Wyko NT3300 Profiling System
1.0
Title
Wyko NT3300 Profiling System (White-light interferometer)

Figure 1 - Wyko NT3300 Profiling
System
2.0
Purpose
This document has specific information about the capabilities,
configuration, and proper operation of the NT3300 white-light-interferometer
profiling system. The analysis software and automation features for the Wyko
are quite extensive, and are therefore not covered in this manual. See the
on-line help or the Wyko reference manual for more details. The machine is easy
to learn to use, but takes time to master. Interferometry is sometimes an art.
If you are new to interferometry (or even if you are quite experienced), you
should always question the validity of the measurement. The thin films we
measure are often transparent at the wavelength we measure with (centered
around 600 nm), and therefore multiple reflections from the substrate can give
bogus measurements.
3.0
Scope
3.1
Measurement Technique
The Wyko NT3300 interferometer determines the profile
of an object using interferometry instead of a stylus. Therefore, the profiles
of released MEMS structures can be measured without destroying them. The Wyko
has a range of objectives from 2X-50X and has an additional zoom from 0.5-2X
called the field-of-view (FOV) objective. There are two measurement techniques:
1) phase-shift interferometry (PSI) that uses a single wavelength of light, and
2) vertical-scanning interferometry (VSI) that uses multiple wavelengths of light.
The PSI mode is used to measure continuous surfaces (surfaces with step-heights
less than lambda/4, or about 150 nm) that are within the depth-of-field of the
objective you are using, and is accurate to about 1 nm (with work, it can be as
good as ~0.1 nm). The VSI mode is good for measuring step heights as high as 5
mm (yes, millimeters!), but has a reduced accuracy of about 10-30 nm. It
measures tall features by scanning the microscope head downwards and measuring
the response of the light intensity of each pixel. Use the VSI mode for
continuous structures that extend beyond the depth-of-field of the objective
you are using (i.e. for cantilevers with large strain gradients).
3.2
Resolution
The Wyko takes nm-resolution static measurements in
the z-axis (along the optical path) and µm-resolution measurements in
the x and y axes. Resolution in the x- and y-axes
is limited by optical diffraction and varies depending on which lens is used.
Best case, it cannot be better than the wavelength of light, lambda, used to
take the measurement (lambda~=600 nm). Because transverse (perpendicular to the
optical axis) resolution is limited by diffraction, the Wyko is NOT a good tool
to determine surface roughness smaller than lambda. An AFM is better suited for
this type of measurement.
3.3
Measurement Limitations
Measurements should be made on one type of material.
When more than one material is encountered, the step height between materials
is not accurate because the phase returned from the materials is not the same.
In the PSI mode, errors of up to ~300 nm (lambda/2) are possible. In VSI mode,
it is quite possible that errors are as large as a few microns. When you have
more than one material (i.e. measuring photoresist step heights or a
deep-trench etch that still has a PR mask) you should verify the measurement
with some other means to build confidence that what you are getting is correct.
If you need very accurate measurements, consider coating the wafer/die with a
thin film of gold or some other reflective material if you can.
3.4
More Measurement
Limitations
As alluded to in the opening section, measuring thin
films can give unreliable results at times. The Wyko has decent software to
determine the upper surface of a structure, but the software has been known to
fail. Always question the validity of the measurement results. It is usually
quite obvious when a measurement is bad if you use your a priori
knowledge of what you are measuring (i.e. a radius-of-curvature of 10 microns
is most likely not accurate).
4.0
Applicable
Documents
4.1
Wyko NT3300 Reference Manual
4.2
On-line help documentation
5.0
Definitions,
Process Terminology, Nomenclature
5.1
PSI:
Phase-Shift Interferometry
5.2
VSI: Vertical-Scanning
Interferometry
5.3
FOV:
Field-Of-View object, and set of lenses that increase the microscope power from
0.5 - 2X.
5.4
The Wyko operator station is shown
in Figure 2. The joystick controls the motorized stage (and microscope head for
tip/tilt) and the rotating control knob controls the microscope head height
(focus).


Figure 2 -
Wyko Operator Station
6.0
Safety
6.1
The Wyko is a relatively safe
machine to use. Care should be taken not to get fingers caught in the motorized
stages. There is an emergency-off button in case of smoke, sparks, fire, etc.
6.2
Equipment Precautions
6.2.1
Never lower the z-axis
without looking at the objectives to make sure they do not crash into your
sample.
