Carbonization reveals size differences in zirconia nanoparticles from various framework structures, suggesting a link to their atomic arrangement.
Templated synthesis is an important avenue for the development and synthesis of porous materials, as it provides a high level of control over the resulting structure. However, this control is difficult to achieve at the atomic level for poorly crystalline or noncrystalline materials, such as metal-organic framework (MOF)-derived carbons. We report the carbonization of three zirconium-based MOFs with different framework and inorganic building unit structures to form zirconia nanoparticles in a carbon matrix. Using a combination of X-ray diffraction, X-ray total scattering, and transmission electron microscopy, we found that the extended Zr-oxo chains of MIL-140C-bpy facilitate the formation of larger and more ordered zirconia nanoparticles. In contrast, the discrete Zr₆-oxo clusters of UiO-67-bpy and Zr-ABTC result in smaller and differently structured nanoparticles.
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Powell et al. (2025) studied this question.
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