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Chinese Physics B

Orientation of KRb molecules in a switched electrostatic field

Yunxia Huang, Shuwu Xu, Xiao-Hua Yang

Published May 1, 2013• 2 citations
Publisher

Abstract

We theoretically investigate the orientation of the cold KRb molecules induced in a switched electrostatic field by numerically solving the full time-dependent Schrödinger equation. The results show that the periodic field-free molecular orientation can be realized for the KRb molecules by rapidly switching off the electrostatic field. Meanwhile, by varying the switching times of the electrostatic field, the adiabatic and nonadiabatic interactions of the molecules with the applied field can be realized. Moreover, the influences of the electrostatic field strength and the rotational temperature to the degree of the molecular orientation are studied. The investigations show that increasing the electrostatic field will increase the degree of the molecular orientation, both in the constant-field regime and in the field-free regime, while the increasing of the rotational temperature of the cold molecules will greatly decrease the degree of the molecular orientation.

DOI
10.1088/1674-1056/22/5/053701

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We theoretically investigate the orientation of the cold KRb molecules induced in a switched electrostatic field by numerically solving the full time-dependent Schrödinger equation. The results show that the periodic field-free molecular orientation can be realized for the KRb molecules by rapidly switching off the electrostatic field. Meanwhile, by varying the switching times of the electrostatic field, the adiabatic and nonadiabatic interactions of the molecules with the applied field can be realized. Moreover, the influences of the electrostatic field strength and the rotational temperature to the degree of the molecular orientation are studied. The investigations show that increasing the electrostatic field will increase the degree of the molecular orientation, both in the constant-field regime and in the field-free regime, while the increasing of the rotational temperature of the cold molecules will greatly decrease the degree of the molecular orientation.
We theoretically investigate the orientation of the cold KRb molecules induced in a switched electrostatic field by numerically solving the full time-dependent Schrdinger equation. The results show that the periodic field-free molecular orientation can be realized for the KRb molecules by rapidly switching off the electrostatic field. Meanwhile, by varying the switching times of the electrostatic field, the adiabatic and nonadiabatic interactions of the molecules with the applied field can be realized. Moreover, the influences of the electrostatic field strength and the rotational temperature to the degree of the molecular orientation are studied. The investigations show that increasing the electrostatic field will increase the degree of the molecular orientation, both in the constant-field regime and in the field-free regime, while the increasing of the rotational temperature of the cold molecules will greatly decrease the degree of the molecular orientation.
We theoretically investigate the orientation of the cold KRb molecules in a weak electrostatic field assisted by a shaped laser pulse. The results show that the slow turn-on and rapid turn-off laser pulse can enhance the molecular orientation of KRb significantly, and a high degree of molecular orientation of more than 0.9 can be obtained when the electrostatic field is as low as 3kV/cm. In addition, the influences of the electrostatic field strength and the parameters of the laser pulse are studied in detail.
The authors present a detailed study of low-temperature collisions between CaD molecules and He atoms in superimposed electric and magnetic fields with arbitrary orientations. Electric fields do not interact with the electron spin of the molecules directly but modify their rotational structure and, consequently, the spin-rotation interactions. The authors examine molecular Stark and Zeeman energy levels as functions of the angle between the fields and show that rotating fields may induce and shift avoided crossings between the Zeeman levels of the rotationally ground and rotationally excited states of the molecule. The dynamics of molecular collisions are extremely sensitive to external fields near these avoided crossings and it is shown that molecular collisions may be controlled by varying both the strength and the relative orientation of the fields. The effects observed in this study are due to interactions of the isolated molecules with external fields so the conclusions should be relevant for collisions of molecules with other atoms or collisions of molecules with each other. This study demonstrates that electric fields may be used to enhance or suppress spin-rotation interactions in molecules. The spin-rotation interactions induce nonadiabatic couplings between states of different total spins in systems of two open-shell species and it is suggested that electric fields might be used for controlling nonadiabatic spin transitions and spin-forbidden chemical reactions of cold molecules in a magnetic trap.
We present a theoretical study of atom-molecule collisions in superimposed electric and magnetic fields and show that dynamics of electronic spin relaxation in molecules at temperatures below 0.5 K can be manipulated by varying the strength and the relative orientation of the applied fields. The mechanism of electric field control of Zeeman transitions is based on an intricate interplay between intramolecular spin-rotation couplings and molecule-field interactions. We suggest that electric fields may affect chemical reactions through inducing nonadiabatic spin transitions and facilitate evaporative cooling of molecules in a magnetic trap.
An electrostatic lattice is composed of many micro-scale traps. It is a powerful tool for manipulating cold polar molecules on a chip with the help of the interaction between the dipole moment and the inhomogeneous electric field. To the best of our knowledge, the existing electrostatic lattice still suffers the nonadiabatic transition that will lead to the escape of molecules from the electrostatic trap. In the paper, we skillfully design the electrode structure to avoid the zero-field zone at the center of every single microtrap, and the nonadiabatic transitions can be prevented. First, we numerically calculate the distribution of the spatial electrostatic field. Then, the influences of voltages on the electric field intensity and the height of the trap center are investigated. We simulate of the trajectory of molecules using the Monte Carlo method and figure out the factors impacting the loading efficiency of our electrostatic lattice. At last, we discuss how the voltages and the loading positions affect the positional distribution of trapped molecules.
Orientation of single and two coupled polar molecules irradiated by a single laser pulse under a conical-well model is investigated theoretically. The orientation of a single hindered rotor shows a periodic behavior. In particular, the amplitude of the oscillation is sensitive to the degree of alternation of the laser field. Crossover from field-free to hindered rotation is observed by varying the hindering angle for different heights of conical wells. For a small hindering potential and angle, time-averaged orientation differs greatly from that for an infinite one. The orientation at a large hindering angle shows irregularlike behavior under strong dipole-dipole interaction. Entanglement induced by the dipole-dipole interaction is also calculated for the coupled-rotor system, in which the time-averaged entropy increases monotonically as the hindering angle is increased. The competition between the confinement effect and dipole interaction is found to dominate the behavior of the coupled-rotor system.