scholarly journals Hidden magnetic order in plutonium dioxide nuclear fuel

2018 ◽  
Vol 20 (32) ◽  
pp. 20943-20951 ◽  
Author(s):  
James T. Pegg ◽  
Ashley E. Shields ◽  
Mark T. Storr ◽  
Andrew S. Wills ◽  
David O. Scanlon ◽  
...  

The magnetic structure of PuO2 has been investigated by computational methods. A hereto unknown longitudinal 3k AFM ground-state that retains Fm3̄m crystal symmetry has been identified.

2012 ◽  
Vol 86 (10) ◽  
Author(s):  
V. Hutanu ◽  
A. Sazonov ◽  
M. Meven ◽  
H. Murakawa ◽  
Y. Tokura ◽  
...  

2017 ◽  
Vol 56 (24) ◽  
pp. 14842-14849 ◽  
Author(s):  
Liurukara D. Sanjeewa ◽  
Vasile O. Garlea ◽  
Michael A. McGuire ◽  
Matthias Frontzek ◽  
Colin D. McMillen ◽  
...  

2000 ◽  
Vol 289-290 ◽  
pp. 32-37 ◽  
Author(s):  
Y Yamamoto ◽  
S Kawarazaki ◽  
Y Miyako ◽  
K Nishiyama ◽  
K Nagamine

2019 ◽  
Author(s):  
Ελένη Αζά

The discovery of materials with coexisting magnetic and ferroelectric orders, has revived theinterest of condensed matter physics and materials’ science communities maintaining the greatpromise of such fundamental mechanisms in devising applications ranging from portablemagnetoelectric (ME) sensors and memories to radar technologies. The present PhD thesis is a study in the field of strongly correlated systems where coupled properties arise from the interplay of charge and spin degrees of freedom over lattice topologies enabling competing magnetic interactions and therefore emergence of coupling of electric and magnetic order. Non-perovskite, two-dimensional (2D) Na-Mn-O oxides are revisited in scope of this in both polycrystalline and large single crystal forms. Among Na-deficient polymorphs, hexagonal α-Na0.7MnO2 (single crystals) has been investigated for the first time as a playground of competing interactions due to mixed Mnvalence (Mn4+ / Mn3+), fostered by Na vacancies in the structure. The competition of FM (Mn3+-Mn4+) and AFM (Mn3+ -Mn3+) interactions is believed to be the origin of the magnetic instability leading to a glassy ground state leaving also their footprint in the dielectric permittivity measurements. Competing FM and AFΜ interactions are also investigated as the origin of the anisotropic magnetic properties witnessed in a-NaxMnO2 (x= 0.96) single crystals. Neutron single crystal experiments show a well-established AFM long range order which vanishes above 26 K whilea coexistent canted antiferromagnetic state persists up to 45 K. In both alpha powders and aNa0.96MnO2 single crystals, the dielectric permittivity suggests the onset of the commensuratemagnetic long range order (T~ 45 K) which in the case of the powders allows a magnetocapacitance effect. Compositional modulations in β-NaMnO2, which are depicted as an intergrowth of α- and βlike oxygen coordinations, are found to trigger a proper-screw magnetic ground state which evolves into collinear commensurate AFM state. Features in the dielectric permittivity coincide with the onset of the commensurate AFM order giving away also the contribution of the α- structural domains. Further understanding of the mechanisms that dictate the relief of frustrated interactions and establishment of magnetic order together with the role of structural complexity in the form of domains or domain-walls is a direction that warrants further exploration as it will help us to resolve whether other coupled electron degrees of freedom are likely to be generated in this family of oxides.


2014 ◽  
Vol 89 (17) ◽  
Author(s):  
Oleg Rivin ◽  
Hagai Shaked ◽  
Arsen Gukasov ◽  
El'ad N. Caspi

COSMOS ◽  
2008 ◽  
Vol 04 (02) ◽  
pp. 131-140 ◽  
Author(s):  
AKIRA MIYAZAKI ◽  
TOSHIAKI ENOKI

The crystal structures and electronic and magnetic properties of conducting molecular magnets developed by our group are reviewed from the viewpoints of our two current strategies for increasing the efficiency of the π–d interaction. (EDTDM)2 FeBr 4 is composed of quasi-one-dimensional donor sheets sandwiched between magnetic anion sheets. The ground state of the donor layer changes from the insulator state to the metallic state by the application of pressure. When it is near to the insulator–metal phase boundary pressure, the magnetic order of the anion spins considerably affects the transport properties of the donor layer. The crystal structure of ( EDO – TTFBr 2)2 FeX 4 ( X = Cl , Br ) is characterized by strong intermolecular halogen–halogen contacts between the organic donor and FeX 4 anion molecules. The presence of the magnetic order of the Fe 3+ spins and relatively high magnetic order transition temperature proves the role of the halogen–halogen contacts as exchange interaction paths.


2012 ◽  
Vol 113 (6) ◽  
pp. 808-814 ◽  
Author(s):  
Manuel Doemer ◽  
Matteo Guglielmi ◽  
Prashanth Athri ◽  
Natalia S. Nagornova ◽  
Thomas R. Rizzo ◽  
...  

Science ◽  
2014 ◽  
Vol 345 (6197) ◽  
pp. 653-656 ◽  
Author(s):  
Mostafa Enayat ◽  
Zhixiang Sun ◽  
Udai Raj Singh ◽  
Ramakrishna Aluru ◽  
Stefan Schmaus ◽  
...  

Spin-polarized scanning tunneling microscopy (SP-STM) has been used extensively to study magnetic properties of nanostructures. Using SP-STM to visualize magnetic order in strongly correlated materials on an atomic scale is highly desirable, but challenging. We achieved this goal in iron tellurium (Fe1+yTe), the nonsuperconducting parent compound of the iron chalcogenides, by using a STM tip with a magnetic cluster at its apex. Our images of the magnetic structure reveal that the magnetic order in the monoclinic phase is a unidirectional stripe order; in the orthorhombic phase at higher excess iron concentration (y > 0.12), a transition to a phase with coexisting magnetic orders in both directions is observed. It may be possible to generalize the technique to other high-temperature superconductor families, such as the cuprates.


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