arXiv subjects

Wolfgang Wernsdorfer

Publications and source records attributed to Wolfgang Wernsdorfer.

69 records · Page 4Linked to original sources

arXiv2016

Studies on the Magnetic Ground State of a Spin Möbius Strip

Here we report the synthesis, structure and detailed characterisation of three n-membered oxovanadium rings, Na$_n$[(V=O)$_n$Na$_n$(H$_2$O)$_n$($α$, $β$, or $γ$-CD)$_2$]$m$H$_2$O (n = 6, 7, or 8), prepared by the reactions of (V=O)SO$_4$$\cdot$$x$H$_2$O with $α$, $β$, or $γ$-cyclodextrins (CDs) and NaOH in water. Their alternating heterometallic vanadium/sodium cyclic core structures were sandwiched between two CD moieties such that O-Na-O groups separated neighbouring vanadyl ions. Antiferromagnetic interactions between the $S$ = 1/2 vanadyl ions led to $S$ = 0 ground states for the even-membered rings, but to two quasi-degenerate $S$ = 1/2 states for the spin-frustrated heptanuclear cluster.

cond-mat.str-el↗

arXiv2013

Supramolecular Spin Valves

Magnetic molecules possess a high potential as building blocks for the design of spintronic devices. Moreover, the use of molecular materials opens the way for the controlled use of bottom-up, e.g. supramolecular, processing techniques combining massively parallel self-fabrication with conventional top-down nanostructuring techniques. The development of solid state spintronic devices based on the giant magnetoresistance (GMR), tunnel magnetoresistance (TMR), and spin valve effects has revolutionized the field of magnetic memory applications. Recently, organic semiconductors were inserted into nanometer sized tunnel junctions allowing enhancement of spin reversal, giant magneto-resistance behaviour was observed in single non-magnetic molecules coupled to magnetic electrodes, and the use of the quantum tunnelling properties of single-molecule magnets (SMMs) in hybrid devices was proposed. Herein, we present an original device in which a non-magnetic molecular quantum dot, made of a single-wall carbon nanotube (SWCNT) contacted with non-magnetic electrodes, is laterally coupled via supramolecular interactions to a TbPc2-SMM (Pc = phthalocyanine), which provides a localized magnetic moment. The conductance through the SWCNT is modulated by sweeping the magnetic field, exhibiting magnetoresistance ratios up to 300% between fully polarized and non-polarized SMMs below 1 K. We thus demonstrate the functionality of a supramolecular spin valve without magnetic leads. Our results open up prospects of circuit-integration and implementation of new device capabilities.

cond-mat.mes-hall↗

arXiv2013

Landau-Zener tunneling of a single Tb3+ magnetic moment allowing the electronic read-out of a nuclear spin

A multi-terminal device based on a carbon nanotube quantum dot was used at very low tem- perature to probe a single electronic and nuclear spin embedded in a bis-phthalocyanine Terbium (III) complex (TbPc2). A spin-valve signature with large conductance jumps was found when two molecules were strongly coupled to the nanotube. The application of a transverse field separated the magnetic signal of both molecules and enabled single-shot read-out of the Terbium nuclear spin. The Landau-Zener (LZ) quantum tunneling probability was studied as a function of field sweep rate, establishing a good agreement with the LZ equation and yielding the tunnel splitting Δ. It was found that ? increased linearly as a function of the transverse field. These studies are an essential prerequisite for the coherent manipulation of a single nuclear spin in TbPc2.

cond-mat.mes-hall↗

arXiv2012

Dynamics and Dissipation induced by Single-Electron Tunneling in Carbon Nanotube Nanoelectromechanical Systems

We demonstrate the effect of single-electron tunneling (SET) through a carbon nanotube quantum dot on its nanomechanical motion. We find that the frequency response and the dissipation of the nanoelectromechanical system (NEMS) to SET strongly depends on the electronic environment of the quantum dot, in particular on the total dot capacitance and the tunnel coupling to the metal contacts. Our findings suggest that one could achieve quality factors of 10$^{6}$ or higher by choosing appropriate gate dielectrics and/or by improving the tunnel coupling to the leads.

cond-mat.mes-hall↗

arXiv2011

First order $0/π$ quantum phase transition in the Kondo regime of a superconducting carbon nanotube quantum dot

