Polyvinylidene Fluoride Based Piezoelectric Composites with Strong Interfacial Adhesion via Click Chemistry for Self-Powered Flexible Sensors.

Achieving relatively uniform dispersion in organic-inorganic composites with overwhelming differences in surface energy is a perennial challenge. Herein, novel eliminated polyvinylidene fluoride (EPVDF)/EPVDF functionalized barium titanate nanoparticles (EPVDF@BT) flexible piezoelectric nanogenerators (PENGs) with strong interfacial adhesion are developed via thermal stretching following sequential click chemistry. Thanks to the strong interfacial adhesion, the optimal PENGs containing ultra-high ß-phase content (97.2%) exhibit not only optimized mechanical and dielectric behaviors but also excellent piezoelectric properties with high piezoelectric output (V = 10.7 V, I = 216 nA), reliable durability (8000 cycles), ultrafast response time (20 ms), and good sensitivity (2.09 nA kPa-1 ), far outperforming most reported PVDF-based composites. Furthermore, COMSOL finite element simulations (FEM) confirm that the elevated stress transfer efficiency induced by the strong interfacial adhesion is the main driving force for enhanced piezoelectric performances. For practical applications, self-powered PENGs can simply but stably capture mechanical energy, drive tiny electronic devices, and serve as potential multifunctional and durable sensors for detecting human physiological motions. This work opens a pioneering avenue to break the trade-offs between piezoelectric and other properties, which is of great importance for developing self-powered flexible sensors.

Efficient Regulation of the Cross-Linking Structure in Polyurethane: Achieving Outstanding Processing and Mechanical Properties for a Wind Turbine Blade.

Although epoxy resin has been extensively used in the field of wind turbine blades, polyurethane has attracted much attention in recent years, due to its potential value of better fatigue resistance, lower processing viscosity and higher strength than epoxy resin blades. Herein, we construct a dense cross-linking structure in polyurethane (PU) based on different amounts of hydroxypropyl methacrylate (HPMA) with low processing viscosity and excellent mechanical properties. By increasing the content of HPMA, the thermal stability of PU is enhanced, but the micro-morphology does not change significantly. When the content of HPMA is 50 g (in 200 g copolymer), the PU sample PH-50 exhibits a viscosity of 70 MPa·s and a gelation time of 120 min at 25 °C, which is sufficient to complete processes like pouring and filling. By post-curing the PH-50 at 80 °C for 2 h, the heat distortion temperature can reach 72 °C, indicating the increase of temperature resistance. The PU copolymers also have excellent mechanical and dynamic thermo-mechanical properties due to the cross-linking structure between PU chains and poly-HPMA chains. Additionally, the PU copolymer has excellent compatibility with various glass fiber fabrics (GFF), showing a good match in the vacuum infusion experiment and great properties in the mechanical test. By compounding PH-50 with GFF, the composite with high strength is easily prepared for a wind turbine blade in various positions. The tensile strengths of the composites are all over 1000 MPa in the 0° direction. Such composites are promising for the future development of wind turbine blades that meet the stringent requirements for outstanding processing and mechanical properties.

Novel Radiochromic Elastomer Dosimeter Based on the Self-Sensitizing Effect of Disulfide Bonds.

γ-Irradiation is a kind of high-energy ionizing ray, which has widespread applications in material, food, and medical industries as well as in the environment. Since this irradiation is invisible, quantitatively monitoring its exposure doses is crucial to irradiated targets. As a type of dosimeter, radiochromic dosimeters can detect γ-irradiation by color changing, and its strategy to realize the radiochromic behavior basically relies on active radicals from radiolysis of an external environmental medium. However, the primary problem of this external environment-mediated sensitization strategy is that it complicates the components of dosimeters. Herein, we present a novel type of self-sensitizing radiochromic poly(urethane-urea) elastomers (PUUEs), where disulfide bonds, serving as radiation-responsive and sensitizing units, are introduced. This is the first attempt to utilize radicals generated from radiolysis of weak bonds in a solid polymer matrix to sensitize color change of dye-doped radiochromic dosimeters. Moreover, it is intriguing that the simultaneously introduced aryl hydrazone bond endows dosimeters with excellent color retention and maintains the Δa* value of 72.9% even after 1 month on the basis of the as-irradiated specimen. Besides, the metathesis of disulfide bonds not only endows dosimeters with better self-healing capability, but also accelerates the postcuring behavior and hydrogen bond reconfiguration, resulting in improved mechanical performance.

