• Fermion@mander.xyz
    link
    fedilink
    English
    arrow-up
    2
    ·
    6 months ago

    I could be wrong, but I think XRD requires very pure crystals of sufficiently large size. That can help you ascertain the structure and composition of something you can synthesize and crystalize, but I don’t believe xrd can image specific regions of interest like single doping sites like this article talks about.

    Synchrotron XRD also has a major drawback in having a very significant equipment requirement that requires being able send samples away for analysis at a dedicated facility. That puts limits on sample preparation and stability time, as well as sharing beam time with lots of other groups.

    It’s been a while since I’ve read up on synchrotron xray diffraction though, so there could be workarounds for some of those limitation or I could be misremembering details.

    • CapeWearingAeroplane@sopuli.xyz
      link
      fedilink
      English
      arrow-up
      3
      ·
      6 months ago

      You’re definitely correct that getting sychrotron time is hard :(

      On the first part though: Yes and no. XRD will tell you about things like strain and unit cell size distribution, so in that sense, you can’t resolve a single doping site. On the other hand, if you have a reaction going on, or some dopant diffusing into your sample, synchrotron XRD is powerful/fast enough that you can “film” how the crystal structure changes in real time. That “film” will be a kind of average of many sites, but can still be focused to a relatively small region (don’t remember exactly how small off the top of my head, but I believe we’re talking nm-scale).