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首页> 外文期刊>Nano letters >Achieving Low Overpotential Li-O-2 Battery Operations by Li2O2 Decomposition through One-Electron Processes
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Achieving Low Overpotential Li-O-2 Battery Operations by Li2O2 Decomposition through One-Electron Processes

机译:通过单电子过程中的Li2O2分解实现低电位的Li-O-2电池操作

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摘要

As a promising high-capacity energy storage technology, Li-O-2 batteries face two critical challenges, poor cycle lifetime and low round-trip efficiencies, both of which are connected to the high overpotentials. The problem is particularly acute during recharge, where the reactions typically follow two-electron mechanisms that are inherently slow. Here we present a strategy that can significantly reduce recharge overpotentials. Our approach seeks to promote Li2O2 decomposition by one-electron processes, and the key is to stabilize the important intermediate of superoxide species. With the introduction of a highly polarizing electrolyte, we observe that recharge processes are successfully switched from a two-electron pathway to a single-electron one. While a similar one-electron route has been reported for the discharge processes, it has rarely been described for recharge except for the initial stage due to the poor mobilities of surface bound superoxide ions (O-2(-)), a necessary intermediate for the mechanism. Key to our observation is the solvation of O-2(-) by an ionic liquid electrolyte (PYR14TESI). Recharge overpotentials as low as 0.19 V at 100 mA/g(carbon) are measured.
机译:作为一种有前途的大容量储能技术,Li-O-2电池面临两个关键挑战,即循环寿命差和往返效率低,这两个方面都与高电势有关。该问题在充电过程中尤为严重,在该过程中,反应通常遵循固有地缓慢的两电子机理。在这里,我们提出一种可以显着降低充电超电势的策略。我们的方法旨在通过单电子过程促进Li2O2的分解,关键是稳定超氧化物类的重要中间体。随着高极化电解质的引入,我们观察到充电过程已成功地从两电子路径切换到单电子路径。尽管已经报道了放电过程中类似的单电子路线,但除了初始阶段,由于表面结合的超氧化物离子(O-2(-))的迁移率很低,因此很少有人描述它可以进行充电,这是制备锂的必要中间体。机制。我们观察的关键是离子液体电解质(PYR14TESI)对O-2(-)的溶剂化作用。在100 mA / g(碳)下测得的充电过电势低至0.19 V.

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