Concerns linked to highly dispersed iron anchored within graphitic carbon nitride, is it a truly promising material to drive heterogeneous photo-Fenton treatments?

The precipitation of iron at pH > 4 is one of the main drawbacks of any Fenton-based process. Among the engineered solutions, the incorporation of iron within the wide cavities of graphitic carbon nitride (g-CN) has recently gained momentum. However, most works employing Fe-g-CN materials usually employ high H<sub>2</sub>O<sub>2</sub> concentrations (>25 mM) to observe considerable pollutant abatements (without or with UV-vis light irradiation, i.e., by heterogeneous dark- or photo-Fenton processes, respectively). To gain further insights into this issue, in this work, Fe-g-CN, with different amounts of iron, were synthesised by thermal polycondensation of melamine and FeCl<sub>3</sub>·6H<sub>2</sub>O as precursors and compared its performance with the g-CN alone. Under UV-A light, a content of 0.2% w/w of iron in the g-CN was optimal to improve the oxidative performances of target pollutants (phenol and sulfamethoxazole 100 μM, respectively), higher Fe-loadings decreased the photocatalytic performances with respect to g-CN. Interestingly, this trend was inversed when adding H<sub>2</sub>O<sub>2</sub> 1 mM, being the pollutant removal by g-CN faster than that by Fe-g-CN (for phenol, k<sub>obs</sub> = 8.02 × 10<sup>-2</sup> min<sup>-1</sup> and 2.83 × 10<sup>-2</sup> min<sup>-1</sup>, respectively), opposed to expectations. Furthermore, HO<sup>•</sup>, HO<sub>2</sub><sup>•</sup> or <sup>1</sup>O<sub>2</sub> were barely detected by Electron Paramagnetic Resonance, indicating that the reactive species should oxidise the g-CN rather than react with the spin traps. Finally, although g-CN oxidation was not observed by typical characterisation techniques (such as FT-IR/ATR), we have observed 6 times more nitrates formation by illuminated Fe-g-CN than g-CN, indicating that iron enhances the self-oxidation of illuminated carbon nitrides. Our results demonstrate that iron incorporation in g-CN might be not as convenient as usually stated in the literature, as the stability of the photocatalyst is drastically reduced, releasing nitrates and possibly decreasing the material's lifetime.

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Publication Details

Journal
Chemosphere
Published
2025-03-04
DOI
https://doi.org/10.1016/j.chemosphere.2025.144255
Citations
2
Primary Topic
Advanced Photocatalysis Techniques
Type
article
Field-Weighted Citation Impact
0.73
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article

Concerns linked to highly dispersed iron anchored within graphitic carbon nitride, is it a truly promising material to drive heterogeneous photo-Fenton treatments?

Fabrizio Caldera, S. Pellegrino, Enzo Laurenti, Iván Sciscenko et al.
2 citations
Chemosphere
Advanced Photocatalysis Techniques
0.73
article

Concerns linked to highly dispersed iron anchored within graphitic carbon nitride, is it a truly promising material to drive heterogeneous photo-Fenton treatments?

Fabrizio Caldera, S. Pellegrino, Enzo Laurenti, Iván Sciscenko, Claudio Minero, Marco Minella
article en
2 citations

Abstract

The precipitation of iron at pH > 4 is one of the main drawbacks of any Fenton-based process. Among the engineered solutions, the incorporation of iron within the wide cavities of graphitic carbon nitride (g-CN) has recently gained momentum. However, most works employing Fe-g-CN materials usually employ high H<sub>2</sub>O<sub>2</sub> concentrations (>25 mM) to observe considerable pollutant abatements (without or with UV-vis light irradiation, i.e., by heterogeneous dark- or photo-Fenton processes, respectively). To gain further insights into this issue, in this work, Fe-g-CN, with different amounts of iron, were synthesised by thermal polycondensation of melamine and FeCl<sub>3</sub>·6H<sub>2</sub>O as precursors and compared its performance with the g-CN alone. Under UV-A light, a content of 0.2% w/w of iron in the g-CN was optimal to improve the oxidative performances of target pollutants (phenol and sulfamethoxazole 100 μM, respectively), higher Fe-loadings decreased the photocatalytic performances with respect to g-CN. Interestingly, this trend was inversed when adding H<sub>2</sub>O<sub>2</sub> 1 mM, being the pollutant removal by g-CN faster than that by Fe-g-CN (for phenol, k<sub>obs</sub> = 8.02 × 10<sup>-2</sup> min<sup>-1</sup> and 2.83 × 10<sup>-2</sup> min<sup>-1</sup>, respectively), opposed to expectations. Furthermore, HO<sup>•</sup>, HO<sub>2</sub><sup>•</sup> or <sup>1</sup>O<sub>2</sub> were barely detected by Electron Paramagnetic Resonance, indicating that the reactive species should oxidise the g-CN rather than react with the spin traps. Finally, although g-CN oxidation was not observed by typical characterisation techniques (such as FT-IR/ATR), we have observed 6 times more nitrates formation by illuminated Fe-g-CN than g-CN, indicating that iron enhances the self-oxidation of illuminated carbon nitrides. Our results demonstrate that iron incorporation in g-CN might be not as convenient as usually stated in the literature, as the stability of the photocatalyst is drastically reduced, releasing nitrates and possibly decreasing the material's lifetime.

ChemosphereVol. 376
University of Turin (IT)
Openalex Percentile: Top 33%
Advanced Photocatalysis Techniques
0.73
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