NASICON LiM2(PO4)3 electrolyte (M = Zr) and electrode (M = Ti) materials for all solid-state Li-ion batteries with high total conductivity and low interfacial resistance

被引:65
作者
El-Shinawi, Hany [1 ]
Regoutz, Anna [2 ]
Payne, David J. [2 ]
Cussen, Edmund J. [3 ]
Corr, Serena A. [1 ]
机构
[1] Univ Glasgow, Sch Chem, WestCHEM, Glasgow G12 8QQ, Lanark, Scotland
[2] Imperial Coll London, Dept Mat, Exhibit Rd, London SW7 2AZ, England
[3] Univ Strathclyde, Dept Pure & Appl Chem, WestCHEM, Glasgow G1 1XL, Lanark, Scotland
基金
英国工程与自然科学研究理事会;
关键词
LITHIUM METAL ANODE; ROOM-TEMPERATURE; SUBSTITUTED LI7LA3ZR2O12; LIZR2(PO4)3; STABILITY; MICROSTRUCTURE; TRANSPORT;
D O I
10.1039/c7ta08715b
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
All solid-state batteries based on NASICON-type LiM2(PO4)(3) electrolyte phases are highly promising owing to their high ionic conductivities and chemical stabilities. Unlike Ti-based phases, extensively studied as Li+ solid electrolyte membranes, LiZr2(PO4)(3) (LZP) is expected to form a stable interface with a metallic lithium anode, a challenge which has posed a serious roadblock to realising safe all solid-state batteries. However, prohibitively large grain boundary resistances are often observed in this material and this issue, combined with processing difficulties in fabricating LZP in dense forms, has impinged on the application of LZP as a solid electrolyte for all solid-state batteries. To overcome these shortcomings and demonstrate the excellent potential of LZP as a solid electrolyte, we have developed a simple approach, based on sol-gel chemistry, to effectively improve the densification of the material leading to higher total conductivity than previously reported (1.0 x 10(-4) S cm(-1) at 80 degrees C) and enabling the investigation of the material as a Li+ solid electrolyte without the need for elaborate post-processing steps. The interfacial resistance decreases dramatically on using thin layers of Au buffer to improve the contact between Li and the LZP surface. The Li/LZP interface shows constant resistance upon Li+ cycling (at 40 mA cm(-2)), despite the formation of a passivation layer of Li3P/Li8ZrO6 on the LZP surface. This is consistent with the prediction that this surface layer serves as a Li+ conductive, solid electrolyte interface between Li and LZP. Finally, an analogue material, LiTi2(PO4)(3), is also introduced and demonstrated as an electrode material for proposed LZP-based all-solid-state batteries.
引用
收藏
页码:5296 / 5303
页数:8
相关论文
共 26 条
  • [21] DIMORPHISM, PHASE-TRANSITIONS, AND TRANSPORT-PROPERTIES IN LIZR2(PO4)3
    SUDREAU, F
    PETIT, D
    BOILOT, JP
    [J]. JOURNAL OF SOLID STATE CHEMISTRY, 1989, 83 (01) : 78 - 90
  • [22] The effects of crystallization parameters on the ionic conductivity of a lithium aluminum germanium phosphate glass-ceramic
    Thokchom, Joykumar S.
    Kumar, Binod
    [J]. JOURNAL OF POWER SOURCES, 2010, 195 (09) : 2870 - 2876
  • [23] Li7La3Zr2O12 Interface Modification for Li Dendrite Prevention
    Tsai, Chill-Long
    Roddatis, Vladimir
    Chandran, C. Vinod
    Ma, Qianli
    Uhlenbruck, Sven
    Bram, Martin
    Heitjans, Paul
    Guillon, Olivier
    [J]. ACS APPLIED MATERIALS & INTERFACES, 2016, 8 (16) : 10617 - 10626
  • [24] Direct Observation of the Interfacial Instability of the Fast Ionic Conductor Li10GeP2S12 at the Lithium Metal Anode
    Wenzel, Sebastian
    Randau, Simon
    Leichtweiss, Thomas
    Weber, Dominik A.
    Sann, Joachim
    Zeier, Wolfgang G.
    Janek, Juergen
    [J]. CHEMISTRY OF MATERIALS, 2016, 28 (07) : 2400 - 2407
  • [25] Interphase formation and degradation of charge transfer kinetics between a lithium metal anode and highly crystalline Li7P3S11 solid electrolyte
    Wenzel, Sebastian
    Weber, Dominik A.
    Leichtweiss, Thomas
    Busche, Martin R.
    Sann, Joachim
    Janek, Juergen
    [J]. SOLID STATE IONICS, 2016, 286 : 24 - 33
  • [26] Li1.2Zr1.9Ca0.1(PO4)3, a room-temperature Li-ion solid electrolyte
    Xie, Hui
    Goodenough, John B.
    Li, Yutao
    [J]. JOURNAL OF POWER SOURCES, 2011, 196 (18) : 7760 - 7762