Hexagonal Boron Nitride Nanosheets Research Articles

Two-Part Surfactant-Assisted Exfoliation of Hexagonal Boron Nitride Nanosheets to Obtain Highly Stable Two-Dimensional Nanomaterial Dispersions

Two-Part Surfactant-Assisted Exfoliation of Hexagonal Boron Nitride Nanosheets to Obtain Highly Stable Two-Dimensional Nanomaterial Dispersions

Thermally Conductive Polydimethylsiloxane-Based Composite with a Three-Dimensional Vertically Aligned Thermal Network Incorporating Hexagonal Boron Nitride Nanosheets and Nanodiamonds.

Thermal interface materials play a pivotal role in efficiently transferring heat from heating devices to thermal management components, thereby reducing the risk of component degradation due to overheating. In this study, we propose a strategy for enhancing the out-of-plane thermal conductivity (TC) of composite materials by fabricating a three-dimensional (3D) thermal network within a polydimethylsiloxane (PDMS) matrix. Specifically, the composite material was designed to incorporate a dense thermal network comprising hexagonal boron nitride nanosheets (BNNSs) and nanodiamonds (NDs). The fabrication process commenced with the preparation of BNNSs through liquid-phase exfoliation, followed by the creation of a 3D BNNSs-NDs/polyimide aerogel thermal framework using a unidirectional solidification ice templating method and subsequent heat treatment. Vacuum impregnation and curing were then employed to finalize the production of the 3D BNNSs-NDs/PDMS composite material. Characterization analyses indicated that the addition of NDs filled the voids between BNNSs, leading to the densification of the thermal framework pore walls and the establishment of additional thermal pathways. Impressively, with concentrations of BNNSs and NDs of 17.99 and 7.71 wt %, respectively, the out-of-plane TC of the 3D BNNSs-NDs/PDMS composite material reached 1.623 W m-1 K-1, marking notable enhancements of 754.21% and 256.70% compared to those of pure PDMS and composites prepared via direct blending with randomly distributed BNNSs and NDs, respectively. Furthermore, the 3D BNNSs-NDs thermal framework improved the compressive strength and the dimensional stability of the composite material. Finite element simulations additionally confirmed the synergistic improvement of the TC achieved through the combination of BNNSs and NDs, demonstrating that the 3D BNNSs-NDs/PDMS composite material displayed superior heat conduction and a greater density of thermal pathways compared to those of its counterparts, including 3D BNNSs/PDMS and 3D NDs/PDMS composite materials. In summary, this work presents a strategy for enhancing the out-of-plane TC of polymer-based composite materials by incorporating vertically aligned thermal networks.

Preparation of Thin-Layered Hexagonal Boron Nitride Nanosheet with Oxygen Doping.

Hexagonal boron nitride nanosheet (h-BNNS), a structural analogue of graphene, possesses remarkable properties such as exceptional electrical insulation, great resistance to corrosion, excellent mechanical strength, and thermal conductivity. Nonetheless, its continued development is still hampered by the lack of a preparation technique with an easy-to-follow procedure and reliable composition and structure control. In this study, we investigated a two-step protocol for uniform size production of thin-layered h-BNNS. By carefully manipulating the crystallization degree during synthesis of h-BN powder and employing subsequent hydrothermal treatment, we successfully obtained h-BNNS with an even thickness of only a few atomic layers. Compared with the broadly used liquid-phase exfoliation process, not only is the thickness significantly decreased but also the yield is considerably elevated to several grams. Moreover, the in-plane O doping content can be adjusted within a relatively wide range. Overall, our finding demonstrates the potential of this approach in facilitating the exploration and utilization of h-BNNS.

