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arXiv:2606.12323

Photon Cycling and Laser Cooling of an Asymmetric Top Molecule

Grace K. Li, Giseok Lee, Jack Mango, Hana Lampson, YongWoong Lee, Winston Wang, Avikar Periwal, Nathaniel B. Vilas, Alexander Frenett, Loïc Anderegg, John M. Doyle

Published Jun 10, 2026• 0 citations
arXivHTMLPDF

Abstract

We realize two-dimensional magnetically-assisted Sisyphus laser cooling of an asymmetric top molecule (ATM), calcium monoamide (CaNH$_2$). Vibrational state closure is achieved with $41.1 \pm 6.3$ photons scatters using optical pumping of the $X[3_1]$ state. Photon-cycling measurements show good agreement with branching ratios determined by dispersed fluorescence spectroscopy. Rotational closure is maintained by driving the $X[1_{11}] \to A [0_{00}]$ transition. The observed absence of additional state leakage channels broadens the scope of molecular laser cooling to include ATMs, which are the most general geometric class of molecules and possess the richest internal structure. Future applications of quantum controlled ATMs include new quantum information platforms and searches for physics beyond the Standard Model.

DOI
10.48550/arxiv.2606.12323

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We present a practical roadmap to achieve optical cycling and laser cooling of asymmetric top molecules (ATMs).Our theoretical analysis describes how reduced molecular symmetry, as compared to diatomic and symmetric nonlinear molecules, plays a role in photon scattering.We present methods to circumvent limitations on rapid photon cycling in these systems.We calculate vibrational branching ratios for a diverse set of asymmetric top molecules and find that many species within a broad class of molecules can be effectively cooled with a manageable number of lasers.We also describe methods to achieve rotationally closed optical cycles in ATMs.Despite significant structural complexity, laser cooling can be made effective by using extensions of the current techniques for linear molecules.Potential scientific impacts of laser-cooled ATMs span frontiers in controlled chemistry, quantum simulation, and searches for physics beyond the Standard Model.
In this dissertation, I present studies of molecules for uses in quantum science ranging from quantum computing and ultracold collisions to controlling organic-inspired molecular species. Starting with a diatomic molecule, calcium monofluoride, we developed an optical tweezer platform for use in quantum computing and demonstrated rotational coherence times significantly longer than measured dipole-enabled gate times. Using the Tweezer platform, we studied ultracold collisions of exactly two molecules and exerted full quantum control over the internal structure of the molecules. The collisions resulted in a rapid loss from the tweezers, leading us to develop a microwave shield to prevent these lossy collisions. The shielding scheme enhanced the rate of elastic collisions enabling the demonstration of forced evaporative cooling. To explore the possible use of larger molecules for quantum science, we studied the rotational structure of an asymmetric top and aromatic molecule, calcium monophenoxide, with the intent of identifying a path toward laser cooling and trapping. We cycled several photons, but theory predicted many more. After eliminating several decay paths, the key loss remained unknown. Applying the same methods to CaNH2_22​, a smaller asymmetric top molecule with similar spatial symmetry, we performed laser cooling. Using CaNH2_22​, we demonstrated photon cycling, and then observed Sisyphus cooling and heating features for the first time using an asymmetric top molecule. This work lays the foundation for future laser-cooling of organic-inspired molecules in an optical tweezer array for applications ranging from quantum computing to quantum chemistry, and precision measurement.
Abstract We demonstrate optical cycling and laser cooling of a cryogenic buffer-gas beam of calcium monohydride (CaH) molecules. We measure vibrational branching ratios for laser cooling transitions for both excited electronic states A and B. Furthermore, we measure that repeated photon scattering via the A ← X transition is achievable at a rate of ∼ 1.6 × 1 0 6 photons s−1 and demonstrate interaction-time limited scattering of ∼ 200 photons by repumping the largest vibrational decay channel. We also demonstrate a sub-Doppler cooling technique, namely the magnetically assisted Sisyphus effect, and use it to cool the transverse temperature of a molecular beam of CaH. Using a standing wave of light, we lower the transverse temperature from 12.2(1.2) mK to 5.7(1.1) mK. We compare these results to a model that uses optical Bloch equations and Monte Carlo simulations of the molecular beam trajectories. This work establishes a clear pathway for creating a magneto-optical trap (MOT) of CaH molecules. Such a MOT could serve as a starting point for production of ultracold hydrogen gas via dissociation of a trapped CaH cloud.
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.
Only bosonic molecular species have been directly laser cooled to date, primarily due to an abundance of bosonic isotopes in nature and to their simpler hyperfine structure. Fermionic molecules provide new opportunities for ultracold chemistry, quantum simulation, and precision measurements. Here we report direct laser cooling of a fermionic molecular isotopologue, calcium monodeuteride (CaD). With a nuclear spin I = 1 , only 5 hyperfine states need to be addressed for rotational closure in optical cycling. These hyperfine states are unresolved for typical experimental linewidths. We present a method for efficiently producing alkaline-earth metal hydrides and deuterides. We demonstrate rotational closure and show magnetically assisted Sisyphus cooling in one dimension for a beam of CaD molecules. Our results indicate that the experimental complexity for laser cooling CaD is similar to that of calcium monohydride (CaH). Laser cooling of CaD is a promising first step for production of ultracold and trapped atomic deuterium. Published by the American Physical Society 2024
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.