Introduction

The focused ion beam (FIB) microscope has gained widespread use in fundamental materials studies and technological applications over the last several years because it offers both high-resolution imaging and flexible micro and nanomachining in a single platform. FIB techniques are used in a variety of applications. In terms of failure analysis, FIB techniques are commonly used in high magnification microscopy, die surface milling or cross-sectioning, and even material deposition.

Background on FIB

A FIB system works very similarly to a scanning electron microscope, except that it uses a finely focused beam of gallium (Ga+) ions instead of the latter's use of electrons. This focused primary beam of gallium ions is rastered on the surface of the material to be analyzed. As it hits the surface, a small amount of material is sputtered, or dislodged, from the surface. The dislodged material may be in the form of secondary ions, atoms, and secondary electrons. These ions, atoms, and electrons are then collected and analyzed as signals to form an image on a screen as the primary beams scans the surface. This image forming capability allows high magnification microscopy .

The higher the primary beam current, the more material is sputtered from the surface. If only high-mag microscopy is intended, only a low-beam operation must be employed. High-beam operation is used to sputter or remove material from the surface, such as during high-precision milling or cross-sectioning of an area on the die.

Resources available in the MOST library

Other Resources

MTU Equipment

The Hitachi FB-2000A FIB uses a beam of focused high-energy (30 kV) gallium ions to remove material in a very controlled manner from inorganic specimens. The FB-2000A is a single beam system; that is, users image the specimen with the same beam used for milling. The column resembles that of an electron microscope and functions very much the same. Control of the ion beam is gained through the Unix workstation and fabrication software system that is designed to support both TEM sample preparation and pattern milling.


Fig.1. Michigan Tech FIB - ACMAL Facicity

Hitachi_FB-2000A_Focussed Ion Beam (FIB) Specifications

Hardware Description Our equipment has the following major hardware:

Operating the FIB

Before you can start

Before you can use the FIB, you must pass and be certified first. The preferred pathway to certification is through the SEM course, MY4200/4201 offered in the fall. If you chose to be trained one-on-one, the time required to train you depends on you and your skills. Students with mechanical aptitude learn faster. Note that the following charges are included for individual training; Salary and fringes for trainer plus the hourly instrument use fee $59/ hour. For details on rates, please visit http://mcff.mtu.edu/acmal/rates/ .

If you are interested in becoming trained to use this equipment, consult Dr. Pearce first and then contact either of the following: Owen P Mills (opmills@mtu.edu) or Felicia Nip (frnip@mtu.edu) in order to get more information.

FIB Operating Procedures

Preliminary Steps

FIB Control panel
Fig.1
  1. Sign-in to the logbook.
  2. Ensure IP1 and IP2 green lights are on (on the front panel below chamber)Fig.1.
  3. Make sure the green lights are on for DP, Water, and Air Press. Make sure the DP Power Switch is on.
  4. Check that both S.C. and S.E.C. Vacuum green lights are on at HIGH vacuum.

NOTE ON SWITCHES:

NOTE ON SAMPLES:

Start Up

FIB login screen
Fig.2
  1. Turn FIB POWER switch ON (to the left of vacuum controls).
  2. At FB-2000A Login screen (see Fig.2);
  1. On the Depo warm up menu;
Depo warm-upmenu
Fig.3
  1. Next is the FIB menu.
  1. Click on the HV button along the top menu. This will initiate the HV sequence and begin the tip reforming process which may take up to 30 minutes.
  1. Iext should be around 3.2-3.4 μA. If not in range, contact staff.
Turning heater-ON
Fig.4
  1. Under the Depo tab, turn Heater ON [Fig.4]
  2. Depo users must wait up to 1 hour until the deposition gun warms to 5.6 VDC, or 2.7 VDC for cold users.

