We have a library of iron oxide nanoparticles doped with different metals and a very thick organic layer. Which would be the best approach to determine the oxidation state of these metals?
The K-edges of your metall atoms are easily accessable and the 10nm organic layer ís no challenge for the x-rays. Core size is no problem but the overall concentration could be too small.
However using a synchrotron as x-ray source could help.
Please have a look at the link.
You 'adress' your metal dopands via the k-edge energy. But therefore it is necessary to have no further Ni, Cu, Zn or Mn in your sample or in the sample support.
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