I've re-run the HR coating designs for both ETM and ITM using interpolated dispersions (presumably at room temperature). The difference is shown in Attachment #1 and Attachment #2.
Basically, all features are still present in both spectral transmission plots, which is consistent with the relatively flat dispersions from 1 to 3 um in Silica and Tantala thin films, but the index corrections of a few percent from low-temperature estimates to room-temperature measured (?) dispersions are able to push the HR transmission up by a few (2-3) times. For instance, the ETM transmission at 2128.2 nm goes up by ~ 3. The new number is still well below what we have requested for phase I so this is in principle not an issue.
A secondary change is the sensitivity (the slope around the specified wavelength) which seems to have increased for the ETM and decreased for the ITM. This was another consideration so I'm running the optimizer to try and minimize this without sacrificing too much in transmission. For this I am using the stack as a first guess in an attempt to run fast optimization. Will post results in a reply to this post.
Alright, I've done a re-optimization targetting a wider T band around 2128 nm. For this I modified the scalar minimization cost to evaluate the curvature term (instead of the slope) around a wide range of 10% (instead of 1%). Furthermore, in prevision of the overall effects of using the updated dispersion, I intentionally optimized for a lower T such that we intentionally overshoot.
The results are in Attachment #1 and Attachment #2.
Sat amp seems to be working just fine. There does seem to be a saturation issue with one of the outputs we may need to change a resistor on the board.
Kind of a silly post, and not very scientific, but we are sticking to it. During our check in today we discussed Mariner suspension frame design concept, and we chose to proceed with MOS-style (4 posts, rectangular footprint).
- We looked at a scaled-up SOS (WIP, lots of things broke, just notice the larger side plates and base - see Attachment 1) and we were not super excited by the aspect ratio of the larger side plates - didn't look super stiff - or the mass of the base.
- We noted that the intermediate mass will need OSEMs, and accommodating those will be easier if there is a larger footprint (as afforded by MOS).
MOS-style it is, moving forward!
Also, Checked In to PDM (see Attachment 2 - filename 40mETMsuspension_small-shields.SLDASM and filepath \llpdmpro\Voyager\mariner 40m cryo upgrade ) the current state of the Mariner suspension concept assembly (using MOS). Other than updating the test mass to the 6" configuration, I didn't do any tidying up, so I'm not perfectly satisfied with the state of the model. This at least puts the assembly in a place where anyone can access and work on it. Progress!
Have been using the 40m Coatings repo code by Gautam (with some modifications to make dichroic designs under Ta2O5_Voyager), as well as the parameters compiled in the Mariner wiki for Silica-tantala thin films. Here are some of the top picks.
For ETM, the target transmissivities are 5.0 ppm @ 2128.2 nm and 50.0 ppm @ 1418.8 nm. After different combinations of differential evolution walkers, numbers of layers, thickness bounds, a couple of different optimization strategies, the optimum design has consistently converged with 19 - 26 layer pairs (total of 38 - 52 layers). The picks are based on the sensitivities, E_field at the boundary, and a qualitatively uniform stack (discarded "insane-looking" solutions). The top picks in Attachment 1 may be a good starting point for a manufacturer. In order of appearance, they are:
For ITM, the target transmissivities are 2000 ppm @ 2128.2 nm and 50.0 ppm @ 1418.8 nm (critically coupled cavity for AUX). The lower trans for 2128.2 nm made this easier faster to converge, although the number of thin film layers was equally centered about ~ 50 layers. Haven't explored as much in the parameter space, but the top picks in Attachment 2 are decent for approaching manufacturer. In order of appearance, they are:
New optima are being found using the same basic code with some modifications, which I summarize below;
Still working to translate all these changes to ITM, but here are samples for some optimum.
I guess you have tried it already - but does enforcing the stacks to be repeating bilayer pairs of the same thickness fail miserably? When doing this for the PR3 optic @1064nm, I found that the performance of a coating in which the layers are repeating bilayers (so only 2 thicknesses + the cap and end are allowed to vary) was not that much worse than the one in which all 38 thicknesses were allowed to vary arbitrarily. Although you are aiming for T=50ppm at the second wavelength (which isn't the harmonic) which is different from the PR3 reqs. This kind of repetitive structure with fewer arbitrary thicknesses may be easier to manufacture (and the optimizer may also converge faster since the dimensionality of the space to be searched is smaller).
Cool starfish 🌟 . What is the interpretation of the area enclosed by the vertices? Is that the (reciprocal) cost? So the better solution maximizes the area enclosed?
Yeah, the magnitudes are the inverse weighted scalar costs (so they lie on the appropriate relative scale) and indeed larger enclosed areas point to better optima. I would be careful though, because the lines connecting the scalar costs depend on the order of the vector elements (for the plot)... so I guess if I take the cost vector and shuffle the order I would get a different irregular polygon, but maybe the area is preserved regardless of the order in which the scalars are displayed...
