Ionic Porous Aromatic Framework as a Self-Degraded Template for the Synthesis of a Magnetic γ-Fe2O3/WO3·0.5H2O Hybrid Nanostructure with Enhanced Photocatalytic Property

An ionic porous aromatic framework is developed as a self-degraded template to synthesize the magnetic heterostructure of γ-Fe2O3/WO3·0.5H2O. The Fe3O4 polyhedron was obtained with the two-phase method first and then reacted with sodium tungstate to form the γ-Fe2O3/WO3·0.5H2O hybrid nanostructure. Under the induction effect of the ionic porous network, the Fe3O4 phase transformed to the γ-Fe2O3 state and complexed with WO3·0.5H2O to form the n-n heterostructure with the n-type WO3·0.5H2O on the surface of n-type γ-Fe2O3. Based on a UV-Visible analysis, the magnetic photocatalyst was shown to have a suitable band gap for the catalytic degradation of organic pollutants. Under irradiation, the resulting γ-Fe2O3/WO3·0.5H2O sample exhibited a removal efficiency of 95% for RhB in 100 min. The charge transfer mechanism was also studied. After the degradation process, the dispersed powder can be easily separated from the suspension by applying an external magnetic field. The catalytic activity displayed no significant decrease after five recycles. The results present new insights for preparing a hybrid nanostructure photocatalyst and its potential application in harmful pollutant degradation.

Synthesis of Transition Metal Dichalcogenides based hybrid nanostructures by thermal decomposition method

In this work, we report synthesis of hybrid nanostructures of Transition Metal Dichalcogenides via thermal decomposition method. Ammonium tetrathiomolybdate was used as not only growth templates but also as starting precursor for synthesis of hybrid nanostructures. The conditions for the synthesizing method were optimized using electron microscopy and x-ray diffraction. In this hybrid nanostructure synthesis, it was found that MoO3 nanorods are interspersed on exfoliated MoS2 nanosheets. The structural and optical properties of the hybrid nanostructure were investigated using transmission electron microscopy (TEM), Scanning electron microscopy (SEM), X-ray diffraction (XRD), Raman spectroscopy and Ultraviolet Visible spectrophotometry (UV-VIS). The hybrid nanostructure of MoO3 on MoS2 shows a band gap of 2.2 eV. It was also found that by tuning the preparation parameters viz temperature of heating and time of heating, the composition of the hybrid nanostructure can be varied.

Enhanced Absorption with Graphene-Coated Silicon Carbide Nanowires for Mid-Infrared Nanophotonics

The mid-infrared (MIR) is an exciting spectral range that also hosts useful molecular vibrational fingerprints. There is a growing interest in nanophotonics operating in this spectral range, and recent advances in plasmonic research are aimed at enhancing MIR infrared nanophotonics. In particular, the design of hybrid plasmonic metasurfaces has emerged as a promising route to realize novel MIR applications. Here we demonstrate a hybrid nanostructure combining graphene and silicon carbide to extend the spectral phonon response of silicon carbide and enable absorption and field enhancement of the MIR photon via the excitation and hybridization of surface plasmon polaritons and surface phonon polaritons. We combine experimental methods and finite element simulations to demonstrate enhanced absorption of MIR photons and the broadening of the spectral resonance of graphene-coated silicon carbide nanowires. We also indicate subwavelength confinement of the MIR photons within a thin oxide layer a few nanometers thick, sandwiched between the graphene and silicon carbide. This intermediate shell layer is characteristically obtained using our graphitization approach and acts as a coupling medium between the core and outer shell of the nanowires.