There has been growing interest in scattering media in recent years, due to their potential applications as solar collectors, photocatalyzers, random lasers and other novel optical devices. Here, we have introduced a novel core–shell scattering medium for a random laser composed of TiO₂@Silica nanoparticles. Higher efficiency, lower laser threshold and long photobleaching lifetime in random lasers were demonstrated. This has introduced a new method or parameter (fraction of absorbed pumping), which opens a new avenue to characterize and study the scattering media. Optical chemical and colloidal stabilities were combined by coating a suitable silica shell onto TiO₂ nanoparticles.

Anderson localization of light and random lasing in this critical regime is an open research frontier, which besides being a basic research topic could also lead to important applications. This article investigates the random laser action at the localization transition in a strongly disordered scattering medium composed of a colloidal suspension of core–shell nanoparticles (TiO₂@Silica) in ethanol solution of Rhodamine 6G. The classical superfluorescence band of the random laser was measured separately by collecting the emission at the back of the samples, showing a linear dependence with pumping fluence without gain depletion. However, frontal collection showed saturation of the absorption and emission. Narrow peaks of approximately equal intensity are observed on top of the classical superfluorescence band, indicating suppression of the interaction between the peaks modes. The linewidth of these peaks is lower than that of the passive modes of the scattering medium. A method called fraction of absorbed pumping allowed us to infer that this peak’s mode (localized modes) is confined to a shallow region near the input-pumping border.

A TiO2@Silica nanoparticle has been introduced in a random laser. TiO2 particles with an average diameter of 0.41 μm were coated with silica shells of different thicknesses. Strong dependency of silica shell thickness on the medium scattering strength was found. A mathematical relationship between the scattering mean free path, random laser threshold, and random laser efficiency was developed. Higher efficiency, lower laser threshold, narrower bandwidth, and longest photobleaching lifetime were obtained in the random laser that had increased silica shell thickness. Optical colloidal stability and light coupling enhancement with scattering particles, provided by silica shell, should lead to improved laser performance.

This paper reports the synthesis of silver nanoparticles coated with porous silica (Ag@Silica NPs) using an assisted laser ablation method. This method is a chemical synthesis where one of the reagents (the reducer agent) is introduced in nanometer form by laser ablation of a solid target submerged in an aqueous solution. In a first step, a silicon wafer immersed in water solution was laser ablated for several minutes. Subsequently, an AgNO3 aliquot was added to the aqueous solution. The redox reaction between the silver ions and ablation products leads to a colloidal suspension of core-shell Ag@Silica NPs. The influence of the laser pulse energy, laser wavelength, ablation time, and Ag+ concentration on the size and optical properties of the Ag@Silica NPs was investigated. Furthermore, the colloidal suspensions were studied by UV–VIS-NIR spectroscopy, X-Ray diffraction, and high-resolution transmission electron microscopy (HRTEM).