B. Coasne's research while affiliated with Massachusetts Institute of Technology and other places

SSCI-VIDE+ING+DFA:CDA:JEC

Progress in computational materials science has allowed the development of realistic models for a wide range of materials including both crystalline and glassy solids. In recent years, with the growing interest in nanoparticles and porous materials, more attention has been devoted to the design of realistic models of glassy surfaces and finely divided materials. The structural disorder in glassy surfaces, however, poses a major challenge which consists of describing such surfaces using computer simulations. In this paper, we show how atomic-scale simulations can be used to develop and investigate the properties of glassy surfaces. We illustrate how both first principles calculations and classical molecular mechanics can be used to follow the trajectory at finite temperature of these systems, and obtain statistical thermodynamic averages to compare against available experiments. Both glassy oxide (silica) and non-oxide (chalcogenide) surfaces are considered.

The hydrogen uptake in hybrid sorbents consisting of n-alkane solvents confined in mesoporous silica aerogel is measured at different temperatures from 273 to 313 K and pressures up to 40 bar. An apparent “oversolubility” effect is observed as the H2 uptake in the hybrid sorbents is much larger than that in bulk solvents. The H2 uptake in the hybrid sorbents is found to increase with increasing temperature, which suggests that the flexibility and conformation of n-alkane molecules confined in the aerogel play a crucial role; high-entropy (disordered) alkane configurations lead to the creation of numerous cavities which make it possible to solubilize a larger number of H2 molecules. This departs from adsorption-driven solubility effects for which the number of solubilized molecules decreases with increasing temperature. For a given temperature and pressure, it is found that the number of solubilized H2 molecules per unit volume increases with decreasing alkane chain length. Such an effect, which is observed for both the bulk alkanes and the alkanes confined in the silica aerogel, can be rationalized by considering the number density of CHx (x = 2 or 3) groups; for a given temperature, the latter number density decreases with decreasing alkane chain length so that the free volume available to solubilize H2 molecules increases.

In this work molecular simulations are used to probe the gas adsorption properties of amorphous chalcogenide nanopores. A realistic atom-scale model, derived by first-principles calculations, of glassy chalcogenide surface is considered for the present study. Nitrogen adsorption and condensation at 77 K in pores of different widths are simulated for characterization purposes. The adsorption of carbon dioxide, methane, hydrogen, and their mixtures is investigated at 298 K. Analysis of the adsorption data shows nice agreement with the prediction of obtained using the Ideal Adsorbed Solution Theory. A detailed comparison with experimental literature data is also proposed and discussed. We also address the effect of the surface chemistry on the gas adsorption by studying both bare and hydrogenated chalcogenide surfaces. We show here that porous glassy chalcogenide exhibits highly selective gas adsorption properties and can strongly discriminate among gases on the basis of their interaction with the chalcogenide surface.

In the present work, the structure and dynamics of IL confined in amorphous silica and chalcogenide pores with different pore sizes are investigated by means of molecular simulation. This work sheds light on the complex behavior of hybrid materials made up of ionic liquid confined in inorganic porous materials.

We study water dynamics at a silica aqueous interface. Both hydrophilic (hydroxylated) surfaces and hydrophobic surfaces (dehydroxylated upon irradiation) have been generated from atomistic simulations. A new method for the calculation of the normal self-diffusion coefficients based on the calculation of mean first passage times is proposed. It uses the Smoluchowski theory of Brownian motion and it takes proper account of the layering of the molecules. In the case of parallel self-diffusion coefficients, a decrease is found compared to the bulk values. It can be described in terms of hydrodynamic boundary conditions induced by the surface confinement. This hydrodynamic explanation is not enough to interpret the case of normal self-diffusion coefficients for which an important diminution is found. Normal self-diffusion coefficients appear to depend strongly on the hydrophilicity of the surface. They tend towards their bulk value only at long distances from the surfaces. The first layer of water molecules is found to be partially adsorbed.

Zirconia-based refractories are ceramics that serve as furnaces for the production of high-quality speciality glasses. These materials are obtained by cooling a melt composed of different oxides and oxide precursors. The microstructure of these refractories consists of monoclinic zirconia embedded in a three-dimensional interconnected amorphous phase. Using mesoscopic Monte Carlo simulations, the present paper addresses the effect of the amount of amorphous phase and temperature on the microstructure of the material. The simulated microstructures resemble those obtained using tomography experiments. A theoretical model describing the electrical behavior of the material as a function of temperature and composition is also reported. In this model, the conductivity of the ZrO2 particles is assumed to be constant, but the overall conductivity of the sample depends on its tortuosity τ. Comparison with experimental data suggests that the present model provides a realistic picture of the electrical behavior of zirconia-based ceramics and leads to quantitative predictions.

National @ INGENIERIE+CDA:DFA:YSC

Water within pores of cementitious materials plays a crucial role in the damage processes of cement pastes, particularly in the binding material comprising calcium-silicate-hydrates (C-S-H). Here, we employed Grand Canonical Monte Carlo simulations to investigate the properties of water confined at ambient temperature within and between C-S-H nanoparticles or "grains" as a function of the relative humidity (%RH). We address the effect of water on the cohesion of cement pastes by computing fluid internal pressures within and between grains as a function of %RH and intergranular separation distance, from 1 to 10 Å. We found that, within a C-S-H grain and between C-S-H grains, pores are completely filled with water for %RH larger than 20%. While the cohesion of the cement paste is mainly driven by the calcium ions in the C-S-H, water facilitates a disjoining behavior inside a C-S-H grain. Between C-S-H grains, confined water diminishes or enhances the cohesion of the material depending on the intergranular distance. At very low %RH, the loss of water increases the cohesion within a C-S-H grain and reduces the cohesion between C-S-H grains. These findings provide insights into the behavior of C-S-H in dry or high-temperature environments, with a loss of cohesion between C-S-H grains due to the loss of water content. Such quantification provides the necessary baseline to understand cement paste damaging upon extreme thermal, mechanical, and salt-rich environments.