6.2.2
Never install software on the
system; it may interfere with the Wyko software.
7.0
Statistical/Process
Data
8.0
Available
Processes, Process Notes
9.0
Operation
9.1
Start Up
9.1.1
The Wyko should be powered down unless
a user was taking measurements just prior to you. Press the green start button
to power up the interferometer and computer. If the power does not come on,
turn the red emergency-off button clockwise (or pull it out), and then press
the power button again. Turn on the computer monitor.
9.1.2
Log on to the computer once it has
booted up.
9.1.3
Enable the Wyko on the wand.
9.1.4
Start the measurement software
from Start->Programs->Wyko->Vision32 or double-click the
Vision32 icon on the desktop.
9.1.5
Let the interferometer warm up
(5-10 minutes should be enough) before continuing.
9.2
Stage Motion
The computer-controlled stage is
controlled with the x/y axis controller shown in Figure 2. Moving the joystick
controller will move the stage when the Wyko software is running. Pressing the
high-speed button and moving the joystick simultaneously will move the stage
faster.
9.3
Focusing
Focus is adjusted by rotating the z-axis controller. Pressing the
high-speed button and rotating the z-axis controller simultaneously will change
the focus much faster. You should always raise the objectives while looking at
the sample monitor when focusing the Wyko. This will prevent you from crashing
them into your sample. To focus, first lower the objective while watching the
object to a distance slightly less than the working distance of the objective
(50X: 2.5 mm, 20X: 3.5 mm, 10X: 6 mm). Then raise the objective slowly while
watching the monitor. You can get a quick estimate if you are close to focus by
looking at the spot the Wyko (or any other microscope for that matter) projects
onto the sample. The microscope is in focus when the spot size is at a minimum
(and the spot has well-defined edges).
9.4
Tilting the Microscope Head
The microscope head can
be tilted in two axes (tip/tilt) to level the sample with respect to the
microscope. Tilt with respect to the microscope objective results in many
interference fringes across the sample. (It is easier to rotate the microscope
head than to tilt the stage.) To adjust tip/tilt, press the tip/tilt button
while moving the joystick. Tilt adjustments are best done after the sample is
in focus and interference fringes are apparent. It is easiest to adjust one
axis at a time. At first, tilt adjustments can be confusing. Practice will make
you an expert in a short amount of time!
9.5
Calibration
The Wyko must be
calibrated every time it is powered up (or once a month for VSI and daily for
PSI, if the machine is on for extended periods). There are two calibrations,
one for PSI mode, and one for VSI mode. You only have to calibrate for the mode
you will use to measure. The following directions explain the calibration
procedure. You must demonstrate calibration to the super user to qualify.
9.5.1
Place the appropriate calibration
standard under the microscope objective and focus on the surface. Best focus is
when the fringes have maximum contrast. For calibration purposes, it does not
matter which objective you use. Lower-power objectives (i.e. 10X) are often
easier to work with because of the larger field-of-view and depth-of-focus.
Figure 3 shows the two types of calibration standards. These standards are very
expensive, a few thousand dollars, and should only be cleaned by staff. Do not
touch the surfaces of the standards. The VSI standard has already been broken
due to misuse. Fortunately the step structure is still in tact so it can still
be used. Please be careful when focusing the microscope.
9.5.2
Open the Measurement Options (Hardware->Measurement
Options…)
9.5.2.1 Select the desired (camera) resolution from the Options page.
9.5.2.2 Select the type of measurement you will be using: VSI or PSI. (It is
often easier to see fringes in the PSI mode because the coherence length is
longer. Once you have focused well enough to see fringes, you can switch to the
VSI mode).
9.5.2.1 Choose an objective. Which one does not matter, but a large field of
view is often helpful (e.g. use the 10X objective).
9.5.2.2 Choose an FOV. Which one does not matter, but a large field of view is
often helpful (e.g. use the 1X FOV).
9.5.2.3 Adjust the intensity (press the Intensity button on the bottom of
the Hardware->Measurement Options page) so that the camera is not
saturated (denoted by red regions on the intensity window). It is necessary to
adjust the intensity before calibrating because of a bug in the software. The
calibration routine lets you adjust intensity, but it resorts to the intensity
before the calibration routine.
