Dear Bartłomiej,

From my intuitive understanding of GSAS-II, I think that the approach suggested 
is that you fit one profile function only because it is ideally supposed to be 
the pure instrumental profile determined from a standard. Then you will model 
deviations from the instrumental profile by using some of the many broadening 
models available in the <Data> tab of each phase (domain size model, mustrain 
model etc). (This names suggest that anything differing from the pure 
instrumental profile is treated as if coming from the microstructure of the 
phase, but obviously the refined values of these models are only physically 
meaningful under certain conditions).

For example you could use the Be substrate also as an internal peak shape 
standard, fit the profile from its peaks only, and then keep it fixed. Finally 
you refine the broadening parameters for the sample phase using the domain size 
model, mustrain model etc.

Kind regards,

Arianna




-----Original Message-----
From: Bartłomiej Gędziorowski <[email protected]> 
Sent: Friday, September 6, 2019 14:09
To: [email protected]
Subject: [GSAS-II] Different profiles for different phases

Hello Everybody,

first of all I'd like to say hello to everybody, because this is my first post 
in this list. My name Is Bartłomiej Gędziorowski, I work at AGH UST in Cracow, 
Poland and I'm a materials scientist.

I worked few years with GSAS+EXPGUI, now from some time I'm migrating to GSASII 
and I cannot find one feature. It is the setting of different profile sets for 
different phases for a single histogram. I have a sample in form of a thin 
layer on a beryllium substrate. As a result on diffractograms I can see both my 
material reflections, quite wide because of sub-micron grains, and very thin 
beryllium. This causes a problem, because I cannot find suitable set of profile 
values for double-phase refinement. I worked it around putting beryllium 
reflections in the background, but that's not a good solution for me. 
The beryllium peaks are very helpful, because they allow to precisely fit 
sample displacement - we use special in-situ cell in which placing sample in 
right position is challenging and we always have some shift. 
For that reason it would be perfect to do a double-phase fit.

I would be grateful for some suggestions how to solve my issue.

Best regards,

--
Bartłomiej Gędzioroski, Ph.D.
AGH University of Science and Technology, Faculty of Energy and Fuels, 
Department of Hydrogen Energy, al. Mickiewicza 30
30-059 Krakow, Poland


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