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Non-encapsulated
Cross Section Basics
Purpose
Cross sections serve two main functions.
Cuts through representative structures within an IC show relationships
of layers and features, such as step coverage, interfaces
between layers, and possibly embedded defects or voids. Precision
cross sections through specific defects often lead to the
process step or mechanism which produced the defect.
Background and Theory
When applicable, non-encapsulated cross
sectioning is simpler and faster than the classical encapsulated
method. Results of non-encapsulated cross sectioning are more
suitable for viewing in a scanning electron microscope.
The passivation layer of the IC provides sufficient encapsulation
of malleable metallization to prevent smearing. Rounding of
the front edge is avoided by using hard, flat grinding and
polishing surfaces. Originally, 600 grit SiC paper was used
to grind to within 20 - 30 µm of the target. Polishing
from that point was accomplished solely and slowly on a glass
disc. (Hammond and Vogel, p 221) However, the need for faster
throughput and the introduction of hard tungsten plugs necessitated
new polishing media and techniques.
Today, the many possible choices for grinding and polishing
media can be confusing. The non-encapsulated process is still
easy to understand and execute. The procedure explained here
is basic, simple and fast. It produces excellent results which
can be imaged on either standard or field emission SEMs.
Equipment
Three variable speed 8 inch (200 mm)
polisher/grinders are recommended for this process. One variable
speed polisher, 10 - 150 RPM, is sufficient; but, frequent
wheel changes with a single polisher will slow down the process.
Required facilities are 120 or 220 volts power, a clean water
supply, and a drain.
Dry nitrogen (or a supply of aerosol cans) is also required
to blow samples dry. A stereo microscope and a metallurgical
microscope are required to check progress.
The only specialty equipment required is a polishing fixture
and sample mount. The process given here is designed specifically
for Accelerated Analysis’ PF101. However, with some
increase in grinding times, the lighter fixtures sold by Technology
Associates can be used.
Regardless of the number of polishers available, several interchangeable
8 inch (200 mm) wheels are recommended for this procedure.
Suggested allocation of nylon or aluminum wheels is suggested
below:
SiC paper (600, 800,
1000, 1200 grit)
1.0 µm Al2O3
on Mylar (or 1.0 µm diamond on Mylar)
0.3 µm Al2O3
on Mylar (or 0.5 µm diamond on Mylar)
0.1 µm diamond
on Mylar
0.05 µm Al2O3
on Mylar
0.1 µm and 0.05 µm diamond suspension on low nap
cloth
Procedure
The general cross sectioning procedure
has been broken down into four main steps: cutting and mounting,
grinding, fine grinding / rough polishing, and polishing.
Cutting
and Mounting
The result of cutting is a piece
of silicon roughly 5 mm (0.25 inches) square. The desired
cross section target should be within 50 µm of one
edge. The silicon piece is then attached to a sample mount
such that the edge containing the target is parallel to
and extending over the edge of the sample mount, as shown
in Fig. 1.
Figure
(1) Silicon piece attached to sample mount with wax. Note:
Target cross section line must extend beyond end of mount. |
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Variations involving diamond saws can
be substituted for the cleaving technique described below. When
the structure to be cross sectioned is large, the break can
be into the structure itself, eliminating all grinding steps.
An excellent example of using a laser to direct the break through
a specific structure is shown by Gajda (p 13).
Determine the desired cross section line. Establish visible
landmarks to use as navigation references. Photograph if necessary.
If suitable landmarks do not exist, create visible marks with
a laser or mechanical probe.
Cleave or
break the wafer parallel to and within 50 µm of the desired
cross section line. This first break creates the edge which
will be ground and polished.
Break away
a strip about 5 mm or 0.25 inches wide including the intended
target. Wider pieces can be polished, but the additional area
reduces effective pressure, and severely decreases removal rates.
Finally break
away about 5 mm or 0.25 inches.
Heat a sample
mount to 125°C. Apply a dot of wax and mount the sample
in cantilever fashion on the sample mount. (See Fig. 1 above.)
Grinding
The purpose of grinding is to rapidly
achieve a surface, one micron away from and parallel to, the
desired cross section line. The surface to be polished should
be flat and scratches should be no greater than those caused
by 1 µm Al2O3 or diamond particles on Mylar. The grinding
procedure typically requires less than 15 minutes including
inspection time.
