Mechanical Strength Research Articles

Interface engineering in CF/Al matrix composites for enhancement in mechanical strength and anti-corrosion properties

Metal matrix composites (MMCs), renowned for their lightweight and exceptional mechanical properties, are currently in high demand. Herein, carbon fiber‑aluminum metal matrix composites (CF/Al MMCs) modified with 4 types of corrosion-barrier interface coatings (CBCs), respectively, including Ni, TiO2, ZnO, and Al2O3 were investigated, and the composites were prepared by squeeze casting technique. The effects of these CBCs on the CF/Al interface reaction and the mechanical properties and electrochemical corrosion resistance of the composites are revealed and discussed thoroughly. It is observed that T300‑carbon fiber reinforced MMCs without any CBCs exhibit low mechanical strength due to the formation of Al4C3 phase induced by strong interaction between fiber and matrix. With CBCs, the formation of Al4C3 was significantly suppressed. Comparatively, the ZnO-coated CF/Al MMCs exhibit the most remarkable enhancement in the mechanical properties with a flexural strength of 796.4 MPa and a modulus of 105.3 GPa, which are approximately 114% and 52.2% higher than those of the counterparts without CBCs, respectively. More importantly, the CF/Al MMCs with CBCs demonstrate superior chemical corrosion resistance, retaining their mechanical performance even after a 7-day immersion in salt solutions. These results provide an important guideline in interface engineering for MMCs with enhanced mechanical properties and electrochemical corrosion resistance.

Development of Multifunctional Sustainable Packaging from Acetylated Cellulose Micro-Nanofibrils (CMNF)

Cellulose micro-nanofibrils (CMNF) with different fibrillation levels were partially acetylated while preserving their morphological and native crystalline structure. The morphological changes due to fibrillation and chemical modification were observed using Time-of-Flight Secondary Ion Mass Spectrometry (ToF-SIMS) and optical profilometry. The change in tensile and burst strength, barrier, and biodegradability profile were investigated which revealed that the mechanical properties of the unmodified CMNF films increased with increase in extent of fibrillation. However, the mechanical strength of the acetylated film decreased with the increase in degree of acetylation. The stretching or folding property of the film increased with the increase in both the fibrillation and acetylation. The contact angle value increased due to a higher degree of fibrillation and acetylation because they increased the hydrophobicity and consequently enhanced the air and water vapor resistance of the unmodified and modified CNF films. Furthermore, all films exhibited the highest resistance against oil and grease, and the biodegradability test substantiated that CNF films were compostable in soil. In total, this work expresses new pathways to enhance the barrier properties of biodegradable CNF films by regulating the degree of fibrillation and acetylation, thus can emerge as sustainable alternatives to for packaging and agriculture applications.

Effect of ratio of desulfurization gypsum to carbide slag on low-carbon phase change composites for energy storage

To recycle industrial wastes sufficiently, this work innovatively proposed a mixture of desulfurization gypsum and carbide slag as skeleton material to fabricate phase-change composites with NaNO3 as phase change material in a mass ratio of 5 to 5. Four phase-change composites were fabricated with different ratio of desulfurization gypsum to carbide slag by the cold compression-hot sintering method, and then key thermal and mechanical properties, microscopic morphology and chemical compatibility between components were investigated in detail. Results show that the mixture of desulfurization gypsum and carbide slag as skeleton material is feasible and reliable and an optimal mass ratio of desulfurization gypsum to carbide slag was obtained to be 3.5 to 1.5; the phase-change composite with the optimal mass ratio possesses good mechanical strength of up to 134.116 MPa and an energy storage capacity of 483.151 J/g in the range of 100 to 400 °C, as well as excellent thermal stability and chemical compatibility between components, inside which the NaNO3 is well encapsulated. Moreover, the phase-change composites fabricated in this work have far low energy consumption and carbon dioxide emission.

