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Mohammad Nadim Kamar

Publications and source records attributed to Mohammad Nadim Kamar.

2 recordsLinked to original sources

Glassy Dynamics of LiCl.6H2O Solution in Nanoporous Media

Understanding how nanoconfinement alters the dynamics of glass-forming aqueous electrolytes is essential for clarifying the interplay among ionic hydration, hydrogen-bond structure, and interfacial effects. Here, LiCl.6H2O was investigated in the bulk and under confinement in SBA-15 mesoporous silica with an average pore diameter of 8 nm. Differential scanning calorimetry, Raman spectroscopy, quasielastic neutron scattering, 1 H spin-lattice relaxation, and pulsed-fieldgradient NMR were combined to probe thermal behavior, hydrogen-bond structure, local mobility, and translational transport over complementary time and length scales. The calorimetric results show that LiCl.6H2O remains glass-forming under confinement, while its thermal signature of the glass transition becomes slightly broader and shifted upward relative to the bulk. Raman spectra in the O-H stretching region indicate that the concentrated LiCl solution possesses a weakened and less tetrahedrally connected hydrogen-bond network compared with bulk water. On the subnanosecond timescale, elastic fixed-window analysis reveals reduced mean-squared displacements under confinement, demonstrating suppressed motional amplitudes inside the pores. Inelastic fixed-window neutron scattering scans analyzed within a jump-diffusion framework yield lower effective translational diffusion coefficients and longer residence times for the confined liquid, indicating that confinement mainly hinders translational escape from transient local environments. 1 H relaxometry further shows that confinement broadens the distribution of local proton fluctuation times, while PFG-NMR confirms that the measured long-range water mobility in bulk LiCl.6H2O solution is reduced relative to bulk water. While the present data do not resolve distinct interfacial and pore-centered populations in confined LiCl.6H2O, its dynamics are markedly altered across timescales, from the glassy to the liquid state, resulting in slower, spatially constrained, and more heterogeneous motions.

cond-mat.mtrl-sci↗

How special are the dynamics of deep eutectic solvents? A Look at the Prototypical Case of Ethaline

We investigated the molecular dynamics of the prototypical deep eutectic solvent (DES) ethaline. We disentangled the different motions of its two constituents, namely choline chloride and ethylene glycol on a spatio-temporal range that extends from sub-nanometer to micrometer distances and from picosecond to millisecond times. This was achieved by a combination of pulsed-field-gradient NMR, time-of-flight, and backscattering quasielastic neutron scattering experiments with isotopically labelled samples. On the micrometer scale, we observe that the translational motions of the two DES constituents obey classical hydrodynamics, with distinct diffusivities that reflect their different hydrodynamic radii. This is no longer valid at the nanometer-scale, where the two DES components present similar short-ranged diffusivities, which indicates a significant effect of their supramolecular association. The sub-nanometer scale motions include jumps that precede Fickian diffusion, and localized dynamics that precede the breaking of the transient cage formed by neighboring molecules. Therein, the spatial amplitude of the localized motions mirrors their different molecular sizes, while their respective correlation times contrast with observations made for other choline-based DES such as glyceline. This result underlines the importance of more subtle effects, such as the different H-bond propensities of the polyol donor, and demonstrate the difficulty to anticipate the nanoscale dynamic behavior of DES from the knowledge of their macroscopic properties.

physics.chem-ph↗