Biomineralization-Inspired Copper Sulfide Decorated Aramid Textiles via In Situ Anchoring toward Versatile Wearable Thermal Management.

Designing smart textiles for personal thermal management (PTM) is an effective strategy for thermoregulation and energy saving. However, the manufacture of versatile high-performance thermal management textiles for complex real-world environments remains a challenge due to the limitations of functional integration, material properties, and preparation procedures. In this study, an aramid fabric based on in situ anchored copper sulfide nanostructure is developed. The textile with excellent solar and Joule heating properties can effectively keep the body warm even at low energy inputs. Meanwhile, the reduced infrared emissivity of the textile decreases the thermal radiation losses and helps to maintain a constant body temperature. Impressively, the textile integrates superb electromagnetic shielding, near-complete UV protection properties, and ideal resistance to fire and bacteria. This work provides a simple strategy for fabricating multi-functional integrated wearable devices with flexibility and breathability, which is highly promising in versatile PTM applications.

Hydroxyapatite/Poly (Butylene Succinate)/Metoprolol Tartrate Composites with Controllable Drug Release and a Porous Structure for Bone Scaffold Application.

Nowadays, it is a challenge for a bone scaffold to achieve controllable drug release and a porous structure at the same time. Herein, we fabricated hydroxyapatite/poly (butylene succinate)/metoprolol tartrate (HA/PBS/MPT) composites via melt blending, aiming to provide the option of an in situ pore-forming strategy. The introduction of HA not only significantly improved the hydrophilicity of the PBS matrix by reducing the hydrophilic contact angle by approximately 36% at a 10% content, but also damaged the integrity of the PBS crystal. Both were beneficial for the penetration of phosphate-buffered saline solution into matrix and the acceleration of MPT release. Accompanied with MPT release, porous structures were formed in situ, and the HA inside the matrix was exposed. With the increase in HA content, the MPT release rate accelerated and the pore size became larger. The in vitro cytocompatibility evaluation indicated that HA/PBS/MPT composites were conductive to the adhesion, growth, and proliferation of MC3T3-E1 cells due to the HA being exposed around the pores. Thus, the MPT release rate, pore size, and cell induction ability of the HA/PBS/MPT composites were flexibly and effectively adjusted by the composition at the same time. By introducing HA, we innovatively achieved the construction of porous structures during the drug release process, without the addition of pore-forming agents. This approach allows the drug delivery system to combine controllable drug release and biocompatibility effectively, offering a novel method for bone repair material preparation. This work might provide a convenient and robust strategy for the fabrication of bone scaffolds with controllable drug release and porous structures.

Comb Polybutadiene with Long Polystyrene Side Chains: A Solution for Tunable Flowability and Enhancing Dielectric Properties in High-Frequency Printed Board Adhesive Films.

Liquid high-vinyl polybutadiene (PB) possessed excellent dielectric properties, rendering them suitable candidates for adhesive films of high-frequency printed boards. However, their inherent low molecular weights resulted in chain slippage and overflow during processing, thereby diminishing the performance of the adhesive films. To address this challenge, we synthesized comb PB with long polystyrene side chains via reversible addition-fragmentation chain transfer (RAFT) polymerization, effectively immobilizing the PB backbone and restricting relative chain slippage. Controlling the length and number of "comb teeth" (styrene side chains) efficiently regulated the flowability of comb PB, achieving distinct flow states. Simultaneously, molecular dynamics simulations revealed that the elongated and inflexible polystyrene side chains of comb PB could create minuscule cavities, which impeded close packing of molecules and led to low dielectric constants (2.39/2.01, 1 MHz/10 GHz) and ultralow dielectric losses (0.0071/0.0016, 1 MHz/10 GHz). Furthermore, a series of printed circuit boards were fabricated using a comb PB adhesive film, and the signal loss was significantly reduced to 48.8% (19 GHz) in comparison with a commercial epoxy adhesive. This study demonstrated the potential of comb PB with polystyrene side chains to achieve desirable flow and dielectric properties by introducing tangles, large volume potential resistance, and microporosity compared with block structures.

