锰
相间
阴极
对偶(语法数字)
原位
钾
材料科学
氧化锰
氧化物
纳米技术
冶金
化学工程
化学
工程类
生物
有机化学
细胞生物学
物理化学
艺术
文学类
作者
Kaixiang Lei,Zhuo Zhu,Zhengxuan Yin,Pengfei Yan,Fujun Li,Jun Chen
出处
期刊:Chem
[Elsevier BV]
日期:2019-11-14
卷期号:5 (12): 3220-3231
被引量:127
标识
DOI:10.1016/j.chempr.2019.10.008
摘要
Summary Mn-based oxides have attracted extensive attention as electrode materials. However, the irreversible phase transition and Mn2+ dissolution result in their structure instability and performance decay. Here, we report dual interphase layers in situ formed on P2-K0.67MnO2 (P2-KMO) in 6.0 M of potassium bis(fluorosulfonyl)amide in diglyme (KFSI/G2) during charging. It is composed of a solid-electrolyte interphase (SEI) and K-poor spinel interlayer on P2-KMO, which are derived from the simultaneous decomposition of 6.0 M KFSI/G2 and disproportionation of surface Mn3+. They cooperatively enable the reversible phase transition of P2↔P″2 in the bulk P2-KMO and mitigate Mn loss. This leads to a high capacity retention of 90.5% and a Coulombic efficiency of 100% after 300 cycles. The investigation highlights the significance of interphase chemistry of electrode materials for potassium-ion batteries and beyond.
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