In this paper we describe a new Mueller matrix (MM) microscope that generalizes and makes quantitative the polarized light microscopy technique. In this instrument all the elements of the MU are simultaneously determined from the analysis in the frequency domain of the time-dependent intensity of the light beam at every pixel of the camera. The variations in intensity are created by the two compensators continuously rotating at different angular frequencies. A typical measurement is completed in a little over one minute and it can be applied to any visible wavelength. Some examples are presented to demonstrate the capabilities of the instrument.

Multiwall carbon nanotubes grown by plasma enhanced chemical vapour deposition were functionalized by H(2)O plasma treatment. Through a controlled functionalization process of the carbon nanotubes (CNTs) we were able to modify and tune their chemical reactivity, expanding the range of potential applications in the field of energy and environment. In particular, different oxygen groups were attached to the surfaces of the nanotubes (e.g. carboxyl, hydroxyl and carbonyl), which changed their physicochemical properties. In order to optimize the main operational parameters of the H(2)O plasma treatment, pressure and power, a Box-Wilson experimental design was adopted. Analysis of the morphology, electrochemical properties and functional groups attached to the surfaces of the CNTs allowed us to determine which treatment conditions were suitable for different applications. After water plasma treatment the specific capacitance of the nanotubes increased from 23 up to 68 F g(-1) at a scan rate of 10 mV s(-1).

In recent years, vertical graphene nanowalls (VGNWs) have gained significant attention due to their exceptional properties, including their high specific surface area, excellent electrical conductivity, scalability, and compatibility with transition metal compounds. These attributes position VGNWs as a compelling choice for various applications, such as energy storage, catalysis, and sensing, driving interest in their integration into next-generation commercial graphene-based devices. Among the diverse graphene synthesis methods, plasma-enhanced chemical vapor deposition (PECVD) stands out for its ability to create large-scale graphene films and VGNWs on diverse substrates. However, despite progress in optimizing the growth conditions to achieve micrometer-sized graphene nanowalls, a comprehensive understanding of the underlying physicochemical mechanisms that govern nanostructure formation remains elusive. Specifically, a deeper exploration of nanometric-level phenomena like nucleation, carbon precursor adsorption, and adatom surface diffusion is crucial for gaining precise control over the growth process. Hydrogen’s dual role as a co-catalyst and etchant in VGNW growth requires further investigation. This review aims to fill the knowledge gaps by investigating VGNW nucleation and growth using PECVD, with a focus on the impact of the temperature on the growth ratio and nucleation density across a broad temperature range. By providing insights into the PECVD process, this review aims to optimize the growth conditions for tailoring VGNW properties, facilitating applications in the fields of energy storage, catalysis, and sensing.

Organizing a post-fossil fuel economy requires the development of sustainable energy carriers. Hydrogen is expected to play a significant role as an alternative fuel as it is among the most efficient energy carriers. Therefore, nowadays, the demand for hydrogen production is increasing. Green hydrogen produced by water splitting produces zero carbon emissions but requires the use of expensive catalysts. Therefore, the demand for efficient and economical catalysts is constantly growing. Transition-metal carbides, and especially Mo₂C, have attracted great attention from the scientific community since they are abundantly available and hold great promises for efficient performance toward the hydrogen evolution reaction (HER). This study presents a bottom-up approach for depositing Mo carbide nanostructures on vertical graphene nanowall templates via chemical vapor deposition, magnetron sputtering, and thermal annealing processes. Electrochemical results highlight the importance of adequate loading of graphene templates with the optimum amount of Mo carbides, controlled by both deposition and annealing time, to enrich the available active sites. The resulting compounds exhibit exceptional activities toward the HER in acidic media, requiring overpotentials of 82 mV at -10 mA/cm² and demonstrating a Tafel slope of 56 mV/dec. The high double-layer capacitance and low charge transfer resistance of these Mo₂C on GNW hybrid compounds are the main causes of the enhanced HER activity. This study is expected to pave the way for the design of hybrid nanostructures based on nanocatalyst deposition on three-dimensional graphene templates.