Zn3Sb4O6F6 and KI-Doped Zn3Sb4O6F6: A Metal Oxyfluoride System for Photocatalytic Activity, Knoevenagel Condensation, and Bacterial Disinfection.

Zn3Sb4O6F6 crystallites were synthesized by a pH-regulated hydrothermal synthetic approach, while doping on Zn3Sb4O6F6 by KI was performed by the "incipient wetness impregnation technique." The effect of KI in Zn3Sb4O6F6 is found with the changes in morphology in the doped compound, i.e., needle-shaped particles with respect to the irregular cuboid and granular shaped in the pure compound. Closer inspection of the powder diffraction pattern of doped compounds also reveals the shifting of Braggs' peaks toward a lower angle and the difference in cell parameters compared to the pure compound. Both metal oxyfluoride comprising lone pair elements and their doped compounds have been successfully applied as photocatalysts for methylene blue dye degradation. Knoevenagel condensation reactions were performed using Zn3Sb4O6F6 as the catalyst and confirmed 99% yield even at 60 °C temperature under solvent-free conditions. Both pure and KI-doped compounds were tested against several standard bacterial strains, i.e., Enterobacter sp., Escherichia coli, Staphylococcus sp., Salmonella sp., Bacillus sp., Proteous sp., Pseudomonas sp., and Klebsiella sp. by the "disk diffusion method" and their antimicrobial activities were confirmed.

Chemiresistive NH3 detection at sub-zero temperatures by polypyrrole- loaded Sn1-xSbxO2 nanocubes.

Chemiresistive gas sensors operate mainly at high temperatures, primarily due to the need of energy for surface adsorption-desorption of analytes. As a result, the operating temperature of the chemiresistive sensors could be reduced only to room temperature. Hence, a plethora of sensing requirements at temperatures below ambient have remained outside the scope of chemiresistive materials. In this work, we have developed an antimony-doped SnO2 nanocube-supported expanded polypyrrole network that could detect low ppm ammonia gas (≤20 ppm) at sub-zero temperatures with high response (∼4), selectivity, and short response and recovery times. The low temperature chemiresistive sensing has been explained in terms of the interplay of an extended conducting network of an in situ deposited polymer, effective transport properties of majority charge carriers and a loosely bound exciton-like electron-hole pair formation and breakage mechanism.

pH-regulated hydrothermal synthesis and characterization of Sb4O5X2 (X = Br/Cl) and its use for the dye degradation of methyl orange both with and without light illumination.

A pH-regulated hydrothermal synthesis method was employed to synthesize Sb4O5Br2 and Sb4O5Cl2 crystallites. Characterization is done by single crystal X-ray diffraction, powder X-ray diffraction, infra-red spectroscopy, scanning electron microscopy and DFT studies. The compounds crystallize in monoclinic symmetry with a P21/c space group. Complete structural analysis of the Sb4O5Br2 compound by using single crystal X-ray diffraction data is performed for the first time and a comparative study with Sb4O5Cl2 is also discussed. The SEM study reveals that the surface morphology changes with the variation of pH for bromide compounds, whereas pH change does not affect the morphology of the chloride analogues. Electronic band structures of the synthesized oxyhalides were investigated in order to understand their catalytic effects in the dye degradation reactions in dark as well as sunlight conditions.

Ferromagnetic Ni1-xVxO1-y Nano-Clusters for NO Detection at Room Temperature: A Case of Magnetic Field-Induced Chemiresistive Sensing.

Surface modulation of functional nanostructures is an efficient way of improving gas sensing properties in chemiresistive materials. However, synthesis methods employed so far in achieving desired performances are cumbersome and energy intensive. Moreover, nano-engineering-induced magnetic properties of these materials which are expected to enhance sensing responses have not been utilized until now in improving their interaction with target gases. In particular for gasses with paramagnetic nature such as NO or NO2, the inherent magnetic property of the chemiresistor might assist in enabling superior sensing performance. In this work, vanadium-doped NiO nano-clusters with ferromagnetic behavior at room temperature have been synthesized by a simple and effective combination of soft chemical routes and employed in efficient and selective detection of paramagnetic NO gas. While NiO is typically anti-ferromagnetic, the nanoscale engineering of NiO- and V-doped NiO samples have been found to tune the inherent anti-ferromagnetic behavior into room-temperature ferromagnetism. Surface modification in terms of formation of nano-clusters led to an increased Brunauer-Emmett-Teller surface area of ∼120 m2/g. The sample Ni0.636V0.364O has been observed to exhibit a selective and high response of ∼98% to 1 ppm NO at room temperature with fast response (14 s) and recovery (95 s). The improved sensing response of this sample compared to other doped NiO variants could be explained in terms of lower remnant magnetic moment of the sample accompanied with higher excess negative charge at the surface. The sensing response of this sample was increased by 30% in the presence of an external magnetic field of 280 gauss, highlighting the importance of magnetic ordering in chemiresistive gas sensing between the magnetic sensor material and target analyte. This material stands as a potential gas sensor with excellent NO detection properties.

Influence of pressure on the transport, magnetic, and structural properties of superconducting Cr0.0009NbSe2 single crystal.

We investigate the superconducting critical current density (J c), transition temperature (T c), and flux pinning properties under hydrostatic pressure (P) for Cr0.0009NbSe2 single crystal. The application of P enhances T c in both electrical resistivity (∼0.38 K GPa-1: 0 ≤ P ≤ 2.5 GPa) and magnetization (∼0.98 K GPa-1: 0 ≤ P ≤ 1 GPa) measurements, which leads to a monotonic increase in J c and flux pinning properties. The field-dependent J c at various temperatures under P is analyzed within the collecting pinning theory and it shows that δT c pinning is the crossover to δl pinning above the critical pressure (P c ∼0.3 GPa). Our systematic analysis of the flux pinning mechanism indicates that both the density of pinning centers and pinning forces greatly increase with the application of P, which leads to an enhancement in the vortex state. Structural studies using synchrotron X-ray diffraction under pressure illustrate a stable hexagonal phase without any significant impurity phase and lattice parameter reduction with P shows highly anisotropic nature.