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Sputtering

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Title: Sputtering


1
Sputtering
Eyal Ginsburg
WW46/02
2
Contents
  • Metallization structure
  • PVD System Overview
  • Sputtering yield, conditioning, methods
  • Film nucleation and growth

3
Contact Metal Lines - SEM
4
Glue Layer (Cont. 1)
5
Aluminum - General
  • Al-alloys thin films were selected for the first
    30 years of the IC industry.
  • They continue to be the most widely used
    materials, although copper.
  • Al has low resistivity (?2.7??-cm), and its
    compatibility with Si and SiO2.
  • Al forms a thin native oxide (Al2O3) on its
    surface upon exposure to oxygen, and affect the
    contact resistance.

6
Aluminum - General (cont.)
  • Al thin films can also suffer from corrosion (ex.
    Al dry etch may leave chlorine residues on Al
    surface and lead to formation of HCl and then
    attack the Al).

7
Aluminum interconnects
  • The material used in interconnects is not pure
    aluminum, but an aluminum alloy. Usually with Cu
    (0.5-2), sometimes with Si.
  • The Cu in Al-alloy slows the electromigration
    (EM) phenomenon. Si slows EM slightly, used in
    contact level to prevent spiking.
  • Al-alloys decrease the melting point, increase
    the resistivity and need to be characterized (ex.
    Dry etch).

8
Metal line stack
  • Usually the metal line contains 4-5 layers
  • Al - This layer makes the contacts with the
    Tungsten plugs. It is the primary current
    carrier.
  • TiN Layer - Creates a barrier between the Al/Cu
    and the Titanium layers because of the increasing
    temperature at a downstream process will increase
    the rate of the reaction of Al with Ti.

9
Metal stack (Cont. 1)
  • Titanium Layer - Provides an alternate current
    path (shunt) around flaws in the primary current
    carrier. And thus improves electromigration
    characteristics.

10
Metal stack (Cont. 2)
  • TiN ARC Layer - This is an anti-reflecting
    coating which aides lithography to keep control
    of critical dimensions and to absorb light during
    the resist exposure. It also functions as a
    hillock suppressant.

11
Metal stack - SEM
Metal line
ILD
TiN
W- Via2
Ti
TiN
Metal line
Al
12
  • PVD System Overview (Endura)

13
Endura PVD system
14
Endura standard mainframe
15
Mainframe Components
  • Preclean Ch. Applies a light. Non selective
    plasma etch to the wafer before the PVD process.
  • Cooldown Ch. Cools the wafer after the PVD
    process.
  • Expansion Ch. (CD) Optionally configured for
    PVD or other processes such as etch.
  • Wafer orienter/degas Ch. Orients the wafer flat
    to a designated angle and degasses the wafer to
    remove water vapor before the preclean process.
  • PVD Ch. DC magnetron sputter deposition
    chambers for depositing materials used in
    interconnects metalization (ex. Al, Ti, TiN,
    TiW).
  • Cassette loadlocks The starting point for wafer
    transfers. Accept 1 cassette with 25 wafers.

16
Vacuum system
  • PVD system uses Ultra-High Vacuum (UHV) to reduce
    particulates and provide purer film qualities.
  • The tool uses staged vacuum regimes to achieve
    UHV.

17
Pressure regions and vacuum stages
18
PVD chambers and pumps
19
  • Sputter deposition for ULSI

20
Sputtering General
  • Sputtering is a term used to describe the
    mechanism in which atoms are ejected from the
    surface of a material when that surface is stuck
    by sufficiency energetic particles.
  • Alternative to evaporation.
  • First discovered in 1852, and developed as a thin
    film deposition technique by Langmuir in 1920.
  • Metallic films Al-alloys, Ti, TiW, TiN,
    Tantalum, Nickel, Cobalt, Gold, etc.

21
Reasons for sputtering
  • Use large-area-targets which gives uniform
    thickness over the wafer.
  • Control the thickness by Dep. time and other
    parameters.
  • Control film properties such as step coverage
    (negative bias), grain structure (wafer temp),
    etc.
  • Sputter-cleaned the surface in vacuum prior to
    deposition.

