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Organic light‐emitting diodes (OLEDs) have garnered increasing attention as a promising candidate for application in next‐generation displays and solid‐state lighting devices. The doping technique commonly used to fabricate light‐emitting layers (EMLs) of OLEDs disperses the emitting material in a host matrix to mitigate aggregation‐induced quenching (ACQ). Alternatively, owing to their high efficiency and ease of manufacture, nondoped OLEDs have been developed as a substitute for doped OLEDs. When fabricating nondoped OLEDs, it is essential to suppress the ACQ effect in the EML and efficiently utilize the generated excitons for radiative decay. Since the discovery of aggregation‐induced emission (AIE) by Tang et al., significant work has been done to improve the stability and efficiency of nondoped OLEDs based on fluorescent AIE luminogens (AIEgens). Fluorescent AIEgens, synthesized using various molecular frameworks, such as silole, tetra/triphenylethylene, tetraphenylpyrazine, and tetraphenylbenzene, exhibit high photoluminescence quantum yields in the solid state. Therefore, many studies have reported that fluorescent AIEgen‐based OLEDs have excellent external quantum efficiency and exhibit emission at various wavelengths, including deep‐blue/blue/green emission. With the development of fluorescent AIEgens, delayed fluorescent AIEgens with efficient triplet utilization through reverse intersystem crossing and AIE properties have been adopted as ideal emitters and used in nondoped OLEDs. This review systematically discusses and summarizes recent reports on the development of AIEgens for nondoped OLEDs by grouping them into fluorescent and delayed fluorescent AIEgens. The purpose of this review is to provide deep insights into the design of novel AIEgens for high‐performance nondoped OLEDs.

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Titania supported vanadomolybdophosphoric acid (VMPA) catalysts with vanadium in different positions, incorporated into the molybdophosphoric acid structure by substituting for molybdenum and cation exchanged on the molybdophosphoric acid surface, were synthesized. The catalysts were characterized by XRD, FT-IR, Raman spectroscopy, TPR, XPS, and ESR techniques. The FT-IR and Raman spectral analyses confirm that the molybdophosphoric acid is present with the Keggin ion structure during modifications. The incorporation of vanadium into the primary or secondary structures of the Keggin heteropoly acid was confirmed by ESR, Raman, and XPS analysis. These catalysts were investigated for the vapor phase ammoxidation of 2-methyl pyrazine and methanol oxidation. The specific location of vanadium in the 12-molybdophosphoric acid was found to affect the catalytic redox performance. The catalyst with vanadium present in the primary structure of the Keggin ion possesses enhanced catalytic redox activity and selectivity compared to when vanadium is present on the Keggin surface for both the ammoxidation and oxidation reactions.

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