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Register a new userHigh Resolution Rydberg Spectroscopy of ultracold Rubidium Atoms
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We present experiments on two-photon excitation of ${rm ^{87}}$Rb atoms to Rydberg states. For this purpose, two continuous-wave (cw)-laser systems for both 780 nm and 480 nm have been set up. These systems are optimized to a small linewidth (well below 1 MHz) to get both an efficient excitation process and good spectroscopic resolution. To test the performance of our laser system, we investigated the Stark splitting of Rydberg states. For n=40 we were able to see the hyperfine levels splitting in the electrical field for different finestructure states. To show the ability of spatially selective excitation to Rydberg states, we excited rubidium atoms in an electrical field gradient and investigated both linewidths and lineshifts. Furthermore we were able to excite the atoms selectively from the two hyperfine ground states to Rydberg states. Finally, we investigated the Autler-Townes splitting of the 5S$_{1/2}$$to$5P$_{3/2}$ transition via a Rydberg state to determine the Rabi frequency of this excitation step.
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We report the observation of dipole-forbidden, but quadrupole-allowed, one-photon transitions to high Rydberg states in Rb. Using pulsed UV excitation of ultracold atoms in a magneto-optical trap, we excite $5s to nd$ transitions over a range of principal quantum numbers $n=27-59$. Compared to dipole-allowed (E1) transitions from $5s to np$, these E2 transitions are weaker by a factor of approximately 2000. We also report measurements of the anomalous $np_{3/2} : np_{1/2}$ fine-structure transition strength ratio for $n=28-75$. Both results are in agreement with theoretical predictions.
The theory of quantum scarring -- a remarkable violation of quantum unique ergodicity -- rests on two complementary pillars: the existence of unstable classical periodic orbits and the so-called quasimodes, i.e., the non-ergodic states that strongly overlap with a small number of the systems eigenstates. Recently, interest in quantum scars has been revived in a many-body setting of Rydberg atom chains. While previous theoretical works have identified periodic orbits for such systems using time-dependent variational principle (TDVP), the link between periodic orbits and quasimodes has been missing. Here we provide a conceptually simple analytic construction of quasimodes for the non-integrable Rydberg atom model, and prove that they arise from a requantisation of previously established periodic orbits when quantum fluctuations are restored to all orders. Our results shed light on the TDVP classical system simultaneously playing the role of both the mean-field approximation and the systems classical limit, thus allowing us to firm up the analogy between the eigenstate scarring in the Rydberg atom chains and the single-particle quantum systems.
We develop and study quantum and semi-classical models of Rydberg-atom spectroscopy in amplitude-modulated optical lattices. Both initial- and target-state Rydberg atoms are trapped in the lattice. Unlike in any other spectroscopic scheme, the modulation-induced ponderomotive coupling between the Rydberg states is spatially periodic and perfectly phase-locked to the lattice trapping potentials. This leads to a novel type of sub-Doppler mechanism, which we explain in detail. In our exact quantum model, we solve the time-dependent Schrodinger equation in the product space of center-of-mass (COM) momentum states and the internal-state space. We also develop a perturbative model based on the band structure in the lattice and Fermis golden rule, as well as a semi-classical trajectory model in which the COM is treated classically and the internal-state dynamics quantum-mechanically. In all models we obtain the spectrum of the target Rydberg-state population versus the lattice modulation frequency, averaged over the initial thermal COM momentum distribution of the atoms. We investigate the quantum-classical correspondence of the problem in several parameter regimes and exhibit spectral features that arise from vibrational COM coherences and rotary-echo effects. Applications in Rydberg-atom spectroscopy are discussed.
All light has structure, but only recently it has become possible to construct highly controllable and precise potentials so that most laboratories can harness light for their specific applications. In this chapter, we review the emerging techniques for high-resolution and configurable optical trapping of ultracold atoms. We focus on optical deflectors and spatial light modulators in the Fourier and direct imaging configurations. These optical techniques have enabled significant progress in studies of superfluid dynamics, single-atom trapping, and underlie the emerging field of atomtronics. The chapter is intended as a complete guide to the experimentalist for understanding, selecting, and implementing the most appropriate optical trapping technology for a given application. After introducing the basic theory of optical trapping and image formation, we describe each of the above technologies in detail, providing a guide to the fundamental operation of optical deflectors, digital micromirror devices, and liquid crystal spatial light modulators. We also describe the capabilities of these technologies for manipulation of trapped ultracold atoms, where the potential is dynamically modified to enable experiments, and where time-averaged potentials can realise more complex traps. The key considerations when implementing time-averaged traps are described.
We experimentally demonstrate optical spectroscopy of magnetically trapped atoms on an atom chip. High resolution optical spectra of individual trapped clouds are recorded within a few hundred milliseconds. Detection sensitivities close to the single atom level are obtained by photoionization of the excited atoms and subsequent ion detection with a channel electron multiplier. Temperature and decay rates of the trapped atomic cloud can be monitored in real time for several seconds with only little detection losses. The spectrometer can be used for investigations of ultracold atomic mixtures and for the development of interferometric quantum sensors on atom chips.
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