Published September 30, 2014 | Version v1
Journal article

A computational study of the double-bands plasmonic light scattering of Al2O3 coated Al nanoshells in the deep-ultraviolet range

Description

Highlights: • The anti-symmetric scattering could be tuned down to the deep-ultraviolet below 200 nm. • The LSPR scattering with high energy is greater than the scattering with low energy. • The double-bands RLS of oxide coated Al nanoshell could be fine tuned by the geometry. - Abstract: The tunable scattering cross section of oxide layer-coated Al nanoshell has been computationally studied as a function of wavelength. The calculation results show that the two resonance light scattering (RLS) peaks of Al nanoshell have higher frequency and greater intensity than that of Au and Ag nanoshell. Both of the two scattering peaks, which are corresponding to anti-symmetric and symmetric plasmon coupling, take place in the ultraviolet range. And the anti-symmetric scattering peak could be tuned down to the deep-ultraviolet wavelength below 200 nm. By increasing radius and dielectric constant of the inner core, or decreasing the thickness of the oxide layer, the anti-symmetric scattering peak with short wavelength could be enhanced and has greater intensity than that of symmetric scattering peak with long wavelength, which is different from that of Au and Ag nanoshells. Obtaining intense RLS peaks from Al nanoshell at deep-ultraviolet region presents a potential for the application of ultra-sensitive biosensing, ultraviolet material characterization, and ultraviolet nanoscale imaging

Availability note (English)

Available from http://dx.doi.org/10.1016/j.apsusc.2014.06.129

Additional details

Identifiers

DOI
10.1016/j.apsusc.2014.06.129;
PII
S0169-4332(14)01434-2;

Publishing Information

Journal Title
Applied Surface Science
Journal Volume
314
Journal Page Range
p. 145-150
ISSN
0169-4332
CODEN
ASUSEE

Optional Information

Copyright
Copyright (c) 2014 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.