اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدPhoto-induced Antiferromagnetic-ferromagnetic Transition and Electronic Structure Modulation in GdBaCo$_2$O$_{5.5}$ Thin Film
72
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We investigate both the ferromagnetic (FM) and antiferromagnetic (AFM) ultrafast dynamics of a strongly correlated oxide system, GdBaCo$_2$O$_{5.5}$ thin film, by time-resolved x-ray magnetic circular dichroism in reflectivity (XMCDR) and resonant magnetic x-ray diffraction (RMXD). A photo-induced AFM-FM transition characterized by an increase of the transient XMCDR beyond the unpumped value and a decay of RMXD was observed. The photon-energy dependence of the transient XMCDR and reflectivity can likely be interpreted as a concomitant photo-induced spinstate transition.
قيم البحث
اقرأ أيضاً
The topological property of SrRu$_2$O$_6$ and isostructural CaOs$_2$O$_6$ under various strain conditions is investigated using density functional theory. Based on an analysis of parity eigenvalues, we anticipate that a three-dimensional strong topol
ogical insulating state should be realized when band inversion is induced at the A point in the hexagonal Brillouin zone. For SrRu$_2$O$_6$, such a transition requires rather unrealistic tuning, where only the $c$ axis is reduced while other structural parameters are unchanged. However, given the larger spin-orbit coupling and smaller lattice constants in CaOs$_2$O$_6$, the desired topological transition does occur under uniform compressive strain. Our study paves a way to realize a topological insulating state in a complex oxide, which has not been experimentally demonstrated so far.
The structural, magnetic and transport properties of the layered RBaCo$_2$O$_{5.5}$ cobaltites are sensitive to the oxygen stoichiometry. In this present study, we report the presence of a low-temperature magnetic glassy state in electron-doped polyc
rystalline YBaCo$_2$O$_{5.5}$ cobaltite. The ac magnetization studies show the absence of conventional spin glass features, while the various dc magnetization studies demonstrate the presence of non-equilibrium magnetic glassy state at low temperature. The magnetic glassy state of this sample results from the kinetic arrest of the first order ferro (or ferri) to antiferromagnetic transition. The role of electron doping in the occurrence of magnetic glassy phenomena is discussed in terms of magnetic phase separation involving the Co3+/Co2+ clusters of the ferrimagnetic phase in the Co3+/Co3+ antiferromagnetic matrix.
We investigate the spin rotational structure of magnetic skyrmions in a tetragonal polar magnet VOSe2O5 via polarized small-angle neutron scattering (SANS). Spin polarization analysis of the scattered neutrons provides consistent evidence for the cyc
loidal spin modulation in all the incommensurate phases at zero and non-zero magnetic field along the c axis, including the triangular skyrmion-lattice phase. In the vicinity of the skyrmion phase, we performed extensive SANS measurements to unravel a field-induced incommensurate phase (IC-2 state). We discuss the possibility of anisotropic double-q state as an alternative spin structure to provisional square skyrmion-lattice state.
We have employed first principles calculations to study the electronic structure and magnetic properties of the low-dimensional phosphates, Ba2Cu(PO4)2 and Sr2Cu(PO4)2. Using the self-consistent tight-binding lin- earized muffin-tin orbital method an
d the Nth order muffin-tin orbital method, we have calculated the various intrachain as well as the interchain hopping parameters between the magnetic ions Cu2+ for both the com- pounds. We find that the nearest-neighbor intrachain hopping t is the dominant interaction suggesting the compounds to be indeed one dimensional. Our analysis of the band dispersion, orbital projected band struc- tures, and the hopping parameters confirms that the Cu2+-Cu2+ super-super exchange interaction takes place along the crystallographic b direction mediated by O-P-O. We have also analyzed in detail the origin of short-range exchange interaction for these systems. Our ab initio estimate of the ratio of the exchange inter- action of Sr2Cu(PO4)2 to that of Ba2Cu(PO4)2 compares excellently with available experimental results.
The high temperature magnetic order in SrRu$_2$O$_6$ was studied by measuring magnetization and neutron powder diffraction with both polarized and unpolarized neutrons. SrRu$_2$O$_6$ crystallizes into the hexagonal lead antimonate (PbSb$_2$O$_6$, spa
ce group textit{P}$overline{3}$1textit{m}) structure with layers of edge-sharing RuO$_6$ octahedra separated by Sr$^{2+}$ ions. SrRu$_2$O$_6$ orders at $T_N$=565,K with Ru moments coupled antiferromagnetically both in-plane and out-of-plane. The magnetic moment is 1.30(2) $mu_mathrm{B}$/Ru at room temperature and is along the crystallographic textit{c}-axis in the G-type magnetic structure. We performed density functional calculations with constrained RPA to obtain the electronic structure and effective intra- and inter-orbital interaction parameters. The projected density of states show strong hybridization between Ru 4$d$ and O 2$p$. By downfolding to the target $t_{2g}$ bands we extracted the effective magnetic Hamiltonian. We performed Monte Carlo simulations to determine the transition temperature as a function of inter- and intra-plane couplings and find weak inter plane coupling, 3% of the intra-plane coupling, permits three dimensional magnetic order at $T_N$. As suggested by the magnetic susceptibility, two-dimensional correlations persist above $T_N$ due to the strong intra-plane coupling.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
