An ideal plasmonic system for hot-electron generation allows the optical excitation of plasmons, limits radiation losses, exhibits strong non-radiative electron damping, and is made from scalable and cost-effective materials. Here we demonstrate the optical excitation of dark interlayer plasmons in bilayers of colloidal gold nanoparticles. This excitation is created by an antiparallel orientation of the dipole moments in the nanoparticle layers; it is expected to exhibit strongly reduced radiative damping. Despite the vanishing dipole moment, an incoming electromagnetic wave that is propagating normal to the surface will excite the dark mode due to field retardation. We observe a strong peak in the absorption spectrum of a colloidal gold bilayer (nanoparticle diameter = 46 nm); this peak is absent for a nanoparticle monolayer. The full width at half maximum of the dark mode is 230 meV for an ideal nanoparticle crystal and 320 meV for the structure produced by self-assembly out of solution. The position and width of the dark plasmon are efficiently tailored by the interparticle distance within the layer, nanoparticle size and layer number. We present time-resolved pump and probe experiments of hot-electron generation by bright and dark bilayer nanoparticle modes.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1039/c8fd00149a | DOI Listing |
ACS Nano
December 2024
School of Materials Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, China.
Ultrafast thermal switches are pivotal for managing heat generated in advanced solid-state applications, including high-speed chiplets, thermo-optical modulators, and on-chip lasers. However, conventional phonon-based switches cannot meet the demand for picosecond-level response times, and existing near-field radiative thermal switches face challenges in efficiently modulating heat transfer across vacuum gaps. To overcome these limitations, we propose an ultrafast thermal switch design based on pump-driven transient polaritons in asymmetric terminals.
View Article and Find Full Text PDFACS Nano
December 2024
Department of Materials Science and Engineering, Technion - Israel Institute of Technology, Haifa 32000, Israel.
Collective optical properties can emerge from an ordered ensemble of emitters due to interactions between the individual units. Superlattices of halide perovskite nanocrystals exhibit collective light emission, influenced by dipole-dipole interactions between simultaneously excited nanocrystals. This coupling changes both the emission energy and rate compared to the emission of uncoupled nanocrystals.
View Article and Find Full Text PDFNanotechnology
December 2024
Department of Physics, King Faisal University, King Faisal University P.O. 380 Ahsaa 31982, Al Ahsa, 31982, SAUDI ARABIA.
An anisotropic plasmonic trimer is proposed as an effective spectroscopic amplifier for the maximum signal enhancement of the Hyper-Raman Scattering (HRS) process. The three-particle system is composed of asymmetric Au nanorings arranged collinearly in a J-aggregate configuration and illuminated by a longitudinally polarized light. The optical properties of the considered trimer have been numerically simulated by the Finite-Difference Time-Domain (FDTD) method.
View Article and Find Full Text PDFJ Cancer Res Clin Oncol
December 2024
Department of Neurosurgery, Faculty of Medicine and University Hospital Carl Gustav Carus, Technische Universität Dresden, Dresden, Germany.
Purpose: Analysis of autofluorescence holds promise for brain tumor delineation and diagnosis. Therefore, we investigated the potential of a commercial confocal laser scanning endomicroscopy (CLE) system for clinical imaging of brain tumors.
Methods: A clinical CLE system with fiber probe and 488 nm laser excitation was used to acquire images of tissue autofluorescence.
J Chem Phys
December 2024
Department of Physics, Stockholm University, AlbaNova University Center, SE-10691 Stockholm, Sweden.
Vibrational polaritons are formed by strong coupling of molecular vibrations and photon modes in an optical cavity. Experiments have demonstrated that vibrational strong coupling can change molecular properties and even affect chemical reactivity. However, the interactions in a molecular ensemble are complex, and the exact mechanisms that lead to modifications are not fully understood yet.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!