催化作用
材料科学
单线态氧
纳米颗粒
石墨烯
碳化
氧气
化学工程
氧化物
电子转移
纳米技术
光化学
化学
冶金
复合材料
扫描电子显微镜
有机化学
工程类
作者
Liqin Chen,Jianjun Liao,Linlin Zhang,Chen Li,Shuhai He,Chengjun Ge
出处
期刊:ACS ES&T water
[American Chemical Society]
日期:2023-01-25
卷期号:3 (2): 542-555
被引量:5
标识
DOI:10.1021/acsestwater.2c00563
摘要
Currently, catalysts with core–shell structures have an important role in catalytic performance and practical applications, but how to simplify the preparation method and a reasonable explanation of the activation mechanism are still lacking. In this work, we obtained highly dispersed and ultrafine laser-induced nitrogen-doped graphene-wrapped iron cobaltate (LI-FeCo2O4@NDG) catalysts by one-step carbonization of iron cobalt metal–organic framework (FeCo-MOF) precursors using a CO2 laser annealing technique under ambient conditions. An LI-FeCo2O4@NDG/peroxymonosulfate (PMS) system achieved a rapid degradation of sulfamethoxazole (SMX) with 92.2% degradation efficiency in 6 min. Meanwhile, LI-FeCo2O4@NDG exhibited low metal leaching (Co, 0.155 mg/L; Fe, 0.008 mg/L) and a high reaction rate constant (k = 0.413 min–1). Most importantly, the ability of the catalyst could achieve nearly 100% utilization and conversion of PMS to singlet oxygen (1O2). The activation mechanism may be explained that the electron pool and interfacial electric field formed by the LI-FeCo2O4@NDG with the core–shell structure could accelerate the electron supply and transfer to the PMS, facilitating the activation of PMS self-decomposition to produce more 1O2. Overall, this work is expected to open a new avenue for the construction of core–shell structures and a new insight for revealing its activation mechanism of PMS.
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