We investigate key quantum characteristics of the mixed spin-(1/2,1,1/2) Heisenberg trimer under the influence of an external magnetic field. Specifically, we analyze the distributions of bipartite and tripartite entanglement quantified through the respective negativities and the ${l}_{1}$ -norm of coherence with the help of rigorous analytical and numerical methods. Our findings suggest that the heterotrinuclear molecular nanomagnet $[{{{\text{Cu}}^{2+}\text{L}}}_{2}{\text{Ni}}^{2+}{({\text{H}}_{2}\text{O})}_{2}]{({\text{ClO}}_{4})}_{2}\ifmmode\cdot\else\textperiodcentered\fi{}3{\text{H}}_{2}\text{O}$, which represents an experimental realization of the mixed spin-(1/2,1,1/2) Heisenberg trimer, exhibits a significant bipartite entanglement between ${\text{Cu}}^{2+}$ and ${\text{Ni}}^{2+}$ magnetic ions along with robust tripartite entanglement among all three constituent ${\text{Cu}}^{2+}{\text{Ni}}^{2+}{\text{Cu}}^{2+}$ magnetic ions. The significant bipartite and tripartite entanglement persists even at relatively high temperatures up to $37\phantom{\rule{0.16em}{0ex}}\text{K}$ and magnetic fields up to $46\phantom{\rule{0.16em}{0ex}}\text{T}$ , whereby the coherence is maintained even at elevated temperatures. It is evidenced that the aforementioned molecular complex with the magnetic core ${\text{Cu}}^{2+}{\text{Ni}}^{2+}{\text{Cu}}^{2+}$ provides an intriguing quantum resource, which exhibits a star-shaped state within the singlet eigenstate at low magnetic fields and W-like state within the triplet eigenstate at moderate magnetic fields.We investigate key quantum characteristics of the mixed spin-(1/2,1,1/2) Heisenberg trimer under the influence of an external magnetic field. Specifically, we analyze the distributions of bipartite and tripartite entanglement quantified through the respective negativities and the ${l}_{1}$-norm of coherence with the help of rigorous analytical and numerical methods. Our findings suggest that the heterotrinuclear molecular nanomagnet $[{{{\text{Cu}}^{2+}\text{L}}}_{2}{\text{Ni}}^{2+}{({\text{H}}_{2}\text{O})}_{2}]{({\text{ClO}}_{4})}_{2}\ifmmode\cdot\else\textperiodcentered\fi{}3{\text{H}}_{2}\text{O}$, which represents an experimental realization of the mixed spin-(1/2,1,1/2) Heisenberg trimer, exhibits a significant bipartite entanglement between ${\text{Cu}}^{2+}$ and ${\text{Ni}}^{2+}$ magnetic ions along with robust tripartite entanglement among all three constituent ${\text{Cu}}^{2+}{\text{Ni}}^{2+}{\text{Cu}}^{2+}$ magnetic ions. The significant bipartite and tripartite entanglement persists even at relatively high temperatures up to $37\phantom{\rule{0.16em}{0ex}}\text{K}$ and magnetic fields up to $46\phantom{\rule{0.16em}{0ex}}\text{T}$, whereby the coherence is maintained even at elevated temperatures. It is evidenced that the aforementioned molecular complex with the magnetic core ${\text{Cu}}^{2+}{\text{Ni}}^{2+}{\text{Cu}}^{2+}$ provides an intriguing quantum resource, which exhibits a star-shaped state within the singlet eigenstate at low magnetic fields and W-like state within the triplet eigenstate at moderate magnetic fields.

arXiv:2407.07037Physical Review AFeb 7, 20258 citations

Excitations in a perfect magnetized quantum spin ladder

A. Zheludev, D. Schmidiger, S. Mühlbauer +7 more

Bulletin of the American Physical SocietyMar 19, 20130 citations

Energy efficient coherent quantum control of nitrogen vacancy (NV) spin with nanoscale magnets

