材料科学
荧光
检出限
纳米技术
调制(音乐)
共价键
多孔性
聚合物
光电子学
费斯特共振能量转移
工作(物理)
共价有机骨架
探测器
金属有机骨架
冷凝
生物传感器
分析物
极限(数学)
表面改性
选择性
纳米颗粒
作者
Jin Yu,Hong Chang,Wendan Luo,Liping Ding,Taihong Liu,Yu Fang
标识
DOI:10.1002/adom.202502848
摘要
Abstract A majority of 2D covalent organic frameworks (COFs) exhibit weak fluorescence in the solid state, and achieving precise donor‐ π ‐acceptor (D‐ π ‐A) strength modulation for high‐performance fluorescence sensing remains a significant challenge. Herein, four fluorescent nanofilms are rationally prepared through an interfacial dynamic condensation strategy. An atomically precise approach is demonstrated to tune D‐ π ‐A strength by incorporating diverse electron‐withdrawing acceptors, which feature different numbers of N ‐heterocyclic atoms and a tailored microenvironment. Beneficial from their high porosity and large surface area, the nanofilms afford channels for rapid mass transfer and abundant responsive nitrogen sites, which in turn realize highly efficient fluorescence detection of a sarin mimic, diethyl chlorophosphate (DCP). Leveraging the key laminated sensor component developed in Fang's group, a detector prototype is integrated and applied to detect DCP selectively and reversibly. It features the merits of rapid turn‐on response (3.0 s), ultrasensitive detection limit (0.066 ppt), and excellent reversibility (55 cycles). Based on the dynamic responses, effective discrimination between DCP and acid interferents can be achieved. This work not only presents a strategy for modulating D‐ π ‐A strength in interfacial nanofilms to achieve turn‐on and ultrasensitive fluorescence detection, but also paves the way for reliable on‐site and real‐time monitoring of nerve agents.
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