Search arXiv⌕ Search
Home/Archive/arXiv

arXiv · cond-mat/0305448

Comment on "X-ray resonant scattering studies of orbital and charge ordering in Pr1-xCaxMnO3"

Joaquin Garcia·Gloria Subias
View original source ↗Read source document ↗Export metadata ↓

Abstract

In a recent published paper [Phys. Rev. B 64, 195133 (2001)], Zimmermann et al. present a systematic x-ray scattering study of charge and orbital ordering phenomena in the Pr1-xCaxMnO3 series with x= 0.25, 0.4 and 0.5. They propose that for Ca concentrations x=0.4 and 0.5, the appearance of (0, k+1/2, 0) reflections are originated by the orbital ordering of the eg electrons in the a-b plane while the (0, 2k+1, 0) reflections are due to the charge ordering among the Mn3+ and Mn4+ ions. Moreover, for small Ca concentrations (x<0.3), the orbital ordering is only considered and it occurs at (0, k, 0) reflections. A rigorous analysis of all these resonance reflections will show the inadequacy of the charge-orbital model proposed to explain the experimental results. In addition, this charge-orbital model is highly inconsistent with the electronic balance. On the contrary, these reflections can be easily understood as arising from the anisotropy of charge distribution induced by the presence of local distortions, i.e. due to a structural phase transition.

Explore related subjects

cond-mat.str-el

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Joaquin Garcia, Gloria Subias. 2003-05-19. Comment on "X-ray resonant scattering studies of orbital and charge ordering in Pr1-xCaxMnO3". https://doi.org/10.1103/physrevb.68.127101

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

KEEP EXPLORING

Related papers

arXiv2026

Real-space determination of orbital states driving successive phase transitions in FeV2O4

Direct experimental access to orbital states in strongly correlated materials remains a major challenge, despite their central role in driving coupled structural and magnetic phase transitions. In systems where electronic correlations, electron-lattice coupling, and relativistic spin-orbit interactions compete on comparable energy scales, even first-principles calculations often yield multiple metastable solutions, hindering the unambiguous identification of the ground state. Here, we demonstrate that the orbital states of the spinel oxide FeV2O4, which possesses active orbital degrees of freedom on both Fe and V ions, are uniquely resolved by combining valence electron density (VED) analysis based on state-of-the-art synchrotron x-ray diffraction with spin-polarized density-functional-theory calculations. Our results reveal that temperature-dependent rearrangements of orbital occupations drive successive structural transitions that accompany collinear and noncoplanar ferrimagnetic orders, establishing a direct correspondence between orbital anisotropy and spin structure. More broadly, this work shows that experimentally determined VED provides a decisive real-space constraint on competing theoretical solutions, offering a powerful and broadly applicable framework for elucidating the microscopic mechanisms of complex phase transitions in strongly correlated electron systems.

cond-mat.str-el↗
arXiv2026

Macroscopic Zero-Mode Manifold Isolated by Quantum Chaos

Chaotic many-body spectra are expected to densely fill their energy window. We show that constrained spin chains with chiral symmetry evade this expectation by hosting an exponentially large manifold of symmetry-protected exact zero modes separated from the surrounding spectrum by a sharp gap at zero energy. The gap is generated by chaotic level repulsion, with width set by the number of zero modes times the mean level spacing. We verify this mechanism in an East-West kinetically constrained chain, develop a minimal random-matrix description, and show how the gap can be detected through linear-response spectroscopy.

cond-mat.str-el↗
arXiv2026

Textures as a phase-transition probe for quantum spin chains

The idea of quantum texture has been recently proposed and used as a tool for quantifying coherences and for quantum gate identification. In this work we offer a study on its usage to quantum phase transitions, demonstrating the rugosity metric as a simple tool for effective phase-transition probing. We establish the link between rugosity in the computational basis and the hierarchy of spin correlators, and analyze rugosities defined in the global ground-state and in ground-states belonging to different magnetization sectors (to which we refer to as global vs symmetry-resolved rugosities) to study the phase diagram of the Heisenberg XXZ model. We find distinct rugosity signatures at both transition points. In particular, a sharp feature appears at $Δ=1$ already for small systems, revealing a pronounced sensitivity of the correlation hierarchy encoded by the texture to this point. Since the BKT transition coincides with the isotropic $SU(2)$ point of the XXZ model, this behavior may reflect a particular sensitivity of rugosity to the structure of the spin-correlation hierarchy at isotropy.

cond-mat.str-el↗