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Ties H. Fikkers

Publications and source records attributed to Ties H. Fikkers.

4 recordsLinked to original sources

2D transverse laser cooling of a hexapole focused beam of cold BaF molecules

A cryogenic buffer gas beam, an electrostatic hexapole lens, and 2D transverse Doppler laser cooling are combined to produce a bright beam of barium monofluoride ($^{138}$Ba$^{19}$F) molecules. Experimental results and trajectory simulations are used to study the laser cooling effect as a function of laser detuning, laser power, laser alignment, and interaction time. A scattering rate of 6.1(1.4) $\times 10^{5}$ s$^{-1}$ on the laser cooling transition is obtained; this is $14 \%$ of the expected maximum, which is attributed to limited control of the magnetic field used to remix dark states. Using 3 tuneable lasers with appropriate sidebands and detuning, each molecule scatters approximately 400 photons during 2D laser cooling, limited by the interaction time and scattering rate. Leaks to dark states are less than 10$\%$. The experimental results are used to benchmark the trajectory simulations to predict the achievable flux 3.5 m downstream for a planned $e$EDM experiment.

physics.atom-ph↗

Manipulating a beam of barium fluoride molecules using an electrostatic hexapole

An electrostatic hexapole lens is used to manipulate the transverse properties of a beam of barium fluoride molecules from a cryogenic buffer gas source. The spatial distribution of the beam is measured by recording state-selective laser-induced fluorescence on an emccd camera, providing insight into the intensity and transverse position spread of the molecular beam. Although the high mass and unfavorable Stark shift of barium fluoride pose a considerable challenge, the number of molecules in the low-field seeking component of the N=1 state that pass a 4 mm diameter aperture 712 mm behind the source is increased by a factor of 12. Furthermore, it is demonstrated that the molecular beam can be displaced by up to +/-5 mm by moving the hexapole lens. Our measurements agree well with numerical trajectory simulations. We discuss how electrostatic lenses may be used to increase the sensitivity of beam experiments such as the search for the electric dipole moment of the electron.

physics.atom-ph↗

A novel method to determine the phase-space distribution of a pulsed molecular beam

We demonstrate a novel method to determine the longitudinal phase-space distribution of a cryogenic buffer gas beam of barium-fluoride molecules based on a two-step laser excitation scheme. The spatial resolution is achieved by a transversely aligned laser beam that drives molecules from the ground state $X^2Σ^+$ to the $A^2Π_{1/2}$ state around 860 nm, while the velocity resolution is obtained by a laser beam that is aligned counter-propagating with respect to the molecular beam and that drives the Doppler shifted $A^2Π_{1/2}$ to $D^2Σ^+$ transition around 797 nm. Molecules in the $D$-state are detected virtually background-free by recording the fluorescence from the $D-X$ transition at 413 nm. As molecules in the ground state do not absorb light at 797 nm, problems due to due to optical pumping are avoided. Furthermore, as the first step uses a narrow transition, this method can also be applied to molecules with hyperfine structure. The measured phase-space distributions, reconstructed at the source exit, show that the average velocity and velocity spread vary significantly over the duration of the molecular beam pulse. Our method gives valuable insight into the dynamics in the source and helps to reduce the velocity and increase the intensity of cryogenic buffer gas beams. In addition, transition frequencies are reported for the $X-A$ and $X-D$ transitions in barium fluoride with an absolute accuracy below 0.3 MHz.

physics.atom-ph↗

Mass and Shape Determination of Optically Levitated Nanoparticles

When introducing a nanoparticle into an optical trap, its mass and shape are not immediately apparent. We combine a charge-based mass measurement with a shape determination method based on light scattering and an analysis of the damping rate anisotropy, all on the same set of silica nanoparticles, trapped using optical tweezers in vacuum. These methods have previously only been used separately, and the mass determination method has not been applied to asymmetric particles before. We demonstrate that the combination of these classification techniques is required to distinguish particles with similar mass but different shape, and vice versa. The ability to identify these parameters is a key step for a range of experiments on precision measurements and sensing using optically levitated nanoparticles.

physics.optics↗