386 words
2 minutes
Correlation Function and the Classical Limit

The correlation function C(t)C(t) is the overlap of a state with its own time-evolved self, so it tells you how quickly a quantum state moves away from where it started. In this post I compute it for a state built as a superposition of energy eigenstates with a Gaussian distribution of energies. What comes out at the end is a very concrete version of the energy-time uncertainty relation.

The setup#

Suppose you have prepared a state ∣α⟩|\alpha\rangle as a superposition of NN energy eigenstates ∣wk⟩|w_k\rangle with a mean energy ω0\omega_0 and a width σω\sigma_\omega:

ck∝e−(ωk−ω0)22σω2c_k \propto e^{-\frac{(\omega_k - \omega_0)^2}{2\sigma_\omega^2}}∣α⟩=∑kck∣wk⟩|\alpha\rangle = \sum_k c_k |w_k\rangle

We want the normalized state and the correlation amplitude C(t)=⟨α∣U(t)∣α⟩C(t) = \langle \alpha | U(t) | \alpha \rangle.

Normalization#

To normalize the state, we require ⟨α∣α⟩=1\langle \alpha | \alpha \rangle = 1:

⟨α∣α⟩=∑k,lck∗cl⟨wk∣wl⟩=∑k∣ck∣2=1\langle \alpha | \alpha \rangle = \sum_{k,l} c_k^* c_l \langle w_k | w_l \rangle = \sum_k |c_k|^2 = 1

Given the proportionality ck=Ae−(ωk−ω0)22σω2c_k = A e^{-\frac{(\omega_k - \omega_0)^2}{2\sigma_\omega^2}}, we find the normalization constant AA:

A=1∑ke−(ωk−ω0)2σω2A = \frac{1}{\sqrt{\sum_k e^{-\frac{(\omega_k - \omega_0)^2}{\sigma_\omega^2}}}}

The Correlation Function#

The time evolution operator is U(t)=e−iHt/ℏU(t) = e^{-iHt/\hbar}. Acting on the state ∣α⟩|\alpha\rangle:

U(t)∣α⟩=∑kcke−iωkt∣wk⟩U(t) |\alpha\rangle = \sum_k c_k e^{-i\omega_k t} |w_k\rangle

The correlation function C(t)C(t) is defined as the overlap between the initial state and the state at time tt:

C(t)=⟨α∣U(t)∣α⟩=∑k∣ck∣2e−iωktC(t) = \langle \alpha | U(t) | \alpha \rangle = \sum_k |c_k|^2 e^{-i\omega_k t}

Using the normalization and the Gaussian coefficients:

C(t)=∑ke−(ωk−ω0)2σω2e−iωkt∑ke−(ωk−ω0)2σω2C(t) = \frac{\sum_k e^{-\frac{(\omega_k - \omega_0)^2}{\sigma_\omega^2}} e^{-i\omega_k t}}{\sum_k e^{-\frac{(\omega_k - \omega_0)^2}{\sigma_\omega^2}}}

Classical Limit#

In the limit of a large number of states (N→∞N \to \infty) and small spacing, we can approximate the sum as an integral:

C(t)≈∫e−(ω−ω0)2σω2e−iωtdω∫e−(ω−ω0)2σω2dωC(t) \approx \frac{\int e^{-\frac{(\omega - \omega_0)^2}{\sigma_\omega^2}} e^{-i\omega t} d\omega}{\int e^{-\frac{(\omega - \omega_0)^2}{\sigma_\omega^2}} d\omega}

The integral in the numerator is the Fourier transform of a Gaussian:

∫−∞∞e−aω2+bωdω=πaeb2/4a\int_{-\infty}^{\infty} e^{-a\omega^2 + b\omega} d\omega = \sqrt{\frac{\pi}{a}} e^{b^2/4a}

After completing the square and performing the integration, we find:

C(t)≈e−iω0te−σω2t2/4C(t) \approx e^{-i\omega_0 t} e^{-\sigma_\omega^2 t^2 / 4}

Interpretation#

The absolute value of the correlation function, ∣C(t)∣=e−σω2t2/4|C(t)| = e^{-\sigma_\omega^2 t^2 / 4}, shows a Gaussian decay. The “correlation time” τ\tau can be defined as the time it takes for ∣C(t)∣|C(t)| to drop to 1/e1/e of its initial value:

τ=2σω\tau = \frac{2}{\sigma_\omega}

So τσω=2\tau \sigma_\omega = 2, which is the energy-time uncertainty relation in about the most concrete form you can get. The broader the spread of energies σω\sigma_\omega (i.e. the less well-defined the energy, which is the more “classical” direction), the faster the state decorrelates.

Correlation Function and the Classical Limit
https://rohankulkarni.me/posts/notes/correlation-function-classical-limit/
Author
Rohan Kulkarni
Published at
2023-07-20
License
CC BY-NC-SA 4.0
Share Post
Comments