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Anisotropically wetting substrates enable useful control of droplet behavior across a range of applications. Usually, these involve chemically or physically patterning the substrate surface, or applying gradients in properties like temperature or electrical field. Here, we show that a flat, stretched, uniform soft substrate also exhibits asymmetric wetting, both in terms of how droplets slide and in their static shape. Droplet dynamics are strongly affected by stretch: glycerol droplets on silicone substrates with a 23\% stretch slide 67\% faster in the direction parallel to the applied stretch than in the perpendicular direction. Contrary to classical wetting theory, static droplets in equilibrium appear elongated, oriented parallel to the stretch direction. Both effects arise from droplet-induced deformations of the substrate near the contact line., Comment: 3 figures

Programming supramolecular assembly in the time domain is a fundamental aspect of the design of biomimetic materials. We achieved the time-controlled sol–gel transition of a poly(vinyl alcohol)–iodine supramolecular complex by generating iodine in situ with a clock reaction. We demonstrate that both the gelation time and the mechanical properties of the resulting hydrogel can be tuned by properly selecting the clock parameters or through competitive iodine complexation., Soft Matter, 17 (5), ISSN:1744-683X, ISSN:1744-6848

Autocatalytic pH clocks can be useful to control self-assembly in the time domain. Their applications are, however, limited by the currently available toolbox. We describe here an approach for the design of a dynamic pH switch that generates intense alkali-to-acid changes after a tailorable lagtime (from minutes to hours), and we demonstrate its application for the time-controlled supramolecular self-assembly of nanofibers., Molecular Systems Design & Engineering, 5 (2), ISSN:2058-9689

Self-regulating materials require embedded control systems. Active networks of enzymes fulfill this function in living organisms, and the development of chemical controls for synthetic systems is still in its infancy. While previous work has focused on enzymatic controls, small-molecule networks have unexplored potential. We describe a simple small-molecule network that is able to produce transient pH cycles with tunable lagtimes and lifetimes, based on coupling the acid-to-alkali methylene glycol-sulfite reaction to 1,3-propanesultone, a slow acid generator. Applied to transient pH-driven supramolecular self-assembly of a perylene diimide, our system matches the flexibility of in vitro enzymatic systems, including the ability to perform repeated cycles of assembly and disassembly., Soft Matter, 16 (3), ISSN:1744-683X, ISSN:1744-6848

Transient self-assembly is a necessary step towards the development of life-like materials. Our approach allows to program pH-driven supramolecular assembly in the time domain with tailorable lag- and life-times, overcoming the limitations of previously described approaches and setting a new standard for active materials design.

Living and engineered systems rely on the stable coexistence of two interspersed liquid phases. Yet, surface tension drives their complete separation. Here, we show that stable droplets of uniform and tunable size can be produced through arrested phase separation in an elastic matrix. Starting with a cross-linked, elastic polymer network swollen by a solvent mixture, we change the temperature or composition to drive demixing. Droplets nucleate and grow to a stable size that is tunable by the network cross-linking density, the cooling rate, and the composition of the solvent mixture. We discuss thermodynamic and mechanical constraints on the process. In particular, we show that the threshold for macroscopic phase separation is altered by the elasticity of the polymer network, and we highlight the role of correlations between nuclei positions in determining the droplet size and polydispersity. This phenomenon has potential applications ranging from colloid synthesis and structural color to phase separation in biological cells., Physical Review X, 8 (1), ISSN:2160-3308

We employ a semiclassical picture to study dynamics in a bosonic Josephson junction with various initial conditions. Phase-diffusion of coherent preparations in the Josephson regime is shown to depend on the initial relative phase between the two condensates. For initially incoherent condensates, we find a universal value for the buildup of coherence in the Josephson regime. In addition, we contrast two seemingly similar on-separatrix coherent preparations, finding striking differences in their convergence to classicality as the number of particles increases., Comment: 18 pages, 8 figures, improved version, pedagogical orientation, 3 extra appendices that are not included in the published version

We consider an atomic Bose-Einstein condensate loaded in a biased double-well trap with tunneling rate K and interatomic interaction U. The Bose-Einstein condensate is prepared such that all N atoms are in the left well. We drive the system by sweeping the potential difference E between the two wells. Depending on the interaction u=NU/K and the sweep rate E, we distinguish three dynamical regimes: adiabatic, diabatic, and sudden and consider the occupation statistics of the final state. The analysis goes beyond mean-field theory and is complemented by a semiclassical picture.