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Register a new userComment on Microscopic magnetic modeling for the S = 1/2 alternating chain compounds Na3Cu2SbO6 and Na2Cu2TeO6 (arXiv:1402.1091)
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In a recent paper by Schmitt et al. (arXiv:1402.1091), signs of two exchange interactions of one-dimensional alternating chains in distorted honeycomb systems of Na3Cu2SbO6 and Na2Cu2TeO6 are argued by theoretical calculations. Although the authors report that they have clarified that the interaction J1a is ferromagnetic between the spins within a structural dimer, and J1b is antiferromagnetic between these dimers, these results have been known for a long time by our two papers, which are cited by Schmitt et al.
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We have measured the specific heat of an S=1/2 antiferromagnetic alternating Heisenberg chain pentafulorophenyl nitronyl nitroxide under magnetic fields up to H>H_C2. This compound has the field-induced magnetic ordered (FIMO) phase between H_C1 and H_C2. Characteristic behaviors are observed depending on the magnetic field up to above H_C2 outside of the H-T boundary for the FIMO. Temperature and field dependence of the specific heat are qualitatively in good agreement with the theoretical calculation on an S=1/2 two-leg ladder. [Wang et al. Phys. Rev. Lett 84 5399 (2000)] This agreement suggests that the observed behaviors are related with the low-energy excitation in the Tomonaga-Luttinger liquid.
We successfully synthesized the zinc-verdazyl complex [Zn(hfac)$_2$]$cdot$($o$-Py-V) [hfac = 1,1,1,5,5,5-hexafluoroacetylacetonate; $o$-Py-V = 3-(2-pyridyl)-1,5-diphenylverdazyl], which is an ideal model compound with an $S$ = 1/2 ferromagnetic-antiferromagnetic alternating Heisenberg chain (F-AF AHC). $Ab$ $initio$ molecular orbital (MO) calculations indicate that two dominant interactions $J_{rm{F}}$ and $J_{rm{AF}}$ form the $S=1/2$ F-AF AHC in this compound. The magnetic susceptibility and magnetic specific heat of the compound exhibit thermally activated behavior below approximately 1 K. Furthermore, its magnetization curve is observed up to the saturation field and directly indicates a zero-field excitation gap of 0.5 T. These experimental results provide evidence for the existence of a Haldane gap. We successfully explain the results in terms of the $S=1/2$ F-AF AHC through quantum Monte Carlo calculations with $|J_{rm{AF}}/J_{rm{F}}|$ = 0.22. The $ab$ $initio$ MO calculations also indicate a weak AF interchain interaction $J$ and that the coupled F-AF AHCs form a honeycomb lattice. The $J$ dependence of the Haldane gap is calculated, and the actual value of $J$ is determined to be less than 0.01$|J_{rm{F}}|$.
We present the results of the magnetization and dielectric constant measurements on untwinned single crystal samples of the frustrated S=1/2 chain cuprate LiCu_2O_2. Novel magnetic phase transitions were observed. A spin flop transition of the spiral spin plane was observed for the field orientations H||a,b. The second magnetic transition was observed at H~15 T for all three principal field directions. This high field magnetic phase is discussed as a collinear spin-modulated phase which is expected for an S=1/2 nearest-neighbor ferromagnetic and next-nearest-neighbor antiferromagnetic chain system.
We have measured the specific heat of the S = 1/2 alternating Heisenberg antiferromagnetic chain compound pentafluorophenyl nitronyl nitroxide in magnetic fields using a single crystal and powder. A sharp peak due to field-induced magnetic ordering (FIMO) is observed in both samples. The H-T phase boundary of the FIMO of the single crystal is symmetric with respect to the central field of the gapless field region HC1 < H < HC2, whereas it is distorted for the powder whose ordering temperatures are lower. An analysis employing calculations based on the finite temperature density matrix renormalization group indicates the possibility of novel incommensurate ordering due to frustration in the powder around the central field.
Static magnetic susceptibility chi, ac susceptibility chi_{ac} and specific heat C versus temperature T measurements on polycrystalline samples of In2VO5 and chi and C versus T measurements on the isostructural, nonmagnetic compound In2TiO5 are reported. A Curie-Wiess fit to the chi(T) data above 175 K for In2VO5 indicates ferromagnetic exchange between V^{4+} (S = 1/2) moments. Below 150 K the chi(T) data deviate from the Curie-Weiss behavior but there is no signature of any long range magnetic order down to 1.8 K. There is a cusp at 2.8 K in the zero field cooled (ZFC) chi(T) data measured in a magnetic field of 100 Oe and the ZFC and field cooled (FC) data show a bifurcation below this temperature. The frequency dependence of the chi_{ac}(T) data indicate that below 3 K the system is in a spin-glass state. The difference Delta C between the heat capacity of In2VO5 and In2TiO5 shows a broad anomaly peaked at 130 K. The entropy upto 300 K is more than what is expected for S = 1/2 moments. The anomaly in Delta C and the extra entropy suggests that there may be a structural change below 130 K in In2VO5.
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