22
Sputtering steps
  • Ions are generated and directed at a target.
  • The ions sputter targets atoms.
  • The ejected atoms are transported to the
    substrate.
  • Atoms condense and form a thin film.

23
Sputtering
  • Coating process that involves the transport of
    material from the target to the wafer. Atoms from
    the target are ejected as a result of momentum
    transfer between incident ions and the target.
    The particles traverse the vacuum chamber and are
    deposited on the wafer.

24
Application of Sputtering
  • Thin film deposition
  • Microelectronics
  • Decorative coating
  • Protective coating
  • Etching of targets
  • Microelectronics patterning
  • Depth profiling microanalysis
  • Surface treatment
  • Hardening
  • Corrosion treatment

25
The billiard ball model
  • There is a probability that atom C will be
    ejected from the surface as a result of the
    surface being stuck by atom A.
  • In oblique angle (45º-90º) there is higher
    probability for sputtering, which occur closer to
    the surface.

26
Sputter yield
  • Defined as the number of atoms ejected per
    incident ion.
  • Typically, range 0.1-3.
  • Determines the deposition rate.
  • Depends on
  • Target material.
  • Mass of bombarding ions.
  • Energy of the bombarding ions.
  • Direction of incidence of ions (angle).
  • Pressure

27
Sputter yield (Cont. 1)
Target materials Al/Cu(0.5)
2
Grain size 200?m
1
Grain size 45?m
28
Sputter yield (Cont. 2)
  • Molecule size need to be about the same size as
    the sputtered material
  • too big cause layer deformation and yield a lot
    of material.
  • too small cause layer deformation w/o ejecting
    atoms. Target deformation Less uniform dep.

29
Sputter yield (Cont. 3)
  • Ion energy Vs. sputter yield

30
Sputter yield (Cont. 4)
  • Sputter yield peaks at lt90º.
  • Atoms leave the surface with cosine distribution.

31
Sputter yield (Cont. 5)
  • Pressure reduction allow better deposited
    atoms/molecules flux flow towards the substrate.
    Expressed by Mean free path which is the
    average distance an atom can move, in one
    direction without colliding at another atom.

32
Process conditions
  • Type of sputtering gas. In purely physical
    sputtering (as opposed to reactive sputtering)
    this limits to noble gas, thus Argon is generally
    the choice.
  • Pressure range usually 2-3 mTorr (by glow
    discharge).
  • Electrical conditions selected to give a max
    sputter yield (Dep rate).

33
Sputter deposition film growth
  • Sputtered atoms have velocities of 3-6E5
    cm/sec and energy of 10-40 eV.
  • Desire many of these atoms deposited upon the
    substrate.
  • Therefore, the spacing is 5-10 mm.
  • The mean free path is usually lt5-10 mm.
  • Thus, sputtered atoms will suffer one or more
    collision with the sputter gas.

34
Sputter dep. film (Cont. 1)
  • The sputter atoms may therefore
  • Arrive at surface with reduce energy (1-2 eV).
  • Be backscattered to target/chamber.
  • The sputtering gas pressure can impact on film
    deposition parameters, such as Dep rate and
    composition of the film.

35
Sputtering additional methods
  • Reactive sputtering
  • RF sputtering
  • Magnetron sputtering
  • Collimated sputtering
  • Hot sputtering

36
Reactive sputtering
  • Reactive gas is introduced into the sputtering
    chamber in addition to the Argon plasma.
  • The compound is formed by the elements of that
    gas combining with the sputter material (Ex.
    TiN).
  • The reaction is usually occurs either on the
    wafer surface or on the target itself.
  • As you add more reactive gas at some point the
    reaction rate exceeds the sputtering rate.
  • At this point the target surface switches from
    clean metal to compound over a short time.

