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Creating a specific shape with hierarchically porous structure of metal-organic frameworks represents an effective strategy to enhance the adsorption and photocatalytic performance yet remains rather challenging. Herein, we present a facile linker competitive coordination induced interface assembly strategy to synthesize a series of star-concave metal-organic frameworks (MOFs) (Fe-MIL-101) with rich hierarchical pores. This strategy of star-concave Fe-MIL-101 depends on the electronegativity difference of the two linkers to produce an in-situ oriented growth with controllable kinetics nucleation and structural evolution. As a result, the optimized star-concave Fe-MIL-101-2 with multiple physical-chemical effects endows enhanced visible-light trapping, preferred charge separation, and optimized the local electronic structure. In comparison with the slightly concave Fe-MIL-101 and solid octahedron Fe-MIL-101-NH2, the star-concave Fe-MIL-101-2 displays a clear superiority in the adsorption-photoreduction of Cr(VI) under visible-light irradiation. Furthermore, the X-ray absorption fine structure spectroscopy, finite element method, and density functional theory calculations are performed to reveal the local electronic structure of star-concave Fe-MIL-101-2, understanding the mechanisms behind the boosting synergistic adsorption-photoreduction of Cr(VI) removal performance. This work provides a new perspective for the rational construction of MOFs-based photocatalysts with high activity for Cr(VI) removal through shape engineering.

This is an open access article under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0, https://creativecommons.org/licenses/by/4.0/).
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