Room-temperature entanglement of the nickel-radical molecular complex (Et3NH)[Ni(hfac)2L]
Jozef Strecka, Elham Shahhosseini Shahrabadi

TL;DR
This study demonstrates that the nickel-radical molecular complex exhibits strong bipartite entanglement at room temperature, making it a promising candidate for molecular qubits in quantum computing.
Contribution
It provides the first experimental and theoretical analysis of room-temperature entanglement in a nickel-radical complex with potential quantum information applications.
Findings
Maintains significant entanglement above 546 K
Strong antiferromagnetic exchange coupling J/kB = 505 K
Entanglement retains about 40% of maximum at room temperature
Abstract
The bipartite entanglement is comprehensively investigated in the mononuclear molecular complex (Et3NH)[Ni(hfac)2L]L, where HL denotes 2-(2-hydroxy-3-methoxy-5-nitrophenyl)-4,4,5,5-tetramethyl-4,5-dihydro-1H-imidazol-3-oxide-1-oxyl and hfacH stands for hexafluoroacetylacetone. From the magnetic point of view, the molecular compound (Et3NH)[Ni(hfac)2L] consists of an exchange-coupled spin-1 Ni2+ magnetic ion and a spin-1/2 nitronyl-nitroxide radical substituted nitrophenol. The nickel-radical molecular complex affords an experimental realization of a mixed spin-(1/2, 1) Heisenberg dimer with a strong antiferromagnetic exchange coupling J/kB = 505 K and two distinct g-factors gRad=2.005 and gNi=2.275. By adopting this set of magnetic parameters we demonstrate that the Zeeman splitting of a quantum ferrimagnetic ground-state doublet due to a weak magnetic field may substantially reinforce…
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