Leskes Michal, Moore Amy J, Goward Gillian R, Grey Clare P
Deparment of Chemistry, University of Cambridge , Lensfield Road, CB2 1EW, Cambridge, United Kingdom.
Department of Chemistry, McMaster University , 1280 Main Street West, Hamilton, Ontario L8S 4M1, Canada.
J Phys Chem C Nanomater Interfaces. 2013 Dec 27;117(51):26929-26939. doi: 10.1021/jp410429k. Epub 2013 Nov 27.
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 O 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. C 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-oxygen battery.
采用多核固态核磁共振方法来研究锂空气电池,监测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。虽然过氧化锂通过氧固态核磁共振(ssNMR)被确定为在基于1,2 - 二甲氧基乙烷(DME)的电解质中首次放电时的主要产物,但它在充电过程中会与碳阴极表面反应形成碳酸盐。碳固态核磁共振为碳阴极表面碳酸盐的形成提供了证据,该碳酸盐在第一个循环的高充电电压下被去除,但在后续循环中会积累。在放电后的阴极中还检测到少量氢氧化锂和甲酸盐,虽然氢氧化锂的形成是可逆的,但甲酸盐会持续存在并在进一步循环时在阴极中积累。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。证明了ssNMR光谱在直接检测电池内产物形成和分解方面的实用性,这是评估用于开发可行锂氧电池的新型电解质、催化剂和阴极材料的必要步骤。