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Appl. Sci. 2016, 6(10), 272; doi:10.3390/app6100272

Novel Luminescent Multilayer Films Containing π-Conjugated Anionic Polymer with Electronic Microenvironment

Beijing Key Laboratory of Materials Utilization of Nonmetallic Minerals and Solid Wastes, National Laboratory of Mineral Materials, School of Materials Science and Technology, China University of Geosciences, Beijing 100083, China
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Author to whom correspondence should be addressed.
Academic Editor: Giorgio Biasiol
Received: 1 August 2016 / Accepted: 19 September 2016 / Published: 27 September 2016
(This article belongs to the Section Materials)
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Abstract

Layered double hydroxides (LDHs), luminescent π-conjugated anionic polymer and montmorillonite (MMT) were orderly assembled into luminescent multilayer films via layer-by-layer self-assembly method. The electronic microenvironment (EME), the structure of which is like a traditional capacitor, can be constructed by exfoliated LDHs or MMT nanosheets. In addition, the rigid inorganic laminated configuration can offer stable surroundings between the interlayers. As a result, we conclude that EME can extend the luminescent lifespans of multilayer films substantially, due to affecting relaxation times of π-conjugated anionic polymer. Consequently, because of the remarkable impact on better photoemission behaviors of luminescent π-conjugated anionic polymer, EME assembled by LDHs or MMT nanosheets have had high hopes attached to them. They are expected to have the potential for designing, constructing, and investigating novel light-emitting thin films. View Full-Text
Keywords: thin films; luminescent; multilayers thin films; luminescent; multilayers
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This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. (CC BY 4.0).

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Wang, T.; Liu, M.; Ma, H. Novel Luminescent Multilayer Films Containing π-Conjugated Anionic Polymer with Electronic Microenvironment. Appl. Sci. 2016, 6, 272.

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