Promethium

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Promethium

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Orbitals and Energies #

Note – these are listed in BINDING ENERGY

 

Pm 3d ≈ 1028 eV

Pm 4s ≈ 331 eV

Pm 4p ≈ 240 eV

Pm 4d ≈ 120 eV

Pm 5s ≈ 38 eV

Pm 5p ≈ 22 eV

Pm 4f ≈ 4 eV

Doublet Separations #

Pm 3d = 26.3 eV

Pm 3p = 113.7 eV

Pm 4d = 4.1 eV

Common Overlaps for Pm 3d #

Zn 2p – At 4s – U 4s – Sb MNN (Al Ka X-rays) – V LMM (Al Ka X-rays)

Auger Energies #

Note – these are listed in KINETIC ENERGY

 

No data

Common Binding Energies – Pm 3d #

Species #

B.E. / eV #

Charge Ref #

Reference #

Theory and Background #

Pm has been rarely studied by XPS due to it’s rarity and radioactivity. In lanthanides the 3d core hole created in an XPS experiment interacts strongly with the partially-filled 4f shell. That interaction produces complex multiplet splitting of the 3d5/2 and 3d3/2 features and often yields multiple main components plus satellites (shake-up / shake-down, charge transfer). This is a general property across the lanthanide series and is crucial for interpreting Pm 3d spectra.[1]  For oxides or compounds where 4f–ligand (e.g., O 2p) hybridization exists, you can get charge-transfer satellites in the 3d region.

Experimental Advice #

Radioactivity from Pm may in theory cause sample damage itself.

Data Analysis Guidance #

Reference Datasets #

 

Coming soon

References #

  1. Bagus, Paul S., et al. “Multiplet splitting for the XPS of heavy elements: Dependence on oxidation state.” Surface Science 643 (2016): 142-149.. Read it online here.