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Understanding the direct transformation from graphite to diamond has been a long-standing challenge with great scientific and practical importance. Previously proposed transformation mechanisms1–3, based on traditional experimental observations that lacked atomistic resolution, cannot account for the complex nanostructures occurring at graphite−diamond interfaces during the transformation4,5. Here we report the identification of coherent graphite−diamond interfaces, which consist of four basic structural motifs, in partially transformed graphite samples recovered from static compression, using high-angle annular dark-field scanning transmission electron microscopy. These observations provide insight into possible pathways of the transformation. Theoretical calculations confirm that transformation through these coherent interfaces is energetically favoured compared with those through other paths previously proposed1–3. The graphite-to-diamond transformation is governed by the formation of nanoscale coherent interfaces (diamond nucleation), which, under static compression, advance to consume the remaining graphite (diamond growth). These results may also shed light on transformation mechanisms of other carbon materials and boron nitride under different synthetic conditions.

The traditional hardness-toughness tradeoff poses a substantial challenge for the development of superhard materials. Due to strong covalent bonds and intrinsic brittleness, the full advantage of microstructure engineering for enhanced mechanical properties requires further exploration in superhard materials. Here heterogeneous diamond-cBN composites were synthesized from a carefully prepared precursor (hBN microflakes uniformly wrapped by onion carbon nanoparticles) through phase transitions under high pressure and high temperature. The synthesized composites inherit the architecture of the precursors: cBN regions with an anisotropic profile that spans several micrometers laterally and several hundred nanometers in thickness are embedded in a nanograined diamond matrix with high-density nanotwins. A significantly high fracture toughness of 16.9 ± 0.8 MPa m

From the perspective of high-temperature applications, materials with excellent high-temperature mechanical properties are always desirable. The present work demonstrates that the binder-free nanopolycrystalline WC ceramic with an average grain size of 103 nm obtained by high-pressure and high-temperature sintering exhibits excellent mechanical properties at both room temperature and high temperature up to 1000 °C. Specifically, the binder-free nanopolycrystalline WC ceramic still maintains a considerably high Vicker hardness HV of 23.4 GPa at 1000 °C, which is only 22% lower than the room temperature HV. This outstanding thermo-mechanical stability is superior to that of typical technical ceramics, e.g. SiC, Si3N4, Al2O3, etc. Nanocrystalline grains with many dislocations, numerous low-energy, highly stable Σ2 grain boundaries, and a relatively low thermal expansion coefficient, are responsible for the observed outstanding high-temperature mechanical properties.

Traditional ceramics or metals cannot simultaneously achieve ultrahigh strength and high electrical conductivity. The elemental carbon can form a variety of allotropes with entirely different physical properties, providing versatility for tuning mechanical and electrical properties in a wide range. Here, by precisely controlling the extent of transformation of amorphous carbon into diamond within a narrow temperature–pressure range, we synthesize an in situ composite consisting of ultrafine nanodiamond homogeneously dispersed in disordered multilayer graphene with incoherent interfaces, which demonstrates a Knoop hardness of up to ~53 GPa, a compressive strength of up to ~54 GPa and an electrical conductivity of 670–1,240 S m–1 at room temperature. With atomically resolving interface structures and molecular dynamics simulations, we reveal that amorphous carbon transforms into diamond through a nucleation process via a local rearrangement of carbon atoms and diffusion-driven growth, different from the transformation of graphite into diamond. The complex bonding between the diamond-like and graphite-like components greatly improves the mechanical properties of the composite. This superhard, ultrastrong, conductive elemental carbon composite has comprehensive properties that are superior to those of the known conductive ceramics and C/C composites. The intermediate hybridization state at the interfaces also provides insights into the amorphous-to-crystalline phase transition of carbon.

GeP5, as the most representative phosphorus-based material in two-dimensional layered phosphorous compounds, has shown a fairly bright application prospect in the field of energy storage because of its ultrahigh electrical conductivity. However, high-yield exfoliation methods and effective structure construction strategies for GeP5 nanosheets are still missing, which completely restricts the further application of GeP5-based nanocomposites. Here, we not only improved the yield of GeP5 nanosheets by a liquid nitrogen-assisted liquid-phase exfoliation technique but also constructed the GeP5@RuO2 nanocomposites with the 0D/2D heterostructure by in situ introduction of ultrafine RuO2 nanoparticles on highly conductive GeP5 nanosheets using a simple hydrothermal synthesis method, and then applying it to micro-supercapacitors (MSCs) as electrode materials through a mask-assisted vacuum filtration technique. It is precisely because of the synergy of the electrical double-layer material, GeP5 nanosheets and the pseudocapacitance material RuO2 nanoparticles that endows the GeP5@RuO2 electrode with outstanding electrochemical performance in micro-supercapacitors with a large specific capacitance of 129.5 mF cm-2/107.9 F cm-3, high energy density of 17.98 μWh cm-2, remarkable long-term cycling stability with 98.4% capacitance retention after 10 000 cycles, the exceptional mechanical stability, outstanding environmental stability, and excellent integration features. This work opens up a new avenue to construct GeP5-based nanocomposites as a most promising novel electrode material for practical application in flexible portable/wearable micro-nanoelectronic devices.