Constructing polyimide-based nanocomposite dielectrics with superior high‐temperature energy storage performance via using ternary structure strategy

To maintain low leakage current and energy storage stability of polyimide at high temperature and electric field, ternary structure strategy is used to construct polyimide-based nanocomposite dielectrics, relating to cross-linked structure, sandwich structure and inorganic filler structure. Based on synergistic effect, energy storage properties of crosslinked polyimide-based sandwich‐structured nanocomposite films is significantly improved, in which cross-linked polyimide composited layers with 2 wt% hexagonal boron nitride nanosheets are selected as two outer insulating layers and cross-linked polyimide composited layer with 1 wt% barium titanate nanoparticles is employed as central polarization layer. When volume ratio of middle polarization layer is 10 % (denoted as N-10 T-N), the maximum Ud of 11.6 J/cm3 and η of 87 % are achieved at room temperature. At 150 °C, the Ud of N-10 T-N is 5.1 J/cm3. This study provides the experience for the development of polyimide dielectrics with high capacitive properties over a wide temperature range.

Fiber Optic Sensor Coated with Multiple Layers of Hexagonal Boron Nitride Nanosheets (BNNS) for the Detection of Volatile Organic Compounds.

Nowadays, volatile organic compound (VOC) detection is imperative to ensure environmental safety in industry and indoor environments, as well as to monitor human health in medical diagnosis. Gas sensors with the best sensor response, selectivity, and stability are in high demand. Simultaneously, the advancement of nanotechnology facilitates novel nanomaterial-based gas sensors with superior sensor characteristics and low power consumption. Recently, boron nitride, a 2D material, has emerged as an excellent candidate for gas sensing and demonstrated exceptional sensing characteristics for new-generation gas sensing devices. Herein, ultrathin porous boron nitride nanosheets (BNNSs) with large lateral sizes were synthesized using a facile synthesis approach, and their material characteristics were investigated utilizing a variety of analytical techniques, including X-ray diffraction, Fourier transform infrared spectroscopy, ultraviolet spectroscopy, X-ray photoelectron spectroscopy, and scanning electron microscopy. A BNNS-coated cladding-modified fiber optic sensor (FOS) probe was prepared and employed for VOC (ammonia, ethanol, and acetone) sensing across concentrations varying from 0 to 300 ppm. The BNNSs-coated FOS demonstrated better selectivity toward 300 ppm ammonia, and specifically annealed BNNSs displayed a maximum sensor response of 55% along with a response/recovery times of 15 s/34 s compared to its counterparts. The superior ammonia sensing performances could be attributed to the formation of ultrathin nanosheets and a porous surface with slit-like features in hexagonal boron nitride.

Hexagonal boron nitride nanosheets/graphene nanoplatelets/cellulose nanofibers-based multifunctional thermal interface materials enabling electromagnetic interference shielding and electrical insulation

Thermal interface materials (TIMs) that block electromagnetic interference (EMI) and current leakage are essential for high-density, high-power devices and compact form factors of electronic and mobility platforms. However, their coupled thermal-electrical-electromagnetic characteristics involve mismatches in thermal conductivity, electrical insulation, and EMI shielding, limiting the multifunctionality. Herein, a sandwich-like structural design that rationally combines graphene nanoplatelets (GNPs), hexagonal boron nitride nanosheets (BNNSs) and cellulose nanofibers (CNFs) is presented toward multifunctional trilayer TIMs enabling high thermal conductivity, EMI shielding, electrical insulation, mechanical compatibility and flame retardancy. The top and bottom BNNSs serve as electrically insulating yet thermally conductive layers while the GNPs in the central layer mitigate EMI and the CNFs as a binder complete the mechanical properties for the lamella-like trilayers. The resulting TIM exhibits a high in-plane thermal conductivity (25.5 W/m·K), and the LED cooling system using the TIM demonstrates the capability of reducing the operating temperature. Furthermore, it shows a high-volume resistivity (4.12 × 1013 Ω cm) and EMI shielding effectiveness (29.0 dB) at X-band frequencies. Its mechanical robustness is confirmed with tensile strength and elongation of 65.0 MPa and 2.36 %, and the high flame retardancy is validated. The outcomes will inspire tailoring multifunctional TIMs using lamellar structures that optimally combine micro/nanomaterials.

