分析物
化学
多路复用
戒指(化学)
分子
荧光
串联(数学)
拉曼散射
生物信息学
分析化学(期刊)
纳米技术
组合化学
拉曼光谱
材料科学
色谱法
有机化学
生物信息学
基因
生物
组合数学
光学
物理
量子力学
生物化学
数学
作者
Lam Bang Thanh Nguyen,Yong Xiang Leong,Charlynn Sher Lin Koh,Shi Xuan Leong,Siew Kheng Boong,Howard Yi Fan Sim,Gia Chuong Phan‐Quang,In Yee Phang,Xing Yi Ling
出处
期刊:Angewandte Chemie
[Wiley]
日期:2022-06-08
卷期号:61 (33): e202207447-e202207447
被引量:61
标识
DOI:10.1002/anie.202207447
摘要
Abstract Gas‐phase surface‐enhanced Raman scattering (SERS) remains challenging due to poor analyte affinity to SERS substrates. The reported use of capturing probes suffers from concurrent inconsistent signals and long response time due to the formation of multiple potential probe–analyte interaction orientations. Here, we demonstrate the use of multiple non‐covalent interactions for ring complexation to boost the affinity of small gas molecules, SO 2 and NO 2 , to our SERS platform, achieving rapid capture and multiplex detection down to 100 ppm. Experimental and in‐silico studies affirm stable ring complex formation, and kinetic investigations reveal a 4‐fold faster response time compared to probes without stable ring complexation capability. By synergizing spectral concatenation and support vector machine regression, we achieve 91.7 % accuracy for multiplex quantification of SO 2 and NO 2 in excess CO 2 , mimicking real‐life exhausts. Our platform shows immense potential for on‐site exhaust and air quality surveillance.
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