Issue 6, 2024

Water structures on acidic zeolites and their roles in catalysis

Abstract

The local reaction environment of catalytic active sites can be manipulated to modify the kinetics and thermodynamic properties of heterogeneous catalysis. Because of the unique physical–chemical nature of water, heterogeneously catalyzed reactions involving specific interactions between water molecules and active sites on catalysts exhibit distinct outcomes that are different from those performed in the absence of water. Zeolitic materials are being applied with the presence of water for heterogeneous catalytic reactions in the chemical industry and our transition to sustainable energy. Mechanistic investigation and in-depth understanding about the behaviors and the roles of water are essentially required for zeolite chemistry and catalysis. In this review, we focus on the discussions of the nature and structures of water adsorbed/stabilized on Brønsted and Lewis acidic zeolites based on experimental observations as well as theoretical calculation results. The unveiled functions of water structures in determining the catalytic efficacy of zeolite-catalyzed reactions have been overviewed and the strategies frequently developed for enhancing the stabilization of zeolite catalysts are highlighted. Recent advancement will contribute to the development of innovative catalytic reactions and the rationalization of catalytic performances in terms of activity, selectivity and stability with the presence of water vapor or in condensed aqueous phase.

Graphical abstract: Water structures on acidic zeolites and their roles in catalysis

Article information

Article type
Review Article
Submitted
16 Oct 2023
First published
19 Feb 2024
This article is Open Access
Creative Commons BY license

Chem. Soc. Rev., 2024,53, 3065-3095

Water structures on acidic zeolites and their roles in catalysis

Q. Liu and J. A. van Bokhoven, Chem. Soc. Rev., 2024, 53, 3065 DOI: 10.1039/D3CS00404J

This article is licensed under a Creative Commons Attribution 3.0 Unported Licence. You can use material from this article in other publications without requesting further permissions from the RSC, provided that the correct acknowledgement is given.

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