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Register a new userConditional Ramsey Spectroscopy with Synchronized Atoms
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We investigate Ramsey spectroscopy performed on a synchronized ensemble of two-level atoms. The synchronization is induced by the collective coupling of the atoms to a heavily damped mode of an optical cavity. We show that, in principle, with this synchronized system it is possible to observe Ramsey fringes indefinitely, even in the presence of spontaneous emission and other sources of individual-atom dephasing. This could have important consequences for atomic clocks and a wide range of precision metrology applications.
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Interaction of atoms with twisted light is the subject of intense experimental and theoretical investigation. In almost all studies, the atom is viewed as a localized probe of the twisted light field. However, as argued in this paper, conceptually novel effects will arise if light-atom interaction is studied in the double-twisted regime with delocalized atoms, that is, either via twisted light absorption by atom vortex beam, or via two-twisted-photon spectroscopy of atoms in a non-vortex but delocalized state. Even for monochromatic twisted photons and for an infinitely narrow line, absorption will occur over a finite range of detuning. Inside this range, a rapidly varying absorption probability is predicted, revealing interference fringes induced by two distinct paths leading to the same final state. The number, location, height and contrast of these fringes can give additional information on the excitation process which would not be accessible in usual spectroscopic settings. Visibility of the predicted effects will be enhanced at the future Gamma factory thanks to the large momenta of ions.
We theoretically investigate the dynamics of a gas of strongly interacting Rydberg atoms subject to a time-domain Ramsey interferometry protocol. The many-body dynamics is governed by an Ising-type Hamiltonian with long range interactions of tunable strength. We analyze and model the contrast degradation and phase accumulation of the Ramsey signal and identify scaling laws for varying interrogation times, ensemble densities, and ensemble dimensionalities.
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.
Optics and interferometry with matter waves is the art of coherently manipulating the translational motion of particles like neutrons, atoms and molecules. Coherent atom optics is an extension of techniques that were developed for manipulating emph{internal} quantum states. Applying these ideas to translational motion required the development of techniques to localize atoms and transfer population coherently between distant localities. In this view position and momentum are (continuouse) quantum mechanical degree of freedom analogous to discrete internal quantum states. In our contribution we start with an introduction into matter-wave optics in section 1, discuss coherent atom optics and atom interferometry techniques for molecular beams in section 2 and for trapped atoms in section 3. In section 4 we then describe tools and experiments that allow us to probe the evolution of quantum states of many-body systems by atom interference.
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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