An Electrochemical Impedance Study of the Capacity Limitations in Na-O2 Cells

被引:38
作者
Knudsen, Kristian B. [1 ,2 ]
Nichols, Jessica E. [2 ,3 ]
Vegge, Tejs [1 ]
Luntz, Alan C. [4 ,5 ]
McCloskey, Bryan D. [2 ,3 ]
Hjelm, Johan [1 ]
机构
[1] Tech Univ Denmark, Dept Energy Convers & Storage, DK-4000 Roskilde, Denmark
[2] Univ Calif Berkeley, Dept Chem & Biomol Engn, Berkeley, CA 94720 USA
[3] Univ Calif Berkeley, Lawrence Berkeley Natl Lab, Energy Storage & Distributed Resources Div, Berkeley, CA 94720 USA
[4] Stanford Univ, Dept Chem Engn, SUNCAT Ctr Interface Sci & Catalysis, 443 Via Ortega, Stanford, CA 94305 USA
[5] SLAC Natl Accelerator Lab, 2575 Sand Hill Rd, Menlo Pk, CA 94025 USA
基金
美国国家科学基金会;
关键词
NONAQUEOUS LI-O-2; SODIUM SUPEROXIDE; GROWTH; ELECTRODES; TRANSPORT; STABILITY; DISCHARGE; SOLVENTS; NAO2; O-2;
D O I
10.1021/acs.jpcc.6b02788
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
Electrochemical impedance spectroscopy, pressure change measurements, and scanning electron microscopy were used to investigate the nonaqueous Na-O-2 cell potential decrease and rise (sudden deaths) on discharge and charge, respectively. To fit the impedance spectra from operating cells, an equivalent circuit model was used that takes into account the porous nature of the positive electrode and is able to distinguish between the electrolyte resistance in the pores and the charge-transfer resistance of the pore walls. The results obtained indicate that sudden death on discharge is caused by, depending on the current density, either accumulation of large NaO2 crystals that eventually block the electrode surface and/or a thin film of NaO2 forming on the cathode surface at the end of discharge, which limits charge-transfer. The commonly observed sudden rise in potential toward the end of charge may be caused by a concentration depletion of NaO2 dissolved in the electrolyte near the cathode surface and/or an accumulation of degradation products on the cathode surface.
引用
收藏
页码:10799 / 10805
页数:7
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