Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/155675
Title: Hybridized surface lattice modes in intercalated 3-disk plasmonic crystals for high figure-of-merit plasmonic sensing
Authors: Tobing, Landobasa Yosef Mario
Soehartono, Alana Mauluidy
Mueller, Aaron David
Yong, Ken-Tye
Fan, Weijun
Zhang, Dao Hua
Keywords: Engineering::Electrical and electronic engineering
Issue Date: 2021
Source: Tobing, L. Y. M., Soehartono, A. M., Mueller, A. D., Yong, K., Fan, W. & Zhang, D. H. (2021). Hybridized surface lattice modes in intercalated 3-disk plasmonic crystals for high figure-of-merit plasmonic sensing. Nanoscale, 13(7), 4092-4102. https://dx.doi.org/10.1039/D0NR07020C
Project: SERC 1720700038 
A1883c0002 
Journal: Nanoscale 
Abstract: Engineering the spectral lineshape of plasmonic modes by various electromagnetic couplings and mode interferences enables significant improvements for plasmonic sensing. However, bulk and surface sensitivities remain constrained by a trade-off arising from their respective dependence on the interaction volume and decay length of the plasmonic mode, making higher bulk sensitivity realized at the expense of reduced surface sensitivity. We propose a new approach to overcome this trade-off by combining near-field and far-field coupling in an intercalated 3-disk plasmonic crystal, where ∼10× higher figure of merit (FoM) and ∼2× higher surface sensitivity can be achieved, in comparison with those achievable by localized surface plasmons. A plasmonic mode with a Q-factor up to ∼110 is demonstrated based on gold 3-disk arrays in the visible spectrum, with a bulk FoM of ∼24 and a surface sensitivity prefactor of ∼13.56. The design and fabrication simplicity of the 3-disk structure highlight its potential for a robust plasmonic sensing platform with a high figure of merit.
URI: https://hdl.handle.net/10356/155675
ISSN: 2040-3364
DOI: 10.1039/D0NR07020C
Rights: © 2021 The Royal Society of Chemistry. All rights reserved. This paper was published in Nanoscale and is made available with permission of The Royal Society of Chemistry.
Fulltext Permission: open
Fulltext Availability: With Fulltext
Appears in Collections:EEE Journal Articles

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