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arXiv:1303.1711 · Physical Review A

Controlled ripple texturing of suspended graphene membranes due to coupling with ultracold atoms

Sofia Ribeiro, Stefan Scheel

Published Nov 26, 2013• 10 citations
arXivHTMLPDF

Abstract

We explore the possibility to create hybrid quantum systems that combine ultracold atoms with graphene membranes. We investigate a setup in which a cold atom cloud is placed close to a free-standing sheet of graphene at distances of a few hundred nanometers. The atoms then couple strongly to the graphene membrane via Casimir-Polder forces. Temporal changes in the atomic state of the atomic cloud changes the Casimir-Polder interaction, thereby leading to the creation of a back-action force in the graphene sheet. This setup provides a controllable way to engineer ripples in a graphene sheet with cold atoms.

DOI
10.1103/physreva.88.052521

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We explore the possibility to create hybrid quantum systems that combine ultracold atoms with graphene membranes. We investigate a setup in which a cold atom cloud is placed close to a free-standing sheet of graphene at distances of a few hundred nanometers. The atoms then couple strongly to the graphene membrane via Casimir-Polder forces. Temporal changes in the atomic state of the atomic cloud changes the Casimir-Polder interaction, thereby leading to the creation of a back-action force in the graphene sheet. This setup provides a controllable way to engineer ripples in a graphene sheet with cold atoms.
This thesis focuses on theoretical quantum optics, with special emphasis on developing protocols in which engineered vacuum forces enable one to construct hybrid systems. In these systems, atoms are combined with solid-state devices in order to take advantage of their unique properties such as long coherence times of atoms and flexibility, tunability, scalability, and fast response offered by solid-state systems. Special attention is given to the study of atom-surface interactions with Rydberg atoms, where exact Fano-type diagonalization of the interaction Hamiltonian is obtained showing that, not only do Rydberg atoms suffer energy shifts, the presence of a surface leads to an alteration and admixture of the unperturbed eigenstates. Of particular interest are dispersion forces on graphene systems. We investigate whether and under which circumstances the Casimir-Polder potential between an atom and a graphene-substrate system is dominated by the interaction with graphene such that the effect of the substrate does not play an important role. We also explore the possibility to create a setup where dispersion forces could be use to bend a graphene sheet. Placing an atom close, at distances of a few hundred nanometers, to a free-standing graphene membrane we show that temporal changes in the atomic state change the Casimir-Polder interaction, thereby leading to the creation of a backaction force in the graphene sheet. Finally, we look at nonlinear atom--surface coupling processes with the aim of proposing a hybrid quantum circuit device in which individual field-excitations can be transferred between atoms and surface polaritons on demand. Deeper investigations of nonlinear processes reveal the existence of a sum rule for two-photon spontaneous decay rates that can be simply understood as a redistribution of photonic modes across the frequency spectrum where the total integrated number of modes is still conserved.
We propose a scheme to actively cool the fundamental flexural (out-of-plane) mode of a graphene sheet via vacuum forces. Our setup consists of a cold-atom cloud placed close to a graphene sheet at distances of a few micrometers. The atoms couple to the graphene membrane via Casimir-Polder forces. By deriving a self-consistent set of equations governing the dynamics of the atomic gas and the flexural modes of the graphene, we show it is possible to cool graphene from room temperatures by actively (laser) cooling an atomic gas. By choosing the right set of experimental parameters we are able to cool a graphene sheet down to $\ensuremath{\sim}60 \ensuremath{\mu}\mathrm{K}$.
We investigate the Casimir force on thin suspended dielectric layers covered with graphene, both theoretically and experimentally. Thermal effects of the Casimir force on graphene occur at separations significantly smaller compared to ordinary metals and dielectrics. At such small separations, the Casimir force is sufficiently strong to be measured experimentally. However, the presence of substrates to support the graphene significantly reduces the enhancement. We show theoretically that replacing the solid substrate beneath graphene with a thin dielectric membrane partially restores this strong thermal dependence. One of the interacting objects is a solid gold plate. The other object is a suspended dielectric membrane made of either 15 nm of silicon oxide or 13 nm silicon nitride, covered with graphene. At a separation of $\sim$500 nm, theoretical predictions yield changes in the Casimir pressure of up to 54 % and 40 % for silicon oxide and silicon nitride, respectively, when the temperature is increased from 10 K to 294 K. Measurements were performed for graphene on a suspended silicon nitride membrane at room temperature, using a gold-coated sphere attached to a cantilever as the force sensor. The measured force gradient is consistent with the theoretical prediction, although the thermal dependence could not be resolved, in part because of uncertainties in the optical properties of silicon nitride. Replacing a bulk substrate with a thin dielectric membrane covered with graphene provides a substantial reduction of the Casimir force, which may facilitate the stable operation of neutral nanomechanical elements at small separations.
We show that thin dielectric films can be used to enhance the performance of passive atomic mirrors by enabling quantum reflection probabilities of over 90% for atoms incident at velocities of ∼1 mm s −1 , achieved in recent experiments. This enhancement is brought about by weakening the Casimir–Polder attraction between the atom and the surface, which induces the quantum reflection. We show that suspended graphene membranes also produce higher quantum reflection probabilities than bulk matter. Temporal changes in the electrical resistance of such membranes, produced as atoms stick to the surface, can be used to monitor the reflection process, non-invasively and in real time. The resistance change allows the reflection probability to be determined purely from electrical measurements without needing to image the reflected atom cloud optically. Finally, we show how perfect atom mirrors may be manufactured from semiconductor heterostructures, which employ an embedded two-dimensional electron gas to tailor the atom–surface interaction and so enhance the reflection by classical means.
We investigate the fluctuation-induced Casimir interactions between two parallel graphene sheets carrying steady-state drift currents. The graphene properties are modeled based on the shifted Fermi disk model to capture the non-equilibrium optical response of the system. We find that the drift current introduces a repulsive correction to the perpendicular to the layers Casimir interaction, thereby reducing the overall attractive force. Although the correction is repulsive, it does not overcome the underlying attraction between the layers. It also generates a lateral force that opposes the carrier flow direction. Both contributions are studied in terms of distance and drift velocity functionalities showing pathways for Casimir force control.
Abstract Sympathetic laser cooling of a single mode graphene membrane coupled to an atomic cloud interacting via Casimir–Polder forces has been recently proposed. Here, we extend this study to the effect of secondary graphene membrane whose frequency may be far or close to resonance. We show that if the two mechanical modes are close together, it is possible to simultaneously cool both modes. Conversely, if the two frequencies are set far apart, the secondary mode does not affect the cooling of the first one. We also study the entanglement properties of the steady-state using the logarithmic negativity. We show how stationary mechanical entanglement between two graphene sheets can be generated by means of vacuum fluctuations. Moreover, we find that, within feasible experimental parameters, large steady-state acoustomechanical entanglement, i.e. entanglement between the phononic and mechanical mode, E N ≈ 5 , can be generated.