Iodine Uptake by Zr-/Hf-Based UiO-66 Materials: The Influence of Metal Substitution on Iodine Evolution.

Many works reported the encapsulation of iodine in metal-organic frameworks as well as the I → I chemical conversion. This transformation has been examined by adsorbing gaseous iodine on a series of UiO-66 materials and the different Hf/Zr metal ratios (0-100% Hf) were evaluated during the evolution of I into I. The influence of the hafnium content on the UiO-66 structure was highlighted by PXRD, SEM images, and gas sorption tests. The UiO-66(Hf) presented smaller lattice parameter ( = 20.7232 Å), higher crystallite size (0.18 ≤ Φ ≤ 3.33 μm), and smaller SSA (818 m·g) when compared to its parent UiO-66(Zr) ─ = 20.7696 Å, 100 ≤ Φ ≤ 250 nm, and SSA = 1262 m·g. The effect of replacing Zr atoms by Hf in the physical properties of the UiO-66 was deeply evaluated by a spectroscopic study using UV-vis, FTIR, and Raman characterizations. In this case, the Hf presence reduced the band gap of the UiO-66, from 4.07 eV in UiO-66(Zr) to 3.98 eV in UiO-66(Hf). Furthermore, the UiO-66(Hf) showed a blue shift for several FTIR and Raman bands, indicating a stiffening on the implied interatomic bonds when comparing to UiO-66(Zr) spectra. Hafnium was found to clearly favor the capture of iodine [285 g·mol, against 230 g·mol for UiO-66(Zr)] and the kinetic evolution of I into I after 16 h of I filtration. Three iodine species were typically identified by Raman spectroscopy and chemometric analysis. These species are as follows: "free" I (206 cm), "perturbed" I (173 cm), and I (115 and 141 cm). It was also verified, by FTIR spectroscopy, that the oxo and hydroxyl groups of the inorganic [MO(OH)] (M = Zr, Hf) cluster were perturbed after the adsorption of I into UiO-66(Hf), which was ascribed to the higher acid character of Hf. Finally, with that in mind and considering that the EPR results discard the possibility of a redox phenomenon involving the tetravalent cations (Hf or Zr), a mechanism was proposed for the conversion of I into I in UiO-66─based on an electron donor-acceptor complex between the aromatic ring of the BDC linker and the I molecule.