ABSTRACT
Zn(II) (complex 1), Cd(II) (complex 2), and Hg(II) (complex 3) complexes have been synthesized using a triply protonated tptz (H3tptz3+) ligand and characterized mainly by single-crystal X-ray analysis. The general formula of all of the complexes is (H3tptz)3+·Cl-·[MCl4]2-·nH2O (where n = 1, 1.5, and 1.5 for complexes 1, 2, and 3, respectively). The crystallographic analysis reveals that the anion···π, anion···π+, and several hydrogen bondingâ¯interactions play a fundamental role in the stabilization of the self-assembled architectures that in turn help to enhance the dimensionality of all of the complexes. In addition, Hirshfeld surfaces and fingerprint plots have been deployed here to visualize the similarities and differences in hydrogen bonding interactions in 1-3, which are very important in forming supramolecular architectures. A density functional theory (DFT) study has been used to analyze and rationalize the supramolecular interactions by using molecular electrostatic potential (MEP) surfaces and combined QTAIM/NCI plots. Then, the device parameters for the complexes (1-3) have been thoroughly investigated by fabricating a Schottky barrier diode (SBD) on an indium tin oxide (ITO) substrate. It has been observed that the device made from complex 2 is superior to those from complexes 1 and 3, which has been explained in terms of band gaps, differences in the electronegativities of the central metal atoms, and the better supramolecular interactions involved. Finally, theoretical calculations have also been performed to analyze the experimental differences in band gaps as well as electrical conductivities observed for all of the complexes. Henceforth, the present work combined supramolecular, photophysical, and theoretical studies regarding group 12 metals in a single frame.
ABSTRACT
We report the synthesis of SnO2/α-Fe2O3 heterostructure thin films by employing two-step processes: galvanic and chemical deposition. Fe2O3 is a narrow band gap semiconductor and has short hole diffusion length. Therefore, the photogenerated electrons and holes are not easy to separate in Fe2O3. Combining Fe2O3 to SnO2, a wide-energy-gap semiconductor having suitable valence band and conduction band position is a promising candidate for the photo catalysts. The chemical modification of this heterostructure was achieved by electro-active Prussian blue (PB) molecule. The photocatalytic activities of SnO2, α-Fe2O3, SnO2/α-Fe2O3, and SnO2/α-Fe2O3-PB thin films were investigated for organic dye degradation. It was observed that the coupled and combined modified systems showed better reactivity compared to individual single-component materials. The electrocatalytic activity of the synthesized thin films has also been studied where hydrogen peroxide (H2O2) was taken as a model compound. Amperometric study also reveals that the couple and combined modified thin films are more effective at sensing hydrogen peroxide (H2O2) than single-component materials.
ABSTRACT
A novel non-enzymatic peroxide sensor has been constructed by using nickel oxide (NiO) thin films as sensing material, which were prepared by a two-step process: (i) electrodeposition of nickel sulfide (NiS) and (ii) thermal air oxidation of as-deposited NiS to NiO. The resultant material is highly porous and comprises interconnected nanofibers. UV-Vis spectroscopy, FTIR spectroscopy, X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and field-emission scanning electron microscopy (FESEM) were used for a complete characterization of nanostructured NiO thin films. Cyclic voltammetry study shows that NiO/ITO electrode facilitates the oxidation of hydrogen peroxide and exhibits excellent catalytic activity towards its sensing. The amperometric study of NiO/ITO was carried out to determine the sensitivity, linear range, detection limit of the proposed sensor. The sensor exhibits prominent electrocatalytic activity toward the oxidation of H2O2 with a wide linear range and a low detection limit. The possible use of the synthesized NiO thin films as an effective photocatalyst for the decomposition of phenol is also discussed.
ABSTRACT
Thin films of nanocrystalline and porous FeS(2) with marcasite phase have been deposited from a greenish-blue iron nitroprusside precursor film, which readily gives FeS(2) on reacting with an aqueous solution of sodium sulfide. High resolution X-ray diffraction (HRXRD) pattern indicated the formation of polycrystalline and orthorhombic (marcasite) phase of FeS(2), whereas the field emission scanning electron microscopy (FESEM) showed the morphology of the films to be consisted of grains of average 25 nm diameter with unevenly distributed numerous pores. Optical characterization (UV-Vis and photoluminescence) revealed significant amount of blueshift in the band gap energy of the deposited material, which is attributed to the strong quantum confinement effect exerted by the FeS(2) nanocrystals. The deposited FeS(2) films showed good photocatalytic activity toward the degradation of Rose Bengal dye and could be found efficient for wastewater treatment.
