اشترك بالحزمة الذهبية واحصل على وصول غير محدود شمرا أكاديميا
تسجيل مستخدم جديدNegative magnetization of Li2Ni2Mo3O12 having a spin system composed of distorted honeycomb lattices and linear chains
74
0
0.0
(
0
)
اسأل ChatGPT حول البحث
ﻻ يوجد ملخص باللغة العربية
We study themagnetism of a spin-1 substance Li2Ni2Mo3O12. The spin system consists of distorted honeycomb lattices and linear chains of Ni2+ spins. Li+ ions enter about 25% and 50% of the honeycomb and chain Ni sites, respectively, creating disorder in both spin subsystems. A magnetic phase transition occurs at Tc = 8.0 K in the zero magnetic field. In low magnetic fields, the magnetization increases rapidly below Tc, decreases below 7 K, and finally becomes negative at low temperatures. We determine the magnetic structure using neutron powder diffraction results. The honeycomb lattices and linear chains show antiferromagnetic and ferromagnetic long-range order, respectively. We investigate static and dynamic magnetic properties using the local probe technique of muon spin relaxation. We discuss the origin of the negative magnetization.
قيم البحث
اقرأ أيضاً
Keeping current interests to identify materials with intrinsic magnetodielectric behavior near room temperature and with novel pyroelectric current anomalies, we report temperature and magnetic-field dependent behavior of complex dielectric permittiv
ity and pyroelectric current for an oxide, Li2Ni2Mo3O12, containing magnetic ions with (distorted) honey-comb and chain arrangement and ordering magnetically below 8 K. The dielectric data reveal the existence of relaxor ferroelectricity behavior in the range 160-240 K and there are corresponding Raman mode anomalies as well in that temperature range. Pyrocurrent behavior is also consistent with this interpretation, with the pyrocurrent peak-temperature interestingly correlating with the poling temperature. 7Li NMR offer an evidence for crystallographic disorder intrinsic to this compound and we therefore conclude that such a disorder is apparently responsible for the randomness of local electric field leading to relaxor ferroelectric property. Another observation of emphasis is that there is a notable decrease in the dielectric constant with the application of magnetic field to the tune of about -2.4% at 300 K, with the magnitude varying mariginally with temperature. Small loss factor values validate intrinsic behavior of the magnetodielectric effect at room temperature.
The characterization and manipulation of deposited magnetic clusters or molecules on surfaces is a prerequisite for their future utilization. In recent years techniques like spin-flip inelastic electron tunneling spectroscopy using a scanning tunneli
ng microscope proved to be very precise in determining e.g. exchange constants in deposited finite spin chains in the meV range. In this article we tackle the problem numerically by investigating the transition from where a pure spin Hamiltonian is sufficient to the point where the interaction with the surface significantly alters the magnetic properties. To this end we study the static, i.e. equilibrium impurity magnetization of antiferromagnetic chains for varying couplings to a conduction electron band of a metal substrate. We show under which circumstances the screening of a part of the system enables one to deduce molecular parameters of the remainder from level crossings in an applied field.
We investigate the ground state magnetization plateaus appearing in spin 1/2 polymerized Heisenberg chains under external magnetic fields. The associated fractional quantization scenario and the exponents which characterize the opening of gapful exci
tations are analyzed by means of abelian bosonization methods. Our conclusions are fully supported by the extrapolated results obtained from Lanczos diagonalizations of finite systems.
We report on the magnetic, thermodynamic, dielectric, and pyroelectric measurements on the hitherto unreported Fe${_4}$Ta${_2}$O${_9}$. This system is seen to exhibit a series of magnetic transitions, many of which are coupled to the emergence of fer
roelectric order, making Fe${_4}$Ta${_2}$O${_9}$ the only genuine multiferroic in its material class. We suggest that the observed properties arise as a consequence of an effective reduction in the dimensionality of the magnetic lattice, with the magnetically active Fe${^{2+}}$ ions preferentially occupying a quasi 2D buckled honeycomb structure. The low temperature $H$-$T$ phase diagram of Fe${_4}$Ta${_2}$O${_9}$ reveals a rich variety of coupled magnetic and ferroelectric phases, in similarity with that observed in the distorted Kagome systems.
The classical Heisenberg model on the trillium and distorted windmill lattices exhibits a degenerate ground state within large-$N$ theory, where the degenerate wavevectors form a surface and line, in 3-dimensional space, respectively. We name such st
ates partially ordered to represent the existence of long-range order along the direction normal to these degenerate manifolds. We investigate the effects of thermal fluctuations using Monte Carlo (MC) methods, and find a first order transition to a magnetically ordered state for both cases. We further show that the ordering on the distorted windmill lattice is due to order by disorder, while the ground state of the trillium lattice is unique. Despite these different routes to the realization of low temperature ordered phases, the static structure factors obtained by large-$N$ theory and MC simulations for each lattice show quantitative agreement in the cooperative paramagnetic regime at finite temperatures. This suggests that a remnant of the characteristic angle-dependent spin correlations of partial order remains above the transition temperatures for both lattices. The possible relevance of these results to $beta$-Mn, CeIrSi, and MnSi is discussed.
سجل دخول لتتمكن من نشر تعليقات
التعليقات
جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
