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Upconversion luminescence of Tm3+ and Yb3+-codoped lutetium oxide nanopowders

Identifieur interne : 000616 ( Pascal/Curation ); précédent : 000615; suivant : 000617

Upconversion luminescence of Tm3+ and Yb3+-codoped lutetium oxide nanopowders

Auteurs : LIQIONG AN [République populaire de Chine] ; JIAN ZHANG [République populaire de Chine] ; MIN LIU [République populaire de Chine] ; SHIWEI WANG [République populaire de Chine]

Source :

RBID : Pascal:08-0402967

Descripteurs français

English descriptors

Abstract

Lutetium oxide nanopowders codoped with Tm3+ and Yb3+ were synthesized by the co-precipitation method. Upconversion luminescence properties of the powder compacts have been investigated upon continuous wave excitation at 980 nm. Blue emission band was observed by naked eye, which was corresponded to the 1G43H6 transition of Tm3+ ions. However, upconversion spectra revealed that the strongest emission was centered at 809 nm, assigned to the 3H43H6 transition. Weak red emission centered at 651.5 nm was attributed to the 1G43F4 transition while considerably weaker ultraviolet emission centered at 361 nm was ascribed to the 1D23H6transition. The dependence of the intensity of upconversion emissions on the pump power implies two-step and three-step excitation mechanisms of the 3H4 and 1G4 levels, respectively. The possible upconversion schemes are discussed in this paper. Lutetium oxide powders can be sintered into transparent ceramics and high intensity of up-converted IR and blue emissions associated with the 3H43H6 and 1G43H6 transitions of Tm3+ in this matrix may offer lasers potential.
pA  
A01 01  1    @0 0925-8388
A03   1    @0 J. alloys compd.
A05       @2 451
A06       @2 1-2
A08 01  1  ENG  @1 Upconversion luminescence of Tm3+ and Yb3+-codoped lutetium oxide nanopowders
A09 01  1  ENG  @1 The 6th International Conference on f-Elements (ICFE-6), September 4-9, 2006, Wrocław, Poland
A11 01  1    @1 LIQIONG AN
A11 02  1    @1 JIAN ZHANG
A11 03  1    @1 MIN LIU
A11 04  1    @1 SHIWEI WANG
A12 01  1    @1 LEGENDZIEWICZ (J.) @9 ed.
A12 02  1    @1 HANUZA (J.) @9 ed.
A12 03  1    @1 MALTA (O.) @9 ed.
A12 04  1    @1 STREK (W.) @9 ed.
A14 01      @1 Shanghai Institute of Ceramics, Chinese Academy of Sciences @2 Shanghai 200050 @3 CHN @Z 1 aut. @Z 2 aut. @Z 3 aut. @Z 4 aut.
A20       @1 538-541
A21       @1 2008
A23 01      @0 ENG
A43 01      @1 INIST @2 1151 @5 354000175013971260
A44       @0 0000 @1 © 2008 INIST-CNRS. All rights reserved.
A45       @0 17 ref.
