Gary K. Klauminzer

Bio: Gary K. Klauminzer is an academic researcher. The author has contributed to research in topics: Raman scattering & Coherent anti-Stokes Raman spectroscopy. The author has an hindex of 3, co-authored 3 publications receiving 233 citations.

Coherent anti‐Stokes Raman spectroscopy (CARS): Improved experimental design and observation of new higher‐order processes

Abstract: The development of the optical and electronic arrangement which has permitted the straightforward measurement of coherent anti‐Stokes Raman spectra (CARS) and of higher‐order processes not previously reported is described in this paper. The CARS spectrum of a dilute solution of diphenyloctatetraene in benzene is presented. This spectrum demonstrates the significantly greater signal‐to‐noise ratio possible with CARS as compared to conventional Raman techniques. Higher‐order Raman spectral excitation studies (HORSES) are described which indicate the presence of a six‐wave or a second‐order four‐wave mixing process.

Resonance enhanced coherent anti-Stokes Raman scattering.

Abstract: Resonance enhancement of coherent anti-Stokes Raman scattering due to the proximity of the laser frequencies to an electronic transition has been demonstrated for dilute solutions of diphenyloctatetrane in benzene. The Raman contribution to the third order susceptibility is shown to be complex near an electronic resonance and the resulting features of the coherent anti-Stokes Raman scattering spectra are discussed in detail. This work represents one step in the demonstration that the high signal to noise ratio, fluorescence rejection, and low average power levels of the coherent anti-Stokes Raman scattering experiment can be used to advantage in Raman studies of dilute solutions and materials of biological interest.

Coherent anti-Stokes Raman scattering (CARS) spectra, with resonance enhancement, of cytochrome c and vitamin B12 in dilute aqueous solution.

Abstract: Coherent anti-Stokes Raman scattering (CARS) spectra have been obtained for ferrocytochrome c and cyano cobalamin in aqueous solution at millimolar concentrations, using a pair of tunable dye lasers pumped by a pulsed nitrogen laser. Resonance enhancement was obtained by tuning the omega1 laser to the visible absorption bands of the samples. The spectral features correspond to those observed in the conventional resonance Raman spectra. It appears that CARS spectroscopy, with its advantageous fluorescence rejection, can be usefully applied to biological samples by exploiting resonance enhancement. While the background scattering from water is 10 times higher than that of benzene and other aromatic solvents, it is actually at the low end of the scale for most liquids. The anomalously low background of aromatic liquids is thought to result from competition by the unusually efficient stimulated Raman scattering which they display. Off-resonance spectra for both cobalamin and cytochrome c contain negative peaks, i.e., absorption bands in the background. These are interpreted as inverse Raman processes induced by the omega1 photons in the presence of the continuum provided by the background scattering. While both CARS and the inverse Raman effect are subject to resonance enhancement, the wavelength dependence of CARS is evidently steeper.

Coherent Anti-Stokes Raman Scattering Microscopy: Instrumentation, Theory, and Applications

Abstract: Coherent anti-Stokes Raman scattering (CARS) microscopy permits vibrational imaging with high-sensitivity, high speed, and three-dimensional spatial resolution. We review recent advances in CARS microscopy, including experimental design, theoretical understanding of contrast mechanisms, and applications to chemical and biological systems. We also review the development of multiplex CARS microspectroscopy, which allows high-speed characterization of microscopic samples, and CARS correlation spectroscopy, which probes fast diffusion dynamics with vibrational selectivity.

A review of the theory and application of coherent anti-Stokes Raman Spectroscopy (CARS)

Abstract: Coherent anti-Stokes Raman spectroscopy (CARS) is a relatively new kind of Raman spectroscopy which is based on a nonlinear conversion of two laser beams into a coherent, laser-like Raman beam of high intensity in the anti-Stokes region. The emission is often many orders of magnitude greater than normal Raman scattering and, because of the coherent and anti-Stokes character of radiation, the method is very useful for obtaining Raman spectra of fluorescing samples, gases in discharges, plasmas, combustion, atmospheric chemistry. In this paper we outline the basic theory behind CARS and describe its unusual effects and drawbacks. We review the research to date on various materials, and indicate the possible future direction, utility and applications of CARS such as surface studies, fluctuation phenomena, reaction dynamics, photochemistry, kinetics, relaxation, and energy transfer.

Coherent Raman spectroscopy

Abstract: A review of the salient features of five coherent Raman techniques is given, including typical spectra produced by each technique. The resonant and nonresonant signal contributions in the monochromatic plane wave limit are calculated for: (1) Coherent AntiStokes Raman Spectroscopy(CARS); (2) a polarization technique referred to as ASTERISK; (3) Raman-induced Kerr-effect Spectroscopy(RIKES); (4) Optically Heterodyned RIKES (OHD-RIKES); (5) Stimulated Raman Spectroscopy (SRS). The relevant noise contribution to each of these techniques is developed within the framework of a comparative signal-to-noise analysis, and realistic detection limits are discussed. The OHD-RIKES technique is selected as the most viable of the coherent Raman techniques which satisfies the following criteria: (A) suppression of nonresonant background signals and enhanced signal-to-noise ratio; (b) simplicity of operation and interpretation of results. This is the first known application of optical heterodyne detection and optimization to coherent Raman spectroscopy, and the principles developed are generally applicable to all forms of third-order nonlinear spectroscopu.