Noble metal nanoparticles have received much attention due to their interesting properties that make them useful in different technical fields. Metallic nanoparticles with optical properties in the near infrared region of the electromagnetic spectrum are of great importance for biological applications, in particular photothermal therapy, as it is greatly enhanced by metallic nanoparticles. However, despite the large amount of work that has been done with metallic nanoparticles for thermal therapy, there is a reduced amount of scientific reports about the photothermal stability of most studied nanoparticles. In this work, hollow Au–Ag bimetallic nanoparticles were synthesized via galvanic replacement reaction, with optical properties that can be tuned systematically along the visible and near infrared region of the spectrum, by changing the pH before the synthesis of the templates and by controlling the amount of gold added for the synthesis of the nanoshells. The synthesized nanoparticles exhibit good photothermal properties when illuminated with an 808 nm laser light. An increase of temperature of nearly 20 °C is achieved after 15 minutes of irradiation. Moreover, the Au–Ag nanoparticles show good reusability even after ten heating/cooling cycles. The nanoparticles also retain their optical properties after 12 hours of continuous irradiation and are able to maintain their photothermal characteristics of increasing the temperature at the same levels during the entire process.
Recently, the paraelectric response of water was investigated in the range 0–100 °C. It showed an almost perfect Curie–Weiss behaviour up to 60 °C, but a slight change in slope of 1/εd versus T at 60 °C was overlooked. In this work, we report optical extinction measurements on metallic (gold and silver) nanoparticles dispersed in water, annealed at various temperatures in the range from 20 to 90 °C. An anomalous response at 60 °C is clearly detectable, which we associate to a subtle structural transformation in the water molecules at that temperature. This water anomaly is also manifested by means of a blue shift in the longitudinal surface plasmon resonance of the metallic nanoparticles for the solutions annealed at temperatures higher than about 60 °C. A reanalysis of 1/εd (T) for water in the whole temperature range leads us to conclude that the water molecule undergoes a subtle transformation from a low temperature (0–60 °C) configuration with a dipole moment μ1 = 2.18 D (close to the molecular dipole moment of ice) to a high temperature (60–100 °C) configuration with μ2 = 1.87 D (identical to the molecular dipole moment in water vapour).
In this work, we used a sequential method of synthesis for gold–silver bimetallic nanoparticles with core@shell structure (Au@AgNPs).Rumex hymenosepalusroot extract (Rh), which presents high content in catechins and stilbenes, was used as reductor agent in nanoparticles synthesis. Size distribution obtained by Transmission Electron Microscopy (TEM) gives a mean diameter of 36 ± 11 nm for Au@AgNPs, 24 ± 4 nm for gold nanoparticles (AuNPs), and 13 ± 3 nm for silver nanoparticles (AgNPs). The geometrical shapes of NPs were principally quasi-spherical. The thickness of the silver shell over AuNPs is around 6 nm and covered by active biomolecules onto the surface. Nanoparticles characterization included high angle annular dark field images (HAADF) recorded with a scanning transmission electron microscope (STEM), Energy-Dispersive X-ray Spectroscopy (EDS), X-Ray Diffraction (XRD), UV–Vis Spectroscopy, Zeta Potential, and Dynamic Light Scattering (DLS). Fourier Transform Infrared Spectrometer (FTIR), and X-ray Photoelectron Spectroscopy (XPS) show that nanoparticles are stabilized by extract molecules. A growth kinetics study was performed using the Gompertz model for microorganisms exposed to nanomaterials. The results indicate that AgNPs and Au@AgNPs affect the lag phase and growth rate ofEscherichia coliandCandida albicansin a dose-dependent manner, with a better response for Au@AgNPs