首页> 外文期刊>The journal of physical chemistry, C. Nanomaterials and interfaces >Role of Li2O2@Li2CO3 Interfaces on Charge Transport in Nonaqueous Li-Air Batteries
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Role of Li2O2@Li2CO3 Interfaces on Charge Transport in Nonaqueous Li-Air Batteries

机译:Li2O2 @ Li2CO3接口在非水锂空气电池中电荷传输中的作用

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The formation and oxidation of the main discharge product in nonaqueous secondary Li-O-2 batteries, that is, Li2O2, has been studied intensively, but less attention has been given to the formation of cathode electrolyte interfaces, which can significantly influence the performance of the Li-O-2 battery. Here we apply density functional theory with the Hubbard U correction (DFT+U) and nonequilibrium Green's function (NEGF) methods to investigate the role of Li2O2@Li2CO3 interface layers on the ionic and electronic transport properties at the oxygen electrode. We show that, for example, lithium vacancies accumulate at the peroxide part of the interface during charge, reducing the coherent electron transport by two to three orders of magnitude compared with pristine Li2O2. During discharge, Li2O2@Li2CO3 interfaces may, however, provide an alternative in-plane channel for fast electron polaron hopping that could improve the electronic conductivity and ultimately increase the practical capacity in nonaqueous Li-O-2 batteries.
机译:已经对非水二次Li-O-2电池主要放电产物Li2O2的形成和氧化进行了深入研究,但对阴极电解质界面的形成的关注却很少,这会显着影响电池的性能。 Li-O-2电池。在这里,我们将密度泛函理论与Hubbard U校正(DFT + U)和非平衡格林函数(NEGF)方法结合使用,以研究Li2O2 @ Li2CO3界面层对氧电极上离子和电子传输性质的作用。我们表明,例如,锂空位在充电过程中聚集在界面的过氧化物部分,与原始Li2O2相比,相干电子传输减少了2至3个数量级。然而,在放电过程中,Li2O2 @ Li2CO3界面可以为快速电子极化子跳跃提供替代的面内通道,从而可以提高电子电导率并最终提高非水Li-O-2电池的实际容量。

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