Probing impact on magnetic behavior of cobalt layer grown on thick MoS 2 layer.

Understanding the metal-semiconductor heterostructure interface is crucial for the development of spintronic devices. One of the prospective candidates and extensively studied semiconductors is molybdenum disulfide (MoS 2 ). Herein, utilizing Kerr microscopy, we investigated the impact of thick MoS 2 on the magnetic properties of the 10 nm Co layer. A comparative study on Co / MoS 2 and Co/Si shows that coercivity increased by 77% and the Kerr signal decreased by 26% compared to Co grown on Si substrate. In addition, the Co domain structure significantly changed when grown on MoS 2 . The plausible reason for the observed magnetic behavior can be that the Co interacts differently at the interface of MoS 2 as compared to Si. Therefore, our studies investigate the interfacial effect on the magnetic properties of Co grown on thick MoS 2 layer. Furthermore, our results will help in developing next-generation spintronic devices.

An overview of green synthesized silver nanoparticles towards bioactive antibacterial, antimicrobial and antifungal applications.

Present review emphatically introduces the synthesis, biocompatibility, and applications of silver nanoparticles (AgNPs), including their antibacterial, antimicrobial, and antifungal properties. A comprehensive discussion of various synthesis methods for AgNPs, with a particular focus on green chemistry mediated by plant extracts has been made. Recent research has revealed that the optical properties of AgNPs, including surface plasmon resonance (SPR), depend on the particle size, as well as the synthesis methods, preparation synthesis parameters, and used reducing agents. The significant emphasis on the use of synthesized AgNPs as antibacterial, antimicrobial, and antifungal agents in various applications has been reviewed. Furthermore, the application areas have been thoroughly examined, providing a detailed discussion of the underlying mechanisms, which aids in determining the optimal control parameters during the synthesis process of AgNPs. Furthermore, the challenges encountered while utilizing AgNPs and the corresponding advancements to overcome them have also been addressed. This review not only summarizes the achievements and current status of plant-mediated green synthesis of AgNPs but also explores the future prospects of these materials and technology in diverse areas, including bioactive applications.

Comparative Study of TiO2, ZnO, and Nb2O5 Photoanodes for Nitro-Substituted Naphthoquinone Photosensitizer-Based Solar Cells.

This research focuses on the first demonstration of NO2Lw (2-hydroxy-3-nitronaphthalene-1,4-dione) as a photosensitizer and TiO2, ZnO, and Nb2O5 as photoanode materials for dye-sensitized solar cells (DSSCs). The metal-free organic photosensitizer (i.e., nitro-group-substituted naphthoquinone, NO2Lw) was synthesized for this purpose. As a photoanode material, metal oxides, such as TiO2, ZnO, and Nb2O5, were selected. The synthesized NO2Lw contains an electron-withdrawing group (-NO2) and anchoring groups (-OH) that exhibit absorption in the visible range. The UV-visible absorbance spectrum of NO2Lw demonstrates the absorption ascribed to ultraviolet and visible region charge transfer. The NO2Lw interacts with the TiO2, ZnO, and Nb2O5 photoanode, as shown by bathochromic shifts in wavelengths in the photosensitizer-loaded TiO2, ZnO, and Nb2O5 photoanodes. FT-IR analysis also studied the bonding interaction between NO2Lw and TiO2, ZnO, and Nb2O5 photoanode material. The TiO2, ZnO, and Nb2O5 photoanodes loaded with NO2Lw exhibit a shift in the wavenumber of the functional groups, indicating that these groups were involved in loading the NO2Lw photosensitizer. The amount of photosensitizer loading was calculated, showing that TiO2 has higher loading than ZnO and Nb2O5 photoanodes; this factor may constitute an increased JSC value of the TiO2 photoanode. The device performance is compared using photocurrent-voltage (J-V) curves; electrochemical impedance spectroscopy (EIS) measurement examines the device's charge transport. The TiO2 photoanode showed higher performance than the ZnO and Nb2O5 photoanodes in terms of photoelectrochemical properties. When compared to ZnO and Nb2O5 photoanodes-based DSSCs, the TiO2 photoanode Bode plot shows a signature frequency peak corresponding to electron recombination rate toward the low-frequency region, showing that TiO2 has a greater electron lifetime than ZnO and Nb2O5 photoanodes based DSSCs.

