High Adhesion Research Articles

Control system and process optimization for electroless nickel plating

A novel method based on mid-frequency vibration is proposed to eliminate coating defects such as bubbles during electroless nickel plating. An automated control system for the plating, enabling precise and stable measurements and adjustments of critical parameters such as plating solution temperature, pH, and nickel ion concentration, is also established, which significantly improves process efficiency and coating quality. Experimental results indicate that the system is capable of realizing stable operation over extended periods. A nonporous nickel–phosphorus coating with a thickness greater than 200 μm is successfully obtained, with high phosphorus content, robust adhesion, and superior machinability.

Anatase‐reinforced PtZn@Silicalite‐1 structured catalysts boosting propane dehydrogenation

AbstractStructured catalysts exhibit the advantages of high diffusion efficiency and low heat transfer resistance, which have attracted increasing attention to non‐adiabatic gas–solid process. However, the metal‐supported coating catalysts face the problems of weaker bond strength and severe sintering, especially under the conditions of large flow rate and high temperature. Herein, metal@Silicalite‐1 structured catalysts with high adhesion and thermal stability were successfully prepared by hydroxylating the substrate with anatase. Rich surface Ti‐OH significantly strengthened the adhesion stability of the zeolite coating. In propane dehydrogenation reaction, the optimized PtZn@S‐1‐15Ti showed a high specific activity of 49.6 molC3H6·molPt−1·s−1 with propylene selectivity above 99% at 600°C. The introduction of anatase accelerated the aggregation of silicon sources and induced nucleation with growth content of zeolite increased by 3.6 times. It breaks the inherent contradiction between high loading amount and strong binding ability of coated catalysts, which broadens the avenues for industrial applications.

Superhydrophobicity With Self-Adaptive Water Pressure Resistance and Adhesion of Pistia Stratiotes Leaf.

Superhydrophobic surfaces are promising for optimizing amphibious aircraft by minimizing water drag and adhesion. Achieving this involves ensuring these surfaces can resist high liquid pressure caused by deep water and fluid flow. Maximizing the solid-liquid contact area is a common strategy to improve liquid pressure resistance. However, this approach inevitably increases solid-liquid adhesion, making it challenging to guarantee a trade-off between the two wetting characteristics. Here, it is found that the Pistia stratiotes leaf exhibits superhydrophobicity with high water pressure resistance and low adhesion, attributed to its self-adaptive deformable microstructure with unique re-entrant features. Under pressure, these microstructures deform to increase the solid-liquid contact area, thereby enhancing water pressure resistance. The re-entrant features elevate the deformation threshold, enabling higher modulus microstructures to achieve adaptive response. This facilitates the recovery of deformed microstructures, restoring the air layer and maintaining low adhesion. Following these concepts, Pistia stratiotes leaf-inspired surfaces are fabricated, achieving an 183% improvement in water impact resistance and an ≈80% reduction in adhesion after overpressure compared to conventional superhydrophobic surfaces. The design principles inspired by Pistia stratiotes promise significant advancements in amphibious aircraft and other trans-media vehicles.

Stainless Steel Deposits on an Aluminum Support Used in the Construction of Packaging and Food Transport Containers

A series of chemical elements from the chemical composition of the packs of liquid food products migrate inside them or they combine with other chemical elements existing in the food, resulting in chemical compounds that worsen the quality of the food. In the present paper, layers of food stainless steel were deposited using thermal arc spraying on an aluminum alloy substrate to stop the migration of aluminum ions inside liquid food products. The physical-chemical and mechanical properties of the protection system: stainless steel layer used in the food industry (suggestively called: food-grade stainless steel)—aluminum substrate were investigated, and then the organoleptic properties of the food liquids that came into contact with the deposit were evaluated. It was found that food-gradestainless steel deposits have low porosity (3.8%) and relatively high adhesion and hardness, which allows complete isolation of the substrate material. The investigations carried out on the properties of food liquids that come into contact with the stainless steel deposit revealed the fact that it perfectly seals the aluminum start. The food-grade stainless steel coating (80T) was much better and safer for preserving dairy products maintaining a constant acidity up to 17 degrees Thorner, wines (with an average acidity of 3.5–4 degrees), juices (with natural pigments), and oils (with a good absorbance level correlated with clarity). This aspect suggests that the created system can be successfully used to manufacture containers for the transport of liquid products.

