用水解缩聚的 3-aminopropyltriethoxysilane 对 1,2,4-三氨基苯分子进行改性,从而增强其光致发光性能

IF 3.3 3区 物理与天体物理 Q2 OPTICS Journal of Luminescence Pub Date : 2024-11-09 DOI:10.1016/j.jlumin.2024.120980
Haowei Tan, Yoshiki Iso, Tetsuhiko Isobe
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引用次数: 0

摘要

在水中具有更长波长和更高光致发光量子产率(PLQY)的小分子染料因其在荧光分析技术中的巨大潜力而日益受到关注。在这里,用 3-aminopropyltriethoxysilane (APTES) 修饰了 1,2,4-三氨基苯(TriAB)红色发光荧光染料,以避免与水分子接触,并抑制水中 O-H 振动引起的荧光淬灭。X 射线衍射仪和傅立叶变换红外吸收光谱证实了水解缩聚 APTES 形成了类似二氧化硅的结构。用水解缩聚 APTES 对 TriAB 进行改性后,粉末状态下会发出橙色荧光,而在改性之前 TriAB 粉末并未发出任何荧光。APTES 改性后的 TriAB 在水中的 PLQY 为 11.1%,高于 TriAB 在水中的 4.5%。这些结果证实,APTES 衍生的类二氧化硅基质可屏蔽 TriAB 与水以及与其他 TriAB 分子之间的分子间相互作用,从而克服荧光淬灭。
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Photoluminescence enhancement of 1,2,4-triaminobenzene molecules by modification with hydrolytically polycondensed 3-aminopropyltriethoxysilane
Small-molecule dyes with longer wavelength and higher photoluminescence quantum yield (PLQY) in water have attracted increasing attention due to their bright potential in fluorescence analysis technologies. Here, a red-emitting fluorescent dye of 1,2,4-triaminobenzene (TriAB) was modified with 3-aminopropyltriethoxysilane (APTES) to avoid contact with water molecules and to suppress fluorescence quenching due to O-H vibrations in water. The formation of a silica-like structure from hydrolytically polycondensed APTES was confirmed by X-ray diffractometry and Fourier-transform infrared absorption spectroscopy. Modification of TriAB with hydrolytically polycondensed APTES induced orange emission in the powder state, although TriAB powder did not exhibit any fluorescence before modification. The PLQY of APTES-modified TriAB in water was 11.1 %, which was higher than that of TriAB in water, 4.5 %. These results confirmed that the APTES derived silica-like matrix shielded TriAB from both water and intermolecular interactions with other TriAB molecules, overcoming fluorescence quenching.
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来源期刊
Journal of Luminescence
Journal of Luminescence 物理-光学
CiteScore
6.70
自引率
13.90%
发文量
850
审稿时长
3.8 months
期刊介绍: The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid. We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.
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