Macroscopic and microscopic Li+ transport parameters in cubic garnet-type "Li6.5La2.5Ba0.5ZrTaO12" as probed by impedance spectroscopy and NMR

被引:61
作者
Narayanan, S. [1 ]
Epp, V. [2 ]
Wilkening, M. [2 ]
Thangadurai, V. [1 ]
机构
[1] Univ Calgary, Dept Chem, Calgary, AB T2N 1N4, Canada
[2] Graz Univ Technol, Inst Chem & Technol Mat, A-8010 Graz, Austria
基金
加拿大创新基金会;
关键词
LITHIUM ION CONDUCTION; DIELECTRIC-RELAXATION; AC CONDUCTIVITY; LI7LA3ZR2O12; CHALLENGES; IDENTIFICATION; CRYSTALLINE; ELECTROLYTE; DIFFUSION;
D O I
10.1039/c2ra01042a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The garnet-type "Li6.5La2.5Ba0.5ZrTaO12", crystallizing with cubic symmetry was prepared according to a conventional solid state synthesis method using metal oxides and salt precursors of high purity. The formation of the "single-phase" garnet-type structure was studied by powder X-ray diffraction (PXRD). Electron microprobe analysis (EMPA) coupled with a wavelength-dispersive spectrometer (WDS) showed a rather homogeneous distribution of Ta ions and Zr ions compared to that of Ba ions and La ions in "Li6.5La2.5Ba0.5ZrTaO12". Li ion dynamics were complementarily studied using variable-temperature AC-impedance spectroscopy and Li-7 NMR measurements. The bulk (ion) conductivities probed are in very good agreement with results reported earlier, illustrating the excellent reproducibility of the Li transport properties of "Li6.5La2.5Ba0.5ZrTaO12". In particular, AC impedance and NMR results indicate that the Li transport process studied is of long-range nature. Finally, the chemical compatibility of the electrolyte "Li6.5La2.5Ba0.5ZrTaO12" was tested with Li2FeMn3O8, being a high-voltage cathode material. As shown by variable-temperature PXRD measurements, the garnet-type structure (bulk) was found to be stable up to 673 K.
引用
收藏
页码:2553 / 2561
页数:9
相关论文
共 51 条
[1]   Fast Li-circle plus conducting ceramic electrolytes [J].
Adachi, GY ;
Imanaka, N ;
Aono, H .
ADVANCED MATERIALS, 1996, 8 (02) :127-+
[2]   THE DETERMINATION OF HOPPING RATES AND CARRIER CONCENTRATIONS IN IONIC CONDUCTORS BY A NEW ANALYSIS OF AC CONDUCTIVITY [J].
ALMOND, DP ;
DUNCAN, GK ;
WEST, AR .
SOLID STATE IONICS, 1983, 8 (02) :159-164
[3]   TEMPERATURE-DEPENDENCE OF THE AC CONDUCTIVITY OF NA BETA-ALUMINA [J].
ALMOND, DP ;
WEST, AR ;
GRANT, RJ .
SOLID STATE COMMUNICATIONS, 1982, 44 (08) :1277-1280
[4]   Synthesis and structure analysis of tetragonal Li7La3Zr2O12 with the garnet-related type structure [J].
Awaka, Junji ;
Kijima, Norihito ;
Hayakawa, Hiroshi ;
Akimoto, Junji .
JOURNAL OF SOLID STATE CHEMISTRY, 2009, 182 (08) :2046-2052
[5]   Structure and ionic conductivity in lithium garnets [J].
Cussen, Edmund J. .
JOURNAL OF MATERIALS CHEMISTRY, 2010, 20 (25) :5167-5173
[6]   The structure of lithium garnets:: cation disorder and clustering in a new family of fast Li+ conductors [J].
Cussen, EJ .
CHEMICAL COMMUNICATIONS, 2006, (04) :412-413
[7]   Fast Li diffusion in crystalline LiBH4 due to reduced dimensionality: Frequency-dependent NMR spectroscopy [J].
Epp, V. ;
Wilkening, M. .
PHYSICAL REVIEW B, 2010, 82 (02)
[8]   Challenges in the development of advanced Li-ion batteries: a review [J].
Etacheri, Vinodkumar ;
Marom, Rotem ;
Elazari, Ran ;
Salitra, Gregory ;
Aurbach, Doron .
ENERGY & ENVIRONMENTAL SCIENCE, 2011, 4 (09) :3243-3262
[9]   Recent developments in cathode materials for lithium ion batteries [J].
Fergus, Jeffrey W. .
JOURNAL OF POWER SOURCES, 2010, 195 (04) :939-954
[10]   Multi-electron reaction materials for high energy density batteries [J].
Gao, Xue-Ping ;
Yang, Han-Xi .
ENERGY & ENVIRONMENTAL SCIENCE, 2010, 3 (02) :174-189