硫杂蒽酮
光化学
系统间交叉
光子上转换
材料科学
量子点
光催化
化学
紫外线
酮
分子
超快激光光谱学
三重态
光谱学
氢原子萃取
光解
量子产额
轨道能级差
接受者
作者
Zhaolong Wang,Xiaoheng Chen,Kaifeng Wu
出处
期刊:Small
[Wiley]
日期:2026-02-13
卷期号:22 (22): e14174-e14174
被引量:1
标识
DOI:10.1002/smll.202514174
摘要
Aromatic ketones have been long adopted as photocatalysts for photochemical synthesis owing to their efficient intersystem crossing and high triplet energy. Most of these ketones, however, absorb at ultraviolet wavelengths with low extinction coefficients, limiting the efficiency and scope of accessible photochemical reactions. Herein, we report the use of low-toxicity (Cd, Pb-free) blue ZnSe-based quantum dots (QDs) to sensitize the triplets of their surface-anchored thioxanthone molecules with high triplet energy of 2.75 eV. Ultrafast spectroscopy unambiguously reveals a stepwise, electron-transfer-mediated triplet energy transfer mechanism. This unusual photosensitization, in conjunction with the unique chemical reactivity of the thioxanthone triplets, allows us to use blue light to drive multiple challenging photochemical and photocatalytic applications: i) visible-to-ultraviolet B photon upconversion with large anti-Stokes shift of 0.8 eV through triplet-triplet annihilation; ii) energy transfer photocatalysis such as the disulfide-ene reaction; iii) reductive aryl dechlorination and C-N coupling enabled by hydrogen abstraction by thioxanthone triplets. This environmentally benign QD-ketone hybrid system will inspire the design of advanced photocatalysts for a variety of energy-demanding photochemical applications.
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