We propose a novel approach for efficient tuning of optical properties of a high refractive index subwavelength nanoparticle with a magnetic Mie-type resonance by means of femtosecond laser irradiation. This concept is based on ultrafast photoinjection of dense (>10(20) cm(-3)) electron-hole plasma within such nanoparticle, drastically changing its transient dielectric permittivity. This allows manipulation by both electric and magnetic nanoparticle responses, resulting in dramatic changes of its scattering diagram and scattering cross section. We experimentally demonstrate 20% tuning of reflectance of a single silicon nanoparticle by femtosecond laser pulses with wavelength in the vicinity of the magnetic dipole resonance. Such a single-particle nanodevice enables designing of fast and ultracompact optical switchers and modulators.
Optical bound states in the continuum (BICs) provide a way to engineer resonant response in photonic crystals with giant quality factors. The extended interaction time in such systems is particularly promising for enhancement of nonlinear optical processes and development of a new generation of active optical devices. However, the achievable interaction strength is limited by the purely photonic character of optical BICs. Here, 1 arXiv:1905.13505v1 [cond-mat.mes-hall] 31 May 2019 we mix optical BIC in a photonic crystal slab with excitons in atomically thin transition metal dichalcogenide MoSe 2 via strong coupling to form exciton-polaritons with Rabi splitting exceeding 27 meV. We experimentally show BIC-like behavior of both upper and lower polariton branches, with complete suppression of radiation into far-field at the BIC wavevector and strongly varying Q-factor in its vicinity. Owing to an effective disorder averaging through motional narrowing, we achieve small polariton linewidth of 2 meV and demonstrate linewidth control via angle and temperature tuning. Our results pave the way towards developing tunable BIC-based polaritonic devices for sensing, lasing, and nonlinear optics. Optical bound states in the continuum (BICs), supported by photonic crystal structures of certain geometries, have received much attention recently as a novel approach to generating extremely spectrally narrow resonant responses. 1,2 Since BICs are uncoupled from the radiation continuum through symmetry protection 3 or resonance trapping, 4 their high quality factors, while reaching 10 5 − 10 6 , can be robust to perturbations of photonic crystal geometric parameters. This enables a broad range of practical applications, including recently demonstrated spectral filtering, 5 chemical and biological sensing, 6,7 and lasing. 4Providing an efficient light-trapping mechanism, optical BICs are particularly attractive for enhancing nonlinear optical effects, with recent theoretical proposals discussing enhanced bistability 8 and Kerr-type focusing nonlinearity. 9 However, for practical realization of these proposals, a significantly stronger material nonlinear susceptibility is needed than generally available in dielectric-based photonic crystals.An attractive approach to the enhancement of effective nonlinearity is through the use of exciton-polaritons -hybrid quasi-particles that inherit both the coherent properties of photonic modes and interaction strength of excitons. 10,11 Hybrid nanophotonic systems incorporating atomically thin transition metal dichalcogenides (TMDs) have proven to be a particularly promising platform owing to their ease of fabrication and possibility of room temperature operation. [12][13][14] In addition to conventional microcavity-based designs, TMD
Dewetting of thin metal films is one of the most widespread method for functional plasmonic nanostructures fabrication. However, simple thermal-induced dewetting does not allow to control degree of nanostructures order without additional lithographic process steps. Here we propose a novel method for lithography-free and large-scale fabrication of plasmonic nanostructures via controllable femtosecond laserinduced dewetting. The method is based on femtosecond laser surface pattering of a thin film followed by a nanoscale hydrodynamical instability, which is found to be very controllable under specific irradiation conditions. We achieve control over degree of nanostructures order by changing laser irradiation parametrs and film thickness. This allowed us to exploit the method for the broad range of applications: resonant light absorbtion and scattering, sensing, and potential improving of thin-film solar cells.
Growth and properties of the self‐catalyzed heterostructured GaP nanowires (NWs) with GaP1 − xAsx insertions in the form of nanodiscs (NDs) grown by means of molecular‐beam epitaxy on Si (111) substrate are studied. To obtain the NDs with the different composition and optoelectronic properties, the ratio of As and P fluxes is varied. Structural properties of the synthesized heterostructures are characterized by means of transmission electron microscopy. Energy dispersive X‐ray spectroscopy is used to study chemical composition of the NDs. The maximum achieved fraction x in the NDs is nearly 60%. Sublinear dependence of As concentration in the ND on the As/P flux ratio is observed and theoretical description for the observed phenomenon is provided. The proposed model can be used to estimate the predicted As/P ratio for the synthesis of GaPAs NDs as well as NWs of the required composition. Microphotoluminescence (μPL) studies demonstrate the appearance of broadband PL signal in the spectral range between 600 and 700 nm, corresponding to the NDs with different compositions. Spectra intensity modulation is found due to longitudinal Fabry–Pérot‐type resonances in the individual NWs.
In this paper we study growth of quasi-one-dimensional GaN nanowires (NWs) and nanotube (NT)-like nanostructures on Si(111) substrates covered with a thin AlN layer grown by means of plasma-assisted molecular beam epitaxy. In the first part of our study we investigate the influence of the growth parameters on the geometrical properties of the GaN NW arrays. First, we find that the annealing procedure carried out prior to deposition of the AlN buffer affects the elongation rate and the surface density of the wires. It has been experimentally demonstrated that the NW elongation rate and the surface density drastically depend on the substrate growth temperature, where 800 °C corresponds to the maximum elongation rate of the NWs. In the second part of the study, we introduce a new dopant-stimulated method for GaN nanotube-like nanostructure synthesis using a high-intensity Si flux. Transmission electron microscopy was used to investigate the morphological features of the GaN nanostructures. The synthesized structures have a hexagonal cross-section and possess high crystal quality. We propose a theoretical model of the novel nanostructure formation which includes the role of the dopant Si. Some of the Si-doped samples were studied with the photoluminescence (PL) technique. The analysis of the PL spectra shows that the highest value of donor concentration in the nanostructures exceeds 5∙1019 cm−3.
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We demonstrate that the use of a GaN seeding layer prepared prior to the growth of epitaxial GaN on Si (111) can lead to the formation of oriented arrays of Y-shaped nanoislands and nanowires and affects the surface density of the nanostructures.
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