Hi Leandro, I suspect you will get several answers to your excellent questions. It's late as I type this and I am looking forward to seeing my pillow, so I am going to respond to just one part of your email.
On Thursday 22 February 2007 20:59, Leandro Langie Araujo wrote: > I've been reading some papers and I can find people who do set the > [nanoparticle]'s deltaE0 to be the same as the crystalline foil as > well as people who report different deltaE0s for NPs relative to the > foil. This confuses me because by setting (or not) deltaE0 we > directly change the correlated variables, delR and C3. This really gets at the heart of why exafs analysis is difficult. You are certainly correct that the deltaE0 is highly correlated with delR and C3. That correlation is hard to avoid in a non-linear analysis as all three terms effect the phase of the calculated chi(k). Most of the tricks that we so-called experts yammer on about on this mailing list have to do with ways of dealing with those strong correlations that are physically sound and statistically defensible. To continue with your example of comparing nanoparticles their bulk analogs, one strategy taken to deal with these correlation is to assert that some parameter will be the same in the bulk as at the nanoscale. By making that assertion -- or, if your prefer, by using prior knowledge of the system -- we reduce the correlation by supplying more information (perhaps in the form of a multiple data set fit) or we remove the correlation by promoting that parameter from "guessed parameter" to "parameter set according to prior knwoledge". To be more specific, we might assert that the changes to the electronic state of the nanoparticles compared to their bulk analog are relatively small -- small enough that we can neglect the effect. Saying that requires that one believes it. It may be true for metallic nanoparticles, but may not be true for, say, semiconductor nanoparticles. If you believe it to be true that the electronic state doesn't change much, then you are well justified in asserting that the E0 for carefully aligned data should be the same. Otherwise, you should lift that constraint and investigate how e0 might be different for your nanoparticles. So what should you do if you are not sure? Well, one strategy might be to do a multiple data set fit using carefully aligned bulk and nano data. Compare the fit using a constrained e0 to the fit where the two e0s float freely. If the free floating e0s make sense given what you know about the electronics of the nanoparticles and they provide a statistically significant improvement to the fit, then probably you should have free floating e0s. If you float the two e0s and they come out the same (within their error bars, of course) then you probably should reintroduce the constraint. The whole time you are doing that, you need to be mindful that, as you say, e0 is correlated to other parameters. The fitting results need to be both reasonable and defensible regardless of how you decide to cast the problem. "Reasonable and defensible" applied to all the parameters, not just e0. Hope that helps, B -- Bruce Ravel ---------------------------------------------- [EMAIL PROTECTED] Molecular Environmental Science Group, Building 203, Room E-165 MRCAT, Sector 10, Advanced Photon Source, Building 433, Room B007 Argonne National Laboratory phone and voice mail: (1) 630 252 5033 Argonne IL 60439, USA fax: (1) 630 252 9793 My homepage: http://cars9.uchicago.edu/~ravel EXAFS software: http://cars9.uchicago.edu/~ravel/software/ _______________________________________________ Ifeffit mailing list Ifeffit@millenia.cars.aps.anl.gov http://millenia.cars.aps.anl.gov/mailman/listinfo/ifeffit