Modification in Toxicity of l-Histidine-Incorporated ZnO Nanoparticles toward Escherichia coli.

This paper presents a comparative study of the toxicity of pristine-ZnO and l-histidine-incorporated ZnO toward Escherichia coli (E. coli) as a Gram-negative model organism. Pristine-ZnO and l-histidine-incorporated ZnO with different l-histidine concentrations were synthesized using an open aqueous solution bath technique. XRD studies revealed the formation of polycrystalline wurtzite ZnO. The average crystallite size of the synthesized l-histidine-incorporated ZnO decreased as the concentration of l-histidine increased. The FTIR spectra showed the presence of Zn-O, CO2-/CO3-, and C-N (only in l-histidine-incorporated ZnO samples) and -OH bond vibration signals in all samples. The chemical purity of all the samples was ensured using XPS analysis. The microbial activity of these samples was investigated using E. coli. The solution with 100 µg/mL ZnO in sterile distilled water showed up to 94% growth inhibition of E. coli, establishing antibacterial activity. However, l-histidine incorporated in ZnO showed reduced antibacterial activity with the increase of the concentration of l-histidine in ZnO. Furthermore, flow cytometry studies during the interaction of ZnO and E. coli confirmed the generation of reactive oxygen species (ROS), validating its antibacterial activity. The interaction of l-histidine-incorporated ZnO and E. coli showed declining ROS with the increase in the l-histidine concentration, indicating a ZnO toxicity reduction.

Comparative Studies on Synthesis, Characterization and Photocatalytic Activity of Ag Doped ZnO Nanoparticles.

In this work, silver (Ag) doped zinc oxide (ZnO) nanoparticles were synthesized using zinc chloride, zinc nitrate, and zinc acetate precursors with (0 to 10) wt % Ag doping by a simple reflux chemical method. The nanoparticles were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy, ultraviolet visible spectroscopy, and photoluminescence spectroscopy. The nanoparticles are studied as a photocatalyst for visible light driven annihilation of methylene blue and rose bengal dyes. The 5 wt % Ag doped ZnO displayed optimum photocatalytic activity toward methylene blue and rose bengal dye degradation at the rate of 13 × 10-2 min-1 and 10 × 10-2 min-1, respectively. Here we report antifungal activity for the first time using Ag doped ZnO nanoparticles against Bipolaris sorokiniana, displaying 45% efficiency for 7 wt % Ag doped ZnO.

Self-biased photodetector using 2D layered bismuth triiodide (BiI3) prepared using the spin coating method.

Layered bismuth triiodide (BiI3) is a 2D material that has emerged as an ideal choice for optical sensors. Although BiI3 has been prepared using vacuum-based deposition techniques, there is a dearth of research studies on synthesizing this material using chemical route. The present work uses a facile spin coating method with varying rotation speeds (rpm) to fabricate BiI3 material thin films for photodetection applications. The structural, optical, and morphological study of BiI3 thin films prepared at 3000-6000 rpm were investigated. XRD analysis indicates formation of BiI3 films and revealed that BiI3 has a rhombohedral crystal structure. FESEM analysis showed that BiI3 films prepared at different rpm are homogeneous, dense, and free from cracks, flaws, and protrusions. In addition, films show an island-like morphology with grain boundaries having different grain sizes, micro gaps, and the evolution of the granular morphology of BiI3 particles. The UV spectroscopy and photoluminescence analysis revealed that BiI3 films strongly absorb light in the visible region of spectra with a high absorption coefficient of ∼104 cm-1, have an optical band gap of ∼1.51 eV. A photodetector was realised using fabricated BiI3 film obtained at an optimum spin speed of 4000 rpm. It showed rapid rise and decay times of 0.4 s and 0.5 s, a responsivity of ∼100 µA W-1, external quantum efficiency of 2.1 × 10-4%, and detectivity of ∼3.69 × 106 Jones at a bias voltage of 0 V. Our results point towards a new direction for layered 2D BiI3 materials for the application in self-biased photodetectors.

Naphthoquinoneoxime-Sensitized Titanium Dioxide Photoanodes: Photoelectrochemical Properties.

