Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Polycrystalline samples of Ln18Li8Rh5O39 (Ln = La, Pr) have been synthesized by the ceramic method and characterized by X-ray and neutron diffraction. The compounds crystallize in the cubic space group Pmn, with a0 approximately 12.1 Angstroms. The unit cell contains four intersecting 111 chains, each comprised of an alternating sequence of face-sharing RhO6 octahedra and LiO6 trigonal prisms. The octahedra located at the points of intersection contain Rh4+, whereas the remainder contain Rh3+; the compounds thus contain a charge-ordered arrangement of the two cations. The polyhedral chains are enclosed in tunnels formed by the Ln-O sublattice. The magnetic properties of the two new compounds are discussed briefly: both are paramagnetic over the temperature range 5 < TK < 300.

Download full-text PDF

Source
http://dx.doi.org/10.1021/ic050949sDOI Listing

Publication Analysis

Top Keywords

charge-ordered arrangement
8
ln18li8rh5o39 mixed-metal
4
mixed-metal oxide
4
oxide charge-ordered
4
arrangement rh3+
4
rh3+ rh4+
4
rh4+ polycrystalline
4
polycrystalline samples
4
samples ln18li8rh5o39
4
ln18li8rh5o39 synthesized
4

Similar Publications

The doped Hubbard model is one of the paradigmatic platforms to engineer exotic quantum many-body states, including charge-ordered states, strange metals, and unconventional superconductors. While undoped and doped correlated phases have been experimentally realized in a variety of twisted van der Waals materials, experiments in monolayer materials, and in particular 1T transition metal dichalcogenides, have solely reached the conventional insulating undoped regime. Correlated phases in monolayer two-dimensional materials have much higher associated energy scales than their twisted counterparts, making doped correlated monolayers an attractive platform for high temperature correlated quantum matter.

View Article and Find Full Text PDF

FeGeTe is a two-dimensional van der Waals material that exhibits ferromagnetic order with a high Curie temperature () of around room temperature. In addition to , two magnetic transitions occur with decreasing temperature, and a charge-ordered state is observed at low temperatures. We employed Ge Kα X-ray fluorescence holography (XFH) for FeGeTe to directly investigate the local structure in the charge-ordered state, i.

View Article and Find Full Text PDF
Article Synopsis
  • The study involves the synthesis of three mixed-valence barium iron fluorides (BaFeF series) using hydrothermal redox reactions, resulting in unique structural characteristics.
  • Each compound showcases different arrangements of FeF units: BaFeF features 1D infinite [FeFeF] double chains, BaFeF contains 1D [FeF] double chains, and BaFeF has a complex 3D framework with isolated FeF units.
  • Magnetic studies reveal that BaFeF undergoes an antiferromagnetic phase transition at ~11 K, while BaFeF exhibits canted antiferromagnetic ordering at ~32.5 K, indicating distinct magnetic properties influenced by their structural configurations.
View Article and Find Full Text PDF

The self-organization of strongly interacting electrons into superlattice structures underlies the properties of many quantum materials. How these electrons arrange within the superlattice dictates what symmetries are broken and what ground states are stabilized. Here we show that cryogenic scanning transmission electron microscopy (cryo-STEM) enables direct mapping of local symmetries and order at the intra-unit-cell level in the model charge-ordered system NdSrMnO.

View Article and Find Full Text PDF

Anharmonic Magnon Excitations in Noncollinear and Charge-Ordered RbFe^{2+}Fe^{3+}F_{6}.

Phys Rev Lett

August 2018

School of Physics and Astronomy and Centre for Science at Extreme Conditions, University of Edinburgh, Edinburgh EH9 3FD, United Kingdom.

RbFe^{2+}Fe^{3+}F_{6} is an example of a charge ordered antiferromagnet where iron sites, with differing valences, are structurally separated into two interpenetrating sublattices. The low temperature magnetically ordered Fe^{2+} (S=2) and Fe^{3+} (S=5/2) moments form a noncollinear orthogonal structure with the Fe^{3+} site displaying a reduced static ordered moment. Neutron spectroscopy on single crystals finds two distinct spin wave branches with a dominant coupling along the Fe^{3+} chain axis (b axis).

View Article and Find Full Text PDF