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A. D. Law
Researcher at Max Planck Society
Publications - 16
Citations - 476
A. D. Law is an academic researcher from Max Planck Society. The author has contributed to research in topics: Radial distribution function & Casimir effect. The author has an hindex of 10, co-authored 16 publications receiving 391 citations. Previous affiliations of A. D. Law include Paracelsus Private Medical University of Salzburg & University of Stuttgart.
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Journal ArticleDOI
Geometry-induced superdiffusion in driven crowded systems.
Olivier Bénichou,Anna S. Bodrova,Dipanjan Chakraborty,Dipanjan Chakraborty,Pierre Illien,A. D. Law,Carlos Mejía-Monasterio,Gleb Oshanin,Raphaël Voituriez +8 more
TL;DR: This work presents and solves analytically a minimal model consisting of a driven TP in a dense, crowded medium in which the motion of particles is mediated by the diffusion of packing defects, called vacancies, and predicts a long-lived superdiffusion which ultimately crosses over to giant diffusive behavior.
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Self-Assembly of Two-Dimensional Colloidal Clusters by Tuning the Hydrophobicity, Composition, and Packing Geometry
TL;DR: By tuning the composition and packing geometry of the mixed monolayer, a rich variety of two-dimensional hexagonal superlattices of mixed A/B or A/C clusters are formed, stabilized by short-ranged electrostatic induced dipole interactions, indicating that the self-assembly process can be effectively controlled.
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Two-dimensional colloidal alloys.
TL;DR: It is found that a rich variety of two-dimensional hexagonal super-lattices of large and small particles can be obtained in this system due to strong and long-range electrostatic repulsions through the nonpolar octane phase.
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Anisotropic Self-Assembly from Isotropic Colloidal Building Blocks.
TL;DR: This work studies the phase behavior of microspheres in the presence of poly(N-isopropylacrylamide) microgels at the air/water interface and demonstrates how complex, anisotropic assembly patterns can be realized from entirely isotropic building blocks by control of the interaction potential.
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Colloidal particles at fluid interfaces: behaviour of isolated particles.
TL;DR: The effects that a variation of the morphology and surface chemistry of a particle can have on its ability to adhere to a liquid interface, from a thermodynamic as well as a kinetic perspective, are explored.