阴极
材料科学
氧化物
平面(几何)
亥姆霍兹自由能
吸附
化学工程
无机化学
纳米技术
化学
物理化学
热力学
有机化学
物理
冶金
几何学
数学
工程类
作者
Mei‐Yan Sun,Bo Liu,Xia Yang,Ya‐Xuan Wang,Yin‐Qi Zheng,Lan Wang,Liang Deng,Lei Zhao,Zhen‐Bo Wang
标识
DOI:10.1002/adma.202311432
摘要
Abstract Sodium layered‐oxides (Na x TMO 2 ) sustain severe interfacial stability issues when subjected to battery applications. Particularly at high potential, the oxidation limits including transition metal dissolution and solid electrolyte interphase reformation are intertwined upon the cathode, resulting in poor cycle ability. Herein, by rearranging the complex and structure of the Helmholtz absorption plane adjacent to Na x TMO 2 cathodes, the mechanism of constructing stable cathode/electrolyte interphase (CEI) to push up oxidation limits is clarified. The strong absorbent fluorinated anions replace the solvents into the inner Helmholtz plane, thereby reorganizing the Helmholtz absorption structure and spontaneously inducing anion‐dominated interphase to envelop more active sites for layered oxides. More importantly, such multi‐component CEI proves effective for the long‐term durability of a series of manganese‐based oxide cathodes, which achieves a 1500‐cycles lifetime against high oxidation voltage limit beyond 4.3 V. This work unravels the key role of breaking high‐oxidation limits in attaining higher energy density of layered‐oxide systems.
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