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On-Surface Carbon Nitride Growth from Polymerization of 2,5,8-Triazido-s-heptazine

[Image: see text] Carbon nitrides have recently come into focus for photo- and thermal catalysis, both as support materials for metal nanoparticles as well as photocatalysts themselves. While many approaches for the synthesis of three-dimensional carbon nitride materials are available, only top-down...

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Detalles Bibliográficos
Autores principales: Krinninger, Matthias, Bock, Nicolas, Kaiser, Sebastian, Reich, Johanna, Bruhm, Tobias, Haag, Felix, Allegretti, Francesco, Heiz, Ueli, Köhler, Klaus, Lechner, Barbara A. J., Esch, Friedrich
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10500973/
https://www.ncbi.nlm.nih.gov/pubmed/37719034
http://dx.doi.org/10.1021/acs.chemmater.3c01030
Descripción
Sumario:[Image: see text] Carbon nitrides have recently come into focus for photo- and thermal catalysis, both as support materials for metal nanoparticles as well as photocatalysts themselves. While many approaches for the synthesis of three-dimensional carbon nitride materials are available, only top-down approaches by exfoliation of powders lead to thin-film flakes of this inherently two-dimensional material. Here, we describe an in situ on-surface synthesis of monolayer 2D carbon nitride films as a first step toward precise combination with other 2D materials. Starting with a single monomer precursor, we show that 2,5,8-triazido-s-heptazine can be evaporated intact, deposited on a single crystalline Au(111) or graphite support, and activated via azide decomposition and subsequent coupling to form a covalent polyheptazine network. We demonstrate that the activation can occur in three pathways, via electrons (X-ray illumination), via photons (UV illumination), and thermally. Our work paves the way to coat materials with extended carbon nitride networks that are, as we show, stable under ambient conditions.