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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

The Structure of Borophosphosilicate Pure Network Former Glasses Studied by Multinuclear NMR Spectroscopy

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Author(s):
Uesbeck, Tobias ; Eckert, Hellmut
Total Authors: 2
Document type: Journal article
Source: Journal of Physical Chemistry C; v. 121, n. 3, p. 1838-1850, JAN 26 2017.
Web of Science Citations: 5
Abstract

New mixed network glasses along the composition line xB(2)O(3)-(30 - x)P2O5-70SiO(2) have been prepared and characterized in terms of their chemical composition, viscosity, and characteristic temperatures. The physical properties have been correlated with structural information, obtained from Raman spectroscopy and advanced B-11, Si-29, and P-31 single and double resonance solid state NMR studies. Both the macroscopic and structural properties show nonlinear changes as a function of composition, with maximal values of the viscometric glass transition temperature near 12-13 mol % B2O3. The structure of phosphorus-rich glasses is dominated by tetrahedral B(4) units linked to three to four phosphorus species and multiple phosphorus environments, including P-(3) (branching phosphate) groups linked to silicon, and P-(4) units forming B-O-P linkages as in boron phosphate, BPO4 (superscripts denote the number of bridging oxygen species). In the boron-rich region, the phosphorus species are exclusively present as P-(4) groups and the boron atoms present in excess of a B/P ratio of unity are present in the form of three-coordinated B-(3) units forming both B-O-B and B-O-Si linkages. While these results document a strong mutual affinity of the boron oxide and phosphorus oxide components, the species concentrations and numbers of B-O-P linkages fall consistently below those numbers expected from a clustering scenario maximizing the number of such connectivities, indicating the absence of macroscopic phase separation. Important differences relative to the previously studied system xAl(2)O(3)-(30 - x)P2O5-70SiO(2) are discussed. (AU)

FAPESP's process: 13/07793-6 - CEPIV - Center for Teaching, Research and Innovation in Glass
Grantee:Edgar Dutra Zanotto
Support Opportunities: Research Grants - Research, Innovation and Dissemination Centers - RIDC