The paper presents a hierarchical deep‑learning framework that integrates compositional, structural, and transport models to screen solid‑state electrolytes. Four modules—L‑G‑DCNN, DenseGNN, MatterSim, and DeePMD—coordinate to evaluate thermodynamics, multi‑property performance, and kinetic transport, outperforming existing methods. Applied to over 30 million candidates, the workflow identifies 97 high‑performance materials, mainly halides, and links Li⁺ jump‑network connectivity to ionic conductivity while highlighting limits for oxide electrolytes.
arXiv:2607. 25597v1 Announce Type: new Abstract: The reactivity of lithium-metal electrolytes arises from the interplay of molecular functional groups, Li$^+$ solvation, and salt-anion participation.
SoLiD26 is a curated dataset of 15.4 million first‑principles atomic structures for solid‑liquid interfaces, comprising up to 576 atoms and 15 chemical elements. The data were generated from density functional theory calculations, mainly ab initio molecular dynamics, and include aqueous coinage metal interfaces, electrode‑electrolyte systems, and bulk references. Each record contains atomic species, positions, cell parameters, periodic boundary conditions, potential energy, and atomic forces, all computed with VASP using the PBE functional and D3 dispersion corrections.
arXiv:2609.14906v1 Announce Type: cross Abstract: The Hohenberg-Kohn theorem establishes that, in principle, the ground state (GS) charge density contains all GS information of a many-electron system...
arXiv:2607. 05736v1 Announce Type: new Abstract: Molecular property prediction often relies on isolated data modalities, where continuous 3D graph neural networks (GNNs) struggle to efficiently capture long-range topological dependencies and exact macroscopic heuristics.
arXiv:2606. 28220v1 Announce Type: new Abstract: Physics-informed neural networks (PINNs) have emerged as a powerful tool for solving nonlinear partial differential equations (PDEs), including battery electrochemical models.
ProtoMI is a literature‑driven framework that learns structural priors from 126 reported boron‑containing electrolyte additives and applies them to screen 179,977 unlabeled candidates. Using graph contrastive learning, it identifies seven interpretable prototypes and adapts them through semi‑supervised contrastive learning, achieving enrichment factors of 9.2–45.6 while evaluating less than 2% of the candidate space. The method led to the discovery of four commercially accessible additives, including TNDB, which improves high‑temperature LiFePO4||graphite cycling by 34.93% and forms protective interphases that suppress solvent decomposition and Fe deposition.
SCALE (Simulation‑Calibrated Amortized Learning for Energy Materials) is a physics‑grounded learning architecture that fuses deterministic scientific operators, experimental calibration, and transformer‑scale inference to accelerate the discovery of energy materials. It converts expensive mechanistic computations and measured data into reusable models for rapid screening, ranking, inverse design, and active learning. In a case study on solid‑state metal‑hydride hydrogen‑storage, SCALE calibrated a phase‑equilibrium capacity operator against 381 experimental anchors, generated 5,000 teacher labels, and used a 2.90‑million‑parameter edge‑biased graph transformer to achieve high surrogate fidelity (MAE 0.0582 wt% H₂, RMSE 0.0833 wt% H₂, R² 0.9927, Pearson r 0.9963) while reducing per‑candidate screening cost by 10⁷–10⁸ times.
arXiv:2608. 00212v1 Announce Type: new Abstract: Spatial atomic layer deposition (SALD) is a leading atmospheric-pressure, high-throughput route to industrial ALD, but design and control are limited by the cost of predicting surface coverage: high-fidelity CFD is far too slow for operating-window scans, while analytic models miss transport modulation such as the gas curtain.
arXiv:2607. 24818v1 Announce Type: cross Abstract: Accurate prediction of crystal properties remains a key challenge in computational materials science.
arXiv:2604. 09320v2 Announce Type: replace-cross Abstract: Mechanistic understanding and rational design of complex chemical systems depend on fast and accurate predictions of electronic structures beyond individual building blocks.
arXiv:2603. 07977v3 Announce Type: replace-cross Abstract: Machine Learning Interatomic Potentials (MLIPs) enable accurate large-scale atomistic simulations, yet improving their expressive capacity efficiently remains challenging.
arXiv:2608.23874v1 Announce Type: cross Abstract: Predicting thermal stability during handling and storage is essential for the design of safe and reliable energetic materials. However, experimental...