Measuring the internal quantum yield of upconversion luminescence for ytterbium-sensitized upconversion phosphors using the ytterbium(iii) emission as an internal standard. Issue 36 (7th September 2018)

• Record Type: Journal Article
• Authors: May, P. Stanley; Baride, Aravind; Hossan, Md Yeathad; Berry, Mary
• Is Part Of: Nanoscale. Volume 10:Issue 36(2018)
• Page Start: 17212
• Page End: 17226
• Publication Date: 2018-09-07
• Subjects: Nanoscience -- Periodicals; Nanotechnology -- Periodicals; 620.505
• DOI: 10.1039/c8nr03538e
• Languages: English
• ISSNs: 2040-3364

Abstract

Abstract : A new method is presented for estimating the internal quantum yield (IQY) of upconversion (UC) luminescence for Yb 3+ -sensitized ETU phosphors. Abstract : A method is presented for estimating the internal quantum yield (IQY) of NIR-to-NIR and NIR-to-visible upconversion (UC) luminescence for Yb 3+ -sensitized energy-transfer upconversion (ETU) phosphors. The method does not require an integrating sphere or a secondary standard, but rather uses the 1 μm emission of the Yb 3+ sensitizer as an internal standard. The method requires the acquisition of the 1 μm emission decay curve of the UC phosphor using low pulse-energy density, an estimation of the radiative decay constant of the 1 μm emission, and emission spectra corrected for instrument response. This method is valid for UC emission spectra acquired via pulsed or continuous wave (cw) excitation. The method is demonstrated for cw excitation to obtain IQY for UC and downshifted luminescence for β-phase NaYF4 : 0.5%Tm, 25%Yb and NaYF4 : 2%Er, 18%Yb nanocrystals (with and without a passivating NaYF4 shell) over a range of excitation irradiance. The corresponding results are consistent with those obtained using integrating spheres and numerical simulations, respectively. For pulsed excitation, an additional alternative method is described which requires acquisition of the 1 μm emission decay curve at each excitation pulse-energy density for which the IQY is to be determined. The proposed methods should be particularly useful for samples having very low absorbance at the excitation wavelength, for which direct determination methods are impractical.