9.5.2.4 Use the default settings for everything else
9.5.3 Press the Calibrate button.
9.5.3.1 Check the Auto Calibrate check box (i.e. do not Verify the
calibration - another bug).
9.5.3.2 Do not check All Modes (again, a bug in the software does not
keep the intensity value you set during the calibration).
9.5.3.3 Be sure to check the View Initial Calibration Value checkbox.
Then, make sure the number, when displayed, is approximately 0.9 on 1X speed,
and 2.7 (about 3 times larger) on 3X speed for the VSI mode, and 34.2 for the
PSI mode. This is necessary to let the calibration converge. If the calibration
fails, it is often necessary to reset this initial calibration value.
9.5.3.4 Click Next, and follow the directions in the dialog box.
9.5.4
VSI Calibration Hints
When doing a VSI calibration, start off in PSI mode. The coherence
length is much longer, which means there is a greater distance over which the
interference fringes appear. Begin by focusing on the sticker. The sticker has
a lot of contrast, so it is easy to focus on. Then move the stage so you are
looking at the metal/glass transition. The spot projected by the Wyko should be
half on the glass and half on the metal. It is easiest to see it from the side
by eye. The glass is thick and transparent. There is a possibility you are now
focused on the bottom surface of the glass. The bottom surface is the wrong
surface, so raise the objective until the edge of the glass is in focus. When
you are in focus, fringes should appear. If they do not appear, move the
objective up and down a little (one or two turns without pressing the fast
button) to get in into best focus. If fringes still do not appear, make sure
you are in PSI mode. Once fringes appear, move the stage so the objective is
over the calibration step. The step will most likely be out of focus now, but
you have an edge to focus on. Refocus until you see fringes. Once you have
fringes, switch to VSI mode. If you lose the fringes, you weren't at best focus,
so readjust the focus until they reappear.
b) a)


Figure 3
a)
PSI-mode calibration standard b)
VSI-mode calibration standard
9.6
Operation
9.6.1
Choose the proper objective to image
your sample with. Rotate the turret using the knurled (rough) ring. NEVER TURN
THE TURRET ON ANY MICROSCOPE USING THE LENSES. Doing so can misalign the
objectives. DO NOT REMOVE THE OBJECTIVES FROM THE TURRET. THEY HAVE BEEN
ADJUSTED SO THEY ARE PARFOCAL WITH EACH OTHER.
9.6.2
Place the sample under the
microscope objective making sure that the objective will not hit the sample. It
is useful to “flatten” the sample by adjusting the tip and tilt of the
interferometer so there are few to no fringes seen on the sample. (The
remaining tilt can be removed during post processing.)
9.6.3
Select the measurement mode, VSI
or PSI, from Hardware->Measurement Options->Options.
9.6.3.1 For PSI mode, focus on the structure until you have the best fringe
contrast.
9.6.3.2 For VSI mode, focus for best fringe contrast on the uppermost part of
the structure.
9.6.3.2.1
Select the proper scan lengths, Backscan
and Length, from Hardware->Measurement Options->VSI Options.
9.6.3.2.2
The scan length Length is
the distance the microscope will scan going down from its present position.
9.6.3.2.3
The scan length Backscan is
the distance the microscope will scan above the present position before it
scans below the present position.
9.6.4
Adjust the intensity, Hardware->Measurement
Options->Intensity, to maximum intensity without saturating the camera
(as seen by regions of red on the intensity screen).
9.6.5
Take the measurement File->New
Measurement
9.6.6
Save the measurement on the local
drive E:<login name>.
9.6.6.1
Do not leave large amounts of data
here. Assume that the data is not safe for more than a day. Transfer the data
to the ZIP drive or the CDRW drive that are located in the computer cabinet
under the Wyko optical head.
9.7
Analysis
9.7.1
Post-processing routines that come
with the Wyko software are extensive and cannot be adequately explained here.
For a better understanding of what is included, experiment with the software
and consult the on-line documentation or the reference manual.
9.7.2
Software
9.7.2.1 The Vision32 analysis software can be installed on your local machine.
Disks with the programs are available for loan from the Microlab office. When
installing the software, select NT2000 for the instrument type and select
workstation mode.
9.8
Shutdown
9.8.1
Disable the Wyko.
9.8.2
Shutdown the computer. Make sure
the computer has completed shutting down before powering off. The computer is
done shutting down when the "Restart" dialog appears on the screen.
