Hello Sebastian:

The figure that you shared is interesting. Here are three observations/ things 
to check:

  1.  Is the integration time per point the same during the in-situ 
measurements? I think that it is otherwise the raw data would not be on the 
same scale as the other scans.
  2.  The raw data shows about the same edge step so I believe you are correct 
and the signal is the same in all the measurements, so somehow during the 
in-situ part additional noise was picked up. Was the in-situ apparatus causing 
some vibrations or noise in the measurement?

Kind regards,
Shelly

From: Ifeffit <ifeffit-boun...@millenia.cars.aps.anl.gov> On Behalf Of 
Sebastian Kunze
Sent: Monday, April 29, 2024 7:17 AM
To: ifeffit@millenia.cars.aps.anl.gov
Subject: [Ifeffit] Origin of noise in Ag K-Edge

Greetings, I recently did in-situ QEXAFS at Ag K-edge, expecting to see 
structure loss starting from crystalline (metallic) state. While we can see 
that, in addition we also see an increase in noise(?) in the xanes region 
(compare start and
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Greetings,

I recently did in-situ QEXAFS at Ag K-edge, expecting to see structure loss 
starting from crystalline (metallic) state. While we can see that, in addition 
we also see an increase in noise(?) in the xanes region (compare start and end 
in the attached image). I am confused by this because the amount of material 
did not change, so I did not expect a difference in the signal/noise ratio at 
the absorption edge. And it is reproducible across several samples, so not 
instrument related. Could anyone point me in the right direction as to what I 
am missing?

Thank you!

Best,
Sebastian Kunze

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