TiO2 nanorods decorated Si nanowire hierarchical structures for UV light activated photocatalytic application.

Water remediation techniques like photolysis have recently piqued the interest of many researchers due to water contamination resulting from heavy industrialization and urbanization. In the current work, as-synthesized TiO2 nanorod decorated vertically aligned silicon nanowire (SiNW) leads to a hierarchical morphological structure formation. The photocatalytic nature of the fabricated SiNW/TiO2 nanoheterojunction is examined by the dye degradation of textile pollutants like methylene blue (MB), rhodamine B (RhB), and eosin B (EB). The catalytic dye degradation investigations revealed that 4 h hydrothermal synthesis of TiO2 on the surface of SiNW (ST4) exhibited excellent catalytic behaviour. In the presence of H2O2 and UV irradiation, the ST4 nanoheterostructure can degrade 98.89% of the model pollutant methylene blue (MB) in 15 min, demonstrating remarkable photocatalytic performance. The direct Z-scheme heterojunction exhibited by the SiNW/TiO2 structure facilitates a more efficient charge transfer mechanism with higher reducing and oxidizing ability leading to enhanced photocatalytic behaviour. The degradation pathway examined by LC-MS studies demonstrated the complete breakdown of the organic MB dye molecules ultimately mineralizing into CO2, H2O, and other inorganic substances. The photocatalyst ST4 exhibited excellent reusability and stability after multiple cycles of dye degradation enabling its use in practical water purification purposes.

Band edge tuned ZnxCd1-xS solid solution nanopowders for efficient solar photocatalysis.

This work highlights the synthesis of zinc blende ZnxCd1-xS ternary solid solutions with a tunable bandgap. Composition dependent band gaps are realized due to the effective band edge tuning of the solid solutions which in turn show decent photocatalytic behaviour. The bandgap of ZnxCd1-xS increases as Zn composition increases. It is interesting to note that the highest catalytic activity is observed for Zn0.8Cd0.2S (Eg = 2.83 eV) in the visible spectra due to the presence of defect states in the bandgap around 2.35 eV which has been explicated according to the results of photoluminescence spectra. Density of states (DOS) analysis provides further theoretical insight into the more negative conduction band edge for x = 0.8 than other samples. It also determines generation of intermediate states due to sulfur vacancy which is responsible for more electron-hole generation and the highest rate of Methyl Orange (MO) degradation under natural sunlight irradiation.