We show that under very general assumptions the adiabatic approximation of the phase of the zeta-regularized determinant of the imaginary-time Schrödinger operator with periodic Hamiltonian is equal to the Berry phase.
Shows that (non-adiabatic) Berry phases in time-independent systems arise for fundamentally different reasons than those for time-dependent systems. For time-independent Hamiltonians the Berry phases are seen to only depend on the chosen cyclic initial state, the Hamiltonian merely providing the appropriate period. The author also discusses two time-dependent examples where the time dependence arises from different sources, namely a two-level atom in an intense laser and a harmonic oscillator with a periodic forcing term.
Berry's (1984) formulation of the topological phase for periodic Hamiltonians is extended to the case of non-adiabatic evolution by proper choice of initial states. This restores a full parallel with the non-adiabatic formalism of Aharonov and Anandan (1987) for periodic orbits in a projective Hilbert space. The Berry phase for the novel example of a single electron in a rigidly rotating octahedral environment is calculated using both this formalism and that used previously by Aharonov and Anandan and by Page (1987).
We introduce a perturbative approach to solving the time-dependent Schr\"odinger equation, named adiabatic perturbation theory (APT), whose zeroth-order term is the quantum adiabatic approximation. The small parameter in the power series expansion of the time-dependent wave function is the inverse of the time it takes to drive the system's Hamiltonian from the initial to its final form. We review other standard perturbative and nonperturbative ways of going beyond the adiabatic approximation, extending and finding exact relations among them, and also compare the efficiency of those methods against the APT. Most importantly, we determine APT corrections to the Berry phase by use of the Aharonov-Anandan geometric phase. We then solve several time-dependent problems, allowing us to illustrate that the APT is the only perturbative method that gives the right corrections to the adiabatic approximation. Finally, we propose an experiment to measure the APT corrections to the Berry phase and show, for a particular spin-1∕2 problem, that to first order in APT the geometric phase should be two and a half times the (adiabatic) Berry phase.