Plasmonic-enhanced photoluminescence in porous silicon with pore-embedded gold nanoparticles fabricated by direct reduction of chloroauric acid

The low efficiency of porous silicon (p-Si) luminescence hinders the development of silicon-based optoelectronic devices. The increase in p-Si emission using near-field enhancement, owing to the incorporation of gold nanoparticles (AuNPs) into the photonic structure, is probably the most viable alternative. However, the coupling of plasmon resonance to p-Si emission is challenging because of the difficulty in controlling the size and location of the AuNPs with respect to the emissive p-Si layer. In this study, AuNPs were synthesized by clean direct reduction of chloroauric acid inside a p-Si photonic structure. As a result, AuNPs could be synthesized all along the pores of the p-Si structure, allowing to obtain a six-fold enhancement of the p-Si photoluminescence, specifically for the emission band at 567 nm owing to the plasmon effect. Possible applications of this hybrid material include light-emitting devices and photoluminescence-based sensors

Room-temperature polariton repulsion and ultra-strong coupling for a non-trivial topological one-dimensional tunable Fibonacci-conjugated porous-Silicon photonic quasi-crystal showing quasi bound-states-in-the-continuum

Room temperature strong coupling from CdSeS/Zn quantum-dots embedded into a tunable porous-silicon Fibonacci-conjugated array could be observed when exciton's energy was tuned either to the photonic-edge or the defect in the middle of the pseudo-bandgap region of the 1D cavity. Both, the photonic-edge and the defect could be identified as topological edge modes and quasi-bound-states-in-the-continuum, where large density of states and field localization over a wider bandwidth produce a broadband Purcell enhancement, helping to optimize the coupling among the exciton and the 1D photonic quasi-crystal despite the natural difficulty to make the quantum dots to penetrate the cavity pores. A clear repulsion among polaritons, amounting to almost 8 meV for in-plane k values when the cavity energy is larger than the exciton one (blue k-detuning), was measured when increasing the incident light fluence, marking the potential of this non-trivial topological array for achieving polariton quantum blockade. Evidence for ultra-strong coupling, where a shift as large as 20 meV, could be found when the defect of the pseudo-bandgap region of the cavity was tuned to the exciton

Controlled Anisotropic Deformation of Ag Nanoparticles by Si Ion Irradiation

The shape and alignment of silver nanoparticles embedded in a glass matrix is controlled using silicon ion irradiation. Symmetric silver nanoparticles are transformed into anisotropic particles whose larger axis is along the ion beam. Upon irradiation, the surface plasmon resonance of symmetric particles splits into two resonances whose separation depends on the fluence of the ion irradiation. Simulations of the optical absorbance show that the anisotropy is caused by the deformation and alignment of the nanoparticles, and that both properties are controlled with the irradiation fluence.Comment: Submitted to Phys. Rev. Lett. (October 14, 2005

Effect of size and composition on the second harmonic generation from lithium niobate powders at different excitation wavelengths

INVESTIGACIÓN DESARROLLADA EN COLABORACIÓN DE RED TEMATICA PRODEP /SEP/MEXICOLiNbO3 microcrystalline systems, possessing almost stoichiometric composition, were produced by varying the temperature and time parameters in the annealing processes following a mechanochemical reaction of raw powders. SHG from these samples, detected for every fundamental wavelength in the range 800-1300 nm, and being maximal at a certain wavelength, λmax, for each sample, has been addressed to a random scattering of the induced nonlinear polarizations. Possible tuning of λmax could be ascribed to control of composition and grain size of the sample. Random orientation of the produced nanocrystallites was verified since no dependence for SHG intensity on incident polarization was observed.PAPIIT-UNAM through grant IN117116 Y “RED PRODEP-SEP Compuestos poliméricos propiedades y aplicaciones 2015-2016

Room-Temperature CsPbBr3_3 Mixed Polaritons States

Light-matter interactions are known to lead to the formation of polariton states through what is called strong coupling, leading to the formation of two hybrid states usually tagged as Upper and Lower Polaritons. Here, we consider a similar interaction between excitons and photons in the realm of strong interactions, with the difference that it enables us to obtain a mixed-polariton state. In this case, the energy of this mixed state is found between the energies of the exciton state and the cavity mode, resulting in an imaginary coupling coefficient related to a specific class of singular points. These mixed states are often considered unobservable, although they are predicted well when the dressed states of a two-level atom are considered. However, intense light confinement can be obtained by using a Bound State in the Continuum, reducing the damping rates, and enabling the observation of mixed states resulting from the correct kind of exceptional point giving place to strong coupling. In this study, using the Transfer Matrix Method, we simulated cavities made of porous silicon coupled with CsPbBr3 perovskite quantum dots to numerically observe the mixed states as well as experimentally, by fabricating appropriate samples. The dispersion relation of the mixed states is fitted using the same equation as that used for strong coupling but considering a complex coupling coefficient, which is directly related to the appropriate type of exceptional point

Ablation and optical third-order nonlinearities in Ag nanoparticles

The optical damage associated with high intensity laser excitation of silver nanoparticles (NPs) was studied. In order to investigate the mechanisms of optical nonlinearity of a nanocomposite and their relation with its ablation threshold, a high-purity silica sample implanted with Ag ions was exposed to different nanosecond and picosecond laser irradiations. The magnitude and sign of picosecond refractive and absorptive nonlinearities were measured near and far from the surface plasmon resonance (SPR) of the Ag NPs with a self-diffraction technique. Saturable optical absorption and electronic polarization related to self-focusing were identified. Linear absorption is the main process involved in nanosecond laser ablation, but non-linearities are important for ultrashort picosecond pulses when the absorptive process become significantly dependent on the irradiance. We estimated that near the resonance, picosecond intraband transitions allow an expanded distribution of energy among the NPs, in comparison to the energy distribution resulting in a case of far from resonance, when the most important absorption takes place in silica. We measured important differences in the ablation threshold and we estimated that the high selectiveness of the SPR of Ag NPs as well as their corresponding optical nonlinearities can be strongly significant for laser-induced controlled explosions, with potential applications for biomedical photothermal processes

Effect of chromophore-chromophore electrostatic interactions in the NLO response of functionalized organic-inorganic sol-gel materials

In the last years, important non-linear optical results on sol-gel and polymeric materials have been reported, with values comparable to those found in crystals. These new materials contain push-pull chromophores either incorporated as guest in a high Tg polymeric matrix (doped polymers) or grafted onto the polymeric matrix. These systems present several advantages; however they require significant improvement at the molecular level - by designing optimized chromophores with very large molecular figure of merit, specific to each application targeted. Besides, it was recently stated in polymers that the chromophore-chromophore electrostatic interactions, which are dependent of chromophore concentration, have a strong effect into their non-linear optical properties. This has not been explored at all in sol-gel systems. In this work, the sol-gel route was used to prepare hybrid organic-inorganic thin films with different NLO chromophores grafted into the skeleton matrix. Combining a molecular engineering strategy for getting a larger molecular figure of merit and by controlling the intermolecular dipole-dipole interactions through both: the tuning of the push-pull chromophore concentration and the control of TEOS (Tetraethoxysilane) concentration, we have obtained a r33 coefficient around 15 pm/V at 633 nm for the classical DR1 azo-chromophore and a r33 around 50 pm/V at 831 nm for a new optimized chromophore structure.Comment: 10 pages, 11 figures, 1 tabl