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The use of metal powders produced by mechanical treatment in various fields, such as catalysis or gas absorption, is often limited by the low specific surface area of the resulting particles. One of the possible solutions for increasing the particle fineness is hydrogen treatment; however, its effect on the structure of mechanically treated powders remains unexplored. In this work, for the first time, a metal-oxide nanocomposite powder was produced by mechanical alloying (MA) in a high-energy planetary ball mill from commercial powders of Zr and Co in the atomic ratio Co:Zr = 53:47 in an inert atmosphere, followed by high-pressure hydrogenation at room temperature. The initial powders and products of alloying and hydrogenation were studied by XRD, 59Co Internal Field NMR, SEM, and HRTEM microscopy with EDX mapping, as well as Raman spectroscopy. MA resulted in significant amorphization of the powders, as well as extensive oxidation of zirconium by water according to the so-called "Fukushima effect". Moreover, an increase in hcp Co sites was observed. 59Co IF NMR spectra revealed the formation of magnetically single-domain cobalt particles after hydrogenation. The crystallite sizes remained unchanged, which was not observed earlier. The pulverization of Co and an increase in hcp Co sites made this nanocomposite suitable for the synthesis of promising Fischer-Tropsch catalysts.

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A simple, synergistic engineering of the conduction band (CB), conductivity, and interface of TiO2-based bilayered electron transport layers (ETLs) via scalable TiO2 and SnO2 nanoparticles processed at low temperature (≤ 100 °C) for regular planar perovskite solar cells (PSCs) was developed. The bottom layer (Lt-TiO2:SnO2 nanocomposite film) was prepared by spin coating from the ethanol suspension of small ground TiO2 nanoparticles with big ground SnO2 nanoparticles as the additive. The top C-SnO2 layer (spin-coated from the concentrated commercial SnO2 nanoparticles (C-SnO2 NPs, 20 wt %, 7 nm in size suspended in H2O)) can be regarded as an interlayer between Lt-TiO2:SnO2 and perovskite (Psk) absorbers. Bilayered Lt-TiO2:SnO2/C-SnO2 ETLs are dense films with a cascade CB, good conductivity, facile electron extraction/transport ability, and a highly hydrophilic surface for depositing high-quality Psk films. Regular planar PSCs based on Lt-TiO2:SnO2/C-SnO2 ETLs combined with a (FAI)0.90(PbI2)0.94(MABr)0.10(PbBr2)0.10 absorber and a spiro-OMeTAD hole transporter achieved the highest power conversion efficiency of 22.04% with a negligible current hysteresis. The champion cell lost less than 3% of the initial efficiency under continuous room lighting (1000 lux) for 1000 h (lost 10% after 2184 h) without encapsulation under an inert atmosphere. Four related low-temperature-processed ETLs (Lt-TiO2/C-SnO2, Lt-C-SnO2, Lt-TiO2:SnO2, and Lt-TiO2) were fabricated using the same metal oxide nanoparticle suspensions and studied simultaneously to reveal the function of each metal oxide in the bilayered Lt-TiO2:SnO2/C-SnO2 ETLs. In the bottom Lt-TiO2:SnO2 layer, small TiO2 nanoparticles were needed for making a dense film, and highly conducting big SnO2 nanoparticles are used to increase the conductivity of ETLs and a handy electron transport path for reducing the charge accumulation and series resistance of the cell. A top C-SnO2 layer (regarded as an interlayer between Psk and Lt-TiO2:SnO2) was used to extract/transport electrons facilely, to form a bilayered ETL with a cascade CB, and to create a hydrophilic surface to deposit high-quality Psk films to enhance the photovoltaic performance of the PSCs. This study provides a blueprint for designing good-performance ETLs for high-efficiency, stable regular planar PSCs using various sized nanoparticles prepared in a very simple and low-cost way.

