printable and flexible electronics.

Transparent and flexible energy supply devices are becoming increasingly important for human interfaces as the Internet of Things (IoT) continues to grow. In this study, self-poled and transparent piezoelectric nanogenerators (ST-PENGs) based on 1H,1H,2H,2H-perfluorodecyltriethoxysilane (PFOES) and polyvinylidene fluoride-co-hexafluoropropylene (PVDF-HFP) composite films were prepared via extrusion printing, where PFOES induces the transformation of PVDF-HFP chains, exhibiting a higher ß-phase content and remarkable piezoelectric properties. The hydrogen bonding interaction between the PVDF-HFP matrix and the PFOES agents causes a clear transition from phase to phase, as evidenced by Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD) results. Moreover, the PFOES content influences the ß-phase content, with 10 wt% of PFOES enabling the induction of the ß-phase content up to 82.7%. The proposed ST-PENGs generate an excellent output voltage, power, and sensitivity of ∼6.2 V, ∼6.9 µW cm-2, and ∼131.3 mV N-1, respectively, exhibiting a record-high improvement compared with previously reported PENGs. These ST-PENGs also offer significant promise in tracking human activity and recovering biomechanical energy. This study may provide insight into the development of transparent and flexible piezoelectric devices to achieve high-performance self-powered electronics.

Screen Printing of Surface-Modified Barium Titanate/Polyvinylidene Fluoride Nanocomposites for High-Performance Flexible Piezoelectric Nanogenerators.

Piezoelectric energy harvesters are appealing for the improvement of wearable electronics, owing to their excellent mechanical and electrical properties. Herein, screen-printed piezoelectric nanogenerators (PENGs) are developed from triethoxy(octyl)silane-coated barium titanate/polyvinylidene fluoride (TOS-BTO/PVDF) nanocomposites with excellent performance based on the important link between material, structure, and performance. In order to minimize the effect of nanofiller agglomeration, TOS-coated BTO nanoparticles are anchored onto PVDF. Thus, composites with well-distributed TOS-BTO nanoparticles exhibit fewer defects, resulting in reduced charge annihilation during charge transfer from inorganic nanoparticles to the polymer. Consequently, the screen-printed TOS-BTO/PVDF PENG exhibits a significantly enhanced output voltage of 20 V, even after 7500 cycles, and a higher power density of 15.6 µW cm-2, which is 200 and 150% higher than those of pristine BTO/PVDF PENGs, respectively. The increased performance of TOS-BTO/PVDF PENGs is due to the enhanced compatibility between nanofillers and polymers and the resulting improvement in dielectric response. Furthermore, as-printed devices could actively adapt to human movements and displayed excellent detection capability. The screen-printed process offers excellent potential for developing flexible and high-performance piezoelectric devices in a cost-effective and sustainable way.

Fabrication of Enzyme-Free and Rapid Electrochemical Detection of Glucose Sensor Based on ZnO Rod and Ru Doped Carbon Nitride Modified Gold Transducer.

Over 3 in 4 adults with diabetes live in low- and middle-income counties and health expenditure also increased 316% over the last 15 years. In this regard, we fabricate low cost, reusable and rapid detection of diabetes sensor based on zinc oxide rod inserted ruthenium-doped carbon nitride (ZnO-g-Ru-C3N4) modified sensor device. Developed sensor device physically and electrochemically characterized using X-ray diffraction (XRD), fourier-transform infrared spectroscopy (FTIR), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), cyclic voltammetry (CV), chronoamperometry (CA) and differential pulse voltammetry (DPV). Sensing device as an effective enzyme-free glucose detection with high sensitivity (346 µA/mM/cm2) over the applied lower potential of +0.26 V (vs. Ag/AgCl), fast response (3 s) and broad linear range of (2-28) mM, coupled with a lower limit of detection (3.5 nM). The biosensing device gives better anti-interference ability with justifiable reproducibility, reusability (single electrode re-use 26 times in physiological buffer and 3 times in serum) and stability. Moreover, the real-time applicability of the sensor device was evaluated in human blood, serum and urine samples.

A fast and label-free detection of hydroxymethylated DNA using a nozzle-jet printed AuNPs@Ti3C2 MXene-based electrochemical sensor.

