O. N. Bakharev

Nuclear Spin Dynamics in the Quantum Regime of a Single-Molecule Magnet

We show that the nuclear spin dynamics in the single-molecule magnet Mn12-ac below 1 K is governed by quantum tunneling fluctuations of the cluster spins, combined with intercluster nuclear spin diffusion. We also obtain the first experimental proof that-surprisingly-even deep in the quantum regime the nuclear spins remain in good thermal contact with the lattice phonons. We propose a simple model for how T-independent tunneling fluctuations can relax the nuclear polarization to the lattice that may serve as a framework for more sophisticated theories.

Quantum tunnelling of magnetization in Mn12-ac studied by 55Mn NMR

Abstract We present an ultra-low temperature study (down to T =20 mK) of the nuclear spin-lattice relaxation (SLR) in the 55 Mn nuclei of the molecular magnet Mn 12 - ac . The nuclear spins act as local probes for the electronic spin fluctuations, due to thermal excitations and to tunnelling events. In the quantum regime (below T ≈0.75 K), the nuclear SLR becomes temperature independent and is driven by fluctuations of the clusters electronic spin due to the quantum tunnelling of magnetization in the ground doublet. The quantitative analysis of the nuclear SLR shows that the presence of fast-tunnelling molecules, combined with nuclear intercluster spin diffusion, plays an important role in the relaxation process.

Spin dynamics and ordering of a cuprate stripe antiferromagnet

In La1.48Nd0.4Sr0.12CuO4 the 139La and 63Cu NQR relaxation rates and signal wipe-out upon lowering temperature are shown to be due to purely magnetic fluctuations. They follow the same renormalized classical behavior as seen in neutron data, when the electronic spins order in stripes, with a small spread in spin stiffness (15% spread in activation energy). The La signal, which reappears at low temperatures, is magnetically broadened and experiences additional wipe-out due to slowing down of the Nd fluctuations.

Magnetic dipolar ordering and relaxation in the high-spin molecular cluster compound Mn6

Few examples of magnetic systems displaying a transition to pure dipolar magnetic order are known to date, and single-molecule magnets can provide an interesting example. The molecular cluster spins and thus their dipolar interaction energy can be quite high, leading to reasonably accessible ordering temperatures, provided the crystal field anisotropy is sufficiently small. This condition can be met for molecular clusters of sufficiently high symmetry, as for the Mn6 compound studied here. Magnetic specific heat and susceptibility experiments show a transition to ferromagnetic dipolar order at T_{c} = 0.16 K. Classical Monte-Carlo calculations indeed predict ferromagnetic ordering and account for the correct value of T_{c}. In high magnetic fields we detected the contribution of the ^{55}Mn nuclei to the specific heat, and the characteristic timescale of nuclear relaxation. This was compared with results obtained directly from pulse-NMR experiments. The data are in good mutual agreement and can be well described by the theory for magnetic relaxation in highly polarized paramagnetic crystals and for dynamic nuclear polarization, which we extensively review. The experiments provide an interesting comparison with the recently investigated nuclear spin dynamics in the anisotropic single molecule magnet Mn12-ac.

First time determination of the microscopic structure of a stripe phase: Low temperature NMR in La2NiO4.17

The experimental observations of stripes in superconducting cuprates and insulating nickelates clearly show the modulation in charge and spin density. However, these have proven to be rather insensitive to the harmonic structure and (site or bond) ordering. Using (139)La NMR in La(2)NiO(4+delta) with delta = 0.17, we show that in the 1/3 hole doped nickelate below the freezing temperature the stripes are strongly solitonic and site ordered with Ni(3+) ions carrying S = 1/2 in the domain walls and Ni(2+) ions with S = 1 in the domains.