PPSM, ENS Cachan, CNRS, Université Paris-Saclay, 94235, Cachan, France.
Dpt Appl. Chem. & Biochem., Kumamoto University, 2-39-1 Kurokami, Chuo-ku, Kumamoto, 860-8555, Japan.
Angew Chem Int Ed Engl. 2016 Mar 7;55(11):3662-6. doi: 10.1002/anie.201510600. Epub 2016 Jan 28.
Controlling or switching the optical signal from a large collection of molecules with the minimum of photons represents an extremely attractive concept. Promising fundamental and practical applications may be derived from such a photon-saving principle. With this aim in mind, we have prepared fluorescent photochromic organic nanoparticles (NPs), showing bright red emission, complete ON-OFF contrast with full reversibility, and excellent fatigue resistance. Most interestingly, upon successive UV and visible light irradiation, the NPs exhibit a complete fluorescence quenching and recovery at very low photochromic conversion levels (<5 %), leading to the fluorescence photoswitching of 420±20 molecules for only one converted photochromic molecule. This "giant amplification of fluorescence photoswitching" originates from efficient intermolecular energy-transfer processes within the NPs.
用最少的光子来控制或切换大量分子的光学信号是一个极具吸引力的概念。从这种节省光子的原理中可能衍生出有前景的基础研究和实际应用。基于这一目标,我们制备了具有明亮红色发射、完全 ON-OFF 对比且具有完全可逆性以及优异抗疲劳性的荧光光致变色有机纳米粒子(NPs)。最有趣的是,在连续的紫外光和可见光照射下,NPs 在非常低的光致变色转换水平(<5%)下表现出完全的荧光猝灭和恢复,导致仅一个转化的光致变色分子即可实现 420±20 个分子的荧光光开关切换。这种“荧光光开关的巨大放大”源自 NPs 内有效的分子间能量转移过程。