Raman microscopy is a powerful analytical technique for materials and life sciences that enables mapping the spatial distribution of the chemical composition of a sample. State-of-the-art Raman microscopes, based on point-scanning frequency-domain detection, have long (∼1s) pixel dwell times, making it challenging to acquire images of a significant area (e.g., 100×100µm). Here we present a compact wide-field Raman microscope based on a time-domain Fourier-transform approach, which enables parallel acquisition of the Raman spectra on all pixels of a 2D detector. A common-path birefringent interferometer with exceptional delay stability and reproducibility can rapidly acquire Raman maps (∼30min for a 250000pixel image) with high spatial (<1µm) and spectral (∼23cm−1) resolutions. Time-domain detection allows us to disentangle fluorescence and Raman signals, which can both be measured separately. We validate the system by Raman imaging plastic microbeads and demonstrate its multimodal operation by capturing fluorescence and Raman maps of a multilayer-WSe2 sample, providing complementary information on the strain and number of layers of the material.

High-throughput multimodal wide-field Fourier-transform Raman microscope

Bassi, A.;Candeo, A.;Genco, A.;Valentini, G.;Vanna, R.
Writing – Review & Editing
;
Manzoni, C.
Ultimo
Conceptualization
2023

Abstract

Raman microscopy is a powerful analytical technique for materials and life sciences that enables mapping the spatial distribution of the chemical composition of a sample. State-of-the-art Raman microscopes, based on point-scanning frequency-domain detection, have long (∼1s) pixel dwell times, making it challenging to acquire images of a significant area (e.g., 100×100µm). Here we present a compact wide-field Raman microscope based on a time-domain Fourier-transform approach, which enables parallel acquisition of the Raman spectra on all pixels of a 2D detector. A common-path birefringent interferometer with exceptional delay stability and reproducibility can rapidly acquire Raman maps (∼30min for a 250000pixel image) with high spatial (<1µm) and spectral (∼23cm−1) resolutions. Time-domain detection allows us to disentangle fluorescence and Raman signals, which can both be measured separately. We validate the system by Raman imaging plastic microbeads and demonstrate its multimodal operation by capturing fluorescence and Raman maps of a multilayer-WSe2 sample, providing complementary information on the strain and number of layers of the material.
2023
Istituto di fotonica e nanotecnologie - IFN
multimodal, wide-field, Fourier-transform, Raman, microscope
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/505146
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