5-hydroxymethylcytosine (5hmC) is a key epigenetic mark in the mammalian genome that has been proposed as a promising cancer biomarker with diagnostic and prognostic potentials. A new type of two-dimensional (2D) material called MXene includes transition metal carbides and nitrides and possesses unique physico-chemical properties suitable for diverse applications, including electrochemical sensors. Here, we report a new nozzle-jet printed electrochemical sensor using gold nanoparticles (AuNPs)@Ti3C2 MXene nanocomposite for the real-time and label-free detection of 5hmC in the genome. We utilized Ti3C2 MXene as a platform to immobilize AuNPs, which have been shown to exhibit different affinity interactions toward 5-methylcytosine (5 mC) and 5hmC, and thus produce distinct electrochemical responses. To fabricate the electrode, a highly conductive and adhesive silver ink was prepared to generate a silver line onto polyethylene terephthalate (PET) substrate using nozzle-jet printing, followed by deposition of AuNPs@Ti3C2 MXene ink at one end via dropcasting. Analyses of morphology and chemical composition showed that all steps of the sensor fabrication were successful. The fabricated sensor coupled with cyclic voltammetry showed excellent performance in distinguishing 5 mC- or 5hmC-enriched cellular genomic DNAs. As a proof-of-concept investigation, we confirmed that our sensor readily and consistently detected 5hmC diminution in multiple tumors, compared to the paired normal tissues. Thus, our simple and cost-effective sensing strategy using printable AuNPs@Ti3C2 MXene ink holds promise for a wide range of practical applications in epigenetic studies as well as clinical settings.

A Screen-Printed Metal Hybrid Composite for Wireless Wind Sensing.

Wind sensing has become a key component in various fields with the growing trend of assessing air conditions for energy conversion. In this study, we demonstrated a wireless screen-printable flexible strain sensor system based on Ag/MWCNT composite for wind sensing. To achieve high printability with the metal hybrid composite for the fabrication of a screen-printed flexible sensor, we systematically investigated the rheological properties, resulting in the high shear thinning and thixotropic behavior of the composite. After confirming the suitability for screen printing, we investigated the performance of the printed strain sensor, obtaining a gauge factor (G.F.) of 2.08 with 90% sensitivity and high durability after 6000 bending cycles. In addition, the sensor showed 98% temperature sensitivity during a wind sensing test due to the intrinsic properties of the metal hybrid composite. In an application based on an IoT system, we verified that the response of the wireless sensor corresponded with that of a wired sensor, indicating the expansion of low-cost, mass-produced screen-printed wind sensors.

Rapid and Label-Free Detection of 5-Hydroxymethylcytosine in Genomic DNA Using an Au/ZnO Nanorods Hybrid Nanostructure-Based Electrochemical Sensor.

Ten-eleven-translocation (TET) proteins modify DNA methylation by oxidizing 5-methylcytosine (5mC) to 5-hydroxymethylcytosine (5hmC). Loss of 5hmC, a widely accepted epigenetic hallmark of cancers, is proposed as a biomarker for early cancer diagnosis and prognosis. Thus, precise quantification of 5hmC holds great potential for diverse clinical applications. DNAs containing 5mC or 5hmC display different adsorption affinity toward the gold surface, thus producing different electrochemical responses. Here a novel, label-free electrochemical sensor based on gold nanoparticles (Au NPs)/zinc oxide nanorods (ZnO NRs) nanostructure for the facile and real-time detection of 5hmC-enriched DNAs is reported. The hybrid structure is fabricated by the vertical hydrothermal growth of ZnO NRs onto indium tin oxide glass substrate, followed by the decoration of ZnO NRs with Au NPs via sputtering. Successful fabrication is confirmed by analyzing the morphology and chemical composition of the sensor. By coupling the fabricated sensor with cyclic voltammetry, its functionality in distinguishing genomic DNAs containing different levels of 5hmC is validated. Notably, the sensor device successfully and consistently detects 5hmC loss in primary hepatocellular carcinoma, compared to the normal tissues. Thus, the novel sensing strategy to assess DNA hydroxymethylation will likely find broad applications in early cancer diagnosis and prognosis evaluation.

Boosting Performance of Self-Polarized Fully Printed Piezoelectric Nanogenerators via Modulated Strength of Hydrogen Bonding Interactions.