Columbite-rich multiphase TiO2 nanoceramics with outstanding mechanical and dielectric properties were successfully prepared through high-pressure sintering by using anatase-type TiO2 as precursor. High-pressure sintering combined with phase transformation assisted consolidation can effectively refine the grain size of the recovered samples. This process is conducive to obtain nanocrystalline columbite-rich TiO2 ceramics with excellent performance. The highest hardness is approximately 12.76 GPa, which is 2.5 times higher than that of ordinary coarse-grained ceramics. The effect of columbite phase on the hardness of multiphase ceramics is discussed. The columbite-rich TiO2 ceramic shows a colossal permittivity (∼8 × 103) and low loss (∼0.2) at 1 kHz and room temperature, which are superior to that of undoped rutile polycrystalline ceramics. This ceramic shows a steadier frequency-dependent dielectric permittivity and loss than rutile TiO2 crystal. These results enrich the fundamental knowledge of columbite-rich TiO2, thereby enabling the exploitation of new applications.

Nanostructured silicon carbide (SiC) materials are expected to have bright prospect in application as high-performance electrode materials with excellent charge–discharge cycling stability. However, the exploration of SiC-based micro-supercapacitors (MSCs) still remains a grand challenge seriously hampered by low areal capacities and complicated multistep production process. Herein, we report that rationally designed SiC/C nanocomposite with hierarchical porous structure and improved electrical conductivity has been realized by a facile and rapid carbothermic reduction using silica sol and sucrose as silicon and carbon source. The amorphous carbon between SiC nanoparticles (NPs) contributes to enlarged surface areas and excellent conductivity, not only ensuring intimate contact between the electrolyte and the electrode but also providing an effective ion highway for electrolyte ions. As a result, MSCs based on SiC/C nanocomposite (Si/C mass ratio of 1:1.5) demonstrate an optimal specific areal capacitance of 11.8 mF cm−2 at 2 mV s−1, outstanding flexibility (104.5% retention of initial capacitance at 180° bending), and superior integration. Most notably, the capacitance remains at 97.3% of the initial value after 50000 charging/discharging cycles, superior to that of most advanced SiC-based MSCs ever reported. This work demonstrates an effective design for hierarchical porous SiC/C nanocomposite for energy storage, which gives significant inspirations on the exploration of high-performance SiC-based MSCs.

Boron carbide (B4C) is an important structural ceramic material, however, the use of this material is limited by its poor sinterability and low fracture toughness. Nano-sized powders have small particle size, high chemical activity and great sintering ability, which can promote the fabrication of the dense B4C ceramics. Herein, by spark plasma sintering (SPS) homemade high-purity nanopowders, single phase B4C ceramics with density close to the theoretical value were prepared. Results showed that the best SPS condition was holding at temperature of 1850 °C for 4 min. Under this condition the sample exhibited enhanced mechanical properties including Vickers hardness of 33.9 GPa, fracture toughness of 3.81 MPa m1/2 and flexure strength of 554.7 MPa. Transmission electron microscopy (TEM) analysis shows that non-coherent twins exist at the grain boundary instead of amorphous phase or second phase, which further confirms the high purity and high densification of the obtained B4C ceramics.

Low dimensional semiconductors can be used for various electronic and optoelectronic devices because of their unique structure and property. In this work, one-dimensional Sb2S3 nanowires (NWs) with high crystallinity were grown via chemical vapor deposition (CVD) technique on SiO2/Si substrates. The Sb2S3 NWs exhibited needle-like structures with inclined cross-sections. The lengths of Sb2S3 nanowires changed from 7 to 13 μm. The photodetection properties of Sb2S3 nanowires were comprehensively and systematically characterized. The Sb2S3 photodetectors show a broadband photoresponse ranging from ultraviolet (360 nm) to near-infrared (785 nm). An excellent specific detectivity of 2.1 × 1014 Jones, high external quantum efficiency of 1.5 × 104 %, sensitivity of 2.2 × 104 cm2W−1 and short response time of less than 100 ms was achieved for the Sb2S3 NW photodetectors. Moreover, the Sb2S3 NWs showed outstanding switch cycling stability that was beneficial to the practical applications. The high-quality Sb2S3 nanowires fabricated by CVD have great application potential in semiconductor and optoelectronic fields.

