多功能电解质添加剂化学实现高性能Li||NMC622电池

IF 5.5 3区 材料科学 Q1 ELECTROCHEMISTRY
Girum Girma Bizuneh , Amir Mahmoud Makin Adam , Chunlei Zhu , Junda Huang , Huaping Wang , Zhongsheng Wang , Daxiong Wu , Lei Guo , Maryam Chafiq , Young Gun Ko
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引用次数: 0

摘要

富镍阴极LiNi0.6Mn0.2Co0.2O2 (NMC622)因其高比容量和低廉的成本被认为是锂金属电池可行的阴极候选材料。然而,由于接口稳定性差,它容易受到容量快速衰减的影响。在这项研究中,我们提出了一种三功能电解质添加剂策略,通过在NMC622阴极上形成坚固的富锂阴极电解质界面(CEI)和在Li阳极上形成固体电解质界面(SEI),以及以4-(三氟甲基)苯甲酸酐(FMBA)为添加剂清除HF以防止电极腐蚀,从而稳定电极/电解质界面。在0.75℃下,Li||NMC622可以稳定运行300次,保留率为78% (140 mA h g-1)。此外,具有FMBA的对称Li||锂电池可以在0.5 mA cm-2的过电位下维持950 h的电镀/剥离。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
High Performance Li||NMC622 Battery Enabled by Multi-Functional Electrolyte Additive Chemistry
Nickel-rich cathode LiNi0.6Mn0.2Co0.2O2 (NMC622) is considered a viable cathode candidate for lithium metal batteries because of its high specific capacity and inexpensive cost. However, it is susceptible to rapid capacity fading because of the poor interface stability. In this study, we presented a tri-functional electrolyte additive strategy for stabilizing electrode/electrolyte interfaces through forming robust LiF-rich cathode electrolyte interphase (CEI) on NMC622 cathode and solid electrolyte interphase (SEI) on Li anode as well as scavenging HF to prevent electrodes from corrosion with 4-(trifluoromethyl) benzoic anhydride (FMBA) as the additive. Li||NMC622 with such additive could stably operate up to 300 cycles with a retention of 78 % (140 mA h g-1) at 0.75 C. Moreover, symmetric Li||Li cell with FMBA could sustain >950 h plating/stripping with narrow overpotential at 0.5 mA cm-2.
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来源期刊
Electrochimica Acta
Electrochimica Acta 工程技术-电化学
CiteScore
11.30
自引率
6.10%
发文量
1634
审稿时长
41 days
期刊介绍: Electrochimica Acta is an international journal. It is intended for the publication of both original work and reviews in the field of electrochemistry. Electrochemistry should be interpreted to mean any of the research fields covered by the Divisions of the International Society of Electrochemistry listed below, as well as emerging scientific domains covered by ISE New Topics Committee.
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