Abstract
We report the synthesis of uniform 2.5 ± 0.4 nm diameter Ce(iii) carbonate clusters deposited on the surface of TiO(2) nanoparticles and characterize them using HAADF-STEM and EELS, as well as UV-Vis and FTIR spectroscopies. This material is a highly proficient catalytic antioxidant for the degradation of photocatalytically generated reactive oxygen species (ROS). We observed an unusual U-shaped pH-dependence in its photoprotection catalytic activity, with an optimum function in the near-neutral pH range of 7.7 ± 0.7. This sharp pH dependence is not observed in previously reported bulk Ce(iii) carbonate materials, and it is also not a consequence of Ce(iii) carbonate cluster decomposition. However, it is consistent with a tandem reaction sequence consisting of a biomimetic superoxide dismutase and catalase function, which is dependent on a balance of protons and hydroxide anions for function. Our dissolution-deposition approach for synthesizing nanoscale Ce(iii) carbonate clusters on TiO(2) should be generalizable to other carbonates and metal-oxide supports.