LiYF4: Yb3+, Ho3+, Ce3+@ 碳量子点复合材料的一步制备及双模发光防伪应用

IF 3.6 3区 物理与天体物理 Q2 OPTICS
Jiantao Lü , Jie Liang , Ting Fan , Yayun Zhou , Tingting Deng , Wenqiang Li
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引用次数: 0

摘要

在荧光防伪领域,单一发光模式的材料容易被伪造,无法满足当前的防伪要求。目前报道的双模发光材料通常需要多步繁琐的合成步骤。本文采用一步水热法制备了 LiYF4:Yb3+、Ho3+、Ce3+ 上转换微米粒子(UCMPs)/碳量子点(CDs)复合材料,大大简化了 CDs 和 UCMPs 的复合工艺。通过改变 Ce3+ 离子的掺杂浓度,可以实现上转换波长(从绿光到 980 纳米激发的红光)。通过 CD 和 UCMPs 的结合,实现了明显的双模发光现象。最后,利用丝网印刷技术制作出三叶草图案,实现了在 365 nm 和 980 nm 激发下的多色发光。这种新型荧光防伪复合材料采用简单环保的一步法合成工艺,有望推动荧光防伪领域的发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

One-step preparation and dual mode luminescence anti-counterfeiting application of LiYF4: Yb3+, Ho3+, Ce3+@ carbon quantum dot composite materials

One-step preparation and dual mode luminescence anti-counterfeiting application of LiYF4: Yb3+, Ho3+, Ce3+@ carbon quantum dot composite materials

In the field of fluorescent anti-counterfeiting, materials with single luminous mode are easy to be forged, which cannot meet the current anti-counterfeiting requirements. Currently reported bimodal light-emitting materials usually require multi-step and tedious synthesis steps. In this paper, LiYF4: Yb3+, Ho3+, Ce3+ upconversion micron particles (UCMPs)/carbon quantum dots (CDs) composite materials were prepared by one-step hydrothermal method, which greatly simplified the composite process of CDs and UCMPs. The upconversion wavelength (from green light to red light excited by 980 nm) can be achieved by changing the doping concentration of Ce3+ ions. Through the combination of CDs and UCMPs, an obvious dual mode luminescence phenomenon was achieved. Finally, screen printing was used to produce a clover pattern, which realized multi-color luminescence under 365 nm and 980 nm excitations respectively. The new fluorescence anti-counterfeiting composites, which uses simple and environmentally friendly one-step synthesis process, is expected to promote the development of fluorescence anti-counterfeiting field.

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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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