Aluminum-Porphyrin Metal-Organic Frameworks for Visible-Light Photocatalytic and Sonophotocatalytic Cr(VI) Reduction.

Abstract

In this study, four isostructural aluminum-based porphyrin metal-organic frameworks [Al-TCPP(M), M = H2 and Zn] with different morphologies and sizes were synthesized by the hydrothermal method. By adjusting the hydrothermal reaction time and the types of porphyrin ligands, Al-TCPP(M) MOFs exhibited diverse morphologies including tetragonal, rectangular, and carambola-like phase. In view of the introduction of porphyrin ligands and the strong coordination effect of Al-O units, Al-TCPP(M) MOFs exhibited good chemical stability, broad visible light harvesting capability, and fast photogenerated charge response. Four Al-TCPP(M) MOFs exhibited excellent photocatalytic activities for Cr(VI) in aqueous solution. Notably, the regulation to the nanoscale carambola-like morphology of Al-TCPP MOFs and metallization of the porphyrin ligand promoted the Cr(VI) photoreduction reaction where the catalytic activity of metallic carambola-like Al-TCPP increased 1.7 times compared to that of nonmetallic tetragonal MOFs. With the assistance of sonophotocatalysis, the Cr(VI) average reduction rates reached 0.658, 0.542, 0.785, and 0.629 mg·L-1·min-1 for Al-TCPP(H2)-24h, Al-TCPP(H2)-72h, Al-TCPP(Zn)-24h, and Al-TCPP(Zn)-72h, which are 1.2-1.4 times higher than that of photocatalysis. UV-vis absorption spectroscopy, electronic spin resonance, and fluorescence spectroscopy experiments demonstrated that the synergistic effect of photochemistry and sonochemistry promoted the transfer of photogenerated electrons from Al-TCPP(M) to Cr(VI), thus enhancing the catalytic activity. The combination of the sonophotocatalytic technology with aluminum-porphyrin MOFs may become an effective strategy to improve MOF-based photocatalytic systems.