Plasmons of magnesium nanodisks and their interactions with a dipole-carrying molecule
Creators
- 1. Department of Physics, Kuwait College of Science And Technology, Doha Area, 7th Ring Road, P.O. Box 27235 (Kuwait)
Description
Magnesium nanostructures have recently emerged as an outstanding material with new and intriguing plasmonic properties. Here we investigate the optical properties of pristine and pyridine adsorbed magnesium nanodisks having diameter spanning in the range of 0.50 nm–2.0 nm. We base our calculations on computationally efficient time-dependent density-functional theory calculations. Our results demonstrate that pristine magnesium nanodisks possess localized surface plasmon resonances. The adsorption of a dipole-carrying molecule significantly alters their plasmonic response due to the strong plasmon splitting, leading to new features in their optical response. We believe that magnesium nanodisks provide a versatile platform for sensing and in the design of novel ultra-sensitive plasmonic devices.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.physe.2018.11.036Additional details
Identifiers
- DOI
- 10.1016/j.physe.2018.11.036;
- PII
- S1386947718314103;
Publishing Information
- Journal Title
- Physica E. Low-Dimensional Systems and Nanostructures (Print)
- Journal Volume
- 108
- Journal Page Range
- p. 296-299
- ISSN
- 1386-9477
INIS
- Country of Publication
- Netherlands
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54126096
- Subject category
- S77: NANOSCIENCE AND NANOTECHNOLOGY;
- Descriptors DEI
- ADSORPTION; DENSITY FUNCTIONAL METHOD; DESIGN; DIPOLES; MAGNESIUM; MOLECULES; NANOSTRUCTURES; OPTICAL PROPERTIES; PLASMONS; PYRIDINE; SURFACES; TIME DEPENDENCE
- Descriptors DEC
- ALKALINE EARTH METALS; AZINES; CALCULATION METHODS; ELEMENTS; HETEROCYCLIC COMPOUNDS; METALS; MULTIPOLES; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; PHYSICAL PROPERTIES; PYRIDINES; QUASI PARTICLES; SORPTION; VARIATIONAL METHODS
Optional Information
- Copyright
- Copyright (c) 2018 Elsevier B.V. All rights reserved.