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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.


Papers
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Journal ArticleDOI
TL;DR: In this study in situ Raman and Fourier transform infrared (FTIR) spectroscopic methods were combined with sorption techniques, electrophoretic mobility measurements, and surface complexation modeling to study the interaction of As(III) and As(V) with amorphous oxide surfaces.

1,181 citations

01 Jan 2008
TL;DR: In this paper, the authors used the Raman spectra of strained graphene to estimate the band gap opening under 1% uniaxial tensile strain on a transparent and flexible substrate.
Abstract: Graphene was deposited on a transparent andflexible substrate, and tensile strain up to0.8% was loaded by stretching the substrate in one direction. Raman spectra of strained graphene show significant red shifts of 2D and G band (27.8 and14.2 cm 1 per 1% strain, respectively) because of the elongation of the carboncarbon bonds. This indicates that uniaxial strain has been successfully applied on graphene. We also proposedthat,byapplyinguniaxialstrainongraphene,tunablebandgapatKpointcanberealized.First-principle calculations predicted a band-gap opening of300 meV for graphene under 1% uniaxial tensile strain. The strained graphene provides an alternative way to experimentally tune the band gap of graphene, which would be more efficient and more controllable than other methods that are used to open the band gap in graphene. Moreover,ourresultssuggestthattheflexiblesubstrateisreadyforsuchastrainprocess,andRamanspectroscopy can be used as an ultrasensitive method to determine the strain.

1,171 citations

Journal ArticleDOI
01 Jul 1997-Nature
TL;DR: In this paper, the effects of exposing single-walled carbon nanotubes to typical electron-donor (potassium, rubidium) and electron-acceptor (iodine, bromine) dopants were investigated.
Abstract: Single-walled carbon nanotubes1 (SWNTs) are predicted to be metallic for certain diameters and pitches of the twisted graphene ribbons that make up their walls2. Chemical doping is expected to substantially increase the density of free charge carriers and thereby enhance the electrical (and thermal) conductivity. Here we use Raman spectroscopy to study the effects of exposing SWNT bundles1 to typical electron-donor (potassium, rubidium) and electron-acceptor (iodine, bromine) dopants. We find that the high-frequency tangential vibrational modes of the carbon atoms in the SWNTs shift substantially to lower (for K, Rb) or higher (for Br2) frequencies. Little change is seen for I2 doping. These shifts provide evidence for charge transfer between the dopants and the nanotubes, indicating an ionic character of the doped samples. This, together with conductivity measurements3, suggests that doping does increase the carrier concentration of the SWNT bundles.

1,162 citations

Journal ArticleDOI
TL;DR: A review of the plasmon-enhanced Raman spectroscopy (PERS) field can be found in this paper, where a new generation of hotspots that are generated from hybrid structures combining PERS-active nanostructures and probe materials are discussed.
Abstract: Since 2000, there has been an explosion of activity in the field of plasmon-enhanced Raman spectroscopy (PERS), including surface-enhanced Raman spectroscopy (SERS), tip-enhanced Raman spectroscopy (TERS) and shell-isolated nanoparticle-enhanced Raman spectroscopy (SHINERS). In this Review, we explore the mechanism of PERS and discuss PERS hotspots — nanoscale regions with a strongly enhanced local electromagnetic field — that allow trace-molecule detection, biomolecule analysis and surface characterization of various materials. In particular, we discuss a new generation of hotspots that are generated from hybrid structures combining PERS-active nanostructures and probe materials, which feature a strong local electromagnetic field on the surface of the probe material. Enhancement of surface Raman signals up to five orders of magnitude can be obtained from materials that are weakly SERS active or SERS inactive. We provide a detailed overview of future research directions in the field of PERS, focusing on new PERS-active nanomaterials and nanostructures and the broad application prospect for materials science and technology. Assisted by rationally designed novel plasmonic nanostructures, surface-enhanced Raman spectroscopy has presented a new generation of analytical tools (that is, tip-enhanced Raman spectroscopy and shell-isolated nanoparticle-enhanced Raman spectroscopy) with an extremely high surface sensitivity, spatial resolution and broad application for materials science and technology.

1,158 citations

Journal ArticleDOI
TL;DR: In this article, Raman spectroscopy and imaging can be used as a quick and unambiguous method to determine the number of layers of a single-layer graphite compared to graphite.
Abstract: Graphene has many unique properties that make it an ideal material for fundamental studies as well as for potential applications. Here we review recent results on the Raman spectroscopy and imaging of graphene. We show that Raman spectroscopy and imaging can be used as a quick and unambiguous method to determine the number of graphene layers. The strong Raman signal of single layer graphene compared to graphite is explained by an interference enhancement model. We have also studied the effect of substrates, the top layer deposition, the annealing process, as well as folding (stacking order) on the physical and electronic properties of graphene. Finally, Raman spectroscopy of epitaxial graphene grown on a SiC substrate is presented and strong compressive strain on epitaxial graphene is observed. The results presented here are highly relevant to the application of graphene in nano-electronic devices and help in developing a better understanding of the physical and electronic properties of graphene.

1,157 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20235,220
202210,775
20214,240
20204,764
20194,957
20184,893