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S. Truppe

Publications and source records attributed to S. Truppe.

17 recordsLinked to original sources

Robust watt-level continuous-wave deep-ultraviolet lasers near 230 nm

Continuous-wave (CW) deep-ultraviolet (DUV) lasers near 230~nm enable laser cooling of AlF, Cd, and Zn, but second-harmonic generation below 237~nm relies in practice on beta-barium borate (BBO), whose walk-off and UV-induced degradation hinder sustained operation. We demonstrate compact, affordable VECSEL-based systems informed by four years of operating 14 DUV cavities in 12 laser systems across six European laboratories. External LBO cavities produce nearly 4~W at 463~nm with 94% cavity efficiency. We compare spherically and elliptically focused Brewster-cut BBO cavities with a normal-incidence AR-coated design. The AR-coated cavity delivers the highest power and efficiency, reaching 1.0~W at 51% cavity and 44% external efficiency; the spherical Brewster cavity reaches 700~mW and maintains constant circulating power over 70~h, while elliptical focusing reduces peak intensity sixfold and improves beam quality, albeit with greater alignment sensitivity. Collaboration-designed DUV optics, AlF spectroscopy, and Cd trapping validate the system.

physics.atom-ph

Magneto-optical trapping of aluminum monofluoride

Magneto-optical trapping of molecules has thus far been restricted to molecules with $^2Σ$ electronic ground states. These species are chemically reactive and only support a simple laser cooling scheme from their first excited rotational level. Here, we demonstrate a magneto-optical trap (MOT) of aluminum monofluoride (AlF), a deeply bound and intrinsically stable diatomic molecule with a $^1Σ^+$ electronic ground state. The MOT operates on the strong A$^1Π\leftarrow{}$X$^1Σ^+$ transition near 227.5~nm, whose Q$(J)$ lines are all rotationally closed. We demonstrate a MOT of about $6\times 10^4$ molecules for the $J=1$ level of AlF, more than $10^4$ molecules for $J=2$ and $3$, and with no fundamental limit in going to higher rotational levels. Laser cooling and trapping of AlF is conceptually similar to the introduction of alkaline-earth atoms into cold atom physics, and is key to leveraging its spin-forbidden a$^3Π\leftarrow{}$X$^1Σ^+$ transition for precision spectroscopy and narrow-line cooling.

physics.atom-ph

A large magneto-optical trap of cadmium atoms loaded from a cryogenic buffer gas beam

We demonstrate rapid loading of a magneto-optical trap (MOT) of cadmium atoms from a pulsed cryogenic helium buffer gas beam, overcoming strong photoionization losses. Using the $ ^1S_0 \rightarrow{} ^1P_1 $ transition at 229 nm, we capture up to $ 1.1(2) \times 10^7$ $^{112}$Cd atoms in 10 ms, achieving a peak density of $2.5 \times 10^{11}$cm$^{-3}$ and a phase-space density of $ 2 \times 10^{-9} $. The large scattering force in the deep ultraviolet enables Zeeman slowing within 5 cm of the trap, yielding a capture velocity exceeding 200 m/s. We measure the MOT trap frequency and damping constant, and determine the absolute photoionization cross section of the $^1P_1 $ state. Photoionization losses are mitigated via dynamic detuning of the trapping light's frequency, allowing efficient accumulation of multiple atomic pulses. Our results demonstrate the benefits of deep-UV (DUV) transitions and cryogenic beams for loading high-density MOTs, especially for species with significant loss channels in their main cooling cycle. The cadmium MOT provides a robust testbed that benchmarks our DUV laser cooling system and establishes the foundation for trapping and cooling polar AlF molecules, which share many optical and structural properties with Cd.

physics.atom-ph

Isotope Shifts in Cadmium as a Sensitive Probe for Physics Beyond the Standard Model

Isotope shifts (ISs) in atomic energy levels are sensitive probes of nuclear structure and new physics beyond the Standard Model. We present an analysis of the ISs of the cadmium atom (Cd I) and singly charged cadmium ion (Cd II). ISs of the 229 nm, 326 nm, 361 nm and 480 nm lines of Cd I are measured with a variety of techniques; buffer-gas-cooled beam spectroscopy, capturing atoms in a magneto-optic-trap, and optical pumping. IS constants for the D1 and D2 lines of Cd II are calculated with high accuracy by employing analytical response relativistic coupled-cluster theory in the singles, doubles and triples approximations. Combining the calculations for Cd II with experiments, we infer IS constants for all low-lying transitions in Cd I. We benchmark these constants as calculated via different many-body methods. Our calculations for Cd II enable nuclear charge radii of Cd isotopes to be extracted with unprecedented accuracy. The combination of our precise calculations and measurements shows that King Plots for Cd I can improve the state-of-theart sensitivity to a new heavy boson by up to two orders of magnitude.

