Journal•ISSN: 0377-0486
Journal of Raman Spectroscopy
Wiley
About: Journal of Raman Spectroscopy is an academic journal published by Wiley. The journal publishes majorly in the area(s): Raman spectroscopy & Raman scattering. It has an ISSN identifier of 0377-0486. Over the lifetime, 7609 publications have been published receiving 188492 citations. The journal is also known as: JRS.
Topics: Raman spectroscopy, Raman scattering, Infrared spectroscopy, Coherent anti-Stokes Raman spectroscopy, Spectroscopy
Papers published on a yearly basis
Papers
More filters
TL;DR: In this paper, the laser power dependence of the spectra of oxides and oxyhydroxides was investigated by using Raman microscopy, and it was shown that increasing laser power causes the characteristic bands of hematite to show up in the spectrum of most of the compounds studied.
Abstract: Hematite (α-Fe2O3), magnetite (Fe3O4), wustite (FeO), maghemite (γ-Fe2O3), goethite (α-FeOOH), lepidocrocite (γ-FeOOH) and δ-FeOOH were studied by Raman microscopy. Such compounds have already been studied by Raman spectroscopy, but there are some disagreements in the reported data. Here, Raman microscopy was employed to investigate the laser power dependence of the spectra of these oxides and oxyhydroxides. Low laser power was used for the reference spectra in order to minimize the risks of spectral changes due to sample degradation. The results obtained show that increasing laser power causes the characteristic bands of hematite to show up in the spectra of most of the compounds studied whereas the hematite spectrum undergoes band broadening and band shifts. © 1997 John Wiley & Sons, Ltd.
2,569 citations
TL;DR: In this paper, the Raman spectra of anatase have been observed in both natural and synthetic crystals and the six Raman active fundamentals predicted by group theory are all observed and assigned.
Abstract: Raman spectra of anatase have been observed in natural and synthetic crystals. Both crystals show the same spectral features. The Raman band occurring at 516 cm−1 at room temperature is split into two peaks centred at 519 cm−1 and 513 cm−1 at low temperature (73 K). The six Raman active fundamentals predicted by group theory are all observed and assigned. The spectra are analyzed by a simple model considering only short-range forces and the calculated vibrational frequencies are in good agreement with the observed Raman frequencies.
1,922 citations
TL;DR: The electromagnetic theory of surface-enhanced Raman spectroscopy (SERS), despite its simplicity, can account for all major SERS observations, including: the need for a nanostructured material as the SERS-active system; the observation that some metals form good SERS active systems while others do not; the observed polarization sensitivity shown by nanoparticle aggregates; and the optical behavior of nanostructure materials in the absence of a molecular adsorbate as mentioned in this paper.
Abstract: The electromagnetic theory of surface-enhanced Raman spectroscopy (SERS), despite its simplicity, can account for all major SERS observations, including: the need for a nanostructured material as the SERS-active system; the observation that some metals form good SERS-active systems while others do not; the observation that strongly interacting metal nanoparticles result in very much more effective SERS-active systems; the observed polarization sensitivity shown by nanoparticle aggregates; and the optical behavior of nanostructured metals in the absence of a molecular adsorbate. By extending the ideas inherent in the electromagnetic model one can also understand the seminal features reported for single-molecule SERS, including the puzzling observation that only a few silver ‘particles’ in an ensemble are ‘hot’ (they are appropriately structured nanoparticle clusters) and that for a hot particle, once one is able to observe SERS, adding more adsorbate does not significantly alter the intensity (once the electromagnetic hot spot is occupied, adding adsorbate to other sites on the nanoparticle cluster will not add greatly to the observed intensity). However, the electromagnetic model does not account for all that is learned through SERS. Molecular resonances, charge-transfer transitions and other processes such as ballistic electrons transiently probing the region where the molecule resides and then modulating electronic processes of the metal as a result certainly contribute to the rich information SERS reports; and by virtue of the fact that these contributions will vary from molecule to molecule, they will constitute the most interesting aspects reported by SERS. But, the overall reason why SERS produces such inordinate enhancements is largely an electromagnetic property of nanostructures. Copyright © 2005 John Wiley & Sons, Ltd.
1,644 citations
TL;DR: A collection of Raman spectra of biomolecules that can serve as references for the interpretation of biological materials is presented in this paper, where the most important components present in a cell are included.
Abstract: Raman spectra of biological materials are very complex, because they consist of signals from all molecules present in cells. In order to obtain chemical information from these spectra, it is necessary to know the Raman patterns of the possible components of a cell. In this paper, we present a collection of Raman spectra of biomolecules that can serve as references for the interpretation of Raman spectra of biological materials. We included the most important components present in a cell: (1) DNA and RNA bases (adenine, cytosine, guanine, thymine and uracil), (2) amino acids (glycine, L-alanine, L-valine, L-serine, L-glutamic acid, L-arginine, L-phenylalanine, L-tyrosine, L-tryptophan, L-histidine, L-proline), (3) fatty acids and fats (lauric acid, myristic acid, palmitic acid, stearic acid, 12-methyltetradecanoic acid, 13-methylmyristic acid, 14-methylpentadecanoic acid, 14-methylhexadecanoic acid, 15-methylpalmitic acid, oleic acid, vaccenic acid, glycerol, triolein, trilinolein, trilinolenin), (4) saccharides (β-D-glucose, lactose, cellulose, D-(+)-dextrose, D-(+)-trehalose, amylose, amylopectine, D-(+)-mannose, D-(+)-fucose, D-(−)-arabinose, D-(+)-xylose, D-(−)-fructose, D-(+)-galactosamine, N-acetyl-D-glucosamine, chitin), (5) primary metabolites (citric acid, succinic acid, fumarate, malic acid, pyruvate, phosphoenolpyruvate, coenzyme A, acetyl coenzyme A, acetoacetate, D-fructose-6-phosphate) and (6) others (β-carotene, ascorbic acid, riboflavin, glutathione). Examples of Raman spectra of bacteria and fungal spores are shown, together with band assignments to the reference products. Copyright © 2007 John Wiley & Sons, Ltd.
1,157 citations
TL;DR: In this article, a series of tables are presented to facilitate rapid determination of the selection rules for vibrational transitions for nuclear site group analysis, where the number of infrared and Raman active modes of each symmetry may be obtained without detailed analysis of the symmetry elements in the crystallographic unit cell or the construction of tables.
Abstract: The group theoretical methods by which the symmetries of normal modes in crystals may be determined are outlined, and a series of tables are presented to facilitate rapid determination of the selection rules for vibrational transitions. Emphasis is placed on the method of nuclear site group analysis in which the number of infrared and Raman active modes of each symmetry may be obtained without detailed analysis of the symmetry elements in the crystallographic unit cell or the construction of tables. By using the tables presented here for most cases identification of the crystallographic space group is sufficient information to allow determination of the vibrational mode selection rules by inspection. Several examples are included in which crystals are analyzed by each of the methods.
1,064 citations