SPI-Modified h-BN Nanosheets-Based Thermal Interface Materials for Thermal Management Applications.

The rising concern over the usage of electronic devices and the operating environment requires efficient thermal interface materials (TIMs) to take away the excess heat generated from hotspots. TIMs are crucial in dissipating undesired heat by transferring energy from the source to the heat sink. Silicone oil (SO)-based composites are the most used TIMs due to their strong bonding and oxidation resistance. However, thermal grease performance is unreliable due to aging effects, toxic chemicals, and a higher percentage of fillers. In this work, TIMs are prepared using exfoliated hexagonal boron nitride nanosheets (h-BNNS) as a nanofiller, and they were functionalized by ecofriendly natural biopolymer soy protein isolate (SPI). The exfoliated h-BNNS has an average lateral size of ∼266 nm. The functionalized h-BNNS/SPI are used as fillers in the SO matrix, and composites are prepared using solution mixing. Hydrogen bonding is present between the organic chain/oxygen in silicone polymer, and the functionalized h-BNNS are evident from the FTIR measurements. The thermal conductivity of h-BNNS/SPI/SO was measured using the modified transient plane source (MTPS) method. At room temperature, the maximum thermal conductivity is 1.162 Wm-1K-1 (833% enhancement) at 50 wt % of 3:1 ratio of h-BNNS:SPI, and the thermal resistance (TR) of the composite is 5.249 × 106 K/W which is calculated using the Foygel nonlinear model. The heat management application was demonstrated by applying TIM on a 10 W LED bulb. It was found that during heating, the 50 wt % TIM decreases the surface temperature of LED by ∼6 °C compared with the pure SO-based TIM after 10 min of ON condition. During cooling, the modified TIM reduces the surface temperature by ∼8 °C under OFF conditions within 1 min. The results indicate that natural polymers can effectively stabilize and link layered materials, enhancing the efficiency of TIMs for cooling electronics and LEDs.

Fabrication of rGO-decorated hBNNS hybrid nanocomposite via organic-inorganic interfacial chemistry for enhanced electrocatalytic detection of carcinoembryonic antigen.

Organic-inorganic hybrid nanocomposites (OIHN), with tailored surface chemistry, offer ultra-sensitive architecture capable of detecting ultra-low concentrations of target analytes with precision. In the present work, a novel nano-biosensor was fabricated, acquainting dynamic synergy of reduced graphene oxide (rGO) decorated hexagonal boron nitride nanosheets (hBNNS) for detection of carcinoembryonic antigen (CEA). Extensive spectroscopic and microscopic analyses confirmed the successful hydrothermal synthesis of cross-linked rGO-hBNNS nanocomposite. Uniform micro-electrodes of rGO-hBNNS onto pre-hydrolyzed ITO were obtained via electrophoretic deposition (EPD) technique at low DC potential (15V). Optimization of antibody incubation time, pH of supporting electrolyte, and immunoelectrode preparation was thoroughly investigated to enhance nano-biosensing efficacy. rGO-modified hBNNS demonstrated 29% boost in electrochemical performance over bare hBNNS, signifying remarkable electro-catalytic activity of nano-biosensor. The presence of multifunctional groups on the interface facilitated stable crosslinking chemistry, increased immobilization density, and enabled site-specific anchoring of Anti-CEA, resulting in improved binding affinity. The nano-biosensor demonstrated a remarkably low limit of detection of 5.47pg/mL (R2 = 0.99963), indicating exceptional sensitivity and accuracy in detecting CEA concentrations from 0 to 50ng/mL. The clinical evaluation confirmed its exceptional shelf life, minimal cross-reactivity, and robust recovery rates in human serum samples, thereby unraveling the potential for early, highly sensitive, and reliable CEA detection.

