In the present study, single phase nickel based disulphide (NiS2) and diselenide (NiSe2) nanostructures were prepared hydrothermally in a short time span (4 h) under subcritical temperature (160 °C). The nanostructures grow in cubic crystal phases. Average crystallite sizes and intrinsic microstrains were determined using Williamson-Hall (W-H) plot analysis. Hollow NiS2 nanospheres and bipyramidal NiSe2 nanostructures are reported that are suitable for surface related applications. Thermal gravimetric analysis (TGA) indicated high stability of the nanostructures at elevated temperatures. Optical studies indicated visible light activeness of the nanostructures exhibiting sharp band edges. The nanostructures are mesoporous in nature with NiS2 and NiSe2 having respectively a large specific surface area of 310 m2/g and 177 m2/g. A primarily work done to determine the electrochemical nature of the nanostructures showed the materials are pseudo-capacitive in nature with specific capacitances of 1022 F/g and 480 F/g respectively for NiS2 and NiSe2. The photo-catalytic activity of the nanostructures was explored against a colourless pollutant; phenol. The nanostructures degraded most of the phenol (>90 %) under visible light illumination and the reusability experiments performed determined industrial value of the photocatalysts.
Mn doping in SrSnO3 perovskite material via hydrothermal process under subcritical conditions is reported for the very first time. The present article aims to carry this perovskite suitable for blue light-emitting diodes (LEDs) and spintronic applications. The influence of various Mn doping percentages on structural, morphological, compositional, optical, photoluminescent, and magnetic properties of SrSnO3 is demonstrated. The perovskite material is grown in an orthorhombic crystal structure having a space symmetry of Pnma along with point group of mmm as determined from the Rietveld refinement. Doping is an excellent way to modify the properties of wide-band-gap perovskite nanostructures. Incorporation of Mn is the result of exact substitution. Morphological studies indicate formation of rodlike structures with thickness in nanoscale dimensions (180-280 nm), and the thickness is a function of doping concentration. The higher doping concentration resulted in enhanced growth of the nanorods. Selected area electron diffraction (SAED) results showed the single-crystal nature of the nanorods. Thermogravimetric analysis (TGA) confirmed the high stability of the material at elevated temperatures. Also, the doped perovskite material is transparent in the visible light, active in the ultraviolet region having a band gap of â¼2.78 eV, and is tuned up to 2.25 eV as the Mn doping concentration reaches 10%. The transfer of excitonic energy from the host material to the dopant Mn2+ ion leads to the formation of spin-forbidden [4T1-6A1] emission. Later on, photoluminescence study indicates an enhancement in luminescence behavior of Mn doped perovskite nanostructures. The Commission Internationale de l'éclairage (CIE) diagram drawn to find the color coordinates of the nanorods determines their suitability for blue LEDs. In addition, Mn doping results the conversion of diamagnetic SrSnO3 into a ferromagnetic material, making the nanorods suitable for spintronic applications.
We present our work on the rapid hydrothermal synthesis of highly crystalline 2D SnS nanostructures. An innovative idea is used in which thioglycolic acid is the sulfur precursor source. Structural studies indicate the material has grown in a single-phase orthorhombic structure. The single-phase formation of the material is also confirmed from the rietveld refinement of the experimental XRD data and by raman spectroscopic analysis. Morphological studies show the formation of 2D sheets having thickness in the nanoscale (100-150 nm) dimensions. Optical absorbance studies show the material is visible-light active exhibiting an indirect bandgap of 1.1 eV and direct band gap â¼1.7 eV. Density functional theory calculations support the experimental bandgap results. Photocatalytic activity of the nanosheets was investigated against methylene blue (MB), rhodamine B (RhB) and methyl orange (MO) dyes employing a solar simulator as the source of photons (light source). The nanosheets were found to photodegrade 80% of MB, 77% of RhB and 60% of MO in 120 min of light illumination. Reusability and post catalytic properties affirm the durability and stability of the nanosheets, which is very important in the context of waste water treatment considering the toxic nature of the effluents from dye industries.
Chalcogenide nanostructures are the materials with diverse applications. Here, we report rapid hydrothermal synthesis of crystalline ZnSe quantum dots (QDs), avoiding the use of toxic chemicals. To the best of our knowledge, this is the first report on very rapid (5 h) hydrothermal synthesis of pristine ZnSe QDs. Elemental selenium is used as a source for selenium. Structural, morphological, compositional, and optical properties of the semiconductor were studied. Structural properties (X-ray diffraction) demonstrate that the particles have grown in a single cubic phase. Morphological studies show formation of agglomerated QDs (4 nm). The material possess stoichiometric ratio of the constituent elements that are uniformly distributed. Selected area electron diffraction (SAED) study indicated the material is polycrystalline in nature. Optical properties demonstrated that the QDs are suitable for optoelectronic devices exhibiting room temperature photoluminescence. Commission Internationale de l'Éclairage (CIE) chromaticity diagram shows the material exhibits violet emission and hence suitable for violet LEDs that have potential ability in clinical applications.
Quantum Dots , Selenium Compounds , Water , X-Ray Diffraction , Zinc Compounds
