Structure and strain relaxation mechanisms of ultrathin epitaxial Pr2O3 films on Si(111) -: art. no. 074906

被引:41
|
作者
Schroeder, T
Lee, TL
Libralesso, L
Joumard, I
Zegenhagen, J
Zaumseil, P
Wenger, C
Lupina, G
Lippert, G
Dabrowski, J
Müssig, HJ
机构
[1] European Synchrotron Radiat Facil, F-38043 Grenoble, France
[2] IHP, D-15236 Frankfurt, Oder, Germany
关键词
D O I
10.1063/1.1883304
中图分类号
O59 [应用物理学];
学科分类号
摘要
The structure of ultrathin epitaxial Pr2O3 films on Si(111) was studied by synchrotron radiation-grazing incidence x-ray diffraction. The oxide film grows as hexagonal Pr2O3 phase with its (0001) plane attached to the Si(111) substrate. The hexagonal (0001) Pr2O3 plane matches the in-plane symmetry of the hexagonal Si(111) surface unit cell by aligning the < 10(1) over bar 0 > Pr2O3 along the < 11(2) over bar > Si directions. The small lattice mismatch of 0.5% results in the growth of pseudomorphic oxide films of high crystalline quality with an average domain size of about 50 nm. The critical thickness t(c) for pseudomorphic growth amounts to 3.0 +/- 0.5 nm. The relaxation of the oxide film from pseudomorphism to bulk behavior beyond t(c) causes the introduction of misfit dislocations, the formation of an in-plane small angle mosaicity structure, and the occurence of a phase transition towards a (111) oriented cubic Pr2O3 film structure. The observed phase transition highlights the influence of the epitaxial interface energy on the stability of Pr2O3 phases on Si(111). A mechanism is proposed which transforms the hexagonal (0001) into the cubic (111) Pr2O3 epilayer structure by rearranging the oxygen network but leaving the Pr sublattice almost unmodified. (C) 2005 American Institute of Physics.
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页数:9
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