eEDM collaboration, P. Aggarwal, Y. Yin, K. Esajas, H. L. Bethlem, A. Boeschoten, A. Borschevsky, S. Hoekstra, K. Jungmann, V. R. Marshall, T. B. Meijknecht, M.… 展开作者
eEDM collaboration, P. Aggarwal, Y. Yin, K. Esajas, H. L. Bethlem, A. Boeschoten, A. Borschevsky, S. Hoekstra, K. Jungmann, V. R. Marshall, T. B. Meijknecht, M. C. Mooij, R. G. E. Timmermans, A. Touwen, W. Ubachs, L. Willmann
We report on the electrostatic trapping of neutral SrF molecules. The molecules are captured from a cryogenic buffer-gas beam source into the moving traps of a 4.5 m long traveling-wave Stark decelerator. The SrF molecules in $X^2Σ^+(v=0, N=1)$ state are brought to rest as the velocity of the moving traps is gradually reduced from 190 m/s to zero. The molecules are held for up to 50 ms in multiple electric traps of the decelerator. The trapped packets have a volume (FWHM) of 1 mm$^{3}$ and a velocity spread of 5(1) m/s which corresponds to a temperature of $60(20)$ mK. Our result demonstrates a factor 3 increase in the molecular mass that has been Stark-decelerated and trapped. Heavy molecules (mass$>$100 amu) offer a highly increased sensitivity to probe physics beyond the Standard Model. This work significantly extends the species of neutral molecules of which slow beams can be created for collision studies, precision measurement and trapping experiments.
We report on the deceleration of a beam of SrF molecules from 290 to 120~m/s. Following supersonic expansion, the molecules in the $X^2Σ$ ($v=0$, $N=1$) low-field seeking states are trapped by the moving potential wells of a traveling-wave Stark decelerator. With a deceleration strength of 9.6 km/s$^2$ we have demonstrated the removal of 85 % of the initial kinetic energy in a 4 meter long modular decelerator. The absolute amount of kinetic energy removed is a factor 1.5 higher compared to previous Stark deceleration experiments. The demonstrated decelerator provides a novel tool for the creat…
We report on the production, deceleration and detection of a SrF molecular beam. The molecules are captured from a supersonic expansion and are decelerated in the X$^2Σ^+ (v=0, N=1)$ state. We demonstrate the removal of up to 40% of the kinetic energy with a 2 meter long modular traveling-wave decelerator. Our results demonstrate a crucial step towards the preparation of ultracold gases of heavy diatomic molecules for precision spectroscopy.
We present experimental results from a new scheme for magneto-optically trapping strontium monofluoride (SrF) molecules, which provides increased confinement compared to our original work. The improved trap employs a new approach to magneto-optical trapping presented by M. Tarbutt, \emph{arXiv preprint} 1409.0244, which provided insight for the first time into the source of the restoring force in magneto-optical traps (MOTs) where the cycling transition includes dark Zeeman sublevels (known as type-II MOTs). We measure a radial spring constant $20\times$ greater than in our original work with …
We present an analysis of the deceleration and trapping of heavy diatomic molecules in low-field seeking states by a moving electric potential. This moving potential is created by a 'ring-decelerator', which consists of a series of ring-shaped electrodes to which oscillating high voltages are applied. Particle trajectory simulations have been used to analyze the deceleration and trapping efficiency for a group of molecules that is of special interest for precision measurements of fundamental discrete symmetries. For the typical case of the SrF molecule in the (N,M) = (2, 0) state, the ring-dec…
We have recently demonstrated static trapping of ammonia isotopologues in a decelerator that consists of a series of ring-shaped electrodes to which oscillating high voltages are applied [Quintero-Pérez et al., Phys. Rev. Lett. 110, 133003 (2013)]. In this paper we provide further details on this traveling wave decelerator and present new experimental data that illustrate the control over molecules that it offers. We analyze the performance of our setup under different deceleration conditions and demonstrate phase-space manipulation of the trapped molecular sample.
