The stretching vibration of a carbon monoxide (CO) molecule is modelled as a…
PHYSICS · Subjective · Fermi University Physics · Quantum Mechanics · Quantum dynamics and its formulations · Quantum dynamics and its formulations
The Structure of Quantum Mechanics, Ch Coherent states, Ehrenfest's theorem and the classical limit
Problem
The stretching vibration of a carbon monoxide (CO) molecule is modelled as a one-dimensional harmonic oscillator in the reduced-mass coordinate x, the departure of the bond length from equilibrium, with reduced mass μ=1.14×10−26kg and angular frequency ω=4.1×1014rads−1. Treat the potential as exactly harmonic, V(x)=21μω2x2, and the motion of the relative coordinate is treated as one-dimensional and undamped. (a) Starting from the Heisenberg equation of motion, derive dtd⟨x^⟩=μ⟨p^⟩ and dtd⟨p^⟩=−⟨V′(x^)⟩, and show the second relation carries no correction term for this potential, for any state, giving ⟨x^⟩¨=−ω2⟨x^⟩ exactly. (b) At t=0 the vibrational state is the coherent state ∣α0⟩, eigenstate of a^ with α0 real and positive, for which ⟨x^⟩0=x0=0.010nm and ⟨p^⟩0=0. Using ⟨α∣x^∣α⟩=2ℏ/μωReα, find α0 numerically. (c) Solve the equation of part (a) with these initial conditions for ⟨x^⟩(t). (d) Starting instead from the number-state expansion of ∣α0⟩ and En=(n+21)ℏω, show directly that U^(t)∣α0⟩=e−iωt/2∣α0e−iωt⟩, recompute ⟨x^⟩(t), confirm it matches (c), and evaluate ⟨x^⟩(t1) at t1=61×ω2π. (e) The real bond follows the Morse potential of the chapter's four-systems worked example, with range 1/a≈43pm, whose restoring force near equilibrium is −V′(x)=−μω2x(1−23ax+⋯). By what fraction does the true force at x0 differ from the harmonic one, and can the answer to (d) be trusted to two significant figures?