Deterministic reversal of single magnetic vortex circulation by an electric field

The ability to control magnetic vortex is critical for their potential applications in spintronic devices.Traditional methods including magnetic field,spin-polarized current etc.have been used to flip the core and/or reverse circulation of vortex.However,it is challenging for deterministic electric-field control of the single magnetic vortex textures with time-reversal broken symmetry and no planar magnetic anisotropy.Here it is reported that a deterministic reversal of single magnetic vortex circulation can be driven back and forth by a space-varying strain in multiferroic heterostructures,which is controlled by using a bi-axial pulsed electric field.Phase-field simulation reveals the mechanism of the emerging magnetoelastic energy with the space variation and visualizes the reversal pathway of the vortex.This deterministic electric-field control of the single magnetic vortex textures demonstrates a new approach to integrate the low-dimensional spin texture into the magnetoelectric thin film devices with low energy consumption.

Anisotropic NdFeB Magnet Fabricated by Single Stroke Hot Deformation

The general hot deformation process consists of two steps, hot pressing and die-upsetting in order to obtain the anisotropic NdFeB magnet. This is the first report that the high anisotropy NdFeB magnets can be fabricated by single stroke hot deforming the isotropic magnet. The magnetic properties of those materials are: coercivity iHc ～11 kOe, remanence Br ～12 kG, and the maximum energy product (BH)max ～28 MG.Oe.

Gate-Voltage-Induced Magnetization Reversal and Tunneling Anisotropic Magnetoresistance in a Single Molecular Magnet with Temperature Gradient

We study the coutrol of gate voltage over the magnetization of a single-molecule magnet （SMM） weakly coupled to a ferromagnetic and a normal metal electrode in the presence of the temperature gradient between two electrodes. It is demonstrated that the SMM＇s magnetization can change periodically with periodic gate voltage due to the driving oI the temperature gradient. Under an appropriate matching of the electrode polarization, the temperature difference and the pulse width of gate voltage, the SMM＇s magnetization can be completely reversed in a period of gate voltage. The corresponding flipping time can be controlled by the system parameters. In addition, we also investigate the tunneling anisotropic magnetoresistance （TAMFt） of the device in the steady state when the ferromagnetic electrode is noncollinear with the easy axis of the SMM, and show the jump characteristic of the TAMR.

Deterministic Generation of Quantum State Transfer Between Spatially Separated Single Molecule Magnets

We propose a new scheme for realizing deterministic quantum state transfer （QST） between two spatially separated single molecule magnets （SMMs） with the framework of cavity quantum eleetrodynamics （QED）. In the present scheme, two SMMs are trapped in two spatially separated optical cavities coupled by an optical fiber. Through strictly numerically simulating, we demonstrate that our scheme is robust with respect to the SMMs＇ spontaneous decay and fiber loss under the conditions of dispersive SMMs-field interaction and strong coupling of cavity fiber. In addition, we also discuss the influence of photon leakage out of cavities and show that our proposal is good enough to demonstrate the generation of QST with high fidelity utilizing the current experimental technology. The present investigation provides research opportunities for realizing QST between solid-state qubits and may result in a substantial impact on the progress of solid-state-based quantum communications network.

Phonon-Assisted Spin Current in Single Molecular Magnet Junctions

Owing to the bistable character of the single molecular magnet （SMM）, it can generate 100% spin-polarized currents even connected with normal （N） leads. In this work, we study the phonon-assisted spin current in N- SMM-N systems. We mainly focus on the interplay of SMM＇s bistable character and electron-phonon coupling. It is found that when SMM is trapped in one of the lowest bistable states, it can generate phonon-assisted spin- polarized currents. At the up-spin transport channel, it is accompanied by a phonon-assisted up-spin current, while at the down-spin transport channel, it is accompanied by a phonon-assisted down-spin current.

