Double shelled titanium dioxide@mesoporous organosilica nanotube as an amphiphilic photoactive nanoreactor for efficient photocatalytic oxidation of styrene.

In this work, we have proposed a strategy to fabricate double-shell nanotubes as amphiphilic photoactive nanoreactors (HTTBPC) through the ordered hybridization of mesoporous organosilicon (PMO) and titanium dioxide (TiO) nanotubes. Unlike the previous rough composite, the heterogeneous structure established between cobalt-porphyrin functionalized PMO and conventional TiO has a staggered matching band gap, which makes it have excellent light harvesting and high carrier separation ability. This is still unexplored. Interestingly, the prepared photocatalysts exhibited superior activity (99%) and benzaldehyde selectivity (94%) in the oxidation of styrene in water at room temperature, which was 3.8 and 2.8 times higher than that of TiO nanotubes and PMO functionalized with cobalt porphyrin, respectively. It was demonstrated that the strong interaction between cobalt porphyrin PMO and TiO improved the separation of photogenerated carriers and the amphiphilic properties of mesoporous organosilica boosted the adsorption of substrate molecules in water, contributing to the significantly enhanced photocatalytic activity. This work provides a design of high-performance photocatalysts for alkene oxidation under green conditions.