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Electrogenerated Thin Films of Microporous Polymer Networks with Remarkably Increased Electrochemical Response to Nitroaromatic Analytes

机译:微孔聚合物网络的电生薄膜对硝基芳族化合物的电化学响应显着提高

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摘要

Thin films of microporous polymer networks (MPNs) have been generated by electrochemical polymerization of a series of multifunctional carbazole-based monomers. The microporous films show high Brunauer-Emmett-Teller (BET) surface areas up to 1300 m(2) g(-1) as directly measured by krypton sorption experiments. A correlation between the number of polymerizable carbazole units of the monomer and the resulting surface area is observed. Electrochemical sensing experiments with 1,3,5-trinitrobenzene as prototypical nitroaromatic analyte demonstrate an up to 180 times increased current response of MPN-modified glassy carbon electrodes in relation to the nonmodified electrode. The phenomenon probably involves intermolecular interactions between the electron-poor nitroaromatic analytes and the electron-rich, high surface area microporous deposits, with the electrochemical reduction at the MPN-modified electrodes being an adsorption-controlled process for low scan rates. We expect a high application potential of such MPN-modified electrodes for boosting the sensitivity of electrochemical sensor devices.
机译:微孔聚合物网络(MPN)的薄膜是通过一系列多官能咔唑基单体的电化学聚合反应生成的。通过k吸附实验直接测量,微孔膜显示高达1300 m(2)g(-1)的高Brunauer-Emmett-Teller(BET)表面积。观察到单体的可聚合咔唑单元的数目与所得表面积之间的相关性。用1,3,5-三硝基苯作为典型的硝基芳香族分析物的电化学传感实验表明,与未修饰的电极相比,MPN修饰的玻璃碳电极的电流响应提高了多达180倍。该现象可能涉及贫电子的硝基芳族分析物与富电子的高表面积微孔沉积物之间的分子间相互作用,而MPN修饰电极上的电化学还原是低扫描速率的吸附控制过程。我们期望这种MPN修饰电极在提高电化学传感器装置的灵敏度方面具有很高的应用潜力。

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