Rational Design of Carbon Nitride Chemical and Photophysical Properties toward Highly Efficent Photocatalysts

Jesús Barrio barriohe@post.bgu.ac.il Menny Shalom
Department of Chemistry and Ilse Katz Institute for Nanoscale Science and Technology, Ben-Gurion University of the Negev, Beer-Sheva, Israel

Over the past few years, graphitic carbon nitride (g-CN) has attracted widespread attention due to its outstanding electronic properties, which have been exploited in various applications, including in photo- and electro-catalysis, heterogeneous catalysis, CO2 reduction, water splitting, light-emitting diodes, and solar cells. g-CN comprises only carbon and nitrogen, and it can be synthesized by several routes. The synthesis of this material can be carried out by polymerization of C and N rich monomers, such like cyanamide, dicyanamide or melamine (1,2). However, the traditional solid state reaction usually yields unordered materials with grain boundaries and low photo-catalytic activity. Recently, we showed a new synthetic path based on the supramolecular preorganization of g-CN monomers by using non-covalent interactions prior their calcinations at high temperatures. The new path results in highly active materials for photocatalytic applications (3) (water splitting (4) and pollutants degradation (5)).

Here we show that by clever design of supramolecular assemblies we can control the chemical, photophysical and catalytic properties of g-CN toward its utilization as photocatalyst for various reactions (6-7). The supramolecular interactions between different starting monomers at different conditions (i.e. solvents) and their role on the materials growth and chemical, photophysical and catalytic properties will be discussed. This work provides new opportunities for the rational design of carbon nitride based photocatalysts for environmental and energy-related applications.

References

  1. Wang, X.; et al. Mater., 2008, 8(1), 76-80.
  2. Thomas, A.; et al. Mater. Chem., 2008, 18, 4893-4908.
  3. Shalom, M.; et al. Am. Chem. Soc. 2013, 135, 7118-7121.
  4. Shalom, M.; et al. Mater. 2014, 26, 5812-5818.
  5. Jordan, T.; et al. ChemCatChem 2015, 7, 2826-2830.
  6. Barrio, J.; Shalom, M. Sci. Semicond. Proc. 2017. DOI: 10.1016/j.mssp.2017.04.015
  7. Barrio, J.; et al. ACS Sustain. Eng. 2017. DOI: 10.1021/acssuschemeng.7b02807








Powered by Eventact EMS