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arXiv:1610.08243 · Journal of Physics B Atomic Molecular and Optical Physics

Laser-coolable polyatomic molecules with heavy nuclei

T A Isaev, Andrei V. Zaitsevskii, E Eliav

Published Sep 26, 2017• 91 citations
arXivHTMLPDF

Abstract

Abstract Recently, a few diatomic and polyatomic molecules have been identified as prospective systems for Doppler/Sisyphus cooling. Doppler/Sisyphus cooling allows us to decrease the kinetic energy of molecules down to μ K temperatures with high efficiency and allows their capture in molecular traps, including magneto-optical traps. Trapped molecules can be used for creating molecular fountains and/or performing controlled chemical reactions, high-precision spectra measurements, and a wealth of other applications. Polyatomic molecules with heavy nuclei are of considerable interest for the ‘new physics’ search outside of the Standard Model and other applications including cold chemistry and photochemistry, quantum informatics, etc. Here, we focus on the radium monohydroxide molecule (RaOH), which is on the one hand amenable to laser cooling and on the other hand opens excellent possibilities for  -odd and  ,  -odd effects research. At present, RaOH is the heaviest polyatomic molecule proposed for direct cooling with lasers.

DOI
10.1088/1361-6455/aa8f34

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Abstract Recently, a few diatomic and polyatomic molecules have been identified as prospective systems for Doppler/Sisyphus cooling. Doppler/Sisyphus cooling allows us to decrease the kinetic energy of molecules down to μ K temperatures with high efficiency and allows their capture in molecular traps, including magneto-optical traps. Trapped molecules can be used for creating molecular fountains and/or performing controlled chemical reactions, high-precision spectra measurements, and a wealth of other applications. Polyatomic molecules with heavy nuclei are of considerable interest for the ‘new physics’ search outside of the Standard Model and other applications including cold chemistry and photochemistry, quantum informatics, etc. Here, we focus on the radium monohydroxide molecule (RaOH), which is on the one hand amenable to laser cooling and on the other hand opens excellent possibilities for  -odd and  ,  -odd effects research. At present, RaOH is the heaviest polyatomic molecule proposed for direct cooling with lasers.
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The rich internal structure of polyatomic molecules has inspired a number of theoretical proposals exploring a myriad of unique scientific and engineering frontiers, including quantum simulation and next-generation searches for physics beyond the standard model. Establishing full control over these complex quantum objects is likely necessary to harness their full potential; however, the same rich internal structure that gives rise to the immense scientific potential of polyatomic molecules also makes manipulating them a daunting task. In the past decade there has been considerable progress in the production, cooling, and control of diatomic species using direct laser cooling and magneto-optical trapping. This dissertation focuses on extending direct laser cooling and trapping to polyatomic molecules. Direct laser cooling of triatomic radical calcium monohydroxide (CaOH) is demonstrated. This molecules is a prototypical example of a broad class of polyatomic molecules that includes symmetric and asymmetric tops. Transverse magneto-optical trapping is demonstrated, establishing the ability to scatter an unprecedented number of photons in a polyatomic species. An understanding of previously unappreciated intricacies of molecular structure is developed, that explains observations of novel vibrational decay pathways. High resolution spectroscopy of hybrid vibrational modes is performed. A laser cooling scheme is constructed that will support future efforts to use the full range of laser cooling and high-fidelity detection techniques required to implement an optical tweezer array of polyatomic molecules. Our experimental efforts demonstrate the feasibility of direct laser cooling applied to CaOH, up ending long-standing assumptions of the inextricable complexity of polyatomic molecules.
Ultracold molecules are a promising platform for a wide range of applications in quantum science, including searches for new particles (beyond the Standard Model), quantum computing and simulation, and studies of ultracold collisions and chemistry. Over the last decade, tremendous progress has been made in developing techniques to trap diatomic molecules (molecules containing only two atoms) and cool them to ultracold temperatures using laser cooling. Polyatomic molecules (molecules containing more than two atoms) provide new, unique scientific opportunities not afforded by their diatomic counterparts and represent the next frontier in laser cooling and quantum science with molecules. In this thesis, we present our work on extending laser cooling and quantum control to polyatomic molecules. We describe our demonstration of laser cooling and the creation of a magneto-optical trap (MOT) of a polyatomic molecule, calcium monohydroxide (CaOH). We further demonstrate loading of the trapped molecules into an optical dipole trap (ODT) and loading of individual CaOH molecules into the conservative