F. Ladieu

Direct experimental evidence of a growing length scale accompanying the glass transition

Understanding glass formation is a challenge, because the existence of a true glass state, distinct from liquid and solid, remains elusive: Glasses are liquids that have become too viscous to flow. An old idea, as yet unproven experimentally, is that the dynamics becomes sluggish as the glass transition approaches, because increasingly larger regions of the material have to move simultaneously to allow flow. We introduce new multipoint dynamical susceptibilities to estimate quantitatively the size of these regions and provide direct experimental evidence that the glass formation of molecular liquids and colloidal suspensions is accompanied by growing dynamic correlation length scales.

Spatial correlations in the dynamics of glassforming liquids : Experimental determination of their temperature dependence

We use recently introduced three-point dynamic susceptibilities to obtain an experimental determination of the temperature evolution of the number of molecules Ncorr that are dynamically correlated during the structural relaxation of supercooled liquids. We first discuss in detail the physical content of three-point functions that relate the sensitivity of the averaged two-time dynamics to external control parameters (such as temperature or density), as well as their connection to the more standard four-point dynamic susceptibility associated with dynamical heterogeneities. We then demonstrate that these functions can be experimentally determined with good precision. We gather available data to obtain the temperature dependence of Ncorr for a large number of supercooled liquids over a wide range of relaxation time scales from the glass transition up to the onset of slow dynamics. We find that Ncorr systematically grows when approaching the glass transition. It does so in a modest manner close to the glass transition, which is consistent with an activation-based picture of the dynamics in glassforming materials. For higher temperatures, there appears to be a regime where Ncorr behaves as a power-law of the relaxation time. Finally, we find that the dynamic response to density, while being smaller than the dynamic response to temperature, behaves similarly, in agreement with theoretical expectations.

Spin glass behavior in an interacting gamma-Fe2O3 nanoparticle system

In this paper we investigate the superspin glass behavior of a concentrated assembly of interacting maghemite nanoparticles and compare it to that of canonical atomic spin glass systems. ac versus temperature and frequency measurements show evidence of a superspin glass transition taking place at low temperature. In order to fully characterize the superspin glass phase, the aging behavior of both the thermo-remanent magnetization (TRM) and ac susceptibility has been investigated. It is shown that the scaling laws obeyed by superspin glasses and atomic spin glasses are essentially the same, after subtraction of a superparamagnetic contribution from the superspin glass response functions. Finally, we discuss a possible origin of this superparamagnetic contribution in terms of dilute spin glass models.

Evidence of growing spatial correlations at the glass transition from nonlinear response experiments.

The ac nonlinear dielectric response chi3(omega,T) of glycerol was measured close to its glass transition temperature T(g) to investigate the prediction that supercooled liquids respond in an increasingly nonlinear way as the dynamics slows down (as spin glasses do). We find that chi3(omega,T) indeed displays several nontrivial features. It is peaked as a function of the frequency omega and obeys scaling as a function of omega tau(T), with tau(T) the relaxation time of the liquid. The height of the peak, proportional to the number of dynamically correlated molecules N(corr)(T), increases as the system becomes glassy, and chi3 decays as a power law of omega over several decades beyond the peak. These findings confirm the collective nature of the glassy dynamics and provide the first direct estimate of the T dependence of N(corr).

Superconducting diamagnetic fluctuations in ropes of carbon nanotubes

We report low-temperature magnetisation measurements on a large number of purified ropes of single wall carbon nanotubes. In spite of a large superparamagnetic contribution due to the small ferromagnetic catalytical particles still present in the sample, at low temperature (

Experimental investigation of superspin glass dynamics

T<0.5K

Ground State of the Kagome-Like S = 1/2 Antiferromagnet Volborthite Cu~3V~2O~7(OH)~2 · 2H~2O

) and low magnetic field (

Measuring thermal effects in femtosecond laser-induced breakdown of dielectrics

H<80 Oe

A method for measuring the nonlinear response in dielectric spectroscopy through third harmonics detection

), a diamagnetic signal is detectable. This low temperature diamagnetism can be interpreted as the Meissner effect in ropes of carbon nanotubes which have previously been shown to exhibit superconductivity from transport measurements.

Low temperature magnetization of the S = 1 2 kagome antiferromagnet Zn Cu 3 ( O H ) 6 Cl 2

Magnetic nanoparticle assemblies in high concentrations can exhibit spin glass like properties in the low temperature phase due to the influence of strong dipolar interactions. To address the question of the extent to which the properties of these “superspin” glasses mimic those of an atomic spin glass, several homogeneously dispersed γ‐Fe2O3 nanoparticle assemblies of varying volume fraction have been studied. In a concentrated sample, the main features of atomic spin glasses have been observed including aging phenomena for which we have proposed a rescaling.