Lossless and Lossy Characterization of the State of Perturbed Anharmonic Diatomics: An Information-Theoretic Compaction of Quantum Dynamics.

A lossless, exact compaction of the time-evolved state of the quantum dynamical system of a perturbed anharmonic molecule is demonstrated using dynamical symmetries. The density matrix of the anharmonic molecule is a linear combination of these symmetries, and it remains so as a time-dependent perturbation is applied. Accurate, unitary-but-approximate, and thereby irreversible compaction is further shown using fewer symmetries, and the fidelity of this lossy compaction is quantified. Perturbations are typically linear in the operators of a Lie algebra. For a Hamiltonian that is also linear, one knows well how to reversibly compact the state of a dynamical system. However, anharmonic vibrations have a finite number of unequally spaced energy levels, and a good description of their spectra typically requires an algebraic-type Hamiltonian that is bilinear in the operators of a Lie algebra. For a bilinear Hamiltonian we show how a matrix-based approach allows us to compact both the populations and the coherences, either exactly reversibly or inexactly irreversibly, with fewer symmetries. A forced Morse oscillator is used as an explicit analytical and numerical example covering the entire range of dynamics from the sudden to the adiabatic limits.