Subscribe to the gold package and get unlimited access to Shamra Academy
Register a new userNonexponential decay of Feshbach molecules
160
0
0.0
(
0
)
Ask ChatGPT about the research
No Arabic abstract
We analyze the temporal behavior of the survival probability of an unstable $^6$Li Feshbach molecule close to the BCS-BEC crossover. We find different instances of nonexponential decay as the magnetic field approaches the resonance value, at which the molecule becomes stable. We observe a transition from an exponential decay towards a regime dominated by a stretched-exponential law.
rate research
Read More
Ultracold molecules have experienced increasing attention in recent years. Compared to ultracold atoms, they possess several unique properties that make them perfect candidates for the implementation of new quantum-technological applications in several fields, from quantum simulation to quantum sensing and metrology. In particular, ultracold molecules of two-electron atoms (such as strontium or ytterbium) also inherit the peculiar properties of these atomic species, above all the possibility to access metastable electronic states via direct excitation on optical clock transitions with ultimate sensitivity and accuracy. In this paper we report on the production and coherent manipulation of molecular bound states of two fermionic $^{173}$Yb atoms in different electronic (orbital) states $^1$S$_0$ and $^3$P$_0$ in proximity of a scattering resonance involving atoms in different spin and electronic states, called orbital Feshbach resonance. We demonstrate that orbital molecules can be coherently photoassociated starting from a gas of ground-state atoms in a three-dimensional optical lattices by observing several photoassociation and photodissociation cycles. We also show the possibility to coherently control the molecular internal state by using Raman-assisted transfer to swap the nuclear spin of one of the atoms forming the molecule, thus demonstrating a powerful manipulation and detection tool of these molecular bound states. Finally, by exploiting this peculiar detection technique we provide first information on the lifetime of the molecular states in a many-body setting, paving the way towards future investigations of strongly interacting Fermi gases in a still unexplored regime.
We study collisions in an optically trapped, pure sample of ultracold Cs$_2$ molecules in various internal states. The molecular gas is created by Feshbach association from a near-degenerate atomic gas, with adjustable temperatures in the nanokelvin range. We identify several narrow loss resonances, which point to the coupling to more complex molecular states and may be interpreted as Feshbach resonances in dimer-dimer interactions. Moreover, in some molecular states we observe a surprising temperature dependence in collisional loss. This shows that the situation cannot be understood in terms of the usual simple threshold behavior for inelastic two-body collisions. We interpret this observation as further evidence for a more complex molecular structure beyond the well-understood dimer physics.
Employing a short-range two-channel description we derive an analytic model of atoms in isotropic and anisotropic harmonic traps at a Feshbach resonance. On this basis we obtain a new parameterization of the energy-dependent scattering length which differs from the one previously employed. We validate the model by comparison to full numerical calculations for Li-Rb and explain quantitatively the experimental observation of a resonance shift and trap-induced molecules in exited bands. Finally, we analyze the bound state admixture and Landau-Zener transition probabilities.
Magnetically tunable Feshbach resonances in ultracold atomic systems are chiefly identified and characterized through time consuming atom loss spectroscopy. We describe an off-resonant dispersive optical probing technique to rapidly locate Feshbach resonances and demonstrate the method by locating four resonances of $^{87}$Rb, between the $|rm{F} = 1, rm{m_F}=1 rangle$ and $|rm{F} = 2, rm{m_F}=0 rangle$ states. Despite the loss features being $lesssim0.1$ G wide, we require only 21 experimental runs to explore a magnetic field range >18 G, where $1~rm{G}=10^{-4}$ T. The resonances consist of two known s-wave features in the vicinity of 9 G and 18 G and two previously unobserved p-wave features near 5 G and 10 G. We further utilize the dispersive approach to directly characterize the two-body loss dynamics for each Feshbach resonance.
We have performed radio-frequency dissociation spectroscopy of weakly bound ^6Li_2 Feshbach molecules using low-density samples of about 30 molecules in an optical dipole trap. Combined with a high magnetic field stability this allows us to resolve the discrete trap levels in the RF dissociation spectra. This novel technique allows the binding energy of Feshbach molecules to be determined with unprecedented precision. We use these measurements as an input for a fit to the ^6Li scattering potential using coupled-channel calculations. From this new potential, we determine the pole positions of the broad ^6Li Feshbach resonances with an accuracy better than 7 times 10^{-4} of the resonance widths. This eliminates the dominant uncertainty for current precision measurements of the equation of state of strongly interacting Fermi gases. For example, our results imply a corrected value for the Bertsch parameter xi measured by Ku et al. [Science 335, 563 (2012)], which is xi = 0.370(5)(8).
Log in to be able to interact and post comments
comments
Fetching comments
Sign in to be able to follow your search criteria
