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arXiv:2506.23507 · Scientific Reports

Optical cycling of MgF molecules within the hyperfine states in X(N=1) state

Kikyeong Kwon, Seunghwan Roh, Youngju Cho, Yongwoong Lee, Eunmi Chae

Published Dec 4, 2025• 0 citations
arXivHTMLPDF

Abstract

Achieving laser cooling of molecules necessitates the establishment of a closed optical cycling transition. In contrast to atoms, molecules exhibit additional vibrational and rotational structures, which must be carefully addressed-alongside hyperfine splittings-when designing the laser frequency scheme for efficient optical cycling. In this work, we investigated optical cycling in MgF molecules on the laser cooling transition, namely [Formula: see text] transition between the electronic ground state ([Formula: see text]) and the electronic excited state ([Formula: see text]). The ground state comprises four hyperfine levels, of which two are unresolved within the excited-state linewidth; the two hyperfine levels in the excited state are also unresolved. Consequently, three laser frequencies suffice to address all transitions. This was realized by generating three independently tunable frequency components using acousto-optic modulators (AOMs). With optimized detunings, power ratios, and total beam power, simultaneous application of all three frequency components increased the total number of scattered photons by up to [Formula: see text] relative to the sum of the individual single-frequency signals. Applying a tilted magnetic field to remix the dark Zeeman states increased the photon yield by an additional factor of [Formula: see text], leading to an overall enhancement of about sevenfold. These results provide quantitative benchmarks for MgF optical cycling and practical guidance for future molecular slowing and magneto-optical trapping experiments.

