Quantum dynamics of a polar rotor acted upon by an electric rectangular pulse of variable duration
arXiv:2105.00978 · doi:10.1080/00268976.2021.1966111
Abstract
As demonstrated in our previous work [J. Chem. Phys. 149, 174109 (2018)], the kinetic energy imparted to a quantum rotor by a non-resonant electromagnetic pulse with a Gaussian temporal profile exhibits quasi-periodic drops as a function of the pulse duration. Herein, we show that this behaviour can be reproduced with a simple waveform, namely a rectangular electric pulse of variable duration, and examine, both numerically and analytically, its causes. Our analysis reveals that the drops result from the oscillating populations that make up the wavepacket created by the pulse and that they are necessarily accompanied by drops in the orientation and by a restoration of the pre-pulse alignment of the rotor. Handy analytic formulae are derived that allow to predict the pulse durations leading to diminished kinetic energy transfer and orientation. Experimental scenarios are discussed where the phenomenon could be utilized or be detrimental.
arXiv comment18 pages, 5 figures. Submitted to the Molecular Physics special issue dedicated to Jürgen Troe
References in corpus (36)
- Quantum computation with trapped polar molecules
- Controlling the quantum stereodynamics of ultracold bimolecular reactions
- Quantum control of molecular rotation
- Manipulation of Molecules with Electromagnetic Fields
- Controlling the hyperfine state of rovibronic ground-state polar molecules
- Enantiomer-Specific State Transfer of Chiral Molecules
- Giant half-cycle attosecond pulses
- Efficient and long-lived field-free orientation of molecules by a single hybrid short pulse
- Control of molecular rotation with a chiral train of ultrashort pulses
- Prospects for Quantum Computing with an Array of Ultracold Polar Paramagnetic Molecules
- Generation of unipolar half-cycle pulse via unusual reflection of a single-cycle pulse from an optically thin metallic or dielectric layer
- Principles of enantio-selective excitation in three-wave mixing spectroscopy of chiral molecules
- Controlling Polar Molecules in Optical Lattices
- Field-free two-direction alignment alternation of linear molecules by elliptic laser pulses
- WavePacket: A Matlab package for numerical quantum dynamics. I: Closed quantum systems and discrete variable representations
- Experimental observation of Anderson localization in laser-kicked molecular rotors
- Ultimate field-free molecular alignment by combined adiabatic-impulsive field design
- WavePacket: A Matlab package for numerical quantum dynamics. II: Open quantum systems, optimal control, and model reduction
- Observation of Bloch oscillations in molecular rotation
- Time-dependent unitary perturbation theory for intense laser driven molecular orientation
- Laser control for the optimal evolution of pure quantum states
- Semiclassical catastrophes and accumulative angular squeezing of a kicked quantum rotor
- Anderson wall and Bloch oscillations in molecular rotation
- Experimental demonstration of coherent control in quantum chaotic systems
- Field-free molecular alignment induced by elliptically polarized laser pulses: non invasive 3 dimensional characterization
- Topology of surfaces for molecular Stark energy, alignment and orientation generated by combined permanent and induced electric dipole interactions
- Supersymmetry and eigensurface topology of the planar quantum pendulum
- Precisely Spun Super Rotors
- Shaping of the time-evolution of field-free molecular orientation by THz laser pulses
- Supersymmetry and eigensurface topology of the spherical quantum pendulum
- Unitary time-dependent superconvergent technique for pulse-driven quantum dynamics
- Conditional quasi-exact solvability of the quantum planar pendulum and of its anti-isospectral hyperbolic counterpart
- Symmetric Tops Subject to Combined Electric Fields: Conditional Quasi-Solvability via the Quantum Hamilton-Jacobi Theory
- Orientation and Alignment Dynamics of Polar Molecule Driven by Shaped Laser Pulses
- Dynamics of polar polarizable rotors acted upon by unipolar electromagnetic pulses: From the sudden to the adiabatic regime
- Pendular trapping conditions for ultracold polar molecules enforced by external electric fields