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arXiv:2109.13484 · Physical Review A

Trapping and binding by dephasing

K. Mukherjee, S. Poddar, Sebastian Wüster

Published Apr 22, 2022• 1 citation
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Abstract

The binding and trapping of particles usually rely on conservative forces, described by unitary quantum dynamics. We show that both can also arise solely from spatially dependent dephasing, the simplest type of decoherence. This can be based on continuous weak position measurements in only selected regions of space, for which we propose a practical realization. For a single particle, we demonstrate a quantum particle in a box based on dephasing. For two particles, we demonstrate their binding despite repulsive interactions, if their molecular states are dephased at large separations only. Both mechanisms are experimentally accessible, as we show for an example with Rydberg atoms in a cold gas background.

DOI
10.1103/physreva.105.l041102

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The binding and trapping of particles usually rely on conservative forces, described by unitary quantum dynamics. We show that both can also arise solely from spatially dependent dephasing, the simplest type of decoherence. This can be based on continuous weak position measurements in only selected regions of space, for which we propose a practical realization. For a single particle, we demonstrate a quantum particle in a box based on dephasing. For two particles, we demonstrate their binding despite repulsive interactions, if their molecular states are dephased at large separations only. Both mechanisms are experimentally accessible, as we show for an example with Rydberg atoms in a cold gas background.
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One of the classic first problems in quantum theory textbooks is that of the particle trapped in a box. Despite the apparent artificiality of the situation, it has quite a few interesting features that we can quickly apply to some more physically plausible situations. The particle in a box is literally an object, such as an electron, trapped inside a ‘box.’ In a realistic physical example, this ‘box’ would be a volume of space bound by some constraining force acting on the particle. For example, an atom is a ‘box’ as far as the orbiting electrons are concerned, with the electrostatic force between the positive protons in the nucleus and the negative electrons providing the constraint. The first move is to assume that the wave function for any particle in the box will have separate spatial and temporal dependencies. One of the key steps in obtaining our wave function was the quantization of the momentum.
In this dissertation I investigate cold Rydberg atoms and molecules in which the angular-momentum character of the quantum states involved strongly influences their properties and dynamics. In the first part I focus on long-range diatomic Rydberg molecules formed by a rubidium D-state Rydberg atom and a second rubidium atom in its ground state. Spectroscopic measurements of molecular binding energies are presented showing the effect of the Rydberg atom size and fine-structure coupling on the molecular potentials. A theoretical model is introduced that takes into account all relevant angular-momentum couplings between the molecular constituents, successfully reproducing experimental observations. Calculations of adiabatic potentials and binding energies, molecular-state lifetimes, electric and magnetic dipole moments are also presented. In the second part, I describe the production and magnetic trapping of cold circular Rydberg atoms. The circular Rydberg atoms are generated out of a cold gas of rubidium using the crossed-fields method and magnetically trapped. The trapping force is employed to induce center-of-mass oscillations of the trapped atom sample. Trap parameters and observed oscillation frequencies are used to measure the magnetic moments of the circular Rydberg atoms. Trap losses and the atomic internal-state evolution in the 300 Kelvin thermal background are also investigated.
We show that Born-Oppenheimer surfaces can intrinsically decohere, implying loss of coherence among constituent electronic basis states. We consider the example of interatomic forces due to resonant dipole-dipole interactions within a dimer of highly excited Rydberg atoms, embedded in an ultracold gas. These forces rely on a coherent superposition of two-atom electronic states, which is destroyed by continuous monitoring of the dimer state through a detection scheme utilizing the background gas atoms. We show that this intrinsic decoherence of the molecular energy surface can gradually deteriorate a repulsive dimer state, causing a mixing of attractive and repulsive character. For sufficiently strong decoherence, a Zeno-like effect causes a complete cessation of interatomic forces. We finally show how short decohering pulses can controllably redistribute population between the different molecular energy surfaces.
We present a method for determining the depth of an atomic or molecular trap of any type. This method relies on a measurement of the trap loss rate induced by collisions with background gas particles. Given a fixed gas composition, the loss rate uniquely determines the trap depth. Because of the ``soft'' long-range nature of the van der Waals interaction, these collisions transfer kinetic energy to trapped particles across a broad range of energy scales, from room temperature to the microkelvin energy scale. The resulting loss rate therefore exhibits a significant variation over an enormous range of trap depths, making this technique a powerful diagnostic with a large dynamic range. We present trap depth measurements of a Rb magneto-optical trap using this method and a different technique that relies on measurements of loss rates during optical excitation of colliding atoms to a repulsive molecular state. The main advantage of the method presented here is its large dynamic range and applicability to traps of any type requiring only knowledge of the background gas density and the interaction potential between the trapped and background gas particles.