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Geometric frustration in ordered lattices of plasmonic nanoelements
Inspired by geometrically frustrated magnetic systems, we present the optical response of three cases of hexagonal lattices of plasmonic nanoelements. All of them were designed using a metal-insulator-metal configuration to enhance absorption of light, with elements in close proximity to exploit nea...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6401306/ https://www.ncbi.nlm.nih.gov/pubmed/30837626 http://dx.doi.org/10.1038/s41598-019-40117-4 |
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author | Conde-Rubio, Ana Fraile Rodríguez, Arantxa Espinha, André Mihi, Agustín Pérez-Murano, Francesc Batlle, Xavier Labarta, Amílcar |
author_facet | Conde-Rubio, Ana Fraile Rodríguez, Arantxa Espinha, André Mihi, Agustín Pérez-Murano, Francesc Batlle, Xavier Labarta, Amílcar |
author_sort | Conde-Rubio, Ana |
collection | PubMed |
description | Inspired by geometrically frustrated magnetic systems, we present the optical response of three cases of hexagonal lattices of plasmonic nanoelements. All of them were designed using a metal-insulator-metal configuration to enhance absorption of light, with elements in close proximity to exploit near-field coupling, and with triangular symmetry to induce frustration of the dipolar polarization in the gaps between neighboring structures. Both simulations and experimental results demonstrate that these systems behave as perfect absorbers in the visible and/or the near infrared. Besides, the numerical study of the time evolution shows that they exhibit a relatively extended time response over which the system fluctuates between localized and collective modes. It is of particular interest the echoed excitation of surface lattice resonance modes, which are still present at long times because of the geometric frustration inherent to the triangular lattice. It is worth noting that the excitation of collective modes is also enhanced in other types of arrays where dipolar excitations of the nanoelements are hampered by the symmetry of the array. However, we would like to emphasize that the enhancement in triangular arrays can be significantly larger because of the inherent geometric incompatibility of dipolar excitations and three-fold symmetry axes. |
format | Online Article Text |
id | pubmed-6401306 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-64013062019-03-08 Geometric frustration in ordered lattices of plasmonic nanoelements Conde-Rubio, Ana Fraile Rodríguez, Arantxa Espinha, André Mihi, Agustín Pérez-Murano, Francesc Batlle, Xavier Labarta, Amílcar Sci Rep Article Inspired by geometrically frustrated magnetic systems, we present the optical response of three cases of hexagonal lattices of plasmonic nanoelements. All of them were designed using a metal-insulator-metal configuration to enhance absorption of light, with elements in close proximity to exploit near-field coupling, and with triangular symmetry to induce frustration of the dipolar polarization in the gaps between neighboring structures. Both simulations and experimental results demonstrate that these systems behave as perfect absorbers in the visible and/or the near infrared. Besides, the numerical study of the time evolution shows that they exhibit a relatively extended time response over which the system fluctuates between localized and collective modes. It is of particular interest the echoed excitation of surface lattice resonance modes, which are still present at long times because of the geometric frustration inherent to the triangular lattice. It is worth noting that the excitation of collective modes is also enhanced in other types of arrays where dipolar excitations of the nanoelements are hampered by the symmetry of the array. However, we would like to emphasize that the enhancement in triangular arrays can be significantly larger because of the inherent geometric incompatibility of dipolar excitations and three-fold symmetry axes. Nature Publishing Group UK 2019-03-05 /pmc/articles/PMC6401306/ /pubmed/30837626 http://dx.doi.org/10.1038/s41598-019-40117-4 Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Conde-Rubio, Ana Fraile Rodríguez, Arantxa Espinha, André Mihi, Agustín Pérez-Murano, Francesc Batlle, Xavier Labarta, Amílcar Geometric frustration in ordered lattices of plasmonic nanoelements |
title | Geometric frustration in ordered lattices of plasmonic nanoelements |
title_full | Geometric frustration in ordered lattices of plasmonic nanoelements |
title_fullStr | Geometric frustration in ordered lattices of plasmonic nanoelements |
title_full_unstemmed | Geometric frustration in ordered lattices of plasmonic nanoelements |
title_short | Geometric frustration in ordered lattices of plasmonic nanoelements |
title_sort | geometric frustration in ordered lattices of plasmonic nanoelements |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6401306/ https://www.ncbi.nlm.nih.gov/pubmed/30837626 http://dx.doi.org/10.1038/s41598-019-40117-4 |
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