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Dive into the research topics where Roland H. Staff is active.

Publication


Featured researches published by Roland H. Staff.


ACS Nano | 2012

Patchy Nanocapsules of Poly(vinylferrocene)-Based Block Copolymers for Redox-Responsive Release

Roland H. Staff; Markus Gallei; Markus Mazurowski; Matthias Rehahn; Rüdiger Berger; Katharina Landfester; Daniel Crespy

Nanocapsules composed of a poly(vinylferrocene)-block-poly(methyl methacrylate) shell and a hydrophobic liquid core are prepared in water. The nanocapsule shells display a patchy structure with poly(vinylferrocene) patches with sizes of 25 ± 3 nm surrounded by poly(methyl methacrylate). The functional nanopatches can be selectively oxidized, thereby influencing the colloidal morphology and introducing polar domains in the nanocapsule shell. The hydrophobic to hydrophilic transition in the redox-responsive nanopatches can be advantageously used to release a hydrophobic payload encapsulated in the core by an oxidation reaction.


Soft Matter | 2011

Phase behavior of binary mixtures of block copolymers and a non-solvent in miniemulsion droplets as single and double nanoconfinement

Roland H. Staff; Patrick Rupper; Ingo Lieberwirth; Katharina Landfester; Daniel Crespy

Nanoparticles consisting of different molecular weight poly(styrene-block-methyl methacrylate) (P(S-b-MMA)) copolymers and nanocapsules consisting of the same copolymers, but additionally with hexadecane as liquid core material were prepared by the miniemulsion process. The dependence of the morphology of block copolymer assemblies on the nanoconfinement was investigated. We introduced two nanoconfinement parameters, that are the nanoparticle diameter D and the shell thickness d; D was controlled by varying the concentration of surfactant in the miniemulsion, while d was controlled by the ratio hexadecane/copolymer. As the diameter D of the high molecular weight (Mw ∼ 203,700 g mol−1) P(S-b-MMA) nanoparticles increased, first Janus-particles (at D 1800 nm) were obtained. Nanocapsules with 0 < d < D also showed an onion-like structure. In both cases the outmost layer was PMMA as identified by XPS and the lamellar thickness was in agreement with theoretical considerations. Nanoparticles and nanocapsules prepared with a low-molecular weight (Mw ∼ 19,500 g mol−1) P(S-b-MMA) displayed patchy structures. This is the first time that the morphology of block copolymers was studied under double nanoconfinement in colloids.


Small | 2013

Particle formation in the emulsion-solvent evaporation process.

Roland H. Staff; David Schaeffel; Andrey Turshatov; Davide Donadio; Hans-Jürgen Butt; Katharina Landfester; Kaloian Koynov; Daniel Crespy

The mechanism of particle formation from submicrometer emulsion droplets by solvent evaporation is revisited. A combination of dynamic light scattering, fluorescence resonance energy transfer, zeta potential measurements, and fluorescence cross-correlation spectroscopy is used to analyze the colloids during the evaporation process. It is shown that a combination of different methods yields reliable and quantitative data for describing the fate of the droplets during the process. The results indicate that coalescence plays a minor role during the process; the relatively large size distribution of the obtained polymer colloids can be explained by the droplet distribution after their formation.


Nano Letters | 2012

Fluorescence Correlation Spectroscopy Directly Monitors Coalescence During Nanoparticle Preparation

David Schaeffel; Roland H. Staff; Hans-Juergen Butt; Katharina Landfester; Daniel Crespy; Kaloian Koynov

Dual color fluorescence cross-correlation spectroscopy (DC FCCS) experiments were conducted to study the coalescence and aggregation during the formation of nanoparticles. To assess the generality of the method, three completely different processes were selected to prepare the nanoparticles. Polymeric nanoparticles were formed either by solvent evaporation from emulsion nanodroplets of polymer solutions or by miniemulsion polymerization. Inorganic nanocapsules were formed by polycondensation of alkoxysilanes at the interface of nanodroplets. In all cases, DC FCCS provided fast and unambiguous information about the occurrence of coalescence and thus a deeper insight into the mechanism of nanoparticle formation. In particular, it was found that coalescence played a minor role for the emulsion-solvent evaporation process and the miniemulsion polymerization, whereas substantial coalescence was detected during the formation of the inorganic nanocapsules. These findings demonstrate that DC FCCS is a powerful tool for monitoring nanoparticles genesis.


Archive | 2013

Recent Advances in the Emulsion Solvent Evaporation Technique for the Preparation of Nanoparticles and Nanocapsules

Roland H. Staff; Katharina Landfester; Daniel Crespy

The emulsion solvent evaporation technique is a method for preparing nanoparticles and nanocapsules that are particularly adapted for applications requiring materials with high purity and low toxicity, such as for biomedicine or electronics. We discuss here new important advances concerning the elucidation of the mechanism of nanoparticle formation, and the synthesis of nanoparticles with new structures or from new polymers.


Macromolecules | 2014

Hydrophobic Nanocontainers for Stimulus-Selective Release in Aqueous Environments

Roland H. Staff; Markus Gallei; Katharina Landfester; Daniel Crespy


Macromolecular Chemistry and Physics | 2012

Preparation and Characterization of Anisotropic Submicron Particles From Semicrystalline Polymers

Roland H. Staff; Ingo Lieberwirth; Katharina Landfester; Daniel Crespy


Macromolecules | 2014

Polymer Janus Nanoparticles with Two Spatially Segregated Functionalizations

Markus Urban; Birger Freisinger; Omayma Ghazy; Roland H. Staff; Katharina Landfester; Daniel Crespy; Anna Musyanovych


Macromolecular Chemistry and Physics | 2012

Chemical Routes Toward Multicompartment Colloids

Daniel Crespy; Roland H. Staff; Tanja Becker; Katharina Landfester


Polymer Chemistry | 2014

Janus nanoparticles with both faces selectively functionalized for click chemistry

Roland H. Staff; Jochen Willersinn; Anna Musyanovych; Katharina Landfester; Daniel Crespy

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Markus Gallei

Technische Universität Darmstadt

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Andrey Turshatov

Karlsruhe Institute of Technology

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