Ion Implantation Chpt 8, #14 - University of Washington · 28 10−15 1 2 1 23 2 2312 1 1 2 eV-cm2...
Transcript of Ion Implantation Chpt 8, #14 - University of Washington · 28 10−15 1 2 1 23 2 2312 1 1 2 eV-cm2...
Class Handout #14 © 1999
EE212 1999-00 1 JDP, MDD, PBG
EE 212 FALL 1999-00
ION IMPLANTATION - Chapter 8
Basic Concepts
• Ion implantation is the dominant method ofdoping used today. In spite of creating enormouslattice damage it is favored because:• Large range of doses - 1011 to 1016 /cm2
• Extremely accurate dose control• Essential for MOS VT control• Buried (retrograde) profiles are possible• Low temperature process• Wide choice of masking materials
• There are also some significant disadvantages:• Damage to crystal• Anomalous transiently enhanced diffusion
(TED) upon annealing this damage• Charging of insulating layers
V
V
Ionsource
Analyzing magnet
Pump
Resolvingaperature
Accelerator
Focus
Neutralbeam gate
Neutraltrap X & Y
scanplates
Wafer
Faraday cup
Q0-30keV
0-200keV
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A. Implant Profiles
• At its heart ion implantation is a random process.• High energy ions (1-1000keV) bombard the
substrate and lose energy through nuclearcollisions and electronic drag forces.
Range R
Projected rangeRP
Vacuum Silicon
• Profiles can often be described by a Gaussiandistribution, with a projected range and standarddeviation. (200keV implants shown below.)
1021
1020
1017
1019
1018
Con
cent
ratio
n (c
m-3
)
0 0.2 0.4 0.6 0.8 1Depth (µm)
SbAs P
B
0.606 CP∆RP
RP
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C x Cx R
RPP
P( ) exp= −
−( )
2
22∆(1)
Q C x dx= ( )∫−∞
∞ or Q R CP P= 2π ∆ (2)
where Q is the dose in ions cm-2 and is measured bythe integrated beam current.
• The ranges and standard deviation ∆Rp of thecommon dopants in randomly oriented silicon areshown below.
0
0.05
0.1
0.15
0.2
0.25
0.3
0.35
0.4
0 40 80 120 160 200
Dep
th (µ
m)
Energy (keV)
B
P
Sb
As
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0
0.02
0.04
0.06
0.08
0.1
0.12
0 40 80 120 160 200
Sta
ndar
d D
evia
tion
(µm
)
Energy (keV)
B
P
Sb
As
• Monte Carlo simulations of the randomtrajectories of a group of ions implanted at a spoton the wafer show the 3-D spatial distribution ofthe ions. (1000 phosphorus ions at 35 keV.)
ImplantBeam
x
y
z
80
40
0
-40
050
-100-50
040
80120
• This appears as an elongated ellipse because mostof the high energy ions undergo only small anglecollisions.
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• Side view shows Rp and ∆Rp while the beamdirection view shows the lateral straggle.
zBeam direction
80
40
0
-40
y
050100 -100-50
y
-40
0
40
80
x
Side view
0 40 80 120
• The two-dimensional distribution is often assumedto be composed of just the product of the verticaland lateral distributions.
C x y C xyRvert, exp( ) = ( ) −
⊥
2
22∆(3)
• Now consider what happens at a mask edge - ifthe mask is thick enough to block the implant, thelateral profile under the mask is determined by thelateral straggle. (35keV and 120keV As implantsat the edge of a poly gate from Alvis et al.)
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• The description of the profile at the mask edge isgiven by a sum of point response Gaussianfunctions, which leads to an error functiondistribution under the mask.
B. Masking Implants
How thick does a mask have to be?
CP*
RP*
Depth
xm
C*(xm)CB
Con
cent
ratio
n
• For masking,
C x Cx R
RCm P
m P
PB
* **
*exp( ) = −
−( )
≤2
22∆
(4)
• Calculating the required mask thickness,
x R RCC
R m Rm P PP
BP P= +
= +* **
* *ln∆ ∆2 (5)
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• The dose that penetrates the mask is given by
R
x R
Rdx
Qerfc
x R
RPP
P
Px
m P
Pm
= − −
∫ = −
∞
2 2 2 2
2
π∆ ∆ ∆*
*
*
*
*exp
(6)
• Real structures may be more complicated becausemask edges or implants are not vertical.