Specimen Exchange

  1. Attach your sample to the holder with carbon tape.
  2. There must always be a holder left in the FIB goniometer.

The following is how to remove either plug or holder from the goniometer: 3 Removal of PLUG:

4 OR Removal of HOLDER:

The following is how to insert the holder into goniometer:

  1. Insertion of HOLDER:

Alignment

LMIS tab Menu
Fig.5
  1. Select the following image parameters:
Area x Zoom 256 x 1
Scan Speed Rapid
Accum 1
  1. Open the LMIS tab and check that the extraction current is around 3.2-3.4 μA. If not, use the slider to adjust it to that level. [Fig.5]
  2. Using the Trackball, locate an area that is suitable for aligning the beams you will be using for your FIB work.
Choosing beam to align
Fig.6
  1. Open the Column Adjustment menu at the top of the screen.
  2. Choosing which beams to align: [Fig.6]
Patterning users Lift-Out Users
M0-20 Beam-01
M0-50 M0-20
M1-50 M0-50
M1-100 M1-50
M1-100
M1-200
M1-300
M1-500


  1. Click the Beam Name pull-down and select a beam to align. Press Continuous scan button.
  2. Reset the Deflector Shift X&Y to zero.
  3. Set the scan AreaxZoom to 256x4 to visualize feature of interest, and then focus. While focusing;
  1. Set the Contrast and Brightness as necessary.

NOTE: You may need to move the specimen constantly when aligning beams with high currents to prevent erosion of the specimen.

10. Click Register to save the beam conditions after aligning each beam.

11. Go on to the next Beam Name and repeat until you have aligned all required beams for your project.

12. Focus and register M0-50.

NOTE: NEVER MAKE CHANGES TO THE APERTURE OR LENS MODE SETTINGS!!.

Lift Out Technique

Lift-out holder
Fig.7
NOTE: You must use the correct holder for lift-out. See Image. [Fig.7]
NOTE: The Lift-Out procedure may be performed over two days instead of one as indicated in the procedure.
  1. Check the eucentric position:
Checking the eucentric position
Fig.8
On holder Z position
Si wafer 200 µm
Si wafer + 1 piece of tape


  1. Return tilt to 0 degrees.
Adjusting the actuator
Fig.9
  1. In the Column Adjustment menu, check that the M0-50 Course Focus is ~21.7. Register then Stop beam.
  1. Press Continuous Scan.
  2. Checking the Depo position:
NOTE: If the gun does not appear, select Nozzle position: Escape. Call gun back in, and re-run procedure.
If this does not work, check that the area is 256x1. If you still do not see the gun, contact Owen Mills for manual adjustments.
NOTE: If the gun appears greater or less than the desired dimensions, call for assistance before proceeding.
Checking the Depo position
Fig.10
Adjusting contrast
Fig.11
  1. Checking the Micro-probe position:
NOTE: If you cannot find the tip, change area to L-Scan and adjust the focus and contrast.
Centering the tip
Fig.12
NOTE: If probe does not come back to the saved position, find the tip. Move only in the L&R directions with the trackball.
Then, move slightly up or down and try the L&R directions again. Repeat until found, then repeat the procedure.
NOTE: The touch occurs when there is a change of contrast on the screen. Although the control board will "beep",
you cannot always rely on this and the probe end may strike the specimen.
Adjusting the tip
Fig.13
Nozzle position
Fig.14
Adjusting probe
Fig.15

Deposition for Lift-Out Technique

  1. Move probe left and lower it enough so it is away from the depo gun.
Fabrication menu
Fig.16
  1. From the Depo menu, select Nozzle position:
  1. Close S.C. AIRLOCK VALVE.
  1. Return to the area to be lifted out.
  2. Select Column Adjustment>File>Quit>OK. Open the Fabrication menu. [Fig. 16]
  3. Set the following parameters:
Area x Zoom 256x8
Beam Beam-01
  1. Press Continuous Scan.
  1. Click the Get Image button.
  2. Check that the depo gun is heated to 6.2 VDC on red voltmeter.

10. Use the DEPO TOOL to draw a rectangular box for the pad. [Fig. 17] & [Fig. 18]

Fabrication menu (DEPO TOOL)
Fig.17
Fabrication menu (PEPO TOOL)
Fig.18
Dimensions 15x3
Time 10-12 min
Scan ← and


NOTE: Make sure the beam name is changed under the Fabrication Condition as well as on the right panel.

