Higher Fracture Strain Research Articles

Robust-adhesion and high-mechanical strength hydrogel for efficient wet tissue adhesion.

Bioadhesive hydrogels show great promise in wound closure due to their minimally invasive nature and ease of use. However, they typically exhibit poor wet adhesion and mechanical properties on wet tissues. Herein, a ready-to-use bioadhesive hydrogel (denoted as PAA-NHS/C-CS) with rapidly robust adhesion and high mechanical strength is developed via a simple one-pot UV crosslinking polymerization of acrylic acid (AA), catechol-functionalized chitosan (C-CS), and acrylic acid N-hydroxysuccinimide ester (AA-NHS ester). Benefitting from the hydrogen bonds and electrostatic attractions formed between PAA-NHS and C-CS, the as-prepared hydrogel exhibits high tensile strength (∼630 kPa), fracture strain (∼1950%), and toughness (∼4250 kJ m-3) in the fully swollen state. Besides, the noncovalent interactions and covalent crosslinking formed between the dual adhesive moieties (the NHS ester and catechol groups) and the tissue surface endow the hydrogel with high shear strength (∼160 kPa), interfacial toughness (∼630 J m-2), and burst pressure (∼447 mmHg) on wet porcine skin. By integrating the high mechanical properties, rapid robust adhesion, and operational convenience, the as-prepared PAA-NHS/C-CS hydrogel shows great promise in wound closure.

Molecular dynamics simulation of bending behavior of B2-FeAl alloy nanowires with different crystallographic orientations

In nanosystems, the metallic nanowires are subjected to significant and cyclic bending deformation upon integration into stretchable and flexible nanoelectronic devices. The reliability and service life of these nanodevices depend fundamentally on the bending mechanical properties of the metallic nanowires that serve as the critical components. A deep understanding of the deformation behavior of the metallic nanowires under bending is not only essential but also imperative for design and manufacture of high-performance nanodevices. To explore the mechanism underlying the bending plasticity of the metallic nanowire, we have conducted a study on the bending deformation of B2-FeAl alloy nanowires with various crystallographic orientations, sizes and cross-sectional shapes by using molecular dynamics simulation. Our results show that the bending behavior of the B2-FeAl alloy nanowires is independent of the size and cross-sectional shape of the nanowire, but it is highly sensitive to its axial orientation. Specifically, both <111>- and <110>-oriented nanowires yield by dislocation nucleation upon bending, in which the <111>-oriented nanowire fails by brittle fracture soon after yielding, while the <110>-oriented nanowire exhibits good ductility due to homogeneous plastic flow raised by continuous nucleation and steady motion of dislocations. In contrast to the aforementioned two nanowires, the bending plasticity of the <001>-oriented nanowire is mediated by stress-induced transformation from B2 to L1<sub>0</sub> phases, which leads to excellent ductility and higher fracture strain. The orientation dependence of bending deformation can be understood by considering the Schmid factor. Moreover, the plastically bent nanowires with <110> and <001> orientations are able to recover to their original shape upon unloading, particularly, the plastic deformation in the <001>-oriented nanowire is recoverable completely via reverse transformation from L1<sub>0</sub> to B2 structures, exhibiting superelasticity. This work elucidates the deformation mechanism of the B2-FeAl alloy nanowire subjected to bending load, which provides a crucial insight for the design and optimization of flexible and stretchable nanodevices based on metallic nanowires.