30 Degree Tilt
Dis
tanc
e (µ
m)
Distance (µm)
30˚ tilt
0 0.2 0.4 0.6 0.8 1.0
0.2
0
-0.2
-0.4
C. Profile Evolution During Annealing
• Comparing Eqn. (1) with the Gaussian profilefrom the last set of notes, we see that ∆Rp isequivalent to 2 Dt . Thus
C x tQ
R Dt
x R
R DtP
P
P
, exp( ) =+( )
−−( )
+( )
2 2 2 22
2
2π ∆ ∆(7)
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∆RP
Implanted
After Diffusion
2Dt
• Thus if the implanted profile is Gaussian, laterthermal cycles produce a Gaussian profile as well(assuming the surface doesn't come into play).
• The only other profile we can calculateanalytically is when the implanted Gaussian isshallow enough that it can be treated as a deltafunction and the subsequent anneal can be treatedas a one-sided Gaussian. (Recall example indiffusion notes.)
1020
1019
Con
cent
ratio
n (c
m-3
)
1018
10170 0.05 0.1 0.15 0.2 0.25 0.3
Depth (µm)
Antimony 360 keV
Boron38 keV
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• Real implanted profiles are more complex.• Light ions backscatter to skew the profile
upwards.• Heavy ions scatter deeper.
• 4 moment descriptions of these profiles are oftenused (with tabulated values for these moments).
Range: RQ
xC x dxP = ( )∫−∞
∞1(8)
Std. Dev: ∆RQ
x R C x dxP P= −( )∫ ( )−∞
∞1 2
(9)
Skewness: γ =−( ) ( )∫
−∞
∞x R C x dx
Q R
P
P
3
3∆(10)
Kurtosis: β =−( ) ( )∫
−∞
∞x R C x dx
Q R
P
P
4
4∆(11)
D. Implants in Real Silicon - Channeling
• At least until it is damaged by the implant, Si is acrystalline material.
• Channeling can produce unexpectedly deepprofiles.
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• Screen oxides and tilting/rotating the wafer canminimize but not eliminate these effects. (7˚ tilt iscommon.)
0 0.1 0.2 0 .3 0 .4 0. 5 0.6 0 .7 0 .8Depth (µm)
Con
cent
ratio
n (c
m-3
) 2 x 1013 cm-2 scaled
2 x 1013 cm-2
2 x 1015 cm-2
1021
1020
1019
1018
1017
1016
1015
• Sometimes a dual Pearson profile description isuseful.
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Modeling of Range Statistics
• The total energy loss during an ion trajectory isgiven by the sum of nuclear and electronic losses(these can be treated independently).
dEdx
N S Sn e= − +( ) (12)
R dxN
dES E S E
R
n e
E= ∫ =
+∫0 0
1 0
( ) ( )(13)
A. Nuclear Stopping
• An incident ion scatters off the core charge on anatomic nucleus, modeled to first order by ascreened Coulomb scattering potential.
V rq Z Z
rra
( ) exp= −
21 2
4πε(14)
TargetRecoil
Incidention
ScatteredIon
• This potential is integrated along the path of theion to calculate the scattering angle. (Look-uptables are often used in practice.)
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• Sn(E) in Eqn. (13) can be approximated by
S E xZ Z
Z Z
mm mn( ) .
/ / /=+( ) +
−2 8 10 15 1 2
12 3
22 3 1 2
1
1 2 eV - cm2
(15)
where Z1, m1 = ion and Z2, m2 = substrate.
B. Non-Local and Local Electronic Stopping
• Drag force caused by charged ion in "sea" ofelectrons (non-local electronic stopping).
Dielectric Medium
Retarding E-field
Vion
• Collisions with electrons around atoms transfersmomentum and results in local electronicstopping.
