Interference microscopic imaging method and interference microscope
A technology of interference microscope and microscope objective lens, which is used in the measurement of phase influence characteristics, material analysis by optical means, instruments, etc., which can solve the problems that the numerical aperture of the objective lens cannot be made too large, and the reference optical path cannot be completely symmetrical.
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Embodiment 1
[0040] refer to figure 1 , which is shown in a structural schematic diagram of an embodiment of an interference microscope in this embodiment, specifically, an interference microscope, including:
[0041] Light source generating device, compensation interference cavity, detection arm, signal acquisition and processing unit; wherein,
[0042] The light source generator includes a light-emitting device S with a spectral width and a first lens L1. In this implementation, the light-emitting device S adopts an LED light source with a central wavelength λ0=850nm and a spectral width Δλ=30nm. The light source is collimated by the first lens L1 to become quasi-parallel light;
[0043] The compensation interference cavity includes a first beam splitter BS1, a first mirror M1, a second mirror M2, a first microscope objective MS1, and the first microscope objective MS1 is located between the first beam splitter BS1 and the second mirror M2 Between, the second reflection mirror M2 is at t...
Embodiment 2
[0051] Such as figure 2 As shown, this embodiment adopts the same compensating interference cavity as that of Embodiment 1, except that the image-transmitting unit Green lens rod or the image-transmitting optical fiber bundle (F-B) is inserted into the detection arm. Both the reference light and the sample light are transmitted in the image transmission unit without changing the optical path difference, so endoscopic interference imaging can be realized. The specific imaging process is consistent with that of Embodiment 1, and will not be repeated here.
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