We rigorously analyze the full tripartite entanglement of a mixed spin-(1/2,1) Heisenberg tetramer in the presence of an external magnetic field. The tetramer consists of two mixed spin-(1/2,1) dimers arranged to form a square plaquette, with distinct exchange couplings J and J1 between spins from the same and different dimers, respectively. The full tripartite entanglement is classified according to the tripartite negativity NABC defined as a geometric mean of all possible bipartite negativities NA|BC, NB|AC, and NC|AB, when the degrees of freedom of the fourth spin D of the tetrapartite system ABCD are traced out. We demonstrate that for J1/J>1, both trimeric subsystems 1/2-1-1 and 1/2-1/2-1 exhibit tripartite entanglement mediated through the central spin. This entanglement becomes more robust upon the application of an external magnetic field. The opposite limit J1/J<1 leads to the spontaneous emergence of full tripartite entanglement solely within the subsystem 1/2-1-1. However, the increasing magnetic field swiftly disrupts the three-particle correlation across the relevant ground-state phase boundary. Additionally, we identify that in the isotropic limit J1/J=1, the ground-state degeneracy significantly reduces the strength of full tripartite entanglement and favors nontrivial subtypes of full nonseparable states with none or just one spin-dimer entanglement. Finally, we discuss in detail the thermal stability of all fully tripartite nonseparable states.
A genuine tripartite entanglement of a mixed spin-(1/2,1) Heisenberg tetramer is rigorously analyzed in a presence of external magnetic field. The couple of mixed spin-(1/2,1) dimers is arranged in a perfect rectangular square plaquette involving two nonequivalent Heisenberg exchange couplings
J and
J1. The degree of a genuine tripartite entanglement is evaluated according to the genuine tripartite negativity
NABC defined as a geometric mean of all possible bipartite negativities corresponding to a decomposition into a single spin and the remaining spin dimer
NA∣BC,
NB∣AC and
NC∣AB after degrees of freedom of the last fourth spin
D are traced out. Due to the symmetry of a mixed spin-(1/2,1) Heisenberg tetramer two different genuine tripartite negativities for the trimeric system
1/2−1−1 and
1/2−1/2−1 were identified. It was found that the genuine tripartite negativity for the interaction ratio
J1/J<1 becomes nonzero solely in the tripartite system
1/2−1−1 at low-enough magnetic fields. The opposite interaction limit
J1/J>1 gives rise to the nonzero genuine tripartite negativity in both tripartite systems in a presence of external magnetic field until the classical ferromagnetic state is achieved. It was shown, that the genuine tripartite negativity of a mixed spin-(1/2,1) Heisenberg tetramer can be detected also at nonzero temperatures. An enhancement of the thermal genuine tripartite negativity through the enlargement of the total spin number of a tripartite system is evidenced. The correlation between the bipartite negativity of two spins and the genuine tripartite negativity is discussed in detail.
The spatial distribution of entanglement within a spin-1/2 Heisenberg star composed from a single central spin and three peripheral spins is examined in the presence of an external magnetic field using the Kambe projection method, which allows an exact calculation of the bipartite and tripartite negativity serving as a measure of the bipartite and tripartite entanglement. Apart from a fully separable polarized ground state emergent at high-enough magnetic fields, the spin-1/2 Heisenberg star exhibits at lower magnetic fields three outstanding nonseparable ground states. The first quantum ground state exhibits the bipartite and tripartite entanglement over all possible decompositions of the spin star into any pair or triad of spins, whereby the bipartite and tripartite entanglement between the central and peripheral spins dominates over that between the peripheral spins. The second quantum ground state has a remarkably strong tripartite entanglement between any triad of spins in spite of the lack of bipartite entanglement. The central spin of the spin star is separable from the remaining three peripheral spins within the third quantum ground state, where the peripheral spins are subject to the strongest tripartite entanglement arising from a two-fold degenerate W-state.
