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Ferrimagnetism

About: Ferrimagnetism is a research topic. Over the lifetime, 7609 publications have been published within this topic receiving 151259 citations.


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Journal ArticleDOI
TL;DR: In this paper, a tutorial of typical magnetic behavior of molecular materials is presented and three distinct models (intramolecular spin coupling through orthogonal orbitals in the same spatial region within a molecule/ion, intermolecular spins coupling through pairwise configuration interaction between spin-containing moieties, and dipole-dipole, through-space interactions) which enable the design of new molecular-based magnetic materials are discussed.
Abstract: Magnets composed of molecular species or polymers and prepared by relatively low-temperature organic synthetic methodologies are a focus of contemporary materials science research. The anticipated properties of such molecular-species-based magnetic materials, particularly in combination with other properties associated with molecules and polymers, may enable their use in future generations of electronic, magnetic, and/or photonic/photronic devices ranging from information storage and magnetic imaging to static and low-frequency magnetic shielding. A tutorial of typical magnetic behavior of molecular materials is presented. The three distinct models (intramolecular spin coupling through orthogonal orbitals in the same spatial region within a molecule/ion, intermolecular spin coupling through pairwise “configuration interaction” between spin-containing moieties, and dipole—dipole, through-space interactions) which enable the design of new molecular-based magnetic materials are discussed. To achieve the required spin couplings for bulk ferro- or ferrimagnetic behavior it is crucial to prepare materials with the necessary primary, secondary, and tertiary structures akin to proteins. Selected results from the worldwide effort aimed at preparing molecular-based magnetic materials by these mechanisms are described. Some organometallic solids comprised of linear chains of alternating metallocenium donors (D) and cyanocarbon acceptors (A) that is, …D•+ A•− D•+ A•−…, exhibit cooperative magnetic phenomena. Bulk ferromagnetic behavior was first observed below the critical (Curie) temperature Tc of 4.8 K for [FeIII(C5Me5)2]•+ [TCNE]•− (Me = methyl; TCNE = tetracyanoethylene). Replacement of FeIII with MnIII leads to a ferromagnet with a Tc of 8.8 K in agreement with mean-field models developed for this class of materials. Replacement with CrIII, however, leads to a ferromagnet with a Tc lowered to 3.65 K which is at variance with this model. Extension to the reaction of a vanadium(o) complex with TCNE leads to the isolation of a magnet with a Tc ≈ 400 K, which exceeds the thermal decomposition temperature of the material. This demonstrates that a magnetic material with a Tc substantially above room temperature is achievable in a molecule/organic/polymeric material. Finally, a new class of one-dimensional ferrimagnetic materials based on metalloporphins is discussed.

1,184 citations

Journal ArticleDOI
14 Apr 2011-Nature
TL;DR: It is found that the ultrafast spin reversal in GdFeCo, where spins are coupled antiferromagnetically, occurs by way of a transient ferromagnetic-like state, which provides a concept for the possibility of manipulating magnetic order on the timescale of the exchange interaction.
Abstract: The dynamics of spin ordering in magnetic materials is of interest for both fundamental understanding and progress in information-processing and recording technology. Radu et al. study spin dynamics in a ferrimagnetic gadolinium–iron–cobalt (GdFeCo) alloy that is optically excited at a timescale shorter than the characteristic magnetic exchange interaction between the Gd and Fe spins. Using element-specific X-ray magnetic circular dichroism spectroscopy, they show that the Gd and Fe spins switch directions at very different timescales. As a consequence, an unexpected transient ferromagnetic state emerges. These surprising observations, supported by simulations, provide a possible new concept of manipulating magnetic order on a timescale of the exchange interaction. Ferromagnetic or antiferromagnetic spin ordering is governed by the exchange interaction, the strongest force in magnetism1,2,3,4. Understanding spin dynamics in magnetic materials is an issue of crucial importance for progress in information processing and recording technology. Usually the dynamics are studied by observing the collective response of exchange-coupled spins, that is, spin resonances, after an external perturbation by a pulse of magnetic field, current or light. The periods of the corresponding resonances range from one nanosecond for ferromagnets down to one picosecond for antiferromagnets. However, virtually nothing is known about the behaviour of spins in a magnetic material after being excited on a timescale faster than that corresponding to the exchange interaction (10–100 fs), that is, in a non-adiabatic way. Here we use the element-specific technique X-ray magnetic circular dichroism to study spin reversal in GdFeCo that is optically excited on a timescale pertinent to the characteristic time of the exchange interaction between Gd and Fe spins. We unexpectedly find that the ultrafast spin reversal in this material, where spins are coupled antiferromagnetically, occurs by way of a transient ferromagnetic-like state. Following the optical excitation, the net magnetizations of the Gd and Fe sublattices rapidly collapse, switch their direction and rebuild their net magnetic moments at substantially different timescales; the net magnetic moment of the Gd sublattice is found to reverse within 1.5 picoseconds, which is substantially slower than the Fe reversal time of 300 femtoseconds. Consequently, a transient state characterized by a temporary parallel alignment of the net Gd and Fe moments emerges, despite their ground-state antiferromagnetic coupling. These surprising observations, supported by atomistic simulations, provide a concept for the possibility of manipulating magnetic order on the timescale of the exchange interaction.

