Correlation-function-based microstructure design of alloy-polymer composites for dynamic dry adhesion tuning in soft gripping

Author:

Xu Yaopengxiao1,Chen Pei-En2,Li Hechao2,Xu Wenxiang13,Ren Yi2,Shan Wanliang4,Jiao Yang1ORCID

Affiliation:

1. Department of Materials Science and Engineering, Arizona State University, Tempe, Arizona 85287, USA

2. Department of Mechanical Engineering, Arizona State University, Tempe, Arizona 85287, USA

3. College of Mechanics and Materials, Hohai University, Nanjing 211100, People’s Republic of China

4. Department of Mechanical and Aerospace Engineering, Syracuse University, Syracuse, New York 13244, USA

Abstract

Tunable dry adhesion is a crucial mechanism in compliant manipulation. The gripping force can be controlled by reversibly varying the physical properties (e.g., stiffness) of the composite via external stimuli. The maximal gripping force Fmaxand its tunability depend on, among other factors, the stress distribution on the gripping interface and its fracture dynamics (during detaching), which in turn are determined by the composite microstructure. Here, we present a computational framework for the modeling and design of a class of binary smart composites containing a porous low-melting-point alloy (LMPA) phase and a polymer phase, in order to achieve desirable dynamically tunable dry adhesion. We employ spatial correlation functions to quantify, model, and represent the complex bi-continuous microstructure of the composites, from which a wide spectrum of realistic virtual 3D composite microstructures can be generated using stochastic optimization. A recently developed volume-compensated lattice-particle method is then employed to model the dynamic interfacial fracture process, where the gripper is detached from the object, to compute Fmaxfor different composite microstructures. We focus on the interface defect tuning mechanism for dry adhesion tuning enabled by the composite, and find that for an optimal microstructure among the ones studied here, a tenfold dynamic tuning of Fmaxbefore and after the thermal expansion of the LMPA phase can be achieved. Our computational results can provide valuable guidance for experimental fabrication of the LMPA–polymer composites.

Funder

National Science Foundation

Publisher

AIP Publishing

Subject

General Physics and Astronomy

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