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arXiv:2006.03484 · Physical Chemistry Chemical Physics

Nondestructive dispersive imaging of rotationally excited ultracold molecules

Qingze Guan, Michael Highman, Η. Meier, Garrett R. Williams, V. W. Scarola, Brian DeMarco, Svetlana Kotochigova, Bryce Gadway

Published Jan 1, 2020• 8 citations
arXivHTMLPDF

Abstract

A barrier to realizing the potential of molecules for quantum information science applications is a lack of high-fidelity, single-molecule imaging techniques. Here, we present and theoretically analyze a general scheme for dispersive imaging of electronic ground-state molecules. Our technique relies on the intrinsic anisotropy of excited molecular rotational states to generate optical birefringence, which can be detected through polarization rotation of an off-resonant probe laser beam. Using 23Na87Rb and 87Rb133Cs as examples, we construct a formalism for choosing the molecular state to be imaged and the excited electronic states involved in off-resonant coupling. Our proposal establishes the relevant parameters for achieving degree-level polarization rotations for bulk molecular gases, thus enabling high-fidelity nondestructive imaging. We additionally outline requirements for the high-fidelity imaging of individually trapped molecules.

DOI
10.1039/d0cp03419c

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A barrier to realizing the potential of molecules for quantum information science applications is a lack of high-fidelity, single-molecule imaging techniques. Here, we present and theoretically analyze a general scheme for dispersive imaging of electronic ground-state molecules. Our technique relies on the intrinsic anisotropy of excited molecular rotational states to generate optical birefringence, which can be detected through polarization rotation of an off-resonant probe laser beam. Using 23Na87Rb and 87Rb133Cs as examples, we construct a formalism for choosing the molecular state to be imaged and the excited electronic states involved in off-resonant coupling. Our proposal establishes the relevant parameters for achieving degree-level polarization rotations for bulk molecular gases, thus enabling high-fidelity nondestructive imaging. We additionally outline requirements for the high-fidelity imaging of individually trapped molecules.
This thesis presents the development of a toolbox for the coherent control of ultracold polar molecules. Such systems of molecules promise the creation of long-lived, highly dipolar quantum gases with applications spanning the fields of quantum state controlled chemistry, quantum information, quantum simulation, and precision measurement. However, the addition of vibrational and rotational degrees of freedom leads to molecular systems being significantly more complex than their widely used atomic counterparts. In this work we demonstrate full control of the quantum state down to the hyperfine level of an optically trapped sample of ultracold bosonic 87Rb133 Cs molecules, and exploit that control to begin an investigation into the collision processes which take place in an ultracold molecular gas. We create a sample of up to ∼ 4000 optically trapped molecules in their rovibronic and hyperfine ground state. We characterise the molecules by measuring their temperature, binding energy, and molecule-frame electric dipole moment. We perform spectroscopy of the first rotationally excited state with hyperfine state resolution using microwaves to determine accurate values of rotational and hyperfine coupling constants. We use coherent π pulses to perform complete transfer population between selected hyperfine levels of the ground, first-excited, and second-excited rotational states. We investigate the effect of the off-resonant light of our optical dipole trap on the rotational and hyperfine structure of the molecules. Through a combination of high-resolution microwave spectroscopy and parametric heating measurements, we characterise the polarisability of the 87Rb133Cs molecule. We demonstrate that coupling between neighbouring hyperfine states manifests in rich structure with many avoided crossings in any rotational state other than the ground state. This coupling may be tuned by rotating the polarisation of the linearly polarised trapping light. Finally, we study the lifetime of polar bosonic 87Rb133Cs molecules in our 3D optical dipole trap. We examine the lifetime of the molecules as a function of dipole trap intensity, magnetic field, and hyperfine and rotational state. Despite the chemical stability of the 87Rb133 Cs molecule, we observe lifetimes of ∼1 s corresponding to 2-body decay rates close to the universal limit.