The effect of layer thickness ratio on the drug release behavior of alternating layered composite prepared by layer-multiplying co-extrusion.

Multi-layered drug delivery (MLDD) system has promising potential to achieve controlled release. However, existing technologies face difficulties in regulating the number of layers and layer-thickness ratio. In our previous works, layer-multiplying co-extrusion (LMCE) technology was applied to regulate the number of layers. Herein, we utilized layer-multiplying co-extrusion technology to modulate the layer-thickness ratio to expand the application of LMCE technology. Four-layered poly (ε-caprolactone)-metoprolol tartrate/poly (ε-caprolactone)-polyethylene oxide (PCL-MPT/PEO) composites were continuously prepared by LMCE technology, and the layer-thickness ratios for PCL-PEO layer and PCL-MPT layer were set to be 1:1, 2:1, and 3:1 just by controlling the screw conveying speed. The in vitro release test indicated that the rate of MPT release increased with decreasing the thickness of the PCL-MPT layer. Additionally, when PCL-MPT/PEO composite was sealed by epoxy resin to eliminate the edge effect, sustained release of MPT was achieved. The compression test confirmed the potential of PCL-MPT/PEO composites as bone scaffolds.

Tetris-Style Stacking Process to Tailor the Orientation of Carbon Fiber Scaffolds for Efficient Heat Dissipation.

As the miniaturization of electronic devices and complication of electronic packaging, there are growing demands for thermal interfacial materials with enhanced thermal conductivity and the capability to direct the heat toward heat sink for highly efficient heat dissipation. Pitch-based carbon fiber (CF) with ultrahigh axial thermal conductivity and aspect ratios exhibits great potential for developing thermally conductive composites as TIMs. However, it is still hard to fabricate composites with aligned carbon fiber in a general approach to fully utilize its excellent axial thermal conductivity in specific direction. Here, three types of CF scaffolds with different oriented structure were developed via magnetic field-assisted Tetris-style stacking and carbonization process. By regulating the magnetic field direction and initial stacking density, the self-supporting CF scaffolds with horizontally aligned (HCS), diagonally aligned and vertically aligned (VCS) fibers were constructed. After embedding the polydimethylsiloxane (PDMS), the three composites exhibited unique heat transfer properties, and the HCS/PDMS and VCS/PDMS composites presented a high thermal conductivity of 42.18 and 45.01 W m-1 K-1 in fiber alignment direction, respectively, which were about 209 and 224 times higher than that of PDMS. The excellent thermal conductivity is mainly ascribed that the oriented CF scaffolds construct effective phonon transport pathway in the matrix. In addition, fishbone-shaped CF scaffold was also produced by multiple stacking and carbonization process, and the prepared composites exhibited a controlled heat transfer path, which can allow more versatility in the design of thermal management system.

Selectively multilayered distribution of stereocomplex crystallite and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) ribbons to achieve highly ductile and strong poly(l-lactide) composites.

