4.6 Article

Background-free imaging of chemical bonds by a simple and robust frequency-modulated stimulated Raman scattering microscopy

Journal

OPTICS EXPRESS
Volume 28, Issue 10, Pages 15663-15677

Publisher

OPTICAL SOC AMER
DOI: 10.1364/OE.391016

Keywords

-

Categories

Funding

  1. National Institute of General Medical Sciences [R01 GM128214, R01 GM132860]
  2. National Science Foundation [1904684]
  3. Direct For Mathematical & Physical Scien
  4. Division Of Chemistry [1904684] Funding Source: National Science Foundation

Ask authors/readers for more resources

Being able to image chemical bonds with high sensitivity and speed, stimulated Raman scattering (SRS) microscopy has made a major impact in biomedical optics. However, it is well known that the standard SRS microscopy suffers from various backgrounds, limiting the achievable contrast, quantification and sensitivity. While many frequency-modulation (FM) SRS schemes have been demonstrated to retrieve the sharp vibrational contrast, they often require customized laser systems and/or complicated laser pulse shaping or introduce additional noise, thereby hindering wide adoption. Herein we report a simple but robust strategy for FM-SRS microscopy based on a popular commercial laser system and regular optics. Harnessing self-phase modulation induced self-balanced spectral splitting of picosecond Stokes beam propagating in standard single-mode silica fibers, a high-performance FM-SRS system is constructed without introducing any additional signal noise. Our strategy enables adaptive spectral resolution for background-free SRS imaging of Raman modes with different linewidths. The generality of our method is demonstrated on a variety of Raman modes with effective suppressing of backgrounds including non-resonant cross phase modulation and electronic background from two-photon absorption or pump-probe process. As such, our method is promising to be adopted by the SRS microscopy community for background-free chemical imaging. (c) 2020 Optical Society of America under the terms of the OSA Open Access Publishing Agreement

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available