AI Article Synopsis

  • Understanding the intricate structures of metal-organic frameworks (MOFs) is crucial for grasping their properties and potential applications.
  • A low-dose imaging technique was successfully used to visualize the atomic structures of the MIL-125 framework, revealing unexpected rotational configurations of titanium-oxygen (Ti-O) nodes that differ from earlier predictions based on X-ray diffraction.
  • The study further detailed the variations in node rotation within MIL-125 and explored related defects through real-space imaging, paving the way for discovering new structural phenomena in other porous materials.

Article Abstract

Resolving the detailed structures of metal organic frameworks is of great significance for understanding their structure-property relation. Real-space imaging methods could exhibit superiority in revealing not only the local structure but also the bulk symmetry of these complex porous materials, compared to reciprocal-space diffraction methods, despite the technical challenges. Here we apply a low-dose imaging technique to clearly resolve the atomic structures of building units in a metal-organic framework, MIL-125. An unexpected node structure is discovered by directly imaging the rotation of Ti-O nodes, different from the unrotated structure predicted by previous X-ray diffraction. The imaged structure and symmetry can be confirmed by the structural simulations and energy calculations. Then, the distribution of node rotation from the edge to the center of a MIL-125 particle is revealed by the image analysis of Ti-O rotation. The related defects and surface terminations in MIL-125 are also investigated in the real-space images. These results not only unraveled the node symmetry in MIL-125 with atomic resolution but also inspired further studies on discovering more unpredicted structural changes in other porous materials by real-space imaging methods.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11322488PMC
http://dx.doi.org/10.1038/s41467-024-51384-9DOI Listing

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