Quantum spin dynamics

Abstract:

© 2019 American Physical Society. The interaction Hamiltonian (Formula Presented) Eq. (14) describing the interaction between the cavity and the electronic system was obtained by expanding the Peierls Hamiltonian in Eq. (A4) up to first order in the small parameter (Formula Presented) All results presented in the paper are consistent with this appro imate interaction Hamiltonian, leading to an effective Hamiltonian that depends quadratically on. However, it turns out that a straightforward improvement of the parameters entering the effective Hamiltonian in Eq. (26) can be obtained by including the second-order term in the Peierls Hamiltonian in Eq. (A4). This term gives rise to modifications of our results that are also of order through a renormalization of the nearest-neighbor hopping amplitude (Formula Presented) The authors would like to thank M. A. Sentef for bringing the importance of the second-order term in Eq. (A4) to our attention.

Abstract:

We show that the macroscopic magnetic and electronic properties of strongly correlated electron systems can be manipulated by coupling them to a cavity mode. As a paradigmatic example we consider the Fermi-Hubbard model and find that the electron-cavity coupling enhances the magnetic interaction between the electron spins in the ground-state manifold. At half filling this effect can be observed by a change in the magnetic susceptibility. At less than half filling, the cavity introduces a next-nearest-neighbor hopping and mediates a long-range electron-electron interaction between distant sites. We study the ground-state properties with tensor network methods and find that the cavity coupling can induce a phase characterized by a momentum-space pairing effect for electrons.

Abstract:

We investigate the low-temperature magnetic properties of the molecule-based chiral spin chain ½CuðpymÞðH2OÞ4SiF6 · H2O (pym ¼ pyrimidine). Electron-spin resonance, magnetometry and heat capacity measurements reveal the presence of staggered g tensors, a rich low-temperature excitation spectrum, a staggered susceptibility, and a spin gap that opens on the application of a magnetic field. These phenomena are reminiscent of those previously observed in nonchiral staggered chains, which are explicable within the sine-Gordon quantum-field theory. In the present case, however, although the sineGordon model accounts well for the form of the temperature dependence of the heat capacity, the size of the gap and its measured linear field dependence do not fit with the sine-Gordon theory as it stands. We propose that the differences arise due to additional terms in the Hamiltonian resulting from the chiral structure of ½CuðpymÞðH2OÞ4SiF6 · H2O, particularly a uniform Dzyaloshinskii-Moriya coupling and a fourfold periodic staggered field.

Abstract:

Coherent control of individual molecular spins in nanodevices is a pivotal prerequisite for fulfilling the potential promised by molecular spintronics. By applying electric field pulses during time-resolved electron spin resonance measurements, we measure the sensitivity of the spin in several antiferromagnetic molecular nanomagnets to external electric fields. We find a linear electric field dependence of the spin states in Cr7Mn, an antiferromagnetic ring with a ground-state spin of S ¼ 1, and in a frustrated Cu3 triangle, both with coefficients of about 2 rad s−1=V m−1. Conversely, the antiferromagnetic ring Cr7Ni, isomorphic with Cr7Mn but with S ¼ 1=2, does not exhibit a detectable effect. We propose that the spinelectric field coupling may be used for selectively controlling individual molecules embedded in nanodevices.