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- At the start of the day perform a high flash and run up the emission.
- Open the beam valve and check there is a beam on the large phosphor screen. Centre with beam shift.
- Insert and centre the largest condenser lens aperture (150μm)
- Ensure the objective lens is at standard focus and bring the sample to Gaussian focus height.
- Select the alpha value which you want to use.
- Select the spot size you with to use.
- Adjust any 2-fold astigmatism in the beam using condenser lens stig.
- Anode wobble and adjust beam deflectors (GunA2) until concentric movement is achieved.
- Go to 1 Mx magnification, find a feature on the sample and wobble the HT. Correct for any movement in the sample with beam align deflectors (CLA2).
- Correct for tilt balance using the tilt wobbler.
- Iterate steps 7-10 if necessary.
- At 1 Mx magnification illuminate a region of amorphous material, spread the beam, insert the One-View camera and lift the viewing screen.
- View a live fft FFT of the image and adjust two fold astigmatism in the objective lens.
- Ensure that the objective lens is set to standard defocus.
- Increase the height of the sample so that the image is under focus and numerous thon rings can be observed.
- Stop the view on Digital Micrograph and press single on the COSMO TEM auto-adjust software.
- Using COSMO software correct 2 fold astigmatism to ≤5nm.
- Set the tableaux angle to the required level and run a tableaux.
- Correct for higher order aberrations.
- Iterate 17-19 as required.
- using the corrector optics panel (make sure the toggle button is on TEM).
- If necessary run the COSMO corrector.
- Insert the required condenser lens aperture for imaging.
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If you leave the microscope please ensure the beam valve is closed. |
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If you leave the microscope for an extended period of time please:
On returning to the microscope:
If your emission current drops significantly during your session you can restore to 15μA by following the above procedure.
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