Physics:Kubo formula

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Short description: Quantum mechanics mathematical equation

The Kubo formula, named for Ryogo Kubo who first presented the formula in 1957,[1][2] is an equation which expresses the linear response of an observable quantity due to a time-dependent perturbation.

Among numerous applications of the Kubo formula, one can calculate the charge and spin susceptibilities of systems of electrons in response to applied electric and magnetic fields. Responses to external mechanical forces and vibrations can be calculated as well.

General Kubo formula

Consider a quantum system described by the (time independent) Hamiltonian H0. The expectation value of a physical quantity at equilibrium temperature T, described by the operator A^, can be evaluated as:

⟨A^⟩=1Z0Tr⁡[ρ^0A^]=1Z0∑n⟨n|A^|n⟩e−βEn,

where β=1/kBT is the thermodynamic beta, ρ^0 is density operator, given by

ρ^0=e−βH^0=∑n|n⟩⟨n|e−βEn

and Z0=Tr⁡[ρ^0] is the partition function.

Suppose now that just after some time t=t0 an external perturbation is applied to the system. The perturbation is described by an additional time dependence in the Hamiltonian:

H^(t)=H^0+V^(t)θ(t−t0),

where θ(t) is the Heaviside function (1 for positive times, 0 otherwise) and V^(t) is hermitian and defined for all t, so that H^(t) has for positive t−t0 again a complete set of real eigenvalues En(t). But these eigenvalues may change with time.

However, one can again find the time evolution of the density matrix ρ^(t) rsp. of the partition function Z(t)=Tr⁡[ρ^(t)], to evaluate the expectation value of

⟨A^⟩=Tr⁡[ρ^(t)A^]Tr⁡[ρ^(t)].

The time dependence of the states |n(t)⟩ is governed by the Schrödinger equation

iℏ∂∂t|n(t)⟩=H^(t)|n(t)⟩,

which thus determines everything, corresponding of course to the Schrödinger picture. But since V^(t) is to be regarded as a small perturbation, it is convenient to now use instead the interaction picture representation, |n^(t)⟩, in lowest nontrivial order. The time dependence in this representation is given by |n(t)⟩=e−iH^0t/ℏ|n^(t)⟩=e−iH^0t/ℏU^(t,t0)|n^(t0)⟩, where by definition for all t and t0 it is: |n^(t0)⟩=eiH^0t0/ℏ|n(t0)⟩

To linear order in V^(t), we have

U^(t,t0)=1−iℏ∫t0tdt′V^(t′).

Thus one obtains the expectation value of A^(t) up to linear order in the perturbation:

⟨A^(t)⟩=⟨A^⟩0−iℏ∫t0tdt′1Z0∑ne−βEn⟨n(t0)|A^(t)V^(t′)−V^(t′)A^(t)|n(t0)⟩,

thus[3]

Kubo formula (general)

⟨A^(t)⟩=⟨A^⟩0−iℏ∫t0tdt′⟨[A^(t),V^(t′)]⟩0


The brackets ⟨⟩0 mean an equilibrium average with respect to the Hamiltonian H0. Therefore, although the result is of first order in the perturbation, it involves only the zeroth-order eigenfunctions, which is usually the case in perturbation theory and moves away all complications which otherwise might arise for t>t0.

The above expression is true for any kind of operators. (see also Second quantization)[4]

Full Derivation of the Kubo formula

An alternative derivation of the Kubo formula begins with the time-dependent Schrödinger equation for a pure state,

iℏ∂∂t|ψ(t)⟩=H^(t)|ψ(t)⟩.

Define the unitary time-evolution operator by

U^(t,t0)|ψ(t0)⟩=|ψ(t)⟩,U^(t0,t0)=I^.

The Schrödinger equation then implies

iℏ∂U^(t,t0)∂t=H^(t)U^(t,t0).

For the time-independent unperturbed Hamiltonian H^0, define

U^0(t)=e−itH^0/ℏ.

Suppose that the complete Hamiltonian is

H^(t)=H^0−F(t)A^,

where F(t) is a real-valued generalized force and A^ is a Hermitian operator. Introduce the interaction picture by writing

U^(t,t0)=U^0(t)U^I(t,t0)U^0†(t0).

The factor U^0†(t0) ensures that U^(t0,t0)=I^ when U^I(t0,t0)=I^. Substitution into the evolution equation gives

iℏ∂U^0(t)∂tU^I(t,t0)U^0†(t0)+iℏU^0(t)∂U^I(t,t0)∂tU^0†(t0)=[H^0−F(t)A^]U^0(t)U^I(t,t0)U^0†(t0).

Since

iℏ∂U^0(t)∂t=H^0U^0(t),

the terms containing H^0 cancel. Multiplying from the left by U^0†(t) and from the right by U^0(t0) gives

iℏ∂U^I(t,t0)∂t=−F(t)U^0†(t)A^U^0(t)U^I(t,t0).

Define the unperturbed time-dependent operator

A^I(t)=U^0†(t)A^U^0(t)=eitH^0/ℏA^e−itH^0/ℏ.