potential an optical tweezer array. We also describe our realization of a new type of MOT developed for molecules, a "conveyor belt MOT", which provides increased compression compared to traditional molecular MOTs and was discovered using numerical simulations of the CaOH MOT that were developed as part of this thesis. The increased MOT density and ODT loading afforded by the conveyor belt MOT provides the density required to perform studies of collisions between ultracold CaOH molecules. We also describe our work on the laser cooling the symmetric top molecule CaOCH₃, opening the possibility for 3-D laser cooling of even larger, more complex molecules into the ultracold regime. With the ability to laser cool and trap CaOH molecules, our most recent work has focused on developing tools for quantum control and on initial explorations of some of the new features afforded by polyatomic molecules. We describe a novel protocol established to perform a measurement of the electron's electric dipole moment ("eEDM"). Looking towards quantum information processing with polyatomic molecules, we create a new type of qubit using parity-doublet states in the bending mode of CaOH and characterize its coherence properties. Finally, we provide a brief outlook towards the future of laser cooling of polyatomic molecules for quantum science and provide a few suggestions for new directions opened up by the work presented in this thesis.
Extending AMO techniques of motional control to heavy polyatomic molecules opens new possibilities for precision measurements of fundamental physics. Though various laser-cooling and deceleration techniques have been applied to diatomic molecules throughout the last decade, their application to more complex molecules has heretofore been focused on light species, leaving generalizability to heavy species an open question. To investigate the high-mass frontier, we here study how to extend motional control to heavy-atom-containing polyatomic molecules. First, we discuss Zeeman-Sisyphus deceleration of YbOH, which can be used to decelerate species capable of scattering only ~10s of photons. Then, we discuss radiative slowing and magneto-optical trapping of SrOH, techniques only extendable to species capable of scattering ∼104\sim10^4∼104 photons. The last work focuses on spectroscopy of nonlinear molecules to assess the viability of extending techniques of motional control to more complex species. We find a dependence of both rotational and vibrational control on symmetry group, and identify a next-generation candidate for laser cooling. We end with a overview tying these projects together, and assessing the future of motional control along mass and complexity axes, including brief suggestions of how complementary methods to those studied here can further expand into the frontiers of molecular control.
Ultracold polyatomic molecules containing heavy nuclei, such as SrOH and YbOH, are sensitive to T- symmetry violating and P-symmetry violating physics beyond the Standard Model through the electron’s electric dipole moment. Furthermore, SrOH is sensitive to ultralight Dark Matter through measuring time variations of fundamental constants. However, in order to make full use of these molecules, they need to be cooled to ultracold temperatures and held in optical traps. We have realized a magneto-optical trap (MOT) of SrOH and used this as the essential element to achieve optical trap- ping in the microKelvin temperature regime. We observed MOT lifetimes approaching 200 ms with temperatures ∼ 1 mK and observed damped oscillations in the MOT. We further cooled the SrOH molecules to ∼ 40 μ K using Λ-enhanced gray molasses, and compressed the cloud to about 100 μm size using the conveyor belt MOT technique. Using this ultracold dense cloud of SrOH, we loaded an optical dipole trap (ODT), with a molecular lifetime of 1.2(1) seconds. In separate experiments with YbOH, which is heavier than SrOH, we demonstrated a novel deceleration method (Zeeman- Sisyphus deceleration) that can slow YbOH to under 20 m/s with only a few photons scattered utilizing high magnetic fields up to 2.5 T. By driving spin-flip transitions at the maxima and minima of the magnetic fields, slowing was achieved, which is a critical first step toward loading of a MOT for this species. We addressed the challenges associated with driving spin-flip transitions in molecules that have molecular perturbations among the electronic excited states and developed an understanding of the physics of such systems that is applicable to a wide range of molecules.
We perform magnetically assisted Sisyphus laser cooling of the triatomic free radical strontium monohydroxide (SrOH). This is achieved with principal optical cycling in the rotationally closed P(N^{''}=1) branch of either the X[over ˜]^{2}Σ^{+}(000)↔A[over ˜]^{2}Π_{1/2}(000) or the X[over ˜]^{2}Σ^{+}(000)↔B[over ˜]^{2}Σ^{+}(000) vibronic transitions. Molecules lost into the excited vibrational states during the cooling process are repumped back through the B[over ˜](000) state for both the (100) level of the Sr-O stretching mode and the (02^{0}0) level of the bending mode. The transverse temperature of a SrOH molecular beam is reduced in one dimension by 2 orders of magnitude to ∼750 μK. This approach opens a path towards creating a variety of ultracold polyatomic molecules by means of direct laser cooling.