Fish‐eye shape prediction with gigacycle fatigue failure

In this paper, a model using the energy approach was established to investigate the formation of fish‐eye shape in the gigacycle fatigue failure. The model was used to predict the size of the fish‐eye formed by a given subsurface inclusion. The predicted results were comparable with the fractography of SNCM439 steel and other experimental results of gigacycle fatigue available in the literature. The current model can capture the fish‐eye shape and can be used to predict the life of crack initiation during fatigue failure.     

Recent Progress on Bioinspired Self‐Propelled Micro/Nanomotors via Controlled Molecular Self‐Assembly

The combination of bottom‐up controllable self‐assembly technique with bioinspired design has opened new horizons in the development of self‐propelled synthetic micro/nanomotors. Over the past five years, a significant advances toward the construction of bioinspired self‐propelled micro/nanomotors has been witnessed based on the controlled self‐assembly technique. Such a strategy permits the realization of autonomously synthetic motors with engineering features, such as sizes, shapes, composition, propulsion mechanism, and function. The construction, propulsion mechanism, and movement control of synthetic micro/nanomotors in connection with controlled self‐assembly in recent research activities are summarized. These assembled nanomotors are expected to have a tremendous impact on current artificial nanomachines in future and hold potential promise for biomedical applications including drug targeted delivery, photothermal cancer therapy, biodetoxification, treatment of atherosclerosis, artificial insemination, crushing kidney stones, cleaning wounds, and removing blood clots and parasites.     

Self‐Propelled Micro/Nanomotors for On‐Demand Biomedical Cargo Transportation

Micro/nanomotors (MNMs) are miniaturized machines that can perform assigned tasks at the micro/nanoscale. Over the past decade, significant progress has been made in the design, preparation, and applications of MNMs that are powered by converting different sources of energy into mechanical force, to realize active movement and fulfill on‐demand tasks. MNMs can be navigated to desired locations with precise controllability based on different guidance mechanisms. A considerable research effort has gone into demonstrating that MNMs possess the potential of biomedical cargo loading, transportation, and targeted release to achieve therapeutic functions. Herein, the recent advances of self‐propelled MNMs for on‐demand biomedical cargo transportation, including their self‐propulsion mechanisms, guidance strategies, as well as proof‐of‐concept studies for biological applications are presented. In addition, some of the major challenges and possible opportunities of MNMs are identified for future biomedical applications in the hope that it may inspire future research.     

Flexible Hard Coating: Glass‐Like Wear Resistant,Yet Plastic‐Like Compliant,Transparent Protective Coating for Foldable Displays

A flexible hard coating for foldable displays is realized by the highly cross‐linked siloxane hybrid using structure–property relationships in organic–inorganic hybridization. Glass‐like wear resistance, plastic‐like flexibility, and highly elastic resilience are demonstrated together with outstanding optical transparency. It provides a framework for the application of siloxane hybrids in protective hard coatings with high scratch resistance and flexibility for foldable displays.     

Magnetically Powered Annelid‐Worm‐Like Microswimmers

A bioinspired magnetically powered microswimmer is designed and experimentally demonstrated by mimicking the morphology of annelid worms. The structural parameters of the microswimmer, such as the surface wrinkling, can be controlled by applying prestrain on substrate for the precise fabrication and consistent performance of the microswimmers. The resulting annelid‐worm‐like microswimmers display efficient propulsion under an oscillating magnetic field, reaching a peak speed of ≈100 µm s^?1. The speed and directionality of the microswimmer can be readily controlled by changing the parameters of the field inputs. Additionally, it is demonstrated that the microswimmers are able to transport microparticles toward a predefined destination, although the translation velocity is inevitably reduced due to the additional hydrodynamic resistance of the microparticles. These annelid‐worm‐like microswimmers have excellent mobility, good maneuverability, and strong transport capacity, and they hold considerable promise for diverse biomedical, chemical sensing, and environmental applications.     

Self‐Propelled Micro/Nanomotors for Sensing and Environmental Remediation

Self‐propelled micro/nanomotors have gained attention for successful application in cargo delivery, therapeutic treatments, sensing, and environmental remediation. Unique characteristics such as high speed, motion control, selectivity, and functionability promote the application of micro/nanomotors in analytical sciences. Here, the recent advancements and main challenges regarding the application of self‐propelled micro/nanomotors in sensing and environmental remediation are discussed. The current state of micro/nanomotors is reviewed, emphasizing the period of the last five years, then their developments into the future applications for enhanced sensing and efficient purification of water resources are extrapolated.     

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.     

