Hard disagree here.

You're using crystallographic parameters to calculate the (intensities and
positions of the) pattern.

To me, that's the core of Rietveld refinement.

You need to apply a peak shape model. Why not apply a model from which you
can extract crystallite parameters?

QPA can then be done on the output of a refinement, eg application of the
internal standard method using the Hill /Howard algorithm.

Its still a Rietveld refinement, I'm not just fitting peaks willy nilly;
they're constrained by a crystal model.


Matthew

On Sat, 13 Jan 2024, 01:48 Alan W Hewat, <[email protected]>
wrote:

> Apart from the record number of atoms, phases, parameters, citations etc
> used to describe just 3 broad peaks, I object to this kind of refinement
> being called "Rietveld refinement". Luca called it "Rietveld-like" in MAUD,
> which was used here, but even that is wrong. The term "Rietveld refinement"
> should be restricted to the refinement of crystallographic parameters -
> cell dimensions, atom coordinates etc. and not applied to quantitative
> analysis of phases, particle size etc. Fitting peaks in powder patterns was
> done before Rietveld, who must be turning in his grave to see his name
> associated with this kind of thing.
>
> ________________________________
> Dr Alan Hewat, NeutronOptics
> Grenoble, FRANCE (from phone)
> [email protected]
> +33.476984168 VAT:FR79499450856
> http://NeutronOptics.com/hewat
> _______________________________
>
>
> On Fri, 12 Jan 2024, 12:57 Le Bail Armel, <[email protected]> wrote:
>
>> Hi,
>>
>> A good candidate for the "worst Rietveld refinement of the year" award :
>>
>> https://pubpeer.com/publications/12069A6AD9D5D34F26031F34705D06
>>
>> Even the difference pattern is totally fabricated.
>>
>> Best
>>
>> Armel
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