生物炭
降级(电信)
兴奋剂
化学
污染
Atom(片上系统)
环境化学
化学工程
材料科学
有机化学
热解
光电子学
生物
工程类
嵌入式系统
电信
计算机科学
生态学
作者
Shutian Lin,Xin-Li Zhang,Yingzhi Chen,Yuanhong Zhong,Gao Cheng,Lin Yu
标识
DOI:10.1016/j.solidstatesciences.2025.107860
摘要
The Fe-N-C catalyst was synthesized using loofah sponge-derived carbon and applied for peroxymonosulfate (PMS) activation to degrade organic pollutants. The catalyst, featuring highly dispersed single-atom Fe on the N-C framework, showed outstanding activity for phenol degradation across a wide pH range. The incorporation of Fe significantly boosted the catalytic performance, achieving rapid degradation of phenol at 20 mg L -1 within 10 minutes, using 0.5 mmol L -1 of PMS and 0.2 g L -1 of catalyst. Electron paramagnetic resonance (EPR) and reactive oxygen quenching experiments identified the singlet oxygen ( 1 O 2 ) and superoxide radical (O 2 •‒ ) as the main reactive oxygen species, with the former playing a key role. It has been demonstrated that the Fe-N x structures were the active sites that facilitated the generation of 1 O 2 , thereby enhancing the catalytic activity of the Fe-N-C materials. The catalyst also effectively addressed pollutants like Rhodamine B and climbazole, indicating its potential for environmental remediation. The synthesis approach for Fe-N-C is applicable to other transition metals, such as Mn, Co, Ni, Cu, and Zn, providing valuable insights for the development of highly efficient and durable M-N-C catalysts. • Fe-N-C catalyst from loofah sponge-derived carbon was successfully synthesized. • Single-atom Fe on the N-C framework boosts phenol degradation at a wide pH range. • 1 O 2 and O 2 •‒ were the main reactive species in Fe-N-C catalyzed system with PMS. • Fe-N x are active sites for facilitating 1 O 2 generation and enhancing the catalysis. • Fe-N-C synthesis method fits other transition metals, advancing M-N-C catalysts.
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