Issue 36, 2011

Novel fabrication of NIR-vis upconversion NaYF4:Ln (Ln = Yb, Er, Tm) crystal layers by a flux coating method

Abstract

High quality upconverting NaYF4:Ln (Ln = Yb, Er, Tm) crystal layers were successfully fabricated directly onto glass substrates at a relatively low temperature of 350 °C by a novel two-step flux coating method. First, mixed pastes of solute (NaF and YF3) and dopants (LnF3) were coated on glass substrates by simple bar-coating, and then flux pastes (NaNO3 or NaNO3–NaF) were coated onto the dopant-containing solute layer. After the two-step coating, raw material-coated substrates were heated at 350 or 400 °C in an electric furnace. To remove the remaining flux, the crystal layers were washed with warm water. Finally, high quality, nanotextured NaYF4:Ln crystal layers with good adhesion were directly grown onto the glass substrates. These crystal layers consisted of densely packed idiomorphic NaYF4:Ln crystals. In particular, individual NaYF4:Ln crystals were typically shaped as hexagonal prisms. The NaYF4:Ln crystal phases depended strongly on the heating conditions, i.e., temperature and time. The NaNO3 and NaNO3–NaF fluxes were effective for the growth of high-quality idiomorphic NaYF4:Ln crystals. Additionally, the upconversion fluorescence properties of NaYF4:Ln crystal layers were controlled by changing dopant types and ratios. The NaYF4:10%Yb,1%Er, NaYF4:50%Yb,1%Er, NaYF4:20%Yb,1%Tm and NaYbF4:1%Er crystal layers emitted green, orange, blue and red fluorescences, respectively, under 980 nm laser irradiation.

Graphical abstract: Novel fabrication of NIR-vis upconversion NaYF4:Ln (Ln = Yb, Er, Tm) crystal layers by a flux coating method

Article information

Article type
Paper
Submitted
28 May 2011
Accepted
12 Jul 2011
First published
09 Aug 2011

J. Mater. Chem., 2011,21, 13847-13852

Novel fabrication of NIR-vis upconversion NaYF4:Ln (Ln = Yb, Er, Tm) crystal layers by a flux coating method

S. Suzuki, K. Teshima, T. Wakabayashi, H. Nishikiori, T. Ishizaki and S. Oishi, J. Mater. Chem., 2011, 21, 13847 DOI: 10.1039/C1JM12390D

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