光子上转换
发色团
材料科学
激发
激子
激发态
量子产额
光电子学
光化学
化学物理
蒽
发光
化学
原子物理学
荧光
光学
物理
量子力学
作者
Prasenjit Mahato,Angelo Monguzzi,Nobuhiro Yanai,Teppei Yamada,Nobuo Kimizuka
出处
期刊:Nature Materials
[Nature Portfolio]
日期:2015-08-03
卷期号:14 (9): 924-930
被引量:114
摘要
The conversion of low-energy light into photons of higher energy based on sensitized triplet-triplet annihilation upconversion (TTA-UC) has emerged as a promising wavelength-shifting methodology because it permits UC at excitation powers as low as the solar irradiance. However, its application has been significantly hampered by the slow diffusion of excited molecules in solid matrices. Here, we introduce metal-organic frameworks (MOFs) that promote TTA-UC by taking advantage of triplet exciton migration among fluorophores that are regularly aligned with spatially controlled chromophore orientations. We synthesized anthracene-containing MOFs with different molecular orientations, and the analysis of TTA-UC emission kinetics unveiled a high triplet diffusion rate with a micrometre-scale diffusion length. Surface modification of MOF nanocrystals with donor molecules and their encapsulation in glassy poly(methyl methacrylate) (PMMA) allowed the construction of molecular-diffusion-free solid-state upconverters, which lead to an unprecedented maximization of overall UC quantum yield at excitation powers comparable to or well below the solar irradiance.
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