FEI Tecnai G2 F20 Operating Procedures Manual

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FEI Tecnai G
 
 

1. Startup

 
 
 
1. Sign-up in the microscope log-book
2. Startup the software if not already running: Start the software in this
sequence:
 
1.
Tecnai User Interface
2.
Digital Micrograph
3.
TIA
(TEM Imaging and Analysis)
 
3. Check the vacuum: Look at the
GUN, COLUMN and CAMERA values should look like the ones below and
highlighted in green. Gun will always be 1 Log.
4. Fill the cold-trap dewar with LN
until it is full. If you are the first user of the day, refill it again after 30 minutes.
Refill the LN
 
 
5. Inserting the specimen holder
Room temperature sample
There are two things to check prior to inserting the specimen holder:
(a) Under the
Search
Control
then Holder. This will reset X, Y, Z, and α on the stage and avoid damaging the
 
2
F20 Operating Procedures
(6/01/2017)
Vacuum
2
at least every 3 hrs to keep it full
2
2
tab, in the
Stage
menu, click on the flap-out menu and click
panel under the
: Cover the screen window first. Fill the dewar
Setup
menu. The

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Summary of Contents for FEI Tecnai G2 F20

  • Page 1 FEI Tecnai G F20 Operating Procedures (6/01/2017)     1. Startup       1. Sign-up in the microscope log-book 2. Startup the software if not already running: Start the software in this sequence:   Tecnai User Interface Digital Micrograph (TEM Imaging and Analysis)  ...
  • Page 2 holder. Wait until the red light on the Compustage is off before proceeding. (b) Remove the objective aperture by sliding the lever to the right. Align the specimen holder with the small pin at approximately 3 o’clock. Carefully insert the end of the specimen holder into the stage until you reach the end. Then rotate clockwise to about 5 o’clock whilst very gently pushing inwards.
  • Page 3   2. Microscope Alignments 1. Eucentric height adjustment (a) Open the column valves under the Setup menu. At a magnification of about 4000- 5000 x, find a noticeable feature on your specimen. (b) Activate the alpha-wobbler. Change the Z height on the right-hand control panel to minimize the image displacement.
  • Page 4 4. Direct Alignments: Under the Tune menu go to Direct Alignments     Perform direct alignments at 50,000X and close to focus on the specimen. (a) Beam Shift alignment: Click on Beam Shift and go to crossover. Center the beam in the middle of the phosphor screen using Multifunction knobs X and Y.
  • Page 5   (c) Rotation Center alignment: Find an identifiable object in your specimen. Click on Rotation Center and minimize its displacement using MF X and Y. (d) Comma free alignment: Use the Orius CCD to go slightly underfocus (-500 nm). Using the live FFT correct Direct Alignments: Comma free alignment X Y.
  • Page 6     3. STEM mode (a) Find an area of interest at a low magnification (~10 k); (b) In the STEM menu click STEM, Diffraction mode will be activated; press the Diffraction button to deactivate the Diffraction mode; (c) Under the Direct Alignments, perform Beam Shift, Beam-Tilt Pivot Points X/Y, and Rotation Center (turn the outer ring of the objective focus know counter-clock wise to...
  • Page 7 Using   t he   F alcon   I I   o n   t he   T ecnai   F 20     1. Perform   a ll   m icroscope   a lignments   o ut   o f   L ow   D ose   2.
  • Page 8     Focal   l ength   ( mm)   2.7   Detector   FEI   F alcon   I I     Physical     p ixel   s ize   ( μm)   14      ...

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