Randomized trial demonstrates molecular-resolution imaging of MOF surfaces, suggesting improved structural analysis capabilities.
Metal–organic frameworks (MOFs) are crystalline porous materials that have attracted widespread interest owing to their chemical versatility and functional properties. Over the past 30 years, MOF structures have been primarily characterized using diffraction‐based methods, which provide ensemble‐averaged information about long‐range order but are not suited to investigating spatially localized, site‐specific structural features. Atomic force microscopy (AFM) at the liquid‐solid interface enables real‐space, molecular‐resolution imaging of MOF crystal surfaces under native conditions, but places stringent demands on sample preparation: crystals must be firmly immobilized and their surfaces preserved in a state compatible with high‐resolution imaging. Here, we present a versatile method to anchor MOF crystals on highly oriented pyrolytic graphite (HOPG) via covalent grafting of aryl‐carboxylate groups. Crystals of different sizes are grown directly on the functionalized substrate and transferred air‐free to the AFM liquid cell, preserving surface integrity by avoiding prior drying or processing. We demonstrate molecular‐resolution imaging on three structurally distinct MOFs: MOF‐5 , HKUST‐1 , and Zn 2 (BDC) 2 (DABCO) . AFM tip‐induced surface refinement generates flat terraces on rough as‐synthesized crystals, and real‐time monitoring of terrace growth dynamics is demonstrated. The chemical versatility and thermal robustness of the grafting strategy make this platform broadly applicable across diverse MOF families.
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Cucinotta et al. (2026) studied this question.
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