4.6 Article

Effect of Molten Salt Synthesis Processing Duration on the Photo- and Radioluminescence of UV-, Visible-, and X-ray-Excitable La2Hf2O7:Eu3+ Nanoparticles

Journal

ACS OMEGA
Volume 3, Issue 7, Pages 7757-7770

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsomega.8b00987

Keywords

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Funding

  1. National Science Foundation under CHE [1710160]
  2. DMR [1523577]
  3. USDA National Institute of Food and Agriculture [2015-38422-24059]
  4. Robert A. Welch Foundation [BX-0048]
  5. United States-India Education Foundation (USIEF) [2268/FNPDR/2017]
  6. Institute of International Education (IIE) [2268/FNPDR/2017]

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Ln(3+)-ion-doped nanomaterials possess excellent properties because of their high color purity, longer excited state lifetime, narrow emission, and large Stokes shifts. In this work, we studied the correlation between the luminescence properties of La2Hf2O7:Eu3+ pyrochlore nanoparticles (NPs) synthesized by a molten salt synthesis (MSS) method at a relatively low temperature and several MSS processing durations (from 1 to 12 h). We synthesized these NPs with different sizes just by changing the MSS processing time without subjecting to high temperature. Raman spectroscopy confirmed the stabilization of the ideal pyrochlore structure of the La2Hf2O7: Eu3+ NPs at various MSS processing durations. The synthesized NPs exhibited bright red emission under UV, visible, and X-ray excitations, highlighting their potential applications as a red phosphor and scintillator. As the MSS processing time was increased from 1 to 12 h, a spectral change in the position of the charge transfer state in the La2Hf2O7:Eu3+ NPs was observed. The sample processed by the MSS with a duration of 3 h exhibited the highest luminescence intensity, which was attributed to its optimum crystals with least surface defects and less agglomeration. The obtained results strongly and unambiguously indicate the brighter side of this new type of pyrochlore-based NPs in the fast growing field of solid-state lighting and scintillator materials.

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