The probability, P(t),
of the irreversible dissipation into a continuous spectrum of an initially (t = 0) localized
(Ψo)
nonstationary state acquires, as time increases, ‘memory’ due to the lower energy
bound of the spectrum, and eventually follows a nonexponential decay (NED).
Regardless of the degree of dependence on energy, the magnitude of this deviation
from exponential decay depends on the degree of proximity to threshold, and on
whether the theory employs a real energy distribution, one form of which is g(E) ≡ ⟨Ψo |δ(H − E)|Ψo ⟩,
or a complex energy distribution, G(E) ≡ ⟨Ψo |(H − E + i0)|Ψo ⟩. It is the
latter that is physically consistent, since it originates from the singularity at t = 0, which breaks
the S-matrix
unitarity, in accordance with the non-Hermitian character of decaying states. In order to
test the quantum mechanical theory, we carried out semiclassical path integral calculations
of the P(t)
for an isolated narrow tunnelling state, whereby the
truncated Fourier transform of a semiclassical Green function,
Gsc(E),
is obtained. The results are in agreement with the analytic results
of quantum mechanics when energy and time asymmetry are
taken into account. It is shown that the analytic structure of
Gsc(E) is [Dregular + Dpole],
where Dpole
is a finite sum over complex poles, which are the complex eigenvalues,
Wn, that the potential
can support. The Wn
are given by En + Δn − (i/2)Γn, where
En
are the real eigenvalues of the corresponding bound potential, Γn are the energy
widths and Δn
are the energy shifts, both expressed in terms of computable semiclassical
quantities. The spherical harmonic oscillator (SHO) with and without angular
momentum, and unstable ground states of diatomic molecules, are treated
as particular cases. The exact spectrum of the SHO is recovered only
when the Kramers–Langer semiclassical expression for the centrifugal
potential is used, thereby bypassing the difficulty of the singularity at r = 0.
The spectrum from the use of the quantal form l(l + 1) reduces to that of
l(l + 1/2)2 in the
limit of large l, i.e., for
orbits far from r = 0.
Using previously computed energies and widths for the vibrational
levels of He22+1σ
g2 1Σ
g+, the application
of two formulae for P(t),
one derived from a Lorentzian real energy distribution and the other from the
corresponding complex energy distribution, shows that, for the lowest level, in the
former case NED starts after about 193 lifetimes, and in the latter after
about 102 lifetimes. The fact that this difference is large should have
consequences for the deeper understanding of irreversibility at the quantum level.