Browsing by Author "Jeng, H. T."

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Bonding anisotropy in multiferroic TbMnO(3) probed by polarization dependent x-ray absorption spectroscopy
(2009-01-26)
Chen, J. M.
;
Lee, J. M.
;
Chen, C. K.
;
Chou, T. L.
;
Lu, K. T.
O K- and Mn L(2,3)-edges x-ray absorption spectra of orthorhombic TbMnO(3) single crystals show strong polarization dependence, in contrast with results of previous experiments on orthorhombic LaMnO(3) and DyMnO(3) thin films that show nearly isotropic spectral structure. First-principles calculations reveal that TbMnO(3) exhibits a zigzag e(g) orbital ordering ground state. The highly distorted MnO(6) octahedron and orbital ordering in TbMnO(3) produce highly anisotropic Mn-O bonding within the ab plane, a frustration of the magnetic ordering, and the formation of complicated incommensurate magnetic structures.
Bonding anisotropy in multiferroic TbMnO3 probed by polarization dependent x-ray absorption spectroscopy
(2009-01-26)
Chen, J. M.
;
Lee, J. M.
;
Chen, C. K.
;
Chou, T. L.
;
Lu, K. T.
O K- and Mn L-2,L-3-edges x-ray absorption spectra of orthorhombic TbMnO3 single crystals show strong polarization dependence, in contrast with results of previous experiments on orthorhombic LaMnO3 and DyMnO3 thin films that show nearly isotropic spectral structure. First-principles calculations reveal that TbMnO3 exhibits a zigzag e(g) orbital ordering ground state. The highly distorted MnO6 octahedron and orbital ordering in TbMnO3 produce highly anisotropic Mn-O bonding within the ab plane, a frustration of the magnetic ordering, and the formation of complicated incommensurate magnetic structures.
Intra- and intersite electronic excitations in multiferroic TbMnO(3) probed by resonant inelastic x-ray scattering
(2010-09-27)
Chen, J. M.
;
Lee, J. M.
;
Huang, S. W.
;
Lu, K. T.
;
Jeng, H. T.
Mn 3d valence states and elementary electronic excitations in single-crystalline TbMnO(3) were probed with resonant inelastic x-ray scattering (RIXS) (or resonant x-ray emission spectroscopy, RXES), polarized x-ray absorption spectra and ab initio electron-structure calculations. Polarized Mn K-edge x-ray absorption spectra of TbMnO(3) crystals exhibit a significant anisotropy along three crystallographic directions, particularly for the white-line region. The 1s3p-RXES spectra obtained at the Mn K edge reveal that the quadrupolar Raman regime is restricted predominantly to below the pre-edge peak whereas the fluorescence regime starts from the first pre-edge peak of 1s -> 3d transitions, indicating a relatively delocalized character of unoccupied Mn 3d states. The additional K beta emission profile at energy loss similar to 62 eV is attributed to the off-site dipole Mn 1s-Mn' 3d and/or Mn 1s-Tb 5d transitions, originating from hybridization between Mn 4p states and neighboring Mn' 3d/Tb 5d states. The off-site dipole transition makes a considerable contribution to the pre-edge region of Mn K-edge spectrum. Three prominent RIXS features at similar to 2.9, 7, and 11 eV were observed. Based on GGA+U calculations, the 7 eV region corresponds to transitions from O 2p states to unoccupied minority Mn 3d states, whereas the 11 eV band is ascribed to transitions from the O 2p band to the empty Tb 5d band. The broad 2.9 eV band is attributed to the coexistence of on-site Mn 3d-Mn 3d and off-site Mn 3d-Mn' 3d transitions.
Intra- and intersite electronic excitations in multiferroic TbMnO3 probed by resonant inelastic x-ray scattering
(2010-09-27)
Chen, J. M.
;
Lee, J. M.
;
Huang, S. W.
;
Lu, K. T.
;
Jeng, H. T.