BIOM-06. NOGGIN CONTRIBUTES TO BRAIN METASTATIC COLONIZATION OF LUNG CANCER CELLS

Abstract Brain metastasis is a common complication among patients with lung cancer, yet the underlying mechanisms remain unclear. In this study, we aimed to investigate the pathogenesis of brain metastasis in lung cancer. We established highly colonizing metastatic lung cancer cells, A549-M2, through multiple implantations of A549 human lung cancer cells in the carotid artery of athymic nude mice. Compared to parental cells (M0), M2 cells demonstrated slower growth in culture plates and soft agar, as well as lower motility and higher adhesion, key characteristics of mesenchymal-epithelial transition (MET). Further analysis revealed that M2 cells exhibited decreased expression of epithelial-mesenchymal transition markers, including ZEB1 and Vimentin. M2 cells also demonstrated reduced invasiveness in co-culture systems. RNA sequencing and gene set enrichment analysis confirmed that M2 cells underwent MET. Intriguingly, depletion of Noggin, a BMP antagonist, was observed in M2 cells, and replenishment of Noggin restored suppressed migration and invasion of M2 cells. In addition, Noggin knockdown in control M0 cells promoted cell attachment and suppressed cell migration, suggesting that Noggin reduction during brain colonization causes inhibition of migration and invasion of metastatic lung cancer cells. Our results suggest that lung cancer cells undergo MET and lose their motility and invasiveness during brain metastatic colonization, which is dependent on Noggin.

Preparation of tannic acid-based recyclable adhesive with high adhesion property, low curing temperature, and environmental tolerance

Tannin-based adhesives have demonstrated promise in decreasing dependence on petrochemical resources linked to formaldehyde-based resins. However, current tannin-based adhesives face challenges due to the incorporation of expensive or toxic reagents such as isocyanate, epoxy, and formaldehyde, as well as the inability to be recycled. This study presents a simple and eco-friendly approach for producing a tannic acid-based recyclable adhesive (TA-BVB) by employing tannic acid and 1,4-butanediol divinyl ether through acetal reactions. The resulting adhesive can be cured at a low temperature of 70℃ and demonstrated high bonding strength on wood and aluminum sheets, measuring 4.45 MPa and 5.44 MPa, respectively. Notably, the adhesive maintained its adhesion strength even under harsh conditions, including high temperatures (100℃), liquid nitrogen (-196℃), and exposure to various solvents. Moreover, the adhesive showcased excellent reusability, retaining over 100 % and 86 % of bonding strength after the first and second rounds of hot pressing, respectively. This adhesive can be repaired using infrared laser irradiation and displayed remarkable mold resistance. This research underscores the potential of tannic acid in developing environmentally friendly, high-performance, recyclable adhesives with versatile applications.

Nanosecond laser interference ablation of fluorine-free aluminum alloy surfaces for dynamic adhesion and static wettability synergistically modulating water collection

Water collection from mist is a potential solution to water scarcity, which is a critical issue worldwide. In this paper, laser interference ablation assisted with stearic acid immersion has been used to achieve synergistic modulation of dynamic adhesion and static wettability for water collection on fluorine-free aluminum alloy surface. The research demonstrates that there is an optimal balance point between dynamic adhesion and static wettability for water collection. This optimal point shifts toward low dynamic adhesion at the high misting rate due to the flooding on metastable surfaces with high dynamic adhesion. In addition, wetting transition induced by tilting is observed on metastable surfaces. The good stability of the proposed fluorine-free surface has been demonstrated by the long-term water collection and long periods of immersion in water. This work can provide theoretical inspiration and a scalable preparation method for green and stable water collection strategies.

Effect of bismuth oxide on radiation shielding and interaction characteristics of polyvinyl alcohol-based polymer: Potential use in medical apron design

This study evaluated radiation shielding and interaction characteristics of polyvinyl alcohol (PVA) polymer separately doped with 10% and 20% Bi2O3 respectively for medical apron design and shielding special electronic installations. Prepared samples were characterized by scanning electron microscopy (SEM) and energy dispersive spectrometry (EDS). The EDS results showed that Carbon (C), Oxygen (O), and bismuth (Bi) elements were the predominant elements present in the prepared samples. The SEM result displaced surface irregularities due to a special bonding matrix between PVA and Bi2O3. Mass attenuation coefficient (MAC), effective atomic number (Zeff), Half value layer (HVL), Mean free path (MFP), Fast neutron removal cross-section (R), Total Mass Stopping Power (TSP), and photon Range (R) of the prepared polymer composites (PV-1Bi and PV-2Bi) were evaluated with XCOM and PHITS computer programs. Results showed that the MAC of the prepared polymer samples was significantly higher than some recently developed composites at 0.662 MeV and 1.25 MeV gamma energy. Therefore, polyvinyl alcohol (PVA) polymer doped with Bi2O3 should be deployed in medical apron design and shielding special electronic installations where flexibility and high adhesion abilities are crucial.