The procedure given below is applicable to all silicon samples,
regardless of composition. However, variations in grinding media
can be entirely satisfactory, as long as the final surface is
flat and contains only very small scratches. The optional diamond
polishing media on Mylar may cut faster, but are not better
than Al2O3 unless the sample contains a high percentage of very
hard material such as tungsten.
| If more than
40 µm of material must be removed to reach the final
cross section line, begin grinding with 600 grit SiC paper.
Insert sample mount with sample into the polishing fixture.
Start the wheel rotation at 60 - 100 RPM and adjust water
to a low but continuous flow. Hold the polishing fixture
by its sides near the back (Teflon block end) between
thumb and finger. Lower the fixture and sample, Teflon
end first, to the rotating wheel. The wheel rotation is
into the sample. (See Fig. 2.) Allow the fixture to exert
pressure of its weight onto the sample. The SiC paper
will show a dark strip behind the sample as material is
removed. Wait 20 - 30 seconds, then check progress.
Figure (2) Hold
polishing fixture between thumb and forefinger such
that wheel rotates into the sample. Allow weight of
the fixture to determine pressure on the sample.
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Adjust
angle of the polishing line with adjustment screw on the
PF101 fixture as desired. Continue until the ground surface
of the sample is within 20 µm of the target line.
(20 µm is about 1/5 of an IC bonding pad.) Clean
the sample with running water before proceeding to the
next step.
Figure (3) Rinse sample and fixture with water between
each step. Grinding technique is the same for every step. |
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Set up the grinder with 800 grit SiC
paper. Maintain wheel rotation at 60 - 100 RPM and keep slow,
continuous water flow. If 600 grit SiC was used prior to this
step, remove at least 10 µm of material to eliminate
the subsurface damage created by the 600 grit grinding. Continue
until the ground surface is within 10 µm of the target
line. (See Fig. 3.) Again, adjust angle of the polishing line
with adjustment screw on the PF101 fixture. Typical time for
this step is 30 - 60 seconds depending on actual size of the
sample.
Set up the grinder with 1200 grit SiC paper. Maintain wheel
rotation at 60 - 100 RPM and keep slow, continuous water flow.
If 800 grit SiC was used prior to this step, remove at least
5 µm of material to eliminate the subsurface damage
created by the 800 grit grinding. Continue until the ground
surface is within 6 µm of the target line. Typical time
for this step is 30 - 60 seconds depending on actual size
of the sample.
Set up the grinder with 1 µm Al2O3 on Mylar. Maintain
wheel rotation at 60 - 100 RPM and keep slow, continuous water
flow. If 1200 grit SiC was used prior to this step, remove
at least 4 microns of material to eliminate the subsurface
damage created by the 800 grit grinding. Continue until the
ground surface is within 2 µm of the target line. Typical
time for this step is 60 seconds depending on actual size
of the sample.
Fine Grinding / Rough Polishing
The purpose of fine grinding / rough
polishing is to remove damage due to 1 µm grinding and
to enter the geometry of interest. For many, if not most applications,
the finish after fine grinding is perfectly adequate to reveal
details of semiconductor structure. This fact makes non-encapsulated
cross sectioning less intimidating. If an error in judgement
of removal rates does not permit further polishing the cross
section can reasonably be declared complete after this "rough
polishing" step. If the cross section is to be viewed
on a standard tungsten filament or LaB6 SEM, the chemical
etching to delineate features can, at the same time, remove
fine details. For example, note that the procedure given by
Hammond and Danyew (p 162) produces excellent results using
0.3 µm Al2O3 as the final polish. The additional step
with 0.1 µm diamond on Mylar achieves a superior finish
without danger of smearing soft metals.
Set up the grinder with 0.3 µm Al2O3 on Mylar. Decrease
wheel rotation to 30 RPM and keep slow, continuous water flow.
Remove at least 1 µm of material. Continue until the
ground surface is within 2 µm of the target line. Typical
time for this step is 60 seconds depending on actual size
of the sample.
Set up the grinder with 0.1 µm diamond on Mylar. (Diamond
is superior to Al2O3 . See NOTE below.) Again, use slow wheel
rotation of 30 RPM and keep slow, continuous water flow. Continue
until the ground surface is within 1.0 - 1.5 µm of the
target line. Typical time for this step is 60 seconds.