We demonstrate simultaneous deceleration and trapping of a cold atomic and molecular mixture. This is the first step towards studies of cold atom-molecule collisions at low temperatures as well as application of sympathetic cooling. Both atoms and molecules are cooled in a supersonic expansion and are loaded into a moving magnetic trap which brings them to rest via the Zeeman interaction from an initial velocity of 375 m/s. We use a beam seeded with molecular Oxygen, and entrain it with Lithium atoms by laser ablation prior to deceleration. The deceleration ends with loading of the mixture int…
A pulsed beam of ground state OH radicals is slowed down using a Stark decelerator and is subsequently loaded into an electrostatic trap. Characterization of the molecular beam production, deceleration and trap loading process is performed via laser induced fluorescence detection inside the quadrupole trap. Depending on details of the trap loading sequence, typically $10^5$ OH ($X^2Π_{3/2}, J=3/2$) radicals are trapped at a density of around $10^7$ cm$^{-3}$ and at temperatures in the 50-500 mK range. The 1/e trap lifetime is around 1.0 second.
We demonstrate loading of SrF molecules into an optical dipole trap (ODT) via in-trap $Λ$-cooling. We find that this cooling can be optimized by a proper choice of relative ODT and $Λ$ beam polarizations. In this optimized configuration, we observe molecules with temperatures as low as 14(1) $μ$K in traps with depths up to 570 $μ$K. With optimized parameters, we transfer $\!\sim\!5$% of molecules from our radio-frequency magneto-optical trap into the ODT, at a density of $\sim\!2\times 10^{9}$ cm$^{-3}$, a phase space density of $\sim\!2\times 10^{-7}$, and with a trap lifetime of $\!\sim\!1$ …
We demonstrate a scheme for magneto-optically trapping strontium monofluoride (SrF) molecules at temperatures one order of magnitude lower and phase space densities three orders of magnitude higher than obtained previously with laser-cooled molecules. In our trap, optical dark states are destabilized by rapidly and synchronously reversing the trapping laser polarizations and the applied magnetic field gradient. The number of molecules and trap lifetime are also significantly improved from previous work by loading the trap with high laser power and then reducing the power for long-term trapping…
Laser cooling and trapping are central to modern atomic physics. The workhorse technique in cold-atom physics is the magneto-optical trap (MOT), which combines laser cooling with a restoring force from radiation pressure. For a variety of atomic species, MOTs can capture and cool large numbers of particles to ultracold temperatures (<1 mK); this has enabled the study of a wide range of phenomena from optical clocks to ultracold collisions whilst also serving as the ubiquitous starting point for further cooling into the regime of quantum degeneracy. Magneto-optical trapping of molecules could p…
Stark deceleration has been utilized for slowing and trapping several species of neutral, ground-state polar molecules generated in a supersonic beam expansion. Due to the finite physical dimension of the electrode array and practical limitations of the applicable electric fields, only molecules within a specific range of velocities and positions can be efficiently slowed and trapped. These constraints result in a restricted phase space acceptance of the decelerator in directions both transverse and parallel to the molecular beam axis; hence, careful modeling is required for understanding and …
We demonstrate feedback control optimization for the Stark deceleration and trapping of neutral polar molecules using evolutionary strategies. In a Stark-decelerator beamline pulsed electric fields are used to decelerate OH radicals and subsequently store them in an electrostatic trap. The efficiency of the deceleration and trapping process is determined by the exact timings of the applied electric field pulses. Automated optimization of these timings yields an increase of 40 % of the number of trapped OH radicals.
