Cryogenic Buffer-gas Beam Research Articles

Hyperfine structure and isotope shifts of the (4s2)S01→(4s4p)P11 transition in atomic zinc

We report absolute frequency, isotope shift, radiative lifetime, and hyperfine structure measurements of the (4s2)S01→(4s4p)P11 (213.8 nm) transition in Zn I using a cryogenic buffer gas beam. Laser-induced fluorescence is collected with two orthogonally oriented detectors to take advantage of differences in the emission pattern of the isotopes. This enables a clear distinction between isotopes whose resonances are otherwise unresolved, and a measurement of the Zn67 hyperfine structure parameters, A(Zn67)=20(2)MHz and B(Zn67)=10(5)MHz. We reference our frequency measurements to an ultralow expansion cavity and achieve an uncertainty at the level of 1 MHz, about 1 percent of the natural linewidth of the transition. Published by the American Physical Society 2024

Direct laser cooling of calcium monohydride molecules

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 photons s−1 and demonstrate interaction-time limited scattering of 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.

Deceleration and Trapping of SrF Molecules.

We report on the electrostatic trapping of neutral SrF molecules. The molecules are captured from a cryogenic buffer-gas beam source into the moving traps of a 4.5-m-long traveling-wave Stark decelerator. The SrF molecules in X^{2}Σ^{+}(v=0,N=1) state are brought to rest as the velocity of the moving traps is gradually reduced from 190 m/s to zero. The molecules are held for up to 50ms in multiple electric traps of the decelerator. The trapped packets have a volume (FWHM) of 1 mm^{3} and a velocity spread of 5(1) m/s, which corresponds to a temperature of 60(20)mK. Our result demonstrates a factor 3 increase in the molecular mass that has been Stark decelerated and trapped. Heavy molecules (mass>100 amu) offer a highly increased sensitivity to probe physics beyond the standard model. This work significantly extends the species of neutral molecules of which slow beams can be created for collision studies, precision measurement, and trapping experiments.

Simulation of cryogenic buffer gas beams

The cryogenic buffer gas beam (CBGB) is an important tool in the study of cold and ultracold molecules. While there are known techniques to enhance desired beam properties, such as high flux, low velocity, or reduced divergence, they have generally not undergone detailed numerical optimization. Numerical simulation of buffer gas beams is challenging, as the relevant dynamics occur in regions where the density varies by orders of magnitude, rendering standard numerical methods unreliable or intractable. Here, we present a hybrid approach to simulating CBGBs that combines gas dynamics methods with particle tracing. The simulations capture important properties such as velocities and divergence across an assortment of designs, including two-stage slowing cells and de Laval nozzles. This approach should therefore be a useful tool for optimizing CBGB designs across a wide range of applications.

Optical cycling, radiative deflection and laser cooling of barium monohydride (138Ba1H)

We present the first experimental demonstration of radiation pressure force deflection and direct laser cooling for barium monohydride (BaH) molecules resulting from multiple photon scattering. Despite a small recoil velocity (2.7 mm s−1) and a long excited state lifetime (137 ns), we use 1060 nm laser light exciting the X → A electronic transition of BaH to deflect a cryogenic buffer-gas beam and reduce its transverse velocity spread. Multiple experimental methods are employed to characterize the optical cycling dynamics and benchmark theoretical estimates based on rate equation models as well as solutions of the Lindblad master equation for the complete multilevel system. Broader implications for laser cooling and magneto-optical trapping of heavy-metal-containing molecules with narrow transition linewidths are presented. Our results pave the way for producing a new class of ultracold molecules—alkaline earth monohydrides—via direct laser cooling and trapping, opening the door to realizing a new method for delivering ultracold hydrogen atoms (Lane 2015 Phys. Rev. A 92, 022511).

Shaped nozzles for cryogenic buffer-gas beam sources

Cryogenic buffer gas beams are important sources of cold molecules. In this work we explore the use of a converging-diverging nozzle with a buffer-gas beam. We find that, under appropriate circumstances, the use of a nozzle can produce a beam with improved collimation, lower transverse temperatures, and higher fluxes per solid angle.

Production of carbon clusters C3 to C12 with a cryogenic buffer-gas beam source.

Cryogenic buffer-gas beam sources are capable of producing intense beams of a wide variety of molecules and have a number of advantages over traditional supersonic expansion sources. In this work, we report on a neon matrix isolation study of carbon clusters produced with a cryogenic buffer-gas beam source. Carbon clusters created by laser ablation of graphite are trapped in a neon matrix and detected with a Fourier-transform infrared spectrometer in the spectral range 4000-1000 cm-1. Through a study of carbon cluster production as a function of various system parameters, we characterize the behavior of the buffer-gas beam source and find that approximately 1011-1012 of each cluster is produced with each pulse of the ablation laser. These measurements demonstrate the usefulness of cryogenic buffer-gas beam sources for producing molecular beams of clusters.

Proposal for Laser Cooling of Complex Polyatomic Molecules.

An experimentally feasible strategy for direct laser cooling of polyatomic molecules with six or more atoms is presented. Our approach relies on the attachment of a metal atom to a complex molecule, where it acts as an active photon cycling site. We describe a laser cooling scheme for alkaline earth monoalkoxide free radicals taking advantage of the phase space compression of a cryogenic buffer-gas beam. Possible applications are presented including laser cooling of chiral molecules and slowing of molecular beams using coherent photon processes.

Radiation pressure force from optical cycling on a polyatomic molecule

We demonstrate multiple photon cycling and radiative force deflection on the triatomic free radical strontium monohydroxide (SrOH). Optical cycling is achieved on SrOH in a cryogenic buffer-gas beam by employing the rotationally closed branch of the vibronic transition . A single repumping laser excites the Sr–O stretching vibrational mode, and photon cycling of the molecule deflects the SrOH beam by an angle of via scattering of ∼100 photons per molecule. This approach can be used for direct laser cooling of SrOH and more complex, isoelectronic species.

Rotational State Microwave Mixing for Laser Cooling of Complex Diatomic Molecules.

We demonstrate the mixing of rotational states in the ground electronic state using microwave radiation to enhance optical cycling in the molecule yttrium (II) monoxide (YO). This mixing technique is used in conjunction with a frequency modulated and chirped continuous wave laser to slow longitudinally a cryogenic buffer-gas beam of YO. We generate a flux of YO below 10 m/s, directly loadable into a three-dimensional magneto-optical trap. This technique opens the door for laser cooling of diatomic molecules with more complex loss channels due to intermediate states.