69 research outputs found
Loss of ultracold 87Rb133Cs molecules via optical excitation of long-lived two-body collision complexes
We show that the lifetime of ultracold ground-state 87Rb133Cs molecules in an optical trap is limited by fast optical excitation of long-lived two-body collision complexes. We partially suppress this loss mechanism by applying square-wave modulation to the trap intensity, such that the molecules spend 75% of each modulation cycle in the dark. By varying the modulation frequency, we show that the lifetime of the collision complex is 0.53 0.06 ms in the dark. We find that the rate of optical excitation of the collision complex is 3þ4 −2 × 103 W−1 cm2 s−1 for λ ¼ 1550 nm, leading to a lifetime of < 100 ns for typical trap intensities. These results explain the two-body loss observed in experiments on nonreactive bialkali molecules
Robust storage qubits in ultracold polar molecules
Quantum states with long-lived coherence are essential for quantum computation, simulation and metrology. The nuclear spin states of ultracold molecules prepared in the singlet rovibrational ground state are an excellent candidate for encoding and storing quantum information. However, it is important to understand all sources of decoherence for these qubits, and then eliminate them, to reach the longest possible coherence times. Here we fully characterize the dominant mechanisms of decoherence for a storage qubit in an optically trapped ultracold gas of RbCs molecules using high-resolution Ramsey spectroscopy. Guided by a detailed understanding of the hyperfine structure of the molecule, we tune the magnetic field to where a pair of hyperfine states have the same magnetic moment. These states form a qubit, which is insensitive to variations in magnetic field. Our experiments reveal a subtle differential tensor light shift between the states, caused by weak mixing of rotational states. We demonstrate how this light shift can be eliminated by setting the angle between the linearly polarized trap light and the applied magnetic field to a magic angle of arccos(1/3–√)≈55∘. This leads to a coherence time exceeding 5.6 s at the 95% confidence level
Ultracold molecules for quantum simulation: rotational coherence in CaF and RbCs
Polar molecules offer a new platform for quantum simulation of systems with long-range interactions, based on the electrostatic interaction between their electric dipole moments. Here, we report the development of coherent quantum state control using microwave fields in CaF and RbCs molecules, a crucial ingredient for many quantum simulation applications. We perform Ramsey interferometry measurements with fringe spacings of and investigate the dephasing time of a superposition of and rotational states when the molecules are confined. For both molecules, we show that a judicious choice of molecular hyperfine states minimises the impact of spatially varying transition-frequency shifts across the trap. For magnetically trapped CaF we use a magnetically insensitive transition and observe a coherence time of 0.61(3)~ms. For optically trapped RbCs we exploit an avoided crossing in the AC Stark shifts and observe a maximum coherence time of 0.75(6)~ms
Search for the decay in the momentum region
We have searched for the decay in the kinematic
region with pion momentum below the peak. One event was
observed, consistent with the background estimate of . This
implies an upper limit on
(90% C.L.), consistent with the recently measured branching ratio of
, obtained using the standard model
spectrum and the kinematic region above the peak. The
same data were used to search for , where is a weakly
interacting neutral particle or system of particles with .Comment: 4 pages, 2 figure
Search for the decay K+ to pi+ gamma gamma in the pi+ momentum region P>213 MeV/c
We have searched for the K+ to pi+ gamma gamma decay in the kinematic region
with pi+ momentum close to the end point. No events were observed, and the 90%
confidence-level upper limit on the partial branching ratio was obtained, B(K+
to pi+ gamma gamma, P>213 MeV/c) < 8.3 x 10-9 under the assumption of chiral
perturbation theory including next-to-leading order ``unitarity'' corrections.
The same data were used to determine an upper limit on the K+ to pi+ gamma
branching ratio of 2.3 x 10-9 at the 90% confidence level.Comment: 15 pages, 3 figures; no change in the results, accepted for
publication in Physics Letters
Enhancing easy-plane anisotropy in bespoke Ni(II) quantum magnets
We examine the crystal structures and magnetic properties of several S = 1 Ni(II) coordination compounds, molecules and polymers, that include the bridging ligands HF2-, AF62- (A = Ti, Zr) and pyrazine or non-bridging ligands F-, SiF62-, glycine, H2O, 1-vinylimidazole, 4-methylpyrazole and 3-hydroxypyridine. Pseudo-octahedral NiN4F2, NiN4O2 or NiN4OF cores consist of equatorial Ni-N bonds that are equal to or slightly longer than the axial Ni-Lax bonds. By design, the zero-field splitting (D) is large in these systems and, in the presence of substantial exchange interactions (J), can be difficult to discriminate from magnetometry measurements on powder samples. Thus, we relied on pulsed-field magnetization in those cases and employed electron-spin resonance (ESR) to confirm D when J 0) and range from ≈ 8-25 K. This work reveals a linear correlation between the ratio d(Ni-Lax)/d(Ni-Neq) and D although the ligand spectrochemical properties may also be important. We assert that this relationship allows us to predict the type of magnetocrystalline anisotropy in tailored Ni(II) quantum magnets
Further search for the decay in the momentum region P < 195 MeV/c
We report the results of a search for the decay
in the kinematic region with momentum MeV/c using the
data collected by the E787 experiment at BNL. No events were observed. When
combined with our previous search in this region, one candidate event with an
expected background of events results in a 90% C.L. upper limit
of on the branching ratio of .
We also report improved limits on the rates of and where are hypothetical, massless, long-lived
neutral particles.Comment: 5 pages, 3 figures, Accepted for publication in Phys. Rev.
Coherent Manipulation of the Internal State of Ultracold 87Rb133Cs Molecules with Multiple Microwave Fields
We explore coherent multi-photon processes in 87Rb133Cs molecules using 3-level lambda and ladder configurations of rotational and hyperfine states, and discuss their relevance to future applications in quantum computation and quantum simulation. In the lambda configuration, we demonstrate the driving of population between two hyperfine levels of the rotational ground state via a two-photon Raman transition. Such pairs of states may be used in the future as a quantum memory, and we measure a Ramsey coherence time for a superposition of these states of 58(9) ms. In the ladder configuration, we show that we can generate and coherently populate microwave dressed states via the observation of an Autler–Townes doublet. We demonstrate that we can control the strength of this dressing by varying the intensity of the microwave coupling field. Finally, we perform spectroscopy of the rotational states of 87Rb133Cs up to N = 6, highlighting the potential of ultracold molecules for quantum simulation in synthetic dimensions. By fitting the measured transition frequencies we determine a new value of the centrifugal distortion coefficient Dv = h × 207.3(2) Hz
Diatomic-py: A Python module for calculating the rotational and hyperfine structure of 1Σ molecules
We present a computer program to calculate the quantised rotational and hyperfine energy levels of diatomic molecules in the presence of dc electric, dc magnetic, and off-resonant optical fields. Our program is applicable to the bialkali molecules used in ongoing state-of-the-art experiments with ultracold molecular gases. We include functions for the calculation of space-fixed electric dipole moments, magnetic moments and transition dipole moments
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