ICFO – The Institute of Photonic Sciences

About: ICFO – The Institute of Photonic Sciences is a facility organization based out in Barcelona, Spain. It is known for research contribution in the topics: Quantum & Quantum entanglement. The organization has 872 authors who have published 1965 publications receiving 56273 citations.

Modulational instability and solitary waves in polariton topological insulators

Abstract: Optical microcavities supporting exciton–polariton quasi-particles offer one of the most powerful platforms for the investigation of the rapidly developing area of topological photonics in general, and of photonic topological insulators in particular. Energy bands of the microcavity polariton graphene are readily controlled by a magnetic field and influenced by the spin-orbit (SO) coupling effects, a combination leading to the formation of linear unidirectional edge states in polariton topological insulators as very recently predicted. In this work we depart from the linear limit of non-interacting polaritons and predict instabilities of the nonlinear topological edge states resulting in the formation of the localized topological quasi-solitons, which are exceptionally robust and immune to backscattering wave packets propagating along the graphene lattice edge. Our results provide a background for experimental studies of nonlinear polariton topological insulators and can influence other subareas of photonics and condensed matter physics, where nonlinearities and SO effects are often important and utilized for applications.

Dissociation of two-dimensional excitons in monolayer WSe2

Abstract: Two-dimensional (2D) semiconducting materials are promising building blocks for optoelectronic applications, many of which require efficient dissociation of excitons into free electrons and holes. However, the strongly bound excitons arising from the enhanced Coulomb interaction in these monolayers suppresses the creation of free carriers. Here, we identify the main exciton dissociation mechanism through time and spectrally resolved photocurrent measurements in a monolayer WSe2 p–n junction. We find that under static in-plane electric field, excitons dissociate at a rate corresponding to the one predicted for tunnel ionization of 2D Wannier–Mott excitons. This study is essential for understanding the photoresponse of 2D semiconductors and offers design rules for the realization of efficient photodetectors, valley dependent optoelectronics, and novel quantum coherent phases. In two-dimensional semiconductors excitons are strongly bound, suppressing the creation of free carriers. Here, the authors investigate the main exciton dissociation pathway in p-n junctions of monolayer WSe2 by means of time and spectrally resolved photocurrent measurements.

Optimization of Nanoparticle-Based SERS Substrates through Large-Scale Realistic Simulations

Abstract: Surface-enhanced Raman scattering (SERS) has become a widely used spectroscopic technique for chemical identification, providing unbeaten sensitivity down to the single-molecule level. The amplification of the optical near field produced by collective electron excitations —plasmons— in nanostructured metal surfaces gives rise to a dramatic increase by many orders of magnitude in the Raman scattering intensities from neighboring molecules. This effect strongly depends on the detailed geometry and composition of the plasmon-supporting metallic structures. However, the search for optimized SERS substrates has largely relied on empirical data, due in part to the complexity of the structures, whose simulation becomes prohibitively demanding. In this work, we use state-of-the-art electromagnetic computation techniques to produce predictive simulations for a wide range of nanoparticle-based SERS substrates, including realistic configurations consisting of random arrangements of hundreds of nanoparticles with var...

Chloride-Induced Thickness Control in CdSe Nanoplatelets

Abstract: Current colloidal synthesis methods for CdSe nanoplatelets (NPLs) routinely yield samples that emit, in discrete steps, from 460 to 550 nm. A significant challenge lies with obtaining thicker NPLs, to further widen the emission range. This is at present typically achieved via colloidal atomic layer deposition onto CdSe cores, or by synthesizing NPL core/shell structures. Here, we demonstrate a novel reaction scheme, where we start from 4.5 monolayer (ML) NPLs and increase the thickness in a two-step reaction that switches from 2D to 3D growth. The key feature is the enhancement of the growth rate of basal facets by the addition of CdCl2, resulting in a series of nearly monodisperse CdSe NPLs with thicknesses between 5.5 and 8.5 ML. Optical characterization yielded emission peaks from 554 nm up to 625 nm with a line width (fwhm) of 9-13 nm, making them one of the narrowest colloidal nanocrystal emitters currently available in this spectral range. The NPLs maintained a short emission lifetime of 5-11 ns. Finally, due to the increased red shift of the NPL band edge photoluminescence excitation spectra revealed several high-energy peaks. Calculation of the NPL band structure allowed us to identify these excited-state transitions, and spectral shifts are consistent with a significant mixing of light and split-off hole states. Clearly, chloride ions can add a new degree of freedom to the growth of 2D colloidal nanocrystals, yielding new insights into both the NPL synthesis as well as their optoelectronic properties.

Universal analytical modeling of plasmonic nanoparticles

Abstract: Control over the optical response of metal nanoparticles and their associated plasmons is currently enabling many promising applications in areas as diverse as biosensing and photocatalysis. In this context, experiments based upon colloid synthesis and nanofabricated structures are assisted by numerical electromagnetic modeling, which supplies predictive simulations, but not the kind of physical intuition needed for exploration of new ideas, such as one finds when simple mathematical expressions can describe a problem. This tutorial review presents and extends a simple analytical simulation method that allows us to accurately describe the optical response of metal nanoparticles, including retardation effects, without the requirement of large computational resources. More precisely, plasmonic extinction spectra and near-field enhancement are described through a small set of real numbers for each nanoparticle shape, which we tabulate for a wide selection of common morphologies. Remarkably, these numbers are independent of size, composition and environment. We further present a compilation of nanoplasmonic experimental data that are excellently described by the simple mathematical expressions here introduced.