Originally posted by Si
Do we define H0 to have the same spectrum as H because it is the only way to get 3.1.12? Or is it an axiom? And is there some physical reason for it? What is the physical interpretation for the eigenstates of H0?
Intuitively, since Ψ
α± are states of non-interacting particles, we should be able to define them in terms of some corresponding set of free particle states Φ
α of a free particle hamiltonian H
0 in a way that they have the same appearance as the Ψ
α±. This means that if we write H = H
0+V, then since the Ψ
α± are eigenstates of the
full physical hamiltonian H, V must be chosen so that the masses appearing in H
0 are the physical masses etc.
Originally posted by Si
This is why Weinberg gives a little "spread" (using g(?)) to these states...
In exp(-iHτ)Ψ on p109, Ψ describes a state seen by an observer at some point
during a collision process. Now, the whole idea of defining scattering amplitudes in terms of in and out states depends on the assumption that the collision process occurs over some
finite interval of time. If Ψ is an energy eigenstate Ψ
α so that we know it's exact energy, by the time-energy uncertainty principle the collision process is spread out across all time, in which case the whole idea of in and out states goes down the toilet. We see this mathematically by noting that in that case exp(-iHτ)Ψ = exp(-iE
ατ)Ψ
α, so that taking τ → ± ∞ achieves nothing since exp(-iE
ατ) is purely oscillatory and so has no limit. Thus, since Ψ
α± are effectively states of non-interacting particles so that 3.1.1 requires they be energy eigenstates of the hamiltonian H, we must consider ∫dαexp(-iE
ατ)g(α)Ψ
α± rather than just individual energy eigenstates Ψ
α±. Therefore, the correspondence between the Ψ
α± and the Φ
α must be given in terms of wave packets: ∫dαexp(-iE
ατ)g(α)Ψ
α± → ∫dαexp(-iE
ατ)g(α)Φ
α for τ → -∞ or τ → +∞ respectively.
Originally posted by Si
The fact that H has two sets of eigenstates even though a Hermitian operator should only have one means that 3.1.11 is not quite correct...
Ψ
α± are states in the same hilbert space (see 1st full paragraph after 3.2.1) and by energy conservation their energy eigenvalues must be equal.