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Title: Plasmonic Spherical Heterodimers: Reversal of Optical Binding Force Based on the Forced Breaking of Symmetry
Authors: Mahdy, M.R.C. 
Danesh, M.
Zhang, T. 
Ding, W.
Rivy, H.M.
Chowdhury, A.B.
Mehmood, M.Q. 
Issue Date: 2018
Publisher: Nature Publishing Group
Citation: Mahdy, M.R.C., Danesh, M., Zhang, T., Ding, W., Rivy, H.M., Chowdhury, A.B., Mehmood, M.Q. (2018). Plasmonic Spherical Heterodimers: Reversal of Optical Binding Force Based on the Forced Breaking of Symmetry. Scientific Reports 8 (1) : 3164. ScholarBank@NUS Repository.
Rights: Attribution 4.0 International
Abstract: The stimulating connection between the reversal of near-field plasmonic binding force and the role of symmetry-breaking has not been investigated comprehensively in the literature. In this work, the symmetry of spherical plasmonic heterodimer-setup is broken forcefully by shining the light from a specific side of the set-up instead of impinging it from the top. We demonstrate that for the forced symmetry-broken spherical heterodimer-configurations: reversal of lateral and longitudinal near-field binding force follow completely distinct mechanisms. Interestingly, the reversal of longitudinal binding force can be easily controlled either by changing the direction of light propagation or by varying their relative orientation. This simple process of controlling binding force may open a novel generic way of optical manipulation even with the heterodimers of other shapes. Though it is commonly believed that the reversal of near-field plasmonic binding force should naturally occur for the presence of bonding and anti-bonding modes or at least for the Fano resonance (and plasmonic forces mostly arise from the surface force), our study based on Lorentz-force dynamics suggests notably opposite proposals for the aforementioned cases. Observations in this article can be very useful for improved sensors, particle clustering and aggregation. � 2018 The Author(s).
Source Title: Scientific Reports
ISSN: 20452322
DOI: 10.1038/s41598-018-21498-4
Rights: Attribution 4.0 International
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