The quantum entanglement measure is determined, for the first time, for a collection of spin-1/2 arranged in a infinite chain with finite temperature and applied to a single-crystal β-\mathrm{T_eVO_4}. The physical quantity proposed here to measure the entanglement is the distance between states by adopting the Hilbert-Schmidt norm. We relate the distance between states with the magnetic susceptibility. The decoherence temperature, above which the entanglement is suppressed, is determined for a system. A correlation among their decoherence temperatures and their respective exchange coupling constants is established, moreover, it is conjectured that the exchange coupling protects the system from decoherence as temperature increases.
The spin-1/2 Ising-Heisenberg trimerized chain in a magnetic field is revisited with the aim to explore the quantum entanglement and non-locality within the exactly solved spin system, which exhibits in a low-temperature magnetization curve two intermediate plateaux at zero and one-third of the saturation magnetization.The groundstate phase diagram involves two quantum (antiferromagnetic, ferrimagnetic I) and two classical (ferrimagnetic II, saturated paramagnetic) phases.We have rigorously calculated the concurrence and Bell function in order to quantify the quantum entanglement and non-locality at zero as well as non-zero temperatures.It is demonstrated that the entanglement can be thermally induced also above the classical ground states unlike the quantum nonlocality, which means that the thermal entanglement is indispensable for a violation of the locality principle.
The entanglement thermal (equilibrium) properties in spin-1/2 Ising-Heisenberg model on an ideal diamond chain is analyzed. Due to the classical character of Ising-type exchange interactions between two neighboring antiferromagnetic Heisenberg dimers, the calculation of quantum entanglement (by tracing out Ising spins) can be performed for each of the dimers separately. The concurrence, as a measure of entanglement is obtained and different regimes depending on the values of exchange interactions are revealed. The effects of the magnetic field are incorporated and critical temperatures corresponding to the vanishing or arising of entanglement are considered.
The entanglement quantum properties of a spin-1/2 Ising-Heisenberg model on a symmetrical diamond chain were analyzed. Due to the separable nature of the Ising-type exchange interactions between neighboring Heisenberg dimers, calculation of the entanglement can be performed exactly for each individual dimer. Pairwise thermal entanglement was studied in terms of the isotropic Ising-Heisenberg model and analytical expressions for the concurrence (as a measure of bipartite entanglement) were obtained. The effects of external magnetic field H and next-nearest neighbor interaction J(m) between nodal Ising sites were considered. The ground state structure and entanglement properties of the system were studied in a wide range of coupling constant values. Various regimes with different values of ground state entanglement were revealed, depending on the relation between competing interaction strengths. Finally, some novel effects, such as the two-peak behavior of concurrence versus temperature and coexistence of phases with different values of magnetic entanglement, were observed.
Exchange interactions in spin systems can give rise to quantum entanglement in the ground and thermal states of the systems. We consider a spin tetramer, with spins of magnitude
21, in which the spins interact via nearest-neighbor, diagonal, and four-spin interactions of strength
J1,
J2, and
K, respectively. The ground- and thermal-state entanglement properties of the tetramer are calculated analytically in the various limiting cases. Both bipartite and multipartite entanglements are considered and a signature of the quantum phase transition (QPT), in terms of the entanglement ratio, is identified. The first-order QPT is accompanied by discontinuities in the nearest-neighbor and diagonal concurrences. The magnetic properties of a
S=21 antiferromagnetic polyoxovanadate compound V12 are well explained by tetramers, with
J2=0,
K=0, in which the spins interact via the isotropic Heisenberg exchange interaction Hamiltonian. Treating the magnetic susceptibility $\ensuremath{\chi}$ as an entanglement witness (EW), an estimate of the lower bound of the critical entanglement temperature
Tc below which entanglement is present in the experimental compound, is determined. Two other cases considered include the symmetric tetramer---i.e., tetrahedron
(J1=J2,K=0)---and the symmetric trimer. In both the cases, there is no entanglement between a pair of spins in the thermal state but multipartite entanglement is present. A second EW based on energy provides an estimate of the entanglement temperature
TE below which the thermal state is definitely entangled. This EW detects bipartite entanglement in the case of the tetramer describing a square of spins (the case of V12 ) and multipartite entanglement in the cases of the tetrahedron and symmetric trimer.