High-Pressure Phase Transition, Pore Collapse, and Amorphization in the Siliceous 1D Zeolite, TON

Year: 2017

Authors: Thibaud JM., Rouquette J., Hermet P., Dziubek K., Gorelli FA., Santoro M., Garbarino G., Alabarse FG., Cambon O., Di Renzo F., van der Lee A., Haines J.

Autors Affiliation: Univ Montpellier, CNRS, ICGM, ENSCM, Montpellier, France; European Lab Non Linear Spect LENS, I-50019 Sesto Fiorentino, Italy; Adam Mickiewicz Univ, Fac Chem, Umultowska 89b, PL-61614 Poznan, Poland; CNR, INO, I-50019 Sesto Fiorentino, Italy; ESRF, 71 Ave Martyrs, F-38000 Grenoble, France; Synchrotron Soleil, St Aubin BP48, F-91192 Gif Sur Yvette, France; Univ Montpellier, CNRS, IEM, Montpellier, France.

Abstract: The siliceous zeolite TON with a 1-D pore system was studied at high pressure by X-ray diffraction, infrared spectroscopy, and DFT calculations. The behavior of this material was investigated using nonpenetrating pressure transmitting media. Under these conditions, a phase transition from the Cmc2(1) to a Pbn2(1) structure occurs at close to 0.6 GPa with doubling of the primitive unit cell based on Rietveld refinements. The pores begin to collapse with a strong increase in their ellipticity. Upon decreasing the pressure below this value the initial structure was not recovered. DFT calculations indicate that the initial empty pore Cmc2(1) phase is dynamically unstable. Irreversible, progressive pressure-induced amorphization occurs upon further increases in pressure up to 21 GPa. These changes are confirmed in the mid-and far-infrared spectra by peak splitting at the Cmc2(1) to Pbn2(1) phase transition and strong peak broadening at high pressure due to amorphization.

Journal/Review: JOURNAL OF PHYSICAL CHEMISTRY C

Volume: 121 (8)      Pages from: 4283  to: 4292

More Information: We are grateful for the support from PICS bilateral project CNR/CNRS (Italy/France), 2014-2016: Multifunctional zeolite/polymer nanocomposites. We acknowledge funding from the Agence Nationale de la Recherche program Investissements dŽavenir in the framework of the contract ANR-10-LABX-05-01 (LabEx CheMlSyst). We also thank the Deep Carbon Observatory (DCO) initiative under the project Physics and Chemistry of Carbon at Extreme Conditions and the Ente Cassa di Risparmio di Firenze under the project Firenze Hydrolab 2. K.D. acknowledges the Polish Ministry of Science and Higher Education.
KeyWords: POWDER DIFFRACTION; FLEXIBILITY; TEMPERATURE; FRAMEWORK; INSERTION; BEHAVIOR; CRYSTAL
DOI: 10.1021/acs.jpcc.6b11594

Citations: 21
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