Issue 47, 2012

Concentration-controlled emission in LaF3:Yb3+/Tm3+nanocrystals: switching from UV to NIR regions

Abstract

The homogeneous LaF3:Yb3+/Tm3+ nanocrystals (NCs) with an average diameter of 5 nm and different doping concentrations (Yb3+: 2–20%, Tm3+: 0.2–1.5%) were synthesized by a simple solvothermal approach. Their emission spectra, luminescent dynamics, and power-dependence of up-conversion (UC) photoluminescence were investigated in detail. Under 980 nm excitation, as-synthesized NCs exhibited interesting emission properties: a broad range of photoluminescence spanning from the ultraviolet (UV, ∼330 nm) to near infrared (NIR, ∼1700 nm) region, as well as the tunable relative intensity of different excited states. These unique UC or down-conversion (DC) emission behaviors were strongly influenced by the doping concentration of Tm3+ and Yb3+ ions within LaF3 NCs. With the increase of the concentration ratio between Yb3+ and Tm3+ ions, the NIR emissions were highly suppressed, but the UV and visible emissions increased quickly. The result demonstrated that such concentration effect was mainly originated from two mechanisms: one was the competition mechanism among the different intermediate exciting levels such as 3F4, 3H4, 1G4 and 1D2, and the other was the cross-relaxation mechanism between the Tm3+ ions. By optimizing the concentration of Tm3+ and Yb3+ ions, multi-photon UC or DC luminescence properties of LaF3:Yb3+/Tm3+ NCs could be facilely tuned from UV to NIR, which will be helpful for their further applications in the field of sensing, imaging, labeling, lighting and displays, etc.

Graphical abstract: Concentration-controlled emission in LaF3:Yb3+/Tm3+ nanocrystals: switching from UV to NIR regions

Article information

Article type
Paper
Submitted
10 Aug 2012
Accepted
28 Sep 2012
First published
01 Oct 2012

J. Mater. Chem., 2012,22, 24698-24704

Concentration-controlled emission in LaF3:Yb3+/Tm3+ nanocrystals: switching from UV to NIR regions

X. Bai, D. Li, Q. Liu, B. Dong, S. Xu and H. Song, J. Mater. Chem., 2012, 22, 24698 DOI: 10.1039/C2JM35403A

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