Vion
Target
e-
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• To first order,
S E cv kEe ion( ) /= = 1 2, k x≅ −0 2 10 15. ev cm1/2 2 (16)
C. Total Stopping Power
Ene
rgy
loss
(ke
V µm
-1)
10
100
1000
10 100 1000Energy (keV)
AsN
BN
SEPN
• The critical energy Ec when the nuclear andelectronic stopping are equal is
B: ≈ 17keVP: ≈ 150keVAs, Sb : > 500keV
Damage Production
• Consider a 30keV arsenic ion, which has a rangeof 25 nm, traversing roughly 100 atomic planes.
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• The number of displaced particles created by anincoming ion is given by
nEE
ionsn
d= =
×=
230 0002 15
1000,
(17)
300 eV Si Knock-on
30 keVAs ion
100 atomic planes
Damage cylinder
t = 0.1 ps
t = 0.5 ps
t = 6.0 ps
• Molecular dynamics simulation of a 5keV Boronion implanted into silicon [de la Rubia, LLNL]
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Amorphization
• For high enough doses, the crystal becomesamorphous and loses all long range order. At thispoint, the arrangement of lattice atoms is randomand the damage accumulation has saturated.
1E15 1.5E15 2E15 4E15 5E15 1E16
0.2µm
Cry
stal
line
Am
orph
ous
Surface
• Cross sectional TEM images of amorphous layerformation with increasing implant dose (300keVSi -> Si) [Rozgonyi]
Damage Annealing
Goals:
• Remove primary damage created by the implantand activate the dopants.
• Restore silicon lattice to its perfect crystallinestate.
• Restore the electron and hole mobility.• Do this without appreciable dopant redistribution.
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10-8 10-6 10-4 10-2 1 100
0.1
1
10
100
Surface Vrecombination
Bulk I&Vrecombination
Surface Irecombination
Initial excess I & V
Ann
hila
ted
I & V
per
impl
ante
d io
n
Seconds
• Bulk and surface recombination take place on ashort time scale.
• "+1" I excess remains. These I coalesce into{311} defects which are stable for longer periods.
• {311} defects anneal out in sec - min at moderatetemperatures (800 - 1000˚C) but eject I ⇒ TED.
<311>
<110>
311 Capture radiusI-dimer
Ribbon-like defect
• Stable dislocation loops can form when thedamage is greater (amorphizing implant - seebelow).
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Solid Phase Epitaxy
• If the substrate is amorphous, it can regrow bySPE.
5 min 10 min 15 min 20 min
Amorphous
100 nm
EORdamage
• Cross sectional TEM images of amorphous layerregrowth at 525˚C, from a 200keV, 6e15 cm-2 Sbimplant [Fletcher].
SPE regrowth
EOR loops
Residualdamage
Max damagebelow
amorphizationthreshold
a/c interface
Implanted Profile
Con
cent
ratio
n
DepthSurface
• BUT - the tail of damage beyond the a/c interfacecan nucleate stable, secondary defects and causetransient enhanced diffusion (TED).
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Dopant Activation
• When the substrate is amorphous, SPE providesan ideal way of repairing the damage andactivating dopants.
• At lower implant doses, activation is much morecomplex because stable defects form.
400 500 600 700 800 900 0
0.2
0.4
0.6
0.8
1.0
TA (˚C)
Sub AmorphousAmorphous
3 x 1012 cm-2
1 x 1015 cm-2
1 x 1014 cm-2
Fra
ctio
n A
ctiv
e
8 x 1012 cm-2
2.5 x 1014
2 x 1015
ReverseAnnealing
1.0
0.1
0.01400 500 600700 800 900 1000
TA (˚C)
Fra
ctio
n A
ctiv
e
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• Plot (above) of fractional activation versus annealtemperature for Boron. The intermediatetemperature range represents reverse annealing.
• Reverse annealing is though to occur because of acompetition between the native interstitial pointdefects and the boron atoms for lattice sites.
Transient Enhanced Diffusion
0 0.08 0.16 0.24 0.32 0.4Depth (µm)
10 sec 1000˚C
2 min 800˚C
Con
cent
ratio
n (c
m-3
)
1019
1018
1017
1016
• TED is the result of interstitial damage from theimplant enhancing the dopant diffusion for a brieftransient period.
