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Efficient energy transfer from inserted CdTe quantum dots to YVO 4:Eu3+ inverse opals: A novel strategy to improve and expand visible excitation of rare earth ions

  • Yongsheng Zhu
  • , Shaobo Cui
  • , Xu Chen
  • , Wen Xu
  • , Pingwei Zhou
  • , Yunfeng Wang
  • , Lin Xu
  • , Hongwei Song
  • , Ling Huang
  • , Wei Huang
  • Jilin University
  • Nanjing Tech University
  • Nanjing University of Posts and Telecommunications

Research output: Contribution to journalArticlepeer-review

17 Scopus citations

Abstract

Rare earth (RE)-based phosphors demonstrate sharp emission lines, long lifetimes and high luminescence quantum yields; thus, they have been employed in various photoelectric devices, such as light-emitting diodes (LEDs) and solar spectral converters. However, their applications are largely confined by their narrow excitation bands and small absorption cross sections of 4f-4f transitions. In this paper, we demonstrate a novel strategy to improve and expand the visible excitation bands of Eu3+ ions through the interface energy transfer (ET) from CdTe quantum dots (QDs) to YVO 4:Eu3+ inverse opal photonic crystals (IOPCs). The significant effects observed in the CdTe QDs/YVO4:Eu3+ IOPCs composites were that the excitation of Eu3+ ions was continuously extended from 450 to 590 nm and that the emission intensity of the 5D0-7FJ transitions was enhanced ∼20-fold, corresponding to the intrinsic 7F1- 5D1 excitation at 538 nm. Furthermore, in the IOPC network, the ET efficiency from the QDs to YVO4:Eu3+ was greatly improved because of the suppression of energy migration among the CdTe QDs, which gave an optimum ET efficiency as high as 47%. Besides, the modulation of photonic stop bands (PSBs) on the radiative transition rates of the QDs and Eu3+ ions was studied, which showed that the decay lifetime constants for Eu3+ ions were independent of PSBs, while those of QDs demonstrated a suppression in the PSBs. Their physical nature was explained theoretically.

Original languageEnglish
Pages (from-to)8075-8083
Number of pages9
JournalNanoscale
Volume6
Issue number14
DOIs
StatePublished - 21 Jul 2014
Externally publishedYes

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