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Synthesis and oxide ion conductivity of lanthanum-europium oxide fluoride, La2Eu2O3F6

Identifieur interne : 000C49 ( PascalFrancis/Curation ); précédent : 000C48; suivant : 000C50

Synthesis and oxide ion conductivity of lanthanum-europium oxide fluoride, La2Eu2O3F6

Auteurs : Masayuki Takashima [Japon] ; Susumu Yonezawa [Japon] ; Marc Leblanc [France]

Source :

RBID : Pascal:03-0071315

Descripteurs français

English descriptors

Abstract

La2Eu2O3F6 was prepared by solid-solid reaction between 1-mol La2O3 and 2-mol EuF3 at 1473 K. The crystal structure of La2Eu2O3F6 was analyzed to be the monoclinic structure (a0=0.403 nm, b0=1.14 nm, c0=0.572 nm, β=135.2°) derived from the fluorite structure. The ionic arrangement was suggested to be somewhat disordered in the La2Eu2O3F6 in contrast to that in the Nd2Eu2O3F6 with highly ordered ionic arrangement. It was assumed that the disorder in La2Eu2O3F6 resulted in the lower oxide conductivity, La2Eu2O3F6 (σ=0.8 S m-1, τO2-=0.7 at 773 K), than that of Nd2Eu2O3F6 (σ=2.0 S m-1, τO2=0.9 at 773 K). La2Eu2O3F6 was stable up to ca. 970 K in air, and converted into LaEuO3 (monoclinic) at 1623 K through the metastable state of La2EuO2F2 (rhombohedral) at ca. 1190 K by the pyrohydrolysis. The electrical conductivity declined due to pyrohydrolysis; LaEuO2F2, σ2.0×10-2 S m-1, LaEuO3, σ7.0×10-5 S m-1 at 873 K.
pA  
A01 01  1    @0 0167-2738
A02 01      @0 SSIOD3
A03   1    @0 Solid state ion.
A05       @2 154-5
A08 01  1  ENG  @1 Synthesis and oxide ion conductivity of lanthanum-europium oxide fluoride, La2Eu2O3F6
A09 01  1  ENG  @1 Materials and Processes for Energy and Environment. Part B
A11 01  1    @1 TAKASHIMA (Masayuki)
A11 02  1    @1 YONEZAWA (Susumu)
A11 03  1    @1 LEBLANC (Marc)
A12 01  1    @1 BADWAL (S. P. S.) @9 ed.
A14 01      @1 Department of Materials Science and Engineering, Faculty of Engineering, Fukui University @2 3-9-1 Bunkyo, Fukui 910-8507 @3 JPN @Z 1 aut. @Z 2 aut.
A14 02      @1 Laboratoire des Fluorures UPRES-A 6010, Faculte des Sciences, Universite du Maine @3 FRA @Z 3 aut.
A15 01      @1 CSIRO Manufacturing and Infrastructure Technology, Private Bag 33 @2 Clayton South, Victoria @3 AUS @Z 1 aut.
A18 01  1    @1 International Society for Solid State Ionics (ISSI) @3 INT @9 patr.
A20       @1 547-553
A21       @1 2002
A23 01      @0 ENG
A43 01      @1 INIST @2 18305 @5 354000106857910770
A44       @0 0000 @1 © 2003 INIST-CNRS. All rights reserved.
A45       @0 12 ref.
A47 01  1    @0 03-0071315
A60       @1 P @2 C
A61       @0 A
A64 01  1    @0 Solid state ionics
A66 01      @0 NLD
