Is it really amorphous content, or is there a whole bunch of very fine 
nanocrystalline stuff or material with a very high defect density that is 
widening the peak?  If the fitter is having trouble matching the peak shape, it 
may be ascribing a fairly arbitrary portion between amorphous and crystalline.

Marcus Mendenhall

Materials Measurement Science Division
National Institute of Science and Technology
100 Bureau Dr. stop 8370 (217/B115)
Gaithersburg, MD 20899 USA
Phone: +1-301-975-8631
during COVID-19 response period:
Home phone: 301-916-5486
Cell: 615-293-3120

> On Mar 3, 2021, at 7:34 AM, François Goutenoire 
> <[email protected]> wrote:
> 
> Dear Rietveld users,
> 
> I have some industrial compound presenting a strong hyper-Lorentzian peak 
> shape (eta=1.1 with HighScore). When we calculate the amorphous content after 
> an internal standard addition, the result is 40%. The micro-absorption effect 
> has been minimized (mu of the internal standard is closed to the compound).
> 
> But with some electronic transmission analysis no amorphous is observed.
> 
> The question is : Does a strong hyper-Lorentzian peak shape could influence 
> quantitative analysis ?
> 
> François
> 
> -- 
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