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A versatile Raman setup with time-gating and fast wide-field imaging capabilities.
Mooij, Bram J A; Schmidt, Robert W; Vijvers, Wouter A J; Ariese, Freek.
Afiliación
  • Mooij BJA; LaserLaB, Faculty of Sciences, Vrije Universiteit Amsterdam, de Boelelaan 1081, 1081 HV, Amsterdam, The Netherlands. Electronic address: bja.mooij@gmail.com.
  • Schmidt RW; LaserLaB, Faculty of Sciences, Vrije Universiteit Amsterdam, de Boelelaan 1081, 1081 HV, Amsterdam, The Netherlands.
  • Vijvers WAJ; Chromodynamics B.V., High Tech Campus 12, 5656 AE Eindhoven, The Netherlands.
  • Ariese F; LaserLaB, Faculty of Sciences, Vrije Universiteit Amsterdam, de Boelelaan 1081, 1081 HV, Amsterdam, The Netherlands.
Spectrochim Acta A Mol Biomol Spectrosc ; 318: 124388, 2024 Oct 05.
Article en En | MEDLINE | ID: mdl-38795525
ABSTRACT
Raman spectroscopy is a well-established method for chemical identification, with a wide variety of applications. The two major limitations are that fluorescence can hamper detection, and that Raman imaging is slow; it typically takes multiple hours to measure even a small surface area. We have developed a multimodal setup that mitigates these limitations. The setup has a point-scanning mode that allows for time-gated as well as continuous Raman spectroscopy, and both modes use an 80 MHz, 532 nm excitation laser with up to 20 W of power. The fluorescence suppression capabilities of the setup were demonstrated by comparing time-gated to continuous detection of a Dracaena leaf. Raman bands showed a 4-8 times improvement in signal-to-background ratio, and one band that was invisible in the continuous measurement, became visible in the time-gated measurement. The setup also has a 4-band simultaneously detected wide-field mode. Using a set of beam splitters, the Raman signal from the sample is split. This signal is imaged onto four separate cameras, each with a specific band-pass filter. The wide-field data were processed using principal component analysis with k-means clustering. To illustrate the wide-field capabilities of the setup, a 1mm2 sample containing aspirin, caffeine and paracetamol was measured using 10 W excitation power. A 10-second measurement enabled identification of the compounds, and a 1-second measurement showed promising results. This brings the setup close to real-time imaging, showing great potential for applications in quality control or for measuring samples that change over time.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Spectrochim Acta A Mol Biomol Spectrosc Asunto de la revista: BIOLOGIA MOLECULAR Año: 2024 Tipo del documento: Article Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Spectrochim Acta A Mol Biomol Spectrosc Asunto de la revista: BIOLOGIA MOLECULAR Año: 2024 Tipo del documento: Article Pais de publicación: Reino Unido