spin dynamic
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2021 ◽  
Vol 127 (9) ◽  
Author(s):  
Giuseppe Bevilacqua ◽  
Valerio Biancalana ◽  
Yordanka Dancheva ◽  
Alessandro Fregosi ◽  
Antonio Vigilante

AbstractThe dynamic response of a parametric system constituted by a spin precessing in a time dependent magnetic field is studied by means of a perturbative approach that unveils unexpected features, and is then experimentally validated. The first-order analysis puts in evidence different regimes: beside a tailorable low-pass-filter behaviour, a band-pass response with interesting potential applications emerges. Extending the analysis to the second perturbation order permits to study the response to generically oriented fields and to characterize several non-linear features in the behaviour of such kind of systems.



2021 ◽  
Vol 10 (5) ◽  
Author(s):  
Luhang Yang ◽  
Adrian Feiguin

We study the nature of the excitations of an antiferromagnetic (AFM) Heisenberg chain with staggered long range interactions using the time-dependent density matrix renormalization group method and by means of a multi-spinon approximation. The chain undergoes true symmetry breaking and develops long range order, transitioning from a gapless spin liquid to a gapless ordered AFM phase. The spin dynamic structure factor shows that the emergence of Néel order can be associated to the formation of bound states of spinons that become coherent magnons. The quasiparticle band leaks out from the two-spinon continuum that is pushed up to higher energies. Our physical picture is also supported by an analysis of the behavior of the excitations in real-time.



2020 ◽  
Vol 49 (25) ◽  
pp. 8672-8683 ◽  
Author(s):  
Prashant Kumar ◽  
H. Khanduri ◽  
Saurabh Pathak ◽  
Arjun Singh ◽  
G. A. Basheed ◽  
...  

Temperature plays a vital role in the hydrothermal synthesis of the nanoparticles. Herein, we have provided a very detailed spin dynamic investigation on the varying size Fe3O4 nanoparticles using FMR technique.



2020 ◽  
pp. 1-1
Author(s):  
Fengxian Wang ◽  
Wei Shen ◽  
Mingming Tian ◽  
Qian Chen ◽  
Zhaocong Huang ◽  
...  
Keyword(s):  




2019 ◽  
Vol 9 (4) ◽  
pp. 630 ◽  
Author(s):  
Soyoung Jekal ◽  
Andreas Danilo ◽  
Dao Phuong ◽  
Xiao Zheng

In atomic GdFe 2 films capped by 4d and 5d transition metals, we show that skyrmions with diameters smaller than 12 nm can emerge. The Dzyaloshinskii–Moriya interaction (DMI), exchange energy, and the magnetocrystalline anisotropy (MCA) energy were investigated based on density functional theory. Since DMI and MCA are caused by spin–orbit coupling (SOC), they are increased with 5d capping layers which exhibit strong SOC strength. We discover a skyrmion phase by using atomistic spin dynamic simulations at small magnetic fields of ∼1 T. In addition, a ground state that a spin spiral phase is remained even at zero magnetic field for both films with 4d and 5d capping layers.



Author(s):  
Soyoung Jekal ◽  
Andreas Danilo ◽  
Dao Phoung ◽  
Xiao Zheng

In atomic GdFe$_2$ films capped by 4$d$ and 5$d$ transition metals, we show that skyrmions with diameters smaller than 12 nm can emerge. The Dzyaloshinskii--Moriya interaction (DMI), exchange energy, and the magnetocrystalline anisotropy (MCA) energy were investigated based on density functional theory. Since DMI and MCA are caused by spin--orbit coupling (SOC), they are increased with 5$d$ capping layers which exhibit strong SOC strength. We discover a skyrmion phase by using atomistic spin dynamic simulations at small magnetic fields of $\sim$1 T. In addition, a ground state that a spin spiral phase is remained even at zero magnetic field for both films with 4$d$ and 5$d$ capping layers.



SPIN ◽  
2018 ◽  
Vol 08 (03) ◽  
pp. 1850014 ◽  
Author(s):  
Zuwei Fu ◽  
Zongzhi Zhang ◽  
Yaowen Liu

Laser-induced magnetization switching in GdFe ferrimagnets strongly depends on the pulse duration. To gain insight into the ferrimagnetic switching process, Landau–Lifshitz–Gilbert (LLG) spin dynamic modeling is performed at an atomistic-level with two sub-lattice systems. The switching dynamics triggered by laser pulses can be considered as two stages: Demagnetization stage by the laser pulse heating and re-magnetization at the cooling down stage after the pulse impulsion. By tuning the laser pulse duration, the intensity of demagnetization can be well controlled, by which the subsequent magnetization switching during the cooling process can be obtained. The simulation results indicate that the occurrence of the transient ferromagnetic-like (TFL) state is necessary during the magnetization switching process. Furthermore, the thermal temperature and heating time play an important role for the ferrimagnetic switching. In the overheating region, the random switching behavior appears because the TFL state is uncontrollable.



SPIN ◽  
2017 ◽  
Vol 07 (01) ◽  
pp. 1740003
Author(s):  
Y. Ren ◽  
Z. Z. Zhang ◽  
T. Min ◽  
Q. Y. Jin

The ultrafast demagnetization processes (UDP) in Ta ([Formula: see text] nm)/TbFeCo (20 nm) films have been studied using the time-resolved magneto-optical Kerr effect (TRMOKE). With a fixed pump fluence of 2 mJ/cm2, for the sample without a Ta underlayer ([Formula: see text][Formula: see text]nm), we observed the UDP showing a two-step decay behavior, with a relatively longer decay time ([Formula: see text] around 3.0 ps in the second step due to the equilibrium of spin-lattice relaxation following the 4[Formula: see text] occupation. As a 10[Formula: see text]nm Ta layer is deposited, the two-step demagnetization still exists while [Formula: see text] decreases to [Formula: see text]1.9[Formula: see text]ps. Nevertheless, the second-step decay ([Formula: see text]) disappears as the Ta layer thickness is increased up to 20 nm, only the first-step UDP occurs within 500 fs, followed by a fast recovery process. The rapid magnetization recovery rate strongly depends on the pump fluence. We infer that the Ta layer provides conduction electrons involving the thermal equilibrium of spin-lattice interaction and serves as heat bath taking away energy from spins of TbFeCo alloy film in UDP.



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