State Expansion of a Levitated Nanoparticle in a Dark Harmonic Potential.

We spatially expand and subsequently contract the motional thermal state of a levitated nanoparticle using a hybrid trapping scheme. The particle's center-of-mass motion is initialized in a thermal state (temperature 155 mK) in an optical trap and then expanded by subsequent evolution in a much softer Paul trap in the absence of optical fields. We demonstrate expansion of the motional state's standard deviation in position by a factor of 24. In our system, state expansion occurs devoid of backaction from photon recoil, making this approach suitable for coherent wave function expansion.

Cavity-mediated long-range interactions in levitated optomechanics.

The ability to engineer cavity-mediated interactions has emerged as a powerful tool for the generation of non-local correlations and the investigation of non-equilibrium phenomena in many-body systems. Levitated optomechanical systems have recently entered the multiparticle regime, which promises the use of arrays of strongly coupled massive oscillators to explore complex interacting systems and sensing. Here we demonstrate programmable cavity-mediated interactions between nanoparticles in vacuum by combining advances in multiparticle optical levitation and cavity-based quantum control. The interaction is mediated by photons scattered by spatially separated particles in a cavity, resulting in strong coupling that is long-range in nature. We investigate the scaling of the interaction strength with cavity detuning and interparticle separation and demonstrate the tunability of interactions between different mechanical modes. Our work will enable the exploration of many-body effects in nanoparticle arrays with programmable cavity-mediated interactions, generating entanglement of motion, and the use of interacting particle arrays for optomechanical sensing.

Fast quantum interference of a nanoparticle via optical potential control.

We introduce and theoretically analyze a scheme to prepare and detect non-Gaussian quantum states of an optically levitated particle via the interaction with light pulses that generate cubic and inverted potentials. We show that this approach allows to operate on sufficiently short time- and length scales to beat decoherence in a regime accessible in state-of-the-art experiments. Specifically, we predict the observation of single-particle interference of a nanoparticle with a mass above 108 atomic mass units delocalized by several nanometers, on timescales of milliseconds. The proposed experiment uses only optical and electrostatic control, and can be performed at about 10-10 mbar and at room temperature. We discuss the prospect of this method for coherently splitting the wavepacket of massive dielectric objects without using either projective measurements or an internal level structure.

Levitated Optomechanics with Meta-Atoms.

We propose to introduce additional control in levitated optomechanics by trapping a meta-atom, i.e., a subwavelength and high-permittivity dielectric particle supporting Mie resonances. In particular, we theoretically demonstrate that optical levitation and center-of-mass ground-state cooling of silicon nanoparticles in vacuum is not only experimentally feasible but it offers enhanced performance over widely used silica particles in terms of trap frequency, trap depth, and optomechanical coupling rates. Moreover, we show that, by adjusting the detuning of the trapping laser with respect to the particle's resonance, the sign of the polarizability becomes negative, enabling levitation in the minimum of laser intensity, e.g., at the nodes of a standing wave. The latter opens the door to trapping nanoparticles in the optical near-field combining red and blue-detuned frequencies, in analogy to two-level atoms, which is of interest for generating strong coupling to photonic nanostructures and short-distance force sensing.

Interaction between an Optically Levitated Nanoparticle and Its Thermal Image: Internal Thermometry via Displacement Sensing.

We propose and theoretically analyze an experiment where displacement sensing of an optically levitated nanoparticle in front of a surface can be used to measure the induced dipole-dipole interaction between the nanoparticle and its thermal image. This is achieved by using a surface that is transparent to the trapping light but reflective to infrared radiation, with a reflectivity that can be time modulated. This dipole-dipole interaction relies on the thermal radiation emitted by a silica nanoparticle having sufficient temporal coherence to correlate the reflected radiation with the thermal fluctuations of the dipole. The resulting force is orders of magnitude stronger than the thermal gradient force, and it strongly depends on the internal temperature of the nanoparticle for a particle-to-surface distance greater than two micrometers. We argue that it is experimentally feasible to use displacement sensing of a levitated nanoparticle in front of a surface as an internal thermometer in ultrahigh vacuum. Experimental access to the internal physics of a levitated nanoparticle in vacuum is crucial to understanding the limitations that decoherence poses to current efforts devoted to preparing a nanoparticle in a macroscopic quantum superposition state.

