Diffraction Limit Sample for Microscope

In summary, the conversation is about trying to reach the diffraction limit with a light microscope. The person has a microscope with a 2000x magnification limit, but is having trouble finding a good sample with two spots. They have tried using their phone's OLED screen, but the pixels are too far apart. They then turned to MEMS Microphones, which have holes that their microscope can easily resolve. However, creating two small holes close together is difficult. The conversation then shifts to discussing the numerical aperture of the person's lenses and suggests trying swabbing the inside of their cheek or looking at diatoms and microspheres. The conversation ends with a clarification about whether the cells or the objects inside them are sub-diffraction
  • #1
entropy111
3
0
Hi all,

So, I'm trying to "hit" the diffraction limit (i.e. view Rayleigh criterion, or Abbe or Sparrow criterion) with my light microscope . Bought the scope off amazon..it's a typical AmScope that has 2000x magnification limit... But the trouble is I can't find a good sample of two spots.

I used my OLED screen on my phone...but the pixels are 85 microns apart...which my microscope can easily resolve.

Then I turned to MEMS Microsphones http://memsjournal.typepad.com/.a/6a00d8345225f869e20147e315f8a1970b-pi

which i have a few samples of...the perforation holes are 10.5 microns in diatemer, separated by approx 5.56 microns. My scope can easily resolve them.


Preparing two small holes 100-600nm apart from one another would be likely too difficult for me to create.

any ideas on how to view Diffraction Limit, or rayleighs criterion, etc?

I was thinking maybe slides created for Two Slits Interference experiments.


Thank you,
 
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  • #2
What's the numerical aperture of your lens?

Something simple to try: swab the inside of your cheek with a q-tip, and wipe the q-tip on a slide. Add a drop of water, cover with a coverslip, and you'll have hundreds of epithelial cells to look at, full of objects below the diffraction limit. Other objects: diatoms, microspheres, soot.
 
  • #3
NA = .1 though I have other lens.

These are the lens i have: http://ecx.images-amazon.com/images/I/51SnU8iFrNL.jpg

the red one on the right is .1, I can vary from there.

Re the Epithelial cells: so the cells themselves are sub-diffraction limit? Or the things inside them are?

Thank you for your reply.
 
  • #4
entropy111 said:
NA = .1 though I have other lens.

These are the lens i have: http://ecx.images-amazon.com/images/I/51SnU8iFrNL.jpg

the red one on the right is .1, I can vary from there.

Re the Epithelial cells: so the cells themselves are sub-diffraction limit? Or the things inside them are?

Thank you for your reply.

The things inside- your set of lenses are well-suited for looking at cells, either from your mouth or from plants- try peeling off a thin layer from an onion, for example.
 
  • #5


I would suggest using a sample with a pattern that has a known distance between the features, such as a resolution test target or a grating slide. These types of samples are specifically designed for testing the limits of microscope resolution and can help you accurately determine the diffraction limit of your microscope. Additionally, using a high-quality objective lens and optimizing your microscope's settings can also improve your ability to resolve smaller features. If creating your own sample with small holes is too difficult, these other options may be more feasible and reliable for testing the diffraction limit of your microscope.
 

Related to Diffraction Limit Sample for Microscope

1. What is the diffraction limit for a microscope sample?

The diffraction limit for a microscope sample is the smallest distance between two points that can be resolved by the microscope. This limit is determined by the wavelength of light being used and the numerical aperture of the objective lens.

2. How is the diffraction limit calculated?

The diffraction limit for a microscope sample can be calculated using the Abbe diffraction formula, which takes into account the wavelength of light, the numerical aperture of the objective lens, and the refractive index of the medium being used.

3. Can the diffraction limit be improved?

Yes, the diffraction limit for a microscope sample can be improved by using a shorter wavelength of light, increasing the numerical aperture of the objective lens, or using specialized techniques such as deconvolution or super-resolution microscopy.

4. What happens if the diffraction limit is exceeded?

If the diffraction limit is exceeded, the microscope will not be able to distinguish between two closely spaced points and they will appear as one blurred point. This can result in a loss of resolution and detail in the image.

5. How does the diffraction limit affect the quality of microscope images?

The diffraction limit directly affects the resolution and clarity of microscope images. A smaller diffraction limit means that finer details can be resolved and the image will appear sharper and more detailed. A larger diffraction limit can result in a lower quality image with less resolution and detail.

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