Self-polarized piezoelectric devices have attracted significant interest owing to their fabrication processes with low energy consumption. Herein, novel poling-free piezoelectric nanogenerators (PENGs) based on self-polarized polyvinylidene difluoride (PVDF) induced by the incorporation of different surface-modified barium titanate nanoparticles (BTO NPs) were prepared via a fully printing process. To reveal the effect of intermolecular interactions between PVDF and NP surface groups, BTO NPs were modified with hydrophilic polydopamine (PDA) and hydrophobic 1H,1H,2H,2H-perfluorodecyltriethoxysilane (PFDTES) to yield PDA-BTO and PFD-BTO, respectively. This study demonstrates that the stronger hydrogen bonding interactions existed in PFD-BTO/PVDF composite film comparative to the PDA-BTO/PVDF composite film induced the higher ß-phase formation (90%), which was evidenced by the XRD, FTIR and DSC results, as well as led to a better dispersion of NPs and improved mechanical properties of composite films. Consequently, PFD-BTO/PVDF-based PENGs without electric poling exhibited a significantly improved output voltage of 5.9 V and power density of 102 µW cm-3, which was 1.8 and 2.9 times higher than that of PDA-BTO/PVDF-based PENGs, respectively. This study provides a promising approach for advancing the search for high-performance, self-polarized PENGs in next-generation electric and electronic industries.

Mortise-tenon joint structured hydrophobic surface-functionalized barium titanate/polyvinylidene fluoride nanocomposites for printed self-powered wearable sensors.

Self-powered wearable sensors exhibiting high sensitivity and flexibility have attracted widespread interest in the field of wearable electronics. Herein, a 3D printing technique was employed to fabricate a fully printed, flexible self-powered sensor with high piezoelectric performance. This printing technique is based on the hydrophobic surface-functionalized barium titanate (FD-BTO)/polyvinylidene fluoride (PVDF) composite film. To strengthen the interface bond between BTO and PVDF, the BTO nanoparticles were surface functionalized using hydrophobic 1H,1H,2H,2H-perfluorodecyltriethoxysilane (PFDTES). As a result, there was an increase in the content of the ß-phase in the PFDTES modified BTO (FD-BTO) nanoparticle composite film. The 3D-printed self-powered sensor based on the optimum FD-BTO/PVDF composite film exhibited excellent sensitivity (61.6 mV kPa-1) with a piezoelectric coefficient (d33) of 69.1 pC/N, which is two-fold higher than that of the unfunctionalized BTO/PVDF counterpart. Additionally, the power sensor displayed excellent mechanical durability in the 20 000 cyclic force tests. In practice, the printed devices were used as a sports wearable device to monitor and analyze athlete motion, and a self-powered printed sensor array (5 × 5), which could effectively detect the pattern image of the external pressure input. The 3D-printed self-powered sensor demonstrated herein can contribute significantly to the applications and the development of printed electronic wearable devices.

Sol⁻Gel-Processed Organic⁻Inorganic Hybrid for Flexible Conductive Substrates Based on Gravure-Printed Silver Nanowires and Graphene.

In this study, an organic⁻inorganic (O⁻I) nanohybrid obtained by incorporating an alkoxysilane-functionalized amphiphilic polymer precursor into a SiO2⁻TiO2 hybrid network was successfully utilized as a buffer layer to fabricate a flexible, transparent, and stable conductive substrate for solution-processed silver nanowires (AgNWs) and graphene under ambient conditions. The resulting O⁻I nanohybrid sol (denoted as AGPTi) provided a transmittance of the spin-coated AgNWs on an AGPTi-coated glass of 99.4% and high adhesion strength after a 3M tape test, with no visible changes in the AgNWs. In addition, AGPTi acted as a highly functional buffer layer, absorbing the applied pressure between the conductive materials, AgNWs and graphene, and rigid substrate, leading to a significant reduction in sheet resistance. Furthermore, gravure-printed AgNWs and graphene on the AGPTi-based flexible substrate had uniform line widths of 490 ± 15 and 470 ± 12 µm, with 1000-cycle bending durabilities, respectively.

The effect of surfactants on electrohydrodynamic jet printing and the performance of organic field-effect transistors.

