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Enhanced two-photon-excited fluorescence from electron donor-acceptor exciplex

机译:来自电子供体 - 受体Exciplex的增强的双光子激发荧光

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摘要

Exciplex-based thermally activated delayed fluorescence (TADF) materials show long luminescence lifetimes and high quantum efficiency by converting the non-radiative triplets into the radiative singlets. Here, strong upconverted fluorescence from the amorphous thin films of TADF donor-acceptor (D-A) exciplexes is observed under near-infrared excitation. The spectroscopic studies demonstrate that the enhanced upconversion in exciplex emission combines a series of excited state processes including the two-photon absorption (TPA) of donors and the TADF of D-A pairs. The comparison between donor-only and D-A systems indicates that the upconversion is greatly facilitated by the energy harvesting mechanisms existing in the exciplex-based TADF materials. The results reveal the formation mechanism of exciplex excited-states following the two-photon excitation in D-A blends, and consequently the potentials of exciplex materials in nonlinear optics applications. Moreover, a maximum D-A distance of similar to 6.9 nm for two-photon excited exciplex formation is obtained.
机译:基于激基复合物的热激活延迟荧光(TADF)材料通过将非辐射三重态转变为辐射单重态,显示出较长的发光寿命和较高的量子效率。在这里,在近红外激发下观察到来自TADF施主-受主(D-A)激基复合物的非晶态薄膜的强上转换荧光。光谱研究表明,激基复合物发射中增强的上转换结合了一系列激发态过程,包括施主的双光子吸收(TPA)和D-a对的TADF。仅供体和D-A系统之间的比较表明,基于激基复合物的TADF材料中存在的能量收集机制极大地促进了上转换。结果揭示了D-A共混物中双光子激发后激基复合物激发态的形成机制,从而揭示了激基复合物材料在非线性光学中的应用潜力。此外,对于双光子激发的激基复合物的形成,获得了类似于6.9 nm的最大D-a距离。

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