4.6 Article

A perovskite-structured aluminium-substituted lithium lanthanum titanate as a potential artificial solid-electrolyte interface for aqueous rechargeable lithium-metal-based batteries

Journal

ELECTROCHIMICA ACTA
Volume 248, Issue -, Pages 232-242

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.electacta.2017.07.110

Keywords

Lithium lanthanum titanate; Lithium-metal batteries; Bilayer solid electrolyte; Protected lithium electrode; Aqueous electrolyte

Funding

  1. Basic Research Program through national foundation of Korea (NRF) [2015R1D1A3A01019399]
  2. leading human resource training program of regional neo industry through national foundation of Korea (NRF) [2017H1D5A1044874]
  3. Materials/Components Technology Development Program [10077287]
  4. Ministry of Trade, Industry & Energy of Korea
  5. National Research Foundation of Korea [2017H1D5A1044874, 2015R1D1A3A01019399] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

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An aluminium-doped lithium lanthanum titanate (A-LLTO) solid electrolyte was prepared using a simple citrate-gel method, and this was followed by a pelletization and the conventional sintering process. When the sintering time was varied at 1350 degrees C for the synthesis of the A-LLTO, the A-LLTO ceramic that was sintered at 1350 degrees C for 6 h exhibited the highest ionic conductivity of 3.17 x 10(-4) S cm(-1) at 25 degrees C. In addition, the stability and durability of the synthesized A-LLTO ceramic was tested through a one-month aqueous-solution immersion for which the pH values were varied between 0 and 14. The stability of the A-LLTO is the highest in the alkaline environment; furthermore, for its use in the aqueous-electrolyte environment, a protected lithium electrode (PLE) structure was made by combining the lithium (Li) metal, a lithium phosphorous oxynitride (LiPON) interlayer, and the A-LLTO, whereby the LiPON interlayer prevented a direct reaction between the Li metal and the A-LLTO. The Li-LiCoO2 and Li-O-2 cells comprising the PLE exhibited a superior electrochemical performance when they were used in the alkaline 1 M LiNO3-electrolyte environment. After 100 cycles of the charge-discharge at the 1C rate, the aqueous Li-LiCoO2 cells maintained 59.3% of the initial capacity with a coulombic efficiency of 98.3%. In addition, the aqueous Li-O-2 cell operated stably for 40 cycles under the limited capacity mode of 0.5 mAh cm (2). The outstanding performance of the Li-metal-based cells originates from the A-LLTO solid electrolyte, due to the latter's high stability, ionic conductivity, and an effective suppression effect regarding the dendritic growth of the Li. (C) 2017 Elsevier Ltd. All rights reserved.

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