Passivation of the La2NiMnO6 double perovskite to hydroxylation by excess nickel, and the fate of the hydroxylated surface upon heating
•Lanthanum nickel manganese oxide formed a double perovskite, LaNi0.5Mn0.5O3.•LaNi0.75Mn0.25O3 phase separated into LaNi0.5Mn0.5O3, NiO and LaNiO3.•Stoichiometric LaNi0.5Mn0.5O3 formed an extensively hydroxylated overlayer.•Heating formed an La2O3 overlayer and did not regenerate the perovskite.•Exc...
Saved in:
Published in: | Applied surface science Vol. 305; pp. 544 - 553 |
---|---|
Main Authors: | , , |
Format: | Journal Article |
Language: | English |
Published: |
Amsterdam
Elsevier B.V
30-06-2014
Elsevier |
Subjects: | |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | •Lanthanum nickel manganese oxide formed a double perovskite, LaNi0.5Mn0.5O3.•LaNi0.75Mn0.25O3 phase separated into LaNi0.5Mn0.5O3, NiO and LaNiO3.•Stoichiometric LaNi0.5Mn0.5O3 formed an extensively hydroxylated overlayer.•Heating formed an La2O3 overlayer and did not regenerate the perovskite.•Excess nickel prevented extensive hydroxylation.
The double perovskites with a total elemental content of LaNi0.5Mn0.5O3 and LaNi0.75Mn0.25O3 were synthesized by solid state methods, although the LaNi0.75Mn0.25O3 material underwent phase separation into NiO, LaNiO3 and LaNi0.5Mn0.5O3. Auger Electron Spectroscopy (AES) and X-ray photoelectron spectroscopy (XPS) indicated substantial lanthanum surface segregation for the LaNi0.5Mn0.5O3 material, which formed an altered La(OH)3 layer 50–100 monolayers in thickness. The La(OH)3 could be removed by Ar+ sputtering to achieve a surface of approximately stoichiometric concentration. Heating the La(OH)3-covered LaNi0.5Mn0.5O3 did not regenerate the double perovskite but rather produced an overlayer of La2O3. While the LaNi0.75Mn0.25O3 material displayed extensive phase separation, the excess nickel appeared to prevent substantial lanthanum surface segregation. |
---|---|
ISSN: | 0169-4332 1873-5584 |
DOI: | 10.1016/j.apsusc.2014.03.134 |