多环芳烃
拉曼光谱
化学
基质(水族馆)
环境化学
红外光谱学
单层
密度泛函理论
光化学
有机化学
计算化学
生物化学
海洋学
光学
物理
地质学
作者
Andrés B. Sánchez-Alvarado,Jingyi Zhou,Peixuan Jin,Oara Neumann,Thomas P. Senftle,Peter Nordlander,Naomi J. Halas
出处
期刊:ACS Nano
[American Chemical Society]
日期:2023-12-08
卷期号:17 (24): 25697-25706
被引量:4
标识
DOI:10.1021/acsnano.3c10746
摘要
Polycyclic aromatic hydrocarbons (PAHs) constitute a class of universally prevalent carcinogenic environmental contaminants. It is increasingly recognized, however, that PAHs derivatized with oxygen, sulfur, or nitrogen functional groups are frequently more dangerous than their unfunctionalized counterparts. This much larger family of chemicals─polycyclic aromatic compounds─PACs─is far less well characterized than PAHs. Using surface-enhanced Raman and IR Absorption spectroscopies (SERS + SEIRA) combined on a single substrate, along with density functional theoretical (DFT) calculations, we show that direct chemical detection and identification of PACs at sub-parts-per-billion concentration can be achieved. Focusing our studies on 9,10-anthraquinone, 5,12-tetracenequinone, 9-nitroanthracene, and 1-nitropyrene as model PAC contaminants, detection is made possible by incorporating a hydroxy-functionalized self-assembled monolayer that facilitates hydrogen bonding between analytes and the SERS + SEIRA substrate. 5,12-Tetracenequinone was detected at 0.3 ppb, and the limit of detection was determined to be 0.1 ppb using SEIRA alone. This approach is straightforwardly extendable to other families of analytes and will ultimately facilitate fieldable chemical detection of these dangerous yet largely overlooked environmental contaminants.
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