By combining inelastic neutron scattering and numerical simulations, we study the quasi-one-dimensional Ising-like quantum antiferromagnet
BaCo2V2O8 in a longitudinal magnetic field applied along the Ising anisotropy, which is also the chain direction. The external field closes the excitation gap due to the magnetic anisotropy, inducing a transition from the N\'eel ordered state to an incommensurate longitudinal spin density wave phase. If the field is increased further, another transition into a transverse antiferromagnetic phase takes place at 9 T due to the competition between longitudinal and transverse correlations. We numerically and experimentally show that the model of XXZ chains connected by a weak interchain interaction well reproduces this transition. We also calculate the dynamical susceptibility and demonstrate that it agrees quantitatively with inelastic neutron scattering measurements. In contrast to the abrupt change of magnetic ordering, the spectra do not change much at the transition at 9 T, and the spin dynamics can be described as a Tomonaga-Luttinger liquid. We also refine the modeling of
BaCo2V2O8 by including a four-site periodic term arising from the crystal structure which enables one to account for an anomaly of the magnetic susceptibility appearing at 19.5 T, as well as for the anticrossing observed in the inelastic neutron scattering spectra.
Abstract Entanglement is a crucial resource for quantum information processing and its detection and quantification is of paramount importance in many areas of current research. Weakly coupled molecular nanomagnets provide an ideal test bed for investigating entanglement between complex spin systems. However, entanglement in these systems has only been experimentally demonstrated rather indirectly by macroscopic techniques or by fitting trial model Hamiltonians to experimental data. Here we show that four-dimensional inelastic neutron scattering enables us to portray entanglement in weakly coupled molecular qubits and to quantify it. We exploit a prototype (Cr7Ni)2 supramolecular dimer as a benchmark to demonstrate the potential of this approach, which allows one to extract the concurrence in eigenstates of a dimer of molecular qubits without diagonalizing its full Hamiltonian.