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Register a new userDirect Observation of a Feshbach-resonance by Coincidence-detection of Ions and Electrons in Penning Ionization Collisions
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Observation of molecular dynamics with quantum state resolution is one of the major challenges in chemical physics. Complete characterization of collision dynamics leads to the microscopic understanding and unraveling of different quantum phenomena such as scattering resonances. We present a new experimental approach for observing molecular dynamics involving neutral particles and ions that is capable in providing state-to-state mapping of the dynamics. We use Penning ionization reaction between argon and metastable helium to generate argon ion and ground state helium atom pairs at separation of several angstroms. The energy of ejected electron carries the information about the initial electronic state of an ion. The coincidence detection of ionic products provides a state resolved description of the post-ionization ion-neutral dynamics. We demonstrate that correlation between the electron and ion energy spectra enables us to directly observe the spin-orbit excited Feshbach resonance state of HeAr$^+$. We measure the lifetime of the quasi-bound HeAr$^+$ A$_2$ state and discuss possible applications of our method.
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We propose and experimentally investigate a scheme for observing Feshbach resonances in atomic quantum gases in situ and with a high temporal resolution of several ten nanoseconds. The method is based on the detection of molecular ions, which are optically generated from atom pairs at small interatomic distances. As test system we use a standard rubidium gas (87Rb) with well known magnetically tunable Feshbach resonances. The fast speed and the high sensitivity of our detection scheme allows to observe a complete Feshbach resonance within one millisecond and without destroying the gas.
We demonstrate a p$-wave optical Feshbach resonance (OFR) using purely long-range molecular states of a fermionic isotope of ytterbium ^{171}Yb, following the proposition made by K. Goyal et al. [Phys. Rev. A 82, 062704 (2010)]. The p-wave OFR is clearly observed as a modification of a photoassociation rate for atomic ensembles at about 5 micro-Kelvins. A scattering phase shift variation of delta eta=0.022 rad is observed with an atom loss rate coefficient K=28.0*10^{-12} cm^3/s.
We demonstrate a double-trap system well suited to study cold collisions between trapped ions and trapped atoms. Using Yb$^+$ ions confined in a Paul trap and Yb atoms in a magneto-optical trap, we investigate charge-exchange collisions of several isotopes for collision energies down to 400 neV (5 mK). The measured rate coefficient of $6 times 10^{-10}$ cm$^{3}$s$^{-1}$, constant over four orders of magnitude in collision energy, is in good agreement with that derived from a semiclassical Langevin model for an atomic polarizability of 143 a.u.
We report on the observation of cold collisions between $^6$Li atoms and Yb$^+$ ions. This combination of species has recently been proposed as the most suitable for reaching the quantum limit in hybrid atom-ion systems, due to its large mass ratio. For atoms and ions prepared in the $^2S_{1/2}$ ground state, the charge transfer and association rate is found to be at least~10$^{3}$ times smaller than the Langevin collision rate. These results confirm the excellent prospects of $^6$Li--Yb$^+$ for sympathetic cooling and quantum information applications. For ions prepared in the excited electronic states $^2P_{1/2}$, $^2D_{3/2}$ and $^2F_{7/2}$, we find that the reaction rate is dominated by charge transfer and does not depend on the ionic isotope nor the collision energy in the range $sim$~1--120~mK. The low charge transfer rate for ground state collisions is corroborated by theory, but the $4f$ shell in the Yb$^+$ ion prevents an accurate prediction for the charge transfer rate of the $^2P_{1/2}$, $^2D_{3/2}$ and $^2F_{7/2}$ states. Using textit{ab initio} methods of quantum chemistry we calculate the atom-ion interaction potentials up to energies of 30$times 10^3$~cm$^{-1}$, and use these to give qualitative explanations of the observed rates.
We demonstrate detection of NaRb Feshbach molecules at high magnetic field by combining molecular photodissociation and absorption imaging of the photofragments. The photodissociation process is carried out via a spectroscopically selected hyperfine Zeeman level correlated with the Na ($3P_{3/2}$) + Rb ($5S_{1/2}$) asymptote which, following spontaneous emission and optical pumping, leads to ground-state atoms in a single level with near unity probability. Subsequent to the dissociation, the number of molecules is obtained by detecting the resultant $^{23}$Na and $^{87}$Rb atoms. We have also studied the heating effect caused by the photodissociation process and optimized the detection protocol for extracting the temperature of the molecular cloud. This method enables the $in~situ$ detection of fast time scale collision dynamics between NaRb Feshbach molecules and will be a valuable capability in studying few-body physics involving molecules.
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