Ductile (Ag,Cu)2(S,Se,Te)-based auxetic metamaterials for sustainable thermoelectric power generation

Sustainable energy solution has resulted in significant interest in thermoelectric power generation, converting waste heat into electricity. However, the practical application of thermoelectric generators has been hindered by issues with their adaptability to arbitrary heat sources and durability in an operational environment. Here, we propose deformable auxetic thermoelectric metamaterials composed of high-entropy (Ag,Cu)2(S,Se,Te) ductile alloys, realized using finite element modelling and three-dimensional (3D) printing. We design a re-entrant auxetic structure with a negative Poisson’s ratio to maximize the mechanical deformability and develop an (Ag,Cu)2(S,Se,Te) particle-based colloidal 3D printable ink, tailored with Te microparticles. The 3D-printed (Ag,Cu)2(S,Se,Te) alloy exhibit a ZT value of 1.15 coupled with high compressive strength (208 MPa) and fracture strain (17.5 %). The fabricated auxetic metamaterials exhibit excellent vibrational stability and adaptability to diverse curved surfaces, realizing efficient power generation on a synclastic curved heat source. Our approach offers a method to design durable and efficient heat recovery devices.

Biomimetic toughening design of 3D-printed polymeric structures: Enhancing toughness through sacrificial bonds and hidden lengths

Spider silk is known for its excellent strength and fracture resistance properties due to its molecular design structure, characterized by sacrificial bonds and hidden lengths. These structures have inspired reinforcements of synthetic polymer materials to enhance toughness. In this study, we mimic these natural toughening mechanisms by designing and manufacturing 3D-printed polymeric structures incorporating overlapping curls consisting of coiling fiber with sacrificial bonds and hidden lengths. Utilizing the liquid rope coiling effect, we manufactured overlapping curls using three polymers: polylactic acid (PLA), liquid crystal polymer (LCP), and polyamide 6 (PA6). Uniaxial tensile tests were performed to characterize the mechanical properties of overlapping curl as a function of geometries, post-treatments, and material constitutive parameters. Our results show that single-sided overlapping curls can fully unfold while double-sided curls are prone to premature failure. Heat-pressure post-treatment was found to significantly increase the load-capacity of the sacrificial bonds by up to ▪ due to increased contact area. However, the defects introduced in the fibre after the break of the sacrificial bonds, make the structure more susceptible to premature failure, limit the complete unfolding of the hidden length, and lead to a decrease up to ▪ of the toughness. To guarantee the complete unfolding of the hidden lengths and improve the toughness, we demonstrate that selecting a polymer material with either high fracture strength (e.g., LCP, ▪) or high fracture strain (e.g., PA6, >2) is crucial, and increase toughness up to ▪ and ▪, respectively.

A ternary calcium silicate bone cement with high mechanical properties and good operability

The treatment of vertebral compression fractures of the spinal necessitates the use of injectable bone repair materials with the adaptive modulus of elasticity. Currently, newly developed injectable self-curing materials for minimally invasive surgery are primarily categorized into calcium phosphate and calcium silicate systems, both of which exhibit excellent biocompatibility. However, calcium phosphate bone cement lacks adequate mechanical properties and the stress does not match between bone and material. Calcium silicate cement has a long curing time, low mechanical strength, and high alkalinity. These deficiencies render them inadequate for meeting clinical requirements. Therefore, we incorporated inorganic disodium phosphate, organic polyvinyl alcohol, and solid component cerium oxide into the matrix phase of tricalcium silicate bone cement to establish a ternary self-curing hydration reinforcement system and produced an organic-inorganic composite injectable bone cement. Even though the composite bone cement has a longer setting time, it exhibited high compressive strength (61.9Mpa) and fracture strain (7.88 %), demonstrating excellent mechanical properties. Furthermore, it also demonstrates good injectable properties (86 %), anti-collapse properties, good biological activity, and outstanding antibacterial properties. The composite bone cement has great potential to develop a new injectable self-curing material to replace PMMA bone cement in clinical vertebral compression fractures.

