211 research outputs found
Entanglement Switch for Dipole Arrays
We propose a new entanglement switch of qubits consisting of electric
dipoles, oriented along or against an external electric field and coupled by
the electric dipole-dipole interaction. The pairwise entanglement can be tuned
and controlled by the ratio of the Rabi frequency and the dipole-dipole
coupling strength. Tuning the entanglement can be achieved for one, two and
three-dimensional arrangements of the qubits. The feasibility of building such
an entanglement switch is also discussed.Comment: 6 pages and 4 figures. To be published on Journal of Chemical Physic
Coherent transfer of photoassociated molecules into the rovibrational ground state
We report on the direct conversion of laser-cooled 41K and 87Rb atoms into
ultracold 41K87Rb molecules in the rovibrational ground state via
photoassociation followed by stimulated Raman adiabatic passage.
High-resolution spectroscopy based on the coherent transfer revealed the
hyperfine structure of weakly bound molecules in an unexplored region. Our
results show that a rovibrationally pure sample of ultracold ground-state
molecules is achieved via the all-optical association of laser-cooled atoms,
opening possibilities to coherently manipulate a wide variety of molecules.Comment: 4 pages, 4 figure
Partial-Transfer Absorption Imaging: A versatile technique for optimal imaging of ultracold gases
Partial-transfer absorption imaging is a tool that enables optimal imaging of
atomic clouds for a wide range of optical depths. In contrast to standard
absorption imaging, the technique can be minimally-destructive and can be used
to obtain multiple successive images of the same sample. The technique involves
transferring a small fraction of the sample from an initial internal atomic
state to an auxiliary state and subsequently imaging that fraction absorptively
on a cycling transition. The atoms remaining in the initial state are
essentially unaffected. We demonstrate the technique, discuss its
applicability, and compare its performance as a minimally-destructive technique
to that of phase-contrast imaging.Comment: 10 pages, 5 figures, submitted to Review of Scientific Instrument
Memory-related cognitive load effects in an interrupted learning task:A model-based explanation
Background: The Cognitive Load Theory provides a well-established framework for investigating aspects of learning situations that demand learners' working memory resources. However, the interplay of these aspects at the cognitive and neural level is still not fully understood. Method: We developed four computational models in the cognitive architecture ACT-R to clarify underlying memory-related strategies and mechanisms. Our models account for human data of an experiment that required participants to perform a symbol sequence learning task with embedded interruptions. We explored the inclusion of subsymbolic mechanisms to explain these data and used our final model to generate fMRI predictions. Results: The final model indicates a reasonable fit for reaction times and accuracy and links the fMRI predictions to the Cognitive Load Theory. Conclusions: Our work emphasizes the influence of task characteristics and supports a process-related view on cognitive load in instructional scenarios. It further contributes to the discussion of underlying mechanisms at a neural level
Dispersion interactions and reactive collisions of ultracold polar molecules
Progress in ultracold experiments with polar molecules requires a clear
understanding of their interactions and reactivity at ultra-low collisional
energies. Two important theoretical steps in this process are the
characterization of interaction potentials between molecules and the modeling
of reactive scattering mechanism. Here, we report on the {\it abinitio}
calculation of isotropic and anisotropic van der Waals interaction potentials
for polar KRb and RbCs colliding with each other or with ultracold atoms. Based
on these potentials and two short-range scattering parameters we then develop a
single-channel scattering model with flexible boundary conditions. Our
calculations show that at low temperatures (and in absence of an external
electric field) the reaction rates between molecules or molecules with atoms
have a resonant character as a function of the short-range parameters. We also
find that both the isotropic and anisotropic van der Waals coefficients have
significant contributions from dipole coupling to excited electronic states.
