Enhanced electrochemical performance of garnet Li7La3Zr2O12 electrolyte by efficient incorporation of LiCl

被引:0
|
作者
Luo, Yali [1 ,2 ]
Dong, Jiaxin [1 ]
Wang, Yuanjun [1 ]
Wang, Zhaoqi [1 ]
Chen, Zi'ang [1 ]
Zhang, He [1 ]
机构
[1] Xuzhou Univ Technol, Sch Mat & Chem Engn, Xuzhou 221018, Jiangsu, Peoples R China
[2] Xuzhou Univ Technol, Res Ctr Waste Reuse & New Energy Technol, Xuzhou 221018, Jiangsu, Peoples R China
关键词
LiCl incorporation; Electrochemical performance; Lithium-sulfur battery; IONIC-CONDUCTIVITY; SOLID-ELECTROLYTE; CERAMIC ELECTROLYTES; LI+ CONDUCTIVITY; LITHIUM; STABILITY; MICROSTRUCTURE; SUBSTITUTION; ADDITIVES; CAPACITY;
D O I
10.1016/j.ceramint.2024.10.015
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Garnet-type Ta-doped Li7La3Zr2O12 (LLZO) lithium-ion-conducting ceramic electrolytes has become the promising and critical candidate for developing the high-energy-density all-solid-state lithium batteries, due to the satisfied Li+ conductivity, stability against metallic lithium anode, and the feasible preparation under ambient air. Here, to further increase the lithium-ion conductivity of LLZO comparable to that of the commercial organic liquid electrolytes, lithium chloride (LiCl) is effectively introduced to synthesize the garnet-type ceramic electrolytes with the nominal composition (Li6.5La3Zr1.5Ta0.5O12)1-x-(LiCl)x (x = 0, 5mol%, 10mol%, 15mol%, 20mol %, and 25mol%) via high-temperature calcination process. The cubic structure with highly conductive performance is confirmed from X-ray diffraction measurement as well as Raman spectra analysis. Structural information is observed according to field emission scanning electron microscope equipped with energy dispersive spectrometer and density measurements. Among above investigated ceramic compositions, the prepared (Li6.5La3Zr1.5Ta0.5O12)0.85-(LiCl)0.15 ceramic electrolyte sheet sintered at 1200 degrees C for 12h presents the roomtemperature Li-ion conductivity of 1.22 x 10-3 S center dot cm- 1 by alternating current (AC) impedance analysis along with the corresponding activation energy of 0.262eV through Arrhenius equation calculation. The electronic conductivity measurements are also done by direct-current polarization to confirm the ionic nature for all investigated ceramics. Furthermore, the Li|(Li6.5La3Zr1.5Ta0.5O12)0.85-(LiCl)0.15 |Li symmetric batteries can possess the small interfacial resistance of 92.3 Omega cm2 and stably run for 1000 h at 0.1 mA cm- 2 without a short circuit at room temperature. The hybridized lithium-sulfur battery with (Li6.5La3Zr1.5Ta0.5O12)0.85-(LiCl)0.15 electrolyte delivered excellent initial room-temperature discharge capacity of 1204mAh center dot g- 1 and 1152 mAh center dot g-1 under the current density of 0.1C and 0.2C respectively, large coulombic efficiency, and great cycling stability. Moreover, the lithium-sulfur batteries also can show excellent cycling performances under different current densities and a good capacity recoverability. The above investigation results suggest that the low-melting-point LiCl incorporation in Li6.5La3Zr1.5Ta0.5O12 electrolyte is an effective measurement to synthesize the cubic and dense Li-stuff garnet ceramic sheets for the high-performance rechargeable next-generation solid-state batteries.
引用
收藏
页码:51055 / 51064
页数:10
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