Polyetherimide nanocomposite with enhanced mechanical, thermal and dielectric properties by incorporating synergistically exfoliated‐chemical functionalization induced hexagonal boron nitride nanosheets

AbstractThe present study aims to improve the mechanical, thermal and dielectric properties of polyetherimide (PEI) nanocomposite via simplified method, involving the creation of a nanocomposite using PEI incorporated with exfoliated‐chemical functionalization induced hexagonal boron nitride nanosheets (BNNS). XRD, FTIR and Raman elucidated the chemical structure of functionalized BNNS and indicated the success preparation of functionalized BNNS. Functionalization effectively improved the compatibility of nanocomposites and contributed to the property improvements. Morphological analysis unveiled a compact and dense microstructure within the nanocomposites in correlation with functionalized BNNS. Broad band dielectric spectroscopy revealed excellent dielectric properties of produced PEI nanocomposite. DMA testing verified a noteworthy enhancement in both Tg and storage modulus upon incorporating of BNNS. In summary, this comprehensive investigation highlights the impact of functionalized BNNS on mechanical, thermal and dielectric properties of developed PEI dielectric nanocomposite and is expected to expand the application of PEI in the field of high‐temperature energy storage.Highlights Polyetherimide (PEI) was used as polymer matrix and boron nitride derivatives as dielectric fillers to prepare PEI dielectric nanocomposite. Due to the influences of dielectric properties by interface polarization effect and the local distribution of electric field of the fillers in PEI matrix, the dielectric constant, breakdown strength and energy storage density of PEI nanocomposites were obviously improved compared with pure PEI. The effects of interfacial interactions between PBNNS and PEI contributes to the uniform dispersion and comprehensive property improvements of PEI dielectric nanocomposites. This work presents a systematic investigation into the fabrication of PEI/BNNS nanocomposite using a one‐step solution blending method, inspiring the research and development of PEI in the energy storage applications areas in the future.

Construction of 3D nanostructures on carbon fiber surfaces by sizing for preparing high‐performance composites

AbstractPoor interfacial adhesion between carbon fibers (CF) and the resin matrix has been a limiting factor in advancing the properties of composites. To address this challenge, this study employs the sizing method to coat carbon nanotubes (CNTs) and hexagonal boron nitride nanosheets (h‐BN) onto the CF surface. The 3D structures formed by strategic of combination 1D and 2D nanomaterials, markedly enhances the mechanical, thermal and frictional properties of CF composites. The results reveal a significant boost in the flexural strength, flexural modulus, interlaminar shear strength and interfacial shear strength of the prepared CF composites, registering increases of 53.96%, 60.41%, 55.58% and 55.35%, respectively. These advancements stem from the heightened surface reactivity and roughness of the fibers, facilitated by the synergistic interactions between CNTs and BN. Furthermore, the thermal conductivity of the composites exhibits a remarkable increase of 63.56%, attributed to the synergistic coupling between CF and BN, establishing an efficient thermal conductivity pathway within the composites. This research provides a highly effective approach for crafting high‐performance CF composites.Highlights Construction of 3D network structures on CF surfaces by the sizing method. Synergistic coupling between BN and CNT enhances composite properties. Synergistic enhancement of friction and thermal properties of CF composites.

Enhancing mechanical property, thermal conductivity, and radiation stability of fluorine rubber through incorporation of hexagonal boron nitride nanosheets

