Coherent Manipulation and Decoherence of S=10 Single-Molecule Magnets
arXiv:0810.1254 · doi:10.1103/PhysRevLett.102.087603
Abstract
We report coherent manipulation of S=10 Fe single-molecule magnets. The temperature dependence of the spin decoherence time measured by high frequency pulsed electron paramagnetic resonance indicates that strong spin decoherence is dominated by Fe spin bath fluctuations. By polarizing the spin bath in Fe single-molecule magnets at magnetic field = 4.6 T and temperature = 1.3 K, spin decoherence is significantly suppressed and extends the spin decoherence time to as long as 712 ns. A second decoherence source is likely due to fluctuations of the nuclear spin bath. This hints that the spin decoherence time can be further extended via isotopic substitution to smaller magnetic moments.
4 pages including 3 figures
References in corpus (13)
- Quantum Computing in Molecular Magnets
- Will spin-relaxation times in molecular magnets permit quantum information processing?
- Quantum Coherence in an Exchange-Coupled Dimer of Single-Molecule Magnets
- Quenching Spin Decoherence in Diamond through Spin Bath Polarization
- Direct Observation of Quantum Coherence in Single-Molecule Magnets
- The effects of nuclear spins on the quantum relaxation of the magnetization for the molecular nanomagnet Fe_8
- Pair-wise decoherence in coupled spin qubit networks
- A multi-frequency high-field pulsed EPR / ENDOR spectrometer
- Quantum Coherence between High Spin Superposition States of Single Molecule Magnet Ni
- Characterization of the S = 9 excited state in Fe8Br8 by Electron Paramagnetic Resonance
- Pump-Probe Experiments on the Single-Molecule Magnet Fe8 : Measurement of Excited Level Lifetimes
- Radiation- and Phonon-Bottleneck-Induced Tunneling in the Fe8 Single-Molecule Magnet
- High frequency EPR on dilute solutions of the single molecule magnet Ni
Cited by in corpus (26)
- Decoherence in Crystals of Quantum Molecular Magnets
- Single-molecule Nanomagnets
- High-frequency and high-field optically detected magnetic resonance of nitrogen-vacancy centers in diamond
- Counteracting dephasing in Molecular Nanomagnets by optimized qudit encodings
- Spin-Orbit Qubits of Rare-Earth-Metal Ions in Axially Symmetric Crystal Fields
- General Magnetic Transition Dipole Moments for Electron Paramagnetic Resonance
- A high-frequency electron paramagnetic resonance spectrometer for multi-dimensional, -frequency and -phase pulsed measurements
- Collective coupling of a macroscopic number of single-molecule magnets with a microwave cavity mode
- Dissipative dynamics in a quantum bistable system: Crossover from weak to strong damping
- Decoherence measurements in crystals of molecular magnets
- Dynamic spin localization and gamma-magnets
- Dzyaloshinsky-Moriya interaction and long life time of the spin state in the Cu triangular spin cluster by inelastic neutron scattering measurements
- Tunable multi-photon Rabi oscillations in an electronic spin system
- Decoherence of intermolecular entanglement in exchange-coupled nanomagnets
- On the size of linear superpositions in molecular nanomagnets
- Thermodynamics of quantum information in noisy polarizers
- Light induced magnetization in a spin S=1 easy-plane antiferromagnetic chain
- Designing quantum error correction codes for practical spin qudit
- Precision ESR Measurements of Transverse Anisotropy in the Single-molecule Magnet Ni
- Spin-Orbit Coupling Fluctuations as a Mechanism of Spin Decoherence
- Manipulating spins of magnetic molecules: Hysteretic behavior with respect to bias voltage
- Sustaining Rabi oscillations by using a phase-tunable image drive
- Entrapment of magnetic micro-crystals for on-chip electron spin resonance studies
- Tunnel magnetoresistance of a supramolecular spin valve
- Sensitive Magnetic Force Detection with a Carbon Nanotube Resonator
- Fault-Tolerant Encoding of Logical Qudits in Spin Systems