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arXiv · 1705.07236

Scan-less confocal phase microscopy based on dual comb spectroscopy of two-dimensional-image-encoding optical frequency comb

Eiji Hase·Takeo Minamikawa·Shuji Miyamoto·Ryuji Ichikawa·Yi-Da Hsieh·Kyuki Shibuya·Yoshiaki Nakajima·Akifumi Asahara·Kaoru Minoshima·Yasuhiro Mizutani·Tetsuo Iwata·Hirotsugu Yamamoto·Takeshi Yasui
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Abstract

Confocal imaging and phase imaging are powerful tools in life science research and industrial inspection. To coherently link the two techniques with different depth resolutions, we introduce an optical frequency comb (OFC) to microscopy. Two-dimensional (2D) image pixels of a sample were encoded onto OFC modes via 2D spectral encoding, in which OFC acted as an optical carrier with a vast number of discrete frequency channels. Then, a scan-less full-field confocal image with a depth resolution of 62.4 um was decoded from a mode-resolved OFC amplitude spectrum obtained by dual-comb spectroscopy. Furthermore, a phase image with a depth resolution of 13.7 nm was decoded from a mode-resolved OFC phase spectrum under the above confocality. The phase wrapping ambiguity can be removed by the match between the confocal depth resolution and the phase wrapping period. The proposed hybrid microscopy approach will be a powerful tool for a variety of applications.

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Eiji Hase, Takeo Minamikawa, Shuji Miyamoto, Ryuji Ichikawa, Yi-Da Hsieh, Kyuki Shibuya, Yoshiaki Nakajima, Akifumi Asahara, Kaoru Minoshima, Yasuhiro Mizutani, Tetsuo Iwata, Hirotsugu Yamamoto, Takeshi Yasui. 2017-05-20. Scan-less confocal phase microscopy based on dual comb spectroscopy of two-dimensional-image-encoding optical frequency comb. https://doi.org/10.1364/optica.5.000634

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