激光阈值
分子内力
分子
激发态
材料科学
质子
光化学
波长
化学
光电子学
原子物理学
物理
量子力学
立体化学
有机化学
作者
Changcun Yan,Yanping Liu,Wan‐Ying Yang,Junjie Wu,Xuedong Wang,Liang‐Sheng Liao
标识
DOI:10.1002/anie.202210422
摘要
Organic molecules which can undergo excited-state intramolecular proton transfer (ESIPT) process have been considered as ideal gain materials for near-infrared organic lasers owing to their effective four-level systems. However, extending lasing wavelength beyond 800 nm with present ESIPT-active gain materials is still in challenge. Herein, we established a molecular design strategy that operates via extending the π-conjugated system of the ESIPT parent core to enhance the cascaded double ESIPT process and thus to achieve the red-shifted six-level system lasing. Concretely, a model molecule with 1,9-dihydroxyanthracene as the ESIPT parent core was designed and synthesized, which was proved to undergo twice cascaded ESIPT processes while the 1,8-dihydroxynaphthalene-based analogue can only undergo once ESIPT process based on DFT calculations and ultrafast dynamics analyses. Finally, a six-level system lasing toward 900 nm was achieved with a low threshold of 27.4 μJ cm-2 .
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