A Dual‐Organic‐Transistor‐Based Tactile‐Perception System with Signal‐Processing Functionality

Organic‐device‐based tactile‐perception systems can open up new opportunities for the next generation of intelligent products. To meet the critical requirements of artificial perception systems, the efficient construction of organic smart elements with integrated sensing and signal processing functionalities is highly desired, but remains a challenge. This study presents a dual‐organic‐transistor‐based tactile‐perception element (DOT‐TPE) with biomimetic functionality by the construction of organic synaptic transistors with integrated sensing transistors. The unique geometry of the DOT‐TPE permits instantaneous sensing of pressure stimuli and synapse‐like processing of an electric signal in a single element. More importantly, these organic‐transistor‐based tactile‐perception elements can be built into arrays to serve as bionic tactile‐perception systems. The combined biomimetic functionality of tactile‐perception systems, together with their promising features of flexibility and large‐area fabrication, makes this work represent a step forward toward novel e‐skin devices for artificial intelligence.     

Scaffold‐Free Liver‐On‐A‐Chip with Multiscale Organotypic Cultures

The considerable advances that have been made in the development of organotypic cultures have failed to overcome the challenges of expressing tissue‐specific functions and complexities, especially for organs that require multitasking and complex biological processes, such as the liver. Primary liver cells are ideal biological building blocks for functional organotypic reconstruction, but are limited by their rapid loss of physiological integrity in vitro. Here the concept of lattice growth used in material science is applied to develop a tissue incubator, which provides physiological cues and controls the 3D assembly of primary cells. The cues include a biological growing template, spatial coculture, biomimetic radial flow, and circulation in a scaffold‐free condition. The feasibility of recapitulating a multiscale physiological structural hierarchy, complex drug clearance, and zonal physiology from the cell to tissue level in long‐term cultured liver‐on‐a‐chip is demonstrated. These methods are promising for future applications in pharmacodynamics and personal medicine.     

Virion‐Like Membrane‐Breaking Nanoparticles with Tumor‐Activated Cell‐and‐Tissue Dual‐Penetration Conquer Impermeable Cancer

Poor drug penetration into tumor cells and tissues is a worldwide difficulty in cancer therapy. A strategy is developed for virion‐like membrane‐breaking nanoparticles (MBNs) to smoothly accomplish tumor‐activated cell‐and‐tissue dual‐penetration for surmounting impermeable drug‐resistant cancer. Tailor‐made dendritic arginine‐rich peptide prodrugs are designed to mimic viral protein transduction domains and globular protein architectures. Attractively, these protein mimics self‐assemble into virion‐like nanoparticles in aqueous solution, having highly ordered secondary structure. Tumor‐specific acidity conditions would activate the membrane‐breaking ability of these virion‐like nanoparticles to perforate artificial and natural membrane systems. As expected, MBNs achieve highly efficient drug penetration into drug‐resistant human ovarian (SKOV3/R) cancer cells. Most importantly, the well‐organized MBNs can pass through endothelial/tumor cells and spread from one cell to another one. Intravenous injection of MBNs into nude mice bearing impermeable SKOV3/R tumors suggests that the MBNs can recognize the tumor tissue after prolonged blood circulation, evoke the membrane‐breaking function for robust transvascular extravasation, and penetrate into the deep tumor tissue. This work provides the first demonstration of sophisticated molecular and supramolecular engineering of virion‐like MBNs to realize the long‐awaited cell‐and‐tissue dual‐penetration, contributing to the development of a brand‐new avenue for dealing with incurable cancers.     

Enhanced Solar‐to‐Hydrogen Generation with Broadband Epsilon‐Near‐Zero Nanostructured Photocatalysts

The direct conversion of solar energy into fuels or feedstock is an attractive approach to address increasing demand of renewable energy sources. Photocatalytic systems relying on the direct photoexcitation of metals have been explored to this end, a strategy that exploits the decay of plasmonic resonances into hot carriers. An efficient hot carrier generation and collection requires, ideally, their generation to be enclosed within few tens of nanometers at the metal interface, but it is challenging to achieve this across the broadband solar spectrum. Here the authors demonstrate a new photocatalyst for hydrogen evolution based on metal epsilon‐near‐zero metamaterials. The authors have designed these to achieve broadband strong light confinement at the metal interface across the entire solar spectrum. Using electron energy loss spectroscopy, the authors prove that hot carriers are generated in a broadband fashion within 10 nm in this system. The resulting photocatalyst achieves a hydrogen production rate of 9.5 µmol h^?1 cm^?2 that exceeds, by a factor of 3.2, that of the best previously reported plasmonic‐based photocatalysts for the dissociation of H₂ with 50 h stable operation.     

