Analysis and information content of quadrupolar NMR in glasses: 25Mg NMR in vitreous MgSiO3 and CaMgSi2O6

Marcos de Oliveira Jr, Hugo Damasceno, Philip Salmon, Hellmut Eckert

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8 Citations (SciVal)

Abstract

The static wideline and high-resolution magic angle spinning (MAS) 25Mg NMR lineshapes measured for isotopically enriched enstatite and diopside glasses indicate a wide distribution of the electric-field gradient (EFG) components at the 25Mg position caused by disorder. The correct characterization of this distribution requires simulations with special attention paid to the experimental parameters. Here, both the static spectra obtained by wideband excitation and the MAS-NMR spectra obtained via rotor-synchronized Hahn spin echo acquisition were successfully simulated with the Czjzek distribution model, using one consistent set of parameters. Average nuclear electric quadrupole coupling constants near 8 MHz and a distribution width around 4 MHz were obtained for both materials, which suggests that earlier results on these glasses need to be re-examined. The results of this study outline a general strategy for characterizing the local environments of strongly coupled quadrupolar nuclei in amorphous and glassy materials. Despite the discrepancies between the interaction parameters extracted from our data and those published in earlier NMR work, the best fit to the data indicate an average isotropic chemical shift near 13 ppm (vs. aqueous MgCl2 solution) for both the enstatite and diopside glasses. Assuming the
applicability of the current database relating the 25Mg chemical shifts with coordination numbers in crystalline compounds, this value suggests that the Mg2+ ions are six-coordinated. This conclusion, however, is based on the
simplifying assumption that the 25Mg spectrum comprises a Czjzek distribution centered at a single isotropic chemical shift value and stands in contrast to the results of recent isotope-selective neutron diffraction studies
which give an average Mg-O coordination number of 4.4–4.5 for both glasses. However, reasonable fits to the MAS-NMR spectra can also be obtained when constraining the average isotropic chemical shift to 50 ppm, a
value typical of four-coordinated Mg. We conclude that multiple Mg sites with different coordination numbers may well be present and that, in the present glasses, 25Mg NMR at typically used spinning rates and magnetic
field strengths (20 kHz, 14.1 T) is not capable of resolving them due to excessive broadening by quadrupolar interactions.
Original languageEnglish
Article number100067
JournalJournal of Magnetic Resonance Open
Volume12-13
Early online date10 Aug 2022
DOIs
Publication statusPublished - 31 Dec 2022

Bibliographical note

Funding of this work by FAPESP, Project number 2013/07793–6, is most gratefully acknowledged. M.O.Jr. and H.E. acknowledge the National Council for Scientific and Technological Development (CNPq, grants n° 311069/2020–7 and 310870/2020–8, respectively). H.D. is grateful for personal fellowship support from CNPq and Nippon Electric Glass. P.S.S. received support from the University of Bath's International Funding Scheme. We thank Laurent Cormier (Paris) for providing the samples and Hesameddin Mohammadi and Rita Mendes da Silva (Bath) for access to their diffraction results prior to publication.

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