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4-Nitrophenol (4-NP) is an extensively utilized industrial chemical and one of major toxic water pollutant. Therefore, there is an urgent need to monitor the levels of 4-NP from environmental samples as well as its eradication are extremely important. Keeping this as a motivation, this research for the first-time reports microwave-assisted cost-effective synthesis of silver oxide (Ag2O)-zinc oxide (ZnO) composite nanocones (CNCs, 80-100 nm) for simultaneous electrochemical detection and photodegradation of 4-NP from aqueous solutions. The Ag2O-ZnO CNCs modified gold electrode was fabricated for electrochemical detection of 4-NP. Such fabricated sensor exhibited a sensitivity of 1.6 µA µM-1cm-2, wide linear detection range of 0.4-26 µM & 28-326 µM, and a low limit of detection of 23 nM. The sensor also exhibited good selectivity in real water samples. Also, an outstanding photocatalytic performance of Ag2O-ZnO CNCs was evaluated towards UV-assisted degradation of 4-NP and organic water pollutant dye, methylene blue. The Ag2O-ZnO CNCs exhibited excellent electro- and photocatalytic activities due to the formation of p-n nano-heterojunction comprising of p-type Ag2O and n-type ZnO semiconductor nanoparticles within the composite. Therefore, herein reported smart CNCs can be projected as applied nano-system for cost-effective and rapid simultaneous detection and removal of 4-NP from aqueous solutions. Such nano-system can be useful for industrial application where detection and removal of 4-NP is a key issue to resolve.

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Many microbial species causing infectious disease all over the world became a social burden and creating threat among community. These microbes possess long lifetime, enhancing mortality and morbidity rate in affected organisms. In this condition, the treatment was ineffective and more chances of spreading of infection into other organisms. Hence, it is necessary to initiate infection control efforts and prevention activities against multidrug resistant microbes, to reduce the death rate of people. Seriously concerning towards this problem progress was shown in developing significant drugs with least side effects. Emergence of nanoparticles and its novelty showed effective role in targeting and destructing microbes well. Further, many research works have shown nanocomposites developed from nanoparticles coupled with other nanoparticles, polymers, carbon material acted as an exotic substance against microbes causing severe loss. However, metal and metal oxide nanocomposites have gained interest due to its small size and enhancing the surface contact with bacteria, producing damage to it. The bactericidal mechanism of metal and metal oxide nanocomposites involve in the production of reactive oxygen species which includes superoxide radical anions, hydrogen peroxide anions and hydrogen peroxide which interact with the cell wall of bacteria causing damage to the cell membrane in turn inhibiting the further growth of cell with leakage of internal cellular components, leading to death of bacteria. This review provides the detailed view on antibacterial activity of metal and metal oxide nanocomposite which possessed novelty due to its physiochemical changes.

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Microelectronic gas-sensor devices were developed for the detection of carbon monoxide (CO), nitrogen dioxides (NO2), ammonia (NH3) and formaldehyde (HCHO), and their gas-sensing characteristics in six different binary gas systems were examined using pattern-recognition methods. Four nanosized gas-sensing materials for these target gases, i.e., Pd-SnO2 for CO, In2O3 for NOX, Ru-WO3 for NH3, and SnO2-ZnO for HCHO, were synthesized using a sol-gel method, and sensor devices were fabricated using a microsensor platform. Principal component analysis of the experimental data from the microelectromechanical systems gas-sensor arrays under exposure to single gases and their mixtures indicated that identification of each individual gas in the mixture was successful. Additionally, the gas-sensing behavior toward the mixed gas indicated that the traditional adsorption and desorption mechanism of the n-type metal oxide semiconductor (MOS) governs the sensing mechanism of the mixed gas systems.

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A novel flake-ball-like magnetic Fe3O4/γ-MnO2 meso-porous nano-composite was synthesized and characterized for defluoridation. Adsorption process, characters, and effects of solution chemistry on the adsorption of flourinion in Fe3O4/γ-MnO2 were evaluated. The results show that the adsorption of fluorinion in the Fe3O4/γ-MnO2 nano-composite is fitted with the Pseudo-first model and the Langmuir model, indicating that the adsorption process of fluorinion in the Fe3O4/γ-MnO2 nano-composite was a physical process and not only controlled by the film diffusion but also controlled by the intra-particle diffusion and surface adsorption. It shows that the adsorption of fluorinion sharply decrease with the increase of pH due to the negative changed surface of Fe3O4/γ-MnO2 in water and the competition of OH- for the active points. The competition from decreases the adsorption of fluoride in the order of Cl- < NO3- < SO42-, which relied on the ratio of charge towards radius (z/r) of the anions, and the negatively charged humic acid competed with fluorinion for the adsorption sites. Based on the adsorption results and the XPS analysis, the OMn bond in the raw adsorbent supported the active site (OMnOH) for fluoride adsorption by forming an OMnF bond on the surface of Fe3O4/γ-MnO2.

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