- Ifeffit - millenia.cars.aps.anl.gov

Postdoc position at Argonne National Laboratory - X-ray characterization of low-temperature fuel cell and electrolyzers
by Myers, Deborah J. 30 Oct '23

30 Oct '23

https://argonne.wd1.myworkdayjobs.com/Argonne_Careers/job/Lemont-IL-USA/Pos…

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Re: [Ifeffit] Differences between Larch and Artemis when performing FEFF calculations
by Ava Rajh 18 Oct '23

18 Oct '23

Hello Matt! thank you for the response. In putting together all the project files for the minimal working example I tested a bunch more .cif files of various materials including different graphite file, and there was no difference in Larch and Athena in any of them (as long as the same FEFF version and input settings are used) as expected. Looking closely at the feff input file for the C.cif I was having trouble with, there were some differences which I haven't noticed when looking through them before. So as far as I am concerned, this was a user error on my part, as the generated input files weren't exactly the same. If I save the input feff file from Larch and use that in Artemis or the other way around, as you suggested, the results match exactly. The compared spectra in my previous message were calculated separately, exported and plotted together. thank you for very much for the help and kind regards, Ava > Message: 1 > Date: Mon, 16 Oct 2023 15:24:26 -0500 > From: Matt Newville <newville(a)cars.uchicago.edu> > To: XAFS Analysis using Ifeffit <ifeffit(a)millenia.cars.aps.anl.gov> > Subject: Re: [Ifeffit] Differences between Larch and Artemis when > performing FEFF calculations > Message-ID: > <CA+7ESbrWm5UoBYggLmi+-WZRU6mn4Y_-z1OBVg57pAu4rsXM7w(a)mail.gmail.com> > Content-Type: text/plain; charset="utf-8" > > Hi Ava, > > I think you'll have to give us more details about what you have done. > The > figures you show are all in R-space, so after at least some > processing... > So, yes, project files and/or scripts would be helpful. Yes, there > can be > subtle changes in the background subtraction (and in the normalization > process too) between Larch and Ifeffit/Athena/Artemis. > > By default, Artemis uses Feff 6.10 and Larch uses Feff 8. For the C K > edge, that could have a noticeable difference, especially in the > placing of > the k=0 value, though I do not know how big that effect would be for C > (graphite?). But also, Artemis and Larch can both read the inputs > from > the other calculations: it might be that this is what you have done to > make the plots, but that wasn't 100% clear to me. > > > > > On Mon, Oct 16, 2023 at 2:08?PM Ava Rajh <ava.rajh(a)ijs.si> wrote: > >> Dear all! >> >> I haven't been able to find a similar question/issue in the previous >> threads, so I hope someone can help me figure out what is going on. >> >> I am trying to fit a Carbon EXAFS spectra, using graphite as a model. >> I >> am first focusing on just the first two single scattering paths, so I >> calculated the theoretical paths with FEFF in Larch and tried using >> them >> to fit the spectra. I was consistently getting slightly lower >> distances >> than expected, but otherwise an OK fit. >> >> The issue is, I tried to compare the analysis with a colleague who is >> using Athena. At first glance the EXAFS spectra, using the exact same >> parameters, looked very similar (but not exactly the exactly the same, >> this I attributed to Larch using a different autobk procedure). I >> would >> have however expected the theoretical paths to match exactly, if they >> were calculated and plotted with the same parameters. But they were >> also >> slightly different. I then downloaded Athena and spent time trying to >> find where the differences come from. If I compare the first two >> calculated shells from Larch with the ones from Athena, with exactly >> the >> same set of test parameters (S02 = 1, E0 = 0, dr1 = 0, s2_1 = 0, dr2 = >> 0, s2_2 = 0), the resulting models do not match. I made sure the paths >> are calculated from the came .cif file in both cases, use FEFF6, have >> the same calculated reference distances, same FT... >> >> So, my main question is, am I missing something important in regards >> to >> calculations, why would the calculated paths be different and which >> one >> would be the "correct" one to use for the fit? And the other question >> would be about the fact that EXAFS spectra of experimental data look >> slightly different using Larch and Athena, am I right in disregarding >> this, or should I dig deeper and find the source of discrepancy? >> >> I am enclosing a plot of just the calculated first two shells from >> Athena and Larch (FT: kmin = 2, kmax = 7.5, Fittting in R space, kw = >> 3, kWindow = Hanning, dk = 1.0, Rmin = 0.6, Rmax = 2.1) along with the >> cif file I ended up using for testing the differences. If it would be >> helpful, I can also provide the project files and larch script I used >> for the dataset, but I am mainly interested in understanding the >> differences seen in the theoretical parts first. I tested this using >> Larch v 0.9.72 and Demeter 0.9.26 >> >> Thank you ver much for the help, and If I need to provide any >> additional >> info please let me know. >> kind regards, Ava >> >> -- >> Ava Rajh_______________________________________________