We study a carbon nanotube quantum dot embedded into a SQUID loop in order to investigate the competition of strong electron correlations with proximity effect. Depending whether local pairing or local magnetism prevails, a superconducting quantum dot will respectively exhibit positive or negative supercurrent, referred to as a 0 or $π$ Josephson junction. In the regime of strong Coulomb blockade, the 0 to $π$ transition is typically controlled by a change in the discrete charge state of the dot, from even to odd. In contrast, at larger tunneling amplitude the Kondo effect develops for an odd charge (magnetic) dot in the normal state, and quenches magnetism. In this situation, we find that a first order 0 to $π$ quantum phase transition can be triggered at fixed valence when superconductivity is brought in, due to the competition of the superconducting gap and the Kondo temperature. The SQUID geometry together with the tunability of our device allows the exploration of the associated phase diagram predicted by recent theories. We also report on the observation of anharmonic behavior of the current-phase relation in the transition regime, that we associate with the two different accessible superconducting states. Our results ultimately reveal the spin singlet nature of the Kondo ground state, which is the key process in allowing the stability of the 0-phase far from the mixed valence regime.

cond-mat.mes-hall↗

arXiv2011

Universal transport signatures in two-electron molecular quantum dots: gate-tunable Hund's rule, underscreened Kondo effect and quantum phase transitions

We review here some universal aspects of the physics of two-electron molecular transistors in the absence of strong spin-orbit effects. Several recent quantum dots experiments have shown that an electrostatic backgate could be used to control the energy dispersion of magnetic levels. We discuss how the generically asymmetric coupling of the metallic contacts to two different molecular orbitals can indeed lead to a gate-tunable Hund's rule in the presence of singlet and triplet states in the quantum dot. For gate voltages such that the singlet constitutes the (non-magnetic) ground state, one generally observes a suppression of low voltage transport, which can yet be restored in the form of enhanced cotunneling features at finite bias. More interestingly, when the gate voltage is controlled to obtain the triplet configuration, spin S=1 Kondo anomalies appear at zero-bias, with non-Fermi liquid features related to the underscreening of a spin larger than 1/2. Finally, the small bare singlet-triplet splitting in our device allows to fine-tune with the gate between these two magnetic configurations, leading to an unscreening quantum phase transition. This transition occurs between the non-magnetic singlet phase, where a two-stage Kondo effect occurs, and the triplet phase, where the partially compensated (underscreened) moment is akin to a magnetically "ordered" state. These observations are put theoretically into a consistent global picture by using new Numerical Renormalization Group simulations, taylored to capture sharp finie-voltage cotunneling features within the Coulomb diamonds, together with complementary out-of-equilibrium diagrammatic calculations on the two-orbital Anderson model. This work should shed further light on the complicated puzzle still raised by multi-orbital extensions of the classic Kondo problem.

cond-mat.mes-hall↗

arXiv2011

Cotunneling through a magnetic single-molecule transistor based on N\atC60

We present an experimental and theoretical study of a magnetic single-molecule transistor based on N@C60 connected to gold electrodes. Particular attention is paid to the regime of intermediate molecule-lead coupling, where cotunneling effects manifest themselves in the Coulomb-blockade regime. The experimental results for the differential conductance as a function of bias, gate voltage, and external magnetic field are in agreement with our analysis of the tunneling rates and provide evidence of magnetic signatures in single-N@C60 devices arising from an antiferromagnetic exchange interaction between the C60 spin and the nitrogen spin.

cond-mat.mes-hall↗

arXiv2009

Observation of the underscreened Kondo effect in a molecular transistor

We present the first quantitative experimental evidence for the underscreened Kondo effect, an uncomplete compensation of a quantized magnetic moment by conduction electrons, as originally proposed by Nozieres and Blandin. The device consists of an even charge spin S = 1 molecular quantum dot, obtained by electromigration of C60 molecules into gold nanogaps and operated in a dilution fridge. The persistence of logarithmic singularities in the low temperature conductance is demonstrated by a comparison to the fully screened configuration obtained in odd charge spin S = 1/2 Coulomb diamonds. We also discover an extreme sensitivity of the underscreened Kondo resonance to magnetic field, that we confirm on the basis of numerical renormalization group calculations.

cond-mat.mes-hall↗

arXiv2009

Optimizing the flux coupling between a nanoSQUID and a magnetic particle using atomic force microscope nanolithography

We present results of Niobium based SQUID magnetometers for which the weak-links are engineered by the local oxidation of thin films using an Atomic Force Microscope (AFM). Firstly, we show that this technique allows the creation of variable thickness bridges with 10 nm lateral resolution. Precise control of the weak-link milling is offered by the possibility to realtime monitor weak-link conductance. Such a process is shown to enhance the magnetic field modulation hence the sensitivity of the magnetometer. Secondly, AFM lithography is used to provide a precise alignment of NanoSQUID weak-links with respect to a ferromagnetic iron dot. The magnetization switching of the near-field coupled particle is studied as a junction of the applied magnetic field direction.

