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APCVD Process: Reactant Transport Dynamics

The document discusses various aspects of chemical vapor deposition (CVD) processes. It describes the transport of reactants and byproducts in atmospheric pressure CVD (APCVD) and the surface chemical reactions that occur. Low pressure CVD (LPCVD) and plasma enhanced CVD (PECVD) are also introduced. Specific examples of depositing polysilicon, silicon dioxide, and silicon nitride using LPCVD and PECVD processes are provided, including common deposition parameters and properties of the deposited films. Unintentional doping from the substrate during epitaxial deposition and autodoping effects are also covered.

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Udai Singh
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0% found this document useful (0 votes)
27 views32 pages

APCVD Process: Reactant Transport Dynamics

The document discusses various aspects of chemical vapor deposition (CVD) processes. It describes the transport of reactants and byproducts in atmospheric pressure CVD (APCVD) and the surface chemical reactions that occur. Low pressure CVD (LPCVD) and plasma enhanced CVD (PECVD) are also introduced. Specific examples of depositing polysilicon, silicon dioxide, and silicon nitride using LPCVD and PECVD processes are provided, including common deposition parameters and properties of the deposited films. Unintentional doping from the substrate during epitaxial deposition and autodoping effects are also covered.

Uploaded by

Udai Singh
Copyright
© All Rights Reserved
We take content rights seriously. If you suspect this is your content, claim it here.
Available Formats
Download as PPT, PDF, TXT or read online on Scribd

A.

Transport of Reactions to
Wafer Surface in APCVD
1. Transport of reactants by forced convection to the deposition region
2. Transport of reactants by diffusion from the main gas stream to the
wafer surface
1. Turbulent flow can produce thickness nonuniformities
2. Depletion of reactants can cause the film thickness to decrease in direction of
gas flow

3. Adsorption of reactants on the wafer surface

APCVD
B. Chemical reaction
1.
2.
3.

Surface migration
Site incorporation on the surface
Desorption of byproducts

C. Removal of chemical byproducts

1. Transport of byproduct through the boundary layer


2. Transport of byproducts by forced convection
away from the deposition region

APCVD
At

steady state if two fluxes are equal

C S CG
The

kS
1
hG

growth rate of the film, v (cm/s), is

F
k S hG CG
v
N k S hG N
Where N is the number of atoms incorporated
into the film per unit volume
For single composition film, this is the density

Mole fraction
The

mole fraction in incorporating


species in the gas phase
CG Partial pressure of the reactant gases
Y

CT
Total gas pressure

where CT is the concentration of all


molecules in the gas phase

Two limiting cases for APCVD


model
Surface

reaction controlled case


(kS<<hG) v CT k Y
N

Mass

transfer or gas-phase diffusion


controlled case (hG<<kS)
CT
v
hGY
N

APCVD

Both cases predict linear growth rates


but they have different coefficients
There is no parabolic growth rate

Surface reaction rate constant is controlled


by Arrhenius-type equation (X=Xoe-E/kT)
Quite temperature sensitive

Mass transfer coefficient is relatively


temperature independent
Sensitive to changes in partial pressures and total gas
pressure

APCVD

Epitaxial deposition of Si

Epitaxial deposition of Si
Slopes

of the reaction-limited graphs are


all the same
activation energy of about 1.6 eV
This implies the reactions are similar; just the
number of atoms is different
There is reason to believe that desorption of H 2
from the surface is the rate limiting step

In

practice

epitaxial Si at high temperatures (mass


transfer regime)
poly-Si is deposited at low temperatures
(reaction limited, low surface mobility)

Deposition of Si
Choice

of gas affect the overall growth rate

Silane (SiH4) is fastest


SiCl4 is the slowest

Growth

rate in the mass transfer regime is


inversely dependent on the square root of
the source gas molecular weight
Growth rate is dependent on the
crystallographic orientation of the wafer
(111) surfaced grow slower than (100)
Results in faceting on nonplanar surfaces

APCVD

In the preceding theory, assumed hG and


Cs were constants
F h C C
1

Real systems are more complex than this


Consider the chamber where wafers lie on
a susceptor (wafer holder).
Stagnant boundary layer, S, is not a constant,
but varies along the length of the reactor
Cs varies with reaction chamber length as
reaction depletes gases

APCVD

APCVD

Effects
Changes

the effective cross section of the


tube, which changes the gas flow rate
Increasing the flow rate reduces the thickness
of the boundary layer and increases the mass
transfer coefficient
Reduces gas diffusion length

To

correct for the gas depletion effect, the


reaction rate is increased along the length
of the tube by imposing an increasing
temperature gradient of about 525 oC

APCVD

Sometimes we wish to dope the thin films


as they are grown (e.g. PSG, BSG, BPSG,
polysilicon, and epitaxial silicon).
Addition of dopants as gases for reaction
AsH3, B2H6, or PH3.