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EXAFS fitting - Reff command not recognized
by van der Veer, Siebe 17 Oct '23

17 Oct '23

Hi all, I'm having an issue where I want to use a * reff (also tried a*reff, a * Reff, a*Reff) as the expression for delta R, but instead of recognizing the command Reff, Larix now considers this a parameter it should fit, whereas in the past it would just use the value for Reff contained in the path in question. Is anyone else experiencing this issue as well and if so, how can I fix this? Best, -- *Siebe van der Veer* | *PhD student* Nanostructures of Functional Oxides | Zernike Institute for Advanced Materials University of Groningen | Nijenborgh 4, 9747 AG Groningen | The Netherlands Email: s.van.der.veer(a)rug.nl |

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Differences between Larch and Artemis when performing FEFF calculations
by Ava Rajh 16 Oct '23

16 Oct '23

Dear all! I haven't been able to find a similar question/issue in the previous threads, so I hope someone can help me figure out what is going on. I am trying to fit a Carbon EXAFS spectra, using graphite as a model. I am first focusing on just the first two single scattering paths, so I calculated the theoretical paths with FEFF in Larch and tried using them to fit the spectra. I was consistently getting slightly lower distances than expected, but otherwise an OK fit. The issue is, I tried to compare the analysis with a colleague who is using Athena. At first glance the EXAFS spectra, using the exact same parameters, looked very similar (but not exactly the exactly the same, this I attributed to Larch using a different autobk procedure). I would have however expected the theoretical paths to match exactly, if they were calculated and plotted with the same parameters. But they were also slightly different. I then downloaded Athena and spent time trying to find where the differences come from. If I compare the first two calculated shells from Larch with the ones from Athena, with exactly the same set of test parameters (S02 = 1, E0 = 0, dr1 = 0, s2_1 = 0, dr2 = 0, s2_2 = 0), the resulting models do not match. I made sure the paths are calculated from the came .cif file in both cases, use FEFF6, have the same calculated reference distances, same FT... So, my main question is, am I missing something important in regards to calculations, why would the calculated paths be different and which one would be the "correct" one to use for the fit? And the other question would be about the fact that EXAFS spectra of experimental data look slightly different using Larch and Athena, am I right in disregarding this, or should I dig deeper and find the source of discrepancy? I am enclosing a plot of just the calculated first two shells from Athena and Larch (FT: kmin = 2, kmax = 7.5, Fittting in R space, kw = 3, kWindow = Hanning, dk = 1.0, Rmin = 0.6, Rmax = 2.1) along with the cif file I ended up using for testing the differences. If it would be helpful, I can also provide the project files and larch script I used for the dataset, but I am mainly interested in understanding the differences seen in the theoretical parts first. I tested this using Larch v 0.9.72 and Demeter 0.9.26 Thank you ver much for the help, and If I need to provide any additional info please let me know. kind regards, Ava -- Ava Rajh

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Re: [Ifeffit] Ifeffit Digest, Vol 248, Issue 2
by bikov＠phys.uni-sofia.bg 13 Oct '23

