Physics:Lorentz oscillator model

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Short description: Theoretical model describing the optical response of bound charges


Electrons are bound to the atomic nucleus analogously to springs of different strengths, AKA springs that are not isotropic, AKA anisotropic.

The Lorentz oscillator model (classical electron oscillator or CEO 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]

Derivation of electron motion

The 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: 𝐅net=𝐅damping+𝐅spring+𝐅driving=md2𝐫dt2mτd𝐫dtk𝐫e𝐄(t)=md2𝐫dt2d2𝐫dt2+1τd𝐫dt+ω02𝐫=em𝐄(t)

where

  • 𝐫 is the displacement of charge from the rest position,
  • t is time,
  • τ is the relaxation time/scattering time,
  • k is a constant factor characteristic of the spring,
  • m is the effective mass of the electron,
  • ω0=k/m is the resonance frequency of the oscillator,
  • e is the elementary charge,
  • 𝐄(t) is the electric field.

For time-harmonic fields: 𝐄(t)=𝐄0eiωt 𝐫(t)=𝐫0eiωt

The stationary solution of this equation of motion is: 𝐫(ω)=emω02ω2iω/τ𝐄(ω)

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

The displacement, 𝐫, induces a dipole moment, 𝐩, given by 𝐩(ω)=e𝐫(ω)=α^(ω)𝐄(ω).

α^(ω) is the polarizability of single oscillator, given by α^(ω)=e2m1(ω02ω2)iω/τ.

Three distinct scattering regimes can be interpreted corresponding to the dominant denominator term in the dipole moment:[5]

Regime Condition Dispersion Scaling Phase Shift
Thomson scattering ω2ωτ,ω02 1
Shneider-Miles scattering ωτ|ω02ω2| ω2 90°
Rayleigh scattering ω02ω2,ωτ ω4 180°

Polarization

The polarization 𝐏 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 𝐏=N𝐩=Nα^(ω)𝐄(ω).

Electric displacement

The electric displacement 𝐃 is related to the polarization density 𝐏 by 𝐃=ε^𝐄=𝐄+4π𝐏=(1+4πNα^)𝐄

Dielectric function

Lorentz oscillator model. The real (blue solid line) and imaginary (orange dashed line) components of relative permittivity are plotted for a single oscillator model with parameters ω0=23.8THz (12.6 μm), s/ω02=3.305, Γ/ω0=0.006, and ε=6.7. These parameters approximate hexagonal silicon carbide.[6]

The complex dielectric function is given the following (in Gaussian units): ε^(ω)=1+4πNe2m1(ω02ω2)iω/τ where 4πNe2/m=ωp2 and ωp 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[7] ε^(ω)=ε+jχjL(ω;ω0,j) where χjL(ω;ω0,j)=sjω0,j2ω2iΓjω and

  • ε 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,
  • sj=ωp2fj and fj is related to the strength of the jth absorption mechanism,
  • Γj=1/τ.

Separating the real and imaginary components, ε^(ω)=ε1(ω)+iε2(ω)=[ε+jsj(ω0,j2ω2)(ω0,j2ω2)2+(Γjω)2]+i[jsj(Γjω)(ω0,j2ω2)2+(Γjω)2]

Complex conductivity

The complex optical conductivity in general is related to the complex dielectric function (in Gaussian units) as σ^(ω)=ω4πi(ε^(ω)1)

Substituting the formula of ε^(ω) in the equation above we obtain σ^(ω)=Ne2mωω/τ+i(ω02ω2)

Separating the real and imaginary components, σ^(ω)=σ1(ω)+iσ2(ω)=Ne2mω2τ(ω02ω2)2+ω2/τ2iNe2m(ω02ω2)ω(ω02ω2)2+ω2/τ2

See also

References

  1. Lorentz, Hendrik Antoon (1909) (in en). The theory of electrons and its applications to the phenomena of light and radiant heat. Bd. XXIX;Bd. 29. New York; Leipzig: B.G. Teubner. OCLC 535812. 
  2. 2.0 2.1 Dressel, Martin; Grüner, George (2002). "Semiconductors" (in en). Electrodynamics of Solids: Optical Properties of Electrons in Matter. Cambridge. pp. 136–172. doi:10.1017/CBO9780511606168.008. ISBN 9780521592536. 
  3. Almog, I. F.; Bradley, M. S.; Bulovic, V. (2011). "The Lorentz Oscillator and its Applications". Massachusetts Institute of Technology. https://ocw.mit.edu/courses/electrical-engineering-and-computer-science/6-007-electromagnetic-energy-from-motors-to-lasers-spring-2011/readings/MIT6_007S11_lorentz.pdf. 
  4. 4.0 4.1 4.2 Colton, John (2020). "Lorentz Oscillator Model". Brigham Young University. https://physics.byu.edu/faculty/colton/docs/phy442-resources/Lorentz-oscillator-model.pdf. 
  5. Patel, Adam (2021). "Thomson and collisional regimes of in-phase coherent microwave scattering off gaseous microplasmas". Scientific Reports 11 (1): 23389. doi:10.1038/s41598-021-02500-y. PMID 34862396. Bibcode2021NatSR..1123389P. 
  6. Spitzer, W. G.; Kleinman, D.; Walsh, D. (1959). "Infrared Properties of Hexagonal Silicon Carbide". Physical Review 113 (1): 127–132. doi:10.1103/PhysRev.113.127. Bibcode1959PhRv..113..127S. https://doi.org/10.1103/PhysRev.113.127. Retrieved 2021-11-24. 
  7. 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. https://doi.org/10.1023/A:1022655309574. Retrieved 2021-11-24.