光子上转换
系统间交叉
蒽
光化学
菁
荧光
激发态
材料科学
激发
光电子学
化学
光学
原子物理学
发光
单重态
物理
量子力学
作者
Xueze Zhao,Shan He,Weijie Chi,Xiaogang Liu,Pengzhong Chen,Wen Sun,Jianjun Du,Jiangli Fan,Xiaojun Peng
标识
DOI:10.1002/advs.202202885
摘要
Abstract Upconverted reactive oxygen species (ROS) photosensitization with one‐photon excitation mode is a promising tactic to elongate the excitation wavelengths of photosensitive dyes to near‐infrared (NIR) light region without the requirement of coherent high‐intensity light sources. However, the photosensitization efficiencies are still finite by the unilateral improvement of excited‐state intersystem crossing (ISC) via heavy‐atom‐effect, since the upconverted efficiency also plays a decisive role in upconverted photosensitization. Herein, a NIR light initiated one‐photon upconversion heavy‐atom‐free small molecule system is reported. The meso‐rotatable anthracene in pentamethine cyanine (Cy5) is demonstrated to enrich the populations in high vibrational–rotational energy levels and subsequently improve the hot‐band absorption (HBA) efficiency. Moreover, the spin–orbit charge transfer intersystem crossing (SOCT‐ISC) caused by electron donated anthracene can further amplify the triplet yield. Benefiting from the above two aspects, the 1 O 2 generation significantly increases with over 2‐fold improved performance compared with heavy‐atom‐modified method under upconverted light excitation, which obtains efficient in vivo phototheranostic results and provides new opportunities for other applications such as photocatalysis and fine chemical synthesis.
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