Deep-ultraviolet Raman spectra of Mars-relevant evaporite minerals under 248.6 nm excitation

1Joseph Razzell Hollis,1,2Schelin Ireland,1William Abbey,3Rohit Bhartia,1Luther W.Beegle
Icarus (in Press) Link to Article []
1NASA Jet Propulsion Laboratory, California Institute of Technology, Pasadena, CA, United States
2University of Hawaii at Mānoa, Mānoa, HI, United States
3Photon Systems Inc., Covina, CA, United States
Copyright Elsevier

We have measured the deep-ultraviolet (DUV) Raman spectra of a number of evaporite minerals that are relevant to lacustrine and fluvial environments found on Earth and Mars, and show that DUV Raman can provide detailed information on elemental composition and crystal structure. The minerals included three borates, eight carbonates, and seven sulfates, with each class of mineral exhibited very distinct spectra under 248.6 nm excitation, dominated by the various internal vibrations of the borate, carbonate or sulfate oxyanion. Peak positions were shifted by markedly lower wavenumbers vs positions reported in the literature for longer wavelengths, a phenomenon we ascribe to the effect of pre-resonance with the oxyanion. Within each class, minerals consisting different metallic cations could be distinguished by the position of the dominant vibrational mode and the relative intensities of the minor modes, ascribed to the electrostatic impact of the cation on the vibrational behavior of the oxyanion. There was also evidence that DUV Raman can reveal minor metallic components even if they are not apparent in XRD, as two of three calcite (CaCO3) samples exhibited a shoulder on the dominant peak consistent with perturbation by Mg. UV absorption by Fe2+/3+ was a major factor in determining measurable signal, with Fe-rich minerals exhibiting weak/undetectable spectra. Understanding the spectra of these evaporite minerals will be essential to interpreting and identifying complex mineral samples using this technique, and represents an important addition to the spectral standards library of DUV Raman spectroscopy.


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