ADHESION OF STEEL CORD WITH CU-ZN-FE COATING IN COBALT-FREE COMPOUND

ABSTRACT The adhesion of steel cord with Cu-Zn-Fe coating in a cobalt-free skim compound in hot and humid conditions was investigated and compared with the current adhesion system consisting of brass-coated steel cord in cobalt-containing skim compound. Standard adhesion tests showed that the adhesion retention of Cu-Zn-Fe–coated cord in a cobalt-free compound was significantly improved with respect to current adhesion system. Advanced characterization of adhesion interphases by field emission scanning electron microscopic examination of cord-compound cross sections and X-ray photoelectron spectroscopy depth profiling revealed that incorporating the Fe element into the coating significantly reduces the dezincification of the metallic coating and prevented excessive growth of adhesion interphase. This results in high adhesion retention of Cu-Zn-Fe–coated steel cord in cobalt-free compound. Furthermore, a hypothesis was proposed to explain how the Fe element decreases the dezincification of the metallic coating in hot and humid conditions. Because Cu-Zn-Fe–coated cord eliminates the need for cobalt salts in the compound, using this cord in cobalt-free compounds generates a completely cobalt-free solution to tackle adhesion degradation and health risks of the current adhesion system.

Rigid-Flexible Coupled Dendritic Molecule Doping: General Approach to Activate Commercial Polymers into Harsh Condition-Tolerant Multi-Reusable Strong Supramolecular Adhesives.

Developing functional adhesives combining strong adhesion, good recyclability and diverse harsh-condition adaptability is a grand challenge. Here, we introduce a general dendritic molecule doping strategy to activate commercial polymers into a new family of supramolecular adhesives integrating high adhesion strength, ultralow temperature, water resistant and multi-reusable properties. Our method involves rational design of a new rigid-flexible coupled dendritic molecule-M4C8OH as a versatile dopant, while simple M4C8OH doping into commercial polymers can modulate internal and external non-covalent interaction to enable H-bonding enhanced interchain cross-linking for tough cohesion along with enhanced interphase interaction. This endows 20 wt % M4C8OH-doped polycaprolactone (PCL) adhesives (PCL-M4C8OH) with improved adhesion strength on various substrates with the maximum increase up to 2.87 times that of PCL. In particular, the adhesion strengths of PCL-M4C8OH on polymethyl methacrylate at 25 °C and -196 °C reach 4.67 and 3.58 MPa-1.9 and 2.3 times those of PCL and superior to diverse commercial adhesives and most reported adhesives. PCL-M4C8OH also displays markedly-improved multi-usability and tolerance against ultralow temperature and diverse wet environments. Mechanism studies reveal the crucial role of M4C8OH molecular structures toward superior adhesion. Our method can be expanded to other polymer matrices, yielding diverse new supramolecular adhesives.

Improving UV protection and retention of photosensitive agrochemicals: Innovative polyurethane-CeO2 hybrid pesticide microcapsules

Photolysis and poor retention significantly decrease the utilization efficiency of photosensitive agrochemicals, leading to considerable ecological and economic losses. We successfully prepared novel pyraclostrobin-loaded polyurethane-inorganic hybrid microcapsules (Pyr@KCeO2-PU MCs) with high adhesion and UV stability by interfacial polymerization. CeO2 nanoparticles (NPs) were incorporated as UV light absorbers, while a silane coupling agent (KH550) was employed for in situ crosslinking of PU with CeO2 NPs, facilitating their dispersion within the PU shell. Characterization results revealed a high encapsulation efficiency of 90 % and uniform sizes (D50 = 915 nm) for the Pyr@KCeO2-PU MCs. Optical property investigations using UV–vis spectroscopy indicated that the integration of CeO2 NPs within the PU shell produced stronger UV absorption bands compared to both Pyr technical (TC) and Pyr@PU MCs. This observation underscores the potential of CeO2 NPs as effective UV absorbers. The anti-photolysis performance of Pyr@KCeO2-PU MCs improved with the addition of CeO2 NPs, yielding a retention rate of Pyr in Pyr@KCeO2-PU MCs that was 1.90 and 1.27 times greater than that of Pyr TC and Pyr@PU MCs, respectively, under UV irradiation. Furthermore, KH550 not only facilitated crosslinking between PU and CeO2 NPs, ensuring uniform distribution of CeO2 NPs on the PU shell surface, but also enhanced wettability and foliar retention. The contact angle of Pyr@KCeO2-PU MCs (32°) was significantly lower than that of Pyr@PU MCs (84°), and Pyr retention on rice leaves was 17.5 mg/cm2 for Pyr@KCeO2-PU MCs, surpassing that of Pyr@PU MCs (9.3 mg/cm2). Additionally, Pyr@KCeO2-PU MCs exhibited superior efficacy against various plant pathogens compared to Pyr TC and Seltima. These findings highlight the potential of Pyr@KCeO2-PU MCs for enhancing pesticide utilization and offer valuable insights for the future development of PU-based pesticide formulations.

