4.8 Article

Ultrafast Plasmonics Beyond the Perturbative Regime: Breaking the Electronic-Optical Dynamics Correspondence

期刊

NANO LETTERS
卷 22, 期 7, 页码 2748-2754

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.nanolett.1c04608

关键词

Plasmonics; Nanooptics; Hot Electrons; Ultrafast Spectroscopy; Ultrafast Nanophotonics

资金

  1. European Union [899673]
  2. Brazilian funding agency Capes
  3. Brazilian funding agency Fapemig
  4. Brazilian funding agency CNPq

向作者/读者索取更多资源

The transient optical response of plasmonic nanostructures is important for studying light harvesting, photocatalytic processes, nonlinear nanophotonics, and all-optical modulation. However, under a nonperturbative excitation regime, the correspondence between the temporal evolution of the dynamic optical signal and the photoexcited hot electrons is not valid.
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.

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