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

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 exf...

Full description

Saved in:
Bibliographic Details
Published in:Chemistry of materials Vol. 35; no. 17; pp. 6762 - 6770
Main Authors: Krinninger, Matthias, Bock, Nicolas, Kaiser, Sebastian, Reich, Johanna, Bruhm, Tobias, Haag, Felix, Allegretti, Francesco, Heiz, Ueli, Köhler, Klaus, Lechner, Barbara A. J., Esch, Friedrich
Format: Journal Article
Language:English
Published: American Chemical Society 12-09-2023
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Description
Summary: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.
Bibliography:ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ISSN:0897-4756
1520-5002
DOI:10.1021/acs.chemmater.3c01030