Mn 3d valence states and elementary electronic excitations in single-crystalline TbMnO3 were probed with resonant inelastic x-ray scattering (RIXS) (or resonant x-ray emission spectroscopy, RXES), polarized x-ray absorption spectra and ab initio electron-structure calculations. Polarized Mn K-edge x-ray absorption spectra of TbMnO3 crystals exhibit a significant anisotropy along three crystallographic directions, particularly for the white-line region. The 1s3p-RXES spectra obtained at the Mn K edge reveal that the quadrupolar Raman regime is restricted predominantly to below the pre-edge peak whereas the fluorescence regime starts from the first pre-edge peak of 1s -> 3d transitions, indicating a relatively delocalized character of unoccupied Mn 3d states. The additional K beta emission profile at energy loss similar to 62 eV is attributed to the off-site dipole Mn 1s-Mn' 3d and/or Mn 1s-Tb 5d transitions, originating from hybridization between Mn 4p states and neighboring Mn' 3d/Tb 5d states. The off-site dipole transition makes a considerable contribution to the pre-edge region of Mn K-edge spectrum. Three prominent RIXS features at similar to 2.9, 7, and 11 eV were observed. Based on GGA+U calculations, the 7 eV region corresponds to transitions from O 2p states to unoccupied minority Mn 3d states, whereas the 11 eV band is ascribed to transitions from the O 2p band to the empty Tb 5d band. The broad 2.9 eV band is attributed to the coexistence of on-site Mn 3d-Mn 3d and off-site Mn 3d-Mn' 3d transitions.
Pressure-dependent electronic structures in multiferroic DyMnO(3): A combined lifetime-broadening-suppressed x-ray absorption spectroscopy and ab initio electronic structure study
(2010-10-21)
Chen, J. M.
;
Lee, J. M.
;
Chou, T. L.
;
Chen, S. A.
;
Huang, S. W.
Variations in the electronic structure and structural distortion in multiferroic DyMnO(3) were probed by synchrotron x-ray diffraction, lifetime-broadening-suppressed x-ray absorption spectroscopy (XAS), and ab initio electronic structure calculations. The refined x-ray diffraction data enabled an observation of a diminished local Jahn-Teller distortion of Mn sites within MnO(6) octahedra in DyMnO(3) on applying the hydrostatic pressure. The intensity of the white line in Mn K-edge x-ray absorption spectra of DyMnO(3) progressively increased with the increasing pressure. With the increasing hydrostatic pressure, the absorption threshold of an Mn K-edge spectra of DyMnO(3) shifted toward a greater energy, whereas the pre-edge line slightly shifted to a smaller energy. We provide the spectral evidence for the pressure-induced bandwidth broadening for manganites. The intensity enhancement of the white line in Mn K-edge spectra is attributed to a diminished Jahn-Teller distortion of MnO(6) octahedra in compressed DyMnO(3). A comparison of the pressure-dependent XAS spectra with the ab initio electronic structure calculations and full calculations of multiple scattering using the code FDMNES shows the satisfactory agreement between experimental and calculated Mn K-edge spectra. (C) 2010 American Institute of Physics. [doi:10.1063/1.3490400]
Pressure-dependent electronic structures in multiferroic DyMnO3: A combined lifetime-broadening-suppressed x-ray absorption spectroscopy and ab initio electronic structure study
(2010-10-21)
Chen, J. M.
;
Lee, J. M.
;
Chou, T. L.
;
Chen, S. A.
;
Huang, S. W.
Variations in the electronic structure and structural distortion in multiferroic DyMnO3 were probed by synchrotron x-ray diffraction, lifetime-broadening-suppressed x-ray absorption spectroscopy (XAS), and ab initio electronic structure calculations. The refined x-ray diffraction data enabled an observation of a diminished local Jahn-Teller distortion of Mn sites within MnO6 octahedra in DyMnO3 on applying the hydrostatic pressure. The intensity of the white line in Mn K-edge x-ray absorption spectra of DyMnO3 progressively increased with the increasing pressure. With the increasing hydrostatic pressure, the absorption threshold of an Mn K-edge spectra of DyMnO3 shifted toward a greater energy, whereas the pre-edge line slightly shifted to a smaller energy. We provide the spectral evidence for the pressure-induced bandwidth broadening for manganites. The intensity enhancement of the white line in Mn K-edge spectra is attributed to a diminished Jahn-Teller distortion of MnO6 octahedra in compressed DyMnO3. A comparison of the pressure-dependent XAS spectra with the ab initio electronic structure calculations and full calculations of multiple scattering using the code FDMNES shows the satisfactory agreement between experimental and calculated Mn K-edge spectra. (C) 2010 American Institute of Physics. [doi:10.1063/1.3490400]
Resonant x-ray emission spectroscopy of multiferroic TbMnO3
(2007-07-30)
Chen, J. M.
