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Doping: Depositing impurities into Si in a controlled manner

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Presentation on theme: "Doping: Depositing impurities into Si in a controlled manner"— Presentation transcript:

1 Doping: Depositing impurities into Si in a controlled manner
Diffusion Doping: Depositing impurities into Si in a controlled manner

2 Overview Diffusion vs Implantation Mechanism,Models Steps Equipment

3 Goal: Controlled Junction Depth
Controlled dopant concentration and profile Preferred location of maximum concentration need not be the surface P+ P+ Drain Source N “well” Wafer (Substrate): P Type

4 Diffusion & Ion Implanatation
Ion Implantation Bombardment of ions SOURCE Ions Electric Field Junction is where N = P Can also be used when doping N in N OXIDE BLOCK Wafer (Substrate)`

5 Diffusion & Ion Implantation
Solid-in-solid high temperatures (1000 C) Distances covered are in um or nm Diffusion OXIDE BLOCK Wafer (Substrate)`

6 Mechanism , Models Substitutional (10-12 cm2/s)
Interstitial replacement (10-6 cm2/s) Interstitial movement Substitutional preferred (better control) Au, Cu diffuse by interstitial mechanism B, P etc by substitutional mechanism Two ideal cases Constant source, limited source Using Fick’s First & second law J = Flux D - Diffusivity of A in B N- Concentration x - distance

7 Models Limited source Constant Source Dose Q = constant
Approx by Delta Fn Constant Source Concentration at x=0 is No Complementary Error Function Total Dose Q

8 Models Constant Source Concentration at x=0 is No
Important Parameter : Dt species, temp and time N0 Concentration Impurity 3 2 1 Distance from Surface

9 Models Limited Source Dose Q Important Parameter : Dt N0
Area under the curve is constant If you normalize, erfc drops faster than Gaussian Concentration Impurity 3 1 2 Distance from Surface

10 Diffusivity Diffusivity Follows Arrhenius behavior
Wafer goes through heating cycles many times in the process Effective Diffusivity * time = sum (Diffusivity * time) Concept of thermal budget

11 Diffusion Max absorption (at a given temp) Usually quite high
Good for emitter and collector, but not for base Not all dopant can contribute to electron/hole near solubility limit Solubility limit in the range of 10 20/cm3 at 1000o C Diffusion into silicon Faster on grain boundaries 10 times in poly silicon Diffusivity in SiO2 usually very low (Segregation occurs)

12 Junction Formation N Carrier Conc Impurity Conc P Jn Distance
from surface

13 Diffusion: Drive In: Dopant re distribution
Deposited dopant must be pushed into Si Re-distribution of dopant Oxidation of exposed Si to protect OXIDATION Dopant Diffusion *Dopant profile changes due to diffusion * Also due to preference for Oxide/Silicon: N-type piles up in Si, P-type depletes in Si

14 Diffusion: Steps Dep Diffusion OXIDE BLOCK 1.Pre Clean
To remove particles Thin oxide grows OXIDE BLOCK 2.HF Etch To remove oxide Not too much! 3.Deposit (pre dep) Deposit enough to be higher than the solubility limit 4.Drive In High temp to enable diffusion inside Si Also forms SiO2 (with high dopant concentration) 2-STEP diffusion (usual) 5.Deglaze (HF Etch) Oxide may act as dopant source in future steps Removing highly doped oxide may be problem (for dry etch)

15 Diffusion: Dep: schematic
Wafers are Horizontal Gas Flow Better Uniformity Less wafers per batch Vertical Poor Uniformity More wafers per batch (or can have smaller chamber) Gas Flow Dummy wafers placed in the beginning & end

16 Doping: Gas phase Dopant can be in Gas/Liquid/Solid state, but is typically carried using N2 in gaseous form *Carrier gas may be bubbled through liquid source *Carrier gas may pass over heated solid source * inert gas can provide volume to maintain laminar flow Chamber Carrier Gas (N2) + Source Reaction gas

17 Doping: Gas phase Reaction/Diffusion Limited Phosphorus oxy chloride
Phosphine Arsenic Oxide Diborane Boron Tribromide

18 Solid phase Solid Source Slugs between wafers
Lower through put Cleaning is issue (slugs can break) Safer to handle(no toxic vapor at room temp) Spin coating (with solvents) Similar to photo resist coating Cost of extra spin/bake steps thickness variations

19 Doping: Solid phase Phosphorous pentoxide Arsenic Oxide
Antimony Tri Oxide Boron Trioxide Tri Methyl Borate (TMB)

20 Issues Side diffusion Maximum dopant concentration is near surface
Increases with temperature/time Limits the space between devices Maximum dopant concentration is near surface ==> majority of current near surface (Surface tends to have max defects) ==> less control Dislocation generation (thermal drive in) Surface contamination (dep) Low dopant concentration and thin junction (small junction depth) are difficult At 0.18 um , junction depth is ~ 40 nm At 0.09 um, junction depth may be 20 nm

21 Issues: Side diffusion
Side diffusion (Lateral Diffusion) BLOCK Wafer (Substrate)` Diffusion OXIDE BLOCK

22 Example of Real systems :
Hitachi systems *Hitachi-Zestone VII *2m x 3m x 3m *300 mm wafer *one wafer at a time * lower thermal budget, * better control, uniformity * low throughput *Hitachi-Vertron V *1m x 3.5m x 3.3m *200 mm wafer *150 wafers at a time * higher thermal budget, * good control, uniformity * high throughput

