| Literature DB >> 27645726 |
Tayro E Acosta-Maeda1, Anupam K Misra1, John N Porter1, David E Bates1, Shiv K Sharma1.
Abstract
We determined Raman cross-sections of various organic liquids and inorganic polyatomic ions in aqueous solutions with a 532 nm pulsed laser using remote Raman systems developed at the University of Hawaii. Using a calibrated integrating sphere as a light source, we converted the intensity counts in the spectrum of the light from the integrating sphere measured with UH remote Raman instrument to spectral radiance. From these data, a response function of the remote Raman instrument was obtained. With the intensity-calibrated instrument, we collected remote Raman data from a standard 1 mm path length fused silica spectrophotometer cell filled with cyclohexane. The measured value of the differential Raman cross-section for the 801 cm-1 vibrational mode of cyclohexane is 4.55 × 10-30 cm2 sr-1 molecule-1 when excited by a 532 nm laser, in good agreement with the values reported in the literature. Using the measured cyclohexane Raman cross-section as a reference and relative Raman mode intensities of the various ions and organic liquids, we calculated the Raman cross-sections of the strongest Raman lines of nitrate, sulfate, carbonate, phosphate ions, and organic liquids by maintaining same experimental conditions for remote Raman detection. These relative Raman cross-section values will be useful for estimating detection capabilities of remote Raman systems for planetary exploration.Entities:
Keywords: Raman cross-section; Raman spectroscopy; planetary science instruments; remote Raman; remote sensing; standoff Raman
Year: 2016 PMID: 27645726 DOI: 10.1177/0003702816668531
Source DB: PubMed Journal: Appl Spectrosc ISSN: 0003-7028 Impact factor: 2.388