We report on a novel bichromatic fluorescent imaging scheme for background-free detection of single CaF molecules trapped in an optical tweezer array. By collecting fluorescence on one optical transition while using another for laser cooling, we achieve an imaging fidelity of 97.7(2)% and a nondestructive detection fidelity of 95.5(6)%. Notably, these fidelities are achieved with a modest photon budget, suggesting that the method could be extended to more complex laser-coolable molecules with less favorable optical cycling properties. We also report on a framework and new methods to characterize various loss mechanisms that occur generally during fluorescent detection of trapped molecules, including two-photon decay and admixtures of higher excited states that are induced by the trapping light. In particular, we develop a novel method to dispersively measure transition matrix elements between electronically excited states. The method could also be used to measure arbitrarily small Franck-Condon factors between electronically excited states, which could significantly aid in ongoing efforts to laser cool complex polyatomic molecules.
We demonstrate a scheme for direct absorption imaging of an ultracold ground-state polar molecular gas near quantum degeneracy. Imaging molecules without closed optical cycling transitions is challenging. Our technique relies on photon-shot-noise-limited absorption imaging on a strong but open bound-bound molecular transition. We present a systematic characterization of this imaging technique. Using this technique combined with time-of-flight expansion, we demonstrate the capability to determine momentum and spatial distributions for the molecular gas. With its capability of imaging molecules in arbitrary external fields, we anticipate that this technique will find many applications in the study of molecular quantum gases.
Abstract We discuss how the internal structure of ultracold molecules, trapped in the motional ground state of optical tweezers, can be used to implement qudits. We explore the rotational, fine and hyperfine structure of 40Ca19F and 87Rb133Cs, which are examples of molecules with 2Σ and 1Σ electronic ground states, respectively. In each case we identify a subset of levels within a single rotational manifold suitable to implement a four-level qudit. Quantum gates can be implemented using two-photon microwave transitions via levels in a neighboring rotational manifold. We discuss limitations to the usefulness of molecular qudits, arising from off-resonant excitation and decoherence. As an example, we present a protocol for using a molecular qudit of dimension d = 4 to perform the Deutsch algorithm.
Abstract We propose a quantum gas microscope for ultracold atoms that enables nondestructive atom detection, thus evading higher-band excitation and change of the internal degrees of freedom. We show that photon absorption of a probe beam cannot be ignored even in dispersive detection to obtain a signal-to-noise ratio greater than unity because of the shot noise of the probe beam under a standard measurement condition. The first scheme we consider for the nondestructive detection, applicable to an atom that has an electronic ground state without spin degrees of freedom, is to utilize a magic-wavelength condition of the optical lattice for the transition for probing. The second is based on the dispersive Faraday effect and squeezed quantum noise and is applicable to an atom with spins in the ground state. In this second scheme, a scanning microscope is adopted to exploit the squeezed state and reduce the effective losses. Application to ultracold ytterbium atoms is discussed.
Ultracold polar molecules possess a manifold of long-lived molecular rotational states, which can be coherently controlled using microwave fields and entangled by the long-range dipole-dipole interactions between molecules. The ability to control these features at the individual molecule level provides a rich toolbox with which to engineer quantum simulations of exotic materials or build a molecular quantum computer. Until recently, this level of single molecule control has eluded researchers due to the challenges inherent in taming the complex internal structure of molecules. In this thesis, we demonstrate full control over the internal quantum states and coherent interactions of individual NaCs molecules in optical tweezers. This platform is based on coherent assembly of ultracold Na and Cs atoms trapped and cooled in separate arrays, before being magnetoassociated at a Feshbach resonance to form weakly-bound molecules. Using high-resolution spectroscopy of electronically excited molecular states, we identify an efficient two-photon pathway to the rovibrational ground state of NaCs that we use to prepare an array of ground state molecules in tweezers. We demonstrate a "magic ellipticity'' technique to eliminate differential light shifts between two molecular rotational states and achieve coherence times of up to 250(40) ms for a superposition of those states. We then show that we can rearrange molecules in an array to eliminate defects and perform single-shot readout of multiple rotational states using controlled molecule dissociation and imaging of constituent atoms at high magnetic field. Finally, we coherently control the dipole-dipole interactions between two molecules, producing a Bell state with a fidelity of 94(3) % and demonstrating a universal entangling iSWAP gate for qubits encoded in molecular hyperfine states.