Naphthoquinoneoxime derivatives, viz., LwOx, 3-hydroxy-4-(hydroxyimino)naphthalen-1 (4H)-one; PthOx, 3-hydroxy-4-(hydroxyimino)-2-methylnaphthalen-1(4H)-one; and Cl_LwOx, 2-chloro-3-hydroxy-4-(hydroxyimino)naphthalen-1(4H)-one, are used in fabrication of dye-sensitized solar cells (DSSCs). The photophysical and electrochemical properties of the sensitizers were studied. The HOMO-LUMO energy gaps of the sensitizers (LwOx, PthOx, and Cl_LwOx) calculated by using the intersection of UV-visible and fluorescence spectra are 2.85, 2.71, and 2.87 eV, respectively. The energy band alignment energy level of the sensitizer, that is, the lowest unoccupied molecular orbital (LUMO) and highest occupied molecular orbital (HOMO), should match with the energy level of the TiO2 conduction band and the redox potential of iodine/triiodide electrolyte to allow smooth electron transfer. The electrochemical characterization of sensitizers was done to find the LUMO and HOMO level of the sensitizer. It shows that the LUMO level of (LwOx, PthOx, and Cl_LwOx) is above the conduction band position of TiO2. Electrochemical impedance spectroscopy was used to study the charge transport resistance and electron lifetime of DSSCs. The charge transport resistance at the TiO2 |electrolyte|counter electrode interface was reduced in the Cl_LwOx device; thus, the electron lifetime of Cl_LwOx was enhanced compared to LwOx and PthOx sensitizers. The fabricated device was characterized using photocurrent density-voltage (J-V) measurement. It is observed that there was an enhancement in the overall power conversion efficiency (η) of the DSSCs fabricated by using Cl_LwOx sensitizers as compared to LwOx and PthOx sensitizer-loaded photoanodes. Enhancement in power conversion efficiency, that is, photovoltage and photocurrent, is achieved due to the chlorine substituent. Thus, the chlorine substituent naphthoquinoneoxime pushes the electron density, enhancing the pushing nature and facilitating the lone pair present in the N-OH moiety to attach to TiO2 more strongly.

Titania Nanorods Embedded with 2-Bromo-3-(methylamino)naphthalene-1,4-dione for Dye-Sensitized Solar Cells.

In a recent study, TiO2 nanorod electrodes were prepared by the hydrothermal approach followed by calcination at various temperatures from 300 to 600 °C. The effects of calcination temperature on the morphological and structural properties were investigated. The novel analogue of aminonaphthoquinone(2R-(n-alkylamino)-1,4-naphthoquinone) photosensitizer, viz. BrA1, 2-bromo-3-(methylamino)naphthalene-1,4-dione was synthesized from 2,3-dibromonaphthalene-1,4-dione. X-ray crystallographic data collection and refinement confirm that BrA1 crystallizes in the triclinic space group P 1̅. After loading BrA1, the photosensitizer on the annealed TiO2 nanorod (TiO2NR) electrodes, the optical properties of the photoanodes showed broadbands in each of the UV and visible regions, which are attributed to the π →π* and n → π* charge-transfer transitions, respectively. The dye-sensitized solar cell (DSSC) system was formed by loading the BrA1 photosensitizer on TiO2NR. The electrochemical impedance spectroscopy (EIS) analyses confirm that calcination temperature improves the charge transportation by lowering the resistance path during the photovoltaic process in TiO2NR (400 °C) photoanode-based DSSCs due to the sufficient photosensitizer adsorption and fast electron injection. Due to the effective light harvesting by the BrA1 photosensitizer and charge transport through the TiO2 nanorod, the power conversion efficiencies (PCE) of the TiO2NR (400 °C/BrA1-based) DSSCs were improved for 2-bromo-3-(methylamino)naphthalene-1,4-dione.

Synthesis, Structural and Optical Properties of ZrBi2Se6 Nanoflowers: A Next-Generation Semiconductor Alloy Material for Optoelectronic Applications.