All-glycerogel stretchable supercapacitor with stable performance in a wide temperature window from −20 to 80 °C

Stretchable supercapacitors (s-SCs) are extensively used in portable and wearable smart electronic devices. However, existing s-SCs exhibit low electrical conductivity/stretchability, weak electrode/electrolyte interfaces, and limited operational temperatures, which severely limit their practical applications. Accordingly, we have developed a stretchable glycerogel supercapacitor (s-GGSC) addressing these limitations. Electrode is fabricated by glycerol-mediated robust integration of poly(vinyl alcohol) and poly(3,4-ethylenedioxythiophene) polystyrene sulfonate through a simple strategy of partial drying–reswelling and thermal annealing. This eliminates the conventional trade-off between electrical conductivity and stretchability and provides adaptability to wide temperature ranges (−20 to 80 °C). A compatible electrolyte is also fabricated using poly(vinyl alcohol), lithium perchlorate, and glycerol. Heat-mediated facile exchange of inter- and intramolecular hydrogen bonding enables robust bonding between the electrode and electrolyte in the developed s-GGSC, thus solving interfacial problems under harsh mechanical conditions. The high electrical conductivity (1089 ± 49 S m−1) and fracture strain (232%) of the electrode preclude the use of an additional current collector. s-GGSC exhibits areal capacitance retentions of 90.92% and 93.27% after 7 d of incubation at −20 and 80 °C, respectively, and excellent cycling stability (81.48% capacitance retention) after 10,000 cycles. Furthermore, the areal capacitance of the device remains constant after intense mechanical deformations, such as bending, twisting, and stretching. s-GGSC outperforms existing flexible and/or stretchable supercapacitors under harsh conditions, confirming its suitability as a potential power source for wearable and stretchable smart electronic devices.

High-Strain-Rate Deformation Behavior of Co0.96Cr0.76Fe0.85Ni1.01Hf0.40 Eutectic High-Entropy Alloy at Room and Cryogenic Temperatures.

The deformation behaviors of Co0.96Cr0.76Fe0.85Ni1.01Hf0.40 eutectic high-entropy alloy (EHEA) under high strain rates have been investigated at both room temperature (RT, 298 K) and liquid nitrogen temperature (LNT, 77 K). The current Co0.96Cr0.76Fe0.85Ni1.01Hf0.40 EHEA exhibits a high yield strength of 740 MPa along with a high fracture strain of 35% under quasi-static loading. A remarkable positive strain rate effect can be observed, and its yield strength increased to 1060 MPa when the strain rate increased to 3000/s. Decreasing temperature will further enhance the yield strength significantly. The yield strength of this alloy at a strain rate of 3000/s increases to 1240 MPa under the LNT condition. Moreover, the current EHEA exhibits a notable increased strain-hardening ability with either an increasing strain rate or a decreasing temperature. Transmission electron microscopy (TEM) characterization uncovered that the dynamic plastic deformation of this EHEA at RT is dominated by dislocation slip. However, under severe conditions of high strain rate in conjunction with LNT, dislocation dissociation is promoted, resulting in a higher density of nanoscale deformation twins, stacking faults (SFs) as well as immobile Lomer-Cottrell (L-C) dislocation locks. These deformation twins, SFs and immobile dislocation locks function effectively as dislocation barriers, contributing notably to the elevated strain-hardening rate observed during dynamic deformation at LNT.

A strategy for high-entropy copper alloys composition design assisted by deep learning based on data reconstruction and network structure optimization

Complex mapping relationships between high-entropy alloy compositions and performances struggle to precisely elucidate by traditional machine learning models, hindering the accurate and efficient design of high-performance alloys. In this work, a novel alloy design strategy combined self-decision deep neural network, data reconstruction with network structure optimization was proposed, which effectively enhanced the model's ability to predict the mapping relationships between high-dimensional composition spaces and mechanical properties of alloy. Compared to other machine learning methods, significantly improves model prediction accuracy (hardness model: 97.98%; strength model: 94.40%). Through above model, the mechanical properties of 308 new (CuNiMn)-X high-entropy copper alloys was studied added other elements such as Al, Ti, Cr, and Fe, which designed and produced a novel (CuNiMn)60Al20Cr20 alloy with high hardness of 474 HV, high compressive strength of 2322 MPa, and high fracture strain of 25.20%. The primary factors influencing alloy performance and their respective thresholds were also quantitatively revealed (hardness: electronegativity deviation (0.02, 0.1) and nuclear charge deviation (0, 0.25); compressive strength: mean nuclear charge (25, 30) and mean atomic radius (134 p.m.)). These findings provide a new perspective and approach for the design and mechanism understanding of high-performance alloys with complex compositions.

