Li Xiaoping, Liu Meng, Wen Lanxuan, Li Rongwei, Liu Yu, Yang Shengjiong, Ding Dahu, Chen Yang, Chen Rongzhi, Xu Shengming
Yanshan Earth Critical Zone and Surface Fluxes Research Station, College of Resources and Environment, University of Chinese Academy of Sciences, Beijing 100049, China.
School of Environmental and Municipal Engineering, Xi'an University of Architecture and TechnologyNo.13, Yanta Road, Xi'an, Shaanxi 710055, China.
Environ Sci Technol. 2025 Jul 8;59(26):13458-13469. doi: 10.1021/acs.est.5c01201. Epub 2025 Jun 25.
Fenton process and activated carbon are widely used for water treatment, yet both encounter significant challenges, such as slow Fe/Fe conversion and rapid adsorbent saturation. Herein, a category of hitherto overlooked dynamic single-atom sites on heteroatom-doped carbons (HDCs) that mitigate the above problems was observed by coupling Fenton and activated carbon. Specifically, the defects on the carbon surface, particularly the heteroatom defects, coordinated with Fe in the bulk solution to form dynamic single-atom sites that simultaneously suppress the Fe hydrolysis and promote the Fe/Fe conversion. This synergy sustains the efficient oxidation process of the coupled system through up to 5 cycles due to the optimized Fe/Fe cycling. Moreover, dynamic single-atom sites enable the continuous removal of adsorbates from the carbon surface, extending the time before adsorption saturation and maintaining nearly 100% efficiency for 480 h. Mechanistic analysis revealed that dynamic single-atom sites optimize the Fe/Fe redox cycle through forming a carbon → ligand atoms → Fe ↔ HO electron flux pathway. Their bidirectional electron flux with HO enhances OH· production, thereby improving the Fenton oxidation process. These findings offer crucial insights for overcoming challenges in environmental engineering technologies and underscore the potential superiority of coupled systems in practical applications.
芬顿法和活性炭被广泛用于水处理,但两者都面临重大挑战,如铁/亚铁转化缓慢和吸附剂快速饱和。在此,通过将芬顿法与活性炭相结合,观察到一类迄今为止被忽视的杂原子掺杂碳(HDCs)上的动态单原子位点,可缓解上述问题。具体而言,碳表面的缺陷,特别是杂原子缺陷,与本体溶液中的铁配位形成动态单原子位点,同时抑制铁水解并促进铁/亚铁转化。由于优化了铁/亚铁循环,这种协同作用使耦合系统的高效氧化过程可持续多达5个循环。此外,动态单原子位点能够持续从碳表面去除吸附质,延长吸附饱和前的时间,并在480小时内保持近100%的效率。机理分析表明,动态单原子位点通过形成碳→配体原子→铁⇔羟基自由基电子通量途径优化铁/亚铁氧化还原循环。它们与羟基自由基的双向电子通量增强了羟基自由基的产生,从而改善了芬顿氧化过程。这些发现为克服环境工程技术中的挑战提供了关键见解,并强调了耦合系统在实际应用中的潜在优势。