Laser cooling and magneto-optical trapping of molecules typically involves multiple transitions driven by several laser frequencies. We analyze how magneto-optical trapping forces depend on the angular momenta, $F_l$ and $F_u$, and the g-factors, $g_l$ and $g_u$, of the lower and upper states. When $F_l > F_u$ the polarizations must be reversed relative to cases where $F_u \ge F_l$. The correct choice of circular polarization depends on the sign of $g_{u}$ but not on the sign of $g_{l}$. If $g_{u}$ is zero there is no trapping force, and the trapping force is very weak whenever $g_u$ is small …
We discuss a possible one-dimensional trapping and cooling of atoms and molecules due to their non-resonant interaction with the counter-propagating light pulses trains. The counter-propagating pulses form a one-dimensional trap for atoms and molecules, and properly chosen the carrier frequency detuning from the transition frequency of the atoms or molecules keeps the "temperature" of the atomic or molecular ensemble close to the Doppler cooling limit. The calculation by the Monte-Carlo wave function method is carried out for the two-level and three-level schemes of the atom's and the molecule…
We describe the production of cold, slow-moving LiH molecules. The molecules are produced in the ground state using laser ablation and supersonic expansion, and 68% of the population is transferred to the rotationally excited state using narrowband radiation at the rotational frequency of 444GHz. The molecules are then decelerated from 420m/s to 53m/s using a 100 stage Stark decelerator. We demonstrate and compare two different deceleration modes, one where every stage is used for deceleration, and another where every third stage decelerates and the intervening stages are used to focus the mol…
We present experiments on decelerating and trapping ammonia molecules using a combination of a Stark decelerator and a traveling wave decelerator. In the traveling wave decelerator a moving potential is created by a series of ring-shaped electrodes to which oscillating high voltages are applied. By lowering the frequency of the applied voltages, the molecules confined in the moving trap are decelerated and brought to a standstill. As the molecules are confined in a true 3D well, this new kind of deceleration has practically no losses, resulting in a great improvement on the usual Stark deceler…
We present a robust, continuous molecular decelerator that employs high magnetic fields and few optical pumping steps. CaOH molecules are slowed, accumulating at low velocities in a range sufficient for loading both magnetic and magneto-optical traps. During the slowing, the molecules scatter only 7 photons, removing around 8 K of energy. Because large energies can be removed with only a few spontaneous radiative decays, this method can be applied to nearly any paramagnetic atomic or molecular species, opening a general path to trapping of complex molecules.
Trapping of atoms and molecules in electrostatic, magnetic and optical traps has enabled studying atomic and molecular interactions on a timescale of many seconds, allowing observations of ultra-cold collisions and reactions. Here we report the first magnetic deceleration and trapping of neutral carbon atoms in a static magnetic trap. When co-trapping the carbon atoms with oxygen molecules in a superconducting trap, the carbon signal decays in a non-exponential manner, consistent with losses resulting from atom-molecule collisions. Our findings pave the way to studying both elastic and inelast…
Beams of helium atoms in Rydberg-Stark states with principal quantum number $n=48$ and electric dipole moments of 4600~D have been decelerated from a mean initial longitudinal speed of 2000~m/s to zero velocity in the laboratory-fixed frame-of-reference in the continuously moving electric traps of a transmission-line decelerator. In this process accelerations up to $-1.3\times10^{7}$~m/s$^2$ were applied, and changes in kinetic energy of $ΔE_{\mathrm{kin}}=1.3\times10^{-20}$~J ($ΔE_{\mathrm{kin}}/e = 83$~meV) per atom were achieved. Guided and decelerated atoms, and those confined in stationar…
The large electric dipole moments associated with highly excited Rydberg states of atoms and molecules make gas-phase samples in these states very well suited to deceleration and trapping using inhomogeneous electric fields. The methods of Rydberg-Stark deceleration with which this can be achieved are reviewed here. Using these techniques, the longitudinal motion of beams of atoms and molecules moving at speeds as high as 2500~m/s have been manipulated, with changes in kinetic energy of up to $|ΔE_{\mathrm{kin}}|=1.3\times10^{-20}$~J ($|ΔE_{\mathrm{kin}}|/e=80$~meV or $|ΔE_{\mathrm{kin}}|/hc=6…
