Erik Kvam M aland Master Thesis in Computer Science May 2015
Selective Etching Using Argon Plasma By: C. Joseph Lust Advisor: Prof. Kvam.
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Transcript of Selective Etching Using Argon Plasma By: C. Joseph Lust Advisor: Prof. Kvam.
Selective Etching Using Argon Plasma
By: C. Joseph LustAdvisor: Prof. Kvam
Overview Objectives Approach Equipment Used Problems Findings
Introduction To selectively etch silicon nitride
and aluminum deposited on a silicon substrate.
Silicon
Silicon Nitide
Aluminum
Approach Cut samples to a size of about
0.75cm by 0.75 cm. Clean samples using acetone and
methanol Use spinner at 4000 rpm to apply
AZ 1518 photoresist Bake at 900 C for 10 minutes
Approach Place mask on sample and expose
to UV light for one minute at a height of four inches
Place in AZ developer for approximately 10 to 15 seconds then rinse in DI water
Bake at 900 C for 10 minutes Use Carbon tape to attach samples
to blank sputter ring
Approach Etch in sputterer using Argon
Plasma for desired time Take off Photoresist using Acetone Used profilometer to measure
height difference
Sputtering Used times of 10 minutes, 20
minutes, 30 minutes, 40 minutes, and 50, minutes, and 60 minutes
Kept pressure at around 80 millitorrs
Kept current at around 15 milliamps
Photoresist The photoresist used was AZ 1518
which is made by Clariant. AZ 1518 is a positive photoresist. When it is exposed to UV light that
part can be removed by using AZ developer.
Positive Resist
Sample to be etched
Resist
Equipment Used Headway Reasearch, Inc Spinner Blak-Ray Longwave ultraviolet
lamp Anatech LTD Hummer 6.2
sputtering system Tencor instruments Alpha-step 200
profilometer
Problems Getting Photoresist on samples
took a couple of attempts to get righto First batch resist just washed away
o Mask wasn’t close enough or no prebakeo Second batch resist wouldn’t come off
o Developer was too diluted
Mask
Before Etching
After Etching for 60 minutes
Findings When using the profilometer, the
sections that were covered by resist were left unharmed. The results were comparable to a sample that had not been used at all.
Findings On the sections of Silicon Nitride
and Aluminum that were exposed, the results were not as expected. While it was being etched the plasma caused the material to rise up. This caused a peaks to form when the profilometer was used.
Findings These peaks were usually between
1 to 3 microns higher then the unetched section. When comparing the different runs there was no pattern between height of the peaks and run time.
Profilometer graph for SiN
-0.5
0
0.5
1
1.5
2
2.5
0 500 1000 1500 2000 2500
microns
microns
Series1
Profilometer graph for Al
-0.5
0
0.5
1
1.5
2
2.5
0 500 1000 1500 2000 2500
microns
microns
Series1
Future Work Try using different pressure and
current for the plasma. Try using a wet etch to selectively
etch the materials.
Acknowledgements Prof. Kvam Mark McCormick Patty Metcalf Purdue University