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J. Richter

Publications and source records attributed to J. Richter.

At least 55 records · Page 3Linked to original sources

Quantum s = 1/2 Antiferromagnets on Archimedean Lattices: The Route from Semiclassical Magnetic Order to Nonmagnetic Quantum States

We investigate ground states of $s$=1/2 Heisenberg antiferromagnets on the eleven two-dimensional (2D) Archimedian lattices by using the coupled cluster method. Magnetic interactions and quantum fluctuations play against each other subtly in 2D quantum magnets and the magnetic ordering is thus sensitive to the features of lattice topology. Archimedean lattices are those lattices that have 2D arrangements of regular polygons and they often build the underlying magnetic lattices of insulating quasi-two-dimensional quantum magnetic materials. Hence they allow a systematic study of the relationship between lattice topology and magnetic ordering. We find that the Archimedian lattices fall into three groups: those with semiclassical magnetic ground-state long-range order, those with a magnetically disordered (cooperative quantum paramagnetic) ground state, and those with a fragile magnetic order. The most relevant parameters affecting the magnetic ordering are the coordination number and the degree of frustration present.

cond-mat.str-el↗

Thermodynamic Properties of the Anisotropic Frustrated Spin-chain Compound Linarite PbCuSO$_4$(OH)$_2$

We present a comprehensive macroscopic thermodynamic study of the quasi-one-dimensional (1D) $s = \tfrac{1}{2}$ frustrated spin-chain system linarite. Susceptibility, magnetization, specific heat, magnetocaloric effect, magnetostriction, and thermal-expansion measurements were performed to characterize the magnetic phase diagram. In particular, for magnetic fields along the b axis five different magnetic regions have been detected, some of them exhibiting short-range-order effects. The experimental magnetic entropy and magnetization are compared to a theoretical modelling of these quantities using DMRG and TMRG approaches. Within the framework of a purely 1D isotropic model Hamiltonian, only a qualitative agreement between theory and the experimental data can be achieved. Instead, it is demonstrated that a significant symmetric anisotropic exchange of about 10% is necessary to account for the basic experimental observations, including the 3D saturation field, and which in turn might stabilize a triatic (three-magnon) multipolar phase.

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Thermodynamics of the two-dimensional frustrated J1-J2 Heisenberg ferromagnet in the collinear stripe regime: Susceptibility and correlation length

We calculate the temperature dependence of the correlation length xi and the uniform susceptibility chi_0 of the frustrated J1-J2 square-lattice Heisenberg ferromagnet in the collinear stripe phase using Green-function technique. The height chi_{max} and the position T(chi_{max}) of the maximum in the chi_0(T) curve exhibit a characteristic dependence on the frustration parameter J2/|J1|, which is well described by power laws, chi_{max}=a(J2-J2^c)^{-nu} and T(chi_{max})=b(J_2-J_2^c), where J2^c = 0.4 and nu is of the order of unity.The correlation length diverges at low temperatures as xi \propto e^{A/T}, where A increases with growing J2/|J1|. We also compare our results with recent measurements on layered vanadium phosphates and find reasonable agreement.

cond-mat.str-el↗

Interplay of inter-chain interactions and exchange anisotropy: Stability of multipolar states in quasi-1D quantum helimagnets

We quantify the instability towards the formation of multipolar states in coupled spin-1/2 chain systems with a frustrating J1-J2 exchange, in parameter regimes that are of directly relevance to edge-shared cuprate spin-chain compounds. Three representative types of inter-chain coupling and the presence of uniaxial exchange anisotropy are considered. The magnetic phase diagrams are determined by Density Matrix Renormalization Group calculations and completed by exact analytic results for the nematic and dipolar phases. We establish that the residual couplings strongly affect the pitch of spiral states and their instability to multipolar phases. Our theoretical results bring to the fore novel candidate materials close to quantum nematic/triatic ordering.