9.8.3
Press the red Emergency Off
button, then rotate it clockwise (or pull it).
9.8.4
Turn off the computer monitor.
10.0
Troubleshooting
Guidelines
If calibration fails, make sure you have checked Auto
Calibrate and have adjusted the intensity before calibrating. If troubles
continue, report the problem on the wand.
11.0
Qualification
Procedures
11.1
Potential new users should arrange
ahead of time to have an existing user review Wyko operation. Casual
questioning (e.g. "Hey, can you review this with me for a moment?")
is not to be considered an official review period.
11.2
The first question that should be
asked is whether Chapter 8.13 - Wyko NT3300 Profiling System of the WAND has
been thoroughly reviewed? If not, insist
that it be reviewed before the meeting.
11.3
The “meeting” between the
qualified user and trainee user should be scheduled for enough time to explain
equipment operation and calibration. Equipment time can be recharged to new
user’s account if necessary.
11.4
Training should be done at least
twice by two different current users and the trainee should demonstrate
calibration and basic operation.
11.5
Superusers will first ask, “who
trained you?” of the new user. “Training” implies adequately following the
training steps outline above. The users identified as being the ones who did
the training will be responsible for the information conveyed by the new user
during the qualification.
12.0
Miscellaneous
Precautions, Guidelines, and General Rules
12.1
Do not lean on the optical stage
or the machine in general.
12.2
Do not turn the knobs on the
mechanical stage when it is powered up.
12.3
Rotate the turret using the
knurled (rough) ring. NEVER TURN THE TURRET ON ANY MICROSCOPE USING THE LENSES.
Doing so can misalign the objectives. This is good practice for all
microscopes, since rotating the turret using the objectives can damage them
over time.
12.4
DO NOT REMOVE THE OBJECTIVES FROM
THE TURRET. THEY HAVE BEEN ADJUSTED SO THEY ARE PARFOCAL WITH EACH OTHER.
12.5
Use PSI mode for continuous
surfaces that are in the depth of focus.
12.6
Use VSI mode for stepped
structures or any other structure that is not completely in the depth of focus.
12.7
Make sure not to crash the
objectives into the structure when focusing or when using the VSI mode. NEVER
focus downward, only upward.
12.8
Do a calibration every time the
machine has been powered up or on a daily basis for PSI and on a monthly basis
for VSI mode.
12.9
The objectives should be parfocal
(they focus at the same height), so when focusing on an object, you can use the
low-magnification objective to find the focus. This is easier since you will
see more structures and the depth of focus is larger for the low-magnification
objective. Then rotate the turret to the lens you need.
12.10
If your structures are highly
curved, use the highest-power objective possible. You can use the 0.5 FOV to
view a larger field if need be. The higher-magnification objectives have a
larger numerical aperture, and can therefore collect a larger angle of incoming
light.
12.11
Never use any kind of sticky stuff
(tape, clay, etc.) to mount your structures or fasten wires. There is an
optical-bench breadboard that can be used to affix wires by using clamps
screwed in with 1/4-20 screws.
12.12
Store your files in the
E:<login name> directory. Please remove files when you are done. If drive
space gets full, files will be deleted randomly to make space.
12.13
Never install software on the
system, it might conflict with they Wyko software or compromise the operating system.
12.14
Optical measurements in general
are not good for surface roughness since the lateral resolution of the
interferometer is not good enough. You should use an AFM for surface-roughness
measurements.
12.15
Never turn the knobs on the stage manually
with the power on.
12.16
Do not lean on the machine.
12.17
To do a screen capture, press
Crtl-PrtScn. The screen capture is stored on the clipboard. You can now paste
it into another program, or open the clipboard and save it as a clipboard file.
12.18
Use the default configuration if
you are having troubles with the software. Store your own configurations in
your own directory E:<login name>. The default configuration is in
c:\...\wyko.ini
13.0
Calibration
Hints
13.1
Use the lowest power lens for the
calibrations (easiest to get the fringes since the depth of focus is longer).
13.2
Click "Auto Calibrate"
when doing a calibration.
13.3
The step feature on the VSI
standard is between the “Wyko” symbols and is etched into the glass.
13.4
Focus at the edge of the
calibration standards so you have a feature to look at.
13.5
For a VSI calibration, find the
fringes with the PSI mode first (it is much easier because the coherence length
of the light is longer), then switch to the VSI mode and find the fringes
again.