氧化还原
阴极
材料科学
锰
无机化学
化学
化学工程
冶金
物理化学
工程类
作者
Zhijun Wu,Chenhui Yan,Panyu Gao,Liaona She,Xin Zhang,Yue Lin,Xuebin Yu,Yongfeng Liu,Wenping Sun,Yinzhu Jiang,Yaxiong Yang,Hongge Pan,Hongge Pan
出处
期刊:Small
[Wiley]
日期:2024-05-19
卷期号:20 (37): e2401645-e2401645
被引量:10
标识
DOI:10.1002/smll.202401645
摘要
Anionic redox chemistry enables extraordinary capacity for Li- and Mn-rich layered oxides (LMROs) cathodes. Unfortunately, irreversible surface oxygen evolution evokes the pernicious phase transition, structural deterioration, and severe electrode-electrolyte interface side reaction with element dissolution, resulting in fast capacity and voltage fading of LMROs during cycling and hindering its commercialization. Herein, a redox couple strategy is proposed by utilizing copper phthalocyanine (CuPc) to address the irreversibility of anionic redox. The Cu-N synergistic effect of CuPc could not only inhibit surface oxygen evolution by reducing the peroxide ion O2 2- back to lattice oxygen O2-, but also enhance the reaction activity and reversibility of anionic redox in bulk to achieve a higher capacity and cycling stability. Moreover, the CuPc strategy suppresses the interface side reaction and induces the forming of a uniform and robust LiF-rich cathode electrolyte, interphase (CEI) to significantly eliminate transition metal dissolution. As a result, the CuPc-enhanced LMRO cathode shows superb cycling performance with a capacity retention of 95.0% after 500 long-term cycles. This study sheds light on the great effect of N-based redox couple to regulate anionic redox behavior and promote the development of high energy density and high stability LMROs cathode.
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