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Spin-1/2 Heisenberg antiferromagnet on an anisotropic kagome lattice

We use the coupled cluster method to study the zero-temperature properties of an extended two-dimensional Heisenberg antiferromagnet formed from spin-1/2 moments on an infinite spatially anisotropic kagome lattice of corner-sharing isosceles triangles, with nearest-neighbor bonds only. The bonds have exchange constants $J_{1}>0$ along two of the three lattice directions and $J_{2} \equiv κJ_{1} > 0$ along the third. In the classical limit the ground-state (GS) phase for $κ< 1/2$ has collinear ferrimagnetic (Néel$'$) order where the $J_2$-coupled chain spins are ferromagnetically ordered in one direction with the remaining spins aligned in the opposite direction, while for $κ> 1/2$ there exists an infinite GS family of canted ferrimagnetic spin states, which are energetically degenerate. For the spin-1/2 case we find that quantum analogs of both these classical states continue to exist as stable GS phases in some regions of the anisotropy parameter $κ$, namely for $0<κ<κ_{c_1}$ for the Néel$'$ state and for (at least part of) the region $κ>κ_{c_2}$ for the canted phase. However, they are now separated by a paramagnetic phase without either sort of magnetic order in the region $κ_{c_1} < κ< κ_{c_2}$, which includes the isotropic kagome point $κ= 1$ where the stable GS phase is now believed to be a topological ($\mathbb{Z}_2$) spin liquid. Our best numerical estimates are $κ_{c_1} = 0.515 \pm 0.015$ and $κ_{c_2} = 1.82 \pm 0.03$.

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The magnetization process of the spin-one triangular-lattice Heisenberg antiferromagnet

We apply the coupled cluster method and exact diagonalzation to study the uniform susceptibility and the ground-state magnetization curve of the triangular-lattice spin-1 Heisenberg antiferromagnet. Comparing our theoretical data for the magnetization curve with recent measurements on the s=1 triangular lattice antiferromagnet Ba3NiSb2O9 we find a very good agreement.

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Flat-Band Ferromagnetism as a Pauli-Correlated Percolation Problem

We investigate the location and nature of the para-ferro transition of interacting electrons in dispersionless bands using the example of the Hubbard model on the Tasaki lattice. This case can be analyzed as a geometric site-percolation problem where different configurations appear with nontrivial weights. We provide a complete exact solution for the 1D case and develop a numerical algorithm for the 2D case. In two dimensions the paramagnetic phase persists beyond the uncorrelated percolation point, and the grand-canonical transition is via a first-order jump to an unsaturated ferromagnetic phase.

cond-mat.stat-mech↗

Ground-state phase diagram of the spin-1/2 square-lattice J1-J2 model with plaquette structure

Using the coupled cluster method for high orders of approximation and Lanczos exact diagonalization we study the ground-state phase diagram of a quantum spin-1/2 J1-J2 model on the square lattice with plaquette structure. We consider antiferromagnetic (J1>0) as well as ferromagnetic (J1<0) nearest-neighbor interactions together with frustrating antiferromagnetic next-nearest-neighbor interaction J2>0. The strength of inter-plaquette interaction lambda varies between lambda=1 (that corresponds to the uniform J1-J2 model) and lambda=0 (that corresponds to isolated frustrated 4-spin plaquettes). While on the classical level (s \to \infty) both versions of models (i.e., with ferro- and antiferromagnetic J1) exhibit the same ground-state behavior, the ground-state phase diagram differs basically for the quantum case s=1/2. For the antiferromagnetic case (J1 > 0) Neel antiferromagnetic long-range order at small J2/J1 and lambda \gtrsim 0.47 as well as collinear striped antiferromagnetic long-range order at large J2/J1 and lambda \gtrsim 0.30 appear which correspond to their classical counterparts. Both semi-classical magnetic phases are separated by a nonmagnetic quantum paramagnetic phase. The parameter region, where this nonmagnetic phase exists, increases with decreasing of lambda. For the ferromagnetic case (J1 < 0) we have the trivial ferromagnetic ground state at small J2/|J1|. By increasing of J2 this classical phase gives way for a semi-classical plaquette phase, where the plaquette block spins of length s=2 are antiferromagnetically long-range ordered. Further increasing of J2 then yields collinear striped antiferromagnetic long-range order for lambda \gtrsim 0.38, but a nonmagnetic quantum paramagnetic phase lambda \lesssim 0.38.

