No Arabic abstract
We investigate the role of topology and distortions in the quantum dynamics of magnetic molecules, using a cyclic spin system as reference. We consider three variants of antiferromagnetic molecular ring, i.e. Cr$_8$, Cr$_7$Zn and Cr$_7$Ni, characterized by low lying states with different total spin $S$. We theoretically and experimentally study the low-temperature behavior of the magnetic torque as a function of the applied magnetic field. Near level crossings, this observable selectively probes quantum fluctuations of the total spin ($S$ mixing) induced by lowering of the ideal ring symmetry. We show that while a typical distortion of a model molecular structure is very ineffective in opening new $S$-mixing channels, the spin topology is a major ingredient to control the degree of $S$ mixing. This conclusion is further substantiated by low-temperature heat capacity measurements.
We investigate theoretically the spin-spin interaction of two-electrons in vertically coupled QDs as a function of the angle between magnetic field and growth axis. Our numerical approach is based on a real-space description of single-particle states in realistic samples and exact diagonalization of carrier-carrier Coulomb interaction. In particular, the effect of the in-plane field component on tunneling and, therefore, spin-spin interaction will be discussed; the singlet-triplet phase diagram as a function of the field strength and direction is drawn.
It is widely admitted that the helical conformation of certain chiral molecules may induce a sizable spin selectivity observed in experiments. Spin selectivity arises as a result of the interplay between a helicity-induced spin-orbit coupling and electric dipole fields in the molecule. From the theoretical point of view, different phenomena might affect the spin dynamics in helical molecules, such as quantum dephasing, dissipation and the role of metallic contacts. Previous studies neglected the local deformation of the molecule about the carrier thus far, but this assumption seems unrealistic to describe charge transport in molecular systems. We introduce an effective model describing the electron spin dynamics in a deformable helical molecule with weak spin-orbit coupling. We find that the electron-lattice interaction allows the formation of stable solitons such as bright solitons with well defined spin projection onto the molecule axis. We present a thorough study of these bright solitons and analyze their possible impact on the spin dynamics in deformable helical molecules.
Scanning tunneling microscopy (STM) can be used to detect inelastic spin transitions in magnetic nano-structures comprising only a handful of atoms. Here we demonstrate that STM can uniquely identify the electrostatic spin crossover effect, whereby the exchange interaction between two magnetic centers in a magnetic molecule changes sign as a function of an external electric field. The fingerprint of such effect is a large drop in the differential conductance as the bias increases. Crucially in the case of a magnetic dimer the spin crossover transition inverts the order between the ground state and the first excited state, but does not change their symmetry. This means that at both sides of the conductance drop associated to the spin crossover transition there are two inelastic transition between the same states. The corresponding conductance steps split identically in a magnetic field and provide a unique way to identify the electrostatic spin crossover.
We address the electronically induced anisotropy field acting on a spin moment comprised in a vibrating magnetic molecule located in the junction between ferromagnetic metals. Under weak coupling between the electrons and molecular vibrations, the nature of the anisotropy can be changed from favoring a high spin (easy axis) magnetic moment to a low spin (easy plane) by applying a temperature difference or a voltage bias across the junction. For unequal spin-polarizations in the ferromagnetic metals it is shown that the character of the anisotropy is essentially determined by the properties of the weaker ferromagnet. By increasing the temperature in this metal, or introducing a voltage bias, its influence can be suppressed such that the dominant contribution to the anisotropy is interchanged to the stronger ferromagnet. With increasing coupling strength between the molecular vibrations and the electrons, the nature of the anisotropy is locked into favoring easy plane magnetism.
Artificial spin ice systems have seen burgeoning interest due to their intriguing physics and potential applications in reprogrammable memory, logic and magnonics. In-depth comparisons of distinct artificial spin systems are crucial to advancing the field and vital work has been done on characteristic behaviours of artificial spin ices arranged on different geometric lattices. Integration of artificial spin ice with functional magnonics is a relatively recent research direction, with a host of promising early results. As the field progresses, studies examining the effects of lattice geometry on the magnonic response are increasingly significant. While studies have investigated the effects of different lattice tilings such as square and kagome (honeycomb), little comparison exists between systems comprising continuously-connected nanostructures, where spin-waves propagate through the system via exchange interaction, and systems with nanobars disconnected at vertices where spin-waves are transferred via stray dipolar-field. Here, we perform a Brillouin light scattering study of the magnonic response in two kagome artificial spin ices, a continuously-connected system and a disconnected system with vertex gaps. We observe distinctly different high-frequency dynamics and characteristic magnetization reversal regimes between the systems, with key distinctions in system microstate during reversal, internal field profiles and spin-wave mode quantization numbers. These observations are pertinent for the fundamental understanding of artificial spin systems and the design and engineering of such systems for functional magnonic applications.