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Structural and ionic transport studies of LiAlyCo1+yO2 nano-structured intercalation compounds

Identifieur interne : 000110 ( PascalFrancis/Curation ); précédent : 000109; suivant : 000111

Structural and ionic transport studies of LiAlyCo1+yO2 nano-structured intercalation compounds

Auteurs : N. Amdouni [France, Tunisie] ; H. Zarrouk [Tunisie] ; F. Soulette [France] ; C. Julien [France]

Source :

RBID : Pascal:05-0330155

Descripteurs français

English descriptors

Abstract

We present the electrochemical features behavior of LiAlyCo1-yO2 (0.0≤y≤0.3) electrodes prepared by "chimie douce" using the citrate route. The phase evolution was studied as a function of the aluminum substitution and the modification on the intercalation and deintercalation of Li ions. The overall electrochemical capacity of the LiAlyCo1-yO2 oxides have been reduced due to the sp metal substitution, however, a more stable charge-discharge cycling performances have been observed when electrodes are charged up to 4.3 V as compared to the performance of the native oxide. For such a cut-off voltage, the charge capacity of the Li//LiAl0.2Co0.8O2 cell is ca. 118 mAh/g. Kinetics characterized by the GITT method show enhancement of the chemical diffusion coefficients upon Al substitution in the LiAlyCo1-yO2 matrix.
pA  
A01 01  1    @0 0161-6374
A05       @2 20
A08 01  1  ENG  @1 Structural and ionic transport studies of LiAlyCo1+yO2 nano-structured intercalation compounds
A09 01  1  ENG  @1 New trends in intercalation compounds for energy storage conversion : Paris, 30 April - 2 May 2003
A11 01  1    @1 AMDOUNI (N.)
A11 02  1    @1 ZARROUK (H.)
A11 03  1    @1 SOULETTE (F.)
A11 04  1    @1 JULIEN (C.)
A12 01  1    @1 ZAGHIB (K.) @9 ed.
A12 02  1    @1 JULIEN (C.M.) @9 ed.
A12 03  1    @1 PRAKASH (J.) @9 ed.
A14 01      @1 LMDH, CNRS-UMR 7603, Université Pierre et Marie Curie, 4 place Jussieu, case 86 @2 75252 Paris @3 FRA @Z 1 aut. @Z 3 aut. @Z 4 aut.
A14 02      @1 LCM, Université de Tunis El Manar, Campus Universitaire @2 2092 El Manar II @3 TUN @Z 1 aut. @Z 2 aut.
A18 01  1    @1 Electrochemical Society. Battery Division @2 Pennington NJ @3 USA @9 patr.
A18 02  1    @1 Electrochemical Society. Energy Technology Division @2 Pennington NJ @3 USA @9 patr.
A20       @1 363-368
A21       @1 2003
A23 01      @0 ENG
A26 01      @0 1-56677-403-9
A43 01      @1 INIST @2 22195 @5 354000124436780440
A44       @0 0000 @1 © 2005 INIST-CNRS. All rights reserved.
A45       @0 18 ref.
A47 01  1    @0 05-0330155
A60       @1 P @2 C
A61       @0 A
A64 01  1    @0 Proceedings - Electrochemical society
A66 01      @0 USA
C01 01    ENG  @0 We present the electrochemical features behavior of LiAlyCo1-yO2 (0.0≤y≤0.3) electrodes prepared by "chimie douce" using the citrate route. The phase evolution was studied as a function of the aluminum substitution and the modification on the intercalation and deintercalation of Li ions. The overall electrochemical capacity of the LiAlyCo1-yO2 oxides have been reduced due to the sp metal substitution, however, a more stable charge-discharge cycling performances have been observed when electrodes are charged up to 4.3 V as compared to the performance of the native oxide. For such a cut-off voltage, the charge capacity of the Li//LiAl0.2Co0.8O2 cell is ca. 118 mAh/g. Kinetics characterized by the GITT method show enhancement of the chemical diffusion coefficients upon Al substitution in the LiAlyCo1-yO2 matrix.
C02 01  X    @0 001D05I03E
C03 01  3  FRE  @0 Batterie électrique @5 05
C03 01  3  ENG  @0 Electric batteries @5 05
C03 02  X  FRE  @0 Lithium ion @5 06
C03 02  X  ENG  @0 Lithium ion @5 06
C03 02  X  SPA  @0 Litio ión @5 06
C03 03  X  FRE  @0 Composé insertion @5 07
C03 03  X  ENG  @0 Intercalation compound @5 07
C03 03  X  SPA  @0 Compuesto inserción @5 07
C03 04  X  FRE  @0 Propriété électrochimique @5 08
C03 04  X  ENG  @0 Electrochemical properties @5 08
C03 04  X  SPA  @0 Propiedad electroquímica @5 08
C03 05  X  FRE  @0 Cathode @5 09
C03 05  X  ENG  @0 Cathode @5 09
C03 05  X  SPA  @0 Cátodo @5 09
C03 06  X  FRE  @0 Matériau électrode @5 10
C03 06  X  ENG  @0 Electrode material @5 10
C03 06  X  SPA  @0 Material electrodo @5 10
C03 07  X  FRE  @0 Lithium oxyde @5 11
C03 07  X  ENG  @0 Lithium oxide @5 11
C03 07  X  SPA  @0 Litio óxido @5 11
C03 08  X  FRE  @0 Aluminium oxyde @5 12
C03 08  X  ENG  @0 Aluminium oxide @5 12
C03 08  X  SPA  @0 Aluminio óxido @5 12
C03 09  X  FRE  @0 Cobalt oxyde @5 13
C03 09  X  ENG  @0 Cobalt oxide @5 13
C03 09  X  SPA  @0 Cobalto óxido @5 13
N21       @1 234
pR  
A30 01  1  ENG  @1 International symposium on new trends in intercalation compounds for energy storage and conversion @3 Paris FRA @4 2003-04-30

