电解质
阴极
亲核细胞
钝化
材料科学
食腐动物
电极
电化学
反应性(心理学)
氧化物
化学工程
氧化剂
无机化学
纳米技术
化学
激进的
有机化学
图层(电子)
物理化学
催化作用
工程类
医学
替代医学
病理
冶金
作者
Baodan Zhang,Lingling Wang,Xiaotong Wang,Shiyuan Zhou,Ang Fu,Yawen Yan,Qingsong Wang,Qingshui Xie,Dong‐Liang Peng,Yu Qiao,Shi‐Gang Sun
标识
DOI:10.1016/j.ensm.2022.09.032
摘要
Triggering O-related anionic redox reactivity can introduce additional capacity in Li-rich layered oxide (LRLO) cathode, while, activated oxygen species also threatens to electrode-electrolyte interface stability. Herein, revealed by in-situ SERS/Raman, we demonstrate that enrichment of superoxo-related species on LRLO surface would significantly aggravate electrolyte degradation by nucleophilic attack, and confuse/deteriorate the architecture of cathode electrolyte interface (CEI) on LRLO. Through rational introducing LiBOB as a boron-contained electrolyte additive, enhanced CEI was achieved with BOB-derived cross-linking and B-F/BxOy polymeric components. More importantly, benefitting from its synergy effect with LiPF6, the sustained release of LiDFOB acts as a superoxo scavenger, which efficiently eliminates related nucleophilic attack. Tailoring the CEI into a uniform, dense, and stable passivate protection front-face, LiBOB additive enhances the cycling stability of LRLO, delivered 92.5% capacity retention (300 cycles). This work arouses reconsideration on the design/modification principle of electrolyte for LRLO cathode, and emphasizes the in-situ superoxo scavenging process.
科研通智能强力驱动
Strongly Powered by AbleSci AI