电解质
锂(药物)
氧气
分解
化学工程
化学
二甲基乙酰胺
化学稳定性
无机化学
材料科学
离子电导率
电导率
电极
有机化学
溶剂
物理化学
医学
工程类
内分泌学
作者
Jin‐Hyuk Kang,Jiwon Park,Moony Na,Rak Hyeon Choi,Hye Ryung Byon
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2022-10-31
卷期号:7 (12): 4248-4257
被引量:12
标识
DOI:10.1021/acsenergylett.2c01796
摘要
Lithium–oxygen (Li-O2) batteries suffer from undesirable chemical reactions. Side products, such as lithium carbonates (Li2CO3), undergo partial decomposition during charging, and their accumulation leads to poor cyclability. Herein, we show significantly improved cyclability by forming peroxodicarbonate (C2O62–) as the soluble discharging product, hence preserving its stability at low temperatures. The Li-O2 cells comprising 10% CO2 gas and tetraglyme electrolyte solution form anhydride-linked C2O62–. However, despite the improved stability of C2O62– at 0 °C, the low ionic conductivity of tetraglyme results in poor cyclability. In contrast, dimethylacetamide-based cells produce peroxo-linked C2O62– and offer over 100 cycles at −10 °C. During cycles, the first charging plateaus belonging to C2O62– oxidation appear consistently at 3.75 V (vs Li/Li+). In addition, Li2CO3 is entirely decomposed during the second charging plateau at 4.45 V. Our results show promise for the development of highly rechargeable Li-O2/CO2 batteries.
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