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Guido L. A. Kusters

Guido L. A. Kusters appears in the imported research catalog. Authorship, coauthor and topic links are available while profile ownership is still unclaimed.

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cond-mat.soft Biological Physics cond-mat.mtrl-sci cond-mat.stat-mech

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preprint2026arXiv

Coexistence of patterned phases in chemically active multicomponent mixtures

Chemically active mixtures exhibit complex patterns that emerge from the interplay of physical interactions and reactions among components. Individually, these two processes are well-understood: Physical interactions can give rise to phase separation, whereas reactions can form reaction-diffusion patterns. To understand the combination of both processes, we identify a Lyapunov functional for a class of chemical reactions. By minimizing this functional, we identify a generalized Gibbs phase rule that governs the number of coexisting patterns, and we demonstrate that complex patterns can be created by the modular combination of independent phases. Our theory unveils complex stationary patterns in chemically active mixtures and provides a framework for analyzing more complex systems.

preprint2022arXiv

Transient response and domain formation in electrically deforming liquid crystal networks

Recently, Van der Kooij and co-workers recognised three distinct, transient regimes in the dynamics of electrically-deforming liquid crystal networks [Van der Kooij et al., Nat. Commun. 10, 1 (2019)]. Based on a Landau-theoretical framework, which encompasses spatially resolved information, we interpret these regimes: initially, the response is dominated by thermal noise, then the top of the film expands, followed by a permeation of this response into the bulk. An important signature of this interpretation is a significant dependence of the regime time scales on film thickness, where we observe a clear thin-film-to-bulk transition. The point of transition coincides with the emergence of spatial inhomogeneities in the bulk, i.e., domain formation, and should be avoided due to the less predictable steady-state expansion it gives rise to. Finally, we show that this domain formation can be suppressed by decreasing the initial thickness of the film, and increasing the linear dimensions of the mesogens, or their orientational order when crosslinked into the network, though this comes at the cost of the deformation magnitude. Our results contribute to achieving finer control over how smart liquid crystal network coatings are activated.