Optical vibrations in sheet silicates

Published under licence by IOP Publishing Ltd
, , Citation E Loh 1973 J. Phys. C: Solid State Phys. 6 1091 DOI 10.1088/0022-3719/6/6/022

0022-3719/6/6/1091

Abstract

Raman scattering up to 1000 cm-1 Stokes shift, and infrared absorption spectra, from 10 cm-1 to 4000 cm-1, of several sheet silicates have been measured at room temperature. The samples are natural crystals of two muscovites, two phlogopites, two talcs, one margarite, one lepidolite, one chlorite and one biotite. The optical vibrational spectra of sheet silicates can be interpreted as molecular vibrations of: (1) the distorted octahedron MO6 with S6 symmetry below 210 cm-1, (2) an isosceles triangle O-H-O of C2 nu symmetry in sheet silicates containing octahedral Al3+ in the range 190 cm-1 to 270 cm-1, (3) a distorted tetrahedron SiO4 of C3 nu symmetry between 300 cm-1 and 1200 cm-1, (4) a combination band between the nu 3(a1) mode of SiO4 at 450 cm-1 with other bands at lower frequencies and (5) the stretching and librations of OH between 400 cm-1 and 3700 cm-1.

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