Patterning molecular scale paramagnets at Au Surface: A root to Magneto-Molecular-Electronics

Few examples of the exploitation of molecular magnetic properties in molecular electronics are known to date. Here we propose the realization of Self assembled monolayers (SAM) of a particular stable organic radical. This radical is meant to be used as a standard molecule on which to prove the validity of a single spin reading procedure known as ESR-STM. We also discuss a range of possible applications, further than ESR-STM, of magnetic monolayers of simple purely organic magnetic molecule.Comment: This preprint is currently partially under revisio

Multi-storey Building Retrofit by ADAS- Equipped Braces

Incorporation of dissipative bracing systems is an emerging seismic retrofit strategy for frame structures. Among the several types of devices currently adopted as passive protection elements, Added Damping and Stiffness (ADAS) steel dissipaters have a well-established tradition. This is a consequence of their plain working principle, based on the elastic-plastic behaviour of the constituting plates, as well as of their relatively easy installation. In spite of this, the design of ADAS dampers is not simple, because it requires a proper balance between the addition of energy dissipation and horizontal translational stiffness. An energy-based design criterion is formulated to this aim in this study, which directly relates the total number of plates of the dissipaters to the supplemental damping energy needed to jointly reduce stress states and storey drifts, expressly taking into account the reduction of the fundamental vibration period due to the stiffening effect of the bracing system. A seismic retrofit intervention is demonstratively designed by applying this criterion for a 6-storey building with reinforced concrete structure, an assessment analysis of which shows poor seismic performance capacities. A comparative analysis among three different installation hypotheses of the ADAS devices allows to select the distribution capable of attaining the best performance of the retrofit measure

Quantum Double and Differential Calculi

We show that bicovariant bimodules as defined by Woronowicz are in one to one correspondence with the Drinfeld quantum double representations. We then prove that a differential calculus associated to a bicovariant bimodule of dimension n is connected to the existence of a particular (n+1)--dimensional representation of the double. An example of bicovariant differential calculus on the non quasitriangular quantum group E_q(2) is developed. The construction is studied in terms of Hochschild cohomology and a correspondence between differential calculi and 1-cocycles is proved. Some differences of calculi on quantum and finite groups with respect to Lie groups are stressed.Comment: Revised version with added cohomological analysis. 14 pages, plain te

Magnetic properties and spin dynamics in single molecule paramagnets Cu6Fe and Cu6Co

The magnetic properties and the spin dynamics of two molecular magnets have been investigated by magnetization and d.c. susceptibility measurements, Electron Paramagnetic Resonance (EPR) and proton Nuclear Magnetic Resonance (NMR) over a wide range of temperature (1.6-300K) at applied magnetic fields, H=0.5 and 1.5 Tesla. The two molecular magnets consist of CuII(saldmen)(H2O)}6{FeIII(CN)6}](ClO4)38H2O in short Cu6Fe and the analog compound with cobalt, Cu6Co. It is found that in Cu6Fe whose magnetic core is constituted by six Cu2+ ions and one Fe3+ ion all with s=1/2, a weak ferromagnetic interaction between Cu2+ moments through the central Fe3+ ion with J = 0.14 K is present, while in Cu6Co the Co3+ ion is diamagnetic and the weak interaction is antiferromagnetic with J = -1.12 K. The NMR spectra show the presence of non equivalent groups of protons with a measurable contact hyperfine interaction consistent with a small admixture of s-wave function with the d-function of the magnetic ion. The NMR relaxation results are explained in terms of a single ion (Cu2+, Fe3+, Co3+) uncorrelated spin dynamics with an almost temperature independent correlation time due to the weak magnetic exchange interaction. We conclude that the two molecular magnets studied here behave as single molecule paramagnets with a very weak intramolecular interaction, almost of the order of the dipolar intermolecular interaction. Thus they represent a new class of molecular magnets which differ from the single molecule magnets investigated up to now, where the intramolecular interaction is much larger than the intermolecular one

Energy Barrier Enhancement by Ligand Substitution in Tetrairon(III) Single Molecule Magnets

A dramatic increase of the energy barrier (Ueff) in tetrairon(III) single-mol. magnets can be achieved by simple chem. modification. Site-specific replacement of the six methoxide bridges in [Fe4(OMe)6(dpm)6] (Hdpm = dipivaloylmethane; Ueff/kB = 3.5 K) with two tripodal 1,1,1-tris(hydroxymethyl)ethane (H3thme) ligands affords [Fe4(thme)2(dpm)6] with Ueff/kB = 15.6(2) K and a magnetic relaxation time exceeding 1000 s at T <0.2 K. The prepd. complex is trigonal, space group R-3c, Z = 6, R1 = 0.0370, R2 = 0.1089

Two fermion relativistic bound states: hyperfine shifts

We discuss the hyperfine shifts of the Positronium levels in a relativistic framework, starting from a two fermion wave equation where, in addition to the Coulomb potential, the magnetic interaction between spins is described by a Breit term. We write the system of four first order differential equations describing this model. We discuss its mathematical features, mainly in relation to possible singularities that may appear at finite values of the radial coordinate. We solve the boundary value problems both in the singular and non singular cases and we develop a perturbation scheme, well suited for numerical computations, that allows to calculate the hyperfine shifts for any level, according to well established physical arguments that the Breit term must be treated at the first perturbative order. We discuss our results, comparing them with the corresponding values obtained from semi-classical expansions.Comment: 16 page

Integrated photonic structures for photon-mediated entanglement of trapped ions

Trapped atomic ions are natural candidates for quantum information processing and have the potential to realize or improve quantum computing, sensing, and networking. These applications often require the collection of individual photons emitted from ions into guided optical modes, in some cases for the production of entanglement between separated ions. Proof-of-principle demonstrations of such photon collection from trapped ions have been performed using high-numerical-aperture lenses and single-mode fibers, but integrated photonic elements in ion-trap structures offer advantages in scalability and manufacturabilty over traditional optics. In this paper we analyze structures monolithically fabricated with an ion trap for collecting single photons from ions, coupling them into integrated waveguides, and manipulating them via interference. We discuss practical considerations for realizing photon-mediated entanglement between trapped ions using these waveguide-based devices.Comment: 17 pages, 6 figures, 2 table