We have performed thermodynamic and neutron scattering measurements on the S=1/2 kagomé lattice antiferromagnet ZnCu3(OH)6Cl2. The susceptibility indicates a Curie-Weiss temperature of theta CW approximately = -300 K; however, no magnetic order is observed down to 50 mK. Inelastic neutron scattering reveals a spectrum of low energy spin excitations with no observable gap down to 0.1 meV. The specific heat at low-T follows a power law temperature dependence. These results suggest that an unusual spin liquid state with essentially gapless excitations is realized in this kagomé lattice system.
Single magnetic atoms on surfaces are the smallest conceivable units for two-dimensional magnetic data storage. Previous experiments on such systems have investigated magnetization curves, the many-body Kondo effect and magnetic excitations in quantum spin systems, but a stable magnetization has not yet been detected for an atom on a non-magnetic surface in the absence of a magnetic field. The spin direction of a single magnetic atom can be fixed by coupling it to an underlying magnetic substrate via the exchange interaction, but it is then difficult to differentiate between the magnetism of the atom and the surface. Here, we take advantage of the orbital symmetry of the spin-polarized density of states of single cobalt atoms to unambiguously determine their spin direction in real space using a combination of spin-resolved scanning tunnelling microscopy experiments and ab initio calculations. By laterally moving atoms on our non-collinear magnetic template, the spin direction can also be controlled while maintaining magnetic sensitivity, thereby providing an approach for constructing and characterizing artificial atomic-scale magnetic structures.
We report magnetocaloric and magnetic-torque evidence that in Cs2CuBr4--a geometrically frustrated Heisenberg S=1/2 triangular-lattice antiferromagnet--quantum fluctuations stabilize a series of spin states at simple increasing fractions of the saturation magnetization Ms. Only the first of these states--at M=1/3Ms--has been theoretically predicted. We discuss how the higher fraction quantum states might arise and propose model spin arrangements. We argue that the first-order nature of the transitions into those states is due to strong lowering of the energies by quantum fluctuations, with implications for the general character of quantum phase transitions in geometrically frustrated systems.
We report a transverse conical spin spiral as the magnetic ground state of a double-layer Mn on a W(110) surface. Using spin-polarized scanning tunneling microscopy, we find a long-range modulation along the [001] direction with a periodicity of 2.4 nm coexisting with a local row-wise antiferromagnetic contrast. First-principles calculations reveal a transverse conical spin-spiral ground state of this system which explains the observed magnetic contrast. The canting of the spins is induced by higher-order exchange interactions, while the spiraling along the [001] direction is due to frustrated Heisenberg exchange and Dzyaloshinskii-Moriya interaction.
With the advent of scanning probe microscopy techniques that involve a tip and a sample in relative motion in the contact or noncontact regime, the microscopic aspects of friction have become a major branch of research called nanotribology. A significant number of recent studies in this field have concentrated on the distinction between electronic and phononic contributions to friction. Here, we are using the combination of spin-polarized scanning tunneling microscopy and single-atom manipulation in order to move individual magnetic atoms over a magnetic template. By monitoring the spin-resolved manipulation traces and comparing them with results of Monte Carlo simulations, we are able to reveal the characteristic friction force variations resulting from the occurrence of spin friction on the atomic scale.
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