Controlling ultracold atoms with laser light has greatly advanced quantum science. The wavelength of light sets a typical length scale for most experiments to the order of 500 nanometers (nm) or greater. In this work, we implemented a super-resolution technique that localizes and arranges atoms on a sub-50-nm scale, without any fundamental limit in resolution. We demonstrate this technique by creating a bilayer of dysprosium atoms and observing dipolar interactions between two physically separated layers through interlayer sympathetic cooling and coupled collective excitations. At 50-nm distance, dipolar interactions are 1000 times stronger than at 500 nm. For two atoms in optical tweezers, this should enable purely magnetic dipolar gates with kilohertz speed.
Controlling ultracold atoms with laser light has greatly advanced quantum science. The wavelength of light sets a typical length scale for most experiments to the order of 500 nanometers (nm) or greater. In this work, we implemented a super-resolution technique that localizes and arranges atoms on a sub-50-nm scale, without any fundamental limit in resolution. We demonstrate this technique by creating a bilayer of dysprosium atoms and observing dipolar interactions between two physically separated layers through interlayer sympathetic cooling and coupled collective excitations. At 50-nm distance, dipolar interactions are 1000 times stronger than at 500 nm. For two atoms in optical tweezers, this should enable purely magnetic dipolar gates with kilohertz speed.
Atomic physics has greatly advanced quantum science, mainly due to the ability to control the position and internal quantum state of atoms with high precision, often at the quantum limit. The dominant tool for this is laser light, which can structure and localize atoms in space (e.g., in optical tweezers, optical lattices, 1D tubes or 2D planes). Due to the diffraction limit of light, the natural length scale for most experiments with atoms is on the order of 500 nm or larger. Here we implement a new super-resolution technique which localizes and arranges atoms on a sub-50 nm scale, without any fundamental limit in resolution. We demonstrate this technique by creating a bilayer of dysprosium atoms, mapping out the atomic density distribution with sub-10 nm resolution, and observing dipolar interactions between two physically separated layers via interlayer sympathetic cooling and coupled collective excitations. At 50 nm, dipolar interactions are 1,000 times stronger than at 500 nm. For two atoms in optical tweezers, this should enable purely magnetic dipolar gates with kHz speed.
Ultracold atoms are an exceptionally versatile platform to test novel physical concepts. They have greatly advanced our understanding of the physics of many-body systems and allowed precision measurements of fundamental constants. They are also a promising architecture for quantum computation and quantum simulation. A key to the practicality of ultra-cold atoms is the ability to image them with high spatial resolution. Available microscopy schemes have reached sufficient resolution to detect individual atoms trapped in optical lattices with submicron spacings, but their spatial resolution is typically limited to about half the wavelength of the imaging light. Now, two independent teams—one led by Cheng Chin from the University of Chicago, Illinois, and the other led by Steve Rolston and Trey Porto from the University of Maryland, College Park —have reported subwavelength-resolution imaging techniques for ultracold atoms. The methods, capable of resolving objects up to 50 times smaller than the optical wavelength, have allowed the teams to map the shape of atomic density distributions on nanometer scales. Nanoscale maps of atomic density will be important observables for probing many-body effects in cold atomic and molecular systems.
This thesis discusses the experiments on 2D dipolar Bose gas of ultracold erbium atoms. Long-range and anisotropic dipole-dipole interaction induces complex orders in quantum many-body systems. Highly magnetic lanthanide atoms such as dysprosium and erbium have the largest magnetic moment in the periodic table, which has attracted significant attention in the past decades. Starting from quantum degenerate dysprosium and erbium atoms, exotic phases like quantum droplets, supersolid, dipolar quantum solid in the Hubbard regime have been studied. However, the 2D dipolar superfluid still remains understudied, despite being theoretically discussed for over two decades. Although tremendous theoretical proposals predict different phenomena in 2D dipolar superfluids, our first interest is to know how the superfluidity emerges in the 2D dipolar gases at finite temperatures. Our observations suggest that the superfluid transition can be well described by the Berezinskii-Kosterlitz-Thouless transition with an effective contact interaction as a function of dipolar orientation. With the 2D dipolar superfluid with strong DDI, we characterized the elementary excitation of the matter: the collective breathing mode. Our measurements establish how the competition between local and nonlocal interaction in strongly dipolar 2D superfluid retains quasi-scale invariance or strongly breaks scale invariance. By further searching the interaction parameters, we created stripes with global coherence, which are the first supersolid stripes in 2D. Experiments including measuring density fluctuation, coherence, and collective mode have been performed to understand the 2D supersolid. At last, we also observe unconventional light scattering from round-disk dipolar BECs, which provides new possibilities for atom optics.
