IR absorbance spectra of olivine

To address this need, we study room temperature absorption spectra of a large suite of olivines evenly spaced across Mg and Fe compositions. We apply the principle that classical dispersion theory may be used to determine peak positions as well as peak widths, strengths and possibly optical function (n({lambda}) and k({lambda})) estimates from absorption spectra of thin film samples of these olivines and two additional isotropic and anisotropic minerals with varying hardness and numbers of spectral bands.

For olivine, we find that this method provides good estimates of peak position and that accounting for asymmetric peak shapes in this way increases the error on full width at half-maximum and oscillator strengths. Values from classical dispersion fits better match published n and k derived from reflectivity of single crystals when the dust proxy is soft and the thickness of the sample is independently constrained. Electronic data and peak parameter trends for the laboratory olivine absorption spectra and the viability of the extracted n and k are discussed with regard to astronomy.