Osteogenerative and corrosion-decelerating teriparatide-mediated strontium–zinc phosphate hybrid coating on biodegradable zinc–copper alloy for orthopaedic applications

Zinc–copper (ZnCu) alloys recently showed great potential as biodegradable materials for bone implants thanks to their excellent mechanical strength, biosafety, and promising bioactivities. However, bare ZnCu alloys exhibited poor cytocompatibility and osteointegration. Moreover, the biological functions of ZnCu remain to be corroborated. Herein, the teriparatide (PTH)-mediated strontium–zinc phosphate (SrZnP) organic–inorganic hybrid coating was fabricated on the surface of ZnCu substrate via a chemical conversion method to contain the release of Zn ions and improve biofunctionality in osteogenesis. The characteristics of the hybrid coating were optimised by adjusting the amount of PTH molecules added. A dense and homogenous coating with micellar crystal micro-/nano-structure was obtained. The coated samples showed a significantly decreased corrosion rate and a more uniform corrosion mode, effectively suppressing the release of Zn2+. Additionally, the coated ZnCu enhanced the proliferation of bone marrow mesenchymal stem cells (BMSCs), promoted the expression of alkaline phosphatase and the formation of calcium nodules, and upregulated the levels of osteogenic-related genes. More important, the hybrid coating activated the classic osteogenic signalling pathway of BMP-2/Smad1/Runx2 and Sirt1/Runx2 to induce the osteogenic differentiation of BMSCs. These appealing features can be mainly attributed to the constituents of released Zn2+, Sr2+, and PTH molecules in the control, as well as the unique topographical characteristics of the coatings. Taken together, the PTH&SrZnP hybrid coating could be a promising option for surface modification of biodegradable metallic Zn for orthopaedic applications.

Ex-situ fabrication of engineered green network of multifaceted bacterial cellulose film with enhanced antimicrobial properties for post-harvest preservation of table grapes

In order to overcome the inherent limitations of pristine bacterial cellulose (BC) as an active food packaging material, this study employs a dual-action approach to ex-situ fabricate a multifaceted green composite of BC through citrus pectin (CP) impregnation and subsequent functionalization with thyme essential oil (TEO) encapsulated CP-TEO active emulsion coating. Among various BC-CP composites studied, BC-CP1 revealed the optimal film formation with homogeneous dense microstructure, enhanced mechanical strength (from 126.37 MPa to 183.24 MPa), and reduced water vapor permeability (WVP) (from 3.69 ×10−11 g.m−1.s−1.Pa−1 to 3.33 ×10−11 g.m−1.s−1.Pa−1). The WVP was further reduced to 2.69 × 10−11 g.m−1.s−1.Pa−1 with the CP-TEO active emulsion coating. The BC-CP1/TEO2 exhibited exceptional antibacterial and antibiofilm characteristics, effective UV-blocking, and improved visible light transmittance. The film demonstrated superior potential in preserving grape quality over 9 days of storage compared to pristine BC and conventional plastic packaging. Thus, the BC-CP1/TEO2 has emerged as an eco-friendly, multi-layered solution for sustainable packaging needs.

PENGARUH KEKUATAN IMPAK DAN TARIK KOMPOSIT BERPENGUAT SERAT SEMBUKAN DENGAN MATRIK EPOXY

Composite is a combination of two or more elements arranged in a certain way to get new properties in matrial. Plants of Pukan (Peaderiafoetida L.) is a kind of wild grass that spreads and grows wild in nature. This study aims to determine the effect of the mechanical strength of the composite reinforced dying in the Healing with epoxy matrix. In this test, using Sembukan fiber as a reinforcement and epoxy as a composite matrial adhesive. The tests include: Tensile tests referring to ASTMD 3039, and Impact Tests referring to ASTMD 256. These tests use fiber volume fractions of 20%, 30%, and 40% with woven fiber orientation. The results showed, the greater the fiber volume fraction, the greater the toughness, the highest toughness was found in the fiber volume fraction variance of 40%, amounting to 0.10396 J/mm2. Same as Tensile testing, the stress increases with increasing fiber volume fraction, ie at 40% fiber at 9,1596 MPa. The influencing factor is none other than the percentage of fibers in the composite increasing the mechanical strength of the matrix. Keywords: Fiber Heal, toughness Impact, Tensile strength.

An injectable and absorbable magnesium phosphate bone cement designed for osteoporotic fractures

Magnesium phosphate cement as a substitute for osteoporotic fracture implants has gained increasing attention from the public. However, lack of sufficient mechanical strength and osteoinductive capacity, rapid setting time and strongly alkaline environment during degradation have hindered its practical application. Hence, a drug carrier system composed of chitosan and teriparatide solution of liquid phase is constructed and compounded into magnesium phosphate cement (CHI-TR MPC). The CHI-TR MPC composites exhibited almost neutral pH, extended setting time, excellent injectability, enhanced compressive strength, and increased porosity. Meanwhile，the CHI-TR MPC scaffold facilitated the controllable release of ions and drugs, promoted osteogenic differentiation and mineralization through its abundant pore structure, and possessed an appropriate degradation rate. Therefore, this CHI-TR MPC scaffold has huge potential for functional biomaterials design and clinical management in the treatment of osteoporotic fractures.