We present a moving-trap Zeeman decelerator (MTZD) for use in molecular beam manipulation and magnetic-trapping experiments of paramagnetic atoms and molecules. The 0.49 m MTZD consists of a combination of a 2D magnetic quadrupole guide and deceleration coils, which together produce an array of 3D magnetic traps. The design is based on that of Trimeche et al. with significant modifications. The 2D quadrupole is driven by fast rising and falling square pulses of current (up to 700 A) of arbitrary lengths of time. The traps can be made to move at velocities from ca. 370 m/s down to zero, which i…
We report on the Stark deceleration and electrostatic trapping of $^{14}$NH ($a ^1Δ$) radicals. In the trap, the molecules are excited on the spin-forbidden $A ^3Π\leftarrow a ^1Δ$ transition and detected via their subsequent fluorescence to the $X ^3Σ^-$ ground state. The 1/e trapping time is 1.4 $\pm$ 0.1 s, from which a lower limit of 2.7 s for the radiative lifetime of the $a ^1Δ, v=0,J=2$ state is deduced. The spectral profile of the molecules in the trapping field is measured to probe their spatial distribution. Electrostatic trapping of metastable NH followed by optical pumping of the t…
Metastable (1s)(2s) $^3{\rm S}_1$ helium atoms produced in a supersonic beam were excited to Rydberg-Stark states (with $n$ in the $27-30$ range) in a cryogenic environment and subsequently decelerated by, and trapped above, a surface-electrode decelerator. In the trapping experiments, the Rydberg atoms were brought to rest in 75~$μ$s and over a distance of 33~mm and kept stationary for times $t_{\mathrm{trap}}$ in the $0-525$~$μ$s range, before being re-accelerated for detection by pulsed field ionization. The use of a home-built valve producing short gas pulses with a duration of about 20~$μ…
There is substantial interest in producing samples of ultracold molecules for possible applications in quantum computation, quantum simulation of condensed matter systems, precision measurements, controlled chemistry, and high precision spectroscopy. A crucial step to obtaining large samples of ultracold, trapped molecules is developing a means to bridge the gap between typical molecular source velocities (~150-600 m/s) and velocities for which trap loading or confinement is possible (~5-20 m/s). Here we show deceleration of a beam of neutral strontium monofluoride (SrF) molecules using radiat…
Cryogenic buffer-gas beams are a promising method for producing bright sources of cold molecular radicals for cold collision and chemical reaction experiments. In order to use these beams in studies of reactions with controlled collision energies, or in trapping experiments, one needs a method of controlling the forward velocity of the beam. A Stark decelerator can be an effective tool for controlling the mean speed of molecules produced by supersonic jets, but efficient deceleration of buffer-gas beams presents new challenges due to longer pulse lengths. Traveling-wave decelerators are unique…
Cold supersonic beams of molecules can be slowed down using a switched sequence of electrostatic field gradients. The energy to be removed is proportional to the mass of the molecules. Here we report deceleration of YbF, which is 7 times heavier than any molecule previously decelerated. We use an alternating gradient structure to decelerate and focus the molecules in their ground state. We show that the decelerator exhibits the axial and transverse stability required to bring these molecules to rest. Our work significantly extends the range of molecules amenable to this powerful method of cool…
A new beamline for Resonant Excitation of Beams with Electromagnetic fields and Lasers (REBEL) and Stopping and Trapping of Radioactive Isotopes for Precision Experiments (STRIPE)
We have developed a source of cold LiH molecules for Stark deceleration and trapping experiments. Lithium metal is ablated from a solid target into a supersonically expanding carrier gas. The translational, rotational and vibrational temperatures are 0.9(0.1) K, 5.9(0.5) K and 468(17) K respectively. Although they have not reached thermal equilibrium with the carrier gas, we estimate that 90% of the LiH molecules are in the ground state, X^{1} Σ^{+} (v=0, J=0). With a single 7 ns ablation pulse, the number of molecules in the ground state is 4.5(1.8)*10^{7} molecules per steradian. A second, d…
