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Single Molecular Magnets

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Presentation on theme: "Single Molecular Magnets"— Presentation transcript:

1 Single Molecular Magnets
Ge,Weihao

2 Introduction What is Single Molecular Magnet?
Configuration: metal atom linked by oxygen, packed in ligands Described as a total single spin; size and anisotropy has great effect Why are they interesting? Theoretical: quantum behavior at mesoscopic level Application: Quantum computer: quantum interference and coherence High-density storage device Internal memory effect high integration Other applications Two kinds of these clusters Big integer spin ½ spin big molecule

3 Superparamagnetism Superparamagnetism Origin of superparamagnetism
paramagnetism below Curie’s temperature large susceptibility superparamagnetism limit Origin of superparamagnetism magnetism: result of spin alignment thermal excitation, ferromagnetism <-> paramagnetism small scale, below Tc: thermal excitation destroys the ordering between the clusters thermal excitation cannot upset alignment within the cluster ferro~ inside & para~ outside => treated as a large spin as a whole Experiment results stepped hysteresis can be found below certain temperature. frequency dependent AC susceptibility

4 Quantum Tunneling Magnetization
Experiment steps found in hysteresis of Mn12 cluster Model two – well model resonant tunneling thermally assisted QTM & pure QTM A commonly used form of Hamiltonian axial anisotropic term Zeeman splitting term transverse anisotropic term Experiments Model A commonly used form of Hamiltonian spins within: Heisenberg model total spin: treated as a large spin QT relaxation also. equally distributed in wells apply magnetic field -> all in 1 well field turned off -> all in 1 well tunnel back, relaxation -> relaxation time

5 Integer Spin SMM: Mn12 Significance Structure Hamiltonian
archeological reason: first synthesized SMM & QTM first observed most widely studied Structure Mn3+, external octagon; Mn4+, internal tetrahedron. Ground state: S=10 Hamiltonian symmetry: lowest even power of transverse terms is 4 transition: probably exist low-ordered odd-powered terms

6 Integer Spin SMM: Fe4 Structure Hamiltonian
Fe3+: centered triangle, C2 symmetry Ground state: S=5 Hamiltonian general form Advantages over Mn12 in application More efficient tunneling longer relaxation time less affected when attached to a surface stability

7 ½ spin big molecule: V15 Structure Experimental result
a center triangle between two hexagons S=1/2, no large energy barrier, large zero field splitting Experimental result hysteresis observed Rabi oscillation coherence time: ~100 μs Theoretical approaches dissipative two-level system: Landau - Zener transition exchange interaction: “spin rotation in a phonon bath” Structure Properties Theoretical approaches two-level model: relatively large zero field splitting ~80mK spin hamiltonian: hexagon cancels by anteferromagnetic coupling; only consider triangle exchange term; anisotropy term; interaction with nuclear spin; zeeman term coherence time limited by nuclear spin

8 Summary General introduction to single molecular magnets
quantum behavior beyond the microscopic scale in these clusters Origin of the magnetism of SMM Quantum Tunneling Magnetization A result of size and anisotropy Integer spin clusters and ½ spin clusters integer: easy to interpreted by large-spin approximation ½ spin: lack of barrier, tunneling caused by spin-phonon interaction long-lived coherence

9 References QTM: Gatteschi,D.; Sessoli,R. “Quantum tunneling magnetization and related phenomena in Molecular Materials.” Angew. Chem.Ed. 42(3), 2003,pp.268 Mn12: Friedman,J., Sarachik,M. “Mesoscopic Measurement of Resonant Magnetization Tunneling in High-Spin Molecules.” PRL, 76(20),1996, pp.3830 Barra, A., et.al. “High-frequency EPR spectra of a molecular nanomagnet: Understanding quantum tunneling of the magnetization.” PRB. 56(13), 1997, pp.8192 Fe4: Accorsi,S., et.al. “Tuning Anisotropy Barriers in a Family of Tetraion(III) Single-Molecule Magnets with an S = 5 Ground State” JACS. 128(14), 2006, pp Wernsdorfer,W., et.al. “X-ray Magnetic Circular Dichroism Picks out Single-Molecule Magnets Suitable for Nanodevices.” Adv.Mater. 21, 2009, pp Sessoli,R., et.al. “Magnetic memory of a single-molecule quantum magnet wired to a gold surface.” Nature Mater. 8, 2009, pp.194 V15: Müller,A., et.al. “Quantum Oscillation in a molecular magnet.” Nature lett. 453, 2008 pp.203 Choirescu, et.al. “Environmental effects on big molecule with spin ½.” J.Appl.Phys.87(9) 2000 pp.5496


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