Charge-transfer in Ferromagnesian Silicates: The Polarized Electronic Spectra of Trioctahedral Micas

D. W. Robbins and R. G. J. Strens
Turner Bros. Asbestos Ltd., P.O. Box 40, Rochdale, Lancashire
School of Physics, The University, Newcastle upon Tyne NE1 7RU

Summary: Polarized spectra (2000 to 25000 Å) have been obtained for fifteen analysed trioctahedral micas covering a wide range of compositions, and including four phlogopites, nine biotites, and two lepidomelanes. Three main contributions to the absorption have been noted: charge transfer from oxygen to ferrous iron throughout the visible and near ultraviolet, charge transfer from ferrous to ferric ions at the red end of the visible spectrum and internal d-d transitions of ferrous ions in the near infrared.

Substitutions in the brucite layer (especially Ti) cause the O → Fe2+ band to broaden, and thus to encroach on the visible region for vibration directions in the plane of the cleavage flake. The transmission window between these bands is further blocked by the Fe2+ → Fe3+ charge-transfer band, which is polarized in the plane of the flake. The overall effect is to produce very strong absorption throughout the visible region for (β, γ) vibration directions, and relatively weak absorption for α, i.e. the observed very strong pleochroism of biotite.

Many features of the spectra of chlorite, amphiboles, and tourmaline, which contain octahedral ions in brucite-like sheets, strips, and fragments respectively, may be interpreted by analogy with biotite.

Two types of solid solution effect are described: substitutional broadening, which is responsible for the extension of the O → Fe2+ band into the visible region in biotites and aluminous ortho-pyroxenes, and substitutional intensification, which permits in solid solutions transitions that are forbidden by the conventional selection rules.

Mineralogical Magazine; March 1972 v. 38; no. 297; p. 551-563; DOI: 10.1180/minmag.1972.038.297.03
© 1972, The Mineralogical Society
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