11. Press Fabrication Start button and run until complete.

12. Use M0-50 to check the deposition quality [Fib. 19]

Fabrication menu (Changing beam name)
Fig.19

13. Under the Stage menu, click C.Copy>Save to save position.

Rough Milling for Lift-Out Technique

  1. Focus and register M1-500 off the area of interest. Use M0-50 to return to the saved position.
  2. Select File>Open:
Q FAB 2 menu
Fig.20
Q FAB2 menu
Fig.21
  1. Focus and register M0-50. At 256x1, manually tilt specimen to 60 degrees and lock position. [Fig. 22]

Fig.22
  1. Return to the saved spot and use 256x4 to focus and register M1-300 for the undercut. Then Get Image.
  2. From the Edit menu, press Clear to remove the QFAB_2 pattern from the screen.
  3. Use the SPUTTER TOOL to draw a rectangular box with the following parameters: [Fig. 23].
Sputter tool menu
Fig.23
AreaxZoom 256x8
Dimensions ~24x2
Time 10 min.
Scan ← and


  1. Place box 6-9μm below the top edge of specimen.
NOTE: Turn the CONTRAST UP to carefully watch both sides of the milling window move towards the center until it is cut through. When complete, press Stop & Close. [Fig. 24] [Fig. 25]

Fig.24

Fig.25
  1. Select M0-50. At 256x1, tilt the sample back to 0 degrees and lock position. [Fig.26]
  2. At 256x4, focus register. Check if the back edges are cut.

Fig.26

Landing the Probe for Lift-Out Technique

  1. Set AreaxZoom to 256x1 and position specimen in the center of the screen.
  2. CALL probe and position the tip of the probe on the far right, but not along the edge of the portion of the specimen to be removed.
NOTE: If you cannot find the probe, change the Area setting to L-SCAN
  1. Set to 256x4 and press BUZ ON on the control board.
  2. Technique for lowering the probe tip: [Fig. 27]

Fig.27

Fig.28
  1. At 256x8, focus and register Beam-01.
  1. Use the DEPO TOOL to draw a rectangle with the following parameters:
Dimensions ~2.5x3
Time 5 min
Scan ↓ and ≡

Fig.29


  1. Place box over the probe tip and press Fabrication Start. [Fig. 28]
  2. You may add another protective layer at the same time.
  1. At 256x8, focus and register M1-100.

10. Press BUZ ON or monitor the TOUCH LED.

11. To cut the micro-bridge, use the SPUTTER TOOL to draw a rectangle with the following parameters [Fig. 29]

Dimensions ~2.7x8.6
Time 5 min
Scan ↓ and

12. Click the Fabrication Start button.

NOTE: If mill is run too long, re-deposition may occur.
NOTE: If TOUCH LED does not turn off, ask for assistance before proceeding to next step.

13. Carefully LO, using SLOW speed first.

This marks a stopping point for users who will perform the Lift out over two days. If performing over one day, continue to Step 14.

If starting from Day 2 of the Lift-Out procedure, repeat:

Section : Alignment for: M0-50, M1-50, Beam-01, M1-100, M1-200, and M1-20 and,
Section : Lift Out Technique Steps 7-10 (Put holder in detent)

14. Open S.C. AIRLOCK VALVE.

15. Load the TEM holder with the Omni Probe grid (the line around the grid should be faced up).


Fig.30

16. Holder should be in the FIB position.

BLUE SECTION IS IF THE OMNIPROBE GRID IS NOT USED, PLACE IN DROP DOWN MENU

17. Roll holder over to the R-T position and find the edge of the grid. 18. At 256x4, focus and register M1-500 for a landing pad.

19. Use the SPUTTER TOOL to create a rectangle with the following parameters:

Dimensions ~25x5
Time 10 min
Scan ← and

PAY ATTENTION TO SPECIAL INSTRUCTIONS FOLLOWING THIS STEP.


