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arXiv:2203.09998

Casimir-Polder interactions of Rydberg atoms with graphene-based van der Waals heterostructures

K. Wongcharoenbhorn, Koller, Christian, Fromhold, Timothy Mark, Li, Weibin

Published Mar 18, 2022• 0 citations
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Abstract

We investigate the thermal Casimir-Polder (CP) potential of \textsuperscript{87}Rb atoms in Rydberg $n$S-states near single- and double-layer graphene. The dependence of the CP potential on parameters such as atom-surface distance, temperature, principal quantum number $n$ and graphene Fermi energy are explored. Through large scale numerical simulations, we show that, in the non-retarded regime, the CP potential is dominated by the non-resonant and evanescent-wave terms which are monotonic, and that, in the retarded regime, the CP potential exhibits spatial oscillations. We identify that the most important contributions to the resonant component of the CP potential come from the $n$S-$n$P and $n$S-$(n-1)$P transitions. Scaling of the CP potential as a function of the principal quantum number and temperature is obtained. A heterostructure comprising hexagonal boron nitride layers sandwiched between two graphene layers is also studied. When the boron nitride layer is sufficiently thin, the CP potential can be weakened by changing the Fermi energy of the top graphene layer. Our study provides insights for understanding and controlling CP potentials experienced by Rydberg atoms near single and multi-layer graphene-based van der Waals heterostructures.

