18 O study of the oxidation of reactively sputtered Ti 1− x Al x N barrier
The preparation of high-permittivity perovskite materials requires high-temperature (550–750 °C) oxidizing environments, providing stringent limitations on the choice of electrode materials. To minimize interdiffusion and oxidation reactions, an electrically conductive diffusion barrier such as Ti 1...
Gespeichert in:
Veröffentlicht in: | Journal of materials research 2001-09, Vol.16 (9), p.2591-2599 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | The preparation of high-permittivity perovskite materials requires high-temperature (550–750 °C) oxidizing environments, providing stringent limitations on the choice of electrode materials. To minimize interdiffusion and oxidation reactions, an electrically conductive diffusion barrier such as Ti
1−
x
Al
x
N is needed below the electrode material (Pt, IrO
2
, RuO
2
…). Ti
1−
x
Al
x
N films were deposited by multitarget reactive sputtering in a mixture of Ar and N
2
. The stability of these films has been investigated under typical conditions for crystallization of perovskite dielectrics. Sample composition was characterized using Rutherford backscattering spectroscopy and nuclear reaction analysis. In particular, the concentration depth profiles of both
18
O and
27
Al were measured before and after RTA treatments via the narrow resonances of
18
O(p,α)
15
N at 151 keV (FWHM = 100 eV) and
27
Al(p,γ)
28
Si at 992 keV (FWHM = 100 eV). The different
18O
excitation curves show that the oxidation resistance increases with Al incorporation. The Al excitation curves indicate a uniform Al content for as-deposited Ti
x
Al
1−
x
N and reveal Al diffusion to the surface during the oxidation process which indicates the formation of an Al-rich oxide layer at the Ti
x
Al
1−
x
N surface, leaving a layer depleted in Al below it. |
---|---|
ISSN: | 0884-2914 2044-5326 |
DOI: | 10.1557/JMR.2001.0356 |