arXiv subjects

Bertrand Vileno

Publications and source records attributed to Bertrand Vileno.

3 recordsLinked to original sources

arXiv2025

Encoding information onto the charge and spin state of a paramagnetic atom using MgO tunnelling spintronics

An electrical current that flows across individual atoms can generate exotic quantum transport signatures in model junctions built using atomic tip or lateral techniques. So far, however, a viable industrial pathway for atom-driven devices has been lacking. Here, we demonstrate that a commercialized device platform can fill this nanotechnological gap. According to conducting tip atomic force microscopy, inserting C atoms into the MgO barrier of a magnetic tunnel junction generates nanotransport paths. Within magnetotransport experiments, this results in quantum interferences, and in Pauli spin blockade effects linked to tunneling magnetoresistance peaks that can be electrically controlled. We report an additional persistent memory effect that we attribute to the charging of a single "gating" C atom that is adjacent to a single C atom forming the microscale junction's effective nanotranport path. Local magnetometry experiments confirm the secondary role of magnetic stray fields on the C atoms. Our results show that, to exhibit atom-level properties, a device need not be nanoscaled, and position MgO tunneling spintronics as a promising platform to industrially implement quantum technologies.

cond-mat.mes-hall↗

arXiv2022

Quantum advantage in a molecular spintronic engine that harvests thermal fluctuation energy

Recent theory and experiments have showcased how to harness quantum mechanics to assemble heat/information engines with efficiencies that surpass the classical Carnot limit. So far, this has required atomic engines that are driven by cumbersome external electromagnetic sources. Here, using molecular spintronics, we propose an implementation that is both electronic and autonomous. Our spintronic quantum engine heuristically deploys several known quantum assets by having a chain of spin qubits formed by the paramagnetic Co centers of phthalocyanine (Pc) molecules electronically interact with electron-spin selecting Fe/C60 interfaces. Density functional calculations reveal that transport fluctuations across the interface can stabilize spin coherence on the Co paramagnetic centers, which host spin flip processes. Across vertical molecular nanodevices, we measure enduring dc current generation, output power above room temperature, two quantum thermodynamical signatures of the engine's processes, and a record 89% spin polarization of current across the Fe/C60 interface. It is crucially this electron spin selection that forces, through demonic feedback and control, charge current to flow against the built-in potential barrier. Further research into spintronic quantum engines, insight into the quantum information processes within spintronic technologies, and retooling the spintronic-based information technology chain, could help accelerate the transition to clean energy.

cond-mat.mes-hall↗

arXiv2017

Disentangling magnetic hardening and molecular spin chain contributions to exchange bias in ferromagnet/molecule bilayers

We performed SQUID and FMR magnetometry experiments to clarify the relationship between two reported magnetic exchange effects arising from interfacial spin-polarized charge transfer within ferromagnetic metal (FM)/molecule bilayers: the magnetic hardening effect, and spinterface-stabilized molecular spin chains. To disentangle these effects, both of which can affect the FM magnetization reversal, we tuned the metal phthalocyanine molecule central site's magnetic moment to selectively enhance or suppress the formation of spin chains within the molecular film. We find that both effects are distinct, and additive. In the process, we 1) extended the list of FM/molecule candidate pairs that are known to generate magnetic exchange effects, 2) experimentally confirmed the predicted increase in anisotropy upon molecular adsorption; and 3) showed that spin chains within the molecular film can enhance magnetic exchange. This magnetic ordering within the organic layer implies a structural ordering. Thus, by distengangling the magnetic hardening and exchange bias contributions, our results confirm, as an echo to progress regarding inorganic spintronic tunnelling, that the milestone of spintronic tunnelling across structurally ordered organic barriers has been reached through previous magnetotransport experiments. This paves the way for solid-state devices studies that exploit the quantum physical properties of spin chains, notably through external stimuli.

cond-mat.mtrl-sci↗