Self‐Assembled Ag‐MXA Superclusters with Structure‐Dependent Mechanical Properties

The low elastic modulus and time‐consuming formation process represent the major challenges that impede the penetration of nanoparticle superstructures into daily life applications. As observed in the molecular or atomic crystals, more effective interactions between adjacent nanoparticles would introduce beneficial features to assemblies enabling optimized mechanical properties. Here, a straightforward synthetic strategy is showed that allows fast and scalable fabrication of 2D Ag‐mercaptoalkyl acid superclusters of either hexagonal or lamellar topology. Remarkably, these ordered superstructures exhibit a structure‐dependent elastic modulus which is subject to the tether length of straight‐chain mercaptoalkyl acids or the ratio between silver and tether molecules. These superclusters are plastic and moldable against arbitrarily shaped masters of macroscopic dimensions, thereby opening a wealth of possibilities to develop more nanocrystals with practically useful nanoscopic properties.     

Variational‐based modeling of micro‐electro‐elasticity with electric field‐driven and stress‐driven domain evolutions

Recently, increasing interest in so‐called functional or smart materials with electromechanical coupling has been shown such as ferroelectric piezoceramics. These materials are characterized by microstructural properties, which can be changed by external stress and electric field stimuli, and hence find use as the active components in sensors and actuators. The electromechanical coupling effects result from the existence and rearrangement of microstructural domains with uniformly oriented electric polarization. The understanding and efficient simulation of these highly nonlinear and dissipative mechanisms, which occur on the microscale of ferroelectric piezoceramics, are a key challenge of the current research. This paper does not offer a substantially new physical model of these phenomena but a new mathematical modeling approach based on a rigorous exploitation of rate‐type variational principles. This provides a new insight in the structure of the coupled problem, where the governing field equations appear as the Euler equations of a variational statement. We outline a variational‐based micro‐electro‐elastic model for the microstructural evolution of both electrically and mechanically driven electric domains in ferroelectric ceramics, which also incorporates the surrounding free space. To this end, we extend recently developed multifield incremental variational principles of electromechanics from local to gradient‐extended dissipative response and specialize it by a Ginzburg–Landau‐type phase field model, where the thickness of the domain walls enters the formulation as a length scale. This serves as a natural starting point for a canonical compact, symmetric finite element implementation, considering the mechanical displacement, the microscopic polarization, and the electric potential induced by the polarization as the primary fields. The latter is defined on both the solid domain and a surrounding free space. Numerical simulations treat domain wall motions for electric field‐driven and stress‐driven loading processes, including the expansion of the electric potential into the free space. Copyright © 2012 John Wiley & Sons, Ltd.     

Few‐Layer Bismuthene with Anisotropic Expansion for High‐Areal‐Capacity Sodium‐Ion Batteries

Bismuth is a promising anode material for state‐of‐the‐art rechargeable batteries due to its high theoretical volumetric capacity and relatively low working potential. However, its charge storage mechanism is unclear, hindering further improvement of the cell performance. Here, using in situ transmission electron microscopy and X‐ray diffraction techniques as well as theoretical analysis, it is found that a large anisotropic volume expansion of 142% occurs along the z‐axis largely due to the alloy reaction during sodiation, significantly reducing the electrochemical performance of bismuth electrodes. To address this problem, ultrathin few‐layer bismuthene with a large aspect ratio is rationally synthesized, and can relieve the expansion strain along the z‐axis. A free‐standing bismuthene/graphene composite electrode with tunable thickness achieves a strikingly stable and high areal sodium storage capacity of 12.1 mAh cm^?2, which greatly exceeds that of most reported electrode materials. The clarification of the charge storage mechanism and the superior areal capacity achieved should facilitate the development of bismuth‐based high‐performance anodes for practical electrochemical energy‐storage applications.     

Mean‐strain 10‐node tetrahedron with energy‐sampling stabilization

In this study, a new mean‐strain 10‐node tetrahedral element is developed using energy‐sampling stabilization. The proposed 10‐node tetrahedron is composed of several four‐node linear tetrahedral elements, four tetrahedra in the corners and four tetrahedra that tile the central octahedron in three possible sets of four‐node linear tetrahedra, corresponding to three different choices for the internal diagonal. The assumed strains are calculated from mean ‘basis function gradients.’ The energy‐sampling technique introduced previously for removing zero‐energy modes in the mean‐strain hexahedron is adapted for the present element: the stabilization energy is evaluated on the four‐corner tetrahedra. The proposed element naturally leads to a lumped‐mass matrix and does not have unphysical low‐energy vibration modes. For simplicity, we limit our developments to linear elasticity with compressible and nearly incompressible material. The numerical tests demonstrate that the present element performs well compared with the classical 10‐node tetrahedral elements for shell and plate structures, and nearly incompressible materials. Copyright © 2016 John Wiley & Sons, Ltd.     