Blending poly(l-lactide) (PLLA) with elastic polymers is an efficient way to obtain highly ductile materials (> 300 %), but it is accompanied by a significant reduction in strength. In this work, a special alternating multilayered composites with alternating stereocomplex crystallite (SC) (PLLA/poly(d-lactide) (PDLA) layer) and highly oriented Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) ribbons (PLLA/PHBV layer) is in situ constructed during laminated structuring process. Experimental results show that in situ formed PHBV ribbons are limitedly distributed in the thickness direction and align parallel to the layer interfaces. More interestingly, not only highly oriented shish crystals but also sparse lamellae of PLLA, which are arrested by SC, shish crystals, and PHBV ribbons, are in situ formed. Compared with sea-island structured composites prepared by traditional compression molding, the alternating multilayered composites show an increase in elongation at break from 8.7 % to 345.1 % and an increase in yield strength from 61.4 MPa to 73.2 MPa. During the tensile testing, the PLLA/PHBV layers firstly form micro-fibrils and micro-voids, driving the molecular chains of the PLLA/PDLA layer to respond in time to external forces through stress transfer of rich continuous layer interfaces. Since shear yielding and plastic deformation can easily penetrate the entire matrix, the alternating multilayered composites go a brittle-ductile transformation and the ductility is improved significantly. The increased strength of the alternating multilayered material is ascribed to the stiff shish crystals and SC. This work provides important guidance for the durable application of strong and ductile PLLA-based materials.

Biocompatible shape-memory poly(propylene carbonate)/silk fibroin blend with body temperature responsiveness.

The high value-added medical applications surely represent the leading edge of the shape-memory materials (SMPs) field. Herein, the biomedical SMPs were easily prepared via incorporating silk fibroin (SF) into poly(propylene carbonate) (PPC) through directly melt blending. Based on the intrinsic glass transition of PPC at ∼37 °C, the blends showed a body temperature responsiveness without a complex procedure for adjusting the switching temperature. By varying the SF content, the blend exhibited tunable shape-memory effects (SME), with a first enhancing but then worsening shape recoverability and a stable and excellent shape fixity. And the blend with 3 wt% SF achieved the best SME, enabling an efficient shape reconfiguration under a 37 °C water bath. It was revealed that SF acted as physical cross-links to connect the PPC chains forming a shape-memory network, thus can well retard irreversible the chain slipping of PPC, leading to the improvement of recoverability. Moreover, the results obtained from cell compatibility testing showed the huge application potential of this material in the biomedical field. This work proposed a facile preparation strategy for developing biocompatible body heat actuated shape-memory materials.

Visualization of Deep Convolutional Neural Networks to Investigate Porous Nanocomposites for Electromagnetic Interference Shielding.

Constructing porous structures in electromagnetic interference (EMI) shielding materials is a common strategy to decrease the secondary pollution caused by the reflection of electromagnetic waves (EMWs). However, the lack of direct analysis methods makes it difficult to fully understand the effect of porous structures on EMI, hindering EMI composites' development. Furthermore, while deep learning techniques, such as deep convolutional neural networks (DCNNs), have significantly impacted material science, their lack of interpretability limits their applications to property predictions and defect detection tasks. Until recently, advanced visualization techniques provided an approach to reveal the relevant information behind DCNNs' decisions. Inspired by it, a visual approach for porous EMI nanocomposite mechanism studies is proposed. This work combines DCNN visualization with experiments to investigate EMI porous nanocomposites. First, a rapid and straightforward salt-leaked cold-pressing powder sintering method is employed to prepare high-EMI CNTs/PVDF composites with various porosities and filler loadings. Notably, the solid sample with 30 wt % loading maintains an ultrahigh shielding effectiveness of 105 dB. The influence of porosity on the shielding mechanism is discussed macroscopically based on the prepared samples. To determine the shielding mechanism, a modified deep residual network (ResNet) is trained on a dataset of scanning electron microscopy (SEM) images of the samples. The Eigen-CAM visualization of the modified ResNet intuitively shows that the amount and depth of the pores impact the shielding mechanisms and that shallow pore structures contribute less to EMW absorption. This work is instructive for material mechanism studies. Besides, the visualization has the potential as a porous-like structure marking tool.

Versatile Melanin-Like Coatings with Hierarchical Structure toward Personal Thermal Management, Anti-Icing/Deicing, and UV Protection.

