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Physical Review A

Effect of the geometric phase on the possible measurement of the electron’s electric dipole moment using molecules confined by a Stark gravitational trap

P. M. Rupasinghe, Neil E. Shafer

Published Sep 24, 2008• 8 citations
Publisher

Abstract

We derive an effective Hamiltonian to account for the geometric phase that occurs in the adiabatic separation of center-of-mass and internal motion of a molecule moving in external fields. We then apply this Hamiltonian to the determination of the coherence time of molecules confined in a region of space by an anisotropic electric field. We show that the coherence time is expected to scale as the load temperature of the molecules squared and that milli-K temperatures are likely to be required for a trapped molecule experiment to compete with a more conventional Ramsey beam resonance experiment.

DOI
10.1103/physreva.78.033427

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Physical Review A•May 6, 2014•1 citation
We derive an effective Hamiltonian to account for the geometric phase that occurs in the adiabatic separation of center-of-mass and internal motion of a molecule moving in external fields. We then apply this Hamiltonian to the determination of the coherence time of molecules confined in a region of space by an anisotropic electric field. We show that the coherence time is expected to scale as the load temperature of the molecules squared and that milli-K temperatures are likely to be required for a trapped molecule experiment to compete with a more conventional Ramsey beam resonance experiment.
Heavy polar molecules can be used to measure the electric dipole moment of the electron, which is a sensitive probe of physics beyond the Standard Model. The value is determined by measuring the precession of the molecule's spin in a plane perpendicular to an applied electric field. The longer this precession evolves coherently, the higher the precision of the measurement. For molecules in a trap, this coherence time could be very long indeed. We evaluate the sensitivity of an experiment where neutral molecules are trapped electrically, and compare this to an equivalent measurement in a molecular beam. We consider the use of a Stark decelerator to load the trap from a supersonic source, and calculate the deceleration efficiency for YbF molecules in both strong-field seeking and weak-field seeking states. With a 1 s holding time in the trap, the statistical sensitivity could be ten times higher than it is in the beam experiment, and this could improve by a further factor of five if the trap can be loaded from a source of larger emittance. We study some effects due to field inhomogeneity in the trap and find that rotation of the electric field direction, leading to an inhomogeneous geometric phase shift, is the primary obstacle to a sensitive trap-based measurement.
Heavy polar molecules can be used to measure the electric dipole moment of the electron, which is a sensitive probe of physics beyond the Standard Model. The value is determined by measuring the precession of the molecule’s spin in a plane perpendicular to an applied electric field. The longer this precession evolves coherently, the higher the precision of the measurement. For molecules in a trap, this coherence time could be very long indeed. We evaluate the sensitivity of an experiment where neutral molecules are trapped electrically, and compare this to an equivalent measurement in a molecular beam. We consider the use of a Stark decelerator to load the trap from a supersonic source, and calculate the deceleration efficiency for YbF molecules in both strong-field seeking and weak-field seeking states. With a 1 s holding time in the trap, the statistical sensitivity could be ten times higher than it is in the beam experiment, and this could improve by a further factor of five if the trap can be loaded from a source of larger emittance. We study some effects due to field inhomogeneity in the trap and find that rotation of the electric field direction, leading to an inhomogeneous geometric phase shift, is the primary obstacle to a sensitive trap-based measurement. 1
Theories are developed to evaluate Larmor frequency shifts, derived from geometric phases, in experiments to measure electric dipole moments (EDM's) of trapped, atoms, molecules, and neutrons. A part of these shifts is proportional to the applied electric field and can be interpreted falsely as an electric dipole moment. A comparison is made between our theoretical predictions for these shifts and some results from our recent experiments, which shows agreement to within the experimental errors of 15%. The comparison also demonstrates that some trapped particle EDM experiments have reached a sensitivity where stringent precautions are needed to minimize and control such false EDM's. Computer simulations of these processes are also described. They give good agreement with the analytical results and they extend the study by investigating the influence of varying surface reflection laws in the hard-walled traps considered. They also explore the possibility to suppress such false EDM's by introducing collisions with buffer gas particles. Some analytic results for frequency shifts proportional to the square of the E\mathbf{E}E field are also given and there are results for the averaging of the B\mathbf{B}B field in the absence of an E\mathbf{E}E field.
In experiments searching for a nonzero electric dipole moment of trapped particles, frequency shifts correlated with an applied electric field can be interpreted as a false signal. One such effect, referred to as the geometric phase effect, is known to occur in a magnetic field that is nonperfectly homogeneous. The increase in sensitivity of experiments demands improved theoretical description of this effect. In the case of fast particles, like atoms at room temperature and low pressure, the validity of established theories was limited to a cylindrical confinement cell in a uniform gradient with cylindrical symmetry. We develop a more general theory valid for an arbitrary shape of the magnetic field as well as for arbitrary geometry of the confinement cell. Our improved theory is especially relevant for experiments measuring the neutron electric dipole moment with an atomic comagnetometer. In this context, we have reproduced and extended earlier numerical studies of the geometric phase effect induced by localized magnetic impurities.
The OH molecule in its ground state presents a versatile platform for precision measurement and quantum information processing. These applications vitally depend on the accurate measurement of transition energies between the OH levels. Significant sources of systematic errors in these measurements are shifts based on the geometric phase arising from the magnetic and electric fields used for manipulating OH. In this article, we present these geometric phases for fields that vary harmonically in time, as in the Ramsey technique. Our calculation of the phases is exact within the description provided by our recent analytic solution of an effective Stark-Zeeman Hamiltonian for the OH ground state. This Hamiltonian has been shown to model experimental data accurately. We find that the OH geometric phases exhibit rich structure as a function of the field rotation rate. Remarkably, we find rotation rates where the geometric phase accumulated by a specific state is zero, or where the relative geometric phase between two states vanishes. We expect these findings to be of importance to precision experiments on OH involving time-varying fields. More specifically, our analysis quantitatively characterizes an important item in the error budget for precision spectroscopy of ground-state OH.