Design and performance of a novel direct Z-scheme NiGa2O4/CeO2 nanocomposite with enhanced sonocatalytic activity

A novel direct Z-scheme NiGa 2 O 4 /CeO 2 nanocomposite was designed and prepared via simple sol-hydrothermal and calcination methods, and its sonocatalytic activity was tested by studying the degradation of a model antimicrobial agent, malachite green (MG), under ultrasonic irradiation. Near complete (96.2%) degradation of MG (at 10 mg/L) could be achieved by the NiGa 2 O 4 /CeO 2 nanocomposite (at 1.0 g/L) after ultrasonic irradiation (40 kHz, 300 W) for 60 min at 25 °C. Under the same conditions, only 51.2 and 72.0% of the MG degraded in the presence of NiGa 2 O 4 and CeO 2 (at 1.0 g/L), respectively. These results demonstrate that the direct Z-scheme NiGa 2 O 4 /CeO 2 nanocomposite has excellent sonocatalytic activity, which is attributed to the matching band-gaps between NiGa 2 O 4 and CeO 2 . The sonocatalytic activity of NiGa 2 O 4 /CeO 2 nanocomposite decreased by 17% after four cycles of reuse, which is indicative of relatively good reusability. Scavenging experiments revealed that sonocatalytic degradation of MG results from the combined action of hydroxyl radicals ( OH) and holes (h + ), with the latter having a greater contribution. The pathways and mechanism of MG degradation were proposed based on the degradation intermediates detected. The results demonstrate that the prepared direct Z-scheme NiGa 2 O 4 /CeO 2 nanocomposite worked as designed and exhibited high and stable sonocatalytic activity during MG degradation, and could thus serve as a promising candidate in sonocatalytic treatment of other organic pollutants in wastewaters. The findings also provide new insights on the mechanism of sonocatalytic degradation and the design of efficient Z-scheme sonocatalysts.