Superhydrophobic photothermal coatings are promising for multifunctional applications due to the efficient use of solar energy, but the current challenge is to seek one easy-to-prepare material with high photothermal performance. Herein, inspired by mussel adhesion and lotus leaf surfaces, we developed superhydrophobic photothermal coatings with hierarchical structure by depositing melanin-like polydopamine (PDA) and dip-coating polydimethylsiloxane (PDMS)/hydrophobic fumed silica (SiO2) sequentially. Benefitting from the efficient photothermal conversion performance of PDA, the coated fabric can rapidly warm up to 100 °C under 100 mW/cm2 sun irradiation. Meanwhile, the coatings show excellent superhydrophobic properties (WCA of 163°), which not only prevent the adhesion of the contaminant from maintaining a long-term and efficient photothermal performance but also help the fabric to own outstanding passive anti-icing and active deicing performances. Furthermore, the superhydrophobic properties of the coatings can be maintained after sandpaper abrasion, repeat tape-peeling, and ultrasonication. In addition, superior UV protection of the coatings can meet the long-term service conditions under outdoor sunlight. The PDA-based superhydrophobic photothermal coatings are believed to inspire new strategies for solar-driven multifunctional applications such as personal thermal management, anti-icing/deicing of variously shaped components, photothermal antibacterial, and so on.

Influence of Alternating Multi-Layered Design on Damping Characteristics of Butyl Rubber Composites and a New Idea for Achieving Wide Temperature Range and High Damping Performance.

This paper investigates the influence of an alternating multi-layered design on the material loss factor and effective temperature range of free/constrained-damping butyl rubber, and then proposes a new method of designing materials with high damping properties and a wide temperature range. First, the wide-temperature rubber IIR-0, the low-temperature rubber IIR-1, the medium-temperature rubber IIR-2, and the high-temperature rubber IIR-3 are prepared and characterized. Second, the influences of an alternating multi-layered design on the damping peak values and temperature range of free damping and micro-constrained damping of the rubber types are investigated. Finally, different methods for broadening the damping temperature range and improving the damping loss factor are discussed. The results show that the loss factor of the alternating multi-layered, constrained damping structure is increased to 0.488, while that of the free-damping structure is increased to 0.845. Their damping-temperature ranges are increased to 89.4 °C and 93.2 °C, respectively. A wide temperature range and high damping performance can be achieved by the alternating multi-layered design of rubber/plastic micro-constrained damping composites.

Sandwich-Structured Surface Coating of a Silver-Decorated Electrospun Thermoplastic Polyurethane Fibrous Film for Excellent Electromagnetic Interference Shielding with Low Reflectivity and Favorable Durability.

Nowadays, high efficiency and low reflection electromagnetic interference (EMI) shielding materials have a wide potential application of electronic fields. However, it is still challenging to achieve long-term durability under external mechanical deformations or other harsh conditions. Herein, sandwich-structured surface coatings with a mixture of polydimethylsiloxane (PDMS)/carboxylated multiwalled carbon nanotube and magnetic ferriferous oxide nanoparticle hybrid fillers (MWCNTs-COOH/Fe3O4, MFs) are introduced onto a silver-decorated electrospun thermoplastic polyurethane (TPU) fibrous film to achieve both outstanding low reflective EMI shielding and favorable durability. The surface coatings not only act as an effective absorbing layer but also provide a micro-nano hierarchical superhydrophobic surface. The resultant film shows a remarkable conductivity (361.0 S/cm), an excellent EMI shielding effectiveness (SE) approaching 85.4 dB, and a low reflection coefficient value of 0.61. Interestingly, the obtained film still maintains an excellent EMI SE even after mechanical deformations or being immersed in strong acidic solution, alkaline solution, and organic solvents for 6 h. This work opens a new avenue for the design of low reflective EMI shielding films under harsh environments.

Switchable Piezoelectricity of Polyvinylidene Fluoride Films Induced by Crystal Transition in Shape Memory Process.