Dynamic mechanical behavior of ultra-high specific strength lightweight Ti61Al16Cr10Nb8V5 multi-principal element alloy

This study investigated the dynamic mechanical property and microstructure evolution of the Ti61Al16Cr10Nb8V5 (Ti61) lightweight multi-principal element alloy(MPEA) with a density of 4.83 g/cm3. After melting and rolling, the Ti61 alloy was composed of a BCC matrix phase and dispersed B2 phase, and also contained a small amount of fine needle-like FCC phase and spherical HCP phase. Mechanical testing of Ti61 alloy revealed that the ultimate tensile strength is about 1223 MPa, and the tensile elongation is about 13.2 %, with a specific strength of around 253 MPa*cm3/g. Dynamic compression testing of Ti61 alloy showed a significant strain rate strengthening effect and excellent fracture strain greater than 50 %. Calculation and microstructural observations indicated that at low strain rates ranging from 10−3/s to 10/s, the strain rate sensitivity of Ti61 alloy was 0.0087, with the main plastic deformation mechanism of dislocation nucleation, dislocation slip, and stacking faults. At high strain rates ranging from 500/s to 5000/s, the strain rate sensitivity raises to 0.0963 and the main deformation mechanism of the Ti61 alloy involved higher-density dislocation nucleation, dislocation slip, stacking faults and twinning. At strain rates of 5000/s, HCP-FCC phase transition accompanied by FCC microtwins and BCC-α2HCP phase transition occurred. Furthermore, dynamic recrystallization also occurred in Ti61 alloy. The HCP-FCC has the orientation of (0001)HCP//(11−1)FCC, [1−210]HCP//[011]FCC. The BCC-α2HCP has the orientation of {101}BCC//{0001}HCP and [111]BCC//[2−1−10]HCP. Twining and phase transition strengthen the yield stress of Ti61 alloy, while dynamic recrystallization reduced the flow stress of Ti61 alloy. Ti61 alloy has high strength, high compression fracture strain, and ultra-high specific strength, which is a new LWMPEA with great application potential in military armor.

Intrinsically Stretchable Organic Photovoltaic Cells with Improved Mechanical Durability and Stability via Dual‐Donor Polymer Blending

AbstractIntrinsically stretchable organic photovoltaic cells (OPVs) have garnered significant attention as crucial devices for powering next‐generation wearable electronics. Despite the rapid power conversion efficiency gains in champion OPVs, their brittle stretchability has failed to meet the demands of the Internet of Things era, severely hindering further development and practical applications. In this regard, a new dual‐donor polymer blending strategy is demonstrated for constructing intrinsically stretchable OPVs by designing a novel high‐molecular–weight conjugated polymer PM6‐HD. This PM6 derivative featuring long alkyl chains can reach a sufficiently high molecular weight and thus exhibits a high fracture strain exceeding 90%, which is ≈12 times higher than the benchmark PM6. Synergistic optimization of mechanical properties and photovoltaic performance in polymer:small molecule and all‐polymer systems constructed from the physical blends of PM6 and PM6‐HD is achieved. Crucially, the resulting intrinsically stretchable OPV demonstrates excellent stretchability and stability, with a record PCE80% strain of 50.3% and the efficiency retention of above 80% even after 1000 cycles of cyclic stretching at high strains. This work contributes to the advancement of intrinsically stretchable OPV technology and opens up new possibilities for its integration into wearable electronic devices.

Solvent-Resistant Adhesive Gel with Thermal Post-Tunability.