13 Oct '23

Dear Edmund Welter, Dear Matt Newville, Thank you for the answers and very informative explanations. With best regards, Konstantin > Send Ifeffit mailing list submissions to > ifeffit(a)millenia.cars.aps.anl.gov > > To subscribe or unsubscribe via the World Wide Web, visit > http://millenia.cars.aps.anl.gov/mailman/listinfo/ifeffit > or, via email, send a message with subject or body 'help' to > ifeffit-request(a)millenia.cars.aps.anl.gov > > You can reach the person managing the list at > ifeffit-owner(a)millenia.cars.aps.anl.gov > > When replying, please edit your Subject line so it is more specific > than "Re: Contents of Ifeffit digest..." > > > Today's Topics: > > 1. Fitting mechanism of Artemis (bikov(a)phys.uni-sofia.bg) > 2. Re: Fitting mechanism of Artemis (Edmund Welter) > 3. Re: Fitting mechanism of Artemis (Matt Newville) > > > ---------------------------------------------------------------------- > > Message: 1 > Date: Fri, 6 Oct 2023 11:09:55 +0300 > From: bikov(a)phys.uni-sofia.bg > To: ifeffit(a)millenia.cars.aps.anl.gov > Subject: [Ifeffit] Fitting mechanism of Artemis > Message-ID: > <1936f567bb85f017cc9aa404a2a49fda.squirrel(a)mail.phys.uni-sofia.bg> > Content-Type: text/plain;charset=utf-8 > > Dear all, > I have a general question regarding the mechanism employed in the fitting > procedures implemented in Artemis. > How exactly is performed a fit? Do we have a fixed > central atom (absorbing/emitting atom) and only the distances to the > neighbors included in the probed pathways are varied, i.e. by varying the > coordinates of the corresponding neighbor atoms, or during > the fitting process Artemis can vary the position of the absorption center > too? Could the procedure be constrained in such a way that the scattering > pathways are adjusted by only varying the coordinates of the central atom? > > With kind regards, > Konstantin Bikov > PhD Student at the Physics Department > of the University of Sofia, Bulgaria > > > > ------------------------------ > > Message: 2 > Date: Fri, 6 Oct 2023 11:05:26 +0200 > From: Edmund Welter <edmund.welter(a)desy.de> > To: ifeffit(a)millenia.cars.aps.anl.gov > Subject: Re: [Ifeffit] Fitting mechanism of Artemis > Message-ID: <1ac7d9c6-e37f-2b17-82c5-bb382af973ba(a)desy.de> > Content-Type: text/plain; charset=UTF-8; format=flowed > > Dear Konstantin, > > why would you want to do that? If you change the distance between A-B > you the distance between B-A changes by the same amount. If you move the > absorber away from let's say the centre of an octaeder you would split > the (next) nearest neighbours shell into different shells with different > distances. If the differences are large enough and the resolution of > your EXAFS spectrum sufficient you would see more than one (first > neighbours) peak in the FT of your EXAFS spectrum. But that would be > another model that you would feed into FEFF before you start your second > fit. Technically you would fneed to define the position of all atoms in > your model in world-coordinates. So the absorber would no longer be at > 0,0,0. I would guess that this would make the computation and the model > more complex or at least less intuitive. > > Best regards, > > Edmund > > > On 06.10.23 10:09, bikov(a)phys.uni-sofia.bg wrote: >> Dear all, >> I have a general question regarding the mechanism employed in the >> fitting >> procedures implemented in Artemis. >> How exactly is performed a fit? Do we have a fixed >> central atom (absorbing/emitting atom) and only the distances to the >> neighbors included in the probed pathways are varied, i.e. by varying >> the >> coordinates of the corresponding neighbor atoms, or during >> the fitting process Artemis can vary the position of the absorption >> center >> too? Could the procedure be constrained in such a way that the >> scattering >> pathways are adjusted by only varying the coordinates of the central >> atom? >> >> With kind regards, >> Konstantin Bikov >> PhD Student at the Physics Department >> of the University of Sofia, Bulgaria >> >> _______________________________________________ >> Ifeffit mailing list >> Ifeffit(a)millenia.cars.aps.anl.gov >> http://millenia.cars.aps.anl.gov/mailman/listinfo/ifeffit >> Unsubscribe: http://millenia.cars.aps.anl.gov/mailman/options/ifeffit > > > ------------------------------ > > Message: 3 > Date: Fri, 6 Oct 2023 11:41:17 -0500 > From: Matt Newville <newville(a)cars.uchicago.edu> > To: XAFS Analysis using Ifeffit <ifeffit(a)millenia.cars.aps.anl.gov> > Subject: Re: [Ifeffit] Fitting