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Clausius–Mossotti relationFrom Wikipedia, the free encyclopedia
The Clausius–Mossotti relation is named after the Italian physicist Ottaviano-
Fabrizio Mossotti, whose 1850 book[1] analyzed the relationship between the
dielectric constants of two different media, and the German physicist Rudolf
Clausius, who gave the formula explicitly in his 1879 book[2] in the context not of
dielectric constants but of indices of refraction. The same formula also arises in
the context of conductivity, in which it is known as Maxwell's formula. It arises
yet again in the context of refractivity, in which it is known as the Lorentz–
Lorenz equation.
The Clausius–Mossotti law applies to the dielectric constant of a dielectric that is
perfect, homogeneous and isotropic. It is the second of the following three
equalities:[3][4]
where
is the dielectric constant of a substance
is the permittivity of a vacuum
is the molar mass of the substance
is its density
is Avogadro's number,
is the molecular polarizability in SI-units (C·m2/V) and
is the molecular polarizability volume (m3 in SI) or the
polarizability in the CGS system of units.[4]
Contents [hide]
1 Clausius–Mossotti factor
2 Derivation
3 Richard Feynman on the Clausius–Mossotti equation
4 Dielectric constant and polarizability
5 References
Clausius–Mossotti factor [edit]
The Clausius–Mossotti factor can be expressed in terms of complex
permittivities:[5][6][7]
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![Page 2: En Wikipedia Org Wiki Clausius–Mossotti Relation](https://reader037.vdocuments.us/reader037/viewer/2022100216/577cbf841a28aba7118dec0c/html5/thumbnails/2.jpg)
where
is the permittivity (the subscript p refers to a lossless dielectric sphere
suspended in a medium m)
is the conductivity
is the angular frequency of the applied electric field
i is the imaginary unit, the square root of -1
In the context of electrokinetic manipulation, the real part of the Clausius–
Mossotti factor is a determining factor for the dielectrophoretic force on a
particle, whereas the imaginary part is a determining factor for the
electrorotational torque on the particle. Other factors are, of course, the
geometries of the particle to be manipulated and the electric field. Whereas
can be directly measured by application of different AC potentials
directly on electrodes,[8] can be measured by electro-rotation
measurements thanks to optical trapping methods.
Derivation [edit]
Assume a simple cubic lattice of polarisable points with polarisability .
Application of an external field will induce a dipole at each site . Due to
symmetry, the local (microscopic) field inside lattice is identical at each lattice
point: .
Away from the lattice points, the electric field is given by:
where the dipole electric field
Richard Feynman on the Clausius–Mossotti equation[edit]
In his Lectures on Physics (Vol.2, Ch32), Richard Feynman has a background
discussion deriving the Clausius–Mossotti Equation, in reference to the index of
refraction for dense materials. He starts with the derivation of an equation for
the index of refraction for gases, and then shows how this must be modified for
dense materials, modifying it, because in dense materials, there are also
electric fields produced by other nearby atoms, creating local fields. In essence,
Feynman is saying that for dense materials the polarization of a material is
proportional to its electric field, but that it has a different constant of
proportionality than that for a gas. When this constant is corrected for a dense
material, by taking into account the local fields of nearby atoms, one ends up
with the Clausius–Mossotti Equation.[9] Feynman states the Clausius–Mossotti
equation as follows:
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,
where
is the number of particles per unit volume of the capacitor,
is the atomic polarizability,
is the refractive index.
Feynman discusses "atomic polarizability" and explains it in these terms: When
there is a sinusoidal electric field acting on a material, there is an induced dipole
moment per unit volume which is proportional to the electric field - with a
proportionality constant that depends on the frequency. This constant is a
complex number, meaning that the polarization does not exactly follow the
electric field, but may be shifted in phase to some extent. At any rate, there is a
polarization per unit volume whose magnitude is proportional to the strength of
the electric field.
Dielectric constant and polarizability [edit]
The polarizability , of an atom is defined in terms of the local electric field at
the atom by
where
is the dipole moment,
is the local electric field at the orbital[clarification needed]
The polarizability is an atomic property, but the dielectric constant will depend
on the manner in which the atoms are assembled to form a crystal. For a non-
spherical atom, will be a tensor.[10]
The polarization of a crystal may be expressed approximately as the product of
the polarizabilities of the atoms times the local electric field:
Now, to relate the dielectric constant to the polarizability, which is what the
Clausius–Mossotti equation (or relation) is all about,[10] one must consider that
the results will depend on the relation that holds between the macroscopic
electric field and the local electric field:
where
is the concentration,
is the polarizability of atoms j,
Local Electrical Field at atom sites .
References [edit]
1. ^ Mossotti, O. F. (1850). Mem. di mathem. e fisica in Modena. 24 11. p. 49.
2. ^ Clausius, R. (1879). Die mechanische U’grmetheorie. 2. p. 62.
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3. ^ Rysselberghe, P. V. (January 1932). "Remarks concerning the Clausius–Mossotti Law". J. Phys. Chem. 36 (4): 1152–1155. doi:10.1021/j150334a007 .
4. ^ a b Atkins, Peter; de Paula, Julio (2010). "Chapter 17". Atkins' PhysicalChemistry. Oxford University Press. p. 622-629. ISBN 978-0-19-954337-3.
5. ^ Hughes, Michael Pycraft (2000). "AC electrokinetics: applications fornanotechnology" . Nanotechnology 11 (2): 124–132.Bibcode:2000Nanot..11..124P . doi:10.1088/0957-4484/11/2/314 .
6. ^ Markov, Konstantin Z. (2000). "Elementary Micromechanics of HeterogeneousMedia". In Konstantin Z. Markov and Luigi Preziosi. 'Heterogeneous Media:Modelling and Simulation' . Boston: Birkhauser. pp. 1–162. ISBN 978-0-8176-4083-5.
7. ^ Gimsa, J. (2001). "Characterization of particles and biological cells by AC-electrokinetics". In A.V. Delgado. Interfacial Electrokinetics and Electrophoresis.New York: Marcel Dekker Inc. pp. 369–400. ISBN 0-8247-0603-X.
8. ^ T. Honegger, K. Berton, E. Picard et D. Peyrade. Determination of Clausius–Mossotti factors and surface capacitances for colloidal particles. Appl. Phys.Lett., vol. 98, no. 18, page 181906, 2011.
9. ^ Feynman, R. P., Leighton, R. B.; Sands, M (1989). Feynman Lectures onPhysics. Vol. 2, chap. 32 (Refractive Index of Dense Materials), sec. 3: AddisonWesley. ISBN 0-201-50064-7.
10. ^ a b Kittel, Charles (1995). Introduction to Solid State Physics (8th ed.). Wiley.ISBN 0-471-41526-X.
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