Magnetization Reversal Process of Single Crystal a-Fe Containing a Nonmagnetic Particle

The magnetization reversal process and hysteresis loops in a single crystal α-iron with nonmagnetic particles are simulated in this work based on the Landau-Lifshitz-Gilbert equation. The evolutions of the magnetic domain morphology are studied, and our analyses show that the magnetization reversal process is affected by the interaction between the moving domain wall and the existing nonmagnetic particles. This interaction strongly depends on the size of the particles, and it is found that particles with a particular size contribute the most to magnetic hardening.

31P Nuclear Magnetic Resonance of Charge-Density-Wave Transition in a Single Crystal of RuP

We perform 31p nuclear magnetic resonance （NMR） measurements on a single crystal of RuP. The anomalies in resistivity at about TA = 270 K and TB = 330 K indicate that two phase transitions occur. The line shape of alp NMR spectra in different temperature ranges is attributed to the charge density distribution. The Knight shift and spin-lattice relaxation rate 1/T1T are measured from 1OK to 30OK. At about TA = 270K, they both decrease abruptly with the temperature reduction, which reveals the gap-opening behavior. Well below TA, they act like the case of normal metal. Charge-density-wave phase transition is proposed to interpret the transition occurring at about TA.

Dephasing of quantum tunnelling in molecular nanomagnets

Dephasing mechanism of quantum tunnelling in molecular magnets has been studied by means of the spin-coherentstate path integral in a mean field approximation. It is found that the fluctuating uncompensated transverse field from the dipolar-dipolar interaction between molecular magnets contributes a random phase to the quantum interference phase. The resulting transition rate is determined by the average tunnel splitting over the random phase. Such a dephasing process leads to the suppression of quenching due to the quantum phase interference, and to the steps due to odd resonances in hysteresis loop survived, which is in good agreement with experimental observations in molecular nanomagnets Fes and Mn12.

Magnetoelastic instability in the XXZ rings with next-nearest neighbour coupling

This paper numerically investigates the magnetoelastic instability in the S = 1/2 {XXZ} rings containing finite spins N with antiferromagnetic nearest-neighbour （{NN}） and next-nearest neighbour （{NNN}） coupling. It finds that, as the {NN} anisotropy Δ1 equals the {NNN} anisotropy ／varDelta2, there exists a critical {NNN} coupling strength J2c（≈0.5）, at which the systems always locate in dimerized phase for arbitrary large spring constant. As Δ1 ／ne Δ2, the values of J2^{／rm c} are dependent on N and the difference of （Δ1-／varDelta2）.

Magnetoelastic Instability in Ring-Shaped Molecule Magnets with Next-Nearest Neighbor Coupling

In considering next-nearest neighbor （NNN） coupling, we numerically investigate the magnetoelastic instability in ring-shaped mesoscopic antiferromagnetic Heisenberg spin 1/2 systems with spin-phonon interaction. The results indicate that, for antiferromagnetic NNN coupling J2, there may be a critical value J2^c, at which the ground state is dimerized for arbitrary lattice spring constant and beyond and below which the magnetoelastic instability behavior is different from each other. The values of J2^c are irrelevant to the system size. For ferromagnetic NNN coupling, only continuous transition is present from dimerized phase to uniform phase as lattice spring constant is increased.

Spin Parity Effect on Magnetic Relaxation by Quantum Tunneling in Nanomagnets

Spin parity effect on magnetic relaxation by quantum tunneling in the biaxial spin model is studied by taking into account the transverse local stray field. It is shown that the square root time dependence in the even resonance occurs in the presence of a distribution of transverse anisotropic parameters, while the odd resonance always shows exponential relaxation. Magnetic relaxation under a sweeping field is also studied. The variation of the relaxation curve with the increasing distribution width of the local stray field for even resonance is qualitatively different from that of the odd resonance. The theoretical result on even resonance is in agreement with experimental results on Fe8 system, while the prediction for odd resonance awaits the experimental verification.

