Many-body models for molecular nanomagnets

We present a flexible and effective ab-initio scheme to build many-body models for molecular nanomagnets, and to calculate magnetic exchange couplings and zero-field splittings. It is based on using localized Foster-Boys orbitals as one-electron basis. We apply this scheme to three paradigmatic systems, the antiferromagnetic rings Cr8 and Cr7Ni and the single molecule magnet Fe4. In all cases we identify the essential magnetic interactions and find excellent agreement with experiments.Comment: 5 pages, 3 figure

Quantum-gate implementation in permanently coupled AF spin rings without need of local fields

We propose a scheme for the implementation of quantum gates which is based on the qubit encoding in antiferromagnetic molecular rings. We show that a proper engineering of the intercluster link would result in an effective coupling that vanishes as far as the system is kept in the computational space, while it is turned on by a selective excitation of specific auxiliary states. These are also shown to allow the performing of single- and two-qubit gates without an individual addressing of the rings by means of local magnetic fields.Comment: To appear in Physical Review Letter

S-mixing and quantum tunneling of the magnetization in molecular nanomagnets

The role of $S$-mixing in the quantum tunneling of the magnetization in nanomagnets has been investigated. We show that the effect on the tunneling frequency is huge and that the discrepancy (more than 3 orders of magnitude in the tunneling frequency) between spectroscopic and relaxation measurements in Fe$_8$ can be resolved if $S$-mixing is taken into account.Comment: REVTEX, 10 pages, 3 jpg figures, to appear in PR

Enhancement of rare-earth--transition-metal exchange interaction in Pr2_{2}Fe17_{17} probed by inelastic neutron scattering

The fundamental magnetic interactions of Pr$_{2}$Fe$_{17}$ are studied by inelastic neutron scattering and anisotropy field measurements. Data analysis confirms the presence of three magnetically inequivalent sites, and reveals an exceptionally large value of the exchange field. The unexpected importance of $J$-mixing effects in the description of the ground-state properties of Pr$_{2}$Fe$_{17}$ is evidenced, and possible applications of related compounds are envisaged.Comment: 4 RevTeX pages, 4 EPS figures. Accepted for publication by Appl. Phys. Lett. (will be found at http://apl.aip.org

Magnetic Susceptibility of Multiorbital Systems

Effects of orbital degeneracy on magnetic susceptibility in paramagnetic phases are investigated within a mean-field theory. Under certain crystalline electric fields, the magnetic moment consists of two independent moments, e.g., spin and orbital moments. In such a case, the magnetic susceptibility is given by the sum of two different Curie-Weiss relations, leading to deviation from the Curie-Weiss law. Such behavior may be observed in d- and f-electron systems with t_{2g} and Gamma_8 ground states, respectively. As a potential application of our theory, we attempt to explain the difference in the temperature dependence of magnetic susceptibilities of UO_2 and NpO_2.Comment: 4 pages, 3 figure

Low-temperature antihydrogen-atom scattering

A simple method to include the strong force in atom-antiatom scattering is presented. It is based on the strong-force scatteringn length between the nucleon and antinucleon. Using this method elastic and annihilation cross sections are calculated for hydrogen-antihydrogen and helium-antihydrogen scattering. The results are compared to first-order perturbation theory using a pseudo potential. The pseudo-potential approach works fairly well for hydrogen-antihydrogen scattering, but fails for helium-antihydrogen scattering where strong-force effects are more prominent.Comment: 9 pages, 2 figures, to be published in Nuclear Instruments and Methods

Molecular engineering of antiferromagnetic rings for quantum computation

The substitution of one metal ion in a Cr-based molecular ring with dominant antiferromagnetic couplings allows to engineer its level structure and ground-state degeneracy. Here we characterize a Cr7Ni molecular ring by means of low-temperature specific-heat and torque-magnetometry measurements, thus determining the microscopic parameters of the corresponding spin Hamiltonian. The energy spectrum and the suppression of the leakage-inducing S-mixing render the Cr7Ni molecule a suitable candidate for the qubit implementation, as further substantiated by our quantum-gate simulations.Comment: To appear in Physical Review Letter

Molecular nanomagnets as quantum simulators

Quantum simulators are controllable systems that can be used to simulate other quantum systems. Here we focus on the dynamics of a chain of molecular qubits with interposed antiferromagnetic dimers. We theoretically show that its dynamics can be controlled by means of uniform magnetic pulses and used to mimic the evolution of other quantum systems, including fermionic ones. We propose two proof-of-principle experiments, based on the simulation of the Ising model in transverse field and of the quantum tunneling of the magnetization in a spin-1 system.Comment: Phys. Rev. Lett., in pres