Green's function (many-body theory)
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In many-body theory, the term Green's function (or Green function) is sometimes used interchangeably with correlation function, but refers specifically to correlators of field operators or creation and annihilation operators.
The name comes from the Green's functions used to solve inhomogeneous differential equations, to which they are loosely related. (Specifically, only two-point 'Green's functions' are Green's functions in the mathematical sense; the linear operator that they invert is the part of the Hamiltonian operator that is quadratic in the fields.)
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[edit] Spatially uniform case
[edit] Basic definitions
Throughout, ζ is + 1 for bosons and − 1 for fermions and denotes either a commutator or anticommutator as appropriate.
The signs of the Green functions have been chosen so that the thermal Green function for a free particle is
and the retarded Green function is
In this section, functions will have their arguments abbreviated as single numbers: and
will be replaced by n.
The imaginary-time Heisenberg operators can be written in terms of Schrödinger operators as
where K = H − μN is the grand-canonical Hamiltonian. Similarly, for the real-time operators,
and .
In imaginary time, the general Green function is defined by
where n signifies . (The imaginary-time variables τn are restricted to the range 0 to β.)
In real time, the definition is
where n signifies .
[edit] Two-point functions
The Green function with a single pair of arguments (n = 1) is referred to as the two-point function, or propagator. In the presence of translational symmetry, it depends only on the difference of its arguments. Taking the Fourier transform with respect to both space and time gives
where the sum is over the appropriate Matsubara frequencies (and the integral involves an implicit factor of (2π) − d, as usual).
In real time, we will explicitly indicate the time-ordered function with a superscript T:
The real-time two-point Green function can be written in terms of `retarded' and `advanced' Green functions, which will turn out to have simpler analyticity properties. The retarded and advanced Green functions are defined by
and
respectively.
They are related to the time-ordered Green function by
where
is the Bose-Einstein or Fermi-Dirac distribution function.
[edit] Imaginary-time ordering and β-periodicity
The thermal Green functions are defined only when both imaginary-time arguments are within the range 0 to β. The two-point Green function has the following properties. (The position or momentum arguments are suppressed in this section.)
Firstly, it depends only on the difference of the imaginary times:
The argument τ − τ' is allowed to run from − β to β.
Secondly, is periodic under shifts of β. Because of the small domain within which the function is defined, this means just
for 0 < τ < β. (Note that the function is antiperiodic for fermions.) Time ordering is crucial for this property, which can be proved straightforwardly, using the cyclicity of the trace operation.
These two properties allow for the Fourier transform representation and its inverse,
Finally, note that has a discontinuity at τ = 0; this is consistent with a long-distance behaviour of
.
[edit] Spectral representation
The propagators in real and imaginary time can both be related to the spectral density (or spectral weight), given by
where refers to a (many-body) eigenstate of the grand-canonical Hamiltonian H − μN, with eigenvalue Eα.
The imaginary-time propagator is then given by
and the retarded propagator by
where the limit as is implied.
The advanced propagator is given by the same expression, but with − iη in the denominator. The time-ordered function can be found in terms of GR and GA. As claimed above, GR(ω) and GA(ω) have simple analyticity properties: the former (latter) has all its poles and discontinuities in the lower (upper) half-plane. The thermal propagator has all its poles and discontinuities on the imaginary ωn axis.
The spectral density can be found very straightforwardly from GR, using the identity
This gives
This furthermore implies that obeys the following relationship between its real and imaginary parts:
where P denotes the principal value of the integral.
The spectral density obeys a sum rule:
which gives
as .
[edit] Hilbert transform
The similarity of the spectral representations of the imaginary- and real-time Green functions allows us to define the function
which is related to and GR by
and
A similar expression obviously holds for GA.
The relation between and
is referred to as a Hilbert transform.
[edit] Proof of spectral representation
We demonstrate the proof of the spectral representation of the propagator in the case of the thermal Green function, defined as
Due to translational symmetry, it is only necessary to consider for τ > 0, given by
Inserting a complete set of eigenstates gives
Since and
are eigenstates of H − μN, the Heisenberg operators can be rewritten in terms of Schr\"odinger operators, giving
Performing the Fourier transform then gives
Momentum conservation allows the final term to be written as (up to possible factors of the volume)
which confirms the expressions for the Green functions in the spectral representation.
The sum rule can be proved by considering the expectation value of the commutator,
and then inserting a complete set of eigenstates into both terms of the commutator:
Swapping the labels in the first term then gives
which is exactly the result of the integration of ρ.
[edit] Non-interacting case
In the non-interacting case, is an eigenstate with (grand-canonical) energy
, where
is the single-particle dispersion relation measured with respect to the chemical potential. The spectral density therefore becomes
From the commutation relations,
with possible factors of the volume again. The sum, which involves the thermal average of the number operator, then gives simply , leaving
The imaginary-time propagator is thus
and the retarded propagator is
[edit] Zero-temperature limit
As , the spectral density becomes
where α = 0 corresponds to the ground state. Note that only the first (second) term contributes when ω is positive (negative).
[edit] General case
[edit] Basic definitions
We can use `field operators' as above, or creation and annihilation operators associated with other single-particle states, perhaps eigenstates of the (noninteracting) kinetic energy. We then use
where ψα is the annihilation operator for the single-particle state α and is that state's wavefunction in the position basis. This gives
with a similar expression for G(n).
[edit] Two-point functions
These depend only on the difference of their time arguments, so that
and
We can again define retarded and advanced functions in the obvious way; these are related to the time-ordered function in the same way as above.
The same periodicity properties as described in above apply to . Specifically,
and
for τ < 0.
[edit] Spectral representation
In this case,
where m and n are many-body states.
The expressions for the Green functions are modified in the obvious ways:
and
Their analyticity properties are identical. The proof follows exactly the same steps, except that the two matrix elements are no longer complex conjugates.
[edit] Noninteracting case
If the particular single-particle states that are chosen are `single-particle energy eigenstates', ie,
then for an eigenstate:
so is :
and so is :
We therefore have
where
We then rewrite
and use the fact that the thermal average of the number operator gives the Bose-Einstein or Fermi-Dirac distribution function.
Finally, the spectral density simplifies to give
- ραβ = 2πδ(ξβ − ω)δαβ,
so that the thermal Green function is
and the retarded Green function is
Note that the noninteracting Green function is diagonal, but this will not be true in the interacting case.
[edit] References
- Negele, J.W. and Orland, H.: Quantum Many-Particle Systems AddisonWesley (1988).
- Abrikosov, A.A., Gorkov, L.P. and Dryaloshinski, I.E.: Methods of Quantum Field Theory in Statistical Physics Englewood Cliffs: Prentice-Hall (1963).