Solid State Multicolor Emission in Substitutional Solid Solutions of Metal-Organic Frameworks

被引:77
|
作者
Newsome, Wesley J. [1 ]
Ayad, Suliman [2 ]
Cordova, Jesus [1 ]
Reinheimer, Eric W. [3 ]
Campiglia, Andres D. [1 ]
Harper, James K. [1 ]
Hanson, Kenneth [2 ]
Uribe-Romo, Fernando J. [1 ]
机构
[1] Univ Cent Florida, Dept Chem, 4111 Libra Dr,Room 251 PSB, Orlando, FL 32816 USA
[2] Florida State Univ, Dept Chem & Biochem, 95 Chieftan Way, Tallahassee, FL 32306 USA
[3] Rigaku Americas Corp, 9009 New Trails Dr, The Woodlands, TX 77381 USA
基金
美国国家科学基金会;
关键词
PROTON-TRANSFER ESIPT; WHITE-LIGHT EMISSION; FUNCTIONAL-GROUPS; FULL-COLOR;
D O I
10.1021/jacs.9b05191
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Preparing crystalline materials that produce tunable organic-based multicolor emission is a challenge due to the inherent inability to control the packing of organic molecules in the solid state. Utilizing multivariate, high-symmetry metal-organic frameworks, MOFs, as matrices for organic-based substitutional solid solutions allows for the incorporation of multiple fluorophores with different emission profiles into a single material. By combining nonfluorescent links with dilute mixtures of red, green, and blue fluorescent links, we prepared zirconia-type MOFs and found that the bulk materials exhibit features of solution-like fluorescence. Our study found that MOFs with a fluorophore link concentration of around 1 mol % exhibit fluorescence with decreased inner filtering, demonstrated by changes in spectral profiles, increased quantum yields, and lifetime dynamics expected for excited-state proton-transfer emitters. Our findings enabled us to prepare organic-based substitutional solid solutions with tunable chromaticity regulated only by the initial amounts of fluorophores. These materials emit multicolor and white light with high quantum yields (similar to 2-14%), high color-rendering indices (>93), long shelf life, and superb hydrolytic stability at ambient conditions.
引用
收藏
页码:11298 / 11303
页数:6
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