Tape-cast Ce-substituted Li7La3Zr2O12 electrolyte for improving electrochemical performance of solid-state lithium batteries

Solid-state lithium-metal batteries (SSLMBs) with a composite solid electrolyte (CSE) have great potential for achieving both high energy density and high safety and are thus promising next-generation energy storage devices. The current bottlenecks are a high electrode/electrolyte interface resistan...

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Veröffentlicht in:Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2022-11, Vol.10 (42), p.22512-22522
Hauptverfasser: Rath, Purna Chandra, Yu-Syuan Jheng, Cheng-Chia, Chen, Chih-Long, Tsai, Yu-Sheng, Su, Chun-Chen, Yang, Rüdiger-A Eichel, Hsieh, Chien-Te, Tai-Chou, Lee, Chang, Jeng-Kuei
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Sprache:eng
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Zusammenfassung:Solid-state lithium-metal batteries (SSLMBs) with a composite solid electrolyte (CSE) have great potential for achieving both high energy density and high safety and are thus promising next-generation energy storage devices. The current bottlenecks are a high electrode/electrolyte interface resistance and the limited Li+ conductivity of the solid electrolyte layer. To reduce the interface resistance, a tape casting method is used to directly deposit a CSE layer (∼20 μm) onto a model LiFePO4 cathode. The CSE slurry infiltrates the cathode layer, forming a Li+ conduction network and ensuring intimate contact between the CSE and the cathode. The tape casting parameters, such as the polymer/Li salt ratio, inorganic filler fraction, and casting thickness, for the CSE layer are investigated. To increase Li+ conductivity, Ce substitution is conducted for Li7La3Zr2−xCexO12, x = 0–0.15. The effects of Ce content on the specific capacity, rate capability, and cycling stability of Li//CSE//LiFePO4 cells are systematically studied. Li7La3Zr1.9Ce0.1O12 (i.e., x = 0.1) is found to be the optimal composition; it outperforms Li7La3Zr2O12 and Li6.25Ga0.25La3Zr2O12 in terms of CSE conductivity and SSLMB charge–discharge performance.
ISSN:2050-7488
2050-7496
DOI:10.1039/d2ta06808g