Suchergebnisse

Nanoscale magnetic systems play a decisive role in areas ranging from biology to spintronics. Although, in principle, THz electron paramagnetic resonance (EPR) provides high-resolution access to their properties, lack of sensitivity has precluded realizing this potential. To resolve this issue, the principle of plasmonic enhancement of electromagnetic fields that is used in electric dipole spectroscopies with great success is exploited, and a new type of resonators for the enhancement of THz magnetic fields in a microscopic volume is proposed. A resonator composed of an array of diabolo antennas with a back-reflecting mirror is designed and fabricated. Simulations and THz EPR measurements demonstrate a 30-fold signal increase for thin film samples. This enhancement factor increases to a theoretical value of 7500 for samples confined to the active region of the antennas. These findings open the door to the elucidation of fundamental processes in nanoscale samples, including junctions in spintronic devices or biological membranes. ; This research has been supported by European Union's Horizon 2020 programme FET-OPEN project PETER, GA 767 227. The Center for Integrated Quantum Science and Technology (IQST), and the Carl Zeiss Foundation are also acknowledged. The authors thank Brno University of Technology (FSI-S-20-6485) and the GAČR project 20–28573S. The authors acknowledge financial support from the Spanish Ministry of Science, Innovation and Universities (national project RTI2018-094830-B-100 and the project MDM-2016-0618 of the Maria de Maeztu Units of Excellence Program) and the Basque Government (grant No. IT1164-19). The authors thank Prof. Sabine Ludwigs and David Neusser for access to the SnowJet cleaner. The authors thank Thomas Keating Ltd. for providing the quasi-optical bench used for the transmission measurements of the PMR. The authors thank Dennis Schäfter for the valuable support provided for the Python scripts and Martin Konečný for useful discussions. Open access funding enabled and organized ...

Hybrid materials consisting of organic semiconductors and molecular quantum bits promise to provide a novel platform for quantum spintronic applications. However, investigations of such materials, elucidating both the electrical and quantum dynamical properties of the same material have never been reported. Here the preparation of hybrid materials consisting of conducting polymers and molecular quantum bits is reported. Organic field-effect transistor measurements demonstrate that the favorable electrical properties are preserved in the presence of the qubits. Chemical doping introduces charge carriers into the material, and variable-temperature charge transport measurements reveal the existence of mobile charge carriers at temperatures as low as 15 K. Importantly, quantum coherence of the qubit is shown to be preserved up to temperatures of at least 30 K, that is, in the presence of mobile charge carriers. These results pave the way for employing such hybrid materials in novel molecular quantum spintronic architectures. ; This work received financial support from the European Union's Horizon 2020 Research and Innovation Programme under Grant Agreement 767227 (FET-OPEN project PETER), the Center for Integrated Quantum Science and Technology (IQST), and the Carl Zeiss Foundation. The authors thank Benjamin Gerlach for experimental contributions at early stages of this work. The authors gratefully acknowledge useful discussions with James Borchert, Tobias Wollandt, and Dr. Hagen Klauk of the Max Planck Institute of Solid State Research in Stuttgart. The authors thank David Weißhaupt (IHT, University of Stuttgart) for cutting the transistor substrates. Open access funding enabled and organized by Projekt DEAL.

Total control over the electronic spin relaxation in molecular nanomagnets is the ultimate goal in the design of new molecules with evermore realizable applications in spin-based devices. For single-ion lanthanide systems, with strong spin–orbit coupling, the potential applications are linked to the energetic structure of the crystal field levels and quantum tunneling within the ground state. Structural engineering of the timescale of these tunneling events via appropriate design of crystal fields represents a fundamental challenge for the synthetic chemist, since tunnel splittings are expected to be suppressed by crystal field environments with sufficiently high-order symmetry. Here, we report the long missing study of the effect of a non-linear (C₄) to pseudo-linear (D₄𝒅) change in crystal field symmetry in an otherwise chemically unaltered dysprosium complex. From a purely experimental study of crystal field levels and electronic spin dynamics at milliKelvin temperatures, we demonstrate the ensuing threefold reduction of the tunnel splitting. ; M.A.S., U.B.H., K.L., and J.Be. acknowledge financial support from the Danish Research Councils for Independent Research (12-125226). M.A.S., U.B.H., M.R, and K.L. acknowledge DANSCATT for financial support for the neutron scattering experiments. For the experiments conducted at FRM II, this project has received funding from the European Union's 7th Framework Programme for research, technological development and demonstration under the NMI3-II Grant number 283883. M.A.S. thanks the Oticon Foundation (16-2669), and the Augustinus Foundation (16-2917) for financial support in relation to a research stay at Institut fur Physikalische Chemie, Universitat Stuttgart, Germany. M.P. and J.v.S. thank the DFG for funding (SL104/5-1). K.S.P. thanks the Danish Research Council for Independent Research for a DFF-Sapere Aude Research Talent grant (4090-00201). E.B., A.A, and, J.Ba. acknowledge the financial support of Spanish MINECO project MAT2017-83468-R. M.J. acknowledges the ...

Total control over the electronic spin relaxation in molecular nanomagnets is the ultimate goal in the design of new molecules with evermore realizable applications in spin-based devices. For single-ion lanthanide systems, with strong spin-orbit coupling, the potential applications are linked to the energetic structure of the crystal field levels and quantum tunneling within the ground state. Structural engineering of the timescale of these tunneling events via appropriate design of crystal fields represents a fundamental challenge for the synthetic chemist, since tunnel splittings are expected to be suppressed by crystal field environments with sufficiently high-order symmetry. Here, we report the long missing study of the effect of a non-linear (C4) to pseudo-linear (D4d) change in crystal field symmetry in an otherwise chemically unaltered dysprosium complex. From a purely experimental study of crystal field levels and electronic spin dynamics at milliKelvin temperatures, we demonstrate the ensuing threefold reduction of the tunnel splitting. ; M.A.S., U.B.H., K.L., and J.Be. acknowledge financial support from the Danish Research Councils for Independent Research (12-125226). M.A.S., U.B.H., M.R, and K.L. acknowledge DANSCATT for financial support for the neutron scattering experiments. For the experiments conducted at FRM II, this project has received funding from the European Union's 7th Framework Programme for research, technological development and demonstration under the NMI3-II Grant number 283883. M.A.S. thanks the Oticon Foundation (16-2669), and the Augustinus Foundation (16-2917) for financial support in relation to a research stay at Institut für Physikalische Chemie, Universität Stuttgart, Germany. M.P. and J.v.S. thank the DFG for funding (SL104/5-1). K.S.P. thanks the Danish Research Council for Independent Research for a DFF-Sapere Aude Research Talent grant (4090-00201). E.B., A.A, and, J.Ba. acknowledge the financial support of Spanish MINECO project MAT2017-83468-R. M.J. acknowledges the Swiss National Science Foundation. ; Peer reviewed