kubikat said:
My lenses are AR coated I think. I was thinking about buying some more lenses (maybe getting the plano-convex ones) and uncoated ones are a lot cheaper... would they still work for what I am doing? I mean the laser I am using is 80 mW and I read that 10 mW is usually enough for trapping, so I can afford losing a lot of power.
And I am not using the IR-viewer (we don't have one)... I use a card. Or just turn the power of the beam down and look at it with naked eye (since the beam is only 780 nm I can see it and looking at it with naked eye makes alignment a lot easier)
Redbelly98 said:
It's good that you have extra power to spare in terms of being able to see the reflected beams.
Hmmm, I'll defer that question to Andy... but it sounds like you could be okay with uncoated ones, if your project budget is tight.
I would use AR coated lenses, for a couple of reasons:
1) Since you can adjust the power output of the diode directly, you can always dial down the trap power that way. Using AR lenses will increase the maximum trap force, which can translate into the ability to trap smaller objects, or objects with a smaller index mismatch.
2) The microscope objective was (most likely) not designed to image 780 nm light, and so the lens aberrations and the transmission will be worse than the visible.
Personally, I can't see 780 nm light directly; I'd have to use an IR viewer (mine's a View-It, genetically identical to the Find-R-Scope). So I'd always run the laser at full power and wear glasses. Plus, I'm not very familiar with your diode source, but I wonder if the beam characteristics change when you dial down so much.
Then, of course, there's the issue of what happens to the scattered light (off a non AR lens)- the light has to go somewhere. My systems have been built on upright microscopes, which places the beam line directly at eye level. This does not make the safety people happy. Again, 780 nm is on the edge of visibility, so you (or someone else using your system) may not have a blink reflex, which could translate into eye damage.
One bit of advice on alignment technique- *always* align to the laser beam. Assuming you are not using a microscope, the alignment steps proceed: shine beam directly onto the sample, then place lens #1 in the path, center and adjust tip/tilt. Then add lens #2, repeat the alignment steps, the add the microscope objective. Once that has all be done, perform final alignment by imaging the focused laser (I replace the samples with a mirror) and adjust first the objective, then lens #2, then lens #1 to minimize the various aberrations.
If you are using a microscope, then first align the beam to the microscope optical axis, then proceed as above. If there are mirrors, align them all prior to adding any lenses. I perform my final alignment by adjusting the mirror tip/tilt, rather than the lenses.
I guess, after all this discussion, I am wondering why the Airy pattern was present at the focus of lens #1 in the first place: can you reproduce the original setup and verify that?