Coherent spatial control of wave packet dynamics on quantum lattices

Quantum lattices are pivotal in the burgeoning fields of quantum materials and information science. Rapid developments in microscopy and quantum engineering allow for preparing and monitoring wave-packet dynamics on quantum lattices with increasing spatial and temporal resolution. Motivated by these emerging research interests, we present an analytical study of wave packet diffusivity and diffusion length on tight-binding quantum lattices subject to stochastic noise. Our analysis points to the crucial role of spatial coherence and predicts a set of novel phenomena: noise can enhance the transient diffusivity and diffusion length of sufficiently extended initial states; A smooth Gaussian initial state spreads slower than a localized initial state; A standing or traveling initial state with large momentum spreads faster than a localized initial state and exhibits a noise-induced peak in the transient diffusivity; The change in the time-dependent diffusivity and diffusion length relative to a localized initial state follows a universal dependence on the Gaussian width. These theoretical predictions and the underlying mechanism of spatial coherence suggest the possibility of controlling the wave packet dynamics on quantum lattices by spatial manipulations, which will have implications for materials science and quantum technologies.Comment: 8 pages, 5 figure

Long-Lasting Orientation of Symmetric-top Molecules Excited by Two-Color Femtosecond Pulses

Impulsive orientation of symmetric-top molecules excited by two-color femtosecond pulses is considered. In addition to the well-known transient orientation appearing immediately after the pulse and then reemerging periodically due to quantum revivals, we report the phenomenon of field-free long-lasting orientation. Long-lasting means that the time averaged orientation remains non-zero until destroyed by other physical effects, e.g. intermolecular collisions. The effect is caused by the combined action of the field-polarizability and field-hyperpolarizability interactions. The dependence of degree of long-lasting orientation on temperature and pulse's parameters is considered. The effect can be measured by means of second (or higher-order) harmonic generation, and may be used to control the deflection of molecules traveling through inhomogeneous electrostatic fields.Comment: 12 pages, 7 figure

Enhanced persistent orientation of asymmetric-top molecules induced by cross-polarized terahertz pulses

We investigate the persistent orientation of asymmetric-top molecules induced by time-delayed THz pulses that are either collinearly or cross polarized. Our theoretical and numerical results demonstrate that the orthogonal configuration outperforms the collinear one, and a significant degree of persistent orientation—approximately 10% at 5 K and nearly 3% at room temperature—may be achieved through parameter optimization. The dependence of the persistent orientation factor on temperature and field parameters is studied in detail. The proposed application of two orthogonally polarized THz pulses is both practical and efficient. Its applicability under standard laboratory conditions lays a solid foundation for future experimental realization of THz-induced persistent molecular orientation

Visualizing coherent molecular rotation in a gaseous medium

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