分子内力
调制(音乐)
期限(时间)
电荷(物理)
传输(计算)
化学物理
化学
生物物理学
材料科学
物理
计算机科学
声学
立体化学
生物
量子力学
并行计算
作者
Fangfang Xiao,Da Lei,Chaogan Liu,Yushu Li,Wenfei Ren,Ji‐Guang Li,Dezhong Li,Baiyi Zu,Xincun Dou
标识
DOI:10.1002/anie.202400453
摘要
Abstract Aggregation‐induced emission (AIE) shows promising performance in chemical sensing relying on the change of the emission behavior of the probe molecule monomers to the aggregated product. However, whether the response contrast could be further boosted by utilizing the emission property of the aggregated probe and the aggregated product remains a big challenge. Here, an exciting AIE probe regulation strategy was proposed by coherently modulating the aggregation behavior and the intramolecular charge transfer (ICT) property of the probes and thus an aggregated‐to‐aggregated colorimetric‐fluorescent dual‐mode detection was achieved. The blue emissive film obtained with the optimal AIE probe has been proven to be effective to recognize the vapor of nerve agent analog DCP in air by emitting a sharp green fluorescence. In addition, a porous polymer‐based wet sensing chip loaded with the probe enables the immediate response to DCP vapor with a limit of detection (LOD) of 1.7 ppb, and it was further integrated into a wearable watch device for long‐term monitoring of DCP vapor up to two weeks. We expect the present probe design strategy would greatly deepen the AIE‐based science and provide new insights for long‐term monitoring sensors toward trace hazardous substances.
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