With the rapid development of wearable self-powered devices, the piezoelectric materials having deformable and switchable characteristics are attracting extensive attention. Herein, the cross-linked polyvinylidene fluoride (cPVDF) was fabricated through an alkali-catalyzed defluorination and chemical cross-linking method by introducing trimethylhexamethylenediamine (THDA). The system filled with 1 wt % THDA (CP1) was proved to possess balanced cross-linking density and crystallinity, which would play a crucial role in achieving a switchable piezoelectric effect. In comparison to pristine PVDF, the cross-linked one exhibited repeatable shape memory characterization due to restrained plastic deformation above the melting transition. Both the shape-fixing and shape-recovery ratios were stably maintained above 90%. More significantly, the thermo-mechanical program also triggered the α-ß-α crystal transition accompanied by the variation of conformational entropy. The largest amount of ß crystals was produced in the temporary shape, whereas the original and recovery shapes were dominated by α crystals. Such structural transition occurred repeatedly in the successive shape memory cycles, which thereby induced the periodic fluctuation of the piezoelectric constant (d33). For the CP1 sample, its d33 was only about 2 pC/N in the original and recovery shapes but reached up to 9.4 pC/N in the temporary shape. When the latter one was fabricated into a piezoelectric device, alternating voltage and current were generated by performing periodic impact force and were demonstrated to be capable of monitoring some pressure-related motions in real time without an external power supply. Finally, the switchable piezoelectric effect of the CP1 at different shape memory stages was further revealed through its electroactive response to the sinusoidal voltage stimulation. This work offers a special perspective in tailoring piezoelectric performance through the structural transition in shape memory progress, which is of great significance for enriching the types and applications of piezoelectric polymers.

Effects of MWCNTs on Char Layer Structure and Physicochemical Reaction in Ethylene Propylene Diene Monomer Insulators.

As one of the most promising ablative fillers, multi-walled carbon nanotubes (MWCNTs) have been used to improve the ablative resistance of Ethylene-Propylene-Diene Monomer (EPDM) insulators by facilitating the carbothermal reduction reaction of silica. However, the contribution of MWCNTs to char layer structure of the insulators was unclear. In this work, the effects of MWCNTs on char layer structure and ablative resistance were investigated in different EPDM-based insulators with and without silica. The results showed that adding only 3 phr MWCNTs can reduce the linear ablation rate of EPDM-based insulators without silica by 31.7%, while 6 phr MWCNTs are required to obtain similar results in EPDM-based insulators with silica. The char layer morphology of the two insulators gradually evolved into a dense porous structure as MWCNTs content increased, but their formation mechanisms were different. The XRD and Raman spectrum showed that different physicochemical reactions occurred around MWCNTs under different charring components. The proposed ablation mechanism was further verified by designing alternating multilayer distribution of MWCNTs and silica. This work can guide the construction of desirable char layer structure for increasing the ablative resistance of EPDM-based insulators.

Constructing oriented two-dimensional fish scale-like Gd@MXene barrier walls in polyvinyl alcohol to achieve excellent neutron shielding properties.

The increasing utilization of nuclear energy and radiation medicine has urged flexible neutron shielding materials for personal protection. However, it was a challenge to manufacture neutron shielding materials with good flexibility and efficient neutron shielding performance. Herein, a new type of hybrid filler named Gd@MXene nanoflakes were successfully synthesized via one step-hydrothermal reaction and used for efficient neutron shielding, which was composed of two-dimensional (2D) Ti3C2Tx-MXene nanoflakes and zero-dimensional Gd nanoparticles (NPs). Inspired by fish scales, the spin coating method was employed to manufacture the film composed of polyvinyl alcohol (PVA) and Gd@MXene, which aligned random Gd@MXene into oriented 2D fish scale-like barrier walls. The 2D fish scale-like Gd@MXene barrier walls scattered the neutron rays multiple times between the nanoflakes, thereby improving the neutron absorption efficiency of Gd atoms. The film showed excellent neutron shielding performance and thermal conductivity; the neutron shielding rate of 20-Gd@MXene/PVA with a thickness of 62 µm was 3.36 times higher than that of pure PVA. The thermal conductivity of Gd@MXene/PVA was nearly 10 times higher than that of pure PVA. This work introduced a novel film for neutron radiation shielding and had potential applications in personal wearable protective equipment.

