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1.
Phys Rev Lett ; 127(16): 167201, 2021 Oct 15.
Artigo em Inglês | MEDLINE | ID: mdl-34723605

RESUMO

A system of magnetic molecules coupled to microwave cavities (LC resonators) undergoes the equilibrium superradiant phase transition. The transition is experimentally observable. The effect of the coupling is first illustrated by the vacuum-induced ferromagnetic order in a quantum Ising model and then by the modification of the magnetic phase diagram of Fe_{8} dipolar crystals, exemplifying the cooperation between intrinsic and photon-induced spin-spin interactions. Finally, a transmission experiment is shown to resolve the transition, measuring the quantum electrodynamical control of magnetism.

2.
Chem Sci ; 12(15): 5621-5630, 2021 Mar 17.
Artigo em Inglês | MEDLINE | ID: mdl-34168797

RESUMO

We explore how to encode more than a qubit in vanadyl porphyrin molecules hosting a S = 1/2 electronic spin coupled to a I = 7/2 nuclear spin. The spin Hamiltonian and its parameters, as well as the spin dynamics, have been determined via a combination of electron paramagnetic resonance, heat capacity, magnetization and on-chip magnetic spectroscopy experiments performed on single crystals. We find low temperature spin coherence times of micro-seconds and spin relaxation times longer than a second. For sufficiently strong magnetic fields (B > 0.1 T, corresponding to resonance frequencies of 9-10 GHz) these properties make vanadyl porphyrin molecules suitable qubit realizations. The presence of multiple equispaced nuclear spin levels then merely provides 8 alternatives to define the '1' and '0' basis states. For lower magnetic fields (B < 0.1 T), and lower frequencies (<2 GHz), we find spectroscopic signatures of a sizeable electronuclear entanglement. This effect generates a larger set of allowed transitions between different electronuclear spin states and removes their degeneracies. Under these conditions, we show that each molecule fulfills the conditions to act as a universal 4-qubit processor or, equivalently, as a d = 16 qudit. These findings widen the catalogue of chemically designed systems able to implement non-trivial quantum functionalities, such as quantum simulations and, especially, quantum error correction at the molecular level.

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