Lithium difluoro(oxalato)borate: A promising salt for lithium metal based secondary batteries?

被引:87
作者
Schedlbauer, T. [1 ]
Krueger, S. [1 ]
Schmitz, R. [1 ]
Schmitz, R. W. [1 ]
Schreiner, C. [1 ]
Gores, H. J. [1 ]
Passerini, S. [1 ]
Winter, M. [1 ]
机构
[1] Univ Munster, Inst Phys Chem, MEET Battery Res Ctr, D-48149 Munster, Germany
关键词
Lithium metal anodes; Lithium difluoro(oxalato)borate; Lithium hexafluorophosphate; SEI-formation; Coulombic efficiency; Surface analysis; ION BATTERIES; ELECTROLYTE-SOLUTIONS; RECHARGEABLE BATTERIES; PROPYLENE CARBONATE; LITHIATED GRAPHITE; CYCLING EFFICIENCY; SOLID-ELECTROLYTE; ORGANIC ADDITIVES; LI; BEHAVIOR;
D O I
10.1016/j.electacta.2013.01.023
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
This work is a comparative study on lithium cycling on copper in solutions based on ethylene carbonate (EC) and diethyl carbonate (DEC) (3:7, by wt.) and two lithium salts, lithium hexafluorophosphate (LiPF6) and lithium difluoro(oxalato)borate (LiDFOB). Coulombic efficiencies of the long term lithium deposition/dissolution experiments and dissolution-rate (D-rate) tests on copper demonstrated clearly the superior behavior of the LiDFOB-based electrolyte. To clarify the impact of the formed solid electrolyte interphase (SEI) on the Coulombic efficiencies achieved in the electrolytes, voltage drop values of the D-rate tests were compared with measured values of conductivities and AC impedance measurements of the electrolytes. The formed SEI has a larger influence on voltage drop values of a cell than the conductivity of the electrolyte. The correlation between surface chemistry, morphology, and Coulombic efficiencies of lithium deposition on copper was investigated by scanning electron microscopy (SEM) and Raman spectroscopy. All methods demonstrated the strong influence of the investigated lithium salts on the lithium deposition/dissolution performance on copper substrates. The LiDFOB-based electrolyte showed superior SEI properties than the LiPF6-based electrolyte. (C) 2013 Elsevier Ltd. All rights reserved.
引用
收藏
页码:102 / 107
页数:6
相关论文
共 57 条
  • [1] DIRECTIONS IN SECONDARY LITHIUM BATTERY RESEARCH-AND-DEVELOPMENT
    ABRAHAM, KM
    [J]. ELECTROCHIMICA ACTA, 1993, 38 (09) : 1233 - 1248
  • [2] Investigation of the Hydrolysis of Lithium Bis[1,2-oxalato(2+O,O′] Borate (LiBOB) in Water and Acetonitrile by Conductivity and NMR Measurements in Comparison to Some Other Borates
    Amereller, Marius
    Multerer, Michael
    Schreiner, Christian
    Lodermeyer, Johannes
    Schmid, Alexander
    Barthel, Josef
    Gores, Heiner J.
    [J]. JOURNAL OF CHEMICAL AND ENGINEERING DATA, 2009, 54 (02) : 468 - 471
  • [3] [Anonymous], 1980, Infrared Characteristic Group Frequencies
  • [4] Review of selected electrode-solution interactions which determine the performance of Li and Li ion batteries
    Aurbach, D
    [J]. JOURNAL OF POWER SOURCES, 2000, 89 (02) : 206 - 218
  • [5] A short review of failure mechanisms of lithium metal and lithiated graphite anodes in liquid electrolyte solutions
    Aurbach, D
    Zinigrad, E
    Cohen, Y
    Teller, H
    [J]. SOLID STATE IONICS, 2002, 148 (3-4) : 405 - 416
  • [6] New insights into the interactions between electrode materials and electrolyte solutions for advanced nonaqueous batteries
    Aurbach, D
    Markovsky, B
    Levi, MD
    Levi, E
    Schechter, A
    Moshkovich, M
    Cohen, Y
    [J]. JOURNAL OF POWER SOURCES, 1999, 81 : 95 - 111
  • [7] IMPEDANCE SPECTROSCOPY OF LITHIUM ELECTRODES .1. GENERAL BEHAVIOR IN PROPYLENE CARBONATE SOLUTIONS AND THE CORRELATION TO SURFACE-CHEMISTRY AND CYCLING EFFICIENCY
    AURBACH, D
    ZABAN, A
    [J]. JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1993, 348 (1-2): : 155 - 179
  • [8] Besenhard J.O., 1999, HDB BATTERY MAT, P618
  • [9] Besenhard JO, 2002, CHEMPHYSCHEM, V3, P155, DOI 10.1002/1439-7641(20020215)3:2<155::AID-CPHC155>3.0.CO
  • [10] 2-S