Their values can differ dramatically from those solely obtained from the
permanent dipole moment. A comparison with recently obtained reaction rates of
fermionic KRb shows that the experimental data can not be
explained by a model where the short-range scattering parameters are
independent of the relative orbital angular momentum or partial wave.Comment: 15 pages, 12 figure
Observation of enhanced rate coefficients in the H + H H + H reaction at low collision energies
The energy dependence of the rate coefficient of the H reaction has been measured in the range of
collision energies between K and
mK. A clear deviation of the rate coefficient from the value expected on the
basis of the classical Langevin-capture behavior has been observed at collision
energies below K, which is attributed to the joint
effects of the ion-quadrupole and Coriolis interactions in collisions involving
ortho-H molecules in the rotational level, which make up 75% of the
population of the neutral H molecules in the experiments. The experimental
results are compared to very recent predictions by Dashevskaya, Litvin, Nikitin
and Troe (J. Chem. Phys., in press), with which they are in agreement.Comment: 14 pages, 3 figure
Loss of molecules in magneto-electrostatic traps due to nonadiabatic transitions
We analyze the dynamics of a paramagnetic, dipolar molecule in a generic
"magneto-electrostatic'' trap where both magnetic and electric fields may be
present. The potential energy that governs the dynamics of the molecules is
found using a reduced molecular model that incorporates the main features of
the system. We discuss the shape of the trapping potentials for different field
geometries, as well as the possibility of nonadiabatic transitions to untrapped
states, i.e., the analog of Majorana transitions in a quadrupole magnetic
atomic trap. Maximizing the lifetime of molecules in a trap is of great concern
in current experiments, and we assess the effect of nonadiabatic transitions on
obtainable trap lifetimes.Comment: 13 pages, 6 figure
Ultracold polar molecules near quantum degeneracy
We report the creation and characterization of a near quantum-degenerate gas
of polar K-Rb molecules in their absolute rovibrational ground
state. Starting from weakly bound heteronuclear KRb Feshbach molecules, we
implement precise control of the molecular electronic, vibrational, and
rotational degrees of freedom with phase-coherent laser fields. In particular,
we coherently transfer these weakly bound molecules across a 125 THz frequency
gap in a single step into the absolute rovibrational ground state of the
electronic ground potential. Phase coherence between lasers involved in the
transfer process is ensured by referencing the lasers to two single components
of a phase-stabilized optical frequency comb. Using these methods, we prepare a
dense gas of polar molecules at a temperature below 400 nK. This
fermionic molecular ensemble is close to quantum degeneracy and can be
characterized by a degeneracy parameter of . We have measured the
molecular polarizability in an optical dipole trap where the trap lifetime
gives clues to interesting ultracold chemical processes. Given the large
measured dipole moment of the KRb molecules of 0.5 Debye, the study of quantum
degenerate molecular gases interacting via strong dipolar interactions is now
within experimental reach
Photoassociative creation of ultracold heteronuclear 6Li40K* molecules
We investigate the formation of weakly bound, electronically excited,
heteronuclear 6Li40K* molecules by single-photon photoassociation in a
magneto-optical trap. We performed trap loss spectroscopy within a range of 325
GHz below the Li(2S_(1/2))+K(4P_(3/2)) and Li(2S_(1/2))+K(4P_(1/2)) asymptotic
states and observed more than 60 resonances, which we identify as rovibrational
levels of 7 of 8 attractive long-range molecular potentials. The long-range
dispersion coefficients and rotational constants are derived. We find large
molecule formation rates of up to ~3.5x10^7s^(-1), which are shown to be
comparable to those for homonuclear 40K_2*. Using a theoretical model we infer
decay rates to the deeply bound electronic ground-state vibrational level
X^1\Sigma^+(v'=3) of ~5x10^4s^(-1). Our results pave the way for the production
of ultracold bosonic ground-state 6Li40K molecules which exhibit a large
intrinsic permanent electric dipole moment.Comment: 6 pages, 4 figures, submitted to EP
Velocity-selected molecular pulses produced by an electric guide
Electrostatic velocity filtering is a technique for the production of
continuous guided beams of slow polar molecules from a thermal gas. We extended
this technique to produce pulses of slow molecules with a narrow velocity
distribution around a tunable velocity. The pulses are generated by
sequentially switching the voltages on adjacent segments of an electric
quadrupole guide synchronously with the molecules propagating at the desired
velocity. This technique is demonstrated for deuterated ammonia (ND),
delivering pulses with a velocity in the range of and a
relative velocity spread of at FWHM. At velocities around
, the pulses contain up to molecules each. The data are
well reproduced by Monte-Carlo simulations, which provide useful insight into
the mechanisms of velocity selection.Comment: 8 pages, 6 figure
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