Local heterogeneity for a Eu3+-doped glass evidenced by time-resolved fluorescence spectroscopy coupled to scanning near-field optical microscopy

被引:5
作者
Grausem, Jerome
Dossot, Manuel
Cremel, Sebastien
Humbert, Bernard
Viala, Francois
Mauchien, Patrick
机构
[1] CNRS, LCPME, UMR 7564, UHP, F-54600 Villers Les Nancy, France
[2] CEA Saclay, DEN, DANS, DPC,SCP, F-91191 Gif Sur Yvette, France
关键词
D O I
10.1021/jp0607317
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Time-resolved fluorescence spectroscopy (TRFS) was applied to an aluminate glass sample doped with Eu3+ cation as a fluorescent probe of the chemical environment and local symmetry. Conventional far-field experiments revealed the presence of two different phases: an amorphous phase featured by a highly disordered environment surrounding the Eu3+ cation and a more ordered polycrystalline phase that exhibits a significant increase in the Eu3+ fluorescence decay time compared to that of the amorphous phase. Near-field fluorescence spectra and decay kinetics were recorded in the frontier region between the two phases using a home-built scanning near-field optical microscope. SNOM-TRFS experiments confirmed the presence of local heterogeneities in this part of the glass at a sub-micrometric spatial scale. Polycrystalline sites featured an important shear-force interaction with the probing fiber optic tip, a longer fluorescence decay time, and a higher Stark splitting of the D-5(0) -> F-7(J) (J = 1-4) electronic transitions of the Eu3+ cations.
引用
收藏
页码:11259 / 11266
页数:8
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