The Lorentz oscillator model describes the optical response of bound charges. The model is named after the Dutch physicist Hendrik Antoon Lorentz. It is a classical, phenomenological model for materials with characteristic resonance frequencies (or other characteristic energy scales) for optical absorption, e.g. ionic and molecular vibrations, interband transitions (semiconductors), phonons, and collective excitations.[1][2]
![](http://upload.wikimedia.org/wikipedia/commons/thumb/b/b9/Atom-spring.svg/220px-Atom-spring.svg.png)
Derivation of electron motion
editThe model is derived by modeling an electron orbiting a massive, stationary nucleus as a spring-mass-damper system.[2][3][4] The electron is modeled to be connected to the nucleus via a hypothetical spring and its motion is damped by via a hypothetical damper. The damping force ensures that the oscillator's response is finite at its resonance frequency. For a time-harmonic driving force which originates from the electric field, Newton's second law can be applied to the electron to obtain the motion of the electron and expressions for the dipole moment, polarization, susceptibility, and dielectric function.[4]
Equation of motion for electron oscillator:
where
- is the displacement of charge from the rest position,
- is time,
- is the relaxation time/scattering time,
- is a constant factor characteristic of the spring,
- is the effective mass of the electron,
- is the resonance frequency of the oscillator,
- is the elementary charge,
- is the electric field.
For time-harmonic fields:
The stationary solution of this equation of motion is:
The fact that the above solution is complex means there is a time delay (phase shift) between the driving electric field and the response of the electron's motion.[4]
Dipole moment
editThe displacement, , induces a dipole moment, , given by
is the polarizability of single oscillator, given by
Polarization
editThe polarization is the dipole moment per unit volume. For macroscopic material properties N is the density of charges (electrons) per unit volume. Considering that each electron is acting with the same dipole moment we have the polarization as below
Electric displacement
editThe electric displacement is related to the polarization density by
Dielectric function
editThe complex dielectric function is given by where and is the so-called plasma frequency.
In practice, the model is commonly modified to account for multiple absorption mechanisms present in a medium. The modified version is given by[6] where and
- is the value of the dielectric function at infinite frequency, which can be used as an adjustable parameter to account for high frequency absorption mechanisms,
- and is related to the strength of the th absorption mechanism,
- .
Separating the real and imaginary components,
Complex conductivity
editThe complex optical conductivity in general is related to the complex dielectric function
Substituting the formula of in the equation above we obtain
Separating the real and imaginary components,
See also
editReferences
edit- ^ Lorentz, Hendrik Antoon (1909). The theory of electrons and its applications to the phenomena of light and radiant heat. Vol. Bd. XXIX, Bd. 29. New York; Leipzig: B.G. Teubner. OCLC 535812.
- ^ a b Dressel, Martin; Grüner, George (2002). "Semiconductors". Electrodynamics of Solids: Optical Properties of Electrons in Matter. Cambridge. pp. 136–172. doi:10.1017/CBO9780511606168.008. ISBN 9780521592536.
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: CS1 maint: location missing publisher (link) - ^ Almog, I. F.; Bradley, M. S.; Bulovic, V. (2011). "The Lorentz Oscillator and its Applications" (PDF). Massachusetts Institute of Technology, Department of Electrical Engineering and Computer Science. Massachusetts Institute of Technology. Retrieved 2021-11-24.
- ^ a b c Colton, John (2020). "Lorentz Oscillator Model" (PDF). Brigham Young University, Department of Physics & Astronomy. Brigham Young University. Retrieved 2021-11-18.
- ^ Spitzer, W. G.; Kleinman, D.; Walsh, D. (1959). "Infrared Properties of Hexagonal Silicon Carbide". Physical Review. 113 (1): 127–132. Bibcode:1959PhRv..113..127S. doi:10.1103/PhysRev.113.127. Retrieved 2021-11-24.
- ^ Zhang, Z. M.; Lefever-Button, G.; Powell, F. R. (1998). "Infrared Refractive Index and Extinction Coefficient of Polyimide Films". International Journal of Thermophysics. 19 (3): 905–916. doi:10.1023/A:1022655309574. S2CID 116271335. Retrieved 2021-11-24.