(ZnS)x(Cu0.1InS1.55) heteronanocrystals with broadband emission as a single component for potential WLEDs

•(ZnS)x(Cu0.1InS1.55) HNCs were synthesized by decomposing ethylxanthate salts.•The dual emission bands can be easily tuned by adding Zn precursor.•The range of the excitation wavelength is consistent with the emission region of commercial near-UV LED chips.•The HNCs can be used as one potential sin...

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Veröffentlicht in:Applied surface science 2015-10, Vol.353, p.263-268
Hauptverfasser: Lu, S.H., Huang, H.Z., Wang, Y.S., Chen, T.F., Wang, A.J., Zheng, D.
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Sprache:eng
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Zusammenfassung:•(ZnS)x(Cu0.1InS1.55) HNCs were synthesized by decomposing ethylxanthate salts.•The dual emission bands can be easily tuned by adding Zn precursor.•The range of the excitation wavelength is consistent with the emission region of commercial near-UV LED chips.•The HNCs can be used as one potential single component to fabricate WLEDs. Semiconductor nanocrystals as a single component for fabricating WLEDs have proven to be a simple and effective alternative. In this paper, (ZnS)x(Cu0.1InS1.55) heteronanocrystals (HNCs) were easily synthesized via a hot injection route using a mixture of ethylxanthate salts as precursors. The as-prepared heteronanocrystals were characterized by X-ray diffraction, transmission electron microscopy, UV–Vis absorption and photoluminescence spectroscopies. The effects of the Zn mole fraction on the crystal structure and optical properties were studied. The absorption of the HNCs shifts to shorter wavelengths with increasing the Zn component. The photoluminescence (PL) spectra with the two broad emissions of blue (about 435nm) and yellow-red (590–643nm) were observed and assigned to the corresponding transition pathways. Their peculiar luminescence with high efficiency shows a quite tunable emission from cool to warm by varying the mole ratios of Zn precursor. The single component based WLED with optical conversion was simply fabricated by coating (ZnS)0.4(Cu0.1InS1.55) HNCs onto a commercial UV-LED. The operation time under UV excitation is derived to be around 4.5h.
ISSN:0169-4332
1873-5584
DOI:10.1016/j.apsusc.2015.06.132