Publications by authors named "Benjamin A Stickler"

Article Synopsis
  • Electric quadrupole traps effectively levitate charged objects, from protons to small particles, influencing their rotational behavior when charge distribution varies.
  • Experiments reveal a shift in motion for microparticles, transitioning from librational to synchronized rotation with the trap drive due to torque effects from the electric quadrupole.
  • This technique showcases versatility by spinning various particles like silicon microrods and microdiamonds, with the latter enabling detailed motion analysis through embedded nitrogen vacancy centers, promising advances in levitated quantum nanomechanics.
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Article Synopsis
  • Optical binding is the interaction between objects affected by laser light, useful for controlling tiny mechanical movements.
  • The study explores the quantum aspects of optical binding and how these effects can be detected in upcoming experiments with levitated nanoparticles.
  • The research also highlights limitations in achieving entanglement through optical binding in free space and suggests methods to overcome these challenges.
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Article Synopsis
  • Matter-wave interferometry with molecules showcases a key quantum phenomenon and has potential for advanced measurements in physical chemistry.
  • A major challenge is developing efficient beam splitting methods that can work with a variety of particles.
  • This research focuses on using intense deep-ultraviolet light to better understand interactions that could lead to new techniques in protein interferometry and enhanced sensing of molecular properties.
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Non-Hermitian dynamics, as observed in photonic, atomic, electrical and optomechanical platforms, holds great potential for sensing applications and signal processing. Recently, fully tuneable non-reciprocal optical interaction has been demonstrated between levitated nanoparticles. Here we use this tunability to investigate the collective non-Hermitian dynamics of two non-reciprocally and nonlinearly interacting nanoparticles.

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Nonlinear mechanical resonators display rich and complex dynamics and are important in many areas of fundamental and applied sciences. Here, we present a general strategy to generate mechanical nonlinearities for trapped particles by transverse driving in a funnel-shaped potential. Employing a trapped ion platform, we study the nonlinear oscillation, bifurcation, and hysteresis of a single calcium ion and demonstrate a 20-fold enhancement of the signal from a zeptonewton-magnitude harmonic force through the effect of vibrational resonance.

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We show theoretically that feedback cooling of two levitated, interacting nanoparticles enables differential sensing of forces and the observation of stationary entanglement. The feedback drives the two particles into a stationary, nonthermal state which is susceptible to inhomogeneous force fields and which exhibits entanglement for sufficiently strong interparticle couplings. We predict that force-gradient sensing at the zepto-Newton per micron range is feasible and that entanglement due to the Coulomb interaction between charged particles can be realistically observed in state-of-the-art setups.

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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.

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Arrays of optically trapped nanoparticles have emerged as a platform for the study of complex nonequilibrium phenomena. Analogous to atomic many-body systems, one of the crucial ingredients is the ability to precisely control the interactions between particles. However, the optical interactions studied thus far only provide conservative optical binding forces of limited tunability.

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Simultaneously cooling the rotational and translational motion of nanoscale dielectrics into the quantum regime is an open task of great importance for sensing applications and quantum superposition tests. Here, we show that the six-dimensional ground state can be reached by coherent-scattering cooling with an elliptically polarized and shaped optical tweezer. We determine the cooling rates and steady-state occupations in a realistic setup and discuss applications for mechanical sensing and fundamental experiments.

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Classical rotations of asymmetric rigid bodies are unstable around the axis of intermediate moment of inertia, causing a flipping of rotor orientation. This effect, known as the tennis racket effect, quickly averages to zero in classical ensembles since the flipping period varies significantly upon approaching the separatrix. Here, we explore the quantum rotations of rapidly spinning thermal asymmetric nanorotors and show that classically forbidden tunneling gives rise to persistent tennis racket dynamics, in stark contrast to the classical expectation.

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We demonstrate Bragg diffraction of the antibiotic ciprofloxacin and the dye molecule phthalocyanine at a thick optical grating. The observed patterns show a single dominant diffraction order with the expected dependence on the incidence angle as well as oscillating population transfer between the undiffracted and diffracted beams. We achieve an equal-amplitude splitting of 14ℏk (photon momenta) and maximum momentum transfer of 18ℏk.

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We present the quantum master equation describing the coherent and incoherent dynamics of a rapidly rotating molecule in the presence of a thermal background gas. The master equation relates the rate of rotational alignment decay and decoherence to the microscopic scattering amplitudes, which we calculate for anisotropic van der Waals scattering. For large rotational energies, we find quantitative agreement of the resulting alignment decay rate with recent superrotor experiments.

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We establish that matter-wave diffraction at near-resonant ultraviolet optical gratings can be used to spatially separate individual conformers of complex molecules. Our calculations show that the conformational purity of the prepared beam can be close to 100% and that all molecules remain in their electronic ground state. The proposed technique is independent of the dipole moment and the spin of the molecule and thus paves the way for structure-sensitive experiments with hydrocarbons and biomolecules, such as neurotransmitters and hormones, which have evaded conformer-pure isolation so far.

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We present the Markovian quantum master equation describing rotational decoherence, friction, diffusion, and thermalization of planar, linear, and asymmetric rotors in contact with a thermal environment. It describes how an arbitrary initial rotation state decoheres and evolves toward a Gibbs-like thermal ensemble, as we illustrate numerically for the linear and the planar top, and it yields the expected rotational Fokker-Planck equation of Brownian motion in the semiclassical limit.

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We derive the Boltzmann equation for the rotranslational dynamics of an arbitrary convex rigid body in a rarefied gas. It yields as a limiting case the Fokker-Planck equation accounting for friction, diffusion, and nonconservative drift forces and torques. We provide the rotranslational friction and diffusion tensors for specular and diffuse reflection off particles with spherical, cylindrical, and cuboidal shape, and show that the theory describes thermalization, photophoresis, and the inverse Magnus effect in the free molecular regime.

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Nanomechanical devices have attracted the interest of a growing interdisciplinary research community, since they can be used as highly sensitive transducers for various physical quantities. Exquisite control over these systems facilitates experiments on the foundations of physics. Here, we demonstrate that an optically trapped silicon nanorod, set into rotation at MHz frequencies, can be locked to an external clock, transducing the properties of the time standard to the rod's motion with a remarkable frequency stability f /Δf of 7.

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We present matter-wave interferometry as a tool to advance spectroscopy for a wide class of nanoparticles, clusters and molecules. The high sensitivity of de Broglie interference fringes to external perturbations enables measurements in the limit of an individual particle absorbing only a single photon on average, or even no photon at all. The method allows one to extract structural and electronic information from the loss of the interference contrast.

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Optical control of nanoscale objects has recently developed into a thriving field of research with far-reaching promises for precision measurements, fundamental quantum physics and studies on single-particle thermodynamics. Here, we demonstrate the optical manipulation of silicon nanorods in high vacuum. Initially, we sculpture these particles into a silicon substrate with a tailored geometry to facilitate their launch into high vacuum by laser-induced mechanical cleavage.

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