Technische Universität München, Chair for Technical Electrochemistry, Department of Chemistry and Catalysis Research Center, Germany.
Forschungszentrum Jülich, Institut für Energie- und Klimaforschung, Grundlagen der Elektrochemie (IEK-9), 52425, Jülich, Germany.
Angew Chem Int Ed Engl. 2016 Jun 6;55(24):6892-5. doi: 10.1002/anie.201602142. Epub 2016 May 4.
Aprotic lithium-oxygen (Li-O2 ) batteries have attracted considerable attention in recent years owing to their outstanding theoretical energy density. A major challenge is their poor reversibility caused by degradation reactions, which mainly occur during battery charge and are still poorly understood. Herein, we show that singlet oxygen ((1) Δg ) is formed upon Li2 O2 oxidation at potentials above 3.5 V. Singlet oxygen was detected through a reaction with a spin trap to form a stable radical that was observed by time- and voltage-resolved in operando EPR spectroscopy in a purpose-built spectroelectrochemical cell. According to our estimate, a lower limit of approximately 0.5 % of the evolved oxygen is singlet oxygen. The occurrence of highly reactive singlet oxygen might be the long-overlooked missing link in the understanding of the electrolyte degradation and carbon corrosion reactions that occur during the charging of Li-O2 cells.
非质子锂-氧(Li-O2)电池近年来因其出色的理论能量密度而引起了广泛关注。一个主要的挑战是由于降解反应导致的较差的可逆性,这些降解反应主要发生在电池充电过程中,目前仍了解甚少。在此,我们表明,在高于 3.5 V 的电势下,Li2O2 氧化会形成单线态氧((1)Δg)。通过与自旋捕获剂反应来检测单线态氧,形成稳定的自由基,然后通过在特制的光谱电化学电池中进行时间和电压分辨的原位电子顺磁共振(EPR)光谱学来观察到该自由基。根据我们的估计,大约有 0.5%的演化氧是单线态氧。高度反应性的单线态氧的出现可能是理解在 Li-O2 电池充电过程中发生的电解质降解和碳腐蚀反应中被长期忽视的缺失环节。