Gongora, J. S. Totero; Miroshnichenko, Andrey E.; Kivshar, Yuri S.; Fratalocchi, Andrea(Nature Communications, Springer Nature, 2017-05-31)[Article]
Nanophotonics is a rapidly developing field of research with many suggestions for a design of nanoantennas, sensors and miniature metadevices. Despite many proposals for passive nanophotonic devices, the efficient coupling of light to nanoscale optical structures remains a major challenge. In this article, we propose a nanoscale laser based on a tightly confined anapole mode. By harnessing the non-radiating nature of the anapole state, we show how to engineer nanolasers based on InGaAs nanodisks as on-chip sources with unique optical properties. Leveraging on the near-field character of anapole modes, we demonstrate a spontaneously polarized nanolaser able to couple light into waveguide channels with four orders of magnitude intensity than classical nanolasers, as well as the generation of ultrafast (of 100 fs) pulses via spontaneous mode locking of several anapoles. Anapole nanolasers offer an attractive platform for monolithically integrated, silicon photonics sources for advanced and efficient nanoscale circuitry.
Gongora, J. S. Totero; Miroshnichenko, Andrey E.; Kivshar, Yuri S.; Fratalocchi, Andrea(Laser & Photonics Reviews, Wiley, 2016-03-18)[Article]
A spaser is a nanoplasmonic counterpart of a laser, with photons replaced by surface plasmon polaritons and a resonant cavity replaced by a metallic nanostructure supporting localized plasmonic modes. By combining analytical results and first-principle numerical simulations, we provide a comprehensive study of the ultrafast dynamics of a spaser. Due to its highly-nonlinear nature, the spaser is characterized by a large number of interacting degrees of freedom, which sustain a rich manifold of different phases we discover, describe and analyze here. In the regime of strong interaction, the system manifests an irreversible ergodic evolution towards the configuration where energy is equally shared among all the available degrees of freedom. Under this condition, the spaser generates ultrafast vortex-like lasing modes that are spinning on the femtosecond scale and whose direction of rotation is dictated by quantum noise. In this regime, the spaser acquires the character of a nanoparticle with an effective spin. This opens up a range of interesting possibilities for achieving unidirectional emission from a symmetric nanostructure, stimulating a broad range of applications for nanoplasmonic lasers as unidirectional couplers and random information sources.
Gongora, J. S. Totero; Miroshnichenko, Andrey E.; Kivshar, Yuri S.; Fratalocchi, Andrea(2017 Conference on Lasers and Electro-Optics Europe & European Quantum Electronics Conference (CLEO/Europe-EQEC), Institute of Electrical and Electronics Engineers (IEEE), 2017-11-02)[Presentation]
One of the main challenges in photonics is the integration of ultrafast coherent sources in silicon compatible platforms at the nanoscale . Generally, the emission of ultra-short pulses is achieved by synchronizing the cavity modes of the system via external active components, such as, e.g., Q-switch or saturable absorbers. Consequently, the required optical setups are complex and difficult to integrate on-chip. To address these difficulties, we propose a novel type of integrated source based on the spontaneous synchronization of several near-field nanolasers. We design our near-field lasers by considering the nonlinear amplification of non-radiating Anapole modes . Anapoles represent an intriguing non-conventional state of radiation, whose excitation is responsible for the formation of scattering suppression states in dielectric nanostructures . Due to their inherent near-field emission properties, an ensemble of anapole-based nanolasers represent an ideal candidate to investigate and tailor spontaneous synchronization phenomena in a silicon-compatible framework. Additionally, their mutual non-linear interaction can be precisely controlled within standard nanofabrication tolerances.
Export search results
The export option will allow you to export the current search results of the entered query to a file. Different
formats are available for download. To export the items, click on the button corresponding with the preferred download format.
By default, clicking on the export buttons will result in a download of the allowed maximum amount of items.
For anonymous users the allowed maximum amount is 50 search results.
To select a subset of the search results, click "Selective Export" button and make a selection of the items you want to export.
The amount of items that can be exported at once is similarly restricted as the full export.
After making a selection, click one of the export format buttons. The amount of items that will be exported is indicated in the bubble next to export format.