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Decoherence in crystals of quantum molecular magnets

Abstract

Quantum decoherence is a central concept in physics. Applications such as quantum information processing depend on understanding it; there are even fundamental theories proposed that go beyond quantum mechanics1,2,3, in which the breakdown of quantum theory would appear as an ‘intrinsic’ decoherence, mimicking the more familiar environmental decoherence processes4. Such applications cannot be optimized, and such theories cannot be tested, until we have a firm handle on ordinary environmental decoherence processes. Here we show that the theory for insulating electronic spin systems can make accurate and testable predictions for environmental decoherence in molecular-based quantum magnets5. Experiments on molecular magnets have successfully demonstrated quantum-coherent phenomena6,7,8 but the decoherence processes that ultimately limit such behaviour were not well constrained. For molecular magnets, theory predicts three principal contributions to environmental decoherence: from phonons, from nuclear spins and from intermolecular dipolar interactions. We use high magnetic fields on single crystals of Fe8 molecular magnets (in which the Fe ions are surrounded by organic ligands) to suppress dipolar and nuclear-spin decoherence. In these high-field experiments, we find that the decoherence time varies strongly as a function of temperature and magnetic field. The theoretical predictions are fully verified experimentally, and there are no other visible decoherence sources. In these high fields, we obtain a maximum decoherence quality-factor of 1.49 × 106; our investigation suggests that the environmental decoherence time can be extended up to about 500 microseconds, with a decoherence quality factor of 6 × 107, by optimizing the temperature, magnetic field and nuclear isotopic concentrations.

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Figure 1: Typical ESR spectra, showing echo intensity as a function of transverse magnetic field, H.
Figure 2: Calculated contributions to the decoherence coming from the coupling to nuclear spins, phonons and magnons.
Figure 3: Measured and calculated decoherence times T 2 in samples 1 and 2, as a function of temperature.

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References

  1. 't Hooft, G. Quantum gravity as a dissipative deterministic system. Class. Quantum Gravity 16, 3263–3279 (1999)

    Article  ADS  MathSciNet  Google Scholar 

  2. Penrose, R. On gravity's role in quantum state reduction. Gen. Relativ. Gravit. 28, 581–600 (1996)

    Article  ADS  MathSciNet  Google Scholar 

  3. Leggett, A. J. Testing the limits of quantum mechanics: motivation, state of play, prospects. J. Phys. Condens. Matter 14, R415–R451 (2002)

    Article  ADS  CAS  Google Scholar 

  4. Stamp, P. C. E. The decoherence puzzle. Stud. Hist. Phil. Mod. Phys. 37, 467–497 (2006)

    Article  MathSciNet  Google Scholar 

  5. Gatteschi, D., Sessoli, R. & Villain, J. Molecular Nanomagnets (Oxford Univ. Press, 2006)

    Book  Google Scholar 

  6. Takahashi, S. et al. Coherent manipulation and decoherence of S = 10 single-molecule magnets. Phys. Rev. Lett. 102, 087603 (2009)

    Article  ADS  Google Scholar 

  7. Bertaina, S. et al. Quantum oscillations in a molecular magnet. Nature 453, 203–206 (2008)

    Article  ADS  CAS  Google Scholar 

  8. Schlegel, C. et al. Direct observation of quantum coherence in single-molecule magnets. Phys. Rev. Lett. 101, 147203 (2008)

    Article  ADS  CAS  Google Scholar 

  9. Leibfried, D., Blatt, R., Monroe, C. & Wineland, D. Quantum dynamics of single trapped ions. Rev. Mod. Phys. 75, 281–324 (2003)

    Article  ADS  CAS  Google Scholar 

  10. Labaziewicz, J. et al. Temperature dependence of electric field noise above gold surfaces. Phys. Rev. Lett. 101, 180602 (2008)

    Article  ADS  Google Scholar 

  11. Xu, X. et al. Optically controlled locking of the nuclear field via coherent dark-state spectroscopy. Nature 459, 1105–1109 (2009)

    Article  ADS  CAS  Google Scholar 

  12. Ladd, T. D. et al. Pulsed nuclear pumping and spin diffusion in a single charged quantum dot. Phys. Rev. Lett. 105, 107401 (2010)

    Article  ADS  Google Scholar 

  13. Takahashi, S. et al. Quenching spin decoherence in diamond through spin bath polarization. Phys. Rev. Lett. 101, 047601 (2008)

    Article  ADS  Google Scholar 

  14. Childress, L. et al. Coherent dynamics of coupled electron and nuclear spin qubits in diamond. Science 314, 281–285 (2006)

    Article  ADS  CAS  Google Scholar 

  15. Hanson, R. et al. Coherent dynamics of a single spin interacting with an adjustable spin bath. Science 320, 352–355 (2008)

