Raman spectroscopy

About: Raman spectroscopy is a research topic. Over the lifetime, 122605 publications have been published within this topic receiving 2891083 citations. The topic is also known as: Raman Spectrum Analysis & spectrum Analysis, Raman.

Infrared and Raman spectroscopy : methods and applications

Abstract: Early history of vibrational spectroscopy general survey of vibrational spectroscopy tools for infrared and Raman spectroscopy vibrational spectroscopy of different classes and states of compounds evaluation procedures special techniques and applications (Part contents)

Raman spectroscopy of diamond and doped diamond.

Abstract: The optimization of diamond films as valuable engineering materials for a wide variety of applications has required the development of robust methods for their characterization. Of the many methods used, Raman microscopy is perhaps the most valuable because it provides readily distinguishable signatures of each of the different forms of carbon (e.g. diamond, graphite, buckyballs). In addition it is non-destructive, requires little or no specimen preparation, is performed in air and can produce spatially resolved maps of the different forms of carbon within a specimen. This article begins by reviewing the strengths (and some of the pitfalls) of the Raman technique for the analysis of diamond and diamond films and surveys some of the latest developments (for example, surface-enhanced Raman and ultraviolet Raman spectroscopy) which hold the promise of providing a more profound understanding of the outstanding properties of these materials. The remainder of the article is devoted to the uses of Raman spectroscopy in diamond science and technology. Topics covered include using Raman spectroscopy to assess stress, crystalline perfection, phase purity, crystallite size, point defects and doping in diamond and diamond films.

Light scattering study of boron nitride microcrystals

Abstract: Raman scattering and x-ray diffraction measurements are used to correlate finite-size effects on the Raman spectra of nonpolar vibrational modes in BN. The BN microcrystalline samples used exhibited domain sizes varying from 4.4 to 78.5 nm in the plane and 1.5 and 47.5 nm perpendicular to the planes. The Raman measurements indicated that the high-frequency ${E}_{2g}$ mode shifted to higher frequency and broadened as the crystallite size decreased. A formulation of the Raman cross section for scattering from nonpolar microcrystals is presented. The development includes evaluation of the susceptibility correlation function over a limited spatial extent. The results indicate that spectral changes are related to the phonon dispersion, and the wave-vector uncertainty is accounted for. The formulation is applied to describe the BN light scattering results, and good agreement was obtained to describe the observed shift in frequency.

Raman spectroscopy of orthorhombic perovskitelike YMnO 3 and LaMnO 3

Abstract: The Raman-active phonons in orthorhombic perovskitelike ${\mathrm{YMnO}}_{3}$ and ${\mathrm{LaMnO}}_{3}$ were studied by measuring Raman spectra in various scattering configurations. The experimental Raman line wave numbers and the expected shapes for the phonon modes were compared to those reported for other perovskitelike compounds with the $\mathrm{Pnma}$ structure and to the results of lattice dynamical calculations. The observed Raman lines in the spectra of ${\mathrm{YMnO}}_{3}$ and ${\mathrm{LaMnO}}_{3}$ were assigned to definite atomic motions. The much larger linewidths and strong variation of the Raman spectra with increasing laser power in the case of ${\mathrm{LaMnO}}_{3}$ provide evidence for a structural instability that may result in a phase transition under laser annealing.

Analysis of the composite structures in diamond thin films by Raman spectroscopy.

Abstract: Diamond and diamondlike thin films produced by various chemical-vapor-deposition processes have been examined using Raman spectroscopy. These films exhibit features in the Raman spectra, suggesting that they are composites of crystalline and amorphous diamond and graphitic structures. The components of this composite structure that contribute to the Raman scattering are discussed in terms of ${\mathrm{sp}}^{2}$- and ${\mathrm{sp}}^{3}$-bonded structures. The use of Raman spectroscopy as a technique for estimating the ${\mathrm{sp}}^{2}$-to-${\mathrm{sp}}^{3}$ bonding ratio is considered. Powder composites of BN-diamond and graphite-diamond have been studied as a means of modeling the films, and a simple theoretical model of the Raman scattering from these samples is proposed. From these results it is shown that it is necessary to make assumptions about the domain size of the graphitic ${\mathrm{sp}}^{2}$ regions. It is found that the Raman scattering associated with ${\mathrm{sp}}^{2}$ bonding in the films is much stronger than that from single-crystalline or microcrystalline graphite structures. Shifts of the vibrational modes are also observed. The optical and vibrational properties of the ${\mathrm{sp}}^{2}$ component in the films implies a different atomic microstructure. A model of the ${\mathrm{sp}}^{2}$-bonding configurations in the films is proposed which may account for the observed features in the Raman spectra.