Specific Process Knowledge/Etch/ICP Metal Etcher: Difference between revisions

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<gallery caption="Standardization images of the shallolr recipe" widths="300px" heights="300px" perrow="2">
<gallery caption="Standardization images of the shallolr recipe" widths="300px" heights="300px" perrow="2">
Image:jmlshal070921 pos1 2mu_09.jpg|The profile of a 2 <math>\mu</math>m trench
Image:WF 2F-6 dec092010-30 nm.jpg.jpg|The 30 nm trenches are somewhat wider due to overexposure of E-beam resist
image:jmlshal070921 pos1 50mu_08.jpg|The profile of a 50 <math>\mu</math>m trench
image:WF 2F-6 dec092010-120 nm.jpg.jpg|The 30 nm trenches are somewhat wider due to overexposure of E-beam resist
</gallery>
</gallery>
It looks like the trenches are closing up as the etch goes deeper, consistent with too much polymer deposition on the sidewall.
The options I would look at are
        1) to reduce the coil power to 700W so that the dc bias of the etch increases & you sputter more of the polymer off.
        2) increase the platen temperature to 40 C so as to reduce polymer condensation on the wafer.
        3) substitute Cl2 for some of the HBr - try a 50: 50 mix of Cl2 / HBr for the main etch with the same total gas flow.  This will reduce the amount      of polymerising species in the plasma & therefore help reduce the amount of sidewall deposition.  I would try these separately.
Just as a sanity check, have you got any pre-etch SEM images of the ZEP?  There's a contradiction in the SEM images  - in that you are seeing what looks to be undercut, whilst the trenches are also closing up.  One effect is consistent with too little polymerisation whilst the other is caused by too much.  The breakthrough step is actually quite a physical & directional etch, which usually doesn't cause an undercut.  What exposed area do you have on the samples?

Revision as of 15:18, 23 February 2011

Etching of nanostructures in silicon using the ICP Metal Etcher

The starting point
Break Gas Cl2 20 sccm
Pressure 2 mTorr, Strike 3 secs @ 5 mTorr
Power 600 W CP, 200 W PP
Temperature 20 degs
Hardware 100 mm Spacers
Time 15 secs
Main Gas HBr 20 sccm
Pressure 2 mTorr, Strike 3 secs @ 5 mTorr
Power 900 W CP, 50 W PP
Temperature 20 degs
Hardware 100 mm Spacers
Time ? secs

ER 200 nm/min, 3:1 over resist. Vertical profile. To improve selectivity to oxide under-layers you can add a small amount of O2 ( e.g 2 sccm if the MFC is small enough). This should not give an undercut.

It looks like the trenches are closing up as the etch goes deeper, consistent with too much polymer deposition on the sidewall.

The options I would look at are

       1) to reduce the coil power to 700W so that the dc bias of the etch increases & you sputter more of the polymer off.
       2) increase the platen temperature to 40 C so as to reduce polymer condensation on the wafer.
       3) substitute Cl2 for some of the HBr - try a 50: 50 mix of Cl2 / HBr for the main etch with the same total gas flow.  This will reduce the amount      of polymerising species in the plasma & therefore help reduce the amount of sidewall deposition.   I would try these separately.

Just as a sanity check, have you got any pre-etch SEM images of the ZEP? There's a contradiction in the SEM images - in that you are seeing what looks to be undercut, whilst the trenches are also closing up. One effect is consistent with too little polymerisation whilst the other is caused by too much. The breakthrough step is actually quite a physical & directional etch, which usually doesn't cause an undercut. What exposed area do you have on the samples?