A47 01  1    @0 08-0402967
A60       @1 P @2 C
A61       @0 A
A64 01  1    @0 Journal of alloys and compounds
A66 01      @0 CHE
C01 01    ENG  @0 Lutetium oxide nanopowders codoped with Tm3+ and Yb3+ were synthesized by the co-precipitation method. Upconversion luminescence properties of the powder compacts have been investigated upon continuous wave excitation at 980 nm. Blue emission band was observed by naked eye, which was corresponded to the 1G43H6 transition of Tm3+ ions. However, upconversion spectra revealed that the strongest emission was centered at 809 nm, assigned to the 3H43H6 transition. Weak red emission centered at 651.5 nm was attributed to the 1G43F4 transition while considerably weaker ultraviolet emission centered at 361 nm was ascribed to the 1D23H6transition. The dependence of the intensity of upconversion emissions on the pump power implies two-step and three-step excitation mechanisms of the 3H4 and 1G4 levels, respectively. The possible upconversion schemes are discussed in this paper. Lutetium oxide powders can be sintered into transparent ceramics and high intensity of up-converted IR and blue emissions associated with the 3H43H6 and 1G43H6 transitions of Tm3+ in this matrix may offer lasers potential.
C02 01  3    @0 001B70H67B
C03 01  3  FRE  @0 Photoluminescence @5 02
C03 01  3  ENG  @0 Photoluminescence @5 02
C03 02  X  FRE  @0 Codopage @5 03
C03 02  X  ENG  @0 Codoping @5 03
C03 02  X  SPA  @0 Codrogado @5 03
C03 03  3  FRE  @0 Coprécipitation @5 04
C03 03  3  ENG  @0 Coprecipitation @5 04
C03 04  X  FRE  @0 Compactage poudre @5 05
C03 04  X  ENG  @0 Powder compaction @5 05
C03 04  X  SPA  @0 Compactación polvo @5 05
C03 05  3  FRE  @0 Transition niveau énergie @5 06
C03 05  3  ENG  @0 Energy-level transitions @5 06
C03 06  X  FRE  @0 Conversion fréquence @5 07
C03 06  X  ENG  @0 Frequency conversion @5 07
C03 06  X  SPA  @0 Conversión frecuencia @5 07
C03 07  3  FRE  @0 Frittage @5 08
C03 07  3  ENG  @0 Sintering @5 08
C03 08  3  FRE  @0 Transfert énergie @5 09
C03 08  3  ENG  @0 Energy transfer @5 09
C03 09  3  FRE  @0 Addition thulium @5 10
C03 09  3  ENG  @0 Thulium additions @5 10
C03 10  3  FRE  @0 Addition ytterbium @5 11
C03 10  3  ENG  @0 Ytterbium additions @5 11
C03 11  3  FRE  @0 Oxyde de lutétium @2 NK @5 15
C03 11  3  ENG  @0 Lutetium oxides @2 NK @5 15
C03 12  X  FRE  @0 Nanopoudre @5 16
C03 12  X  ENG  @0 Nanopowder @5 16
C03 12  X  SPA  @0 Nanopolvo @5 16
N21       @1 259
pR  
A30 01  1  ENG  @1 International Conference on f-Elements (ICFE-6) @2 6 @3 Wrocław POL @4 2009-09-04

