RESUMEN
Plasmonic metasurfaces exhibiting collective responses known as surface lattice resonances (SLRs) show potential for realizing flat photonic components for wavelength-selective processes, including lasing and optical nonlinearities. However, postfabrication tuning of SLRs remains challenging, limiting the applicability of SLR-based components. Here, we demonstrate how the properties of high quality factor SLRs are easily modified by breaking the symmetry of the nanoparticle surroundings. We break the symmetry by changing the refractive index of the overlying immersion oil by controlling the ambient temperature of the device. We show that a modest temperature change of 10 °C can increase the quality factor of the SLR from 400 to 750. Our results demonstrate accurate and reversible modification of the properties of the investigated SLRs, paving the way toward tunable SLR-based photonic devices. More generally, we show how symmetry breaking of the environment can be utilized for efficient and potentially ultrafast modification of the SLR properties.
RESUMEN
We report the performance of a graphene-enhanced THz grating fabricated by depositing a gold layer on the femtosecond micromachined SiO2 substrate. The morphology of the gold plated patterned substrate was studied by scanning electron microscopy (SEM) and atomic force microscopy (AFM), while the quality of the chemical vapor deposition (CVD) graphene was evaluated by Raman spectroscopy. The electromagnetic (EM) response of the metasurface comprising the graphene sheet and the gold plated substrate was studied by THz time domain spectroscopy in the 100 GHz-1 THz frequency range. We employed the finite elements method (FEM) to model the metasurface EM response by adjusting the ac conductivity of the gold layer covering the patterned SiO2 substrate to reproduce the measured transmission/reflection spectra. The results of the numerical simulation reveal the impact of the imperfectness of the gold layer on the performance of the THz metasurface. The experimental results are well described in terms of the Drude-Smith model of metal conductivity that takes into account the anisotropic scattering of the carriers in thin metal films.
RESUMEN
We performed the investigation of the polarization-sensitive photocurrent generated in silver-palladium metal-semiconductor nanocomposite films under irradiation with nanosecond laser pulses at the wavelength of 2600 nm. It is shown that in both the transverse and the longitudinal configuration, the surface photogalvanic (SPGE) and photon drag effects (PDE) contribute to the observed photocurrent. However, the temporal profile of the transverse photocurrent pulse is monopolar at any polarization and angle of incidence, while the temporal profile of the longitudinal photocurrent pulse depends on the polarization of the excitation beam. Specifically, the irradiation of the film with the s-polarized excitation beam produces a monopolar photoresponse, while at p-polarized excitation, the photoresponse is bipolar, having a short front and long tail. Obtained experimental results are in agreement with the developed phenomenological theory, which describes transverse and longitudinal photocurrents due to SPGE and PDE in terms of relevant second-order nonlinear susceptibilities and allows us to obtain their dependences on the angle of incidence and polarization of the excitation laser beam. The pronounced dependence of the photocurrent on the angle of incidence and polarization of the excitation beam opens avenues toward the development of polarization- and position-sensitive detectors for industrial and space applications.
RESUMEN
We report on the observation of the helicity-dependent photoresponse of the 20-µm-thick silver-palladium (Ag/Pd) nanocomposite films. In the experiment, 120 fs pulses of Ti:S laser induced in the film an electric current perpendicular to the incidence plane. The photoinduced current is a linear function of the incident beam power, and its sign depends on the beam polarization and angle of incidence. In particular, the current is zero for the p- and s-polarized beams, while its sign is opposite for the right- and left-circularly polarized beams. By comparing experimental results with theoretical analysis, we show that the photoresponse of the Ag/Pd nanocomposite originates from the photon drag effect.
RESUMEN
We report on a high performance nonlinear optical filter for the telecommunication window that employs detonation nanodiamonds (NDs). The nanosecond Z-scan experiments revealed that the heavy water ND suspensions enable strong optical limiting in the wavelength range of 1400-1675 nm. We observed an enhancement of the optical limiting performance in the blue part of the communication window. In particular, at the wavelength of 1400 nm the transmittance of the 2 mm thick sample with 4.5 wt. % ND concentration is suppressed by 45% for the input fluence of 3.8 J/cm(2). The proposed nonlinear optical filter employs the phenomena of the nonlinear absorption and the nonlinear light scattering in ND suspensions.
RESUMEN
We report on the optical limiting (OL) in stable aqueous suspensions of detonation nanodiamond (ND) clusters with average size of 50, 110, and 320 nm. The nanosecond Z-scan measurements at wavelength of 532 nm revealed that the larger the cluster size, the better the OL performance and the higher the ray stability of the ND suspension. Our analysis showed that the nonlinear scattering and the nonlinear absorption are the dominant mechanisms of OL in aqueous ND suspensions.