scholarly journals Sensing properties of lattice resonances of 2D metal nanoparticle arrays: An analytical model

2013 ◽  
Vol 21 (22) ◽  
pp. 27490 ◽  
Author(s):  
Barbora Špačková ◽  
Jiří Homola
2013 ◽  
Vol 3 (6) ◽  
pp. 794 ◽  
Author(s):  
Susan Derenko ◽  
René Kullock ◽  
Zhi Wu ◽  
Andrew Sarangan ◽  
Christiane Schuster ◽  
...  

2014 ◽  
Vol 2 (4) ◽  
pp. 394-399 ◽  
Author(s):  
Edgar Palacios ◽  
Aiqing Chen ◽  
Jonathan Foley ◽  
Stephen K. Gray ◽  
Ulrich Welp ◽  
...  

2007 ◽  
Vol 39 (5) ◽  
pp. 411-422 ◽  
Author(s):  
Masaya Mitsuishi ◽  
Miki Ishifuji ◽  
Hiroshi Endo ◽  
Hiroyuki Tanaka ◽  
Tokuji Miyashita

Nanomaterials ◽  
2019 ◽  
Vol 9 (4) ◽  
pp. 531 ◽  
Author(s):  
Uldis Malinovskis ◽  
Raimonds Poplausks ◽  
Donats Erts ◽  
Kerstin Ramser ◽  
Sigitas Tamulevičius ◽  
...  

This study demonstrates a new, robust, and accessible deposition technique of metal nanoparticle arrays (NPAs), which uses nanoporous anodic alumina (NAA) as a template for capillary force-assisted convective colloid (40, 60, and 80 nm diameter Au) assembly. The NPA density and nanoparticle size can be independently tuned by the anodization conditions and colloid synthesis protocols. This enables production of non-touching variable-density NPAs with controllable gaps in the 20–60 nm range. The NPA nearest neighbor center distance in the present study was fixed to 100 nm by the choice of anodization protocol. The obtained Au NPAs have the resonant scattering maxima in the visible spectral range, with a refractometric sensitivity, which can be tuned by the variation of the array density. The thickness of the NAA layer in an Aluminum-NAA-NPA multilayer system enables further tuning of the resonance frequency and optimization for use with specific molecules, e.g., to avoid absorption bands. Applicability of the mentioned multilayers for colorimetric refractive index (RI) sensing is demonstrated. Their use as Surface-Enhanced Raman Scattering (SERS) substrates is tested using hemoglobin as a biological probe molecule.


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