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Stability of advanced functional materials subjected to extreme conditions involving ion bombardment, radiation, or reactive chemicals is crucial for diverse applications. Here we demonstrate the excellent stability of wafer-scale thin films of vertically aligned hexagonal BN nanosheets (hBNNS) exposed to high-energy ions and reactive atomic oxygen representative of extreme conditions in space exploration and other applications. The hBNNS are fabricated catalyst-free on wafer-scale silicon, stainless steel, copper and glass panels at a lower temperature of 400 °C by inductively coupled plasma (ICP) assisted chemical vapor deposition (CVD) and subsequently characterized. The resistance of BNNS to high-energy ions was tested by immersing the samples into the plasma plume at the anode of a 150 W Hall Effect Thruster with BNNS films facing Xenon ions, revealing that the etching rate of BNNS is 20 times less than for a single-crystalline silicon wafer. Additionally, using O2/Ar/H2 plasmas to simulate the low Earth orbit (LEO) environment, it is demonstrated that the simulated plasma had very weak influence on the hBNNS surface structure and thickness. These results validate the strong potential of BNNS films for applications as protective, thermally conductive and insulating layers for spacecrafts, electric plasma satellite thrusters and semiconductor optoelectronic devices. [ABSTRACT FROM AUTHOR]

Hexagonal boron nitride (h -BN) is an extraordinarily tough material that is chemically and thermally resistant to extreme environments, uniquely electrically insulating yet possessing exceptionally high thermal conductivity. Owing to these exotic and outstanding properties, and the ability to be controllably fabricated at large-scale, various architectures of low-dimensional h -BN have emerged as promising candidates for a myriad of applications. This review provides a comprehensive and holistic account of the most widely utilized fabrication techniques with emphasis on new advancements for various forms of nano-BN architectures ranging from 0D quantum dots, 1D nanotubes and nanoribbons, 2D nanosheets and 3D frameworks of BN. These techniques encompass improved synthesis progresses by chemical vapor deposition, scalable forms of exfoliation, bottom-up and top-down hydrothermal/solvothermal processes and assembly of 3D structures by freeze-casting. Furthermore, the functional properties and utilization of these nano-BN architectures for various novel and evolving applications including thermal management for modern electronics, deep ultraviolet optoelectronics, single photon quantum emitters, protective coatings against corrosion, high-performance polymer dielectrics, space instrumentation, drug delivery, tissue engineering and biosensing are extensively elaborated. Finally, several major challenges and limitations of the existing fabrication technologies that hinder further upscaling and commercialization are highlighted, which offer new opportunities for the development of advanced BN nanostructures toward diverse emerging and future applications. [Display omitted] • Recent impactful developments on the synthesis and assembly techniques of various nano-BN architectures are discussed. • Their functional properties and prospective applications are summarized. • Strategies and challenges towards further upscaling and commercialization are proposed. [ABSTRACT FROM AUTHOR]

Porous polymeric foams as dielectric layer for highly sensitive capacitive based pressure sensors have been extensively explored owing to their excellent flexibility and elasticity. Despite intensive efforts, most of previously reported porous polymer foams still suffer from difficulty in further lowering the attainable density limit of ≈0.1 g cm−3 while retaining high sensitivity and compressibility due to the limitations on existing fabrication techniques and materials. Herein, utilizing 3D interconnected networks of few‐layer hexagonal boron nitride foams (h‐BNFs) as supporting frameworks, lightweight and highly porous BN/polydimethylsiloxane composite foams (BNF@PDMS) with densities reaching as low as 15 mg cm−3 and permittivity close to that of air are fabricated. This is the lightest PDMS‐based foam reported to date. Owing to the synergistic effects between BN and PDMS, these lightweight composite foams possess excellent mechanical resilience, extremely high compressibility (up to 95% strain), good cyclic performance, and superelasticity. Being electrically nonconductive, the potential application of BNF@PDMS as a dielectric layer for capacitive sensors is further demonstrated. Remarkably, the as‐fabricated device can perform multiple sensing functions such as noncontact touch sensor, environmental monitoring sensor, and high sensitivity pressure sensor that can detect extremely low pressures of below 1 Pa. [ABSTRACT FROM AUTHOR]

In this work, we report for the first time a simple approach to fabricate 3D reduced graphene oxide/boron nitride (rGO/BN) sponges with no additional chemical cross-linkers. Encouragingly, such sponge possesses higher compressibility and better recoverability in both air and organic solvents as compared to the bare rGO sponge. The as-prepared rGO/BN sponge also exhibits excellent water resistance and high oil absorption capability, achieving up to 170 times its own weight toward a wide range of environmental contaminants. Especially, the absorbed oil can be easily removed by the absorption–squeezing process which is cost effective and environmental friendly for oil collection. Most importantly, the underlying reasons for the remarkable mechanical properties, excellent oil absorption capabilities have been analysed and revealed in depth. These exceptional characteristics together with the ease of scalable synthesis make the as-prepared 3D rGO/BN sponge show many promising applications ranging from tissue engineering, sensors, catalysis, energy storage and conversion to environmental remediation. [ABSTRACT FROM AUTHOR]

Reduced graphene oxide (rGO)/boron nitride (BN) composite films were successfully fabricated by facile vacuum filtration and subsequent thermal treatment. Their morphology, structure and electrochemical performance were systematically characterized by field emission scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, Raman spectroscopy, cyclic voltammetry, galvanostatic charge/discharge and electrochemical impedance spectroscopy. Importantly, the as-prepared rGO/BN composite film with a 2 wt.% BN content as binder-free anode material for lithium ion batteries (LIBs) exhibited a high reversible capacity of 278 mAh·g −1 at a high current density of 100 mA·g −1 , high rate capability, and high capacity retention over the first 200 cycles. The enhanced electrochemical performances of rGO/BN composite film are attributed to the unique structure and the synergistic effects between layered BN and graphene, which favored electrolyte penetration and buffered the volume expansion during the lithiation and delithiation process. In addition, this work not only provides a versatile strategy for fabrication of other graphene-based films, but also shows the potential promise of rGO/BN composite film for other energy storage devices. [ABSTRACT FROM AUTHOR]