Resonant tunnelling of the magnetization in molecular crystal of [（Mn1-xCrx）12O12 （CH3COO）16（H2O）4]·2CH3COOH·4H2O（x=0,0.03,0.04,0.05）

The quantum tunnelling of magnetization （QTM） in single crystals of the single molecule magnet （Mn1-xCrx）12- Ac （x=0, 0.03, 0.04, 0.05） has been investigated. In comparison with its parent Mnl2-Ac, a greater rate of magnetization relaxation and a lower effective potential-energy barrier have been observed in Cr-doping samples. This modulation of QTM due to the Cr-doping could be attributed to the small change of Sz due to the smaller spin of Cr itself and additional intrinsic but distributed transverse and longitudinal anisotropy raised by a subtle change of the local environment in the magnetic Mn12 core.

Magnetic anisotropy in 5d transition metal-porphyrin molecules

Single molecule magnets(SMMs) with large magnetic anisotropy energy(MAE) have great potential applications in magnetic recording.Using the first-principles calculations,we investigate the MAE of 5 d transition metal-porphyrin-based SMMs by using the PBE and PBE+U with different U values,respectively.The results indicate that W-P,Re-P,Os-P,and Ir-P possess the considerably large MAE among 5 d TM-P SMMs.Furthermore,the MAE of 5 d TM-P can be facilely manipulated by tensile strain.The reduction of the absolute value of MAE for Ir-P molecule caused by tensile strain makes it easier to implement the writing operation.The decreasing of the occupation number of minority-spin channels of Ir-d_(x^(2)-y^(2)) orbital leads the MAE to decrease when the tensile strain increases.

Anisotropic magnetocaloric effect in a dysprosium(Ⅲ) single-molecule magnet——Commemorating the 100th anniversary of the birth of Academician Guangxian Xu

Dysprosium compounds with high magnetic anisotropy are widely studied as single molecule magnets(SMMs).Here the anisotropic magnetocaloric effect in a Dy(Ⅲ)SMM,{[Dy(OSiMe_(3))_(2)(4-Mepy)5(BPh_(4))]0.5 Toluene},was studied by single crystals.Angular dependent magnetization can be observed at 300 K because of its high magnetic anisotropy.SMM behavior measured along the easy axis direction is identical to that of the polycrystalline sample.Rotating magnetization from the easy axis to the hard plane gives a maximum magnetic entropy change(-ΔSR)of 3.05 J/(kg·K)at 19 K atΔB=5 T,which enables the Dy(Ⅲ)SMM to be used as a low-temperature rotating magnetic refrigerant.

Calixarene-supported hexadysprosium cluster showing single molecule magnet behavior

The syntheses, crystal structures, magnetic and luminescent properties of three isornorphous compounds [LnIII6（,u4-O）2（C4A）2- （NO3）2（HCOO）2（CH30）2（DMF）4（CH3OH）4] （Ln = Gd （1）, Tb （2） and Dy （3）; H4C4A = p-tert-butylcalix[4]arene） are reported. These three compounds are featured with the sandwich-like units constructed by two tail-to-tail calixarene molecules and an in-between Lnm6 octahedron. The DyTM compound exhibits both single molecule magnet behavior and photoluminescence.

Single molecule magnetic behavior and photo-enhanced proton conductivity in a series of photochromic complexes

Molecules with multifunctional properties are of immense interest in hybrid materials, while challenges still existed because of the limited compatibility of multiple functionalities in a single system. In this work, a series of metal-organic complexes were synthesized and characterized under the assembly of electron donor phosphonate, electron acceptor polypyridine ligand and spin carrier rare earth ions. All the compounds exhibited remarkable and reversible responses with photochromism and photomodulated fluorescence, originated from photogenerated radicals via electron transfer from phosphonates to polypyridine ligands. For the Dy analog, slow magnetic relaxation was observed at cryogenic temperature, indicating the single-molecule magnetic behavior. Furthermore, photogenerated radicals could enhance the proton conductive behavior, with about 2 times larger in magnitude after light irradiation for Dy and Y compounds. The introduction of photoluminescence, magnetism and proton conduction into metallic phosphonates can provide potential applications for photochromic materials.

