Nanodiffraction using 4D-STEM has become a key technique for quantitative nanoscale structural mapping in materials research, yet interpreting its high-dimensional datasets in structurally complex materials remains a major bottleneck. Existing analysis workflows typically rely on structural models, manual annotation, predefined classes, or sample-specific heuristics, limiting their ability to characterize heterogeneous complex materials. Here, we introduce DINO4DSTEM, a self-supervised machine learning framework that automatically discovers structurally meaningful states directly from raw diffraction data. Without structural models, manual labels, a predefined number of classes, or system-specific parameter tuning, the framework learns representations that organize diffraction patterns by their intrinsic structural similarities, transforming large collections of low-dose measurements into quantitative nanoscale structure maps. Across diverse datasets, DINO4DSTEM consistently identifies the dominant structural degrees of freedom, providing segmentation without human supervision. We applied the framework to the crystallization of indomethacin, a beam-sensitive, multidomain pharmaceutical system, revealing that crystallinity emerges from a partially ordered precursor and spans a continuous spectrum of structural order. The discovered nanoscale structural states are mapped to reveal the evolution of order across the specimen quantitatively. By replacing task-specific analysis with general self-supervised representation learning, DINO4DSTEM provides a broadly applicable framework for quantitative nanoscale structural mapping in complex materials, enabling the discovery of emergent structural organization in heterogeneous, beam-sensitive systems.
Heterogeneous interfaces dictate the performance and degradation of functional materials, making it essential to link local structural variations with macroscopic failure mechanisms to guide future materials design. Yet structural heterogeneity, phase overlap, and local disorder produce highly convoluted diffraction si...
Hao-Ran Zhang, Zian Mao, Shu-Fen Chu et al.· 0 citations
Metal-organic frameworks (MOFs) and MOF-like porous materials exhibit vast structural diversity and support critical applications in gas storage, separations, and catalysis. Predictive modeling remains difficult because their structure-property relationships are multiscale and cage-like, governed by both local chemical...
Covalent organic frameworks (COFs) are highly ordered, porous organic materials whose reticular construction from tailored nodes and linkers enables atomic-level control over structure and function. The design space of COFs is vast with virtually unlimited combinations of nodes, linkers, and functional groups. Interpre...
Alathea E. Davies, O. Adesina, Isabella M. Valdez et al.· Journal of Chemical Theory a...· 1 citation
Proteins that reversibly adopt multiple stable folds challenge the classical sequence–structure paradigm, yet their discovery remains limited because fold switching is difficult to detect experimentally and current computational methods fail to resolve the underlying conformationally plastic regions. Here we present Mo...
A deep-learning-enabled dual-mode CSP framework that simultaneously supports two complementary tasks: predicting stable crystal structures for given elemental compositions and identifying chemically viable elemental substitutions for a predefined crystal topology is proposed.
Chen Qin, Xiang-Yan Luo, Zhi-Xiang Fan et al.· Inorganic Chemistry· 0 citations
The assembly of nanodiamonds (NDs) dictates their emergent structural and functional states, yet the atomistic mechanisms governing this process remain largely unresolved. In this work, the facet-dependent interactions and temperature-regulated aggregation of NDs are investigated through large-scale deep potential mo...
Rui He, Jing-Shuang Dang· Journal of Physical Chemistr...· 0 citations
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