TY - JOUR
T1 - Broadband Coherent Raman Scattering Microscopy
AU - Polli, Dario
AU - Kumar, Vikas
AU - Valensise, Carlo M.
AU - Marangoni, Marco
AU - Cerullo, Giulio
N1 - KAUST Repository Item: Exported on 2021-04-13
Acknowledged KAUST grant number(s): OSR-2016-CRG5-3017-01
Acknowledgements: This work has been supported by European Research Council Consolidator Grant VIBRA (ERC-2014-CoG 648615), Horizon2020 GRAPHENE Flagship (785219), and KAUST (OSR-2016-CRG5-3017-01).
This publication acknowledges KAUST support, but has no KAUST affiliated authors.
PY - 2018/7/31
Y1 - 2018/7/31
N2 - Spontaneous Raman (SR) microscopy allows label-free chemically specific imaging based on the vibrational response of molecules; however, due to the low Raman scattering cross section, it is intrinsically slow. Coherent Raman scattering (CRS) techniques, by coherently exciting vibrational oscillators in the focal volume, increase signal levels by several orders of magnitude under appropriate conditions. In its single-frequency version, CRS microscopy has reached very high imaging speeds, up to the video rate; however, it provides information which is not sufficient to distinguish spectrally overlapped chemical species within complex heterogeneous systems, such as cells and tissues. Broadband CRS combines the acquisition speed of CRS with the information content of SR, but it is technically very demanding. In this Review, the current state of the art in broadband CRS microscopy, both in the coherent anti-Stokes Raman scattering (CARS) and the stimulated Raman scattering (SRS) versions are reviewed. Different technical solutions for broadband CARS and SRS, working both in the frequency and in the time domains, are compared and their merits and drawbacks assessed.
AB - Spontaneous Raman (SR) microscopy allows label-free chemically specific imaging based on the vibrational response of molecules; however, due to the low Raman scattering cross section, it is intrinsically slow. Coherent Raman scattering (CRS) techniques, by coherently exciting vibrational oscillators in the focal volume, increase signal levels by several orders of magnitude under appropriate conditions. In its single-frequency version, CRS microscopy has reached very high imaging speeds, up to the video rate; however, it provides information which is not sufficient to distinguish spectrally overlapped chemical species within complex heterogeneous systems, such as cells and tissues. Broadband CRS combines the acquisition speed of CRS with the information content of SR, but it is technically very demanding. In this Review, the current state of the art in broadband CRS microscopy, both in the coherent anti-Stokes Raman scattering (CARS) and the stimulated Raman scattering (SRS) versions are reviewed. Different technical solutions for broadband CARS and SRS, working both in the frequency and in the time domains, are compared and their merits and drawbacks assessed.
UR - http://hdl.handle.net/10754/668683
UR - http://doi.wiley.com/10.1002/lpor.201800020
UR - http://www.scopus.com/inward/record.url?scp=85053207057&partnerID=8YFLogxK
U2 - 10.1002/lpor.201800020
DO - 10.1002/lpor.201800020
M3 - Article
SN - 1863-8880
VL - 12
SP - 1800020
JO - Laser & Photonics Reviews
JF - Laser & Photonics Reviews
IS - 9
ER -