Machine Learning Based Identification of Solvents from Post-Desiccation Patterns

Liquid crystal textures encode rich structural information, yet mapping these images to mesophase identity remains challenging because visually similar patterns can arise from distinct structures. Here we present a simple, interpretable representation that maps textures to a 75-dimensional frequency vector of two-by-two ordinal patterns, grouped into eleven symmetry-based types to characterize a large-scale dataset spanning seven mesophases. Combined with a simple machine learning classifier, this lightweight representation yields near-perfect phase recognition, including the difficult distinction between smectic A and smectic B mesophases. Our approach generalizes to unseen compounds and accurately distinguishes between phase identity and material origin. Unlike deep learning methods, each ordinal pattern is readily interpretable, and model explanations augmented with network visualizations of pattern interactions reveal the specific types and pairwise dependencies that drive each mesophase decision, providing compact, physically meaningful summaries of texture determinants. These results establish two-by-two ordinal patterns as an interpretable and scalable tool for liquid crystal image analysis, with potential applications to other complex patterned systems in materials science.

X-ray diffraction (XRD) is a experimental technique for determining the phase composition and structure of crystalline materials. However, interpreting XRD patterns is challenging, particularly in high-throughput materials discovery, where many novel materials may need to be characterized and no reference patterns are available. Consequently, machine learning is increasingly used to accelerate and automate the analysis while reducing errors associated with human interpretation. We propose a multi-decision framework for XRD phase analysis that integrates representation learning, similarity-based retrieval, and explainable decision support within a unified reference database. A convolutional autoencoder learns compact latent representations of XRD patterns that preserve structural similarity while remaining robust to variations arising from experimental noise and measurement conditions. By integrating multiple decision pathways within a shared latent space, the framework moves beyond single-label prediction toward ranked and interpretable phase analysis that mirrors expert practice. During inference, complementary decision mechanisms are applied, including latent-space classification and retrieval, explanation-guided similarity using Integrated Gradients, and composition-based similarity search. These mechanisms generate ranked candidate phase lists that are aggregated into a final prediction with an associated confidence score. Experiments on synthetic datasets demonstrate strong predictive performance, achieving 98.85,% accuracy for crystal system classification and 95.82,% accuracy for space group prediction on the test set, while maintaining robustness under realistic perturbations. The framework supports reliable, analyst-friendly identification of crystal phases and structures in high-throughput and exploratory materials discovery settings.

Most machine-learning interatomic potentials (MLIPs) are trained on gas-phase data, which limits their use for chemistry in solution. Here, we introduce AnySolv, a transferable implicit solvation potential that provides solvent-dependent energy and force corrections to existing gas-phase potentials without retraining them. It is trained on 1.4 million solvation energies and forces computed with density functional theory (DFT) and SMD in 36 solvents, spanning charged, open-shell, and transition-state structures. Because solvents are represented by continuous physical descriptors, AnySolv supports 179 solvents, including those absent from training. On external benchmarks, AnySolv reproduces DFT-SMD solvation energies to 2-4 meV mean absolute error at more than three orders of magnitude lower cost, and it matches the accuracy of DFT-SMD against experimental solvation free energies. This enables screening of the mechanisms of 120 nucleophilic aromatic substitution reactions in six phases as well as molecular dynamics simulations that reproduce the experimentally observed solvent-dependent conformational preferences of alanine dipeptide. By providing transferable solvation corrections to existing MLIPs, AnySolv enables scalable simulations of solvent-dependent chemical reactivity and molecular dynamics.