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<div type="abstract" xml:lang="en">We present the electrochemical features behavior of LiAl
<sub>y</sub>
Co
<sub>1-y</sub>
O
<sub>2</sub>
(0.0≤y≤0.3) electrodes prepared by "chimie douce" using the citrate route. The phase evolution was studied as a function of the aluminum substitution and the modification on the intercalation and deintercalation of Li ions. The overall electrochemical capacity of the LiAl
<sub>y</sub>
Co
<sub>1-y</sub>
O
<sub>2</sub>
oxides have been reduced due to the sp metal substitution, however, a more stable charge-discharge cycling performances have been observed when electrodes are charged up to 4.3 V as compared to the performance of the native oxide. For such a cut-off voltage, the charge capacity of the Li//LiAl
<sub>0.2</sub>
Co
<sub>0.8</sub>
O
<sub>2</sub>
cell is ca. 118 mAh/g. Kinetics characterized by the GITT method show enhancement of the chemical diffusion coefficients upon Al substitution in the LiAl
<sub>y</sub>
Co
<sub>1-y</sub>
O
<sub>2</sub>
matrix.</div>
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nano-structured intercalation compounds</s1>
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<sub>y</sub>
Co
<sub>1-y</sub>
O
<sub>2</sub>
(0.0≤y≤0.3) electrodes prepared by "chimie douce" using the citrate route. The phase evolution was studied as a function of the aluminum substitution and the modification on the intercalation and deintercalation of Li ions. The overall electrochemical capacity of the LiAl
<sub>y</sub>
Co
<sub>1-y</sub>
O
<sub>2</sub>
oxides have been reduced due to the sp metal substitution, however, a more stable charge-discharge cycling performances have been observed when electrodes are charged up to 4.3 V as compared to the performance of the native oxide. For such a cut-off voltage, the charge capacity of the Li//LiAl
<sub>0.2</sub>
Co
<sub>0.8</sub>
O
<sub>2</sub>
cell is ca. 118 mAh/g. Kinetics characterized by the GITT method show enhancement of the chemical diffusion coefficients upon Al substitution in the LiAl
<sub>y</sub>
Co
<sub>1-y</sub>
O
<sub>2</sub>
matrix.</s0>
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<s5>10</s5>
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<s5>11</s5>
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<s0>Lithium oxide</s0>
<s5>11</s5>
</fC03>
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<s0>Litio óxido</s0>
<s5>11</s5>
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<s0>Aluminium oxyde</s0>
<s5>12</s5>
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<s5>12</s5>
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<s5>13</s5>
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<s5>13</s5>
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<fA30 i1="01" i2="1" l="ENG">
<s1>International symposium on new trends in intercalation compounds for energy storage and conversion</s1>
<s3>Paris FRA</s3>
<s4>2003-04-30</s4>
</fA30>
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   |texte=   Structural and ionic transport studies of LiAlyCo1+yO2 nano-structured intercalation compounds
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