催化作用
扩展X射线吸收精细结构
化学
密度泛函理论
Atom(片上系统)
煅烧
扫描透射电子显微镜
苯酚
X射线光电子能谱
无机化学
结晶学
物理化学
光化学
吸收光谱法
材料科学
透射电子显微镜
化学工程
纳米技术
计算化学
有机化学
嵌入式系统
工程类
物理
量子力学
计算机科学
作者
Yu Yin,Lei Shi,Wenlang Li,Xuning Li,Hong Wu,Zhimin Ao,Wenjie Tian,Shaomin Liu,Shaobin Wang,Hongqi Sun
标识
DOI:10.1021/acs.est.9b03342
摘要
The maximization of the numbers of exposed active sites in supported metal catalysts is important to achieve high reaction activity. In this work, a simple strategy for anchoring single atom Fe on SBA-15 to expose utmost Fe active sites was proposed. Iron salts were introduced into the as-made SBA-15 containing the template and calcined for simultaneous decomposition of the iron precursor and the template, resulting in single atom Fe sites in the nanopores of SBA-15 catalysts (SAFe-SBA). X-ray diffraction (XRD), UV-vis diffuse reflectance spectroscopy (UV-vis DRS), high-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM), and extended X-ray absorption fine structure (EXAFS) imply the presence of single atom Fe sites. Furthermore, EXAFS analysis suggests the structure of one Fe center with four O atoms, and density functional theory calculations (DFT) simulate this structure. The catalytic performances of SAFe-SBA were evaluated in Fenton-like catalytic oxidation of p-hydroxybenzoic acid (HBA) and phenol. It was found that the single atom SAFe-SBA catalysts displayed superior catalytic activity to aggregated iron sites (AGFe-SBA) in both HBA and phenol degradation, demonstrating the advantage of SAFe-SBA in catalysis.
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