NOTE
Until this step, SiC, Al2O3, or diamond could be used interchangeably
with little effect on the end result. However, for this final
approach into the defect or geometry of interest, diamond
is preferable because of its sharp, clean cutting properties.
Polishing
The purpose of polishing is to remove
all scratches and to leave the exposed cross section without
artifacts from the grinding and polishing sequence. Additionally,
the completed cross section should be exactly centered on
the contact, via, or other feature in the target. Polishing
will remove very little material (2 µm or less) and
can not remove any deep scratches or damage created by grinding
too close to the desired finish with course abrasives. However,
polishing will remove surface scratches from the 0.1 µm
diamond. Polishing can expose very subtle details otherwise
lost in polishing artifacts.
Polishing is most important when the cross section is to be
viewed in a high-resolution field emission SEM (FESEM). High
resolution and low accelerating voltage FESEMs can image cross
sections as polished or with very light delineation etches.
The details of polishing depend on the composition of the
sample:
Si,
SiO2, and Al with/without thin barrier metal layers
Set
up the grinder/polisher with 0.05 µm Al2O3 on
Mylar. Adjust wheel rotation to 30 RPM and keep slow,
continuous water flow. Polish for 30 seconds or until
0.1 µm diamond scratches are removed. Repeat if
necessary and material permits.
The final polishing step uses the same 0.05 µm
Al2O3 set up to remove the streaks which may trail from
edges of metal or polysilicon lines. For this step hold
the polishing fixture between thumb and finger such
that the wheel rotates into the Teflon block end of
the fixture. Lower the sample to the wheel, Teflon end
first, and polish for 30 seconds. (See Fig. 4.)
Figure (4) Final polish, if necessary, with fixture
held in reverse direction on 0.05 µm AL2O3. (Never
grind in reverse direction!)
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Inspect, clean by rolling a cotton
tip saturated with soapy water over the polished surface and
top. Rinse with copious flow of water and blow dry.
Si, SiO2, and metallization including
tungsten plugs or layers
Set up the grinder/polisher with low
nap cloth. Place a circular track of 0.1 or 0.05 µm
diamond suspension on a damp wheel. Adjust wheel rotation
to 70 - 100 RPM. Do not use water. Polish for 30 seconds.
Repeat as necessary.
Inspect, clean by rolling a cotton tip saturated with soapy
water over the polished surface and top. Rinse with copious
flow of water and blow dry.
General Comments
The grinding procedure given involves
several short steps. Certainly, satisfactory results can be
obtained by grinding longer with fewer steps. However, the
procedure will be tedious if overall grind time is increased
by using fine grit to remove material slowly. Additionally,
if grinding time is excessive, material removal rate may decrease
as media wears and be difficult to judge.
Cross sections wider than the recommended 0.25 inches width
will require significantly longer grinding and polishing times.
Do not use worn out grinding media. Be aware of increased
removal rate when going from worn to fresh media. Surprisingly,
even fresh, finer grit polishing media may have a faster removal
rate than coarser, worn media.
Even if a cleaved edge is close to the desired final line
such that no grinding is required, a brief grind on 1200 grit
SiC is recommended to make a flat surface. Grind only as necessary
to create a flat surface, even if a portion of the surface
remains untouched. Jagged edges on a cleaved sample, if not
removed, will scratch away the Al2O3 or diamond.
End Notes
JJ Gajda, FG Trudeau, JA Wade, "Semiconductor
Structure Enhancement for SEM Analysis," Proceedings
of the International Symposium for Testing and Failure Analysis,
1981.
BR Hammond and RR Danyew, "A Microfinishing Technique
for Semiconductor Failure Analysis," Proceedings of the
International Symposium for Testing and Failure Analysis,
1988.
BR Hammond and TR Vogel, "Non-encapsulated Microsectioning
as a Construction and Failure Analysis Tool," Proceedings
of the 20th International Reliability Physics Symposium, 1982.
P Kasuba, "A Technique for Achieving Ultra-Smooth Chip
Cross Sections," Proceedings of the 21st International
Symposium for Testing and Failure Analysis, 1995.
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