Preparation and Characterization of Sol–Gel-Driven LixLa3Zr2O12 Solid Electrolytes and LiCoO2 Cathodes for All-Solid-State Lithium-Ion Batteries

2020 ◽  
Vol 20 (11) ◽  
pp. 7002-7009
Author(s):  
Gwan Hyeon Kim ◽  
Min Ji Kim ◽  
Hae Been Kim ◽  
Ji Heon Ryu ◽  
Hee Chul Lee

In the current study, we prepared a LixLa3Zr2O12 ((Al, Ta) LLZO) powder doped with 0.2 mol of Al and Ta using the sol-gel method and subsequently used it to fabricate solid electrolyte pellets. In pellets with lithium content of 6.2 and 6.82 mol, a cubic phase and a lithium-deficient pyrochlore mixed-phase were respectively observed. However, when the lithium content was 8.06 mol, a lithium-excess phase was also observed. Meanwhile, at 7.44 mol lithium, the (Al, Ta) LLZO ceramic pellets showed a pure cubic garnet phase with no secondary phase. When lithium was added excessively, a non-granular morphology was observed at the (Al, Ta) LLZO fracture surface in which the grains were tightly bonded by the liquid phase formed during sintering. Nyquist plots of the pellets showed that the effect of grain boundaries was eliminated and the pellets exhibited a high lithium ion conductivity of 4.26 × 10−4 S/cm. Using spin coating and multi-step heat treatment, we deposited LiCoO2 (LCO) thin films on (Al, Ta) LLZO pellets to form cathodes. There was no significant interdiffusion between the LCO cathode and (Al, Ta) LLZO solid electrolyte and morphological analysis indicted that a thin interfacial layer (~10 nm) was formed between the LCO and the electrolyte. Finally, we demonstrated an all-solid-state rechargeable battery in the form of a coin cell comprising of an LCO cathode, Li metal anode, and (Al, Ta) LLZO solid electrolyte, which could yield a discharge capacity of ~100 mAh/g.

Author(s):  
Seonggyu Cho ◽  
Shinho Kim ◽  
Wonho Kim ◽  
Seok Kim ◽  
Sungsook Ahn

Considering the safety issues of Li ion batteries, all-solid-state polymer electrolyte has been one of the promising solutions. In this point, achieving a Li ion conductivity in the solid state electrolytes comparable to liquid electrolytes (>1 mS/cm) is particularly challenging. Employment of polyethylene oxide (PEO) solid electrolyte has not been not enough in this point due to high crystallinity. In this study, hybrid solid electrolyte (HSE) systems are designed with Li1.3Al0.3Ti0.7(PO4)3(LATP), PEO and Lithium hexafluorophosphate (LiPF6) or Lithium bis(trifluoromethanesulfonyl)imide (LiTFSI). Hybrid solid cathode (HSC) is also designed using LATP, PEO and lithium cobalt oxide (LiCoO2, LCO)—lithium manganese oxide (LiMn2O4, LMO). The designed HSE system displays 3.0 × 10−4 S/cm (55 ℃) and 1.8 × 10−3 S/cm (23 ℃) with an electrochemical stability as of 6.0 V without any separation layer introduction. Li metal (anode)/HSE/HSC cell in this study displays initial charge capacity as of 123.4/102.7 mAh/g (55 ℃) and 73/57 mAh/g (25 °C). To these systems, Succinonitrile (SN) has been incorporated as a plasticizer for practical secondary Li ion battery system development to enhance ionic conductivity. The incorporated SN effectively increases the ionic conductivity without any leakage and short-circuits even under broken cell condition. The developed system also overcomes the typical disadvantages of internal resistance induced by Ti ion reduction. In this study, optimized ionic conductivity and low internal resistance inside the Li ion battery cell have been obtained, which suggests a new possibility in the secondary Li ion battery development.


Micromachines ◽  
2021 ◽  
Vol 12 (2) ◽  
pp. 134
Author(s):  
Minji Kim ◽  
Gwanhyeon Kim ◽  
Heechul Lee

The rapidly growing Li-ion battery market has generated considerable demand for Li-ion batteries with improved performance and stability. All-solid-state Li-ion batteries offer promising safety and manufacturing enhancements. Herein, we examine the effect of substitutional doping at three cation sites in garnet-type Li7La3Zr2O12 (LLZO) oxide ceramics produced by a sol–gel synthesis technique with the aim of enhancing the properties of solid-state electrolytes for use in all-solid-state Li-ion batteries. Building on the results of mono-doping experiments with different doping elements and sites—Al, Ga, and Ge at the Li+ site; Rb at the La3+ site; and Ta and Nb at the Zr4+ site—we designed co-doped (Ga, Al, or Rb with Nb) and tri-doped (Ga or Al with Rb and Nb) samples by compositional optimization, and achieved a LLZO ceramic with a pure cubic phase, almost no secondary phase, uniform grain structure, and excellent Li-ion conductivity. The findings extend the current literature on the doping of LLZO ceramics and highlight the potential of the sol–gel method for the production of solid-state electrolytes.


2016 ◽  
Vol 284 ◽  
pp. 1-6 ◽  
Author(s):  
Takashi Teranishi ◽  
Yuki Ishii ◽  
Hidetaka Hayashi ◽  
Akira Kishimoto

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
A-Young Kim ◽  
Florian Strauss ◽  
Timo Bartsch ◽  
Jun Hao Teo ◽  
Jürgen Janek ◽  
...  

AbstractWhile still premature as an energy storage technology, bulk solid-state batteries are attracting much attention in the academic and industrial communities lately. In particular, layered lithium metal oxides and lithium thiophosphates hold promise as cathode materials and superionic solid electrolytes, respectively. However, interfacial side reactions between the individual components during battery operation usually result in accelerated performance degradation. Hence, effective surface coatings are required to mitigate or ideally prevent detrimental reactions from occurring and having an impact on the cyclability. In the present work, we examine how surface carbonates incorporated into the sol–gel-derived LiNbO3 protective coating on NCM622 [Li1+x(Ni0.6Co0.2Mn0.2)1–xO2] cathode material affect the efficiency and rate capability of pellet-stack solid-state battery cells with β-Li3PS4 or argyrodite Li6PS5Cl solid electrolyte and a Li4Ti5O12 anode. Our research data indicate that a hybrid coating may in fact be beneficial to the kinetics and the cycling performance strongly depends on the solid electrolyte used.


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