In-situ constructing highly oriented ductile poly(3-hydroxybutyrate-co-3-hydroxyvalerate) nanoribbons: Towards strong, ductile, and good heat-resistant polylactic-based composites.

It remains a great challenge to manufacture polylactic (PLA) with high strength, ductility, and heat resistance simultaneously. Herein, PLA/poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) nanoribboned composites, the highly oriented PHBV nanoribbons decorated by the PLA lamella, are successfully achieved through the multistage stretching extrusion (MSE) system. SEM confirms that in-situ highly oriented PHBV nanoribbons are achieved by biaxial-stretching field during the MSE process. Through investigating crystalline architecture of PLA/PHBV nanoribboned composites, it is found that the stiff shish and sparse lamellae of PLA are obtained under the coupling effect of PHBV nanoribbons and biaxial-stretching field. DMA reveals partial compatibility between PLA and PHBV. Interestingly, during tensile test, PHBV nanoribbons show high flexibility and synergistically facilitate the stretch of semi-rigid chains of PLA by an effective interfacial interaction. Consequently, even they both are extremely brittle, PLA/PHBV nanoribboned composites exhibit excellent strength (82.9 MPa) and ductility (186.7 %), compared with pure PLA (71.4 MPa and 12.3 %). Additionally, due to the promotion of the crystallization of PLA, PLA/PHBV nanoribboned composites show excellent heat resistance (E'140°C > 350 MPa). The nanoribboned composites are of immense significance, which provide significant guidance for the simultaneous enhancement of ductility and strength of polymer materials.

Advances in hydrogels for stem cell therapy: regulation mechanisms and tissue engineering applications.

Stem cell therapy has shown unparalleled potential in tissue engineering, but it still faces challenges in the regulation of the stem cell fate. Inspired by the native stem cell niche, a variety of engineered hydrogels with programmed physicochemical properties have been developed to achieve flexible and controlled regulation of the stem cell fate, greatly enhancing the clinical application prospects of stem cell therapy in tissue regeneration. Here, the recent advances in hydrogels for stem cell therapy are summarized. The mechanism by which hydrogels regulate the stem cell fate is first presented, followed by the application of hydrogel/stem cell therapies in tissue engineering, including bone tissue engineering, skin wound healing and central nervous system regeneration. Finally, the current challenges and future prospects of hydrogel/stem cell therapies in tissue engineering are discussed. The purpose of this review is to provide a reference for the crossover and integration of hydrogels and stem cells in the field of tissue engineering.

Microporous Formation Mechanism of Biaxial Stretching PA6/PP Membranes with High Porosity and Uniform Pore Size Distribution.

The low porosity and wide pore size distribution of biaxial stretching PP microporous membranes continue to be the primary impediments to their industrial application. To solve this problem, there is a critical and urgent need to study the micropore-forming mechanism of PP membranes. In this research, the interfacial micropore formation mechanism of PA6/PP membranes during biaxial stretching was investigated. PA6/PP membranes containing spherical PA6 and fibrillar PA6 were found to exhibit different interfacial micropore formation mechanisms. Numerous micropores were generated in the PA6/PP membranes, containing PA6 spherical particles via the interface separation between the PP matrix and PA6 spherical particles during longitudinal stretching. Subsequent transverse stretching further expanded the two-phase interface, promoting the breakdown and fibrosis of the PP matrix and forming a spider-web-like microporous structure centered on spherical PA6 particles. In PA6/PP membranes with PA6 fibers, fewer micropores were generated during longitudinal stretching, but the subsequent transverse stretching violently separated the PA6 fibers, resulting in a dense fiber network composed of PA6 fibers interwoven with PP fibers. Crucially, the PA6/PP biaxial stretching of microporous membranes presented an optimized pore structure, higher porosity, narrower pore size distribution, and better permeability than ß-PP membranes. Furthermore, this study explored a new approach to the fabrication of high-performance PA6/PP microporous membranes, with good prospects for potential industrial application.