cond-mat.str-el↗

Decorated Shastry-Sutherland lattice in the spin-1/2 magnet CdCu2(BO3)2

We report the microscopic magnetic model for the spin-1/2 Heisenberg system CdCu2(BO3)2, one of the few quantum magnets showing the 1/2-magnetization plateau. Recent neutron diffraction experiments on this compound [M. Hase et al., Phys. Rev. B 80, 104405 (2009)] evidenced long-range magnetic order, inconsistent with the previously suggested phenomenological magnetic model of isolated dimers and spin chains. Based on extensive density-functional theory band structure calculations, exact diagonalizations, quantum Monte Carlo simulations, third-order perturbation theory, as well as high-field magnetization measurements, we find that the magnetic properties of CdCu2(BO3)2 are accounted for by a frustrated quasi-2D magnetic model featuring four inequivalent exchange couplings: the leading antiferromagnetic coupling J_d within the structural Cu2O6 dimers, two interdimer couplings J_t1 and J_t2, forming magnetic tetramers, and a ferromagnetic coupling J_it between the tetramers. Based on comparison to the experimental data, we evaluate the ratios of the leading couplings J_d : J_t1 : J_t2 : J_it = 1 : 0.20 : 0.45 : -0.30, with J_d of about 178 K. The inequivalence of J_t1 and J_t2 largely lifts the frustration and triggers long-range antiferromagnetic ordering. The proposed model accounts correctly for the different magnetic moments localized on structurally inequivalent Cu atoms in the ground-state magnetic configuration. We extensively analyze the magnetic properties of this model, including a detailed description of the magnetically ordered ground state and its evolution in magnetic field with particular emphasis on the 1/2-magnetization plateau. Our results establish remarkable analogies to the Shastry-Sutherland model of SrCu2(BO3)2, and characterize the closely related CdCu2(BO3)2 as a material realization for the spin-1/2 decorated anisotropic Shastry-Sutherland lattice.

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The frustrated Heisenberg antiferromagnet on the checkerboard lattice: the $J_{1}$--$J_{2}$ model

We study the ground-state (gs) phases of the spin-half anisotropic planar pyrochlore (or crossed chain) model using the coupled cluster method (CCM). The model is a frustrated antiferromagnetic (AFM) $J_{1}$--$J_{2}$ system on the checkerboard lattice, with nearest-neighbor exchange bonds $J_{1}>0$ and next-nearest-neighbor bonds $J_{2} \equiv κJ_{1} > 0$. Using various AFM classical ground states as CCM model states we present results for their gs energy, average on-site magnetization, and susceptibilities to plaquette valence-bond crystal (PVBC) and crossed-dimer valence-bond crystal (CDVBC) ordering. We show that the state with Neel ordering is the gs phase for $κ< κ_{c_1} \approx 0.80 \pm 0.01$, but that none of the fourfold set of AFM states selected by quantum fluctuations at $O(1/s)$ in a large-$s$ analysis (where $s$ is the spin quantum number) from the infinitely degenerate set of AFM states that form the gs phase for the classical version of the model (for $κ>1$) survives the quantum fluctuations to form a stable magnetically-ordered gs phase for the spin-half case. The Neel state becomes susceptible to PVBC ordering at or very near to $κ= κ_{c_1}$, and the fourfold AFM states become infinitely susceptible to PVBC ordering at $κ= κ_{c_2} \approx 1.22 \pm 0.02$. In turn, we find that these states become infinitely susceptible to CDVBC ordering for all values of $κ$ above a certain critical value at or very near to $κ= κ_{c_2}$. We thus find a Neel-ordered gs phase for $κ<κ_{c_1}$, a PVBC-ordered phase for $κ_{c_1} < κ< κ_{c_2}$, and a CDVBC-ordered phase for $κ> κ_{c_2}$. Both transitions are probably direct ones, although we cannot exclude very narrow coexistence regions confined to $0.79 \lesssim κ\lesssim 0.81$ and $1.20 \lesssim κ\lesssim 1.22$ respectively.

cond-mat.str-el↗

Ground-state phases of the frustrated spin-1/2 $J_{1}$--$J_{2}$--$J_{3}$ Heisenberg ferromagnet ($J_{1}<0$) on the honeycomb lattice with $J_{3}=J_{2}>0$

We study the ground-state (gs) properties of the frustrated spin-1/2 $J_{1}$--$J_{2}$--$J_{3}$ Heisenberg model on a honeycomb lattice with ferromagnetic (FM) nearest-neighbor ($J_{1}=-1$) exchange and frustrating antiferromagnetic (AFM) next-nearest-neighbor ($J_{2}>0$) and next-next-nearest-neighbor ($J_{3}>0$) exchanges, for the case $J_{3}=J_{2}$. We use the coupled cluster method in high orders of approximation, complemented by the exact diagonalization of a lattice with 32 sites, and calculate the gs energy, magnetic order parameter, and spin-spin correlation functions. We find a quantum phase transition between regions characterized by FM order and a form of AFM ("striped") collinear order at $J^{c}_{2} \approx 0.1095 \pm 0.0005$. We compare results for the FM case (with $J_{1}=-1$) to previous results for the corresponding AFM case (with $J_{1}=+1$). While the magnetic order parameters behave similarly for the FM and the AFM models for large values of the frustration parameter $J_{2}$, there are considerable differences between them for $J_{2}/|J_{1}| \lesssim 0.6$. For example, the quasiclassical collinear magnetic long-range order for the AFM model (with $J_{1}=+1$) breaks down at $J^{c_{2}}_{2} \approx 0.60$, whereas the "equivalent" point for the FM model (with $J_{1}=-1$) occurs at $J^{c}_{2} \approx 0.11$. Unlike in the AFM model (with $J_{1}=+1$), where a plaquette valence-bond crystal phase intrudes between the two corresponding quasiclassical AFM phases (with Néel and striped order) for $J^{c_{1}}_{2} < J_{2} < J^{c_{2}}_{2}$, with $J^{c_{1}}_{2} \approx 0.47$, we find no clear indications in the FM model for an intermediate magnetically disordered phase between the phases exhibiting FM and striped order. Instead, the evidence points strongly to a direct first-order transition between the two ordered phases of the FM model.

