Lindhard theory

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In condensed matter physics, Lindhard theory[1] is a method of calculating the effects of electric field screening by electrons in a solid. It is based on quantum mechanics (first-order perturbation theory) and the random phase approximation. It is named after Danish physicist Jens Lindhard, who first developed the theory in 1954.[2][3][4]

Thomas–Fermi screening, plasma oscillations and Friedel oscillations can be derived as a special case of the more general Lindhard formula. In particular, Thomas–Fermi screening is the limit of the Lindhard formula when the wavevector (the reciprocal of the length-scale of interest) is much smaller than the Fermi wavevector, i.e. the long-distance limit.[1] The Lorentz–Drude expression for the plasma oscillations are recovered in the dynamic case (long wavelengths, finite frequency).

This article uses cgs-Gaussian units.

Lindhard function

Static Lindhard function F(x). Its derivative has a logarithmic divergence at x=1 (dashed line).

The term

χ(𝐪,ω)=∑𝐤f𝐤+𝐪−f𝐤ℏ(ω+iδ)+E𝐤+q−E𝐤

is a response function known as Lindhard function. Here f𝐤 is the Fermi–Dirac distribution function for electrons in thermodynamic equilibrium, E𝐤=ℏ2k2/2m is the kinetic energy with wave vector 𝐤, m is the electron mass and δ is a positive infinitesimal constant,.

Zero temperature functions

At zero temperature, f𝐤(T=0)=Θ(kF−|𝐤|) is a Heaviside step function, where k𝐅 is the Fermi wave vector associated to the Fermi energy EF=ℏ2kF2/2m. The sum can be carried out in the continuous limit using analytic continuation, resulting in χ(𝐪,ω)=ℱ(|𝐪|/2kF,iℏ(ω+iδ)/4EF), where in 3 dimensions can be written as[5]

ℱ(x,y)=12+18x[1−(x−yx)2]log⁡|x−y/x+1x−y/x−1|+18x[1−(x+yx)2]log⁡|x+y/x+1x+y/x−1|.

In the static limit, when ω→0, we have that χ(𝐪,0)=ℱ(|𝐪|/2kF,0)=F(|𝐪|/2k𝐅), where

F(x)=12+1−x24xlog⁡|x+1x−1|

is the (static) Lindhard function.[6] This function derivative diverges at x=1. Also F(x→0)=1. Note that F(x) also appears in the calculation of the ground state energy of jellium when using Hartree–Fock method.[7]

Formula for the dielectric function

The electron-electron Coulomb potential V(𝐫)=e2/|𝐫|, where e is the elementary charge, can be written in Fourier space as V𝐪=4πe2/|𝐪|2 (where 𝐪 is the wave vector), then the effective single particle potential is

Veff(𝐪)=V𝐪ϵ(𝐪).

The Lindhard formula for the longitudinal dielectric function is then given by

ϵ(𝐪,ω)=1−V𝐪χ(𝐪,ω),

where χ(𝐪,ω) is Lindhard function.

This Lindhard formula is valid also for nonequilibrium distribution functions. It can be obtained by first-order perturbation theory and the random phase approximation (RPA).

To understand the Lindhard formula, consider some limiting cases in 2 and 3 dimensions. The 1-dimensional case is also considered in other ways.

Long wavelength limit

In the long wavelength limit (𝐪→0), Lindhard function reduces to

ϵ(𝐪=0,ω)≈1−ωpl2ω2,

where ωpl2=4πe2NL3m is the three-dimensional plasma frequency (in SI units, replace the factor 4π by 1/ϵ0.) For two-dimensional systems,

ωpl2(𝐪)=2πe2nqϵm.

This result recovers the plasma oscillations from the classical dielectric function from Drude model and from quantum mechanical free electron model.

Template:Math proof Template:Hidden begin First, consider the long wavelength limit (q→0).