Spin-Controlled Quantum Interference of Levitated Nanorotors.

We describe how to prepare an electrically levitated nanodiamond in a superposition of orientations via microwave driving of a single embedded nitrogen-vacancy (NV) center. Suitably aligning the magnetic field with the NV center can serve to reach the regime of ultrastrong coupling between the NV and the diamond rotation, enabling single-spin control of the particle's three-dimensional orientation. We derive the effective spin-oscillator Hamiltonian for small amplitude rotation about the equilibrium configuration and develop a protocol to create and observe quantum superpositions of the particle orientation. We discuss the impact of decoherence and argue that our proposal can be realistically implemented with near-future technology.

Ponderomotive Squeezing of Light by a Levitated Nanoparticle in Free Space.

A mechanically compliant element can be set into motion by the interaction with light. In turn, this light-driven motion can give rise to ponderomotive correlations in the electromagnetic field. In optomechanical systems, cavities are often employed to enhance these correlations up to the point where they generate quantum squeezing of light. In free-space scenarios, where no cavity is used, observation of squeezing remains possible but challenging due to the weakness of the interaction, and has not been reported so far. Here, we measure the ponderomotively squeezed state of light scattered by a nanoparticle levitated in a free-space optical tweezer. We observe a reduction of the optical fluctuations by up to 25% below the vacuum level, in a bandwidth of about 15 kHz. Our results are explained well by a linearized dipole interaction between the nanoparticle and the electromagnetic continuum. These ponderomotive correlations open the door to quantum-enhanced sensing and metrology with levitated systems, such as force measurements below the standard quantum limit.

Mechanical Squeezing via Unstable Dynamics in a Microcavity.

We theoretically show that strong mechanical quantum squeezing in a linear optomechanical system can be rapidly generated through the dynamical instability reached in the far red-detuned and ultrastrong coupling regime. We show that this mechanism, which harnesses unstable multimode quantum dynamics, is particularly suited to levitated optomechanics, and we argue for its feasibility for the case of a levitated nanoparticle coupled to a microcavity via coherent scattering. We predict that for submillimeter-sized cavities the particle motion, initially thermal and well above its ground state, becomes mechanically squeezed by tens of decibels on a microsecond timescale. Our results bring forth optical microcavities in the unresolved sideband regime as powerful mechanical squeezers for levitated nanoparticles, and hence as key tools for quantum-enhanced inertial and force sensing.

Probing Surface-Bound Atoms with Quantum Nanophotonics.

Quantum control of atoms at ultrashort distances from surfaces would open a new paradigm in quantum optics and offer a novel tool for the investigation of near-surface physics. Here, we investigate the motional states of atoms that are bound weakly to the surface of a hot optical nanofiber. We theoretically demonstrate that with optimized mechanical properties of the nanofiber these states are quantized despite phonon-induced decoherence. We further show that it is possible to influence their properties with additional nanofiber-guided light fields and suggest heterodyne fluorescence spectroscopy to probe the spectrum of the quantized atomic motion. Extending the optical control of atoms to smaller atom-surface separations could create opportunities for quantum communication and instigate the convergence of surface physics, quantum optics, and the physics of cold atoms.

Quantum Acoustomechanics with a Micromagnet.

We show theoretically how to strongly couple the center-of-mass motion of a micromagnet in a harmonic potential to one of its acoustic phononic modes. The coupling is induced by a combination of an oscillating magnetic field gradient and a static homogeneous magnetic field. The former parametrically couples the center-of-mass motion to a magnonic mode while the latter tunes the magnonic mode in resonance with a given acoustic phononic mode. The magnetic fields can be adjusted to either cool the center-of-mass motion to the ground state or to enter into the strong quantum coupling regime. The center of mass can thus be used to probe and manipulate an acoustic mode, thereby opening new possibilities for out-of-equilibrium quantum mesoscopic physics. Our results hold for experimentally feasible parameters and apply to levitated micromagnets as well as micromagnets deposited on a clamped nanomechanical oscillator.

Cavity-Based 3D Cooling of a Levitated Nanoparticle via Coherent Scattering.

