Relative efficiency of SHG vs SFG

  • #1
fevemo
3
1
TL;DR Summary
Is a SHG process (936 nm to 468 nm) similar in efficiency to a SFG process (850 nm+1040 nm to 468 nm) assuming same properties of the two lasers (both fs pulsed, same focal spot, same polarization, etc.?
I am trying to align two ~100-140 fs pulsed lasers, one at 1040 nm and one between 750-950 nm through a working custom 2p microscope. The end goal is to do stimulated Raman (CARS and SRS) which requires the two beams to be coincident and the pulses to be perfectly synchronized in time, however for now I am testing using a crystal that generates second harmonics signal.

To find the temporal alignment I look at the blue channel (~475 nm) signal from the microscope and maximize the SFG signal coming from the crystals when both the laser beams are enabled (1040 nm + 850 nm) by moving a delay line for the 1040 nm beam. This procedure works well and I can consistently find a small (200-300 fs) window where the SFG signal is clearly visible. This signal scales linearly with the power of each laser which reassures me it is in fact SFG.

Now the problem I am facing is that once I try to get some CARS/SRS signal there is practically none, even with samples that should generate very large responses. Going back to SFG I noticed that the efficiency is significantly lower than just setting the tunable beam to 936 nm. To get a similar intensity from SFG I need almost 10x more power on the sample than when using SHG with a single 936 nm beam (68 mW vs 7.4 mW). Obviously, I would expect for a single beam to be more efficient than two superimposed beams of different wavelengths, but 10x more power feels like too much. Is this an indicator that the focal points of the two beams are barely overlapping or is the 10x lower efficiency within reason for a properly aligned setup?

P.S.: I am aware CARS and SRS are usually done with ps pulsed lasers because of the spectral resolution required, I'm not concerned about resolution at the moment and fs-based CARS and SRS have been shown to work and even generate a stronger signal in some cases. Also, to add to the mystery, a previous version of this setup worked and gave me a decent SRS signal.
 
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  • #2
I wonder if this is a dispersion thing because the wavelengths are different. Besides the sources, sample(s), and detectors what other optical elements are in your beam path?
 
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  • #3
Andy Resnick said:
I wonder if this is a dispersion thing because the wavelengths are different. Besides the sources, sample(s), and detectors what other optical elements are in your beam path?
Yes, maybe walkoff losses? SFG can sometimes work better if the beams aren't colinear.
 
  • #4
DaveE said:
Yes, maybe walkoff losses? SFG can sometimes work better if the beams aren't colinear.
Another good guess- it depends on the nonlinear crystal and specific phase matching condition.
 
  • #5
Thanks for the replies!

Andy Resnick said:
I wonder if this is a dispersion thing because the wavelengths are different. Besides the sources, sample(s), and detectors what other optical elements are in your beam path?
This has definitely been one of my suspects.
The current setup has the 1040 beam going through a delay line with ~10 silver mirrors, a 2X beam shrinker (to compensate for the divergence of the extra path length), and then joins the tunable beam using a notch filter. After that they both go through a beam expander (not ideal IMO), ~8 more mirrors, and then the microscope (scan + tube lenses, galvos, dichroic mirror, objective)

Some extra info that might be relevant:
  • The laser has GDD pre-compensation for the tunable beam and the best SFG signal is obtained when using the maximum pre-compensation possible (15000 fs2)
  • Using a very old GRENUILLE (FROG) device I estimate both of the beams are still under 160fs before they enter the microscope.
DaveE said:
Yes, maybe walkoff losses? SFG can sometimes work better if the beams aren't colinear.
I had never heard of this but I suspect I have observed it as slightly misaligning the 1040nm beam yields a better SFG signal under the objective. Now I know not to use this as a proxy to improving the SRS signal as there would be no walk-off in that case.

I realized after my original post that my current setup is probably introducing additional divergence for the 1040nm beam as I had the 2X beam shrinker mounted near the exit of the laser, meaning I was shrinking the beam from ~2mm to ~1mm. Could this be the source of issues? In the original implementation (which gave me SRS signal) the same beam shrinker was mounter after several meters of optical path, shrinking the beam from ~5mm to ~2.5mm.
 
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  • #6
fevemo said:
Thanks for the replies!


This has definitely been one of my suspects.
The current setup has the 1040 beam going through a delay line with ~10 silver mirrors, a 2X beam shrinker (to compensate for the divergence of the extra path length), and then joins the tunable beam using a notch filter. After that they both go through a beam expander (not ideal IMO), ~8 more mirrors, and then the microscope (scan + tube lenses, galvos, dichroic mirror, objective)
Wow- that's a lot of mirrors. Are the mirrors first surface or coated? Also, I'm not sure what your total power loss from the < 100% reflectivity would be, it could be significant. I assume the beam expander and beam shrinker are refractive devices?

fevemo said:
I realized after my original post that my current setup is probably introducing additional divergence for the 1040nm beam as I had the 2X beam shrinker mounted near the exit of the laser, meaning I was shrinking the beam from ~2mm to ~1mm. Could this be the source of issues? In the original implementation (which gave me SRS signal) the same beam shrinker was mounter after several meters of optical path, shrinking the beam from ~5mm to ~2.5mm.
Doubtful? In my mind it's more of a question about etendue. If there's no difference in etendue regardless of where the beam shrinker is (which seems reasonable... unless there's vignetting, for example), then the change of beam divergence post-shrink should be the same in both cases.

What about the dichroic(s) int he microscope- can they properly handle the various wavelengths?
 
  • #7
Andy Resnick said:
Wow- that's a lot of mirrors. Are the mirrors first surface or coated? Also, I'm not sure what your total power loss from the < 100% reflectivity would be, it could be significant.
They're all protected silver mirrors from Thorlabs which have ~97% reflectivity at 1040nm. I have measured ~40% power loss through the delay line and ~60% power loss through the common path to the objective. This is not a big concern as we have enough power at the objective (>600mW for both beams, out of the laser we get ~2W on the tunable beam and ~4W on the fixed 1040nm).

Andy Resnick said:
I assume the beam expander and beam shrinker are refractive devices?
Correct, beam shrinker is just a f200mm lens + f100mm lens and the beam expander is similar but I don't remember the exact focal lengths (~4X expansion, could be f75mm and f300mm).

Andy Resnick said:
Doubtful? In my mind it's more of a question about etendue. If there's no difference in etendue regardless of where the beam shrinker is (which seems reasonable... unless there's vignetting, for example), then the change of beam divergence post-shrink should be the same in both cases.
So I quickly tested going back to the previous order and it was way easier to align the beam shrinker such that after the beam expander (which unfortunately I can't touch) the fixed beam was collimated and ~6mm in diameter which is exactly what I want.
With this setup I also managed to get some SRS and CARS signals, although they are still weaker than expected. I didn't have time yet to quantify how the SFG signal compares to the SHG signal now, but it looks similar to the results mentioned above. I have a strong suspicion that the source of the issue is around this, either beam diameter or collimation, however it is still not clear to me why the position of the beam shrinker affects the SRS signal.

Andy Resnick said:
What about the dichroic(s) int he microscope- can they properly handle the various wavelengths?
They should be, we use the microscope extensively for two-photon imaging and it works well. IIRC the dichroics are designed specifically for multiphoton imaging so they have low GDD and work all the way from 750nm to 1300nm.

Also, thanks again for taking the time to think dwell on my issues!
 

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