Raman Spectroscopy

Raman spectroscopy ( /ˈrɑːmən/; named after Sir C. V. Raman) is a spectroscopic technique used to observe vibrational, rotational, and other low-frequency modes in a system. It relies on inelastic scattering, or Raman scattering, of monochromatic light, usually from a laser in the visible, near infrared, or near ultraviolet range. The laser light interacts with molecular vibrations, phonons or other excitations in the system, resulting in the energy of the laser photons being shifted up or down. The shift in energy gives information about the vibrational modes in the system. Infrared spectroscopy yields similar, but complementary, information.

Typically, a sample is illuminated with a laser beam. Light from the illuminated spot is collected with a lens and sent through a monochromator. Wavelengths close to the laser line due to elastic Rayleigh scattering are filtered out while the rest of the collected light is dispersed onto a detector.

Spontaneous Raman scattering is typically very weak, and as a result the main difficulty of Raman spectroscopy is separating the weak inelastically scattered light from the intense Rayleigh scattered laser light. Historically, Raman spectrometers used holographic gratings and multiple dispersion stages to achieve a high degree of laser rejection. In the past, photomultipliers were the detectors of choice for dispersive Raman setups, which resulted in long acquisition times. However, modern instrumentation almost universally employs notch or edge filters for laser rejection and spectrographs (either axial transmissive (AT), Czerny-Turner (CT) monochromator, or FT (Fourier transform spectroscopy based), and CCD detectors.

There are a number of advanced types of Raman spectroscopy, including surface-enhanced Raman, resonance Raman, tip-enhanced Raman, polarised Raman, stimulated Raman (analogous to stimulated emission), transmission Raman, spatially offset Raman, and hyper Raman.

The Raman effect occurs when light impinges upon a molecule and interacts with the electron cloud and the bonds of that molecule. For the spontaneous Raman effect, which is a form of light scattering, a photon excites the molecule from the ground state to a virtual energy state. When the molecule relaxes it emits a photon and it returns to a different rotational or vibrational state. The difference in energy between the original state and this new state leads to a shift in the emitted photon's frequency away from the excitation wavelength. The Raman effect, which is a light scattering phenomenon, should not be confused with absorption (as with fluorescence) where the molecule is excited to a discrete (not virtual) energy level.

If the final vibrational state of the molecule is more energetic than the initial state, then the emitted photon will be shifted to a lower frequency in order for the total energy of the system to remain balanced. This shift in frequency is designated as a Stokes shift. If the final vibrational state is less energetic than the initial state, then the emitted photon will be shifted to a higher frequency, and this is designated as an Anti-Stokes shift. Raman scattering is an example of inelastic scattering because of the energy transfer between the photons and the molecules during their interaction.

A change in the molecular polarization potential — or amount of deformation of the electron cloud — with respect to the vibrational coordinate is required for a molecule to exhibit a Raman effect. The amount of the polarizability change will determine the Raman scattering intensity. The pattern of shifted frequencies is determined by the rotational and vibrational states of the sample. This dependence on the polarizability differs from Infrared spectroscopy where the interaction between the molecule and light is determined by the dipole moment; this contrasting feature allows to analyze transitions that might not be IR active via Raman spectroscopy, as exemplified by the rule of mutual exclusion in centrosymmetric molecules.

Read more about Raman Spectroscopy:  History, Raman Shift, Applications, Microspectroscopy, Polarized Analysis, Variations

Other articles related to "raman spectroscopy, spectroscopy, raman":

Spatially Offset Raman Spectroscopy
... Spatially Offset Raman Spectroscopy (SORS) is a variant of Raman spectroscopy that allows highly accurate chemical analysis of objects beneath obscuring surfaces, such as tissue ... Raman spectroscopy relies on inelastic scattering events of monochromatic light to produce a spectrum characteristic of a sample ...
Preservation Of Illuminated Manuscripts - Inks and Pigments - Identification
... XRF) Particle induced x-ray emission (PIXE-α) Raman spectroscopy Raman spectroscopy Raman spectroscopy analyzes the molecular vibrations of the pigments and uses this data to map out its ... other non-invasive identification techniques the results of Raman spectroscopy are much more certain ...
Raman Spectroscopy - Variations
... Several variations of Raman spectroscopy have been developed ... surface-enhanced Raman), to improve the spatial resolution (Raman microscopy), or to acquire very specific information (resonance Raman) ... Surface Enhanced Raman Spectroscopy (SERS) - Normally done in a silver or gold colloid or a substrate containing silver or gold ...
Selective Chemistry Of Single-walled Nanotubes - Spectroscopy and Functionalization - Raman Spectroscopy
... Raman spectroscopy is a powerful technique with wide ranging applications in carbon nanotube studies ... Some important Raman features are radial breathing mode (RBM), tangential mode (G-band), and disorder-related mode ...
Spectroscopy - Other Types
... Other types of spectroscopy are distinguished by specific applications or implementations Auger spectroscopy is a method used to study surfaces of materials on a micro-s ... Cavity ring down spectroscopy Circular Dichroism spectroscopy Coherent anti-Stokes Raman spectroscopy (CARS) is a recent technique that has high sensitivity and powerful applications for in vivo spectroscopy ... Cold vapour atomic fluorescence spectroscopy Correlation spectroscopy encompasses several types of two-dimensional NMR spectroscopy ...