4.7 Article

SCM-25: A Zeolite with Ordered Meso-cavities Interconnected by12x12x10-Ring Channels Determined by 3D Electron Diffraction

Journal

INORGANIC CHEMISTRY
Volume 61, Issue 10, Pages 4371-4377

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.1c03632

Keywords

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Funding

  1. National Key R&D Program of China [2017YFB0702800]
  2. National Natural Science Foundation of China [21802168]
  3. China Petrochemical Corporation (Sinopec Group)
  4. Swedish Research Council (VR) [2017-04321]
  5. Knut and Alice Wallenberg Foundation (KAW) [2012-0112]
  6. Swedish Research Council [2017-04321] Funding Source: Swedish Research Council

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A novel porous germanosilicate SCM-25 with large accessible cavities via widepore windows has been synthesized. It has a high surface area and thermal stability. The study also proposes a potential postsynthetic strategy for the preparation of zeolites with ordered meso-cavities.
Zeolites with large cavities that are accessible via widepore windows are desirable but very rare. They have been dominantlyused as catalysts in industry. Here we report a novel porousgermanosilicate SCM-25, the zeolite structure containing orderedmeso-cavities (29.9x7.6x6.0 A3) interconnected by 10- and 12-ringchannels. SCM-25 was synthesized as nanosized crystals by using asimple organic structure-directing agent (OSDA). Three-dimensional(3D) electron diffraction shows that SCM-25 crystallizes in theorthorhombic space groupCmmmwitha= 14.62 A,b= 51.82 A,c=13.11 A, which is one of the zeolites with the largest unit celldimensions. We demonstrate that 3D electron diffraction is a powerfultechnique for determining the complex structure of SCM-25,including the disorders and distributions of framework atoms silicon and germanium. SCM-25 has a high surface area (510 m2/g) and high thermal stability (700 degrees C). Furthermore, we propose a potential postsynthetic strategy for the preparation of zeoliteswith ordered meso-cavities by applying the ADOR (assembly-disassembly-organization-reassembly) approach.

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