DOI
10.1038/s41598-025-28774-0

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Achieving laser cooling of molecules necessitates the establishment of a closed optical cycling transition. In contrast to atoms, molecules exhibit additional vibrational and rotational structures, which must be carefully addressed-alongside hyperfine splittings-when designing the laser frequency scheme for efficient optical cycling. In this work, we investigated optical cycling in MgF molecules on the laser cooling transition, namely [Formula: see text] transition between the electronic ground state ([Formula: see text]) and the electronic excited state ([Formula: see text]). The ground state comprises four hyperfine levels, of which two are unresolved within the excited-state linewidth; the two hyperfine levels in the excited state are also unresolved. Consequently, three laser frequencies suffice to address all transitions. This was realized by generating three independently tunable frequency components using acousto-optic modulators (AOMs). With optimized detunings, power ratios, and total beam power, simultaneous application of all three frequency components increased the total number of scattered photons by up to [Formula: see text] relative to the sum of the individual single-frequency signals. Applying a tilted magnetic field to remix the dark Zeeman states increased the photon yield by an additional factor of [Formula: see text], leading to an overall enhancement of about sevenfold. These results provide quantitative benchmarks for MgF optical cycling and practical guidance for future molecular slowing and magneto-optical trapping experiments.
We demonstrate radiative force deflection by using an optical cycling of the $X{\phantom{\rule{0.16em}{0ex}}}^{2}{\mathrm{\ensuremath{\Sigma}}}_{1/2}^{+}\ensuremath{-}A{\phantom{\rule{0.16em}{0ex}}}^{2}{\mathrm{\ensuremath{\Pi}}}_{1/2}$ electronic transition in diatomic molecule magnesium monofluoride (MgF). For the (0,0) and (0,1) bands of the electronic transition, the Franck-Condon factors---obtained by the dispersed laser-induced fluorescence spectrum---are f00=0.972{f}_{00}=0.972f00​=0.972 and f01=0.028{f}_{01}=0.028f01​=0.028, which suggests that the vibrational branching is quasiclosed. Furthermore, the dark Zeeman sublevels are destabilized by applying an external magnetic field. The cycling fluorescence is clearly observed to reveal that the molecular beam is deflected by 4.9 mm via scattering $\ensuremath{\sim}200$ photons per molecule. This work is encouraging toward laser cooling and magneto-optical trapping of MgF molecules.
Laser cooling and trapping are central to modern atomic physics. It has been roughly three decades since laser cooling techniques produced ultracold atoms, leading to rapid advances in a vast array of fields and a number of Nobel prizes. Prior to the work presented in this thesis, laser cooling had not yet been extended to molecules because of their complex internal structure. However, this complexity makes molecules potentially useful for a wide range of applications. The first direct laser cooling of a molecule and further results we present here provide a new route to ultracold temperatures for molecules. In particular, these methods bridge the gap between ultracold temperatures and the approximately 1 kelvin temperatures attainable with directly cooled molecules (e.g. with cryogenic buffer gas cooling or decelerated supersonic beams). Using the carefully chosen molecule strontium monofluoride (SrF), decays to unwanted vibrational states are suppressed. Driving a transition with rotational quantum number R=1 to an excited state with R'=0 eliminates decays to unwanted rotational states. The dark ground-state Zeeman sublevels present in this specific scheme are remixed via a static magnetic field. Using three lasers for this scheme, a given molecule should undergo an average of approximately 100,000 photon absorption/emission cycles before being lost via unwanted decays. This number of cycles should be sufficient to load a magneto-optical trap (MOT) of molecules. In this thesis, we demonstrate transverse cooling of an SrF beam, in both Doppler and a Sisyphus-type cooling regimes. We also realize longitudinal slowing of an SrF beam. Finally, we detail current progress towards trapping SrF in a MOT. Ultimately, this technique should enable the production of large samples of molecules at ultracold temperatures for molecules chemically distinct from competing methods.
We present a theoretical study of magneto-optical trapping (MOT) force exerted on magnesium monofluoride (MgF) with three-dimensional rate equations, in which we have considered the complex vibrational and rotational levels and the effects of small internal splittings and degeneracies, including fine and hyperfine structures and the magnetic quantum numbers. We investigate the feasibility of MOT for MgF with a very small excited-state ggg factor $(\phantom{\rule{4pt}{0ex}}{g}_{e}=\ensuremath{-}0.0002)$ and a large radiative decay rate $(\mathrm{\ensuremath{\Gamma}}=2\ensuremath{\pi}\ifmmode\times\else\texttimes\fi{}22\phantom{\rule{0.16em}{0ex}}\mathrm{MHz})$ for the electronic transition of $X{\phantom{\rule{0.16em}{0ex}}}^{2}{\mathrm{\ensuremath{\Sigma}}}^{+}$ to $A{\phantom{\rule{0.16em}{0ex}}}^{2}{\mathrm{\ensuremath{\Pi}}}_{1/2}$ states. We also optimize the MOT with reference to the three-, four-, and more-frequency component models with various polarization configurations and detunings. By applying the dual-frequency arrangement to more than one hyperfine level, we suggest a configuration of the (3+1)(3+1)(3+1)-frequency components for achieving the MOT of MgF.
Cold and ultracold molecules are highly desirable for a diverse range of applications in physics and chemistry such as precision measurements, tests of fundamental physics, quantum simulation and information processing, quantum chemistry, and the physics of strongly correlated quantum matter. Laser cooling is usually infeasible in molecules because their rotational and vibrational transitions make is difficult to come up with a closed scattering cycle. Recently, a narrow range of diatomic molecules, one of which is CaF, has been shown to possess a convenient electronic structure and a highly-diagonal Franck-Condon matrix and thus be amenable to laser cooling. This thesis describes experiments on laser cooling of CaF radicals produced in a supersonic source. We first investigate the increased fluorescence when multi-frequency resonant light excites the molecules from the four hyperfine levels of the ground X²∑+(N = 1, v = 0) state to the first excited A²π½ (J’ = 1=2; v’ = 0) state. The number of photons scattered per molecule increases significantly from one or two in the single frequency case to more than 50 before the molecules get pumped into the X²∑+(N = 1; v = 1) state. We demonstrate laser cooling and slowing of CaF using counter-propagating laser light which causes the molecules to scatter more than a thousand photons on the X (N = 1, v = 0, 1) <->A (J’ = 1=2; v’ = 0) transition. The effect of the laser cooling is to slow a group of molecules from 600 ms-1 to about 580 ms-1 and to narrow their velocity distribution from an initial temperature of 3 K down to 300 mK. In addition, chirping the frequency of the cooling light to keep it on resonance with the decelerating molecules doubles the deceleration and further compresses the velocity distribution. The effect of the laser cooling is limited by the optical pumping of molecules in the X (N = 1, v = 2) state.
For laser-cooling considerations, we have theoretically investigated the electronic, rovibrational, and hyperfine structures of the BaF molecule. The highly diagonal Franck-Condon factors and the branching ratios for all possible transitions within the lowest-lying four electronic states have also been calculated. Meanwhile, the mixing between the metastable ${A}^{{\ensuremath{'}}^{2}}\mathrm{\ensuremath{\Delta}}$ and ${A}^{2}\mathrm{\ensuremath{\Pi}}$ states and, further, the lifetime of the $\mathrm{\ensuremath{\Delta}}$ state have been estimated since the loss procedure via the $\mathrm{\ensuremath{\Delta}}$ state might fatally break the main quasicycling $\mathrm{\ensuremath{\Sigma}}\ensuremath{-}\mathrm{\ensuremath{\Pi}}$ transition for cooling and trapping. The resultant hyperfine splittings of each rovibrational state in the ${X}^{2}{\mathrm{\ensuremath{\Sigma}}}^{+}$ state provide benchmarks for sideband modulations of the cooling and repumping lasers and the remixing microwaves to address all necessary levels. The calculated Zeeman shift and ggg factors for both XXX and AAA states serve as benchmarks for selection of the trapping laser polarizations. Our study paves the way for future laser cooling and magneto-optical trapping of the BaF molecule.
In red-detuned magneto-optical traps (MOTs) of molecules, sub-Doppler heating competes with Doppler cooling, resulting in high temperature and low density. A solution is offered by the blue-detuned MOT where sub- Doppler cooling dominates and the cloud is compressed. Several blue-detuned molecular MOTs have been implemented. A recent implementation relies on a pair of orthogonally polarized components whose frequency separation is smaller than the transition linewidth. We identify the trapping force in these MOTs. At a certain magnetic field, there is a state that is dark to the laser propagating in one direction, but not to the counterpropagating one. This Zeeman-induced dark state (ZIDS) sets up an imbalance in the photon scattering rate, leading to a restoring force. We also study the role of the moving lattices generated by the closely spaced frequency components of the light. We show that there is a velocity-dependent force that drives the molecules toward the speeds of these moving lattices, and that over a relevant range of magnetic fields this combines with the ZIDS force to transport molecules toward the center of the MOT. Here, gray molasses cooling, assisted by nonadiabatic transitions driven by the time-varying polarization of the light field, cools the molecules toward zero velocity. We study these mechanisms for model systems with simple level structures and then extend them to molecules with ground-state hyperfine structure.