Department of Energy Engineering, Hanyang University , Seoul 04763, Republic of Korea.
ACS Appl Mater Interfaces. 2018 Jan 10;10(1):526-533. doi: 10.1021/acsami.7b14279. Epub 2017 Dec 28.
As a substitute for the current lithium-ion batteries, rechargeable lithium oxygen batteries have attracted much attention because of their theoretically high energy density, but many challenges continue to exist. For the development of these batteries, understanding and controlling the main discharge product LiO (lithium peroxide) are of paramount importance. Here, we comparatively analyzed the amount of LiO in the cathodes discharged at various discharge capacities and current densities in dimethyl sulfoxide (DMSO) and tetraethylene glycol dimethyl ether (TEGDME) solvents. The precise assessment entailed revisiting and revising the UV-vis titration analysis. The amount of LiO electrochemically formed in DMSO was less than that formed in TEGDME at the same capacity and even at a much higher full discharge capacity in DMSO than in TEGDME. On the basis of our analytical experimental results, this unexpected result was ascribed to the presence of soluble LiO-like intermediates that remained in the DMSO solvent and the chemical transformation of LiO to LiOH, both of which originated from the inherent properties of the DMSO solvent.
作为当前锂离子电池的替代品,可充电锂氧电池因其理论上的高能量密度而引起了广泛关注,但仍存在许多挑战。对于这些电池的发展,理解和控制主要的放电产物 LiO(过氧化锂)至关重要。在这里,我们比较分析了在二甲基亚砜(DMSO)和四乙二醇二甲醚(TEGDME)溶剂中以不同放电容量和电流密度放电的阴极中 LiO 的含量。精确的评估需要重新审视和修订 UV-vis 滴定分析。在相同容量下,DMSO 中电化学形成的 LiO 量少于 TEGDME 中形成的 LiO 量,甚至在 DMSO 中的完全放电容量比在 TEGDME 中高得多的情况下也是如此。基于我们的分析实验结果,这种出乎意料的结果归因于存在可溶的 LiO 样中间体,它们残留在 DMSO 溶剂中,以及 LiO 向 LiOH 的化学转化,这两者都源于 DMSO 溶剂的固有性质。