TY - JOUR
T1 - Efficient energy transfer from inserted CdTe quantum dots to YVO 4:Eu3+ inverse opals
T2 - A novel strategy to improve and expand visible excitation of rare earth ions
AU - Zhu, Yongsheng
AU - Cui, Shaobo
AU - Chen, Xu
AU - Xu, Wen
AU - Zhou, Pingwei
AU - Wang, Yunfeng
AU - Xu, Lin
AU - Song, Hongwei
AU - Huang, Ling
AU - Huang, Wei
PY - 2014/7/21
Y1 - 2014/7/21
N2 - 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.
AB - 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.
UR - http://www.scopus.com/inward/record.url?scp=84903640733&partnerID=8YFLogxK
U2 - 10.1039/c4nr01845a
DO - 10.1039/c4nr01845a
M3 - 文章
AN - SCOPUS:84903640733
SN - 2040-3364
VL - 6
SP - 8075
EP - 8083
JO - Nanoscale
JF - Nanoscale
IS - 14
ER -