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Register a new userMolecular engineering of antiferromagnetic rings for quantum computation
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The substitution of one metal ion in a Cr-based molecular ring with dominant antiferromagnetic couplings allows to engineer its level structure and ground-state degeneracy. Here we characterize a Cr7Ni molecular ring by means of low-temperature specific-heat and torque-magnetometry measurements, thus determining the microscopic parameters of the corresponding spin Hamiltonian. The energy spectrum and the suppression of the leakage-inducing S-mixing render the Cr7Ni molecule a suitable candidate for the qubit implementation, as further substantiated by our quantum-gate simulations.
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Surfaces are at the frontier of every known solid. They provide versatile supports for functional nanostructures and mediate essential physicochemical processes. Being intimately related with 2D materials, interfaces and atomically thin films often feature distinct electronic states with respect to the bulk, which are key for many relevant properties, such as catalytic activity, interfacial charge-transfer, or crystal growth mechanisms. Of particular interest is reducing the surface electrons dimensionality and spread with atomic precision, to induce novel quantum properties via lateral scattering and confinement. Both atomic manipulation and supramolecular principles provide access to custom-designed molecular superlattices, which tailor the surface electronic landscape and influence fundamental chemical and physical properties at the nanoscale. Herein, we review the confinement of surface state electrons focusing on their interaction with molecule-based scaffolds created by molecular manipulation and self-assembly protocols under ultrahigh vacuum conditions. Starting from the quasi-free 2D electron gas present at the (111)-terminated surface planes of noble metals, we illustrate the enhanced molecule-based structural complexity and versatility compared to simple atoms. We survey low-dimensional confining structures in the form of artificial lattices, molecular nanogratings or quantum dot arrays, which are constructed upon appropriate choice of their building constituents. Whenever the realized (metal-)organic networks exhibit long-range order, modified surface band structures with characteristic features emerge, revealing intriguing physical properties, such as discretization, quantum coupling or energy and effective mass renormalization. Such collective electronic states can be additionally modified by positioning guest species at the voids of open nanoarchitectures [...].
Presented are magnetization measurements on a crystal of Cr7Ni antiferromagnetic rings. Irradiation with microwaves at frequencies between 1 and 10 GHz leads to observation of very narrow resonant photon absorption lines which are mainly broadened by hyperfin interactions. A two-pulse hole burning technique allowed us to estimate the characteristic energy diffusion time.
Bottom-up prepared carbon nanostructures appear as promising platforms for future carbon-based nanoelectronics, due to their atomically precise and versatile structure. An important breakthrough is the recent preparation of nanoporous graphene (NPG) as an ordered covalent array of graphene nanoribbons (GNRs). Within NPG, the GNRs may be thought of as 1D electronic nanochannels through which electrons preferentially move, highlighting NPGs potential for carbon nanocircuitry. However, the {pi}-conjugated bonds bridging the GNRs give rise to electronic cross-talk between the individual 1D channels, leading to spatially dispersing electronic currents. Here, we propose a chemical design of the bridges resulting in destructive quantum interference, which blocks the cross-talk between GNRs in NPG, electronically isolating them. Our multiscale calculations reveal that injected currents can remain confined within a single, 0.7 nm wide, GNR channel for distances as long as 100 nm. The concepts developed in this work thus provide an important ingredient for the quantum design of future carbon nanocircuitry.
We outline a range of proposals on using quantum rings and nanohelices for terahertz device implementations. We show that an Aharonov-Bohm quantum ring system and a double-gated quantum ring system both permit control over the polarization properties of the associated terahertz radiation. In addition, we review the superlattice properties of a mathematically similar system, that of a nanohelix in external electric fields, which reveals negative differential conductance.
We demonstrated theoretically that a circularly polarized electromagnetic field substantially modifies electronic properties of a periodical chain of quantum rings. Particularly, the field opens band gaps in the electron energy spectrum of the chain, generates edge electron currents and induces the Fano-like features in the electron transport through the finite chain. These effects create physical prerequisites for the development of optically controlled nanodevices based on a set of coupled quantum rings.
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