Cyano-substituted oligo (alpha-phenylenevinylene)-1,4-bis(R-cyano-4-diphenylaminostyryl)-2,5-diphenylbenzene (CNDPASDB) molecules are studied in solution and aggregate state by time-resolved fluorescence techniques. CNDPASDB exhibits a strong solvent polarity dependent characteristic of aggregation-induced emission (AIE). By time-dependent spectra, the gradual transition from local excited state to intramolecular charge transfer state with the increasing solvent polarity is clearly resolved. The transition time in high polarity solvent DMF is very fast, around 0.5 ps, resulting in a low fluorescence quantum yield. While in aggregate state, the intramolecular torsion is restricted and the local environment becomes less polar. Thus, the intramolecular charge transfer state is eliminated and efficient AIE occurs.
Hybrid metal halide perovskites have been paid enormous attentions in photophysics research, whose excellent performances were attributed to their intriguing charge carriers proprieties. However, it still remains far from satisfaction in the comprehensive understanding of perovskite charge-transport properities, especially about trap-assisted recombination process. In this Letter, through time-resolved transient absorption (TA) and photoluminescence (PL) measurements, we provided a relative comprehensive investigation on the charge carriers recombination dynamics of CH3NH3PbBr3 (MAPbBr3) perovskite films and quantum dots (QDs), especially about trap-assisted recombination. It was found that the integral recombination mode of MAPbBr3 films was highly sensitive to the density distribution of generated charge carriers and trap states. Additional, Trap effects would be gradually weakened with elevated carrier densities. Furthermore, the trap-assisted recombination can be removed from MAPbBr3 QDs through its own surface passivation mechanism and this specialty may render the QDs as a new material in illuminating research. This work provides deeper physical insights into the dynamics processes of MAPbBr3 materials and paves a way toward more light-harvesting applications in future.
Graphene quantum dots (GQDs) have recently emerged as a promising type of low‐toxicity, high‐biocompatibility, and chemically inert fluorescence probe with a high resistance to photobleaching. They are a prospective substitution for organic materials in light‐emitting devices (LED), enabling the predicted concept of much brighter and more robust carbon LED (CLED). However, the mechanism of GQD emission remains an open problem despite extensive studies conducted so far, which is becoming the greatest obstacle in the route of technical improvement of GQD quantum efficiency. This problem is solved by the combined usage of femtosecond transient absorption spectroscopy and femtosecond time‐resolved fluorescence dynamics measured by a fluorescence upconversion technique, as well as a nanosecond time‐correlated single‐photon counting technique. A fluorescence emission‐associated dark intrinsic state due to the quantum confinement of in‐plane functional groups is found in green‐fluorescence graphene quantum dots by the ultrafast dynamics study, and the two characteristic fluorescence peaks that appear in all samples are attributed to independent molecule‐like states. This finding establishes the correlation between the quantum confinement effect and molecule‐like emission in the unique green‐fluorescence graphene quantum dots, and may lead to innovative technologies of GQD fluorescence enhancement, as well as its broad industrial application.
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