Abstract: The research on renewable energy is actively looking into electrocatalysts based on transition metal chalcogenides because nanostructured electrocatalysts support the higher intrinsic activity for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). A major technique for facilitating the conversion of renewable and sustainable energy is electrochemical water splitting. The aim of the review is to discuss the revelations made when trying to alter the internal and external nanoarchitectures of chalcogenides-based electrocatalysts to enhance their performance. To begin, a general explanation of the water-splitting reaction is given to clarify the key factors in determining the catalytic performance of nanostructured chalcogenides-based electrocatalysts. To delve into the many ways being employed to improve the HER's electrocatalytic performance, the general fabrication processes utilized to generate the chalcogenides-based materials are described. Similarly, to enhance the OER performance of chalcogenides-based electrocatalysts, the applied complementary techniques and the strategies involved in designing the bifunctional water-splitting electrocatalysts (HER and OER) are explained. As a conclusive remark, the challenges and future perspectives of chalcogenide-based electrocatalysts in the context of water splitting are summarized.

Abstract: In recent years, Two-Dimensional (2D) materials have gained significant attention for their distinctive physical and chemical properties, positioning them as promising contenders for the next generation of electronic technologies. One notable group within these materials is MXenes, which have exhibited remarkable breakthroughs across various technological domains, including catalysis, renewable energy, electronics, sensors, fuel cells, and supercapacitors. By making subtle modifications to the surface termination, introducing metal ions, precise etching timing, and applying surface functionalization, the characteristics of MXenes can be fine-tuned to achieve desired band structures, rendering them suitable for sensor design. This review focuses on the strategic development of gas sensors based on Field-Effect Transistors (FETs), thoroughly examining the latest progress in MXene-based material design and addressing associated challenges and future prospects. The review aims to provide a comprehensive overview of MXene, summarizing its current applications and advancements in FET-based gas sensing.

Abstract: Human performance enhancing drugs (PEDs), frequently used in sport competitions, are strictly prohibited by the World Anti-Doping Agency (WADA). Biological samples collected from ath-letes and regular patients are continuously tested regarding the identification and/or quantification of the banned substances. Current work is focused on the application of a new analytical method, molecularly imprinted nanoparticles (nanoMIPs), to detect and determine concentrations of certain prohibited drugs, such as B-blockers, in water and human urine samples. These medications are used in the treatment of cardiovascular conditions, negative effects of adrenaline (helping to relief stress), and hypertension (slowing down the pulse and softening the arteries). They can also significantly increase muscle relaxation and improve heart efficiency. The new method of the detection and quantification of B-blockers is based on synthesis, characterization, and implementation of nanoMIPs (so-called plastic antibodies). It offers numerous advantages over the traditional methods, including high binding capacity, affinity, and selectivity for target molecules. Additionally, the whole process is less complicated, cheaper, and better controlled. The size and shape of the nanoMIPs is evaluated by dynamic light scattering (DLS) and transmission electron microscope (TEM). The affinity and selectivity of the nanoparticles are investigated by competitive pseudo enzyme-linked immunosorbent assay (pseudo-ELISA) similar to common immunoassays employing natural antibodies. To provide reliable results towards either doping detection or therapeutic monitoring using the minimal invasive method, the qualitative and quantitative analysis of these drugs is performed in water and human urine samples. It is demonstrated that the assay can detect B-blockers in water within the linear range 1 nmolmiddotL(-1)-1 mmolmiddotL(-1) for atenolol with the detection limit 50.6 ng mL(-1), and the linear range 1 mmolmiddotL(-1)-10 mmolmiddotL(-1) for labetalol with the detection limit of 90.5 ngmiddotmL(-1). In human urine samples, the linear range is recorded in the concentration range 0.1 mmolmiddotL(-1)-10 nmolmiddotL(-1) for atenolol and 1 mmolmiddotL(-1)-10 nmolmiddotL(-1) for labetalol with a detection limit of 61.0 ngmiddotmL(-1)for atenolol and 99.4 ngmiddotmL(-1) for labetalol.

Abstract: Validating methodology formerly reported, polythiophene electrosynthesised as nanowires from the monomer and some of its oligomers is now described. The work is conducted on a platinum electrode previously modified with a template that tunes the polymer growth inside the confined space of the pores. In addition, it was confirmed that the use of larger chain-length oligomers as starting unit helps to obtain more homogeneous wires, although its adhesion to the supporting substrate works against. Characterisation allows to verify the morphology and to confirm higher levels of doping/undoping of the nanostructures as compared to the corresponding bulky deposits, which points to improved macroscopic properties. It is demonstrated that this strategy allows obtaining nanowires of very small diameter, ranging from 2.8 to 4.0 nm; thus demonstrating that the use of this approach enables the direct obtainment of nanowires upon the electrode surface, with the obvious advantage that this implies.

Abstract: Ag-CdO composites are still one of the most commonly used electrical contact materials in low-voltage applications owing to their excellent electrical and mechanical properties. Nevertheless, considering the restriction on using Cd due to its toxicity, it is necessary to find alternative materials that can replace these composites. In this study, the synthesis of Ag-ZnO alloys from Ag-Zn solid solutions was investigated by hot mechanochemical processing. The hot mechanochemical processing was conducted in a modified attritor mill at 138 degrees C under flowing O-2 at 1200 cm(3)/min for 3.0 h. The microstructure and phase evolution were investigated using X-ray diffractometry, field emission gun scanning electron microscopy and transmission electron microscopy. The results suggest that it is possible to complete the oxidation of Ag-Zn solid solution by hot mechanochemical processing at a low temperature and short time. This novel synthesis route can produce Ag-ZnO composites with a homogeneous distribution of nanoscale ZnO precipitates, which is impossible to achieve using the conventional material processing methods. Considering the fact that the fundamental approach to improving electric contact material performance resides in obtaining uniform dispersion of the second-phase in the Ag matrix, this new processing route could open the possibility for Ag-ZnO composites to replace non-environmentally friendly Ag-CdO.

