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Riek C, Kocher C, Zirak P, et al. Stimulated Raman scattering microscopy by Nyquist modulation of a two-branch ultrafast fiber source. Opt Lett. 2016;41(16):3731-4doi: 10.1364/OL.41.003731.
Riek, C., Kocher, C., Zirak, P., Kölbl, C., Fimpel, P., Leitenstorfer, A., Zumbusch, A., & Brida, D. (2016). Stimulated Raman scattering microscopy by Nyquist modulation of a two-branch ultrafast fiber source. Optics letters, 41(16), 3731-4. https://doi.org/10.1364/OL.41.003731
Riek, Claudius, et al. "Stimulated Raman scattering microscopy by Nyquist modulation of a two-branch ultrafast fiber source." Optics letters vol. 41,16 (2016): 3731-4. doi: https://doi.org/10.1364/OL.41.003731
Riek C, Kocher C, Zirak P, Kölbl C, Fimpel P, Leitenstorfer A, Zumbusch A, Brida D. Stimulated Raman scattering microscopy by Nyquist modulation of a two-branch ultrafast fiber source. Opt Lett. 2016 Aug 15;41(16):3731-4. doi: 10.1364/OL.41.003731. PMID: 27519075.
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Opt Lett. 2016 Aug 15;41(16):3731-4. doi: 10.1364/OL.41.003731.

Stimulated Raman scattering microscopy by Nyquist modulation of a two-branch ultrafast fiber source.

Optics letters

Claudius Riek, Claudius Kocher, Peyman Zirak, Christoph Kölbl, Peter Fimpel, Alfred Leitenstorfer, Andreas Zumbusch, Daniele Brida

PMID: 27519075 DOI: 10.1364/OL.41.003731

Abstract

A highly stable setup for stimulated Raman scattering (SRS) microscopy is presented. It is based on a two-branch femtosecond Er:fiber laser operating at a 40 MHz repetition rate. One of the outputs is directly modulated at the Nyquist frequency with an integrated electro-optic modulator (EOM). This compact source combines a jitter-free pulse synchronization with a broad tunability and allows for shot-noise limited SRS detection. The performance of the SRS microscope is illustrated with measurements on samples from material science and cell biology.

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