mechanism of Artemis > Message-ID: > <CA+7ESbpV-FtSVhjEpoTdV72ntx4wAibjZHqZdeAq7ShpSZZiiw(a)mail.gmail.com> > Content-Type: text/plain; charset="utf-8" > > Hi Konstantin, > > > > On Fri, Oct 6, 2023 at 3:11?AM <bikov(a)phys.uni-sofia.bg> wrote: > >> Dear all, >> I have a general question regarding the mechanism employed in the >> fitting >> procedures implemented in Artemis. >> How exactly is performed a fit? > > > > That is a pretty open-ended question to be able to answer with precision. > Is the question more about how fitting works in general, or about what is > modeled and allowed to change in the mode for EXAFS? > > There are plenty of writeups and resources on both topics, including > program documentation. > > Do we have a fixed central atom (absorbing/emitting atom) and only the >> distances to the >> neighbors included in the probed pathways are varied, i.e. by varying >> the >> coordinates of the corresponding neighbor atoms, or during >> the fitting process Artemis can vary the position of the absorption >> center >> too? > > > > Within the context of the software here, the answer is sort of that the > central atom is fixed. > > The way we model EXAFS is effectively (more below, as some might object > to > this) as a 1-dimensional problem. Single scattering EXAFS depends only on > the scalar distance between the atoms (or path length for the > photo-electron). Now, some aspects of EXAFS scattering definitely depend > on more than just distance. The Z of the scattering atom definitely has a > large effect. The angle of the X-ray polarization vector with the > three-dimensional bond direction can also have an effect. These are > folded into the scattering amplitude and phase shift. But even the > disorder terms, sigma^2, and so on, are really capturing the disorder in > R, > not the 3-D disorder. > > For sure, multiple-scattering paths will have 3D information baked into > them. With Feff and the way we use it, this 3D info *is* folded into the > scattering amplitudes and phase shifts calculated for a path and all we > really vary is the distribution of path lengths for those paths. > > In 1-D, it does not matter whether the absorber or scatterer moves, the > only thing that matters is the distance. In fact, to the extent that > neighboring atoms move together in the same direction, there is no effect > on the EXAFS -- an atom in a solution or melt will have EXAFS (it might be > weak, but it does not fall to 0 at a phase transition). EXAFS is much > more > sensitive to "optical phonons" (neighboring atoms moving in opposite > direction) than to "acoustic phonons" (neighboring atoms moving in the > same > direction). > > Now, one can take a reverse-monte-carlo approach: calculate a lot of > different local structures, sum the EXAFS for each calculation, and see > which is best. One can also do something sort of in-between: calculate > a > set of "undistorted paths" and one or more sets of "distorted paths" and > then do a linear (or for some multiple-scattering case, quadratic) model > to > combine these. > > > Could the procedure be constrained in such a way that the scattering >> pathways are adjusted by only varying the coordinates of the central >> atom? >> > > Yes. In fact, this has been done several times. If you imagine a metal > ion > (let's say Ti) surrounded by six neighbors (let's say O) in an octahedron, > a common thing to try to model is if that Ti atom moves away from the > center of the octahedron, say in a perovskite-like structure. > > For the simplest case (ie, what I would start with ;)), you could > calculate > the EXAFS with Ti at the center of a perfect octahedron and get 6 > equivalent paths, and add those to give the EXAFS. If the octahedron is > distorted, you might have 2, 3, 4, or 6 paths. Let's go all the way to > "general" 6 paths. Each path would use a different Feff calculation (or > a > copy). You would not be limited to varying the change in each of the six > path lengths (our 'delr' parameter) to have the same delr for all paths. > Instead, you could define 3 new fitting variables, let's say "dx", "dy", > and "dz" for the displacement of the absorbing Ti from the position used > in > the Feff calculation (let's just call that "origin"). > > If you only have "dz", then one path gets shorter by dz, one gets longer > by > dz, and the other four get longer by sqrt(reff*2 + dz**2), where "reff" is > the magic "R used for each path Feff calculation. I'll leave the more > general case for you ;). > > Hope that gets you started, > > --Matt >

