Abstract:As rubber-like elastomers have led to scientific breakthroughs in soft, stretchable characteristics-based wearable, implantable electronic devices or relevant research fields, developments of degradable elastomers with comparable mechanical properties could bring similar technological innovations in transient, bioresorbable electronics or expansion into unexplored areas. Here, we introduce ultra-stretchable, biodegradable elastomers capable of stretching up to ~1600% with outstanding properties in toughness, t… Show more
“…Degradability is an essential property of transient electronic materials. Gelatin is a water-soluble, biodegradable biopolymer, typically degrading by thermal and enzymatic degradation. , Here, an enzymatic degradation was performed to evaluate the potential of Gel- g -P3HT-2 for use in biomedical applications, e.g., in implantable electronics. ,− In vitro enzymatic degradation of gelatin is usually conducted in the PBS solution using collagenases, which are one of the three main subfamilies of human matrix metalloproteinases (MMPs) and are enzymes that can cleave the peptide bonds in the extracellular matrix of mammalian organ systems . In the degradation of Gel- g -P3HT-2, collagenase type II was utilized to perform the enzymatic degradation of gelatin, which is expected to specifically cleave amine (peptide) bonds in the gelatin backbone of the Gel- g -P3HT .…”
As transient electronics continue to advance, the demand for new materials has given rise to the exploration of conducting polymer (CP)-based electronic materials. The big challenge lies in balancing conductivity while introducing controlled degradable properties into CP-based transient materials. In response to this, we present in this work a concept of using conducting polymers attached to an enzymatically biodegradable biopolymer to create transient polymer electronics materials. Specifically, poly(3hexyl thiophene) (P3HT) is covalently grafted onto biopolymer gelatin, affording graft copolymer gelatin-graf t-poly(3-hexyl thiophene) (termed Gel-g-P3HT). The thin films of Gel-g-P3HT that were produced by optimized processing solvent (THF/H 2 O cosolvent) showed enhanced π−π stacking domains of P3HT, resulting in semiconducting thin films with good electroactivity. Due to the presence of amide bonds in the gelatin backbone, Gel-g-P3HT underwent degradation over a period of 5 days, resulting in the formation of amphiphilic micellar nanoparticles that are biocompatible and nontoxic. The potential of these conductive and degradable graft copolymers was demonstrated in a pressure sensor. This research paves the way for developing biocompatible and enzymatically degradable polymer materials based on P3HT, enabling the next generation of transient polymer electronics for diverse applications, such as skin, implantable, and environmental electronics.
“…Degradability is an essential property of transient electronic materials. Gelatin is a water-soluble, biodegradable biopolymer, typically degrading by thermal and enzymatic degradation. , Here, an enzymatic degradation was performed to evaluate the potential of Gel- g -P3HT-2 for use in biomedical applications, e.g., in implantable electronics. ,− In vitro enzymatic degradation of gelatin is usually conducted in the PBS solution using collagenases, which are one of the three main subfamilies of human matrix metalloproteinases (MMPs) and are enzymes that can cleave the peptide bonds in the extracellular matrix of mammalian organ systems . In the degradation of Gel- g -P3HT-2, collagenase type II was utilized to perform the enzymatic degradation of gelatin, which is expected to specifically cleave amine (peptide) bonds in the gelatin backbone of the Gel- g -P3HT .…”
As transient electronics continue to advance, the demand for new materials has given rise to the exploration of conducting polymer (CP)-based electronic materials. The big challenge lies in balancing conductivity while introducing controlled degradable properties into CP-based transient materials. In response to this, we present in this work a concept of using conducting polymers attached to an enzymatically biodegradable biopolymer to create transient polymer electronics materials. Specifically, poly(3hexyl thiophene) (P3HT) is covalently grafted onto biopolymer gelatin, affording graft copolymer gelatin-graf t-poly(3-hexyl thiophene) (termed Gel-g-P3HT). The thin films of Gel-g-P3HT that were produced by optimized processing solvent (THF/H 2 O cosolvent) showed enhanced π−π stacking domains of P3HT, resulting in semiconducting thin films with good electroactivity. Due to the presence of amide bonds in the gelatin backbone, Gel-g-P3HT underwent degradation over a period of 5 days, resulting in the formation of amphiphilic micellar nanoparticles that are biocompatible and nontoxic. The potential of these conductive and degradable graft copolymers was demonstrated in a pressure sensor. This research paves the way for developing biocompatible and enzymatically degradable polymer materials based on P3HT, enabling the next generation of transient polymer electronics for diverse applications, such as skin, implantable, and environmental electronics.
“…Additionally, methods such as reducing sensor thickness, decreasing the sensor's Young's modulus, and optimizing sensor structural design can all enhance the flexibility of flexible resistive tactile sensors. 38,39…”
Section: Principle Of Flexible Resistive Tactile Sensorsmentioning
The widespread integration of sensors into our everyday existence has paved the path for groundbreaking progress across various domains, including healthcare, robotics, and human-computer interaction. In this context, flexible resistive...
“…1–3 If no measures are taken to address this issue, it is projected that waste plastics will double within the next 20 years, reaching 33 billion tons by 2050. 4,5 While various bio-based and biodegradable polymers have been developed as alternatives to non-biodegradable plastics, 6–9 a significant amount of non-biodegradable waste plastics persists, accumulating on land and in the oceans without decomposing. The primary culprits behind plastic pollution are petrochemical-based polymers with a carbon–carbon backbone, mainly polyethylene, polypropylene, polyvinyl chloride and polystyrene (PS).…”
Vacuum pyrolysis of waste polystyrene foam over a spirit lamp flame for 20 minutes produced 98% pure styrene without needing fractionation or purification, which promises a convenient closed-loop chemical recycling system.
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