摘要
The SiO2-Fe3O4 core-shell nanostructures were synthesized by sol-gel chemistry. The morphological features of the nanostructures were examined by field emission scanning electron microscopy which revealed the core-shell nature of the nanoparticles. X-ray diffraction studies evidenced the formation of SiO2-Fe3O4 core-shell nanostructures with high degree of homogeneity. The elemental composition of the SiO2-Fe3O4 core-shell nanostructures was determined by energy-dispersive X-ray spectroscopy analysis. Fourier transform infrared spectroscopy showed the Si-O-Fe stretching vibrations. On analysis of the optical properties with UV-Vis spectra and Tauc＇s plot, it was found that the band gap of SiO2-Fe3O4 core-shell nanostructures diminished to 1.5 eV. Investigation of the electrical properties of the core-shell nanostructures using field-dependent conductivity measurements presented a significant increase in photoconductivity as compared to those of its single components, thereby rendering them as promising candidates for application as photo- electrodes in dye-sensitized solar cells.
The SiO2-Fe3O4 core-shell nanostructures were synthesized by sol-gel chemistry. The morphological features of the nanostructures were examined by field emission scanning electron microscopy which revealed the core-shell nature of the nanoparticles. X-ray diffraction studies evidenced the formation of SiO2-Fe3O4 core-shell nanostructures with high degree of homogeneity. The elemental composition of the SiO2-Fe3O4 core-shell nanostructures was determined by energy-dispersive X-ray spectroscopy analysis. Fourier transform infrared spectroscopy showed the Si-O-Fe stretching vibrations. On analysis of the optical properties with UV-Vis spectra and Tauc＇s plot, it was found that the band gap of SiO2-Fe3O4 core-shell nanostructures diminished to 1.5 eV. Investigation of the electrical properties of the core-shell nanostructures using field-dependent conductivity measurements presented a significant increase in photoconductivity as compared to those of its single components, thereby rendering them as promising candidates for application as photo- electrodes in dye-sensitized solar cells.