DOI
10.48550/arxiv.2203.09998

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We investigate the thermal Casimir-Polder (CP) potential of \textsuperscript{87}Rb atoms in Rydberg nnnS-states near single- and double-layer graphene. The dependence of the CP potential on parameters such as atom-surface distance, temperature, principal quantum number nnn and graphene Fermi energy are explored. Through large scale numerical simulations, we show that, in the non-retarded regime, the CP potential is dominated by the non-resonant and evanescent-wave terms which are monotonic, and that, in the retarded regime, the CP potential exhibits spatial oscillations. We identify that the most important contributions to the resonant component of the CP potential come from the nnnS-nnnP and nnnS-(n−1)(n-1)(n−1)P transitions. Scaling of the CP potential as a function of the principal quantum number and temperature is obtained. A heterostructure comprising hexagonal boron nitride layers sandwiched between two graphene layers is also studied. When the boron nitride layer is sufficiently thin, the CP potential can be weakened by changing the Fermi energy of the top graphene layer. Our study provides insights for understanding and controlling CP potentials experienced by Rydberg atoms near single and multi-layer graphene-based van der Waals heterostructures.
We investigate the thermal Casimir-Polder (CP) potential of 87Rb^{87}\mathrm{Rb}87Rb atoms in Rydberg nSnSnS-states near single- and double-layer graphene, and briefly look into the lifetimes near graphene-hexagonal boron nitride (hBN) multilayered structures. The dependence of the CP potential on parameters such as atom-surface distance, temperature, principal quantum number nnn, and graphene Fermi energy are explored. Through large-scale numerical simulations, we show that, in the nonretarded regime, the CP potential is dominated by the nonresonant and evanescent-wave terms which are monotonic, and that, in the retarded regime, the CP potential exhibits spatial oscillations. We identify that the most important contributions to the resonant component of the CP potential come from the $nS\text{\ensuremath{-}}nP$ and $nS\text{\ensuremath{-}}(n\ensuremath{-}1)P$ transitions. Scaling of the CP potential as a function of the principal quantum number and temperature is obtained. A heterostructure comprising hexagonal boron nitride layers sandwiched between two graphene layers is also studied. When the boron nitride layer is sufficiently thin, the CP potential can be weakened by changing the Fermi energy of the top graphene layer. Our study provides insights for understanding and controlling CP potentials experienced by Rydberg atoms near single- and multilayer graphene-based van der Waals heterostructures.
We develop a microscopic description of the fluctuation-mediated Casimir-Polder (CP) shifts on a 'test' two-level atom placed near a two-dimensional atomic array of two-level atoms. We derive the resonant and off-resonant CP potentials experienced by the excited test atom using fourth-order perturbation theory, under the assumption that the test atom resonance is far detuned from those of the array atoms. The total potential on the test atom can be described as the sum of the pairwise resonant and off-resonant potentials resulting from its interaction with the individual atoms of the array. We analyze the asymptotic scaling of CP shifts as a function of the test atom-array separation, and its dependence on various system parameters: array spacing and size, and dipole orientation of the array atoms. Our results bridge the description of CP potential across two distinct regimes: (i) from a single-atom limit where we recover the well-known two-atom Van der Waals potential, (ii) to a macroscopic boundary limit, where we demonstrate new asymptotic scaling laws. We demonstrate that these scaling laws can be tuned via the microscopic parameters of the atomic array, establishing atomically-controlled arrays as a versatile platform for tailoring fluctuation-induced QED phenomena.
The Casimir-Polder (CP) effect -- the force between a neutral atom and an uncharged conducting plate in empty space -- is an intriguing consequence of quantum vacuum fluctuations. The typically attractive CP potential crosses over from a scaling of z−3z^{-3}z−3 at short separations to z−4z^{-4}z−4 at long distances, where retardation effects due to the finite speed of light become important. At intermediate distances, where the atom--surface separation is of the order of the wavelength of the dominant atomic transition, experiments have so far relied on indirect methods, such as diffraction or quantum reflection, to observe the CP effect. Here, we directly reveal the CP force between strontium atoms and a dielectric surface via the induced shifts in the atomic energy levels in the intermediate regime. We spectroscopically probe the CP-induced kHz-frequency shift of ultracold atoms confined by a magic-wavelength optical lattice at 189(2)~nm from the surface -- on the scale of the dominant 461-nm transition. Our measurements agree well with QED calculations and differ from the short-range approximation, while excluding the long-distance one. This paves the way for studying the CP effect across various surface properties and geometries, as well as exploring the tensor nature of the atom-surface potential -- all important for the development of hybrid atomic optical-magnetic quantum devices.
The modification of quantum fluctuations by a surface of finite reflectivity shifts the energy levels of atoms and changes their radiative properties (Casimir-Polder effect). At nanometric distances away from a surface (near field), the Casimir-Polder energy shift is given by −C3/z3 (where C3 is the van der Waals coefficient and z is the atom-surface distance) corresponding to the interaction of the fluctuating atomic dipole with its surface induced image. Near field Rydberg-surface interactions are of fundamental interest because the atomic size, scaling as n∗2 (where n∗ is the principle quantum number corrected by the quantum defect), is no longer negligible compared to the atom-surface separation, z. In this case, the dipole approximation, (−C3/z3 law of interaction), is no longer valid and higher-order terms, corresponding to the interaction of the fluctuation quadrupole with its own image, need to be taken into account. Quadrupole interaction terms in the atom-surface interaction manifest themselves with a novel distance dependence of z5 that has not been experimentally investigated yet1. Casimir-Polder experiments were first performed with low-lying Rydberg states (n= 10-14), demonstrating the −C3/z3 law of interaction2. Nevertheless, more recent experiments with high-lying rubidium Rydbergs (n=32-43)3 were not in agreement with Casimir-Polder theory thus highlighting the need for further experimental studies.
Understanding the Casimir-Polder (CP) attraction between ultracold atoms and dielectric surfaces is of fundamental importance to the design and miniaturization of atom chips [1] and for understanding quantum reflection from, and sticking to, the surface [2 - 6]. So far, calculations have focussed on planar dielectrics, either semi-infinite or of finite width [7-9], and non-planar geometries including corrugated surfaces [10], spheres and carbon nanotubes [11-12]. Here, we present a simple scheme, based on the Pairwise-Summation (PWS) approximation, for estimating the CP interaction between a ground-state alkali atom and a dielectric volume of arbitrary shape. The PWS approximation integrates the van der Waals interaction between two ground-state atoms over the many atoms in the surface volume. We relate the microscopic polarizability of atoms in the surface to the bulk dielectric constant via the Clausius-Mossotti relation within the Lorentz local-field theory. We find that the CP potential depends strongly on both the geometry and density of the surface, which modify the fluctuation spectrum of the electromagnetic field that couples the alkali atoms to the dielectric. We compare our results with known analytical expressions for the CP potential near planar surfaces and use them to investigate how BECs interact with, and may quantum reflect from, curvilinear surface structures.
At nanometer separation, the dominant interaction between an atom and a material surface is the fluctuation-induced Casimir-Polder potential. We demonstrate that slow atoms crossing a silicon nitride transmission nanograting are a remarkably sensitive probe for that potential. A 15% difference between nonretarded (van der Waals) and retarded Casimir-Polder potentials is discernible at distances smaller than 51 nm. We discuss the relative influence of various theoretical and experimental parameters on the potential in detail. Our work paves the way to high-precision measurement of the Casimir-Polder potential as a prerequisite for understanding fundamental physics and its relevance to applications in quantum-enhanced sensing.