37
Reactive sput. (Cont. 1)
  • The transition in target chemistry changes
    sputtering conditions dramatically !

38
Reactive sput. (Cont. 2)
  • Typical compounds deposited by reactive
    sputtering

Target Reactive Gas Compound
Al O2 Al2O3
Al N2 AlN
Ti O2 TiO2
Ti N2 TiN
Si N2 Si3N4
Ta O2 Ta2O5
Zn O2 ZnO
In-Sn O2 In2O3-SnO2
39
RF sputtering
  • DC sputter deposition is not suitable for
    insulator deposition, because the positive
    charge on the target surface rejects the ion flux
    and stop the sputtering process.
  • RF voltages can be coupled capacitively through
    the insulating target to the plasma, so
    conducting electrodes are not necessary.
  • The RF frequency is high enough to maintain the
    plasma discharge.

40
RF sputtering (Cont. 1)
  • During the first few complete cycles more
    electrons than ions are collected at each
    electrode (high mobility), and cause to negative
    charge to be buildup on the electrodes.
  • Thus, both electrodes maintain a steady-state DC
    potential that is negative with respect to plasma
    voltage, Vp.
  • A positive Vp aids the transport of the slower
    positive ions and slow down the negative
    electrodes.

41
RF sputtering (Cont. 2)
  • The induced negative biasing of the target due to
    RF powering means that continuous sputtering of
    the target occurs throughout the RF cycle.
  • But it is also means that this occurs at both
    electrodes.

42
RF sputtering (Cont. 3)
  • The wafer will be sputtered at the same rate as
    the target since the voltage drops would be the
    same at both electrodes for symmetric system.
  • It would thus be very difficult to deposit any
    material in that way.
  • Smaller electrode requires a higher RF current
    density to maintain the same total current as the
    larger electrode.

43
RF sputtering (Cont. 4)
  • By making the area of the target electrode
    smaller than the other electrode, the voltage
    drop at the target electrode will be much greater
    than at the other electrode.
  • Therefore almost all the sputtering will occur at
    the target electrode.

44
RF sputtering (Cont. 5)
  • We also use RF sputtering to clean out bottoms of
    Contacts and Vias before the actual deposition.
  • Remove native oxides and etch residues from
    Contacts/Vias.
  • During this step, a controlled thickness of
    surface material is sputtered off the wafer,
    removing any contaminants or native oxide.
  • A film can then be sputter deposited immediately
    afterward without breaking the vacuum.
  • This process was done in the pre-clean chamber.
  • This may also be done by BIAS SPUTTERING
    (reversing the electrical connections).

45
Magnetron sputtering
  • Here magnets are used to increase the percentage
    of electrons that take part in ionization events,
    increase probability of electrons striking Ar,
    increase electron path length, so the ionization
    efficiency is increased significantly.
  • Another reasons to use magnets
  • Lower voltage needed to strike plasma.
  • Controls uniformity.
  • Reduce wafer heating from electron bombardment.
  • Increased deposition rate

46
Magnetron sputtering (Cont. 1)
  • Lower voltage
  • Magnets produce magnetic field
  • Magnetic field make an electron go in curved path
    (helix)
  • Curved paths are longer ? more collisions
  • More collisions make more ions ? easier to strike
    plasma.
  • Controls uniformity
  • Electrons paths are more curved near stronger
    magnetic field.
  • More ions collide with target in regions of high
    magnetic field.
  • More ion collisions lead to more target atoms
    sputtering.
  • More magnets near edge/center makes edge/center
    thick deposition.

47
Magnetron sputtering (Cont. 2)
  • A magnetic field is applied at right angle to
    electric field by placing large magnets behind
    the target.
  • This traps the electrons near the target surface,
    and causes them to move in spiral motion until
    the collide with an Ar atom.
  • Dep rate increases up to 10-100 times faster than
    without magnetron configuration.

48
Magnetron sput (Cont. 3)
  • Magnetron sputtering can be done in either DC or
    RF modes, but the former is more common.
  • Target erodes rapidly in the ring region
    resulting in a deep groove in the target face,
    which cause to non-uniformity film.

