The role of fundamental characteristics of porous systems (binding energy, specific surface area and multilayer adsorption) in designing an efficient hydrogen adsorbent is discussed. We analyze why the amount of hydrogen adsorbed in all known materials is much lower than required for mobile applications and what are possible strategies to increase it. Further we report new ab initio calculations demonstrating possible ways of chemical modification of graphene fragments which can lead to the substantial increase of hydrogen binding to the graphene-based surface. Such Open Carbon Frameworks, substituted and functionalized at the fragments' edge may theoretically adsorb, at ambient temperature and relatively low pressure (60-100 bar), the amount of hydrogen necessary for mobile applications.

Graphene, known as one carbon layer material, holds attractive properties due to its hexagonal lattice, also called honeycomb structure. Since the seminal work on mechanically exfoliated few layer graphene, more growth processes were explored: Chemical Vapor Deposition (CVD) on metals or on silicon carbide (SiC); chemical reduction of graphene oxides and SiC sublimation. In contrast to the other graphene growth techniques, thermal decomposition of SiC provides wafer-scale homogeneous graphene spontaneously forming on semi-insulating substrate. SiC sublimation is the most promising option to achieve the transfer free and wafer-scale graphene. Furthermore, graphene/SiC is compatible with lithography techniques for further applications; thereby epitaxial graphene on SiC is a potential candidate for nanoelectronics. Until now, monolayer graphene growth by SiC sublimation at a pressure closed to the atmospheric pressure (around 900 mbar) and at high temperature (>1650°C) is well known . However, to obtain films with different and controlled characteristics such as the number of graphene layers or the type of doping by controlling the growth parameters remains challenging. We will present the initial growth stages from buffer layer to monolayer graphene on SiC (0001) as a function of the temperature at low pressure (10 mbar). A reproducible synthesis of low p-type doped monolayer graphene was optimized (few 10^11 cm-2). The p-type doping are obtained here on the bare samples without any post-growth process such as lithography. A prototypal HTA-100 furnace developed by Annealsys Company has allowed the synthesis of these original samples. All the samples were characterized by Raman spectroscopy and Atomic Force Microscopy (AFM). In addition, transport measurements (at room temperature and low temperature with high magnetic field) were carried out in the case of continuous monolayer graphene films showing especially characteristics of Quantum Hall Effect.

Liquid phase encapsulation of α-sexithiophene (6T) molecules inside individualized single-walled carbon nanotubes (SWCNTs) is investigated using Ramanimaging and spectroscopy. By taking advantage of the strong Raman response of this system, we probe the encapsulation isotherms at 30°C and 115°C using a statistical ensemble of SWCNT deposited on a Si/SiO2 substrate. Two distinct and sequential stages ofencapsulation are observed: Stage 1 is a one-dimensional (1D) aggregation of 6T alignedhead-to-tail inside the nanotube and stage 2 proceeds with the assembly of a second row, giving pairs of aligned 6Ts stacked together side-by-side. The experimental data are fitted using both Langmuir (type VI) and Ising models, in which the single-aggregate (stage 1) forms spontaneously whereas the pair-aggregate (stage 2) is endothermic in toluene with formation enthalpy of 8Hpair = 260±20 meV. Tunable Raman spectroscopy for each stage reveals a bathochromic shift of the molecular resonance of the pair-aggregate, which is consistent with strong inter-molecular coupling and suggestive of J-type aggregation. This quantitative Raman approach is sensitive to roughly 10 molecules per nanotube andprovides direct evidence of molecular entry from the nanotube ends. These insights into the encapsulation process guide the preparation of well-defined 1D molecular crystals having tailored optical properties.

Recycling route toward electro-active silicone composites has been explored. We studied the dependence of the E-J characteristics on the aggregate content in the polymer matrix. Formulations with 35 vol.% MOV aggregates in the 200-375 µm range exhibit reliable nonlinear behavior with a switching voltage of 175 ± 30 V/mm. This opens a way to valorize varistors based on zinc oxide (ZnO) ceramics.

Chemical vapor deposition has proved to be successful in producing graphene samples on silicon carbide (SiC) homogeneous at the centimeter scale in terms of Hall conductance quantization. Here, we report on the realization of co-planar diffusive Al/ monolayer graphene/ Al junctions on the same graphene sheet, with separations between the electrodes down to 200 nm. Robust Josephson coupling has been measured for separations not larger than 300 nm. Transport properties are reproducible on different junctions and indicate that graphene on SiC substrates is a concrete candidate to provide scalability of hybrid Josephson graphene/superconductor devices.

Infrared response on a carbon nanotube is weak because this homonuclear allotrope of carbon does not bear permanent dipoles. Here, we report the discovery of an exaltation of the infrared absorption response in single-walled carbon nanotubes from dye molecule interactions. A study performed on dimethylquaterthiophene confined into the hollow core of single-walled carbon nanotubes or π-stacked at the outer surface of the latter leads to a symmetry breaking, allowing us to probe interactions between both subsystems. The nature of these interactions is discussed taking into account the tube diameter. This new phenomenon opens a new route to detect weak vibrations thanks to a confinement effect.