Fig.31

At this point, reposition the box and re-run so that you are milling the specimen and not the vacuum! Continue with stopping and repositioning until your depth of cut is at least 15 µm and flat. You must repeat until the width equals ~10 µm. 20. To check the width:

21. Focus and register M0-50. Under Stage menu, select C.

22. Turn on BUZ ON and HOLD OFF


Fig.32

23. Move stage to upper edge of entire holder by moving the holder down so it is barely on, or even off the screen.

24. To land the sample, use the technique described in Section Landing the Probe Step #4 [Fig. 31]

25. At 256x8, focus and register Beam-01

26. Use the DEPO TOOL to draw a rectangle with the following parameters: [Fig. 32]

Dimensions ~6x3 (varies)
Time 5 min
Scan ← and

Fig.33


Place box on the upper left edge and press Fabrication Start. You may add another 3x5 rectangle for 5 min. on the same or different edge. [33]

27. At 256x8, focus and register beam M1-200.

28. Use the SPUTTER TOOL to draw a rectangle with the following parameters:

Dimensions ~6x3
Time 5 min
Scan ← and


Place the box over the top edge of probe. Observe the mill and press Stop & Close when you hear the "beep."

29. Move the probe up and press ESC on the control board to remove probe.

30. Focus and register M0-50 to observe the results.

Fine Milling for Lift-Out Technique


Fig.34
NOTE: It is very important that you are focused and registered at this step.
  1. Click Get Image. At 256x8, focus and registerM1-200.
  2. Use the SPUTTER TOOL to draw a rectangle with the following parameters: [Fig. 34]
Dimensions ~11x2
Time At least 4 min. per edge
Scan ← and


Place the box on the upper edge of the protective pad and press Fabrication Start. OBSERVE: THE WHITE PORTION (THE TAPER) SHOULD GRADUALLY DISSAPPEAR.

NOTE: Repeat the two preceding steps as necessary, alternating the mill on the upper and lower edge on the taper only,

until specimen measures 1 µm. [Fig. 35] [Fig. 36]

Fig.35
  1. At 32x2, focus and register M1-100.
  2. Repeat steps 2 -3 until the specimen is 0.6 µm
  3. Focus and register M1-50.
  4. Repeat steps 2 -3 until the specimen is 0.2-0.3 µm [Fig. 37]
  5. Focus and register M1-50 or M0-50.
  6. Final milling:
Dimensions ~11x0.5
Time At least 4 min. per edge
Scan ↑ and ≡ (away from edge)



Fig.36

Correctly position box on the upper edge

NOTE: After changing the area to 32x8, only adjust the box VERTICALLY
Dimensions ~11x0.5
Time At least 4 min. per edge
Scan ↓ and ≡ (away from edge)



Fig.37

REMINDER: After changing the area to 32x8, only adjust the box VERTICALLY

a. Change area to 32x8 and press Fabrication Start.

b. Change to 32x1 and Speed: Rapid.

c. Change area to 32x8 and focus. You may need to change the Speed: 5.

d. The final specimen should be 50-70 nm.

Tungsten Deposition

NOTE: Drift is always down. Use Speed: RAPID.
  1. Load specimen and focus.
  1. Pull the specimen HOLDER rod into the detent position (See Section 3.5 Step 8)
  2. Insert the DEPO gun and focus on the DEPO gun nozzle.
  1. 3-5 coarse clicks to the left of the focus slider should return you to the recorded sample focus.
  2. Move the DEPO gun out and then in again to check positioning.
  1. Put both the specimen back and the DEPO gun back in for a final check.

Bitmap Image Milling (SEM/TEM)

NOTE: Only import 256 bitmap files with a proper 3½ in. floppy disk.
  1. To Upload a Pattern:

Loop Time and Dwell Time will automatically change according to your chosen settings. Loop Time= Dwell Time x #Deflection Points and Total Time (min.) = Loop Time x Frame Number.

  1. To Create a New Pattern:

NOTE: DO NOT USE THE POLYGON DRAWING TOOL. The software will not allow you to exit the drawing mode and the system will need to be re-started.

Using the NPGS Software

NPGS, Nanometer Pattern Generation System, allows a user to create a nanometer pattern on a sample. Generally the beam parameters used are found on the last page of the FIB manual under the "Beam Mode" column "M1", using an aperture size of 100µm. Zoom is set at 566x. The center-to-center value is set to 3.69nm.
The calibration of the FIB is dependent on the densities of the samples. This procedure is specific for the construction of wave guides. The standard line does is between 80 and 100, producing depths between 500 and 600 nm.