;
Chen, C. K.
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Chou, T. L.
;
Jarrige, I.
;
Ishii, H.
The Mn 3d valence states in single-crystalline TbMnO3 were probed using x-ray absorption spectroscopy and resonant x-ray emission spectroscopy (RXES). The polarized Mn K-edge x-ray absorption spectra show a strong polarization dependence, particularly for the white line region, indicating the strong anisotropic Mn-O bonding within the ab plane in TbMnO3. The RXES data obtained at the Mn K edge clearly reveal that unoccupied Mn 3d states exhibit a relatively delocalized character, stemming from hybridization of the Mn 3d states with the neighboring Mn 4p orbitals. The authors demonstrated that resonant x-ray emission spectroscopy is able to characterize the degree of localization of the unoccupied states or hole carriers in manganites.
Strong orbital polarization in orthorhombic DyMnO(3): A combined x-ray linear dichroism and ab initio electronic structure study
(2010-05-15)
Chen, J. M.
;
Hu, Z.
;
Jeng, H. T.
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Chin, Y. Y.
;
Lee, J. M.
We present a combined experimental and theoretical study on the Mn 3d orbital occupation in orthorhombic DyMnO(3) single crystals. We have observed a very strong polarization dependence in the Mn L(2,3) x-ray absorption spectra, indicative for a distinct anisotropic orbital occupation. Ab initio electronic-structure calculations clearly infer the existence of a strong orbital polarization in the e(g) band with a staggered d(3x2-r2)/d(3y2-r2)-type ordering pattern in the ab plane. This finding is in excellent agreement with a quantitative analyis of the spectra using the atomic multiplet cluster approach.
Strong orbital polarization in orthorhombic DyMnO3: A combined x-ray linear dichroism and ab initio electronic structure study
(2010-05-15)
Chen, J. M.
;
Hu, Z.
;
Jeng, H. T.
;
Chin, Y. Y.
;
Lee, J. M.
We present a combined experimental and theoretical study on the Mn 3d orbital occupation in orthorhombic DyMnO3 single crystals. We have observed a very strong polarization dependence in the Mn L-2,L-3 x-ray absorption spectra, indicative for a distinct anisotropic orbital occupation. Ab initio electronic-structure calculations clearly infer the existence of a strong orbital polarization in the e(g) band with a staggered d(3x2-r2)/d(3y2-r2)-type ordering pattern in the ab plane. This finding is in excellent agreement with a quantitative analyis of the spectra using the atomic multiplet cluster approach.
The unconventional doping in YBa2Cu3O7-x/La0.7Ca0.3MnO3 heterostructures by termination control
(2017-01-16)
Tra, V. T.
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Huang, R.
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Gao, X.
;
Chen, Y. -J.
;
Liu, Y. T.
In strongly correlated oxides, heterostructures provide a powerful route to manipulate the charge, spin, orbital, and lattice degrees of freedom to create distinctive functionalities. In this work, we have achieved atomically precise interface control in YBa2Cu3O7-x/La0.7Ca0.3MnO3 (YBCO/LCMO) heterostructures and find a hidden effective doping. This mechanism is responsible for higher Tc in the sample with the MnO2-terminated interface than in that with the La0.7Ca0.3O-terminated interface. The MnO2-terminated sample also shows a larger magnetic moment of Mn together with a lower valence state. For more than a decade, the control of T-c in these heterostructures prior to this work has been solely via the variation of YBCO or LCMO thickness. This work hints at an alternative way of exploiting and exploring the interactions between superconductivity and magnetism in this system. Published by AIP Publishing.