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 (8)
- Will spin-relaxation times in molecular magnets permit quantum information processing?
- Quenching Spin Decoherence in Diamond through Spin Bath Polarization
- Direct Observation of Quantum Coherence in Single-Molecule Magnets
- Pair-wise decoherence in coupled spin qubit networks
- A multi-frequency high-field pulsed EPR / ENDOR spectrometer
- 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