Dynamic covalent bonds enabled recyclable chitosan oligosaccharide-based wood adhesive with high adhesion and anti-mildew performances

Biomass wood adhesives have emerged as a promising alternative to traditional synthetic resins due to their ability to address issues related to formaldehyde pollution and reliance on petrochemical resources. However, these adhesives are generally not recyclable and require high curing temperatures. Herein, a novel eco-friendly, strong, and recyclable chitosan oligosaccharide (CS)-based wood adhesive named CS-PB was developed using CS, lignin-derived 3,4-dihydroxybenzaldehyde, and 1,4-phenylenediboronic acid. The cohesive strength and recyclability of the adhesive were significantly enhanced by the dynamic borate ester and imine networks formed through catalyst-free covalent cross-linking. The adhesive exhibited a maximum bonding strength of 5.60 MPa, surpassing many synthetic and biomass adhesives. Moreover, the recycled adhesive retained 88 % of its original strength. Even under extreme conditions such as 100 °C, −196 °C the CS-PB adhesive can still maintain high bonding strength. Notably, the CS-PB adhesive demonstrated low-temperature curing properties, achieving a high bonding strength of 5.21 MPa when cured at 90 °C, since imine bonds can be formed under mild conditions. Furthermore, the adhesive displayed excellent mildew resistance attributed to the synergistic effects of amino, boronic acid, and benzene rings. The proposed straightforward design strategy provides valuable insights for constructing high-strength and recyclable biomass adhesives.

Gelation embolism agents suppress clinical TACE-incited pro-metastatic microenvironment against hepatocellular carcinoma progression

Current embolic agents in transcatheter arterial chemoembolization (TACE) of hepatocellular carcinoma (HCC) encounter instability and easy leakage, discounting TACE efficacy with residual HCC. Moreover, clinical TACE aggravates hypoxia and pro-metastatic microenvironments, rendering patients with HCC poor prognosis. Herein, we developed Zein-based embolic agents that harness water-insoluble but ethanol-soluble Zein to encompass doxorubicin (DOX)-loaded mesoporous hollow MnO2 (HMnO2). The conditions and capacity of HMnO2 to generate reactive oxygen species (ROS) were assayed. Mechanical examinations of Zein-HMnO2@DOX were performed to evaluate its potential as the embolic agent. Invitro experiments were carried out to evaluate the effect of Zein-HMnO2@DOX on HCC. The subcutaneous HCC mouse model and rabbit VX2 HCC model were established to investigate its anti-tumor and anti-metastasis efficacy and explore its potential anti-tumor mechanism. The high adhesion and crosslinking of Zein with HMnO2@DOX impart Zein-HMnO2@DOX with strong mechanical strength to resist deformation and wash-off. Zein gelation and HMnO2 decomposition in response to water and acidic tumor microenvironment, respectively, enable continuous DOX release and Fenton-like reaction for reactive oxygen species (ROS) production and O2 release to execute ROS-enhanced TACE. Consequently, Zein-based embolic agents outperform clinically-used lipiodol to significantly inhibit orthotopic HCC growth. More significantly, O2 release down-regulates hypoxia inducible factor (HIF-1α), vascular endothelial growth factor (VEGF) and glucose transporter protein 1 (GLUT1), which thereby re-programmes TACE-aggravated hypoxic and pro-metastatic microenvironments to repress HCC metastasis towards lung. Mechanistic explorations uncover that such Zein-based TACE agents disrupt oxidative stress, angiogenesis and glycometabolism pathways to inhibit HCC progression. This innovative work not only provides a new TACE agent for HCC, but also establishes a new strategy to ameliorate TACE-aggravated hypoxia and metastasis motivation against clinically-common HCC metastasis after TACE operation. Excellent Young Science Fund for National Natural Science Foundation of China (82022033); National Natural Science Foundation of China (Grant No. 82373086, 82102761); Major scientific and technological innovation project of Wenzhou Science and Technology Bureau (Grant No. ZY2021009); Shanghai Young Top-Notch Talent.

