76 research outputs found

    Role of dipolar and exchange interactions in the positions and widths of EPR transitions for the single-molecule magnets Fe8 and Mn12

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    We examine quantitatively the temperature dependence of the linewidths and line shifts in electron paramagnetic resonance experiments on single crystals of the single-molecule magnets Fe8_8 and Mn12_{12}, at fixed frequency, with an applied magnetic field along the easy axis. We include inter-molecular spin-spin interactions (dipolar and exchange) and distributions in both the uniaxial anisotropy parameter DD and the Land\'{e} gg-factor. The temperature dependence of the linewidths and the line shifts are mainly caused by the spin-spin interactions. For Fe8_8 and Mn12_{12}, the temperature dependence of the calculated line shifts and linewidths agrees well with the trends of the experimental data. The linewidths for Fe8_8 reveal a stronger temperature dependence than those for Mn12_{12}, because for Mn12_{12} a much wider distribution in DD overshadows the temperature dependence of the spin-spin interactions. For Fe8_8, the line-shift analysis suggests two competing interactions: a weak ferromagnetic exchange coupling between neighboring molecules and a longer-ranged dipolar interaction. This result could have implications for ordering in Fe8_8 at low temperatures.Comment: published versio

    Spin-Wave Description of Nuclear Spin-Lattice Relaxation in Mn_{12}O_{12} Acetate

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    In response to recent nuclear-magnetic-resonance (NMR) measurements on the molecular cluster Mn_{12}O_{12} acetate, we study the nuclear spin-lattice relaxation rate 1/T_1 developing a modified spin-wave theory. Our microscopic new approach, which is distinct from previous macroscopic treatments of the cluster as a rigid spin of S=10, not only excellently interprets the observed temperature and applied-field dependences of 1/T_1 for ^{55}Mn nuclei but also strongly supports the ^{13}C NMR evidence for spin delocalization over the entire molecule.Comment: to be published in Phys. Rev. Lett., 4 pages, 4 figures embedde

    Semiconductive and Photoconductive Properties of the Single Molecule Magnets Mn12_{12}-Acetate and Fe8_8Br8_8

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    Resistivity measurements are reported for single crystals of Mn12_{12}-Acetate and Fe8_8Br8_8. Both materials exhibit a semiconductor-like, thermally activated behavior over the 200-300 K range. The activation energy, EaE_a, obtained for Mn12_{12}-Acetate was 0.37 Âą\pm 0.05 eV, which is to be contrasted with the value of 0.55 eV deduced from the earlier reported absorption edge measurements and the range of 0.3-1 eV from intramolecular density of states calculations, assuming 2Ea2E_a= EgE_g, the optical band gap. For Fe8_8Br8_8, EaE_a was measured as 0.73 Âą\pm 0.1 eV, and is discussed in light of the available approximate band structure calculations. Some plausible pathways are indicated based on the crystal structures of both lattices. For Mn12_{12}-Acetate, we also measured photoconductivity in the visible range; the conductivity increased by a factor of about eight on increasing the photon energy from 632.8 nm (red) to 488 nm (blue). X-ray irradiation increased the resistivity, but EaE_a was insensitive to exposure.Comment: 7 pages, 8 figure

    Nuclear spin-lattice relaxation in ferrimagnetic clusters and chains: A contrast between zero and one dimensions

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    Motivated by ferrimagnetic oligonuclear and chain compounds synthesized by Caneschi et al., both of which consist of alternating manganese(II) ions and nitronyl-nitroxide radicals, we calculate the nuclear spin-lattice relaxation rate 1/T_1 employing a recently developed modified spin-wave theory. 1/T_1 as a function of temperature drastically varies with the location of probe nuclei in both clusters and chains, though the relaxation time scale is much larger in zero dimension than in one dimension. 1/T_1 as a function of an applied field in long chains forms a striking contrast to that in finite clusters, diverging with decreasing field like inverse square root at low temperatures and logarithmically at high temperatures.Comment: to be published in Phys. Rev. B 68 August 01 (2003

    High frequency resonant experiments in Fe8_8 molecular clusters

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    Precise resonant experiments on Fe8_{8} magnetic clusters have been conducted down to 1.2 K at various tranverse magnetic fields, using a cylindrical resonator cavity with 40 different frequencies between 37 GHz and 110 GHz. All the observed resonances for both single crystal and oriented powder, have been fitted by the eigenstates of the hamiltonian H=−DSz2+ESx2−gμBH⋅S{\cal H}=-DS_z^2+ES_x^2-g\mu_B{\bf H}\cdot {\bf S}. We have identified the resonances corresponding to the coherent quantum oscillations for different orientations of spin S = 10.Comment: to appear in Phys.Rev. B (August 2000

    Magnetic Field Effects on the Far-Infrared Absorption in Mn_12-acetate

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    We report the far-infrared spectra of the molecular nanomagnet Mn_12-acetate (Mn_12) as a function of temperature (5-300 K) and magnetic field (0-17 T). The large number of observed vibrational modes is related to the low symmetry of the molecule, and they are grouped together in clusters. Analysis of the mode character based on molecular dynamics simulations and model compound studies shows that all vibrations are complex; motion from a majority of atoms in the molecule contribute to most modes. Three features involving intramolecular vibrations of the Mn_12 molecule centered at 284, 306 and 409 cm-1 show changes with applied magnetic field. The structure near 284 cm−1^{-1} displays the largest deviation with field and is mainly intensity related. A comparison between the temperature dependent absorption difference spectra, the gradual low-temperature cluster framework distortion as assessed by neutron diffraction data, and field dependent absorption difference spectra suggests that this mode may involve Mn motion in the crown.Comment: 5 pages, 4 figures, PRB accepte

    Detailed single crystal EPR lineshape measurements for the single molecule magnets Fe8Br and Mn12-ac

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    It is shown that our multi-high-frequency (40-200 GHz) resonant cavity technique yields distortion-free high field EPR spectra for single crystal samples of the uniaxial and biaxial spin S = 10 single molecule magnets (SMMs) [Mn12O12(CH3COO)16(H2O)4].2CH3COOH.4H2O and [Fe8O2(OH)12(tacn)6]Br8.9H2O. The observed lineshapes exhibit a pronounced dependence on temperature, magnetic field, and the spin quantum numbers (Ms values) associated with the levels involved in the transitions. Measurements at many frequencies allow us to separate various contributions to the EPR linewidths, including significant D-strain, g-strain and broadening due to the random dipolar fields of neighboring molecules. We also identify asymmetry in some of the EPR lineshapes for Fe8, and a previously unobserved fine structure to some of the EPR lines for both the Fe8 and Mn12 systems. These findings prove relevant to the mechanism of quantum tunneling of magnetization in these SMMs.Comment: Phys. Rev. B, accepted with minor revision

    Equal Sensitivity of the Two Strands of øX174 Replicative DNA to Breakage by Ionizing Radiation

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    The supertwisted, double-stranded, replicative intermediate of øX174 DNA (RFI) has been used to determine whether one of the two strands of the double helix is uniquely sensitive to induction of single-strand breaks by ionizing radiation. This could result from a particularly sensitive base sequence or a transfer of energy to a specific location of the DNA molecule. The results indicate that both strands of the double helix are equally broken, even though their base compositions are significantly different. If there are “hot spots” in the strands, then they are present in equal amounts in each strand
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