Polyol-assisted hydrothermal synthesis of Mn-doped α - Fe2O3(MFO) nanostructures: Spin disorder-induced magnetism and photocatalytic properties.

Hierarchical nanostructures play an important role in environmental clean-up and sustainability applications. The magnetic and photocatalytic characteristics of flower-like Mn-doped α-Fe2O3 nanostructures were prepared by using a polyol-assisted hydrothermal method. Crystallite sizes are in the range of 35-42 nm, and the existence of 3D hierarchical nanostructures was observed in FESEM pictures. The optical band gap energy varies between 2.08 and 2.16 eV, while XPS examination exposes the ions' charge states and validates Mn3+ inclusion in the Fe3+ lattice. At room temperature, the addition of Mn to α-Fe2O3 results in a spin disorder ferromagnetism and coercivity of about 600 Oe was achieved. Methylene blue (MB) dye solution degraded by 92% when 2.5% Mn doped with α-Fe2O3 under visible conditions for 120 min irradiation time.

Visible light photocatalytic and magnetic properties of V doped α-Fe2O3 (VFO) nanoparticles synthesized by polyol assisted hydrothermal method.

Vanadium-doped α-Fe2O3 nanoparticles (VFO nanoparticles) were prepared by polyol-assisted hydrothermal method. The impact on the structure, optical, magnetic and photocatalytic properties of α-Fe2O3 nanoparticles were studied by varying the vanadium concentration from 1 to 5%. XRD analysis confirms the presence of hematite phase with hexagonal structure and estimates the nanocrystals size as ∼26-38 nm. FESEM and TEM reveal the formation of 3D flower-like morphology bundled with 2D nanoflakes. The estimated band gap energy was in the range 2.01 eV-2.12 eV. XPS study shows the presence of vanadium in V4+ oxidation state in VFO nanoparticles. VSM study shows a non-saturated hysteresis loop with weak ferromagnetic behavior for all the VFO nanoparticles. 5% V doped α-Fe2O3 nanoparticles (5%VFO nanoparticles) exhibited superior visible light driven photocatalytic activity compared to other samples.

Optical behavior and sensor activity of Pb ions incorporated ZnO nanocrystals.

We present the synthesis and characterization of nanocrystalline ZnO doped with Pb in different concentrations. The structural and chemical compositions of the products are characterized by XRD, XPS, EDS and FT-IR spectroscopy. The observed results suggest that Pb ions (Pb(2+) and Pb(4+)) are successfully incorporated into the lattice position of Zn(2+) ions in ZnO. The optical properties of the products are studied by UV-Vis and room temperature PL measurements. The PL emission spectra of ZnO:Pb, show the intensity quenching for both the UV and visible emissions. The influence of Pb on controlling the size and morphology of ZnO is studied by FESEM and confirmed by HRTEM. Amperometric response shows that ZnO incorporated with 0.075M of Pb ions has enhanced sensor activity for H2O2 than the undoped product.

Luminance behavior of Ce3+ doped ZnS nanostructures.

We report the synthesis and characterization of undoped and various levels of Ce(3+) doped ZnS nanocrystal. The structure and size of the products were studied by X-ray diffraction (XRD). The existence of functional groups was identified by Fourier transform infrared spectrometry (FT-IR). The UV-Visible measurements reveal that the synthesized products are blue shifted when compared with bulk phase of ZnS as a result of quantum confinement effect. The PL studies show an enhancement in the intensity of emission band in the UV region on increased Ce(3+) doping. The morphology of the products was evaluated by Field emission scanning electron microscope (FESEM) and High resolution transmission electron microscopy (FESEM). The presence of Ce(3+) was confirmed by Energy dispersive spectral analysis (EDS). The thermal stability of pure and doped products was analyzed by thermo gravimetric and differential thermal analysis (TG-DTA).