For the denominator of the Lindhard formula,

E𝐤+𝐪−E𝐤=ℏ22m(k2+2𝐤⋅𝐪+q2)−ℏ2k22m≃ℏ2𝐤⋅𝐪m,

and for the numerator,

f𝐤+𝐪−f𝐤≃𝐪⋅∇𝐤f𝐤.

Inserting these into the Lindhard formula and taking the limit of δ→0, we obtain

ϵ(0,ω)≃1+V𝐪∑𝐤,iqi∂f𝐤∂kiℏω0−ℏ2𝐤⋅𝐪m≃1+V𝐪ℏω0∑𝐤,iqi∂f𝐤∂ki(1+ℏ𝐤⋅𝐪mω0)≃1+V𝐪ℏω0∑𝐤,iqi∂f𝐤∂kiℏ𝐤⋅𝐪mω0=1+V𝐪ℏω02∫d2k(L2π)2∑i,jqi∂f𝐤∂kiℏkjqjmω0=1+V𝐪L2mω022∫d2k(2π)2∑i,jqiqjkj∂f𝐤∂ki=1+V𝐪L2mω02∑i,jqiqj2∫d2k(2π)2kj∂f𝐤∂ki=1−V𝐪L2mω02∑i,jqiqjnδij=1−2πe2ϵqL2L2mω02q2n=1−ωpl2(𝐪)ω02,

where we used E𝐤=ℏϵ𝐤, V𝐪=2πe2ϵqL2 and ωpl2(𝐪)=2πe2nqϵm. Template:Hidden end

Static limit

Consider the static limit (ω+iδ→0).

The Lindhard formula becomes

ϵ(𝐪,ω=0)=1−V𝐪∑𝐤f𝐤+𝐪−f𝐤E𝐤+𝐪−E𝐤.

Inserting the above equalities for the denominator and numerator, we obtain

ϵ(𝐪,0)=1−V𝐪∑𝐤,iqi∂f∂kiℏ2𝐤⋅𝐪m=1−V𝐪∑𝐤,iqi∂f∂kiℏ2𝐤⋅𝐪m.

Assuming a thermal equilibrium Fermi–Dirac carrier distribution, we get

∑iqi∂f𝐤∂ki=−∑iqi∂f𝐤∂μ∂E𝐤∂ki=−∑iqikiℏ2m∂f𝐤∂μ

here, we used E𝐤=ℏ2k22m and ∂E𝐤∂ki=ℏ2kim.

Therefore,

ϵ(𝐪,0)=1+V𝐪∑𝐤,iqikiℏ2m∂f𝐤∂μℏ2𝐤⋅𝐪m=1+V𝐪∑𝐤∂f𝐤∂μ=1+4πe2ϵq2∂∂μ1L3∑𝐤f𝐤=1+4πe2ϵq2∂∂μNL3=1+4πe2ϵq2∂n∂μ≡1+κ2q2.

Here, κ is the 3D screening wave number (3D inverse screening length) defined as

κ=4πe2ϵ∂n∂μ.

Then, the 3D statically screened Coulomb potential is given by

Vs(𝐪,ω=0)≡V𝐪ϵ(𝐪,0)=4πe2ϵq2L3q2+κ2q2=4πe2ϵL31q2+κ2.

And the inverse Fourier transformation of this result gives

Vs(r)=∑𝐪4πe2L3(q2+κ2)ei𝐪⋅𝐫=e2re−κr

known as the Yukawa potential. Note that in this Fourier transformation, which is basically a sum over all 𝐪, we used the expression for small |𝐪| for every value of 𝐪 which is not correct.

Statically screened potential(upper curved surface) and Coulomb potential(lower curved surface) in three dimensions

For a degenerated Fermi gas (T=0), the Fermi energy is given by

EF=ℏ22m(3π2n)23,

So the density is

n=13π2(2mℏ2EF)32.

At T=0, EF≡μ, so ∂n∂μ=32nEF.

Inserting this into the above 3D screening wave number equation, we obtain

κ=4πe2ϵ∂n∂μ=6πe2nϵEF.

This result recovers the 3D wave number from Thomas–Fermi screening.