The interaction-picture evolution equation is therefore

iℏ∂U^I(t,t0)∂t=−F(t)A^I(t)U^I(t,t0),

or equivalently,

∂U^I(t,t0)∂t=−1iℏF(t)A^I(t)U^I(t,t0).

Integrating from t0 to t gives

U^I(t,t0)−U^I(t0,t0)=−1iℏ∫t0tdt′F(t′)A^I(t′)U^I(t′,t0).

Using the boundary condition

U^I(t0,t0)=I^,

one obtains the exact integral equation

U^I(t,t0)=I^−1iℏ∫t0tdt′F(t′)A^I(t′)U^I(t′,t0).

This equation is iterative because the unknown evolution operator also appears inside the integral. For a sufficiently weak perturbation, linear response is obtained by replacing U^I(t′,t0) inside the integral by I^. To first order in F,

U^I(t,t0)=I^−1iℏ∫t0tdt′F(t′)A^I(t′)+𝒪(F2).

This is the first-order term of the Dyson series. Its adjoint is

U^I†(t,t0)=I^+1iℏ∫t0tdt′F(t′)A^I(t′)+𝒪(F2).

For another observable B^, define its unperturbed time dependence by

B^I(t)=U^0†(t)B^U^0(t).

Because the equilibrium density operator commutes with U^0(t0), the outer free-evolution factors cancel inside the equilibrium trace. It is therefore sufficient to consider

B^tot(t)=U^I†(t,t0)B^I(t)U^I(t,t0).

Substituting the first-order expressions for U^I and U^I† gives

B^tot(t)=[I^+1iℏ∫t0tdt′F(t′)A^I(t′)]B^I(t)×[I^−1iℏ∫t0tdt′F(t′)A^I(t′)]+𝒪(F2).

Discarding terms of second and higher order yields

B^tot(t)=B^I(t)+1iℏ∫t0tdt′F(t′)[A^I(t′),B^I(t)]+𝒪(F2).

The equilibrium average is defined by

⟨X^⟩0=1Z0Tr⁡(e−βH^0X^),Z0=Tr⁡(e−βH^0).

Averaging the preceding equation gives

⟨B^tot(t)⟩0=⟨B^I(t)⟩0+1iℏ∫t0tdt′F(t′)⟨[A^I(t′),B^I(t)]⟩0+𝒪(F2).

Since the equilibrium density operator commutes with H^0,

⟨B^I(t)⟩0=⟨B^⟩0.

Equilibrium correlation functions are also invariant under a common translation of both time arguments:

⟨[A^I(t′),B^I(t)]⟩0=⟨[A^,B^I(t−t′)]⟩0.

Define the response function

ϕAB(t)=1iℏ⟨[A^,B^I(t)]⟩0.

It follows that

ϕAB(t−t′)=1iℏ⟨[A^I(t′),B^I(t)]⟩0.

Taking t0→−∞, with the perturbation switched on adiabatically, and writing ⟨B^(t)⟩=⟨B^tot(t)⟩0, gives the Kubo formula

⟨B^(t)⟩=⟨B^⟩0+∫−∞tdt′F(t′)ϕAB(t−t′).

Equivalently, the linear response Green's function can be defined as

GAB(t)=ϕAB(t)θ(t).

The response can then be written as a convolution over all times,

δ⟨B^(t)⟩=∫−∞∞dt′F(t′)GAB(t−t′).

The Heaviside function ensures causality: the response at time t depends only on values of the perturbation at earlier times.[5]

See also

References

  1. ↑ Kubo, Ryogo (1957). "Statistical-Mechanical Theory of Irreversible Processes. I. General Theory and Simple Applications to Magnetic and Conduction Problems". J. Phys. Soc. Jpn. 12 (6): 570–586. doi:10.1143/JPSJ.12.570. http://journals.jps.jp/doi/pdf/10.1143/JPSJ.12.570. 
  2. ↑ Kubo, Ryogo; Yokota, Mario; Nakajima, Sadao (1957). "Statistical-Mechanical Theory of Irreversible Processes. II. Response to Thermal Disturbance". J. Phys. Soc. Jpn. 12 (11): 1203–1211. doi:10.1143/JPSJ.12.1203. 
  3. ↑ Bruus, Henrik; Flensberg, Karsten; Flensberg, ØRsted Laboratory Niels Bohr Institute Karsten (2004-09-02) (in en). Many-Body Quantum Theory in Condensed Matter Physics: An Introduction. OUP Oxford. ISBN 978-0-19-856633-5. https://books.google.com/books?id=v5vhg1tYLC8C. 
  4. ↑ Mahan, GD (1981). Many-particle physics. New York: Springer. ISBN 0306463385. 
  5. ↑ Kubo, Ryogo (1957). "Statistical-Mechanical Theory of Irreversible Processes. I. General Theory and Simple Applications to Magnetic and Conduction Problems". Journal of the Physical Society of Japan 12 (6): 570–586. doi:10.1143/JPSJ.12.570.