
Understanding the Fundamentals of Microporosity Upgrading in Zeolites: Increasing Diffusion and Catalytic Performances
Author(s) -
Qin Zhengxing,
Zeng Shu,
Melinte Georgian,
Bučko Tomáš,
Badawi Michael,
Shen Yanfeng,
Gilson JeanPierre,
Ersen Ovidiu,
Wei Yingxu,
Liu Zhongmin,
Liu Xinmei,
Yan Zifeng,
Xu Shutao,
Valtchev Valentin,
Mintova Svetlana
Publication year - 2021
Publication title -
advanced science
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.388
H-Index - 100
ISSN - 2198-3844
DOI - 10.1002/advs.202100001
Subject(s) - zeolite , mesoporous material , faujasite , sodalite , catalysis , diffusion , chemical engineering , porosity , materials science , chemistry , organic chemistry , composite material , thermodynamics , physics , engineering
Hierarchical zeolites are regarded as promising catalysts due to their well‐developed porosity, increased accessible surface area, and minimal diffusion constraints. Thus far, the focus has been on the creation of mesopores in zeolites, however, little is known about a microporosity upgrading and its effect on the diffusion and catalytic performance. Here the authors show that the “birth” of mesopore formation in faujasite (FAU) type zeolite starts by removing framework T atoms from the sodalite (SOD) cages followed by propagation throughout the crystals. This is evidenced by following the diffusion of xenon (Xe) in the mesoporous FAU zeolite prepared by unbiased leaching with NH 4 F in comparison to the pristine FAU zeolite. A new diffusion pathway for the Xe in the mesoporous zeolite is proposed. Xenon first penetrates through the opened SOD cages and then diffuses to supercages of the mesoporous zeolite. Density functional theory (DFT) calculations indicate that Xe diffusion between SOD cage and supercage occurs only in hierarchical FAU structure with defect‐contained six‐member‐ring separating these two types of cages. The catalytic performance of the mesoporous FAU zeolite further indicates that the upgraded microporosity facilitates the intracrystalline molecular traffic and increases the catalytic performance.