AbstractFluorine rubber (FKM) stands as a pivotal sealing material extensively employed in aerospace and nuclear industries. However, its efficacy will be seriously affected by ionizing radiation. Enhancing its radiation resistance becomes imperative to uphold the stability and safety of associated equipment. This study introduced hexagonal boron nitride (h‐BN) into the FKM as radioprotective fillers through mechanical blending. The interfacial interaction between matrix and h‐BN, the mechanical performances, thermal properties, and radiation stability of composites were systematically examined. Noteworthy findings highlight the presence of robust interaction forces between h‐BN and the matrix, leading to increased crosslink density and improved mechanical properties. The tensile strength of composite with 10 phr fillers (BN/FKM‐10) increased by 30% compared to that of pure FKM. Simultaneously, the introduction of h‐BN greatly enhanced thermal conductivity and radiation stability. The absorbed dose required to achieve a 50% reduction in elongation at break of BN/FKM‐10 surpassed that of FKM by 1.69 times. These results underscore the potential of incorporating h‐BN to simultaneously enhance the mechanical performance, thermal property, and radiation resistance of fluorine rubber.Highlights The chemical interaction force between h‐BN and FKM was confirmed. FKM composites tensile strength was enhanced by h‐BN as an additive crosslinker. The incorporation of h‐BN improves FKM composites thermal conductivity. The radiation resistance of FKM composites has been improved with h‐BN.

Strategies for optimizing interfacial thermal resistance of thermally conductive hexagonal boron nitride/polymer composites: A review

AbstractWith the continuous development of high‐end electronic information technologies such as 5G communications, thermal management is an urgent issue in the electronic and circuit industries due to the miniaturization, functionalization and integration. Recently, polymer‐based composites with the fillers of hexagonal boron nitride (h‐BN) have been regarded as promising candidates resulting from their excellent thermal conductivity (TC), good insulation and remarkable comprehensive properties. However, the high surface inertness of h‐BN itself, incompatibility with matrix and other fillers and mismatch of phonon‐spectrum will bring about the matrix/filler and filler/filler interfacial thermal resistance (ITR), which will greatly decline the TC of the composites, and limit their thermal management ability. Therefore, how to design, regulate and improve the interfacial states in composites and eventually enhance the TC is a current challenge. Researchers have made great effort to reduce the ITR of the composites to improve their TC. However, a comprehensive summary and analysis of researches on the improvement methods of the interface states in composites in the past 3 years is still lacking. In this work, the commonly used mechanism models, and simulation methods for calculating and predicting TC was summarized. From perspectives of Synthesis of h‐BNNs, modification, orientation, bridging and three‐dimensional structures construction, we reviewed strategies for improving the interface states in composites, and focused on the ITR regulation and TC improvement. The improvement effects of various methods on TC were compared. The development trend of high TC composite materials was prospected.Highlights Crystallinity, defect, size, flatness, thickness of hexagonal boron nitride nanosheets (BNNSs) affect interfacial thermal resistance (ITR). Nature of interaction between adjacent layers of BNNS need exploited. Interface and defect are root cause of extra phonon scattering. Shape, density, surface area, distribution and compatibility reduce ITR. Theory, model, simulation methods need developed on different levels.

Functionalized boron nitride nanosheets and their polypropylene nanocomposites: influence on thermal, mechanical, rheological and wear behaviour

ABSTRACT The few-layer hexagonal boron nitride (hBN) nanosheets with hydroxyl (−OH) functional group at edges are synthesized using heat treatment of micron size hBN powder followed by sonication. These nanosheets are modified with a silane coupling agent, 3-Aminopropyl,triethoxysilane (APTES). The synthesized hBN nanosheets are mixed with the PP matrix using twin-screw extrusion followed by injection moulding. In case of APTES-modified hBN nanosheets incorporation in the PP matrix with PP-grafted maleic anhydride (PP-g-MA) shows the formation of an imide bond between the MA functional group of PP-g-MA and the amine group of APTES modified hBN nanosheets revealing compatibilization. The flow behaviour index values are lower for hBN nanosheets filled PP nanocomposites showing the improved processability from Rheological characterization. The few-layered – OH and APTES modified hBN nanosheet incorporation in the PP matrix improves the tensile and thermal properties. The incorporation of APTES modified hBN nanosheet in the PP matrix shows an increase in tensile modulus (18.1%) and tensile strength (8.1%) respectively. Wear studies show the incorporation of – OH and APTES modified hBN nanosheets in the PP matrix decreases the coefficient of friction and wear rate significantly. The wear rate at 4 min of wear testing for modified hBN nanosheet in the PP nanocomposites is ~ 96% less in comparison with neat PP. The wear mechanism is established from wear measurements and scanning electron microscopy (SEM) of worn-out wear surfaces of PP nanocomposites.