cond-mat.supr-con↗

arXiv2009

Contacting individual Fe(110) dots in a single electron-beam lithography step

We report on a new approach, entirely based on electron-beam lithography technique, to contact electrically, in a four-probe scheme, single nanostructures obtained by self-assembly. In our procedure, nanostructures of interest are localised and contacted in the same fabrication step. This technique has been developed to study the field-induced reversal of an internal component of an asymmetric Bloch domain wall observed in elongated structures such as Fe(110) dots. We have focused on the control, using an external magnetic field, of the magnetisation orientation within Néel caps that terminate the domain wall at both interfaces. Preliminary magneto-transport measurements are discussed demonstrating that single Fe(110) dots have been contacted.

cond-mat.mtrl-sci↗

arXiv2008

Supplementary Information: Quantum phase transition in a single-molecule quantum dot

Quantum criticality is the intriguing possibility offered by the laws of quantum mechanics when the wave function of a many-particle physical system is forced to evolve continuously between two distinct, competing ground states. This phenomenon, often related to a zero-temperature magnetic phase transition, can be observed in several strongly correlated materials such as heavy fermion compounds or possibly high-temperature superconductors, and is believed to govern many of their fascinating, yet still unexplained properties. In contrast to these bulk materials with very complex electronic structure, artificial nanoscale devices could offer a new and simpler vista to the comprehension of quantum phase transitions. This long-sought possibility is demonstrated by our work in a fullerene molecular junction, where gate voltage induces a crossing of singlet and triplet spin states at zero magnetic field. Electronic tunneling from metallic contacts into the $\rm{C_{60}}$ quantum dot provides here the necessary many-body correlations to observe a true quantum critical behavior.

cond-mat.mes-hall↗

arXiv2008

Quantum phase transition in a single-molecule quantum dot

cond-mat.mes-hall↗

arXiv2008

Out-of-equilibrium singlet-triplet Kondo effect in a single C_60 quantum dot

We have used an electromigration technique to fabricate a $\rm{C_{60}}$ single-molecule transistor (SMT). Besides describing our electromigration procedure, we focus and present an experimental study of a single molecule quantum dot containing an even number of electrons, revealing, for two different samples, a clear out-of-equilibrium Kondo effect. Low temperature magneto-transport studies are provided, which demonstrates a Zeeman splitting of the finite bias anomaly.

cond-mat.mes-hall↗

arXiv2003

Hexacyanometalate Molecular Chemistry : Trinuclear CrNi2 Complexes; MicroSQUID Magnetisation Studies of Intermolecular Interactions

Three different CrNi2 complexes were synthesized. They differ from each other by the nature of the terminal ligand and of the counter anion : [Cr(CN)4[CN-Ni(tetren)]2]Cl, that crystallizes in two different crystallographic systems and [Cr(CN)4[CN-Ni(dienpy2)]2](ClO4). The ground state spin value is 7/2 for the three systems (ferromagnetic interaction between chromium(III) and nickel(II) ions). The magnetisation of the three CrNi2 complexes was measured using an array of micro-SQUIDs in a temperature range between 0.04 K and 7 K, under a magnetic field up to 1 T. The three samples present a three dimensional magnetic ordering. The correlation between the structure and the intermolecular coupling is analysed in terms of steric hindrances of the terminal ligand, orientation of the molecules in the unit cell (canted structure) and crystal symmetry.

cond-mat.mes-hall↗

arXiv2001

The First Cobalt Single-Molecule Magnet

The first cobalt molecule to function as a single-molecule magnet, [Co4(hmp)4(MeOH)4Cl4], where hmp- is the anion of hydroxymethylpyridine, is reported. The core of the molecule consists of four Co(II) cations and four hmp- oxygen atoms ions at the corners of a cube. Variable-field and variable-temperature magnetization data have been analyzed to establish that the molecule has a S=6 ground state with considerable negative magnetoanisotropy. Single-ion zero-field interactions (DSz2) at each cobalt ion are the origin of the negative magnetoanisotropy. A single-crystal of the compound was studied by means of a micro-SQUID magnetometer in the range of 0.040-1.0K. Hysteresis was found in the magnetization versus magnetic field response of this single crystal. It is concluded that this is the first cobalt molecule to function as a single-molecule magnet.

cond-mat.mes-hall↗