23 Example of Real systems : Protemp
Protemp system picture

24 Gettering To remove unwanted impurities
Try to get them to the back of wafer Defects Ar implant Dep SiN/SiO2 (stress) Oxygen during crystal growth (intrinsic) High Conc P on back of wafer

25 Measurement Sheet Resistance (average)
Four point probe, VDP (Van der Pauw) Bevel Interference Dye SIMS

26 Diffusion: Summary Diffusion Temp, Time, Thermal budget
Doping (more important for older nodes) Relevant for all nodes 2 step (constant source, limited source) Solid/Liq/Gas

27 Ion Implantation “Somewhat similar” to Sputtering
Dopant goes inside the silicon sputtering deposits on the surface Used for controlled doping concentration profile (depth) Equipment Mechanism Issues Summary

28 Equipment Schematic from © Peter van Zant

29 1. Ion Source Gas or solid source (no liquid source)
Solid heated to obtain vapor (P2O5) effectively gas source Mass flow meters (to control the flow better) Gas usually Fluorine based Ionization chamber low pressure (milli/ micro torr) to ionize and minimize contamination heated filament (thermionic emission) positively charged ions created

30 2. Analyzing Selection, analyzing, mass analyzing, ion separation
Similar to Mass Spectroscope Usually the second stage (before acceleration) Magnetic field to control the path Charge to Mass Ratio Some of the species from BF3 source Selection of B+

31 3. Acceleration Acceleration needed for implantation
Positive ions accelerated with ring anodes Energy range: 5 keV for low, 2 MeV for high Medium current : 1 mA High current: 10 mA Current ~ Dose Beam Focus (magnetic/electric) SOI 100 mA High Current Oxygen High energy ==> high throughput few seconds per wafer 10 mA High Current Beam Current Low Energy High Energy Low Current 1 mA keV MeV Accln Energy

32 4. Scanning Beam size ~ 1 sqr cm Wafer size 200 mm or 300 mm Issues:
neutral atoms need to be removed because... dose calculated by current integrator Electrical (beam) scanning & Mechanical (wafer) scanning Beam Scan:(medium current) beam moves outside the wafer for turn controlling XY plates may be destroyed by discharge Rotate wafer for uniformity Wafer scan: (high current) Beam shuttering: (electrical/mechanical) turn beam off when not on wafer

33 5. Target chamber End chamber low particle, high vacuum Wafer held on
clamp (more particles) OR ESC (less particles) Anti-static devices on the chamber Integrate the current to measure dose For 2+ ions, divide by 2 and so on... Wafer charging: minimize by connecting wafer to ground (with a charge counter) dielectrics may get damaged use flood gun to provide electron (and count it in measurement)

34 Stopping cross section
Electrons attract the +vely charged ions Nuclei repel the +vely charged ions Mechanism Inelastic collision: Electron (ionization) Nuclear (nuclear reactions) Elastic collision Electron Nuclear (atom substitution) Stopping cross section vs energy (plots from web) At low energy Nuclear collisions predominant At high energy electronic collisions predominant Variation in ‘stopping cross section’ Gaussian profile expected (projected range Rp)

35 Implantation Mask with Photoresist or oxide
resist for medium and low energy, moderate dose high energy/high dose: increase in temp Resist re-flow Cross link (for organics) less soluble (stripping an issue) Faraday Cage Retain secondary electron from wafer Otherwise, wafer under dosed -Ve Bias e-

36 Issue: Transverse Straggle
implant Gaussian OXIDE BLOCK Transverse Straggle (Diffraction) Even in implantation, dopants present in lateral direction

37 Channeling Some ions will move through “channels” without experiencing
nuclear or electron collision for a “long” time ==> No Gaussian Profile

38 Channeling 1. Hold the wafer at an angle (~ 8 degree)
Also causes “shadow” ==> increase transverse straggle(called undercut) BLOCK ==> Too much angle is also a problem Shadow Undercut

39 Channeling 2. Dep amorphous material on the top It has to be very thin
and not stop ions implant OXIDE BLOCK 3. Damage top of wafer and make it amorphous (eg high energy silicon implant)

40 Channeling 4. Increase temperature ==> reduce channel cross section
Channeling critical angle ~ (Z/E) 1/2 ==> Low energy implants more likely to channel

41 TED Transient Enhanced Diffusion ©Solid State Technology
Damage during implantation ==> point defects (vacancies) interstitial silicon atoms reduced during anneal Channel dopant diffuse to surface ==> VT modification ©Solid State Technology

42 RTA Anneal to heal the damage Diffusion during anneal an issue
High temp repair is faster than anneal Repair energy barrier 5 eV, diffusion barrier 3 or 4 eV 1. Adiabatic (laser, heats surface , < micro sec) profile control difficult (not used) 2. Thermal flux ( micro to 1 sec) laser, ebeam, flash lamp surface+bulk heating rapid cooling ==> point defects 3. Iso thermal (W-Halogen lamp) 30 sec (1100 C)

43 Diffusion vs Ion Implantation
Dep+Diffusion: depends on chemical nature and solubility Implantation: on energy of ion beam Expensive Better Control of junction depth, dose, profile Less ‘transverse straggle’


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