In many 2D materials reported thus far, the forces confining atoms in a 2D plane are often strong interactions, such as covalent bonding. Herein, the first demonstration that hydrogen (H)-bonding can be utilized to assemble polydiacetylene (a conductive polymer) toward a 2D material, which is stable enough to be free-standing, is shown. The 2D material is well characterized by a large number of techniques (mainly different microscopy techniques). The H-bonding allows splitting of the material into ribbons, which can reassemble, similar to a zipper, leading to the first example of a healable 2D material. Moreover, such technology can easily create 2D, organic, conductive nanowire arrays with sub-2-nm resolution. This material may have potential applications in stretchable electronics and nanowire cross-bar arrays.
Single‐crystalline {100} faceted TiC is of great significance in theory to a large number of engineering applications owing to its extraordinary catalytic properties. However, the {111} planes are prevalent in conventional TiC powders given their favorable thermodynamic stability during the initial low stoichiometric growth stage. Herein, a disproportionation–decomposition strategy is developed to directly produce Ti and C atoms to synthesize single‐crystalline {100} faceted TiC powders. Outstanding electrochemical performance of TiC {100} crystal planes in terms of the hydrogen evolution reaction is evidenced by an overpotential of 392 mV at 10 mA cm−2, which is 52% lower than that of randomly faceted TiC counterparts (815 mV).
Carbon and oxygen isotope ratios (δ13C and δ18O) were measured in annual tree-ring cellulose samples dated from 1756 to 2015 CE. These samples were extracted from Chinese pine (Pinus tabulaeformis Carr.) trees located in a semi-arid region of north-central China. We found that tree-ring δ13C and δ18O values both recorded similar climatic signals (e.g., temperature and moisture changes), but found that tree-ring δ13C exhibited a stronger relationship with mean temperature, precipitation, average relative humidity, self-calibrating Palmer drought severity index (scPDSI), and standard precipitation evaporation index (SPEI) than δ18O during the period 1951–2015 CE. The strongest correlation observed was between tree-ring δ13C and scPDSI (previous June to current May), which explains ~43% of the variance. The resulting 130-year reconstruction reveals severe drought events in the 1920s and a sustained drying trend since the 1980s. This hydroclimate record based on tree-ring δ13C data also reveals similar dry and wet events to other proxy data (i.e., tree-ring width and historical documentation) that have allowed reconstructions to be made across the northern fringe of the Asian summer monsoon region. Our results suggest that both large-scale modes of climate variability (e.g., El Niño-Southern Oscillation, Pacific Decadal Oscillation, and North Atlantic Oscillation) and external forcing (e.g., solar variability) may have modulated moisture variability in this region. Our results imply that the relationship between tree-ring δ18O and local climate is less well-characterized when compared to δ13C and may be affected more strongly by the influences of these different atmospheric circulation patterns. In this semi-arid region, tree-ring δ13C appears to represent a better tool with which to investigate historical moisture changes (scPDSI).
Preparation of high melting point sphere is of great practical value and remains a great challenge. Herein, for the first time a delicate chemical vapor deposition (CVD) process was developed for fabricating spherical TiN and TiC powders, which can hardly be attainable by conventional processes. The big equilibrium constant and released heats are key parameters for obtaining spherical TiN and TiC powders by the CVD process. Sphericity and crystallinity of these spherical powders can be controlled by adjusting nucleation and growth. The optimal TiN spheres (diameter 0.46 μm, sphericity 0.89) and TiC spheres (diameter 0.52 μm, sphericity 0.87) were obtained at 850°C under N2 and H2 and CH4, respectively. The design ideas explore a novel way to fabricate high melting point spheres.
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