Abstract

Multicolor ZnO quantum dots (QDs) were synthesized and further modified with hydrophobic hexadecyltrimethoxysilane (HDS) and then hydrophilic aminopropyltriethoxysilane (APS) bilayers, resulting in amine-functionalized ZnO@HDS@APS nanocomposites with tunable fluorescence from blue to green yellow. Systematic investigations verify that the resulting ZnO@HDS@APS could display extremely high stability in aqueous media and unexpectedly, dramatically-enhanced fluorescence intensities, which are about 10-fold higher than those of bare ZnO QDs. The feasibility of the as-prepared ZnO nanocomposites for blood, cell, and tissue imaging was preliminarily demonstrated, promising the wide bio-applications for cell or tissue imaging, proteome analysis, drug delivery, and molecular labeling.

Highlights

  • Multicolor ZnO quantum dots (QDs) were synthesized and further modified with hydrophobic hexadecyltrimethoxysilane (HDS) and hydrophilic aminopropyltriethoxysilane (APS) bilayers, resulting in amine-functionalized ZnO@HDS@APS nanocomposites with tunable fluorescence from blue to green yellow

  • Here, a bi-silanization modification route was conducted for multicolor ZnO QDs

  • Multicolor ZnO QDs were initially synthesized by the modified sol-gel route of ultrasonic chemistry at 0uC with varying [LiOH]/[Zn21] ratios

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Summary

Results

The surface silanization route has been currently employed to modify ZnO QDs, but showing the stable luminescence in non-aqueous media or organic solution only[16,30]. The developed bi-silanization strategy was employed for the modification of several kinds of multicolor ZnO QDs, which were synthesized at varying [LiOH]/[Zn21] ratios of 2.5, 2.1, 1.7, 1.3, and 1.0 in ethanol, resulting in functionalized ZnO@ HDS@APS nanocomposites with tunable fluorescence from blue to green yellow (see Fig. 7). The resulting functionalized ZnO@HDS@APS nanocomposites could present tunable fluorescence from blue to green yellow They could enjoy aqueous ultrastability and surface functionalization and unexpectedly, the dramatically-enhanced fluorescence intensities, which are about 10 times higher than those of bare ZnO QDs. The topological structure and composition changes and optical performances of the as-prepared ZnO@HDS@APS in ethanol and water were systematically demonstrated versus ZnO QDs by using TEM imaging, XRD, IR spectra, UV-vis spectra, and fluorescence spectra. Such a facile bi-silanization route should be extended for the modification of varying nanomaterials like a variety of QDs to enhance their fluorescence, surface functionalization, and aqueous stability for the optical and biological applications on a large scale

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