扩展X射线吸收精细结构
光催化
材料科学
X射线光电子能谱
氧烷
光谱学
铜
吸收光谱法
无机化学
分析化学(期刊)
催化作用
化学
化学工程
有机化学
工程类
冶金
物理
量子力学
作者
Tihana Čižmar,Ivana Panžić,Ivana Capan,Andreja Gajović
标识
DOI:10.1016/j.apsusc.2021.151026
摘要
We investigated the role of Cu(II) ions, their local atomic structure and chemical state in the Cu-modified immobilized nanostructured TiO2 photocatalysts used for imidacloprid degradation under UV/VIS-radiation. Catalyst samples were prepared via electrochemical anodization and modified with different Cu concentrations (0.2–1 M). The catalysts’ structure and morphology were characterized by X-ray diffraction, Raman spectroscopy, Scanning Electron Microscopy and Energy Dispersive X-ray spectroscopy, UV–VIS-NIR spectroscopy, Photoluminescence spectroscopy and X-ray absorption spectroscopy: extended X-ray absorption fine structure and X-ray absorption near edge structure. The EXAFS results indicate formation of Ti–O–Cu connections, suggesting that the Cu(II) cations are attached to TiO2 surface which contributes to the photocatalytic activity improvement, i.e. Cu(II) ions are free electron traps that reduce high recombination rate of photo generated charge carriers. The results here demonstrate the role of Cu(II) cations on photocatalytic activity of the [email protected]2 photocatalyst.
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