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In Situ Neutron Diffraction Monitoring of Li7La3Zr2O12 Formation: Toward a Rational Synthesis of Garnet Solid Electrolytes
被引:99
|作者:
Rao, R. Prasada
[1
]
Gu, Wenyi
[1
]
Sharma, Neeraj
[2
]
Peterson, Vanessa K.
[2
]
Avdeev, Maxim
[2
]
Adams, Stefan
[1
,3
]
机构:
[1] Natl Univ Singapore, Dept Mat Sci & Engn, Singapore 117575, Singapore
[2] Australian Nucl Sci & Technol Org, Bragg Inst, Kirrawee Dc, NSW 2232, Australia
[3] ASTAR, IMRE, Singapore 117602, Singapore
基金:
新加坡国家研究基金会;
关键词:
LITHIUM ION CONDUCTION;
POWDER DIFFRACTOMETER;
CRYSTAL-STRUCTURE;
PHASE-TRANSITION;
LOCAL-STRUCTURE;
LI5LA3M2O12;
M;
STABILITY;
NB;
DYNAMICS;
EXCHANGE;
D O I:
10.1021/acs.chemmater.5b00149
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:
The favorable combination of fast-ionic conductivity and high electrochemical stability of Li-stuffed garnet type Li7La3Zr2O12 (LLZ) makes this material a promising candidate for applications as a solid-state electrolyte in high-energy-density batteries. However, a widespread technical use of LLZ is impeded by difficulty in reliable formation and densification of the pure fast-ion conducting phase. The present study of the phase-formation process enables rational fabrication procedures to be devised based on a thorough understanding of the complex phase formation of LLZ. In situ neutron powder diffraction monitoring of the phase formation revealed an influence of the partial melting of precursors on the formation of the fast-ion conducting phase, indicating that in the typical synthesis route LLZ is not formed in a solid-state reaction but from a partial carbonate melt that decomposes on further heating. The cooling rate critically influences lithium ordering and ionic conductivity.
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页码:2903 / 2910
页数:8
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