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arXiv:2002.04650 · Optica

Optical levitation using broadband light

Anisur Rahman, P. F. Barker

Published Jul 2, 2020• 7 citations
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Abstract

The ability to create dynamic, tailored optical potentials has become important across fields ranging from biology to quantum science. We demonstrate a method for the creation of arbitrary optical tweezer potentials using the broadband spectral profile of a superluminescent diode combined with the chromatic aberration of a lens. A tunable filter, typically used for ultrafast laser pulse shaping, allows us to manipulate the broad spectral profile and therefore the optical tweezer potentials formed by focusing of this light. We characterize these potentials by measuring the Brownian motion of levitated nanoparticles in vacuum and also demonstrate interferometric detection and feedback cooling of the particle’s motion. This simple and cost-effective technique will enable wide application and allow rapid modulation of the optical potential landscape in excess of megahertz frequencies.

DOI
10.1364/optica.392210

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The ability to create dynamic, tailored optical potentials has become important across fields ranging from biology to quantum science. We demonstrate a method for the creation of arbitrary optical tweezer potentials using the broadband spectral profile of a superluminescent diode combined with the chromatic aberration of a lens. A tunable filter, typically used for ultrafast laser pulse shaping, allows us to manipulate the broad spectral profile and therefore the optical tweezer potentials formed by focusing of this light. We characterize these potentials by measuring the Brownian motion of levitated nanoparticles in vacuum and also demonstrate interferometric detection and feedback cooling of the particle’s motion. This simple and cost-effective technique will enable wide application and allow rapid modulation of the optical potential landscape in excess of megahertz frequencies.
The ability to create dynamic, tailored optical potentials has become important across fields ranging from biology to quantum science. We demonstrate a method for the creation of arbitrary optical tweezer potentials using the broadband spectral profile of a superluminescent diode combined with the chromatic aberration of a lens. A tunable filter, typically used for ultrafast laser pulse shaping, allows us to manipulate the broad spectral profile and therefore the optical tweezer potentials formed by focusing of this light. We characterize these potentials by measuring the Brownian motion of levitated nanoparticles in vacuum and also demonstrate interferometric detection and feedback cooling of the particle’s motion. This simple and cost-effective technique will enable wide application and allow rapid modulation of the optical potential landscape in excess of megahertz frequencies.
The superposition of frequency-shifted Laguerre-Gauss modes can produce a rotating saddlelike intensity profile. When spinning fast enough, the optical forces produced by this structured light saddle generate a dynamically stable equilibrium point capable of trapping nanoparticles in a high vacuum, akin to a Paul trap but with its unique characteristics. We analyze the stability conditions and center-of-mass motion, dynamics and cooling of a nanoparticle levitated in the optical saddle trap. We expect the optical saddle to find applications in levitated optomechanics experiments requiring fast parametric modulation and inverted squeezing potential landscapes.
Realizing a large-scale fully controllable quantum system is a challenging task in current physical research and has broad applications. Ultracold atom and molecule arrays in optical tweezers in vacuum have been used for quantum simulation, quantum metrology and quantum computing. Recently, quantum ground state cooling of the center-of-mass motion of a single optically levitated nanoparticle in vacuum was demonstrated, providing unprecedented opportunities for studying macroscopic quantum mechanics and precision measurements. In this work, we create a reconfigurable optically-levitated nanoparticle array in vacuum. Our optically-levitated nanoparticle array allows full control of individual nanoparticles to form an arbitrary pattern and detect their motion. As a concrete example, we choose two nanoparticles without rotation signals from an array to synthesize a nanodumbbell in-situ by merging them into one trap. The nanodumbbell synthesized in-situ can rotate beyond 1 GHz. Our work provides a new platform for studying macroscopic many-body physics.
We combine optical tweezers with feedback to impose arbitrary potentials on a colloidal particle. The feedback trap detects a particle's position, calculates a force based on an imposed “virtual potential,” and shifts the trap center to generate the desired force. We create virtual harmonic and double-well potentials to manipulate particles. The harmonic potentials can be chosen to be either weaker or stiffer than the underlying optical trap. Using this flexibility, we create an isotropic trap in three dimensions. Finally, we show that we can create a virtual double-well potential with fixed well separation and adjustable barrier height. These are accomplished at length scales down to 11 nm, a feat that is difficult or impossible to create with standard optical-tweezer techniques such as time sharing, dual beams, or spatial light modulators.
Nanoparticles levitated in high vacuum are isolated from the surrounding environment and thus can be used in various applications, including quantum physics research. We demonstrated optical levitation of a nanoparticle, which was trapped without cooling at a pressure of 4.5 × 10 −3 Pa, using a single aspheric lens with a large numerical aperture (= 0.9) and 1030-nm laser. We also activated parametric feedback cooling to trap the particle at a pressure of 5.8 × 10 −4 Pa. This experimental system will be useful for studying nanoparticles in ultrahigh vacuum and for building a mixed system with laser-cooled atoms.
We study theoretically the creation of an optical centrifuge for the controlled rotation of levitated nanorotors within an optical tweezer. The optical centrifuge's motion is simulated by rapidly rotating the linear polarization of the tightly focused optical field used to form an optical trap. We show that nanorotors, formed by anisotropic nanoparticles levitated within a trap, can be accelerated to well-defined rotational rates in excess of 100 MHz over durations of hundreds of microseconds. The initial conditions required for stable acceleration, based on optical trap properties and the anisotropic susceptibility of the nanorotor are established and confirmed by numerical simulations. We also present initial experiments that have developed tools for the rapid angular acceleration of the polarization vector of the linearly polarized beam that is required to create the centrifuge. We show that over acceleration durations in the 100 μ s range, high rotational speeds could be achieved in modest vacuum.