Now that I have a proper (homebrewed) fume hood decapping is a lot easier and safer. No fumes to breathe, and a nice thick sash between me and the beaker of hot acid if something goes wrong. That said, I still wear goggles, gloves, and a lab coat as per SOP.
For the new process I am using sulfuric acid as it's much cheaper than nitric. (Concentrated sulfuric of an acceptable quality can be purchased as a drain cleaner, while nitric must be mail-ordered with special hazmat shipping fees). The downside is that sulfuric cannot be used for live decapsulation (at least not easily) since it takes so long. For bare-die decaps it's by far the most cost-effective option, though.
The first step, as is usual for bare-die decaps, is to put them in a beaker of acid, cover with a watch glass or petri dish to slow down evaporation losses. and heat.
View through the sash of my fume hood as the acid warms up |
Close up of beaker on the hot plate |
Later in the decap |
At this point all that has to be done is to leave the chips to cook for a while. I was running at only around 100C (150-200 is more common) so it took an hour or two.
Before I get to the results, a warning as to what you're dealing with here. While pouring the used acid off into another beaker to pull the dies out with tweezers, I spilled a drop on a kimwipe I had in the hood. This was the result:
H2SO4 + organics = bad |
Top metal of FT232RL |
Wiki page: http://siliconpr0n.org/archive/doku.php?id=ftdi_ft232rl
Are they usable after this process or would I need to use nitric for that?
ReplyDeleteI plan on erasing fuses/eeproms with UV!
Thanks
The dies are usable in theory for probing etc but the package and leadframe are destroyed. This process is for bare die recovery for imaging, not sample prep for microprobing.
ReplyDeletehttp://siliconpr0n.org/wiki/doku.php?id=decap:epoxy_acid#hno3_on_preheated_chip is what I'd use if I wanted to probe.