Recently, piezoelectric characteristics have been a research focus for 2D materials because of their broad potential applications. Black phosphorus (BP) is a monoelemental 2D material predicted to be piezoelectric because of its highly directional properties and non‐centrosymmetric lattice structure. However, piezoelectricity is hardly reported in monoelemental materials owing to their lack of ionic polarization, but piezoelectric generation is consistent with the non‐centrosymmetric structure of BP. Theoretical calculations of phosphorene have explained the origin of piezoelectric polarization among P atoms. However, the disappearance of piezoelectricity in multilayer 2D material generally arises from the opposite orientations of adjacent atomic layers, whereas this effect is limited in BP lattices due to their spring‐shaped space structure. Here, the existence of in‐plane piezoelectricity is experimentally reported for multilayer BP along the armchair direction. Current–voltage measurements demonstrate a piezotronic effect in this orientation, and cyclic compression and release of BP flakes show an intrinsic current output as large as 4 pA under a compressive strain of −0.72%. The discovery of piezoelectricity in multilayer BP can lead to further understanding of this mechanism in monoelemental materials.
Currently, most of the mechanoluminescence (ML) phosphors strongly depend on postirradiation stimulation using ultraviolet light (denoted as “UV exposure” from hereon) to show the ML. However, only a few transition metal cations are proven to be effective luminescence centers, which hinder the development of more ML phosphors. This study reports a self‐recoverable deep‐red‐to‐near‐infrared ML using Cr3+‐doped LiGa5O8 phosphor with fully recoverable ML performance. The ML performance can be further optimized by tuning the trap redistributions by codoping the phosphor with Al3+ and Cr3+ cations. Theoretical calculations reveal the important role of Cr dopants in the modulation of local electronic environments for achieving the ML. Owing to the induced interelectronic levels and shallow electron trap distributions, the electron recombination efficiency is enhanced both through direct tunneling and energy transfer toward the dopant levels. Moreover, the ML of Cr3+‐doped LiGa5O8 can penetrate a 2‐mm‐thick pork slice, showing that it can have wide‐ranging in vivo applications, including the optical imaging of intracorporal stress/strain distribution and dynamics. Therefore, this work fabricates a novel ML material with self‐recoverable luminescence in an extended wavelength range, increasing the number of potential ML candidates and promoting the fundamental understanding and practical applications of ML materials.
Tactile sensors with multimode sensing ability are cornerstones of artificial skin for applications in humanoid robotics and smart prosthetics. However, the intuitive and interference-free reading of multiple tactile signals without involving complex algorithms and calculations remains a challenge. Herein a pressure–temperature bimodal tactile sensor without any interference is demonstrated by combining the fundamentally different sensing mechanisms of optics and electronics, enabling the simultaneous and independent sensing of pressure and temperature with the elimination of signal separation algorithms and calculations. The bimodal sensor comprises a mechanoluminescent hybrid of ZnS–CaZnOS and a poly(3,4-ethylenedioxythiophene):poly(styrene sulfonate) (PEDOT:PSS) thermoresistant material, endowing the unambiguous transduction of pressure and temperature into optical and electrical signals, respectively. This device exhibits the highest temperature sensitivity of −0.6% °C–1 in the range of 21–60 °C and visual sensing of the applied forces at a low limitation of 2 N. The interference-free and light-emitting characteristics of this device permit user-interactive applications in robotics for encrypted communication as well as temperature and pressure monitoring, along with wireless signal transmission. This work provides an unexplored solution to signal interference of multimodal tactile sensors, which can be extended to other multifunctional sensing devices.
Edible gliadin nanoparticles (GNPs) were fabricated using the anti-solvent method. They possessed unique high foamability and foam stability. An increasing concentration of GNPs accelerated their initial adsorption speed from the bulk phase to the interface and raised the viscoelastic modulus of interfacial films. High foamability (174.2 ± 6.4%) was achieved at the very low concentration of GNPs (1 mg/mL), which was much better than that of ovalbumin and sodium caseinate. Three stages of adsorption kinetics at the air/water interface were characterized. First, they quickly diffused and adsorbed at the interface, resulting in a fast increase of the surface pressure. Then, nanoparticles started to fuse into a film, and finally, the smooth film became a firm and rigid layer to protect bubbles against coalescence and disproportionation. These results explained that GNPs had good foamability and high foam stability simultaneously. That provides GNPs as a potential candidate for new foaming agents applied in edible and biodegradable products.
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