scholarly journals Some aspects of the theory of magnets with competing double exchange and superexchange interactions

1998 ◽  
Vol 58 (13) ◽  
pp. 8617-8626 ◽  
Author(s):  
D. I. Golosov ◽  
M. R. Norman ◽  
K. Levin
Keyword(s):  
Double Exchange ◽  
Exchange And Superexchange Interactions

On the strength of the double exchange and superexchange interactions in La0.67Ca0.33Mn1-yFeyO3 - an NMR and Mössbauer study

2006 ◽  
Vol 243 (1) ◽  
pp. 259-262 ◽  
Author(s):  
J. Przewoźnik ◽  
Cz. Kapusta ◽  
J. Żukrowski ◽  
K. Krop ◽  
M. Sikora ◽  
...  
Keyword(s):  
Double Exchange ◽  
Mössbauer Study ◽  
Exchange And Superexchange Interactions

Heisenberg and double exchange in iron mixed valence [Fe6S6]+ supercluster

1997 ◽  
Vol 90 (3) ◽  
pp. 445-463 ◽  
Author(s):  
M. CZERWINSKI ◽  
J. DĄBROWSKI
Keyword(s):  
Mixed Valence ◽  
Double Exchange

Double exchange model and the unique properties of the manganites

2001 ◽  
Vol 171 (2) ◽  
pp. 121 ◽  
Author(s):  
Yurii A. Izyumov ◽  
Yu.N. Skryabin
Keyword(s):  
Double Exchange ◽  
Exchange Model

Magnetic Ordering via Itinerant Ferromagnetism in a Metal-Organic Framework

2020 ◽  
Author(s):  
Jesse Park ◽  
Brianna Collins ◽  
Lucy Darago ◽  
Tomce Runcevski ◽  
Michael Aubrey ◽  
...  
Keyword(s):  
Charge Transport ◽  
Magnetic Order ◽  
Metal Organic Framework ◽  
Metal Organic Frameworks ◽  
Magnetic Ordering ◽  
Double Exchange ◽  
Itinerant Ferromagnetism ◽  
Organic Solids ◽  
Metal Organic ◽  
Organic Framework

<b>Materials that combine magnetic order with other desirable physical attributes offer to revolutionize our energy landscape. Indeed, such materials could find transformative applications in spintronics, quantum sensing, low-density magnets, and gas separations. As a result, efforts to design multifunctional magnetic materials have recently moved beyond traditional solid-state materials to metal–organic solids. Among these, metal–organic frameworks in particular bear structures that offer intrinsic porosity, vast chemical and structural programmability, and tunability of electronic properties. Nevertheless, magnetic order within metal–organic frameworks has generally been limited to low temperatures, owing largely to challenges in creating strong magnetic exchange in extended metal–organic solids. Here, we employ the phenomenon of itinerant ferromagnetism to realize magnetic ordering at <i>T</i><sub>C</sub> = 225 K in a mixed-valence chromium(II/III) triazolate compound, representing the highest ferromagnetic ordering temperature yet observed in a metal–organic framework. The itinerant ferromagnetism is shown to proceed via a double-exchange mechanism, the first such observation in any metal–organic material. Critically, this mechanism results in variable-temperature conductivity with barrierless charge transport below <i>T</i><sub>C</sub> and a large negative magnetoresistance of 23% at 5 K. These observations suggest applications for double-exchange-based coordination solids in the emergent fields of magnetoelectrics and spintronics. Taken together, the insights gleaned from these results are expected to provide a blueprint for the design and synthesis of porous materials with synergistic high-temperature magnetic and charge transport properties. </b>

A Combined Spin-Flip and IP/EA Approach for Handling Spin and Spatial Degeneracies: Application to Double Exchange Systems

2018 ◽  
Author(s):  
Shannon Houck ◽  
Nicholas Mayhall
Keyword(s):  
Single Molecule ◽  
Double Exchange ◽  
Computational Effort ◽  
Strongly Correlated ◽  
Single Molecule Magnets ◽  
New Approach ◽  
Spin Flip ◽  
Model Hamiltonian ◽  
Simultaneous Existence ◽  
Exchange Parameters

