Crystal nuclei and structural correlations in two-dimensional colloidal mixtures: experiment versus simulation

We examine binary mixtures of superparamagnetic colloidal particles confined to a two-dimensional water-air interface both by real-space experiments and Monte-Carlo computer simulations at high coupling strength. In the simulations, the interaction is modelled as a pairwise dipole-dipole repulsion. While the ratio of magnetic dipole moments is fixed, the interaction strength governed by the external magnetic field and the relative composition is varied. Excellent agreement between simulation and experiment is found for the partial pair distribution functions including the fine structure of the neighbour shells at high coupling. Furthermore local crystal nuclei in the melt are identified by bond-orientational order parameters and their contribution to the pair structure is discussed

The experimental realization of a two-dimensional colloidal model system

We present the technical details of an experimental method to realize a model system for 2D phase transitions and the glass transition. The system consists of several hundred thousand colloidal super-paramagnetic particles confined by gravity at a flat water-air interface of a pending water droplet where they are subjected to Brownian motion. The dipolar pair potential and therefore the system temperature is not only known precisely but also directly and instantaneously controllable via an external magnetic field B. In case of a one component system of monodisperse particles the system can crystallize upon application of B whereas in a two component system it undergoes a glass transition. Up to 10000 particles are observed by video microscopy and image processing provides their trajectories on all relative length and time scales. The position of the interface is actively regulated thereby reducing surface fluctuations to less than one micron and the setup inclination is controlled to an accuracy of 1 microrad. The sample quality being necessary to enable the experimental investigation of the 2D melting scenario, 2D crystallization, and the 2D glass transition, is discussed.Comment: 13 pages, 11 figure

Dynamics of particles and cages in an experimental 2D glass former

We investigate the dynamics of a glass forming 2D colloidal mixture and show the existence of collective motions of the particles. We introduce a mean square displacement MSD with respect to the nearest neighbors which shows remarkable deviations from the usual MSD quantifying the individual motion of our particles. Combined with the analysis of the self part of the Van Hove function this indicates a coupled motion of particles with their cage as well as intra cage hopping processes.Comment: Submitted to EP

Partial clustering prevents global crystallization in a binary 2D colloidal glass former

A mixture of two types of super-paramagnetic colloidal particles with long range dipolar interaction is confined by gravity to a flat interface of a hanging water droplet. The particles are observed by video microscopy and the dipolar interaction strength is controlled via an external magnetic field. The system is a model system to study the glass transition in 2D, and it exhibits partial clustering of the small particles. This clustering is strongly dependent on the relative concentration $\xi$ of big and small particles. However, changing the interaction strength $\Gamma$ reveals that the clustering does not depend on the interaction strength. The partial clustering scenario is quantified using Minkowski functionals and partial structure factors. Evidence that partial clustering prevents global crystallization is discussed

Local crystalline order in a 2D colloidal glass former

A mixture of two types of super-paramagnetic colloidal particles with long-range dipolar interaction is confined by gravity to a flat interface of a hanging water droplet. The particles are observed by video microscopy and the dipolar interaction strength is controlled by an external magnetic field. The local structure as obtained by pair correlation functions and bond order statistics is investigated as a function of system temperature and relative concentration. Although the system has no long-range order and exhibits glassy dynamics, different types of stable crystallites coexist. The local order of the globally disordered structure is explained by a small set of specific crystal structures. The statistics of crystal unit cells show a continuous increase of local order with decreasing system temperature as well as a dependence on sample history and local composition

Correlation between dynamical heterogeneities, structure and potential-energy distribution in a 2D amorphous solid

We investigate the collective properties of particles in a 2D experimental system which consists of a bi-disperse mixture of colloidal particles confined at an air/water interface. We find a direct correlation between structure and dynamical heterogeneities in this system: particles belonging to locally ordered structures have lower potential energy and are slower than other particles. In a more general way we show that particles with high potential energy are dominating the dynamics especially in the α-relaxation regime