High-efficiency Lithium Metal Stabilization and Polysulfide Suppression in Li-S Battery Enabled by Weakly Solvating Solvent.

Lithium-sulfur batteries (LSBs) are considered a highly promising next-generation energy storage technology due to their exceptional energy density and cost-effectiveness. However, the practical use of current LSBs is hindered primarily by issues related to the "shuttle effect" of lithium polysulfide (LiPS) intermediates and the growth of lithium dendrites. In strongly solvating electrolytes, the solvent-derived solid electrolyte interphase (SEI) lacks mechanical strength due to organic components, leading to ineffective lithium dendrite suppression and severe LiPS dissolution and shuttling. In contrast, the weakly solvating electrolyte (WSE) can create an anion-derived SEI layer which can enhance compatibility with lithium metal anode, and restricting LiPS solubility. Herein, a WSE consisting of 0.4м LiTFSI in the mixture of 1,4-dioxane (DX):dimethoxymethane (DMM) is designed to overcome the issues associated with LSB. Surface analyses confirmed the formation of a beneficial SEI layer rich in LiF, enabling homogeneous lithium deposition with an average Coulombic efficiency CE exceeding 99% over 100 cycles. Implementing the low-concentration WSE in Li||SPAN cells yielded an impressive initial specific capacity of 671mAhg-1. This research highlights the advantages of WSE and offers the pathway for cost-effective electrolyte development, enabling the realization of high-performance LSBs.

Dynamically Cross-Linked Double-Network Hydrogels with Matched Mechanical Properties and Ideal Biocompatibility for Artificial Blood Vessels.

Vessel transplantation is currently considered the "gold standard" treatment for cardiovascular disease. However, ideal artificial vascular grafts should possess good biocompatibility and mechanical strength that match those of native autologous vascular tissue to promote in vivo tissue regeneration. In this study, a series of dynamic cross-linking double-network hydrogels and the resultant hydrogel tubes were prepared. The hydrogels (named PCO), composed of rigid poly(vinyl alcohol) (PVA), flexible carboxymethyl chitosan (CMCS), and a cross-linker of aldehyde-based β-cyclodextrin (OCD), were formed in a double-network structure with multiple dynamical cross-linking including dynamic imine bonds, hydrogen bonds, and microcrystalline regions. The PCO hydrogels exhibited superior mechanical strength, good network stability, and fatigue resistance. Additionally, it demonstrated excellent cell and blood compatibility. The results showed that the introduction of CMCS/OCD led to a significant increase in the proliferation rate of endothelial cells seeded on the surface of the hydrogel. The hemolysis rate in the test was lower than 0.3%, and both protein adsorption and platelet adhesion were reduced, indicating an excellent anticoagulant function. The plasma recalcification time test results showed that endogenous coagulation was alleviated to some extent. When formed into blood vessels and incubated with blood, no thrombus formation was observed, and there was minimal red blood cell aggregation. Therefore, this novel hydrogel tube, with excellent mechanical properties, exhibits antiadhesive characteristics toward blood cells and proteins, as well as antithrombotic properties, making it hold tremendous potential for applications in the biomedical and engineering fields.

Cellulose fibres enhance the function of hemostatic composite medical sealants.

Tissue adhesives and sealants offer promising alternatives to traditional wound closure methods, but the existing trade-off between biocompatibility and strength is still a challenge. The current study explores the potential of a gelatin-alginate-based hydrogel, cross-linked with a carbodiimide, and loaded with two functional fillers, the hemostatic agent kaolin and cellulose fibres, to improve the hydrogel's mechanical strength and hemostatic properties for use as a sealant. The effect of the formulation parameters on the mechanical and physical properties was studied, as well as the biocompatibility and microstructure. The incorporation of the two functional fillers resulted in a dual micro-composite structure, with uniform dispersion of both fillers within the hydrogel, and excellent adhesion between the fillers and the hydrogel matrix. This enabled to strongly increase the sealing ability and the tensile strength and modulus of the hydrogel. The fibres' contribution to the enhanced mechanical properties is more dominant than that of kaolin. A combined synergistic effect of both fillers resulted in enhanced sealing ability (247%), tensile strength (400%), and Young's modulus (437%), compared to the unloaded hydrogel formulation. While the incorporation of kaolin almost did not affect the physical properties of the hydrogel, the incorporation of the fibres strongly increased the viscosity and decreased the gelation time and swelling degree. The cytotoxicity tests indicated that all studied formulations exhibited high cell viability. Hence, the studied new dual micro-composite hydrogels may be suitable for medical sealing applications, especially when it is needed to get a high sealing effect within a short time. The desired hemostatic effect is obtained due to kaolin incorporation without affecting the physical properties of the sealant. Understanding the effects of the formulation parameters on the hydrogel's properties enables the fitting of optimal formulations for various medical sealing applications.

