Laser-induced cavitation (LIC) bubbles and the shockwaves they form upon collapse are destructive to nearby solid boundaries, making them of interest for biomedical and industrial applications. Furthermore, the LIC bubbles provide spatial control that can be tuned by the bubble size, collapse time and shockwave intensity. The inclusion of plasmonic nanoparticles, such as gold nanoparticles (GNP) in the liquids where LIC bubbles are formed, can further enhance the absorption of light, allowing for bubble formation at lower laser energies. However, the effect of the physical properties of such liquids on LIC bubble dynamics remains unknown. In this study, the dynamics of LIC bubbles in water-ethanol, water-glycerol, and water-GNP solutions were investigated by simultaneous high-speed shadowgraphy and spatial transmittance modulation. The first set of experiments demonstrated that LIC bubbles induced in the GNP solutions led to more efficient cavitation formation with lower fluence compared to solutions without GNPs, thereby producing higher-intensity pressure waves. A second set of experiments was conducted to determine the surface tension of GNP solutions at room temperature and was found to be 70.62 mN/m. With this information, and the corresponding values reported in the literature for ethanol and glycerol, we aimed at discerning the role of surface tension and viscosity on the dynamics of LIC bubbles, apart from the enhanced optical absorption of the GNP solutions. We observed that the optical breakdown threshold for plasma formation was reduced by 18% in GNP solutions as compared to DI water and 10.4% compared to ethanol, and the intensity of initial shockwaves in the GNP solutions was much higher than those in DI water. This enhanced intensity of shockwaves in GNP solutions compared to DI water opens a new avenue for the enhancement of cancer cell treatment and anti-bacterial applications in the biomedical field and the enhancement of the laser ablation technique in the industrial setting.

The “Window to the Brain” is a transparent cranial implant under development, based on nanocrystalline yttria‐stabilized zirconia (nc‐YSZ) transparent ceramic material. Previous work has demonstrated the feasibility of this material to facilitate brain imaging over time, but the long‐term stability of the material over decades in the body is unknown. In this study, the low‐temperature degradation (LTD) of nc‐YSZ of 3, 6, and 8 mol % yttria is compared before and after accelerated ageing treatments following ISO standards for assessing the ageing resistance of zirconia ceramics. After 100 hr of accelerated ageing (equivalent to many decades of ageing in the body), the samples do not show any signs of phase transformation to monoclinic by X‐ray diffraction and micro‐Raman spectroscopy. Moreover, the mechanical hardness of the samples did not decrease, and changes in optical transmittance from 500 to 1000 nm due to ageing treatments was minimal (below 3% for all samples), and unlikely to be due to phase transformation of surface crystals to monoclinic. These results indicate the nc‐YSZ has excellent ageing resistance and can withstand long‐term implantation conditions without exhibiting LTD.

In this work, we present an extensive comparative study between novel titanium nitride nanoparticles (TiN NPs) and commercial gold nanorods (GNR), both dispersed in water and exposed to a pulsed laser‐induced cavitation process. The optical density, shockwave emission, and bubble formation of these solutions were investigated using shadowgraphy, spatial transmittance modulation, and acoustic measurements. TiN nanoparticle solutions exhibited high stability undser a periodic nanosecond pulsed‐laser irradiation, making these nanomaterials promising agents for high‐power applications. In addition, they demonstrated a stronger nonlinear absorption compared to the GNR solutions, and plasma formation at lower laser energies. This study advances our understanding of the optical properties of TiN and discusses significant differences compared to gold, with important implications for future applications of this material in water treatment, nonlinear signal converting, and laser‐induced cavitation for medical implementations, among others.

Titanium nitride nanoparticles have become a research interest due to their distinguished optical and photothermal properties. Furthermore, the search for nanoparticle solutions with tunable nonlinear optical properties for laser‐based applications is critical. More specifically, third order optical nonlinearities such as reverse saturable absorption, optical liming, and self‐focusing are important in the biomedical and electronics fields. The optical nonlinearities of titanium nitride plasmonic nanoparticles are investigated as a function of material concentration in water solutions. Furthermore, the effect of nanoparticle clustering on optical nonlinearities is investigated by fabricating micrometer‐sized clusters of ≈50 nm titanium nitride particles. These studies demonstrate that the nonlinear absorption coefficient increases linearly with concentration. However, clusters require higher concentrations compared to the freestanding nanoparticles to exhibit similar nonlinear absorption coefficient and optical density. Similarly, the optical limiting threshold for titanium nitride nanoparticles appears to be lower compared to the cluster solutions, which is impacted by the collective scattering of nanoparticles and high reverse saturable absorption. In addition, self‐focusing is observed in the continuous resonant regime. This study provides an in‐depth analysis of the nonlinear optical properties of titanium nitride, with relevant consequences for applications such as sensor protection and photothermal therapy.