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Machine learning interatomic potential (MLIP) is an emerging technique that has helped achieve molecular dynamics simulations with unprecedented balance between efficiency and accuracy. Recently, the body of MLIP literature has been growing rapidly, which propels the need to automatically process relevant information for researchers to understand and utilize. Named entity recognition (NER), a natural language processing technique that identifies and categorizes information from texts, may help summarize key approaches and findings of relevant papers. In this work, we develop an NER model for MLIP literature by fine‐tuning a pre‐trained language model. To streamline text annotation, we build a user‐friendly web application for annotation and proofreading, which is seamlessly integrated into the training procedure. Our model can identify technical entities with an F1 score of 0.8 for new MLIP paper abstracts using only 60 training paper abstracts and up to 0.75 for scientific texts on different topics. Notably, some “errors” in predictions are actually reasonable decisions, showcasing the model's ability beyond what the performance metrics indicate. This work demonstrates the linguistic capabilities of the NER approach in processing textual information of a specific scientific domain and has the potential to accelerate materials research using language models and contribute to a user‐centric workflow. 

Abstract Biopolymers and bioinspired materials contribute to the construction of intricate hierarchical structures that exhibit advanced properties. The remarkable toughness and damage tolerance of such multilevel materials are conferred through the hierarchical assembly of their multiscale (i.e., atomistic to macroscale) components and architectures. Here, the functionality and mechanisms of biopolymers and bio‐inspired materials at multilength scales are explored and summarized, focusing on biopolymer nanofibril configurations, biocompatible synthetic biopolymers, and bio‐inspired composites. Their modeling methods with theoretical basis at multiple lengths and time scales are reviewed for biopolymer applications. Additionally, the exploration of artificial intelligence‐powered methodologies is emphasized to realize improvements in these biopolymers from functionality, biodegradability, and sustainability to their characterization, fabrication process, and superior designs. Ultimately, a promising future for these versatile materials in the manufacturing of advanced materials across wider applications and greater lifecycle impacts is foreseen. 

The flexibility of metal–organic frameworks (MOFs) affects their gas adsorption and diffusion properties. However, reliable force fields for simulating flexible MOFs are lacking. As a result, most atomistic simulations so far have been carried out assuming rigid MOFs, which inevitably overestimates the gas adsorption energy. Here, we show that this issue can be addressed by applying a machine-learning potential, trained on quantum chemistry data, to atomistic simulations. We find that inclusion of flexibility is particularly important for simulating CO2 chemisorption in MOFs with coordinatively unsaturated metal sites. Specifically, we demonstrate that the diffusion of CO2 in a flexible Mg-MOF-74 structure is about one order of magnitude faster than in a rigid one, challenging the rigid-MOF assumption in previous simulations.