Introduction To Ion Implantation Dr. Lynn Fuller, Dr. Renan Turkman DR Robert Pearson DR Robert Pearson
Introduction To Ion Implantation Dr. Lynn Fuller, Dr. Renan Turkman DR Robert Pearson DR Robert Pearson
Introduction To Ion Implantation Dr. Lynn Fuller, Dr. Renan Turkman DR Robert Pearson DR Robert Pearson
INTRODUCTION TO ION IMPLANTATION Dr. Lynn Fuller, Dr. Renan Turkman Dr Robert Pearson
Webpage: http://people.rit.edu/lffeee Rochester Institute of Technology 82 Lomb Memorial Drive Rochester, NY 14623-5604 Tel (585) 475-2035 Fax (585) 475-5041 Email: [email protected]
Department webpage: http://www.microe.rit.edu
Rochester Institute of Technology Microelectronic Engineering
10-12-11 implant.ppt
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Ion Implantation
Varian 400
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OUTLINE Principles of Ion Implantation Generate a focused beam of ions to be implanted (B+, P+ or As+) Accelerate the ions Scan the ion beam over the wafer Implant dose Ion Implantation Equipment Plasma source and ion extraction Ion selection Accelerating column End station Low and high (beam) current implanters
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OUTLINE Implanted Dopant Profiles Dopant ion-substrate interactions Post implant anneal Dopant concentration profiles Implanted Dopant Profiles (continued) Channeling Implanting through thin film layers (e.g. oxide) Masking against ion implants
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INTRODUCTION Ion implant is used to put specific amounts of n-type and p-type dopants (Dose) into a semiconductor. The dose is accurately measured during implantation giving outstanding control and repeatability. Specific regions can be implanted using a variety of masking materials including photoresist. Ion implantation is basically a low temperature process. Ion implant can deliver lower doses than chemical doping (predeposit). Dose can be as low as 1011 /cm2 In today's advanced integrated circuits ion implantation is used for all doping applications. (with a few exceptions)
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BASICS
F = qE + q ( v x B )
Example 1: Example 2: vy + v B w/m2 v
+
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vx
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GENERATION OF A DOPANT GAS PLASMA Source Gas Molecule + e Dopant Ion + (Other Atoms, Molecules and/or Radicals) + e + e Example : Boron Trifluoride as B source BF3 + e B+ + F2 + F + e + e Other dissociative ionizations result in the generation of B10+,F+, BF2+ The dopant ion sources commonly used in silicon processing are boron trifluoride BF3, phosphine PH3, arsenic pentafluoride AsF5, arsine AsH3 .
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Solenoid N
BF3 e B+ e BF2+
Gas feed
M v 2 / 2 = q Vext
(positive) ions
2qVext m
Ion Implantation
TYPICAL SOURCE SET UP Pressure Extraction Voltage Extraction Current Arc Voltage Arc Current Filament Current Filament Voltage Solenoid Current 30mT 33 KV 0.8 mA 2000 V 50 mA 150 A 20 V 3.0 A
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e-
+
Filament Anode
Extraction Outlet
+ +
Velocity - v
Electrons boil off the filament and ionize the gas. Solenoid make electrons follow a spiral path increasing ionization
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SELECTION OF THE IONS TO BE IMPLANTED The ions are extracted from the source and analyzed in a magnetic field. The Lorentz force makes the ions take a curved path with a radius of curvature that depends on the mass of each ionic species. By adjusting the magnetic field strength, only the selected ions will enter the accelerating column. N Heavy Ions S Light Ions Selected Ions
Analyzing Magnet
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q ( xB) = M 2 / R R=M / q B
2qVext m
B
Magnetic Field
Heavier ions
M /q = R2 B2 / (2 Vext)
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Ion Implantation
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100
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BF2+
100
F+ BF+
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E field
Resolving Aperture Vacc Ground
Column length =
Final Kinetic Energy of the Ion = q ( Vext + Vacc ) Example: Vext = 30 KV Vacc = 70 KV Energy of the Ion= E= 100 KeV
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ACCELERATION OF THE IONS An acceleration voltage is applied across the column giving the ions their final kinetic energy. This voltage should be adjustable.
This shows 14 equal acceleration plates. If the desired acceleration was 70KeV each section would contribute 5000 volts for example.
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BF2 IMPLANTS Boron mass = 11 Fluorine mass = 19 BF2 mass = 49 The energy divides by mass so 100 KeV BF2 is equivalent to 22.4 KeV B11 implant BF2 peak is larger than B11 peak giving more current and shorter time for large dose implants BF2 can give shallow implants BF2 reduces channeling (explained in following pages)
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SCANNING THE BEAM Scanning of the beam The focused ion beam is scanned over the wafer in a highly controlled manner in order to achieve uniform doping. Either the wafer or the beam could be stationary.
