过电位
钝化
氧化还原
电化学
电解质
阴极
化学工程
分解
化学
材料科学
电池(电)
无机化学
电极
纳米技术
物理化学
有机化学
热力学
图层(电子)
功率(物理)
工程类
物理
作者
Hao Wan,Yingjie Sun,Jia Yu,Qianqi Shi,Yongchun Zhu,Yitai Qian
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2022-06-22
卷期号:15 (9): 8101-8108
被引量:5
标识
DOI:10.1007/s12274-022-4490-4
摘要
Low discharge capacity and poor cycle stability are the major obstacles hindering the operation of Li-O2 batteries with high-energy-density. These obstacles are mainly caused by the cathode passivation behaviours and the accumulation of by-products. Promoting the discharge process in solution and accelerating the decomposition of discharge products and by-products are able to alleviate above problems to some extent. Herein, chiral salen-Co(II) complex, (1R,2R)-(-)-N,N-bis(3,5-di-t-butylsalicylidene)-1,2-cyclohexanediaminocobalt(II) (Co(II)) as a multi-functional redox mediator was introduced into electrolyte to induce solution phase formation of Li2O2 and catalyze the oxidation of Li2O2 and main by-products Li2CO3. Due to the Co(II) has the solvation effect towards Li+, it can drive solution phase formation of Li2O2, to prevent electrode from passivation and then increase the discharge capacity with a high Li2O2 yield of 96.09 %. Furthermore, the Co(II) possesses suitable redox couple potentials, and it does so while simultaneously boosting the oxidization of Li2O2 and the decomposition of Li2CO3, reducing charge overpotential, and promoting cycle lifespan. Thereby, a cell with Co(II) achieved a long cycling stability at low charge plateau (3.66 V) over 252 cycles with a specific capacity of 500 mAh·gcarbon−1.
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