Md. Fahim F. Chowdhury, Adi Jung, Léa La Spina +3 more

We investigate coherent quantum control of a nitrogen vacancy (NV) center in diamond with microwave fields generated from a nanoscale magnet that is proximal to the NV center. Our results show remarkable coherent control with high contrast Rabi oscillations using nearfield microwaves from shape anisotropic nanomagnets of lateral dimensions down to 200 nm x 180 nm, driven remotely by surface acoustic wave (SAW) excitation that is at least 400 times and potentially 4 orders of magnitude more energy efficient than generating microwaves with an antenna. Furthermore, we show that varying the acoustic power driving such nanomagnets can achieve control over Rabi frequency. We also report spin-lattice relaxation time T1 is 103 +/-0.5 micro-seconds, the spin-spin relaxation time T2 is 1.23+/-0.29 micro-seconds, and the Ramsey coherence time T2* is 218+/-27 nanoseconds measured using microwave pulses generated by such nanomagnets. The use of the nanoscale magnets to implement highly localized and energy efficient coherent quantum control can replace thermally noisy microwave circuits and demonstrate a path to scalable quantum computing and sensing with NV-defects in diamond and other spin qubits.We investigate coherent quantum control of a nitrogen vacancy (NV) center in diamond with microwave fields generated from a nanoscale magnet that is proximal to the NV center. Our results show remarkable coherent control with high contrast Rabi oscillations using nearfield microwaves from shape anisotropic nanomagnets of lateral dimensions down to 200 nm x 180 nm, driven remotely by surface acoustic wave (SAW) excitation that is at least 400 times and potentially 4 orders of magnitude more energy efficient than generating microwaves with an antenna. Furthermore, we show that varying the acoustic power driving such nanomagnets can achieve control over Rabi frequency. We also report spin-lattice relaxation time T1 is 103 +/-0.5 micro-seconds, the spin-spin relaxation time T2 is 1.23+/-0.29 micro-seconds, and the Ramsey coherence time T2* is 218+/-27 nanoseconds measured using microwave pulses generated by such nanomagnets. The use of the nanoscale magnets to implement highly localized and energy efficient coherent quantum control can replace thermally noisy microwave circuits and demonstrate a path to scalable quantum computing and sensing with NV-defects in diamond and other spin qubits.

arXiv:2407.14018Jul 19, 20241 citation

Quantum Dynamics of Molecular Nanomagnets in a Resonant Cavity and the Maser Effect

César Augusto Dartora, G. G. Cabrera

We study the dynamics of molecular nanomagnets through a fully quantum mechanical model describing high-spin and high-anisotropy magnetic molecules subjected to a time-dependent magnetic field along the quantization axis, which continuously inverts the population of spin states. Crystals of molecular nanomagnets placed inside a resonant cavity interact with a quantized electromagnetic field. Relaxation of excited states takes place by means of spin-photon interaction, allowing stimulated emission of radiation and creating a maser effect.We study the dynamics of molecular nanomagnets through a fully quantum mechanical model describing high-spin and high-anisotropy magnetic molecules subjected to a time-dependent magnetic field along the quantization axis, which continuously inverts the population of spin states. Crystals of molecular nanomagnets placed inside a resonant cavity interact with a quantized electromagnetic field. Relaxation of excited states takes place by means of spin-photon interaction, allowing stimulated emission of radiation and creating a maser effect.

arXiv:cond-mat/0609205Sep 8, 20060 citations

{l}_{1}

-norm of coherence with the help of rigorous analytical and numerical methods. Our findings suggest that the heterotrinuclear molecular nanomagnet $[{{{\text{Cu}}^{2+}\text{L}}}_{2}{\text{Ni}}^{2+}{({\text{H}}_{2}\text{O})}_{2}]{({\text{ClO}}_{4})}_{2}\ifmmode\cdot\else\textperiodcentered\fi{}3{\text{H}}_{2}\text{O}$, which represents an experimental realization of the mixed spin-(1/2,1,1/2) Heisenberg trimer, exhibits a significant bipartite entanglement between

{\text{Cu}}^{2+}

and

{\text{Ni}}^{2+}

magnetic ions along with robust tripartite entanglement among all three constituent

{\text{Cu}}^{2+}{\text{Ni}}^{2+}{\text{Cu}}^{2+}

magnetic ions. The significant bipartite and tripartite entanglement persists even at relatively high temperatures up to

37\phantom{\rule{0.16em}{0ex}}\text{K}

and magnetic fields up to

46\phantom{\rule{0.16em}{0ex}}\text{T}

, whereby the coherence is maintained even at elevated temperatures. It is evidenced that the aforementioned molecular complex with the magnetic core

{\text{Cu}}^{2+}{\text{Ni}}^{2+}{\text{Cu}}^{2+}

provides an intriguing quantum resource, which exhibits a star-shaped state within the singlet eigenstate at low magnetic fields and W-like state within the triplet eigenstate at moderate magnetic fields.