49
Collimated sputtering
  • During the PVD process, metal atoms are sputtered
    at all angles. The standard process deposits
    metal on all areas of the process kit and at
    various angles on the wafer.
  • A small range of arrival angles during deposition
    can cause nonuniform film.
  • This leads to poor bottom coverage of small
    geometry, high aspect ratio contacts and vias as
    the holes seal off at the top before filling up
    at the bottom.

50
Collimated sput. (Cont. 1)
  • One way to improve this by having a narrow range
    of arrival angles, while atoms arriving
    perpendicularly to the wafer.
  • This method called collimated sputtering (first
    proposed in 1992).
  • A hexagonal holes plate is placed between the
    target and the wafer.

51
Collimated sput. (Cont. 2)
  • As the sputtered atoms travel through the
    collimator toward the wafer, only those with
    nearly normal incidence trajectory will continue
    to strike the wafer.
  • The collimator thus acts as a physical filter to
    low angle sputter atoms.

52
Collimated sput. (Cont. 3)
  • 70-90 of atoms are filtered and therefore the
    Dep rate is significantly reduced.
  • In addition the collimator should be cleaned and
    replaced, resulting additional downtime of the
    tool COST.
  • Suitable for contact and barrier layers where lot
    of material is not needed to be deposited.
  • Benefit with cover the bottom of Vias.

53
Collimated sput. (Cont. 4)
  • The next figure shows the bottom coverage of
    collimated sputtering compared to conventional
    versus contact aspect ratio.

54
Hot sputtering
  • Hot sputtering is a method used to fill spaced
    during deposition as well as to improve overall
    coverage.
  • The basic idea is to heat the substrate to
    450-500ºC during deposition.
  • Surface diffusion is significantly increased so
    that filling in spaces, smoothing edges and
    planarization are accomplished, driven by surface
    energy reduction.
  • The temperature in Via planarization processes is
    generally lower than that in contact to protect
    previously deposited Al layers.

55
Hot sputtering (Cont. 1)
  • The lower power in the hot aluminum step
    increases the length of time that the Al atoms
    can diffuse, increasing the distance that they
    travel before they stop.
  • Usually, a thin cold deposition is done first
    with substrate at room temperature, which has
    better adhesion to the underlying material.
  • Then is followed by hot PVD deposition.
  • Main drawbacks is the relatively high temp.
    (reaction, thermal-budget, etc).

56
  • Film Nucleation and Growth

57
Things affect film structure
  • The things that control grain structure are
  • Substrate
  • Base pressure (or contamination level)
  • Deposition temperature
  • Deposition rate
  • Later processing temperature
  • Process pressure (collisions)

58
Film microstructure
  • The film microstructure gives a graphic
    representative of how changing process pressure
    and wafer temperature affects the structure of a
    PVD film.

59
Grain size
Al grains - AFM photos. What is the reason for
the differences between these pictures ?
A. B.
60
What happened to this Ti target ?
61
Target malfunction
  • Ti target was warped near the edge of the target
  • The root cause the flatness of the backing
    plates, being out of specification. The epoxy did
    not adhere to the blank. During sputtering, the
    area where the epoxy did not adhere to the blank
    experienced high temperatures that could no
    longer be dissipated by the backing plate due to
    the minimal contact to the blank. Thus, as the
    area in question became hotter, the more likely
    that assembly warped.

62
The crystal structure of Ti
  • HCP up to 882 C
  • BCC above 882 C

63
Dep rate Vs. KWHR
64
Where to Get More Information
  • S. Wolf, Silicon Processing for the VLSI era, Vol
    1-2.
  • Peter Van Zant, Microchip Fabrication.
  • Stephen A. Campbell, The science and engineering
    of microelectronic fabrication.
  • J. D. Plummer, M. D. Deal and P.B. Griffin,
    Silicon VLSI technology.
  • J.L. Vossen and W. Kern, Thin film processing II.
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