阴极
材料科学
锂(药物)
磷酸
化学工程
镍
储能
降级(电信)
容量损失
相间
电解质
电极
电化学
纳米技术
冶金
化学
电气工程
生物
物理
工程类
内分泌学
物理化学
功率(物理)
医学
量子力学
遗传学
作者
Qiang Xie,Arumugam Manthiram
标识
DOI:10.1021/acs.chemmater.0c02374
摘要
With an increased energy density and cost advantage, ultrahigh-nickel layered oxides (LiNixM1 – xO2, x = 0.9–1.0) are becoming a front-runner as cathodes for next-generation lithium-based batteries, yet their commercialization is blocked both by severe capacity fade and exponentially aggravated air degradation. Thus, it is imperative to find effective solutions to address these issues simultaneously. Here, a significant enhancement in both cycling and air storage stability of the ultrahigh-Ni cathode LiNi0.94Co0.06O2 is achieved via a distinctive phosphoric acid treatment strategy. The modified cathode displays remarkably improved capacity retention (from 36 to 80% after 1000 cycles) and rate capability (from 0 to 105 mA h g–1 at a 30C rate) in pouch cells. Impressively, the modified cathode, after air storage for 450 days, maintains the morphology and 92% of the initial capacity of the fresh sample with excellent cyclability. Comprehensive interphase and structural analyses reveal that the enhanced electrochemical performance is due to a highly stabilized electrode/electrolyte interphase that suppresses electrode corrosion and lattice reconstruction. The excellent air stability results from an adsorption-buffering effect enabled by phosphoric acid to air attack. The study demonstrates an engineering pathway to improve cycling and air stability, facilitating the practical viability of high-capacity, affordable, ultrahigh-Ni cathodes in lithium-based batteries.
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