电解质
阴极
溶解
硼
相间
材料科学
分解
离子
化学工程
电极
化学
分析化学(期刊)
物理化学
有机化学
遗传学
生物
工程类
作者
Zhaoyu Sun,Fangkun Li,Jieying Ding,Zhiye Lin,Mengqing Xu,Min Zhu,Jun Liu
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2023-05-04
卷期号:8 (6): 2478-2487
被引量:26
标识
DOI:10.1021/acsenergylett.3c00324
摘要
Commercial LIBs have the problem of instability interface of electrolyte/cathode at high voltage and high temperature. This work reports a novel series of electron-defect boron compounds to construct stable interfaces of LCO/electrolyte. The results of theoretical calculation indicate that compounds of DPD scaffold can win in the competitive oxidation decomposition for interface regulation. F-rich and B-rich interface is designed by modifying the functional group of DPD scaffold. This strategy of in situ interface design successfully suppresses the dissolution of harmful transition metal ions and the nucleophilic reaction between electrolyte and cathode. Li/LCO cell can remain stable at high voltage (4.5 V) and high temperature (70 °C) in commercial carbonate electrolyte after DPD-F interphase formation. Meanwhile, faster Li+ extraction and insertion kinetics of DPD-F-interface make the Li/LCO cell stable at 4.6 V. Spectral characterizations and theoretical calculations uncover the secret of the forming process of this DPD-F-interface.
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