New insights into the mechanism of coupled photocatalysis and Fenton-based processes using Fe surface-modified TiO2 nanotube layers: The case study of caffeine degradation

TiO2 nanotube (TNT) layers are prepared via electrochemical anodization of Ti foil in ethylene glycol-based electrolyte containing fluoride ions. Using spin-coating of Fe(III) precursor solutions of different concentra-tions (10 mu M to 10 mM), iron surface-modified TNT (Fe-TNT) layers are formed after annealing at 450 degrees C for 2 h in air. The Fe-TNT layers are comprehensively characterized by XRD, SEM, DRS and XPS. To identify and assess the contribution of photocatalysis and Fenton-based processes that are simultaneously triggered by Fe-TNT layers, degradation of caffeine is investigated in the dark and under UVA with and without the presence of 500 mu M H2O2. It has been found that in the presence of H2O2 under UVA, 100 mu M Fe-TNT can degrade 67 % of caffeine after 3 h, of which 4 % is from photolysis, 23.5 % from photocatalysis and 39.5 % from Fenton-based processes. It is important to note that Fenton-based reactions are due to the iron leaching, while the main reactive oxygen species are identified as hydroxyl radicals. In addition, the main degradation by-products are identified by LC-MS and IC-MS techniques, thus leading to the proposal of different degradation pathways of caffeine. To sum up, the research's findings provide novel insights into the concept of photochemical versatility, which is only obliquely explored in the corpus of previous research.

Automated summary

TiO2 nanotube (TNT) layers were prepared using electrochemical anodization, and Fe-TNT layers were formed by spin-coating Fe(III) precursor solutions and annealing. The contribution of photocatalysis and Fenton-based processes in the degradation of caffeine was investigated. 67% of caffeine degradation was achieved by 100 mu M Fe-TNT under UVA with the presence of H2O2, with 4% from photolysis, 23.5% from photocatalysis, and 39.5% from Fenton-based processes.