Abstract

In this work, the functionalization of ZnS quantum dots using the thiol group of l-cysteine for different concentrations has been reported. Chemical precipitation method was used for the synthesis of nascent as well as l-cysteine functionalized ZnS quantum dots for optimized values of pH and molar concentrations of the precursors. Morphological studies were done by X-ray diffraction (XRD) and TEM. Optical measurements were done by UV–visible, Fourier transform infrared (FTIR) and energy resolved photoluminescence studies. Particle size was calculated by using Brus equation. Appreciable changes in morphological and optical properties of ZnS quantum dots were observed in few cases. XRD results shows that, the primary crystallite size decreases with increasing the capping concentration, however, the crystal structure remain same for all the used concentrations of l-cysteine. UV–visible analysis shows that band gap and particle size is also tunable with l-cysteine capping. FTIR studies confirmed l-cysteine capping on the surface of quantum dots. As l-cysteine is non toxic and stable compound, the surface modification of ZnS quantum dots with l-cysteine not only prevents the aggregation of quantum dots but also make them available for the interaction with the target materials and make them suitable for specific biomedical applications.

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