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Register a new userA quantum sensor for atom-surface interactions below 10 $mu$m
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We report about the realization of a quantum device for force sensing at micrometric scale. We trap an ultracold $^{88}$Sr atomic cloud with a 1-D optical lattice, then we place the atomic sample close to a test surface using the same optical lattice as an elevator. We demonstrate precise positioning of the sample at the $mu$m scale. By observing the Bloch oscillations of atoms into the 1-D optical standing wave, we are able to measure the total force on the atoms along the lattice axis, with a spatial resolution of few microns. We also demonstrate a technique for transverse displacement of the atoms, allowing to perform measurements near either transparent or reflective test surfaces. In order to reduce the minimum distance from the surface, we compress the longitudinal size of the atomic sample by means of an optical tweezer. Such system is suited for studies of atom-surface interaction at short distance, such as measurement of Casimir force and search for possible non-Newtonian gravity effects.
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We describe the fabrication and construction of a setup for creating lattices of magnetic microtraps for ultracold atoms on an atom chip. The lattice is defined by lithographic patterning of a permanent magnetic film. Patterned magnetic-film atom chips enable a large variety of trapping geometries over a wide range of length scales. We demonstrate an atom chip with a lattice constant of 10 $mu$m, suitable for experiments in quantum information science employing the interaction between atoms in highly-excited Rydberg energy levels. The active trapping region contains lattice regions with square and hexagonal symmetry, with the two regions joined at an interface. A structure of macroscopic wires, cut out of a silver foil, was mounted under the atom chip in order to load ultracold $^{87}$Rb atoms into the microtraps. We demonstrate loading of atoms into the square and hexagonal lattice sections simultaneously and show resolved imaging of individual lattice sites. Magnetic-film lattices on atom chips provide a versatile platform for experiments with ultracold atoms, in particular for quantum information science and quantum simulation.
The distance-dependence of the anisotropic atom-wall interaction is studied. The central result is the 1/z^6 quadrupolar anisotropy decay in the retarded Casimir-Polder regime. Analysis of the transition region between non-retarded van der Waals regime (in 1/z^3) and Casimir-Polder regime shows that the anisotropy cross-over occurs at very short distances from the surface, on the order of 0.03 Lambda, where Lambda is the atom characteristic wavelength. Possible experimental verifications of this distance dependence are discussed.
The noncontact (van der Waals) friction is an interesting physical effect which has been the subject of controversial scientific discussion. The direct friction term due to the thermal fluctuations of the electromagnetic field leads to a friction force proportional to 1/Z^5 where Z is the atom-wall distance). The backaction friction term takes into account the feedback of thermal fluctuations of the atomic dipole moment onto the motion of the atom and scales as 1/Z^8. We investigate noncontact friction effects for the interactions of hydrogen, ground-state helium and metastable helium atoms with alpha-quartz (SiO_2), gold (Au) and calcium difluorite (CaF_2). We find that the backaction term dominates over the direct term induced by the thermal electromagnetic fluctuations inside the material, over wide distance ranges. The friction coefficients obtained for gold are smaller than those for SiO_2 and CaF_2 by several orders of magnitude.
Mid infrared (MIR) photonics is a key region for molecular physics [1]. High-resolution spectroscopy in the 1--10 {mu}m region, though, has never been fully tackled for the lack of widely-tunable and practical light sources. Indeed, all solutions proposed thus far suffer from at least one of three issues: they are feasible only in a narrow spectral range; the power available for spectroscopy is limited; the frequency accuracy is poor. Here, we present a setup for high-resolution spectroscopy that can be applied in the whole 1--10 {mu}m range by combining the power of quantum cascade lasers (QCLs) and the accuracy achievable by difference frequency generation using an OP-GaP crystal. The frequency is measured against a primary frequency standard using the Italian metrological fibre link network. We demonstrate the performance of the setup by measuring a vibrational transition in a highly-excited metastable state of CO around 6 {mu}m with 11 digits of precision, four orders of magnitude better than the value available in the literature [2].
Quantum metrology enables some of the most precise measurements. In the life sciences, diamond-based quantum sensing has enabled a new class of biophysical sensors and diagnostic devices that are being investigated as a platform for cancer screening and ultra-sensitive immunoassays. However, a broader application in the life sciences based on nanoscale nuclear magnetic resonance spectroscopy has been hampered by the need to interface highly sensitive quantum bit (qubit) sensors with their biological targets. Here, we demonstrate a new approach that combines quantum engineering with single-molecule biophysics to immobilize individual proteins and DNA molecules on the surface of a bulk diamond crystal that hosts coherent nitrogen vacancy qubit sensors. Our thin (sub-5 nm) functionalization architecture provides precise control over protein adsorption density and results in near-surface qubit coherence approaching 100 {mu}s. The developed architecture remains chemically stable under physiological conditions for over five days, making our technique compatible with most biophysical and biomedical applications.
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