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Academic and industrial efforts have focused on developing energy storage devices for wearable and portable electronics using low-cost, scalable, and sustainable materials and approaches. In this work, commercially available stretch-broken carbon fiber yarns (SBCFYs) were hybridized with mixed phases of 1 T and 2H MoS2 nanosheets via conventional and microwave-assisted heating (CAH, MAH) without the use of binders to fabricate symmetric freestanding 1D fiber-shaped supercapacitors (FSCs). Electrochemical characterization performed in a three-electrode configuration showed promising results with specific capacitance values of 184.41 and 180.02 F·g−1, at 1 mV·s−1 for CAH and MAH, respectively. Furthermore, after performing 3000 CV cycles at 100 mV·s−1, the capacitance retention was 79.5% and 95.7%, respectively. Using these results as a reference, symmetric 1D FSCs were fabricated by pairing hybridized SBCFYs with MoS2 by MAH. The devices exhibited specific capacitances of approximately 58.60 ± 3.06 F·g−1 at 1 mV·s−1 and 54.81 ± 7.34 F·g−1 at 0.2 A·g−1 with the highest power density achieved being 15.17 W·g−1 and energy density of 5.06×10–4 Wh·g−1. In addition, five 1D FSCs were hand-stitched and connected in series onto a cotton fabric. These supercapacitors could power a temperature and humidity sensor for up to six minutes, demonstrating the practicality and versatility of the prepared 1D FSCs for powering future electronic systems. [ABSTRACT FROM AUTHOR]

Laser-induced graphene (LIG) is as a promising material for flexible microsupercapacitors (MSCs) due to its simple and cost-effective processing. However, LIG-MSC research and production has been centered on non-sustainable polymeric substrates, such as polyimide. In this work, it is presented a cost-effective, reproducible, and robust approach for the preparation of LIG structures via a one-step laser direct writing on chromatography paper. The developed strategy relies on soaking the paper in a 0.1 M sodium tetraborate solution (borax) prior to the laser processing. Borax acts as a fire-retardant agent, thus allowing the laser processing of sensitive substrates that other way would be easily destroyed under the high-energy beam. LIG on paper exhibiting low sheet resistance (30 Ω sq−1) and improved electrode/electrolyte interface was obtained by the proposed method. When used as microsupercapacitor electrodes, this laser-induced graphene resulted in specific capacitances of 4.6 mF cm−2 (0.015 mA cm−2). Furthermore, the devices exhibit excellent cycling stability (> 10,000 cycles at 0.5 mA cm−2) and good mechanical properties. By connecting the devices in series and parallel, it was also possible to control the voltage and energy delivered by the system. Thus, paper-based LIG-MSC can be used as energy storage devices for flexible, low-cost, and portable electronics. Additionally, due to their flexible design and architecture, they can be easily adapted to other circuits and applications with different power requirements. [ABSTRACT FROM AUTHOR]

The technological potential of poly(methyl methacrylate) (PMMA)-based composite films doped with lanthanide-doped sol–gel derived ionosilicas (IS-Ln) previously proposed for luminescent down-shifting (LDS) and luminescent solar concentrator (LSC) layers connected to photovoltaic (PV) cells is extended here to electrochromic devices (ECDs), targeting the fabrication of single energy harvesting/conversion/management LSC-LDS/PV/ECD systems. These integrated devices have foreseen application in the windows of future zero-energy buildings of smart cities. The proof-of-concept is given with the report of the electro-optical performance of an ECD comprising an optimized electrolyte film composed of PMMA, IS-Nd, and IS-Eu, and the 1-butyl-3-methylimidazolium hexafluorophosphate ionic liquid. This amorphous electrolyte is stable below 160 °C, exhibits high ionic conductivity (2.13 × 10−4 and 8.76 × 10−4 S cm−1 at room temperature and 44 °C, respectively), and emits in the visible (red color) and near-infrared (NIR) spectral regions. The device demonstrated fast switching speed (50 s) and high transparency in the visible-to-NIR spectral regions (transmittance (T) = 79/96/89/77% at 555/1000/1500/1650 nm in the as-prepared state, respectively). Upon application of ±2.5 V for 200 cycles, at the same wavelengths, the Tbleached/Tcolored values were 44/28, 46/26, 39/20, and 27/9%, respectively, and the coloration efficiency (CE) values CEin/CEout values were −302/+181, −381/+228, −446/+267 and −734/+440 cm2 C−1, respectively. Highlights: Red-emitting ECDs enabling dynamic control of sunlight and offering uninterrupted heat emission were fabricated. The ECD electrolyte composition was based on the formulation used previously for films acting both as LDS and LSC layers. The electrolyte included PMMA, Nd3+/Eu3+-doped ionosilicas, and 1-butyl-3-methylimidazolium hexafluorophosphate. The electrolyte is amorphous, exhibits good ionic conductivity, and emits in the visible (red color) and NIR regions. The ECD performance proves its applicability in an integrated LSC-LDS/PV/ECD system. [ABSTRACT FROM AUTHOR]

The extracellular matrix (ECM) of engineered human cardiac tissues corresponds to simplistic biomaterials that allow tissue assembly, or animal derived off-the-shelf non-cardiac specific matrices. Decellularized ECM from human cardiac tissue could provide a means to improve the mimicry of engineered human cardiac tissues. Decellularization of cardiac tissue samples using immersion-based methods can produce acceptable cardiac ECM scaffolds; however, these protocols are mostly described for animal tissue preparations. We have tested four methods to decellularize human cardiac tissue and evaluated their efficiency in terms of cell removal and preservation of key ECM components, such as collagens and sulfated glycosaminoglycans. Extended exposure to decellularization agents, namely sodium dodecyl sulfate and Triton-X-100, was needed to significantly remove DNA content by approximately 93% in all human donors. However, the biochemical composition of decellularized tissue is affected, and the preservation of ECM architecture is donor dependent. Our results indicate that standardization of decellularization protocols for human tissue is likely unfeasible, and a compromise between cell removal and ECM preservation must be established in accordance with the scaffold's intended application. Notwithstanding, decellularized human cardiac ECM supported human induced pluripotent-derived cardiomyocyte (hiPSC-CM) attachment and retention for up to 2 weeks of culture, and promoted cell alignment and contraction, providing evidence it could be a valuable tool for cardiac tissue engineering. [ABSTRACT FROM AUTHOR]

