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arXiv:1605.06055 · New Journal of Physics

An intense, cold, velocity-controlled molecular beam by frequency-chirped laser slowing

Stefan Truppe, H. J. Williams, Noah J. Fitch, Moritz Hambach, Thomas E. Wall, E. A. Hinds, B. E. Sauer, Michael R. Tarbutt

Published Jan 31, 2017• 78 citations
arXivHTMLPDF

Abstract

Using frequency-chirped radiation pressure slowing, we precisely control the velocity of a pulsed CaF molecular beam down to a few m s –1 , compressing its velocity spread by a factor of 10 while retaining high intensity: at a velocity of 15 m s –1 the flux, measured 1.3 m from the source, is 7 × 10 5 molecules per cm 2 per shot in a single rovibrational state. The beam is suitable for loading a magneto-optical trap or, when combined with transverse laser cooling, improving the precision of spectroscopic measurements that test fundamental physics. We compare the frequency-chirped slowing method with the more commonly used frequency-broadened slowing method.

DOI
10.1088/1367-2630/aa5ca2

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Using frequency-chirped radiation pressure slowing, we precisely control the velocity of a pulsed CaF molecular beam down to a few m s –1 , compressing its velocity spread by a factor of 10 while retaining high intensity: at a velocity of 15 m s –1 the flux, measured 1.3 m from the source, is 7 × 10 5 molecules per cm 2 per shot in a single rovibrational state. The beam is suitable for loading a magneto-optical trap or, when combined with transverse laser cooling, improving the precision of spectroscopic measurements that test fundamental physics. We compare the frequency-chirped slowing method with the more commonly used frequency-broadened slowing method.
From studies of fundamental physics to quantum technologies the production of ultracold molecules will have a huge impact across a range of applications. For many years laser cooling, which became an invaluable tool in cold atomic physics, was deemed to be too impractical for application to molecules. Nevertheless, laser cooling has now been demonstrated for a few molecular species. Using a frequency-chirped laser slowing technique, the velocity distribution of a pulse of CaF molecules is compressed and slowed from 180 m/s to about 10 m/s. These slow molecules are then captured in a magneto-optical trap. I present measurements that show how the number of molecules, the photon scattering rate, the oscillation frequency, damping constant, temperature, cloud size and lifetime depend on the key parameters of the magneto-optical trap, especially the intensity and detuning of the main cooling laser. The trap contains up to 2*10^4 molecules, the maximum photon scattering rate is 2.5*10^6 s-1 per molecule, the maximum oscillation frequency is 100 Hz, the maximum damping constant is 500 s^-1, and the minimum rms radius of the trapped cloud is 1.5 mm. A minimum temperature of 730 microkelvin is obtained by ramping down the laser intensity to lower values. To reach lower temperatures, the cloud is loaded into a blue-detuned optical molasses, which cools the molecules to 55 microkelvin, well below the Doppler-limiting temperature. I characterise the cooling process and suggest the sub-Doppler mechanisms responsible. These ultracold molecules are the optically pumped into a single quantum state, and coherently transferred between selected hyperfine components of the ground and first-excited rotational states. Finally, the ultracold, state-selected molecules are loaded into a magnetic trap that has a lifetime of about 1 s.
Laser cooling and trapping in a magneto-optical trap (MOT) have been essential to the success of cold atom physics in the last decades. Recently, the application of the same techniques to molecules has begun. The complexity of even a simple diatomic molecule makes laser cooling difficult, but promises new applications in many areas of research. In this thesis I describe the development of the first three-dimensional MOT of calcium fluoride (CaF) molecules. First, a cryogenic buffer gas source was set up, producing a pulsed beam of 9.3*10^10 molecules per steradian per pulse with forward velocities around 170 m/s. A similar source for very large molecules was set up during a 5 month internship at the University of Vienna. Next, the molecular pulse was slowed down to the capture velocity of a MOT using chirped laser slowing, resulting in about 7*10^5 CaF molecules passing through the typical MOT volume of 1 cm^3 at velocities of 15+-5 m/s. A new deceleration method, called Zeeman-Sisyphus deceleration, was also investigated. In this method molecules move through a spatially varying magnetic field and are optically pumped between low- and high-field seeking states in such as a way that they are always losing kinetic energy. The method promises to deliver more slow molecules because the molecules are guided transversely as they are decelerated. A small prototype was built and the optical pumping step was tested successfully. Finally, 7.6*10^3 CaF molecules were trapped in a MOT and cooled to a temperature of 8.5 mK. The radial trap frequency is 2 pi*130 Hz and the damping constant is beta=9.5*10^2 s^-1. The lifetime is about 100 ms and depends strongly on the scattering rate. This MOT is an an ideal starting point for a wide range of new experiments with ultracold molecules.
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.
We demonstrate deceleration of a beam of neutral strontium monofluoride molecules using radiative forces. Under certain conditions, the deceleration results in a substantial flux of detected molecules with velocities ≲50 m/s. Simulations and other data indicate that the detection of molecules below this velocity is greatly diminished by transverse divergence from the beam. The observed slowing, from ∼140 m/s, corresponds to scattering ≳10(4) photons. We also observe longitudinal velocity compression under different conditions. Combined with molecular laser cooling techniques, this lays the groundwork to create slow and cold molecular beams suitable for trap loading.