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 I2 → I3 – 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 evolu...

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Veröffentlicht in:ACS applied materials & interfaces 2022-07, Vol.14 (26), p.29916-29933
Hauptverfasser: Andrade, Pedro H. M., Henry, Natacha, Volkringer, Christophe, Loiseau, Thierry, Vezin, Hervé, Hureau, Matthieu, Moissette, Alain
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Sprache:eng
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Zusammenfassung:Many works reported the encapsulation of iodine in metal–organic frameworks as well as the I2 → I3 – 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 I2 into I3 –. 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 (a = 20.7232 Å), higher crystallite size (0.18 ≤ Φ ≤ 3.33 μm), and smaller SSABET (818 m2·g–1) when compared to its parent UiO-66­(Zr)  a = 20.7696 Å, 100 ≤ Φ ≤ 250 nm, and SSABET = 1262 m2·g–1. 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–1, against 230 g·mol–1 for UiO-66­(Zr)] and the kinetic evolution of I2 into I3 – after 16 h of I2 filtration. Three iodine species were typically identified by Raman spectroscopy and chemometric analysis. These species are as follows: “free” I2 (206 cm–1), “perturbed” I2 (173 cm–1), and I3 – (115 and 141 cm–1). It was also verified, by FTIR spectroscopy, that the oxo and hydroxyl groups of the inorganic [M6O4(OH)4] (M = Zr, Hf) cluster were perturbed after the adsorption of I2 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 (Hf4+ or Zr4+), a mechanism was proposed for the conversion of I2 into I3 – in UiO-66based on an electron donor–acceptor complex between the aromatic ring of the BDC linker and the I2 molecule.
ISSN:1944-8244
1944-8252
DOI:10.1021/acsami.2c07288