ZrBi2Se6 nanoflower-like morphology was successfully prepared using a solvothermal method, followed by a quenching process for photoelectrochemical water splitting applications. The formation of ZrBi2Se6 was confirmed by field emission scanning electron microscopy (FE-SEM), X-ray diffraction (XRD), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). The estimated value of work function and band gap were found to be 5.5 and 2.26 eV measured using diffuse reflection spectroscopy and ultraviolet photoelectron spectroscopy, suggesting the potential candidate for water splitting. The highest current density of 9.7 µA/cm2 has been observed for the ZrBi2Se6 photoanode for the applied potential of 0.5 V vs SCE. The flat-band potential value was -0.46 V, and the 1.85 nm width of the depletion region is estimated from the Mott-Schottky (MS) analysis. It also reveals that the charge carrier density for the ZrBi2Se6 nanoflowers is 4.8 × 1015 cm-3. The negative slope of the MS plot indicates that ZrBi2Se6 is a p-type semiconductor. It was observed that ZrBi2Se6 nanoflowers had a high charge transfer resistance of ∼730 kΩ and equivalent capacitance of ∼40 nF calculated using electrochemical impedance spectroscopy (EIS) measurements. Using chronoamperometry, the estimated rise time and decay time were 50 ms and 0.25 s, respectively, which reveals the fast photocurrent response and excellent PEC performance of the ZrBi2Se6 photoanode. Furthermore, an attempt has been made to explain the PEC activity of ZrBi2Se6 nanoflowers using an energy band diagram. Thus, the initial results on ZrBi2Se6 nanoflowers appear promising for the PEC activity toward water splitting.

Multifunctional Cu2SnS3 Nanoparticles with Enhanced Photocatalytic Dye Degradation and Antibacterial Activity.

We present a simplistic, ultrafast, and facile hydrothermal deposition of ternary Cu2SnS3 nanoparticles (CTS NPs). The fabricated CTS NPs show superior antimicrobial and photocatalytic activities. In the presence of UV-Visible illumination, methylene blue (MB) dye was studied for photocatalytic dye degradation activity of CTS NPs. Excellent efficiency is shown by incorporating CTS NPs to degrade MB dye. There is a ~95% decrease in the absorbance peak of the dye solution within 120 min. Similarly, CTS NPs tested against three bacterial strains, i.e., B. subtilis, S. aureus, P. vulgaris, and one fungal strain C. albicans, defining the lowest inhibitory concentration and zone of inhibition, revealed greater antimicrobial activity. Hence, it is concluded that the CTS NPs are photocatalytically and antimicrobially active and have potential in biomedicine.

A Facile Chemical Synthesis of PbTe Nanostructures at Room Temperature.

Thermoelectric (TE) materials are possible solutions of the current problems in the energy sector to overcome environmental pollution, increasing energy demand and the decline of natural resources. Thermoelectric materials are a promising alternative for the conversion of waste heat to electricity. Nanocrystalline PbTe powder was synthesized by a simple chemical method at room temperature and systematically investigated at various durations as samples A1-A5. Fourier Transform infrared spectroscopy (FTIR), x-ray diffraction (XRD), microstructural analysis by scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS) confirmed the composition of the samples. TE parameters as thermo-emf of samples A1-A5 and electrical conductivity were measured. The cyclic voltammetry gives a band gap of 0.25 eV, which is in agreement with the optical band gap of the material. The A4 sample has an average crystal size of 36 nm with preferred orientation in (200) verifying the cubic morphology. The obtained TE parameters are beneficial for the non-uniform TE materials which might be due to strong current boundary scattering and extremely low thermal conductivity of the samples.

A Look Behind the Scenes at COVID-19: National Strategies of Infection Control and Their Impact on Mortality.

(1) Background: The severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) began spreading across the globe in December and, as of 9 July 2020, had inflicted more than 550,000 deaths. Public health measures implemented to control the outbreak caused socio-economic havoc in many countries. The pandemic highlighted the quality of health care systems, responses of policymakers in harmony with the population, and socio-economic resilience factors. We suggest that different national strategies had an impact on mortality and case count. (2) Methods: We collected fatality data for 17 countries until 2 June 2020 from public data and associated these with implemented containment measures. (3) Results: The outcomes present the effectiveness of control mechanisms in mitigating the virus for selected countries and the UAE as a special case. Pre-existing conditions defined the needed public health strategies and fatality numbers. Other pre-existing conditions, such as temperature, humidity, median age, and low serum 25-hydroxyvitamin D (25(OH)D) concentrations played minor roles and may have had no direct impact on fatality rates. (4) Conclusions: Prevention, fast containment, adequate public health strategies, and importance of indoor environments were determining factors in mitigating the pandemic. Development of public health strategies adapted to pre-existing conditions for each country and community compliance with implemented policies ensure the successful control of pandemics.