Y
Scan Patterns
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ELECTROSTATIC BEAM SCANNING I) Electrostatic scanning (low/medium beam current implanters. I < 1mA)
Vy Vertical Scan Vx Si wafer
Horizontal Scan
This type of implanter is suitable for low dose implants. The beam current is adjusted to result in t=10 sec./wafer. With scan frequencies in the 100 Hz range, good implant uniformity is achieved with reasonable throughput.
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MECHANICAL BEAM SCANNING Mechanical Scanning (high beam current implanters. I > 1 mA )
Stationary Ion Beam Beam Size = 20 cm2 Si wafer
Excellent wafer cooling needed. Substantial load/unload time. 15 - 25 wafers /disc. Excellent throughput for high dose implants.
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IMPLANT DOSE The implant dose is the number of ions implanted per unit area (cm2) of the wafer. If a beam current I is scanned for a time t , the total implanted charge Q = ( I x t ). For a dose ,the total number of implanted ions is (Scan , area As x ). Since each ion is singly positively charged, this corresponds to a total charge of (q x As x ). Q= It = q As => = Dose = I t / ( q As ) ions/cm2
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Faraday Cup
XL I Current Integrator
Scan Position
XR
XR Wafer Holder
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ion beam
Idt = q =As q
back plate VFaraday
DOSE MONITORING
Vsuppression ( - 500 V )
cup
( - 100 V )
I + Integrator
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COMPLETE SYSTEM
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DOPANT ION-SUBSTRATE INTERACTIONS Upon entering the substrate, the ion slows down due to nuclear and electronic stopping. Nuclear stopping : Nuclear stopping is due to the energy transfer from the ion to Si nuclei. The interaction may be strong enough to displace the Si atom from its site ( only 15 eV needed to displace one Si atom ). The displaced Si atom may even have enough kinetic energy to displace several other Si atoms. Arsenic and Phosphorous ions lose their energy mostly by nuclear stopping. They cause substantial Si crystal damage when the implant dose exceeds 5E13/cm2.
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Ion at rest
Projected Range Rp
Electronic stopping is due to the energy transfer from the ion to the electrons of the host Si crystal. Boron ions lose their energy mostly by electronic stopping. Electronic stopping does not cause crystal damage.
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POST IMPLANT ANNEAL The damaged crystal needs to be restored. This is typically achieved by 900 C, 30 min. furnace anneals or 1150 C, 30 sec. rapid thermal anneals. The interstitial dopant ions become substitutional, thus donating carriers. The interstitial (displaced) silicon atoms become substitutional ,thus removing the defects that trap carriers and/or affect their mobility. During the post implant anneal, dopant ions diffuse deeper into silicon. This must be minimized to maintain shallow junctions.
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Trend: higher the dose, the more disorder, thus the higher the final temperature required for full activation
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} From Curves
Ni
I mqA dt
Cbackground
Approximation N = Ni xi
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As
10-1
B P
10-2 10
Sb
100 Implantation Energy (KeV)
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0.1
B
0.01
P As Sb
0.001 10
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1,000
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CALCULATIONS
Using the equations on the previous pages: Find: Xj sheet Rho implant time surface conc. average doping
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30keV 100keV
Simple Gaussian
300keV 800keV
1017 0 0.2 0.4 0.6 0.8 1.0 1.2 1.4 1.6 1.8 2.0
Depth in m
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VT ADJUST IMPLANT Assume that the total implant is shallow (within Wdmax) +/- Vt = q Dose*/Cox where Dose* is the dose that is added to the Si Cox is gate oxide capacitance/cm2 Boron gives + shift Cox = or / Xox Phosphorous gives - shift Example: To shift +1.0 volts implant Boron through 1000 kooi oxide at an energy to place the peak of the implant at the oxide/silicon interface. Let Xox= 200 . Dose = Vt Cox/q =(1.0)(3.9)(8.85E-14)/(1.6E-19)(200E-8)=1.08E12 ions/cm2 but multiply by 2 since goes into silicon and in Kooi oxide so dose setting on the implanter is 2.16E12 ions/cm2
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Relative degree of openness of the silicon crystal for ions moving in <111>, <100> and <110> directions
unchanneled ion: > cr
(110)
(100)
(111)
: entrance angle
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Channeling process
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The implanted dose C(x) dx is about the same with or without channeling. But along the channeled profile is smaller than along the unchanneled profile. Since the sheet resistance Rs is defined as: Rs= [ q (x) C(x)dx ]-1 = [q C(x)dx]-1 (where is the average effective mobility) Rs is
smaller in regions where channeling occurs.