Micrometer‐Thin Nanocellulose Foils for 3D Organic Electronics

AbstractCellulose is a natural polymer with great properties such as high optical transparency and mechanical strength, flexibility, and biodegradability. Hence, cellulose‐based foils are suitable for the replacement of synthetic polymers as substrate materials in organic electronics. This article reports the fabrication of ultrathin, free‐standing cellulose foils by spraying aqueous 2,2,6,6‐tetramethylpiperidine‐1‐oxyl‐nanocellulose (TEMPO) fibrils ink layer‐by‐layer on a hot substrate using a movable spray nozzle. The resulting foils are only 2 ± 1 µm in thickness with an average basis weight of 1.9 g m−2, which ranges in the same scale as the world's thinnest paper. The suitability of these ultra‐thin nanocellulose foils as a sustainable substrate material for organic electronic applications is demonstrated by testing the foils resistance against organic solvents. Furthermore, silver nanowires (AgNWs) and the blend poly(3,4‐ethylenedioxythiophene):polystyrene sulfonate (PEDOT:PSS) are integrated into the foils, and the foils are molded into 3D paper structures in order to create conductive, paper‐based building blocks for organic electronics.

Surface modification of biomedical titanium alloy for hard tissue repair and reconstruction

In biomedical applications, various materials are used, including metals and their alloys, polymers and ceramics. Among them, titanium (Ti) and titanium alloys are widely utilised in implant materials due to their excellent corrosion resistance and high mechanical strength. However, despite these advantages, titanium is biologically inert and does not integrate well with human cells. Therefore, surface modification of titanium implants plays a crucial role in determining the rate of osseointegration and the overall success of the implants. The primary objective of this review is to provide a detailed introduction to surface modification technologies for titanium alloy implants. The aim is to enhance the biological activity, wear resistance, corrosion resistance and antibacterial properties and reduce the release of ions from the implants. By modifying the surface of titanium implants, it is possible to create a more favourable environment for cell adhesion, proliferation and differentiation. Various techniques, such as physical methods (e.g. sandblasting, acid etching) and chemical methods (e.g. surface oxidation, plasma treatment) can be employed to modify the surface properties of titanium implants. These surface modification techniques can enhance the interaction between the implant and the surrounding biological environment, promoting osseointegration and improving the long-term stability of the implant. Additionally, surface modifications can help reduce the release of potentially harmful ions from the implant, minimise bacterial adhesion and improve the overall biocompatibility of the implant. In conclusion, surface modification of titanium alloy implants is a critical aspect of biomedical engineering. By improving the biocompatibility of titanium implants, these modifications contribute to the success and longevity of implants used in hard tissue repair and reconstruction.

Preparation of Geopolymers with Nanosilica and Water-in-Air Pickering Emulsion: Mechanisms Underlying Its Rheology, Polymerization, and Strength.

Geopolymers are alkaline-activated aluminosilicate binders recognized as a promising alternative to traditional Portland cement due to their significantly lower greenhouse emissions, energy consumption, and carbon footprint. However, the challenge is meeting or exceeding the strength of Portland cement concrete while being prepared within a desired setting time and possessing workable rheology. A "water-in-air" Pickering emulsion, also called dry water, was prepared by stabilizing water droplets with hydrophobic nano silica and using them to control the geopolymer's strength, setting time, and workability. The mechanisms that underlie the effects of dry water on the rheology, setting, and strength were studied in detail through a combination of rheological, thermal, morphological, chemical, and microstructural assessments. A reduction in the viscosity and yield shear stress manifests in a higher flow diameter, principally due to the particle size coarsening in the precursor and the flowability of hydrophobic nano silica. There was a rapid rise in temperature during the setting process as the dry water temporarily increased the local alkalinity in the mixture, which boosted the dissolution of the precursor and, hence, the reaction. Outcomes from X-ray diffraction, thermogravimetric analysis, and Fourier-transform infrared confirm the highest degree of polycondensation for the principal N-A-S-H framework in mixtures containing dry water. These eventually correspond to a denser microstructure under scanning electron microscopy and, in turn, a superior mechanical strength. Depending on the unique combination of characteristics, including size coarsening, temporary water encapsulation, microfilling effect, and supplementary silica source, dry water resolves the "trade-off" between geopolymer's fresh and hardened properties when introducing nanoparticles.

