Investigation of Fluorinated Amides for Solid-Electrolyte Interphase Stabilization in Li-O2 Batteries Using Amide-Based Electrolytes

被引:70
作者
Bryantsev, Vyacheslav S. [1 ]
Giordani, Vincent [1 ]
Walker, Wesley [1 ]
Uddin, Jasim [1 ]
Lee, Ilkeun [2 ]
van Duin, Adri C. T. [3 ]
Chase, Gregory V. [1 ]
Addison, Dan [1 ]
机构
[1] Liox Power Inc, Pasadena, CA 91106 USA
[2] Univ Calif Riverside, Dept Chem, Riverside, CA 92521 USA
[3] Penn State Univ, Dept Nucl & Mech Engn, State Coll, PA 16802 USA
关键词
RAY PHOTOELECTRON-SPECTROSCOPY; PROPYLENE CARBONATE SOLUTIONS; LITHIUM-OXYGEN BATTERY; IMPEDANCE SPECTROSCOPY; AIR BATTERIES; SURFACE; METAL; SOLVENTS; BEHAVIOR; XPS;
D O I
10.1021/jp402844r
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
Solvent and electrode stability is critical for the successful development of the rechargeable, organic electrolyte Li-O-2 (air) battery. Straight-chain alkyl amides, such as N,N-dimethylacetamide (DMA), show superior stability at the O-2 cathode compared to organic carbonates and glymes, but these solvents do not form a stable solid electrolyte interphase (SEI) to prevent a sustained reaction with Li metal. In this work, we use electrochemical impedance spectroscopy and cycling tests on a symmetric Li/electrolyte/Li cell to determine the ability of several fluorinated amide solvents to stabilize the lithium/electrolyte interface. The LiTFSI/N,N-dimethyltrifluoroacetamide (DMTFA) system shows the smallest interfacial impedance and the lowest polarization for Li dissolution and deposition. We present quantum chemical calculations indicating that a-fluorinated alkyl amides are reduced on Li to form insoluble LiF with no or little activation energy. XPS analysis confirms the presence of LiF in the SEI on Li metal exposed to DMTFA, which is likely to play an important role in stabilizing the lithium/electrolyte interface. The improved stability of a metallic Li anode in a rechargeable Li-O-2 battery with LiTFSI/DMA electrolyte is demonstrated using 2% DMTFA as the SE1-stabilizing additive.
引用
收藏
页码:11977 / 11988
页数:12
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