Structural evolution of high zirconia aluminosilicate glasses

M. Ficheux (1, 2) , E. Burov (1) , G. Aquilanti (3) , N. Trcera (4) , V. Montouillout (5) , L. Cormier (2)

1 SVI - Surface du Verre et Interfaces
2 IMPMC_PALM - Propriétés des amorphes, liquides et minéraux [IMPMC]
3 ESRF - European Synchrotron Radiation Facility
4 SSOLEIL - Synchrotron SOLEIL
5 CEMHTI - Conditions Extrêmes et Matériaux : Haute Température et Irradiation

We report a detailed structural investigation of Ca-Na aluminosilicate glasses containing 0-20 wt% ZrO2 using X-ray absorption spectroscopy, Raman spectroscopy and 27 Al and 29 Si NMR. The X-ray absorption spectroscopy data reveal that Zr is predominantly present in ZrO6 octahedra but a significant Zr coordination change occurs with increasing ZrO2 content. Though Al and Zr are competing to be surrounded by charge balancing cations, 27 Al NMR data do not show the presence of high-coordinated Al species; thus charge-balancing cations are preferentially localized close to AlO4 tetrahedra rather than Zr polyhedra, explaining the increase in Zr coordination number that ultimately leads to limit Zr solubility in glasses. Raman and 29 Si NMR data indicates that Zr atoms are linked to the silicate network with a trend for higher degree of network connectivity at high zirconia content. Change in network connectivity and in Zr environment provide insights to understand chemical durability or crystallization in glasses.

Domaines: Matière Condensée [cond-mat]; Matériaux

M. Ficheux, E. Burov, G. Aquilanti, N. Trcera, V. Montouillout, et al.. Structural evolution of high zirconia aluminosilicate glasses. Journal of Non-Crystalline Solids, 2020, 539, pp.120050. ⟨10.1016/j.jnoncrysol.2020.120050⟩. ⟨hal-02873725⟩