Search arXiv⌕ Search

arXiv · cond-mat/0609101

Observation and resonant x-ray optical interpretation of multi-atom resonant photoemission effects in O 1s emission from NiO

Abstract

We present experimental and theoretical results for the variation of the O 1s intensity from a NiO(001) surface as the excitation energy is varied through the Ni 2p1/2,3/2 absorption resonances, and as the incidence angle of the radiation is varied from grazing to larger values. For grazing incidence, a strong multi-atom resonant photoemission (MARPE) effect is seen on the O 1s intensity as the Ni 2p resonances are crossed, but its magnitude decreases rapidly as the incidence angle is increased. Resonant x-ray optical (RXRO) calculations are found to predict these effects very well, although the experimental effects are found to decrease at higher incidence angles faster than those in theory. The potential influence of photoelectron diffraction effects on such measurements are also considered, including experimental data with azimuthal-angle variation and corresponding multiple-scattering-diffraction calculations, but we conclude that they do not vary beyond what is expected on the basis of the change in photoelectron kinetic energy. Varying from linear polarization to circular polarization is found to enhance these effects in NiO considerably, although the reasons are not clear. We also discuss the relationship of these measurements to other related interatomic resonance experiments and theoretical developments, and make some suggestions for future studies in this area.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

N. Mannella, S. -H. Yang, B. S. Mun, F. J. Garcia de Abajo, A. W. Kay, B. C. Sell, M. Watanabe, H. Ohldag, E. Arenholz, A. T. Young, Z. Hussain, M. A. Van Hove, C. S. Fadley. 2006-09-05. Observation and resonant x-ray optical interpretation of multi-atom resonant photoemission effects in O 1s emission from NiO. https://doi.org/10.1103/physrevb.74.165106

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Geometry-Induced Effective Tight-Binding Hamiltonians for Phononic Systems: Mode Conversion and SSH-Like Physics

We present a framework that maps harmonic vibrational systems onto effective multi-orbital tight-binding Hamiltonians, establishing a direct correspondence between phononic degrees of freedom and graph-based lattice models. Within this mapping, the Cartesian displacement components of each mass become internal orbitals, while elastic interactions generate effective onsite energies and hopping amplitudes determined by the geometry of the system. This representation enables the application of numerical and conceptual tools originally developed for electronic transport to the study of phononic systems. The method is first applied to a monoatomic chain containing an angular bend. For this benchmark system, analytical expressions for the polarization-resolved transmission and reflection probabilities are derived and compared against calculations performed using a recursive scattering-matrix method within the mapped tight-binding representation. Excellent agreement is obtained, validating the mapping and demonstrating its ability to describe geometry-induced mode conversion and the influence of evanescent states. We then investigate zigzag chains, where alternating bond orientations generate effective dimerized Hamiltonians reminiscent of the Su--Schrieffer--Heeger (SSH) model. Although the uniform zigzag chain develops a spectral gap, no localized edge states are observed. We show that modified boundary parameters generated by the phononic mapping suppress the edge-state formation expected from the ideal SSH picture. Introducing a geometric domain wall restores localized domain-wall states inside the gap, which give rise to resonant transmission channels across an otherwise insulating frequency window. The resonance energies remain robust against system-size variations and the corresponding transmission approaches unity.

cond-mat.other↗

THz-Driven Quantum Ionic Magnetism in a Quantum Paraelectric SrTiO3

Magnetic moments carried by rotating ionic motion in crystals are becoming recognized as an important contribution to magnetism, angular momentum transport, and optical activity. However, efficient approaches to their dynamical control are lacking. Here, we report THz-driven generation and optical detection of quantum ionic magnetism in quantum paraelectric SrTiO3. We observe an oscillatory ionic magnetization without a corresponding oscillatory polarization, contradicting from the classical relation M~PXdP/dt while its suppression above the quantum paraelectric regime points to a quantum ionic origin. Analysis shows that this effect results from the beating between quantum ionic eigenstates whose degeneracy is lifted due to the directional symmetry breaking by the THz pulse. The presented approach provides a pathway for the ultrafast control of ionic magnetization in quantum materials for spintronic and thermotronic applications.

cond-mat.other↗

Resonantly Enhanced Multiphonon Scattering and Local Orbital-Phonon Coupling in Bulk and Thin Flakes of 2D Single Crystals of Antiferromagnetic (NixFe1-x)2P2S6

Orbital degrees of freedom play a pivotal role in shaping the physical properties of two-dimensional (2D) van der Waals magnetic systems, strongly influencing electron-phonon coupling and intermediate-state dynamics. In this study, we present a comprehensive temperature and thickness-dependent Raman investigation of the single crystals of 2D van der Waals antiferromagnetic series (NixFe1-x)2P2S6. Utilizing Raman spectroscopy, we explore the interplay between local orbital excitations and lattice vibrations, observing higher-order phonon modes extending up to the fourth order. We observe an anomalously high and weakly temperature-dependent intensity ratio of these higher-order modes relative to low-energy first-order phonons. Theoretical cluster calculations and Franck-Condon modelling reveal that these features originate from resonantly enhanced multiphonon scattering mediated by localized intermediate Ni 3d8 multiplet excitations. The local orbital occupancy of these intermediate states couples strongly to lattice coordinates, providing a selective enhancement mechanism for specific phonon channels. Notably, these higher-order features are absent in the end-member Fe2P2S6. This distinction reflects the charge-transfer character of Ni2P2S6, which places optical transitions in resonance with local multiplet states, contrasted with the Mott-Hubbard insulator regime in Fe-rich analogues. Our findings clarify the microscopic origin of high-frequency Raman scattering in transition metal thiophosphates and underscore the central role of local orbital-phonon interactions in 2D correlated magnets.

cond-mat.other↗