• It is the dominant effect today that determinesjunction depths in shallow profiles.
• It is anomalous diffusion, because profiles candiffuse more at low temperatures than at hightemperatures for the same Dt.
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• The basic model for TED assumes that all theimplant damage recombines rapidly, leaving only1 interstitial generated per dopant atom when thedopant atom occupies a substitutional site (the +1model) [Giles].
Con
cent
ratio
n (c
m-3
)
1019
1018
1017
1016
1020
1021
As profile
Boron profiles
InitialFinal
0 0.05 0.1 0.15 0.2 0.25 0.3 0.35 0.4Depth (microns)
• TED effects may be very non-local. Here the Asprofile recrystallizes by SPE without much TED.The buried boron layer is drastically affected bythe +1 interstitials in the As tail region.
Atomic Level Understanding Of TED
• {311} clusters form rapidly and then are stable forextended periods (sec - min), driving TED byemitting I while they shrink.
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1011
1013
1015
Si
Sel
f-In
ters
titia
l Den
sity
(cm
-3)
1017
1019
0 0.2 0.4 0.6 0.8 1Depth (µm)
+1 Initial Damage10-6 sec
10-5
10-410-3
10-2
10-1
• By 0.1 sec (750˚C), the {311} defects haveformed and CI is down to ≈ 1013 cm-3 (SUPREM).
• But CI*≈ 108 cm-3 at 750˚C, so the enhancement is
> 105!
Si
Sel
f-In
ters
titia
l Den
sity
(cm
- 2)
815˚C738˚C705˚C670˚C
1 102 104 1061011
1012
1013
1014
1015
Time (seconds)
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• This enhancement decays over a time period ofsec - min as the {311} clusters break up.
• Given this picture, we can model the {311}behavior as follows:
I Cl Cln n+ ⇔ +1 (18)
where Cln is a cluster with n interstitials.
− = = −
= −
∂∂
∂∂
Ct
Clt
k C Cl k Cl
growth shrinkage
If I r (19)
• The most important part of the transient is whilethe {311} clusters are evaporating I, maintaininga constant supersaturation of I.
• During this period, dopant diffusivityenhancements are ≈ constant and given by (seetext):
C
C a C
E EkT
I
I I
b Fmax
* exp= − −
1
4 3 0π(20)
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500 600 700 800 900 1000 1100 1200Temperature C̊
106
105
104
102
103
Inte
rstit
ial S
uper
satu
ratio
n C
Imax
/CI*
Estimating the Duration of TED
• Over time the interstitial supersaturation decays tozero and TED ends.
1021
1020
1019
1017
1018
Con
cent
ratio
n (c
m-3
)
1016
105
104
As-implanted1
10
100
1000
0 0.1 0.2 0.3 0.4 0.5Depth (µm)
Interstitial Supersaturation R
atio
1 min, 750 C̊
10 min, 750̊ C
• Example - Boron TED. Note that CI/ CI* has
dropped from 104 to 102 in 10 min at 750˚C.
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• The excess I diffuse into the bulk and recombineat the surface.
RP Diffusionflux
Surface
CImax
SurfaceRecombination
Flux
Dose Q
• The flux towards the surface is d C RI I Pmax / where
RP is the range of the implant.• The time to dissolve the clusters is given by the
dose divided by the flux (see text):
τ πenh
P
I
ba R Qd
EkT
=
4 3exp (21)
500 600 700 800 900 1000 1100 1200Temperature ˚C
106
104
102
10-2
1
Tim
e (s
econ
ds)
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• Thus the general picture of TED that emerges is:
QP
τenh
Time
Enh
ance
men
t
10
100
1000
10,000
1
{311} s decay
Steady-state
Rapidexponential
decayCIm
ax/C
I*
• Because the {311} clusters exist for longer timesat low T, there can actually be greater dopantmotion during low T anneals.
1021
1020
1019
1018
Con
cent
ratio
n (c
m-3
)
1017
1016
104
105
0 0.1 0.2 0.3 0.4 0.5 0.6Depth (µm)
700C
800C
700C800C
900C
900C
Interstitial Supersaturation R
atio
1000
100
10
1