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Two kinds of triphenylamine‐derived solid‐state emissive carbon dots (CDs) with orange and yellow color are facilely synthesized through solvothermal treatment, taking advantage of the nonplanar structure and good carrier mobility of triphenylamine unit. Theoretical calculations show that the triphenylamine structure could greatly inhibit the direct π–π stacking of aromatic skeletons and enhance the fluorescence properties of CDs in aggregation state. By adopting the CDs as single emissive layer, high‐performance orange‐color and green‐color electroluminescent light‐emitting diodes (LEDs) are successfully fabricated, with maximum brightness of 9450/4236 cd m−2, high current efficiency of 1.57/2.34 cd A−1 and low turn‐on voltage of 3.1/3.6 eV are respectively achieved. Significantly, white‐color LED device is further prepared. This work provides a universal platform for the construction of novel solid‐state emissive CDs with significant applications in photoelectric device. [ABSTRACT FROM AUTHOR]

In this work, graphite and diamond are successfully introduced into Al melts and TiC is in situ-synthesized based on reactive wetting. It is found that the microstructures of the prepared TiC-reinforced Al composites are varied with the change in carbon sources and their sizes. TiC particles tend to form agglomerations in the composites prepared by both graphite and diamond, but the size of the TiC particles as well as their agglomerations will decrease with the decrease in the carbon source size. In addition, the Ti-C reaction is also difficult to fully carry out due to the influence of the Al-C reaction. As a result, in addition to TiC particles, Al4C3 will also be present in the composites prepared by graphite, especially when the size of graphite is large. As for the composites prepared by diamond, diamond@Al4C3@TiC core–shell particles will form when the size of the diamond is large, such as 10 μm in this work, and these particles will transform into Al4C3@TiC core–shell particles when the size of the diamond is decreased. [ABSTRACT FROM AUTHOR]

The development of efficient red bandgap emission carbon quantum dots (CQDs) for realizing high‐performance electroluminescent warm white light‐emitting diodes (warm‐WLEDs) represents a grand challenge. Here, the synthesis of three red‐emissive electron‐donating group passivated CQDs (R‐EGP‐CQDs): R‐EGP‐CQDs‐NMe2, ‐NEt2, and ‐NPr2 is reported. The R‐EGP‐CQDs, well soluble in common organic solvents, display bright red bandgap emission at 637, 642, and 645 nm, respectively, reaching the highest photoluminescence quantum yield (QY) up to 86.0% in ethanol. Theoretical investigations reveal that the red bandgap emission originates from the rigid π‐conjugated skeleton structure, and the ‐NMe2, ‐NEt2, and ‐NPr2 passivation plays a key role in inducing charge transfer excited state in the π‐conjugated structure to afford the high QY. Solution‐processed electroluminescent warm‐WLEDs based on the R‐EGP‐CQDs‐NMe2, ‐NEt2, and ‐NPr2 display voltage‐stable warm white spectra with a maximum luminance of 5248–5909 cd m−2 and a current efficiency of 3.65–3.85 cd A−1. The warm‐WLEDs also show good long‐term operational stability (L/L0 > 80% after 50 h operation, L0: 1000 cd m−2). The electron‐donating group passivation strategy opens a new avenue to realizing efficient red bandgap emission CQDs and developing high‐performance electroluminescent warm‐WLEDs. [ABSTRACT FROM AUTHOR]