化学
降级(电信)
污染物
罗丹明B
氧化还原
光化学
电子转移
亚甲蓝
甲基橙
氧气
活性氧
超氧化物
催化作用
环境化学
化学工程
激进的
橙色(颜色)
单线态氧
动力学
小学(天文学)
无机化学
过氧二硫酸盐
作者
Pengxu Chang,Xue Li,Chunhui Song,Bingyi Yue,Ningning Xuan,Gang Cheng
出处
期刊:Langmuir
[American Chemical Society]
日期:2026-03-09
卷期号:42 (11): 7897-7906
标识
DOI:10.1021/acs.langmuir.5c06467
摘要
Contact-electro-catalysis (CEC), which induces electron transfer via contact electrification at solid-liquid interfaces to efficiently generate reactive oxygen species (ROS), represents a promising method for the degradation of organic pollutants. However, the low concentration of ROS generated solely by electron transfer at the solid-liquid interface limits the efficient degradation of pollutants. In this study, Fe2+ was introduced into the CEC system to construct a Contact-electro-catalysis Fenton (CEC-Fenton) system, which enhances the concentration of ROS. The addition of Fe2+ provides a pathway for electron transfer, which facilitates the generation of ROS, while the Fe2+/Fe3+ redox cycling supporting the sustained production of ROS. Methyl orange (MO) was employed as a model pollutant to evaluate the catalytic degradation performance. The degradation rate of MO in the CEC-Fenton system can reach up to 0.4 min-1, which is 33 times higher than that in the traditional CEC system. The method exhibits broad-spectrum degradation capabilities for organic pollutants with degradation rates for Methylene Blue (MB) and Rhodamine B (RhB) enhanced by factors of 4.6 and 6.1, respectively. The superior performance of this method for azo pollutants originates from protonation-induced activation of the azo bond. The superoxide anion radical (·O2-) was identified as the primary ROS, whose generation was significantly promoted by the introduction of Fe2+ ions. This project offers a method for increasing the concentration of ROS within the CEC systems.
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