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Ultrafast Plasmonics Beyond the Perturbative Regime: Breaking the Electronic-Optical Dynamics Correspondence
[Image: see text] The transient optical response of plasmonic nanostructures has recently been the focus of extensive research. Accurate prediction of the ultrafast dynamics following excitation of hot electrons by ultrashort laser pulses is of major relevance in a variety of contexts from the study...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9011396/ https://www.ncbi.nlm.nih.gov/pubmed/35343692 http://dx.doi.org/10.1021/acs.nanolett.1c04608 |
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author | Schirato, Andrea Crotti, Giulia Gonçalves Silva, Mychel Teles-Ferreira, Danielle Cristina Manzoni, Cristian Proietti Zaccaria, Remo Laporta, Paolo de Paula, Ana Maria Cerullo, Giulio Della Valle, Giuseppe |
author_facet | Schirato, Andrea Crotti, Giulia Gonçalves Silva, Mychel Teles-Ferreira, Danielle Cristina Manzoni, Cristian Proietti Zaccaria, Remo Laporta, Paolo de Paula, Ana Maria Cerullo, Giulio Della Valle, Giuseppe |
author_sort | Schirato, Andrea |
collection | PubMed |
description | [Image: see text] The transient optical response of plasmonic nanostructures has recently been the focus of extensive research. Accurate prediction of the ultrafast dynamics following excitation of hot electrons by ultrashort laser pulses is of major relevance in a variety of contexts from the study of light harvesting and photocatalytic processes to nonlinear nanophotonics and the all-optical modulation of light. So far, all studies have assumed the correspondence between the temporal evolution of the dynamic optical signal, retrieved by transient absorption spectroscopy, and that of the photoexcited hot electrons, described in terms of their temperature. Here, we show both theoretically and experimentally that this correspondence does not hold under a nonperturbative excitation regime. Our results indicate that the main mechanism responsible for the breaking of the correspondence between electronic and optical dynamics is universal in plasmonics, being dominated by the nonlinear smearing of the Fermi–Dirac occupation probability at high hot-electron temperatures. |
format | Online Article Text |
id | pubmed-9011396 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-90113962022-04-18 Ultrafast Plasmonics Beyond the Perturbative Regime: Breaking the Electronic-Optical Dynamics Correspondence Schirato, Andrea Crotti, Giulia Gonçalves Silva, Mychel Teles-Ferreira, Danielle Cristina Manzoni, Cristian Proietti Zaccaria, Remo Laporta, Paolo de Paula, Ana Maria Cerullo, Giulio Della Valle, Giuseppe Nano Lett [Image: see text] The transient optical response of plasmonic nanostructures has recently been the focus of extensive research. Accurate prediction of the ultrafast dynamics following excitation of hot electrons by ultrashort laser pulses is of major relevance in a variety of contexts from the study of light harvesting and photocatalytic processes to nonlinear nanophotonics and the all-optical modulation of light. So far, all studies have assumed the correspondence between the temporal evolution of the dynamic optical signal, retrieved by transient absorption spectroscopy, and that of the photoexcited hot electrons, described in terms of their temperature. Here, we show both theoretically and experimentally that this correspondence does not hold under a nonperturbative excitation regime. Our results indicate that the main mechanism responsible for the breaking of the correspondence between electronic and optical dynamics is universal in plasmonics, being dominated by the nonlinear smearing of the Fermi–Dirac occupation probability at high hot-electron temperatures. American Chemical Society 2022-03-28 2022-04-13 /pmc/articles/PMC9011396/ /pubmed/35343692 http://dx.doi.org/10.1021/acs.nanolett.1c04608 Text en © 2022 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Schirato, Andrea Crotti, Giulia Gonçalves Silva, Mychel Teles-Ferreira, Danielle Cristina Manzoni, Cristian Proietti Zaccaria, Remo Laporta, Paolo de Paula, Ana Maria Cerullo, Giulio Della Valle, Giuseppe Ultrafast Plasmonics Beyond the Perturbative Regime: Breaking the Electronic-Optical Dynamics Correspondence |
title | Ultrafast Plasmonics Beyond the Perturbative Regime:
Breaking the Electronic-Optical Dynamics Correspondence |
title_full | Ultrafast Plasmonics Beyond the Perturbative Regime:
Breaking the Electronic-Optical Dynamics Correspondence |
title_fullStr | Ultrafast Plasmonics Beyond the Perturbative Regime:
Breaking the Electronic-Optical Dynamics Correspondence |
title_full_unstemmed | Ultrafast Plasmonics Beyond the Perturbative Regime:
Breaking the Electronic-Optical Dynamics Correspondence |
title_short | Ultrafast Plasmonics Beyond the Perturbative Regime:
Breaking the Electronic-Optical Dynamics Correspondence |
title_sort | ultrafast plasmonics beyond the perturbative regime:
breaking the electronic-optical dynamics correspondence |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9011396/ https://www.ncbi.nlm.nih.gov/pubmed/35343692 http://dx.doi.org/10.1021/acs.nanolett.1c04608 |
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