New assignments of Raman spectra of tetrahedra and the effects of electronegativity. II. Silicate glasses

Our density functional theory calculations (by GAUSSIAN) on the Si4O104− moiety and Na4Si4O10 molecule reproduce the experimental Raman frequencies and relative intensities for the three A1 modes in the experimental Raman spectra of Na2Si2O5 and BaSi2O5 crystals and glasses. Taking the center of mas...

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Main Authors: G. Michael Bancroft, Philip A. W. Dean, Grant S. Henderson, H. Wayne Nesbitt
Format: Article
Language:English
Published: AIP Publishing LLC 2023-12-01
Series:AIP Advances
Online Access:http://dx.doi.org/10.1063/5.0173021
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author G. Michael Bancroft
Philip A. W. Dean
Grant S. Henderson
H. Wayne Nesbitt
author_facet G. Michael Bancroft
Philip A. W. Dean
Grant S. Henderson
H. Wayne Nesbitt
author_sort G. Michael Bancroft
collection DOAJ
description Our density functional theory calculations (by GAUSSIAN) on the Si4O104− moiety and Na4Si4O10 molecule reproduce the experimental Raman frequencies and relative intensities for the three A1 modes in the experimental Raman spectra of Na2Si2O5 and BaSi2O5 crystals and glasses. Taking the center of mass into consideration, accompanied by visualization using GaussView, these calculations provide a firm assignment of these three peaks: the 1060 cm−1 peak to the Si-NBO stretch (NBO = Si–O or Si–O–Na), the ∼600 cm−1 peak to the Si-BO stretch (BO = Si–O–Si), and the ∼500 cm−1 peak to the Si-BO-Si bend. Our GAUSSIAN calculations on modified “non-equilibrium” SiO44− tetrahedra, constrained to have the same Si–O bond lengths and O–Si–O bond angles as in the Si4O104− moiety, confirm the above-mentioned assignment and show reasonable agreement with the experimental Raman frequencies and relative intensities. We then examine the regular trends in the Si-NBO and Si-BO stretch frequencies for all Qn (n = 0–4) species in silicate glasses and crystals. The large systematic change in the differences between these frequencies (Δ1) is explained by electronic changes within the SiO4 tetrahedron. For example, the larger Δ1 for the Q3 tetrahedra than the Q2 tetrahedra is due to the changes in Si, BO, and NBO electron densities on the tetrahedral Si and O atoms, as measured by Si 2p and O 1s x-ray photoelectron spectra. This trend strongly suggests that the Si-BO stretch frequency for the Q4 species in v-SiO2 should be ∼500 cm−1, close to the A1 breathing mode frequency of 495 cm−1 for four membered rings previously assigned.
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spelling doaj.art-790bd40c431e4fd68c8ac123794c68c92024-01-03T19:51:07ZengAIP Publishing LLCAIP Advances2158-32262023-12-011312125216125216-1210.1063/5.0173021New assignments of Raman spectra of tetrahedra and the effects of electronegativity. II. Silicate glassesG. Michael Bancroft0Philip A. W. Dean1Grant S. Henderson2H. Wayne Nesbitt3Department of Chemistry, University of Western Ontario, London, Ontario N6A 5B7, CanadaDepartment of Chemistry, University of Western Ontario, London, Ontario N6A 5B7, CanadaDepartment of Earth Sciences, University of Toronto, Toronto, Ontario M5S 3B1, CanadaDepartment of Earth Sciences, University of Western Ontario, London, Ontario N6A 5B7, CanadaOur density functional theory calculations (by GAUSSIAN) on the Si4O104− moiety and Na4Si4O10 molecule reproduce the experimental Raman frequencies and relative intensities for the three A1 modes in the experimental Raman spectra of Na2Si2O5 and BaSi2O5 crystals and glasses. Taking the center of mass into consideration, accompanied by visualization using GaussView, these calculations provide a firm assignment of these three peaks: the 1060 cm−1 peak to the Si-NBO stretch (NBO = Si–O or Si–O–Na), the ∼600 cm−1 peak to the Si-BO stretch (BO = Si–O–Si), and the ∼500 cm−1 peak to the Si-BO-Si bend. Our GAUSSIAN calculations on modified “non-equilibrium” SiO44− tetrahedra, constrained to have the same Si–O bond lengths and O–Si–O bond angles as in the Si4O104− moiety, confirm the above-mentioned assignment and show reasonable agreement with the experimental Raman frequencies and relative intensities. We then examine the regular trends in the Si-NBO and Si-BO stretch frequencies for all Qn (n = 0–4) species in silicate glasses and crystals. The large systematic change in the differences between these frequencies (Δ1) is explained by electronic changes within the SiO4 tetrahedron. For example, the larger Δ1 for the Q3 tetrahedra than the Q2 tetrahedra is due to the changes in Si, BO, and NBO electron densities on the tetrahedral Si and O atoms, as measured by Si 2p and O 1s x-ray photoelectron spectra. This trend strongly suggests that the Si-BO stretch frequency for the Q4 species in v-SiO2 should be ∼500 cm−1, close to the A1 breathing mode frequency of 495 cm−1 for four membered rings previously assigned.http://dx.doi.org/10.1063/5.0173021
spellingShingle G. Michael Bancroft
Philip A. W. Dean
Grant S. Henderson
H. Wayne Nesbitt
New assignments of Raman spectra of tetrahedra and the effects of electronegativity. II. Silicate glasses
AIP Advances
title New assignments of Raman spectra of tetrahedra and the effects of electronegativity. II. Silicate glasses
title_full New assignments of Raman spectra of tetrahedra and the effects of electronegativity. II. Silicate glasses
title_fullStr New assignments of Raman spectra of tetrahedra and the effects of electronegativity. II. Silicate glasses
title_full_unstemmed New assignments of Raman spectra of tetrahedra and the effects of electronegativity. II. Silicate glasses
title_short New assignments of Raman spectra of tetrahedra and the effects of electronegativity. II. Silicate glasses
title_sort new assignments of raman spectra of tetrahedra and the effects of electronegativity ii silicate glasses
url http://dx.doi.org/10.1063/5.0173021
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