The effect of uniaxial single-ion anisotropy on quantum entanglement is rigorously quantified using negativity in a mixed spin-(1,1/2,1) Heisenberg trimer, accounting for different exchange coupling constants between identical and distinct spins. Bipartite negativities between the single-spin entity and the remaining spin dimer are analyzed alongside the global tripartite negativity (gTN) of the whole trimer under the effect of an external magnetic field and both easy-axis and easy-plane types of single-ion anisotropy. Interestingly, the single-ion anisotropy significantly influences the degree of entanglement by altering the stability regions of energetically preferred ground states and it may also introduce additional phases in the overall ground-state phase diagram. Moreover, even an arbitrarily small single-ion anisotropy is sufficient to generate global tripartite entanglement in a state that remains biseparable in the isotropic limit. Finally, the thermal stability of entanglement is discussed in detail, including the emergence of a peculiar local minimum at finite temperatures. The obtained theoretical results may offer deeper insights into bipartite and tripartite entanglement in trimetallic Ni2+-Cu2+-Ni2+molecular compounds.
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.
The concept of negativity is adapted in order to explore the quantum and thermal entanglement of the mixed spin-(1/2,S) Heisenberg dimers in presence of an external magnetic field. The mutual interplay between the spin size S, XXZ exchange and uniaxial single-ion anisotropy is thoroughly examined with a goal to tune the degree and thermal stability of the pairwise entanglement. It turns out that the antiferromagnetic spin-(1/2,S) Heisenberg dimers exhibit higher degree of entanglement and higher threshold temperature in comparison with their ferromagnetic counterparts when assuming the same set of model parameters. The increasing spin magnitude S accompanied with an easy-plane uniaxial single-ion anisotropy can enhance not only the thermal stability but simultaneously the degree of entanglement. It is additionally shown that the further enhancement of a bipartite entanglement can be achieved in the mixed spin-(1/2,S) Heisenberg dimers, involving half-odd-integer spins S. Under this condition the thermal negativity saturates at low-enough temperatures in its maximal value regardless of the magnitude of half-odd-integer spin S. The magnetic field induces consecutive discontinuous phase transitions in the mixed spin-(1/2,S) Heisenberg dimers with S>1, which are manifested in a surprising oscillating magnetic-field dependence of the negativity observed at low enough temperature.
Bipartite quantum and thermal entanglement is quantified within pure and mixed states of a mixed spin-(
1/2,1) Heisenberg dimer with the help of negativity. It is shown that the negativity, which may serve as a measure of the bipartite entanglement at zero as well as nonzero temperatures, strongly depends on intrinsic parameters---for instance, exchange and uniaxial single-ion anisotropy---in addition to extrinsic parameters such as temperature and magnetic field. It turns out that a rising magnetic field unexpectedly reinforces the bipartite entanglement due to the Zeeman splitting of energy levels, which lifts the twofold degeneracy of the quantum ferrimagnetic ground state. The maximal bipartite entanglement is thus reached within a quantum ferrimagnetic phase at sufficiently low but nonzero magnetic fields under the assumption that the gyromagnetic
g factors of the spin-1/2 and spin-1 magnetic ions are equal and the uniaxial single-ion anisotropy is half of the exchange constant. It is suggested that the heterodinuclear complex $[\mathrm{Ni}(\mathrm{dpt})({\mathrm{H}}_{2}\mathrm{O})\mathrm{Cu}(\mathrm{pba})]\ifmmode\cdot\else\textperiodcentered\fi{}2{\mathrm{H}}_{2}\mathrm{O}$ [pba = 1,3-propylenebis(oxamato) and dpt = bis-(3-aminopropyl)amine], which affords an experimental realization of the mixed spin-(
1/2,1) Heisenberg dimer, remains strongly entangled up to relatively high temperatures (about 115 K) and magnetic fields (about 140 T) that are comparable with the relevant exchange constant.