A self-healing multispectral transparent adhesive peptide glass.

Despite its disordered liquid-like structure, glass exhibits solid-like mechanical properties1. The formation of glassy material occurs by vitrification, preventing crystallization and promoting an amorphous structure2. Glass is fundamental in diverse fields of materials science, owing to its unique optical, chemical and mechanical properties as well as durability, versatility and environmental sustainability3. However, engineering a glassy material without compromising its properties is challenging4-6. Here we report the discovery of a supramolecular amorphous glass formed by the spontaneous self-organization of the short aromatic tripeptide YYY initiated by non-covalent cross-linking with structural water7,8. This system uniquely combines often contradictory sets of properties; it is highly rigid yet can undergo complete self-healing at room temperature. Moreover, the supramolecular glass is an extremely strong adhesive yet it is transparent in a wide spectral range from visible to mid-infrared. This exceptional set of characteristics is observed in a simple bioorganic peptide glass composed of natural amino acids, presenting a multi-functional material that could be highly advantageous for various applications in science and engineering.

Conductive Peptide-Based MXene Hydrogel as a Piezoresistive Sensor.

Wearable pressure sensors have become increasingly popular for personal healthcare and motion detection applications due to recent advances in materials science and functional nanomaterials. In this study, a novel composite hydrogel is presented as a sensitive piezoresistive sensor that can be utilized for various biomedical applications, such as wearable skin patches and integrated artificial skin that can measure pulse and blood pressure, as well as monitor sound as a self-powered microphone. The hydrogel is composed of self-assembled short peptides containing aromatic, positively- or negatively charged amino acids combined with 2D Ti3C2Tz MXene nanosheets. This material is low-cost, facile, reliable, and scalable for large areas while maintaining high sensitivity, a wide detection range, durability, oxidation stability, and biocompatibility. The bioinspired nanostructure, strong mechanical stability, and ease of functionalization make the assembled peptide-based composite MXene-hydrogel a promising and widely applicable material for use in bio-related wearable electronics.

MXene-Based Ceramic Nanocomposites Enabled by Pressure-Assisted Sintering.

As MXenes become increasingly widespread, approaches to utilize this versatile class of 2D materials are sought. Recently, there has been growing interest in incorporating MXenes into metal or ceramic matrices to create advanced nanocomposites. This study presents a facile approach of mixing MXene with ceramic particles followed by pressure-assisted sintering to produce bulk MXene/ceramic nanocomposites. The effect of MXene addition on the densification behavior and properties of nanocomposites was explored through the Ti3C2Tz/alumina model system. We discovered that the presence of MXene altered the densification behavior and significantly enhanced the densification rate at low temperatures. In-depth microstructural characterization showed a homogeneous distribution of Ti3C2Tz MXene at the alumina grain boundaries. The Ti3C2Tz/alumina nanocomposites exhibited electrical conductivity but reduced hardness. We also demonstrated that using multilayered Ti3C2Tz as a precursor can produce composites with plate-like TiCx morphology. This work provides a conceptual approach for utilizing the diversity and versatility of MXenes in creating tunable advanced nanocomposites.