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聚苯胺-氧化铁纳米杂化膜作为多功能无标记电化学和生物磁传感器用于儿茶酚。

Polyaniline-iron oxide nanohybrid film as multi-functional label-free electrochemical and biomagnetic sensor for catechol.

机构信息

Department of Metallurgical Engineering & Materials Science, Indian Institute of Technology Bombay, Powai, Mumbai 400076, Maharashtra, India.

出版信息

Anal Chim Acta. 2013 Sep 17;795:8-14. doi: 10.1016/j.aca.2013.07.043. Epub 2013 Jul 31.

DOI:10.1016/j.aca.2013.07.043
PMID:23998532
Abstract

Polyaniline-iron oxide magnetic nanohybrid was synthesized and characterized using various spectroscopic, microstructural and electrochemical techniques. The smart integration of Fe3O4 nanoparticles within the polyaniline (PANI) matrix yielded a mesoporous nanohybrid (Fe3O4@PANI) with high surface area (94 m(2) g(-1)) and average pore width of 12.8 nm. Catechol is quasi-reversibly oxidized to o-quinone and reduced at the Fe3O4@PANI modified electrodes. The amperometric current response toward catechol was evaluated using the nanohybrid and the sensitivity and detection limit were found to be 312 μA μL(-1) and 0.2 nM, respectively. The results from electrochemical impedance spectroscopy (EIS) indicated that the increased solution resistance (Rs) was due to elevated adsorption of catechol on the modified electrodes. Photoluminescence spectra showed ligand-to-metal charge transfer (LMCT) between p-π orbitals of the phenolate oxygen in catechol and the d-σ* metal orbital of Fe3O4@PANI nanohybrid. Potential dependent spectroelectrochemical behavior of Fe3O4@PANI nanohybrid toward catechol was studied using UV/vis/NIR spectroscopy. The binding activity of the biomagnetic particles to catechol through Brownian relaxation was evident from AC susceptibility measurements. The proposed sensor was used for successful recovery of catechol in tap water samples.

摘要

聚吡咯-氧化铁磁性纳米杂化材料是通过各种光谱、微观结构和电化学技术合成和表征的。将 Fe3O4 纳米粒子智能地整合到聚吡咯(PANI)基质中,得到了具有高表面积(94 m(2) g(-1))和平均孔径为 12.8nm 的介孔纳米杂化材料(Fe3O4@PANI)。邻苯二酚在 Fe3O4@PANI 修饰电极上被准可逆地氧化为邻苯醌并还原。通过纳米杂化材料评估了对邻苯二酚的安培电流响应,灵敏度和检测限分别为 312μAμL(-1)和 0.2nM。电化学阻抗谱(EIS)的结果表明,溶液电阻(Rs)的增加是由于邻苯二酚在修饰电极上的吸附增加所致。光致发光光谱显示邻苯二酚中的酚氧的 p-π 轨道与 Fe3O4@PANI 纳米杂化材料的 d-σ*金属轨道之间存在配体到金属的电荷转移(LMCT)。使用紫外/可见/近红外光谱研究了 Fe3O4@PANI 纳米杂化材料对邻苯二酚的电位依赖性光谱电化学行为。通过交流磁化率测量,明显看出生物磁性颗粒通过布朗松弛与邻苯二酚的结合活性。该传感器成功用于自来水中邻苯二酚的回收。

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