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Pascal:08-0402967

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<term>Codoping</term>
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<term>Energy transfer</term>
<term>Energy-level transitions</term>
<term>Frequency conversion</term>
<term>Lutetium oxides</term>
<term>Nanopowder</term>
<term>Photoluminescence</term>
<term>Powder compaction</term>
<term>Sintering</term>
<term>Thulium additions</term>
<term>Ytterbium additions</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Photoluminescence</term>
<term>Codopage</term>
<term>Coprécipitation</term>
<term>Compactage poudre</term>
<term>Transition niveau énergie</term>
<term>Conversion fréquence</term>
<term>Frittage</term>
<term>Transfert énergie</term>
<term>Addition thulium</term>
<term>Addition ytterbium</term>
<term>Oxyde de lutétium</term>
<term>Nanopoudre</term>
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<div type="abstract" xml:lang="en">Lutetium oxide nanopowders codoped with Tm
<sup>3+</sup>
and Yb
<sup>3+</sup>
were synthesized by the co-precipitation method. Upconversion luminescence properties of the powder compacts have been investigated upon continuous wave excitation at 980 nm. Blue emission band was observed by naked eye, which was corresponded to the
<sup>1</sup>
G
<sub>4</sub>
<sup>3</sup>
H
<sub>6</sub>
transition of Tm
<sup>3+</sup>
ions. However, upconversion spectra revealed that the strongest emission was centered at 809 nm, assigned to the
<sup>3</sup>
H
<sub>4</sub>
<sup>3</sup>
H
<sub>6</sub>
transition. Weak red emission centered at 651.5 nm was attributed to the
<sup>1</sup>
G
<sub>4</sub>
<sup>3</sup>
F
<sub>4</sub>
transition while considerably weaker ultraviolet emission centered at 361 nm was ascribed to the
<sup>1</sup>
D
<sub>2</sub>
<sup>3</sup>
H
<sub>6</sub>
transition. The dependence of the intensity of upconversion emissions on the pump power implies two-step and three-step excitation mechanisms of the
<sup>3</sup>
H
<sub>4</sub>
and
<sup>1</sup>
G
<sub>4</sub>
levels, respectively. The possible upconversion schemes are discussed in this paper. Lutetium oxide powders can be sintered into transparent ceramics and high intensity of up-converted IR and blue emissions associated with the
<sup>3</sup>
H
<sub>4</sub>
<sup>3</sup>
H
<sub>6</sub>
and
<sup>1</sup>
G
<sub>4</sub>
<sup>3</sup>
H
<sub>6</sub>
transitions of Tm
<sup>3+</sup>
in this matrix may offer lasers potential.</div>
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</fA66>
<fC01 i1="01" l="ENG">
<s0>Lutetium oxide nanopowders codoped with Tm
<sup>3+</sup>
and Yb
<sup>3+</sup>
were synthesized by the co-precipitation method. Upconversion luminescence properties of the powder compacts have been investigated upon continuous wave excitation at 980 nm. Blue emission band was observed by naked eye, which was corresponded to the
<sup>1</sup>
G
<sub>4</sub>
<sup>3</sup>
H
<sub>6</sub>
transition of Tm
<sup>3+</sup>
ions. However, upconversion spectra revealed that the strongest emission was centered at 809 nm, assigned to the
<sup>3</sup>
H
<sub>4</sub>
<sup>3</sup>
H
<sub>6</sub>
transition. Weak red emission centered at 651.5 nm was attributed to the
<sup>1</sup>
G
<sub>4</sub>
<sup>3</sup>
F
<sub>4</sub>
transition while considerably weaker ultraviolet emission centered at 361 nm was ascribed to the
<sup>1</sup>
D
<sub>2</sub>
<sup>3</sup>
H
<sub>6</sub>
transition. The dependence of the intensity of upconversion emissions on the pump power implies two-step and three-step excitation mechanisms of the
<sup>3</sup>
H
<sub>4</sub>
and
<sup>1</sup>
G
<sub>4</sub>
levels, respectively. The possible upconversion schemes are discussed in this paper. Lutetium oxide powders can be sintered into transparent ceramics and high intensity of up-converted IR and blue emissions associated with the
<sup>3</sup>
H
<sub>4</sub>
<sup>3</sup>
H
<sub>6</sub>
and
<sup>1</sup>
G
<sub>4</sub>
<sup>3</sup>
H
<sub>6</sub>
transitions of Tm
<sup>3+</sup>
in this matrix may offer lasers potential.</s0>
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<s0>Transition niveau énergie</s0>
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<s0>Energy-level transitions</s0>
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<s0>Transfert énergie</s0>
<s5>09</s5>
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<s0>Energy transfer</s0>
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<s0>Addition thulium</s0>
<s5>10</s5>
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<s0>Thulium additions</s0>
<s5>10</s5>
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<s0>Addition ytterbium</s0>
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<fC03 i1="10" i2="3" l="ENG">
<s0>Ytterbium additions</s0>
<s5>11</s5>
</fC03>
<fC03 i1="11" i2="3" l="FRE">
<s0>Oxyde de lutétium</s0>
<s2>NK</s2>
<s5>15</s5>
</fC03>
<fC03 i1="11" i2="3" l="ENG">
<s0>Lutetium oxides</s0>
<s2>NK</s2>
<s5>15</s5>
</fC03>
<fC03 i1="12" i2="X" l="FRE">
<s0>Nanopoudre</s0>
<s5>16</s5>
</fC03>
<fC03 i1="12" i2="X" l="ENG">
<s0>Nanopowder</s0>
<s5>16</s5>
</fC03>
<fC03 i1="12" i2="X" l="SPA">
<s0>Nanopolvo</s0>
<s5>16</s5>
</fC03>
<fN21>
<s1>259</s1>
</fN21>
</pA>
<pR>
<fA30 i1="01" i2="1" l="ENG">
<s1>International Conference on f-Elements (ICFE-6)</s1>
<s2>6</s2>
<s3>Wrocław POL</s3>
<s4>2009-09-04</s4>
</fA30>
</pR>
</standard>
</inist>
</record>

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