Surface reactions now include

Dissociation of the added doping gases


Lattice site incorporation of dopants
Coverage of dopant atoms by the other atoms
in the film

APCVD

Another problem, common in CMOS


production, is unintentional doping of
lightly doped epitaxial Si when depositing
them on a highly doped Si substrate.
Occurs by diffusion because of the high deposition
temperatures (8001000oC)

Growth rate of the deposited layers is


usually much faster than diffusion rates
(vt >> Dt), the semi-infinite diffusion
model can be applied
C
x
C x, t erfc

2 Dt

APCVD

Mass transport on to deposited


films

Atoms can outgas or be transported by carrier


gas from the substrate into the gas stream and
get re-deposited downstream
The process is called autodoping

Empirical expression to describe autodoping


x

Cautodoping C exp
L concentration and
C*S is an effective substrate surface
*
S

L is an experimentally determined parameter


As film grows in thickness, dopant must diffuse
through more film and less dopant enters gas phase.

Autodoping

Autodoping from the backside, edges, or


other sources usually results in a relatively
constant level.

This is because the source of dopant does


not diminish as quickly but is at a much
lower level.

APCVD
The left part of the
curve arises from
the out-diffusion
from the substrate
The straight line
part arises from
the front-side
autodiffusion
The background
(constant) part is
from backside
autodoping

In APCVD
It is critical to deliver the same gas flows to all the
wafers in order to produce the same growth rates
Wafers placed side-by-side

In LPCVD
Mass transfer coefficient is higher as the diffusion
distance of reactants is increased.
the boundary layer thickness slightly increased as P
decreases

DG 1
hG

S
P

Reactions are limited by ks where adsorption on


wafer surface is key limiting step.
Wafers can be stacked parallel to one another
Note that this arrangement will provide a higher throughput

LPCVD

PECVD

There are some cases where temperature


requirements (thermal budget) will not
allow high-temperature depositions
E.g., depositing Si3N4 or SiO2 after Al
APCVD and LPCVD do not produce good quality
films ~ 450oC

Reaction produced in a plasma ignited


using an inert gas between two electrodes
The sample may be heated
Usually between 200-450 oC

PECVD

PECVD
Ideally

suited to rapidly varying the film


composition and properties during
deposition
Apply a potential and an AC signal (13.56
MHz) across a low pressure of the inlet
gases
The processes that occur are complicated and
very difficult to model
The resultant products are very far from
thermodynamic equilibrium
Generates high concentration of particulates
Pinhole density is a problem if chamber is not routinely
cleaned.

PECVD
Oxynitride

Oxide

Microfluidic Channels formed by PECVD

CVD

LPCVD
PECVD

LPCVD

Polysilicon

Deposited by thermal decomposition of silane (SiH4)


Deposition temperature range 580-650C
SiH4 (vapor) = Si (solid) + 2H2 (gas)

A typical set of deposition parameters:

Temperature: 620C
Pressure: 0.2-1.0 torr
SiH4 flow rate ~ 250sccm
Deposition rate = 8-10nm/min

Doping of film
In-situ (during deposition) by the addition of dopant gases
such as phophine, arsine, and diborane
Often doped after deposition by diffusion or ion implantation
Typically highly doped to achieve low resistance
interconnections
0.01-0.001 ohm-cm can be obtained in diffusion-doped
polysilicon.

Silicon dioxide

Variety of methods (PECVD, LPCVD, APCVD)

Index of refraction is used to determine the quality.


Can be doped or undoped

Oxide doped with 5-15% by weight of various dopants can be


used as a diffusion source.

PECVD oxide

SiH4 (gas) + 2N2O (gas) SiO2 (solid) + 2N2 (gas) + 2H2 (gas)
Temperature: 200-400C
Deposition rate of 900nm/min is achievable
Not a good step coverage
Controllable film stress (compressive)
Contains hydrogen (SiOH)
Used for deposition over metals

LPCVD oxide using dichlorosilane

SiCl2H2 + 2N2O SiO2 + 2N2 + 2HCl


Temperatures ~ 900C
Good step coverage
Compressive stress used to stress-compensate LPCVD nitride

Oxide
LPCVD oxide using tetraethylorthosilicate
(TEOS) (liquid source)

Si(OC2H5)4 SiO2 (solid) + 4C2H4 (gas) + 2H2O (gas)


Deposited at temperatures between 650-750C
Excellent uniformity and step coverage

Silicon nitride

Variety of methods (PECVD, LPCVD, APCVD)

Can be used as an oxidation mask (LPCVD)


An excellent barrier to moisture and sodium contamination
(PECVD)
PECVD nitride

SiH4 (gas) + NH3 (gas) SixNyHz (solid) + H2 (gas)


Deposition temperature: 200-400C
Deposition rate of 20-50nm/min
Not a good step coverage
Controllable film stress

Changes after high temperature anneal due to H 2 out-diffusion

LPCVD nitride using dichlorosilane

2SiCl2H2 (gas) + 4NH3 (gas) Si3N4 (solid) + 6H2 (gas)


Deposition temperatures: 700-800C
Good step coverage
Tensile stress
Better resistivity (1016 ohm-cm) and dielectric strength (10
MV/cm) compared to PECVD nitride films (106-1015 ohm-cm
and 1-5MV/cm)

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