C01 01    ENG  @0 La2Eu2O3F6 was prepared by solid-solid reaction between 1-mol La2O3 and 2-mol EuF3 at 1473 K. The crystal structure of La2Eu2O3F6 was analyzed to be the monoclinic structure (a0=0.403 nm, b0=1.14 nm, c0=0.572 nm, β=135.2°) derived from the fluorite structure. The ionic arrangement was suggested to be somewhat disordered in the La2Eu2O3F6 in contrast to that in the Nd2Eu2O3F6 with highly ordered ionic arrangement. It was assumed that the disorder in La2Eu2O3F6 resulted in the lower oxide conductivity, La2Eu2O3F6 (σ=0.8 S m-1, τO2-=0.7 at 773 K), than that of Nd2Eu2O3F6 (σ=2.0 S m-1, τO2=0.9 at 773 K). La2Eu2O3F6 was stable up to ca. 970 K in air, and converted into LaEuO3 (monoclinic) at 1623 K through the metastable state of La2EuO2F2 (rhombohedral) at ca. 1190 K by the pyrohydrolysis. The electrical conductivity declined due to pyrohydrolysis; LaEuO2F2, σ2.0×10-2 S m-1, LaEuO3, σ7.0×10-5 S m-1 at 873 K.
C02 01  3    @0 001B60F30H
C02 02  3    @0 001B60A66F1
C03 01  3  FRE  @0 Conductivité ionique @5 02
C03 01  3  ENG  @0 Ionic conductivity @5 02
C03 02  3  FRE  @0 Structure cristalline @5 03
C03 02  3  ENG  @0 Crystal structure @5 03
C03 03  3  FRE  @0 Phase métastable @5 05
C03 03  3  ENG  @0 Metastable phases @5 05
C03 04  3  FRE  @0 Conductivité électrique @5 06
C03 04  3  ENG  @0 Electrical conductivity @5 06
C03 05  X  FRE  @0 Polyèdre coordination @5 07
C03 05  X  ENG  @0 Coordination polyhedron @5 07
C03 05  X  SPA  @0 Poliedro coordinación @5 07
C03 06  3  FRE  @0 Diffraction RX @5 08
C03 06  3  ENG  @0 XRD @5 08
C03 07  3  FRE  @0 TGA @5 09
C03 07  3  ENG  @0 TGA @5 09
C03 08  X  FRE  @0 Méthode électrochimique @5 10
C03 08  X  ENG  @0 Electrochemical method @5 10
C03 08  X  SPA  @0 Método electroquímico @5 10
C03 09  3  FRE  @0 Lanthane Oxyfluorure @2 NC @2 NA @5 11
C03 09  3  ENG  @0 Lanthanum Oxyfluorides @2 NC @2 NA @5 11
C03 10  3  FRE  @0 Europium Oxyfluorure @2 NC @2 NA @5 12
C03 10  3  ENG  @0 Europium Oxyfluorides @2 NC @2 NA @5 12
C03 11  3  FRE  @0 Composé quaternaire @5 13
C03 11  3  ENG  @0 Quaternary compounds @5 13
C03 12  3  FRE  @0 Etude expérimentale @5 14
C03 12  3  ENG  @0 Experimental study @5 14
C03 13  3  FRE  @0 La2Eu2O3F6 @4 INC @5 53
C03 14  3  FRE  @0 Eu F La O @4 INC @5 54
C03 15  3  FRE  @0 6630H @2 PAC @4 INC @5 56
C03 16  3  FRE  @0 6166F @2 PAC @4 INC @5 57
C07 01  3  FRE  @0 Lanthanide composé @5 48
C07 01  3  ENG  @0 Rare earth compounds @5 48
C07 02  3  FRE  @0 Composé minéral @5 49
C07 02  3  ENG  @0 Inorganic compounds @5 49
N21       @1 041
N82       @1 PSI
pR  
A30 01  1  ENG  @1 SSI 2001 International Conference on Solid State Ionics @3 Cairns AUS @4 2001-07-08