    Article  ADS  CAS  Google Scholar 

  16. Leggett, A. J. et al. Dynamics of the dissipative two-state system. Rev. Mod. Phys. 59, 1–85 (1987)

    Article  ADS  CAS  Google Scholar 

  17. Prokof'ev, N. V. & Stamp, P. C. E. Theory of the spin bath. Rep. Prog. Phys. 63, 669–726 (2000)

    Article  ADS  CAS  Google Scholar 

  18. Morello, A., Stamp, P. C. E. & Tupitsyn, I. S. Pairwise decoherence in coupled spin qubit networks. Phys. Rev. Lett. 97, 207206 (2006)

    Article  ADS  Google Scholar 

  19. Wieghardt, K., Pohl, K., Jibril, I. & Huttner, G. Hydrolysis products of the monomeric amine complex (C6H15N3)FeCl3: the structure of the octameric iron(III) cation of [(C6H15N3)6Fe8(µ3–O)2(µ 2–OH)12]Br7 · 8H2O. Angew. Chem. Int. Edn Engl. 23, 77–78 (1984)

    Article  Google Scholar 

  20. Hahn, E. L. Spin echoes. Phys. Rev. 80, 580–594 (1950)

    Article  ADS  Google Scholar 

  21. van Tol, J., Brunel, L. C. & Wylde, R. J. A quasioptical transient electron spin resonance spectrometer operating at 120 and 240 GHz. Rev. Sci. Instrum. 76, 074101 (2005)

    Article  ADS  Google Scholar 

  22. Morley, G. W., Brunel, L. C. & van Tol, J. A multifrequency high-field pulsed electron paramagnetic resonance/electron-nuclear double resonance spectrometer. Rev. Sci. Instrum. 79, 064703 (2008)

    Article  ADS  Google Scholar 

  23. Stamp, P. C. E. & Tupitsyn, I. S. Coherence window in the dynamics of quantum nanomagnets. Phys. Rev. B 69, 014401 (2004)

    Article  ADS  Google Scholar 

  24. Yao, W., Liu, R. B. & Sham, L. J. Theory of electron spin decoherence by interacting spins in a quantum dot. Phys. Rev. B 74, 195301 (2006)

    Article  ADS  Google Scholar 

  25. Morello, A., Bakharev, O. N., Brom, H. B., Sessoli, R. & de Jongh, L. J. Nuclear Spin Dynamics in the Quantum regime of a single molecule magnet. Phys. Rev. Lett. 93, 197202 (2004)

    Article  ADS  CAS  Google Scholar 

  26. Cuccoli, A. et al. Dipolar interaction and incoherent quantum tunneling: a Monte Carlo study of magnetic relaxation. Europhys. J. B. 12, 39–46 (1999)

    ADS  CAS  Google Scholar 

  27. Tupitsyn, I. S., Stamp, P. C. E. & Prokofev, N. V. Hole digging in ensembles of tunneling molecular magnets. Phys. Rev. B 69, 132406 (2004)

    Article  ADS  Google Scholar 

  28. Hill, S. et al. D-strain, g-strain, and dipolar interactions in the Fe8 and Mn12 single molecule magnets: an EPR lineshape analysis. Int. J. Mod. Phys. B 16, 3326–3329 (2002)

    Article  ADS  CAS  Google Scholar 

  29. Park, K. et al. Effects of D-strain, g-strain, and dipolar interactions on EPR linewidths of the molecular magnets Fe8 and Mn12 . Phys. Rev. B 65, 014426 (2001)

    Article  ADS  Google Scholar 

  30. Barra, A. L., Gatteschi, D. & Sessoli, R. High-frequency EPR spectra of [Fe8O2(OH)12(tacn)6]Br8: a critical appraisal of the barrier for the reorientation of the magnetization in single-molecule magnets. Chem. Eur. J. 6, 1608–1614 (2000)

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This work was supported by the NSF (DMR-0520481, DMR-0703925), the Keck Foundation (S.T. and J.v.T.), NSERC, CIFAR, PITP, the John E. Fetzer Memorial Trust (grant D21-C62) and the Center for Philosophy and the Natural Sciences, California State University, Sacramento (I.S.T. and P.C.E.S.). The National High Magnetic Field Laboratory is supported by NSF Cooperative Agreement DMR-0654118, by the State of Florida, and by the DOE.

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S.T., I.S.T. and P.C.E.S. contributed to the writing of the manuscript. S.T., I.S.T. and P.C.E.S. conceived the ESR experiments. The ESR measurements were carried out by S.T. and J.v.T. The theoretical work was done by I.S.T. and P.C.E.S. C.C.B and D.N.H. synthesized Fe8 crystals and performed X-ray diffraction measurements.

Corresponding authors

Correspondence to S. Takahashi or P. C. E. Stamp.

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The authors declare no competing financial interests.

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Takahashi, S., Tupitsyn, I., van Tol, J. et al. Decoherence in crystals of quantum molecular magnets. Nature 476, 76–79 (2011). https://doi.org/10.1038/nature10314

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