Establishing a reliable method to form scalable neutral-atom platforms is an essential cornerstone for quantum computation, quantum simulation and quantum many-body physics. Here we demonstrate a real-time transport of single atoms using holographic microtraps controlled by a liquid-crystal spatial light modulator. For this, an analytical design approach to flicker-free microtrap movement is devised and cold rubidium atoms are simultaneously rearranged with 2N motional degrees of freedom, representing unprecedented space controllability. We also accomplish an in situ feedback control for single-atom rearrangements with the high success rate of 99% for up to 10 μm translation. We hope this proof-of-principle demonstration of high-fidelity atom-array preparations will be useful for deterministic loading of N single atoms, especially on arbitrary lattice locations, and also for real-time qubit shuttling in high-dimensional quantum computing architectures.

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We present an entanglement scheme for Rydberg atoms using the van der Waals interaction phase induced by Ramsey-type pulsed interactions. This scheme realizes not only controlled phase operations between atoms at a distance larger than Rydberg blockade distance, but also various counter-intuitive entanglement examples, including two-atom entanglement in the presence of a closer third atom and W -state generation for partially-blockaded three atoms. Experimental realization is conducted with single rubidium atoms loaded in an array of optical tweezer dipole traps, to demonstrate the proposed entanglement generations and measurements.

Experimentally observed quantum few-body dynamics of neutral atoms excited to a Rydberg state are numerically analyzed with Lindblad master equation formalism. For this, up to five rubidium atoms are trapped with optical tweezers, arranged in various two-dimensional configurations, and excited to Rydberg 67S state in the nearest-neighbor blockade regime. Their coherent evolutions are measured with time-varying ground-state projections. The experimental results are analyzed with a model Lindblad equation with the homogeneous and inhomogeneous dampings determined by systematic and statistical error analysis. The coherent evolutions of the entangled systems are successfully reproduced by the resulting model analysis for the experimental results with optimal parameters in consistent with external calibrations.PACS numbers:

Rydberg-atom quantum simulators are of keen interest because of their possibilities towards high-dimensional qubit architectures. Here we report three-dimensional conformation spectra of quantum-Ising Hamiltonian systems with programmed qubit connections. With a Rydberg-atom quantum simulator, various connected graphs, in which vertices and edges represent atoms and blockaded couplings, respectively, are constructed in two or three-dimensional space and their eigenenergies are probed during their topological transformations. Star, complete, cyclic, and diamond graphs, and their geometric intermediates, are tested for four atoms and antiprism structures for six atoms. Spectroscopic resolution (∆E/E) less than 10% is achieved and the observed energy level shifts and merges through structural transformations are in good agreement with the model few-body quantum-Ising Hamiltonian.

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We present an experimental investigation of ultrafast-laser driven Rabi oscillations of atomic rubidium. Since the broadband spectrum of an ultrafast laser pulse simultaneously couples all the electronic hyperfine transitions between the excited and ground states, the complex excitation linkages involved with the D1 or D2 transition are energy degenerate. Here, by applying the MorrisShore transformation, it is shown that this multi-state system is reduced to a set of independent two-state systems and dark states. In experiments performed by ultrafast laser interactions of atomic rubidium in the strong interaction regime, we demonstrate that the ultrafast dynamics of the considered multi-state system is governed by a sum of at most two decoupled Rabi oscillations when this system interacts with ultrafast laser pulses of any polarization state. We further show the implication of this result to possible controls of photo-electron polarizations.

The chirped-pulse interaction in the adiabatic coupling regime induces cyclic permutations of the energy states of a three-level system in the V -type configuration, which process is known as the three-level chirped rapid adiabatic passage. Here we show that a spectral hole in a chirped pulse can turn on and off one of the two adiabatic crossing points of this process, reducing the system to an effective two-level system. The given hybrid adiabatic-nonadiabatic transition results in selective excitation of the three-level system, controlled by the laser intensity and spectral position of the hole as well as the sign of the chirp parameter. Experiments are performed with shaped femtosecond laser pulses and the three lowest energy-levels (5S 1/2 , 5P 1/2 , and 5P 3/2 ) of atomic rubidium ( 85 Rb), of which the result shows good agreement with the theoretically analyzed dynamics. The result indicates that our method, being combined with the ordinary chirped-RAP, implements an adiabatic transitions between the two excited states. Furthermore the laser intensity-dependent control may have applications including selective excitations of atoms or ions arranged in space when being used in conjunction with laser beam profile programming.