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Label-free fluorescence platform based on SiO2-coated CdTeS quantum dots for trace analysis of Ag+ in environmental water.
Xiao, Junhui; Yao, Wen; Yan, Dongxu; Yang, Jie; Qiu, Ziyin; Wang, Lishi; Guo, Xinrong.
Afiliação
  • Xiao J; Dongguan Key Laboratory of Public Health Laboratory Science, School of Public Health, Guangdong Medical University, Dongguan, 523808, China; School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, 510641, China.
  • Yao W; Dongguan Key Laboratory of Public Health Laboratory Science, School of Public Health, Guangdong Medical University, Dongguan, 523808, China.
  • Yan D; School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, 510641, China.
  • Yang J; Dongguan Key Laboratory of Public Health Laboratory Science, School of Public Health, Guangdong Medical University, Dongguan, 523808, China.
  • Qiu Z; School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, 510641, China.
  • Wang L; School of Chemistry and Chemical Engineering, South China University of Technology, Guangzhou, 510641, China. Electronic address: wanglsh@scut.edu.cn.
  • Guo X; Dongguan Key Laboratory of Public Health Laboratory Science, School of Public Health, Guangdong Medical University, Dongguan, 523808, China. Electronic address: guoxinr@gdmu.edu.cn.
Talanta ; 278: 126469, 2024 Oct 01.
Article em En | MEDLINE | ID: mdl-38944942
ABSTRACT
In this study, a core-shell structural nano-composite material, namely CdTeS@SiO2, is synthesized by a simple silanization of Te-doped CdS quantum dots (CdTeS QDs). Through SiO2 capping, CdTeS QDs not only improve the fluorescence performance effectively, but also greatly enhance the anti-interference ability in the environment. Based on its excellent optical properties, a novel fluorescence sensor is constructed for the ultramicro detection of Ag+. The fluorescence of CdTeS@SiO2 is strongly quenched in the presence of Ag+ and shows good linearity in the range of 0.005-5.0 µmol L-1 with a detection limit as low as 1.6 nmol L-1. This is mainly due to its unique quenching mechanism Ag+ destroys the spherical structure of SiO2 and promotes the formation of non-radiative electron-hole pairs through electron transfer, leading to fluorescence quenching. At the same time, it competes with Cd for Te, S and MPA on the CdTeS surface, forming Ag-Te, Ag-S and Ag-MPA complexes attached to the CdTeS surface leading to wavelength red-shift. The feasibility of the proposed sensor is demonstrated through spiking experiments, which confirmed the potential value of the constructed fluorescence probe for real-world applications in detecting Ag+ in environmental water.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2024 Tipo de documento: Article