<div>Many multiconfigurational systems, such as single-molecule magnets, are difficult to study using traditional computational methods due to the simultaneous existence of both spin and spatial degeneracies. In this work, a new approach termed n-spin-flip Ionization Potential/Electron Affinity (<i>n</i>SF-IP or <i>n</i>SF-EA) is introduced which combines the spin-flip method of Anna Krylov with particle-number changing IP/EA methods. We demonstrate the efficacy of the approach by applying it to the strongly-correlated N<sub>2</sub><sup>+</sup> as well as several double exchange systems. We also demonstrate that when these systems are well-described by a double exchange model Hamiltonian, only 1SF-IP/EA is required to extract the double exchange parameters and accurately predict energies for the low-spin states. This significantly reduces the computational effort for studying such systems. The effects of including additional excitations (using a RAS-<i>n</i>SF-IP/EA scheme) are also examined, with particular emphasis on hole and particle excitations.</div>

A Combined Spin-Flip and IP/EA Approach for Handling Spin and Spatial Degeneracies: Application to Double Exchange Systems

2018 ◽  
Author(s):  
Shannon Houck ◽  
Nicholas Mayhall
Keyword(s):  
Single Molecule ◽  
Double Exchange ◽  
Computational Effort ◽  
Strongly Correlated ◽  
Single Molecule Magnets ◽  
New Approach ◽  
Spin Flip ◽  
Model Hamiltonian ◽  
Simultaneous Existence ◽  
Exchange Parameters

<div>Many multiconfigurational systems, such as single-molecule magnets, are difficult to study using traditional computational methods due to the simultaneous existence of both spin and spatial degeneracies. In this work, a new approach termed n-spin-flip Ionization Potential/Electron Affinity (<i>n</i>SF-IP or <i>n</i>SF-EA) is introduced which combines the spin-flip method of Anna Krylov with particle-number changing IP/EA methods. We demonstrate the efficacy of the approach by applying it to the strongly-correlated N<sub>2</sub><sup>+</sup> as well as several double exchange systems. We also demonstrate that when these systems are well-described by a double exchange model Hamiltonian, only 1SF-IP/EA is required to extract the double exchange parameters and accurately predict energies for the low-spin states. This significantly reduces the computational effort for studying such systems. The effects of including additional excitations (using a RAS-<i>n</i>SF-IP/EA scheme) are also examined, with particular emphasis on hole and particle excitations.</div>

Effect of Sr Doping on Structure and Emittance of La1-xSrxMnO3 Smart Thermal Control Films

2014 ◽  
Vol 602-603 ◽  
pp. 902-905
Author(s):  
Yong Jun Shen ◽  
Chuan Bin Wang ◽  
Ling Li ◽  
Qiang Shen ◽  
Lian Meng Zhang
Keyword(s):  
Thin Film ◽  
Smooth Surface ◽  
Pulsed Laser ◽  
Double Exchange ◽  
Thermal Control ◽  
Laser Deposition ◽  
Lanthanum Manganite ◽  
Infrared Emissivity ◽  
Control Material ◽  
Double Exchange Interaction

Sr-doped lanthanum manganite (La1-xSrxMnO3) is characteristic of thermochromic, which can act as a smart thermal control material used in the variable-emittance devices. In the present study, La1-xSrxMnO3 thin films were prepared on MgO(100) substrates by pulsed laser deposition, and the effect of Sr-doping (x = 0 ~ 0.4) on the structure and infrared emissivity was investigated. Single-phased La1-xSrxMnO3 films with (100)-orientation were obtained, which showed a dense texture with smooth surface. The ratio of Mn4+/Mn3+ in the films was increased with increasing Sr doping, leading to the enhancement in double-exchange interaction and electrical conductivity. As a result, the phase transition from metal to insulator was observed with the increasing of test temperature. For the La0.8Sr0.2MnO3 thin film, a large value of emittance (De = 0.28) was obtained, indicating good variable-emittance by appropriate Sr doping.

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