cond-mat.str-el↗

The Heisenberg antiferromagnet on the kagome lattice with arbitrary spin: A high-order coupled cluster treatment

Starting with the sqrt{3} x sqrt{3} and the q=0 states as reference states we use the coupled cluster method to high orders of approximation to investigate the ground state of the Heisenberg antiferromagnet on the kagome lattice for spin quantum numbers s=1/2,1,3/2,2,5/2, and 3. Our data for the ground-state energy for s=1/2 are in good agreement with recent large-scale density-matrix renormalization group and exact diagonalization data. We find that the ground-state selection depends on the spin quantum number s. While for the extreme quantum case, s=1/2, the q=0 state is energetically favored by quantum fluctuations, for any s>1/2 the sqrt{3} x sqrt{3} state is selected. For both the sqrt{3} x sqrt{3} and the q=0 states the magnetic order is strongly suppressed by quantum fluctuations. Within our coupled cluster method we get vanishing values for the order parameter (sublattice magnetization) M for s=1/2 and s=1, but (small) nonzero values for M for s>1. Using the data for the ground-state energy and the order parameter for s=3/2,2,5/2, and 3 we also estimate the leading quantum corrections to the classical values.

cond-mat.str-el↗

Thermodynamics of the frustrated one-dimensional spin-1/2 Heisenberg ferromagnet in a magnetic field

We calculate the low-temperature thermodynamic quantities (magnetization, correlation functions, transverse and longitudinal correlation lengths, spin susceptibility, and specific heat) of the frustrated one-dimensional spin-half J1-J2 Heisenberg ferromagnet, i.e. for J2< 0.25|J1|, in an external magnetic field using a second-order Green-function formalism and full diagonalization of finite systems. We determine power-law relations for the field dependence of the position and the height of the maximum of the uniform susceptibility. Considering the specific heat at low magnetic fields, two maxima in its temperature dependence are found.

cond-mat.str-el↗

The J1-J2 Heisenberg model at and close to its z=4 quantum critical point

We study the frustrated J1-J2 Heisenberg model with ferromagnetic nearest neighbor coupling J1<0 and antiferromagnetic next-nearest neighbor coupling J2>0 at and close to the z=4 quantum critical point (QCP) at J1/J2=-4. The J1-J2 model plays an important role for recently synthesized chain cuprates as well as in supersymmetric Yang Mills theories. We study the thermodynamic properties using field theory, a modified spin-wave theory as well as numerical density-matrix renormalization group calculations. Furthermore, we compare with results for the classical model obtained by analytical methods and Monte-Carlo simulations. As one of our main results we present numerical evidence that the susceptibility at the QCP seems to diverge with temperature T as chi ~ T^{-1.2} in the quantum case in contrast to the classical model where chi ~ T^{-4/3}.

cond-mat.str-el↗

Electron hole - phonon interaction and structural changes in La0.9Sr0.1FeO3 by temperature dependent conductivity and valence band photoemission spectros-copy

Electric conductivity and structural details of the hole-doped polaron conductor La0.9Sr0.1FeO3 (LSF10) are reported. The conductivity of a single crystal shows an exponential increase with temperature with a maxi-mum of 100 S/cm at 700 K and with activation energy of about 375 meV, and a decrease for higher temperatures that follows a power law. The exponential increase of the electric conductivity for 300 K {\leg} T {\leg} 700 is accompanied by a shift of spectral weight in the photoemission valence band towards the Fermi level, indicative of a strong electron-phonon interaction. The subsequent decrease of the conductivity for T > 700 K is accompanied by a reversible phase transformation from orthorhombic to rhombohedral symmetry. The decreasing conductivity for T > 700 K is likely due to the reduction of the iron due to oxygen loss causing a decreasing hole concentration, as evidenced by a substantial chemical shift in the Fe K-shell x-ray absorption spectra. Two additional fine structures in the conductivity data at 357 K, this is, a small temperature reversible jump in the conductivity, and at 573 K, a slight reversible increase of the polaron activation energy, are correlated with an exceptionally strong decrease in spectral valence band intensity near the Fermi level, and with the onset of a corresponding structural transition.

cond-mat.str-el↗

Thermodynamics of the one-dimensional frustrated Heisenberg ferromagnet with arbitrary spin

The thermodynamic quantities (spin-spin correlation functions <{\bf S}_0{\bf S}_n>, correlation length ξ, spin susceptibility χ, and specific heat C_V) of the frustrated one-dimensional J1-J2 Heisenberg ferromagnet with arbitrary spin quantum number S below the quantum critical point, i.e. for J2< |J1|/4, are calculated using a rotation-invariant Green-function formalism and full diagonalization as well as a finite-temperature Lanczos technique for finite chains of up to N=18 sites. The low-temperature behavior of the susceptibility χ and the correlation length ξ is well described by χ= (2/3)S^4 (|J1|-4J2) T^{-2} + A S^{5/2} (|J1|-4J2)^{1/2} T^{-3/2} and ξ= S^2 (|J1|-4J2) T^{-1} + B S^{1/2} (|J1|-4J2)^{1/2} T^{-1/2} with A \approx 1.1 ... 1.2 and B \approx 0.84 ... 0.89. The vanishing of the factors in front of the temperature at J2=|J1|/4 indicates a change of the critical behavior of χ and ξ at T \to 0. The specific heat may exhibit an additional frustration-induced low-temperature maximum when approaching the quantum critical point. This maximum appears for S=1/2 and S=1, but was not found for S>1.

cond-mat.str-el↗

The spin-half Heisenberg antiferromagnet on two Archimedian lattices: From the bounce lattice to the maple-leaf lattice and beyond

We investigate the ground state of the two-dimensional Heisenberg antiferromagnet on two Archimedean lattices, namely, the maple-leaf and bounce lattices as well as a generalized $J$-$J'$ model interpolating between both systems by varying $J'/J$ from $J'/J=0$ (bounce limit) to $J'/J=1$ (maple-leaf limit) and beyond. We use the coupled cluster method to high orders of approximation and also exact diagonalization of finite-sized lattices to discuss the ground-state magnetic long-range order based on data for the ground-state energy, the magnetic order parameter, the spin-spin correlation functions as well as the pitch angle between neighboring spins. Our results indicate that the "pure" bounce ($J'/J=0$) and maple-leaf ($J'/J=1$) Heisenberg antiferromagnets are magnetically ordered, however, with a sublattice magnetization drastically reduced by frustration and quantum fluctuations. We found that magnetic long-range order is present in a wide parameter range $0 \le J'/J \lesssim J'_c/J $ and that the magnetic order parameter varies only weakly with $J'/J$. At $J'_c \approx 1.45 J$ a direct first-order transition to a quantum orthogonal-dimer singlet ground state without magnetic long-range order takes place. The orthogonal-dimer state is the exact ground state in this large-$J'$ regime, and so our model has similarities to the Shastry-Sutherland model. Finally, we use the exact diagonalization to investigate the magnetization curve. We a find a 1/3 magnetization plateau for $J'/J \gtrsim 1.07$ and another one at 2/3 of saturation emerging only at large $J'/J \gtrsim 3$.

cond-mat.str-el↗

Saturation field of frustrated chain cuprates: broad regions of predominant interchain coupling

An efficient and precise thermodynamic method to extract the interchain coupling (IC) of spatially anisotropic 2D or 3D spin-1/2 systems from their empirical saturation field H_s (T=0) is proposed. Using density-matrix renormalization group, hard-core boson, and spin-wave theory we study how H_s is affected by an antiferromagnetic (AFM) IC between frustrated chains described in the J_1-J_2-spin model with ferromagnetic 1st and AFM 2nd neighbor in-chain exchange. A complex 3D-phase diagram has been found. For Li2CuO2 and Y2Ca2Cu5O10, we show that H_s is solely determined by the IC and predict H_s approx 61 T for the latter.Using H_s approx 55 T from our high-field pulsed measurements one reads out a weak IC for Li2CuO2 close to that from neutron scattering.

cond-mat.str-el↗