physics.atom-ph

The chemistry of AlF and CaF production in buffer gas sources

In this work, we explore the role of chemical reactions on the properties of buffer gas-cooled molecular beams. In particular, we focus on scenarios relevant to the formation of AlF and CaF via chemical reactions between the Ca and Al atoms ablated from a solid target in an atmosphere of a fluorine-containing gas, in this case, SF6 and NF3. Reactions are studied following an ab initio molecular dynamics approach, and the results are rationalized following a tree-shaped reaction model based on Bayesian inference. We find that NF3 reacts more efficiently with hot metal atoms to form monofluoride molecules than SF6. In addition, when using NF3, the reaction products have lower kinetic energy, requiring fewer collisions to thermalize with the cryogenic helium. Furthermore, we find that the reaction probability for AlF formation is much higher than for CaF across a broad range of temperatures.

physics.comp-ph

Hyperfine resolved optical spectroscopy of the A$^2Π\leftarrow $X$^2Σ^+$ transition in MgF

We report on hyperfine-resolved laser spectroscopy of the A$^2Π\leftarrow $X$^2Σ^+$ transition of MgF, relevant for laser cooling. We recorded 25 rotational transitions with an absolute accuracy of better than 20 MHz, assigned 56 hyperfine lines and determined precise rotational, fine and hyperfine structure parameters for the A$^2Π$ state. The radiative lifetime of the A$^2Π$ state was determined to be 7.2(3) ns, in good agreement with \textit{ab initio} calculations. The transition isotope shift between bosonic isotopologues of the molecule is recorded and compared to predicted values within the Born-Oppenheimer approximation. We measured the Stark effect of selected rotational lines of the A$^2Π\leftarrow $X$^2Σ^+$ transition by applying electric fields of up to 10.6 kV cm$^{-1}$ and determined the permanent electric dipole moments of $^{24}$MgF in its ground X$^2Σ^+$ and first excited A$^2Π$ states to be $μ_X=$2.88(20) D and $μ_A=$3.20(22) D, respectively. Based on these measurements, we caution for potential losses from the optical cycling transition, due to electric field induced parity mixing in the excited state. In order to scatter $10^4$ photons, the electric field must be controlled to below 1 V cm$^{-1}$.

physics.atom-ph

Spectroscopic characterization of aluminum monofluoride with relevance to laser cooling and trapping

Here we report on spectroscopic measurements of the aluminum monofluoride molecule (AlF) that are relevant to laser cooling and trapping experiments. We measure the detailed energy level structure of AlF in the X$^1Σ^+$ electronic ground state, in the A$^1Π$ state, and in the metastable a$^3Π$ state. We determine the rotational, vibrational and electronic branching ratios from the A$^1Π$ state. We also study how the rotational levels split and shift in external electric and magnetic fields. We find that AlF is an excellent candidate for laser cooling on any Q-line of the A$^1Π$ - X$^1Σ^+$ transition and for trapping at high densities.

physics.atom-ph

Magnetic trapping and coherent control of laser-cooled molecules

We demonstrate coherent microwave control of the rotational, hyperfine and Zeeman states of ultracold CaF molecules, and the magnetic trapping of these molecules in a single, selectable quantum state. We trap about $5\times 10^{3}$ molecules for 2 s at a temperature of 65(11) $μ$K and a density of $1.2 \times 10^{5}$ cm$^{-3}$. We measure the state-specific loss rate due to collisions with background helium.

physics.atom-ph

A buffer gas beam source for short, intense and slow molecular pulses

Experiments with cold molecules usually begin with a molecular source. We describe the construction and characteristics of a cryogenic buffer gas source of CaF molecules. The source emits pulses with a typical duration of 240 $μ$s, a mean speed of about 150 m/s, and a flux of $5\times 10^{10}$ molecules per steradian per pulse in a single rotational state.

physics.atom-ph

Characteristics of a magneto-optical trap of molecules

We present the properties of a magneto-optical trap (MOT) of CaF molecules. We study the process of loading the MOT from a decelerated buffer-gas-cooled beam, and how best to slow this molecular beam in order to capture the most molecules. We determine 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 MOT, especially the intensity and detuning of the main cooling laser. We compare our results to analytical and numerical models, to the properties of standard atomic MOTs, and to MOTs of SrF molecules. We load up to $2 \times 10^4$ molecules, and measure a maximum scattering rate of $2.5 \times 10^6$ s$^{-1}$ per molecule, a maximum oscillation frequency of 100 Hz, a maximum damping constant of 500 s$^{-1}$, and a minimum MOT rms radius of 1.5 mm. A minimum temperature of 730 $μ$K is obtained by ramping down the laser intensity to low values. The lifetime, typically about 100 ms, is consistent with a leak out of the cooling cycle with a branching ratio of about $6 \times 10^{-6}$. The MOT has a capture velocity of about 11 m/s.