Cyanide-bridged single molecule magnet based on a manganese(Ⅲ) complex with TTF-fused Schiff base ligand

Reaction of [Mn（TTF-salphen）][OAc] （TTF-salphen2=2,2＇-（（2-（4,5-bis（methylthio）-1,3-dithiol-2-ylidene）-1,3-benzodithiole- 5,6-diyl）bis（nitrilomethylidyne）bis（pbenolate）dianion） and the cyanometalate building blocks [n-Bu4N][（Tp）Fe（CN）3] （Tp =Tris（pyrazolyl）hydroborate） or [n-Bu4N][Ru（salen）（CN）2] （salen2 =N,N＇-ethylenebis（salicylideneimine）dianion） resulted in the formation of two redox-active complexes, the dinuclear heterometallic complex [（Tp）Fe（CN）3Mn（TTF-salphen）＇CH3OH] （1） and the one dimensional complex [Ru（salen）（CN）2Mn（TTF-salphen）]n （2）. Both complexes were characterized by X-ray crystallography and solid state electrochemistry, in addition to static and dynamic magnetic measurements. Antiferromagnetic couplings are found to be operative between metal ion centers bridged by cyanide in both complexes. Complex 1 exhibited field-induced SMM behavior with an energy barrier of 13.8 K. The introduction of the redox-active TTF unit into cyanidebridged complexes with interesting magnetic properties renders them promising candidates for the construction of new hybrid inorganic-organic materials.

Multi-step shot noise spectrum induced by a local large spin

We use non-equilibrium Green＇s function method to analyze the shot noise spectrum of artificial single molecular magnets（ASMM） model in the strong spin–orbit coupling limit in sequential tunneling regime, mainly focusing on the effects of local large spin. In the linear response regime, the shot noise shows 2S ＋ 1 peaks and is strongly spin-dependent.In the nonlinear response regime, one can observe 2S ＋ 1 steps in shot noise and Fano factor. In these steps one can see the significant enhancement effect due to the spin-dependent multi-channel process of local large spin, which reduces electron correlations.

Boosting the proton conduction in a magnetic dysprosium-organic framework by introducing conjugate NH_(4)^(+)-NH_(3)pairs

Metal-organic frameworks(MOFs)with inherent porosity and suspended acidic groups are promising proton conducting materials in water or aqua-ammonia media.Herein we report a new lanthanide phosphonate,namely,Dy_(2)(amp_(2)H_(2))_(2)(mal)(H_(2)O)_(2)·5H2O(MDAF-6).It possesses a 3D open-framework structure,and shows a high NH_(3)adsorption capacity of 142.4 cm^(3)/g at P/P0=0.98 at 298 K due to acid-base interaction.Interestingly,the proton conductivity of MDAF-6-NH3 is enhanced by five orders of magnitude compared to MDAF-6 after 8.5 h exposure in saturated NH_(3)-H_(2)O vapor,indicating the importance of coexistent conjugate acid-base pairs of H_(3)O+-H_(2)O and NH_(4)^(+)-NH_(3)in promoting proton conduction.Magnetic studies of MDAF-6 revealed slow magnetization relaxation under zero dc field,characteristic of singlemolecule magnet behavior.This work provides not only a new multifunctional MOF material,but also a new strategy to improve proton conduction in aqua-ammonia medium.

Thermo-induced structural transformation with synergistic optical and magnetic changes in ytterbium and erbium complexes

Dinuclear ytterbium and erbium based bifunction complexes Ln_(2) L_(2)(depma_(2))Cl_(2)(1-Ln,Ln=Yb and Er,H_(2) L=N~1,N~3-bis(salicylideneimino)diethylenetriamine,depma_(2)=dimerized 9-diethyl-phosphonomethylanthracene)are reported.They undergo thermo-induced consecutive phase transitions,first the dissociation of depma_(2) ligand forming LnL(depma)Cl(2-Ln)and then the release of chloroethane forming LnL(epma)(3-Ln,epma=9-ethylphosphonomethylanthrancene).The structural transformations are accompanied with synergetic switch of the luminescence in visible and NIR regions and also magnetic dynamics.