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Russell Thomas

Publications and source records attributed to Russell Thomas.

3 recordsLinked to original sources

Continuous thermochemical sources of AlF 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 $5\times 10^{15}$ 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.

physics.atom-ph

Hyperfine structure and isotope shifts of the $^1P_1 \leftarrow{} ^{1}S_0$ transition in atomic zinc

We report absolute frequency, isotope shift, radiative lifetime and hyperfine structure measurements of the $^1P_1 \leftarrow{} ^{1}S_0$ (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 clear distinction between isotopes whose resonances are otherwise unresolved, and a measurement of the fermion hyperfine structure parameters, $A(^{67}$Zn)$=20(2)$ MHz and $B(^{67}$Zn)$=10(5)$ 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.

physics.atom-ph

High-resolution isotope-shift spectroscopy of Cd I

We present absolute frequency measurements of the ${}^{1}\text{P}_1 \leftarrow {}^{1}\text{S}_0$ ($229$nm) and ${}^{3}\text{P}_1 \leftarrow {}^{1}\text{S}_0$ ($326$nm) transitions for all naturally occurring isotopes of cadmium. The isotope shifts and hyperfine intervals of the fermionic isotopes are determined with an accuracy of 3.3MHz. We find that quantum interference in the laser-induced fluorescence spectra of the ${}^{1}\text{P}_1 \leftarrow {}^{1}\text{S}_0$ transition causes an error of up to 29(5)MHz in determining the hyperfine splitting, when not accounted for with an appropriate model. Using a King-plot analysis, we extract the field- and mass-shift parameters and determine nuclear charge radius differences for the fermions. The lifetime of the $^1\text{P}_1$ state is determined to be 1.60(5)ns by measuring the natural linewidth of the ${}^{1}\text{P}_1 \leftarrow {}^{1}\text{S}_0$ transition. These results resolve significant discrepancies among previous measurements.

physics.atom-ph