ترغب بنشر مسار تعليمي؟ اضغط هنا

BaV3O8: A possible Majumdar-Ghosh system with S=1/2

272   0   0.0 ( 0 )
 نشر من قبل Tanmoy Chakrabarty
 تاريخ النشر 2013
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

BaV3O8 contains both magnetic V4+(S=1/2) ions and non-magnetic V5+(S=0) ions. The V4+ ions are arranged in a coupled Majumdar-Ghosh chain like network. Our magnetic susceptibility chi(T) data fit well with the Curie-Weiss formula in the temperature range of 80-300K and it yields a Curie constant C=0.39cm3K/mole-V4+ and an antiferromagnetic Weiss temperature theta=-26K. The chi(T) curve shows a broad maximum at T~25K indicative of short-range order (SRO) and an anomaly corresponding to long-range order (LRO) at TN~6K. The value of the frustration index (f=mod[theta/TN]~5) suggests that the system is moderately frustrated. Above the LRO temperature the experimental magnetic susceptibility data match well with the coupled Majumdar-Ghosh chain model with the ratio of the nnn (next-nearest neighbor) to nn (nearest neighbor) magnetic coupling alpha=2 and Jnnn/kB=40K. In a mean-field approach when considering the inter-chain interactions, we obtain the total inter-chain coupling to be about 16K. The LRO anomaly at TN is also observe in the specific heat Cp(T) data and is not sensitive to an applied magnetic field up to 90kOe. A 51V NMR signal corresponding to the non-magnetic vanadium was observed. Anomalies at 6K were observed in the variation with temperature of the 51V NMR linewidth and in the spin-lattice relaxation rate 1/T1, indicating that they are sensitive to the LRO onset and fluctuations at the magnetic V sites. The existence of two components (one short and another long) is observed in the spin-spin relaxation rate 1/T2 data in the vicinity of TN. The shorter component seems to be intimately connected with the magnetically ordered state. We suggest that both magnetically ordered and non-long range ordered (non-LRO) regions coexist in this compound below the long range ordering temperature.



قيم البحث

اقرأ أيضاً

We present an analysis of the entanglement characteristics in the Majumdar-Ghosh (MG) or $J_{1}$-$J_{2}$ Heisenberg model. For a system consisting of up to 28 spins, there is a deviation from the scaling behaviour of the entanglement entropy characte rizing the unfrustrated Heisenberg chain as soon as $J_{2} >0.25$. This feature can be used as an indicator of the dimer phase transition that occurs at $J_{2} = J_{2}^{*} approx 0.2411 J_{1}$. Additionally, we also consider entanglement at the MG point $J_{2}=0.5 J_{1}$.
We consider the application of the recursion method to the calculation of one-particle Greens functions for strongly correlated systems and propose a new way how to extract the information about the infinite system from the exact diagonalisation of s mall clusters. Comparing the results for several cluster sizes allows us to establish those Lanczos coefficients that are not affected by the finite size effects and provide the information about the Greens function of the macroscopic system. The analysis of this bulk-related subset of coefficients supplemented by alternative analytic approaches allows to infer their asymptotic behaviour and to propose an approximate analytical form for the terminator of the Greens function continued fraction expansion for the infinite system. As a result, the Greens function acquires the branch cut singularity corresponding to the incoherent part of the spectrum. The method is applied to the spectral function of one-hole in the Majumdar-Ghosh model (the one-dimensional $ t-J-J^{prime}$ model at $J^{prime}/J=1/2$). For this model, the branch cut starts at finite energy $omega_0$, but there is no upper bound of the spectrum, corresponding to a linear increase of the recursion coefficients. Further characteristics of the spectral function are band gaps in the middle of the band and bound states below $omega_0$ or within the gaps. The band gaps arise due to the period doubling of the unit cell and show up as characteristic oscillations of the recursion coefficients on top of the linear increase.
We report the synthesis and characterization of Li2ZnV3O8, which is a new Zn-doped LiV2O4 system containing only tetravalent vanadium. A Curie-Weiss susceptibility with a Curie-Weiss temperature of <theta>CW ~214 K suggests the presence of strong ant iferromagnetic correlations in this system. We have observed a splitting between the zero-field cooled ZFC and field cooled FC susceptibility curves below 6 K. A peak is present in the ZFC curve around 3.5 K suggestive of spin-freezing . Similarly, a broad hump is also seen in the inferred magnetic heat capacity around 9 K. The consequent entropy change is only about 8% of the value expected for an ordered S = 1=2 system. This reduction indicates continued presence of large disorder in the system in spite of the large <theta>CW, which might result from strong geometric frustration in the system. We did not find any temperature T dependence in our 7Li nuclear magnetic resonance NMR shift down to 6 K (an abrupt change in the shift takes place below 6 K) though considerable T-dependence has been found in literature for LiV2O4- undoped or with other Zn/Ti contents. Consistent with the above observation, the 7Li nuclear spin-lattice relaxation rate 1/T1 is relatively small and nearly T-independent except a small increase close to the freezing temperature, once again, small compared to undoped or 10% Zn or 20% Ti-doped LiV2O4.
CuSiO_3, isotypic to the spin - Peierls compound CuGeO_3, was discovered recently as a metastable decomposition product of the silicate mineral dioptase, Cu_6Si_6O_{18}cdot6H_2O. We investigated the physical properties of CuSiO_3 using susceptibility , magnetization and specific heat measurements on powder samples. The magnetic susceptibility chi(T) is reproduced very well above T = 8 K by theoretical calculations for an S=1/2 antiferromagnetic Heisenberg linear chain without frustration (alpha = 0) and a nearest - neighbor exchange coupling constant of J/k_{B} = 21 K, much weaker than in CuGeO_3. Below 8 K the susceptibility exhibits a substantial drop. This feature is identified as a second - order phase transition at T_{0} = 7.9 K by specific heat measurements. The influence of magnetic fields on T_{0} is weak, and ac - magnetization measurements give strong evidence for a spin - flop - phase at mu_0H_{SF} ~ 3 T. The origin of the magnetic phase transition at T_{0} = 7.9 K is discussed in the context of long - range antiferromagnetic order (AF) versus spin - Peierls(SP)order. Susceptibility and specific heat results support the AF ordered ground state. Additional temperature dependent ^{63,65}Cu nuclear quadrupole resonance experiments have been carried out to probe the Cu^{2+} electronic state and the spin dynamics in CuSiO_3.
In this joint experimental and theoretical work magnetic properties of the Cu$^{2+}$ mineral szenicsite Cu$_3$(MoO$_4$)(OH)$_4$ are investigated. This compound features isolated triple chains in its crystal structure, where the central chain involves an edge-sharing geometry of the CuO$_4$ plaquettes, while the two side chains feature a corner-sharing zig-zag geometry. The magnetism of the side chains can be described in terms of antiferromagnetic dimers with a coupling larger than 200 K. The central chain was found to be a realization of the frustrated antiferromagnetic $J_1$-$J_2$ chain model with $J_1simeq 68$ K and a sizable second-neighbor coupling $J_2$. The central and side chains are nearly decoupled owing to interchain frustration. Therefore, the low-temperature behavior of szenicsite should be entirely determined by the physics of the central frustrated $J_1$-$J_2$ chain. Our heat-capacity measurements reveal an accumulation of entropy at low temperatures and suggest a proximity of the system to the Majumdar-Ghosh point of the antiferromagnetic $J_1$-$J_2$ spin chain, $J_2/J_1=0.5$.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا