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Register a new userQuantized antiferromagnetic spin waves in the molecular Heisenberg ring CsFe$_8$
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We report on inelastic neutron scattering (INS) measurements on the molecular spin ring CsFe$_8$, in which eight spin-5/2 Fe(III) ions are coupled by nearest-neighbor antiferromagnetic Heisenberg interaction. We have recorded INS data on a non-deuterated powder sample up to high energies at the time-of-flight spectrometers FOCUS at PSI and MARI at ISIS, which clearly show the excitation of spin waves in the ring. Due to the small number of spin sites, the spin-wave dispersion relation is not continuous but quantized. Furthermore, the system exhibits a gap between the ground state and the first excited state. We have modeled our data using exact diagonalization of a Heisenberg-exchange Hamiltonian together with a small single-ion anisotropy term. Due to the molecules symmetry, only two parameters $J$ and $D$ are needed to obtain excellent agreement with the data. The results can be well described within the framework of the rotational-band model as well as antiferromagnetic spin-wave theories.
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Large single crystals of the new compound SrMn$_2$V$_2$O$_8$ have been grown by the floating-zone method. This transition-metal based oxide is isostructural to SrNi$_2$V$_2$O$_8$, described by the tetragonal space group $I4_1cd$. Magnetic properties were investigated by means of susceptibility, magnetization, and specific heat measurements. The title compound behaves like a one-dimensional magnetic system above the ordering temperature ($T_N$ = 43 K). The magnetic ground state can be described as a classical long-range ordered antiferromagnet with weak anisotropy.
Linear Heisenberg antiferromagnets (HAFs) are chains of spin-$S$ sites with isotropic exchange $J$ between neighbors. Open and periodic boundary conditions return the same ground state energy in the thermodynamic limit, but not the same spin $S_G$ when $S ge 1$. The ground state of open chains of N spins has $S_G = 0$ or $S$, respectively, for even or odd N. Density matrix renormalization group (DMRG) calculations with different algorithms for even and odd N are presented up to N = 500 for the energy and spin densities $rho(r,N)$ of edge states in HAFs with $S = 1$, 3/2 and 2. The edge states are boundary-induced spin density waves (BI-SDWs) with $rho(r,N)propto(-1)^{r-1}$ for $r=1,2,ldots N$. The SDWs are in phase when N is odd, out of phase when N is even, and have finite excitation energy $Gamma(N)$ that decreases exponentially with N for integer $S$ and faster than 1/N for half integer $S$. The spin densities and excitation energy are quantitatively modeled for integer $S$ chains longer than $5 xi$ spins by two parameters, the correlation length $xi$ and the SDW amplitude, with $xi = 6.048$ for $S = 1$ and 49.0 for $S = 2$. The BI-SDWs of $S = 3/2$ chains are not localized and are qualitatively different for even and odd N. Exchange between the ends for odd N is mediated by a delocalized effective spin in the middle that increases $|Gamma(N)|$ and weakens the size dependence. The nonlinear sigma model (NL$sigma$M) has been applied the HAFs, primarily to $S = 1$ with even N, to discuss spin densities and exchange between localized states at the ends as $Gamma(N) propto (-1)^N exp(-N/xi)$...
We demonstrate that Kondo-Heisenberg systems, consisting of itinerant electrons and localized magnetic moments (Kondo impurities), can be used as a principally new platform to realize scalar chiral spin order. The underlying physics is governed by a competition of the Ruderman-Kittel-Kosuya-Yosida (RKKY) indirect exchange interaction between the local moments with the direct Heisenberg one. When the direct exchange is weak and RKKY dominates the isotropic system is in the disordered phase. A moderately large direct exchange leads to an Ising-type phase transition to the phase with chiral spin order. Our finding paves the way towards pioneering experimental realizations of the chiral spin liquid in low dimensional systems with spontaneously broken time reversal symmetry.
We solve the quantum-mechanical antiferromagnetic Heisenberg model with spins positioned on vertices of the truncated icosahedron using the density-matrix renormalization group (DMRG). This describes magnetic properties of the undoped C$_{60}$ fullerene at half filling in the limit of strong on-site interaction $U$. We calculate the ground state and correlation functions for all possible distances, the lowest singlet and triplet excited states, as well as thermodynamic properties, namely the specific heat and spin susceptibility. We find that unlike the exactly solvable C$_{20}$ to C$_{32}$, the lowest excited state is a triplet rather than a singlet, indicating a reduced frustration due to the presence of many hexagon faces and the separation of the pentagon faces. This implies that frustration may be tuneable within the fullerenes by changing their size. The spin-spin correlations are much stronger along the hexagon bonds and rapidly decrease with distance, so that the molecule is large enough not to be correlated across its whole extent. The specific heat shows a high-temperature peak and a low-temperature shoulder reminiscent of the Kagome lattice, while the spin susceptibility shows a single broad peak and is very close to the one of C$_{20}$.
An efficient density matrix renormalization group (DMRG) algorithm is presented for the Bethe lattice with connectivity $Z = 3$ and antiferromagnetic exchange between nearest neighbor spins $s= 1/2$ or 1 sites in successive generations $g$. The algorithm is accurate for $s = 1$ sites. The ground states are magnetic with spin $S(g) = 2^g s$, staggered magnetization that persists for large $g > 20$ and short-range spin correlation functions that decrease exponentially. A finite energy gap to $S > S(g)$ leads to a magnetization plateau in the extended lattice. Closely similar DMRG results for $s$ = 1/2 and 1 are interpreted in terms of an analytical three-site model.
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