Color tuning via adjusting the dye-loading capacity of a polymer

Color tuning from monomer emission to aggregate emission was accomplished by vacuum thermal evaporation of N,N'-di(n-butyl)quinacridone onto UV-cured photopolymer (NOA-63) with different exposure time. The diffusion of dye molecules into the polymer matrix can be controlled by varying the curin...

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Bibliographische Detailangaben
Veröffentlicht in:Langmuir : the ACS journal of surfaces and colloids. - 1985. - 25(2009), 8 vom: 21. Apr., Seite 4352-5
1. Verfasser: Hu, Wei (VerfasserIn)
Weitere Verfasser: Lu, Nan, Shi, Shoulei, Wang, Yandong, Wang, Yue, Cui, Zhanchen, Huang, Xiaohua, Liu, Yu, Xu, Miaojun, Chi, Lifeng
Format: Online-Aufsatz
Sprache:English
Veröffentlicht: 2009
Zugriff auf das übergeordnete Werk:Langmuir : the ACS journal of surfaces and colloids
Schlagworte:Journal Article
Beschreibung
Zusammenfassung:Color tuning from monomer emission to aggregate emission was accomplished by vacuum thermal evaporation of N,N'-di(n-butyl)quinacridone onto UV-cured photopolymer (NOA-63) with different exposure time. The diffusion of dye molecules into the polymer matrix can be controlled by varying the curing time, which induces the change in the mole ratio between the monomers that are molecularly dispersed into polymer and the aggregates that are shielded on the polymer surface. On the basis of this principle, dual-color and multicolor luminescence patterning were demonstrated by depositing dye molecules onto photolithographically patterned NOA-63 with binary masks and grayscale masks, respectively
Beschreibung:Date Completed 07.07.2009
Date Revised 15.04.2009
published: Print
Citation Status PubMed-not-MEDLINE
ISSN:1520-5827
DOI:10.1021/la900543g