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<title xml:lang="en" level="a">Synthesis and oxide ion conductivity of lanthanum-europium oxide fluoride, La
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
</title>
<author>
<name sortKey="Takashima, Masayuki" sort="Takashima, Masayuki" uniqKey="Takashima M" first="Masayuki" last="Takashima">Masayuki Takashima</name>
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<s1>Department of Materials Science and Engineering, Faculty of Engineering, Fukui University</s1>
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<s3>JPN</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
</inist:fA14>
<country>Japon</country>
</affiliation>
</author>
<author>
<name sortKey="Yonezawa, Susumu" sort="Yonezawa, Susumu" uniqKey="Yonezawa S" first="Susumu" last="Yonezawa">Susumu Yonezawa</name>
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<s1>Department of Materials Science and Engineering, Faculty of Engineering, Fukui University</s1>
<s2>3-9-1 Bunkyo, Fukui 910-8507</s2>
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<sZ>1 aut.</sZ>
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<name sortKey="Leblanc, Marc" sort="Leblanc, Marc" uniqKey="Leblanc M" first="Marc" last="Leblanc">Marc Leblanc</name>
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<title xml:lang="en" level="a">Synthesis and oxide ion conductivity of lanthanum-europium oxide fluoride, La
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
</title>
<author>
<name sortKey="Takashima, Masayuki" sort="Takashima, Masayuki" uniqKey="Takashima M" first="Masayuki" last="Takashima">Masayuki Takashima</name>
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<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
</inist:fA14>
<country>Japon</country>
</affiliation>
</author>
<author>
<name sortKey="Yonezawa, Susumu" sort="Yonezawa, Susumu" uniqKey="Yonezawa S" first="Susumu" last="Yonezawa">Susumu Yonezawa</name>
<affiliation wicri:level="1">
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<s1>Department of Materials Science and Engineering, Faculty of Engineering, Fukui University</s1>
<s2>3-9-1 Bunkyo, Fukui 910-8507</s2>
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<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
</inist:fA14>
<country>Japon</country>
</affiliation>
</author>
<author>
<name sortKey="Leblanc, Marc" sort="Leblanc, Marc" uniqKey="Leblanc M" first="Marc" last="Leblanc">Marc Leblanc</name>
<affiliation wicri:level="1">
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<s1>Laboratoire des Fluorures UPRES-A 6010, Faculte des Sciences, Universite du Maine</s1>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
</inist:fA14>
<country>France</country>
</affiliation>
</author>
</analytic>
<series>
<title level="j" type="main">Solid state ionics</title>
<title level="j" type="abbreviated">Solid state ion.</title>
<idno type="ISSN">0167-2738</idno>
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<date when="2002">2002</date>
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<term>Coordination polyhedron</term>
<term>Crystal structure</term>
<term>Electrical conductivity</term>
<term>Electrochemical method</term>
<term>Europium Oxyfluorides</term>
<term>Experimental study</term>
<term>Ionic conductivity</term>
<term>Lanthanum Oxyfluorides</term>
<term>Metastable phases</term>
<term>Quaternary compounds</term>
<term>TGA</term>
<term>XRD</term>
</keywords>
<keywords scheme="Pascal" xml:lang="fr">
<term>Conductivité ionique</term>
<term>Structure cristalline</term>
<term>Phase métastable</term>
<term>Conductivité électrique</term>
<term>Polyèdre coordination</term>
<term>Diffraction RX</term>
<term>TGA</term>
<term>Méthode électrochimique</term>
<term>Lanthane Oxyfluorure</term>
<term>Europium Oxyfluorure</term>
<term>Composé quaternaire</term>
<term>Etude expérimentale</term>
<term>La2Eu2O3F6</term>
<term>Eu F La O</term>
<term>6630H</term>
<term>6166F</term>
</keywords>
