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Ion Implantation
Ion Implantation
Process by which energetic impurity
atoms can be introduced into single
crystal substrate in order to change
its electronic properties.
Ion Implantation and Controlled Doping
of Impurities
In this process the ions are accelerated to high
energies and allowed to impact the silicon
surfaces.
Because of inherent energy they penetrate into
the lattice and are placed inside the silicon
lattice.
Dr. G. Eranna Integrated Circuit Fabrication Technology © CEERI Pilani
Advantages
Extremely accurate dose control
Tailor made and well controlled doping profile
 large range-of doses-1011
to 1016
/cm2
 Low Temperature process
 Wide choice of masking materials (Oxide, PR, Metal)
 Clean environment (Mass separation, vacuum)
 Non-Equilibrium process (conc. Excess of S.S. limit)
Ion Implantation
Disadvantages
• Highly sophisticated and costly.
• Damage to semiconductor.
• Dopant redistribution during
Annealing
• Charging of insulating layers.
• Photoresist heating and hard to strip.
Ion Implantation System
V
V
Ion
source
Analyzing magnet
Pump
Resolving
aperature
Accelerator
Focus
Neutral
beam gate
Neutral
trap X & Y
scan
plates
Wafer
Faraday cup
Q0-30keV
0-200keV
ION IMPLANTATION
CEERI PILANI, INDIA
Dr. G. Eranna Integrated Circuit Fabrication Technology © CEERI Pilani
Ion Implanter
Implant Profiles
• At its heart ion implantation is a random process.
• High energy ions (1-1000 keV) bombard the substrate and lose
energy through nuclear collisions and electronic drag forces.
Range
R
Projected range
RP
Vacuum Silicon
•The projected range describes the peak of the implanted profile
Implant Profiles
• Profiles can often be described by a Gaussian distribution,
with a projected range and standard deviation. (200keV
implants shown.)
C(x) =CP exp −
x−RP( )
2
2∆RP
2








1021
1020
1017
1019
1018
Concentration(cm-3)
0 0.2 0.4 0.6 0.8 1
Depth (µm)
Sb
As P
B
0.606CP
∆RP
RP
Q = C x()
−∞
∞
∫ dx
Q =2π∆RP CP
(1)
(2)
or
where Q is the dose in ions cm-2
and is measured by the
integrated beam current.
Implant Profiles
Depth(µm)
Implant Profiles
StandardDeviation(µm)
Implant Profiles
Ranges and standard deviation ∆Rp of dopants in
randomly oriented silicon
Implant Profiles
• Monte Carlo simulations of the random trajectories of a group
of ions implanted at a spot on the wafer show the 3-D spatial
distribution of the ions. (1000 phosphorus ions at 35 keV.)
Implant
Beam
x
y
z
80
40
0
-40
0
50
-100
-50
0
40
80
120
Implant Profiles
• Side view shows depth distribution Rp and ∆Rp while the beam
direction view shows the lateral straggle.
z
Beam direction
80
40
0
-40
y
050100 -100-50
y
-40
0
40
80
x
Side view
0 40 80 120
Implant Profiles
• The two-dimensional distribution near window edge is often
assumed to be composed of just the product of the vertical and
lateral distributions.
C x,y( )=Cvert x()exp −
y2
2∆R⊥
2





 (3)
• Now consider what happens at a mask edge - if the mask is thick
enough to block the implant, the lateral profile under the mask is
determined by the lateral straggle.
• The description of the profile at the mask edge is given by a sum
of point response functions with Gaussian form of Eq (3) above.
Masking Implants
• How thick does a mask have to be?
• For masking,
C*
xm( )=CP
*
exp −
xm −RP
*
( )
2
2∆RP
* 2










≤CB
CP
*
RP
*
Depth
xm
C*(xm)CB
Concentration
(4)
For an efficient masking, the
thickness of the mask should be
large enough that the tail of
implant profile in Si is at some
specified background conc.
Qp
Masking Implants
• Setting C*(xm)= CB and solving for the required mask
thickness,
xm =RP
*
+∆RP
*
2ln
CP
*
CB





=RP
*
+m∆RP
* (5)
• The dose that penetrates the mask is given by
QP =
Q
2π∆RP
*
exp−
x−RP
*
2∆RP
*







xm
∞
∫
2
dx =
Q
2
erfc
xm −RP
*
2 ∆RP
*





 (6)
• Parameter m indicates that the mask thickness should be equal to the
range + some multiple m times the standard deviation in masking material
Since the integral or sum of Gaussian
function can be described as an error
function
Profile : High tilt Angle
• Real structures may be even more complicated because mask edges
are not vertical.
• High tilt angle implant for halo doping to minimize short channel
effect
30DegreeTilt
Distance(µm)
Distance(µm)
30Þtilt
0 0.2 0.4 0.6 0.8 1.0
0.2
0
-0.2
-0.4
TSUPREM
50Kev P
Profile Evolution During Annealing
• The only other profile we can calculate analytically is when the
implanted Gaussian is shallow enough that it can be treated as a
delta function and the subsequent anneal can be treated as a
one-sided Gaussian. (Recall example in Dopant Diffusion )
DeltaFunction
DoseQ
(Initial Profile)
Imaginary
DeltaFunction
DoseQ
Diffused
Gaussian
Virtual
Diffusion
x
0
C x,t( )=
Q
πDt
exp −
x2
4Dt





