The Sudden Death Phenomena in Nonaqueous Na-O2 Batteries

被引:42
|
作者
Nichols, Jessica E.
McCloskey, Bryan D. [1 ]
机构
[1] Univ Calif Berkeley, Dept Chem & Biomol Engn, Berkeley, CA 94720 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2017年 / 121卷 / 01期
基金
美国国家科学基金会;
关键词
DISCHARGE PRODUCTS; SODIUM SUPEROXIDE; ELECTROCHEMICAL IMPEDANCE; CELL CHEMISTRY; AIR BATTERIES; LI-O-2; LITHIUM; NAO2; LIMITATIONS; INSIGHTS;
D O I
10.1021/acs.jpcc.6b09663
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
Metal-air (O-2) batteries have been intensely studied over the past decade as potential high-energy alternatives to current state-of-the-art Li-ion batteries. Although Li-O-2 batteries possess higher theoretical specific energies, Na-O-2 cells have been reported to achieve higher capacities on discharge and exhibit much lower overpotentials on charge than analogous Li-O-2 cells. Nevertheless, sudden and large overpotential increases ("sudden deaths") occur in Na-O-2 cells on both discharge and charge, substantially limiting achievable capacity on discharge and increasing the average charge voltage, thereby reducing round-trip energy efficiency. In this work, we unravel the origins of these sudden death phenomena, which have been previously linked to the electrochemistry occurring at the cathode. On discharge, the maximum capacity was limited by pore clogging at low current densities and by surface passivation at high current densities, with concentration polarization playing only a small role in limiting the achievable capacity. On charge, the discharge and charge current densities were both found to influence the attainable capacity prior to sudden death. We propose a charge mechanism consistent with our data, where a concerted surface oxidation mechanism and a dissolution-oxidation mechanism both contribute to the observed overpotentials. Sudden death on charge is proposed to occur when these two pathways cannot support the applied current rate.
引用
收藏
页码:85 / 96
页数:12
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