Abstract
A photocatalyst TiO2/Ti-BPDC-Pt is developed with a self-grown TiO2/Ti-metal–organic framework (MOF) heterojunction, i.e., TiO2/Ti-BPDC, and selectively anchored high-density Pt single-atomic cocatalysts on Ti-BPDC for photocatalytic hydrogen evolution. This intimate heterojunction, growing from the surface pyrolytic reconstruction of Ti-BPDC, works in a direct Z-scheme, efficiently separating electrons and holes. Pt is selectively anchored on Ti-BPDC by ligands and is found in the form of single atoms with loading up to 1.8 wt %. The selective location of Pt is the electron-enriched domain of the heterojunction, which further enhances the utilization of the separated electrons. This tailored TiO2/Ti-BPDC-Pt shows a significantly enhanced activity of 12.4 mmol g−1 h−1 compared to other TiO2- or MOF-based catalysts. The structure-activity relationship further proves the balance of two simultaneously exposed domains of heterojunctions is critical to fulfilling this kind of catalyst.
