RESUMEN
A series of carbon dots@exfoliated layered double hydroxides (CDs@LDH) composites were hydrothermally fabricated by Mg/Al LDH and formamide. The results of FTIR, UV-vis, and XPS spectra in company with HRTEM images showed that crystalline nano CDs formed on the single layer of LDH by Mg-C bond. With the increase of solvothermal reaction time from 2 to 6 h, the band gap and the binding energy of aminic and graphitic N species of CDs@LDH composites decreased, whereas the crystallinity increased. The fluorescence peaks of CDs@LDH composites could be deconvoluted into short-wavelength (416 nm) and large-wavelength (443 nm) components by Gaussian function, and the fluorescence intensities of both components enhanced with the extension of the solvothermal reaction time. The simultaneous enhancements of fluorescence lifetime and quantum yield resulted from the relatively high electron density in graphitic nitrogen of CDs@LDH, whereas the reduction of nonradiative rate was due to the high crystallinity in the carbon core of CDs@LDH. A strong exciton-lattice interaction also has been validated based on the excitation and emission spectra of CDs@LDH, so the fluorescence emission of CDs@LDH composite was heavily related to its crystalline carbon core and nitrogen-containing groups. CDs@LDH with high nitrogen-containing exhibited a superior detection property for Cu2+ ion sensing with the linear range of 26.90 ~ 192.20 µM and a limit of detection of 0.1957 µM. The photo-induced electron transfer (PET) process dominated the fluorescence quenching of CDs@LDH by Cu2+ ion since the fluorescence lifetime decreased with the increase of Cu2+ ion concentration.
RESUMEN
Two novel Eu(III) complexes constructed by maleopimaric acid anhydride (MPA) and 2,2'-bipyridyl (Bpy) / 1, 10-phenanthroline (Phen), named as MPA-Bpy-Eu / MPA-Phen-Eu, have been synthesized by a one-step precipitation method. FTIR, UV, TG, elemental analysis, XPS, and ESI-MS revealed the successful coordination of Eu(III) ions with MPA and Bpy / Phen through Eu-O and Eu-N bonds, respectively. Introducing MPA into coordinate structure increased the electron cloud density in 3d5/2 orbit of Eu(III) ions, enhanced the absolute quantum yields of MPA-Bpy-Eu (89.27%) and MPA-Phen-Eu (94.41%), and decreased the full width at half maxima of 5D0 â 7F2 transitions of MPA-Bpy-Eu (2.23 nm) and MPA-Phen-Eu (2.93 nm), respectively. The fluorescence quenching experiments showed that there was a good linear relationship between the relative fluorescence intensity of MPA-Bpy-Eu and gallic acid (GA) concentration in acetonitrile solution in the range of 0 to 8.41 × 10-2 mM. The results of UV-vis spectra, the fluorescence lifetimes, and the quantum yields demonstrated that the dynamic quenching model played a major role in the quenching process of GA on MPA-Bpy-Eu. The quenching process of GA on MPA-Phen-Eu involved dual fluorescence quenching mechanistic pathways, including static and dynamic models.