ZnO/CuSCN Nano-Heterostructure as a Highly Efficient Field Emitter: a Combined Experimental and Theoretical Investigation.

We report the synthesis of two-dimensional porous ZnO nanosheets, CuSCN nanocoins, and ZnO/CuSCN nano-heterostructure thin films grown on fluorine-doped tin oxide substrates via two simple and low-cost solution chemical routes, i.e., chemical bath deposition and successive ionic layer adsorption and reaction methods. Detail characterizations regarding the structural, optoelectronic, and morphological properties have been carried out, which reveal high-quality and crystalline synthesized materials. Field emission (FE) investigations performed at room temperature with a base pressure of 1 × 10-8 mbar demonstrate superior FE performance of the ZnO/CuSCN nano-heterostructure compared to the isolated porous ZnO nanosheets and CuSCN nanocoins. For instance, the turn-on field required to draw a current density of 10 µA/cm2 is found to be 2.2, 1.1, and 0.7 V/µm for the ZnO, CuSCN, and ZnO/CuSCN nano-heterostructure, respectively. The observed significant improvement in the FE characteristics (ultralow turn-on field of 0.7 V/µm for an emission current density of 10 µA/cm2 and the achieved high current density of 2.2 mA/cm2 at a relatively low applied electric field of 1.8 V/µm) for the ZnO/CuSCN nano-heterostructure is superior to the isolated porous ZnO nanosheets, CuSCN nanocoins, and other reported semiconducting nano-heterostructures. Complementary first-principles density functional theory calculations predict a lower work function for the ZnO/CuSCN nano-heterostructure (4.58 eV), compared to the isolated ZnO (5.24 eV) and CuSCN (4.91 eV), validating the superior FE characteristics of the ZnO/CuSCN nano-heterostructure. The ZnO/CuSCN nanocomposite could provide a promising class of FE cathodes, flat panel displays, microwave tubes, and electron sources.

Effect of photoanode surface coverage by a sensitizer on the photovoltaic performance of titania based CdS quantum dot sensitized solar cells.

In spite of the promising design and architecture, quantum dot sensitized solar cells (QDSSCs) have a long way to go before they attain the actual projected photoconversion efficiencies. Such an inferior performance displayed by QDSSCs is primarily because of many unwanted recombination losses of charge carriers at various interfaces of the cell. Electron recombination due to back electron transfer at the photoanode/electrolyte interface is an important one that needs to be addressed, to improve the efficiency of these third generation nanostructured solar cells. The present work highlights the importance of conformal coverage of CdS quantum dots (QDs) on the surface of the nanocrystalline titania photoanode in arresting such recombinations, leading to improvement in the performance of the cells. Using the successive ionic layer adsorption and reaction (SILAR) process, photoanodes are subjected to different amounts of CdS QD sensitization by varying the number of cycles of deposition. The sensitized electrodes are characterized using UV-visible spectroscopy, cyclic voltammetry and transmission electron microscopy to evaluate the extent of surface coverage of titania electrodes by QDs. Sandwich solar cells are then fabricated using these electrodes and characterized employing electrochemical impedance spectroscopy and J-V characteristics. It is observed that maximum solar cell efficiency is obtained for photoanodes with conformal coating of QDs and any further deposition of sensitizer leads to QD aggregation and so reduces the performance of the solar cells.

Nanocrystalline TiO2/ZnO thin films: fabrication and application to dye-sensitized solar cells.

Nanocrystalline TiO2 thin films composed of densely packed grains were deposited onto indium-doped tin oxide (ITO)-coated glass substrates at room temperature using a chemical bath deposition technique. A layer-by-layer (LbL) process was utilized to obtain a 1.418-microm-thick TiO2/ZnO structure. The TiO2 surface was super-hydrophilic, but its hydrophilicity decreased considerably after ZnO deposition. Other TiO2/ZnO films were studied to assess their suitability as photoelectrodes in dye-sensitized solar cells (DSSCs).