We have developed a continuous SrF radical beam for the loading of helium buffer gas cooling. The SrF molecules are efficiently generated by high-temperature chemical reaction of the solid precursor SrF(2) with boron in a graphite oven. The beam properties are characterized with laser-induced fluorescence spectroscopic method. We obtain a molecular flux of up to 2.1x10(15) sr(-1) s(-1) at the detection region for all rotational states. The dependence of the flux on oven temperature suggests that even higher flux is possible if a higher temperature in the oven is achieved.
We have developed a continuous SrF radical beam for the loading of helium buffer gas cooling. The SrF molecules are efficiently generated by high-temperature chemical reaction of the solid precursor SrF(2) with boron in a graphite oven. The beam properties are characterized with laser-induced fluorescence spectroscopic method. We obtain a molecular flux of up to 2.1x10(15) sr(-1) s(-1) at the detection region for all rotational states. The dependence of the flux on oven temperature suggests that even higher flux is possible if a higher temperature in the oven is achieved.
We demonstrate and characterize a cryogenic buffer gas-cooled molecular beam source capable of producing bright beams of free radicals and refractory species. Details of the beam properties (brightness, forward velocity distribution, transverse velocity spread, rotational and vibrational temperatures) are measured under varying conditions for the molecular species SrF. Under typical conditions we produce a beam of brightness 1.2 × 10(11) molecules/sr/pulse in the X(2)Σ(+)(v = 0, N(rot) = 0) state, with 140(m/s) forward velocity and a rotational temperature of ≈ 1 K. This source compares favorably to other methods for producing beams of free radicals and refractory species for many types of experiments. We provide details of construction that may be helpful for others attempting to use this method.
We demonstrate a cryogenic buffer gas-cooled molecular beam source capable of producing bright, continuous beams of cold and slow free radicals via laser ablation over durations of up to 60 seconds. The source design uses a closed liquid helium reservoir as a large thermal mass to minimize heating and ensure reproducible beam properties during operation. Under typical conditions, the source produces beams of our test species SrF, containing $5\ifmmode\times\else\texttimes\fi{}{10}^{12}$ molecules per steradian per second in the $X{\phantom{\rule{0.16em}{0ex}}}^{2}\mathrm{\ensuremath{\Sigma}}(v=0,N=1)$ state with a rotational temperature of 1.0(2) K and a forward velocity of 140m/s. The beam properties are robust and unchanged for multiple cell exit geometries, but depend critically on the helium buffer gas flow rate, which must be $\ensuremath{\ge}10$ standard cubic centimeters per minute to produce bright, continuous beams of molecules for an ablation repetition rate of 55 Hz.
We realize a continuous, intense, cold molecular and atomic beam source based on buffer-gas cooling. Hot vapor (up to 600 K) from an oven is mixed with cold (15 K) neon buffer gas, and then emitted into a high-flux beam. The novel use of cold neon as a buffer gas produces a forward velocity distribution and low-energy tail that is comparable to much colder helium-based sources. We expect this source to be trivially generalizable to a very wide range of atomic and molecular species with significant vapor pressure below 1000 K. The source has properties that make it a good starting point for laser cooling of molecules or atoms, cold collision studies, trapping, or nonlinear optics in buffer-gas-cooled atomic or molecular gases. A continuous guided beam of cold deuterated ammonia with a flux of 3×10\\(^{11}\\) ND\\(_{3}\\) molecules s\\(^{−1}\\) and a continuous free-space beam of cold potassium with a flux of 1×10\\(^{16}\\) K atoms s\\(^{−1}\\) are realized.
We realize a continuous, intense, cold molecular and atomic beam source based on buffer-gas cooling. Hot vapor (up to 600 K) from an oven is mixed with cold (15 K) neon buffer gas, and then emitted into a high-flux beam. The novel use of cold neon as a buffer gas produces a forward velocity distribution and low-energy tail that is comparable to much colder helium-based sources. We expect this source to be trivially generalizable to a very wide range of atomic and molecular species with significant vapor pressure below 1000 K. The source has properties that make it a good starting point for laser cooling of molecules or atoms, cold collision studies, trapping, or nonlinear optics in buffer-gas-cooled atomic or molecular gases. A continuous guided beam of cold deuterated ammonia with a flux of 3 × 10 11 ND 3 molecules s −1 and a continuous free-space beam of cold potassium with a flux of 1 × 10 16 K atoms s −1 are realized.
A novel cryogenic MgF molecular beam, characterized by high flux and exceptional stability, has been successfully generated within a helium buffer gas environment. This achievement is facilitated by the innovative use of an in-cell stepper motor, which continuously rotates the sample rod during laser ablation. Through meticulous optimization of the ablation laser energy, the position of the ablation spot, and the gas flow rate, among other critical parameters, the resulting MgF beam exhibits a remarkable forward velocity of 209 m/s and an impressive brightness of approximately 1.36 × 1012 molecules per pulse per steradian per internal state. Subsequent attempts at one-dimensional Doppler cooling of the MgF beam have been made, with theoretical calculations closely aligning with experimental outcomes. These findings demonstrate a significant compression in the transverse spatial distribution of the molecular beam, from 7.8 to 6.5 mm, and a substantial cooling of the transverse temperature, from 8.1 to 5.6 mK. This work lays a crucial foundation for the advancement of molecular slowing and magneto-optical trapping techniques for MgF molecules.
The AlF molecule, currently subject to laser cooling and trapping efforts, has the advantage that it can be efficiently produced in a thermochemical reaction between sublimated aluminum trifluoride and aluminum metal. Here we present a series of experiments with continuous molecular beam sources of AlF, utilising this reaction. We demonstrate a compact AlF molecular beam oven whose total far-field brightness is 5×1015 molecules per steradian per second at 923~K, just below the melting temperature of aluminum metal. The continuous output from the oven begins to exceed the peak brightness of a jet-cooled, ablation-based supersonic AlF source for the v=0, J=7 level, and we obtain an excellent signal-to-noise ratio with the oven in pulsed laser ionisation spectroscopy experiments. By delivering flux from the oven into a cryogenic Ne buffer gas cell, we lower the rotational temperature of the beam to around 30~K and reduce its most probable forward velocity from 600~ms−1 to 200~ms−1. In addition, we demonstrate that AlF can be made in a simple dispenser package, and observe that molecules thermalise to the laboratory temperature after colliding with vacuum chamber walls of the experiment. The resulting transient AlF vapour may enable direct loading of a molecular magneto-optical trap.