Lightweight and elastically deformable soft materials that are thermally conductive are critical for emerging applications in wearable computing, soft robotics, and thermoregulatory garments. To overcome the fundamental heat transport limitations in soft materials, room temperature liquid metal (LM) has been dispersed in elastomer that results in soft and deformable materials with unprecedented thermal conductivity. However, the high density of LMs (>6 g cm−3) and the typically high loading (⩾85 wt%) required to achieve the desired properties contribute to the high density of these elastomer composites, which can be problematic for large‐area, weight‐sensitive applications. Here, the relationship between the properties of the LM filler and elastomer composite is systematically studied. Experiments reveal that a multiphase LM inclusion with a low‐density phase can achieve independent control of the density and thermal conductivity of the elastomer composite. Quantitative design maps of composite density and thermal conductivity are constructed to rationally guide the selection of filler properties and material composition. This new multiphase material architecture provides a method to fine‐tune material composition to independently control material and functional properties of soft materials for large‐area and weight‐sensitive applications.
Soft, elastically deformable composites with liquid metal (LM) droplets can enable new generations of soft electronics, robotics, and reconfigurable structures. However, techniques to control local composite microstructure, which ultimately governs material properties and performance, is lacking. Here a direct ink writing technique is developed to program the LM microstructure (i.e., shape, orientation, and connectivity) on demand throughout elastomer composites. In contrast to inks with rigid particles that have fixed shape and size, it is shown that emulsion inks with LM fillers enable in situ control of microstructure. This enables filaments, films, and 3D structures with unique LM microstructures that are generated on demand and locked in during printing. This includes smooth and discrete transitions from spherical to needle‐like droplets, curvilinear microstructures, geometrically complex embedded inclusion patterns, and connected LM networks. The printed materials are soft (modulus < 200 kPa), highly deformable (>600 % strain), and can be made locally insulating or electrically conductive using a single ink by controlling the process conditions. These capabilities are demonstrated by embedding elongated LM droplets in a soft heat sink, which rapidly dissipates heat from high‐power LEDs. These programmable microstructures can enable new composite paradigms for emerging technologies that demand mechanical compliance with multifunctional response.
more » « less- NSF-PAR ID:
- 10445355
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Advanced Materials
- Volume:
- 34
- Issue:
- 20
- ISSN:
- 0935-9648
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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Abstract In this study, we discuss the characterization and quantification of composite microstructures formed by the external field manipulation of high aspect ratio magnetic particles in an elastomeric matrix. In our prior work, we have demonstrated that the simultaneous application of electric and magnetic fields on hard magnetic particles with geometric anisotropy can create a hierarchy of structures at different length scales, which can be used to achieve a wide range of properties. We aim to characterize these hierarchical structures and relate them to final composite properties so we can achieve our ultimate goal of designing a material for a prescribed performance. The complex particle structures are formed during processing by using electric and magnetic fields, and they are then locked-in by curing the polymer matrix around the particles. The model materials used in the study are barium hexaferrite (BHF) particles and polydimethylsiloxane (PDMS) elastomer. BHF was selected for its hard magnetic properties and high geometric anisotropy. PDMS was selected for its good mechanical properties and its tunable curing kinetics. The resulting BHF-PDMS composites are magnetoactive, i.e., they will deform and actuate in response to magnetic fields. In order to investigate the resulting particle orientation, distribution and alignment and to predict the composite’s macro scale properties, we developed techniques to quantify the particle structures.
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Important findings show 1) the ability to control structure using a combination of external electric, magnetic and thermal fields; 2) that electric fields promote long range order while magnetic fields promote short-range order; and 3) the resulting hierarchical structure greatly influence bulk material properties. Manipulating particles in a composite material is technologically important because changes in microstructure can alter the properties of the bulk material. The multifield processing we investigate here can form the basis for next generation additive manufacturing platforms where desired properties are tailored locally through in-situ hierarchical control of particle arrangements.