Exploring the Potential of Sustainable Biopolymers as a Shield against Electromagnetic Radiations.

The increasing demand for biodegradable and environmentally friendly materials is shifting the focus from traditional polymer composites to biocomposites in various applications, especially in electromagnetic shielding. Effective utilization of biopolymers demands improved properties and can be achieved to a certain extent by functionalization. Biopolymers such as cellulose, polylactic acid, and starch are some of the potential candidates for mitigating electromagnetic pollution in next-generation electronic devices because of their high aspect ratio, flexibility, light weight, high mechanical strength, thermal stability, and tunable microwave absorption to the electromagnetic interference (EMI) shielding composites. This Review provides an overview of the current advancements in EMI shielding materials and outlines recent research on EMI shielding composites that utilize various biodegradable polymer structures.

Impact of Sacrificial Hydrogen Bonds on the Structure and Properties of Rubber Materials: Insights from All-Atom Molecular Dynamics Simulations.

The inclusion of sacrificial hydrogen bonds is crucial for advancing high-performance rubber materials. However, the molecular mechanisms governing the impact of these bonds on material properties remain unclear, hindering progress in advanced rubber material research. This study employed all-atom molecular dynamics simulations to thoroughly investigate how hydrogen bonds affect the structure, dynamics, mechanics, and linear viscoelasticity of rubber materials. As the modified repeating unit ratio (β) increased, both interchain and intrachain hydrogen bond content rose, with interchain bonds playing a predominant role. This physical cross-linking network formed through interchain hydrogen bonds restricts molecular chain movement and relaxation and raises the glass transition temperature of rubber. Within a certain content of hydrogen bonds, the mechanical strength increases with increasing β. However, further increasing β leads to a subsequent decrease in the mechanical performance. Optimal mechanical properties were observed at β = 6%. On the other hand, a higher β value yields an elevated stress relaxation modulus and an extended stress relaxation plateau, signifying a more complex hydrogen-bond cross-linking network. Additionally, higher β increases the storage modulus, loss modulus, and complex viscosity while reducing the loss factor. In summary, this study successfully established the relationship between the structure and properties of natural rubber containing hydrogen bonds, providing a scientific foundation for the design of high-performance rubber materials.

Zr-based bulk metallic glasses in PBF-LB/M: near-polished surface quality in the as-built state

AbstractThis study investigates the relationship between varying contour scanning parameters and their impact on both surface characteristics and mechanical performance of the glass-forming Zr59.3Cu28.8Al10.4Nb1.5 produced via PBF-LB/M. Near-polished surface states with Ra values below 1 µm were achieved. The study identifies increased laser power as a key factor in reducing the surface roughness, while repetitive scanning exhibits only marginal improvements in surface quality. Partial crystallization on the surface of the amorphous samples is found on the as-built surfaces. However, it appears to be confined to depths below 50 µm. Impressively, the material showcases large mechanical strength in the as-built condition, evidenced by a high flexural strength of 2.2 GPa combined with approximately 1% plastic deformation. These findings offer initial insights into optimizing additive manufacturing processes for BMGs, guiding the enhancement of both surface quality and mechanical robustness in Zr-based metallic glass fabricated via PBF-LB/M techniques.

Preparation of α-calcium sulfate hemihydrate with high mechanical strength from natural fibrous gypsum in KCl-mediated glycerol-water solution

Natural fibrous gypsum is a kind of high-quality gypsum resources, whose high-value added utilization pathway is to be transformed to α-calcium sulfate hemihydrate (α-HH), a cementitious material that can react with water to form pastes with mechanical strength. In this work, α-HH was prepared from natural fibrous gypsum in KCl mediated glycerol-water solution under mild condition. KCl played a simultaneous function on regulating the phase-transition kinetics, morphology and comprehensive strength of α-HH. Addition of low concentration of KCl prominently retarded the nucleation and growth rate of α-HH and decreased its aspect ratio due to the formation of syngenite on the side faces. While further increase of KCl concentration accelerated the nucleation and growth rate and decreased the crystal sizes. In the presence of 0.04 M KCl, the prepared α-HH presented a hexagonal prism shape with a length / width of 257.69–579.71 μm / 13.13–36.61 μm, and its dry comprehensive strength had reached 38.1 MPa that was comparable to those prepared in commercial, chloride and nitrate system. Altogether, the foreign ion-free glycerol-water solution contributed to transforming natural fibrous gypsum to α-HH with high purity and high mechanical strength.

