Surface modification of bioceramic materials by covalent immobilization of biomolecules is a promising way to improve their bioactivity. This approach implies the use of organic anchors to introduce functional groups on the inorganic surface on which the biomolecules will be immobilized. In this process, the density and surface distribution of biomolecules, and in turn the final biological properties, are strongly influenced by those of the anchors. We propose a new approach based on Raman 2D mapping to evidence the surface distribution of organosilanes, frequently used as anchors on biomaterial surfaces on hydroxyapatite and silicated hydroxyapatite ceramics. Unmodified and silanized ceramic surfaces were characterized by means of contact angle measurements, atomic force microscopy (AFM) and Raman mapping. Contact angle measurements and AFM topographies confirmed the surface modification. Raman mapping highlighted the influence of both the ceramic’s composition and silane functionality (i.e., the number of hydrolysable groups) on the silane surface distribution. The presence of hillocks was shown, evidencing a polymerization and/or an aggregation of the molecules whatever the silane and the substrates were. The substitution of phosphate groups by silicate groups affects the covering, and the spots are more intense on SiHA than on HA.

Channel temperature has a strong impact on the performance of a microwave power transistor. In this paper, various methods, including electrical measurements, optical analysis, and FEM simulations, were employed to perform both transient and steady-state thermal characterization of GH15 2 × 150 µm transistors from UMS foundry (United Monolithic Semiconductors, France). The transient study allowed for the extraction of thermal time constants according to which the temperature in the transistor changes. The steady-state study provided the hotspot temperature. As the channel is physically inaccessible, direct thermal measurement at the hotspot is not possible, in order to extract the temperature of this hotspot, different measurement methods are combined by simulation, which is calibrated based on the measurements, resulting in a well-adjusted thermal model. This calibrated model enabled the extraction of temperature at any location within the device’s structure, particularly at the hotspot. The measurement and simulation results have shown that the hotspot temperature can be 30% higher than the temperature of the nearest external surface for high dissipated power levels.

In the field of non-oxide ceramics, the polymer-derived ceramic (PDC) approach appears to be very promising, especially for obtaining easily shaped and homogeneous materials in terms of structure and composition. However, in order to reach a suitable form during the process, it is often necessary to study the rheology of preceramic polymers while they are modified during polymerisation or crosslinking reactions. Given this need in the understanding of the real-time rheology of macromolecules during their synthesis, a rheometer coupled with both an infrared spectrometer and a Raman probe is described as a powerful tool for monitoring in situ synthesised polycarbosilanes. Indeed, this original device allows one to control the viscosity of a hyberbranched polycarbosilane from defined difunctional and tetrafunctional monomers. Meanwhile, it links this evolution to structural modifications in the macromolecular structure (molar masses, dispersity and conformation), based on SEC-MALS analyses, synchronised by the monomer conversion determined by using Raman and infrared spectroscopies, a common denominator of the aforementioned instrumental platform.