Enhanced photocatalytic degradation of sulfadiazine under LED light using Pd-decorated g-C3N4: Structure–activity relationship, mechanism, and toxicity assessment
Graphitic carbon nitride (g-C 3 N 4 ) is a sustainable photocatalyst, however, its practical application is severely limited by rapid charge recombination and insufficient redox capability. In this work, a Pd x OCN-y photocatalyst was synthesized via photoreduction and evaluated under LED irradiation. The Pd 8 OCN-3 sample exhibited superior performance toward sulfadiazine (SDZ) degradation, achieving 90% removal within 180 min, with a reaction rate 6.53 times higher than that of pristine g-C 3 N 4 . The enhanced activity was attributed to increased surface area, narrowed bandgap, improved charge separation, and suppressed electron–hole recombination. Radical scavenging tests indicated •O 2 − and •OH as the dominant reactive species. Pd 8 OCN-3 also demonstrated high stability and recyclability across multiple cycles. Additionally, phytotoxicity assays using mung bean germination confirmed the reduced toxicity of degradation products, in agreement with QSAR-based predictions. This study not only elucidates the structure–activity relationship of Pd x OCN-y but also provides a viable strategy for designing highly efficient and eco-safe photocatalysts for antibiotic-contaminated wastewater treatment. • An oxygen-doped Pd-decorated g-C 3 N 4 were fabricated successfully. • A high SDZ degradation efficiency of 90% was achieved. • The Pd 8 OCN-3 enables a fast separation of photogenerated charge carriers. • Growth performance of mung bean and toxicity evaluation of degradation intermediates were presented.
Authors
- Oanh T.K. Nguyen
- Vinh Huu Nguyen
- Taeyoon Lee
- Trinh Duy Nguyen
Institutions
- Trường ĐH Nguyễn Tất Thành (VN)
- Pukyong National University (KR)
Publication Details
- Journal
- Journal of Water Process Engineering
- Published
- 2026-02-05
- DOI
- https://doi.org/10.1016/j.jwpe.2026.109606
- Primary Topic
- Advanced Photocatalysis Techniques
- Type
- article
- Field-Weighted Citation Impact
- 0.00