</textClass>
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<front>
<div type="abstract" xml:lang="en">La
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
was prepared by solid-solid reaction between 1-mol La
<sub>2</sub>
O
<sub>3</sub>
and 2-mol EuF
<sub>3</sub>
at 1473 K. The crystal structure of La
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
was analyzed to be the monoclinic structure (a
<sub>0</sub>
=0.403 nm, b
<sub>0</sub>
=1.14 nm, c
<sub>0</sub>
=0.572 nm, β=135.2°) derived from the fluorite structure. The ionic arrangement was suggested to be somewhat disordered in the La
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
in contrast to that in the Nd
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
with highly ordered ionic arrangement. It was assumed that the disorder in La
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
resulted in the lower oxide conductivity, La
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
(σ=0.8 S m
<sup>-1</sup>
, τO
<sup>2-</sup>
=0.7 at 773 K), than that of Nd
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
(σ=2.0 S m
<sup>-1</sup>
, τO
<sup>2</sup>
=0.9 at 773 K). La
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
was stable up to ca. 970 K in air, and converted into LaEuO
<sub>3</sub>
(monoclinic) at 1623 K through the metastable state of La
<sub>2</sub>
EuO
<sub>2</sub>
F
<sub>2</sub>
(rhombohedral) at ca. 1190 K by the pyrohydrolysis. The electrical conductivity declined due to pyrohydrolysis; LaEuO
<sub>2</sub>
F
<sub>2</sub>
, σ2.0×10
<sup>-2</sup>
S m
<sup>-1</sup>
, LaEuO
<sub>3</sub>
, σ7.0×10
<sup>-5</sup>
S m
<sup>-1</sup>
at 873 K.</div>
</front>
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<fA08 i1="01" i2="1" l="ENG">
<s1>Synthesis and oxide ion conductivity of lanthanum-europium oxide fluoride, La
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
</s1>
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<s1>Materials and Processes for Energy and Environment. Part B</s1>
</fA09>
<fA11 i1="01" i2="1">
<s1>TAKASHIMA (Masayuki)</s1>
</fA11>
<fA11 i1="02" i2="1">
<s1>YONEZAWA (Susumu)</s1>
</fA11>
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<s1>LEBLANC (Marc)</s1>
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<s9>ed.</s9>
</fA12>
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<s1>Department of Materials Science and Engineering, Faculty of Engineering, Fukui University</s1>
<s2>3-9-1 Bunkyo, Fukui 910-8507</s2>
<s3>JPN</s3>
<sZ>1 aut.</sZ>
<sZ>2 aut.</sZ>
</fA14>
<fA14 i1="02">
<s1>Laboratoire des Fluorures UPRES-A 6010, Faculte des Sciences, Universite du Maine</s1>
<s3>FRA</s3>
<sZ>3 aut.</sZ>
</fA14>
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<sZ>1 aut.</sZ>
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<s1>547-553</s1>
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<s1>2002</s1>
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<fA60>
<s1>P</s1>
<s2>C</s2>
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</fA61>
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<s0>Solid state ionics</s0>
</fA64>
<fA66 i1="01">
<s0>NLD</s0>
</fA66>
<fC01 i1="01" l="ENG">
<s0>La
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
was prepared by solid-solid reaction between 1-mol La
<sub>2</sub>
O
<sub>3</sub>
and 2-mol EuF
<sub>3</sub>
at 1473 K. The crystal structure of La
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
was analyzed to be the monoclinic structure (a
<sub>0</sub>
=0.403 nm, b
<sub>0</sub>
=1.14 nm, c
<sub>0</sub>
=0.572 nm, β=135.2°) derived from the fluorite structure. The ionic arrangement was suggested to be somewhat disordered in the La
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
in contrast to that in the Nd
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
with highly ordered ionic arrangement. It was assumed that the disorder in La
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
resulted in the lower oxide conductivity, La
