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Mixed halide perovskites undergo phase segregation, manifested as spectral red-shifting of photoluminescence spectra under illumination. In the iodine-bromide mixed perovskites, the origin of the low-energy luminescence is related to iodine-enriched domains formation. Such domains create favorable bands for the induced carrier funneling into them. Despite the phase segregation process is crucial for mixed halide perovskite-based optoelectronics, numerous gaps exist within the understanding of this phenomenon. One such gap pertains to the emergence of temporary and intermediate photoluminescence peaks during the initial stages of phase segregation. However, these peaks appear only within the first few seconds of illumination. Nevertheless, the decreasing temperature may prolong these initial stages. In this work, we carry out a detailed study of the temperature dependence of anion segregation in MAPbBr_2I and MAPbBr2.5I0.5 halide perovskites, to obtain a deeper comprehension of segregation processes, particularly during their initial stages. The temporal evolution of low-temperature photoluminescence reveals the undergoing of the intermediate stage during the segregation process and temperature-related phase transition from orthorhombic to tetragonal phase. To complement the phase segregation study, the temperature dependence of time-resolved photoluminescence spectroscopy is provided, allowing us to estimate the change in the photoluminescence lifetimes for the initial and segregated peaks with temperature., 28 pages, 7 figures

All-dielectric nanophotonics becomes a versatile tool for various optical applications, including nanothermometry and optical heating. Its general concept includes excitation of Mie resonances in nonplasmonic nanoparticles. However, the potential of resonant dielectric nanoparticles in drug delivery applications still have not been fully realized. Here, optically resonant dielectric iron oxide nanoparticles ($\alpha$-Fe$_2$O$_3$ NPs) are employed for remote rupture of microcontainers used as drug delivery platform. It is theoretically and experimentally demonstrated, that $\alpha$-Fe$_2$O$_3$ NPs has several advantages in light-to-heat energy conversion comparing to previously used materials, such as noble metals and silicon, due to the broader spectral range of efficient optical heating, and in enhancement of thermally sensitive Raman signal. The $\alpha$-Fe$_2$O$_3$ NPs embedded into the wall of universal drug carriers, polymer capsules, are used to experimentally determine the local temperature of the capsule rupture upon laser irradiation (170$^o$C). As a proof of principle, we successfully show the delivery and remote release of anticancer drug vincristine upon lowered laser irradiation (4.0$\times$10$^4$~W/cm$^2$) using polymer capsules modified with the $\alpha$-Fe$_2$O$_3$ NPs. The biological tests were performed on two primary cell types: (i) carcinoma cells, as an example of malignant tumor, and (ii) human stem cells, as a model of healthy cells. The developed delivery system consisting of polymer capsules modified with the dielectric nanoparticles provides multifunctional platform for remote drug release and temperature detection.

All-dielectric subwavelength structures utilizing Mie resonances provide a novel paradigm in nanophotonics for controlling and manipulating light. So far, only spontaneous emission enhancement was demonstrated with single dielectric nanoantennas, whereas stimulated emission was achieved only in large lattices supporting collective modes. Here, we demonstrate the first single-particle all-dielectric monolithic nanolaser driven by Mie resonances in visible and near-IR frequency range. We employ halide perovskite CsPbBr$_3$ as both gain and resonator material that provides high optical gain (up to $\sim 10^4$ cm$^{-1}$) and allows simple chemical synthesis of nanocubes with nearly epitaxial quality. Our smallest non-plasmonic Mie-resonant single-mode nanolaser with the size of 420 nm operates at room temperatures and wavelength 535 nm with linewidth $\sim 3.5$ meV. These novel lasing nanoantennas can pave the way to multifunctional photonic designs for active control of light at the nanoscale.

Nanoantennas for highly efficient excitation and manipulation of surface waves at nanoscale are key elements of compact photonic circuits. However, previously implemented designs employ plasmonic nanoantennas with high Ohmic losses, relatively low spectral resolution, and complicated lithographically made architectures. Here we propose an ultracompact and simple dielectric nanoantenna (silicon nanosphere) allowing for both directional launching of surface plasmon polaritons on a thin gold film and their demultiplexing with a high spectral resolution. We show experimentally that mutual interference of magnetic and electric dipole moments supported by the dielectric nanoantenna results in opposite propagation of the excited surface waves whose wavelengths differ by less than 50 nm in the optical range. Broadband reconfigurability of the nanoantennas operational range is achieved simply by varying the diameter of the silicon sphere. Moreover, despite subwavelength size ($, Comment: added relevant references; fixed typos in Supplementary eq. 8,9,11