We experimentally realize cavity cooling of all three translational degrees of motion of a levitated nanoparticle in vacuum. The particle is trapped by a cavity-independent optical tweezer and coherently scatters tweezer light into the blue detuned cavity mode. For vacuum pressures around 10^{-5} mbar, minimal temperatures along the cavity axis in the millikelvin regime are observed. Simultaneously, the center-of-mass (c.m.) motion along the other two spatial directions is cooled to minimal temperatures of a few hundred millikelvin. Measuring temperatures and damping rates as the pressure is varied, we find that the cooling efficiencies depend on the particle position within the intracavity standing wave. This data and the behavior of the c.m. temperatures as functions of cavity detuning and tweezer power are consistent with a theoretical analysis of the experiment. Experimental limits and opportunities of our approach are outlined.

Radiation Reaction of a Jiggling Dipole in a Quantum Electromagnetic Field.

We show how to derive a consistent quantum theory of radiation reaction of a nonrelativistic point-dipole quantum oscillator by including the dynamical fluctuations of the position of the dipole. The proposed nonlinear theory displays neither runaway solutions nor acausal behavior without requiring additional assumptions. Furthermore, we show that quantum (zero-point) fluctuations of the electromagnetic field are necessary to satisfy the second law of thermodynamics. Our results are obtained by developing a nonperturbative technique involving a weak-coupling approximation at the level of the effective action.

Ultrashort Pulses for Far-Field Nanoscopy.

We show that ultrashort pulses can be focused, in a particular instant, to a spot size given by the wavelength associated with its spectral width. For attosecond pulses this spot size is within the nanometer scale. Then we show that a two-level system can be left excited after interacting with an ultrashort pulse whose spectral width is larger than the transition frequency, and that the excitation probability depends not on the field amplitude but on the field intensity. The latter makes the excitation profile have the same spot size as the ultrashort pulse. This unusual phenomenon is caused by quantum electrodynamics in the ultrafast light-matter interaction regime since the usually neglected counterrotating terms describing the interaction with the free electromagnetic modes are crucial for making the excitation probability nonzero and depend on the field intensity. These results suggest that a train of coherent attosecond pulses could be used to excite fluorescent markers with nanoscale resolution. The detection of the light emitted after fluorescence-or any other method used to detect the excitation-could then lead to a new scheme for far-field light nanoscopy.

Strong single-photon coupling in superconducting quantum magnetomechanics.

We show that the inductive coupling between the quantum mechanical motion of a superconducting microcantilever and a flux-dependent microwave quantum circuit can attain the strong single-photon nanomechanical coupling regime with feasible experimental parameters. We propose to use a superconducting strip, which is in the Meissner state, at the tip of a cantilever. A pickup coil collects the flux generated by the sheet currents induced by an external quadrupole magnetic field centered at the strip location. The position-dependent magnetic response of the superconducting strip, enhanced by both diamagnetism and demagnetizing effects, leads to a strong magnetomechanical coupling to quantum circuits.

Prediction of protein-protein interactions using distant conservation of sequence patterns and structure relationships.

MOTIVATION: Given that association and dissociation of protein molecules is crucial in most biological processes several in silico methods have been recently developed to predict protein-protein interactions. Structural evidence has shown that usually interacting pairs of close homologs (interologs) physically interact in the same way. Moreover, conservation of an interaction depends on the conservation of the interface between interacting partners. In this article we make use of both, structural similarities among domains of known interacting proteins found in the Database of Interacting Proteins (DIP) and conservation of pairs of sequence patches involved in protein-protein interfaces to predict putative protein interaction pairs. RESULTS: We have obtained a large amount of putative protein-protein interaction (approximately 130,000). The list is independent from other techniques both experimental and theoretical. We separated the list of predictions into three sets according to their relationship with known interacting proteins found in DIP. For each set, only a small fraction of the predicted protein pairs could be independently validated by cross checking with the Human Protein Reference Database (HPRD). The fraction of validated protein pairs was always larger than that expected by using random protein pairs. Furthermore, a correlation map of interacting protein pairs was calculated with respect to molecular function, as defined in the Gene Ontology database. It shows good consistency of the predicted interactions with data in the HPRD database. The intersection between the lists of interactions of other methods and ours produces a network of potentially high-confidence interactions.