Highly charged inorganic-organic colloidal core-shell particles.

Highly defined, hybrid inorganic-organic colloidal core-shell particles consisting of a silica core and a shell of fluorinated acrylate are prepared in a two-step route. The core-shell structure of the particles is investigated by means of small-angle X-ray scattering (SAXS). Because of highly acidic sulfonic acid surface groups resulting from the radical initiator sodium peroxodisulfate at the organic shell, long-range electrostatic interactions lead to the formation of liquidlike mesostructures. Increasing the effective interaction by reducing the next-neighbor distances induces a freezing of the liquidlike structures, i.e., a transition to crystalline and glassy structures. Because of the high electron density in the core and the fluorinated polymer shell, these particles are strong X-ray scatterers. In combination with the large number of effective charges and the outstanding monodispersity, these core-shell particles are a promising model system for the investigation of the glass transition by photon correlation spectroscopy employing coherent X-rays.

Spatially resolved investigation of solution cast nanoparticle films by X-ray scattering and multidimensional data set classification.

A combinatorial high-throughput approach is used to investigate a solution cast gradient consisting of colloidal gold nanoparticles on top of a silicon substrate by means of a X-ray nanobeam. Classification algorithms are used to reveal and visualize structural transitions from a frozen colloidal solution to a well-defined nanostructure. Prominent length scales on the order of 100 nm are observed. A periodic change in the nanostructure along the gradient is explained by a simplified stick-slip model.

Fast two-dimensional detection for X-ray photon correlation spectroscopy using the PILATUS detector.

The first X-ray photon correlation spectroscopy experiments using the fast single-photon-counting detector PILATUS (Paul Scherrer Institut, Switzerland) have been performed. The short readout time of this detector permits access to intensity autocorrelation functions describing dynamics in the millisecond range that are difficult to access with charge-coupled device detectors with typical readout times of several seconds. Showing no readout noise the PILATUS detector enables measurements of samples that either display fast dynamics or possess only low scattering power with an unprecedented signal-to-noise ratio.

X-ray cross correlation analysis uncovers hidden local symmetries in disordered matter.

We explore the different local symmetries in colloidal glasses beyond the standard pair correlation analysis. Using our newly developed X-ray cross correlation analysis (XCCA) concept together with brilliant coherent X-ray sources, we have been able to access and classify the otherwise hidden local order within disorder. The emerging local symmetries are coupled to distinct momentum transfer (Q) values, which do not coincide with the maxima of the amorphous structure factor. Four-, 6-, 10- and, most prevalently, 5-fold symmetries are observed. The observation of dynamical evolution of these symmetries forms a connection to dynamical heterogeneities in glasses, which is far beyond conventional diffraction analysis. The XCCA concept opens up a fascinating view into the world of disorder and will definitely allow, with the advent of free electron X-ray lasers, an accurate and systematic experimental characterization of the structure of the liquid and glass states.

Hard X ray holographic diffraction imaging.

We determine the absolute electron density of a lithographically grown nanostructure with 25 nm resolution by combining hard x-ray Fourier transform holography with iterative phase retrieval methods. While holography immediately reveals an unambiguous image of the object, we deploy in addition iterative phase retrieval algorithms for pushing the resolution close to the diffraction limit. The use of hard (8 keV) x rays eliminates practically all constraints on sample environment and enables a destruction-free investigation of relatively thick or buried samples, making holographic diffraction imaging a very attractive tool for materials science. We note that the technique is ideally suited for subpicosecond imaging that will become possible with the emerging hard x-ray free-electron lasers.

Field induced anisotropy of charged magnetic colloids: a rescaled mean spherical approximation study.

The liquidlike structure of colloidal suspensions with both electrostatic and magnetic interactions is investigated by means of small angle x-ray scattering (SAXS) dependent on an external magnetic field. For weak magnetic interactions, without external field, the magnetic dipoles are randomly oriented. Under this condition, isotropic structures are observed. In an external field, however, the magnetic momenta arrange parallel to the external field and induce anisotropic liquidlike structures. For weak magnetic interactions, the structure factor can be described within the framework of the rescaled mean spherical approximation. Due to the high experimental accuracy of synchrotron SAXS, from the anisotropic distortion of liquidlike structures, interparticle forces smaller than 10(-15) N can easily be detected.

Structure and dynamics of electrostatically interacting magnetic nanoparticles in suspension.

We investigate the structure and dynamics of charge-stabilized CoFe(2)O(4)-SiO(2) core-shell magnetic nanoparticles in suspensions. Small angle x-ray scattering and x-ray photon correlation spectroscopy allow us to analyze the intraparticle (core-shell) and interparticle structure of the suspension, as well as their dynamic and hydrodynamic behavior. Due to the weak magnetic interactions, the liquidlike structure is governed by screened Coulomb interactions. The hydrodynamic interactions of the measured systems are significantly stronger than predicted by current theories.