McCloskey Bryan D, Garcia Jeannette M, Luntz Alan C
†IBM Research, Almaden Research Center, San Jose, California 95120, United States.
‡SUNCAT, SLAC National Accelerator Laboratory, Menlo Park, California 94025, United States.
J Phys Chem Lett. 2014 Apr 3;5(7):1230-5. doi: 10.1021/jz500494s. Epub 2014 Mar 24.
We present a comparative study of nonaqueous Li-O2 and Na-O2 batteries employing an ether-based electrolyte. The most intriguing difference between the two batteries is their respective galvanostatic charging overpotentials: a Na-O2 battery exhibits a low overpotential throughout most of its charge, whereas a Li-O2 battery has a low initial overpotential that continuously increases to very high voltages by the end of charge. However, we find that the inherent kinetic Li and Na-O2 overpotentials, as measured on a flat glassy carbon electrode in a bulk electrolysis cell, are similar. Measurement of each batteries' desired product yield, YNaO2 and YLi2O2, during discharge and rechargeability by differential electrochemical mass spectrometry (DEMS) indicates that less chemical and electrochemical decomposition occurs in a Na-O2 battery during the first Galvanostatic discharge-charge cycle. We therefore postulate that reactivity differences (Li2O2 being more reactive than NaO2) between the major discharge products lead to the observed charge overpotential difference between each battery.
我们展示了一项使用醚基电解质的非水锂氧电池和钠氧电池的对比研究。这两种电池之间最引人注目的差异在于它们各自的恒电流充电过电势:钠氧电池在其大部分充电过程中表现出低过电势,而锂氧电池具有低初始过电势,该过电势在充电结束时持续增加到非常高的电压。然而,我们发现,在本体电解池中在平坦的玻碳电极上测量的固有动力学锂和钠氧过电势是相似的。通过差分电化学质谱法(DEMS)测量每个电池在放电和再充电过程中的期望产物产率YNaO₂和YLi₂O₂,表明在第一个恒电流充放电循环期间,钠氧电池中发生的化学和电化学分解较少。因此,我们推测主要放电产物之间的反应性差异(Li₂O₂比NaO₂更具反应性)导致了每个电池之间观察到的充电过电势差异。