• Sharma, J. K.
• Dhupar, Anu
• Sharma, Vandana
• Kumar, Suresh

Abstract

<jats:title>Abstract</jats:title><jats:p>In the present work, mixed structure Zn(S,O) nanoparticles have been synthesized using solution based chemical coprecipitation technique. Two different zinc sources (Zn(CH<jats:sub>3</jats:sub>COO)<jats:sub>2</jats:sub>·2H<jats:sub>2</jats:sub>O and ZnSO<jats:sub>4</jats:sub>·7H<jats:sub>2</jats:sub>O) and one sulfur source (CSNH<jats:sub>2</jats:sub>NH<jats:sub>2</jats:sub>) have been used as primary chemical precursors for the synthesis of the nanoparticles in the presence and absence of a capping agent (EDTA). The structural, morphological, compositional and optical properties of the nanoparticles have been analyzed using X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), Fourier transmission infra-red (FT-IR) and UV-Visible (UV-Vis) spectroscopy. XRD revealed the formation of mixed phases of c-ZnS, h-ZnS and h-ZnO in the synthesized nanoparticles. The surface morphology was analyzed from SEM micrographs which showed noticeable changes due to the effect of EDTA. EDX analysis confirmed the presence of zinc, sulfur and oxygen in Zn(S,O) nanoparticles. FT-IR spectra identified the presence of characteristic absorption peaks of ZnS and ZnO along with other functional group elements. The optical band gap values were found to vary from 4.16 eV to 4.40 eV for Zn(S,O) nanoparticles which are higher in comparison to the band gap values of bulk ZnS and ZnO. These higher band gap values may be attributed to the mixed structure of Zn(S,O) nanoparticles.</jats:p>

Topics

• nanoparticle
• surface
• phase
• scanning electron microscopy
• x-ray diffraction
• Oxygen
• zinc
• Energy-dispersive X-ray spectroscopy