4.6 Article

Ferrous to Ferric Transition in Fe-Phthalocyanine Driven by NO2 Exposure

期刊

CHEMISTRY-A EUROPEAN JOURNAL
卷 27, 期 10, 页码 3526-3535

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.202004932

关键词

molecular spintronics; oxidation state; phthalocyanine; surface science; XMCD

资金

  1. University of Padova [CARL-SID17 BIRD2017-UNIPD]
  2. European Research Council (ERC) under the European Union's Horizon 2020 research and innovation programme [725767]
  3. Projekt DEAL
  4. European Research Council (ERC) [725767] Funding Source: European Research Council (ERC)

向作者/读者索取更多资源

Iron phthalocyanine has unique magnetic properties due to the open-shell electronic structure of the central metal ion, making it a valuable catalyst in various reactions. Surface deposition on Cu(100) alters the charge distribution and magnetic properties of the molecule, affecting the spin state of the iron ion. Exposure to different doses of NO2 at room temperature at the metalorganic/metal interface results in three different spin configurations, demonstrating the tunability of the magnetic properties of the iron ion.
Due to its unique magnetic properties offered by the open-shell electronic structure of the central metal ion, and for being an effective catalyst in a wide variety of reactions, iron phthalocyanine has drawn significant interest from the scientific community. Nevertheless, upon surface deposition, the magnetic properties of the molecular layer can be significantly affected by the coupling occurring at the interface, and the more reactive the surface, the stronger is the impact on the spin state. Here, we show that on Cu(100), indeed, the strong hybridization between the Fe dstates of FePc and the sp-band of the copper substrate modifies the charge distribution in the molecule, significantly influencing the magnetic properties of the iron ion. The FeII ion is stabilized in the low singlet spin state (S= 0), leading to the complete quenching of the molecule magnetic moment. By exploiting the FePc/Cu(100) interface, we demonstrate that NO2 dissociation can be used to gradually change the magnetic properties of the iron ion, by trimming the gas dosage. For lower doses, the FePc film is decoupled from the copper substrate, restoring the gas phase triplet spin state (S= 1). A higher dose induces the transition from ferrous to ferric phthalocyanine, in its intermediate spin state, with enhanced magnetic moment due to the interaction with the atomic ligands. Remarkably, in this way, three different spin configurations have been observed within the same metalorganic/metal interface by exposing it to different doses of NO2 at room temperature.

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