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Green-synthesized Cu 2 O nanoaggregates incorporated on β-cyclodextrin for catalytic reduction and electrochemical sensing
Journal of the Iranian Chemical Society ( IF 2.2 ) Pub Date : 2020-06-08 , DOI: 10.1007/s13738-020-01954-7
Jaise Mariya George , Beena Mathew

Abstract

Microwave-assisted methods are facile synthetic routes for the synthesis of nanoparticles. Cu2O nanoaggregates (Cu2O NA) were synthesized using Bauhinia purpurea (B. purpurea) leaf extract via microwave method. The incorporation of Cu2O NA in β-cyclodextrin generated Cu2O-β-CD nanocomposite (Cu2O-β-CD NC). The structure and morphology of the Cu2O-β-CD NC were investigated using characterization techniques like Fourier transform infrared spectroscopy, X-ray photoelectron spectroscopy, X-ray diffraction, scanning electron microscopy, transmission electron microscopy, and atomic force microscopy. The crystallines Cu2O NA and Cu2O-β-CD NC have size 30.65 and 19.73 nm, respectively. The Cu2O-β-CD NC revealed excellent catalytic activities for the reduction of nitro aromatic compounds in the presence of NaBH4. Gold electrode modified with Cu2O-β-CD NC is effective for the sensing levofloxacin. The electrocatalytic performance of the modified electrode was optimized, and the limit of detection was found to be 6.93 nM. The synergistic effect between the semiconductor Cu2O nanoaggregates and high adsorption capability of β-CD provided a better platform for the fast degradation of 4-nitrophenol and enhanced sensitivity for the determination of levofloxacin.

Graphic abstract



中文翻译:

β-环糊精中绿色合成的Cu 2 O纳米聚集体,用于催化还原和电化学传感

摘要

微波辅助方法是合成纳米颗粒的简便合成途径。利用紫荆花B. purpurea)叶提取物通过微波法合成了Cu 2 O纳米聚集体(Cu 2 O NA)。Cu的掺入2 öNA在β环糊精生成的Cu 2 O-β-CD纳米复合材料(铜2 O-β-CD NC)。的Cu的结构和形态2使用的表征技术像傅里叶变换红外光谱,X射线光电子能谱法,X射线衍射O-β-CD NC进行了调查,扫描电子显微镜,透射电子显微镜和原子力显微镜。晶体Cu 2ÒNA和Cu 2 O-β-CD NC分别具有大小30.65 19.73和纳米。在Cu 2 O-β-CD NC揭示了硝基芳族化合物的硼氢化钠中的存在降低优异的催化活性4。与铜修饰的金电极2 O-β-CD NC是有效的所述感测的左氧氟沙星。优化了修饰电极的电催化性能,发现极限为6.93 nM。半导体Cu 2 O纳米聚集体与β-CD的高吸附能力之间的协同效应为4-硝基苯酚的快速降解提供了更好的平台,并提高了左氧氟沙星的测定灵敏度。

图形摘要

更新日期:2020-06-08
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