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Monitoringthe Electrochemical Processes in the Lithium–AirBattery by Solid State NMR Spectroscopy

机译:监控方式锂空气中的电化学过程固态NMR光谱法测定电池

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摘要

A multi-nuclear solid-state NMR approach is employed to investigate the lithium–air battery, to monitor the evolution of the electrochemical products formed during cycling, and to gain insight into processes affecting capacity fading. While lithium peroxide is identified by 17O solid state NMR (ssNMR) as the predominant product in the first discharge in 1,2-dimethoxyethane (DME) based electrolytes, it reacts with the carbon cathode surface to form carbonate during the charging process. 13C ssNMR provides evidence for carbonate formation on the surface of the carbon cathode, the carbonate being removed at high charging voltages in the first cycle, but accumulating in later cycles. Small amounts of lithium hydroxide and formate are also detected in discharged cathodes and while the hydroxide formation is reversible, the formate persists and accumulates in the cathode upon further cycling. The results indicate that the rechargeability of the battery is limited by both the electrolyte and the carbon cathode stability. The utility of ssNMR spectroscopy in directly detecting product formation and decomposition within the battery is demonstrated,a necessary step in the assessment of new electrolytes, catalysts,and cathode materials for the development of a viable lithium–oxygenbattery.
机译:采用多核固态NMR方法研究锂-空气电池,监视循环过程中形成的电化学产物的演变,并深入了解影响容量衰减的过程。过氧化锂通过 17 固态NMR(ssNMR)鉴定为基于1,2-二甲氧基乙烷(DME)的电解质首次放电的主要产物,但它与碳阴极表面反应形成充电过程中碳酸盐。 13 C ssNMR为碳阴极表面形成碳酸盐提供了证据,碳酸盐在第一个循环中以高充电电压被除去,但在随后的循环中积累。在放电的阴极中还检测到少量的氢氧化锂和甲酸锂,尽管氢氧化物的形成是可逆的,但甲酸根在进一步循环后仍会保留并累积在阴极中。结果表明,电池的可充电性受到电解质和碳阴极稳定性的限制。展示了ssNMR光谱在直接检测电池内产品形成和分解中的用途,评估新电解质,催化剂的必要步骤,和阴极材料,用于开发可行的锂氧电池。

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