染料-Er3+ 直接能量转移用于增强 10 纳米以下 NaErF4 的上转换和下转换发光能力

IF 11.3 1区 化学 Q1 CHEMISTRY, PHYSICAL ACS Catalysis Pub Date : 2024-11-12 DOI:10.1021/acs.nanolett.4c04539
Fei Zhao, Huan Ling, Wenrui Zhang, Yunxiang Zhang, Qian Liu
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引用次数: 0

摘要

染料敏化可通过改善光收集来增强镧系元素纳米粒子的发光效果。通常情况下,Yb3+ 可作为能量桥,但只在一个转变中吸收,由于光谱重叠的要求,染料的选择受到限制(λex > 700 nm)。相比之下,发射体 Er3+ 的能级跨度从紫外到近红外,因此非常适合多色激发。我们开发了一种使用氰基染料直接敏化 Er3+ 上转换发光(UCL)和下转换发光(DCL)的策略。与单独的纳米粒子(Er-NPs)相比,在 980 纳米激发下,Cy5 的增强效果最好,UCL 和 DCL 分别提高了 1942 倍和 70 倍。由于界面能量传递增强,较小的 Er-NPs 表现出更亮的染料敏化发光。2 nm 的惰性外壳能产生最亮的 UCL,而较厚的外壳则能改善 DCL。在 2H11/2 (525 nm) 和 2P3/2 (408 nm) 处的染料敏化 Er3+ 发射实现了温度监测,最大灵敏度 (Sa) 为 3.69%/K。这种方法在光学温度传感和医学成像方面具有巨大潜力。
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Dye-to-Er3+ Direct Energy Transfer for Enhancing Up- and Down-conversion Luminescence in Sub-10 nm NaErF4
Dye sensitization enhances the luminescence of lanthanide nanoparticles by improving light-harvesting. Typically, Yb3+ serves as an energy bridge but absorbs at a single transition, limiting dyes’ options (λex > 700 nm) due to the spectral overlap requirement. In contrast, the emitter Er3+ spans energy levels from UV to NIR, making it ideal for multicolor excitation. We developed a strategy to directly sensitize Er3+ upconversion (UCL) and downconversion luminescence (DCL) by using cyanine dyes. Cy5 demonstrated the greatest enhancement, achieving a 1942-fold UCL and 70-fold DCL increase compared to nanoparticles alone (Er-NPs) under 980 nm excitation. Smaller Er-NPs exhibited brighter dye-sensitized luminescence due to enhanced interfacial energy transfer. A 2 nm inert shell produced the brightest UCL, while thicker shells improved DCL. Dye-sensitized Er3+ emissions at 2H11/2 (525 nm) and 2P3/2 (408 nm) enabled temperature monitoring with a maximum sensitivity (Sa) of 3.69%/K. This approach holds significant potential for optical temperature sensing and medical imaging.
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来源期刊
ACS Catalysis
ACS Catalysis CHEMISTRY, PHYSICAL-
CiteScore
20.80
自引率
6.20%
发文量
1253
审稿时长
1.5 months
期刊介绍: ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels. The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.
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