Abstract
In this study, a composite photocatalyst comprising a thin carbon layer and highly dispersed cobalt active sites derived from ZIF-L and modified g-C3N4 (CN), was synthesized using a vacuum calcination method. The composite of Co-NC@CN, demonstrated impressive tetracycline (TC) degradation activity (nearly 80%), both in controlled experiments and in real river water conditions. Experimental visualization and characterization results indicated that the carbon layer and the unique cobalt species, with their Co3+/Co2+ redox capability, enhanced the migration and transfer efficiency of photogenerated carriers, as well as the NC improved TC adsorption. Additionally, free radical capture experiments and electron spin resonance (ESR) confirmed that superoxide radicals (.O2−), hydroxyl radical (.OH) and holes (h+) are the primary active species involved in the TC degradation process. Further analysis using liquid chromatography mass spectrometry (LC-MS) and diffuse reflectance in situ Fourier-transform infrared spectroscopy (Drifts-FTIR) provided detailed insights into the degradation process and the intermediate products formed. This research offers a promising approach to synthesizing sunlight-driven composite photocatalysts for the treatment of real wastewater.
| Original language | English |
|---|---|
| Article number | 117088 |
| Number of pages | 12 |
| Journal | Journal of Photochemistry and Photobiology A: Chemistry |
| Volume | 476 |
| DOIs | |
| Publication status | Published - 1 Jul 2026 |
UN SDGs
This output contributes to the following UN Sustainable Development Goals (SDGs)
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SDG 6 Clean Water and Sanitation
User-Defined Keywords
- Photocatalytic degradation
- Tetracycline
- Emerging pollutants
- N-doped carbon
- Intermediate products
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