Dissipative Landau-Zener transition with decoherence rate

An innovative microscopic model with a minimal number of parameters: tunneling splitting gap, external field sweeping velocity, and decoherence rate is used to describe dynamics of the dissipative Landau-Zener transition in the presence of the decoherence. In limiting cases, the derived equation of motion gives rise to the well-known Landau-Zener and Kayanuma formula. In a general case, the description demonstrates a non-monotonic flipping probability with respect to the sweeping velocity, which is also found in some other models. This non-monotony can be explained by considering the competition and timescale of the quantum tunneling, crossing period, and decoherence process. The simplicity and robustness of the theory offer a practical and novel description of the Landau-Zener transition. In addition, it promises an alternative method to the electron paramagnetic resonance in measuring the effective decoherence rate of relevant quantum systems.Comment: 8 pages, 2 figure

Quantum tunneling of magnetization in molecular spin

We examine the quantum tunneling of magnetization in molecular spin in weak interaction with a bath subject to Redfield master equation. By designing a microscopic model for a multilevel spin system using only a generic Hamiltonian and applying stationary approximation for excited doublets/singlets, we derive a key equation of motion for the quantum tunneling of magnetization process which is applicable in the whole temperature domain. From this equation, we find that in general three tunneling rates are needed to accurately describe the quantum tunneling process. More importantly, behavior of the quantum tunneling in the intermediate temperature domain where there exists a transition between incoherent and coherent quantum tunneling is also unraveled for the first time. Limiting cases at low and high temperature and/or low magnetic field are also worked out where some popular well-known results are reproduced. Last but not least, a new interpretation of the quantum tunneling of magnetization is proposed where we reveal the similarity between this relaxation process with a driven damped harmonic oscillator.Comment: 11 pages, 5 figure

Coherence/incoherence transition temperature in molecular spin

We examine the coherence/incoherence transition temperature of a generic molecular spin. Our results demonstrates that a molecular spin with a high coherence/incoherence transition temperature should possess a low spin number and low axiality, or high spin number and high axiality. Interestingly, the latter is better protected from the magnetic noises than the former and thus be the best candidate for a robust electron-based molecular spin qubit/qudit. The transition temperature can be further optimized if a large non-axial component of the spin Hamiltonian exists.Comment: 8 pages, 6 figure

Single Crystal Investigations Unravel the Magnetic Anisotropy of the “Square-In Square” Cr4Dy4 SMM Coordination Cluster

In the search for new single molecule magnets (SMM), i.e., molecular systems that can retain their magnetization without the need to apply an external magnetic field, a successful strategy is to associate 3d and 4f ions to form molecular coordination clusters. In order to efficiently design such systems, it is necessary to chemically project both the magnetic building blocks and the resultant interaction before the synthesis. Lanthanide ions can provide the required easy axis magnetic anisotropy that hampers magnetization reversal. In the rare examples of 3d/4f SMMs containing CrIII ions, the latter turn out to act as quasi-isotropic anchors which can also interact via 3d-4f coupling to neighbouring Ln centres. This has been demonstrated in cases where the intramolecular exchange interactions mediated by CrIII ions effectively reduce the efficiency of tunnelling without applied magnetic field. However, describing such high nuclearity systems remains challenging, from both experimental and theoretical perspectives, because the overall behaviour of the molecular cluster is heavily affected by the orientation of the individual anisotropy axes. These are in general non-collinear to each other. In this article, we combine single crystal SQUID and torque magnetometry studies of the octanuclear [Cr4Dy4(μ3-OH)4(μ-N3)4(mdea)4(piv)8]·3CH2Cl2 single molecule magnet (piv=pivalate and mdea=N-methyldiethanol amine). These experiments allowed us to probe the magnetic anisotropy of this complex which displays slow magnetization dynamics due to the peculiar arrangement of the easy-axis anisotropy on the Dy sites. New ab initio calculations considering the entire cluster are in agreement with our experimental results

Modifying the properties of 4f single-ion magnets by peripheral ligand functionalisation

We study the ligand-field splittings and magnetic properties of three Er-III single-ion magnets which differ in the peripheral ligand sphere but exhibit similar first coordination spheres by inelastic neutron scattering (INS) and SQUID magnetometry. The INS spectra of the three compounds are profoundly different pointing at a strong response of the magnetic behavior tominor structural changes, as they are e. g. encountered when depositing molecules on surfaces. The observation of several magnetic excitations within the J = 15/2 ground multiplet together with single-crystal magnetic measurements allows for the extraction of the sign and magnitude of all symmetry-allowed Stevens parameters. The parameter values and the energy spectrum derived from INS are compared to the results of state-of-the-art ab initio CASSCF calculations. Temperature-dependent alternating current (ac) susceptibility measurements suggest that the magnetisation relaxation in the investigated temperature range of 1.9 K < T < 5 K is dominated by quantum tunnelling of magnetisation and two-phonon Raman processes. The possibility of observing electron paramagnetic resonance transitions between the ground-state doublet states, which can be suppressed in perfectly axial single-ion magnets, renders the studied systems interesting as representations of quantum bits

The OpenMolcas Web: A Community-Driven Approach to Advancing Computational Chemistry

The developments of the open-source OpenMolcas chemistry software environment since spring 2020 are described, with a focus on novel functionalities accessible in the stable branch of the package or via interfaces with other packages. These developments span a wide range of topics in computational chemistry and are presented in thematic sections: electronic structure theory, electronic spectroscopy simulations, analytic gradients and molecular structure optimizations, ab initio molecular dynamics, and other new features. This report offers an overview of the chemical phenomena and processes OpenMolcas can address, while showing that OpenMolcas is an attractive platform for state-of-the-art atomistic computer simulations