Abstract: A promising sustainable energy storage characteristic is achieved in redox additive electrolyte by developing strict blend of one dimensional (1D) and two dimensional (2D) structures. Hydrothermal reaction is followed to obtain the desired morphology. Two dimensional (2D) reduced graphene oxide (rGO) is added into the redox reaction between potassium permanganate and sodium nitrite to obtain nanocomposite comprising 1D and 2D blended structures of MnO2/rGO. Their structures and morphologies are studied by XRD, Raman and HRTEM analyses, respectively. The pseudocapacitive behaviour is studied in a redox additive electrolyte comprising KOH and K3Fe(CN)(6). The effect of electrolytic concentration was studied by varying the concentration of K3Fe(CN)6. The specific capacity is considerably enhanced up to 1741 F/g, 8.75 A/g with increase in concentration of K3Fe (CN)6. The role of redox couple [Fe(CN)(6)](3)-/[Fe(CN)(6)](4)-played a key role in adding the charge movement across the electrode which tuned well with the manganese ions to obtain one of the most promising pseudo-capacitances from the developed 1D and 2D blended structures of MnO2/rGO. For in-depth analysis of Fe ions movement, a symmetric supercapacitor cell is constructed to achieve a commendable specific capacitance of 216 F/g at 3.75 A/g. Prolong cycling hinted decreasing electrolytic interfacial layers resulting in fast reversible ki-netics of Fe(III) -> Fe(II) ions to achieve astonishing capacity retention of 127% after 3000 cycles.

Abstract: Nanocrystalline Ni (Ni-nc) obtained by mechanical milling may present improved mechanical properties paired with high abrasion resistance. Different sintering processes were used to consolidate Nanocrystaline Ni: hot pressed (HP) and hot-isostatic pressed (HIP). The microstructure, mechanical properties, and tribological were evaluated to compare the processes. X-ray diffraction patterns showed that HIP-consolidated specimens had larger crystallite sizes and 37% less microstrain when compared to the HP specimens. The nanohardness of the HIP specimens was also carried out and it was 50% lower than that of HP specimens, whereas its coefficient of friction found was 25% higher. These results show the advantages of the HP process over the HIP since the high pressure. The low sintering temperature of HP inhibited the grain growth, which leads excellent mechanical and tribological properties of Ni. (C) 2020 Elsevier B.V. All rights reserved.

Abstract: Elemental powders of Cu and Ni, binary alloys (Cu-Ni and Cu-Zr) and ternary alloy (Cu-Ni-Zr) obtained by mechanical alloying and uniaxial compaction hot microstructure and mechanical properties were investigated. The alloys studied were: pure Cu, pure Ni, binary alloys (Cu-Ni; Cu-Zr) and ternary alloys (Cu-Ni-Zr) under the same mechanical milling and hot pressing conditions. The samples were analyzed by X-ray diffraction (XRD), scanning electron microscope (SEM); the mechanical properties were studied by compression tests and hardness in Vickers scale (HV0.5) on polished surfaces at room temperature. According to XRD results, hot pressing process crystallite size increase and microstrain decreases in the compact samples due to the release of crystalline defects. The compacted samples have porosity of approximately 20%. The milling powder samples have a higher hardness than the unmilled samples, this because during milling crystal defects are incorporated together with the microstructural refinement. Ternary alloy is the one with the highest hardness of all systems studied, reaching 689 HV0.5. In compression tests determined a strain 5 %, Zr-containing samples become more fragile presenting the lowest values of compressive strength. In contrast, samples of Ni and Cu-Ni binary alloy are more resistant to compression.

Abstract: Geosynthetics are composite materials manufactured using different types of polymeric fibres, usually employed as anti-reflective cracking systems in asphalt pavements. Materials that compose geosynthetics can be damaged due to mechanical and thermal effects produced during the installation process under hot mix asphalts. In this paper, different polymeric fibres extracted from geosynthetics have been evaluated using nanoindentation tests. The main objective was to evaluate the effect of installation process (dynamic compaction and thermal damage) on the mechanical behaviour of individual polymeric fibres at nano-scale. To do this, elastic modulus (E) and hardness (H) of three different polymeric fibres commonly used in geosynthetics (polypropylene, polyester and polyvinyl-alcohol), in two testing directions and under two different states have been studied. Main conclusions of this work are that mechanical properties of geosynthetics individual fibres can change after installation, producing changes in the behaviour of geosynthetics at macro-scale with consequences in the pavement functionality, and that these changes are different depending on the material that composed the fibres. (C) 2016 Elsevier Ltd. All rights reserved.

Abstract: The simultaneous determination of hydroquinone and catechol was conducted in aqueous and real samples by means of differential pulse voltammetry (DPV) using a glassy carbon electrode modified with Gold Nanoparticles (AuNP) and functionalized multiwalled carbon nanotubes by drop coating. A good response was obtained in the simultaneous determination of both isomers through standard addition to samples prepared with analytical grade water and multivariate calibration by partial least squares (PLS) in winery wastewater fortified with HQ and CT from 4.0 to 150.00 mu M. A sensitivity of 0.154 mu A mu M-1 and 0.107 mu A mu M-1, and detection limits of 4.3 and 3.9 mu M were found for hydroquinone and catechol, respectively. We verified the reliability of the developed method by simultaneously screening analytes in spiked tap water and industrial wastewater, achieving recoveries over 80%. In addition, this paper demonstrates the applicability of chemometric tools for the simultaneous quantification of both isomers in real matrices, obtaining prediction errors of lower than 10% in fortified wastewater.