Asymmetrical Oxide Experiment
With this new understanding of pore size and porosity control, I think we have a lot more flexibility on picking more optimal film conditions.
With this new understanding of pore size and porosity control, I think we have a lot more flexibility on picking more optimal film conditions.
I coated the pncSi samples from W683 (no RTP) with Bovine Serum Albumin (BSA) in Tris-EDTA buffer. Three different concentrations were used: 1 mg/ml, 5 mg/ml and 10 mg/ml (usual range of BSA conc. used for coating Si surfaces). The samples were left in BSA solution for 45-60 mins at room temperature and almost dried,…
Today I etched wafer 621, which is the pair to 620. While w620 has a relatively low pinhole density, w621 shows a much higher occurence of defects. Since the front-end processing and thermal treatment was identical for these wafers, I believe that the variability lies in the etch process. Looking at the two wafers side-by-side,…
Introduction Throughout my rotation, I have been working on the dialysis project with Alec. The goal was to set up a multi-pass system to analyze the membrane’s ability to separate different molecules in blood. The critical separation is between β2-microglobulin (12 kDa) and albumin (66 kDa) – β2-microglobulin is a large toxin that needs to…
Introduction & Motivation A subset of cancer cells has mutations that generate proteins recognized by the immune system as foreign, triggering the immune-mediated clearance of those cells. To avoid this fate, cancer cells can evolve mechanisms to suppress this antitumor response via the regulation of immune checkpoint pathways. Immune checkpoints describe mechanisms that are in…
I have three monolith experiments to report, one of which was successful. In all three cases, I was able to make a pore, though it took about 5 times longer than it would have for the NPN-tented chips. This is likely a consequence of the reduced exposed membrane area in the monolith case, which is…
Tweaking simulation was not bringing it any closer to the experimental shown in the last post. This led me to try the experimental once more. I set up the same system and used 1:2 dilution of the standard protein mixture. I then homogenized the retentate and filtrate and ran 10 ul of each on a…
Comments are closed.
very interesting- this really suggests we should do a series with increasingly thinner top oxide layers- eventually going to the agglomeration regime Joe has seen. Can we do this quickly, with say 20, 15, 10, and 5 nm oxide?
could you also email me the figure as I am having a hard time trying to import it. Thanks,
P. Fauchet
Sure, I also updated the post so the figure can be loaded as bigger image. I haven’t posted in so long on the blog I forgot how to get the images set right.
Charles
I am puzzled as to why 719 falls between the two other samples – or perhaps why 720 shows a higher porosity and average pore size than the 2 others. If one goal is to make high porosity samples that have very small pores, your results suggest that we should increase the thickness of both oxide layers- can someone try this?
I’m not sure why 720 shows a higher porosity and average pore size. I suspect that the thicker bottom oxide might promote pore size and porosity.
Increasing both top and bottom oxide has usually shown a decrease in pore size and porosity.