Synthesis of Pore-Wall-Modified Stable COF/TiO2 Heterostructures via Site-Specific Nucleation for an Enhanced Photoreduction of Carbon Dioxide

Constructing stable heterostructures with appropriate active site architectures in covalent organic frameworks (COFs) can improve the active site accessibility and facilitate charge transfer, thereby increasing the catalytic efficiency. Herein, a pore-wall modification strategy is proposed to achieve regularly arranged TiO2 nanodots (approximate to 1.82 nm) in the pores of COFs via site-specific nucleation. The site-specific nucleation strategy stabilizes the TiO2 nanodots as well as enables the controlled growth of TiO2 throughout the COFs' matrix. In a typical process, the pore wall is modified and site-specific nucleation is induced between the metal precursors and the organic walls of the COFs through a careful ligand selection, and the strongly bonded metal precursors drive the confined growth of ultrasmall TiO2 nanodots during the subsequent hydrolysis. This will result in remarkably improved surface reactions, owing to the superior catalytic activity of TiO2 nanodots functionalized to COFs through strong N-Ti-O bonds. Furthermore, density functional theory studies reveal that pore-wall modification is beneficial for inducing strong interactions between the COF and TiO2 and results in a large energy transfer via the N-Ti-O bonds. This work highlights the feasibility of developing stable COF and metal oxide based heterostructures via organic wall modifications to produce carbon fuels by artificial photosynthesis.

Automated summary

Constructing stable heterostructures with regularly arranged TiO2 nanodots in covalent organic frameworks (COFs) via pore-wall modification strategy improves active site accessibility and catalytic efficiency. Density functional theory studies reveal that pore-wall modification induces strong interactions between COF and TiO2, resulting in large energy transfer via N-Ti-O bonds. This work demonstrates the feasibility of developing stable COF and metal oxide heterostructures for artificial photosynthesis.