An official website of the United States government
Abstract Mechanoresponsive color‐changing materials that can reversibly and resiliently change color in response to mechanical deformation are highly desirable for diverse modern technologies in optics, sensors, and robots; however, such materials are rarely achieved. Here, a fatigue‐resistant mechanoresponsive color‐changing hydrogel (FMCH) is reported that exhibits reversible, resilient, and predictable color changes under mechanical stress. At its undeformed state, the FMCH remains dark under a circular polariscope; upon uniaxial stretching of up to six times its initial length, it gradually shifts its color from black, to gray, yellow, and purple. Unlike traditional mechanoresponsive color‐changing materials, FMCH maintains its performance across various strain rates for up to 10 000 cycles. Moreover, FMCH demonstrates superior mechanical properties with fracture toughness of 3000 J m−2, stretchability of 6, and fatigue threshold up to 400 J m−2. These exceptional mechanical and optical features are attributed to FMCH's substantial molecular entanglements and desirable hygroscopic salts, which synergistically enhance its mechanical toughness while preserving its color‐changing performance. One application of this FMCH as a tactile sensoris then demonstrated for vision‐based tactile robots, enabling them to discern material stiffness, object shape, spatial location, and applied pressure by translating stress distribution on the contact surface into discernible images.
more »
« less
Deformation Rate‐Adaptive Conducting Polymers and Composites
Abstract Materials are more easily damaged during accidents that involve rapid deformation. Here, a design strategy is described for electronic materials comprised of conducting polymers that defies this orthodox property, making their extensibility and toughness dynamically adaptive to deformation rates. This counterintuitive property is achieved through a morphology of interconnected nanoscopic core–shell micelles, where the chemical interactions are stronger within the shells than the cores. As a result, the interlinked shells retain material integrity under strain, while the rate of dissociation of the cores controls the extent of micelle elongation, which is a process that adapts to deformation rates. A prototype based on polyaniline shows a 7.5‐fold increase in ultimate elongation and a 163‐fold increase in toughness when deformed at increasing rates from 2.5 to 10 000% min−1. This concept can be generalized to other conducting polymers and highly conductive composites to create “self‐protective” soft electronic materials with enhanced durability under dynamic movement or deformation.
more »
« less
- PAR ID:
- 10409189
- Publisher / Repository:
- Wiley Blackwell (John Wiley & Sons)
- Date Published:
- Journal Name:
- Small
- Volume:
- 19
- Issue:
- 35
- ISSN:
- 1613-6810
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
More Like this
-
-
Abstract Bioelectronic devices sense or deliver information at the interface between living systems and electronics by converting biological signals into electronic signals and vice‐versa. Biological signals are typically carried by ions and small molecules. As such, ion conducting materials are ideal candidates in bioelectronics for an optimal interface. Among these materials, ion conducting polymers that are able to uptake water are particularly interesting because, in addition to ionic conductivity, their mechanical properties can closely match the ones of living tissue. In this review, we focus on a specific subset of ion‐conducting polymers: proton (H+) conductors that are naturally derived. We first provide a brief introduction of the proton conduction mechanism, and then outline the chemical structure and properties of representative proton‐conducting natural biopolymers: polysaccharides (chitosan and glycosaminoglycans), peptides and proteins, and melanin. We then highlight examples of using these biopolymers in bioelectronic devices. We conclude with current challenges and future prospects for broader use of natural biopolymers as proton conductors in bioelectronics and potential translational applications.more » « less
-
Semicrystalline poly(l-lactide) (PLLA) is a leading biosourced, compostable alternative to conventional plastics but lacks sufficient toughness for many applications. Chain alignment via uniaxial stretching may be used to toughen PLLA but often creates anisotropic materials that are tough in the machine direction (MD) but brittle in the transverse direction (TD). This work reports uniaxially stretched films of PLLA blended with 3 wt % poly(ethylene oxide)-block-poly(butylene oxide) (PEO-PBO), which exhibit as much as a 5-fold increase in toughness in the TD compared to similarly stretched neat PLLA films─and elucidates the impact of PEO–PBO particles on the relationship between stretching, crystallization behavior, and resultant mechanical properties. Faster stretching rates were correlated with higher yield stress and a greater degree of crystallite alignment in the PEO–PBO/PLLA blends. This trend highlights the synergistic relationship between crystallinity and chain alignment and suggests a competing mechanism of heterogeneous crystallite nucleation around PEO–PBO particles. Importantly, PEO–PBO/PLLA exhibited a TD elongation at break of 36%, five times greater than the value of similarly stretched neat PLLA and even greater than the corresponding MD value of either material. Taken together, these findings demonstrate that uniaxial stretching of PEO–PBO/PLLA blends produces biaxially tough films, with the fastest stretching conditions producing the greatest enhancement in TD toughness.more » « less
-
Abstract Soft materials with reversible electrical and mechanical properties are critical for the development of advanced bioelectronics that can distinguish between different rates of applied strain and eliminate performance degradation over many cycles. However, the current paradigm in mechano‐electronic devices involves measuring changes in electrical current based on the accumulation of strain within a conductive material that alters the geometry through which electrons flow. Attempts have been made to incorporate soft materials like liquid metals and concentrated solutions of conjugated polymers and salts to overcome materials degradation but are limited in their ability to detect changes in the rate of the applied strain. Herein, the anisotropic electrical performance of a soft semiconducting composite prepared with silver‐coated microspheres dispersed within a swollen copolymer gel is demonstrated. This composite exhibits an electrical response proportional to the magnitude of the applied shear force to enable a rate‐of‐strain dependent conductivity. Furthermore, a 100‐fold increase in the conductivity of the composite is observed when the electric field is oriented parallel to the flow direction. This improvement in the electrical response can be attributed to the enhanced alignment of microspheres in viscoelastic media and can be leveraged in the development of mechanically responsive electronic devices.more » « less
-
null (Ed.)Owing to their excellent mechanical flexibility, mixed-conducting electrical property, and extraordinary chemical turnability, conjugated polymers have been demonstrated to be an ideal bioelectronic interface to deliver therapeutic effect in many different chronic diseases. This review article summarizes the latest advances in implantable electronics using conjugated polymers as electroactive materials and identifies remaining challenges and opportunities for developing electronic medicine. Examples of conjugated polymer-based bioelectronic devices are selectively reviewed in human clinical studies or animal studies with the potential for clinical adoption. The unique properties of conjugated polymers are highlighted and exemplified as potential solutions to address the specific challenges in electronic medicine.more » « less
