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Matías Gerard

Publications and source records attributed to Matías Gerard.

2 recordsLinked to original sources

Microdroplet Generator Surrogate Enhancement and Inverse Design Through an Uncertainty-Guided Framework

Microfluidic droplet generation is critical for many applications, yet efficient device design in high-dimensional parameter spaces remains computationally prohibitive due to complex multiphase flow dynamics. This work presents a unified methodology that couples adaptive surrogate enhancement with simulation-driven inverse design. High-fidelity Volume-of-Fluid simulations provide ground-truth data, while neural network ensembles predict flow regimes and droplet diameters. Ensemble-based uncertainty quantification identifies epistemic uncertainty using consensus levels for regime classification and the coefficient of variation for diameter prediction, revealing that uncertainty concentrates near regime transition boundaries where physics is highly sensitive to parameter perturbations. A physics-informed enrichment strategy targets these critical zones and addresses class imbalances by deploying additional targeted simulations and retraining the surrogates forming the ensembles. A framework that integrates Particle Swarm Optimization for constrained inverse design, balancing accuracy with predictive confidence and physical consistency is therefore proposed. Validation on independent test datasets demonstrates that the enriched ensembles achieve higher accuracy, with the fraction of predictions within the 0-3% error range on droplet diameter nearly doubling, and high-error cases (above 10%) dropping substantially. The inverse design procedure reliably identifies physically realizable configurations meeting target droplet sizes. This approach significantly reduces computational costs while ensuring reliable predictions, offering a framework with potential applicability to the optimization of a broad range of microfluidic systems.

physics.flu-dyn↗

GQD-AdsNet: Graph Neural Networks Unlock Rapid Exploration of Transition Metal Adsorption on Graphene Quantum Dots

In recent years, interest in single-atom catalysts supported on carbon-based structures has grown considerably due to their high catalytic activity and efficient uses of metal atoms. However, the design and characterization of these materials through first-principles calculations are computationally expensive, limiting the exploration of a large number of possible configurations. Here, we developed a framework based on graph neural networks (GNNs) to predict the adsorption energies of transition metals on graphene quantum dots (GQDs). The model was trained using data obtained from density functional theory calculations and achieved an $R^2$ of 0.906 with an MAE of 0.101 eV, while reducing computational cost by roughly six orders of magnitude relative to DFT. This methodology provides an efficient tool for the accelerated screening and rational design of new catalysts based on carbon nanostructures.

cond-mat.mtrl-sci↗