Graphene Oxide-Supported Lanthanide Metal–Organic Frameworks with Boosted Stabilities and Detection Sensitivities

镧系元素 化学 金属有机骨架 双癸酸 荧光 水溶液 石墨烯 氧化物 复合数 光致发光 天线效应 纳米技术 化学工程 发光 物理化学 有机化学 材料科学 吸附 复合材料 光电子学 孢子 离子 工程类 物理 生物 量子力学 植物
作者
Yuan-Jun Tong,Lu-Dan Yu,Jiating Zheng,Guifeng Liu,Yu‐Xin Ye,Siming Huang,Guosheng Chen,Huangsheng Yang,Cheng Wen,Songbo Wei,Jianqiao Xu,Fang Zhu,Janusz Pawliszyn,Gangfeng Ouyang
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:92 (23): 15550-15557 被引量:43
标识
DOI:10.1021/acs.analchem.0c03562
摘要

The photoluminescent (PL) properties of lanthanide metal–organic frameworks (Ln-MOFs) are intrinsically subtle to water molecules, which remains the major challenge that severely limits their applications as fluorescent probes in aqueous samples. Herein novel composite fluorescent probes were prepared by growing Ln-MOFs (Tb-MOF, Eu-MOF, and Tb/Eu-MOF) on carboxylated porous graphene oxide (PGO-COOH). The 3D thorny composites presented significantly longer fluorescent lifetimes and higher quantum yields than that of the bare Ln-MOFs and exhibited long-term PL stabilities in aqueous samples up to 15 days. The stable and improved PL properties demonstrated that the highly hybrid composite structures protected the MOF components from the adverse effects of water. Furthermore, the unexpected antenna effect of the PGO-COOH substrate on Ln3+ was supposed to be another reason for the improved PL properties. The composites present ultralow detection limits as low as 5.6 nM for 2,4-dinitrotoluene and 2.3 nM for dipicolinic acid as turn-off and ratiometric fluorescent probes, respectively, which was attributed to the incoporation of PGO-COOH that dramatically enahnced inner filter effects and effectively protected the energy transfer process in the MOF components from the interference of the surrounding water. This work presents an effective strategy for creating ultrasensitive and stable fluorescent probes based on Ln-MOFs for applications in aqueous samples.
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