Dry Etching 09
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Transcript of Dry Etching 09
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520/530/580.495
Microfabrication Laboratoryand
520.773Advanced Topics in
Fabrication and Microengineering
Lecture 9
Dry Etching
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Reading for this lecture:(1) May, Chapter 5.2
(2) Williams paper
HW #6: Due Nov. 6
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HFH+
F-
H2OF-
H+H2O
H2OHFHF
Wet Etch
CF4
CF5-CF2
2+
CF4
SF6F
CF3+
Dry Etch
Wet Etching vs Dry Etching
In wet etchants, the etch reactants come form a liquid sourceIn dry etchants, the etch reactants come form a gas or vaporphase source and are typically ionized
-Atoms or ions from the gas are the reactive species thatetch the exposed film
Selectivity : In general, dry etching has less selectivity than wet etching
Anisotropy: In general, dry etching has higher degree of anisotropy than
wet etchingEtch Rate: In general, dry etch has lower etch than wet etching
Etch Control: Dry etching is much easier to start and stop than wetetching
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Etch Mechanism
The slowest dominates !!!
Generation of etching species-Without generating the etching speciesetching will not proceed
Diffusion to surfaces-etching species must get to the surfaceto react with the thin or substrate molecules-the mechanics of getting to the surface canlimit aspect ratio, undercuttig, uniformity
Adsorption-can also effect aspect ratio
Reaction:-strong function of temperature(Arrhenius relationship)
-obviously effect the etch rate
Desorption-can stop etch if the reacted species is notvolatile
Diffusion to bulk gas-can lead to non-uniform etching due to dilution of
un-reacted etching species
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Gas Phase Etch
Reactive Gas
- Gas adsorbs on the surface, diassociates, and then reacts
Xenon Difluoride Etching
XeF2 Adsorb Xe + 2 F
Particular features of XeF2 etching-extremely selective-fast etch rate-isotropic
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RF-Plasma-Based Dry EtchingA plasma is fully or partially ionized gas composed of equal numbers of positive
and negative charges and a different number of unionized molecules.A plasma is produced when an electric field of sufficient magnitude is applied to agas, causing the gas to break down and become ionized.
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Materials Etch Gases Etch Products
Si, SiO2, Si3N4 CF4, SF6, NF3 SiF4
Si Cl2, CCl2F2 SiCl2, SiCl4
Al BCl3, CCL4, SiCl4, Cl2 AlCl3, Al2Cl6
Organics O2, O2 + CF4 CO, CO2, H2O, HF
other: (W, Ta, Mo..) CF4 WF6,..
Dry Etch Chemistries
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Types of Dry Etching Processes
( 1 torr = 1 mmHg)
Types of Etching Methods Geometry Selectivity Excitation Energy Pressure
Gas/vapor Etching Chemical Isotropic Very high noneHigh(760-1torr)
Plasma Etching Chemical Isotropic High 10's to 100's of WattsMedium
(>100 mtorr)
Reactive ion EtchingChemical &Physical
Directional Fair 100's of WattsLow(10-100 mtorr)
Sputtering Etching Physical Directional Low 100's to 1000's of Watts Low(~10 mtorr)
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Degree of Anisotropy
Degree of Anisotropy
vvf
fR
R
tR
tR
h
lA 11 111 ==
For isotropic etching:R
l= R
vandAf= 0
For anisotropic etching:R
l= 0andAf= 1
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Dry Etching Si/SiO2 in F-Based Gases and Plasmas
Prominent etch chemistry in ICs & MEMSCF4 does not etch Si (does not chemisorb) but F2 gas willetch Si with etch products SiF2 and SiF4
Plasma is needed to generate F that must penetrateSiF2-like surface
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Dependence of Etch Rate and Si/SiO2 Selectivityon O2 /CF4 Ratio
Even with plasma the etch rate is slow-insufficient F concentration
Adding O2 to the plasma can increase F concentrationO + CF3 COF2 + F then O+COF2 CO2 + 2F
Etch rate maximizes around 12% O2
Etch rate decreases at higher O2concentrations
-Dilution of F concentration with
overly abundant O2-Trend is similar for SiO2
Etch rate is higher for Si
Si/SiO2 selectivity is good
Isotropic etching
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Adding H2 drastically lowers Si etch rate-lowers F concentration (H+ + F +e- HF)-Nearly 0 at 40% H
2
However, etch rate of SiO2 remains nearlyconstant
Allows etch selectivity to be increasedtremendously
Mechanism for increased selectivity has two
components-deposition of a non-volatile residue-role of O2 in etching of SiO2
Dependence of Etch Rate and SiO2/Si Selectivity
on H2 /CF4 Ratio
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Increase of Degree of AnisotropyFormation of Sidewall Passivating Films
Formation of nonvalatile fluorocarbonsthat deposit on the surfaces (Polymerization)
The deposit can only be removed byphysical collisions with incident ions
Fluorocarbon films deposits on allsurfaces, but the ion velocity is nearlyvertical. As a result, as the etchingproceeds there is little ion bombardment
of the sidewalls and the fluorocarbon filmaccumulates
Adding hydrogen encourages the formationof the fluorocarbon films because hydrogenscavenge fluorine, creating a carbon-rich plasma(same thing happened when C2F6 is usedinstead of CF4 )
Less accumulation is observed on SiO2 than Sisurfaces
Tradeoff betweenSi/SiO2 selectivityandAnisotropy
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Controlling Polymerization through F/C-Ratio
Higher F/C-ratio leads to more etching
Lower F/C-ratio leads to morepolymerization
Can be determined by the gas used
Adding H2 consumes F leads topolymerization
Adding O2
consumes C leads toetching
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Dry Etching Organic Films
O2 plasmas can remove organic films with high selectivity
Adding CF4 can increase etch rate and lowers variation-but selectivity can be reduced if too much is added
Etchrat
eofPloymid
e(um/min)
%va
riationofetc
hrate
etch rate
% etch rate variation
% CF4 added O2
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Damage in Reactive Ion Etching (RIE)
Typical ion flux of 1015 ions/cm2 are delivered at energies of
300 to 700 eV in a RIE.
After a typical etch in a carbon containing RIE, the top 30 isheavily damaged, with an extensive concentration of Si-C bonds.
RIE processes done in a hydrogen-containing ambient also have Si-Hdefects that can be observed as deep
as 300 .
Hydrogen may penetrate severalmicrons into the surface where it candeactivate dopants in the substrate.