Difference between revisions of "EBSD using JEOL 7100F FEG-SEM"

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All samples for EBSD must be polished using the procedure outlined here or to a similar quality before EBSD.
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All samples for EBSD must be polished using the procedure outlined [[AM Sample Preparation for SRAS and EBSD| 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.
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They also need to be thoroughly cleaned using the procedure outlined [[How to clean a sample prior to lithography | 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.
 
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.
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==Installing the sample==
 
==Installing the sample==
  
Check if sample is in “Specimen Exchange” position
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Check if the sample is in the “Specimen Exchange” position
  
 
VENT the specimen exchange chamber
 
VENT the specimen exchange chamber
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Move ion cleaning head out
 
Move ion cleaning head out
  
=SEM=
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==SEM==
  
 
Fill the reservoir with liquid nitrogen
 
Fill the reservoir with liquid nitrogen
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Select the area you want to map
 
Select the area you want to map
  
Once area is selected (based on grain size) pick a suitable step size and time
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Once the area is selected (based on grain size) pick a suitable step size and time
  
 
''Settings''
 
''Settings''
  
Pick resolution you want
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Pick the resolution you want
  
 
✔ Store Patterns
 
✔ Store Patterns
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✔ Acquire post-acquisition image
 
✔ Acquire post-acquisition image
  
=Removign the sample=
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=Removing the sample=
  
 
Retract EBSD detector
 
Retract EBSD detector
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Switch Dynamic focus off
 
Switch Dynamic focus off
  
Wear latex gloves. Once the sample has stopped moving used the stick and pull the sample out
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'''Wear latex gloves'''. Once the sample has stopped moving used the stick and pull the sample out
  
 
VENT the specimen exchange chamber
 
VENT the specimen exchange chamber
  
Open door, remove the sample from the chamber, close the door
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Open the door, remove the sample from the chamber, close the door
  
 
EVAC the chamber
 
EVAC the chamber

Latest revision as of 09:20, 20 August 2021

All samples for EBSD must be polished using the procedure outlined here or to a similar quality before EBSD.

They also need to be thoroughly cleaned using the procedure outlined here or similar.

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.


Installing the sample

Check if the sample is in the “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 ( or greater for a better resolution of the background IMAGE ONLY)

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 the area is selected (based on grain size) pick a suitable step size and time

Settings

Pick the resolution you want

✔ Store Patterns

✔ Beam off after scan

✔ Acquire post-acquisition image

Removing 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 the door, remove the sample from the chamber, close the door

EVAC the chamber