The first step is to get beam into the microscope chamber.
Go to some relatively large beamline slit settings (like
200/200/0 slits, for ENS_I=200
m,
EXS_I=200
m, and EXSY_I wide
open). Look in the upstream inboard viewport; you should see
the snout as a long metal tube with a glass section in its
middle (see Fig. A.2).
Inside this glass section is a mirror that lets you
look down the direction of the beam path towards the exit
window between the beamline vacuum and the inside of the
STXM IV chamber. You should be able to see beam on the
phosphor around the exit window, and adjust the chamber
accordingly.
If the microscope is close to being aligned, you can simply
monitor the flux on a detector to evaluate the alignment
of the microscope chamber to the beam. If you are really
starting from the beginning, you will need to remove the
zone plate and OSA (see Sec. 2.4),
and scan a 5-10
m diameter pinhole as the sample to
evaluate the illumination of the exit window.
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Start with the ZP and OSA removed. From the
File
Edit Alignment
menu in SM, select Insert laser. This
will move the detector platform so that beam should pass
between detector D1 and the VLM, and strike a phosphor
plate located in front of an alignment laser. (You may
have to move the detector platform around a bit to
make sure x-rays are hitting on the phosphor alongside
but not directly at the
mm laser aperture).
Now select Insert photodiode from the Edit Alignment
menu, so that beam
strikes the IRD silicon photodiode. You should get
a signal comparable to what is shown in
Table A.3.
Update values of photodiode_xdet_um and
photodiode_ydet_um in the alignment
file; see
Sec. B.1.