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CHANNELING IS NON UNIFORM ACROSS THE WAFER Due to beam scan angle s and/or the wafer flex angle f, the entrance angle of ions varies across the wafer. The resulting channeling variations cause the sheet resistance to vary across the wafer. These Rs variations can be as much as 25 % across a wafer. As the extent of local channeling is difficult to control, channeling must be prevented.
BEAM BEAM
Wafer
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Wafer
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PREVENTING CHANNELING Channeling does not occur if there is significant implant damage that turns the implanted layer into an amorphous one. Heavy ions like P31 and As75 at large doses do not show channeling. Light ions and/or low dose implants are prone to channeling. In such instances, channeling can be prevented by: 1) Implanting through a thin amorphous layer (e.g. oxide). 2) Tilting and twisting the wafer to close crystal openness as seen by the ion beam. 3) Implanting heavy, but electrically inactive species like Si or Ar prior to the actual dopant implant. The pre-implant implant turns the wafer surface into an amorphous layer.
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CHANNELING Implanting Through Thin Films In addition to channeling prevention, implanting through a thin film layer (e.g. few 100 A of SiO2) offers the following advantages: 1) It prevents photoresist residues/deposits from reaching the silicon surface. The resist residues deposited on the thin film can subsequently be etched away with that film (e.g. SiO2 dipped in B.O.E.)
resist deposit resist resist
oxide
Silicon Wafer
2) It prevents excessive evaporation (out-gassing) of volatile species (e.g. As) during implant damage anneals.
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MASKING AGAINST ION IMPLANTS Various thin films can be used to mask against ion implants : resist, oxide, nitride, polysilicon, etc. The most widely used combination is resist over the oxide. 1 to 1.5 m thick resist blocks most of the ion implants encountered in silicon processing.Silicon dioxide slows down the ions at about the same rate as silicon does. Silicon nitride is a much stronger barrier to ions than silicon.
Dopant Density Implant Doping O X I D E
RESIST
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MASKING WITH PHOTORESIST, POLY, AND OXIDE B11, Dose = 2 E15, E = 50 KeV
P-well
N-well
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0 1 0 0
KeV
2961.954 Angstroms
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BF2 Implant at 80 A in Varian 400 without a water cooled chuck Note: Varian 350D can do implants up to 300 A with no photoresist damage because of wafer cooling
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ION IMPLANT VS. CHEMICAL SOURCE PREDEPOSIT Advantages of Ion Implant Low dose introduction of dopants is possible. In chemical source predeposits dose values less than 5E13/cm2 are not achievable. Ion implant dose control is possible down to 1E11/cm2. High dose introduction is not limited to solid solubility limit values. Dose control is very precise at all levels. Excellent doping uniformity is achieved across the wafer and from wafer to wafer. Done in high vacuum, it is a very clean process step (except for out gassing resist particulates due to excessive local power input ). Drawbacks of Ion Implant It requires very expensive equipment ( $1M or more). At high dose values, implant throughput is less than in the case of chemical source predep.
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LECTURE REVIEW Principles of Ion Implantation The implant depth controlled by the energy E of the ions Dopant density primarily controlled by the implant dose Ion Implantation equipment Low current implanters High current implanters Implanted Dopant Profiles Nuclear stopping and implant damage Post implant anneal Gaussian doping profiles Channeling and its prevention Thin film coverage of the wafer surface Advantages and Drawbacks of Ion Implantation
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REFERENCES 1. Silicon Processing for the VLSI Era Volume I, S. Wolf and R.N. Tauber, Lattic Press, Sunset Beach, CA, 1986. 2. The Science and Engineering of Microelectronic Fabrication, S.A. Campbell, Oxford University Press, New York, NY, 1996. 3. VLSI Technology, Edited by S.M. Sze, McGraw-Hill Book Company, 1983.
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HOMEWORK ION IMPLANT 1: The implant depth is controlled by the a) beam size b) acceleration voltage c) beam current d) implant time 2: The volume density of implanted dopants is controlled by the a) plasma density b) beam size and implant time c) implant time only d) beam current and implant time 3: In using low current implanters that process one wafer at a time, the optimal implant time per wafer (i.e. best uniformity / throughput compromise) a) 1 s b) 10 s c) 50 s d) 100 s 4: True or false? Channeling is a serious problem when implanting AS75 ions at a dose = 5x1015/cm2. 5: In CMOS processing, threshold adjust doping can be made by a) chemical source predep only b) ion implant only c) either chemical source predep or ion implant. 6: Calculate the implant dose and energy needed to make the pmos Vt of -1 volt for the following device parameters. N+ Poly gate, 250 gate oxide, 2E16 cm-3 substrate doping, Nss=3.4E11.
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