期刊
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
卷 62, 期 1, 页码 126-135出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.iecr.2c02521
关键词
-
Designing and synthesizing high-efficiency and stable heterogeneous catalysts for the electro-Fenton process continues to be a challenge. In this study, a co-doped Ce and N metal-organic framework MIL-101(Fe) catalyst was successfully synthesized. The catalyst exhibited a high degradation rate for dyes, competitive stability, and reusability. The design concept of co-doping to produce abundant active sites can be extended to other porous materials for the development of heterogeneous electro-Fenton catalysts.
Design and synthesis of high-efficiency and stable heterogeneous catalysts for the electro-Fenton process remain challenging. In this study, a co-doped Ce and N metal-organic framework MIL-101(Fe) heterogeneous catalyst (Ce/N-MIL-101(Fe) was synthesized by a facile one-step solvothermal method. Polyvinyl pyrrolidone played dual roles during the fabrication process, which not only acted as a nitrogen source for doping but also prevented MIL101(Fe) molecules from aggregating and reinforcing the formation crystal with a complete polyhedral crystal shape. The introduction of Ce significantly enhanced the density of active sites and promoted the Fe3+/ Fe2+ cycle of the reaction system. Owing to the specific structure and properties, the rate of electron transfer in the catalytic process was significantly promoted. The synthesized Ce/N-MIL-101(Fe) catalyst exhibited a high degradation rate for dyes (>98%) with competitive stability and reusability. Moreover, compared with common electro-Fenton catalysts usually operated in a limited pH range of 3.0-6.0, the working pH range of Ce/N-MIL-101(Fe) was widened up to 10.0. The design concept for producing abundant active sites with co-doping into frameworks can be extended to more heterogeneous electro-Fenton catalysts constituted by other porous materials.
作者
我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。
推荐
暂无数据