View source for Depolarization ratio

{{Short description|Intensity ratio between perpendicular component and parallel component of Raman scattered light}}
{{Other uses|Depolarization (disambiguation)}}

In [[Raman spectroscopy]], the '''depolarization ratio''' is the [[Intensity (physics)|intensity]] ratio between the perpendicular component and the parallel component of Raman scattered light.<ref name=Allemand>{{cite journal |last= Allemand |first= Charly D. |date= 1970 |title= Depolarization Ratio Measurements in Raman Spectrometry |journal= Applied Spectroscopy |volume= 24 |issue= 3 |pages= 348–353 |doi= 10.1366/000370270774371552 |bibcode= 1970ApSpe..24..348A |s2cid= 97660984 }}</ref>

Early work in this field was carried out by [[George Placzek]], who developed the theoretical treatment of bond polarizability.<ref name=Long>{{cite journal |last= Long |first= D. A. |date= Apr 8, 1953 |title= Intensities in Raman Spectra. I. A Bond Polarizability Theory |journal= Proceedings of the Royal Society of London. Series A, Mathematical and Physical Sciences |volume= 217 |issue= 1129 |pages= 203–221 |jstor= 99022 |doi= 10.1098/rspa.1953.0057 |bibcode= 1953RSPSA.217..203L |s2cid= 97491664 }}</ref>

The Raman scattered light is emitted by the stimulation of the [[electric field]] of the incident light. Therefore, the direction of the vibration of the electric field, or [[Polarization (waves)|polarization]] direction, of the scattered light might be expected to be the same as that of the incident light. In reality, however, some fraction of the Raman scattered light has a polarization direction that is perpendicular to that of the incident light. This component is called the '''{{dfn|perpendicular component}}'''. Naturally, the component of the Raman scattered light whose polarization direction is parallel to that of the incident light is called the '''{{dfn|parallel component}}''', and the Raman scattered light consists of the parallel component and the perpendicular component.

The ratio of the peak intensity of the parallel and perpendicular component is known as the depolarization ratio ({{mvar|ρ}}), defined in [[#equation-1|equation 1]].<ref name=PE>{{cite web|author= PerkinElmer, Inc. |date= 2008 |title= Raman Polarization Accessory for the RamanStation 400 |type= Technical Note |url= http://las.perkinelmer.com/content/relatedmaterials/productnotes/PRD_RamanPolarizationAccessory4RamanStation400.pdf |accessdate= 5 Jan 2019 |archive-url= https://web.archive.org/web/20101226211117/http://las.perkinelmer.com/content/relatedmaterials/productnotes/PRD_RamanPolarizationAccessory4RamanStation400.pdf |archive-date= 26 December 2010 |url-status= dead}}</ref>

{{Equation|1=\rho = \frac{ I_{perpendicular} }{ I_{parallel} } \quad\textrm{or}\quad \frac{ I_{depolarized} }{ I_{polarized} } |id=1}}

For example, a spectral band with a peak of intensity 10 units when the polarizers are parallel, and an intensity 1 unit when the polarizers are perpendicular, would have a depolarization ratio of 1/10 = 0.1, which corresponds to a highly polarized band.

The value of the depolarization ratio of a Raman band depends on the [[symmetry]] of the molecule and the normal vibrational mode, in other words, the [[point group]] of the molecule and its [[irreducible representation]] to which the [[normal mode]] belongs. Under Placzek's polarizability approximation, it is known that the depolarization ratio of a totally symmetric vibrational mode is less than 0.75, and that of the other modes equals 0.75. A Raman band whose depolarization ratio is less than 0.75 is called a '''{{dfn|polarized band}}''', and a band with a depolarization ratio equal to or greater than 0.75 is called a '''{{dfn|depolarized band}}'''.<ref name=Banwell>{{cite book |last1= Banwell |first1= Colin N. |last2= McCash |first2= Elaine M. |date= 1994 |title= Fundamentals of Molecular Spectroscopy |edition= 4th |publisher= McGraw–Hill |pages= 117–118 |isbn= 0-07-707976-0 }}</ref><ref>{{cite book |last1= Atkins |first1= Peter |last2= de Paula |first2= Julio |date= 2006 |title= Physical Chemistry |edition= 8th |publisher= W. H. Freeman |page= [https://archive.org/details/atkinsphysicalch00pwat/page/464 464] |isbn= 0-7167-8759-8 |author-link= Peter Atkins |url-access= registration |url= https://archive.org/details/atkinsphysicalch00pwat/page/464 }}</ref>

For a [[spherical top]] molecule in which all three axes are equivalent, symmetric vibrations have Raman spectral bands which are completely polarized ({{math|1=''ρ'' = 0}}). An example is the symmetric stretching or "breathing" mode of [[methane]] ({{chem2|CH4}}) in which all four {{chem2|C\sH}} bonds vibrate in phase. However, for the asymmetric mode in which one {{chem2|C\sH}} bond stretches while the other three contract, the Raman scattered radiation is depolarized.<ref name=Banwell/>

For molecules of lower symmetry ([[Rotational spectroscopy#Classification of molecular rotors|symmetric tops or asymmetric tops]]), a vibration with the full [[molecular symmetry|symmetry of the molecule]] leads to a polarized or partially polarized Raman band ({{math|''ρ'' < 0.75}}), while a less symmetric vibration yields a depolarized band ({{math|''ρ'' ≥ 0.75}}).<ref name=Banwell/>

==References==
<references/>

{{Raman spectroscopy|state=expanded}}

[[Category:Raman spectroscopy]]
[[Category:Ratios]]


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