Cancer Modeling‐on‐a‐Chip with Future Artificial Intelligence Integration

Cancer is one of the leading causes of death worldwide, despite the large efforts to improve the understanding of cancer biology and development of treatments. The attempts to improve cancer treatment are limited by the complexity of the local milieu in which cancer cells exist. The tumor microenvironment (TME) consists of a diverse population of tumor cells and stromal cells with immune constituents, microvasculature, extracellular matrix components, and gradients of oxygen, nutrients, and growth factors. The TME is not recapitulated in traditional models used in cancer investigation, limiting the translation of preliminary findings to clinical practice. Advances in 3D cell culture, tissue engineering, and microfluidics have led to the development of “cancer‐on‐a‐chip” platforms that expand the ability to model the TME in vitro and allow for high‐throughput analysis. The advances in the development of cancer‐on‐a‐chip platforms, implications for drug development, challenges to leveraging this technology for improved cancer treatment, and future integration with artificial intelligence for improved predictive drug screening models are discussed.     

Quasi‐Hodgkin–Huxley Neurons with Leaky Integrate‐and‐Fire Functions Physically Realized with Memristive Devices

Artificial neurons with functions such as leaky integrate‐and‐fire (LIF) and spike output are essential for brain‐inspired computation with high efficiency. However, previously implemented artificial neurons, e.g., Hodgkin–Huxley (HH) neurons, integrate‐and‐fire (IF) neurons, and LIF neurons, only achieve partial functionality of a biological neuron. In this work, quasi‐HH neurons with leaky integrate‐and‐fire functions are physically demonstrated with a volatile memristive device, W/WO₃/poly(3,4‐ethylenedioxythiophene): polystyrene sulfonate/Pt. The resistive switching behavior of the device can be attributed to the migration of protons, unlike the migration of oxygen ions normally involved in oxide‐based memristors. With multifunctions similar to their biological counterparts, quasi‐HH neurons are advantageous over the reported HH and LIF neurons, demonstrating their potential for neuromorphic computing applications.     

Inkjet‐Printed High‐Performance Flexible Micro‐Supercapacitors with Porous Nanofiber‐Like Electrode Structures

Flexible planar micro‐supercapacitors (MSCs) with unique loose and porous nanofiber‐like electrode structures are fabricated by combining electrochemical deposition with inkjet printing. Benefiting from the resulting porous nanofiber‐like structures, the areal capacitance of the inkjet‐printed flexible planar MSCs is obviously enhanced to 46.6 mF cm^?2, which is among the highest values ever reported for MSCs. The complicated fabrication process is successfully averted as compared with previously reported best‐performing planar MSCs. Besides excellent electrochemical performance, the resultant MSCs also show superior mechanical flexibility. The as‐fabricated MSCs can be highly bent to 180° 1000 times with the capacitance retention still up to 86.8%. Intriguingly, because of the remarkable patterning capability of inkjet printing, various modular MSCs in serial and in parallel can be directly and facilely inkjet‐printed without using external metal interconnects and tedious procedures. As a consequence, the electrochemical performance can be largely enhanced to better meet the demands of practical applications. Additionally, flexible serial MSCs with exquisite and aesthetic patterns are also inkjet‐printed, showing great potential in fashionable wearable electronics. The results suggest a feasible strategy for the facile and cost‐effective fabrication of high‐performance flexible MSCs via inkjet printing.     

Plasmon‐Enhanced Spectroscopies with Shell‐Isolated Nanoparticles

Shell‐isolated nanoparticle‐enhanced Raman spectroscopy (SHINERS), due to its versatility, has been able to break the long‐term limitations of the material‐ and substrate‐specific generalities in the traditional field of surface‐enhanced Raman spectroscopy. With a shell‐isolated work principle, this method provides an opportunity to investigate successfully in surface, biological systems, energetic materials, and environmental sciences. Both the shell material and core morphology are being improved continuously to meet the requirements in diverse systems, such as the electrochemical studies at single crystal electrode surfaces, in situ monitoring of photoinduced reaction processes, practical applications in energy conversion and storage, inspections in food safety, and the surface‐enhanced fluorescence. Predictably, the concept of shell‐isolated nanoparticle‐enhancement could be expanded to the wider range for the performance of plasmon‐enhanced spectral modifications.