Plasmonic excitations in quantum-sized sodium nanoparticles studied by time-dependent density functional calculations
arXiv:1307.3631 · doi:10.1103/PhysRevB.88.155437
Abstract
The plasmonic properties of sphere-like bcc Na nanoclusters ranging from Na to Na have been studied by real-time time-dependent local density approximation calculations. The optical absorption spectrum, density response function and static polarizability are evaluated. It is shown that the effect of the ionic background (ionic species and lattice) of the clusters accounts for the remaining discrepancy in the principal (surface plasmon) absorption peak energy between the experiments and previous calculations based on a jellium background model. The ionic background effect also pushes the critical cluster size where the maximum width of the principal peak occurs from Na predicted by the previous jellium model calculations to Na. In the volume mode clusters (Na, Na, Na, Na and Na) in which the density response function is dominated by an intense volume mode, a multiple absorption peak structure also appears next to the principal peak. In contrast, the surface mode clusters of greater size (Na, Na, Na and Na) exhibit a smoother and narrower principal absorption peak because their surface plasmon energy is located well within that of the unperturbed electron-hole transitions, and their density responses already bear resemblance to that of classical Mie theory. Moreover, it is found that the volume plasmon that exist only in finite size particles, gives rise to the long absorption tail in the UV region. This volume plasmon manifests itself in the absorption spectrum even for clusters as large as Na with an effective diameter of 3.0 nm.
References in corpus (5)
- A time-dependent density functional theory scheme for efficient calculations of dynamic (hyper)polarizabilities
- Surface plasmon in metallic nanoparticles: renormalization effects due to electron-hole excitations
- Lifetime of the first and second collective excitations in metallic nanoparticles
- Photoabsorption by Volume Plasmons in Metal Nanoclusters
- Coupling of Surface and Volume Dipole Oscillations in C-60 Molecules
Cited by in corpus (9)
- Resonance shifts and spill-out effects in self-consistent hydrodynamic nanoplasmonics
- Kohn-Sham decomposition in real-time time-dependent density-functional theory: An efficient tool for analyzing plasmonic excitations
- Quantum Hydrodynamic Theory for Plasmonics: Impact of the Electron Density Tail
- Ab-initio nanoplasmonics: The impact of atomic structure
- Real-Time Quantum Dynamics of Long-Range Electronic Excitation Transfer in Plasmonic Nanoantennas
- Laplacian-Level Quantum Hydrodynamic Theory for Plasmonics
- Plasmonic modes of polygonal particles calculated using a quantum hydrodynamics method
- Formation of normal surface plasmon modes in small sodium nanoparticles
- An eigenvalue approach to quantum plasmonics based on a self-consistent hydrodynamics method