拉曼光谱
光谱学
荧光
相干反斯托克斯拉曼光谱
荧光光谱法
分子振动
激发态
分子
分析化学(期刊)
红外光谱学
化学
材料科学
拉曼散射
光学
原子物理学
物理
色谱法
量子力学
有机化学
作者
Phillip C. McCann,K. Hiramatsu,Keisuke Goda
标识
DOI:10.1021/acs.jpclett.1c01741
摘要
Fluorescence-encoded vibrational spectroscopy has become increasingly more popular by virtue of its high chemical specificity and sensitivity. However, current fluorescence-encoded vibrational spectroscopy methods lack sensitivity in the low-frequency region, which if addressed could further enhance their capabilities. Here, we present a method for highly sensitive low-frequency fluorescence-encoded vibrational spectroscopy, termed fluorescence-encoded time-domain coherent Raman spectroscopy (FLETCHERS). By first exciting molecules into vibrationally excited states and then promoting the vibrating molecules to electronic states at varying times, the molecular vibrations can be encoded onto the emitted time-domain fluorescence intensity. We demonstrate the sensitive low-frequency detection capability of FLETCHERS by measuring vibrational spectra in the lower fingerprint region of rhodamine 800 solutions as dilute as 250 nM, which is ∼1000 times more sensitive than conventional vibrational spectroscopy. These results, along with further improvement of the method, open up the prospect of performing single-molecule vibrational spectroscopy in the low-frequency region.
科研通智能强力驱动
Strongly Powered by AbleSci AI