IBM Almaden Research Center, San Jose, California 95120, United States.
J Am Chem Soc. 2011 Nov 16;133(45):18038-41. doi: 10.1021/ja207229n. Epub 2011 Oct 21.
Heterogeneous electrocatalysis has become a focal point in rechargeable Li-air battery research to reduce overpotentials in both the oxygen reduction (discharge) and especially oxygen evolution (charge) reactions. In this study, we show that past reports of traditional cathode electrocatalysis in nonaqueous Li-O(2) batteries were indeed true, but that gas evolution related to electrolyte solvent decomposition was the dominant process being catalyzed. In dimethoxyethane, where Li(2)O(2) formation is the dominant product of the electrochemistry, no catalytic activity (compared to pure carbon) is observed using the same (Au, Pt, MnO(2)) nanoparticles. Nevertheless, the onset potential of oxygen evolution is only slightly higher than the open circuit potential of the cell, indicating conventional oxygen evolution electrocatalysis may be unnecessary.
多相电催化已成为可再充电锂-空气电池研究的焦点,以降低氧气还原(放电)和特别是氧气析出(充电)反应中的过电势。在本研究中,我们表明,过去关于非水锂-O2 电池中传统阴极电催化的报告确实是正确的,但与电解质溶剂分解有关的气体析出是被催化的主要过程。在二甘醇二甲醚中,Li2O2 的形成是电化学的主要产物,使用相同的(Au、Pt、MnO2)纳米粒子,在纯碳的情况下,没有观察到催化活性(相比)。然而,氧气析出的起始电位仅略高于电池的开路电位,表明传统的氧气析出电催化可能是不必要的。