Anisotropic orbital occupation and Jahn-Teller distortion of orthorhombic YMnO3 epitaxial films: A combined experimental and theoretical study on polarization-dependent x-ray absorption spectroscopy

The b-axis oriented orthorhombic YMnO3 (o-YMnO3) epitaxial films on a YAlO3 (010) substrate were fabricated with pulsed-laser deposition. The anisotropic orbital occupation and Jahn-Teller (JT) distortion of an o-YMnO3 film were investigated with polarization-dependent x-ray absorption spectra and c...

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Veröffentlicht in:The Journal of chemical physics 2014-04, Vol.140 (15)
Hauptverfasser: Haw, Shu-Chih, Lee, Jenn-Min, Chen, Shin-Ann, Lu, Kueih-Tzu, Lin, Pao-An, Lee, Chih-Hao, Lee, Ming-Tao, Pi, Tun-Wen, Hu, Zhiwei, Chen, Jin-Ming
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Sprache:eng
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Zusammenfassung:The b-axis oriented orthorhombic YMnO3 (o-YMnO3) epitaxial films on a YAlO3 (010) substrate were fabricated with pulsed-laser deposition. The anisotropic orbital occupation and Jahn-Teller (JT) distortion of an o-YMnO3 film were investigated with polarization-dependent x-ray absorption spectra and configuration-interaction multiplet-cluster calculations. A significant energy difference, ∼3.8 eV, for the main white line along E//b and E//a in polarization-dependent Mn K-edge spectra of o-YMnO3 indicates an extraordinary JT distortion and significant anisotropic Mn–O bonding within the ab plane in the o-YMnO3 film. Most importantly, although the orbital occupation of 3d electrons in o-YMnO3 films is almost the same as that in single crystalline o-DyMnO3, the JT distortion of o-YMnO3 films is larger than that of single crystalline o-DyMnO3, deduced from the multiplet calculations. We speculate that this JT distortion predominantly contributes to the origin of the cycloidal spin deformation in bulk o-YMnO3, because of a suppressed nearest-neighbor superexchange interaction and an enhanced next-nearest-neighbor superexchange interaction. These complementary results provide insight into the origin of the E-type magnetic configuration of o-YMnO3.
ISSN:0021-9606
1089-7690
DOI:10.1063/1.4871114