Reassignment of electronic transitions in the laser-activated spectrum of nanocrystalline Y2O3:Er3+
Reassignment of electronic transitions in the laser-activated spectrum of nanocrystalline Y2O3:Er3+
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DOI:
10.1016/j.jlumin.2017.12.053
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发表时间:
2018-04
影响因子:
3.6
通讯作者:
D. Engelsen;G. Fern;T. Ireland;J. Silver
中科院分区:
文献类型:
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作者:
D. Engelsen;G. Fern;T. Ireland;J. Silver
The laser-activated spectra of nanocrystalline Y2O3:Er3+recorded at various temperatures and two excitation energies are described and analysed herein. Based on recently published modified values of the C2-type Stark splitting of Er3+in the cubic Y2O3lattice, the Er3+multiplets in the observed spectra have been re-assigned. The upconversion routes of three2H11/2→4I15/2hot bands from4S3/2Kramers doublets have been traced, based on an Arrhenius-type analysis of these hot bands. We observed 5 peaks in the2H11/2→4I15/2hot band region with a different temperature behaviour. These bands belong to the2P3/2→4I9/2multiplet and their deviating temperature behaviour has been explained in terms of a cross relaxation mechanism. From the ratio between the laser-activated spectra that were recorded at different excitation energies we concluded that the two-photon absorption process becomes more efficient upon increasing the excitation energy. We have also put forward an explanation for the gradual broadening of the fluorescence bands of the2H11/2→4I15/2multiplet in going from 518 nm to 542 nm. The higher Stark splitting levels are due to a stronger electrostatic field of the host lattice and experience therefore a higher electron-phonon interaction, which explains the observed increase of FWHM at larger wavelengths.