Reaction mechanism studies towards effective fabrication of lithium-rich anti-perovskites Li3OX (X = Cl, Br)

被引:92
作者
Li, Shuai [1 ]
Zhu, Jinlong [1 ]
Wang, Yonggang [1 ]
Howard, John W. [1 ]
Lu, Xujie [2 ,3 ]
Li, Yutao [4 ,5 ]
Kumar, Ravhi S. [1 ]
Wang, Liping [1 ]
Daemen, Luke L. [6 ]
Zhao, Yusheng [1 ]
机构
[1] Univ Nevada, High Pressure Sci & Engn Ctr, Las Vegas, NV 89154 USA
[2] Los Alamos Natl Lab, Ctr Integrated Nanotechnol, Los Alamos, NM 87545 USA
[3] Los Alamos Natl Lab, Earth & Environm Sci Div, Los Alamos, NM 87545 USA
[4] Univ Texas Austin, Mat Res Program, ETC9-184, Austin, TX 78712 USA
[5] Univ Texas Austin, Texas Mat Inst, ETC9-184, Austin, TX 78712 USA
[6] Oak Ridge Natl Lab, Spallat Neutron Source, Oak Ridge, TN 37831 USA
关键词
Solid electrolyte; Lithium-ion battery; Lithium-rich anti-perovskite; Solid-state reaction; IONIC-CONDUCTIVITY; LI; CHALLENGES; TRANSPORT;
D O I
10.1016/j.ssi.2015.11.027
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
Lithium-rich anti-perovskites (LiRAPs), with general formula Li3OX (X = Cl, Br), recently reported as superionic conductors with 3-dimensional Li+ migrating channels, are emerging as promising candidates for solid electrolytes in all-solid-state lithium-ion batteries (LIBs). However, great challenges remain in the fabrication of pure LiRAPs due to difficulties such as low yield, impurity phases, thermodynamic instabilities, and moisture sensitivity. In this work, we thoroughly studied the formation mechanism of Li3OCl and Li3OBr using various solid-state reaction routes. Different experimental strategies were developed to improve the syntheses, namely, for the purposes of phase stability, phase purity, and large-scale production. One feasible method is to use the strong reducing agents Li metal or LiH to eliminate the OH species. The results show that LiH is more effective than Li metal, mainly due to negatively charged H- and reaction uniformity. The other successful method employs a solid diffusion approach using Li2O and LiX as the starting reagents, thereby avoiding OH entirely; ball milling of reagents under Ar atmosphere was utilized to decrease initial grain size and increase the reaction rate. Fourier transform infrared spectroscopy (FTIR), thermal analyses, and first-principles calculations were performed to give indications on the reaction pathway. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:14 / 19
页数:6
相关论文
共 30 条
  • [1] [Anonymous], ADV ENERGY MAT
  • [2] [Anonymous], THESIS
  • [3] Building better batteries
    Armand, M.
    Tarascon, J. -M.
    [J]. NATURE, 2008, 451 (7179) : 652 - 657
  • [4] THE AC CONDUCTIVITY OF POLYCRYSTALLINE LISICON, LI2+2XZN1-XGEO4, AND A MODEL FOR INTERGRANULAR CONSTRICTION RESISTANCES
    BRUCE, PG
    WEST, AR
    [J]. JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1983, 130 (03) : 662 - 669
  • [5] First principles methods using CASTEP
    Clark, SJ
    Segall, MD
    Pickard, CJ
    Hasnip, PJ
    Probert, MJ
    Refson, K
    Payne, MC
    [J]. ZEITSCHRIFT FUR KRISTALLOGRAPHIE, 2005, 220 (5-6): : 567 - 570
  • [6] Phase Stability and Transport Mechanisms in Antiperovskite Li3OCl and Li3OBr Superionic Conductors
    Emly, Alexandra
    Kioupakis, Emmanouil
    Van der Ven, Anton
    [J]. CHEMISTRY OF MATERIALS, 2013, 25 (23) : 4663 - 4670
  • [7] Challenges in the development of advanced Li-ion batteries: a review
    Etacheri, Vinodkumar
    Marom, Rotem
    Elazari, Ran
    Salitra, Gregory
    Aurbach, Doron
    [J]. ENERGY & ENVIRONMENTAL SCIENCE, 2011, 4 (09) : 3243 - 3262
  • [8] INFRARED STUDIES OF APATITES .1. VIBRATIONAL ASSIGNMENTS FOR CALCIUM, STRONTIUM, AND BARIUM HYDROXYAPATITES UTILIZING ISOTOPIC-SUBSTITUTION
    FOWLER, BO
    [J]. INORGANIC CHEMISTRY, 1974, 13 (01) : 194 - 207
  • [9] FAST NA+-ION TRANSPORT IN SKELETON STRUCTURES
    GOODENOUGH, JB
    HONG, HYP
    KAFALAS, JA
    [J]. MATERIALS RESEARCH BULLETIN, 1976, 11 (02) : 203 - 220
  • [10] The Li-Ion Rechargeable Battery: A Perspective
    Goodenough, John B.
    Park, Kyu-Sung
    [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2013, 135 (04) : 1167 - 1176