Published June 2021 | Version v1
Journal article

Comparative investigation on upconversion luminescence properties of Lu2O3:Er/Yb and Lu2O2S:Er/Yb phosphors

  • 1. School of Materials Science and Chemical Engineering, Ningbo University, Ningbo, Zhejiang, 315211 (China)
  • 2. School of Metallurgy Engineering, Liaoning Institute of Science and Technology, Benxi, Liaoning, 117004 (China)
  • 3. Research Center for Functional Materials, National Institute for Materials Science, Tsukuba, Ibaraki, 305-0044 (Japan)
  • 4. Key Laboratory of Photoelectric Materials and Devices of Zhejiang Province, Ningbo, 315211 (China)

Description

A series of (Lu0.99xEr0.01Ybx)2O3 and (Lu0.99xEr0.01Ybx)2O2S (x = 0 - 0.1) phosphor particles are prepared to investigate their upconversion luminescence properties. Under 980 nm pumping laser, the two phosphors both exhibit strong green emission at ≈ 520 - 573 nm and weak red emission at ≈ 648 - 688 nm arising from 4S3/2/2H11/24I15/2 and 4F9/24I15/2 transitions of Er3+, respectively. The optimum concentrations of Yb3+ sensitizers are found to be 1.0 at% in oxide and 0.5 at% in oxysulfide, and their corresponding CIE chromaticity coordinates are (0.29, 0.69) and (0.33, 0.65). The Lu2O2S:Er/Yb phosphor exhibits ≈42 times higher luminescence intensity than the Lu2O3:Er/Yb contrast. More Yb3+ addition further increases the proportion of red emission by the cross-relaxation between adjacent Yb3+ and Er3+ and the multiphonon relaxation. The luminescence intensities of the two phosphors gradually increase as the laser output power increases and the upconversion mechanisms are both identified to be two-phonon processes. The Lu2O2S:Er/Yb phosphor has a shorter lifetime than the Lu2O3:Er/Yb counterpart, whereas the lifetime for the red emission is longer than that for the green emission in each case. (© 2021 Wiley‐VCH GmbH)

Additional details

Identifiers

Publishing Information

Journal Title
Physica Status Solidi. A, Applications and Materials Science (Online)
Journal Volume
218
Journal Issue
11
Journal Page Range
p. 1-7
ISSN
1862-6319
CODEN
PSSABA

Optional Information

Notes
AID: 2100014