Thin-film formation for promoting the potential of luminescent lanthanide coordination complexes

被引:19
|
作者
Hasegawa, Miki [1 ,2 ]
Ishii, Ayumi [2 ,3 ,4 ]
机构
[1] Aoyama Gakuin Univ, Dept Chem & Biol Sci, Coll Sci & Engn, Chuo Ku, 5-10-1 Fuchinobe, Sagamihara, Kanagawa 2525258, Japan
[2] Aoyama Gakuin Univ, Mirai Mol Mat Design Inst, Coll Sci & Engn, Chuo Ku, 5-10-1 Fuchinobe, Sagamihara, Kanagawa 2525258, Japan
[3] Toin Univ Yokohama, Grad Sch Engn, Aoba Ku, 1614 Kurogane Cho, Yokohama, Kanagawa 2258503, Japan
[4] Japan Sci & Technol Agcy JST, Precursory Res Embryon Sci & Technol PRESTO, 4-1-8 Honcho, Kawaguchi, Saitama 3320012, Japan
关键词
Lanthanide compounds; Luminescence; Interfacial complexation; Film formation; Core-shell nanoparticles; LANGMUIR-BLODGETT-FILMS; OPTICAL WAVE-GUIDE; UP-CONVERSION LUMINESCENCE; EXCITATION-ENERGY TRANSFER; GAS-SENSING PROPERTIES; RARE-EARTH COMPLEXES; LB FILMS; PHOTOELECTRIC CONVERSION; POLARIZED EMISSION; EUROPIUM COMPLEX;
D O I
10.1016/j.ccr.2020.213458
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Molecular thin films that are periodically layered and core-shell type nanoparticles with interfacial coordination are observed in lanthanide complexes via organic photo-antennae. The layer structures of Eu complexes induced the linearly polarized luminescence (LPL) of ff-transitions by using the Langmuir-Blodgett technique. The aforementioned was achieved due to the independent existence of Eu and the interpretation of the transition dipole moment localized on chromophores in the layers. The chain structure of the complexes was sequentially deposited on the substrates, but exhibited no LPL due to the formation of dome-like chain aggregates. The interfacial coordination can adopt various combinations of nanoparticles (e.g., SiO2, TiO2, and Ln(2)O(3)) with different lanthanides and various types of organic shells to induce upconversion even with low-power light or efficient photomultiplying photodetection. The divalent Eu ion demonstrated high stability. (C) 2020 Elsevier B.V. All rights reserved.
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页数:17
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