Surfactant assisted surface studies of zinc sulfide nanoparticles
• Polydisperse ZnS nanoparticles are successfully synthesized by chemical route using CTAB as a surfactant. • CTAB does not influence the crystal structure of ZnS nanoparticles but the lattice contraction occurs between the Zn–S. • PL emissions are observed around 387, 410, 489, and 528nm. All these...
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Published in | Applied surface science Vol. 257; no. 23; pp. 9846 - 9851 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier B.V
15.09.2011
Elsevier |
Subjects | |
Online Access | Get full text |
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Summary: | • Polydisperse ZnS nanoparticles are successfully synthesized by chemical route using CTAB as a surfactant. • CTAB does not influence the crystal structure of ZnS nanoparticles but the lattice contraction occurs between the Zn–S. • PL emissions are observed around 387, 410, 489, and 528nm. All these transitions correspond to surface vacancies and defect states. • Raman peaks at 320, 615, and 700cm−1 are found. These are observed due to surface phonon mode.
We report a simple soft chemical method for the synthesis of ZnS nanoparticles using varying concentration of cationic surfactant CTAB and examine its surface properties. Powder X-ray diffraction, UV–vis spectroscopy, photoluminescence spectroscopy, selective area electron diffraction, and transmission electron microscopy are used to characterize the as prepared ZnS nanoparticles. XRD and TEM measurements show the size of polydispersed ZnS nanoparticles is in the range of 2–5nm with cubic phase structure. The photoluminescence spectrum of ZnS nanoparticles exhibits four fluorescence emission peaks centered at 387nm, 412nm, 489nm and 528nm showing the application potential for the optical devices. In Raman spectra of ZnS nanoparticles, the modes around 320, 615 and 700cm−1 are observed. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 |
ISSN: | 0169-4332 1873-5584 |
DOI: | 10.1016/j.apsusc.2011.06.046 |