Search arXivSearch

arXiv · 2609.15417

From bending to stretching driven peeling of heterogeneous adhesives

Abstract

We study theoretically the peeling behavior of adhesives. Adopting a fracture mechanics approach, we derive the equation of motion of the adhesion front propagating at the interface between the adhesive and the substrate from which the peel strength is inferred. The originality of our approach lies in the description of the interplay during peeling between the stretching and the bending modes of deformation of the adhesive that is described as a F{\''o}ppl-Von Karman's thin film. Considering first a straight adhesion front, we retrieve the most salient feature of homogeneous adhesives, namely a peeling angle dependent peel strength driven by bending at large angles and by stretching at low angles. We also derive the shape of the adhesive that can be described using a single bending length scale derived from our model. We then investigate the impact of adhesion heterogeneities. We evidence that the deformations of the adhesion front are governed by a non-local interface elasticity the strength of which decreases with the peeling angle. This phenomenon reflects the transition between a stretching dominated peeling at low angle to a bending driven peeling at large angles that is captured in our model. This transition impacts the stability of adhesive fronts that relaxe more slowly from perturbations and gives rise to a stronger toughening effect in presence of a disorder distribution of adhesion energy at low peeling angles. Overall, this study sheds light on the central role played the elastic deformations of adhesives on their peeling behavior. The proposed framework unfolds the complex interplay between the deformation of adhesives and the peeling driving force that may be leveraged to engineer heterogeneous adhesives with enhanced properties. It also provides rich insights on the mechanisms underlying the emergence of non-local elasticity in interface problems.

Explore related subjects

Keep this discovery

Explore connections, maps & timelines

BibTeXRIS

Laurent Ponson. 2026-09-14. From bending to stretching driven peeling of heterogeneous adhesives. https://arxiv.org/abs/2609.15417

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

KEEP EXPLORING

Related papers

Towards ultra-scaled nanoelectronics using the zipper material system $Bi_2O_2Se/Bi_2SeO_5$

Two-dimensional (2D) materials could overcome the scaling bottleneck of nanoelectronics by enabling atomically thin channels, superior electrostatic control, and reduced short-channel effects. However, progress is limited by the lack of semiconductor–insulator interfaces being simultaneously scalable, stable, and reliable. Conventional 2D interfaces are often low quality or require transferring dissimilar materials, limiting reproducibility and scalability. We show that the zipper heterostructure formed by the high-mobility 2D semiconductor Bi 2 O 2 Se and its native high- κ oxide Bi 2 SeO 5 addresses these challenges, providing an atomically sharp, chemically matched interface with excellent electrostatics and promising scaling potential. We further present the first comprehensive multiscale assessment of Bi 2 O 2 Se/Bi 2 SeO 5 transistors targeting thermal stability, reliability, and scalability by linking atomic-scale structure and defects to device-level behavior across four transistor generations (top-gated, fin, and two gate-all-around architectures). Benchmarking against IRDS-2035 targets indicates that Bi 2 O 2 Se/Bi 2 SeO 5 devices could deliver high drive current with low gate leakage under aggressive scaling, potentially surpassing the targets in the upper-bound region of the sensitivity analysis. Finally, we identify oxygen-related oxide defects as the dominant origin of hysteresis consistent with a beneficial role of encapsulation and oxygen-rich annealing. Together, our findings support the potential of this zipper material system as a technologically-credible and manufacturing-relevant platform for future nanoelectronics.

cond-mat.mtrl-sci

Influence of Heterogeneity on the Response of Architected Metamaterials

Architected metamaterials like foams and lattices exhibit complex responses governed by microstructural instabilities, localization, and phase-transition-like phenomena. Their behavior is further affected by heterogeneities inherent in their microstructure often caused through manufacturing processes. In this study we extend a gradient-enhanced, nonlocal continuum formulation to incorporate stochastic material heterogeneity through Gaussian random fields imposed on selected constitutive parameters. The framework enables independent control of both the amplitude and spatial correlation of material fluctuations while preserving thermodynamic consistency and regularization of localization. It also introduces a characteristic lengthscale ratio between the nonlocal and correlation lengthscales, that enables modeling at the limit of random or spatially correlated microstructures. Finite element simulations of confined compression and indentation show that heterogeneity fundamentally alters phase nucleation, localization morphology, and macroscopic response. Overall, the proposed framework provides a unified approach for linking stochastic material variability to instability-driven mechanics in architected metamaterials, enabling improved understanding of imperfection sensitivity, stability and design. It showcases how heterogeneity alone can influence characteristic features of the response, such as stability, slope of the plateau region, and elimination of the initial elastic regime.

cond-mat.mtrl-sci

Structural, electronic, and optical properties of hexagonal GeSn from density functional theory

Unlike cubic GeSn, which undergoes an indirect-to-direct bandgap transition only above a finite Sn concentration, lonsdaleite (2H) germanium is an intrinsic direct-gap semiconductor. We employ first-principles density functional theory to investigate the structural, electronic, and optical properties of 2H-Ge$_{1-x}$Sn$_{x}$ random alloys in the dilute Sn regime ($x \le 0.10$). Substitutional disorder is modeled using 48-atom special quasirandom structure (SQS) supercells, and the coherent effective band structure is recovered via spectral band unfolding. We show that the semiconducting alloy configurations retain a direct bandgap at the $Γ$ point, with a moderate, nearly linear reduction of the bandgap in the dilute regime that shifts the fundamental absorption edge toward the mid-infrared. As the gap approaches zero, its calculated value becomes increasingly sensitive to the atomic configuration and supercell size. Evaluation of the optical transition matrix elements shows that the polarization anisotropy characteristic of pristine 2H-Ge remains observable under dilute Sn alloying. Although alloy disorder relaxes the crystal selection rules, the band edge response remains dominated by light polarized perpendicular to the crystal $c$ axis, whereas the parallel component remains weaker. These results identify dilute hexagonal GeSn as a tunable direct-gap system with a strongly polarization-dependent optical response in the infrared.

cond-mat.mtrl-sci