Engineering of nonlinear optical response in nanostructures is one of the key topics in nanophotonics, as it allows for broad frequency conversion at the nanoscale. Nevertheless, the application of the developed designs is limited by either high cost of their manufacturing or low conversion efficiencies. This paper reports on the efficient second-harmonic generation in a free-standing GaP nanowire array encapsulated in a polymer membrane. Light coupling with optical resonances and field confinement in the nanowires together with high nonlinearity of GaP material yield a strong second-harmonic signal and efficient near-infrared (800−1200 nm) to visible upconversion. The fabricated nanowire-based membranes demonstrate high flexibility and semitransparency for the incident infrared radiation, allowing utilizing them for infrared imaging, which can be easily integrated into different optical schemes without disturbing the visualized beam.

We propose a novel type of tunable Yagi-Uda nanoantenna composed of metal-dielectric (AgGe) core-shell nanoparticles. We show that, due to the combination of two types of resonances in each nanoparticle, such hybrid Yagi-Uda nanoantenna can operate in two different regimes. Besides the conventional nonresonant operation regime at low frequencies, characterized by highly directive emission in the forward direction, there is another one at higher frequencies caused by hybrid magneto-electric response of the core-shell nanoparticles. This regime is based on the excitation of the van Hove singularity, and emission in this regime is accompanied by high values of directivity and Purcell factor within the same narrow frequency range. Our analysis reveals the possibility of flexible dynamical tuning of the hybrid nanoantenna emission pattern via electron-hole plasma excitation by 100 femtosecond pump pulse with relatively low peak intensities ∼200 MW/cm 2 .

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The electric field of high-intensity ultrashort laser pulses substantially perturbs electron subsystem of a crystal and affects its band structure. Laser-driven oscillations of electrons and holes are frequently referred to as a major mechanism of the perturbation in dielectrics and semiconductors. New physical effects arise when the band structure is modified by an ultrashort pulse of the oscillations driven by a few-cycle laser pulse. Assuming the laser-pulse envelope varies slowly compared to the carrier frequency, we derive analytical relations for the laser-modified band structure by utilizing the Keldysh cycle-averaged non-perturbative approach under the approximation of constant effective mass. Formation of indirect-gap transient bands, suppression of the nonlinear absorption on the leading edge of a laser pulse, and cycle-averaged photo-current generation driven by the pulse envelope are predicted. Analytical scaling with six laser and material parameters is obtained. The reported results establish the limits of validity of the Keldysh photoionization model and advance understanding of the fundamental effects involved in high-intensity ultrafast laser-solid interactions.