 (8)
Profile Evolution During Annealing
• Comparing Eqn. (1) with the Diffusion Gaussian profile, we see
that ∆Rp is equivalent to . ThusDt2
C x,t( )=
Q
2π∆RP
2
+2Dt( )
exp −
x−RP( )
2
2 ∆RP
2
+2Dt( )








(7)
²R P
Implanted
After Diffusion
2Dt
Evolution of
a Gaussian
Profile after
annealing
Profile Evolution During Annealing
• Real implanted profiles are more complex.
• Light ions backscatter to skew the profile up.
• Heavy ions scatter deeper.Concentration(cm-3
)
Amorphous Silicon
Dr. G. Eranna Integrated Circuit Fabrication Technology © CEERI Pilani
• Gaussian distribution often match the central region of the
implanted profiles .
• B distribution is skewed toward surface resulting significant
deviations in the tail of the distribution
Profile Evolution During Annealing
• 4 moment descriptions of these profiles are often used (with
tabulated values for these moments).
Range: RP =
1
Q
xC x()
−∞
∞
∫ dx
Std. Dev: ∆RP =
1
Q
x −RP( )
−∞
∞
∫
2
C x()dx
Skewness: γ=
x −RP( )
3
C x( )dx
−∞
∞
∫
Q ∆RP
3
Kurtosis: β=
x −RP( )
4
C x( )dx
−∞
∞
∫
Q ∆RP
4
(9)
(10)
(11)
(12)
• Channeling can produce unexpectedly deep profiles
Implants in Real Silicon - Channeling
• Channeled profile is composed of two portions. Main peak+
channeled part. Accurate modeling requires additional parameter
to specify the ratio of the dose in main &channeled profile
• Note that the channeling decreases in the high dose implant (green
curve) because damage blocks the channels.
B Implant: <100>
Zero Tilt
35KeV
ION IMPLANTATION
CEERI PILANI,INDIA
Non-Local and Local Electronic Stopping
Dielectric Medium
Retarding E-field
• Drag force caused by charged ion in “sea” of electrons (non-local electronic
stopping).
• Collisions with electrons around atoms transfers momentum and results in local
electronic stopping.
CEERI PILANI, INDIA
8.1. microtech ion implant,1,2
8.1. microtech ion implant,1,2
8.1. microtech ion implant,1,2

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8.1. microtech ion implant,1,2

