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用于选择性测定多环芳烃电子给体-受体陷阱的两用表面增强拉曼光谱传感器

Dual-Purpose SERS Sensor for Selective Determination of Polycyclic Aromatic Compounds Electron Donor-Acceptor Traps.

作者信息

Eremina Olga E, Sergeeva Elena A, Ferree Mariia V, Shekhovtsova Tatyana N, Goodilin Eugene A, Veselova Irina A

机构信息

Chemistry Department, Lomonosov Moscow State University, 1 Lenin Hills, Moscow 119991, Russia.

Faculty of Materials Science, Lomonosov Moscow State University, 1 Lenin Hills, Moscow 119991, Russia.

出版信息

ACS Sens. 2021 Mar 26;6(3):1057-1066. doi: 10.1021/acssensors.0c02294. Epub 2021 Feb 2.

Abstract

Toxic, carcinogenic, and mutagenic properties of polycyclic aromatic hydrocarbons (PAHs) and environmental pollution caused by polycyclic aromatic sulfur heterocycles (PASHs) postulate the importance of their selective and sensitive determination in environmental and oil fuel samples. Surface-enhanced Raman spectroscopy (SERS) opens up an avenue toward multiplex analysis of complex mixtures, however not every molecule gives high enhancement factors and, thus, cannot be reliably detected SERS. However, the sensitivity can be drastically increased by additional resonant enhancement as a result of the analyte absorption band overlapping with the surface plasmon band of nanoparticles (NPs) and the laser excitation wavelength. Using this idea, we developed a dual-purpose SERS sensor based on trapping the target PAHs and PASHs into colored charge-transfer complexes (CTCs) with selected organic π-acceptor molecules on the surface of AgNPs. Studying, computing, and then comparing stability constants of the formed CTC served as a powerful explanation and prediction tool for a wise choice of π-acceptor indicator systems for the further silver surface modification. Moreover, we show that CTC formation can be effectively utilized for increasing both selectivity and sensitivity by simple liquid-liquid extraction prior to SERS measurements. For the first time, the dual-purpose SERS sensor allowed determination of two different classes of polycyclic aromatic fuel components down to 10 nM concentration, lower than that restricted by the ASTM regulation, and demonstrated multi-purpose capabilities of the developed approach.

摘要

多环芳烃(PAHs)的毒性、致癌性和致突变性以及多环芳族硫杂环化合物(PASHs)造成的环境污染表明,在环境和石油燃料样品中对它们进行选择性和灵敏测定具有重要意义。表面增强拉曼光谱(SERS)为复杂混合物的多重分析开辟了一条途径,然而并非每个分子都具有高增强因子,因此无法通过SERS可靠检测。不过,由于分析物吸收带与纳米颗粒(NPs)的表面等离子体带以及激光激发波长重叠,通过额外的共振增强可大幅提高灵敏度。基于这一理念,我们开发了一种两用SERS传感器,该传感器通过将目标PAHs和PASHs捕获到与AgNPs表面选定的有机π受体分子形成的有色电荷转移络合物(CTCs)中。研究、计算并比较所形成CTCs的稳定常数,可为明智选择用于进一步银表面修饰的π受体指示剂系统提供有力的解释和预测工具。此外,我们表明,在SERS测量之前,通过简单的液液萃取,CTCs的形成可有效地用于提高选择性和灵敏度。首次,这种两用SERS传感器能够测定低至10 nM浓度的两类不同的多环芳烃燃料成分,低于美国材料与试验协会(ASTM)规定的限制,并展示了所开发方法的多功能性。

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