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Arnaud Le Pottier

Publications and source records attributed to Arnaud Le Pottier.

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↗

Efficient integration of self-assembled organic monolayer tunnel barriers in large area pinhole-free magnetic tunnel junctions

Magneto-transport properties in hybrid magnetic tunnel junctions (MTJs) integrating self-assembled monolayers (SAMs) as tunnel barriers are critically influenced by spinterface effects, which arise from the electronic properties at ferromagnet (FM)/SAM interfaces. Understanding the mechanisms governing spinterface formation in well-controlled model systems is essential for the rational design of efficient molecular spintronic devices. However, the fabrication of FM/SAM/FM systems remains a significant challenge due to the difficulty in preventing electrical shorts through the SAM tunnel barrier during top FM electrode deposition. In this study, we address these challenges by developing model hybrid MTJs incorporating alkanethiol SAM tunnel barriers grafted under ultra-high vacuum conditions onto single-crystalline Fe(001) bottom electrodes. A soft-landing deposition method is used for the deposition of a top Co FM electrode. The deposition process and the electronic properties of the FM/SAM interfaces are first studied by spatially integrated X-ray photoelectron spectroscopy. Furthermore, ballistic electron emission microscopy (BEEM) and spectroscopy are used to investigate the lateral homogeneity of the organic barrier. Optimal soft-landing deposition conditions allows the preparation of homogeneous Co/SAM interfaces with no evidence of metal diffusion through the SAM at the nanoscale. These observations are further confirmed at the micron-scale by the high-yield patterning of large area (5*5um2) MTJs presenting fingerprints of electron tunneling through the SAM. These findings provide critical insights into the fabrication and optimization of molecular spintronic devices, paving the way for advancements in hybrid MTJ technology.

physics.app-ph↗