Filters

20203

More filters

2020 - 20223
Reset filters

Settings

Author: Kuhrt, Robert × Has files: Yes ×

Search Results

Now showing 1 - 3 of 3
  • Thumbnail Image
    Item
    Integrated molecular diode as 10 MHz half-wave rectifier based on an organic nanostructure heterojunction
    ([London] : Nature Publishing Group UK, 2020) Li, Tianming; Bandari, Vineeth Kumar; Hantusch, Martin; Xin, Jianhui; Kuhrt, Robert; Ravishankar, Rachappa; Xu, Longqian; Zhang, Jidong; Knupfer, Martin; Zhu, Feng; Yan, Donghang; Schmidt, Oliver G.
    Considerable efforts have been made to realize nanoscale diodes based on single molecules or molecular ensembles for implementing the concept of molecular electronics. However, so far, functional molecular diodes have only been demonstrated in the very low alternating current frequency regime, which is partially due to their extremely low conductance and the poor degree of device integration. Here, we report about fully integrated rectifiers with microtubular soft-contacts, which are based on a molecularly thin organic heterojunction and are able to convert alternating current with a frequency of up to 10 MHz. The unidirectional current behavior of our devices originates mainly from the intrinsically different surfaces of the bottom planar and top microtubular Au electrodes while the excellent high frequency response benefits from the charge accumulation in the phthalocyanine molecular heterojunction, which not only improves the charge injection but also increases the carrier density.
  • Thumbnail Image
    Item
    Charge transfer characteristics of F6TCNNQ–gold interface
    (Chichester [u.a.] : Wiley, 2020) Kuhrt, Robert; Hantusch, Martin; Knupfer, Martin; Büchner, Bernd
    The metal–organic interface between polycrystalline gold and hexafluorotetracyanonaphthoquinodimethane (F6TCNNQ) was investigated by photoelectron spectroscopy with the focus on the charge transfer characteristics from the metal to the molecule. The valence levels, as well as the core levels of the heterojunction, indicate a full electron transfer and a change in the chemical environment. The changes are observed in the first F6TCNNQ layers, whereas for further film growth, only neutral F6TCNNQ molecules could be detected. New occupied states below the Fermi level were observed in the valence levels, indicating a lowest unoccupied molecular orbital (LUMO) occupation due to the charge transfer. A fitting of the spectra reveals the presence of a neutral and a charged F6TCNNQ molecules, but no further species were present.
  • Thumbnail Image
    Item
    Synthesis and charge transfer characteristics of a ruthenium–acetylide complex
    (London : Royal Society of Chemistry, 2020) Kuhrt, Robert; Ho, Po-Yuen; Hantusch, Martin; Lissel, Franziska; Blacque, Olivier; Knupfer, Martin; Büchner, Bernd
    A novel ruthenium–acetylide complex was synthesised and characterised in solid state and solution. Thin films of the complex were evaporated on silver and gold foils in ultra high vacuum in order to probe the electronic properties with photoemission spectroscopy. The charge transfer characteristics of the complex with the strong acceptor F6TCNNQ were investigated by UV-vis absorption in solution as well as at an interface with photoemission spectroscopy. A new excitation in the former optical gap of the pristine materials was probed in solution. Moreover, it was possible to identify the oxidised complex as well as the reduced acceptor by X-ray photoemission spectroscopy. In particular, our data reveal that oxidation of the complex mainly occurs at the Ru centre. The charge transfer can be characterised as localised and mainly ionic although signs of a reaction of the acceptors aminogroups with the ruthenium–acetylide complex were found.