Adhesives have received extensive attention in flexible bioelectronics, wearable electronic medical devices, and biofuel cells. However, it is a challenge to achieve late regulation of performance once polymer-based gels are formed. Here, a double-network organogel composed of a hydrophilic and hydrophobic polymer network and a polyamide acid network was successfully prepared. In diverse liquid environments (including isopropyl alcohol, glycerol, epichlorohydrin, n-propanol, dichloromethane, triethanolamine, ethanol absolute, hydrogen peroxide, and ethyl acetate), the organogel adhesive demonstrated remarkable properties. It exhibits a strong tensile strength of 200 kPa, a high fracture strain reaching 560%, and an impressive adhesion strength of 38 kPa. In addition, the organogel demonstrates exceptional adhesive properties toward polytetrafluoroethylene, plastics, metals, rubber, and glass. Note that the organogel could also regulate adhesive and tough performance by thermally triggering a cyclization reaction even after the organogel has been formed. The strategy provides a new idea for designing soft materials with post-tunability.

Tailoring the non-coherent interfacial precipitation to overcome the trade-off between strength-ductility and impact energy release in Ti–Zr–Hf–Nb–Ta high entropy alloy

The energetic high-entropy alloys have brought a new idea for the development of new energetic structural materials (ESMs) with high energy density and excellent mechanical properties. However, the energetic high-entropy alloys exhibit a significant trade-off between strength-ductility and impact energy release efficiency. Here, we develop a new strategy to introduce non-coherent interfacial nanoprecipitates into the Ti–Zr-Hf-Nb-Ta BCC energetic high-entropy alloy, which can not only exert the precipitation strengthening mechanism to maintain excellent mechanical properties, but also transform the local shear fracture into multiple cracks along the grain boundary to promote energy release. The nanoprecipitation-strengthened energetic high-entropy alloy achieved a four-times greater fireball area generated by impact energy release than that of the single-phase BCC alloy, while maintaining an excellent mechanical property combination of high dynamic compression strength (1787 MPa) and high fracture strain (40 %). The results provide new insights into the development of energetic high-entropy alloys with superior impact energy release and strength-ductility synergy.

Strong, tough and anisotropic bioinspired hydrogels.

Soft materials are widely used in tissue engineering, soft robots, wearable electronics, etc. However, it remains a challenge to fabricate soft materials, such as hydrogels, with both high strength and toughness that are comparable to biological tissues. Inspired by the anisotropic structure of biological tissues, a novel solvent-exchange-assisted wet-stretching strategy is proposed to prepare anisotropic polyvinyl alcohol (PVA) hydrogels by tuning the macromolecular chain movement and optimizing the polymer network. The reinforcing and toughening mechanisms are found to be "macromolecule crystallization and nanofibril formation". These hydrogels exhibit excellent mechanical properties, such as extremely high fracture stress (12.8 ± 0.7 MPa) and fracture strain (1719 ± 77%), excellent modulus (4.51 ± 0.76 MPa), high work of fracture (134.47 ± 9.29 MJ m-3), and fracture toughness (305.04 kJ m-2) compared with other strong hydrogels and even natural tendons. In addition, excellent conductivity, strain sensing capability, water retention, freezing resistance, swelling resistance, and biocompatibility can also be achieved. This work provides a new and effective method to fabricate multifunctional anisotropic hydrogels with high tunable strength and toughness with potential applications in the fields of regenerative medicine, flexible sensors, and soft robotics.

Super flexible, self-healing, and self-adhesive double network hydrogel reinforced by okara cellulose nanofibrils

Inspired by the mussel, tannic acid (TA) was modified onto the surface of self-made cellulose nanofibrils (CNFs) to prepare TA@CNFs, which was introduced into borax crosslinked polyvinyl alcohol (PVA) to prepare PTC double-network hydrogel with self-healing properties. Through the comparative observation of TEM images and infrared spectra before and after tannic acid modification, the formation of TA@CNFs was proved. The introduction of TA@CNFs greatly increases the fracture stress of PTC hydrogel, which is more than 10 times higher than that of PVA hydrogel without TA@CNFs, and has high fracture strain (1723 %). Moreover, PTC hydrogel has the ability of rapid self-healing, which can heal to the original form within two minutes. In addition, the temperature response ability of PTC hydrogel makes it capable of reshaping. The self-adhesion ability of PTC hydrogel enables it to adhere to the human epidermis to detect motion signals, as sensitive and as stable as a flexible sensor.