Attached is a cartoon partial view into the heat load experienced by the Mariner assembly.
The omnigraffle file with more explicit arrow labelling in the 'layers' tab is available here. The dashed red lines along to top represent vacuum chamber radiation incident on all sides of the OS/IS, not just from the top. Off picture to the right is the BS, left is the beam tube/ETM chamber -- hence the lower absored laser power (solid line) absorbtion (PR power + no HR coating absorption).
Missing or wrong
Yesterday, I did two rounds of slowly heating 4 samples to the maximum hot plate temperature. This was to formally test if my success with a single sample earlier in the week was a fluke. Note that the hot plate takes about 10-15 minutes to reach a stable temperature when it is turned up one notch.
I bonded 4 samples by putting methanol in the gap between the glass slides and letting it dry to create a gap.
Starting at room temperature, I heated the slides on each setting for roughly 15 minutes, then let them cool down naturally over the course of an hour. 3 broke broke at medium heat, and 1 survived the whole process. I belive these broke because the bonds were weaker and I heated them slightly too quickly. In previous tests, I would manually switch the hot plate on and off, but I wanted to see if the hot plate could heat up slow enough on its own.
I bonded 4 samples by scrubbing the slides with methanol, using a compressed air duster to blow off the fibers, rubbing them together with the pressure of my fingers, and repeating this whole procedure until they stuck (it took 2-4 repeats).
Starting at room temperature, I heated the slides on each setting for exactly 20 minutes, then let them cool down naturally over the course of an hour. All of them survived to the maximum temperature (the pictures show them at the start and end of the heating, note the temperature). I credit this to the stronger bonding proceedure and the extra 5 minutes for them to adjust to the temperature. I did not turn the hot plate on or off at any point, I just let it heat up at its own rate.
I cannot tell if the bonds are stronger. The size and shape of the Newtons rings did not change.
[Paco, Nina, Aidan]
We ran our stack emissivity calculation on different AR stacks to try and make a decision for the TM barrel coatings. This code has yet to be validated by cross checking against tmm as suggested by Chris. The proposed layer structures by Aidan and Nina are:
Attachments # 1-3 show the emissivity curves for these simple dielectric stacks. Attachment #4 shows the extinction coefficient data used for the three different materials. The next step is to validate these results with tmm, but so far it looks like TiO2 might be a good absorbing film option.
I have to question whether this passes a sanity test. Surely in the case of Stack 2, the 10um thick Ta2O5 will absorb the majority of the incident radiation before it reaches the SiO2 layer beneath. It should at least be similar to just absorption in Ta2O5 with some Fresnel reflection from the AIr-Ta2O5 interface.
For example, at around 18um, K~2, so the amplitude attenuation factor in a 10um thick layer is 160,000x or a gain of 6E-6. So whatever is under the Ta2O5 layer should be irrelevant - there is negligible reflection.
Agree with this. Quickly running tmm on the same "stacks" gave the Attachment #1-3. (Ignore the vertical axis units... will post corrected plots) and extend the wavelength range to 100 um.
Today we looked at possible locations for where we will be setting up Mariner Suspension and Cryo chamber. The first option was the far left table in the CAML lab but it seems that there is going to be an issue with height clearance, so we have come up with another solution which takes a table from Koji's lab which is 3'x4' ft and moving it into CAML lab in the back right of the lab. To move the table we may need to call facilities to help us because we will most likely need to take the table apart to get it out of the lab. The aisle space in Koji's lab is about 43 inches, but the doorway, which is the tightest space, is 35 inches.
After we have set up the table in CAML we are planning on moving the Chamber in DOPO-lab to CAML. We plan to use skyhook with has a load limit of 500lbs/227kg this should be more than enough to move the chamber. We still need to get the wheeled base for skyhook we are in the works in doing so.
Also, We want to remove the previous setup from the chamber and leave it at DOPO-lab. Stephen is going to figure out how to keep it clean (sort of). Besides these transportation logistics, I am also working on the electronics as an immediate task and the electrical arrangement in the chamber.
to do list
- Check the table height
- Check the chamber height (base/cap)
- Check how much the chamber cap needs to be lifted (so that we can remove it)
- Is the weight capacity sufficient?
- B246/QIL Skyhook
- OMC Lab
Table moving effort in the OMC lab: See https://nodus.ligo.caltech.edu:8081/OMC_Lab/412
The ETM wedge of 0.5deg will allow us to separate the AR reflections. We will be OK with the ITM wedge of 0.5deg too. 0.36 deg for ITM is also OK, but not for the ETM.
- Attachment 1 shows the deflection of the 2128mn and 1418nm beams by the test mass wedge. Here, the wedge angle of 1deg was assumed as a reference. For the other wedge angle, simply multiply the new number (in deg) to the indicated values for the displacement and angle.
