The field of molecular spintronics exploits the properties of organic molecules possessing a magnetic moment, either native in the form of radicals or induced by the insertion of transition metal ...magnetic ions. To realize logic or storage molecular spin-tronics devices, molecules with stable different magnetic states should be deposited on a substrate, and switching between the states controllably achieved. By means of a first-principles calculations, we have devised a functional molecule exhibiting different magnetic states upon structural changes induced by current injection. We investigate the prototypical case of non-planar M-Phthalocyanine (MPc), where M is a transition-metal ion belonging to the 4d and 5d series. We find that for ZrPc and HfPc deposited on a graphene decorated Ni(111) substrate, two different structural conformations could be stabilized, for which the molecules attain different magnetic states depending on the position of the M ion - whether above the Pc or between the Pc and the substrate -, acting therefore as molecular magnetic button. Our work indicates an intuitive way to engineer a magnetic molecular switch with tailored properties, starting from the knowledge of the basic atomic properties of elements and surfaces.
The strength of electronic correlation effects in the spin-dependent electronic structure of ferromagnetic bcc Fe(110) has been investigated by means of spin and angle-resolved photoemission ...spectroscopy. The experimental results are compared to theoretical calculations within the three-body scattering approximation and within the dynamical mean-field theory, together with one-step model calculations of the photoemission process. This comparison indicates that the present state of the art many-body calculations, although improving the description of correlation effects in Fe, give too small mass renormalizations and scattering rates thus demanding more refined many-body theories including nonlocal fluctuations.
Learning the art of exploiting the interplay between different units at the atomic scale is a fundamental step in the realization of functional nano-architectures and interfaces. In this context, ...understanding and controlling the magnetic coupling between molecular centers and their environment is still a challenging task. Here we present a combined experimental-theoretical work on the prototypical case of the bis(phthalocyaninato)-lanthanide(III) (LnPc2) molecular nanomagnets magnetically coupled to a Ni substrate. By means of X-ray magnetic circular dichroism we show how the coupling strength can be tuned by changing the Ln ion. The microscopic parameters of the system are determined by ab-initio calculations and then used in a spin Hamiltonian approach to interpret the experimental data. By this combined approach we identify the features of the spin communication channel: the spin path is first realized by the mediation of the external (5d) electrons of the Ln ion, keeping the characteristic features of the inner 4 f orbitals unaffected, then through the organic ligand, acting as a bridge to the external world.
We present a density-functional theoretical investigation of the electronic and magnetic properties of octametallic Cr-based molecular antiferromagnetic rings. The presence of the divalent magnetic ...ion M unbalances the charge and the spin of the parent Cr8 ring, leading to a finite total spin in the molecules. Results are presented for Cr8, i.e., Cr8F8(O2CH)16 (1), and for Cr7M rings belonging to two different derivatives, i.e., Me2NH2Cr7MF8(O2CH)16, with M = Ni, Mn, Fe, and Cu, and MeCH3 (2, “green” derivative), and Cr7 NiF3(C6H10NO5)(O2CH)15 (H2O) (3, “purple” derivative). Exchange interaction parameters have been extracted from broken-symmetry calculations and compared with the available experiments; in agreement with them, we find that exchange parameters are rather similar in the two derivatives, although somewhat larger in the “purple” derivative. The analysis of the electronic properties shows some differences depending on M, in particular in the size of the highest occupied molecular orbital to lowest unoccupied molecular orbital (HOMO−LUMO) gaps. For all the “green” rings we observe that the HOMOs are localized on the divalent ion site, while the HOMOs for the “purple” Cr7Ni have a more delocalized nature; LUMOs, instead, are, except for “green” Cr7Cu, localized on the Cr atoms opposite to the M site. We discuss how these findings may show up in terms of an asymmetric I−V curve in molecular junctions working in the sequential tunneling regime, or help in discerning the orientation of the molecules with respect to a surface, in scanning tunneling experiments.
Background
Erythematous papulopustular eruption (EPPE) is the most frequent skin adverse event to epidermal growth factor receptor (EGFR) inhibitors but its histopathologic features have been poorly ...studied. As EPPE is a strong predictor of patient's treatment response, the EPPE histopathologic features and their correlations with skin eruption severity and involved drug were investigated.
Method
An involved skin biopsy was carried out in 39 informed patients treated with EGFR inhibitors (mainly cetuximab and erlotinib). The cutaneous changes in hematoxylin‐eosin stained sections were evaluated.
Results
The EPPE to EGFR inhibitors is histopathologically characterized by neutrophilic subcorneal or intraepidermal pustules and polymorphous infiltrate of the superficial dermis during the earliest phases and by lymphocytic perifolliculitis and/or suppurative folliculitis at a later phase. The widespread dermis inflammation was more frequent in severe EPPEs and in patients treated with cetuximab, while the hair follicle inflammation was observed only in mild/moderate EPPEs.
Conclusion
Our study shows the histopathologic signs of EPPE and their correlation with clinical severity and the offending drug.
We report an in-depth study on how spin information propagates at supramolecular scale through a family of heteroaromatic linkers. By density-functional theory calculations, we rationalize the ...behavior of a series of Cr7Ni dimers for which we are able to systematically change the aromatic linker thus tuning the strength of the magnetic interaction, as experimentally shown by low temperature micro-SQUID and specific heat measurements. We also predict a cos2 dependence of the magnetic coupling on the twisting angle between the aromatic cycles in bicyclic linkers, a mechanism parallel to charge transport on similar systems L. Venkataraman et al., Nature (London) 442, 904 (2006).
The ICARUS T600 detector, with about 500 tons of active mass, is the largest Liquid Argon Time Projection Chamber (LAr TPC) ever realised. In 2013 ICARUS concluded an about 4 years long experiment ...with the T600 detector at the LNGS underground laboratory, taking data both with the CNGS neutrino beam and cosmic rays. This very successful experiment demonstrated the high spatial and energy resolutions, electron/photon separation and particle identification capabilities (via dE/dx vs range measurements) of the LAr technology. ICARUS Collaboration refurbished the T600 at CERN, in order to move it to FNAL in the framework of the SBN experiment, to serve as far detector in studies on the short baseline neutrino oscillations. A fundamental part of ICARUS is the light collection system, made of 360 Hamamatsu R5912-MOD, 8 in. diameter, PMT's. This system is dedicated to three tasks: the generation of a light based trigger signal, the identification of the time of occurrence (t0) of each interaction with high time precision and the initial recognition of event topology for fast event selection purposes.
Using first-principles calculations we demonstrate sizable exchange coupling between a magnetic molecule and a magnetic substrate via a graphene layer. As a model system we consider cobaltocene (CoCp ...sub(2)) adsorbed on graphene deposited on Ni(111). We find that the magnetic coupling is antiferromagnetic and is influenced by the molecule structure, the adsorption geometry, and the stacking of graphene on the substrate. We show how the coupling can be tuned by the intercalation of a magnetic monolayer, such as Fe or Co, between graphene and Ni(111). We identify the leading mechanism responsible for the coupling to be the spatial and energy matching of the frontier orbitals of CoCp sub(2) and graphene close to the Fermi level. Graphene plays the role of an electronic decoupling layer while allowing effective spin communication between molecule and substrate.