Abstract:
Environmental remediation via semiconductor heterogeneous photocatalysis is one of the
outstanding and sustainable strategies to control the water pollution by series of redox reactions
taking place at semiconductors surface. Tailoring photocatalytic materials to meet the increasing
global energy demands and challenges related to decontamination of environment has been a
very electrifying prospect for material chemists. Two major processes that limit the activity of
any photocatalyst are the charge carrier recombination process as well as its UV light activity (as
it comprises only 5% of solar spectrum). Hematite (α-Fe2O3), due to favorable visible light active
band gap (i.e. 2.1 eV), has turned out to be hot material for diverse scientific applications related
to energy generation, energy storage, sensors and environmental pollution alleviation etc.
However, the photocatalytic efficiency of α-Fe2O3 is limited by the small life span of the light
generated charge carriers (<10 ps). So our major concern is the engineering hematite
photocatalyst with enhanced photodegradation of environmental pollutant. Herein, we report the
synthesis of the novel α-Fe2O3 based Photocatalysts like α-Fe2O3/ ZnO, α-Fe2O3 /ZnTe and α-
Fe2O3 /ZnSe via hydrothermal approach. X-ray Diffraction (XRD) spectroscopy was used to
analyze the crystal structure, purity and phase of the heterostructured photocatalysts. Moreover,
various crystalline parameters of synthesized photocatalysts were also calculated using XRD
data. Morphological analysis was carried out via Scanning Electron Microscope (SEM). The
elemental composition and purity of the synthesized photocatalysts was confirmed using EDX
spectroscopy. The alignment of energy levels is an important parameter to determine the
pathway of photocatalytic reactions and it was determined with the help of UV-Visible/DRS
spectroscopy as well as XPS analysis. Finally, the as-synthesized heterostructures were used for
the photocatalytic degradation of Congo red dye. The priority order of heterostructures according
to photocatalytic activity is α-Fe2O3/ ZnO < α-Fe2O3 /ZnSe < α-Fe2O3 /ZnTe. α-Fe2O3/ZnTe
showed maximum degradation efficiency up to 97%. The higher photocatalytic degradation
efficiency was attributed to the synergistic effect and efficient charge carrier separation due to
formation of Type-II configuration.