Mechanism Insights in Anticorrosion Performance of Waterborne Epoxy Coatings Reinforced by PEI-Functionalized Boron Nitride Nanosheets.

Functionalized hexagonal boron nitride nanosheets (BNNSs) have arisen as compelling anticorrosive additives, yet the precise mechanism of their corrosion resistance enhancement in coatings remains unclear. Here, polyethylenimine functionalized BNNSs (PEI-BNNSs) with approximately 6-11 layers were prepared through a "one-step" method. Then, the PEI-BNNSs/Waterborne epoxy (WEP) composite coatings were incorporated via the waterborne latex blending method for the anticorrosion of the Q235 substrate. The impedance modulus (|Z|f = 0.01 Hz) of 0.5 wt % PEI-BNNSs/WEP composite coating soaked in 3.5 wt % NaCl solution for 35 days increased by 4 orders of magnitude compared to pure WEP coating, exhibiting exceptional long-term resistance against corrosion. The positron annihilation lifetime spectroscopy and corrosion product analysis demonstrated that the reinforced anticorrosion capabilities are not solely ascribed to the "tortuous path effect" arising from BNNSs impermeability. These mechanisms also encompass the reduction in free volume fraction and radius of the free volume cavities within the composite coating brought about by the PEI molecules. Additionally, the increase in coating adhesion, promoted by PEI, plays an important role in augmenting the barrier properties against corrosive agents. This study provided a full comprehension of the role played by functionalized BNNSs in fortifying the anticorrosion attributes of WEP coatings.

Coupled interaction of exfoliated hexagonal boron nitride nanosheets decorated with MoS2 nanoflowers to enrich electrochemical activities for hybrid supercapacitor applications

Recently, two-dimensional (2D) based electrode materials have been attracted more due to their layered structure, flexibility, increased surface-to-volume ratio, and rapid ion transport properties. Here, the exfoliated h-BN-MoS2 nanocomposites have been developed through the liquid phase exfoliation method assisted to hydrothermal technique. The structure and phases of the synthesized nanocomposites have been studied by XRD analysis. From Raman analysis, the E2g peak is blue-shifted, which confirms the successful formation of exfoliated h-BN nanosheets. The in-depth morphology of the as-prepared exfoliated h-BN-MoS2 nanocomposites have been analyzed by HR-TEM study, in that the exfoliated h-BN nanosheets consisting of 2D-nanoplatelets were successfully decorated with MoS2 nanoflowers. The electrochemical behaviors of the prepared electrodes have been studied in three-electrode systems by CV, EIS, and GCD analysis. As a result, the exfoliated h-BN-MoS2 nanocomposites deliver excellent specific capacity (Cs1) of 411.5 C/g at 10 mV/s scan rate and good capacitive retention of 89.9% after 4000 cycles. From Trasatti analysis, the as-obtained nanocomposites exhibit 571.4 C/g of total (QTo*), 180.9 C/g of outer (Qou*), and 390.4 C/g of inner (Qin*) specific capacity values respectively. In addition, the exfoliated h-BN-MoS2//AC hybrid supercapacitor device (HSC) have been developed, which delivers 196.6 C/g of good specific capacity at 1 A/g current density, and excellent energy density (ED) of 46.1 Wh/kg at the corresponding power density (PD) of 844.9 W/kg. Also, the fabricated device demonstrates 86% of better capacitive retention and 107.2% coulombic efficiency after 2000 charge and discharge cycles. Thus, the ion intercalation and deintercalation through the loosely stacked exfoliated h-BN nanosheets covered with MoS2 nanoflowers manifest excellent charge storage mechanisms in the developed nanocomposite electrode material, thus utilizing them as a promising material for high-power technologies.

