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Influence of Strontium Oxide on Structural Transformations in Diopside-Based Glass-Ceramics Assessed by Diverse Structural Tools

Title data

Reddy, Allu Amarnath ; Tulyaganov, Dilshat U. ; Mather, Glenn C. ; Rodriguez-López, Sonia ; Das, Subrata ; Pascual, María J. ; Muñoz, Francisco ; Siegel, Renée ; Senker, Jürgen ; Ferreira, José M. F.:
Influence of Strontium Oxide on Structural Transformations in Diopside-Based Glass-Ceramics Assessed by Diverse Structural Tools.
In: The Journal of Physical Chemistry C. Vol. 119 (May 2015) Issue 21 . - pp. 11482-11492.
ISSN 1932-7455
DOI: https://doi.org/10.1021/acs.jpcc.5b02475

Abstract in another language

A full understanding of the structural glass variations and of the nucleation and growth of crystalline phases in glass-ceramics (GCs) induced by compositional changes is highly relevant for applications such as sealants for solid oxide fuel cells, bio- and dental materials, and photonics. Systematic substitution of Ca with Sr in diopside (Di-CaMgSi2O6) has a significant impact on the crystalline-phase assemblage after heat treating at 850 degrees C for 500 h. A high percentage of Di crystallized from Sr-free glass; however, with increasing Sr content the tendency toward crystallization decreased, and Sr-akermanite (Sr-Ak) was preferentially crystallized. In this study, the structural transformations in the Di-based-GC system upon the substitution of calcium with strontium have been examined by X-ray powder diffraction (XRD), Si-29 and Al-27 magic angle spinning (MAS)-nuclear magnetic resonance (NMR), and Raman spectroscopies. XRD Rietveld refinement results indicate that up to a maximum of similar to 25 at. % of Sr occupies the Ca site of the Di structure. Al-27 MAS NMR spectra reveal that most of the Al exists in amorphous glassy phase after crystallization. Measured mean quadrupolar coupling constant values augment with increasing Sr content, indicating an increase in order in the glassy phase, which is manifested by a strong preference of Mg2+ for nonbridging oxygens (NBO), resulting in the formation MgO4 tetrahedra. At higher Sr substitution levels (>50%), the decrease in Mg2+ coordination from six to four is evident from the decrease in average Mg-O bond lengths and the systematic variation in intensity of characteristic Mg-O Raman vibrational bands.

Further data

Item Type: Article in a journal
Refereed: Yes
Institutions of the University: Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Chair Anorganic Chemistry III > Chair Anorganic Chemistry III - Univ.-Prof. Dr. Jürgen Senker
Faculties
Faculties > Faculty of Biology, Chemistry and Earth Sciences
Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry
Faculties > Faculty of Biology, Chemistry and Earth Sciences > Department of Chemistry > Chair Anorganic Chemistry III
Result of work at the UBT: No
DDC Subjects: 500 Science > 540 Chemistry
Date Deposited: 26 Jul 2016 12:58
Last Modified: 12 Jun 2019 05:56
URI: https://eref.uni-bayreuth.de/id/eprint/33646