Construction of novel phosphonate-based MOF/P–TiO2 heterojunction photocatalysts: enhanced photocatalytic performance and mechanistic insight

Abstract

Development of highly efficient photocatalysts for photocatalysis research has been a hot research area in recent years. Herein, the phosphate-based metal organic framework (MOF)/P–TiO₂ hybrid composites (MOF_x/P–TiO₂) were first synthesized using the phosphonate-based MOF [Cd(H₂L)]_n (H₄L = 2,5-dimethylbenzene-1,4-diylbis(methylene)diphosphonic acid) and phosphated mesoporous TiO₂ beads (P–TiO₂) using a versatile step-by-step self-assembly strategy for environmental remediation. The results showed that the Cd-MOF loading content in the MOF_x/P–TiO₂ has an important influence on the degradation of pollutants, and the hybrid materials could significantly enhance the photocatalytic activity for the photo-oxidative degradation of RhB (97.6% in 25 min over MOF_1.5/P–TiO₂) and the reduction of Cr(VI) (96.1% in 60 min over MOF_0.5/P–TiO₂) in comparison with the single-component Cd-MOF or P–TiO₂. The enhancement of the photocatalytic activity of MOF_x/P–TiO₂ could be mainly attributed to: (i) the strong light absorption capacity, and (ii) the effective photogenerated charge separation and transfer through the coupled heterojunction interfaces of P–TiO₂ and Cd-MOF. Furthermore, the results verified that the matched band structure of P–TiO₂ and Cd-MOF could induce a superfast Z-scheme interfacial charge transfer path. Therefore, a reasonable Z-scheme charge transfer mechanism was proposed based on the active species trapping experiments and the results of electron spin resonance (ESR). More importantly, MOF_0.5/P–TiO₂ and MOF_1.0/P–TiO₂ possess a good stability and reusability after recycling five times owing to the high chemical stability of the Cd-MOF, P–TiO₂ and heterojunctions. The present work provides a promising approach to construct direct Z-scheme porous heterojunctions for elimination of environmental pollutants.