Ex situ synthesis and optical properties of ZnO-PbS nanocomposites
- Authors
- Ntwaeaborwa, O. M.; Kroon, R. E.; Kumar, V.; Dubroca, T.; Ahn, J. -P.; Park, J. -K.; Swart, H. C.
- Issue Date
- 2009-11
- Publisher
- PERGAMON-ELSEVIER SCIENCE LTD
- Citation
- JOURNAL OF PHYSICS AND CHEMISTRY OF SOLIDS, v.70, no.11, pp.1438 - 1442
- Abstract
- Zinc oxide (ZnO) and lead sulphide (PbS) nanoparticles separately synthesized by a precipitation method were combined by an ex situ route to prepare ZnO-PbS nanocomposites with different molar ratios of ZnO and PbS. The structure and morphology of the ZnO, PbS and ZnO-PbS samples were analyzed with X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM). A UV-vis spectrophotometer was used to collect the absorption and 325 nm He-Cd and 488 nm Ar lasers were used to collect the photoluminescence data from the samples. ZnO nanoparticles showed a broad and stable emission peak at similar to 570 nm, while a strongly quantum confined emission from PbS nanoparticles was detected at similar to 1344-1486 nm. The ZnO-PbS nanocomposites exhibited dual emission in the visible and near-infrared (NIR) regions that is associated with defects and recombination of excitonic centres in the ZnO and PbS nanoparticles, respectively. The PL intensity of the visible emission from the ZnO-PbS nanocomposite was shown to increase when the ZnO to PbS molar ratio was 5:1 and the emission was almost quenched at molar ratios of 1:1 and 1:5. For different molar ratios of ZnO to PbS, the PL intensity of the NIR emission from the ZnO-PbS nanocomposites was more intense than that of PbS nanoparticles. (C) 2009 Elsevier Ltd. All rights reserved.
- Keywords
- QUANTUM DOTS; NANOPARTICLES; PHOTOLUMINESCENCE; TEMPERATURE; GROWTH; QUANTUM DOTS; NANOPARTICLES; PHOTOLUMINESCENCE; TEMPERATURE; GROWTH; Nanocomposites; Sol-gel; Absorption; Photolumiscence
- ISSN
- 0022-3697
- URI
- https://pubs.kist.re.kr/handle/201004/132011
- DOI
- 10.1016/j.jpcs.2009.08.009
- Appears in Collections:
- KIST Article > 2009
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