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Quantum Chemistry

Attosecond correlated electron dynamics at C60 giant plasmon resonance

arXiv
Authors: Shubhadeep Biswas, Andrea Trabattoni, Philipp Rupp, Maia Magrakvelidze, Mohamed El-Amine Madjet, Umberto De Giovannini, Mattea C. Castrovilli, Mara Galli, Qingcao Liu, Erik P. Månsson, Johannes Schötz, Vincent Wanie, François Légaré, Pawel Wnuk, Mauro Nisoli, Angel Rubio, Himadri S. Chakraborty, Matthias F. Kling, Francesca Calegari

Year

2021

Paper ID

41194

Status

Preprint

Abstract Read

~2 min

Abstract Words

151

Citations

N/A

Abstract

Fullerenes have unique physical and chemical properties that are associated with their delocalized conjugated electronic structure. Among them, there is a giant ultra-broadband - and therefore ultrafast - plasmon resonance, which for C60 is in the extreme-ultraviolet energy range. While this peculiar resonance has attracted considerable interest for the potential downscaling of nanoplasmonic applications such as sensing, drug delivery and photocatalysis at the atomic level, its electronic character has remained elusive. The ultrafast decay time of this collective excitation demands attosecond techniques for real-time access to the photoinduced dynamics. Here, we uncover the role of electron correlations in the giant plasmon resonance of C60 by employing attosecond photoemission chronoscopy. We find a characteristic photoemission delay of up to 200 attoseconds pertaining to the plasmon that is purely induced by coherent large-scale correlations. This result provides novel insight into the quantum nature of plasmonic resonances, and sets a benchmark for advancing nanoplasmonic applications.

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  • This paper contributes to the Quantum Chemistry research area in the Quantum Articles archive.
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  • Fullerenes have unique physical and chemical properties that are associated with their delocalized conjugated electronic structure.

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