Issue 62, 2024

New trends in nanoparticle exsolution

Abstract

Many relevant high-temperature chemical processes require the use of oxide-supported metallic nanocatalysts. The harsh conditions under which these processes operate can trigger catalyst degradation via nanoparticle sintering, carbon depositions or poisoning, among others. This primarily affects metallic nanoparticles created via deposition methods with low metal–support interaction. In this respect, nanoparticle exsolution has emerged as a promising method for fabricating oxide-supported nanocatalysts with high interaction between the metal and the oxide support. This is due to the mechanism involved in nanoparticle exsolution, which is based on the migration of metal cations in the oxide support to its surface, where they nucleate and grow as metallic nanoparticles partially embedded in the oxide. This anchorage confers high robustness against sintering or coking-related problems. For these reasons, exsolution has attracted great interest in the last few years. Multiple works have been devoted to proving the high catalytic stability of exsolved metallic nanoparticles in several applications for high-temperature energy storage and conversion. Additionally, considerable attention has been directed towards understanding the underlying mechanism of metallic nanoparticle exsolution. However, this growing field has not been limited to these types of studies and recent discoveries at the forefront of materials design have opened new research avenues. In this work, we define six new trends in nanoparticle exsolution, taking a tour through the most important advances that have been recently reported.

Graphical abstract: New trends in nanoparticle exsolution

Article information

Article type
Feature Article
Submitted
25 Apr 2024
Accepted
10 Jun 2024
First published
11 Jun 2024
This article is Open Access
Creative Commons BY-NC license

Chem. Commun., 2024,60, 7987-8007

New trends in nanoparticle exsolution

A. J. Carrillo, A. López-García, B. Delgado-Galicia and J. M. Serra, Chem. Commun., 2024, 60, 7987 DOI: 10.1039/D4CC01983K

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