Effect of graphene sheet diameter on the microstructure and properties of copper-plated graphene-reinforced 6061-aluminum matrix composites

Herein, graphene with two different average sheet diameters was ultrasonically dispersed, mechanically stirred, and copper-plated. The pretreated graphene was mixed with 6061-aluminum (6061Al) powder to fabricate copper-plated graphene (0.5 wt%) reinforced 6061Al matrix composites by spark plasma sintering. The resulting composites were characterized in terms of their microstructure, tensile properties, electrical conductivity, and thermal conductivity. The incorporation of graphene facilitated load transfer and hindered dislocation movement, thereby enhancing the mechanical properties of the composites. Notably, the composite reinforced by larger-sized graphene achieved a favorable combination of high tensile strength (218 MPa) and fracture strain (17.2 %). Moreover, the addition of graphene also ameliorated the electrical conductivity of 6061Al. The composite reinforced by the larger-sized graphene achieved the highest electrical conductivity of 47.7 %IACS, attributed to the formation of a wider range of conductive channels. Additionally, the introduction of larger-sized graphene increased the thermal conductivity of 6061Al from 161.4 W/(m·K) to 183.2 W/(m·K), whilst the smaller-sized graphene contributed to a modest enhancement of 15.3 W/(m·K). In conclusion, graphene with a larger sheet diameter exhibits a remarkable reinforcement effect on the overall performance of 6061Al.

A light-responsive poly(urethane-urea) actuator with room temperature self-healing performance

Light-responsive actuators with self-healing properties and super mechanical strength at room temperature are critical for practical applications. However, optimizing both of these properties on a single actuator is extremely challenging. Herein, a novel light-responsive poly(urethane-urea) actuator (PIBS-0.75) with room temperature self-healing performance has been successfully prepared. The PIBS-0.75 light-responsive actuator not only exhibits excellent self-healing properties (heals for 8 h at room temperature and regains 91.16 % of its original tensile strength), but also shows high tensile strength (15.52 MPa) and good fracture strain (over 600 %). Moreover, a bionic light-responsive device with room temperature self-healing properties has been successfully fabricated to imitate human gestures of greeting. By incorporating the room temperature self-healing ability into the light-responsive actuator, this work would pave a new way for the development of durable and sustainable light-responsive actuators.

Towards ultra-high strength dual-phase steel with excellent damage tolerance: The effect of martensite volume fraction

Ultra-high strength (> 1 GPa) dual-phase (DP) steels have been extensively investigated in literature. Yet, the damage tolerance of these DP steels remains mostly unexplored, whereas this parameter is crucial for the sheet formability and anti-crushing performance. In this work, a medium-Mn DP steel was proposed in order to develop strong but damage-resistant DP steel by refining the microstructure. Ultra-fine grained (< 1 µm) DP steels were obtained by a simple cold rolling and intercritical annealing process. The developed DP steel can achieve an outstanding ultimate tensile strength (UTS) of over 1470 MPa with appreciable elongation to failure (EtF) of over 9 % when the martensite volume fraction (Vm) is 55 %. Higher Vm results in higher strength. However, the fracture strain, which is connected with damage tolerance, decreases significantly with increasing Vm, and it is even much lower than that of a full-martensite steel. Furthermore, the necking behaviour transfers from diffuse plus localized necking to diffuse necking with increasing Vm. The sufficient ferrite content in the proposed DP1470 steel enables void growth after nucleation, consequently leading to the occurrence of localized necking and higher fracture strain. Thus, a moderate Vm ranging from 45 % to 65 % is suggested for the development of a 1470 MPa grade DP steel with excellent damage tolerance.

Accelerated Design for High-Entropy Alloys Based on Machine Learning and Multiobjective Optimization.