In this work, we developed a facile synthetic process for the fabrication of porous heterojunction Fe2O3/TiO2 using a two-step method to be employed as a visible light photocatalyst. In the first step, porous TiO2 thin films were successfully prepared by a sol–gel method using polyethylene glycol (PEG). The porous TiO2 thin film was further annealed and then decorated with nanoparticles of Fe2O3 using the direct electrodeposition method. The photocatalysts were structurally investigated by scanning electron microscopy (SEM), atomic force microscopy (AFM), X-ray diffraction (XRD) and Raman spectroscopy. The Fe2O3/TiO2 heterojunction presented both an anatase TiO2 phase and rhombohedric structure of hematite α-Fe2O3. The optical properties have been investigated for all the materials, in which the TiO2 material present in porous heterojunction exhibited a remarkable absorption and red shift in the visible region from 3.2 to 3.0 eV compared to the pure heterojunction Fe2O3/TiO2. Moreover, the electrochemical behavior of the samples was investigated. Photocatalytic activity was assessed from methylene blue degradation with remarkable degradability performance under visible light. The photodegradation of the porous heterojunction Fe2O3/TiO2 exhibited an enhanced photodegradation up to 70% after 150 min of irradiation. [ABSTRACT FROM AUTHOR]

A new strategy for the surface modification of bacterial cellulose (BC) through the combination of oxygen plasma deposition and silanization with trichloromethyl silane (TCMS) is described. The combined use of the two techniques modifies both the surface roughness and energy and therefore maximizes the obtained hydrophobic effect. These modified membranes were characterized by Scanning Electron Microscopy (SEM), water contact angle measurements, Fourier-transform infrared spectroscopy (FTIR-ATR) and X-ray photoelectron spectroscopy (XPS), and its cytotoxic potential was investigated using both indirect and direct contact in vitro studies. The obtained results suggest an effective conjugation of TCMS to the surface of BC, leading to a highly hydrophobic surface, with a water contact angle of approximately 130º. It is also demonstrated that this is a stable and durable surface modification strategy, since BC remained hydrophobic even after 6 months, in dry conditions or after being submerged in distilled water for about a month. Importantly, this surface modification revealed no short-term cytotoxic effects on L929 and hDNFs cells. Altogether, these data indicate the successful development of a surface modification method that can be applied to BC, enabling the production of a biodegradable and hydrophobic platform that can be applied to different areas of research and industry. [ABSTRACT FROM AUTHOR]

This paper presents a behavioral model for amorphous indium-gallium-zinc oxide thin-film transistor using artificial neural network (ANN) based equivalent circuit (EC) approach to predict static and dynamic behavior of the device. In addition, TFT parasitic capacitances (C and C) characterization through measurements is also reported. In the proposed model, an EC is derived from the device structure, in terms of electrical lumped elements. Each electrical element in the EC is modeled with an ANN. Then these ANNs are connected together as per the EC and implemented in Verilog-A. The proposed model performance is validated by comparing the circuit simulation results with the measured response of a simple common-source amplifier, which has shown 12.2 dB gain, 50 μW power consumption and 85 kHz 3-dB frequency with a power supply of 6 V. The same circuit is tested as an inverter and its response is also presented up to 50 kHz, from both simulations and measurements. These results show that the model is capable of capturing both small and large signal behavior of the device to good accuracy, even including the harmonic distortion of the signal (that emphasizes the nonlinear behavior of the parasitic capacitance), making the model suitable for IC design. [ABSTRACT FROM AUTHOR]

Throughout the last decade, the expansion of food testing has been gradually moving towards ordinary high throughput screening methods performed on-site. The demand for point-of-care testing, able to distinguish molecular signatures with high accuracy, sensitivity and specificity has been significantly increasing. This new requirement relies on the on-site detection and monitorization of molecular signatures suitable for the surveillance of food production and processing. The widespread use of antibiotics has contributed to disease control of livestock but has also created problems for the dairy industry and consumers. Its therapeutic and subtherapeutic use has increased the risk of contamination in milk in enough concentrations to cause economic losses to the dairy industry and have a health impact in highly sensitive individuals. This study focuses on the development of a simple Surface-Enhanced Raman Spectroscopy (SERS) method for fast high throughput screening of tetracycline (TET) in milk. For this, we integrate a paper-based low-cost, fully recyclable and highly stable SERS platform, with a minimal sample preparation protocol. A two-microliter sample of milk solutions spiked with TET (from 0.01 to 1000 ppm) is dried on a silver nanoparticle coated cardboard substrate and measured via a Raman spectrophotometer. The SERS substrate showed to be extremely stable with a shelf life of several months. A global spectrum principal component analysis approach was used to test all the detected vibrational modes and their correlation with TET concentration. Peak intensity ratios (455 cm−1/1280 cm−1 and 874 cm−1/1397 cm−1) were found to be correlated with TET concentrations in milk, achieving a sensitivity as low as 0.1 ppm. Results indicate that this SERS method combined with portable Raman spectrometer is a potential tool that can be used on-site for the monitoring of TET residues and other antibiotics. [ABSTRACT FROM AUTHOR]