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arXiv:1604.06539 · Physical review. B./Physical review. B

Probing molecular spin clusters by local measurements

Filippo Troiani, Matteo G. A. Paris

Published Sep 16, 2016• 19 citations
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Abstract

We address the characterization of molecular nanomagnets at the quantum level and analyze the performance of local measurements in estimating the physical parameters in their spin Hamiltonians. To this aim, we compute key quantities in quantum estimation theory, such as the classical and the quantum Fisher information, in the prototypical case of a heterometallic antiferromagnetic ring. We show that local measurements, performed only on a portion of the molecule, allow a precise estimate of the parameters related to both magnetic defects and avoided level crossings.

DOI
10.1103/physrevb.94.115422

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We address the characterization of molecular nanomagnets at the quantum level and analyze the performance of local measurements in estimating the physical parameters in their spin Hamiltonians. To this aim, we compute key quantities in quantum estimation theory, such as the classical and the quantum Fisher information, in the prototypical case of a heterometallic antiferromagnetic ring. We show that local measurements, performed only on a portion of the molecule, allow a precise estimate of the parameters related to both magnetic defects and avoided level crossings.
The present paper discusses the use of two information-theoretical quantities—namely, the classical and quantum Fisher information—in the context of molecular magnetism. These functions quantify the suitability of a given observable to the estimation of a physical parameter and provide the highest precision allowed by quantum mechanics in such an estimation process. The quantum Fisher information also quantifies the degree of macroscopicity of a quantum state. As illustrative examples of such applications, we compute the classical and quantum Fisher information of the Fe 4 molecular nanomagnet, used as a probe of an applied magnetic field or as a platform for generating Schrödinger cat states.
We address quantum metrology in critical spin chains with anisotropy and Dzyaloshinskii-Moriya (DM) interaction, and show how local and quasi-local measurements may be exploited to characterize global properties of the systems. In particular, we evaluate the classical (magnetization) and quantum Fisher information of the relevant parameters for the density matrix of a single spin and that of a pair of spins ranging from nearest to sixth-nearest neighbors, to the limiting case of very distant spins. Our results allow us to elucidate the role of the different parameters and to individuate the optimal working regimes for the precise characterization of the system, also clarifying the effects of correlations on the estimation precision.
Abstract We address quantum characterization of anisotropic spin chains in the presence of anti-symmetric exchange, and investigate whether the Hamiltonian parameters of the chain may be estimated with precision approaching the ultimate limit imposed by quantum mechanics. At variance with previous approaches, we focus on the information that may be extracted by measuring only two neighboring spins rather than a global observable on the entire chain. We evaluate the Fisher information (FI) of a two-spin magnetization measure, and the corresponding quantum Fisher information (QFI), for all the relevant parameters, i.e. the spin coupling, the anisotropy, and the Dzyaloshinskii–Moriya (DM) parameter. Our results show that the reduced system made of two neighboring spins may be indeed exploited as a probe to characterize global properties of the entire system. In particular, we find that the ratio between the FI and the QFI is close to unit for a large range of the coupling values. The DM coupling is beneficial for coupling estimation, since it leads to the presence of additional bumps and peaks in the FI and QFI, which are not present in a model that neglects exchange interaction and may be exploited to increase the robustness of the overall estimation procedure. Finally, we address the multiparameter estimation problem, and show that the model is compatible but sloppy, i.e. both the Uhlmann curvature and the determinant of the QFI matrix vanish. Physically, this means that the state of the system actually depends only on a reduced numbers of combinations of parameters, and not on all of them separately.
Antiferromagnetic spin rings represent prototypical realizations of highly correlated, low-dimensional systems. Here we theoretically show how the introduction of magnetic defects by controlled chemical substitutions results in a strong spatial modulation of spin-pair entanglement within each ring. Entanglement between local degrees of freedom (individual spins) and collective ones (total ring spins) are shown to coexist in exchange-coupled ring dimers, as can be deduced from general symmetry arguments. We verify the persistence of these features at finite temperatures, and discuss them in terms of experimentally accessible observables.
Molecular nanomagnets are compounds characterized by a high-spin magnetic core that is protected by organic ligands. They have recently gained attention as potential quantum information carriers in solid-state quantum computing platforms, simultaneously exhibiting classical macroscopic properties and quantum features in light of their complex nature and configuration. Addressing the condition when they manifest unquestionable quantum behavior is key to guarantee their effectiveness as resources for quantum information processing. We address the quantumness of molecular nanomagnets using a recently formulated criterion [cf. Krisnanda et al., Phys. Rev. Lett. 119, 120402 (2017)] demonstrating that these systems exhibit an intrinsic quantum nature, as evidenced by their ability to generate and enhance quantum correlations between two non-interacting probes. Our analysis, which is performed addressing various dynamical regimes, paves the way to the design of experimentally viable tests of non-classicality in multipartite registers consisting of ensembles of molecular nanomagnets.
Molecular nanomagnets are compounds characterized by a high-spin magnetic core that is protected by organic ligands. They have recently gained attention as potential quantum information carriers in solid-state quantum computing platforms, simultaneously exhibiting classical macroscopic properties and quantum features in light of their complex nature and configuration. Addressing the condition when they manifest unquestionable quantum behavior is key to guarantee their effectiveness as resources for quantum information processing. We address the quantumness of molecular nanomagnets using a recently formulated criterion [T. Krisnanda , ] demonstrating that these systems exhibit an intrinsic quantum nature, as evidenced by their ability to generate and enhance quantum correlations between two noninteracting probes. Our analysis, which is performed addressing various dynamical regimes, paves the way to the design of experimentally viable tests of nonclassicality in multipartite registers consisting of ensembles of molecular nanomagnets.