Magnetic FeO-encapsulated VAN@MIL-101(Fe) with mixed-valence sites and mesoporous structures as efficient bifunctional water splitting photocatalysts.

Fe3O4/VAN@MIL-101(Fe) with both mesoporous and mixed-valence Fe3+/Fe2+ structures was controllably synthesized in the synthesis of MIL-101(Fe), and it was used as a bifunctional photocatalyst in both oxygen evolution reactions (OERs) and hydrogen evolution reactions (HERs) of photocatalytic water splitting. By the reduction of auxiliary ligand vanillin (VAN) and the introduction of Fe3O4, the mixed-valence Fe3+/Fe2+ structure in Fe3O4/VAN@MIL-101(Fe) was obtained, which improves the band gap of the Fe3+ reactive active center and increases the separation efficiency of photogenerated carriers. Owing to the partial difference in the structure between VAN and ligand terephthalic acid (H2BDC), hierarchical porous and vacant structures were effectively improved in Fe3O4/VAN@MIL-101(Fe), which can induce more active sites to adsorb more water molecules and shorten the electron-hole migration distance to improve the transfer efficiency of photogenerated carriers. Therefore, Fe3O4/VAN@MIL-101(Fe) presents excellent photocatalytic activities for improving the O2 and H2 production rate up to 360 000 μmol g-1 h-1 and 584 μmol g-1 h-1, respectively. Meanwhile, Fe3O4/VAN@MIL-101(Fe) maintains the excellent catalytic activity in OERs and HERs after recycling for 5 times. Moreover, the introduction of magnetic Fe3O4 nanoplates into Fe3O4/VAN@MIL-101(Fe) can make it easily recyclable by magnetic separation, which can maximize its performance.