Abstract

Chemical warfare agents are toxic chemicals that require rapid, easy‐to‐use, sensitive, and selective sensors to countermeasure. Simulants, such as dimethyl methyl phosphonate (DMMP), are used to test the effectiveness of sensors toward nerve agents. Metal organic frameworks (MOFs) offer large surface area and selective accessibility to active sites making them appealing for chemical sensing applications. In this work, we propose a fast, facile, direct synthesis method for manufacturing fluorescent MOFs with high sensitivity and selectivity. Zr‐BDC is synthesized with 1, 4‐benzenedicarboxylic acid (BDC) as an organic ligand and zirconium (Zr) metal. Fluorescent materials are then encapsulated in a novel and rapid in situ approach with strong solvents. X‐ray diffraction, UV–visible spectroscopy, Fourier‐transform infrared spectroscopy, and Raman spectroscopy are used to verify the successful formation of fluorescent MOFs. Compared to other methods, the gel synthesis method helps to control crystal growth leading to higher BET surface areas of ~1150 m2 g−1 for Zr‐BDC and 850 m2 g−1 for ZrQ@Zr‐BDC. Titration experiments show the sensitivity of the material to DMMP down to 8.3 nM with a highly linear response. Enhanced fluorescence and occupation of mesopores by ZrQ enable lower limit of detection than those of comparable works in literature. The encapsulation mechanism also prevents substantial defects that would otherwise lead to water adsorption.

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