No abstract

Integrating elasticity of polymer and electrical conductivity of filler is widely used for the fabrication of composite foams or aerogels as compressible pressure sensors. Due to their poor interface interaction,...

We report a success in synthesizing high entropy silicides (HES) compounds and manufacturing well-densified HES ceramics through spark plasma sintering. For a designed chemical formula as (Ti0.2Zr0.2Nb0.2Mo0.2W0.2)Si2, the as-synthesized HES showed a formula as (Ti0.22Zr0.06Nb0.29Mo0.22W0.21)Si2 with zirconium partially oxidized into zirconia. Doping with aluminum resulted in a HES with the same composition, promoted formation of ZrSi2 and Al2O3. XRD analysis of as-synthesized HES is well supported by the calculated diffraction data based on a 2x3x1 supercell with HCP crystal structure and experimental chemical composition. The cations in this HES crystal structure can occupy their positions randomly with little change of its lattice parameters and formation enthalpy.

Self-healable flexible sensing materials are extensively investigated for their potential use in human motion detection, healthcare monitoring, and other fields. However, the existing self-healable flexible sensing materials have limited their application in real life due to the weak stability of the conductive network and the difficulty in balancing stretchability and self-healing performances. In this paper, a flexible sensor with skin-like properties was prepared by composing a polymer composite hydrogel with a multiple network structure consisting of polyaniline, polyvinyl alcohol, chitosan, and phytic acid. The composite hydrogel was tested and proved to own high mechanical properties (stretchability ≈ 565%, strength ≈ 1.4 MPa), good electrical conductivity (0.214 S cm–1), excellent self-healing properties (>99% healing efficiency in a 4 h healing period), and antibacterial properties. It had high sensitivity and a wide sensing range for strain and pressure, making it possible to manufacture multifunctional flexible sensors with comprehensive performance exceeding that of most flexible sensing materials. Notably, this polymer composite hydrogel can be manufactured in a large area and at a low cost, which is beneficial for its further application in many fields.

Constructing a three-dimensional (3D) conductive network in a polymer matrix is a common method for preparing flexible sensors. However, the previously reported methods for constructing a 3D conductive network generally have shortcomings such as uncontrollable processes and insufficient network continuity, which limit the practical application of this method. In this work, we report a method for constructing a dual 3D conductive network. The carbon nanotube/graphene oxide co-continuous network (primary network) was introduced on the surface of the waste silicone rubber particles (WSRPs) through the adhesion of polydopamine (PDA), and then WSRPs were bonded into a porous skeleton using nanocellulose. The carbon fiber/carbon ball interconnection network (secondary network) was constructed in liquid silicone rubber (LSR) through the interaction of host–guest dendrimers and was filled into the WSRP skeleton. The dual 3D conductive network structure endowed the sensor with high electrical and thermal conductivity, outstanding stability, and excellent durability. In addition, the sensor showed high strain sensitivity and excellent stability when detecting human body temperature and motion behavior, and the pressure distribution can be spatially mapped through the sensor matrix. These demonstrations give our sensor high potential in the fields of smart devices, body monitoring, and human–machine interfaces.