ISSN:
1089-7690
Source:
AIP Digital Archive
Topics:
Physics
,
Chemistry and Pharmacology
Notes:
We derive the condition for a time dependent quantum system to exhibit an exact or higher order adiabatic time evolution. To this end, the concept of adiabaticity is first analyzed in terms of the transformation properties of the time-dependent Schrödinger equation under a general unitary transformation Uˆ(t). The system will follow an adiabatic time evolution, if the transformed Hamiltonian, Kˆ(t)=Uˆ°HˆUˆ−i(h-dash-bar)Uˆ°Uˆ, is divisible into an effective Hamiltonian hˆ(t), defining adiabatic quasistationary states, and an interaction term Ωˆ(t), whose effect on the adiabatic states exactly cancels the nonadiabatic couplings arising from the adiabatic states' parametric dependence on the time. This decoupling condition, which ensures adiabaticity in the system's dynamics, can be expressed in a state independent manner, and governs the choice of the unitary operator Uˆ(t), as well as the construction of the effective Hamiltonian hˆ(t). Using a restricted class of unitary transformations, the formalism is applied to the time evolution of an atomic or molecular system in interaction with a spatially uniform electromagnetic field, and gives an adiabatic approximation of higher order to the solutions of the semiclassical Schrödinger equation for this system. The adiabatic approximation so obtained exhibits two properties that make it suitable for the studies of intense field molecular dynamics: It is valid for any temporal profile of the field, and improves further as the field intensity increases, as reflected in the weakening of the associated residual nonadiabatic couplings with increasing field strength.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1063/1.455963
