Ultracold molecular gases are promising as an avenue to rich many-body physics, quantum chemistry, quantum information, and precision measurements. This richness, which flows from the complex internal structure of molecules, makes the creation of ultracold molecular gases using traditional methods (laser plus evaporative cooling) a challenge, in particular due to the spontaneous decay of molecules into dark states. We propose a way to circumvent this key bottleneck using an all-optical method for decelerating molecules using stimulated absorption and emission with a single ultrafast laser. We further describe single-photon cooling of the decelerating molecules that exploits their high dark state pumping rates, turning the principal obstacle to molecular laser cooling into an advantage. Cooling and deceleration may be applied simultaneously and continuously to load molecules into a trap. We discuss implementation details including multilevel numerical simulations of strontium monohydride. These techniques are applicable to a large number of molecular species and atoms with the only requirement being an electric dipole transition that can be accessed with an ultrafast laser.
Ultracold molecular gases are promising as an avenue to rich many-body physics, quantum chemistry, quantum information, and precision measurements. This richness, which flows from the complex internal structure of molecules, makes the creation of ultracold molecular gases using traditional methods (laser plus evaporative cooling) a challenge, in particular due to the spontaneous decay of molecules into dark states. We propose a way to circumvent this key bottleneck using an all-optical method for decelerating molecules using stimulated absorption and emission with a single ultrafast laser. We further describe single-photon cooling of the decelerating molecules that exploits their high dark state pumping rates, turning the principal obstacle to molecular laser cooling into an advantage. Cooling and deceleration may be applied simultaneously and continuously to load molecules into a trap. We discuss implementation details including multilevel numerical simulations of strontium monohydride. These techniques are applicable to a large number of molecular species and atoms with the only requirement being an electric dipole transition that can be accessed with an ultrafast laser.
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.
Molecules controlled at the single-quantum-state level offer wide-ranging applications spanning many of the frontiers of modern physics. Within the past decade, simple diatomic molecules have been brought under full quantum control both via assembly from pre-cooled atoms and by direct laser cooling. Polyatomic molecules\footnote{Molecules that contain three or more atoms.} have attracted focus as novel quantum resources providing distinct advantages (and challenges) compared to both atoms and diatomic molecules. For example, nearly all polyatomic molecules have long-lived states that can be fully polarized at low applied electric fields. These and other features generic to polyatomic molecules can be applied to quantum simulation, quantum chemistry, and tests of fundamental physics beyond the Standard Model. While these structural features of polyatomic molecules are highly promising for applications, they complicate the process of bringing molecules under full quantum control. In this thesis, we describe a series of experimental and theoretical advances toward the production of ultracold complex polyatomic molecules. We demonstrate the first laser cooling of the polyatomic radical ytterbium monohydroxide (YbOH), a promising candidate to search for particles and interactions beyond the Standard Model of particle physics. We develop a novel deceleration technique (``Zeeman-Sisyphus deceleration") capable of slowing molecular beams to trappable velocities while scattering fewer than 10 optical photons. This deceleration method is demonstrated using CaOH molecules, a lighter analog of YbOH. In order to determine a viable pathway to full three-dimensional cooling and trapping of YbOH, we develop a spectroscopic technique to measure vibrational branching ratios with relative intensity sensitivity around 1 part in 105, approximately two orders of magnitude beyond the previous state of the art. We also perform the first spectroscopic observations and characterizations of the related molecule ytterbium monomethoxide, YbOCH3, a promising species to probe beyond-the-Standard-Model physics. In addition, we show theoretically that an entire class of asymmetric top molecules can be laser cooled using essentially the same techniques used for much simpler species. Measurements of the vibrational branching ratios for a few prototypical asymmetric to molecules (CaSH and CaNH2) are presented to confirm these predictions.
