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Register a new userNonadiabatic transitions in electrostatically trapped ammonia molecules
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Nonadiabatic transitions are known to be major loss channels for atoms in magnetic traps, but have thus far not been experimentally reported upon for trapped molecules. We have observed and quantified losses due to nonadiabatic transitions for three isotopologues of ammonia in electrostatic traps, by comparing the trapping times in traps with a zero and a non-zero electric field at the center. Nonadiabatic transitions are seen to dominate the overall loss rate even for samples at relatively high temperatures of 10-50 mK.
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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-P{e}rez 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.
Anomalously large linear and quadratic Zeeman shifts are measured for weakly bound ultracold $^{88}$Sr$_2$ molecules near the intercombination-line asymptote. Nonadiabatic Coriolis coupling and the nature of long-range molecular potentials explain how this effect arises and scales roughly cubically with the size of the molecule. The linear shifts yield nonadiabatic mixing angles of the molecular states. The quadratic shifts are sensitive to nearby opposite $f$-parity states and exhibit fourth-order corrections, providing a stringent test of a state-of-the-art textit{ab initio} model.
We present a novel method for engineering an optical clock transition that is robust against external field fluctuations and is able to overcome limits resulting from field inhomogeneities. The technique is based on the application of continuous driving fields to form a pair of dressed states essentially free of all relevant shifts. Specifically, the clock transition is robust to magnetic shifts, quadrupole and other tensor shifts, and amplitude fluctuations of the driving fields. The scheme is applicable to either a single ion or an ensemble of ions, and is relevant for several types of ions, such as $^{40}mathrm{Ca}^{+}$, $^{88}mathrm{Sr}^{+}$, $^{138}mathrm{Ba}^{+}$ and $^{176}mathrm{Lu}^{+}$. Taking a spherically symmetric Coulomb crystal formed by 400 $^{40}mathrm{Ca}^{+}$ ions as an example, we show through numerical simulations that the inhomogeneous linewidth of tens of Hertz in such a crystal together with linear Zeeman shifts of order 10~MHz are reduced to form a linewidth of around 1~Hz. We estimate a two-order-of-magnitude reduction in averaging time compared to state-of-the art single ion frequency references, assuming a probe laser fractional instability of $10^{-15}$. Furthermore, a statistical uncertainty reaching $2.9times 10^{-16}$ in 1~s is estimated for a cascaded clock scheme in which the dynamically decoupled Coulomb crystal clock stabilizes the interrogation laser for an $^{27}mathrm{Al}^{+}$ clock.
We investigate the rovibrational population redistribution of polar molecules in the electronic ground state induced by spontaneous emission and blackbody radiation. As a model system we use optically trapped LiCs molecules formed by photoassociation in an ultracold two-species gas. The population dynamics of vibrational and rotational states is modeled using an ab-initio electric dipole moment function and experimental potential energy curves. Comparison with the evolution of the v=3 electronic ground state yields good qualitative agreement. The analysis provides important input to assess applications of ultracold LiCs molecules in quantum simulation and ultracold chemistry.
Optical trapping of molecules with long coherence times is crucial for many protocols in quantum information and metrology. However, the factors that limit the lifetimes of the trapped molecules remain elusive and require improved understanding of the underlying molecular structure. Here we show that measurements of vibronic line strengths in weakly and deeply bound $^{88}$Sr$_2$ molecules, combined with textit{ab initio} calculations, allow for unambiguous identification of vibrational quantum numbers. This, in turn, enables the construction of refined excited potential energy curves that inform the selection of magic wavelengths which facilitate long vibrational coherence. We demonstrate Rabi oscillations between far-separated vibrational states that persist for nearly 100 ms.
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