Effect of hyaluronic acid on the formation of acellular dermal matrix-based interpenetrating network sponge scaffolds for accelerating diabetic wound healing through photothermal warm bath

Adequate vascularization essential for delivering nutrients critical to wound healing, yet impaired angiogenesis is a major barrier in diabetic wound repair. This study investigates the impact of hyaluronic acid on interpenetrating network sponge scaffolds derived from an acellular dermal matrix, with the aim of enhancing vascularization and healing of diabetic wounds via photothermal warm bath therapy. We prepared three-dimensional porous sponges (H1P4D2@DFO) using molecular interpenetration and ion crosslinking of porcine acellular dermal matrix (PADM), hyaluronic acid, and polydopamine nanoparticles loaded with deferoxamine mesylate (PDA@DFO). This resulting extracellular matrix-based sponge demonstrated properties suitable for wound repair, including high cell adhesion, biocompatibility, bioactivity, porosity (85 %), and water absorption (4500 %). The near-infrared (NIR) photothermal effect of PDA@DFO and the sustained release of deferoxamine mesylate (DFO) enhanced wound vascularization within the wound site. These findings suggest that our sponge scaffold can simulate skin-like structures and establish a supportive microenvironment conducive to microvascular reconstruction. By combining the photothermal warm bath approach with the scaffold's tailored 3D structure, we observed enhanced angiogenesis and accelerated diabetic wound healing, indicating potential clinical applications of these scaffolds in chronic wound management.

A novel bonding strategy of hydrogel on titanium alloy for marine antifouling engineering: multiple antifouling mechanisms and DFT calculations

Marine biofouling is one of the biggest problems for titanium alloys and rutile TiO2 coatings in marine engineering applications. Hydrogel materials are a novel and environmentally benign antifouling strategy, but they cannot be stabilized on alloy surfaces to provide long-term protection. Focusing on the challenges of bonding at the hydrogel-alloy interface, a PAA/PHEMA composite hydrogel containing Cu2O@PEG powder was strongly bonded to the titanium alloy by forming chemical bonds with APTES. The composite hydrogel still achieves an adhesion strength of 60-70 kPa after 7 days of immersion. The samples maintained a stable copper ion leaching rate of 2.61~3.76μg·cm-2·d-1 after 21 days of immersion. The coating-modified titanium alloys showed a 100% bactericidal rate within three hours of contact with different bacteria and exhibited a high anti-algal adhesion rate of up to 99%. In addition, the attachment mode of APTES on rutile TiO2 was clarified for the first time by Density Functional Theory (DFT) calculations. According to DFT calculations, the adsorption energy of APTES on Ti-TiO2 is -747.025kJ/mol, and the adsorption energy of acrylic acid on TiO2-APTES is -535.152kJ/mol. The chemical bonding connection between the hydrogel-alloy interface, as a novel interface bonding strategy, would be expected to broaden the application of titanium alloy in marine engineering.

Functional organic adlayers for controlling the adhesion strength of electrolessly deposited copper on super-engineering plastics

Effective metallization of super-engineering plastics such as liquid crystal polymers (LCP) and polyphenylene sulfides (PPS) via electroless deposition of copper thin films is an important step in the manufacturing of a wide range of devices. Copper deposition typically requires a pre-treatment step involving chemical and/or mechanical roughening to ensure high adhesion at the polymer/Cu interface; however such treatments are detrimental to patterns and topographic features of the polymer that possess µm resolution and/or high aspect ratio. Herein, we demonstrate that it is possible to regulate and improve adhesion of electrolessly deposited copper thin films at LCP and PPS materials via multilayer functionalization with aryldiazonium cations of a p-aminobenzoic acid precursor. We first demonstrate that aryldiazonium grafting conditions can be optimized to overcome the chemical inertness of LCP/PPS without resorting to harsh oxidative or mechanical treatments. We then show that the density of Ar-COOH groups can be regulated by modifying the number of functionalization cycles. X-ray photoelectron spectroscopy studies shows that this has a clear impact on the composition of the catalytic nanoparticle layer required for copper deposition. Adhesion strength studies demonstrate that such changes translate into improved adhesion strengths without any adverse effects on surface roughness. Control experiments with alternative chemical moieties suggest that specific chemical interactions between catalytic seeds and grafted carboxylate groups play an important role in the observed improved adhesion.

