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Ionothermal Synthesis of Crystalline, Condensed, Graphitic Carbon Nitride

MPS-Authors

Bojdys,  Michael J.
Max Planck Society;

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Müller,  Jens Oliver
Inorganic Chemistry, Fritz Haber Institute, Max Planck Society;

Antonietti,  Markus
Max Planck Society;

Thomas,  Arne
Max Planck Society;

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Citation

Bojdys, M. J., Müller, J. O., Antonietti, M., & Thomas, A. (2008). Ionothermal Synthesis of Crystalline, Condensed, Graphitic Carbon Nitride. Chemistry - A European Journal, 14(27), 8177-8182. doi:10.1002/chem.200800190.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0010-FF09-7
Abstract
Herein we report the synthesis of a crystalline graphitic carbon nitride, or g-C3N4, obtained from the temperature-induced condensation of dicyandiamide (NH2C(NH)NHCN) by using a salt melt of lithium chloride and potassium chloride as the solvent. The proposed crystal structure of this g-C3N4 species is based on sheets of hexagonally arranged s-heptazine (C6N7) units that are held together by covalent bonds between C and N atoms which are stacked in a graphitic, staggered fashion, as corroborated by powder X-ray diffractometry and high-resolution transmission electron microscopy.