arXiv subjects

Veacheslav Vieru

Publications and source records attributed to Veacheslav Vieru.

6 recordsLinked to original sources

arXiv2021

Rectangle-like hysteresis in a Dysprosium Metallacrown Magnet with Linear F-Dy-F Anisotropic Moiety

Single-molecule magnets (SMMs) exhibiting open hysteresis loops may potentially apply to molecule-based information processing and storage. However, the capacity to retain magnetic memory is always limited by zero-field quantum tunneling of magnetization (QTM). Herein, a well-designed dysprosium metallacrown SMM, consisting of an endohedral approximate linear F-Dy-F strong anisotropic moiety in a peripheral [15-MCNi-5] metallacrown (MC), is reported with the largest reversal barrier of 1060 cm-1 among d-f SMMs. Rectangle-like hysteresis loops are observed with the huge squareness (remanence/saturation magnetization) up to 97% at 2 K. More importantly, zero-field QTM step is phenomenologically removed by minimizing the dipole coupling and hyperfine interactions. The results demonstrate for the first time that zero-field QTM step can be eliminated via manipulating the ligand field and vanishing the external magnetic perturbations, which illuminates a promising blueprint for developing high-performance SMMs.

cond-mat.mes-hall↗

arXiv2020

Ferromagnetic kinetic exchange interaction in magnetic insulators

The superexchange theory predicts dominant antiferromagnetic kinetic interaction when the orbitals accommodating magnetic electrons are covalently bonded through diamagnetic bridging atoms/groups. Here we show that explicit consideration of magnetic and (leading) bridging orbitals, together with the electron transfer between the former, reveals a strong ferromagnetic kinetic exchange contribution. First principle calculations show that it is comparable in strength with antiferromagnetic superexchange in a number of magnetic materials with diamagnetic metal bridges. In particular, it is responsible for a very large ferromagnetic coupling ($-10$ meV) between the iron ions in a Fe$^{3+}$-Co$^{3+}$-Fe$^{3+}$ complex.

cond-mat.str-el↗

arXiv2020

Field-induced oscillation of magnetization blocking in holmium metallacrown magnet

Single-molecule magnets (SMMs) are promising elements for quantum informatics. In the presence of strong magnetic anisotropy, they exhibit magnetization blocking - a magnetic memory effect at the level of a single molecule. Recent studies have shown that the SMM performance scales with the height of magnetization blocking barrier. By employing molecular engineering this can be significantly modified, remaining independent from other external factors such as magnetic field. Taking advantage of hyperfine coupling of electronic and nuclear spins further enhances their functionality, however, a poor understanding of relaxation mechanisms in such SMMs limits the exploitation of nuclear-spin molecular qubits. Here we report the opening discovery of field-dependent oscillation of the magnetization blocking barrier in a new holmium metallacrown magnet driven by the switch of relaxation mechanisms involving hyperfine interaction. Single-crystal magnetic hysteresis measurements combined with first-principles calculations reveal an activated temperature dependence of magnetic relaxation dominated either by incoherent quantum tunneling of magnetization at anti-crossing points of exchange-hyperfine states or by Orbach-like processes at crossing points. We demonstrate that these relaxation mechanisms can be consecutively switched on and off by increasing the external field, which paves a way for manipulating the magnetization dynamics of SMMs using hyperfine interaction.

cond-mat.mes-hall↗

arXiv2018

Spin-orbital-lattice entangled states in cubic $d^1$ double perovskites

Interplay of spin-orbit coupling and vibronic coupling on heavy $d^1$ site of cubic double perovskites is investigated by ab initio calculations. The stabilization energy of spin-orbital-lattice entangled states is found comparable to or larger than the exchange interactions, suggesting the presence of Jahn-Teller dynamics in the systems. In Ba$_2$YMoO$_6$, the pseudo JT coupling enhances the mixing of the ground and excited spin-orbit multiplet states, which results in strong temperature dependence of effective magnetic moments. The entanglement of the spin and lattice degrees of freedom induces a strong magneto-elastic response. This multiferroic effect is at the origin of the recently reported breaking of local point symmetry accompanying the development of magnetic ordering in Ba$_2$NaOsO$_6$.

cond-mat.str-el↗

arXiv2017

Zeeman interaction and Jahn-Teller effect in $Γ_8$ multiplet

We present a thorough analysis of the interplay of magnetic moment and the Jahn-Teller effect in the $Γ_8$ cubic multiplet. We find that in the presence of dynamical Jahn-Teller effect, the Zeeman interaction remains isotropic, whereas the $g$ and $G$ factors can change their signs. The static Jahn-Teller distortion also can change the sign of these $g$ factors as well as the nature of the magnetic anisotropy. Combining the theory with state-of-the-art {\it ab initio} calculations, we analyzed the magnetic properties of Np$^{4+}$ and Ir$^{4+}$ impurity ions in cubic environment. The calculated $g$ factors of Np$^{4+}$ impurity agree well with experimental data. The {\it ab initio} calculation predicts strong Jahn-Teller effect in Ir$^{4+}$ ion in cubic environment and the strong vibronic reduction of $g$ and $G$ factors.

cond-mat.mtrl-sci↗

arXiv2016

Giant exchange interaction in mixed lanthanides

Combining strong magnetic anisotropy with strong exchange interaction is a long standing goal in the design of quantum magnets. The lanthanide complexes, while exhibiting a very strong ionic anisotropy, usually display a weak exchange coupling, amounting to only a few wavenumbers. Recently, an isostructural series of mixed Ln$^{3+}$-N$_2^{3-}$-Ln$^{3+}$ (Ln $=$ Gd, Tb, Dy, Ho, Er) have been reported, in which the exchange splitting is estimated to reach hundreds wavenumbers. The microscopic mechanism governing the unusual exchange interaction in these compounds is revealed here by combining detailed modeling with density-functional theory and {\it ab initio} calculations. We find it to be basically kinetic and highly complex, involving non-negligible contributions up to seventh power of total angular momentum of each lanthanide site. The performed analysis also elucidates the origin of magnetization blocking in these compounds. Contrary to general expectations the latter is not always favored by strong exchange interaction.

cond-mat.str-el↗