4.6 Article

Degradation and chemical stability of graphitic carbon nitride during ultraviolet light irradiation

Journal

MATERIALS CHEMISTRY AND PHYSICS
Volume 308, Issue -, Pages -

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.matchemphys.2023.128252

Keywords

Graphitic carbon nitride; Degradation; UV irradiation; XPS

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In this study, graphitic carbon nitride (g-C3N4) was synthesized through the pyrolysis of urea at 450 degrees C for 2 h. The degradation of g-C3N4 under UV irradiation was investigated using multiple analytical techniques, including XPS, FTIR, ToF-SIMS, nitrogen adsorption-desorption isotherm, and PL spectroscopy.
Graphitic carbon nitride (g-C3N4) was synthesized by pyrolysis of urea at 450 degrees C for 2 h. X-ray diffraction and transmission electron microscopy confirmed the formation of the stacked hexagonal layers and platelet-like structure of g-C3N4. The sample was irradiated by ultraviolet (UV, 370 nm) light for about 62 h and X-ray photoelectron spectroscopy (XPS), Fourier transform infrared spectroscopy (FTIR), time-of-flight secondary ion mass spectroscopy (ToF-SIMS), Nitrogen adsorption-desorption isotherm, and photoluminescence spectroscopy (PL) were used to investigate the degradation. XPS spectra of C 1s electrons revealed four components associated with adventitious carbon, the -C & EQUIV;N group, heptazine/triazine and carboxyl/carbonate species. Quantitative XPS analysis indicated an increase in the peak areas associated with the -C & EQUIV;N group and carboxyl/carbonate species, accompanied by a decrease in the areas of the components associated with the heptazine/triazine and adventitious carbon. XPS spectra of N 1s were fitted using four components which were assigned to pyridinic nitrogen (C-N=C), nitrile group (N & EQUIV;C), amine groups (NHx) and tertiary nitrogen (N-(C)3). The relative areas of peaks associated with the amine and nitrile groups have slightly increased after UV irradiation whereas the peak associated with pyridinic nitrogen decreased. FTIR spectra suggested a reduction in the C-N and C=N heterocycle bonds and slight variation in the C & EQUIV;N bonds after UV irradiation. BET analysis revealed that the surface area and pore volume have decreased after irradiation. ToF-SIMS analysis indicate the formation of NOx, CNO, NHx, and C4H3NO2 species after irradiation. PL spectra of the g-C3N4 showed a broad blue-green emission which was fitted using three bands and ascribed to the & delta;*-LP, & pi;-LP, and & pi;-& pi;* transitions within the bandgap. During UV irradiation, the g-C3N4 powder lost about 22% of its blue-green emission intensity after nearly 45 h and then remained stable for further irradiation time. This study confirmed the degradation of g-C3N4 under UV irradiation, which should be further studied for better integration of this material in photoexcited applications.

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