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Re: [Ifeffit] Contents of Ifeffit digest...
by charvi singhvi 06 Oct '23

06 Oct '23

Dear Team, I want to subscribe to the Ifeffit mailing list. I am very new to XAS analysis and I aim to gain expertise in it. I have visited ESRF beamline recently and have promising data. I need to do a proper analysis in order to extract useful information. Your help through this mailing list is much appreciated. Kind Regards Charvi Charvi Singhvi c/o Prof. Vivek Polshettiwar Graduate Student Department of Chemical Sciences (DCS), Tata Institute of Fundamental Research (TIFR), Homi Bhabha Road, Colaba, Mumbai 400005 India Phone: +91-22-2278 2986/2051 Email: charvi.singhvi(a)tifr.res.in Home page: https://www.nanocat.co.in/ https://www.tifr.res.in/~dcs

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Fitting mechanism of Artemis
by bikov＠phys.uni-sofia.bg 06 Oct '23

06 Oct '23

Dear all, I have a general question regarding the mechanism employed in the fitting procedures implemented in Artemis. How exactly is performed a fit? Do we have a fixed central atom (absorbing/emitting atom) and only the distances to the neighbors included in the probed pathways are varied, i.e. by varying the coordinates of the corresponding neighbor atoms, or during the fitting process Artemis can vary the position of the absorption center too? Could the procedure be constrained in such a way that the scattering pathways are adjusted by only varying the coordinates of the central atom? With kind regards, Konstantin Bikov PhD Student at the Physics Department of the University of Sofia, Bulgaria

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Larch 0.9.72
by Matt Newville 03 Oct '23

03 Oct '23

Hi Folks, It's been a few months since the last release, but Larch 0.9.72 is now available. There have been several fixes and a few new features. The XAS analysis GUI application has been renamed from the rather dull name of "XAS Viewer" to "Larix" (the genus of trees for the Larch family). We (well, mostly Mauro Rovezzi and others at ESRF) put in a lot of effort over the summer to generate FDMNES inputs from structural information (CIF files, structural information from the Materials Project). This effort to convert structure information to input files for Feff, FDMNES, etc. has been evolving over the past several months, and there will probably be more done on this in the coming months. If you are interested in getting involved, let us know. There are new binary installer scripts for Windows, MacOS, and even Linux, and the "GetLarch" scripts have been updated too. These all will now install a Python 3.11 environment. Although installation is not fast, it is somewhat faster than it has been in the past due to using the Mamba variation of the Anaconda Python tools. More release notes are at https://github.com/xraypy/xraylarch/releases/tag/0.9.72 If you have a fairly recent version of Larch installed, you should be informed that a new version is available, and be prompted to install or run the Larch Updater script. Let us know if you have any troubles with this version or questions, comments, or suggestions for improvements! --Matt

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TiOx K-edge spectra
by Rebecca Katharina Pittkowski 20 Sep '23

20 Sep '23

Dear community, I am preparing a teaching exercise for a course on nano-structure characterization, and I was hoping that someone has some K-edge spectra of titanium oxide nanoparticles lying around that I could reuse for the course. I have been through the NIMS Material Data Repository and found some useful references but it would be great to have a nano-sized example as well. That could very well be from a published article, which I could include in the teaching. Thanks for any input. Greetings from Copenhagen, Rebecca Rebecca K. Pittkowski Tenure-track Assistant Professor University of Copenhagen Center for High Entropy Alloy Catalysis Department of Chemistry Universitetsparken 5 2100 Copenhagen Ø DENMARK Rebecca.pittkowski(a)chem.ku.dk [/var/folders/gc/lhyz4xy96q77x4sbrrh4l46r0000gn/T/com.microsoft.Outlook/WebArchiveCopyPasteTempFiles/cidimage009.png(a)01D5C49F.F68E4220]

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P K-edge EXAFS
by Marcelo Eduardo Alves 15 Sep '23

15 Sep '23

Hi there, I begin by examining phosphorus adsorption by goethite, hematite, and gibbsite. Why is it difficult, if not impossible, to obtain EXAFS spectra at the P-K edge that can be properly used, i.e., spectra with a high signal-to-noise ratio, especially for dilute samples? Would it be possible to use arsenic as a phosphorus proxy to get conclusions from As K-edge EXAFS data that could be extended to P? Thank you.

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