All images and figs are in the Image gallery below

  1. Close initial NPGS Window and re-open the program by clicking on the NPGS Menu shortcut on the desktop.
  1. Wait 40 seconds for calibration. The FIB only calibrates once per day. [Fig 2.jpg]
  2. Click on DesignCAD files in the upper right pull down bar [Fig 3.jpg]
  3. Click DesignCAD express and hit any key to continue. [Fig 4.jpg]
  4. Click on the line icon in the upper left. [Fig 5.jpg]
  5. Draw a horizontal pattern on the screen.
  6. Click on the line and press Ctrl+I, a window will open to allow the parameters to be set in the "Vector" window.
  1. To make an array,
  1. In the NPGS: Make Array Function" windows that appears, enter the following data:
Number of columns:1 [Fig 10.jpg]
Column Spacing (If there are more than one)
Number of rows: 600 [Fig 11.jpg]
Row spacing: 0.35μm (If there are more than 1) [Fig 12.jpg]
The color of your rows and columns can be changed, but hit (N) twice to proceed.
Changing the color of lines and columns defines a different layer to be imaged and this is generally not desired.

YOU ALWAYS NEED TO SET THE PATTERN IN THE MIDDLE OF THE SCREEN.

10. Click on the pull down bar at the top of the screen labeled NPGS>MaxMag>"O" to change/set the origin of the array. [Fig 13.jpg], [Fig 14.jpg], [Fig 15.jpg] 11. Click on the pull down bar at the top of the screen labeled NPGS

12. Click on the pull down bar at the top of the screen labeled NPGS

At this time, you may choose to close this program if you wish. [Fig 19.jpg], [Fig 20.jpg]

13.Right click on the file in the Nanometer Pattern Generator window.

The user should enter the following parameters for creating a wave guide pattern as shown in the picture: [Fig 21.jpg], [Fig 22.jpg]

Layer 1: Normal Writing

Origin Offset: 0,0
Magnification: 566
Center-to-Center Distance: 3.69 nm
Line Spacing: 3.69 nm
Configuration Parameter: 1
Measured Beam Current (Read off of the FIB): 522.0 pA
Multiple Pass Mode: Disable
Line Dose: 100 nC/cm

14. Save the file again in "Runfiles" as the same name used before if preferred.

15. Change "Display file types" to "Run files". [Fig 24.jpg]

16. Select you file and click on DAC(+10,+10) near the bottom left of the window. [Fig 25.jpg]

17. Press "NPGS Mode" in the left column.

18. Click on "Process Run File" near the upper left of the screen.

19. Start the FIB and NPGS at the same time. Spacebar will start the NPGS software. [Fig 26.jpg]

20. Press Esc to manually stop the imaging, or if everything is correct, wait for the timer on the screen to run down.

21. Click FIB Mode in the left column to see your pattern on the Hitachi monitor.

Image gallery

Unloading

  1. Remove the HOLDER by pulling it straight out till it stops,

Wait until you see the SEM SEC open and then gently pull the HOLDER free from the goniometer.

  1. Replace the PLUG.

Shutdown

  1. Select the Stage folder and click Home.
  1. Click File
  1. Click HV to turn off the high voltage.
  2. Close the S.C. AIRLOCK VALVE from the vacuum control panel on the column console beside you.
  3. Click the Exit button to close the FB-2000A software.
  1. See Step #3 above for instructions on removing and replacing the specimen holders.

ALWAYS REMOVE AND REPLACE HOLDERS WITH THE FIB POWER ON.

  1. After a Specimen Holder or Plug is replaced into the goniometer,
  1. Pick up your tools and clean the specimen preparation area.
  1. Swipe out of the computer system and sign the logbook, noting any problems you encountered.

IMPORTANT: !YOU MUST STOP THE FIB AFTER THE IMAGING IS COMPLETE OR THE SAMPLE MAY BE DAMAGED!!. Acknowledgement

The information in this protocol was contributed by the ACMAL staff, Felicia Nip and Owen Mills
Page data
License CC-BY-SA-3.0
Language English ()
Related 0 subpages, 0 pages link here
Views 256 page views (analytics)
Created May 19, 2013 by Jephias Gwamuri
Last edit November 28, 2025 by StandardWikitext bot