Praseodymium • Lanthanide Rare Earth
Primary XPS region: Pr3d
Overlapping regions: Cu2p
Binding energies of common chemical states:
|Chemical state||Binding energy Pr3d5/2|
|Pr metal||932 eV|
- Collect entire Pr3d region (up to 990eV), making sure both Pr3d5/2 and Pr3d3/2 components are acquired.
- There is direct overlap between Pr3d and Cu2p peaks.
- Although Pr3d/Cu2p peaks have strong overlap, Pr3d spin-orbit components have a 3:2 intensity ratio compared to a 2:1 ratio for Cu2p.
- Check for the weaker Cu3p peak at 75eV.
- Check the positions of Pr and Cu Auger peaks (primary Cu LMM peak at kinetic energy is 918eV, compared to primary Pr peak at kineitic energy is 690eV).
Date of discovery: 1885
Name origin: Greek prasios and didymos
Discoverer: C.F. Aver von Welsbach
Obtained from: salts
Melting point: 1208 K
Boiling point: 3400 K
Molar volume: 20.8 × 10-6 m3/mol
Shell structure: 2,8,18,21,8,2
Electron configuration: [Xe]6s24f3
Oxidation state: 3
Crystal structure: hexagonal
Praseodymium should be stored under a light mineral oil or sealed in plastic, as it will develop a green coating which, in return, exposes more metal to oxidation. First discovered in 1885 by German chemist C. F. Auer von Welsbach, praseodymium’s primary use is as an alloying agent combined with magnesium to create high-strength metals for aircraft engines. Praseodymium is also a necessary element for studio lighting and projector lights used in the motion picture industry. This element forms the core of carbon arc lights. Praseodymium gives glasses and enamels a yellowish color. The element has no known biological role.
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