Achievement of all-optical ultrafast signal modulation and routing by a low-loss nanodevice is a crucial step towards an ultracompact optical chip with high performance. Here, we propose a specifically designed silicon dimer nanoantenna, which is tunable via photoexcitation of dense electron-hole plasma with ultrafast relaxation rate. Basing on this concept, we demonstrate the effect of beam steering up to 20 degrees via simple variation of incident intensity, being suitable for ultrafast light routing in an optical chip. The effect is demonstrated both in the visible and near-IR spectral regions for silicon and germanium based nanoantennas. We also reveal the effect of electron-hole plasma photoexcitation on local density of states (LDOS) in the dimer gap and find that the orientation averaged LDOS can be altered by 50\%, whereas modification of the projected LDOS can be even more dramatic: almost 500\% for transverse dipole orientation. Moreover, our analytical model sheds light on transient dynamics of the studied nonlinear nanoantennas, yielding all temporal characteristics of the proposed ultrafast nanodevice. The proposed concept paves the ways to creation of low-loss, ultrafast, and compact devices for optical signal modulation and routing.

Optically generated electron-hole plasma in high-index dielectric nanostructures was demonstrated as a means of tuning of their optical properties. However, until now an ultrafast operation regime of such plasma driven nanostructures has not been attained. Here, we perform pump-probe experiments with resonant silicon nanoparticles and report on dense optical plasma generation near the magnetic dipole resonance with ultrafast (about 2.5 ps) relaxation rate. Basing on experimental results, we develop an analytical model describing transient response of a nanocrystalline silicon nanoparticle to an intense laser pulse and show theoretically that plasma induced optical nonlinearity leads to ultrafast reconfiguration of the scattering power pattern. We demonstrate 100 fs switching to unidirectional scattering regime upon irradiation of the nanoparticle by an intense femtosecond pulse. Our work lays the foundation for developing ultracompact and ultrafast all-optical signal processing devices.

Hybrid nanophotonics based on metal-dielectric nanostructures unifies the advantages of plasmonics and all-dielectric nanophotonics providing strong localization of light, magnetic optical response and specifically designed scattering properties. Here we demonstrate a novel approach for fabrication of ordered hybrid nanostructures via femtosecond laser melting of asymmetrical metal-dielectric (Au-Si) nanoparticles created by lithographical methods. The approach allows selective reshaping of the metal components of the hybrid nanoparticles without affecting dielectric ones. We apply the developed approach for tuning of the hybrid nanostructures scattering properties in the visible range. The experimental results are supported by molecular dynamics simulation and numerical solving of Maxwell equations., Comment: Published in Advanced Materials

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 laser-induced 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., to be published in Laser and Photonics Reviews. arXiv admin note: substantial text overlap with arXiv:1505.03041

We propose a novel concept for efficient dynamic tuning of optical properties of a high refractive index subwavelength nanoparticle with a magnetic Mie-type resonance by means of femtosecond laser radiation. This concept is based on ultrafast generation of electron-hole plasma within such nanoparticle, drastically changing its transient dielectric permittivity. This allows to manipulate by both electric and magnetic nanoparticle responses, resulting in dramatic changes of its extinction cross section and scattering diagram. Specifically, we demonstrate the effect of ultrafast switching-on a Huygens source in the vicinity of the magnetic dipole resonance. This approach enables to design ultrafast and compact optical switchers and modulators based on the "ultrafast magnetic light" concept., Silicon nanoparticles, femtosecond laser pulses, magnetic light

A novel method for single-step, lithography-free, and large-scale laser writing of nanoparticle-based plasmonic structures has been developed. Changing energy of femtosecond laser pulses and thickness of irradiated gold film it is possible to vary diameter of the gold nanoparticles, while the distance between them can be varied by laser scanning parameters. This method has an advantage over the most previously demonstrated methods in its simplicity and versatility, while the quality of the structures is good enough for many applications. In particular, resonant light absorbtion/scattering and surface-enhanced Raman scattering have been demonstrated on the fabricated nanostructures.

A discrete pattern of the low-frequency acoustic emission spectrum under conditions of high-temperature plastic deformation of aluminum is analyzed. It is attributed to re-distribution of vibrational energy of the primary acoustic signal over resonant vibrations of standing waves of the resonators. In a low-stability crystal medium, standing-wave oscillations initiate elementary deformation displacements in a certain material volume. The linear dimensions of this volume are related to the length of the standing wave, thus determining the macroscopic scale of correlation. The correlated deformation displacements in turn generate acoustic signals, whose interference results in the formation of a single acoustic signal of abnormally high amplitude. In a low-stability state of the crystal lattice, activation of the elementary plastic shears could result from a combined action of static forces, thermal fluctuations and dynamic forces of standing acoustic waves.