Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/95210
Title: Analysis of time resolved femtosecond and femtosecond/picosecond coherent anti-Stokes Raman spectroscopy : application to toluene and Rhodamine 6G
Authors: Niu, Kai
Lee, Soo-Ying
Issue Date: 2012
Source: Niu, K., & Lee, S. Y. (2012). Analysis of time resolved femtosecond and femtosecond/picosecond coherent anti-Stokes Raman spectroscopy : application to toluene and Rhodamine 6G. The Journal of Chemical Physics, 136(6).
Series/Report no.: The Journal of Chemical Physics
Abstract: The third-order polarization for coherent anti-Stokes Raman scattering (CARS) from a pure state is described by 48 terms in perturbation theory, but only 4 terms satisfy the rotating wave approximation. They are represented by Feynman dual time-line diagrams and four-wave mixing energy level diagrams. In time-resolved (tr) fs and fs/ps CARS from the ground vibrational state, one resonant diagram, which is the typical CARS term, with three field interactions—pump, Stokes, followed by probe—on the ket is dominant. Using the separable, displaced harmonic oscillators approximation, an analytic result is obtained for the four-time correlation function in the CARS third-order polarization. Dlott's phenomenological expression for off-resonance CARS from the ground vibrational state is derived using a three-state model. We calculated the tr fs and fs/ps CARS for toluene and Rhodamine 6G (R6G), initially in the ground vibrational state, to compare with experimental results. The observed vibrational features and major peaks for both tr fs and fs/ps CARS, from off-resonance (for toluene) to resonance (for R6G) pump wavelengths, can be well reproduced by the calculations. The connections between fs/ps CARS, fs stimulated Raman spectroscopy, and impulsive stimulated scattering for toluene and R6G are discussed.
URI: https://hdl.handle.net/10356/95210
http://hdl.handle.net/10220/9181
ISSN: 0021-9606
DOI: 10.1063/1.3682470
Rights: © 2012 American Institute of Physics. This paper was published in The Journal of Chemical Physics and is made available as an electronic reprint (preprint) with permission of American Institute of Physics. The paper can be found at the following official DOI: [http://dx.doi.org/10.1063/1.3682470]. One print or electronic copy may be made for personal use only. Systematic or multiple reproduction, distribution to multiple locations via electronic or other means, duplication of any material in this paper for a fee or for commercial purposes, or modification of the content of the paper is prohibited and is subject to penalties under law.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:SPMS Journal Articles

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