Selective Probing of Gaseous Ammonia Using Red-Emitting Carbon Dots Based on an Interfacial Response Mechanism

被引:63
作者
Jiang, Bang-Ping [1 ]
Zhou, Bo [1 ]
Shen, Xing-Can [1 ]
Yu, Yun-Xiang [1 ]
Ji, Shi-Chen [1 ]
Wen, Chang-Chun [1 ]
Liang, Hong [1 ]
机构
[1] Guangxi Normal Univ, Sch Chem & Pharmaceut Sci, Key Lab Chem & Mol Engn Med Resources, Minist Educ, Guilin 541004, Peoples R China
关键词
carbon dots; gaseous ammonia; red-emitting fluorescence; sensing mechanism; solid-state fluorescence sensing; surface chemistry; LABEL-FREE DETECTION; FLUORESCENT SENSING PLATFORM; RESONANCE ENERGY-TRANSFER; GRAPHENE QUANTUM DOTS; FULL-COLOR EMISSION; ONE-STEP SYNTHESIS; ONE-POT SYNTHESIS; HYDROTHERMAL TREATMENT; NANODOTS; GREEN;
D O I
10.1002/chem.201502731
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Solid-state fluorescence sensing is one of the most appealing detection techniques because of its simplicity and convenience in practical operation. Herein, we report the development of a red-emitting carbon dots (RCDs)-based material as a solid-state fluorescence sensor for the selective probing of gaseous ammonia. The RCDs were prepared by a low-cost, one-step carbonization method using sugar cane bagasse as the carbon precursor. The pristine RCDs were then directly coated on polyvinylidene fluoride membrane to produce a new fluorescence sensor capable of selectively distinguishing toxic gaseous ammonia from other analyte vapors through sensitive fluorescence quenching with a low detection limit. More importantly, the interfacial response mechanism occurring on the surface of the RCDs has been studied by X-ray photoelectron spectroscopy, Fourier-transform infrared spectroscopy, and Raman measurements. The results indicate that fluorescence quenching in the RCDs might result from ammonia-induced Michael addition through insertion of N into the C=C group and deprotonation of the carboxyl group. To the best of our knowledge, this is the first report that provides clear insight into the mechanism of surface chemistry on CDs in the solid state.
引用
收藏
页码:18993 / 18999
页数:7
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