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María Andrea Barral

Publications and source records attributed to María Andrea Barral.

2 recordsLinked to original sources

Material and thermal properties of MgCl2 molten salt by ab initio and machine-learning molecular-dynamics simulations

We study the structural, thermophysical and dynamical properties of molten MgCl2 over a wide temperature range using Ab Initio Molecular Dynamics (AIMD) and molecular dynamics simulations based on machine-learning interaction potentials (MLIPs). MLIPs can achieve near-AIMD accuracy at a fraction of the computational cost, enabling simulations of larger systems and longer timescales. This opens up the possibility of studying the system under out-of-equilibrium conditions, which in turn allows for the calculation of physical properties, such as the thermal conductivity or viscosity, that cannot be obtained reliably for the typical time and length scales accessible to AIMD. We follow two complementary approaches to develop and evaluate the MLIPs. Firstly, we develop a Deep Potential (DP) from scratch using AIMD trajectories at different temperatures. Secondly, we also evaluate two out-of-the-box foundation models and a fine-tuned version of one of them. The fine-tuning is performed using configurations from the AIMD trajectories originally used to train the Deep Potential. We compare the predictions of the trained DP, the foundation models and AIMD simulations with the available experimental data and provide a comprehensive calculation of the most important physical quantities of molten MgCl2. We compute densities, radial and angular distribution functions, thermal conductivity, heat capacity, viscosity and diffusion coefficients over the 1000-1600 K temperature range. This range is relevant to important technological applications such as thermal energy storage, generation IV nuclear reactors and concentrated solar power systems. Finally, we briefly review the accuracy and performance of the different MLIPs versions used throughout the work.

cond-mat.soft↗

Open-Shell Molecules as Sensitive Probes of Spin-Orbit-Controlled Surface Electronic Structure

Open-shell molecules are highly sensitive probes of correlated oxide surfaces because their partially occupied frontier orbitals strongly amplify subtle changes in adsorbate-substrate hybridization. Combining infrared reflection-absorption spectroscopy with hybrid density functional theory including non-collinear magnetism and spin-orbit coupling, we show that inclusion of spin-orbit coupling is essential to reproduce the vibrational spectrum of NO adsorbed on UO$_2$(111) by suppressing an otherwise artificial overhybridization between the NO frontier orbitals and uranium 5f states. While spin-orbit coupling determines the position of the N-O stretching and, dispersion-driven intermolecular interactions account for its asymmetric broadening at monolayer coverage. These results establish open-shell molecules as sensitive probes of spin-orbit-controlled surface electronic structure and identify NO/UO$_2$(111) as a stringent benchmark for electronic-structure methods describing open-shell molecule-surface interactions.

cond-mat.mtrl-sci↗