Spectral-focusing CARS spectroscopy driven by an all-PM-fiber gain-managed nonlinear amplifier

We demonstrate a spectral-focusing coherent anti-Stokes Raman scattering (SF-CARS) spectroscopy system driven by a single all-fiber gain-managed nonlinear amplification laser. By exploiting the synergistic interplay between self-phase modulation and normal group-velocity dispersion in the gain fiber, the source directly delivers spectrally broadened pulses with an intrinsically linear chirp (pulse energy >100 nJ), eliminating external pulse stretchers and chirp-matching optics. Leveraging the intrinsic delay–frequency mapping, we achieve broadband SF-CARS detection covering a significant portion of the fingerprint region (500–1200 cm−1) with a spectral resolution of ∼13 cm−1. The system capability for sensitive and multiplex chemical analysis is validated by measurements of gaseous SF6 and liquid mixtures of benzene and DMSO. These results establish a compact, robust excitation architecture that advances SF-CARS toward turn-key coherent Raman spectroscopy and high-speed multi-component imaging.

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Publication Details

Journal
Applied Physics Letters
Published
2026-06-29
DOI
https://doi.org/10.1063/5.0326655
Primary Topic
Spectroscopy Techniques in Biomedical and Chemical Research
Type
article
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Spectral-focusing CARS spectroscopy driven by an all-PM-fiber gain-managed nonlinear amplifier

Jiahui Peng, Qi Xu, Z L Li, Kun Chen et al.
Applied Physics Letters
Spectroscopy Techniques in Biomedical and Chemical Research
article

Spectral-focusing CARS spectroscopy driven by an all-PM-fiber gain-managed nonlinear amplifier

Jiahui Peng, Qi Xu, Z L Li, Kun Chen, Jinlong Zheng, Mingtao Peng, Zhijie Shi, Jing Li
article en

Abstract

We demonstrate a spectral-focusing coherent anti-Stokes Raman scattering (SF-CARS) spectroscopy system driven by a single all-fiber gain-managed nonlinear amplification laser. By exploiting the synergistic interplay between self-phase modulation and normal group-velocity dispersion in the gain fiber, the source directly delivers spectrally broadened pulses with an intrinsically linear chirp (pulse energy >100 nJ), eliminating external pulse stretchers and chirp-matching optics. Leveraging the intrinsic delay–frequency mapping, we achieve broadband SF-CARS detection covering a significant portion of the fingerprint region (500–1200 cm−1) with a spectral resolution of ∼13 cm−1. The system capability for sensitive and multiplex chemical analysis is validated by measurements of gaseous SF6 and liquid mixtures of benzene and DMSO. These results establish a compact, robust excitation architecture that advances SF-CARS toward turn-key coherent Raman spectroscopy and high-speed multi-component imaging.

Applied Physics LettersVol. 128(26)
Wuhan National Laboratory for Optoelectronics (CN), Huazhong University of Science and Technology (CN)
Affordable and clean energy
Openalex Percentile: Top 6%
Spectroscopy Techniques in Biomedical and Chemical Research
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