Reaction mechanisms of Li0.30La0.57TiO3 powder with ambient air: H+/Li+ exchange with water and Li2CO3 formation

被引:54
作者
Boulant, Anthony [2 ]
Bardeau, Jean Francois [2 ]
Jouanneaux, Alain [2 ]
Emery, Joel [2 ]
Buzare, Jean-Yves [2 ]
Bohnke, Odile [1 ]
机构
[1] Univ Maine, Inst Rech Ingn Mol & Mat Fonct, Lab Oxydes & Fluorures, CNRS,UMR 6010,FR 2575, F-72085 Le Mans 9, France
[2] Univ Maine, Inst Rech Ingn Mol & Mat Fonct, Lab Phys Etat Condense, CNRS,UMR 6087,FR 2575, F-72085 Le Mans 9, France
关键词
LITHIUM-ION BATTERIES; CO2; ABSORPTION; CARBON-DIOXIDE; MAGNETIC-RESONANCE; PEROVSKITE; SURFACE; OXIDES; NUCLEAR; NMR; LI3XLA2/3-X-SQUARE-1/3-2XTIO3;
D O I
10.1039/b924684c
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The proton/lithium exchange property of the lithium lanthanum titanate Li0.30La0.57TiO3 ( named LLTO) is shown to occur at room temperature under ambient air. The H-1 and Li-7 MAS NMR, TGA analysis and IR spectroscopy techniques are used to probe reaction mechanisms. XRPD analysis gives evidence of the topotactic character of this exchange reaction. As for exchange in aqueous solution, it is shown that Li0.30La0.57TiO3 is able to dissociate water on the grain surface and then to exchange H+ for Li+ into the perovskite structure. Lithium hydroxide is then formed on the grain surface and afterwards reacts with CO2 contained in air to form Li2CO3. It is shown that this mechanism is reversible. When the aged sample ( aging in air for 5 months at room temperature) is annealed at 400 degrees C for two hours, the initial LLTO sample is totally recovered, a mass loss is observed and the carbonate signal in IR spectra disappears, demonstrating the reversibility of the carbonation reaction process.
引用
收藏
页码:3968 / 3975
页数:8
相关论文
共 46 条
[1]   Proton insertion in spinel lithium manganates and the effect of manganese substitution [J].
Aitchison, P ;
Ammundsen, B ;
Bell, T ;
Jones, D ;
Rozière, J ;
Burns, G ;
Berg, H ;
Tellgren, R ;
Thomas, J .
PHYSICA B, 2000, 276 :847-848
[2]  
BELOUS AG, 1987, ZH NEORG KHIM+, V32, P283
[3]   New process of preparation, structure, and physicochemical investigations of the new titanyl phosphate Ti2O(H2O)(PO4)2 [J].
Benmokhtar, S. ;
El jazoulia, A. ;
Chaminade, J. P. ;
Gravereau, P. ;
Menetrier, M. ;
Bouree, F. .
JOURNAL OF SOLID STATE CHEMISTRY, 2007, 180 (10) :2713-2722
[4]   Topotactic H+/Li+ ion exchange on La2/3-xLi3xTiO3:: New metastable perovskite phases La2/3-xTiO3-3x(OH)3x and La2/3-xTiO3-3x/2 obtained by further dehydration [J].
Bhuvanesh, NSP ;
Bohnke, O ;
Duroy, H ;
Crosnier-Lopez, MP ;
Emery, J ;
Fourquet, JL .
MATERIALS RESEARCH BULLETIN, 1998, 33 (11) :1681-1691
[5]   FACTORS INFLUENCING RATE OF CARBON DIOXIDE REACTION WITH LITHIUM HYDROXIDE [J].
BORYTA, DA ;
MAAS, AJ .
INDUSTRIAL & ENGINEERING CHEMISTRY PROCESS DESIGN AND DEVELOPMENT, 1971, 10 (04) :489-&
[6]  
BOULANT A, 2009, THESIS U MAINE LE MA
[7]   Efficient Ion Exchange of H+ for Li+ in (Li0.30La0.57□0.13)TiO3 Perovskite in Water: Protons As a Probe for Li Location [J].
Boulant, Anthony ;
Maury, Pierre ;
Emery, Joel ;
Buzare, Jean-Yves ;
Bohnke, Odile .
CHEMISTRY OF MATERIALS, 2009, 21 (11) :2209-2217
[8]   RAMAN AND INFRARED SPECTRAL STUDIES OF ANHYDROUS LI2CO3 AND NA2CO3 [J].
BROOKER, MH ;
BATES, JB .
JOURNAL OF CHEMICAL PHYSICS, 1971, 54 (11) :4788-+
[9]   THE INFRA-RED SPECTRA AND STRUCTURES OF LI2CO3 AND ANHYDROUS NA2CO3 [J].
BUIJS, K ;
SCHUTTE, CJH .
SPECTROCHIMICA ACTA, 1961, 17 (9-10) :927-932
[10]   INFRARED SPECTROSCOPIC IDENTIFICATION OF SPECIES ARISING FROM REACTIVE ADSORPTION OF CARBON OXIDES ON METAL-OXIDE SURFACES [J].
BUSCA, G ;
LORENZELLI, V .
MATERIALS CHEMISTRY, 1982, 7 (01) :89-126