Influence of hydrogen bonding interactions, entanglement, and covalent crosslinking on the viscoelasticity of acrylic viscoelastomers containing urea group

The structure–property relationship of acrylic clear viscoelastomer films (acrylic CVFs) as foldable optical clear adhesives (OCAs) has always been unclear. In our work, a series of acrylic CVFs with different hydrogen-bonding interactions (H-bondings) and cross-linking densities (namely, CL-H-copolymers) were synthesized. The effects of entanglement, H-bonding, and covalent crosslinking on the recovery and adhesive properties of CL-H copolymers were analyzed by rheology, equilibrium swelling, and tensile stress–strain tests (tensile tests). The structural parameter Mx/MeH was obtained by combining the affine deformation model, the Flory-Rehner equation, and the UCM-Gent model, where Mx is the molecular weight between covalent crosslinkers and MeH is the a physical crosslinking molecular weight affected by H-bondings. The experimental results showed that the CL-H-copolymers had an obvious dependence on Mx/MeH. Recovery properties tended to stabilize (>90 %) at Mx/MeH < 1, while adhesion strengths continued to decrease with decreasing Mx/MeH. This conclusion and methodology are instructive for the design of foldable OCAs with high elasticity and high adhesion performance.

АДГЕЗИВНАЯ АКТИВНОСТЬ МИКРООРГАНИЗМОВ К СТОМАТОЛОГИЧЕСКИМ МАТЕРИАЛАМ ДЛЯ 3D ПЕЧАТИ И ВАКУУМНОЙ ФОРМОВКИ

Relevance: The adhesive activity of the oral microbiome to new generation materials is the subject of study by the global medical community, and the issue of choosing structural materials is still being discussed in the scientific community and is of a controversial nature. Objective: To study the adhesion of representatives of the oral microbiome to samples of modern dental materials under experimental conditions (in vitro). Materials and methods: Samples of photopolymer resins for 3D printing: Dental Crown LCD, Dental Sand A1-A2, Dental Clear Pro, (n=30), (1-3 groups), thermoforming plates for vacuum forming: EV Gasket Bleaching 080, Bioplast multicolor 3.0*123 mm, Bioplast color 3.0*125 mm (n=30), (groups 4-6); clinical isolates of the microbiome as test strains: Staphylococcus aureus, Streptococcus oralis, Neisseria subflava, Actinomyces oris, Candida albicans (n=5). Research methods: experimental, microbiological, cultural, analytical and statistical. Results: The degree of adhesion of representatives of the oral microbiome to the studied structural materials is in the range from 0 to 4.91 (Ia) and depends on both the species composition of the microbiome and the physico-chemical properties of the materials. The high adhesion index for all microbiota groups was noted for vacuum forming materials (4.91), and the lowest was Dental Crown LCD (0), which makes it possible to recommend it for practical use. Conclusions: The choice of structural material should be made, including taking into account the adhesive activity of the oral microbiome in order to reduce the risk of complications. It is recommended to give preference to materials with a low adhesive activity index.

Balancing Interfacial Toughness and Intrinsic Dissipation for High Adhesion and Thermal Conductivity of Polymer-Based Thermal Interface Materials.

In recent years, adhesive thermal interface materials have attracted much attention because of their reliable adhesion properties on most substrates, preventing moisture, vibration impact, or chemical corrosion damage to components and equipment, as well as solving the heat dissipation problem. However, thermal interface materials have a huge contradiction between strong adhesion and high thermal conductivity. Here, we report a polymer-based thermal interface material consisting of polydimethylsiloxane/spherical aluminum fillers, which possesses both adhesion properties (adhesion strength of 3.59 MPa and adhesion toughness of 1673 J m-2 and enhanced thermal conductivity of 3.90 W m-1 K-1). These excellent properties are attributed to the modified chain structure by introducing acrylate accelerators into the polydimethylsiloxane network, thereby striking a balance between interfacial toughness and intrinsic dissipation. The addition of thermally conductive aluminum fillers not only increases the thermal conductivity but also improves the bulk energy dissipation of the thermal interface material. This work provides a novel strategy for designing a novel thermal interface material, leading to new ideas in long-term applications in high-power electronics.

Plant-Derived Hydrogels with High Stretchability and Adhesion for Multifunctional Sensors

Plant-Derived Hydrogels with High Stretchability and Adhesion for Multifunctional Sensors