Urea-Derived Carbon Nitride Fragmentation: A Route to Melem-Based Superstructures
Urea-derived graphitic carbon nitride (g-C3N4) underwent chemical treatment in a strongly oxidizing H2SO4/HNO3/H2O2 environment, followed by dialysis against water. XRD and SEM measurements revealed significant disruption of the layered polymeric framework, including loss of hydrogen-bond-mediated order, partial depolymerization into melem-based units, and the formation of rod-like melem hydrate superstructures. FTIR spectra indicated that chemical treatment resulted in the loss of the heptazine structure and the emergence of melem/triazine vibrations. Consistent disruption of the C–N framework was also observed in XPS spectra, which showed a reduced contribution of nitrogen species associated with inter-triazine bridging. Mott–Schottky analysis yielded potential values suggesting the presence of additional electronic states in the chemically treated sample. This aligns with EPR spin-trapping results, which showed approximately a 2.5-fold decrease in superoxide radical anion generation upon visible light irradiation compared with the parent compound, attributed to both reduced visible-light absorption and trapping of photogenerated electrons in defect states.
Authors
- Jugoslav B. Krstić (ORCID: https://orcid.org/0000-0003-0321-0698)
- Tatjana D. Vulić
- Miloš Mojović (ORCID: https://orcid.org/0000-0002-1868-9913)
- Nadica D. Abazović (ORCID: https://orcid.org/0000-0003-0718-5186)
- Mirjana I. Čomor (ORCID: https://orcid.org/0000-0002-7222-4500)
- Zorica D. Mojović (ORCID: https://orcid.org/0000-0003-4804-0776)
- Milica V. Carević (ORCID: https://orcid.org/0000-0002-7212-4438)
Institutions
- University of Belgrade (RS)
- Institute of General and Physical Chemistry (RS)
- Vinča Institute of Nuclear Sciences (RS)
- Institute of Chemistry, Technology and Metallurgy (RS)
Publication Details
- Journal
- Polymers
- Published
- 2026-10-28
- DOI
- https://doi.org/10.3390/polym18212664
- Primary Topic
- Advanced Photocatalysis Techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Science Fund of the Republic of Serbia