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Register a new userEfficient Optical Manipulation of Janus Particles by Optical Nanofibers
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Added by
Cindy Liza Esporlas
Publication date
2021
fields
Physics
and research's language is
English
Authors
Cindy Esporlas
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Small composite objects, known as Janus particles, drive sustained scientific interest primarily targeted at biomedical applications, where such objects act as micro- or nanoscale actuators, carriers, or imaging agents. The major practical challenge is to develop effective methods for manipulation of Janus particles. The available long-range methods mostly rely on chemical reactions or thermal gradients, therefore having mediocre precision and strong dependency on the content and properties of the carrier fluid. To tackle these limitations, we propose the manipulation of Janus particles (here, silica microspheres half-coated with gold) by optical forces in the evanescent field of an optical nanofiber. We find that Janus particles exhibit stronger transverse localization and faster propulsion compared to all-dielectric particles of the same size. The propulsion speed recorded for a 3-$mu$m particle with a 20-nm-thick gold cap averages at 2~$mu$m/s per 1~mW of optical power, reaching 133 body length/s at 200~mW going through the nanofiber.
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We review our recent progress in the production and characterization of tapered optical fibers with a sub-wavelength diameter waist. Such fibers exhibit a pronounced evanescent field and are therefore a useful tool for highly sensitive evanescent wave spectroscopy of adsorbates on the fiber waist or of the medium surrounding. We use a carefully designed flame pulling process that allows us to realize preset fiber diameter profiles. In order to determine the waist diameter and to verify the fiber profile, we employ scanning electron microscope measurements and a novel accurate in situ optical method based on harmonic generation. We use our fibers for linear and non-linear absorption and fluorescence spectroscopy of surface-adsorbed organic molecules and investigate their agglomeration dynamics. Furthermore, we apply our spectroscopic method to quantum dots on the surface of the fiber waist and to caesium vapor surrounding the fiber. Finally, towards dispersive measurements, we present our first results on building and testing a single-fiber bi-modal interferometer.
We present a procedure for reproducibly fabricating ultrahigh transmission optical nanofibers (530 nm diameter and 84 mm stretch) with single-mode transmissions of 99.95 $ pm$ 0.02%, which represents a loss from tapering of 2.6 $,times ,$ 10$^{-5}$ dB/mm when normalized to the entire stretch. When controllably launching the next family of higher-order modes on a fiber with 195 mm stretch, we achieve a transmission of 97.8 $pm$ 2.8%, which has a loss from tapering of 5.0 $,times ,$ 10$^{-4}$ dB/mm when normalized to the entire stretch. Our pulling and transfer procedures allow us to fabricate optical nanofibers that transmit more than 400 mW in high vacuum conditions. These results, published as parameters in our previous work, present an improvement of two orders of magnitude less loss for the fundamental mode and an increase in transmission of more than 300% for higher-order modes, when following the protocols detailed in this paper. We extract from the transmission during the pull, the only reported spectrogram of a fundamental mode launch that does not include excitation to asymmetric modes; in stark contrast to a pull in which our cleaning protocol is not followed. These results depend critically on the pre-pull cleanliness and when properly following our pulling protocols are in excellent agreement with simulations.
We investigate trapping geometries for cold, neutral atoms that can be created in the evanescent field of a tapered optical fibre by combining the fundamental mode with one of the next lowest possible modes, namely the HE21 mode. Counter propagating red-detuned HE21 modes are combined with a blue-detuned HE11 fundamental mode to form a potential in the shape of four intertwined spirals. By changing the polar- ization from circular to linear in each of the two counter-propagating HE21 modes simultaneously the 4-helix configuration can be transformed into a lattice configuration. The modification to the 4-helix configuration due to unwanted excitation of the the T E01 and T M01 modes is also discussed.
Developing angular trapping methods, which will enable optical tweezers to rotate a micronized bead, is of great importance for the studies of biomacromolecules during a wide range of torque-generation processes. Here we report a novel controlled angular trapping method based on composite Janus particles. We used a chemically synthesized Janus particle, which consists of two hemispheres made of polystyrene (PS) and poly(methyl methacrylate) (PMMA) respectively, as a model system to demonstrate this method. Through computational and experimental studies, we demonstrated the feasibility to control the rotation of a Janus particle in a linearly polarized laser trap. Our results showed that the Janus particle aligned its two hemispheres interface parallel to the laser propagation direction as well as the laser polarization direction. In our experiments, the rotational state of the particle can be easily and directly visualized by using a CMOS camera, and does not require complex optical detection system. The rotation of the Janus particle in the laser trap can be fully controlled in real time by controlling the laser polarization direction. Our newly developed angular trapping technique has the great advantage of easy implementation and real time controllability. Considering the easy chemical synthesis of Janus particles and implementation of the angular trapping, this novel method has the potential of becoming a general angular trapping method. We anticipate that this new method will significantly broaden the availability of angular trapping in the biophysics community, and expand the scope of the research that can be enabled by the angular trapping approach.
We theoretically investigate the optical force exerted on an isotropic particle illuminated by a superposition of plane waves. We derive explicit analytical expressions for the exerted force up to quadrupolar polarizabilities. Based on these analytical expressions, we demonstrate that an illumination consisting of two tilted plane waves can provide a full control on the optical force. In particular, optical pulling, pushing and lateral forces can be obtained by the proper tuning of illumination parameters. Our findings might unlock multiple applications based on a deterministic control of the spatial motion of small particles.
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