Subwavelength atomic tweezer arrays, in which atoms can be positioned at distances smaller than their emission wavelength, have been proposed as a versatile platform to study collective emission phenomena, such as superradiance and subradiance. Experimentally, the realization of such arrays has been a challenge as typical emission wavelengths in the visible or near-infrared are short compared to typical tweezer spacings in the micrometer range. Here, we use 88Sr atoms in optical tweezer arrays to access a mid-infrared transition at 2,923 nm (5s5p3P2→5s4d3D3). We identify a magic trapping wavelength at 597.14(3) nm and demonstrate single-atom preparation and imaging with high fidelity. In addition, using 2,923 nm light, we demonstrate resolved-sideband cooling of tweezer-trapped strontium. Beyond enabling studies of collective emission phenomena in flexible arrangements of atoms, our platform opens novel opportunities for dipolar many-body physics and enhanced control over Rydberg dynamics and the strontium fine-structure qubit.
The entry into the new millennium was marked in the quantum community by the first experimental realizations of the Bose-Einstein condensation of atoms in a vapor, achieved in different research groups. Twenty-five years later, such systems are 'routinely' produced and are the core of many experiments. At the frontier between condensed matter their y, quantum optics, and atomic physics, ultra-cold atoms are subjects of high scientific interest.Ultra-cold gas can be trapped in optical lattices, giving a realistic way of experimentally realizing a new range of lattice Hamiltonians, that are used to simulate condensed matter systems. In these simulations, ultra-cold atoms are used to mimic the behavior of electrons in a solid-state material and could be used to simulate a wide range of complex condensed matter phenomena, such as the fractional quantum Hall effect, topological insulators, and high-temperature superconductivity.In order to study such systems, diffraction-limited quantum gas microscopes have emerged as a way to manipulate and detect atoms trapped in lattice potentials. Using far-field interference, experiments have mainly been restricted to a lattice spacing of 500 nm. This limits the speed of dynamics of all physical processes.Higher energy regimes could be accessed by reducing the lattice spacing. For this purpose, one of the long-term goals of the team is to trap atoms in the near-field of a surface and to make use of the Casimir-Polder forces to shape sub-wavelength potentials. Thanks to nano-fabrication capabilities, the spacing can be reduced to a few tens of nanometers. However, this requires to adapt the imaging techniques to observe cold-atoms with sub-wavelength spatial resolutions.In this PhD thesis, I report first on the advances toward implementing an atom chip in our experiment, which will serve as an integrated platform to manipulate the quantum gas. I present simulations and study an experimental solution allowing the cloud to be transported to the near-field. The method is based on the interference of a laser radiation in the near field of a rotating surface. It has been fully simulated, and the limitations have been numerically and experimentally assessed. I conclude this part by presenting the first model of chip that has been fabricated.In a second part, I report on the development of a sub-wavelength imaging method of cold Rubidium 87 atoms which is based on excited state dressing. I detail the concept of this nano-metric spatial resolution method and apply it to super-resolve a single longitudinal wave function trapped in a tight lattice that exhibits a width below 30 nm.
Optical lattices serve as fundamental building blocks for atomic quantum technology. However, the scale and resolution of these lattices are diffraction-limited to the light wavelength. In conventional lattices, achieving tight confinement of single sites requires high laser intensity, which unfortunately leads to reduced coherence due to increased scattering. This article presents a novel approach for creating an atomic optical lattice with a sub-wavelength spatial structure. The potential is generated by leveraging the nonlinear optical response of three-level Rydberg-dressed atoms, which allows us to overcome the diffraction limit of the driving fields. The resulting lattice comprises a three-dimensional array of ultra-narrow Lorentzian wells over nanometer scales. These unprecedented scales can now be accessed through a hybrid scheme that combines the dipolar interaction and optical twist of atomic eigenstates. The interaction-induced two-body resonance that forms the trapping potential, only occurs at a peculiar laser intensity, localizing the trap sites to ultra-narrow regions over the standing-wave driving field. The feasibility study shows that single-atom confinement in Lorentzian sites with 3nm width, and 37MHz depth are realizable with available lasers. The development of these ultra-narrow trapping techniques holds great promise for applications such as Rydberg-Fermi gates, atomtronics, quantum walks, Hubbard models, and neutral-atom quantum simulation.