显色的
化学
丙酮
检出限
光化学
分析物
产量(工程)
肉眼
辐照
激进的
级联
色谱法
有机化学
材料科学
物理
核物理学
冶金
作者
Jingkai Liang,Hua Li,Junren Wang,Haili Yu,Yi He
标识
DOI:10.1021/acs.analchem.0c00149
摘要
The signal of the traditional chromogenic systems is directly proportional to analyte concentration, leading to an unsatisfactory sensitivity. Herein, we report a cascade chromogenic system to realize exponential amplification of colorimetric signal through coupling chemical oxidation with photoinduced radical chain reaction. The chemical oxidation of o-phenylenediamine (OPD) by Fe3+ generates Fe2+ and photoactive 2,3-diaminophenazine (DAP). Under blue-light irradiation, DAP initiates the formation of holes and H2O2 that reacts with Fe2+ to hydroxyl radicals (·OH) and Fe3+ via an intersystem crossing (ISC) process. Moreover, the holes oxidize water to yield ·OH as well. The resulting ·OH and regenerated Fe3+ in turn oxidize OPD to yield more DAP, leading to a self-propagating reaction cycle that continues to proceed until all the OPD molecules are consumed, along with a distinct color change from colorless to yellow. Through the generation of the complex between DAP and acetone that limits the ISC process, and therefore quenches the colorimetric signal, the highly sensitive and selective naked-eye detection of acetone is achieved from 50 μM to 3 mM, with a limit of detection of 35 μM. Additionally, the feasibility of this colorimetric assay to detect acetone in real water samples is also demonstrated.
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