Please use this identifier to cite or link to this item: https://doi.org/10.1021/acs.nanolett.5b02302
Title: Cavity-Assisted Manipulation of Freely Rotating Silicon Nanorods in High Vacuum
Authors: Kuhn, S
Asenbaum, P
Kosloff, A
Sclafani, M
Stickler, B.A
Nimmrichter, S 
Hornberger, K
Cheshnovsky, O
Patolsky, F
Arndt, M
Keywords: Nanoparticles
Nanorods
Rotation
Rotational flow
Thermodynamics
Cavity optomechanics
Intracavity fields
Nano-scale objects
Optical manipulation
Precision measurement
Quantum physics
Rotational motion
Silicon substrates
Silicon
Issue Date: 2015
Publisher: American Chemical Society
Citation: Kuhn, S, Asenbaum, P, Kosloff, A, Sclafani, M, Stickler, B.A, Nimmrichter, S, Hornberger, K, Cheshnovsky, O, Patolsky, F, Arndt, M (2015). Cavity-Assisted Manipulation of Freely Rotating Silicon Nanorods in High Vacuum. Nano Letters 15 (8) : 5604-5608. ScholarBank@NUS Repository. https://doi.org/10.1021/acs.nanolett.5b02302
Rights: Attribution 4.0 International
Abstract: 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. We manipulate and trace their center-of-mass and rotational motion through the interaction with an intense intracavity field. Our experiments show that the anisotropy of the nanorotors leads to optical forces that are three times stronger than on silicon nanospheres of the same mass. The optical torque experienced by the spinning rods will enable cooling of the rotational motion and torsional optomechanics in a dissipation-free environment. © 2015 American Chemical Society.
Source Title: Nano Letters
URI: https://scholarbank.nus.edu.sg/handle/10635/183881
ISSN: 1530-6984
DOI: 10.1021/acs.nanolett.5b02302
Rights: Attribution 4.0 International
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