Polyaniline-wrapped h-boron nitride nanosheets as anticorrosive filler in epoxy coatings for substantially enhanced protection of mild steel

Excellent impermeability, electronic insulation, thermal stability, and high surface area of hexagonal boron nitride nanosheets (h-BNNS) promise immense potential for corrosion inhibition when coated on the metal substrate. However, the interfacial incompatibility of h-BNNS with polymeric coating matrix has been a major challenge to utilize h-BNNS for metal protection against corrosive environments. In the present work, surface-functionalities-enriched h-BNNS prepared by alkali hydroxides molten salt-induced exfoliation of h-BN powder is used for in-situ growth of polyaniline-emeraldine salt (PANI-ES) by oxidative polymerization of aniline to prepare the h-BNNS-PANI-ES nanocomposites. The excellent compatibility of nitrogen functionalities of h-BNNS-PANI-ES nanocomposites with highly polar epoxy matrix strengthened the coating by enhancement of elastic modulus and hardness. The thoroughly dispersed h-BNNS-PANI-ES nanocomposites into epoxy coating notably enhanced the corrosion inhibition properties in an accelerated corrosive environment (3.5 % saline water). The electrochemical measurements showed eleven-fold rise in total impedance by h-BNNS-PANI-ES nanocomposites compared to PANI-ES-based epoxy coating, highlighting the role of h-BNNS as a structural barrier to protect the underlying mild steel substrate against corrosion. Moreover, mild steel coated with h-BNNS-PANI-ES nanocomposites remained intact even after ten days of exposure to salty fog, demonstrating the potential of such coatings for industrial applications.

Pearl-inspired self-extinguishing, thermal-conductive, and robust thermoplastic polyurethane composite by strengthening inter-layer packing

Fabricating thermoplastic polyurethanes (TPU) that exhibit self-extinguishing properties alongside strong mechanical characteristics and high thermal conductivity represents a challenging yet imperative endeavor within both scientific research and industrial applications. Enhancing the thermal conductivity of composites necessitates meticulous attention to surface treatment and the orientation of chemically inert hexagonal boron nitride nanosheets (BNNS). In this study, BNNS are treated by Strengthening inter-layer packing, which enriches the mechanical enhancement mechanism of the “brick-mortar” structure of natural pearl layers. The treatments use copper hydroxyethylidene diphosphonate and melamine hydroxyethylidene diphosphonate, which have a synergistic flame retardancy. Self-extinguishing TPU films with strong mechanical strength (57 MPa) and high thermal conductivity (9.12 W m−1 K−1) are produced when the functional particles are oriented to create multiple synergistic effects with the TPU simultaneously. Furthermore, when comparing CP0.02/MP@BNNS-TPU composite film to BNNS-TPU film, the limiting oxygen index of TPU composites increased to 30.2 %, and there was a significant decrease in both the peak and total heat releases (77.2 % and 80.6 %, respectively), meeting the UL-94 V-0 standard. This work offers a fresh method for creating self-extinguishing materials with high heat conductivity and robust mechanical characteristics.

Simultaneous enhancements in strength and ductility of hexagonal BN nanosheet reinforced AlSi10Mg composites

We herein report fabrication of hexagonal boron nitride nanosheet (BNNS) reinforced AlSi10Mg composites using a combination of spark plasma sintering (SPS) and hot rolling, the microstructure and mechanical properties of the resulting composites were investigated. The obtained composites present dense microstructure with BNNS uniform distribution. Trace amounts of in-situ interfacial-reaction products such as AlN, AlB2 are observed to endow BNNS-Al interface with good adhesive strength, the interfacial reactions are greatly governed by atom competitive diffusion. In comparison with monolithic AlSi10Mg alloy, the BNNS/AlSi10Mg composites display simultaneous improvements in tensile strength and ductility. In particular, the AlSi10Mg composite with 0.5 wt% BNNS addition exhibits a yield strength of ∼221 MPa and an elongation of ∼8.3 %, representing enhancements of ∼12.7 % and ∼29.7 %, respectively. The possible synergetic strengthening and toughening mechanisms of the resulting composites are discussed based on the test results.