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
(σ=0.8 S m
<sup>-1</sup>
, τO
<sup>2-</sup>
=0.7 at 773 K), than that of Nd
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
(σ=2.0 S m
<sup>-1</sup>
, τO
<sup>2</sup>
=0.9 at 773 K). La
<sub>2</sub>
Eu
<sub>2</sub>
O
<sub>3</sub>
F
<sub>6</sub>
was stable up to ca. 970 K in air, and converted into LaEuO
<sub>3</sub>
(monoclinic) at 1623 K through the metastable state of La
<sub>2</sub>
EuO
<sub>2</sub>
F
<sub>2</sub>
(rhombohedral) at ca. 1190 K by the pyrohydrolysis. The electrical conductivity declined due to pyrohydrolysis; LaEuO
<sub>2</sub>
F
<sub>2</sub>
, σ2.0×10
<sup>-2</sup>
S m
<sup>-1</sup>
, LaEuO
<sub>3</sub>
, σ7.0×10
<sup>-5</sup>
S m
<sup>-1</sup>
at 873 K.</s0>
</fC01>
<fC02 i1="01" i2="3">
<s0>001B60F30H</s0>
</fC02>
<fC02 i1="02" i2="3">
<s0>001B60A66F1</s0>
</fC02>
<fC03 i1="01" i2="3" l="FRE">
<s0>Conductivité ionique</s0>
<s5>02</s5>
</fC03>
<fC03 i1="01" i2="3" l="ENG">
<s0>Ionic conductivity</s0>
<s5>02</s5>
</fC03>
<fC03 i1="02" i2="3" l="FRE">
<s0>Structure cristalline</s0>
<s5>03</s5>
</fC03>
<fC03 i1="02" i2="3" l="ENG">
<s0>Crystal structure</s0>
<s5>03</s5>
</fC03>
<fC03 i1="03" i2="3" l="FRE">
<s0>Phase métastable</s0>
<s5>05</s5>
</fC03>
<fC03 i1="03" i2="3" l="ENG">
<s0>Metastable phases</s0>
<s5>05</s5>
</fC03>
<fC03 i1="04" i2="3" l="FRE">
<s0>Conductivité électrique</s0>
<s5>06</s5>
</fC03>
<fC03 i1="04" i2="3" l="ENG">
<s0>Electrical conductivity</s0>
<s5>06</s5>
</fC03>
<fC03 i1="05" i2="X" l="FRE">
<s0>Polyèdre coordination</s0>
<s5>07</s5>
</fC03>
<fC03 i1="05" i2="X" l="ENG">
<s0>Coordination polyhedron</s0>
<s5>07</s5>
</fC03>
<fC03 i1="05" i2="X" l="SPA">
<s0>Poliedro coordinación</s0>
<s5>07</s5>
</fC03>
<fC03 i1="06" i2="3" l="FRE">
<s0>Diffraction RX</s0>
<s5>08</s5>
</fC03>
<fC03 i1="06" i2="3" l="ENG">
<s0>XRD</s0>
<s5>08</s5>
</fC03>
<fC03 i1="07" i2="3" l="FRE">
<s0>TGA</s0>
<s5>09</s5>
</fC03>
<fC03 i1="07" i2="3" l="ENG">
<s0>TGA</s0>
<s5>09</s5>
</fC03>
<fC03 i1="08" i2="X" l="FRE">
<s0>Méthode électrochimique</s0>
<s5>10</s5>
</fC03>
<fC03 i1="08" i2="X" l="ENG">
<s0>Electrochemical method</s0>
<s5>10</s5>
</fC03>
<fC03 i1="08" i2="X" l="SPA">
<s0>Método electroquímico</s0>
<s5>10</s5>
</fC03>
<fC03 i1="09" i2="3" l="FRE">
<s0>Lanthane Oxyfluorure</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>11</s5>
</fC03>
<fC03 i1="09" i2="3" l="ENG">
<s0>Lanthanum Oxyfluorides</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>11</s5>
</fC03>
<fC03 i1="10" i2="3" l="FRE">
<s0>Europium Oxyfluorure</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>12</s5>
</fC03>
<fC03 i1="10" i2="3" l="ENG">
<s0>Europium Oxyfluorides</s0>
<s2>NC</s2>
<s2>NA</s2>
<s5>12</s5>
</fC03>
<fC03 i1="11" i2="3" l="FRE">
<s0>Composé quaternaire</s0>
<s5>13</s5>
</fC03>
<fC03 i1="11" i2="3" l="ENG">
<s0>Quaternary compounds</s0>
<s5>13</s5>
</fC03>
<fC03 i1="12" i2="3" l="FRE">
<s0>Etude expérimentale</s0>
<s5>14</s5>
</fC03>
<fC03 i1="12" i2="3" l="ENG">
<s0>Experimental study</s0>
<s5>14</s5>
</fC03>
<fC03 i1="13" i2="3" l="FRE">
<s0>La2Eu2O3F6</s0>
<s4>INC</s4>
<s5>53</s5>
</fC03>
<fC03 i1="14" i2="3" l="FRE">
<s0>Eu F La O</s0>
<s4>INC</s4>
<s5>54</s5>
</fC03>
<fC03 i1="15" i2="3" l="FRE">
<s0>6630H</s0>
<s2>PAC</s2>
<s4>INC</s4>
<s5>56</s5>
</fC03>
<fC03 i1="16" i2="3" l="FRE">
<s0>6166F</s0>
<s2>PAC</s2>
<s4>INC</s4>
<s5>57</s5>
</fC03>
<fC07 i1="01" i2="3" l="FRE">
<s0>Lanthanide composé</s0>
<s5>48</s5>
</fC07>
<fC07 i1="01" i2="3" l="ENG">
<s0>Rare earth compounds</s0>
<s5>48</s5>
</fC07>
<fC07 i1="02" i2="3" l="FRE">
<s0>Composé minéral</s0>
<s5>49</s5>
</fC07>
<fC07 i1="02" i2="3" l="ENG">
<s0>Inorganic compounds</s0>
<s5>49</s5>
</fC07>
<fN21>
<s1>041</s1>
</fN21>
<fN82>
<s1>PSI</s1>
</fN82>
</pA>
<pR>
<fA30 i1="01" i2="1" l="ENG">
<s1>SSI 2001 International Conference on Solid State Ionics</s1>
<s3>Cairns AUS</s3>
<s4>2001-07-08</s4>
</fA30>
</pR>
</standard>
</inist>
</record>

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