- Attachment 2 shows the simplified layout of the test masses for the calculation of the wedge angle. Here the ITM and ETM are supposed to be placed at the center of the in-vacuum tables. Considering the presence of the cryo baffles, we need to isolate the pick-off beam on the BS table. There we can place a black glass (or similar) beam dump to kill the AR reflection. For the ETM trans, the propagation length will be too short for in-vacuum dumping of the AR reflection. We will need to place a beam baffle on the transmon table.
- I've assumed the cavity parameter of L=38m and RoC(ETM)=57m (This yields the Rayleigh range zR=27m). The waist radii (i.e. beam radii at the ITM) for the 2128nm and 1418nm beams are 4.3mm and 3.5mm, while the beam radii at the ETM are 7.4mm and 6.0mm, respectively,
- Attachment 3: Our requirement is that the AR reflection of the ALS (1418nm) beam can be dumped without clipping the main beam.
If we assume the wedge angle of 0.5deg, the opening of the main and AR beams will be (2.462+4.462)*0.5 = 3.46 deg. Assuming the distance from the ETM to the in-air trans baffle is 45" (=1.14m), the separation of the beams will become 69mm. The attached figure shows how big the separation is compared with the beam sizes. I declare that the separation is quite comfortable. As the main and AR beams are distributed on both sides of the optic (i.e. left and right), I suppose that the beams are not clipped by the optical window of the chamber. But this should be checked.
Note that the 6w size for the 2128nm beam is 44mm. Therefore, the first lens for the beam shrinkage needs to be 3" in dia, and even 3" 45deg BS/mirrors are to be used after some amount of beam shrinkage.
- Attachment 4 (Lower): If we assume the same ITM wedge angle of 0.5deg as the ETM, both the POX/POY and the AR beams will have a separation of ~100mm. This is about the maximum acceptable separation to place the POX/POY optics without taking too much space on the BS chamber.
- Attachment 4 (Upper): Just as a trial, the minimum ITM wedge angle of 0.36deg was checked, this gives us the PO beam ~3" separated from the main beam. This is still comfortable to deal with these multiple beams from the ITM/
Note that I am just testing out different techniques, so I have not set up the thermocouples to precisely measure the temperatue.
On Tuesday, I developed a new method of putting water, isopropanol, or methanol on one slide then squishing the other slide on top of it to fill the gap with the afformentioned liquid. The slides are slippery at first, but as they dried, which took about 15 minutes, the bond forms. The bonds were strong enough that I could just barely push the slides appart by applying pressure to the side using my thumbs. I prepared 4 samples this way, 2 with iso and 2 with meth. I took one of each and heated them on Medium for 30 minutes under the brass hunk with the aluminum square on the bottom and copper foil on both sides of the samples. Earlier in the day, I tried heating them without the weight on top, but the heat just broke the bond. I took the remain two and set them aside as controls.
On Thursday, I returned to check the bonds. The heated samples had broken. I intented to check on Wednesday, but I was sick from food poisoning, so I do not know whether the bonds broke immediately after heating or due to sitting for an extra day. For the control samples, one also had a broken bond, but the other had become even stronger.
I noticed that, when the slides are successfully bonded, the shape and appearance of the Newton's rings change, which can be seen in the pictures. I speculate that the circles on the unbroken control are the bonded regions. Ideally, we want to see no Newton's rings.
I was thinking about how fast we can cool the test mass. No matter how we improve the emissivity of the test mass and the cryostat, there is a theoretical limitation. I wanted to calculate it as a reference to know how good the cooling is in an experiment.
We have a Si test mass of 300K in a blackbody cryostat with a 0K shield. How fast can we cool the test mass?
Then assume the specific heat is linear as
The actual Cp follows a nonlinear function (cf Debye model), but this is not a too bad assumption down to ~100K.
Then the differential equation can be analytically solved:
where the characteristic time of t0 is
Here T_0 is the initial temperature, cp0 is the slope of the specific heat (Cp(T_0) = c_p0 T_0). epsilon is the emissivity of the test mass, sigma is Stefan Boltzmann constant, A is the radiating surface area, and m is the mass of the test mass.
Up to the characteristic time, the cooling is slow. Then the temperature falls sqrt(t) after that.
As the surface-volume ratio m/A becomes bigger for a larger mass, in general, the cooling of the bigger mass requires more time.
For the QIL 4" mass, Mariner 150mm mass, and the Voyager 450mm mass, t0 is 3.8hr, 5.6hr, and 33.7hr respectively.
This is the fundamental limit for radiation cooling. Thus, we have to use conductive cooling if we want to accelerate the cooling further more than this curve.
Just a general update of what I have been up to deriving Lagrange for double pendulum system and also been looking at code that koji gave to me I've add comment to some of the code also working on my report.
Almost done with coil driver boards
Update of my current work I have finished one coil driver board and started on the last two that I need here is the progress and Ideally, I'll finish by tomorrow.
For our optical contacting, Jennifer and I are starting out with glass (microscope slides), with the setup in the EE shop next to the drill press (photos from Jennifer to follow).
Some interesting links: