Yb3+ Ions Distribution in YAG Nanoceramics Analyzed by Both Optical and TEM-EDX Techniques

被引:27
作者
Boulon, Georges [1 ]
Guyot, Yannick [1 ]
Guzik, Malgorzata [2 ]
Epicier, Thierry [3 ]
Gluchowski, Pawel [4 ]
Hreniak, Dariusz [4 ]
Strek, Wieslaw [4 ]
机构
[1] Univ Lyon, ILM, UMR UCB Lyon CNRS 5306 1, F-69622 Villeurbanne, France
[2] Univ Wroclaw, Fac Chem, PL-50383 Wroclaw, Poland
[3] Univ Lyon, INSA Lyon, UMR CNRS 5510, MATEIS, F-69621 Villeurbanne, France
[4] Polish Acad Sci, Inst Low Temp & Struct Res, PL-50422 Wroclaw, Poland
关键词
YTTRIUM-ALUMINUM-GARNET; HIGH-PRESSURE; ND-YAG; SPECTROSCOPIC PROPERTIES; LUMINESCENT PROPERTIES; DOPED YAG; Y3AL5O12; NANOCRYSTALLINE; BULK; CERAMICS;
D O I
10.1021/jp502882j
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
We show the approach in the structural and spectroscopic analysis of Yb3+-doped YAG nanoceramics prepared using the low temperature-high pressure sintering technique (LTHP) by conjugation of both TEM-EDX and optical techniques. Pressure sintering dependences of absorption, emission, and decays are analyzed and interpreted. The sample pressurized at 8 GPa for sintering is characterized by the highest transparency and confirms the Y3Al5O12 garnet structure of the grains of similar to 21 nm average size. Yb3+ ion distribution has been analyzed by both TEM-EDX evaluation in grains and grain boundaries and spectroscopy of Yb3+ pairs of small population from the co-operative luminescence phenomenon. EDX analysis at the TEM scale provides unambiguous results on a clear tendency of almost uniform Yb3+ distribution. An important new observation has been made at 4 K and room temperature with the F-2(7/2) -> F-2(5/2) 0-phonon absorption line located at 975.7 nm, in addition of the 0-phonon line of the YAG structure of grains at 968 nm similar to that of bulky YAG single crystals. We have discussed the origin of this new 0-phonon line relaxing only by nonradiative transitions and conclude that this line might be assigned to Yb3+ distorted sites on the grain surfaces.
引用
收藏
页码:15474 / 15486
页数:13
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