Ultracold matter offers a unique capability to reach the best high-precision spectroscopy measurements and leads to exciting perspectives in many different areas of science and technology. Molecules, thanks to their complex spectra, couple with a broader range of photons compared to atoms, so they are extremely attractive for fundamental science or to design new quantum technologies. However, to date, only a few molecular species have been brought to temperatures of the order of the microkelvin. This was done by laser cooling, a process that has been demonstrated only for species featuring an unpaired electron that does not participate to the chemical bond. \n \nA different approach, which is indifferent to the molecule electronic structure and thus potentially universal, is sympathetic cooling, where neutral molecules are cooled in a bath of ultracold atoms. However, inelastic collisions between molecules and the coolant is a major obstacle that has hindered the advances of this method thus far. Trapping the molecules in their absolute ground state would circumvent this problem or at least greatly simplify it. In this thesis we simulate the feasibility of an experiment in which metastable CO molecules are first slowed down to a few m/s with a microstructured Stark decelerator, then they are stopped by a strong DC electrical barrier and finally they are transferred irreversibly to their absolute ground state and captured in an optical trap. \nUnfortunately, the results of the simulations indicate that the total number of molecules that can be accumulated in the optical trap is rather low, far behind the observation threshold. Therefore, we concluded that other approaches to produce ultracold molecules must to be searched.
Different from atoms, molecules have unique properties, and play an important role in the research of atomic, molecular and optical physics. Cold molecules have important applications in science and have been studied for more than 20 years. But traditional methods, such as the Stark decelerator, have hit a bottleneck: it is hard to increase the phase space density of molecules. Extending the direct laser-cooling technique to new molecular species has recently been a hot topic and also a big challenge. In this review paper, on one hand, we make a brief review to recent progresses on the direct laser cooling of polar molecules. On the other hand, a demonstration on the feasibility of laser cooling BaF molecule has been experimentally illustrated, including the analysis on the molecular energy levels, measurements of the high-resolution spectroscopy, efficient pre-cooling and state preparation via buffer-gas cooling and detailed investigations on the molcule-light interactions. All these results not only pave the way for future laser-cooling and -trapping experiments, but also serve as a reference for the laser-cooling explorations on new molecular species.
We present a study of Sisyphus cooling of molecules: The scattering of a single photon removes a substantial amount of the molecular kinetic energy and an optical pumping step allows one to repeat the process. A review of the produced cold molecules so far indicates that the method can be implemented for most of them, making it a promising method able to produce a large sample of molecules at sub-mK temperatures. Considerations of the required experimental parameters, for instance the laser power and linewidth or the trap anisotropy and dimensionality, are given. Rate equations, as well as scattering and dipolar forces, are solved using kinetic Monte Carlo methods for several lasers and several levels. For NH molecules, such detailed simulation predicts a 1000-fold temperature reduction and an increase of the phase-space density by a factor of 107. Even in the case of molecules with both low Franck-Condon coefficients and a nonclosed pumping scheme, 60% of trapped molecules can be cooled from 100 mK to sub-mK temperatures in a few seconds. Additionally, these methods can be applied to continuously decelerate and cool a molecular beam.
Ultracold polar molecules have emerged as promising platforms for quantum simulation, quantum information science, precision measurements of fundamental symmetry violations, and quantum chemistry. Over the past decade, rapid progress in direct laser cooling of molecules has enabled new capabilities such as magneto-optical traps (MOTs), sub-Doppler cooling, and optical dipole traps (ODTs), expanding the quantum toolbox with ultracold molecules of complex internal structures and strong dipolar interactions. This thesis presents the design, construction, and operation of an experiment on ultracold strontium monofluoride (88Sr19F) molecules, demonstrating state-of-the-art techniques for molecular laser cooling and trapping. The apparatus integrates a broad range of technical sub-systems, including cryogenics, ultra-high vacuum, optics, electronics, and automated laboratory control software. SrF molecules produced in a slowed cryogenic buffer gas beam are captured into a dual-frequency MOT. Subsequent Λ-enhanced gray molasses cooling reduces the molecule temperature to as low as 5 μK. A novel blue-detuned MOT is also implemented to further compress the molecular cloud, increasing the density by a factor of ∼ 400. At this high density, SrF molecules are efficiently loaded into an ODT, a tight, conservative trap with long lifetimes. Population transfer between different rotational levels is achieved via optical pumping and coherent microwave control, yielding ∼ 0.8 ms coherence time in Rabi oscillation and ∼ 90 % transfer efficiency. This thesis also describes the development of an ultracold rubidium (87Rb) atom experiment, in which a loading rate of ∼ 10^10 atoms/s into a radio-frequency (RF) MOT is demonstrated. A modular two-dimensional MOT serves as the Rb source and can be seamlessly integrated into the SrF apparatus, opening the possibility for future studies of co-trapping and sympathetic cooling of SrF molecules with atoms. The results presented in this thesis establish an experimental foundation for exploring new frontiers in ultracold molecular physics.