Core-shell 3D printed biodegradable calcium phosphate cement—Alginate scaffolds for possible bone regeneration applications

The core/shell 3D printing process using CPC and alginate is intended to create biodegradable scaffolds that have a similar stability to bone tissue and also offer sufficient and continuous antibiotic release. In this way, a patient-specific and patient-friendly process will be established, which should optimally support the human organism in its regeneration. To generate the best possible strength values, the printed scaffolds underwent various post-treatments and were then tested in a material test. The test methods included self-setting, storage in a drying cabinet with a water-saturated atmosphere at 37°C, followed by incubation in PBS, freeze-drying, and coating the samples with alginate. Additionally, a degradation test at pH 7.4 and pH 5 was carried out to test stability under in vitro conditions. It was shown that the untreated and freeze-dried samples failed at a maximum load of 30–700 N, while the remaining scaffolds could withstand a load of at least 2,000 N. At this failure load, most of the test series showed an average deformation of 43.95%. All samples, therefore, remained below the strength of cancellous bone. However, based on a 20% load after surgery, the coated scaffolds represented the best possible alternative, with a Young’s modulus of around 1.71 MPa. We were able to demonstrate that self-setting occurs in core-shell printed CPC/alginate scaffolds after only 1 day, and that mass production is possible. By coating with alginate, the compressive strength could be increased without the need for additional post-treatment. The mechanical strength was sufficient to be available as a scaffold for bone regeneration and additionally as a drug delivery device for future applications and experiments.

Self-healing property of a gel-elastomer two-phase composite material

While self-healing silicones are required for many practical applications, conventional methods of incorporating self-healability in silicones involve generation of bond-forming moieties within the backbone of the oligomer itself. Such processes involve multiple synthesis steps that turn the silicone expensive and less amenable for scale-up. In contrast, hydrogels can be made self-healing by different simple yet robust chemical routes. Hydrogels however lack mechanical strength, necessary for most engineering applications. To meet the above need, we have introduced here a novel two-phase material, consisting of self-healing hydrogel droplets embedded as microscopic healers inside the continuous matrix of silicone. The hydrogel phase, consisting of starch and polyvinyl alcohol (PVA) as the oligomers and multivariate borate ion as the crosslinker is dispersed in silicone oligomer mixed with the curing agent and both phases are allowed to crosslink. Controlled fracture tests on the resultant crosslinked material show that two cut surfaces of it get joined instantaneously with the tensile failure stress reaching as high as 35 kPa; this material remains healable also over ten cycles of incision and reattachment. The hydrogel can act also as an external glue to heal two incised surfaces of the two-phase composite to achieve durable fracture strength and thereby help forming different polygonal structures with angled joints. We have demonstrated also bio-compatibility of the two-phase material thereby opening up its possible use in large variety of biomedical applications.

Dynamic Covalent BondsRegulate Zinc Plating/Stripping Behaviors for High-Performance Zinc Ion Batteries.

Artificial interfaces provide a comprehensive approach to controlling zinc dendrite and surface corrosion in zinc-based aqueous batteries (ZABs). However, due to consistent volume changes during zinc plating/stripping, traditional interfacial layers cannot consistently adapt to the dendrite surface, resulting in uncontrolled dendrite growth and hydrogen evolution. Herein, dynamic covalent bonds exhibit the Janus effect towards zinc deposition at different current densities, presenting a holistic strategy for stabilizing zinc anode. The PBSC intelligent artificial interface consisting of dynamic B-O covalent bonds is developed on zinc anode to mitigate hydrogen evolution and restrict dendrite expansion. Owing to the reversible dynamic bonds, PBSC exhibits shape self-adaptive characteristics at low current rates, which rearranges the network to accommodate volume changes during zinc plating/stripping, resisting hydrogen evolution. Moreover, the rapid association of B-O dynamic bonds enhances mechanical strength at dendrite tips, presenting a shear-thickening effect and suppressing further dendrite growth at high current rates. Therefore, the assembled symmetrical battery with PBSC maintains a stable cycle of 4500 hours without significant performance degradation and the PBSC@Zn||V2O5 pouch cell demonstrates a specific capacity exceeding 170 mAh g-1. Overall, the intelligent interface with dynamic covalent bonds provides innovative approaches for zinc anode interfacial engineering and enhances cycling performance.