Peroxymonosulfate enhanced photocatalytic degradation of organic dye by metal-free TpTt-COF under visible light irradiation

• Published in: Scientific reports 2024-04, Vol.14 (1), p.8183-8183, Article 8183
• Main Authors: Xu, Nong, Liu, Kaixuan, Liu, Qiao, Wang, Qing, Zhu, Anzheng, Fan, Long
• Format: Article
• Language: English
• Subjects: 639/166/898; 639/301/299/890; Biodegradation; Comparative analysis; Dyes; Electrons; Environmental cleanup; Environmental degradation; Free radicals; Harsh environments; Humanities and Social Sciences; Irradiation; multidisciplinary; Photocatalysis; Photodegradation; Science; Science (multidisciplinary); Synergistic effect; Titanium dioxide; Water pollution
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-024-58761-w

Recently, the activation of persulfate (PDS) by non-metallic photocatalysts under visible light has attracted significant interest in applications in environmental remediation. This study presents a pioneering investigation into the combined application of the TpTt-COF and PMS for visible light degradation of organic dyes. Synthesized orange TpTt-COF monomers exhibit exceptional crystallinity, a 2D structure, and notable stability in harsh conditions. The broad visible light absorption around a wavelength of 708 nm. The TpTt-COF emerges as a promising candidate for photocatalytic dye degradation. The study addresses high charge recombination in the TpTt-COF, highlighting the crucial role of its electron donor and acceptor for the PMS activation. Comparative analyses against traditional photocatalytic materials, such as the metal-free carbon-based material g-C 3 N 4 and transition metal-containing TiO 2 , demonstrate TpTt-COF's superior performance, generating diverse free radicals. In simulated experiments, the TpTt-COF's degradation rate surpasses PMS-combined g-C 3 N 4 by 13.9 times. and 1.6 times higher than the TpTt-COF alone. Remarkably, the TpTt-COF maintains high activity under harsh environments. Investigations into the degradation mechanism and the TpTt-COF's reusability reveal its efficiency and stability. Under visible light, TpTt-COF facilitates efficient electron–hole separation. Combining the TpTt-COF with PMS produces various radicals, ensuring effective separation and a synergistic effect. Radical quenching experiments confirm the pivotal role of O 2 - · radicals, while ·OH and SO 4 - · radicals intensify the degradation. After five cycles, TpTt-COF maintains an impressive 83.2% degradation efficiency. This study introduces an efficient photocatalytic system mediated by PMS and valuable insights into governing mechanisms for organic pollutant degradation in water environments.