The development of stable and low-cost catalysts with high reactivity to replace Pt-based ones is the central focus but challenging for hydrogen evolution reaction (HER). The incorporation of single atoms into two-dimensional (2D) supports has been demonstrated as an effective strategy because of the highly active single atomic sites and extremely large surface area of two-dimensional materials. However, the doping of single atoms is normally performed on the surface suffering from low stability, especially in acidic media. Moreover, it is experimentally challenging to produce monolayered 2D materials with atomic doping. Here, we propose a strategy to incorporate single foreign Fe atoms to substitute W atoms in sandwiched two-dimensional WS2. Because of the charge transfer between the doped Fe atom and its neighboring S atoms on the surface, the proximate S atoms become active for HER. Our theoretical prediction is later verified experimentally, showing an enhanced catalytic reactivity of Fe-doped WS2 in HER with the Volmer-Heyrovsky mechanism involved. We refer to this strategy as proximity catalysis, which is expected to be extendable to more sandwiched two-dimensional materials as substrates and transition metals as dopants.

Here a series of sp2-sp3 BxNx+1 (x = 1, 2, 3, 4, 5, 6) structures was constructed. These structures can be viewed as diamond-like BN blocks connected by single N-N bonds. Elastic constants and phonon dispersion curves confirm that all of the proposed structures are mechanically and dynamically stable. These structures all possess metallicity originating from the conductive channels formed by sp2-hybridized N atoms and adjacent sp3-hybridized B and N atoms. These structures exhibit tunable mechanical properties with a regular change in the sp2/sp3 ratio. The theoretical Vickers hardness increases and the ductility decreases as the number of diamond-like BN blocks increases, gradually approaching those of c-BN. Moreover, the convex hull at ambient pressure and 50 GPa indicates that high pressure is beneficial in the synthesis of these B-N phases. The simulated X-ray diffraction patterns of these structures were also calculated to provide more information for further experiments.

As the most primitive vertebrates, lampreys are significant in understanding the early origin and evolution of the vertebrate innate and adaptive immune systems. The complement system is a biological response system with complex and precise regulatory mechanisms and plays an important role in innate and adaptive immunity. It consists of more than 30 distinct components, including intrinsic components, regulatory factors, and complement receptors. Complement system is the humoral backbone of the innate immune defense and complement-like factors have also been found in cyclostomes. Our knowledge as such in lamprey has dramatically increased in the recent years. The searching for complement components in the reissner lamprey Lethenteron reissneri genome database, together with published data, has unveiled the existence of all the orthologues of mammalian complement components identified thus far, including the complement regulatory proteins and complement receptors, in lamprey. This review, summarizes the key themes and recent updates on the complement system of agnathans and discusses the individual complement components of lampreys, and critically compare their functions to that of mammalian complement components. Interestingly, the adaptive immune system of agnathans differs from that of gnathostomes. Lamprey complement components also display some distinctive features, such as lampreys are characterized by the variable lymphocyte receptors (VLRs)-based alternative adaptive immunity. This review may serve as important literature for deducing the evolution of the immune system from invertebrates to vertebrates.

A previous study reported an observed unidentified graphite/hexagonal boron nitride (hBN) superlattice structure in special multilayer heterojunction devices via cross-sectional transmission electron microscopy [Haigh S. J. et al., Nat. Mater. 2012, 11, 764-767]. In this letter, we designed and confirmed two possible graphite/hBN superlattice structures (AA and Ab), which were probably the structures observed by the aforementioned experiment. The formation enthalpies of both structures were negative, indicating that they could be successfully synthesized as the previous experiment reported. The results also showed that both structures possessed dynamic stability and elastic stability. Importantly, the theoretical interlayer distances of AA and Ab were 3.34 and 3.30 A, respectively, which were consistent with the experimental value of 3.32 A. The X-ray diffraction patterns and Raman spectra of both structures were simulated to aid in distinguishing them. This study on the atomic structure of the graphite/hBN superlattice lays a foundation for further research and application of this material.

Recent experiments reported a substantial toughening of nanotwinned diamond (nt-diamond) composite with coherently interfaced diamond polytypes (different stacking sequences). This discovery emphasizes the diversity of graphite-like structures in carbon onion precursors for synthesizing nt-diamond composite. We designed five new graphitic polytypes to investigate structural diversity in graphitic systems. Under ambient pressure, the energies of all the proposed polytypes are between those of graphite (AB structure) and a previously predicted AA structure. Dynamic and elastic stability results showed that four structures (AB'C', AB'D', AAB and ABCB) can be stable under ambient pressure. These four structures all have a large interlayer distance comparable to those in carbon onion and turbostratic graphite. Chiral graphitic structures (AB'D' and AB'C') with reversible electrical properties under slight stress might be responsible for the controversy about the bandgap of graphitic samples. Therefore, these four structures are most likely to be a part of the structures existing in carbon onion and turbostratic graphite or are structural defects in graphitic samples.