Abstract
Absorption of both the excitation and Raman scattered light by the sample (self-absorption) is common in UV Raman spectroscopy and sometimes in visible and FT-Raman spectroscopy due to electronic or vibrational excitation. Self-absorption affects Raman bands and usually results in a non-linear relationship between the Raman intensity and sample concentration. This paper compares quantitative analysis methods for Raman measurements of absorbing liquid and solid samples. Methods based on both internal and external standards can be used to correct for self-absorption. Examples including both liquid (1-methylnaphthalene/isooctane) and solid (V/δ-Al2O 3) systems were used to compare the effectiveness of these methods. The results show that as long as certain restrictions on the use of these analysis methods are satisfied, the self-absorption problem in Raman spectroscopy can be accurately corrected.
Original language | English (US) |
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Pages (from-to) | 40-47 |
Number of pages | 8 |
Journal | Catalysis Today |
Volume | 113 |
Issue number | 1-2 |
DOIs | |
State | Published - Mar 30 2006 |
Funding
This work is financially supported by ATHENA and the Chemical Sciences, Geosciences and Biosciences Division, Office of Basic Energy Sciences, Office of Science, U.S. Department of Energy under Grant No. DE-FG02-97ER14789. The Athena project is funded by the Engineering & Physical Sciences Research Council (EPSRC) of the UK and Johnson Matthey plc.
Keywords
- Absorption
- Correction
- Diffuse reflectance
- External standard
- Internal standard
- Quantitative analysis
- Raman spectroscopy
- Scattering
ASJC Scopus subject areas
- Catalysis
- General Chemistry