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CERAMICS INTERNATIONAL · 2024 ·Vol. 51 ·期 12 ·16749-16757 · IF 5.1

Doping lanthanides towards improvement in self-trapped excitons emission and multiple emission color of Cs2KInCl6 double perovskites

Yihan Liu,Yingjie Mao,Zhichao Zhang,Kai Liu,Denghui Xu,Jun Zhou

Lead-free double perovskites (DPs), characterized by their low toxicity, broad emission spectra and excellent stability, have emerged as highly promising doped hosts with significant potential for visible light applications. However, achieving rich and distinctive multiple photoluminescent (PL) emission through doping with various lanthanide (Ln 3+ ) ions remains a formidable challenge. In this work, we explored the luminescent properties of Cs 2 KInCl 6 , which exhibits intrinsic broad self-trapped excitons (STEs) emission centered at 500 nm. By doping Ln 3+ ions (Dy 3+ , Sm 3+ , and Tb 3+ ) into Cs 2 KInCl 6 , multiple emission could be realized, along with energy transfer (ET) from the intrinsic STEs to Tb 3+ and Sm 3+ ions. Notably, the incorporation of Tb 3+ ions enhanced exciton-phonon coupling and lattice vibrations , resulting in strengthened STEs emission. Furthermore, tunable emission from green to yellow was achieved through multiple ET processes in Cs 2 KInCl 6 :Tb 3+ ,Sm 3+ by co-doping Tb 3+ and Sm 3+ . This work not only offers new insights into enhancing STEs emission in DPs, but also imparts Cs 2 KInCl 6 with tunable PL properties, which makes it a promising candidate for multicolor light-emitting devices.

研究领域: 材料科学 · 光物理学 · 无机化学 · 发光材料 · 半导体材料
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Advanced Optical Materials · 2021 ·Vol. 10 ·期 3 ·2101843 · IF 9.926

Programmable Broadband Responsive Lanthanide-Doped Nanoarchitecture for Information Encryption

Ziyu Chen,Jiaxin Yang,Rui Xu,Zejia Zhao,Xu Sang,Lisa Liu,Ming Feng,Feng Song,Yonghong He,Wei Huang

Optical encryption provides a significant implementation strategy for information security, which can be ascribed to multichannel, simple operation, and high security. Multiple responsive luminescent material has emerged as an ideal candidate for optical encryption, owing to intelligent responsive ability and unclonable security. Herein, a structural doping strategy is developed in the layer-by-layer self-assembly process to elevate the maneuverability of light-emitting color and mode. By encapsulating lanthanide doped inorganic matrix and layered hydroxide with PMA, the recognizable red-orange fluorescence can be produced in the invisible region, and realizes the conversion of yellow and green fluorescence in visible region. Meanwhile, both excitation source and emission color can be used as distinguishable encryption means, which enables structural doping complex to be multiplexed and encoded with high capacity and complexity. Furthermore, asymmetrically and symmetrically coded flexible labels with specific color sequence are prepared by brushing process, and specific encryption key are set to ensure the nonlinearity of cryptosystem. Through the integration of dual-mode and adjustable light response codes constructed by structural doping strategy, multidimensional high-level information encryption can be realized, which opens up a deep exploration in the field of information security for the application of multifunctional optical properties of light response materials.

研究领域: 材料科学 · 纳米科技 · 光学工程 · 信息安全 · 功能材料 · 光子学 · 智能材料
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JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2015 · IF 3.368

Photofunctional hybrids of lanthanide functionalized bio-MOF-1 for fluorescence tuning and sensing

Xiang Shen,Bing Yan

A series of luminescent Ln 3+ @bio-MOF-1 (Ln   =   Eu, Tb, bio-MOF-1   =   Zn 8 (ad) 4 (BPDC) 6 O⋅2Me 2 NH 2 (ad   =   adeninate, BPDC   =   biphenyldicarboxylate)) are synthesized via postsynthetic cation exchange by encapsulating lanthanide ions into an anionic metal–organic framework (MOF), and their photophysical properties are studied. After loading 2-thenoyltrifluroacetone (TTA) as sensitized ligand by a gas diffusion (“ship-in-bottle”) method, it is found that the luminescent intensity of Eu 3+ is enhanced. Especially, when loading two different lanthanide cations into bio-MOF-1, the luminescent color can be tuned to close white (light pink) light output. Additionally, bio-MOF-1 and Eu 3+ @bio-MOF-1 are selected as representative samples for sensing metal ions . When bio-MOF-1 is immersed in the aqueous solutions of different metal ions , it shows highly sensitive sensing for Fe 3+ as well as Eu 3+ @bio-MOF-1 immersed in the DMF solutions of different metal ion. The results are benefit for the further application of functionalized bio-MOFs in practical fields.

研究领域: 无机化学 · 材料科学 · 分析化学 · 纳米生物技术 · 光物理学 · 配位化学
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CHEMICAL ENGINEERING JOURNAL · 2023 · IF 15.1

Upconverted luminescence from lanthanide-doped ferroelectrics for optical storage and triple-mode temperature probing

Haisheng Chen,Wenwen Chen,Jiaying Shen,Xiaona Du,Tianhong Zhou,Zhengang Dong,Taiyu Bian,Jiaxing Guo,Yiyang Wen,Yuanlin Liang,Zhenping Wu,Yang Zhang

Developing smart luminescent materials with desirable and tunable characteristics has always been an overriding priority of fluorescence technology. However, huge challenges encompass the single functionality of the luminescent materials and the traditional chemical synthetic techniques with rigorously controlling over the miscellaneous experimental conditions and variables. Herein, the lanthanide-doped bismuth-layered ferroelectric (Na 0.5 Bi 0.5 ) 0.96 Er 0.04 Bi 2 Nb 2 O 9.02 has been prepared to be utilized as a platform that not only serves the in-situ and reversible tailoring of the upconverted emission via physical methods, but also enable the versatile functionalities such as photomemory and multi-modal temperature sensing. High luminescent contrast that can reach up to 83.7 % before and after the 405 nm irradiation has been realized on the basis of the photochromic phenomenon of the as-prepared (Na 0.5 Bi 0.5 ) 0.96 Er 0.04 Bi 2 Nb 2 O 9.02 sample, and the fundamental application in the photomemory has been exhibited. Moreover, the performances of triple-mode thermometry built on the fluorescent intensity ratio techniques ( 2 H 11/2 / 4 S 3/2 and 4 S 3/2 / 4 F 9/2 ) as well as the lifetime of the 4 S 3/2 excited state of the Er 3+ ion have been investigated in carefulness, with the maximal relative sensitivities of 1.22 % K −1 at 300 K, 0.92 % K −1 at 510 K, and 0.18 % K −1 at 450 K, respectively. Our results provide significant insights into the methodology of physically modulating the upconversion luminescence, and offer a glamorous pathway for multifunctional high-end applications.

研究领域: 材料科学 · 光学工程 · 功能材料 · 纳米光子学 · 传感技术 · 固态物理 · 智能材料
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