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March 21, 2026Journal of the American Chemical Society5 citations

A Stable Mesoporous Zeolite with Superlarge 36-Ring Channels

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AGAimin GongCNChenyang NieHDHaodi Ding

Key Points

  • To develop a mesoporous zeolite with superlarge pore sizes and investigate its structural characteristics and catalytic properties.
  • Synthesized JU-69 zeolite using a phosphonium surfactant-like OSDA.
  • Utilized three-dimensional electron diffraction to determine the structure.
  • Employed atomic-resolution imaging (electron ptychography) for validation.
  • Assessed thermal stability and metal anchoring capabilities of the zeolite.
  • JU-69 zeolite features the largest pore apertures observed at 19.5 Å × 25.2 Å.
  • Achieved a framework density of 9.53 T per 1000 ų.
  • Demonstrated thermal stability up to 900 °C.
  • Active Pd/JU-69 catalysts effective in hydrogenating bulky molecules.

Abstract

Expanding zeolite pore sizes beyond the microporous regime has long been limited by conventional organic structure-directing agents (OSDAs). Here we report JU-69, a mesoporous pure-silica zeolite that features one-dimensional 36-ring channels, representing the largest apertures (19.5 Å × 25.2 Å) observed in any known TO4-based zeolite framework and an ultralow framework density of 9.53 T per 1000 Å3 (T: tetrahedral framework atom). A surfactant-like phosphonium OSDA with bulky head groups and a long alkyl chain directs columnar assemblies that template long-range-ordered mesoporous walls. Three-dimensional electron diffraction reveals a trigonal framework built from three composite building units (CBUs), including cas and two previously unknown CBUs that generate chiral clover arrangements and circular 36-ring pores. The structure is further validated by atomic-resolution real-space imaging using electron ptychography. JU-69 exhibits thermal stability up to 900 °C and periodically arranged silanol groups that enable efficient metal anchoring, demonstrated by active Pd/JU-69 catalysts for bulky molecule hydrogenation. This work establishes a pathway for designing crystalline mesoporous zeolites with unprecedented structural openness.

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Cite This Study

Gong et al. (2026) studied this question.

synapsesocial.com/papers/69be37866e48c4981c6773edhttps://doi.org/10.1021/jacs.6c01322
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