High-entropy alloys (HEAs) with high hardness and high ductility can be considered as candidates for wear-resistant applications. However, designing novel HEAs with multiple desired properties using traditional alloy design methods remains challenging due to the enormous composition space. In this work, we proposed a machine-learning-based framework to design HEAs with high Vickers hardness (H) and high compressive fracture strain (D). Initially, we constructed data sets containing 172,467 data with 161 features for D and H, respectively. Four-step feature selection was performed, with the selection of 12 and 8 features for the D and H prediction models based on the optimal algorithms of the support vector machine (SVR) and light gradient boosting machine (LightGBM), respectively. The R2 of the well-trained models reached 0.76 and 0.90 for the 10-fold cross validation. Nondominated sorting genetic algorithm version II (NSGA-II) and virtual screening were employed to search for the optimal alloying compositions, and four recommended candidates were synthesized to validate our methods. Notably, the D of three candidates have shown significant improvements compared to the samples with similar H in the original data sets, with increases of 135.8, 282.4, and 194.1% respectively. Analyzing the candidates, we have recommended suitable atomic percentage ranges for elements such as Al (2-14.8 at %), Nb (4-25 at %), and Mo (3-9.9 at %) in order to design HEAs with high hardness and ductility.

Development of bioinspired damage-tolerant calcium phosphate bulk materials

ABSTRACT Improving the damage tolerance and reliability of ceramic artificial bone materials, such as sintered bodies of hydroxyapatite (HAp), that remain in vivo for long periods of time is of utmost importance. However, the intrinsic brittleness and low damage tolerance of ceramics make this challenging. This paper reports the synthesis of highly damage tolerant calcium phosphate-based materials with a bioinspired design for novel artificial bones. The heat treatment of isophthalate ion-containing octacalcium phosphate compacts in a nitrogen atmosphere at 1000°C for 24 h produced an HAp/β-tricalcium phosphate/pyrolytic carbon composite with a brick-and-mortar structure (similar to that of the nacreous layer). This composite exhibited excellent damage tolerance, with no brittle fracture upon nailing, likely attributable to the specific mechanical properties derived from its unique microstructure. Its maximum bending stress, maximum bending strain, Young’s modulus, and Vickers hardness were 11.7 MPa, 2.8 × 10‒ 2, 5.3 GPa, and 11.7 kgf/mm2, respectively. The material exhibited a lower Young’s modulus and higher fracture strain than that of HAp-sintered bodies and sintered-body samples prepared from pure octacalcium phosphate compacts. Additionally, the apatite-forming ability of the obtained material was confirmed in vitro, using a simulated body fluid. The proposed bioinspired material design could enable the fabrication of highly damage tolerant artificial bones that remain in vivo for long durations of time.

Ultrahigh tough, self-healing copolymer elastomer crosslinked by reversible imine system

Improvement of toughness is still a challenge for self-healing materials. Most of self-healing materials difficultly balance the mechanical and self-healing property. Here, a molecular design strategy of copolymer is proposed based on three combinations of reversible imine bond, chain motion and thermosensitive hydrogen bond together. The approach initially forms a co-continuous microphase separation structure and then cross-linked by aromatic imine via esterification reaction and Schiff base reaction, which features efficient self-healing, ultrahigh strength and toughness. The resultant elastomer exhibits a high stress at break (≈3 MPa) and high fracture strain (≈600 %). Additionally, the elastomer can reach 95 % self-healing efficiency after healing at 100 °C for 12 h. Extra reversible imine crosslinking displays a doubly promotion for fracture stress, and unchanging strain as well as 1times increase for self-healing efficiency, compared with merely chain motion and hydrogen bonding. This elastomer can be successfully spun into stretchable, conductive, self-healing filaments with core-shell structure by wet spinning and coating methods. It shows excellent corrosion resistance against NaCl, and conductive and self-healing property after coating by PANI polymer. This new type of self-healing polymer is promising to expand the application in future tissue engineering, soft robotics, and biomedical devices.