physics.atom-ph

Molecules cooled below the Doppler limit

The ability to cool atoms below the Doppler limit -- the minimum temperature reachable by Doppler cooling -- has been essential to most experiments with quantum degenerate gases, optical lattices and atomic fountains, among many other applications. A broad set of new applications await ultracold molecules, and the extension of laser cooling to molecules has begun. A molecular magneto-optical trap has been demonstrated, where molecules approached the Doppler limit. However, the sub-Doppler temperatures required for most applications have not yet been reached. Here we cool molecules to 50 uK, well below the Doppler limit, using a three-dimensional optical molasses. These ultracold molecules could be loaded into optical tweezers to trap arbitrary arrays for quantum simulation, launched into a molecular fountain for testing fundamental physics, and used to study ultracold collisions and ultracold chemistry.

physics.atom-ph

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

Using frequency-chirped radiation pressure slowing, we precisely control the velocity of a pulsed CaF molecular beam down to a few m/s, compressing its velocity spread by a factor of 10 while retaining high intensity: at a velocity of 15~m/s the flux, measured 1.3~m from the source, is 7$\times$10$^{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.

physics.atom-ph

A high quality, efficiently coupled microwave cavity for trapping cold molecules

We characterize a Fabry-Perot microwave cavity designed for trapping atoms and molecules at the antinode of a microwave field. The cavity is fed from a waveguide through a small coupling hole. Focussing on the compact resonant modes of the cavity, we measure how the electric field profile, the cavity quality factor, and the coupling efficiency, depend on the radius of the coupling hole. We measure how the quality factor depends on the temperature of the mirrors in the range from 77 to 293K. The presence of the coupling hole slightly changes the profile of the mode, leading to increased diffraction losses around the edges of the mirrors and a small reduction in quality factor. We find the hole size that maximizes the intra-cavity electric field. We develop an analytical theory of the aperture-coupled cavity that agrees well with our measurements, with small deviations due to enhanced diffraction losses. We find excellent agreement between our measurements and finite-difference time-domain simulations of the cavity.

physics.atom-ph

Vibrational branching ratios and hyperfine structure of $^{11}$BH and its suitability for laser cooling

The simple structure of the BH molecule makes it an excellent candidate for direct laser cooling. We measure the branching ratios for the decay of the ${\rm A}^{1}Π(v'=0)$ state to vibrational levels of the ground state, ${\rm X}^{1}Σ^{+}$, and find that they are exceedingly favourable for laser cooling. We verify that the branching ratio for the spin-forbidden transition to the intermediate ${\rm a}^{3}Π$ state is inconsequentially small. We measure the frequency of the lowest rotational transition of the X state, and the hyperfine structure in the relevant levels of both the X and A states, and determine the nuclear electric quadrupole and magnetic dipole coupling constants. Our results show that, with a relatively simple laser cooling scheme, a Zeeman slower and magneto-optical trap can be used to cool, slow and trap BH molecules.

physics.atom-ph

Microwave spectroscopy of Lambda-doublet transitions in the ground state of CH

The Lambda-doublet transitions in CH at 3.3 and 0.7 GHz are unusually sensitive to variations in the fine-structure constant and the electron-to-proton mass ratio. We describe methods used to measure the frequencies of these transitions with Hz-level accuracy. We produce a pulsed supersonic beam of cold CH by photodissociation of CHBr3, and we measure the microwave transition frequencies as the molecules propagate through a parallel-plate transmission line resonator. We use the molecules to map out the amplitude and phase of the standing wave field inside the transmission line. We investigate velocity-dependent frequency shifts, showing that they can be strongly suppressed through careful timing of the microwave pulses. We measure the Zeeman and Stark effects of the microwave transitions, and reduce systematic shifts due to magnetic and electric fields to below 1 Hz. We also investigate other sources of systematic uncertainty in the experiment.

physics.atom-ph

Measurement of the lowest millimetre-wave transition frequency of the CH radical

The CH radical offers a sensitive way to test the hypothesis that fundamental constants measured on earth may differ from those observed in other parts of the universe. The starting point for such a comparison is to have accurate laboratory frequencies. Here we measure the frequency of the lowest millimetre-wave transition of CH, near 535 GHz, with an accuracy of 0.6 kHz. This improves the uncertainty by roughly two orders of magnitude over previous determinations and opens the way for sensitive new tests of varying constants.

physics.atom-ph

A search for varying fundamental constants using Hz-level frequency measurements of cold CH molecules

Many modern theories predict that the fundamental constants depend on time, position, or the local density of matter. We develop a spectroscopic method for pulsed beams of cold molecules, and use it to measure the frequencies of microwave transitions in CH with accuracy down to 3 Hz. By comparing these frequencies with those measured from sources of CH in the Milky Way, we test the hypothesis that fundamental constants may differ between the high and low density environments of the Earth and the interstellar medium. For the fine structure constant we find Δα/α= (0.3 +/- 1.1)*10^{-7}, the strongest limit to date on such a variation of α. For the electron-to-proton mass ratio we find Δμ/μ= (-0.7 +/- 2.2) * 10^{-7}. We suggest how dedicated astrophysical measurements can improve these constraints further and can also constrain temporal variation of the constants.

physics.atom-ph