  • 2. Ion Implantation Process by which energetic impurity atoms can be introduced into single crystal substrate in order to change its electronic properties.
  • 3. Ion Implantation and Controlled Doping of Impurities In this process the ions are accelerated to high energies and allowed to impact the silicon surfaces. Because of inherent energy they penetrate into the lattice and are placed inside the silicon lattice. Dr. G. Eranna Integrated Circuit Fabrication Technology © CEERI Pilani
  • 4. Advantages Extremely accurate dose control Tailor made and well controlled doping profile  large range-of doses-1011 to 1016 /cm2  Low Temperature process  Wide choice of masking materials (Oxide, PR, Metal)  Clean environment (Mass separation, vacuum)  Non-Equilibrium process (conc. Excess of S.S. limit) Ion Implantation
  • 5. Disadvantages • Highly sophisticated and costly. • Damage to semiconductor. • Dopant redistribution during Annealing • Charging of insulating layers. • Photoresist heating and hard to strip.
  • 6. Ion Implantation System V V Ion source Analyzing magnet Pump Resolving aperature Accelerator Focus Neutral beam gate Neutral trap X & Y scan plates Wafer Faraday cup Q0-30keV 0-200keV
  • 8. Dr. G. Eranna Integrated Circuit Fabrication Technology © CEERI Pilani Ion Implanter
  • 9. Implant Profiles • At its heart ion implantation is a random process. • High energy ions (1-1000 keV) bombard the substrate and lose energy through nuclear collisions and electronic drag forces. Range R Projected range RP Vacuum Silicon •The projected range describes the peak of the implanted profile
  • 10.
  • 11. Implant Profiles • Profiles can often be described by a Gaussian distribution, with a projected range and standard deviation. (200keV implants shown.) C(x) =CP exp − x−RP( ) 2 2∆RP 2         1021 1020 1017 1019 1018 Concentration(cm-3) 0 0.2 0.4 0.6 0.8 1 Depth (µm) Sb As P B 0.606CP ∆RP RP Q = C x() −∞ ∞ ∫ dx Q =2π∆RP CP (1) (2) or where Q is the dose in ions cm-2 and is measured by the integrated beam current.
  • 14. Implant Profiles Ranges and standard deviation ∆Rp of dopants in randomly oriented silicon
  • 15. Implant Profiles • Monte Carlo simulations of the random trajectories of a group of ions implanted at a spot on the wafer show the 3-D spatial distribution of the ions. (1000 phosphorus ions at 35 keV.) Implant Beam x y z 80 40 0 -40 0 50 -100 -50 0 40 80 120
  • 16. Implant Profiles • Side view shows depth distribution Rp and ∆Rp while the beam direction view shows the lateral straggle. z Beam direction 80 40 0 -40 y 050100 -100-50 y -40 0 40 80 x Side view 0 40 80 120
  • 17. Implant Profiles • The two-dimensional distribution near window edge is often assumed to be composed of just the product of the vertical and lateral distributions. C x,y( )=Cvert x()exp − y2 2∆R⊥ 2       (3) • Now consider what happens at a mask edge - if the mask is thick enough to block the implant, the lateral profile under the mask is determined by the lateral straggle. • The description of the profile at the mask edge is given by a sum of point response functions with Gaussian form of Eq (3) above.
  • 18. Masking Implants • How thick does a mask have to be? • For masking, C* xm( )=CP * exp − xm −RP * ( ) 2 2∆RP * 2           ≤CB CP * RP * Depth xm C*(xm)CB Concentration (4) For an efficient masking, the thickness of the mask should be large enough that the tail of implant profile in Si is at some specified background conc. Qp
  • 19. Masking Implants • Setting C*(xm)= CB and solving for the required mask thickness, xm =RP * +∆RP * 2ln CP * CB      =RP * +m∆RP * (5) • The dose that penetrates the mask is given by QP = Q 2π∆RP * exp− x−RP * 2∆RP *        xm ∞ ∫ 2 dx = Q 2 erfc xm −RP * 2 ∆RP *       (6) • Parameter m indicates that the mask thickness should be equal to the range + some multiple m times the standard deviation in masking material Since the integral or sum of Gaussian function can be described as an error function
  • 20. Profile : High tilt Angle • Real structures may be even more complicated because mask edges are not vertical. • High tilt angle implant for halo doping to minimize short channel effect 30DegreeTilt Distance(µm) Distance(µm) 30Þtilt 0 0.2 0.4 0.6 0.8 1.0 0.2 0 -0.2 -0.4 TSUPREM 50Kev P
  • 21. Profile Evolution During Annealing • The only other profile we can calculate analytically is when the implanted Gaussian is shallow enough that it can be treated as a delta function and the subsequent anneal can be treated as a one-sided Gaussian. (Recall example in Dopant Diffusion ) DeltaFunction DoseQ (Initial Profile) Imaginary DeltaFunction DoseQ Diffused Gaussian Virtual Diffusion x 0 C x,t( )= Q πDt exp − x2 4Dt       (8)
  • 22. Profile Evolution During Annealing • Comparing Eqn. (1) with the Diffusion Gaussian profile, we see that ∆Rp is equivalent to . ThusDt2 C x,t( )= Q 2π∆RP 2 +2Dt( ) exp − x−RP( ) 2 2 ∆RP 2 +2Dt( )         (7) ²R P Implanted After Diffusion 2Dt Evolution of a Gaussian Profile after annealing
  • 23. Profile Evolution During Annealing • Real implanted profiles are more complex. • Light ions backscatter to skew the profile up. • Heavy ions scatter deeper.Concentration(cm-3 ) Amorphous Silicon
  • 24. Dr. G. Eranna Integrated Circuit Fabrication Technology © CEERI Pilani • Gaussian distribution often match the central region of the implanted profiles . • B distribution is skewed toward surface resulting significant deviations in the tail of the distribution
  • 25. Profile Evolution During Annealing • 4 moment descriptions of these profiles are often used (with tabulated values for these moments). Range: RP = 1 Q xC x() −∞ ∞ ∫ dx Std. Dev: ∆RP = 1 Q x −RP( ) −∞ ∞ ∫ 2 C x()dx Skewness: γ= x −RP( ) 3 C x( )dx −∞ ∞ ∫ Q ∆RP 3 Kurtosis: β= x −RP( ) 4 C x( )dx −∞ ∞ ∫ Q ∆RP 4 (9) (10) (11) (12)
  • 26. • Channeling can produce unexpectedly deep profiles
  • 27. Implants in Real Silicon - Channeling • Channeled profile is composed of two portions. Main peak+ channeled part. Accurate modeling requires additional parameter to specify the ratio of the dose in main &channeled profile • Note that the channeling decreases in the high dose implant (green curve) because damage blocks the channels. B Implant: <100> Zero Tilt 35KeV
  • 28.
  • 29.
  • 31. Non-Local and Local Electronic Stopping Dielectric Medium Retarding E-field • Drag force caused by charged ion in “sea” of electrons (non-local electronic stopping). • Collisions with electrons around atoms transfers momentum and results in local electronic stopping.
  • 32.