AI Article Synopsis

  • The study focuses on the magnetic and electronic transport properties of a newly synthesized dinuclear Cu(ii)-naphthoisoamethyrin complex (PyCu), noting that little research has been done on similar systems with expanded porphyrins.
  • Using Density Functional Theory (DFT) and wave function methods, the research reveals that the magnetic interaction between the metal centers in PyCu is primarily ferromagnetic, with a coupling constant J of 14.2 cm.
  • The study further explores the spin-resolved transport properties of a device incorporating PyCu and gold nano-wires, suggesting its potential applications in spintronics.

Article Abstract

Although the magnetic and transport properties of molecular junction systems composed of metalled porphyrins or phthalocyanines have been broadly studied in recent years, to date no studies have been devoted to evaluate the aforementioned properties in junction systems featuring metalled expanded porphyrins as active elements. The present work reports a detailed theoretical study of the magnetic and electronic transport properties of the recently synthesized dinuclear Cu(ii)-naphthoisoamethyrin complex (PyCu). This is the first work on performing these kinds of studies using a magnetically coupled metallic expanded porphyrin as a molecular kernel. DFT and wave function-based methods have been used to determine the nature of the magnetic interaction between the metallic centres, characterized by the exchange coupling constant J, showing that although this was found to be weakly antiferromagnetic, after an exhaustive analysis it turns out that the coupling has a ferromagnetic nature with a value of J = 14.2 cm. Once the magnetic ground state of PyCu was rigorously established, the spin resolved transport properties of the device composed of the expanded porphyrin attached to two gold nano-wires were studied by means of the combination of DFT and the nonequilibrium Green's function formalism, in order to explore PyCu prospects as a possible spintronic device.

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Source
http://dx.doi.org/10.1039/c9dt01312aDOI Listing

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