School of Environmental Science and Engineering, Suzhou University of Science and Technology, Suzhou, Jiangsu, 215009, China; School of Mechanical Science and Engineering, Northeast Petroleum University, Daqing, Heilongjiang, 163318, China.
School of Mechanical Science and Engineering, Northeast Petroleum University, Daqing, Heilongjiang, 163318, China.
Environ Res. 2024 Sep 15;257:119295. doi: 10.1016/j.envres.2024.119295. Epub 2024 May 31.
Doping with nitrogen atoms can improve the catalytic activity of activated carbon cathodes in electro-Fenton systems, but currently there is a lack of understanding of the catalytic mechanism, which limits the further development of high-performance activated carbon cathodes. Here, a multi-scale exploration was conducted using density functional theory and experimental methods to investigate the mechanism of different nitrogen doping types promoting the redox performance of activated carbon cathodes and the degradation of phenol. The density functional theory results indicate that the introduction of nitrogen atoms enhances the binding ability between carbon substrates and oxygen-containing substances, promotes the localization of surrounding electrons, and makes it easier for O to bind with protons and catalyze the hydrogenation reaction of *OOH. Due to its weak binding ability with oxygen-containing substances, AC is difficult to form HO, resulting in a tendency towards the 4eORR pathway. The binding energy between graphite-N carbon substrate and pyridine-N carbon substrate with *OOH is closer to the volcano top, so graphite n and pyridine n can better promote the selectivity of activated carbon for 2e-ORR. In addition, the calculation results also indicate that pyrrole-N and graphite-N are more capable of catalyzing the reaction energy barrier between ·OH and phenol. Finally, the simulation results were used to guide the modification of nitrogen doped activated carbon and experimental verification was carried out. The degradation results of phenol confirmed the efficient synergistic effect between different types of nitrogen doping, and the NAC-800 electrode exhibited efficient and stable characteristics. This work provides a guiding strategy for further developing stable and highly selective activated carbon cathode materials.
用氮原子掺杂可以提高电芬顿系统中活性炭阴极的催化活性,但目前对其催化机制的了解还很有限,这限制了高性能活性炭阴极的进一步发展。在这里,我们使用密度泛函理论和实验方法进行了多尺度探索,以研究不同氮掺杂类型促进活性炭阴极氧化还原性能和苯酚降解的机理。密度泛函理论的结果表明,氮原子的引入增强了碳底物与含氧物质之间的结合能力,促进了周围电子的局域化,使 O 更容易与质子结合并催化OOH 的加氢反应。由于其与含氧物质的结合能力较弱,AC 很难形成 HO,导致倾向于 4eORR 途径。石墨-N 碳底物与吡啶-N 碳底物与OOH 的结合能更接近火山顶,因此石墨 n 和吡啶 n 可以更好地促进活性炭对 2e-ORR 的选择性。此外,计算结果还表明,吡咯-N 和石墨-N 更能够催化·OH 和苯酚之间的反应能垒。最后,模拟结果被用于指导氮掺杂活性炭的改性,并进行了实验验证。苯酚的降解结果证实了不同类型氮掺杂之间的高效协同作用,并且 NAC-800 电极表现出高效和稳定的特性。这项工作为进一步开发稳定和高选择性的活性炭阴极材料提供了指导策略。