Turning on the machine:
1. Turning the switch, like starting the car
2. Turn on chiller, to the top position
Sample preparation:
Clean the stage with IPA first
Use carbon tape (conductive, should look into how biological samples are made, sputtering with gold) , press the four corners
When using carbon tape: not too much, because the sample might be damaged when you remove it; not too little, because the sample might fall off the stage when tilted.
IMPORTANT: remember your sample position! Better to draw it on the paper
3. Check whether the SEM machine has warmed up or not, then turn on monitor
4. Put sample in, EVAC
the number ( the 7-segment display) will go down to zero
PREEVAC->HT READY (at this stage you can run the current)
5. press HT
Current button ( 12 o'clock or 1 o'clock position) Max: 1 o'clock
6. Turn the left monitor on, initial magnitude: X3000
How to tilt the stage?
Command-> stage t50
50 is the angle, t means to tilt; r means to rotate.
Adjust the focus:
WOBB, should be minimized (by adjusting the handle near the sample container, one is x position, one is y position)
ACCV (from MENU): increase the value, max: 15kV
Or using "stigmatism"
when adjusting the focus, use small particles
Taking pics:
SL3---the highest quality (this would take up one disk)
ALBUM (on monitor) ---save
TV2--sampling on a higher speed, used the adjust the position of the sample
if the frozen pic has bad quality, or not conformal, reduce the voltage
Turning off the SEM:
1. recude current to 0
press HT
2. LSP1
3. increase Magnitude to max: x300,000
turn off left monitor
4. VENT
5. turn right monitor off
wait until you can take the sample out
put chamber in EVAC again, wait until it's HT READY, or pressure goes to 0
Then turn off SEM and chiller
Thu, 27 Sep 2018 10:09:51 -0600
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