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Optical image amplification in dual-comb microscopy
Dual-comb microscopy (DCM), based on a combination of dual-comb spectroscopy (DCS) with two-dimensional spectral encoding (2D-SE), is a promising method for scan-less confocal laser microscopy giving an amplitude and phase image contrast with the confocality. However, signal loss in a 2D-SE optical...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239846/ https://www.ncbi.nlm.nih.gov/pubmed/32433533 http://dx.doi.org/10.1038/s41598-020-64927-z |
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author | Mizuno, Takahiko Tsuda, Takuya Hase, Eiji Tokizane, Yu Oe, Ryo Koresawa, Hidenori Yamamoto, Hirotsugu Minamikawa, Takeo Yasui, Takeshi |
author_facet | Mizuno, Takahiko Tsuda, Takuya Hase, Eiji Tokizane, Yu Oe, Ryo Koresawa, Hidenori Yamamoto, Hirotsugu Minamikawa, Takeo Yasui, Takeshi |
author_sort | Mizuno, Takahiko |
collection | PubMed |
description | Dual-comb microscopy (DCM), based on a combination of dual-comb spectroscopy (DCS) with two-dimensional spectral encoding (2D-SE), is a promising method for scan-less confocal laser microscopy giving an amplitude and phase image contrast with the confocality. However, signal loss in a 2D-SE optical system hampers increase in image acquisition rate due to decreased signal-to-noise ratio. In this article, we demonstrated optical image amplification in DCM with an erbium-doped fiber amplifier (EDFA). Combined use of the image-encoded DCS interferogram and the EDFA benefits from not only the batch amplification of amplitude and phase images but also significant rejection of amplified spontaneous emission (ASE) background. Effectiveness of the optical-image-amplified DCM is highlighted in the single-shot quantitative nanometer-order surface topography and the real-time movie of polystyrene beads dynamics under water convection. The proposed method will be a powerful tool for real-time observation of surface topography and fast dynamic phenomena. |
format | Online Article Text |
id | pubmed-7239846 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-72398462020-05-29 Optical image amplification in dual-comb microscopy Mizuno, Takahiko Tsuda, Takuya Hase, Eiji Tokizane, Yu Oe, Ryo Koresawa, Hidenori Yamamoto, Hirotsugu Minamikawa, Takeo Yasui, Takeshi Sci Rep Article Dual-comb microscopy (DCM), based on a combination of dual-comb spectroscopy (DCS) with two-dimensional spectral encoding (2D-SE), is a promising method for scan-less confocal laser microscopy giving an amplitude and phase image contrast with the confocality. However, signal loss in a 2D-SE optical system hampers increase in image acquisition rate due to decreased signal-to-noise ratio. In this article, we demonstrated optical image amplification in DCM with an erbium-doped fiber amplifier (EDFA). Combined use of the image-encoded DCS interferogram and the EDFA benefits from not only the batch amplification of amplitude and phase images but also significant rejection of amplified spontaneous emission (ASE) background. Effectiveness of the optical-image-amplified DCM is highlighted in the single-shot quantitative nanometer-order surface topography and the real-time movie of polystyrene beads dynamics under water convection. The proposed method will be a powerful tool for real-time observation of surface topography and fast dynamic phenomena. Nature Publishing Group UK 2020-05-20 /pmc/articles/PMC7239846/ /pubmed/32433533 http://dx.doi.org/10.1038/s41598-020-64927-z Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Mizuno, Takahiko Tsuda, Takuya Hase, Eiji Tokizane, Yu Oe, Ryo Koresawa, Hidenori Yamamoto, Hirotsugu Minamikawa, Takeo Yasui, Takeshi Optical image amplification in dual-comb microscopy |
title | Optical image amplification in dual-comb microscopy |
title_full | Optical image amplification in dual-comb microscopy |
title_fullStr | Optical image amplification in dual-comb microscopy |
title_full_unstemmed | Optical image amplification in dual-comb microscopy |
title_short | Optical image amplification in dual-comb microscopy |
title_sort | optical image amplification in dual-comb microscopy |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7239846/ https://www.ncbi.nlm.nih.gov/pubmed/32433533 http://dx.doi.org/10.1038/s41598-020-64927-z |
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