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Loading-Driven Diffusion Pathway Selectivity in Zeolites with Continuum Intersecting Channels. | LitMetric

Loading-Driven Diffusion Pathway Selectivity in Zeolites with Continuum Intersecting Channels.

J Phys Chem Lett

State Key Laboratory of Magnetic Resonance and Atomic and Molecular Physics, National Center for Magnetic Resonance in Wuhan, Key Laboratory of Magnetic Resonance in Biological Systems, Innovation Academy for Precision Measurement Science and Technology, Chinese Academy of Sciences, Wuhan 430071, P. R. China.

Published: April 2023

AI Article Synopsis

  • The study focuses on how diffusion processes in zeolites affect heterogeneous catalysis, particularly with unique zeolites that have "continuum intersecting channels."
  • At lower molecular loading, smaller channels facilitate more efficient diffusion due to strong adsorption sites and molecular reorientation at intersections.
  • As molecular loading increases, larger channels become preferred for transport because they have lower diffusion barriers, allowing for control over diffusion pathways, which could improve product separation in catalysis.

Article Abstract

The diffusion processes in zeolites are important for heterogeneous catalysis. Herein, we show that unique zeolites with "continuum intersecting channels" (e.g., BEC, POS, and SOV), in which two intersections are proximal, are greatly significant to the diffusion process with spontaneous switching of the diffusion pathway under varied loading. At low loading, the synergy of strong adsorption sites and molecular reorientation in intersections contribute to almost exclusive molecular diffusion in smaller channels. With an increase in molecular loading, the adsorbates are transported preferentially in larger channels mainly due to the lower diffusion barrier inside continuum intersection channels. This work demonstrates the ability to adjust the prior diffusion pathway by controlling the molecular loading, which may be beneficial for the separation of the product and byproduct in heterogeneous catalysis.

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Source
http://dx.doi.org/10.1021/acs.jpclett.3c00698DOI Listing

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