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Register a new userThe Competition between Staggered Field and Antiferromagnetic Interactions in Cugeo3:Fe
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The EPR spectra along different crystallographic axes for single crystals of CuGeO3 containing 1% of Fe impurity have been studied in the frequency range 60-360 GHz at temperatures 0.5-30 K. The analysis based on the Oshikawa-Affleck (OA) theory suggests that the temperature dependences of the line width and g-factor are formed as a result of the competition between interchain antiferromagnetic interactions and staggered Zeeman energy. It is found that staggered magnetic moments in CuGeO3:Fe are located predominantly along b axis.
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A pressure and temperature dependent Raman study of the vibrational and spin dynamics in CuGeO3 is presented. A new low temperature, high pressure phase has been identified, and a pressure-temperature phase-diagram is proposed for CuGeO3. The pressure dependence of the effective exchange interaction, of the spin-Peierls gap, and of the spin-Peierls temperature strongly supports a model in which next nearest neighbor interactions stabilise the SP ground state. The Raman data allow for a quantitative estimate of the pressure dependence of the next nearest neighbor interactions.
Naturally occuring or man-made systems displaying periodic spatial modulations of their properties on a nanoscale constitute superlattices. Such modulated structures are important both as prototypes of simple nanotechnological devices and as particular examples of emerging spatial inhomogeneity in interacting many-electron systems. Here we investigate the effect different types of modulation of the system parameters have on the ground-state energy and the charge-density distribution of the system. The superlattices are described by the inhomogeneous attractive Hubbard model, and the calculations are performed by density-functional and density-matrix renormalization group techniques. We find that modulations in local electric potentials are much more effective in shaping the systems properties than modulations in the attractive on-site interaction. This is the same conclusions we previously (Phys. Rev. B 71, 125130) obtained for repulsive interactions, suggesting that it is not an artifact of a specific state, but a general property of modulated structures.
Inelastic neutron scattering was used to measure the magnetic field dependence of spin excitations in the antiferromagnetic S=1/2 chain CuCl_2 2(dimethylsulfoxide) (CDC) in the presence of uniform and staggered fields. Dispersive bound states emerge from a zero-field two-spinon continuum with different finite energy minima at wave numbers q=pi and q_i approx pi (1-2<S_z>). The ratios of the field dependent excitation energies are in excellent agreement with predictions for breather and soliton solutions to the quantum sine-Gordon model, the proposed low-energy theory for S=1/2 chains in a staggered field. The data are also consistent with the predicted soliton and n=1,2 breather polarizations and scattering cross sections.
We study $S=1/2$ dimer excitation in a coupled chain and dimer compound Cu$_2$Fe$_2$Ge$_4$O$_{13} by inelastic neutron scattering technique. The Zeeman split of the dimer triplet by a staggered field is observed at low temperature. With the increase of temperature the effect of random field is detected by a drastic broadening of the triplet excitation. Basic dynamics of dimer in the staggered and random fields are experimentally identified in Cu$_2$Fe$_2$Ge$_4$O$_{13}.
The synchronization of charge oscillations after photoexcitation that has been realized through the emergence of an electronic breathing mode on dimer lattices is studied here from the viewpoint of the competition between interactions and randomness. We employ an extended Hubbard model at three-quarter filling on a simple dimer lattice and add random numbers to all transfer integrals between nearest-neighbor sites. Photoinduced dynamics are calculated using the time-dependent Schrodinger equation by the exact diagonalization method. Although the randomness tends to unsynchronize charge oscillations on different bonds during and after photoexcitation, sufficiently strong on-site repulsion $U$ overcomes this effect and synchronizes these charge oscillations some time after strong photoexcitation. The degree of synchronization is evaluated using an order parameter that is derived from the time profiles of the current densities on all bonds. As to the nearest-neighbor interaction $V$, if $V$ is weakly attractive, it increases the order parameter by facilitating the charge oscillations. The relevance of these findings to previously reported experimental and theoretical results for the organic conductor $kappa$-(bis[ethylenedithio]tetrathiafulvalene)$_2$Cu[N(CN)$_2$]Br is discussed.
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