827 citations

Journal ArticleDOI
07 Jun 1991-Science
TL;DR: Threedimensional antiferromagnetic exchange of the donor and acceptor spins resulting in ferrimagnetic behavior appears to be the mode of magnetic coupling.
Abstract: The reaction of bis(benzene)vanadium with tetracyanoethylene, TCNE, affords an insoluble amorphous black solid that exhibits field-dependent magnetization and hysteresis at room temperature. The critical temperature could not be estimated as it exceeds 350 kelvin, the thermal decomposition temperature of the sample. The empirical composition of the reported material is V(TCNE)x.Y(CH(2)Cl(2)) with x approximately 2 and Y approximately 1/2. On the basis of the available magnetic and infrared data, threedimensional antiferromagnetic exchange of the donor and acceptor spins resulting in ferrimagnetic behavior appears to be the mode of magnetic coupling.

802 citations

Journal ArticleDOI
03 Dec 1993-Science
TL;DR: A simple orbital model was used to predict the electronic structure of the metal ions required to achieve a high ordering temperature, and the synthesis and magnetic properties of two compounds, [Cr5(CN)12].10H2O and Cs0.75 [Cr2.125( CN)6]�5H2 O, are reported, together with the strategy for further work.
Abstract: Molecular-based magnets with high magnetic-ordering temperatures, T(c), can be obtained by mild chemistry methods by focusing on the bimetallic and mixed-valence transition metal micro-cyanide of the Prussian blue family. A simple orbital model was used to predict the electronic structure of the metal ions required to achieve a high ordering temperature. The synthesis and magnetic properties of two compounds, [Cr(5)(CN)(12)].10H(2)O and Cs(0.75) [Cr(2.125)(CN)(6)].5H(2)O, which exhibited magnetic-ordering temperatures of 240 and 190 kelvin, respectively, are reported, together with the strategy for further work.

753 citations

Journal ArticleDOI
TL;DR: The results show the possibility of inducing a macroscopic ferrimagnetic state in multilayered graphene just by randomly removing single C atoms.
Abstract: Atomic vacancies have a strong impact in the mechanical, electronic, and magnetic properties of graphenelike materials. By artificially generating isolated vacancies on a graphite surface and measuring their local density of states on the atomic scale, we have shown how single vacancies modify the electronic properties of this graphenelike system. Our scanning tunneling microscopy experiments, complemented by tight-binding calculations, reveal the presence of a sharp electronic resonance at the Fermi energy around each single graphite vacancy, which can be associated with the formation of local magnetic moments and implies a dramatic reduction of the charge carriers' mobility. While vacancies in single layer graphene lead to magnetic couplings of arbitrary sign, our results show the possibility of inducing a macroscopic ferrimagnetic state in multilayered graphene just by randomly removing single C atoms.

727 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023372
2022766
2021359
2020358
2019369
2018353