| Literature DB >> 30150399 |
Kyle D Chapkin1,2, Luca Bursi2,3, Grant J Stec2,4, Adam Lauchner1,2, Nathaniel J Hogan1,2, Yao Cui1,2, Peter Nordlander1,2,3,5, Naomi J Halas6,2,3,4.
Abstract
Polycyclic aromatic hydrocarbon (PAH) molecules are essentially graphene in the subnanometer limit, typically consisting of 50 or fewer atoms. With the addition or removal of a single electron, these molecules can support molecular plasmon (collective) resonances in the visible region of the spectrum. Here, we probe the plasmon dynamics in these quantum systems by measuring the excited-state lifetime of three negatively charged PAH molecules: anthanthrene, benzo[ghi]perylene, and perylene. In contrast to the molecules in their neutral state, these three systems exhibit far more rapid decay dynamics due to the deexcitation of multiple electron-hole pairs through molecular plasmon "dephasing" and vibrational relaxation. This study provides a look into the distinction between collective and single-electron excitation dynamics in the purely quantum limit and introduces a conceptual framework with which to visualize molecular plasmon decay.Entities:
Keywords: excited-state dynamics; lifetime; molecular plasmons; plasmonicity; plasmonics
Year: 2018 PMID: 30150399 PMCID: PMC6140484 DOI: 10.1073/pnas.1805357115
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205