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Carbon nitride based materials: more than just a support for single-atom catalysis

Journal

CHEMICAL SOCIETY REVIEWS
Volume 52, Issue 15, Pages 4878-4932

Publisher

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2cs00806h

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Recently, single-atom catalysis (SAC), the missing link between homogeneous and heterogeneous catalysis, has been discovered. Carbon nitride (CN)-based materials, which can trap metal atoms in nitrogen-rich coordination sites, have emerged as promising supports for preparing SACs. This review covers the recent advances in SACs supported by CN materials, including characterization techniques, synthetic methods, and their photocatalytic applications. The two-way relationship between single-atoms and CN supports, where the single-atoms can modify the electronic properties of the CN support and vice versa, is emphasized.
Recently, the missing link between homogeneous and heterogeneous catalysis has been found and it was named single-atom catalysis (SAC). However, the SAC field still faces important challenges, one of which is controlling the bonding/coordination between the single atoms and the support in order to compensate for the increase in surface energy when the particle size is reduced due to atomic dispersion. Excellent candidates to meet this requirement are carbon nitride (CN)-based materials. Metal atoms can be firmly trapped in nitrogen-rich coordination sites in CN materials, which makes them a unique class of hosts for preparing single-atom catalysts (SACs). As one of the most promising two-dimensional supports to stabilize isolated metal atoms, CN materials have been increasingly employed for preparing SACs. Herein, we will cover the most recent advances in single-atoms supported by CN materials. In this review, the most important characterization techniques and the challenges faced in this topic will be discussed, and the commonly employed synthetic methods will be delineated for different CN materials. Finally, the catalytic performance of SACs based on carbon nitrides will be reviewed with a special focus on their photocatalytic applications. In particular, we will prove CN as a non-innocent support. The relationship between single-atoms and carbon nitride supports is two-way, where the single-atoms can change the electronic properties of the CN support, while the electronic features of the CN matrix can tune the catalytic activity of the single sites in photocatalytic reactions. Finally, we highlight the frontiers in the field, including analytical method development, truly controlled synthetic methods, allowing the fine control of loading and multi-element synthesis, and how understanding the two-way exchange behind single-atoms and CN supports can push this topic to the next level.

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