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Optimization of Fiber Amplifier Design for Stimulated Raman Scattering Microscopy

  • Christian H. Allen
  • , Ahmed M. Othman
  • , Justin R. Gagnon
  • , Teresa Buragina
  • , Hussein Kotb
  • , Sangeeta Murugkar

Research output: Contribution to journalArticlepeer-review

Abstract

Spectral focusing is a rapid, reliable, and simple method for acquiring hyperspectral coherent Raman images using chirped femtosecond lasers. Previous work has demonstrated the use of a parabolic fiber amplifier for Stokes pulse amplification, which increases the bandwidth of Stokes pulses in stimulated Raman scattering (SRS) microscopy with spectral focusing, thereby expanding the spectral range. However, determining the optimal parameters of the fiber amplifier design — such as fiber lengths, input pump power, and peak power of the input Stokes pulse being amplified — has not been explored in depth for this application. In this study, we performed numerical simulations to find the ideal fiber amplifier parameters to address this limitation. We constructed a Stokes pulse fiber amplifier (SPFA) using fiber section lengths that produced the optimal combination of high-power spectral density, spectral bandwidth, chirp rate, and chirp linearity for the amplified Stokes pulse, and verified the results empirically. We demonstrate the high-quality performance of the SRS microscope with the integrated SPFA for imaging biological samples with a spectral range increased to 400 cm-1 from the typical 200 cm-1 without such amplification. This work provides valuable insights and detailed analysis for those looking to build similar systems, offering important information that has not been thoroughly addressed in previous literature.

Original languageEnglish
Article number7100110
JournalIEEE Journal of Selected Topics in Quantum Electronics
Volume32
Issue number4
DOIs
StatePublished - 2026

Funding

This work was supported by the Government of Canada’s Natural Sciences and Engineering Research Council (NSERC) of Canada under Grant RGPIN-2022-04897 (SM). The authors would like to thank to Prof. Hanan Anis at University of Ottawa for the loan of the optical spectrum analyzer, and to Dr. Vinita Chauhan at Health Canada for lab equipment. Thanks to Olay Chen and Max Pijacki at Carleton University for help with the electronic circuit for the OPM unit of the SPFA. Thanks to Dr. Premkumari Kumarathasan and Dr. Nazila Nazemof at Health Canada for the SHSY5Y cell samples and Prof. Alfonso Abizaid in the Department of Neuroscience at Carleton University for the frozen mouse ear skin tissue samples. Received 2 May 2025; revised 28 August 2025; accepted 28 September 2025. Date of publication 1 October 2025; date of current version 15 October 2025. This work was supported by the Government of Canada’s Natural Sciences and Engineering Research Council (NSERC) of Canada under Grant RGPIN-2022-04897 (SM). (Corresponding authors: Christian H. Allen; Sangeeta Murugkar.) Christian H. Allen was with the Department of Physics, Carleton University, Ottawa, ON K1S5B6, Canada. He is now with the Molecular and Cellular Imaging group at Oak Ridge National Laboratory, Oak Ridge, TN 37831 USA (e-mail: [email protected]).

Keywords

  • Stimulated Raman scattering (SRS) microscopy
  • chirp
  • microscopy
  • optical amplification
  • optics
  • pulsed lasers
  • ytterbium doped fiber amplifier

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