In this article, we report on the direct writing of multi-walled carbon nanotube (MWCNT) composite inks based on three different surfactants via the electrohydrodynamic (EHD) jet printing technique. All three surfactants, including two types of polymeric surfactants and an ionic surfactant, successfully dispersed the MWCNTs in the ink medium. Although the MWCNT composite with the ionic surfactant could not be printed by the EHD process, the MWCNT composites with polymeric surfactants could be successfully printed using this technique. Furthermore, the printed lines exhibited different electrical and electronic characteristics, depending on the type of surfactant. A large amount of the poly(4-styrenesulfonic acid) (PSS) surfactant was required to disperse the MWCNTs in ethanol, whereas a smaller amount of polymeric Triton X-100 (TX100) was required to obtain a MWCNT composite suspension in distilled water, and therefore, the printed lines of the latter provided higher conductivities. In addition, the surface potential and charge carrier injection properties of the EHD-printed MWCNT lines depended on the type of surfactant in the MWCNT composite. Finally, organic field-effect transistors (OFETs) employing source/drain electrodes based on MWCNT/surfactant composites exhibited opposing electrical characteristics depending on the type of surfactant. The MWCNT/PSS lines showed excellent electrical performance when used as electrodes in p-type OFETs, whereas the MWCNT/TX100 lines exhibited excellent performance when used as electrodes in n-type OFETs.

Electrohydrodynamic printing for scalable MoS2 flake coating: application to gas sensing device.

Scalable sub-micrometer molybdenum disulfide ([Formula: see text]) flake films with highly uniform coverage were created using a systematic approach. An electrohydrodynamic (EHD) printing process realized a remarkably uniform distribution of exfoliated [Formula: see text] flakes on desired substrates. In combination with a fast evaporating dispersion medium and an optimal choice of operating parameters, the EHD printing can produce a film rapidly on a substrate without excessive agglomeration or cluster formation, which can be problems in previously reported liquid-based continuous film methods. The printing of exfoliated [Formula: see text] flakes enabled the fabrication of a gas sensor with high performance and reproducibility for [Formula: see text] and [Formula: see text].

Wettability Contrast Gravure Printing.

Silicon gravure patterns are engineered to have cells that are wettable and lands that are not wettable by aqueous inks. This strategy allows excess ink on the lands to be removed without using a doctor blade. Using an aqueous silica ink, continuous lines as narrow as 1.2 µm with 1.5 µm space are gravure printed.

Screen Printing of Highly Loaded Silver Inks on Plastic Substrates Using Silicon Stencils.

Screen printing is a potential technique for mass-production of printed electronics; however, improvement in printing resolution is needed for high integration and performance. In this study, screen printing of highly loaded silver ink (77 wt %) on polyimide films is studied using fine-scale silicon stencils with openings ranging from 5 to 50 µm wide. This approach enables printing of high-resolution silver lines with widths as small as 22 µm. The printed silver lines on polyimide exhibit good electrical properties with a resistivity of 5.5×10(-6) Ω cm and excellent bending tolerance for bending radii greater than 5 mm (tensile strains less than 0.75%).

Fluorinated polyimide gate dielectrics for the advancing the electrical stability of organic field-effect transistors.

Organic field-effect transistors (OFETs) that operated with good electrical stability were prepared by synthesizing fluorinated polyimide (PI) gate dielectrics based on 6FDA-PDA-PDA PI and 6FDA-CF3Bz-PDA PI. 6FDA-PDA-PDA PI and 6FDA-CF3Bz-PDA PI contain 6 and 18 fluorine atoms per repeat unit, respectively. These fluorinated polymers provided smooth surface topographies and surface energies that decreased as the number of fluorine atoms in the polymer backbone increased. These properties led to a better crystalline morphology in the semiconductor film grown over their surfaces. The number of fluorine atoms in the PI backbone increased, the field-effect mobility improved, and the threshold voltage shifted toward positive values (from -0.38 to +2.21 V) in the OFETs with pentacene and triethylsilylethynyl anthradithiophene. In addition, the highly fluorinated polyimide dielectric showed negligible hysteresis and a notable gate bias stability under both a N2 environment and ambient air.

Gravure printing of graphene for large-area flexible electronics.

Gravure printing of graphene is demonstrated for the rapid production of conductive patterns on flexible substrates. Development of suitable inks and printing parameters enables the fabrication of patterns with a resolution down to 30 µm. A mild annealing step yields conductive lines with high reliability and uniformity, providing an efficient method for the integration of graphene into large-area printed and flexible electronics.