<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>10(69)</volume><submitter>Khanna A</submitter><pubmed_abstract>The short-range structure of 20BaO-80TeO&lt;sub>2&lt;/sub> glass was studied &lt;i>in situ&lt;/i> by high pressure neutron diffraction and high pressure Raman spectroscopy. Neutron diffraction measurements were performed at the PEARL instrument of the ISIS spallation neutron source up to a maximum pressure of 9.0 ± 0.5 GPa. The diffraction data was analysed &lt;i>via&lt;/i> reverse Monte Carlo simulations and the changes in the glass short-range structural properties, Ba-O, Te-O and O-O bond lengths and speciation were studied as a function of pressure. Te-O co-ordination increases from 3.51 ± 0.05 to 3.73 ± 0.05, Ba-O coordination from 6.24 ± 0.19 to 6.99 ± 0.34 and O-O coordination from 6.00 ± 0.05 to 6.69 ± 0.06 with an increase in pressure from ambient to 9.0 GPa. &lt;i>In situ&lt;/i> high pressure Raman studies found that the ratio of intensities of the two bands at 668 cm&lt;sup>-1&lt;/sup> and 724 cm&lt;sup>-1&lt;/sup> increases from 0.99 to 1.18 on applying pressure up to 19.28 ± 0.01 GPa, and that these changes are due to the conversion of TeO&lt;sub>3&lt;/sub> into TeO&lt;sub>4&lt;/sub> structural units in the tellurite network. It is found that pressure causes densification of the tellurite network by the enhancement of co-ordination of cations, and an increase in distribution of Te-O and Ba-O bond lengths. The original glass structure is restored upon the release of pressure.</pubmed_abstract><journal>RSC advances</journal><pagination>42502-42511</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9057973</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>&lt;i>In situ&lt;/i> high pressure neutron diffraction and Raman spectroscopy of 20BaO-80TeO&lt;sub>2&lt;/sub> glass.</pubmed_title><pmcid>PMC9057973</pmcid><pubmed_authors>Bull CL</pubmed_authors><pubmed_authors>Hirdesh</pubmed_authors><pubmed_authors>Khanna A</pubmed_authors><pubmed_authors>Funnell NP</pubmed_authors><pubmed_authors>Tyagi S</pubmed_authors><pubmed_authors>Kaur A</pubmed_authors></additional><is_claimable>false</is_claimable><name>&lt;i>In situ&lt;/i> high pressure neutron diffraction and Raman spectroscopy of 20BaO-80TeO&lt;sub>2&lt;/sub> glass.</name><description>The short-range structure of 20BaO-80TeO&lt;sub>2&lt;/sub> glass was studied &lt;i>in situ&lt;/i> by high pressure neutron diffraction and high pressure Raman spectroscopy. Neutron diffraction measurements were performed at the PEARL instrument of the ISIS spallation neutron source up to a maximum pressure of 9.0 ± 0.5 GPa. The diffraction data was analysed &lt;i>via&lt;/i> reverse Monte Carlo simulations and the changes in the glass short-range structural properties, Ba-O, Te-O and O-O bond lengths and speciation were studied as a function of pressure. Te-O co-ordination increases from 3.51 ± 0.05 to 3.73 ± 0.05, Ba-O coordination from 6.24 ± 0.19 to 6.99 ± 0.34 and O-O coordination from 6.00 ± 0.05 to 6.69 ± 0.06 with an increase in pressure from ambient to 9.0 GPa. &lt;i>In situ&lt;/i> high pressure Raman studies found that the ratio of intensities of the two bands at 668 cm&lt;sup>-1&lt;/sup> and 724 cm&lt;sup>-1&lt;/sup> increases from 0.99 to 1.18 on applying pressure up to 19.28 ± 0.01 GPa, and that these changes are due to the conversion of TeO&lt;sub>3&lt;/sub> into TeO&lt;sub>4&lt;/sub> structural units in the tellurite network. It is found that pressure causes densification of the tellurite network by the enhancement of co-ordination of cations, and an increase in distribution of Te-O and Ba-O bond lengths. The original glass structure is restored upon the release of pressure.</description><dates><release>2020-01-01T00:00:00Z</release><publication>2020 Nov</publication><modification>2025-04-04T14:49:29.913Z</modification><creation>2025-04-04T14:49:29.913Z</creation></dates><accession>S-EPMC9057973</accession><cross_references><pubmed>35516775</pubmed><doi>10.1039/d0ra07867k</doi></cross_references></HashMap>