Aperture settings for microscope objective simulation

  • 10 November 2021
  • 4 replies
  • 780 views

Hello, 

 

I am new to Zemax OpticStudio. I’m currently working on the simulate the existing microscope objective we have in the lab. However, I am not sure what will be the best aperture settings for the Zemax simulation. 

I used Object Space NA because I have the specs of the microscope objective as 10X with NA0.25. Can I ask if the Object Space NA will be the most suitable choice for the aperture settings in my scenario because I do not need to do any optimisation of the lens data.

Another issue is if I used Object Space NA will have some light rays not converged to the image plane. Is that will be a problem? 

I have attached the Zemax simulation file here. 

Many thanks.  

 


4 replies

Userlevel 7
Badge +2

Hi Kevin,

 

For this kind of exercise, I would use the Float By Stop Size aperture definition, and if you want to make a forward model, you might be required to enable ray-aiming.

Under this aperture definition, you can fix your STOP semi-diameter and OpticStudio will fill it. How do you know the aperture size? If you know the objective lens manufacturer, you can deduce the focal length of their tube lens. The most popular ones are 200 mm for Nikon, Leica, Mitutoyo, and Thorlabs, 180 mm for Olympus, and 164.5 mm for Zeiss. Since you have the magnification (10X), and the magnification is the ratio between the tube lens and objective lens focal length, you can deduce your objective lens focal length. For example, if you have a Nikon objective, your objective focal length is 200 / 10 = 10 mm. Then, the NA is the sine of half the acceptance angle, which is calculated as atan( semi-diameter / focal length ). Therefore semi-diameter = tan( asin( NA ) ) * focal length = 2.582 mm.

As for your other issue, you seem to have fixed the semi-diameter of your lenses, therefore it puts an aperture on them (you can read (aper) in the left column) and if the rays don’t pass through the aperture, they are terminated.

Let me know if this helps, and take care,

 

David

Hi David, 

 

Thanks so much for your quick reply. I think I fixed the STOP semi-diameter and changed the aperture settings as you mentioned. It works fine and thanks again for pointing out the issues and comprehensive explaination. 

 

Many thanks and have a nice day, 

Kevin 

Userlevel 7
Badge +3

Also, use Cosine-Cubed Apodization of the pupil to include the non-uniform pupil illumination produced by a point source irradiating a close pupil.

  • M
Userlevel 7
Badge +2

That’s really interesting @Mark.Nicholson! Could you elaborate on this particular topic? I’m thinking about the case of fluorescence microscopy, where a fluorophore would emit light uniformly. Would you still use the cosine-cubed, and why this one in particular?

Thank you in advance, and take care,

 

David

Reply