In quantum mechanics, the correlation function C(t) provides deep insights into the evolution of a state and its departure from classical behavior. This problem examines a state prepared as a superposition of energy eigenstates with a Gaussian distribution of energies.
Suppose you have prepared a state ∣α⟩ as a superposition of N energy eigenstates ∣wk⟩ with a mean energy ω0 and a width σω:
ck∝e−2σω2(ωk−ω0)2∣α⟩=∑kck∣wk⟩
Our goal is to compute the normalized state and the correlation amplitude C(t)=⟨α∣U(t)∣α⟩.
In the limit of a large number of states (N→∞) and small spacing, we can approximate the sum as an integral:
C(t)≈∫e−σω2(ω−ω0)2dω∫e−σω2(ω−ω0)2e−iωtdω
The integral in the numerator is the Fourier transform of a Gaussian:
∫−∞∞e−aω2+bωdω=aπeb2/4a
After completing the square and performing the integration, we find:
C(t)≈e−iω0te−σω2t2/4
The absolute value of the correlation function, ∣C(t)∣=e−σω2t2/4, shows a Gaussian decay. The “correlation time” τ can be defined as the time it takes for ∣C(t)∣ to drop by 1/e:
τ=σω2
This relationship, τσω=2, is a manifestation of the energy-time uncertainty principle. As the width of the energy distribution σω increases (more “classical” or less well-defined energy), the state de-correlates much faster.