| 1. |
- Carstensen, Hauke, et al.
(författare)
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Phase formation in colloidal systems with tunable interaction
- 2015
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Ingår i: Physical Review E. Statistical, Nonlinear, and Soft Matter Physics. - 1539-3755 .- 1550-2376. ; 92:1
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Tidskriftsartikel (refereegranskat)abstract
- Self-assembly is one of the most fascinating phenomena in nature and is one key component in the formation of hierarchical structures. The formation of structures depends critically on the interaction between the different constituents, and therefore the link between these interactions and the resulting structure is fundamental for the understanding of materials. We have realized a two-dimensional system of colloidal particles with tunable magnetic dipole forces. The phase formation is studied by transmission optical microscopy and a phase diagram is constructed. We report a phase transition from hexagonal to random and square arrangements when the magnetic interaction between the individual particles is tuned from antiferromagnetic to ferrimagnetic.
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| 2. |
- Carstensen, Hauke, et al.
(författare)
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Self-assembly and percolation in two dimensional binary magnetic colloids
- 2022
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Ingår i: Soft Matter. - : Royal Society of Chemistry (RSC). - 1744-683X .- 1744-6848. ; 18:33, s. 6222-6228
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Tidskriftsartikel (refereegranskat)abstract
- We study the self-assembly of branching-chain networks and crystals in a binary colloidal system with tunable interactions. The particle positions are extracted from microscopy images and order parameters are extracted by image processing and statistical analysis. With these, we construct phase diagrams with respect to particle density, ratio and interaction. In order to draw a more complete picture, we complement the experiments with computer simulations. We establish a region in the phase diagram, where bead ratios and interactions are symmetric, promoting percolated structures.
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| 3. |
- Carstensen, Hauke
(författare)
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Self-assembly of magnetic particles
- 2018
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Doktorsavhandling (övrigt vetenskapligt/konstnärligt)abstract
- Self-assembly is the spontaneous formation of larger structures from small building blocks. This process is driven and determined by the interactions between the constituents. Examples of self assembly are found almost everywhere and, in particular, biological systems in general rely on a hierarchical formation of structures over a range of length scales. Technologically, self-assembly can be used to form mesoscopic structures and artificial crystals. In the case of particles with micrometer size suspended in a liquid phase, it is possible to use optical microscopy for the the investigation of self-assembly.In this thesis, the self-assembly of microbeads with tunable magnetic interactions is studied, based on the statistic analysis of microscope images and computer simulations. Magnetic and non-magnetic microbeads are suspended in a ferrofluid, which is a dispersion of magnetic nanoparticles in water. As a result, the magnetic properties of the microbeads in the ferrofluid are altered and can be described by effective magnetic susceptibilities and magnetic dipole moments, which can be tuned continuously. The liquid is confined between glass slides and effectively the microbeads are studied in a 2D geometry under a magnetic field, applied either in- or out-of-plane. The resulting structures are detected by image analysis algorithms, analyzed and correlated to the dipolar interaction between the beads, as well as to macroscopic quantities, like the particle density and ratio. For the in-plane field a phase transition from square to hexagonal lattice is observed. This phase transition is explained by the change in dipole interaction between the microbeads as the moments change from anti-parallel to parallel alignment. For the out-of-plane field the situation becomes diverse and more phases appear. It turns out that the phase formation in this case is strongly dependent on the bead ratio, density and interactions.We identify regions in the phase diagram, where isolated beads, percolated structures, and crystals dominate. To cover a wide parameter range the experiments are complemented by computer simulations. The tools developed in this thesis enable us to construct phase diagrams extracted from direct imaging and dependence on the extracted relevant parameters.
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| 4. |
- Carstensen, Hauke, et al.
(författare)
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Statistical analysis of phase formation in 2D colloidal systems
- 2018
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Ingår i: The European Physical Journal E Soft matter. - : SPRINGER. - 1292-8941 .- 1292-895X. ; 41:1
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Tidskriftsartikel (refereegranskat)abstract
- Colloidal systems offer unique opportunities for the study of phase formation and structure since their characteristic length scales are accessible to visible light. As a model system the two-dimensional assembly of colloidal magnetic and non-magnetic particles dispersed in a ferrofluid (FF) matrix is studied by transmission optical microscopy. We present a method to statistically evaluate images with thousands of particles and map phases by extraction of local variables. Different lattice structures and long-range connected branching chains are observed, when tuning the effective magnetic interaction and varying particle ratios.
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| 5. |
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| 6. |
- Shi, Liyang, et al.
(författare)
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Dynamic Coordination Chemistry Enables Free Directional Printing of Biopolymer Hydrogel
- 2017
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Ingår i: Chemistry of Materials. - : American Chemical Society (ACS). - 0897-4756 .- 1520-5002. ; 29, s. 5816-5823
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Tidskriftsartikel (refereegranskat)abstract
- Three-dimensional (3D) printing is a promising technology to develop customized biomaterials in regenerative medicine. However, for the majority of printable biomaterials (bioinks) there is always a compromise between excellent printability of fluids and good mechanical properties of solids. 3D printing of soft materials based on the transition from a fluid to gel state is challenging because of the difficulties to control such transition as well as to maintain uniform conditions three-dimensionally. To solve these challenges, a facile chemical strategy for the development of a novel hydrogel bioink with shear-thinning and self-healing properties based on dynamic metal-ligand coordination bonds is presented. The non-covalent cross-linking allows easy extrusion of the bioink from a reservoir without changing of its bulk mechanical properties. The soft hydrogel can avoid deformation and collapse using omnidirectional embedding of the printable hydrogel into a support gel bath sharing the same cross-linking chemistry. After combination with photo-initiated covalent cross-linking, it enables manufacturing of hydrogel structures with complex shapes and precise location of chemically attached ligands. Living cells can be entrapped in the new printable hydrogel and survive the following in situ photocross-linking. The presented printable hydrogel mate-rial expands the existing tool-box of bioinks for generation of in vitro 3D tissue-like structures and direct in vivo 3D printing.
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