Orthorhombic YMnO3 thin films with (200), (020), and (001) orientations were, respectively, obtained by pulsed laser deposition on SrTiO3(110), LaAlO3(110), and SrTiO3(001) substrates. The results demonstrate that the strain between film and substrate can serve as an alternative in transforming the thermodynamically stable hexagonal YMnO3 into the orthorhombic phase, which previously could be obtained with high-pressure high temperature syntheses and epitaxy-stabilized thin film processes. More importantly, these films allow us, for the first time, to unambiguously disclose the intrinsic magnetic property along different crystallographic orientations. Our results show that, although the antiferromagnetic (AFM) ordering remains the same, there is an additional spin reordering transition which is very much dependent on the crystallographic orientation along which the measuring field was applied and on the in-plane crystallographic alignment of the films. Detailed analyses indicate that the origin of the observed second reordering may be due to some strain-induced canted AFM state instead of the incommensurate lock-in transitions conceived previously.
5 September 2007 in Journal of Applied Crystallography
Single-crystal atomic-layer-deposited (ALD) Y\(_{\mathrm{2}}\)O\(_{\mathrm{3}}\) films 2 nm thick were epitaxially grown on molecular beam epitaxy (MBE) GaAs(001)-4 \(\times\) 6 and GaAs(111)A-2 \(\times\) 2 reconstructed surfaces. The in-plane epitaxy between the ALD-oxide films and GaAs was observed using \textit{in-situ} reflection high-energy electron diffraction in our uniquely designed MBE/ALD multi-chamber system. More detailed studies on the crystallography of the hetero-structures were carried out using high-resolution synchrotron radiation X-ray diffraction. When deposited on GaAs(001), the Y\(_{\mathrm{2}}\)O\(_{\mathrm{3}}\) films are of a cubic phase and have (110) as the film normal, with the orientation relationship being determined: Y\(_{\mathrm{2}}\)O\(_{\mathrm{3}}\)(\(110\))[\(001\)][\(\overline{1}10\)]//GaAs(\(001\))[\(110\)][\(1\overline{1}0\)]. On GaAs(\(111\))A, the Y\(_{\mathrm{2}}\)O\(_{\mathrm{3}}\) films are also of a cubic phase with (\(111\)) as the film normal, having the orientation relationship of Y\(_{\mathrm{2}}\)O\(_{\mathrm{3}}\)(\(111\))[\(2\overline{1}\overline{1}\)] [\(01\overline{1}\)]//GaAs (\(111\)) [\(\overline{2}11\)][\(0\overline{1}1\)]. The relevant orientation for the present/future integrated circuit platform is (\(001\)). The ALD-Y\(_{\mathrm{2}}\)O\(_{\mathrm{3}}\)/GaAs(\(001\))-4 \(\times\) 6 has shown excellent electrical properties. These include small frequency dispersion in the capacitance-voltage CV curves at accumulation of ~7% and ~14% for the respective p- and n-type samples with the measured frequencies of 1 MHz to 100 Hz. The interfacial trap density (Dit) is low of ~10\(^{12}\) cm\(^{−2}\)eV\(^{−1}\) as extracted from measured quasi-static CVs. The frequency dispersion at accumulation and the D\(_{it}\) are the lowest ever achieved among all the ALD-oxides on GaAs(\(001\)).