Difference between revisions of "EBSD using JEOL 7100F FEG-SEM"
Don Milesh (talk | contribs) (Created page with "All samples for EBSD must be polished using the procedure outlined here or to a similar quality before EBSD. http://optics.eee.nottingham.ac.uk/wiki/AM_Sample_Preparation_for_...") |
Don Milesh (talk | contribs) m |
||
Line 6: | Line 6: | ||
Finally, you could use the plasma cleaner (upstairs in the sample prep room of the NMRC), but the ion cleaning head does a similar job. | Finally, you could use the plasma cleaner (upstairs in the sample prep room of the NMRC), but the ion cleaning head does a similar job. | ||
+ | |||
Contact Elisabeth Steer <pczeds@exmail.nottingham.ac.uk> if you want to use the plasma cleaner. | Contact Elisabeth Steer <pczeds@exmail.nottingham.ac.uk> if you want to use the plasma cleaner. | ||
Revision as of 11:23, 19 January 2018
All samples for EBSD must be polished using the procedure outlined here or to a similar quality before EBSD. http://optics.eee.nottingham.ac.uk/wiki/AM_Sample_Preparation_for_SRAS_and_EBSD
They also need to be thoroughly cleaned using the procedure outlined here or similar. http://optics.eee.nottingham.ac.uk/wiki/How_to_clean_a_sample_prior_to_lithography
Finally, you could use the plasma cleaner (upstairs in the sample prep room of the NMRC), but the ion cleaning head does a similar job.
Contact Elisabeth Steer <pczeds@exmail.nottingham.ac.uk> if you want to use the plasma cleaner.
Contact Martin Roe <epzmjr@exmail.nottingham.ac.uk> for SEM training.
Contact Nigel Neate <epzncn@exmail.nottingham.ac.uk> for EBSD training.
Contents
Installing the sample
Check if sample is in “Specimen Exchange” position
VENT the specimen exchange chamber
Wear latex gloves. Open door, place sample in chamber, close the door
(Place the area you want to EBSD closest to the outer edge of the door/closest to you when the door is shut)
EVAC the chamber
Using the plasma cleaner
Move ion cleaning head in
Open valve on top of the argon bottle (2-3 turns) to open it, wait 5 seconds and close it
Set voltage, time and hit START
Move ion cleaning head out
SEM
Fill the reservoir with liquid nitrogen
Wear latex gloves. Move sample into chamber using the stick
Wait for chamber vacuum to go down to 10-4
Switch beam ON
Mechanical Alignment (Beam)
Check dynamic focus is off
Apature 3 (or 2) 50μm (or70) Spot size 8 Filter 3
Set working distance to 10mm
Go to about 30,000 mag
Hit ALIGN
Align using the mechanical X and Y nobs on the SEM
Alignment (Sample)
Change working distance to 20mm and Spot size 11
Hit ALIGN
Go to about 2000 mag
Align using the X and Y nobs on the control panel
Set tilt to 70deg
Switch on Dynamic Focus
Focus the centre then the top
EBSD
Move detector into 180-188 max – 195 absolute MAX
Find your region of interest and close the camera
Recheck focus and dynamic focus
Scan image
Settings
Image scan size 1024
Dwell time 35
✔ SE
☐ BSE
✔ FSE
✔ Auto
✔ Tilt centre
Optimise pattern Binning 4x4 Gain 15 Hit Auto exposure 90% signal strength ✔ Auto background ✔ Static background Frame average Check static background (300)
Optimise Solver Settings No of bands 6 MIN Hough resolution 40-60 MAD as low as possible
Acquire Map Select the area you want to map Once area is selected (based on grain size) pick a suitable step size and time Settings Pick resolution you want ✔ Store Patterns ✔ Beam off after scan ✔ Acquire post-acquisition image
Removign the sample
Retract EBSD detector
Click Specimen Exchange position on the SEM window
Switch Dynamic focus off
Wear latex gloves. Once the sample has stopped moving used the stick and pull the sample out
VENT the specimen exchange chamber
Open door, remove the sample from the chamber, close the door
EVAC the chamber