No Arabic abstract
We studied the magnetic properties, in particular dynamics, of the correlated spins associated with natural defects in the organic spin chain compounds ($o$-DMTTF)$_2X$ ($X$ = Br, Cl) by means of electron spin resonance (ESR) spectroscopy. Both materials exhibit spin-Peierls transitions at temperatures around 50 K [P. Foury-Leylekian et al. Phys. Rev. B 84, 195134 (2011)], which allow a separation of the properties of defects inside the chains from the magnetic response of the spin chains. Indeed, continuous wave ESR measurements performed over a wide temperature range evidence the evolution of the spin dynamics from being governed by the spins in the chains at elevated temperatures to a low-temperature regime which is dominated by defects within the spin-dimerized chains. Such defects polarize the antiferromagnetically coupled spins in their vicinity, thereby leading to a finite local alternating magnetization around the defect site which can be described in terms of a soliton, i.e. a spin 1/2 quasiparticle built of many correlated spins, pinned to the defect. In addition, contributions of triplon excitations of the spin-dimerized state to the ESR response below the transition temperature were observed which provides a spectroscopic estimate for the spin-gap of the studied systems. Moreover, details of spin dynamics deep in the spin-Peierls phase were investigated by pulse ESR experiments which revealed Rabi-oscillations as signatures of coherent spin dynamics. From a comparison of the characteristic damping times of the Rabi oscillations with measurements of the spin relaxation times by means of primary-echo decay and CPMG methods it becomes evident that inhomogeneities in local magnetic fields strongly contribute to the soliton decoherence.
We present a multi-frequency Electron Spin Resonance (ESR) study in the range of 4 GHz to 420 GHz of the quasi-one-dimensional, non-dimerized, quarter-filled Mott insulators, delta-(EDT-TTF-CONMe_2)_2X (X=AsF_6, Br). In the high temperature orthorhombic phase above T~190 K, the magnitude and the temperature dependence of the high temperature spin susceptibility are described by a S = 1/2 Heisenberg antiferromagnetic chain with J_AsF6=298 K and J_Br=474 K coupling constants for X=AsF_6 and Br respectively. We estimate from the temperature dependence of the line width an exchange anisotropy, J/J of ~2 * 10^{-3}. The frequency dependence of the line width and the g-shift have an unusual quadratic dependence in all crystallographic orientations that we attribute to an antisymmetric exchange (Dzyaloshinskii--Moriya) interaction.
Raman spectroscopy is used to study magnetic excitations in the quasi one dimensional $S=1/2$ quantum spin systems Cu(Qnx)(Cl$_{1-x}$Br$_x$)$_2$. The low energy spectrum is found to be dominated by a two-magnon continuum as expected from the numerical calculations for the Heisenberg spin ladder model. The continuum shifts to higher energies as more Br is introduced. The cutoff of the scattering increases faster than the onset indicating that the increase of exchange constant along the leg is the main effect on the magnetic properties. The upper and lower continuum thresholds are measured as a function of Br content across the entire range and compared to estimates based on previous bulk studies. We observe small systematic deviations that are discussed.
We present a comparative study of the coupled-tetrahedra quantum spin systems Cu2Te2O5X2, X=Cl, Br (Cu-2252(X)) and the newly synthesized Cu4Te5O12Cl4 (Cu-45124(Cl)) based on ab initio Density Functional Theory calculations. The magnetic behavior of Cu-45124(Cl) with a phase transition to an ordered state at a lower critical temperature T$_c$=13.6K than in Cu-2252(Cl) (T$_c$=18K) can be well understood in terms of the modified interaction paths. We identify the relevant structural changes between the two systems and discuss the hypothetical behavior of the not yet synthesized Cu-45124(Br) with an ab initio relaxed structure using Car-Parrinello Molecular Dynamics.
We have investigated the charge ordering phase of the quasi one dimensional quantum antiferromagnet (TMTTF)$_2X$ ($X=$ SbF$_6$, AsF$_6$ and PF$_6$) using high fields/frequencies electron paramagnetic resonance. In addition to the uniform displacement of the counter anions involved in the charge order phase, we report the existence of a superlattice between the spin chains in the direction $c$, caused by the space modulation of the charge order. When the field is high enough, the magnetic decoupling of the spin chains allows us to estimate the interaction between the chains, $J_c<1$~mK, three orders of magnitude lower than expected from the mean field theory.
The paper presents the Electron Paramagnetic Resonance study of defects in the spin chain o- (DMTTF)2X family using continuous wave and pulsed techniques. The defects in spin chains are strongly correlated and present similar microscopic structure as a molecular magnet. By means of 2D-HYSCORE and DFT calculations we show a strong reduction of hyperfine coupling between the defects and the nuclear spin bath. We assume that the reduction is due to the Heisenberg exchange interaction which screens the effect of the nuclei.