Mesh‐Like Carbon Nanosheets with High‐Level Nitrogen Doping for High‐Energy Dual‐Carbon Lithium‐Ion Capacitors

Li‐ion capacitors (LICs) have demonstrated great potential for bridging the gap between lithium‐ion batteries and supercapacitors in electrochemical energy storage area. The main challenge for current LICs (contain a battery‐type anode as well as a capacitor‐type cathode) lies in circumventing the mismatched electrode kinetics and cycle degradation. Herein, a mesh‐like nitrogen (N)‐doped carbon nanosheets with multiscale pore structure is adopted as both cathode and anode for a dual‐carbon type of symmetric LICs to alleviate the above mentioned problems via a facile and green synthesis approach. With rational design, this dual‐carbon LICs exhibits a broad high working voltage window (0–4.5 V), an ultrahigh energy density of $218.4\mathrm{Wh}{\mathrm{kg}}^{–1}{}_{\mathrm{electrodes}}$ ( $229.8\mathrm{Wh}{\mathrm{L}}^{–1}{}_{\mathrm{electrodes}}$), the highest power density of $22.5\mathrm{kW}{\mathrm{kg}}^{–1}{}_{\mathrm{electrodes}}$ ( $23.7\mathrm{kW}{\mathrm{L}}^{–1}{}_{\mathrm{electrodes}}$) even under an ultrahigh energy density of $97.5\mathrm{Wh}{\mathrm{kg}}^{–1}{}_{\mathrm{electrodes}}$ ( $102.6\mathrm{Wh}{\mathrm{L}}^{–1}{}_{\mathrm{electrodes}}$), as well as reasonably good cycling stability with capacity retention of 84.5% (only 0.0016% capacity loss per cycle) within 10 000 cycles under a high current density of 5 A g^?1. This study provides an efficient method and option for the development of high performance LIC devices.     

Translocation Pathway‐Dependent Assembly of Streptavidin‐ and Antibody‐Binding Filamentous Virus‐Like Particles

Compared to well‐tolerated p3 fusion, the display of fast‐folding proteins fused to the minor capsid p7 and the major capsid p8, as well as in vivo biotinylation of biotin acceptor peptide (AP) fused to p7, are found to be markedly inefficient using the filamentous phage. Here, to overcome such limitations, the effect of translocation pathways, amber mutation, and phage and phagemid display systems on p7 and p8 display of antibody‐binding domains are examined, while comparing the level of in vivo biotinylation of AP fused to p7 or p3. Interestingly, the in vivo biotinylation of AP occurs only in p3 fusion and the fast‐folding antibody‐binding scaffolds fused to p7 and p8 are best displayed via a twin‐arginine translocation pathway in TG1 cells. The lower the expression level of the wild‐type p8 and the smaller the size of the guest protein, the better the display of Z‐domain fused to the recombinant p8. The in vivo biotinylated multifunctional filamentous virus‐like particles can be vertically immobilized on streptavidin (SAV)‐coated microspheres to resemble cellular microvilli‐like structures, which reportedly enhance protein–protein interactions due to dramatically expanded flexible surface area.     

Thread‐Like Radical‐Polymerization via Autonomously Propelled (TRAP) Bots

Micromotor‐mediated synthesis of thread‐like hydrogel microstructures in an aqueous environment is presented. The study utilizes a catalytic micromotor assembly (owing to the presence of a Pt layer), with an on‐board chemical reservoir (i.e., polymerization mixture), toward thread‐like radical‐polymerization via autonomously propelled bots (i.e., TRAP bots). Synergistic coupling of catalytically active Pt layer, together with radical initiators (H₂O₂ and FeCl₃ (III)), and PEGDA monomers preloaded into the TRAP bot, results in the polymerization of monomeric units into elongated thread‐like hydrogel polymers coupled with self‐propulsion. Interestingly, polymer generation via TRAP bots can also be triggered in the absence of hydrogen peroxide for cellular/biomedical application. The resulting polymeric hydrogel microstructures are able to entrap living cells (NIH 3T3 fibroblast cells), and are easily separable via a centrifugation or magnetic separation (owing to the presence of a Ni layer). The cellular biocompatibility of TRAP bots is established via a LIVE/DEAD assay and MTS cell proliferation assay (7 days observation). This is the first study demonstrating real‐time in situ hydrogel polymerization via an artificial microswimmer, capable of enmeshing biotic/abiotic microobjects in its reaction environment, and lays a strong foundation for advanced applications in cell/tissue engineering, drug delivery, and cleaner technologies.     

A Controlled Design of Ripple‐Like Polyamide‐6 Nanofiber/Nets Membrane for High‐Efficiency Air Filter

The filtration capacity of fibrous media for airborne particles is restricted by their thick diameter, low porosity, and limited frontal area. The ability to solve this problem would have broad technological implications for various air filtration applications; despite many past efforts, it remains a great challenge to achieve. Herein, a facile and scalable strategy to fabricate the ripple‐like polyamide‐6 nanofiber/nets (PA‐6 NF/N) air filter via combining electrospinning/netting technique with receiving substrate design is demonstrated. This proposed approach allows the scaffold filaments to orderly embed into 2D PA‐6 nanonets layer with Steiner‐tree structures and nanoscale diameter of ≈20 nm, resulting in the ripple‐like membrane with extremely small pore size, highly porous structure, and hugely extended frontal surface, by facilely adjusting its pleat span and pleat pitch. These unique structural advantages enable the ripple‐like PA‐6 NF/N filter to filtrate the ultrafine particles with high removal efficiency of 99.996%, low air resistance of 95 Pa, and robust quality factor of >0.11 Pa^?1; using its superlight weight of 0.9 g m^?2 and physical sieving manner. This approach has the potentialities to give rise to a novel generation of filter media displaying enhanced filtration capacity for various applications thanks to their nanoscale features and designed macrostructures.     

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.