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Carbon nanospheres with dual-color emission and their application in ratiometric pyrophosphate sensing.
Wang, Zhong-Xia; Gao, Yuan-Fei; Yu, Xian-He; Kong, Fen-Ying; Wang, Wen-Juan; Lv, Wei-Xin; Wang, Wei.
Affiliation
  • Wang ZX; School of Chemistry and Chemical Engineering, Yancheng Institute of Technology, Yancheng 224051, China. wangw@ycit.edu.cn.
Analyst ; 144(2): 550-558, 2019 Jan 14.
Article in En | MEDLINE | ID: mdl-30411742
ABSTRACT
Herein, we employ pH-dependent solubility equilibrium to develop the one-pot aqueous synthesis of dual-color emission fluorescent carbon nanosphere (DFCSs) with novel physicochemical properties. Unexpectedly, some of the DFCSs have a regular nanosphere shape, containing uniform carbon dots (∼20 nm) on their surface. This may be attributed to the change in the surface composition of the carbon nanospheres under the strong alkaline conditions (pH 13), which results in dual-wavelength emission by single-wavelength excitation. Interestingly, the fluorescence intensities of the two emission peaks of the DFCSs at 315/410 nm can be simultaneously quenched upon the addition of Co2+ due to the strong coordination between Co2+ and the O-containing luminescent groups from the carbon dots and DFCSs. Also, the results demonstrate that one Co2+ simultaneously combines with two chromophoric groups. Furthermore, the quenched DFCSs exhibit high sensitivity for pyrophosphate (PPi) in the range of 0.075-200.0 µM through a fluorescence recovery process, which can be attributed to the stronger Co2+-O[double bond, length as m-dash]P bond. This results in the removal of Co2+ from the surface of DFCSs-Co2+ system via competitive adsorption interactions. Meanwhile, this sensor shows high selectivity for PPi over mercapto amino acid and phosphate in aqueous solution. These results indicate the DFCSs can act as a dual-signal PPi-selective sensor via a ratiometric competitive mechanism.

Full text: 1 Database: MEDLINE Language: En Year: 2019 Type: Article

Full text: 1 Database: MEDLINE Language: En Year: 2019 Type: Article