For reference, Debye–Hückel screening describes the non-degenerate limit case. The result is κ=4πe2nβϵ, known as the 3D Debye–Hückel screening wave number.

In two dimensions, the screening wave number is

κ=2πe2ϵ∂n∂μ=2πe2ϵmℏ2π(1−e−ℏ2βπn/m)=2me2ℏ2ϵfk=0.

Note that this result is independent of n.


Template:Hidden begin Consider the static limit (ω+iδ→0). The Lindhard formula becomes

ϵ(𝐪,0)=1−V𝐪∑𝐤f𝐤−𝐪−f𝐤E𝐤−𝐪−E𝐤.

Inserting the above equalities for the denominator and numerator, we obtain

ϵ(𝐪,0)=1−V𝐪∑𝐤,i−qi∂f∂ki−ℏ2𝐤⋅𝐪m=1−V𝐪∑𝐤,iqi∂f∂kiℏ2𝐤⋅𝐪m.

Assuming a thermal equilibrium Fermi–Dirac carrier distribution, we get

∑iqi∂f𝐤∂ki=−∑iqi∂f𝐤∂μ∂E𝐤∂ki=−∑iqikiℏ2m∂f𝐤∂μ.

Therefore,

ϵ(𝐪,0)=1+V𝐪∑𝐤,iqikiℏ2m∂f𝐤∂μℏ2𝐤⋅𝐪m=1+V𝐪∑𝐤∂f𝐤∂μ=1+2πe2ϵqL2∂∂μ∑𝐤f𝐤=1+2πe2ϵq∂∂μNL2=1+2πe2ϵq∂n∂μ≡1+κq.

κ is 2D screening wave number(2D inverse screening length) defined as

κ=2πe2ϵ∂n∂μ.

Then, the 2D statically screened Coulomb potential is given by

Vs(𝐪,ω=0)≡V𝐪ϵ(𝐪,0)=2πe2ϵqL2qq+κ=2πe2ϵL21q+κ.

It is known that the chemical potential of the 2-dimensional Fermi gas is given by

μ(n,T)=1βln⁡(eℏ2βπn/m−1),

and ∂μ∂n=ℏ2πm11−e−ℏ2βπn/m. Template:Hidden end

Formula for the magnetic susceptibility

As with the dielectric function, the magnetic susceptibility χ𝐌 for an electron gas can be calculated as

χM(𝐪,ω)=2μB2χ(𝐪,ω)

where μB is the Bohr magneton.[6]

In the static limit,

χM(𝐪,ω)≈2μB2∫|𝐤|<kF(∂f𝐤∂E𝐤)d3k=μB2mkFπ,

which corresponds to the spin susceptibility of Pauli paramagnetism.[6]

Screening experiments on one dimensional systems

This time, consider some generalized case for lowering the dimension. The lower the dimension is, the weaker the screening effect. In lower dimension, some of the field lines pass through the barrier material wherein the screening has no effect. For the 1-dimensional case, we can guess that the screening affects only the field lines which are very close to the wire axis.

In real experiment, we should also take the 3D bulk screening effect into account even though we deal with 1D case like the single filament. The Thomas–Fermi screening has been applied to an electron gas confined to a filament and a coaxial cylinder.[8] For a K2Pt(CN)4Cl0.32·2.6H20 filament, it was found that the potential within the region between the filament and cylinder varies as e−keffr/r and its effective screening length is about 10 times that of metallic platinum.[8]

See also

References

Template:Reflist

General

  1. ↑ 1.0 1.1 N. W. Ashcroft and N. D. Mermin, Solid State Physics (Thomson Learning, Toronto, 1976)
  2. ↑ Template:Cite journal
  3. ↑ Template:Cite journal
  4. ↑ Template:Cite journal
  5. ↑ Template:Cite book
  6. ↑ 6.0 6.1 6.2 Template:Cite book
  7. ↑ Template:Cite book
  8. ↑ 8.0 8.1 Template:Cite journal