A novel annulated dinuclear dizinc phthalocyanine cross-linked h-BN polyamides for efficient photocatalytic levofloxacin removal from real pharmaceutical wastewater

The alignment of the strong visible-light harvesting phthalocyanine and its metal derivatives onto wide-gap semiconductors has been recognized as a bright approach to fabricate highly effective photocatalysts for energy conversation and environmental restoration. However, the practical application of phthalocyanine-sensitized photocatalysts depends on their incorporation mode between phthalocyanine and basic materials. In this work, a novel high-effective dinuclear zinc (II) phthalocyanine-sensitized photocatalyst is fabricated via covalent immobilization of (Bis(82,112,152-tri-(6-oxyl-2-carboxyl)-naphthaoxytribenzo)[g,l,q]-5,10,15,20-tetraazaporphrinno[b,e]benzene) dizinc (II), (ZnTcPc)2 onto the amino functionalized hexagonal boron nitride (–NH2-h-BN) nanosheets for the first time by a facile condensation strategy. The optimized 9%(ZnTcPc)2/h-BN polymer displays remarkably improved photocatalytic activity in levofloxacin degradation from different aqueous solutions with long-term stability under visible-light illumination. Its decomposition rates reach 81.4%, 71.7% and 90.8% in deionized water, tap water and real pharmaceutical wastewater, respectively. It is approximately 7 times than that of bare h-BN nanosheets in deionized water. The detailed experimental data indicate that the critical role of for improving visible-light harvesting and photoinduced electron transfer capability of h-BN acted by the strongly chemical bond constructed between (ZnTcPc)2 and –NH2-h-BN. The improved photocatalytic mechanism for levofloxacin removal over 9%(ZnTcPc)2/h-BN polymer is proposed according to the results of ESR, UV–vis and fluorescence measurements. Therefore, this unique combination approach affords a carefully designed molecular photocatalyst with great potential application in environmental remediation.

High-Throughput and Scalable Exfoliation of Large-Sized Ultrathin 2D Materials by Ball-Milling in Supercritical Carbon Dioxide.

The 2D materials exhibit numerous technological applications, but their scalable production is a core challenge. Herein, ball milling exfoliation in supercritical carbon dioxide (scCO2) and polystyrene (PS) is demonstrated to completely exfoliate hexagonal boron nitride nanosheets (BNNSs), graphene, molybdenum disulfide (MoS2), and tungsten disulfide (WS2). The exfoliation yield of 91%, 93%, 92%, and 92% and average aspect ratios of 743, 565, 564, and 502 for BNNSs, graphene, MoS2, and WS2, respectively, are achieved. Integrating exfoliated BNNSS in the polystyrene matrix, 3768 % thermal conductivity in the axial direction and 316% in the cross-plane direction at 12wt.% loading is increased. Also, the in-plane and cross-plane electrical conductivity of 6.3×10-4Sm-1 and 6.6×10-3Sm-1, respectively, and the electromagnetic interference (EMI) of 63.3 dB is achieved by exfoliated graphene nanosheets based composite. High thermal and electrical conductivities and EMI shielding are attributed to the high aspect ratio and ultrathin morphology of the exfoliated nanosheets, which exert high charge mobility and form better the percolation network in the composite films due to their high surface area. The process demonstrate herein can produce substantial quantities of diverse 2D nanosheets for widespread commercial utilization.