We investigate experimentally magnetic frustration effects in thermally active artificial kagome spin ice. Starting from a paramagnetic state, the system is cooled down below the Curie temperature of the constituent material. The resulting magnetic c
onfigurations show that our arrays are locally brought into the so-called spin ice 2 phase, predicted by at-equilibrium Monte Carlo simulations and characterized by a magnetic charge crystal embedded in a disordered kagome spin lattice. However, by studying our arrays on a larger scale, we find unambiguous signature of an out-of-equilibrium physics. Comparing our findings with numerical simulations, we interpret the efficiency of our thermalization procedure in terms of kinetic pathways that the system follows upon cooling and which drive the arrays into degenerate low-energy manifolds that are hardly accessible otherwise.
The hole-doped kagome lattice of Cu2+ ions in LaCuO2.66 was investigated by nuclear quadrupole resonance (NQR), electron spin resonance (ESR), electrical resistivity, bulk magnetization and specific heat measurements. For temperatures above ~180 K, t
he spin and charge properties show an activated behavior suggestive of a narrow-gap semiconductor. At lower temperatures, the results indicate an insulating ground state which may or may not be charge ordered. While the frustrated spins in remaining patches of the original kagome lattice might not be directly detected here, the observation of coexisting non-magnetic sites, free spins and frozen moments reveals an intrinsically inhomogeneous magnetism. Numerical simulations of a 1/3-diluted kagome lattice rationalize this magnetic state in terms of a heterogeneous distribution of cluster sizes and morphologies near the site-percolation threshold.
By considering the constrained motion of classical spins in a geometrically frustrated magnet, we find a dynamical freezing temperature below which the system gets trapped in metastable states with a frozen moment and dynamical heterogeneities. The r
esidual collective degrees of freedom are strongly correlated, and by spontaneously forming aggregates, they are unable to reorganize the system. The phase space is then fragmented in a macroscopic number of disconnected sectors (broken ergodicity), resulting in self-induced disorder and thermodynamic anomalies, measured by the loss of a finite configurational entropy. We discuss these results in the view of experimental results on the kagome compounds, SrCr(9p)Ga(12-9p)O19, (H30)Fe3(SO4)2(OH)6, Cu3V2O7(OH)2.2H2O and Cu3BaV2O8(OH)2.
