Search arXiv⌕ Search

arXiv · 2507.07639

Geometry-Dependent Adhesion in Transparent, Monodomain Liquid Crystal Elastomers

Abstract

Elastomeric pressure-sensitive adhesives (PSAs) form adhesive bonds under light pressure. Liquid crystal elastomers (LCEs) are exciting PSA candidates as they can impart both anisotropy and temperature-dependence to adhesion, but the full potential of their anisotropic adhesion is unexplored. Here, identical side-chain LCEs, produced as transparent isotropic or nematic films are investigated; the latter aligned in homeotropic or planar geometries. Their room-temperature adhesion, determined through a 90-degree peel test, is consistent with theoretical predictions and strongest in a planar geometry (peeled parallel to the director) with adhesive force per unit length of 0.67 Nmm-1. In contrast, adhesion of the planar perpendicular, isotropic and homeotropic films is 62.5%, 38.5% and 23.0% lower, respectively. The surface contribution to adhesion is identical for all films, confirming that the variation in adhesion is determined solely by the bulk LCE alignment controlled during film preparation. A temperature-dependent adhesion factor is determined from 0 Celsius to 80 Celsius using dynamic mechanical analysis, and found to be in excellent agreement with the peel data at room temperature. Molecular relaxations active above the glass transition temperature are dominant in determining LCE adhesion. The results show that side-chain LCEs can function as transparent, tunable, broad-temperature smart PSAs

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Aidan Street, Devesh Mistry, Johan Mattsson, Helen F. Gleeson. 2025-07-10. Geometry-Dependent Adhesion in Transparent, Monodomain Liquid Crystal Elastomers. https://arxiv.org/abs/2507.07639

Cite the original work for its findings. Save a collection to share your selection of sources.

KEEP EXPLORING

Related papers

Control of filament network rigidity by the condensation of crowding molecules

Understanding how liquid-liquid phase separation impacts the mechanics of filament networks is a fundamental physical problem at the heart of biological cellular processes and soft material design. While a few theoretical mechanisms have been proposed, a clear demonstration of the direct coupling of phase separation to the overall network stiffness is missing. We report experiments that reveal a universal mechanism by which the condensation of macromolecular crowders induces a rigidity transition in a model filament network. We reconstituted stiff sterically interacting helical filaments and polymeric crowders. Initially, the macromolecules were uniformly dissolved and the filaments formed bundles that assembled a rigid entangled network. Once the crowders condensed into droplets, the network structure lost its rigidity and its mechanical response weakened by an order-of-magnitude. The subsequent dissolution of the condensates was accompanied by the re-establishment of rigidity. Our results show that crowder phase separation modulates the mechanics of filament networks by tuning the osmotic pressure holding the network together. This principle may serve as a paradigm for devising dynamically tunable filamentous materials.

cond-mat.soft↗

Speed up of passive tracers in mixtures with active chemical reactions

Diffusivity of passive tracers in complex mixtures is widely relevant for industrial applications and for probing biological systems. Interactions with the surrounding medium typically generate a drag force that suppresses tracer diffusion, although self-propulsion can accelerate tracers via active fluctuations. Similar effects are not understood in mixtures with particle conversion and exchange, although these are particularly relevant in biological contexts, where actively driven reactions prevail. By studying a thermodynamically consistent model of chemical reactions in mixtures, we show that reactions provide an additional relaxation pathway that suppresses interaction-induced memory, reducing the drag on tracers and restoring their diffusivity toward the value expected in the absence of solutes. Moreover, active reactions generate nonequilibrium fluctuations that can push tracer diffusivity beyond this limit, an effect we confirm with particle-based simulations. Our results identify chemical activity as a distinct route to controlling mass transport and offer a framework for interpreting microrheology experiments in chemically active mixtures.

cond-mat.soft↗

Diffusion of charged rods across 3D varying section channels

We analyze the transport of rod-like particles by diffusion and drift in a three-dimensional channel with varying circular or elliptic cross section. Applying the Fick-Jacobs approximation to the transport equation of the particles' probability distribution, we derive an effective one-dimensional substitute model and the associated free energy profile. Our results show that the data for the mean first passage time of rods, once expressed as a function of the effective free energy barrier, collapse onto the same master curve as obtained for point or spherical particles. The observed universality provides a simple framework for predicting transport times of anisotropic particles in confined geometries without resolving the full multidimensional dynamics.

cond-mat.soft↗